Related gene-specific medical variations for Gene (Select 29992) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2323588	NM_013439.3(PILRA):c.203G>A (p.Arg68Lys)	LOC129998933, PILRA (R68K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1244384	NM_013439.3(PILRA):c.232A>G (p.Arg78Gly)	LOC129998933, PILRA (R78G)	Single nucleotide variant (missense variant)	not provided	GBenign