Related gene-specific medical variations for Gene (Select 9801) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2354584	NM_014763.4(MRPL19):c.23G>C (p.Gly8Ala)	LOC112841599, MRPL19 (G8A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337294	NM_014763.4(MRPL19):c.64G>T (p.Ala22Ser)	LOC112841599, MRPL19 (A22S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235597	NM_014763.4(MRPL19):c.37A>G (p.Met13Val)	LOC112841599, MRPL19 (M13V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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