FAM13B
family with sequence similarity 13 member B
Summary
Predicted to enable GTPase activator activity. Predicted to be involved in regulation of small GTPase mediated signal transduction. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2532317125 | 5:137,276,032 | G/A | — | uncertain significance |
| rs142996518 | 5:137,278,591 | C/T | — | uncertain significance |
| rs201081598 | 5:137,278,641 | G/C | — | uncertain significance |
| rs1214316563 | 5:137,278,655 | A/G | — | uncertain significance |
| rs981215960 | 5:137,278,829 | T/G | — | uncertain significance |
| rs2532431808 | 5:137,278,884 | T/C | — | uncertain significance |
| rs1282985348 | 5:137,278,893 | T/G | — | uncertain significance |
| rs2532432324 | 5:137,278,901 | G/C | — | uncertain significance |
| rs2532515668 | 5:137,281,607 | C/G | — | uncertain significance |
| rs916082428 | 5:137,284,789 | G/A | — | uncertain significance |
| rs772160288 | 5:137,284,829 | G/A | — | uncertain significance |
| rs143483187 | 5:137,288,391 | T/C | — | uncertain significance |
| rs552806662 | 5:137,289,063 | G/C | — | uncertain significance |
| rs541684906 | 5:137,289,152 | A/C | — | uncertain significance |
| rs559691371 | 5:137,289,877 | A/G | — | uncertain significance |
| rs146263439 | 5:137,289,912 | C/T | — | uncertain significance |
| rs375120542 | 5:137,289,913 | G/A | — | uncertain significance |
| rs371205351 | 5:137,289,939 | C/T | — | uncertain significance |
| rs370704588 | 5:137,289,961 | A/G | — | uncertain significance |
| rs758370925 | 5:137,289,979 | G/A | — | uncertain significance |
| rs746862214 | 5:137,289,986 | C/A | — | uncertain significance |
| rs1023859739 | 5:137,290,020 | C/T | — | uncertain significance |
| rs575496727 | 5:137,295,347 | G/A | — | uncertain significance |
| rs1186135369 | 5:137,295,433 | C/T | — | uncertain significance |
| rs139240453 | 5:137,295,445 | C/T | — | uncertain significance |
| rs2532961702 | 5:137,295,866 | G/A | — | uncertain significance |
| rs934027036 | 5:137,298,095 | T/A | — | uncertain significance |
| rs1011884563 | 5:137,298,155 | C/T | — | uncertain significance |
| rs947619062 | 5:137,320,972 | C/A | — | uncertain significance |
| rs754365820 | 5:137,321,029 | A/C | — | uncertain significance |
| rs139752546 | 5:137,321,064 | T/A | — | uncertain significance |
| rs149905723 | 5:137,323,997 | T/C | — | uncertain significance |
| rs1246481738 | 5:137,342,680 | T/C | — | uncertain significance |
| rs573294558 | 5:137,342,781 | T/A | — | uncertain significance |
| rs1782745424 | 5:137,342,805 | T/C | — | uncertain significance |
| rs887064504 | 5:137,342,836 | C/A | — | uncertain significance |
| rs755226222 | 5:137,347,517 | T/C | — | uncertain significance |
| rs772213036 | 5:137,347,529 | T/C | — | uncertain significance |
| rs113331339 | 5:137,351,159 | A/C | intron variant | — |
| rs147001729 | 5:137,354,020 | A/G | — | uncertain significance |
| rs148088678 | 5:137,354,051 | C/T | — | uncertain significance |
| rs754701574 | 5:137,354,668 | C/T | — | uncertain significance |
| rs1451125084 | 5:137,354,680 | T/C | — | uncertain significance |
| rs10479170 | 5:137,356,013 | G/A | intron variant | — |
| rs17171711 | 5:137,364,795 | C/T | regulatory region variant | — |
| rs13355516 | 5:137,380,603 | A/G | downstream gene variant | — |
| rs148378888 | 5:137,383,078 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.