C4orf17
chromosome 4 open reading frame 17
Known Variants11 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs13126513 | 4:100,444,684 | T/A | — | — |
| rs7697177 | 4:100,445,786 | A/G | intron variant | — |
| rs7689584 | 4:100,448,121 | T/A | — | — |
| rs10007975 | 4:100,448,824 | C/T | intron variant | — |
| rs28444681 | 4:100,449,973 | C/A | intron variant | — |
| rs1397320372 | 4:100,451,011 | G/T | — | uncertain significance |
| rs1417597081 | 4:100,451,060 | A/C | — | likely benign |
| rs34500159 | 4:100,453,237 | T/G | intron variant | — |
| rs12648614 | 4:100,453,576 | G/C | — | — |
| rs7688705 | 4:100,456,834 | C/T | intron variant | — |
| rs13131565 | 4:100,459,555 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.