MEI1
meiotic double-stranded break formation protein 1
Summary
Predicted to be involved in meiosis I. Predicted to act upstream of or within germ cell development; meiotic nuclear division; and meiotic spindle organization. Implicated in gestational trophoblastic neoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants117 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200470322 | 22:42,095,573 | A/C | — | uncertain significance |
| rs73424975 | 22:42,095,603 | G/A | — | benign |
| rs1438525823 | 22:42,095,621 | G/T | — | uncertain significance |
| rs200066340 | 22:42,095,644 | C/T | — | likely benign |
| rs763022939 | 22:42,095,649 | T/A | — | uncertain significance |
| rs147348682 | 22:42,095,658 | T/G | missense variant | — |
| rs2147166774 | 22:42,095,683 | C/G | — | uncertain significance |
| rs191014345 | 22:42,095,711 | G/C | — | benign |
| rs113760609 | 22:42,095,725 | G/A | — | benign |
| rs781134339 | 22:42,099,439 | C/G | — | uncertain significance |
| rs777693156 | 22:42,101,512 | A/G | — | likely benign |
| rs2147229895 | 22:42,101,554 | T/G | — | uncertain significance |
| rs374686480 | 22:42,110,023 | A/G | — | uncertain significance |
| rs188195414 | 22:42,110,049 | C/T | — | benign |
| rs535628064 | 22:42,110,050 | C/T | — | uncertain significance |
| rs369777935 | 22:42,110,051 | G/A | — | likely benign |
| rs201845294 | 22:42,110,066 | A/C | — | uncertain significance |
| rs1243243017 | 22:42,112,076 | T/A | — | uncertain significance |
| rs1293918641 | 22:42,112,135 | C/T | — | uncertain significance |
| rs367633748 | 22:42,112,159 | C/T | — | likely benign |
| rs1462918376 | 22:42,114,088 | G/T | — | uncertain significance |
| rs201371126 | 22:42,114,112 | C/A | — | uncertain significance |
| rs146685300 | 22:42,114,160 | A/G | — | likely benign |
| rs199530721 | 22:42,114,195 | G/A | — | uncertain significance |
| rs367643570 | 22:42,114,203 | C/T | — | uncertain significance |
| rs111250833 | 22:42,117,705 | C/T | downstream gene variant | — |
| rs764983701 | 22:42,120,000 | C/G | — | uncertain significance |
| rs969555682 | 22:42,120,028 | A/G | — | likely benign |
| rs748043340 | 22:42,120,052 | C/T | — | uncertain significance |
| rs776083441 | 22:42,125,717 | A/G | — | uncertain significance |
| rs2147546924 | 22:42,125,735 | C/G | — | uncertain significance |
| rs2518837459 | 22:42,126,585 | G/T | — | uncertain significance |
| rs760187909 | 22:42,126,620 | T/A | — | uncertain significance |
| rs1043792591 | 22:42,128,248 | G/C | — | likely pathogenic |
| rs199669858 | 22:42,128,253 | C/T | — | likely benign |
| rs2071930440 | 22:42,128,260 | G/T | — | uncertain significance |
| rs1330085474 | 22:42,128,298 | C/A | — | uncertain significance |
| rs61735670 | 22:42,128,343 | G/C | — | benign |
| rs1569203272 | 22:42,128,349 | G/A | — | pathogenic |
| rs200643171 | 22:42,128,468 | C/T | — | likely benign |
| rs767158440 | 22:42,128,529 | G/A | — | uncertain significance |
| rs779015950 | 22:42,128,564 | G/A | — | uncertain significance |
| rs5751148 | 22:42,139,078 | A/G | — | benign |
| rs201744413 | 22:42,139,155 | G/A | — | uncertain significance |
| rs758200303 | 22:42,139,164 | A/C | — | uncertain significance |
| rs950522878 | 22:42,141,061 | G/T | — | uncertain significance |
| rs199977360 | 22:42,141,069 | G/A | — | likely pathogenic |
| rs1286941272 | 22:42,141,912 | A/C | — | uncertain significance |
| rs759849031 | 22:42,148,613 | G/A | — | uncertain significance |
| rs780353765 | 22:42,149,972 | G/A | — | uncertain significance |
| rs201405312 | 22:42,149,994 | A/G | — | likely benign |
| rs17002655 | 22:42,154,386 | G/C | — | benign |
| rs370762110 | 22:42,154,409 | C/G | — | likely benign |
| rs8141939 | 22:42,154,430 | T/C | — | benign |
| rs55997605 | 22:42,154,546 | A/G | — | benign |
| rs2050033 | 22:42,159,229 | G/T | — | benign |
| rs192926292 | 22:42,159,249 | G/A | — | uncertain significance |
| rs200561206 | 22:42,159,254 | C/T | — | uncertain significance |
| rs374402462 | 22:42,159,282 | A/G | — | uncertain significance |
| rs1358888285 | 22:42,159,305 | A/G | — | uncertain significance |
| rs560803410 | 22:42,159,320 | C/T | — | uncertain significance |
| rs754822453 | 22:42,166,690 | A/G | — | likely benign |
| rs769690676 | 22:42,166,695 | G/A | — | uncertain significance |
| rs61737623 | 22:42,166,724 | G/A | — | benign |
| rs141292262 | 22:42,166,729 | C/T | — | uncertain significance |
| rs779161476 | 22:42,166,816 | C/T | — | uncertain significance |
| rs2518218065 | 22:42,166,870 | G/A | — | uncertain significance |
| rs368487670 | 22:42,166,879 | T/C | — | uncertain significance |
| rs1415687636 | 22:42,166,886 | G/T | — | uncertain significance |
| rs199854922 | 22:42,166,894 | G/A | — | likely benign |
| rs904261125 | 22:42,166,913 | T/A | — | uncertain significance |
| rs142374178 | 22:42,166,956 | C/T | — | likely benign |
| rs17002665 | 22:42,172,118 | T/A | — | benign |
| rs2518286266 | 22:42,172,123 | C/G | — | uncertain significance |
| rs369397468 | 22:42,172,131 | A/G | — | uncertain significance |
| rs373331979 | 22:42,172,133 | A/G | — | uncertain significance |
| rs767568961 | 22:42,172,164 | C/A | — | uncertain significance |
| rs370759463 | 22:42,172,209 | G/A | — | uncertain significance |
| rs373012181 | 22:42,172,228 | C/A | — | likely benign |
| rs956781246 | 22:42,172,233 | A/C | — | uncertain significance |
| rs761020157 | 22:42,174,715 | C/T | — | uncertain significance |
| rs61737655 | 22:42,174,779 | A/G | — | benign |
| rs1022692834 | 22:42,174,806 | C/T | — | likely benign |
| rs5758466 | 22:42,176,059 | G/A | intron variant | — |
| rs1363918205 | 22:42,177,279 | C/T | — | likely benign |
| rs73163330 | 22:42,177,317 | A/G | — | benign |
| rs896233517 | 22:42,177,322 | C/G | — | uncertain significance |
| rs1221368017 | 22:42,177,323 | G/A | — | uncertain significance |
| rs1027885503 | 22:42,177,375 | C/T | — | uncertain significance |
| rs774484158 | 22:42,177,691 | G/T | — | uncertain significance |
| rs759523790 | 22:42,177,784 | C/G | — | uncertain significance |
| rs754021162 | 22:42,177,811 | G/A | — | uncertain significance |
| rs6002481 | 22:42,177,816 | C/A | — | benign |
| rs200125287 | 22:42,177,822 | T/C | — | likely benign |
| rs190911941 | 22:42,180,353 | C/T | — | uncertain significance |
| rs755478970 | 22:42,180,382 | A/G | — | uncertain significance |
| rs12484839 | 22:42,180,400 | A/G | — | likely benign |
| rs375815319 | 22:42,180,611 | G/C | — | likely pathogenic |
| rs779527170 | 22:42,180,638 | G/A | — | uncertain significance |
| rs372447858 | 22:42,180,734 | C/T | — | uncertain significance |
Showing 100 of 117 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.