ClinVar Miner

List of variants in gene combination KIRREL2, NPHS1 reported as likely pathogenic for Finnish congenital nephrotic syndrome

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Total variants: 4
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HGVS dbSNP
NM_004646.3(NPHS1):c.-475_-468delGAGAGAGA rs139954720
NM_004646.3(NPHS1):c.45del (p.Leu16fs) rs1555764281
NM_004646.3(NPHS1):c.58+1G>A rs386833954
NM_004646.3(NPHS1):c.58+1G>T rs386833954

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