CCSER1
coiled-coil serine rich protein 1
Summary
Implicated in cocaine dependence. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7655515 | 4:91,091,035 | A/T | — | — |
| rs6813752 | 4:91,099,481 | T/G | — | — |
| rs769598269 | 4:91,229,442 | G/C | — | uncertain significance |
| rs749883935 | 4:91,229,475 | C/T | — | uncertain significance |
| rs757408650 | 4:91,229,548 | C/T | — | uncertain significance |
| rs768562667 | 4:91,229,678 | G/C | — | uncertain significance |
| rs770685942 | 4:91,229,796 | A/G | — | uncertain significance |
| rs371096921 | 4:91,229,812 | A/C | — | uncertain significance |
| rs763258132 | 4:91,230,115 | C/T | — | uncertain significance |
| rs750217480 | 4:91,230,145 | G/A | — | uncertain significance |
| rs756008404 | 4:91,230,148 | C/T | — | uncertain significance |
| rs1441157245 | 4:91,230,192 | A/G | — | uncertain significance |
| rs571706888 | 4:91,230,297 | G/A | — | uncertain significance |
| rs372404975 | 4:91,230,367 | C/G | — | uncertain significance |
| rs536916903 | 4:91,230,373 | C/T | — | uncertain significance |
| rs1277317247 | 4:91,230,409 | G/A | — | uncertain significance |
| rs2545850380 | 4:91,230,444 | T/C | — | likely benign |
| rs202060801 | 4:91,230,448 | C/T | — | uncertain significance |
| rs763793102 | 4:91,230,504 | G/A | — | uncertain significance |
| rs772767980 | 4:91,230,733 | A/G | — | uncertain significance |
| rs373458356 | 4:91,230,754 | C/T | — | uncertain significance |
| rs773041636 | 4:91,234,040 | C/T | — | uncertain significance |
| rs778767642 | 4:91,234,125 | A/G | — | uncertain significance |
| rs2545890412 | 4:91,234,163 | A/G | — | uncertain significance |
| rs7656001 | 4:91,243,865 | G/C | — | — |
| rs7658082 | 4:91,245,506 | T/A | — | — |
| rs1078765 | 4:91,251,649 | A/T | — | — |
| rs2546617661 | 4:91,321,245 | T/G | — | uncertain significance |
| rs753443542 | 4:91,389,430 | T/C | — | uncertain significance |
| rs187200046 | 4:91,401,611 | C/T | intron variant | — |
| rs148791548 | 4:91,511,483 | C/A | intron variant | — |
| rs115416376 | 4:91,513,257 | C/T | intron variant | — |
| rs545663449 | 4:91,549,187 | T/C | — | uncertain significance |
| rs368111669 | 4:91,549,202 | A/G | — | uncertain significance |
| rs776399571 | 4:91,549,216 | G/C | — | uncertain significance |
| rs202243228 | 4:91,549,288 | A/C | — | uncertain significance |
| rs373209732 | 4:91,549,361 | A/G | — | uncertain significance |
| rs200214194 | 4:91,645,066 | G/A | — | uncertain significance |
| rs201489889 | 4:91,645,114 | C/T | — | uncertain significance |
| rs17186106 | 4:91,703,241 | G/T | regulatory region variant | — |
| rs72879447 | 4:91,768,979 | A/T | intron variant | — |
| rs13125074 | 4:91,808,902 | G/A | intron variant | — |
| rs10018425 | 4:91,810,508 | T/C | intron variant | — |
| rs750392023 | 4:91,844,594 | A/G | — | uncertain significance |
| rs1531404 | 4:91,954,794 | C/G | intron variant | — |
| rs6532271 | 4:92,003,897 | C/G | — | — |
| rs1209980526 | 4:92,007,117 | G/T | — | uncertain significance |
| rs1277909353 | 4:92,007,118 | A/T | — | uncertain significance |
| rs76504638 | 4:92,007,129 | T/C | — | benign |
| rs553908921 | 4:92,250,808 | C/T | — | — |
| rs4128705 | 4:92,283,771 | T/G | intron variant | — |
| rs11933531 | 4:92,415,529 | G/A | intron variant | — |
| rs72886312 | 4:92,492,783 | A/G | intron variant | — |
| rs1356886887 | 4:92,519,769 | A/G | — | uncertain significance |
| rs758195665 | 4:92,519,775 | A/G | — | uncertain significance |
| rs1351965447 | 4:92,519,785 | T/G | — | uncertain significance |
| rs1327494584 | 4:92,519,969 | C/T | — | uncertain significance |
| rs199543790 | 4:92,519,972 | G/A | — | uncertain significance |
| rs374138135 | 4:92,520,014 | G/A | — | uncertain significance |
| rs990925563 | 4:92,520,015 | A/C | — | uncertain significance |
| rs1764706647 | 4:92,520,017 | G/A | — | uncertain significance |
| rs779227303 | 4:92,520,060 | C/T | — | likely benign |
| rs1459883027 | 4:92,520,099 | A/G | — | uncertain significance |
| rs2546021917 | 4:92,520,107 | A/G | — | uncertain significance |
| rs2546021966 | 4:92,520,135 | G/T | — | uncertain significance |
| rs887530915 | 4:92,520,169 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.