ClinVar Miner

List of variants in gene combination KIRREL2, NPHS1 reported as uncertain significance 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_004646.3(NPHS1):c.-31C>T rs376050812
NM_004646.3(NPHS1):c.-57G>T rs140404523
NM_004646.3(NPHS1):c.-61G>A rs75799457
NM_004646.3(NPHS1):c.41T>C (p.Leu14Pro) rs1060499706
NM_004646.3(NPHS1):c.65C>T (p.Ala22Val) rs116617171

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