"OMIM"[submitter] AND "LOC114827827"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 126846	NM_006172.4(NPPA):c.449G>A (p.Arg150Gln)	LOC114827827, NPPA +1 more (R150Q)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 6 +1 more	GConflicting classifications of pathogenicity
Select item 126847	NM_006172.4(NPPA):c.190A>C (p.Ser64Arg)	LOC114827827, NPPA +1 more (S64R)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 6 +3 more	GBenign/Likely benign