List of variants reported as likely benign for Deficiency of steroid 11-beta-monooxygenase by Department of Human Genetics, Laborarztpraxis Dres. Walther, Weindel und Kollegen

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000497.4(CYP11B1):c.1122-20A>G	rs61752794	0.01636
NM_000497.4(CYP11B1):c.243C>T (p.Tyr81=)	rs9657022	0.00712
NM_000497.4(CYP11B1):c.1144C>T (p.Leu382=)	rs5293	0.00007
NM_000497.4(CYP11B1):c.1120C>A (p.Arg374=)	rs61752786

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