Related gene-specific medical variations for Gene (Select 83547) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314326	NM_031430.3(RILP):c.373G>A (p.Asp125Asn)	LOC125177403, RILP (D125N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314324	NM_031430.3(RILP):c.412G>A (p.Gly138Ser)	LOC125177403, RILP (G138S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2606260	NM_031430.3(RILP):c.418G>A (p.Glu140Lys)	LOC125177403, RILP (E140K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592600	NM_031430.3(RILP):c.365G>C (p.Arg122Pro)	LOC125177403, RILP (R122P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296190	NM_031430.3(RILP):c.289C>T (p.Arg97Cys)	LOC125177403, RILP (R97C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207315	NM_031430.3(RILP):c.321G>T (p.Gln107His)	LOC125177403, RILP (Q107H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar