ClinVar Miner

List of variants in gene ADGRV1 reported as uncertain significance by Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_032119.4(ADGRV1):c.12212G>A (p.Arg4071Gln) rs202190568
NM_032119.4(ADGRV1):c.13231+4G>C rs778080956
NM_032119.4(ADGRV1):c.13382A>G (p.His4461Arg) rs182698253
NM_032119.4(ADGRV1):c.17987G>T (p.Trp5996Leu) rs544077645
NM_032119.4(ADGRV1):c.3509A>G (p.Tyr1170Cys) rs188772875
NM_032119.4(ADGRV1):c.4377C>T (p.Asp1459=) rs745380273
NM_032119.4(ADGRV1):c.564G>C (p.Glu188Asp) rs377529304
NM_032119.4(ADGRV1):c.8572A>G (p.Ile2858Val) rs41308297

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.