CRAMP1
cramped chromatin regulator 1
Summary
Predicted to enable chromatin binding activity. Predicted to be involved in pattern specification process. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants89 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs971145177 | 16:1,664,674 | G/A | — | uncertain significance |
| rs926923881 | 16:1,664,696 | G/A | — | uncertain significance |
| rs1343092066 | 16:1,664,743 | G/A | — | uncertain significance |
| rs1268155436 | 16:1,664,771 | G/A | — | uncertain significance |
| rs1258251649 | 16:1,664,812 | G/A | — | uncertain significance |
| rs1049843132 | 16:1,664,821 | G/A | — | uncertain significance |
| rs1007968040 | 16:1,664,825 | C/T | — | uncertain significance |
| rs2508834752 | 16:1,664,840 | A/C | — | uncertain significance |
| rs1011131956 | 16:1,664,846 | C/T | — | uncertain significance |
| rs1396748134 | 16:1,664,848 | T/G | — | uncertain significance |
| rs2508834898 | 16:1,664,890 | C/T | — | uncertain significance |
| rs762499648 | 16:1,664,924 | G/A | — | uncertain significance |
| rs766748223 | 16:1,664,942 | C/T | — | uncertain significance |
| rs959779059 | 16:1,664,945 | T/C | — | uncertain significance |
| rs1189367719 | 16:1,664,969 | C/T | — | uncertain significance |
| rs530251818 | 16:1,669,580 | A/G | — | — |
| rs1043739025 | 16:1,676,058 | G/A | — | uncertain significance |
| rs954424216 | 16:1,676,097 | A/G | — | uncertain significance |
| rs749735014 | 16:1,687,881 | G/A | — | uncertain significance |
| rs9925938 | 16:1,689,227 | G/T | intron variant | — |
| rs2547918333 | 16:1,702,517 | A/T | — | uncertain significance |
| rs779955361 | 16:1,705,281 | G/A | — | uncertain significance |
| rs2547919728 | 16:1,705,300 | T/G | — | uncertain significance |
| rs79007183 | 16:1,705,794 | G/A | intron variant | — |
| rs202240948 | 16:1,705,879 | G/A | — | uncertain significance |
| rs757848793 | 16:1,705,924 | C/T | — | likely benign |
| rs2547920094 | 16:1,705,937 | G/T | — | uncertain significance |
| rs772594351 | 16:1,706,046 | G/A | — | uncertain significance |
| rs2547920158 | 16:1,706,050 | G/A | — | uncertain significance |
| rs571857474 | 16:1,706,079 | G/C | — | uncertain significance |
| rs757338395 | 16:1,706,149 | C/T | — | uncertain significance |
| rs370408080 | 16:1,706,173 | G/T | — | uncertain significance |
| rs772810276 | 16:1,706,181 | C/T | — | uncertain significance |
| rs372160619 | 16:1,706,194 | C/T | — | likely benign |
| rs2547920247 | 16:1,706,212 | G/T | — | uncertain significance |
| rs373720836 | 16:1,706,242 | C/T | — | uncertain significance |
| rs777765671 | 16:1,706,303 | G/C | — | uncertain significance |
| rs371446549 | 16:1,706,365 | G/A | — | likely benign |
| rs377597921 | 16:1,706,406 | G/C | — | uncertain significance |
| rs776911598 | 16:1,706,418 | G/A | — | uncertain significance |
| rs978777791 | 16:1,706,485 | A/G | — | uncertain significance |
| rs542745050 | 16:1,706,497 | C/T | — | uncertain significance |
| rs760066089 | 16:1,706,502 | A/G | — | uncertain significance |
| rs763282564 | 16:1,706,517 | G/A | — | uncertain significance |
| rs767241110 | 16:1,706,529 | C/G | — | uncertain significance |
| rs2547920589 | 16:1,706,544 | T/C | — | uncertain significance |
| rs368181087 | 16:1,706,562 | C/T | — | uncertain significance |
| rs371731624 | 16:1,706,595 | A/G | — | likely benign |
| rs758033308 | 16:1,706,616 | G/A | — | likely benign |
| rs191084422 | 16:1,706,656 | C/T | — | uncertain significance |
| rs757340231 | 16:1,706,779 | G/A | — | uncertain significance |
| rs1376658973 | 16:1,706,808 | G/A | — | uncertain significance |
| rs545529729 | 16:1,706,889 | G/A | — | uncertain significance |
| rs565235725 | 16:1,706,892 | C/T | — | uncertain significance |
| rs903823727 | 16:1,706,893 | G/A | — | uncertain significance |
| rs372279645 | 16:1,706,905 | G/T | — | uncertain significance |
| rs745825658 | 16:1,706,910 | G/A | — | uncertain significance |
| rs541352163 | 16:1,706,944 | T/G | — | uncertain significance |
| rs2547920925 | 16:1,706,949 | A/G | — | uncertain significance |
| rs1300041980 | 16:1,709,932 | C/A | — | uncertain significance |
| rs762190804 | 16:1,710,001 | C/T | — | uncertain significance |
| rs1433219826 | 16:1,710,017 | T/C | — | uncertain significance |
| rs112404892 | 16:1,710,037 | C/A | — | uncertain significance |
| rs915938562 | 16:1,710,038 | C/T | — | uncertain significance |
| rs2036842516 | 16:1,712,641 | T/C | — | uncertain significance |
| rs1232269585 | 16:1,712,767 | G/T | — | uncertain significance |
| rs753123955 | 16:1,715,115 | A/G | — | uncertain significance |
| rs375018736 | 16:1,716,476 | C/A | — | uncertain significance |
| rs372834355 | 16:1,716,527 | G/A | — | uncertain significance |
| rs61741505 | 16:1,716,534 | C/T | — | uncertain significance |
| rs745884113 | 16:1,716,540 | C/T | — | uncertain significance |
| rs1477638466 | 16:1,716,549 | G/A | — | uncertain significance |
| rs201157275 | 16:1,716,596 | G/A | — | likely benign |
| rs768371106 | 16:1,717,342 | G/A | — | uncertain significance |
| rs766728095 | 16:1,718,000 | C/G | — | uncertain significance |
| rs777708207 | 16:1,718,026 | C/T | — | uncertain significance |
| rs757328704 | 16:1,718,027 | C/T | — | uncertain significance |
| rs1016400262 | 16:1,718,108 | C/T | — | uncertain significance |
| rs2547926635 | 16:1,719,004 | G/A | — | uncertain significance |
| rs750593408 | 16:1,719,010 | G/A | — | uncertain significance |
| rs1347846882 | 16:1,719,020 | C/T | — | uncertain significance |
| rs200956828 | 16:1,719,041 | G/T | — | uncertain significance |
| rs370509468 | 16:1,719,067 | C/A | — | uncertain significance |
| rs774926972 | 16:1,719,089 | A/C | — | uncertain significance |
| rs780359215 | 16:1,719,142 | G/A | — | uncertain significance |
| rs2547927484 | 16:1,720,739 | C/T | — | uncertain significance |
| rs2036944471 | 16:1,723,904 | G/T | — | uncertain significance |
| rs751287265 | 16:1,723,940 | G/A | — | uncertain significance |
| rs954450533 | 16:1,723,946 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.