SCFD2
sec1 family domain containing 2
Summary
Predicted to be involved in intracellular protein transport and vesicle-mediated transport. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs59649036 | 4:53,741,175 | T/C | intron variant | — |
| rs2529987206 | 4:53,752,015 | T/C | — | uncertain significance |
| rs1577797710 | 4:53,752,018 | G/A | — | uncertain significance |
| rs190973042 | 4:53,752,023 | G/T | — | uncertain significance |
| rs141706393 | 4:53,752,026 | C/T | — | uncertain significance |
| rs199859310 | 4:53,752,027 | G/A | — | uncertain significance |
| rs2898681 | 4:53,757,000 | G/A | intron variant | — |
| rs188539274 | 4:53,759,966 | C/T | intron variant | — |
| rs756841381 | 4:53,773,692 | C/T | — | likely benign |
| rs1432561326 | 4:53,773,709 | G/A | — | uncertain significance |
| rs537337307 | 4:53,773,751 | T/C | — | uncertain significance |
| rs301127 | 4:53,795,612 | A/T | intron variant | — |
| rs11735529 | 4:53,858,948 | C/G | intron variant | — |
| rs765333492 | 4:53,887,270 | T/C | — | — |
| rs574753165 | 4:53,977,261 | A/G | — | — |
| rs183241934 | 4:54,006,927 | A/C | intron variant | — |
| rs758412900 | 4:54,011,523 | G/A | — | uncertain significance |
| rs1446252293 | 4:54,011,633 | T/C | — | uncertain significance |
| rs761040570 | 4:54,011,709 | A/T | — | uncertain significance |
| rs757328503 | 4:54,011,731 | T/A | — | uncertain significance |
| rs67349114 | 4:54,020,326 | G/A | intron variant | — |
| rs10005818 | 4:54,047,047 | C/A | — | — |
| rs4346703 | 4:54,048,517 | A/T | — | — |
| rs6554074 | 4:54,086,162 | G/C | — | — |
| rs28822987 | 4:54,095,794 | G/A | intron variant | — |
| rs755983150 | 4:54,140,024 | T/C | — | uncertain significance |
| rs147079371 | 4:54,140,057 | G/C | — | uncertain significance |
| rs371033093 | 4:54,140,097 | G/A | — | uncertain significance |
| rs2550534020 | 4:54,140,108 | G/C | — | uncertain significance |
| rs200719400 | 4:54,140,115 | G/A | — | uncertain significance |
| rs2550534182 | 4:54,140,136 | T/C | — | uncertain significance |
| rs530067701 | 4:54,140,153 | C/T | — | uncertain significance |
| rs192499281 | 4:54,140,156 | G/A | — | likely pathogenic |
| rs13130986 | 4:54,142,695 | A/G | intron variant | — |
| rs1481818 | 4:54,147,973 | T/C | regulatory region variant | — |
| rs4864743 | 4:54,150,471 | A/C | — | — |
| rs188378292 | 4:54,167,694 | G/A | intron variant | — |
| rs138747864 | 4:54,179,841 | G/A | — | uncertain significance |
| rs2550586333 | 4:54,179,902 | C/T | — | uncertain significance |
| rs71597835 | 4:54,200,100 | G/A | — | — |
| rs62324336 | 4:54,207,262 | C/A | intron variant | — |
| rs7699124 | 4:54,212,467 | G/C | intron variant | — |
| rs6826663 | 4:54,217,607 | T/C | intron variant | — |
| rs533514727 | 4:54,218,789 | G/A | — | uncertain significance |
| rs138103715 | 4:54,218,811 | C/T | — | uncertain significance |
| rs1560462230 | 4:54,218,822 | A/C | — | uncertain significance |
| rs1734260189 | 4:54,218,825 | G/A | — | uncertain significance |
| rs765285823 | 4:54,218,850 | T/C | — | uncertain significance |
| rs142133865 | 4:54,218,919 | G/T | — | uncertain significance |
| rs374835467 | 4:54,218,927 | A/G | — | uncertain significance |
| rs112124703 | 4:54,220,173 | C/T | intron variant | — |
| rs62325967 | 4:54,220,470 | G/C | — | — |
| rs751333327 | 4:54,231,304 | C/A | — | uncertain significance |
| rs147960965 | 4:54,231,342 | G/A | — | uncertain significance |
| rs543070692 | 4:54,231,343 | C/T | — | uncertain significance |
| rs2550646747 | 4:54,231,415 | C/G | — | uncertain significance |
| rs2550646770 | 4:54,231,424 | G/A | — | uncertain significance |
| rs750241792 | 4:54,231,521 | C/A | — | uncertain significance |
| rs905613421 | 4:54,231,709 | C/G | — | uncertain significance |
| rs1161676694 | 4:54,231,715 | C/T | — | uncertain significance |
| rs377417669 | 4:54,231,883 | C/T | — | uncertain significance |
| rs2550647860 | 4:54,231,898 | G/T | — | uncertain significance |
| rs779055152 | 4:54,231,966 | G/T | — | uncertain significance |
| rs759850496 | 4:54,232,041 | C/G | — | uncertain significance |
| rs765552938 | 4:54,232,042 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.