ANKRD35
ankyrin repeat domain 35
Summary
Predicted to enable actin binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs782188282 | 1:145,555,742 | G/C | — | uncertain significance |
| rs893779352 | 1:145,555,750 | T/C | — | uncertain significance |
| rs147155265 | 1:145,555,756 | G/T | — | uncertain significance |
| rs782479053 | 1:145,555,799 | G/T | — | uncertain significance |
| rs782562570 | 1:145,555,807 | C/T | — | uncertain significance |
| rs782294282 | 1:145,555,821 | C/T | — | uncertain significance |
| rs782403820 | 1:145,556,674 | A/G | — | uncertain significance |
| rs587737472 | 1:145,556,677 | A/G | — | uncertain significance |
| rs1553740453 | 1:145,557,048 | G/A | — | uncertain significance |
| rs2526423521 | 1:145,557,101 | G/T | — | uncertain significance |
| rs587723709 | 1:145,557,362 | C/A | — | — |
| rs1204406545 | 1:145,558,242 | A/G | — | uncertain significance |
| rs201520134 | 1:145,558,244 | C/T | — | uncertain significance |
| rs145335153 | 1:145,558,486 | G/A | — | uncertain significance |
| rs143368139 | 1:145,558,501 | G/A | — | uncertain significance |
| rs138703494 | 1:145,558,835 | G/A | — | uncertain significance |
| rs1193647861 | 1:145,558,863 | C/T | — | uncertain significance |
| rs370459651 | 1:145,558,914 | G/A | — | uncertain significance |
| rs2526408253 | 1:145,560,122 | A/G | — | uncertain significance |
| rs781812215 | 1:145,560,148 | G/A | — | uncertain significance |
| rs757009603 | 1:145,560,244 | C/T | — | uncertain significance |
| rs781974125 | 1:145,560,248 | G/A | — | uncertain significance |
| rs149985268 | 1:145,560,893 | G/C | — | conflicting classifications of pathogenicity |
| rs587733369 | 1:145,560,908 | C/A | — | uncertain significance |
| rs972549417 | 1:145,561,240 | G/T | — | uncertain significance |
| rs782777832 | 1:145,561,244 | G/A | — | likely benign |
| rs782326861 | 1:145,561,310 | T/C | — | uncertain significance |
| rs1387838405 | 1:145,561,382 | A/G | — | likely benign |
| rs150927897 | 1:145,561,399 | C/T | — | uncertain significance |
| rs782246266 | 1:145,561,541 | G/C | — | uncertain significance |
| rs140831880 | 1:145,561,552 | T/A | — | uncertain significance |
| rs782312525 | 1:145,561,568 | G/A | — | uncertain significance |
| rs2526399770 | 1:145,561,610 | C/A | — | uncertain significance |
| rs1653927887 | 1:145,561,675 | G/C | — | uncertain significance |
| rs587691367 | 1:145,561,757 | C/A | — | uncertain significance |
| rs1408588484 | 1:145,561,769 | C/A | — | uncertain significance |
| rs143964722 | 1:145,561,782 | G/T | — | uncertain significance |
| rs201815402 | 1:145,561,841 | G/C | — | uncertain significance |
| rs782399862 | 1:145,561,873 | G/A | — | uncertain significance |
| rs2526397758 | 1:145,561,903 | G/A | — | uncertain significance |
| rs782233086 | 1:145,561,939 | C/T | — | uncertain significance |
| rs140295711 | 1:145,561,945 | C/A | — | uncertain significance |
| rs1653910333 | 1:145,561,972 | G/C | — | uncertain significance |
| rs782680168 | 1:145,562,152 | G/C | — | uncertain significance |
| rs1553739129 | 1:145,562,225 | G/C | — | uncertain significance |
| rs781959537 | 1:145,562,284 | C/G | — | uncertain significance |
| rs2526394250 | 1:145,562,321 | G/A | — | likely benign |
| rs2526393911 | 1:145,562,390 | T/G | — | likely benign |
| rs2526392882 | 1:145,562,468 | A/G | — | likely benign |
| rs142514686 | 1:145,562,528 | G/C | — | uncertain significance |
| rs1553738963 | 1:145,562,574 | C/A | — | uncertain significance |
| rs992740040 | 1:145,562,662 | C/G | — | uncertain significance |
| rs369201218 | 1:145,562,727 | G/T | — | uncertain significance |
| rs1653852236 | 1:145,562,891 | A/G | — | uncertain significance |
| rs587764944 | 1:145,563,077 | C/T | — | uncertain significance |
| rs2526373204 | 1:145,566,692 | G/C | — | uncertain significance |
| rs944959443 | 1:145,566,734 | G/C | — | uncertain significance |
| rs148940814 | 1:145,566,740 | C/T | — | uncertain significance |
| rs374436917 | 1:145,566,741 | G/A | — | uncertain significance |
| rs587692787 | 1:145,566,759 | T/C | — | uncertain significance |
| rs377017276 | 1:145,567,094 | G/A | — | likely benign |
| rs1163644596 | 1:145,567,718 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.