ClinVar Miner

List of variants in gene AXDND1, NPHS2 studied for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP
NM_144696.6(AXDND1):c.3032-12C>T rs1553313479
NM_144696.6(AXDND1):c.3032-1819A>C rs376637418
NM_144696.6(AXDND1):c.3032-1830C>T rs1057516523
NM_144696.6(AXDND1):c.3032-1848G>A rs869312747
NM_144696.6(AXDND1):c.3032-1853C>A rs201408880
NM_144696.6(AXDND1):c.3032-1859dup
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.3032-1908C>T rs751767084
NM_144696.6(AXDND1):c.3032-1910C>T rs1553312833
NM_144696.6(AXDND1):c.3032-1911A>T rs967339926
NM_144696.6(AXDND1):c.3032-21A>T rs775006954
NM_144696.6(AXDND1):c.3032-3048T>C rs377374469
NM_144696.6(AXDND1):c.3032-3051_3032-3050del rs774075788
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.3032-3116T>A
NM_144696.6(AXDND1):c.3032-3121G>C rs1553312393
NM_144696.6(AXDND1):c.3032-3135del rs775170915
NM_144696.6(AXDND1):c.3032-3141G>A rs1410592
NM_144696.6(AXDND1):c.3032-3151G>A rs763818901
NM_144696.6(AXDND1):c.3032-3152C>T rs776859868
NM_144696.6(AXDND1):c.3032-3166G>A rs748203170
NM_144696.6(AXDND1):c.3032-3208_3032-3197del rs1553312282
NM_144696.6(AXDND1):c.3032-3225T>C rs3818587
NM_144696.6(AXDND1):c.3032-3249dup rs1057516900
NM_144696.6(AXDND1):c.3032-32C>G rs369697947
NM_144696.6(AXDND1):c.3032-3318_3032-3313del rs1553312159
NM_144696.6(AXDND1):c.3032-3393C>G rs1410591
NM_144696.6(AXDND1):c.3032-3496C>T rs1410590
NM_144696.6(AXDND1):c.3032-3512C>T rs114905610
NM_144696.6(AXDND1):c.3032-3539C>T rs2274623
NM_144696.6(AXDND1):c.3032-3548G>C rs193266499
NM_144696.6(AXDND1):c.3032-3597T>C rs2274622
NM_144696.6(AXDND1):c.3032-3679G>T rs886045595
NM_144696.6(AXDND1):c.3032-3767T>C rs1060775

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