ClinVar Miner

List of variants in gene combination AXDND1, NPHS2 reported as uncertain significance 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: 16
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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.3032-1853C>A rs201408880
NM_144696.6(AXDND1):c.3032-1908C>T rs751767084
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.3032-3121G>C rs1553312393
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.3032-32C>G rs369697947
NM_144696.6(AXDND1):c.3032-3318_3032-3313del rs1553312159
NM_144696.6(AXDND1):c.3032-3512C>T rs114905610
NM_144696.6(AXDND1):c.3032-3548G>C rs193266499
NM_144696.6(AXDND1):c.3032-3679G>T rs886045595

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