ANKAR
ankyrin and armadillo repeat containing
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants82 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs775763584 | 2:190,541,245 | C/G | — | uncertain significance |
| rs2468880219 | 2:190,541,257 | A/G | — | uncertain significance |
| rs568618403 | 2:190,541,401 | G/A | — | uncertain significance |
| rs1463599164 | 2:190,541,464 | C/T | — | uncertain significance |
| rs1386647771 | 2:190,541,481 | G/A | — | uncertain significance |
| rs77970584 | 2:190,541,492 | T/G | — | benign |
| rs140832996 | 2:190,541,497 | T/C | — | uncertain significance |
| rs140425516 | 2:190,541,646 | G/A | — | uncertain significance |
| rs374314519 | 2:190,541,776 | C/T | — | uncertain significance |
| rs191951749 | 2:190,554,222 | C/G | intron variant | — |
| rs144939402 | 2:190,554,267 | A/G | — | benign |
| rs745502581 | 2:190,554,398 | C/G | — | uncertain significance |
| rs1237090325 | 2:190,554,483 | G/T | — | uncertain significance |
| rs1257706311 | 2:190,554,566 | G/T | — | uncertain significance |
| rs773295578 | 2:190,554,643 | A/G | — | uncertain significance |
| rs1462812174 | 2:190,557,121 | G/A | — | uncertain significance |
| rs1214301643 | 2:190,557,885 | T/C | — | uncertain significance |
| rs148779806 | 2:190,557,894 | A/G | — | likely benign |
| rs16831876 | 2:190,557,908 | G/A | — | benign |
| rs115747871 | 2:190,559,712 | A/C | — | benign |
| rs138942918 | 2:190,559,731 | A/G | — | likely benign |
| rs530882331 | 2:190,559,766 | G/C | — | uncertain significance |
| rs772916051 | 2:190,560,888 | G/A | — | uncertain significance |
| rs148013275 | 2:190,560,942 | C/T | — | uncertain significance |
| rs762042057 | 2:190,560,990 | A/C | — | uncertain significance |
| rs142004571 | 2:190,561,003 | A/T | — | likely benign |
| rs78506934 | 2:190,561,062 | G/A | — | uncertain significance |
| rs190755713 | 2:190,561,075 | G/A | — | uncertain significance |
| rs200744384 | 2:190,569,763 | C/T | — | uncertain significance |
| rs533853538 | 2:190,569,778 | G/A | — | uncertain significance |
| rs773469547 | 2:190,569,812 | G/A | — | uncertain significance |
| rs766973234 | 2:190,569,848 | G/T | — | uncertain significance |
| rs2469076003 | 2:190,569,859 | A/G | — | uncertain significance |
| rs754714133 | 2:190,569,870 | C/T | — | likely benign |
| rs372479146 | 2:190,569,886 | G/A | — | likely benign |
| rs921893517 | 2:190,571,731 | T/C | — | uncertain significance |
| rs2469089666 | 2:190,571,767 | G/C | — | uncertain significance |
| rs538288193 | 2:190,571,794 | T/A | — | uncertain significance |
| rs147390101 | 2:190,571,797 | A/G | — | benign |
| rs150827562 | 2:190,575,775 | A/C | — | uncertain significance |
| rs530022067 | 2:190,575,816 | G/A | — | uncertain significance |
| rs371771252 | 2:190,575,819 | A/G | — | uncertain significance |
| rs2041006291 | 2:190,584,397 | C/A | — | uncertain significance |
| rs142330212 | 2:190,584,400 | T/C | — | likely benign |
| rs74586089 | 2:190,584,410 | G/A | — | benign |
| rs745767391 | 2:190,584,417 | G/A | — | uncertain significance |
| rs2469190162 | 2:190,584,496 | A/G | — | uncertain significance |
| rs748244897 | 2:190,585,442 | A/T | — | uncertain significance |
| rs142304483 | 2:190,585,448 | A/C | — | uncertain significance |
| rs777089877 | 2:190,585,471 | A/C | — | uncertain significance |
| rs200831821 | 2:190,585,486 | C/A | — | uncertain significance |
| rs767058996 | 2:190,585,493 | G/T | — | uncertain significance |
| rs757357867 | 2:190,592,627 | G/C | — | uncertain significance |
| rs769165318 | 2:190,592,672 | T/G | — | uncertain significance |
| rs369248930 | 2:190,592,699 | G/A | — | uncertain significance |
| rs746058223 | 2:190,592,756 | A/T | — | uncertain significance |
| rs142352023 | 2:190,592,760 | C/T | — | benign |
| rs755187735 | 2:190,593,019 | A/T | — | uncertain significance |
| rs779737213 | 2:190,593,080 | G/C | — | uncertain significance |
| rs139078107 | 2:190,593,090 | G/A | — | uncertain significance |
| rs758070365 | 2:190,593,491 | C/T | — | uncertain significance |
| rs1474142779 | 2:190,593,545 | T/C | — | uncertain significance |
| rs2468535202 | 2:190,597,857 | T/C | — | uncertain significance |
| rs761649640 | 2:190,597,896 | C/T | — | uncertain significance |
| rs2468536439 | 2:190,597,951 | A/G | — | uncertain significance |
| rs1378312591 | 2:190,602,410 | A/T | — | uncertain significance |
| rs752651499 | 2:190,602,461 | G/A | — | uncertain significance |
| rs200941909 | 2:190,602,524 | T/G | — | uncertain significance |
| rs143926631 | 2:190,606,152 | A/C | — | benign |
| rs12053254 | 2:190,607,153 | T/C | downstream gene variant | — |
| rs80227981 | 2:190,608,005 | G/A | — | likely benign |
| rs149628527 | 2:190,608,053 | C/T | — | uncertain significance |
| rs762171341 | 2:190,608,138 | T/G | — | uncertain significance |
| rs374330017 | 2:190,608,146 | C/A | — | uncertain significance |
| rs2468638383 | 2:190,609,494 | T/G | — | uncertain significance |
| rs61744814 | 2:190,609,504 | C/T | — | benign |
| rs754991846 | 2:190,611,244 | C/T | — | uncertain significance |
| rs2044197350 | 2:190,611,301 | A/G | — | likely benign |
| rs112668352 | 2:190,611,304 | A/T | — | benign |
| rs2468668592 | 2:190,611,315 | C/T | — | uncertain significance |
| rs144149897 | 2:190,611,328 | C/A | — | uncertain significance |
| rs751815466 | 2:190,611,340 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.