C3810401[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1080824	NM_006172.4(NPPA):c.375G>A (p.Leu125=)	LOC114827827, NPPA +1 more	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 6 +1 more	GLikely benign
Select item 948535	NM_006172.4(NPPA):c.319C>T (p.Arg107Ter)	LOC114827827, NPPA +1 more (R107*)	Single nucleotide variant (nonsense)	Atrial fibrillation, familial, 6 +1 more	GUncertain significance
Select item 240293	NM_006172.4(NPPA):c.253G>A (p.Gly85Arg)	LOC114827827, NPPA +1 more (G85R)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 6 +1 more	GUncertain significance
Select item 469605	NM_006172.4(NPPA):c.197C>T (p.Pro66Leu)	LOC114827827, NPPA +1 more (P66L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 126847	NM_006172.4(NPPA):c.190A>C (p.Ser64Arg)	NPPA, NPPA-AS1 +1 more (S64R)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 6 +2 more	GBenign/Likely benign
Select item 944170	NM_006172.4(NPPA):c.25G>A (p.Val9Met)	LOC114827827, NPPA (V9M)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 6 +1 more	GUncertain significance

ClinVar