Related gene-specific medical variations for Gene (Select 129932866) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3101416	NM_003272.4(GPR137B):c.113C>A (p.Pro38His)	GPR137B, LOC129932866 (P38H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473288	NM_003272.4(GPR137B):c.14G>T (p.Arg5Leu)	GPR137B, LOC129932866 (R5L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456280	NM_003272.4(GPR137B):c.131G>C (p.Gly44Ala)	GPR137B, LOC129932866 (G44A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301971	NM_003272.4(GPR137B):c.40G>A (p.Gly14Ser)	GPR137B, LOC129932866 (G14S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235009	NM_003272.4(GPR137B):c.146A>C (p.Tyr49Ser)	GPR137B, LOC129932866 (Y49S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228487	NM_003272.4(GPR137B):c.65A>G (p.Asp22Gly)	GPR137B, LOC129932866 (D22G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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