ClinVar Miner

List of variants in gene ARID2 reported by ITMI

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_152641.4(ARID2):c.2764A>G (p.Thr922Ala) rs114470162 0.00760
NM_152641.4(ARID2):c.4492G>A (p.Ala1498Thr) rs116531573 0.00536
NM_152641.4(ARID2):c.4300G>T (p.Ala1434Ser) rs150136669 0.00436
NM_152641.4(ARID2):c.4705G>A (p.Ala1569Thr) rs78712333 0.00128
NM_152641.4(ARID2):c.4510C>T (p.Arg1504Trp) rs140500006 0.00112
NM_152641.4(ARID2):c.1808C>T (p.Ala603Val) rs144928351 0.00100
NM_152641.4(ARID2):c.1759A>G (p.Ser587Gly) rs78128744 0.00090
NM_152641.4(ARID2):c.1472C>G (p.Thr491Ser) rs149755754 0.00071
NM_152641.4(ARID2):c.292G>A (p.Glu98Lys) rs140285438 0.00038
NM_152641.4(ARID2):c.4945G>C (p.Val1649Leu) rs201268655 0.00036
NM_152641.4(ARID2):c.2428G>C (p.Ala810Pro) rs74916892 0.00019
NM_152641.4(ARID2):c.28C>A (p.Pro10Thr) rs560068535 0.00007
NM_152641.4(ARID2):c.3068C>T (p.Pro1023Leu) rs577713771 0.00004
NM_152641.4(ARID2):c.4223A>G (p.Lys1408Arg) rs374602869 0.00002
NM_152641.4(ARID2):c.2579A>G (p.Asn860Ser) rs147193304 0.00001
NM_152641.4(ARID2):c.3118G>A (p.Val1040Ile) rs587778055 0.00001
NM_152641.4(ARID2):c.4438G>C (p.Gly1480Arg) rs587778056 0.00001
NM_152641.4(ARID2):c.227T>G (p.Phe76Cys) rs587778057

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.