FHAD1
forkhead associated phosphopeptide binding domain 1
Summary
Predicted to act upstream of or within apoptotic process and spermatogenesis. Located in sperm flagellum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants95 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2523327160 | 1:15,578,300 | G/C | — | uncertain significance |
| rs936755602 | 1:15,578,336 | C/G | — | uncertain significance |
| rs938070787 | 1:15,578,348 | A/T | — | uncertain significance |
| rs865938662 | 1:15,578,372 | A/G | — | uncertain significance |
| rs1355603897 | 1:15,598,901 | G/T | — | uncertain significance |
| rs1470892662 | 1:15,598,906 | G/A | — | uncertain significance |
| rs756645134 | 1:15,615,958 | C/G | — | uncertain significance |
| rs1390234778 | 1:15,615,977 | C/A | — | uncertain significance |
| rs563528811 | 1:15,616,022 | C/T | — | uncertain significance |
| rs778250154 | 1:15,616,073 | C/T | — | uncertain significance |
| rs781623345 | 1:15,616,088 | G/A | — | uncertain significance |
| rs548188217 | 1:15,616,138 | C/T | — | uncertain significance |
| rs1309795593 | 1:15,623,219 | C/G | — | uncertain significance |
| rs376640150 | 1:15,623,221 | G/A | — | uncertain significance |
| rs2524983379 | 1:15,623,282 | A/C | — | uncertain significance |
| rs1012646814 | 1:15,627,737 | C/T | — | uncertain significance |
| rs551228538 | 1:15,627,749 | T/C | — | uncertain significance |
| rs547058385 | 1:15,627,803 | G/A | — | uncertain significance |
| rs202211467 | 1:15,627,824 | G/A | — | uncertain significance |
| rs986204492 | 1:15,627,870 | A/T | — | uncertain significance |
| rs763424963 | 1:15,635,152 | C/T | — | uncertain significance |
| rs747370305 | 1:15,635,164 | G/A | — | uncertain significance |
| rs977003394 | 1:15,635,195 | G/C | — | uncertain significance |
| rs1460111149 | 1:15,635,220 | G/A | — | uncertain significance |
| rs930335951 | 1:15,639,672 | C/T | — | uncertain significance |
| rs760661446 | 1:15,642,885 | A/G | — | likely benign |
| rs1002911650 | 1:15,642,962 | C/T | — | uncertain significance |
| rs949369192 | 1:15,651,020 | G/A | — | uncertain significance |
| rs1487960230 | 1:15,653,612 | C/T | — | uncertain significance |
| rs1163164780 | 1:15,654,864 | C/T | — | uncertain significance |
| rs751922129 | 1:15,654,875 | G/A | — | uncertain significance |
| rs1444754825 | 1:15,654,884 | G/A | — | uncertain significance |
| rs376980078 | 1:15,654,906 | C/T | — | uncertain significance |
| rs953798262 | 1:15,655,938 | A/G | — | uncertain significance |
| rs943726679 | 1:15,668,288 | G/A | — | uncertain significance |
| rs780767246 | 1:15,668,333 | G/A | — | uncertain significance |
| rs75416704 | 1:15,668,372 | G/C | — | uncertain significance |
| rs773986688 | 1:15,671,588 | G/A | — | uncertain significance |
| rs1336583545 | 1:15,671,607 | G/A | — | likely benign |
| rs140526241 | 1:15,671,640 | G/A | — | likely benign |
| rs1569868224 | 1:15,671,648 | A/G | — | likely benign |
| rs1688362414 | 1:15,671,665 | C/G | — | uncertain significance |
| rs771376794 | 1:15,671,919 | C/T | — | uncertain significance |
| rs1207987939 | 1:15,671,954 | G/A | — | uncertain significance |
| rs367965718 | 1:15,671,981 | G/A | — | uncertain significance |
| rs2524153488 | 1:15,671,984 | C/G | — | uncertain significance |
| rs764165573 | 1:15,671,999 | C/G | — | uncertain significance |
| rs954423986 | 1:15,672,008 | C/T | — | uncertain significance |
| rs1418344098 | 1:15,675,556 | G/A | — | uncertain significance |
| rs367725625 | 1:15,675,574 | G/A | — | uncertain significance |
| rs552503130 | 1:15,678,717 | C/T | — | — |
| rs1048002428 | 1:15,679,392 | C/G | — | uncertain significance |
| rs199936638 | 1:15,679,404 | G/A | — | likely benign |
| rs555623090 | 1:15,679,421 | A/T | — | likely benign |
| rs940838651 | 1:15,679,439 | A/C | — | uncertain significance |
| rs189802196 | 1:15,684,661 | C/G | — | uncertain significance |
| rs1228180928 | 1:15,684,670 | T/C | — | uncertain significance |
| rs979426429 | 1:15,684,726 | G/T | — | uncertain significance |
| rs759178039 | 1:15,686,976 | C/G | — | uncertain significance |
| rs374013797 | 1:15,686,987 | A/G | — | uncertain significance |
| rs777926804 | 1:15,687,051 | C/A | — | uncertain significance |
| rs183879616 | 1:15,687,052 | G/A | — | uncertain significance |
| rs1048098355 | 1:15,687,055 | T/G | — | uncertain significance |
| rs759581263 | 1:15,687,070 | A/G | — | uncertain significance |
| rs528012255 | 1:15,687,121 | G/A | — | uncertain significance |
| rs372934958 | 1:15,687,169 | G/A | — | uncertain significance |
| rs369049977 | 1:15,689,156 | C/T | — | uncertain significance |
| rs557275213 | 1:15,689,157 | G/A | — | likely benign |
| rs2524799757 | 1:15,689,163 | C/G | — | uncertain significance |
| rs201087260 | 1:15,689,182 | A/T | — | uncertain significance |
| rs553006400 | 1:15,689,205 | G/A | — | uncertain significance |
| rs373444389 | 1:15,692,403 | C/A | — | uncertain significance |
| rs370758843 | 1:15,694,012 | C/G | — | uncertain significance |
| rs1483859086 | 1:15,694,053 | G/A | — | uncertain significance |
| rs936914239 | 1:15,695,991 | G/A | — | uncertain significance |
| rs181011016 | 1:15,701,013 | G/A | — | uncertain significance |
| rs549212254 | 1:15,701,014 | A/G | — | uncertain significance |
| rs761167442 | 1:15,701,027 | G/T | — | uncertain significance |
| rs1254170305 | 1:15,701,029 | G/A | — | uncertain significance |
| rs749109875 | 1:15,701,041 | G/A | — | uncertain significance |
| rs200167745 | 1:15,701,092 | C/T | — | uncertain significance |
| rs1184165026 | 1:15,701,098 | T/C | — | uncertain significance |
| rs557799240 | 1:15,702,099 | A/G | — | uncertain significance |
| rs779918824 | 1:15,702,102 | A/G | — | uncertain significance |
| rs553014783 | 1:15,702,225 | C/A | — | uncertain significance |
| rs1038902536 | 1:15,707,198 | C/T | — | uncertain significance |
| rs974483148 | 1:15,707,227 | G/A | — | likely benign |
| rs533051999 | 1:15,707,236 | A/C | — | uncertain significance |
| rs1014781198 | 1:15,707,281 | A/G | — | uncertain significance |
| rs555980613 | 1:15,707,812 | A/G | — | uncertain significance |
| rs371335103 | 1:15,708,525 | C/T | — | uncertain significance |
| rs1219799332 | 1:15,708,636 | G/A | — | uncertain significance |
| rs770990473 | 1:15,708,675 | A/G | — | uncertain significance |
| rs375422050 | 1:15,708,679 | G/A | — | uncertain significance |
| rs1261285246 | 1:15,723,902 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.