HMGXB3
HMG-box containing 3
Summary
This gene is one of the non-canonical high mobility group (HMG) genes. The encoded protein contains an HMG-box domain found in DNA binding proteins such as transcription factors and chromosomal proteins. [provided by RefSeq, Aug 2011]
Known Variants82 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1312619257 | 5:149,384,420 | A/G | — | uncertain significance |
| rs2113721678 | 5:149,384,554 | T/C | — | uncertain significance |
| rs2480827145 | 5:149,386,125 | T/C | — | uncertain significance |
| rs542202858 | 5:149,386,198 | A/T | — | uncertain significance |
| rs2480827312 | 5:149,386,208 | C/T | — | uncertain significance |
| rs147119330 | 5:149,386,304 | T/C | intron variant | — |
| rs1283462636 | 5:149,389,771 | G/C | — | uncertain significance |
| rs577757155 | 5:149,389,785 | C/T | — | uncertain significance |
| rs754476196 | 5:149,389,786 | G/A | — | uncertain significance |
| rs201990590 | 5:149,389,789 | G/T | — | uncertain significance |
| rs753868898 | 5:149,389,831 | C/A | — | uncertain significance |
| rs749619104 | 5:149,389,866 | C/T | — | uncertain significance |
| rs540550790 | 5:149,389,893 | A/T | — | uncertain significance |
| rs1755798809 | 5:149,389,896 | G/A | — | uncertain significance |
| rs1470387897 | 5:149,389,912 | C/T | — | uncertain significance |
| rs142114383 | 5:149,389,968 | G/A | — | benign |
| rs766294433 | 5:149,390,016 | G/A | — | uncertain significance |
| rs759407035 | 5:149,390,079 | T/G | — | uncertain significance |
| rs2480834246 | 5:149,390,160 | A/G | — | uncertain significance |
| rs75657424 | 5:149,390,276 | G/C | downstream gene variant | — |
| rs138303033 | 5:149,391,845 | T/C | — | benign |
| rs771950032 | 5:149,391,860 | A/G | — | uncertain significance |
| rs956208478 | 5:149,391,863 | A/C | — | uncertain significance |
| rs1375374208 | 5:149,398,169 | G/T | — | uncertain significance |
| rs1050187008 | 5:149,398,192 | G/A | — | uncertain significance |
| rs188995699 | 5:149,403,964 | C/T | — | uncertain significance |
| rs2113741285 | 5:149,403,972 | G/C | — | uncertain significance |
| rs111881981 | 5:149,404,041 | A/G | — | uncertain significance |
| rs2480858844 | 5:149,404,080 | A/T | — | uncertain significance |
| rs542849731 | 5:149,404,131 | C/T | — | uncertain significance |
| rs747578064 | 5:149,404,152 | A/G | — | likely benign |
| rs61743767 | 5:149,404,193 | C/T | — | benign |
| rs116169796 | 5:149,405,813 | A/G | regulatory region variant | — |
| rs1003247898 | 5:149,406,325 | G/A | — | uncertain significance |
| rs753629527 | 5:149,406,357 | A/G | — | uncertain significance |
| rs2480863204 | 5:149,406,370 | T/G | — | uncertain significance |
| rs565914929 | 5:149,406,394 | G/A | — | uncertain significance |
| rs2480863510 | 5:149,406,421 | C/T | — | uncertain significance |
| rs1331449930 | 5:149,406,436 | C/G | — | uncertain significance |
| rs1185477737 | 5:149,406,613 | T/C | — | uncertain significance |
| rs2304069 | 5:149,406,733 | G/C | — | — |
| rs184700209 | 5:149,407,264 | C/T | downstream gene variant | — |
| rs186497515 | 5:149,410,319 | T/A | — | benign |
| rs538858627 | 5:149,410,361 | G/A | — | uncertain significance |
| rs775858327 | 5:149,410,364 | A/G | — | uncertain significance |
| rs2480876388 | 5:149,412,087 | A/G | — | uncertain significance |
| rs1346273497 | 5:149,412,088 | C/A | — | uncertain significance |
| rs1756405006 | 5:149,412,126 | A/T | — | uncertain significance |
| rs1443522255 | 5:149,412,165 | T/C | — | uncertain significance |
| rs192284552 | 5:149,412,239 | A/C | upstream gene variant | — |
| rs543100056 | 5:149,416,271 | C/T | — | uncertain significance |
| rs752578660 | 5:149,416,272 | G/A | — | uncertain significance |
| rs375400628 | 5:149,416,346 | G/A | — | uncertain significance |
| rs368659948 | 5:149,416,389 | A/G | — | uncertain significance |
| rs757165444 | 5:149,417,007 | G/A | — | uncertain significance |
| rs1352644016 | 5:149,420,361 | G/A | — | uncertain significance |
| rs1216637591 | 5:149,420,400 | G/C | — | uncertain significance |
| rs374063819 | 5:149,421,527 | G/A | — | uncertain significance |
| rs2480903460 | 5:149,425,175 | C/G | — | uncertain significance |
| rs573343251 | 5:149,425,197 | G/A | — | uncertain significance |
| rs1756789904 | 5:149,427,193 | G/A | — | uncertain significance |
| rs1267328631 | 5:149,427,287 | G/C | — | uncertain significance |
| rs1247412160 | 5:149,428,171 | G/C | — | uncertain significance |
| rs2480909962 | 5:149,428,190 | C/G | — | uncertain significance |
| rs1756817602 | 5:149,428,225 | A/G | — | uncertain significance |
| rs1756862939 | 5:149,429,957 | C/G | — | uncertain significance |
| rs542312116 | 5:149,431,387 | C/T | — | uncertain significance |
| rs1041633108 | 5:149,431,412 | C/T | — | uncertain significance |
| rs1228606932 | 5:149,431,440 | C/G | — | uncertain significance |
| rs188426859 | 5:149,431,476 | C/T | — | likely benign |
| rs201732673 | 5:149,431,477 | G/A | — | likely benign |
| rs548707805 | 5:149,431,498 | G/A | — | uncertain significance |
| rs1384567851 | 5:149,431,528 | C/T | — | uncertain significance |
| rs912666320 | 5:149,431,531 | C/T | — | uncertain significance |
| rs746842753 | 5:149,431,542 | C/G | — | uncertain significance |
| rs374466435 | 5:149,431,547 | A/G | — | uncertain significance |
| rs1272564280 | 5:149,431,549 | G/A | — | uncertain significance |
| rs546754586 | 5:149,431,612 | C/T | — | uncertain significance |
| rs1459192010 | 5:149,431,645 | C/T | — | uncertain significance |
| rs367831679 | 5:149,431,674 | C/T | — | likely benign |
| rs574897162 | 5:149,431,678 | C/T | — | uncertain significance |
| rs1483835261 | 5:149,431,748 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.