List of variants in gene NPHS1 reported as uncertain significance by GeneDx

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_004646.4(NPHS1):c.697A>G (p.Thr233Ala)	rs35238405	0.00270
NM_004646.4(NPHS1):c.1151T>C (p.Met384Thr)	rs114112112	0.00091
NM_004646.4(NPHS1):c.1620G>C (p.Ala540=)	rs375861433	0.00042
NM_004646.4(NPHS1):c.1183G>A (p.Gly395Ser)	rs372069596	0.00015
NM_004646.4(NPHS1):c.3455C>T (p.Thr1152Met)	rs143145248	0.00009
NM_004646.4(NPHS1):c.609-10C>T	rs763508503	0.00004
NM_004646.4(NPHS1):c.1040G>A (p.Gly347Glu)	rs386833862
NM_004646.4(NPHS1):c.1606T>C (p.Ser536Pro)	rs1555762694
NM_004646.4(NPHS1):c.2020C>A (p.Pro674Thr)	rs2146822238
NM_004646.4(NPHS1):c.2437G>A (p.Ala813Thr)
NM_004646.4(NPHS1):c.3024A>G (p.Arg1008=)	rs1131691606
NM_004646.4(NPHS1):c.644T>A (p.Leu215Gln)	rs755962215
NM_004646.4(NPHS1):c.673G>C (p.Glu225Gln)
NM_004646.4(NPHS1):c.710T>C (p.Leu237Pro)	rs373835033

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