Variants in gene NPHS2 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_014625.4(NPHS2):c.686G>A (p.Arg229Gln)	rs61747728	0.02796
NM_014625.4(NPHS2):c.413G>A (p.Arg138Gln)	rs74315342	0.00054
NM_014625.4(NPHS2):c.643C>T (p.Gln215Ter)	rs778055996	0.00003
NM_014625.4(NPHS2):c.714G>T (p.Arg238Ser)	rs748812981	0.00003
NM_014625.4(NPHS2):c.503G>A (p.Arg168His)	rs530318579	0.00001
NM_014625.4(NPHS2):c.535-1G>T	rs1291398331	0.00001
NM_014625.4(NPHS2):c.156del (p.Thr53fs)	rs1272948499
NM_014625.4(NPHS2):c.451+2T>A	rs786204708
NM_014625.4(NPHS2):c.452del	rs1250670041
NM_014625.4(NPHS2):c.502C>T (p.Arg168Cys)	rs786204583
NM_014625.4(NPHS2):c.586C>T (p.Arg196Ter)	rs12568913
NM_014625.4(NPHS2):c.685C>T (p.Arg229Ter)	rs1057516414
NM_014625.4(NPHS2):c.738+2T>C	rs1212702104

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