ClinVar Miner

List of variants reported as benign for GRM6-related retinopathy by Genome-Nilou Lab

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000843.4(GRM6):c.1308T>C (p.Thr436=) rs4701014 0.98353
NM_000843.4(GRM6):c.1131C>T (p.Asp377=) rs2071246 0.74455
NM_000843.4(GRM6):c.1500+23A>G rs2256966 0.57932
NM_000843.4(GRM6):c.176A>C (p.Gln59Pro) rs2645329 0.57334
NM_000843.4(GRM6):c.1392A>G (p.Gly464=) rs11746675 0.57251
NM_000843.4(GRM6):c.1353T>C (p.Asn451=) rs2067011 0.50613
NM_000843.4(GRM6):c.1227C>T (p.Tyr409=) rs2645339 0.49941
NM_000843.4(GRM6):c.2196G>A (p.Thr732=) rs2071247 0.18181

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.