Related gene-specific medical variations for Gene (Select 3167) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3106353	NM_005519.2(HMX2):c.797A>G (p.Asn266Ser)	HMX2, LOC124416925 (N266S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106352	NM_005519.2(HMX2):c.658G>C (p.Ala220Pro)	HMX2, LOC124416925 (A220P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608826	NM_005519.2(HMX2):c.731G>A (p.Arg244His)	HMX2, LOC124416925 (R244H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242593	NM_005519.2(HMX2):c.803A>G (p.Tyr268Cys)	HMX2, LOC124416925 (Y268C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222906	NM_005519.2(HMX2):c.746C>T (p.Pro249Leu)	HMX2, LOC124416925 (P249L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 779127	NM_005519.2(HMX2):c.665C>G (p.Ala222Gly)	HMX2, LOC124416925 (A222G)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar