ClinVar Miner

List of variants reported as benign for Finnish congenital nephrotic syndrome by Genome Diagnostics Laboratory, University Medical Center Utrecht

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_004646.4(NPHS1):c.349G>A (p.Glu117Lys) rs3814995 0.25613
NM_004646.4(NPHS1):c.2289C>T (p.Val763=) rs437168 0.15697
NM_004646.4(NPHS1):c.3230A>G (p.Asn1077Ser) rs4806213 0.10689
NM_004646.4(NPHS1):c.1223G>A (p.Arg408Gln) rs33950747 0.04436

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