ClinVar Miner

List of variants in gene ARID1B reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
NM_020732.3(ARID1B):c.1019C>T (p.Ala340Val) rs878853084
NM_020732.3(ARID1B):c.1542+19G>C rs374013482
NM_020732.3(ARID1B):c.3025+6C>T rs148976215
NM_020732.3(ARID1B):c.3345+11G>A rs368322992
NM_020732.3(ARID1B):c.4234T>G (p.Ser1412Ala) rs145516400
NM_020732.3(ARID1B):c.5545C>A (p.Pro1849Thr) rs779490460
NM_020732.3(ARID1B):c.6272T>C (p.Ile2091Thr) rs878852997
NM_020732.3(ARID1B):c.921_923CGG[9] (p.Gly319dup) rs587779747
NM_020732.3(ARID1B):c.962_964GAG[9] (p.Gly328dup) rs747790383

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.