Related gene-specific medical variations for Gene (Select 58530) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3292351	NM_021246.4(LY6G6D):c.64A>T (p.Met22Leu)	LY6G6D, LY6G6F-LY6G6D (M22L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121621	NM_021246.4(LY6G6D):c.397G>A (p.Gly133Arg)	LY6G6D, LY6G6F-LY6G6D (G133R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121620	NM_021246.4(LY6G6D):c.376C>A (p.Leu126Ile)	LY6G6D, LY6G6F-LY6G6D (L126I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537380	NM_021246.4(LY6G6D):c.133G>A (p.Gly45Ser)	LY6G6D, LY6G6F-LY6G6D (G294S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454318	NM_021246.4(LY6G6D):c.74A>G (p.Tyr25Cys)	LY6G6D, LY6G6F-LY6G6D (Y25C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355064	NM_021246.4(LY6G6D):c.115G>A (p.Val39Met)	LY6G6D, LY6G6F-LY6G6D (V39M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249926	NM_021246.4(LY6G6D):c.137G>A (p.Arg46Lys)	LY6G6D, LY6G6F-LY6G6D (R295K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2222241	NM_021246.4(LY6G6D):c.217G>A (p.Ala73Thr)	LY6G6D, LY6G6F-LY6G6D (A73T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar