ClinVar for Gene (Select 115072896) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 320

<< First< Prev

Page of 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3358509	NM_019844.4(SLCO1B3):c.1666_1669del (p.Ile556fs)	SLCO1B3, SLCO1B3-SLCO1B7 (I528fs +1 more)	Deletion (frameshift variant)	SLCO1B3-related disorder	GUncertain significance
Select item 3357272	NM_019844.4(SLCO1B3):c.1154C>T (p.Thr385Met)	SLCO1B3, SLCO1B3-SLCO1B7 (T357M +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 3356506	NM_019844.4(SLCO1B3):c.1815C>T (p.Asn605=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3356221	NM_019844.4(SLCO1B3):c.1648A>G (p.Thr550Ala)	SLCO1B3, SLCO1B3-SLCO1B7 (T522A +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 3355885	NM_019844.4(SLCO1B3):c.1136-6T>A	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related disorder	GLikely benign
Select item 3355109	NM_019844.4(SLCO1B3):c.1244C>T (p.Ser415Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (S387L +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 3353004	NM_019844.4(SLCO1B3):c.1150C>A (p.Pro384Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (P356T +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 3352662	NM_019844.4(SLCO1B3):c.227-5dup	SLCO1B3, SLCO1B3-SLCO1B7	Duplication (intron variant)	SLCO1B3-related disorder	GLikely benign
Select item 3352259	NM_019844.4(SLCO1B3):c.1865+10C>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related disorder	GLikely benign
Select item 3351019	NM_019844.4(SLCO1B3):c.141_143del (p.Ile47del)	SLCO1B3, SLCO1B3-SLCO1B7 (I19del +1 more)	Deletion (inframe_deletion)	SLCO1B3-related disorder	GLikely benign
Select item 3349276	NM_019844.4(SLCO1B3):c.509T>C (p.Met170Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (M142T +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 3345603	NM_019844.4(SLCO1B3):c.1065T>G (p.Ser355=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3320360	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-44413C>T	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3320358	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-18592C>G	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3320357	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-23953T>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3320356	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-18511C>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3320355	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-23955G>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3320354	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-18512G>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3320353	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-45745T>C	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3320352	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-18421C>T	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3320351	NM_019844.4(SLCO1B3):c.1289G>A (p.Cys430Tyr)	SLCO1B3, SLCO1B3-SLCO1B7 (C402Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320350	NM_019844.4(SLCO1B3):c.358T>C (p.Tyr120His)	SLCO1B3, SLCO1B3-SLCO1B7 (Y120H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320349	NM_019844.4(SLCO1B3):c.80T>G (p.Phe27Cys)	SLCO1B3, SLCO1B3-SLCO1B7 (F27C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165815	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-48071G>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165814	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-20266G>C	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165813	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-23787C>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165812	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-23817T>C	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165811	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-44044T>C	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165810	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-44108G>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165809	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-44112G>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165808	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-44121A>G	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165807	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-44341C>T	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165806	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-44356T>G	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165805	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-45827C>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165804	NM_001371097.1(SLCO1B3-SLCO1B7):c.1976C>T (p.Thr659Met)	SLCO1B3-SLCO1B7, SLCO1B7 (T659M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165803	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-12781T>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165802	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-12809C>T	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3165801	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-18425T>G	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165800	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-18434G>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165799	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-18497A>G	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3165798	NM_019844.4(SLCO1B3):c.97G>A (p.Ala33Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (A5T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165797	NM_019844.4(SLCO1B3):c.745C>T (p.Pro249Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (P249S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165796	NM_019844.4(SLCO1B3):c.646G>A (p.Gly216Arg)	SLCO1B3, SLCO1B3-SLCO1B7 (G188R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165795	NM_019844.4(SLCO1B3):c.1982A>G (p.Asn661Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (N633S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165794	NM_019844.4(SLCO1B3):c.1180G>A (p.Gly394Arg)	SLCO1B3, SLCO1B3-SLCO1B7 (G366R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165793	NM_019844.4(SLCO1B3):c.1141A>G (p.Ile381Val)	SLCO1B3, SLCO1B3-SLCO1B7 (I353V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165792	NM_019844.4(SLCO1B3):c.1056T>G (p.Phe352Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (F324L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3061660	NM_019844.4(SLCO1B3):c.1863T>C (p.Phe621=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3060445	NM_019844.4(SLCO1B3):c.1672T>C (p.Leu558=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3054796	NM_019844.4(SLCO1B3):c.1866-9T>C	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related disorder	GLikely benign
Select item 3052155	NM_019844.4(SLCO1B3):c.1956A>G (p.Gln652=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant +1 more)	SLCO1B3-related disorder	GLikely benign
Select item 3051441	NM_019844.4(SLCO1B3):c.840G>A (p.Pro280=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3050120	NM_019844.4(SLCO1B3):c.1714A>G (p.Met572Val)	SLCO1B3, SLCO1B3-SLCO1B7 (M544V +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GLikely benign
Select item 3050106	NM_019844.4(SLCO1B3):c.1809C>G (p.Ser603=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3048853	NM_019844.4(SLCO1B3):c.1136-13_1136-9del	SLCO1B3, SLCO1B3-SLCO1B7	Deletion (intron variant)	SLCO1B3-related disorder	GLikely benign
Select item 3048222	NM_019844.4(SLCO1B3):c.482-10G>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related disorder	GLikely benign
Select item 3047856	NM_019844.4(SLCO1B3):c.226+5C>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related disorder	GLikely benign
Select item 3046175	NM_019844.4(SLCO1B3):c.1498-9del	SLCO1B3, SLCO1B3-SLCO1B7	Deletion (intron variant)	SLCO1B3-related disorder	GLikely benign
Select item 3045857	NM_019844.4(SLCO1B3):c.1980C>T (p.Asp660=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant +1 more)	SLCO1B3-related disorder	GLikely benign
Select item 3045044	NM_019844.4(SLCO1B3):c.153C>T (p.Ser51=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3032943	NM_019844.4(SLCO1B3):c.1290C>T (p.Cys430=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3032765	NM_019844.4(SLCO1B3):c.1328A>G (p.Asp443Gly)	SLCO1B3, SLCO1B3-SLCO1B7 (D415G +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 3032630	NM_019844.4(SLCO1B3):c.948A>G (p.Lys316=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3032507	NM_019844.4(SLCO1B3):c.1068T>C (p.Phe356=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3032132	NM_019844.4(SLCO1B3):c.702C>T (p.Tyr234=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3032033	NM_019844.4(SLCO1B3):c.489A>T (p.Val163=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3031908	NM_019844.4(SLCO1B3):c.1371T>C (p.Ser457=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3031104	NM_019844.4(SLCO1B3):c.300T>C (p.Gly100=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3030685	NM_019844.4(SLCO1B3):c.342A>G (p.Pro114=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related disorder	GLikely benign
Select item 3030300	NM_019844.4(SLCO1B3):c.1136-4C>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related disorder	GLikely benign
Select item 3029790	NM_019844.4(SLCO1B3):c.1827_1830del (p.Gln610fs)	SLCO1B3, SLCO1B3-SLCO1B7 (Q582fs +1 more)	Deletion (frameshift variant)	SLCO1B3-related disorder	GUncertain significance
Select item 3029090	NM_019844.4(SLCO1B3):c.1258T>G (p.Leu420Val)	SLCO1B3, SLCO1B3-SLCO1B7 (L392V +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GLikely benign
Select item 2921058	NM_019844.4(SLCO1B3):c.1732G>C (p.Val578Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (V550L +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2920903	NM_019844.4(SLCO1B3):c.1464A>G (p.Gly488=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	Rotor syndrome	GLikely benign
Select item 2920881	NM_019844.4(SLCO1B3):c.1843A>G (p.Ile615Val)	SLCO1B3, SLCO1B3-SLCO1B7 (I615V +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2920821	NM_019844.4(SLCO1B3):c.1200C>A (p.Phe400Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (F372L +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2636745	NM_019844.4(SLCO1B3):c.485G>A (p.Cys162Tyr)	SLCO1B3, SLCO1B3-SLCO1B7 (C134Y +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 2635830	NM_019844.4(SLCO1B3):c.1226A>G (p.Lys409Arg)	SLCO1B3, SLCO1B3-SLCO1B7 (K381R +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 2634724	NM_019844.4(SLCO1B3):c.143T>C (p.Met48Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (M20T +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 2634168	NM_019844.4(SLCO1B3):c.482-6C>A	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related disorder	GUncertain significance
Select item 2633485	NM_019844.4(SLCO1B3):c.1825G>A (p.Ala609Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (A581T +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 2632059	NM_019844.4(SLCO1B3):c.1720T>C (p.Phe574Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (F546L +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 2631904	NM_019844.4(SLCO1B3):c.1123A>C (p.Asn375His)	SLCO1B3, SLCO1B3-SLCO1B7 (N347H +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 2629244	NM_019844.4(SLCO1B3):c.763G>C (p.Val255Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (V227L +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related disorder	GUncertain significance
Select item 2620875	NM_019844.4(SLCO1B3):c.1997T>C (p.Met666Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (M666T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605496	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-51569G>T	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2598255	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-18529T>G	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2585172	NM_019844.4(SLCO1B3):c.83A>C (p.Lys28Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (K28T)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2554492	NM_001371097.1(SLCO1B3-SLCO1B7):c.1883T>C (p.Leu628Ser)	SLCO1B3-SLCO1B7, SLCO1B7 (L628S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543360	NM_019844.4(SLCO1B3):c.647G>T (p.Gly216Val)	SLCO1B3, SLCO1B3-SLCO1B7 (G188V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536184	NM_019844.4(SLCO1B3):c.4G>A (p.Asp2Asn)	SLCO1B3, SLCO1B3-SLCO1B7 (D2N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515683	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-15125A>G	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2515453	NM_019844.4(SLCO1B3):c.1615G>C (p.Ala539Pro)	SLCO1B3, SLCO1B3-SLCO1B7 (A511P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511599	NM_019844.4(SLCO1B3):c.292G>C (p.Gly98Arg)	SLCO1B3, SLCO1B3-SLCO1B7 (G98R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511223	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-48017C>T	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2495623	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-15156G>A	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2495124	NM_019844.4(SLCO1B3):c.1730T>A (p.Met577Lys)	SLCO1B3, SLCO1B3-SLCO1B7 (M577K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491157	NM_019844.4(SLCO1B3):c.1987A>G (p.Arg663Gly)	SLCO1B3, SLCO1B3-SLCO1B7 (R635G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476101	NM_001371097.1(SLCO1B3-SLCO1B7):c.1866-23808A>C	SLCO1B3-SLCO1B7, SLCO1B7	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2470180	NM_019844.4(SLCO1B3):c.697A>C (p.Met233Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (M233L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 4