"PreventionGenetics, part of Exact Sciences"[submitter] AND "ABCG1"[ge - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3035683	NM_207627.2(ABCG1):c.12G>A (p.Thr4=)	ABCG1	Single nucleotide variant (synonymous variant +1 more)	ABCG1-related disorder	GBenign
Select item 3053330	NM_016818.3(ABCG1):c.-38GCC[15]	ABCG1	Microsatellite (5 prime UTR variant +1 more)	ABCG1-related disorder	GBenign
Select item 3041521	NM_016818.3(ABCG1):c.-38GCC[11]	ABCG1	Microsatellite (5 prime UTR variant +1 more)	ABCG1-related disorder	GBenign
Select item 3037187	NM_016818.3(ABCG1):c.-38GCC[12]	ABCG1	Microsatellite (5 prime UTR variant +1 more)	ABCG1-related disorder	GBenign
Select item 3059271	NM_016818.3(ABCG1):c.-38GCC[9]	ABCG1	Microsatellite (5 prime UTR variant +1 more)	ABCG1-related disorder	GBenign
Select item 3059244	NM_016818.3(ABCG1):c.-38GCC[8]	ABCG1	Microsatellite (5 prime UTR variant +1 more)	ABCG1-related disorder	GBenign
Select item 3053710	NM_016818.3(ABCG1):c.-38GCC[6]	ABCG1	Microsatellite (5 prime UTR variant +1 more)	ABCG1-related disorder	GBenign
Select item 3047646	NM_016818.3(ABCG1):c.-38GCC[5]	ABCG1	Microsatellite (5 prime UTR variant +1 more)	ABCG1-related disorder	GLikely benign
Select item 3044620	NM_016818.3(ABCG1):c.9T>C (p.Cys3=)	ABCG1	Single nucleotide variant (synonymous variant +1 more)	ABCG1-related disorder	GBenign
Select item 3044875	NM_016818.3(ABCG1):c.138G>A (p.Thr46=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GLikely benign
Select item 3046123	NM_016818.3(ABCG1):c.183G>A (p.Thr61=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GLikely benign
Select item 719214	NM_016818.3(ABCG1):c.286+4G>A	ABCG1	Single nucleotide variant (intron variant)	ABCG1-related disorder +1 more	GBenign
Select item 3060995	NM_016818.3(ABCG1):c.339G>A (p.Leu113=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GBenign
Select item 711761	NM_016818.3(ABCG1):c.447C>G (p.Pro149=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder +1 more	GBenign
Select item 3056609	NM_016818.3(ABCG1):c.538-6C>T	ABCG1	Single nucleotide variant (intron variant)	ABCG1-related disorder	GBenign
Select item 3047290	NM_016818.3(ABCG1):c.609G>A (p.Ala203=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GLikely benign
Select item 3052439	NM_016818.3(ABCG1):c.771G>A (p.Ser257=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GLikely benign
Select item 3037791	NM_016818.3(ABCG1):c.993C>T (p.Gly331=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GBenign
Select item 3035558	NM_016818.3(ABCG1):c.1072G>A (p.Gly358Arg)	ABCG1 (G336R +4 more)	Single nucleotide variant (missense variant)	ABCG1-related disorder	GBenign
Select item 3049998	NM_016818.3(ABCG1):c.1173G>A (p.Thr391=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GLikely benign
Select item 3039074	NM_016818.3(ABCG1):c.1344C>T (p.Phe448=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GLikely benign
Select item 786373	NM_016818.3(ABCG1):c.1368G>C (p.Ala456=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder +1 more	GBenign
Select item 3044829	NM_016818.3(ABCG1):c.1722C>T (p.Phe574=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GBenign
Select item 3039239	NM_016818.3(ABCG1):c.1842C>T (p.Asp614=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder	GLikely benign
Select item 740389	NM_016818.3(ABCG1):c.1929C>T (p.Leu643=)	ABCG1	Single nucleotide variant (synonymous variant)	ABCG1-related disorder +1 more	GLikely benign

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Items: 25