ClinVar Miner

List of variants in gene ADAM17 reported as benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003183.6(ADAM17):c.604A>G (p.Arg202Gly) rs2230818 0.06968
NM_003183.6(ADAM17):c.844-5T>C rs201461814 0.00624
NM_003183.6(ADAM17):c.484A>G (p.Lys162Glu) rs34431503 0.00362
NM_003183.6(ADAM17):c.81C>T (p.Gly27=) rs138046330 0.00034
NM_003183.6(ADAM17):c.451-20G>A rs190898474 0.00026
NM_003183.6(ADAM17):c.362-9dup rs769247529
NM_003183.6(ADAM17):c.958-13del rs34863481
NM_003183.6(ADAM17):c.958-34dup rs34863481
NM_003183.6(ADAM17):c.97+15del

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.