FCGBP
Fc gamma binding protein
Summary
Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants398 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs556429522 | 19:40,354,340 | C/T | — | uncertain significance |
| rs761968771 | 19:40,354,384 | T/C | — | uncertain significance |
| rs376090141 | 19:40,354,411 | T/C | — | uncertain significance |
| rs930534198 | 19:40,354,465 | T/C | — | uncertain significance |
| rs765387728 | 19:40,354,480 | A/C | — | uncertain significance |
| rs1339752876 | 19:40,354,510 | A/C | — | uncertain significance |
| rs780021060 | 19:40,354,519 | C/T | — | likely benign |
| rs367675319 | 19:40,357,439 | C/T | — | uncertain significance |
| rs752541180 | 19:40,357,595 | C/T | — | uncertain significance |
| rs571193281 | 19:40,357,600 | G/A | — | uncertain significance |
| rs767623890 | 19:40,357,611 | G/A | — | likely benign |
| rs148773345 | 19:40,357,682 | C/T | — | uncertain significance |
| rs763924280 | 19:40,357,694 | T/C | — | uncertain significance |
| rs200520932 | 19:40,357,727 | C/T | — | likely benign |
| rs368974681 | 19:40,360,875 | T/C | — | uncertain significance |
| rs759774406 | 19:40,360,909 | C/A | — | uncertain significance |
| rs139526217 | 19:40,360,936 | C/T | — | uncertain significance |
| rs1026537999 | 19:40,360,939 | A/G | — | uncertain significance |
| rs184463001 | 19:40,360,974 | G/A | — | uncertain significance |
| rs374766909 | 19:40,360,981 | C/G | — | uncertain significance |
| rs745822010 | 19:40,361,041 | C/T | — | uncertain significance |
| rs776691909 | 19:40,362,748 | C/T | — | uncertain significance |
| rs145591797 | 19:40,362,774 | G/A | missense variant | — |
| rs780105651 | 19:40,362,795 | C/T | — | uncertain significance |
| rs201350567 | 19:40,362,825 | G/A | — | uncertain significance |
| rs1184682524 | 19:40,362,827 | G/A | — | likely benign |
| rs148882021 | 19:40,362,841 | C/T | — | uncertain significance |
| rs750135861 | 19:40,362,849 | C/T | — | uncertain significance |
| rs201686360 | 19:40,362,909 | C/T | — | uncertain significance |
| rs928826668 | 19:40,362,919 | C/T | — | uncertain significance |
| rs757481557 | 19:40,362,943 | G/A | — | uncertain significance |
| rs368275854 | 19:40,363,015 | C/T | — | likely benign |
| rs551862975 | 19:40,363,037 | G/T | — | uncertain significance |
| rs1212077416 | 19:40,363,128 | C/T | — | uncertain significance |
| rs771608901 | 19:40,363,134 | C/T | — | likely benign |
| rs748386056 | 19:40,363,188 | C/T | — | uncertain significance |
| rs140298192 | 19:40,363,221 | C/T | — | uncertain significance |
| rs372154389 | 19:40,363,240 | G/A | — | uncertain significance |
| rs984835095 | 19:40,363,272 | G/C | — | uncertain significance |
| rs369490842 | 19:40,363,872 | C/T | — | uncertain significance |
| rs779728798 | 19:40,363,913 | A/G | — | uncertain significance |
| rs140593694 | 19:40,364,065 | G/A | — | likely benign |
| rs138481755 | 19:40,364,075 | C/G | — | uncertain significance |
| rs542656820 | 19:40,364,103 | C/T | — | uncertain significance |
| rs200818506 | 19:40,364,123 | C/G | — | uncertain significance |
| rs147171686 | 19:40,364,124 | G/C | — | uncertain significance |
| rs762789511 | 19:40,364,151 | C/T | — | uncertain significance |
| rs377388299 | 19:40,364,211 | G/A | — | uncertain significance |
| rs765553575 | 19:40,364,253 | C/G | — | uncertain significance |
| rs200368344 | 19:40,364,283 | C/T | — | uncertain significance |
| rs749258935 | 19:40,364,304 | C/T | — | uncertain significance |
| rs201042086 | 19:40,364,355 | C/T | — | uncertain significance |
| rs375814373 | 19:40,364,409 | A/G | — | uncertain significance |
| rs1337104307 | 19:40,366,042 | C/T | — | uncertain significance |
| rs2513415436 | 19:40,366,063 | G/A | — | uncertain significance |
| rs1203924078 | 19:40,366,066 | C/A | — | uncertain significance |
| rs758454117 | 19:40,366,109 | A/G | — | uncertain significance |
| rs201558688 | 19:40,366,117 | C/T | — | uncertain significance |
| rs201656539 | 19:40,366,142 | C/T | — | uncertain significance |
| rs771508776 | 19:40,366,143 | G/C | — | uncertain significance |
| rs749793074 | 19:40,366,187 | C/T | — | likely benign |
| rs141202081 | 19:40,366,189 | T/A | — | uncertain significance |
| rs748108404 | 19:40,366,234 | G/A | — | uncertain significance |
| rs62106923 | 19:40,366,247 | C/T | — | uncertain significance |
| rs774323088 | 19:40,366,252 | G/C | — | uncertain significance |
| rs139954370 | 19:40,366,255 | T/A | — | uncertain significance |
| rs4029191 | 19:40,366,257 | C/T | — | likely benign |
| rs370511470 | 19:40,366,282 | G/C | — | uncertain significance |
| rs1969697286 | 19:40,366,315 | T/C | — | likely benign |
| rs1429477393 | 19:40,366,319 | C/T | — | uncertain significance |
| rs146237226 | 19:40,366,334 | A/G | — | uncertain significance |
| rs760618440 | 19:40,366,352 | C/T | — | uncertain significance |
| rs202238471 | 19:40,366,376 | G/A | — | uncertain significance |
| rs748304167 | 19:40,366,408 | A/G | — | uncertain significance |
| rs148970533 | 19:40,366,458 | A/G | — | likely benign |
| rs749388257 | 19:40,366,463 | A/G | — | uncertain significance |
| rs772702980 | 19:40,366,483 | G/A | — | uncertain significance |
| rs768623814 | 19:40,366,529 | G/C | — | uncertain significance |
| rs141638527 | 19:40,366,553 | C/T | — | uncertain significance |
| rs1221982971 | 19:40,367,317 | C/T | — | uncertain significance |
| rs1253369433 | 19:40,367,447 | G/A | — | uncertain significance |
| rs759726402 | 19:40,367,758 | C/T | — | uncertain significance |
| rs1161055950 | 19:40,367,759 | G/A | — | uncertain significance |
| rs777521353 | 19:40,367,805 | A/C | — | uncertain significance |
| rs200140260 | 19:40,368,356 | G/C | — | uncertain significance |
| rs757413278 | 19:40,368,375 | G/C | — | uncertain significance |
| rs1416156340 | 19:40,368,420 | C/T | — | uncertain significance |
| rs776385904 | 19:40,368,476 | A/G | — | uncertain significance |
| rs554417983 | 19:40,368,525 | C/T | — | uncertain significance |
| rs778769857 | 19:40,368,608 | C/G | — | uncertain significance |
| rs768991113 | 19:40,368,680 | T/C | — | uncertain significance |
| rs199714018 | 19:40,368,684 | G/A | — | uncertain significance |
| rs144631134 | 19:40,368,707 | C/T | — | uncertain significance |
| rs755114213 | 19:40,368,719 | T/C | — | uncertain significance |
| rs138525431 | 19:40,368,764 | T/C | — | uncertain significance |
| rs759513585 | 19:40,368,834 | C/G | — | uncertain significance |
| rs1411945974 | 19:40,370,205 | C/G | — | uncertain significance |
| rs1322010732 | 19:40,370,206 | C/G | — | uncertain significance |
| rs756777952 | 19:40,370,266 | C/T | — | uncertain significance |
| rs781059374 | 19:40,370,289 | C/G | — | uncertain significance |
Showing 100 of 398 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.