ClinVar Miner

List of variants in gene GRIP1 reported as likely benign for autosomal recessive disease

Included ClinVar conditions (1196):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001366722.1(GRIP1):c.*655_*657dup rs138816960 0.01583
NM_001366722.1(GRIP1):c.2606G>A (p.Arg869Gln) rs145115262 0.00595
NM_001366722.1(GRIP1):c.*1314G>A rs144894732 0.00409
NM_001366722.1(GRIP1):c.2880G>A (p.Ser960=) rs181527317 0.00242
NM_001366722.1(GRIP1):c.2283G>A (p.Ser761=) rs200863167 0.00168
NM_001366722.1(GRIP1):c.2381T>G (p.Met794Arg) rs144494437 0.00155
NM_001366722.1(GRIP1):c.1645A>G (p.Ile549Val) rs201867922 0.00148
NM_001366722.1(GRIP1):c.160G>A (p.Val54Ile) rs199768740 0.00087
NM_001366722.1(GRIP1):c.2886G>A (p.Pro962=) rs375330927 0.00038
NM_001366722.1(GRIP1):c.1199-7C>G rs200313638 0.00029
NM_001366722.1(GRIP1):c.55+9C>A rs199740150 0.00025
NM_001366722.1(GRIP1):c.*234G>A rs541596282 0.00024
NM_001366722.1(GRIP1):c.579-8C>T rs375593950 0.00024
NM_001366722.1(GRIP1):c.1687+12T>C rs151041073 0.00023
NM_001366722.1(GRIP1):c.1688-3T>C rs185129168 0.00021
NM_001366722.1(GRIP1):c.1791A>G (p.Gly597=) rs768730046 0.00006
NM_001366722.1(GRIP1):c.162C>T (p.Val54=) rs759704197 0.00003
NM_001366722.1(GRIP1):c.1389G>A (p.Gly463=) rs200499586 0.00002
NM_001366722.1(GRIP1):c.*499A>G rs572566894 0.00001
NM_001366722.1(GRIP1):c.*1261dup rs35499444
NM_001366722.1(GRIP1):c.*1299_*1301dup rs200995788
NM_001366722.1(GRIP1):c.*1524_*1527del rs148261691
NM_001366722.1(GRIP1):c.*647_*650dup rs200677568
NM_001366722.1(GRIP1):c.*695_*697dup rs201977256
NM_001366722.1(GRIP1):c.1355-10_1355-8del rs148083271
NM_001366722.1(GRIP1):c.1787C>G (p.Pro596Arg) rs200955760
NM_001366722.1(GRIP1):c.418+14C>A rs79994510

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.