Related gene-specific medical variations for Gene (Select 57007) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2403469	NM_020311.3(ACKR3):c.137C>T (p.Thr46Met)	ACKR3, LOC126806571 (T46M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390217	NM_020311.3(ACKR3):c.92C>T (p.Thr31Met)	ACKR3, LOC126806571 (T31M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304849	NM_020311.3(ACKR3):c.136A>G (p.Thr46Ala)	ACKR3, LOC126806571 (T46A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227260	NM_020311.3(ACKR3):c.166G>A (p.Val56Ile)	ACKR3, LOC126806571 (V56I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208233	NM_020311.3(ACKR3):c.230A>G (p.Tyr77Cys)	ACKR3, LOC126806571 (Y77C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 709371	NM_020311.3(ACKR3):c.190G>C (p.Val64Leu)	ACKR3, LOC126806571 (V64L)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar