ClinVar Miner

List of variants reported as likely benign for Finnish congenital nephrotic syndrome by Counsyl

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Total variants: 8
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HGVS dbSNP
NM_004646.3(NPHS1):c.1339G>A (p.Glu447Lys) rs28939695
NM_004646.3(NPHS1):c.2262G>A (p.Gly754=) rs267605438
NM_004646.3(NPHS1):c.2398C>T (p.Arg800Cys) rs114896482
NM_004646.3(NPHS1):c.2869G>C (p.Val957Leu) rs114849139
NM_004646.3(NPHS1):c.3418C>A (p.Arg1140Ser) rs143092783
NM_004646.3(NPHS1):c.43G>C (p.Gly15Arg) rs73928330
NM_004646.3(NPHS1):c.563A>T (p.Asn188Ile) rs145125791
NM_004646.3(NPHS1):c.65C>T (p.Ala22Val) rs116617171

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