APBA3
amyloid beta precursor protein binding family A member 3
Summary
The protein encoded by this gene is a member of the X11 protein family. It is an adapter protein that interacts with the Alzheimer's disease amyloid precursor protein. This gene product is believed to be involved in signal transduction processes. This gene is a candidate gene for Alzheimer's disease. [provided by RefSeq, Jul 2008]
Known Variants71 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1356226308 | 19:3,751,032 | A/G | — | uncertain significance |
| rs199580985 | 19:3,751,035 | C/T | — | uncertain significance |
| rs370153267 | 19:3,751,055 | A/G | — | uncertain significance |
| rs144976844 | 19:3,751,062 | G/A | — | uncertain significance |
| rs1419324827 | 19:3,751,073 | G/A | — | uncertain significance |
| rs368800499 | 19:3,751,189 | C/T | — | uncertain significance |
| rs1415014709 | 19:3,751,239 | A/C | — | uncertain significance |
| rs373218431 | 19:3,751,245 | C/G | — | uncertain significance |
| rs1040773212 | 19:3,751,262 | A/C | — | uncertain significance |
| rs201075992 | 19:3,751,270 | G/A | — | uncertain significance |
| rs372902488 | 19:3,751,293 | C/T | — | uncertain significance |
| rs778982034 | 19:3,751,297 | C/T | — | uncertain significance |
| rs531106233 | 19:3,751,299 | G/A | — | uncertain significance |
| rs148643624 | 19:3,751,311 | C/T | — | uncertain significance |
| rs141313948 | 19:3,751,464 | C/T | — | uncertain significance |
| rs756584046 | 19:3,751,476 | G/A | — | uncertain significance |
| rs545628345 | 19:3,751,478 | C/T | — | uncertain significance |
| rs376088061 | 19:3,751,515 | C/T | — | uncertain significance |
| rs889414556 | 19:3,751,530 | C/A | — | uncertain significance |
| rs754594706 | 19:3,751,535 | G/A | — | uncertain significance |
| rs773106862 | 19:3,751,547 | G/A | — | uncertain significance |
| rs752377456 | 19:3,752,507 | C/T | — | uncertain significance |
| rs778886620 | 19:3,752,525 | G/A | — | uncertain significance |
| rs200943992 | 19:3,752,565 | C/T | — | uncertain significance |
| rs993390811 | 19:3,752,589 | G/A | — | uncertain significance |
| rs2512297181 | 19:3,752,610 | G/T | — | uncertain significance |
| rs781530250 | 19:3,752,613 | C/T | — | uncertain significance |
| rs769900594 | 19:3,752,616 | C/T | — | uncertain significance |
| rs749859490 | 19:3,752,657 | C/G | — | uncertain significance |
| rs1488946377 | 19:3,752,666 | G/A | — | uncertain significance |
| rs1360096932 | 19:3,752,699 | C/T | — | uncertain significance |
| rs774810791 | 19:3,752,703 | G/A | — | uncertain significance |
| rs200682478 | 19:3,752,877 | C/T | — | likely benign |
| rs766370183 | 19:3,752,981 | A/G | — | uncertain significance |
| rs12609548 | 19:3,753,656 | T/C | — | — |
| rs368746082 | 19:3,753,771 | C/T | — | uncertain significance |
| rs972092446 | 19:3,753,785 | C/T | — | uncertain significance |
| rs761296824 | 19:3,753,824 | G/A | — | uncertain significance |
| rs751236971 | 19:3,753,843 | G/A | — | uncertain significance |
| rs373142621 | 19:3,753,851 | G/A | — | uncertain significance |
| rs146035497 | 19:3,754,058 | C/T | — | likely benign |
| rs139904607 | 19:3,754,071 | C/A | — | uncertain significance |
| rs774635160 | 19:3,754,075 | G/A | — | uncertain significance |
| rs973647620 | 19:3,754,200 | C/T | — | uncertain significance |
| rs764194208 | 19:3,754,201 | G/A | — | uncertain significance |
| rs572429772 | 19:3,754,204 | C/T | — | uncertain significance |
| rs749088363 | 19:3,754,215 | C/T | — | likely benign |
| rs1224473166 | 19:3,754,228 | T/C | — | uncertain significance |
| rs748772419 | 19:3,754,287 | G/A | — | uncertain significance |
| rs376765289 | 19:3,754,303 | C/T | — | uncertain significance |
| rs1033794488 | 19:3,754,313 | G/T | — | uncertain significance |
| rs866125587 | 19:3,754,333 | C/G | — | uncertain significance |
| rs55941146 | 19:3,754,338 | A/C | missense variant | — |
| rs200666451 | 19:3,759,565 | G/C | — | uncertain significance |
| rs1179085651 | 19:3,759,570 | G/A | — | uncertain significance |
| rs763080424 | 19:3,759,597 | C/A | — | uncertain significance |
| rs34690145 | 19:3,759,702 | T/C | — | benign |
| rs200510985 | 19:3,759,728 | C/T | — | uncertain significance |
| rs374857161 | 19:3,759,748 | G/A | — | uncertain significance |
| rs2037122453 | 19:3,759,839 | G/A | — | uncertain significance |
| rs769019461 | 19:3,759,853 | C/G | — | uncertain significance |
| rs202201416 | 19:3,759,856 | G/C | — | uncertain significance |
| rs141202109 | 19:3,759,874 | T/C | — | uncertain significance |
| rs773522332 | 19:3,759,899 | G/T | — | uncertain significance |
| rs372283413 | 19:3,759,938 | G/A | — | uncertain significance |
| rs149463753 | 19:3,760,061 | G/A | — | uncertain significance |
| rs2512308562 | 19:3,760,066 | G/A | — | uncertain significance |
| rs199883480 | 19:3,760,130 | C/T | — | likely benign |
| rs750809585 | 19:3,760,187 | C/T | — | uncertain significance |
| rs201096128 | 19:3,760,214 | C/G | — | uncertain significance |
| rs776734372 | 19:3,760,240 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.