List of variants in gene NPHS1 reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004646.4(NPHS1):c.1022G>C (p.Ser341Thr)	rs976105039
NM_004646.4(NPHS1):c.1873G>T (p.Ala625Ser)	rs1973122430
NM_004646.4(NPHS1):c.791C>A (p.Pro264Gln)	rs34982899

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