ClinVar Miner

List of variants reported as likely pathogenic for adrenal gland disease by Center for Human Genetics, Inc

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NM_000244.3(MEN1):c.1064+2T>C rs1555164946
NM_000244.3(MEN1):c.113C>T (p.Ser38Phe) rs794728616
NM_000244.3(MEN1):c.3G>A (p.Met1Ile) rs786204242
NM_003000.2(SDHB):c.600G>A (p.Trp200Ter) rs397516836
NM_003002.4(SDHD):c.18_21del (p.Leu7fs) rs1555186662

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.