GAS6
growth arrest specific 6
Summary
This gene encodes a gamma-carboxyglutamic acid (Gla)-containing protein thought to be involved in the stimulation of cell proliferation. This gene is frequently overexpressed in many cancers and has been implicated as an adverse prognostic marker. Elevated protein levels are additionally associated with a variety of disease states, including venous thromboembolic disease, systemic lupus erythematosus, chronic renal failure, and preeclampsia. [provided by RefSeq, Aug 2014]
Known Variants81 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1402296854 | 13:114,523,859 | G/A | — | uncertain significance |
| rs2502859085 | 13:114,523,931 | A/C | — | uncertain significance |
| rs750814570 | 13:114,523,962 | C/T | — | uncertain significance |
| rs755543652 | 13:114,523,972 | C/T | — | likely benign |
| rs141047065 | 13:114,523,994 | G/A | — | likely benign |
| rs1337973210 | 13:114,524,943 | C/T | — | uncertain significance |
| rs7400002 | 13:114,524,944 | A/G | synonymous variant | — |
| rs199700915 | 13:114,524,966 | C/T | — | benign |
| rs73583241 | 13:114,524,979 | C/T | — | benign |
| rs371536576 | 13:114,524,985 | C/T | — | uncertain significance |
| rs929257792 | 13:114,525,021 | C/T | — | uncertain significance |
| rs74663534 | 13:114,525,022 | G/A | — | benign |
| rs1010087610 | 13:114,525,044 | A/G | — | uncertain significance |
| rs1038795104 | 13:114,525,048 | C/G | — | uncertain significance |
| rs79807310 | 13:114,525,074 | G/A | — | benign |
| rs1009810756 | 13:114,525,093 | C/T | — | uncertain significance |
| rs751493237 | 13:114,525,098 | C/T | — | uncertain significance |
| rs146664338 | 13:114,525,123 | G/T | — | uncertain significance |
| rs9604498 | 13:114,525,938 | C/T | — | — |
| rs2502867841 | 13:114,526,361 | T/G | — | uncertain significance |
| rs1393590464 | 13:114,526,376 | T/C | — | uncertain significance |
| rs770488795 | 13:114,526,409 | C/T | — | likely benign |
| rs368447635 | 13:114,526,410 | G/A | — | uncertain significance |
| rs7992146 | 13:114,526,503 | C/T | — | benign |
| rs74118435 | 13:114,526,504 | G/A | — | benign |
| rs1436431613 | 13:114,526,506 | C/T | — | likely benign |
| rs7400722 | 13:114,527,838 | G/A | intron variant | — |
| rs9577873 | 13:114,528,255 | G/T | — | — |
| rs1180214588 | 13:114,529,989 | G/A | — | uncertain significance |
| rs199698744 | 13:114,530,014 | A/C | — | uncertain significance |
| rs2051559513 | 13:114,530,019 | C/T | — | likely benign |
| rs767144171 | 13:114,530,025 | G/A | — | uncertain significance |
| rs553417045 | 13:114,530,031 | G/A | — | uncertain significance |
| rs2502882357 | 13:114,530,062 | C/T | — | uncertain significance |
| rs1803628 | 13:114,530,114 | G/A | synonymous variant | — |
| rs2502882578 | 13:114,530,124 | A/G | — | uncertain significance |
| rs78437382 | 13:114,530,125 | G/A | — | benign |
| rs766387009 | 13:114,531,612 | C/T | — | uncertain significance |
| rs1566356866 | 13:114,531,615 | C/T | — | uncertain significance |
| rs142494562 | 13:114,531,660 | T/C | — | uncertain significance |
| rs748784454 | 13:114,531,662 | C/T | — | uncertain significance |
| rs1273516388 | 13:114,531,675 | C/T | — | uncertain significance |
| rs9604463 | 13:114,531,911 | A/C | — | — |
| rs7400417 | 13:114,533,746 | G/C | — | — |
| rs202194869 | 13:114,535,304 | C/T | — | uncertain significance |
| rs544430070 | 13:114,535,322 | C/T | — | uncertain significance |
| rs373825026 | 13:114,535,337 | G/A | — | uncertain significance |
| rs140003424 | 13:114,535,418 | T/C | — | likely benign |
| rs776076149 | 13:114,535,614 | G/C | — | uncertain significance |
| rs200207558 | 13:114,535,710 | C/T | — | uncertain significance |
| rs201605000 | 13:114,535,733 | G/A | — | benign |
| rs8191974 | 13:114,537,517 | C/T | splice region variant | — |
| rs1566361188 | 13:114,537,531 | G/A | — | uncertain significance |
| rs1227695105 | 13:114,537,542 | C/T | — | likely benign |
| rs1412044561 | 13:114,537,561 | C/T | — | uncertain significance |
| rs148333937 | 13:114,537,564 | C/A | — | uncertain significance |
| rs1566361230 | 13:114,537,568 | C/T | — | uncertain significance |
| rs755823762 | 13:114,537,569 | G/C | — | uncertain significance |
| rs78824256 | 13:114,537,621 | C/T | missense variant | — |
| rs762983181 | 13:114,537,627 | T/G | — | uncertain significance |
| rs2138635462 | 13:114,537,640 | C/T | — | uncertain significance |
| rs770982123 | 13:114,538,488 | C/G | — | uncertain significance |
| rs146159446 | 13:114,538,506 | G/T | — | uncertain significance |
| rs145586332 | 13:114,538,515 | G/A | — | benign |
| rs200327303 | 13:114,538,526 | G/C | — | uncertain significance |
| rs555084854 | 13:114,538,581 | G/A | — | uncertain significance |
| rs191607985 | 13:114,539,975 | G/A | regulatory region variant | — |
| rs199802250 | 13:114,541,072 | C/T | — | uncertain significance |
| rs767644656 | 13:114,541,134 | C/T | — | uncertain significance |
| rs12868938 | 13:114,541,617 | C/T | — | — |
| rs139682172 | 13:114,542,707 | C/T | — | uncertain significance |
| rs752400830 | 13:114,542,757 | A/G | — | uncertain significance |
| rs2502922275 | 13:114,542,772 | G/A | — | likely benign |
| rs1594201778 | 13:114,542,805 | G/A | — | uncertain significance |
| rs9604490 | 13:114,542,942 | C/T | downstream gene variant | — |
| rs9604489 | 13:114,542,957 | C/A | — | — |
| rs75973359 | 13:114,544,756 | G/A | — | — |
| rs774822461 | 13:114,549,538 | G/A | — | uncertain significance |
| rs6602906 | 13:114,565,522 | G/A | regulatory region variant | — |
| rs768755984 | 13:114,566,588 | C/T | — | uncertain significance |
| rs2051994736 | 13:114,566,854 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.