ClinVar Miner

List of variants in gene combination KIRREL2, NPHS1 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: 4
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HGVS dbSNP
NM_004646.3(NPHS1):c.-170T>C rs401824
NM_004646.3(NPHS1):c.-81C>G rs73928331
NM_004646.3(NPHS1):c.43G>C (p.Gly15Arg) rs73928330
NM_004646.3(NPHS1):c.65C>T (p.Ala22Val) rs116617171

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