ClinVar Miner

List of variants in gene NPHS2 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_014625.3(NPHS2):c.-51G>T rs12406197
NM_014625.3(NPHS2):c.-52C>G rs78541594
NM_014625.3(NPHS2):c.124G>A (p.Gly42Arg) rs559836164
NM_014625.3(NPHS2):c.288C>T (p.Ser96=) rs3738423
NM_014625.3(NPHS2):c.451+22dup rs748179295

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