Related gene-specific medical variations for Gene (Select 126805746) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3178087	NM_032027.3(TM2D1):c.76G>C (p.Val26Leu)	LOC126805746, TM2D1 (V26L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178086	NM_032027.3(TM2D1):c.122G>C (p.Gly41Ala)	LOC126805746, TM2D1 (G41A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358166	NM_032027.3(TM2D1):c.25C>T (p.Pro9Ser)	LOC126805746, TM2D1 (P9S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351592	NM_032027.3(TM2D1):c.29C>T (p.Ser10Phe)	LOC126805746, TM2D1 (S10F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346462	NM_032027.3(TM2D1):c.97T>G (p.Trp33Gly)	LOC126805746, TM2D1 (W33G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313673	NM_032027.3(TM2D1):c.58G>A (p.Val20Ile)	LOC126805746, TM2D1 (V20I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248328	NM_032027.3(TM2D1):c.146A>G (p.Glu49Gly)	LOC126805746, TM2D1 (E49G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar