HORMAD2
HORMA domain containing 2
Summary
Predicted to be involved in meiotic cell cycle and meiotic sister chromatid cohesion. Located in centrosome; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4820827 | 22:30,477,589 | T/C | upstream gene variant | — |
| rs2412970 | 22:30,486,826 | A/G | intron variant | — |
| rs4823071 | 22:30,492,300 | A/G | intron variant | — |
| rs2412971 | 22:30,494,371 | G/A | intron variant | — |
| rs376899418 | 22:30,494,841 | G/A | — | uncertain significance |
| rs34305723 | 22:30,494,847 | G/C | — | benign |
| rs373835705 | 22:30,494,907 | G/T | — | uncertain significance |
| rs1409240185 | 22:30,494,941 | G/T | — | uncertain significance |
| rs9614144 | 22:30,501,486 | T/A | upstream gene variant | — |
| rs718772 | 22:30,504,207 | A/C | — | — |
| rs4823073 | 22:30,512,258 | G/A | regulatory region variant | — |
| rs775025324 | 22:30,517,770 | A/G | — | uncertain significance |
| rs757118057 | 22:30,517,997 | A/T | — | uncertain significance |
| rs748056519 | 22:30,518,009 | C/G | — | uncertain significance |
| rs1922494344 | 22:30,518,111 | G/T | — | uncertain significance |
| rs747662890 | 22:30,518,132 | C/T | — | uncertain significance |
| rs1922498417 | 22:30,518,142 | G/A | — | uncertain significance |
| rs761939996 | 22:30,518,165 | G/A | — | uncertain significance |
| rs4823075 | 22:30,519,152 | T/C | intron variant | — |
| rs4823076 | 22:30,519,414 | G/A | intron variant | — |
| rs2412972 | 22:30,519,825 | T/G | — | — |
| rs5763790 | 22:30,522,413 | G/C | intron variant | — |
| rs4820829 | 22:30,524,248 | C/T | intron variant | — |
| rs5763793 | 22:30,526,632 | G/T | intron variant | — |
| rs2412973 | 22:30,529,631 | C/A | downstream gene variant | — |
| rs5763800 | 22:30,533,409 | A/G | intron variant | — |
| rs9608847 | 22:30,536,056 | T/A | — | — |
| rs2412974 | 22:30,539,821 | C/T | intron variant | — |
| rs2412975 | 22:30,540,590 | T/C | regulatory region variant | — |
| rs1468176 | 22:30,544,516 | G/T | — | — |
| rs4823077 | 22:30,545,149 | A/G | intron variant | — |
| rs5763821 | 22:30,549,071 | A/C | — | — |
| rs4336042 | 22:30,552,511 | G/A | intron variant | — |
| rs5763842 | 22:30,568,738 | G/C | — | — |
| rs1003342 | 22:30,570,022 | A/G | intron variant | — |
| rs201105081 | 22:30,572,073 | T/C | — | uncertain significance |
| rs2518035431 | 22:30,572,124 | C/T | — | uncertain significance |
| rs190493501 | 22:30,572,145 | A/G | — | likely benign |
| rs777114888 | 22:30,572,152 | A/G | — | uncertain significance |
| rs5753037 | 22:30,581,722 | C/G | — | — |
| rs9625935 | 22:30,581,860 | A/T | intron variant | — |
| rs5753039 | 22:30,583,711 | T/A | intron variant | — |
| rs5753043 | 22:30,588,041 | A/T | — | — |
| rs1807711 | 22:30,591,169 | G/C | — | — |
| rs2412980 | 22:30,592,069 | T/A | — | — |
| rs713875 | 22:30,592,487 | C/T | — | — |
| rs962322 | 22:30,593,412 | A/T | — | — |
| rs5763882 | 22:30,597,426 | A/T | — | — |
| rs2412981 | 22:30,600,065 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.