ClinVar Miner

List of variants in gene combination CYP11B2, LOC106799834 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (962):
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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_000498.3(CYP11B2):c.*1047C>T rs886062739
NM_000498.3(CYP11B2):c.*1277G>A
NM_000498.3(CYP11B2):c.*1340T>A
NM_000498.3(CYP11B2):c.*204C>G rs773811282
NM_000498.3(CYP11B2):c.*205G>A
NM_000498.3(CYP11B2):c.*25A>C
NM_000498.3(CYP11B2):c.*298C>A
NM_000498.3(CYP11B2):c.*299G>A rs528171695
NM_000498.3(CYP11B2):c.*431A>C rs886062742
NM_000498.3(CYP11B2):c.*504C>T rs201487778
NM_000498.3(CYP11B2):c.*566C>T rs375938097
NM_000498.3(CYP11B2):c.*579T>C rs559136479
NM_000498.3(CYP11B2):c.*591T>G
NM_000498.3(CYP11B2):c.*613C>T
NM_000498.3(CYP11B2):c.*743C>T rs886062741
NM_000498.3(CYP11B2):c.*746G>A rs570202161
NM_000498.3(CYP11B2):c.*759A>T
NM_000498.3(CYP11B2):c.*789G>A rs61763990
NM_000498.3(CYP11B2):c.*876C>A
NM_000498.3(CYP11B2):c.*879G>A
NM_000498.3(CYP11B2):c.*972C>G rs886062740
NM_000498.3(CYP11B2):c.*993A>G
NM_000498.3(CYP11B2):c.1006G>A (p.Val336Met) rs373369254
NM_000498.3(CYP11B2):c.1021C>T (p.Arg341Cys) rs562670189
NM_000498.3(CYP11B2):c.1039G>A (p.Ala347Thr) rs746708275
NM_000498.3(CYP11B2):c.1086G>C (p.Leu362=) rs763197267
NM_000498.3(CYP11B2):c.1136G>T (p.Gly379Val)
NM_000498.3(CYP11B2):c.1201-9C>G
NM_000498.3(CYP11B2):c.1216T>G (p.Phe406Val)
NM_000498.3(CYP11B2):c.1343G>A (p.Arg448His)
NM_000498.3(CYP11B2):c.1398+10C>T
NM_000498.3(CYP11B2):c.1441A>T (p.Ile481Leu)
NM_000498.3(CYP11B2):c.1454A>G (p.Tyr485Cys)
NM_000498.3(CYP11B2):c.157C>T (p.Leu53=)
NM_000498.3(CYP11B2):c.256C>G (p.Pro86Ala) rs200283987
NM_000498.3(CYP11B2):c.280C>T (p.Pro94Ser)
NM_000498.3(CYP11B2):c.342G>A (p.Glu114=) rs779683417
NM_000498.3(CYP11B2):c.352G>A (p.Ala118Thr) rs372556807
NM_000498.3(CYP11B2):c.395+10G>A rs193166276
NM_000498.3(CYP11B2):c.424T>C (p.Leu142=) rs199988205
NM_000498.3(CYP11B2):c.427C>T (p.Arg143Trp)
NM_000498.3(CYP11B2):c.449C>T (p.Ser150Leu)
NM_000498.3(CYP11B2):c.477G>A (p.Pro159=) rs375242946
NM_000498.3(CYP11B2):c.529C>T (p.Leu177=) rs577489337
NM_000498.3(CYP11B2):c.591A>G (p.Ile197Met) rs886062744
NM_000498.3(CYP11B2):c.595+15G>T rs886062743
NM_000498.3(CYP11B2):c.674A>G (p.His225Arg) rs144140791
NM_000498.3(CYP11B2):c.743T>C (p.Ile248Thr) rs4547
NM_000498.3(CYP11B2):c.752A>G (p.Lys251Arg) rs752962897
NM_000498.3(CYP11B2):c.796T>G (p.Tyr266Asp)
NM_000498.3(CYP11B2):c.800-14T>C rs563246146
NM_000498.3(CYP11B2):c.844C>T (p.Arg282Cys) rs774989997
NM_000498.3(CYP11B2):c.845G>A (p.Arg282His)
NM_000498.3(CYP11B2):c.924T>C (p.Ser308=)
NM_000498.3(CYP11B2):c.979C>T (p.Leu327Phe)
NM_000498.3(CYP11B2):c.9C>A (p.Leu3=) rs148205451

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