ClinVar Miner

List of variants in gene ARID1B reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_020732.3(ARID1B):c.1685T>A (p.Ile562Asn) rs1057522610
NM_020732.3(ARID1B):c.2371+5G>A rs1554298239
NM_020732.3(ARID1B):c.2372-2A>C rs1057524160
NM_020732.3(ARID1B):c.2699C>T (p.Pro900Leu) rs1057521656
NM_020732.3(ARID1B):c.2960C>G (p.Ser987Cys) rs780818465
NM_020732.3(ARID1B):c.3007A>G (p.Met1003Val) rs764460073
NM_020732.3(ARID1B):c.3748A>C (p.Lys1250Gln) rs1057522635
NM_020732.3(ARID1B):c.3851G>T (p.Gly1284Val) rs149389876
NM_020732.3(ARID1B):c.6519G>C (p.Gln2173His) rs1057522604
NM_020732.3(ARID1B):c.971G>C (p.Gly324Ala) rs1057522183
NM_020732.3(ARID1B):c.980G>C (p.Gly327Ala) rs1455234951

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.