LOC101927636
uncharacterized LOC101927636
Known Variants16 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs74590858 | 4:144,833,153 | C/G | coding sequence variant | — |
| rs2440811 | 4:144,847,751 | A/T | — | — |
| rs13130548 | 4:144,859,478 | C/T | intron variant | — |
| rs187768945 | 4:144,866,682 | C/T | intron variant | — |
| rs193216971 | 4:144,881,247 | T/C | intron variant | — |
| rs4835095 | 4:144,881,584 | A/C | — | — |
| rs4835097 | 4:144,881,840 | A/G | intron variant | — |
| rs28504375 | 4:144,885,138 | T/C | — | — |
| rs12648849 | 4:144,885,825 | A/T | intron variant | — |
| rs191457647 | 4:144,890,251 | G/A | intron variant | — |
| rs11931330 | 4:144,891,961 | G/A | intron variant | — |
| rs7681300 | 4:144,892,983 | T/A | intron variant | — |
| rs6814613 | 4:144,894,206 | G/T | — | — |
| rs60428870 | 4:144,896,336 | G/A | intron variant | — |
| rs6827598 | 4:144,901,168 | C/T | — | — |
| rs4835473 | 4:144,903,572 | A/C | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.