ARID3A
AT-rich interaction domain 3A
Summary
This gene encodes a member of the ARID (AT-rich interaction domain) family of DNA binding proteins. It was found by homology to the Drosophila dead ringer gene, which is important for normal embryogenesis. Other ARID family members have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation, and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1021489100 | 19:929,579 | G/A | — | likely benign |
| rs3746142 | 19:929,637 | G/A | — | uncertain significance |
| rs372928434 | 19:929,640 | C/T | — | uncertain significance |
| rs757309861 | 19:929,641 | G/A | — | likely benign |
| rs745854452 | 19:929,647 | G/A | — | uncertain significance |
| rs780064122 | 19:929,655 | C/T | — | uncertain significance |
| rs768209693 | 19:929,658 | G/A | — | uncertain significance |
| rs201419429 | 19:929,686 | G/A | — | uncertain significance |
| rs781483243 | 19:929,694 | C/T | — | uncertain significance |
| rs116393241 | 19:929,763 | G/T | — | uncertain significance |
| rs774786700 | 19:929,784 | C/T | — | uncertain significance |
| rs370403414 | 19:929,791 | C/T | — | uncertain significance |
| rs375623283 | 19:929,805 | G/A | — | likely benign |
| rs765015703 | 19:929,812 | G/A | — | likely benign |
| rs375496194 | 19:929,824 | C/T | — | uncertain significance |
| rs772606131 | 19:929,889 | G/A | — | uncertain significance |
| rs145848515 | 19:930,721 | A/C | — | — |
| rs2511978024 | 19:932,431 | G/A | — | uncertain significance |
| rs546907163 | 19:932,458 | G/A | — | uncertain significance |
| rs1568355573 | 19:932,512 | G/A | — | uncertain significance |
| rs749403652 | 19:932,599 | C/T | — | uncertain significance |
| rs2511979024 | 19:932,626 | G/T | — | uncertain significance |
| rs894864274 | 19:932,638 | C/T | — | uncertain significance |
| rs373775705 | 19:932,639 | G/A | — | uncertain significance |
| rs2511979169 | 19:932,662 | C/T | — | likely benign |
| rs776380486 | 19:932,665 | G/A | — | uncertain significance |
| rs2511979479 | 19:932,725 | G/T | — | uncertain significance |
| rs2159128 | 19:950,380 | G/T | intron variant | — |
| rs2512023360 | 19:960,123 | A/G | — | uncertain significance |
| rs2512031241 | 19:964,351 | C/G | — | uncertain significance |
| rs2240615 | 19:964,434 | A/G | — | benign |
| rs771180105 | 19:965,053 | A/C | — | uncertain significance |
| rs368267576 | 19:966,608 | G/A | — | uncertain significance |
| rs751888436 | 19:966,626 | C/T | — | uncertain significance |
| rs61735586 | 19:966,714 | A/G | — | benign |
| rs548635209 | 19:966,749 | C/T | — | uncertain significance |
| rs140181068 | 19:966,787 | C/T | — | uncertain significance |
| rs772133293 | 19:966,788 | G/A | — | uncertain significance |
| rs1376966400 | 19:966,809 | A/G | — | uncertain significance |
| rs115920176 | 19:966,831 | G/A | — | benign |
| rs537786817 | 19:968,410 | G/A | — | uncertain significance |
| rs142537557 | 19:968,441 | C/T | — | uncertain significance |
| rs2512042171 | 19:968,450 | A/G | — | uncertain significance |
| rs146132253 | 19:968,475 | G/A | — | likely benign |
| rs2512042283 | 19:968,476 | G/A | — | uncertain significance |
| rs201677585 | 19:971,908 | C/T | — | uncertain significance |
| rs2512050839 | 19:971,935 | G/A | — | uncertain significance |
| rs138086881 | 19:971,936 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.