List of variants in gene CYP11B1 reported as likely pathogenic for adrenal gland disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000497.4(CYP11B1):c.125C>T (p.Pro42Leu)	rs193922538	0.00008
NM_000497.4(CYP11B1):c.124C>T (p.Pro42Ser)	rs104894069	0.00001
NM_000497.4(CYP11B1):c.187G>C (p.Asp63His)	rs5282	0.00001
NM_000497.4(CYP11B1):c.235T>A (p.Phe79Ile)	rs1489638195	0.00001
NM_000497.4(CYP11B1):c.264G>A (p.Met88Ile)	rs193922539	0.00001
NM_000497.4(CYP11B1):c.1019T>G (p.Leu340Arg)
NM_000497.4(CYP11B1):c.1466T>C (p.Leu489Ser)
NM_000497.4(CYP11B1):c.147del (p.Trp49fs)	rs748867146
NM_000497.4(CYP11B1):c.168G>A (p.Trp56Ter)	rs1383321200
NM_000497.4(CYP11B1):c.217C>T (p.Gln73Ter)	rs1554653675
NM_000497.4(CYP11B1):c.281C>T (p.Pro94Leu)	rs104894070
NM_000497.4(CYP11B1):c.304C>T (p.Gln102Ter)	rs1554653551
NM_000497.4(CYP11B1):c.360del (p.Arg120fs)
NM_000497.4(CYP11B1):c.395+1G>C	rs1554653514
NM_000497.4(CYP11B1):c.422G>T (p.Arg141Leu)
NM_000497.4(CYP11B1):c.800G>A (p.Gly267Asp)

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