ClinVar Miner

List of variants in gene CYP7B1 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: 28
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HGVS dbSNP
NM_004820.5(CYP7B1):c.*111G>A rs140646421
NM_004820.5(CYP7B1):c.*337T>G rs118000312
NM_004820.5(CYP7B1):c.*402A>T rs189470710
NM_004820.5(CYP7B1):c.*529A>G rs113473170
NM_004820.5(CYP7B1):c.-11G>A rs886063077
NM_004820.5(CYP7B1):c.-144C>T rs191075257
NM_004820.5(CYP7B1):c.-73A>C rs72554625
NM_004820.5(CYP7B1):c.-89C>G rs6994347
NM_004820.5(CYP7B1):c.-99G>C rs886063078
NM_004820.5(CYP7B1):c.1018C>T (p.His340Tyr) rs757698965
NM_004820.5(CYP7B1):c.1162C>T (p.Arg388Ter) rs72554620
NM_004820.5(CYP7B1):c.123-19dup rs8192895
NM_004820.5(CYP7B1):c.1233G>A (p.Glu411=) rs369566738
NM_004820.5(CYP7B1):c.125G>A (p.Arg42Lys) rs375384257
NM_004820.5(CYP7B1):c.1310G>A (p.Cys437Tyr) rs886063072
NM_004820.5(CYP7B1):c.1323G>A (p.Pro441=) rs201281307
NM_004820.5(CYP7B1):c.1456C>T (p.Arg486Cys) rs116171274
NM_004820.5(CYP7B1):c.204G>A (p.Arg68=) rs377119798
NM_004820.5(CYP7B1):c.209T>A (p.Met70Lys) rs886063075
NM_004820.5(CYP7B1):c.260-15dup rs8192896
NM_004820.5(CYP7B1):c.261A>G (p.Gly87=) rs886063074
NM_004820.5(CYP7B1):c.349A>G (p.Lys117Glu) rs368626966
NM_004820.5(CYP7B1):c.522T>C (p.Ser174=) rs371522442
NM_004820.5(CYP7B1):c.56T>C (p.Leu19Pro) rs72554624
NM_004820.5(CYP7B1):c.929G>A (p.Arg310Gln) rs201867790
NM_004820.5(CYP7B1):c.92T>A (p.Leu31Gln) rs886063076
NM_004820.5(CYP7B1):c.957T>C (p.Arg319=) rs886063073
NM_004820.5(CYP7B1):c.971G>A (p.Arg324His) rs59035258

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