ClinVar Miner

List of variants in gene combination CYP21A2, LOC106780800 reported as likely benign for adrenal gland disease

Included ClinVar conditions (131):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_000500.9(CYP21A2):c.1287C>T (p.Cys429=) rs193922543
NM_000500.9(CYP21A2):c.203-46C>T rs6452
NM_000500.9(CYP21A2):c.292+37T>A rs184177366
NM_000500.9(CYP21A2):c.292+45_292+46insTGT rs1422458709
NM_000500.9(CYP21A2):c.292+56T>G rs543633765
NM_000500.9(CYP21A2):c.293-136C>T rs1582301685
NM_000500.9(CYP21A2):c.327C>G (p.Ser109=) rs193922545
NM_000500.9(CYP21A2):c.342C>T (p.Ser114=) rs193922546

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