WDFY4
WDFY family member 4
Summary
Predicted to be involved in antigen processing and presentation. Predicted to act upstream of or within with a positive effect on CD8-positive, alpha-beta T cell activation. Predicted to act upstream of or within cellular response to virus. Predicted to be located in early endosome and endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants249 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs748945050 | 10:49,917,836 | A/G | — | likely benign |
| rs765608663 | 10:49,917,970 | C/T | — | uncertain significance |
| rs749750781 | 10:49,917,971 | G/A | — | likely benign |
| rs2492178371 | 10:49,928,075 | G/T | — | uncertain significance |
| rs373178324 | 10:49,928,116 | G/A | — | uncertain significance |
| rs923754849 | 10:49,928,150 | C/T | — | uncertain significance |
| rs763116265 | 10:49,929,314 | C/T | — | uncertain significance |
| rs142533169 | 10:49,929,353 | G/A | — | likely benign |
| rs930604383 | 10:49,929,357 | A/T | — | uncertain significance |
| rs762680599 | 10:49,929,363 | A/G | — | uncertain significance |
| rs757961242 | 10:49,929,401 | G/A | — | uncertain significance |
| rs989917824 | 10:49,931,482 | C/T | — | uncertain significance |
| rs1056070442 | 10:49,931,512 | C/T | — | uncertain significance |
| rs2492227877 | 10:49,931,518 | T/G | — | uncertain significance |
| rs1231622084 | 10:49,931,527 | A/G | — | uncertain significance |
| rs906529055 | 10:49,931,553 | C/A | — | uncertain significance |
| rs1019279683 | 10:49,931,602 | T/C | — | uncertain significance |
| rs111563360 | 10:49,931,615 | G/A | — | benign |
| rs368696574 | 10:49,933,965 | G/C | — | uncertain significance |
| rs1413949384 | 10:49,933,971 | C/T | — | uncertain significance |
| rs1416225271 | 10:49,934,061 | G/C | — | uncertain significance |
| rs1372171878 | 10:49,934,074 | T/C | — | uncertain significance |
| rs2492280136 | 10:49,935,517 | A/G | — | uncertain significance |
| rs1402783006 | 10:49,935,543 | G/C | — | uncertain significance |
| rs1443044404 | 10:49,935,556 | C/T | — | uncertain significance |
| rs139225815 | 10:49,935,560 | C/T | — | likely benign |
| rs41281997 | 10:49,935,566 | C/G | — | likely benign |
| rs2132315078 | 10:49,935,568 | C/T | — | uncertain significance |
| rs75030191 | 10:49,935,589 | G/A | — | uncertain significance |
| rs1014384563 | 10:49,935,631 | C/T | — | uncertain significance |
| rs370136528 | 10:49,935,641 | C/T | — | uncertain significance |
| rs1378713519 | 10:49,935,643 | G/T | — | uncertain significance |
| rs11101442 | 10:49,936,336 | C/A | — | — |
| rs367638233 | 10:49,937,498 | C/A | — | uncertain significance |
| rs1247737206 | 10:49,937,535 | G/T | — | uncertain significance |
| rs372539984 | 10:49,937,615 | G/T | — | uncertain significance |
| rs1241932639 | 10:49,939,337 | C/A | — | uncertain significance |
| rs368232022 | 10:49,939,347 | C/T | — | uncertain significance |
| rs76028336 | 10:49,939,475 | C/T | — | uncertain significance |
| rs759592071 | 10:49,939,538 | C/T | — | uncertain significance |
| rs1314406426 | 10:49,939,550 | C/T | — | uncertain significance |
| rs979440074 | 10:49,939,577 | C/T | — | uncertain significance |
| rs1171125948 | 10:49,941,984 | G/A | — | uncertain significance |
| rs2492375547 | 10:49,941,991 | C/G | — | likely benign |
| rs1589481174 | 10:49,942,020 | C/T | — | uncertain significance |
| rs1440445524 | 10:49,942,035 | C/A | — | benign |
| rs2492402147 | 10:49,943,939 | C/T | — | uncertain significance |
| rs768416100 | 10:49,943,948 | G/C | — | uncertain significance |
| rs866785917 | 10:49,943,963 | A/G | — | uncertain significance |
| rs767484076 | 10:49,944,008 | T/G | — | uncertain significance |
| rs986469898 | 10:49,951,047 | G/A | — | uncertain significance |
| rs747294517 | 10:49,951,106 | G/A | — | uncertain significance |
| rs2492480211 | 10:49,951,164 | C/A | — | uncertain significance |
| rs150767682 | 10:49,951,202 | G/T | — | uncertain significance |
| rs745889402 | 10:49,951,206 | C/T | — | uncertain significance |
| rs565353811 | 10:49,951,211 | C/T | — | uncertain significance |
| rs759195843 | 10:49,951,273 | G/T | — | uncertain significance |
| rs1387089115 | 10:49,951,328 | C/A | — | uncertain significance |
| rs771860003 | 10:49,951,329 | G/A | — | likely benign |
| rs2492483895 | 10:49,951,343 | A/G | — | uncertain significance |
| rs1331731680 | 10:49,951,344 | C/G | — | uncertain significance |
| rs538098816 | 10:49,951,410 | G/A | — | uncertain significance |
| rs2492485871 | 10:49,951,436 | G/A | — | likely benign |
| rs1054619684 | 10:49,951,437 | G/C | — | uncertain significance |
| rs766875496 | 10:49,951,475 | C/T | — | uncertain significance |
| rs542558497 | 10:49,951,559 | C/T | — | uncertain significance |
| rs1008002494 | 10:49,951,583 | C/G | — | uncertain significance |
| rs1322980120 | 10:49,968,409 | C/T | — | uncertain significance |
| rs72789234 | 10:49,968,492 | G/A | — | benign |
| rs1348846634 | 10:49,982,569 | C/T | — | uncertain significance |
| rs200635264 | 10:49,982,638 | A/C | — | uncertain significance |
| rs115706447 | 10:49,982,649 | C/T | — | benign |
| rs750671752 | 10:49,982,659 | C/T | — | uncertain significance |
| rs1331955636 | 10:49,982,705 | C/T | — | uncertain significance |
| rs12242384 | 10:49,983,819 | C/T | — | benign |
| rs2492822382 | 10:49,984,836 | G/A | — | uncertain significance |
| rs76547526 | 10:49,984,879 | C/T | — | benign |
| rs558367284 | 10:49,984,915 | C/T | — | uncertain significance |
| rs996278469 | 10:49,984,924 | C/T | — | uncertain significance |
| rs2492824721 | 10:49,984,986 | G/A | — | uncertain significance |
| rs2066052443 | 10:49,985,033 | T/G | — | benign |
| rs10857636 | 10:49,985,110 | C/T | intron variant | — |
| rs560423094 | 10:49,986,751 | C/T | — | uncertain significance |
| rs895581784 | 10:49,986,752 | G/A | — | uncertain significance |
| rs184936138 | 10:49,986,778 | G/A | — | uncertain significance |
| rs750281279 | 10:49,986,811 | G/A | — | uncertain significance |
| rs965493144 | 10:49,986,821 | G/A | — | uncertain significance |
| rs766404213 | 10:49,986,829 | G/A | — | uncertain significance |
| rs1419500555 | 10:49,986,863 | A/G | — | uncertain significance |
| rs144344845 | 10:49,988,002 | G/T | — | uncertain significance |
| rs780213095 | 10:49,988,015 | C/G | — | uncertain significance |
| rs1487555589 | 10:49,988,022 | C/A | — | uncertain significance |
| rs745873051 | 10:49,988,054 | C/G | — | uncertain significance |
| rs2066167831 | 10:49,988,108 | A/C | — | uncertain significance |
| rs917239998 | 10:49,988,148 | T/G | — | uncertain significance |
| rs370570628 | 10:49,994,700 | C/T | — | uncertain significance |
| rs779518009 | 10:49,994,735 | G/A | — | uncertain significance |
| rs368218858 | 10:49,994,745 | A/G | — | uncertain significance |
| rs1045711198 | 10:49,994,759 | A/G | — | uncertain significance |
| rs1291731783 | 10:49,994,774 | G/C | — | uncertain significance |
Showing 100 of 249 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.