Variants in gene NPHS1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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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.1339G>A (p.Glu447Lys)	rs28939695	0.00067
NM_004646.4(NPHS1):c.1747G>A (p.Glu583Lys)	rs147641617	0.00059
NM_004646.4(NPHS1):c.803G>A (p.Arg268Gln)	rs115308424	0.00052
NM_004646.4(NPHS1):c.2869G>C (p.Val957Leu)	rs114849139	0.00044
NM_004646.4(NPHS1):c.1802G>C (p.Gly601Ala)	rs114615449	0.00041
NM_004646.4(NPHS1):c.1183G>A (p.Gly395Ser)	rs372069596	0.00015

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