ClinVar Miner

List of variants in gene LOC108863620, STAR studied for primary adrenal insufficiency

Included ClinVar conditions (19):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_000008.11:g.38150990G>A rs16887226 0.01566
NM_000349.3(STAR):c.-70G>T rs370257148 0.00031
NM_000349.2(STAR):c.-255G>T rs567801443 0.00011
NM_000349.2(STAR):c.-152G>A rs1196346446 0.00001
NM_000349.2(STAR):c.-249C>A rs886062906
NM_000349.3(STAR):c.-16C>T rs779983468
NM_000349.3(STAR):c.5_11del (p.Leu2fs)

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.