List of variants in gene NPHS2 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_014625.4(NPHS2):c.413G>A (p.Arg138Gln)	rs74315342	0.00054
NM_014625.4(NPHS2):c.378+1G>A	rs762631237	0.00001
NM_014625.4(NPHS2):c.264del (p.Glu90fs)
NM_014625.4(NPHS2):c.28dup (p.Arg10fs)	rs1553316670
NM_014625.4(NPHS2):c.371G>A (p.Cys124Tyr)	rs2125790095
NM_014625.4(NPHS2):c.378G>C (p.Lys126Asn)	rs267598208
NM_014625.4(NPHS2):c.451+2T>A	rs786204708
NM_014625.4(NPHS2):c.451+3A>T
NM_014625.4(NPHS2):c.714G>C (p.Arg238Ser)	rs748812981
NM_014625.4(NPHS2):c.738+1G>T

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