Related gene-specific medical variations for Gene (Select 5514) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3217401	NM_002714.4(PPP1R10):c.62G>A (p.Arg21Gln)	LOC126859644, PPP1R10 (R21Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531233	NM_002714.4(PPP1R10):c.106A>G (p.Ser36Gly)	LOC126859644, PPP1R10 (S36G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance