List of variants in gene NPHS1 reported as uncertain significance by UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004646.4(NPHS1):c.1486C>A (p.Arg496Ser)	rs373264146	0.00011
NM_004646.4(NPHS1):c.710T>A (p.Leu237Gln)	rs373835033	0.00011
NM_004646.4(NPHS1):c.2344G>A (p.Glu782Lys)	rs549487912	0.00002
NM_004646.4(NPHS1):c.1240A>G (p.Thr414Ala)	rs1973174583

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