List of variants in gene CYP11A1 reported as benign for not provided

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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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000781.3(CYP11A1):c.1435-179A>G	rs2279357	0.69072
NM_000781.3(CYP11A1):c.991-268G>A	rs7173655	0.52113
NM_000781.3(CYP11A1):c.426-283T>C	rs11632698	0.48366
NM_000781.3(CYP11A1):c.991-190G>C	rs12917295	0.48220
NM_000781.3(CYP11A1):c.269+49C>A	rs28681535	0.27895
NM_000781.3(CYP11A1):c.269+123T>C	rs12442401	0.26853
NM_000781.3(CYP11A1):c.425+132G>A	rs1484215	0.05609
NM_000781.3(CYP11A1):c.270-73G>A	rs113729254	0.01968
NM_000781.3(CYP11A1):c.939C>T (p.Phe313=)	rs4986873	0.01114
NM_000781.3(CYP11A1):c.535G>A (p.Val179Ile)	rs58174009	0.00436
NM_000781.3(CYP11A1):c.235G>A (p.Val79Ile)	rs143655263	0.00303
NM_000781.3(CYP11A1):c.1167C>T (p.Pro389=)	rs138177167	0.00268
NM_000781.3(CYP11A1):c.830-14C>G	rs190239248	0.00251
NM_000781.3(CYP11A1):c.438C>T (p.Ala146=)	rs141920628	0.00189
NM_000781.3(CYP11A1):c.417C>T (p.Val139=)	rs141998085	0.00110
NM_000781.3(CYP11A1):c.93G>A (p.Arg31=)	rs141127674	0.00083
NM_000781.3(CYP11A1):c.1158-5C>T	rs377242922	0.00009
NM_000781.3(CYP11A1):c.366C>T (p.Leu122=)	rs530494910	0.00006
NM_000781.3(CYP11A1):c.1195G>T (p.Val399Leu)
NM_000781.3(CYP11A1):c.1237-16G>C
NM_000781.3(CYP11A1):c.269+121dup	rs11350546
NM_000781.3(CYP11A1):c.269+134_269+138del	rs11350546
NM_000781.3(CYP11A1):c.269+138del	rs11350546
NM_000781.3(CYP11A1):c.270-251C>G	rs6495096
NM_000781.3(CYP11A1):c.625+9del
NM_000781.3(CYP11A1):c.930G>A (p.Lys310=)
NM_000781.3(CYP11A1):c.990+213T>C	rs58712424

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