Related gene-specific medical variations for Gene (Select 347736) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3315748	NM_001363941.2(ARMC8):c.1735A>C (p.Ile579Leu)	ARMC8, NME9 (I506L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129673	NM_001363941.2(ARMC8):c.1648A>G (p.Ser550Gly)	ARMC8, NME9 (S519G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129672	NM_001363941.2(ARMC8):c.1528A>G (p.Ser510Gly)	ARMC8, NME9 (S443G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346415	NM_001363941.2(ARMC8):c.1408G>A (p.Val470Ile)	ARMC8, NME9 (V397I +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277142	NM_001363941.2(ARMC8):c.1996A>G (p.Met666Val)	ARMC8, NME9 (M624V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1331617	NM_001363941.2(ARMC8):c.1998G>C (p.Met666Ile)	NME9, ARMC8 (M593I +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

ClinVar