Related gene-specific medical variations for Gene (Select 22913) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3151338	NM_016732.3(RALY):c.820C>T (p.Arg274Trp)	LOC126863016, RALY (R258W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151337	NM_016732.3(RALY):c.575C>T (p.Thr192Met)	LOC126863016, RALY (T192M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386743	NM_016732.3(RALY):c.739G>A (p.Gly247Ser)	LOC126863016, RALY (G247S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357183	NM_016732.3(RALY):c.620G>A (p.Arg207His)	LOC126863016, RALY (R191H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204500	NM_016732.3(RALY):c.665A>G (p.Lys222Arg)	LOC126863016, RALY (K222R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 747105	NM_016732.3(RALY):c.705T>C (p.Gly235=)	LOC126863016, RALY	Single nucleotide variant (synonymous variant)	not provided	GBenign

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