ClinVar Miner

List of variants in gene combination AXDND1, NPHS2 reported as likely pathogenic for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_144696.6(AXDND1):c.3032-1830C>T rs1057516523
NM_144696.6(AXDND1):c.3032-1887G>A
NM_144696.6(AXDND1):c.3032-1891_3032-1890del rs749740335
NM_144696.6(AXDND1):c.3032-1895G>A rs1057517164
NM_144696.6(AXDND1):c.3032-1898C>T rs1490010141
NM_144696.6(AXDND1):c.3032-1904C>T rs200482683
NM_144696.6(AXDND1):c.3032-1907G>A rs74315348
NM_144696.6(AXDND1):c.3032-1910C>T rs1553312833
NM_144696.6(AXDND1):c.3032-1911A>T rs967339926
NM_144696.6(AXDND1):c.3032-3059T>G rs1031744496
NM_144696.6(AXDND1):c.3032-3060C>T rs776016942
NM_144696.6(AXDND1):c.3032-3077G>A rs199506378
NM_144696.6(AXDND1):c.3032-3135del rs775170915
NM_144696.6(AXDND1):c.3032-3151G>A rs763818901
NM_144696.6(AXDND1):c.3032-3249dup rs1057516900

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