Related gene-specific medical variations for Gene (Select 283554) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3101430	NM_001099652.2(GPR137C):c.7G>A (p.Val3Met)	GPR137C, LOC130055645 (V3M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101427	NM_001099652.2(GPR137C):c.26C>T (p.Ala9Val)	GPR137C, LOC130055645 (A9V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517537	NM_001099652.2(GPR137C):c.125C>T (p.Pro42Leu)	GPR137C, LOC130055645 (P42L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409313	NM_001099652.2(GPR137C):c.20G>C (p.Gly7Ala)	GPR137C, LOC130055645 (G7A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237879	NM_001099652.2(GPR137C):c.41C>T (p.Pro14Leu)	GPR137C, LOC130055645 (P14L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227334	NM_001099652.2(GPR137C):c.58C>G (p.Pro20Ala)	GPR137C, LOC130055645 (P20A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222745	NM_001099652.2(GPR137C):c.56A>C (p.Glu19Ala)	GPR137C, LOC130055645 (E19A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar