GOLGB1
golgin B1
Summary
Enables RNA binding activity. Involved in protein localization to pericentriolar material. Located in Golgi apparatus and endoplasmic reticulum-Golgi intermediate compartment. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants172 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758007679 | 3:121,383,383 | T/C | — | uncertain significance |
| rs771045916 | 3:121,383,403 | C/T | — | uncertain significance |
| rs745651336 | 3:121,383,410 | G/A | — | uncertain significance |
| rs138614748 | 3:121,383,792 | G/C | — | uncertain significance |
| rs763348140 | 3:121,383,807 | A/C | — | uncertain significance |
| rs367875657 | 3:121,383,834 | C/G | — | uncertain significance |
| rs530077580 | 3:121,386,324 | G/A | — | uncertain significance |
| rs748027283 | 3:121,386,329 | A/T | — | uncertain significance |
| rs144495540 | 3:121,386,377 | T/A | — | uncertain significance |
| rs547521254 | 3:121,386,414 | C/T | — | likely benign |
| rs755051134 | 3:121,386,989 | T/C | — | uncertain significance |
| rs150865762 | 3:121,388,060 | G/A | — | uncertain significance |
| rs375281562 | 3:121,388,079 | G/C | — | uncertain significance |
| rs538255158 | 3:121,388,094 | C/A | — | uncertain significance |
| rs114033767 | 3:121,388,141 | C/T | — | uncertain significance |
| rs6783463 | 3:121,392,196 | A/G | intron variant | — |
| rs6791046 | 3:121,394,707 | A/G | intron variant | — |
| rs778615178 | 3:121,395,832 | C/A | — | uncertain significance |
| rs534528475 | 3:121,395,859 | C/G | — | uncertain significance |
| rs943410058 | 3:121,396,216 | C/A | — | uncertain significance |
| rs780927705 | 3:121,396,259 | A/G | — | uncertain significance |
| rs2547006341 | 3:121,396,273 | T/C | — | uncertain significance |
| rs142286671 | 3:121,409,523 | G/T | — | uncertain significance |
| rs1407516934 | 3:121,409,697 | G/T | — | likely benign |
| rs116823792 | 3:121,409,832 | G/A | — | likely benign |
| rs1041846011 | 3:121,409,861 | T/C | — | uncertain significance |
| rs371463845 | 3:121,409,902 | A/G | — | uncertain significance |
| rs1024838788 | 3:121,409,912 | C/A | — | uncertain significance |
| rs2547126745 | 3:121,409,999 | T/C | — | uncertain significance |
| rs1420450752 | 3:121,410,179 | C/G | — | uncertain significance |
| rs201201678 | 3:121,410,188 | C/T | — | uncertain significance |
| rs765883541 | 3:121,410,304 | T/C | — | uncertain significance |
| rs371984492 | 3:121,410,352 | G/A | — | uncertain significance |
| rs114926530 | 3:121,410,436 | C/T | — | likely benign |
| rs929887612 | 3:121,410,628 | T/C | — | uncertain significance |
| rs373840289 | 3:121,410,778 | C/T | — | uncertain significance |
| rs1942469507 | 3:121,410,808 | A/C | — | uncertain significance |
| rs184326685 | 3:121,410,811 | A/C | — | uncertain significance |
| rs754180819 | 3:121,411,027 | C/A | — | uncertain significance |
| rs2547138327 | 3:121,411,059 | C/T | — | uncertain significance |
| rs547801884 | 3:121,411,103 | C/T | — | uncertain significance |
| rs766829822 | 3:121,411,114 | G/A | — | uncertain significance |
| rs1427977435 | 3:121,411,139 | T/C | — | uncertain significance |
| rs1942517031 | 3:121,411,223 | T/C | — | uncertain significance |
| rs201961145 | 3:121,411,341 | T/G | — | uncertain significance |
| rs1225002499 | 3:121,411,345 | C/T | — | uncertain significance |
| rs1942536173 | 3:121,411,414 | T/C | — | uncertain significance |
| rs756018283 | 3:121,412,595 | T/C | — | uncertain significance |
| rs186004105 | 3:121,412,682 | C/G | — | uncertain significance |
| rs56162367 | 3:121,412,702 | A/G | — | uncertain significance |
| rs762036228 | 3:121,412,703 | C/T | — | uncertain significance |
| rs200441477 | 3:121,412,705 | T/C | — | uncertain significance |
| rs144414434 | 3:121,412,749 | G/C | — | uncertain significance |
| rs116407164 | 3:121,412,885 | T/A | — | uncertain significance |
| rs372538328 | 3:121,413,146 | C/T | — | uncertain significance |
| rs770806221 | 3:121,413,361 | C/G | — | uncertain significance |
| rs759858442 | 3:121,413,593 | T/A | — | uncertain significance |
| rs947220068 | 3:121,413,615 | T/C | — | uncertain significance |
| rs202244897 | 3:121,413,629 | G/A | — | uncertain significance |
| rs370926720 | 3:121,413,639 | A/G | — | uncertain significance |
| rs1045699257 | 3:121,413,860 | T/C | — | uncertain significance |
| rs1332096335 | 3:121,413,905 | G/A | — | uncertain significance |
| rs776086667 | 3:121,413,947 | A/C | — | uncertain significance |
| rs749115112 | 3:121,414,007 | G/A | — | likely benign |
| rs547309448 | 3:121,414,101 | G/C | — | uncertain significance |
| rs140861121 | 3:121,414,165 | C/A | — | uncertain significance |
| rs1371915267 | 3:121,414,230 | T/C | — | uncertain significance |
| rs759392269 | 3:121,414,233 | C/G | — | uncertain significance |
| rs372673093 | 3:121,414,263 | G/A | — | uncertain significance |
| rs778839292 | 3:121,414,507 | T/G | — | uncertain significance |
| rs767187541 | 3:121,414,654 | G/C | — | uncertain significance |
| rs1413843182 | 3:121,414,688 | T/A | — | uncertain significance |
| rs148168566 | 3:121,414,735 | C/T | — | likely benign |
| rs144067683 | 3:121,414,805 | G/A | — | uncertain significance |
| rs2547190138 | 3:121,414,841 | T/A | — | uncertain significance |
| rs767990835 | 3:121,414,856 | T/C | — | uncertain significance |
| rs768917337 | 3:121,414,961 | T/A | — | uncertain significance |
| rs139019364 | 3:121,414,971 | A/G | — | uncertain significance |
| rs766705613 | 3:121,415,006 | T/C | — | uncertain significance |
| rs373673263 | 3:121,415,043 | C/T | — | uncertain significance |
| rs376708356 | 3:121,415,054 | T/C | — | uncertain significance |
| rs143141179 | 3:121,415,084 | T/C | — | uncertain significance |
| rs373428621 | 3:121,415,088 | T/C | — | uncertain significance |
| rs754130998 | 3:121,415,098 | T/G | — | uncertain significance |
| rs200956055 | 3:121,415,111 | A/G | — | uncertain significance |
| rs2547194100 | 3:121,415,204 | A/T | — | uncertain significance |
| rs139168908 | 3:121,415,291 | C/T | — | uncertain significance |
| rs2547197217 | 3:121,415,437 | C/G | — | uncertain significance |
| rs753608867 | 3:121,415,451 | T/G | — | uncertain significance |
| rs372212899 | 3:121,415,454 | C/T | — | uncertain significance |
| rs148696334 | 3:121,415,471 | G/C | — | uncertain significance |
| rs571510013 | 3:121,415,507 | T/C | — | uncertain significance |
| rs139068595 | 3:121,415,540 | T/C | — | uncertain significance |
| rs2547198820 | 3:121,415,543 | G/A | — | uncertain significance |
| rs370467346 | 3:121,415,603 | G/A | — | uncertain significance |
| rs33988592 | 3:121,415,610 | G/A | missense variant | — |
| rs139646586 | 3:121,415,642 | A/G | — | uncertain significance |
| rs144385283 | 3:121,415,714 | C/G | — | likely benign |
| rs1158250232 | 3:121,415,726 | T/C | — | uncertain significance |
| rs2547201501 | 3:121,415,727 | C/A | — | uncertain significance |
Showing 100 of 172 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.