FAM120A
family with sequence similarity 120 member A
Summary
Enables RNA binding activity. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants82 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs115641885 | 9:96,213,660 | G/T | — | benign |
| rs371621692 | 9:96,213,821 | C/T | — | benign |
| rs1264109130 | 9:96,214,304 | G/A | — | uncertain significance |
| rs756246014 | 9:96,214,310 | G/A | — | uncertain significance |
| rs79629992 | 9:96,214,863 | A/G | — | benign |
| rs1055710 | 9:96,214,928 | G/A | — | benign |
| rs7869969 | 9:96,217,447 | A/T | — | — |
| rs10821129 | 9:96,222,617 | G/A | intron variant | — |
| rs10821130 | 9:96,223,572 | C/T | intron variant | — |
| rs10992746 | 9:96,231,171 | T/C | intron variant | — |
| rs753254507 | 9:96,233,526 | A/G | — | uncertain significance |
| rs372486496 | 9:96,233,690 | A/T | — | likely benign |
| rs4744242 | 9:96,236,711 | G/T | intron variant | — |
| rs10821135 | 9:96,238,578 | C/T | — | benign |
| rs10821136 | 9:96,238,731 | C/T | — | benign |
| rs10992751 | 9:96,239,090 | C/T | intron variant | — |
| rs10821140 | 9:96,253,169 | C/A | intron variant | — |
| rs10992756 | 9:96,253,439 | T/C | intron variant | — |
| rs2297376 | 9:96,259,582 | C/T | — | benign |
| rs140702495 | 9:96,259,820 | G/A | — | uncertain significance |
| rs1859626437 | 9:96,259,869 | C/G | — | uncertain significance |
| rs2542176410 | 9:96,261,100 | T/A | — | uncertain significance |
| rs17532098 | 9:96,262,725 | C/T | intron variant | — |
| rs10821143 | 9:96,263,813 | G/C | regulatory region variant | — |
| rs78046549 | 9:96,268,478 | C/T | intron variant | — |
| rs565665150 | 9:96,273,196 | G/A | — | — |
| rs2991382 | 9:96,278,093 | G/C | — | benign |
| rs554405587 | 9:96,278,098 | C/T | — | benign |
| rs572817649 | 9:96,278,099 | G/A | — | benign |
| rs200536689 | 9:96,278,291 | C/T | — | benign |
| rs753419624 | 9:96,278,292 | G/A | — | uncertain significance |
| rs756859159 | 9:96,278,296 | C/T | — | uncertain significance |
| rs201107481 | 9:96,278,297 | G/A | — | likely benign |
| rs376718875 | 9:96,278,371 | C/T | — | uncertain significance |
| rs1021681998 | 9:96,278,379 | A/G | — | uncertain significance |
| rs775564340 | 9:96,278,442 | A/G | — | uncertain significance |
| rs77023914 | 9:96,278,474 | C/T | — | benign |
| rs1482581124 | 9:96,278,544 | G/A | — | uncertain significance |
| rs202133201 | 9:96,278,575 | G/A | — | benign |
| rs145963492 | 9:96,278,672 | C/T | — | benign |
| rs4744253 | 9:96,278,784 | T/G | — | benign |
| rs57391036 | 9:96,289,231 | G/A | — | benign |
| rs10739950 | 9:96,289,269 | C/T | — | benign |
| rs1564345557 | 9:96,289,523 | A/C | — | uncertain significance |
| rs1999386 | 9:96,289,743 | C/T | — | benign |
| rs147279211 | 9:96,291,646 | G/A | — | likely benign |
| rs1459403900 | 9:96,291,662 | G/A | — | uncertain significance |
| rs758248723 | 9:96,291,705 | T/C | — | uncertain significance |
| rs10761232 | 9:96,292,025 | A/T | — | benign |
| rs10761233 | 9:96,292,166 | A/G | — | benign |
| rs2542346616 | 9:96,294,443 | A/G | — | uncertain significance |
| rs2542346726 | 9:96,294,461 | A/G | — | uncertain significance |
| rs10992779 | 9:96,304,656 | A/G | intron variant | — |
| rs1861769399 | 9:96,305,582 | C/A | — | uncertain significance |
| rs749235071 | 9:96,305,651 | G/T | — | uncertain significance |
| rs60219039 | 9:96,305,982 | T/C | — | benign |
| rs112735065 | 9:96,312,581 | G/A | — | benign |
| rs530741109 | 9:96,312,921 | C/T | — | uncertain significance |
| rs761530286 | 9:96,312,941 | C/T | — | uncertain significance |
| rs7038564 | 9:96,313,012 | C/T | — | benign |
| rs181025485 | 9:96,318,823 | C/T | — | uncertain significance |
| rs966789 | 9:96,319,143 | C/A | — | benign |
| rs1469095194 | 9:96,320,173 | G/A | — | uncertain significance |
| rs372774194 | 9:96,320,184 | A/G | — | uncertain significance |
| rs368196789 | 9:96,320,197 | C/T | — | uncertain significance |
| rs140826080 | 9:96,320,233 | C/T | — | likely benign |
| rs150176698 | 9:96,320,239 | C/T | — | uncertain significance |
| rs776255744 | 9:96,320,920 | C/T | — | uncertain significance |
| rs2542443770 | 9:96,323,415 | G/A | — | uncertain significance |
| rs2542444072 | 9:96,323,480 | G/C | — | uncertain significance |
| rs1399493866 | 9:96,323,483 | C/T | — | uncertain significance |
| rs77734990 | 9:96,324,152 | G/A | downstream gene variant | — |
| rs16909308 | 9:96,326,356 | G/A | — | benign |
| rs1862566196 | 9:96,326,536 | C/T | — | uncertain significance |
| rs1862570514 | 9:96,326,610 | C/G | — | uncertain significance |
| rs369844257 | 9:96,326,634 | G/A | — | uncertain significance |
| rs370300082 | 9:96,326,660 | C/G | — | uncertain significance |
| rs756652801 | 9:96,326,676 | G/A | — | likely benign |
| rs368992682 | 9:96,326,725 | C/T | — | uncertain significance |
| rs764574027 | 9:96,326,776 | G/A | — | uncertain significance |
| rs4330749 | 9:96,327,118 | T/A | — | benign |
| rs11975 | 9:96,327,691 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.