ClinVar Miner

List of variants in gene COL11A2 reported as likely benign by PreventionGenetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_080679.2(COL11A2):c.1291-10G>C rs182657680
NM_080679.2(COL11A2):c.1659C>T (p.Pro553=) rs2229786
NM_080679.2(COL11A2):c.2015C>T (p.Pro672Leu) rs150877886
NM_080679.2(COL11A2):c.2263-5del rs555657704
NM_080679.2(COL11A2):c.3210A>G (p.Gly1070=) rs530771165
NM_080679.2(COL11A2):c.3294C>A (p.Asn1098Lys) rs141967872
NM_080679.2(COL11A2):c.353G>C (p.Arg118Pro) rs41268014
NM_080679.2(COL11A2):c.4137T>A (p.Gly1379=) rs143186319
NM_080679.2(COL11A2):c.4320C>T (p.Leu1440=) rs758306963
NM_080679.2(COL11A2):c.4362A>G (p.Thr1454=) rs34055850
NM_080679.2(COL11A2):c.4750-7C>G rs200548977

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.