Related gene-specific medical variations for Gene (Select 56834) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3132795	NM_032989.3(BAD):c.94T>G (p.Ser32Ala)	BAD, GPR137 (S32A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492154	NM_032989.3(BAD):c.193G>A (p.Gly65Arg)	BAD, GPR137 (G65R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481755	NM_032989.3(BAD):c.236G>T (p.Gly79Val)	BAD, GPR137 (G79V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459152	NM_032989.3(BAD):c.246C>G (p.Asp82Glu)	BAD, GPR137 (D82E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2381722	NM_032989.3(BAD):c.-8-15A>G	BAD, GPR137 (C9R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2339129	NM_032989.3(BAD):c.146G>A (p.Ser49Asn)	BAD, GPR137 (S49N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337374	NM_032989.3(BAD):c.97G>A (p.Gly33Ser)	BAD, GPR137 (G33S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233535	NM_032989.3(BAD):c.244G>A (p.Asp82Asn)	BAD, GPR137 (D82N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar