ANKRD44
ankyrin repeat domain 44
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs745351850 | 2:197,854,335 | C/T | — | uncertain significance |
| rs1468139974 | 2:197,854,366 | C/A | — | uncertain significance |
| rs199697684 | 2:197,854,368 | T/C | — | uncertain significance |
| rs1414227313 | 2:197,858,355 | C/T | — | uncertain significance |
| rs2075960080 | 2:197,858,361 | C/A | — | uncertain significance |
| rs1300829029 | 2:197,858,376 | T/C | — | uncertain significance |
| rs767303463 | 2:197,858,378 | C/T | — | uncertain significance |
| rs908514972 | 2:197,858,381 | G/A | — | uncertain significance |
| rs751962730 | 2:197,863,075 | A/C | — | uncertain significance |
| rs371185609 | 2:197,863,104 | T/G | — | uncertain significance |
| rs754775802 | 2:197,863,131 | T/C | — | uncertain significance |
| rs768009425 | 2:197,863,772 | G/A | — | uncertain significance |
| rs771910566 | 2:197,865,168 | C/T | — | uncertain significance |
| rs758412435 | 2:197,865,195 | G/C | — | uncertain significance |
| rs1456098208 | 2:197,870,444 | G/A | — | uncertain significance |
| rs371039552 | 2:197,870,552 | G/A | — | uncertain significance |
| rs771884805 | 2:197,870,630 | A/G | — | uncertain significance |
| rs769745487 | 2:197,872,607 | C/T | — | uncertain significance |
| rs2468917224 | 2:197,872,613 | T/C | — | uncertain significance |
| rs2468917341 | 2:197,872,622 | A/G | — | uncertain significance |
| rs61752171 | 2:197,873,693 | C/G | — | uncertain significance |
| rs377187711 | 2:197,873,701 | G/A | — | uncertain significance |
| rs762365926 | 2:197,873,749 | T/C | — | uncertain significance |
| rs752754385 | 2:197,878,436 | C/A | — | uncertain significance |
| rs750730223 | 2:197,889,922 | C/A | — | uncertain significance |
| rs4850755 | 2:197,927,372 | C/T | intron variant | — |
| rs779440775 | 2:197,943,456 | C/G | — | uncertain significance |
| rs780285037 | 2:197,943,494 | C/T | — | uncertain significance |
| rs1368550050 | 2:197,943,495 | G/A | — | uncertain significance |
| rs772774703 | 2:197,946,372 | G/A | — | uncertain significance |
| rs572639484 | 2:197,946,418 | A/G | — | uncertain significance |
| rs1055370463 | 2:197,946,444 | G/A | — | uncertain significance |
| rs146056112 | 2:197,948,105 | T/C | — | uncertain significance |
| rs762483495 | 2:197,948,136 | G/A | — | uncertain significance |
| rs143689324 | 2:197,948,160 | C/T | — | uncertain significance |
| rs139336667 | 2:197,948,166 | C/A | — | uncertain significance |
| rs2469332282 | 2:197,949,541 | A/G | — | likely pathogenic |
| rs2469343044 | 2:197,951,412 | C/G | — | uncertain significance |
| rs761634548 | 2:197,951,459 | T/C | — | uncertain significance |
| rs540800015 | 2:197,986,092 | T/A | — | uncertain significance |
| rs138806991 | 2:197,986,178 | C/T | — | uncertain significance |
| rs146931928 | 2:197,986,225 | G/A | — | uncertain significance |
| rs563202124 | 2:197,987,459 | T/C | — | uncertain significance |
| rs745315250 | 2:197,987,468 | G/A | — | uncertain significance |
| rs771897169 | 2:197,987,507 | T/A | — | uncertain significance |
| rs1286948145 | 2:197,990,107 | A/G | — | uncertain significance |
| rs766048697 | 2:197,990,134 | C/T | — | uncertain significance |
| rs887105517 | 2:197,990,588 | G/T | — | uncertain significance |
| rs2468637222 | 2:198,001,330 | C/A | — | uncertain significance |
| rs1298744000 | 2:198,001,344 | A/G | — | uncertain significance |
| rs984944268 | 2:198,001,377 | A/G | — | uncertain significance |
| rs16863455 | 2:198,093,346 | C/G | intron variant | — |
| rs4435471 | 2:198,095,767 | G/A | intron variant | — |
| rs4850425 | 2:198,152,786 | T/A | — | — |
| rs1896857 | 2:198,164,530 | A/G | intron variant | — |
| rs1246954672 | 2:198,175,319 | G/A | — | uncertain significance |
| rs1444706195 | 2:198,175,324 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.