Related gene-specific medical variations for Gene (Select 256586) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3121727	NM_153374.3(LYSMD2):c.223G>A (p.Val75Ile)	LOC130057059, LYSMD2 (V75I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121726	NM_153374.3(LYSMD2):c.194G>T (p.Gly65Val)	LOC130057059, LYSMD2 (G65V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121725	NM_153374.3(LYSMD2):c.193G>A (p.Gly65Ser)	LOC130057059, LYSMD2 (G65S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121723	NM_153374.3(LYSMD2):c.154T>C (p.Tyr52His)	LOC130057059, LYSMD2 (Y52H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327454	NM_153374.3(LYSMD2):c.182C>T (p.Pro61Leu)	LOC130057059, LYSMD2 (P61L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315543	NM_153374.3(LYSMD2):c.80C>T (p.Pro27Leu)	LOC130057060, LYSMD2 (P27L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar