MANSC1
MANSC domain containing 1
Summary
Predicted to be located in membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759504988 | 12:12,483,010 | C/T | — | uncertain significance |
| rs1174788972 | 12:12,483,095 | C/T | — | uncertain significance |
| rs1355595608 | 12:12,483,139 | G/A | — | uncertain significance |
| rs1298054441 | 12:12,483,163 | C/A | — | uncertain significance |
| rs1044407496 | 12:12,483,174 | C/A | — | uncertain significance |
| rs2497387633 | 12:12,483,175 | T/G | — | uncertain significance |
| rs149414243 | 12:12,483,193 | G/A | — | uncertain significance |
| rs754057612 | 12:12,483,208 | G/C | — | uncertain significance |
| rs373449442 | 12:12,483,282 | G/C | — | uncertain significance |
| rs749024750 | 12:12,483,295 | G/A | — | uncertain significance |
| rs1481244881 | 12:12,483,298 | A/G | — | uncertain significance |
| rs558339880 | 12:12,483,323 | C/A | — | uncertain significance |
| rs759881826 | 12:12,483,325 | G/A | — | uncertain significance |
| rs765732772 | 12:12,483,329 | G/C | — | uncertain significance |
| rs377422017 | 12:12,483,377 | G/A | — | uncertain significance |
| rs530824976 | 12:12,483,415 | G/C | — | uncertain significance |
| rs201432430 | 12:12,483,418 | G/A | — | uncertain significance |
| rs758425146 | 12:12,483,419 | T/A | — | uncertain significance |
| rs1369824089 | 12:12,483,448 | G/A | — | uncertain significance |
| rs2497388470 | 12:12,483,449 | G/A | — | uncertain significance |
| rs994737129 | 12:12,483,509 | T/G | — | uncertain significance |
| rs370523906 | 12:12,483,528 | C/A | — | uncertain significance |
| rs2497388790 | 12:12,483,553 | G/A | — | likely benign |
| rs749710243 | 12:12,483,583 | G/A | — | likely benign |
| rs1315240465 | 12:12,483,623 | C/T | — | uncertain significance |
| rs1483566138 | 12:12,483,640 | C/T | — | uncertain significance |
| rs373927498 | 12:12,483,681 | A/C | — | uncertain significance |
| rs199652536 | 12:12,483,693 | C/A | — | likely benign |
| rs1376447756 | 12:12,483,701 | A/G | — | likely benign |
| rs774291026 | 12:12,483,748 | T/G | — | uncertain significance |
| rs200832213 | 12:12,483,755 | A/G | — | uncertain significance |
| rs375298595 | 12:12,483,765 | G/A | — | likely benign |
| rs2497389385 | 12:12,483,779 | A/T | — | uncertain significance |
| rs141156998 | 12:12,483,802 | G/A | — | uncertain significance |
| rs556197994 | 12:12,483,809 | C/T | — | likely benign |
| rs776538136 | 12:12,491,373 | C/T | — | uncertain significance |
| rs781151296 | 12:12,491,465 | C/T | — | uncertain significance |
| rs2497400267 | 12:12,491,483 | A/C | — | uncertain significance |
| rs773715083 | 12:12,496,034 | T/C | — | uncertain significance |
| rs761117307 | 12:12,496,038 | T/G | — | uncertain significance |
| rs531342550 | 12:12,496,118 | G/A | — | uncertain significance |
| rs146513379 | 12:12,496,120 | T/C | — | benign |
| rs56829405 | 12:12,496,935 | G/T | — | — |
| rs57725255 | 12:12,499,023 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.