ClinVar Miner

List of variants in gene INSR reported as uncertain significance by Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP
NM_000208.3(INSR):c.2388G>C (p.Arg796Ser) rs78433961
NM_000208.3(INSR):c.2498G>A (p.Arg833Gln) rs777565396
NM_000208.3(INSR):c.2665C>T (p.Arg889Trp) rs76077021
NM_000208.3(INSR):c.3775G>A (p.Asp1259Asn) rs369102740

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.