Variants in gene combination CYP11B1, LOC106799833 with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000497.4(CYP11B1):c.1098T>G (p.Arg366=)	rs61752769	0.02016
NM_000497.4(CYP11B1):c.1353T>C (p.Leu451=)	rs5316	0.01232
NM_000497.4(CYP11B1):c.1014G>A (p.Gln338=)	rs151335623	0.00158
NM_000497.4(CYP11B1):c.743C>T (p.Thr248Ile)	rs34620645	0.00095
NM_000497.4(CYP11B1):c.459T>C (p.Ala153=)	rs61751150	0.00079
NM_000497.4(CYP11B1):c.554C>G (p.Thr185Ser)	rs566921201	0.00035
NM_000497.4(CYP11B1):c.1451T>A (p.Val484Asp)	rs374517238	0.00009
NM_000497.4(CYP11B1):c.1120C>A (p.Arg374=)	rs61752786
NM_000497.4(CYP11B1):c.1266C>T (p.Arg422=)	rs4998902

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.