ClinVar Miner

List of variants in gene ARID1B reported as benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
NM_017519.2(ARID1B):c.1336_1338CCG[6] (p.Pro450dup) rs572236007
NM_017519.2(ARID1B):c.945_947AGG[3] (p.Gly319del) rs587779748
NM_017519.2(ARID1B):c.962_964GAG[7] (p.Gly328del) rs747790383
NM_020732.3(ARID1B):c.1285A>G (p.Met429Val) rs199948752
NM_020732.3(ARID1B):c.1927-3T>A rs116661275
NM_020732.3(ARID1B):c.1977C>T (p.Pro659=) rs146240413
NM_020732.3(ARID1B):c.2172G>A (p.Ala724=) rs3734441
NM_020732.3(ARID1B):c.3025+6C>T rs148976215
NM_020732.3(ARID1B):c.3399C>T (p.Thr1133=) rs142391292
NM_020732.3(ARID1B):c.3459G>A (p.Glu1153=) rs61745451
NM_020732.3(ARID1B):c.3946G>A (p.Gly1316Arg) rs199674889
NM_020732.3(ARID1B):c.4014-7A>G rs112318565
NM_020732.3(ARID1B):c.4632G>A (p.Pro1544=) rs61738955
NM_020732.3(ARID1B):c.5207A>C (p.Glu1736Ala) rs149518409
NM_020732.3(ARID1B):c.5802C>T (p.Ile1934=) rs142499766
NM_020732.3(ARID1B):c.5922C>T (p.Ile1974=) rs112703040
NM_020732.3(ARID1B):c.6654C>T (p.His2218=) rs183572405
NM_020732.3(ARID1B):c.736G>A (p.Gly246Ser) rs375160616

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.