Related gene-specific medical variations for Gene (Select 6236) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3156365	NM_004165.3(RRAD):c.40C>G (p.Arg14Gly)	LOC130059165, RRAD (R14G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612292	NM_004165.3(RRAD):c.222G>C (p.Glu74Asp)	LOC130059165, RRAD (E74D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353526	NM_004165.3(RRAD):c.120G>A (p.Met40Ile)	LOC130059165, RRAD (M40I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349538	NM_004165.3(RRAD):c.164C>A (p.Ala55Asp)	LOC130059165, RRAD (A55D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297957	NM_004165.3(RRAD):c.155C>T (p.Thr52Ile)	LOC130059165, RRAD (T52I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272079	NM_004165.3(RRAD):c.22A>G (p.Ser8Gly)	LOC130059165, RRAD (S8G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242100	NM_004165.3(RRAD):c.35G>C (p.Gly12Ala)	LOC130059165, RRAD (G12A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar