LOC101929710
uncharacterized LOC101929710
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs918629 | 5:95,301,463 | G/A | upstream gene variant | — |
| rs116635225 | 5:95,325,151 | G/A | regulatory region variant | — |
| rs28638396 | 5:95,392,883 | A/G | — | — |
| rs189699485 | 5:95,406,805 | C/T | intron variant | — |
| rs6895146 | 5:95,418,381 | T/C | downstream gene variant | — |
| rs7734985 | 5:95,428,684 | G/A | intron variant | — |
| rs13188879 | 5:95,440,104 | T/C | — | — |
| rs6865400 | 5:95,442,153 | C/T | — | — |
| rs76994357 | 5:95,447,169 | C/T | intron variant | — |
| rs189211114 | 5:95,483,338 | A/C | intron variant | — |
| rs4869266 | 5:95,486,940 | A/G | intron variant | — |
| rs192282934 | 5:95,509,336 | G/A | intron variant | — |
| rs13179048 | 5:95,542,726 | C/A | downstream gene variant | — |
| rs36101807 | 5:95,549,286 | G/T | coding sequence variant | — |
| rs528483907 | 5:95,562,531 | A/G | — | — |
| rs55745974 | 5:95,566,562 | A/T | intron variant | — |
| rs10064683 | 5:95,567,760 | G/A | intron variant | — |
| rs59600058 | 5:95,581,979 | G/T | — | — |
| rs115378930 | 5:95,600,166 | G/A | intron variant | — |
| rs201281936 | 5:95,606,717 | A/C | — | — |
| rs5869713 | 5:95,625,645 | T/A | — | — |
| rs17085593 | 5:95,630,705 | C/G | regulatory region variant | — |
| rs116165012 | 5:95,636,741 | A/G | intron variant | — |
| rs7700756 | 5:95,637,861 | T/G | — | — |
| rs182740838 | 5:95,641,330 | C/G | intron variant | — |
| rs13162665 | 5:95,642,519 | T/G | intron variant | — |
| rs35247507 | 5:95,688,542 | A/G | intron variant | — |
| rs36115340 | 5:95,689,064 | A/G | intron variant | — |
| rs144489757 | 5:95,694,609 | C/G | intron variant | — |
| rs1820177 | 5:95,696,429 | C/G | — | — |
| rs1820176 | 5:95,696,585 | T/C | intron variant | — |
| rs169241 | 5:95,697,940 | A/T | intron variant | — |
| rs55838622 | 5:95,711,605 | A/C | intron variant | — |
| rs10476553 | 5:95,718,846 | G/C | intron variant | — |
| rs7716123 | 5:95,794,422 | A/T | intron variant | — |
| rs114627901 | 5:95,810,659 | G/A | intron variant | — |
| rs3853209 | 5:95,834,313 | G/A | intron variant | — |
| rs72774885 | 5:95,840,231 | T/G | — | — |
| rs261985 | 5:95,842,987 | C/A | intron variant | — |
| rs261982 | 5:95,843,763 | C/G | — | — |
| rs17086188 | 5:95,845,854 | A/G | regulatory region variant | — |
| rs6556925 | 5:95,848,503 | C/A | intron variant | — |
| rs261967 | 5:95,850,250 | A/C | intron variant | — |
| rs2611732 | 5:95,855,576 | A/G | intron variant | — |
| rs2570467 | 5:95,856,679 | A/G | upstream gene variant | — |
| rs12514158 | 5:95,857,763 | C/G | — | — |
| rs4869139 | 5:95,858,668 | G/A | upstream gene variant | — |
| rs34976806 | 5:95,866,511 | C/G | — | — |
| rs1459843 | 5:95,867,223 | C/A | intron variant | — |
| rs112530420 | 5:95,871,370 | T/C | — | — |
| rs261223 | 5:95,901,046 | A/T | — | — |
| rs8180437 | 5:95,915,723 | G/T | — | — |
| rs111281774 | 5:95,954,057 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.