FAM149A
family with sequence similarity 149 member A
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs553268511 | 4:187,024,178 | G/A | — | — |
| rs575756168 | 4:187,026,611 | G/C | synonymous variant | — |
| rs188599451 | 4:187,028,676 | G/A | — | — |
| rs145574097 | 4:187,030,203 | A/G | intron variant | — |
| rs144397908 | 4:187,042,762 | A/G | intron variant | — |
| rs72708991 | 4:187,050,312 | C/T | — | — |
| rs777545200 | 4:187,073,135 | A/T | — | uncertain significance |
| rs180922588 | 4:187,074,543 | T/G | upstream gene variant | — |
| rs551131214 | 4:187,074,821 | C/G | — | uncertain significance |
| rs140771382 | 4:187,074,872 | G/A | — | likely benign |
| rs765703561 | 4:187,074,888 | C/T | — | likely benign |
| rs767332237 | 4:187,074,916 | C/A | — | uncertain significance |
| rs370460098 | 4:187,075,711 | C/T | — | uncertain significance |
| rs756192368 | 4:187,075,759 | T/C | — | uncertain significance |
| rs1429410541 | 4:187,075,786 | A/G | — | uncertain significance |
| rs1464793359 | 4:187,075,788 | G/C | — | uncertain significance |
| rs192140289 | 4:187,077,156 | A/T | — | uncertain significance |
| rs746650008 | 4:187,077,189 | C/A | — | likely benign |
| rs147196705 | 4:187,077,200 | T/A | — | likely benign |
| rs140463493 | 4:187,077,204 | G/A | — | likely benign |
| rs139661959 | 4:187,077,222 | C/T | — | uncertain significance |
| rs368472968 | 4:187,077,231 | C/T | — | uncertain significance |
| rs754712900 | 4:187,077,233 | C/T | — | uncertain significance |
| rs149745987 | 4:187,077,234 | G/A | missense variant | — |
| rs201494456 | 4:187,077,278 | G/A | — | uncertain significance |
| rs113168248 | 4:187,078,745 | G/A | — | likely benign |
| rs144890576 | 4:187,078,749 | T/C | — | uncertain significance |
| rs569838275 | 4:187,078,793 | G/A | — | likely benign |
| rs754659146 | 4:187,078,857 | G/A | — | likely benign |
| rs7684001 | 4:187,081,313 | G/T | — | — |
| rs79537217 | 4:187,084,023 | T/G | — | uncertain significance |
| rs1488121665 | 4:187,084,024 | A/G | — | uncertain significance |
| rs779900401 | 4:187,084,071 | C/T | — | uncertain significance |
| rs781205660 | 4:187,084,081 | C/T | — | uncertain significance |
| rs377734857 | 4:187,084,099 | C/T | — | uncertain significance |
| rs770780746 | 4:187,084,585 | A/G | — | uncertain significance |
| rs752129593 | 4:187,084,628 | C/T | — | uncertain significance |
| rs200534330 | 4:187,084,630 | G/A | — | uncertain significance |
| rs768842672 | 4:187,084,648 | C/T | — | uncertain significance |
| rs139445329 | 4:187,084,649 | G/A | — | uncertain significance |
| rs144224944 | 4:187,084,729 | T/C | — | uncertain significance |
| rs201562459 | 4:187,084,737 | A/C | — | uncertain significance |
| rs149087810 | 4:187,086,508 | G/A | — | uncertain significance |
| rs766263720 | 4:187,086,515 | A/G | — | likely benign |
| rs751343265 | 4:187,086,517 | A/C | — | likely benign |
| rs375398673 | 4:187,086,553 | T/A | — | uncertain significance |
| rs141878617 | 4:187,086,560 | C/G | — | uncertain significance |
| rs750494973 | 4:187,086,581 | G/A | — | likely benign |
| rs142852013 | 4:187,086,598 | C/T | — | uncertain significance |
| rs369423322 | 4:187,086,601 | G/A | — | uncertain significance |
| rs138746162 | 4:187,086,607 | C/T | — | uncertain significance |
| rs180692842 | 4:187,087,452 | C/A | downstream gene variant | — |
| rs188655304 | 4:187,088,042 | G/A | downstream gene variant | — |
| rs563008928 | 4:187,088,132 | G/A | — | uncertain significance |
| rs772113067 | 4:187,088,159 | C/T | — | uncertain significance |
| rs775628305 | 4:187,088,161 | A/G | — | likely benign |
| rs200559570 | 4:187,088,183 | C/T | — | uncertain significance |
| rs753211748 | 4:187,088,185 | C/T | — | uncertain significance |
| rs148580222 | 4:187,088,186 | G/A | — | uncertain significance |
| rs778368758 | 4:187,088,192 | G/A | — | uncertain significance |
| rs778676220 | 4:187,088,198 | G/T | — | uncertain significance |
| rs759549686 | 4:187,088,220 | G/T | — | likely benign |
| rs145087000 | 4:187,088,345 | C/T | — | uncertain significance |
| rs577429380 | 4:187,088,350 | C/G | — | uncertain significance |
| rs180926224 | 4:187,090,900 | C/T | downstream gene variant | — |
| rs755205050 | 4:187,093,095 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.