ClinVar Miner

List of variants in gene CYP11B1 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (962):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP
NM_000497.3(CYP11B1):c.*1164G>A rs886062735
NM_000497.3(CYP11B1):c.*1209C>T rs757505651
NM_000497.3(CYP11B1):c.*1358T>C rs886062734
NM_000497.3(CYP11B1):c.*1435T>C rs551125657
NM_000497.3(CYP11B1):c.*1590G>C rs886062733
NM_000497.3(CYP11B1):c.*1622C>T rs543935807
NM_000497.3(CYP11B1):c.*1770A>T rs369448045
NM_000497.3(CYP11B1):c.*245C>G rs538608688
NM_000497.3(CYP11B1):c.*400C>T rs61752801
NM_000497.3(CYP11B1):c.*485C>G rs886062737
NM_000497.3(CYP11B1):c.*495C>T rs886062736
NM_000497.3(CYP11B1):c.*613A>G rs1137480
NM_000497.3(CYP11B1):c.*670A>C rs879537131
NM_000497.3(CYP11B1):c.*737C>T rs748684062
NM_000497.3(CYP11B1):c.*848C>T rs149520110
NM_000497.3(CYP11B1):c.*857T>C rs370725779
NM_000497.3(CYP11B1):c.*901G>A rs748103274
NM_000497.3(CYP11B1):c.104T>C (p.Val35Ala) rs201951316
NM_000497.3(CYP11B1):c.187G>C (p.Asp63His) rs5282
NM_000497.3(CYP11B1):c.235T>A (p.Phe79Ile) rs1489638195
NM_000497.3(CYP11B1):c.243C>T (p.Tyr81=) rs9657022
NM_000497.3(CYP11B1):c.346T>G (p.Trp116Gly) rs772733691
NM_000497.3(CYP11B1):c.374A>G (p.His125Arg) rs757389720
NM_000497.3(CYP11B1):c.375C>G (p.His125Gln) rs201137503
NM_000497.3(CYP11B1):c.385G>A (p.Val129Met) rs377423817
NM_000497.3(CYP11B1):c.395+9C>T rs61751140
NM_000497.4(CYP11B1):c.*1012A>C
NM_000497.4(CYP11B1):c.*1253G>T
NM_000497.4(CYP11B1):c.*1264A>C
NM_000497.4(CYP11B1):c.*1296A>G
NM_000497.4(CYP11B1):c.*1313C>T
NM_000497.4(CYP11B1):c.*1476G>C
NM_000497.4(CYP11B1):c.*1511C>T
NM_000497.4(CYP11B1):c.*1550C>T
NM_000497.4(CYP11B1):c.*1623G>C
NM_000497.4(CYP11B1):c.*1929A>C
NM_000497.4(CYP11B1):c.*1944G>A
NM_000497.4(CYP11B1):c.*1979G>A
NM_000497.4(CYP11B1):c.*244C>T
NM_000497.4(CYP11B1):c.*317T>C
NM_000497.4(CYP11B1):c.*345C>A
NM_000497.4(CYP11B1):c.*390A>G
NM_000497.4(CYP11B1):c.*516A>T
NM_000497.4(CYP11B1):c.*596C>A
NM_000497.4(CYP11B1):c.*607C>T
NM_000497.4(CYP11B1):c.*614C>T
NM_000497.4(CYP11B1):c.*946G>A
NM_000497.4(CYP11B1):c.107T>G (p.Leu36Arg)
NM_000497.4(CYP11B1):c.206A>G (p.His69Arg)
NM_000497.4(CYP11B1):c.218A>G (p.Gln73Arg)
NM_000497.4(CYP11B1):c.244G>A (p.Asp82Asn)
NM_000497.4(CYP11B1):c.263T>C (p.Met88Thr)
NM_000497.4(CYP11B1):c.334A>C (p.Ser112Arg)
NM_000497.4(CYP11B1):c.395+6C>T rs553707049

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