"Ambry Genetics"[submitter] AND "LOC123038185"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3320367	NM_005630.3(SLCO2A1):c.1381G>C (p.Asp461His)	LOC123038185, SLCO2A1 (D461H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3165823	NM_005630.3(SLCO2A1):c.1297A>G (p.Thr433Ala)	LOC123038185, SLCO2A1 (T433A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance