| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs371009290 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849413 | ACATTTGGAAAGATA[A/C]AAAAACTGACCATTC | 92912 |
| rs371079070 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843987 | TTTCCCCCGCGACTT[G/T]CCCATCCCAGGCCGG | 92912 |
| rs371132532 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889133 | TAGCCCAGTAGGAGA[A/G]TTAAAGAGTGGAAGA | 92912 |
| rs371190207 | snp | A/G/T | 3.2987e-05 | 0.00406108 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868918 | GTGCATATTTGTTCT[A/G/T]TATAGCCCTGGCAGA | 92912 |
| rs371296076 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872518 | AGGGGTATTCAAATT[C/T]TTTGTTTTCTTTTCC | 92912 |
| rs371303974 | snp | C/T | 0.000181038 | 0.00951243 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879218 | ACAGGACCCCATATA[C/T]TTCCAGTGGGGTGCG | 92912 |
| rs371309574 | snp | C/T | 3.35954e-05 | 0.00409836 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878065 | CTTTGCAATGGTAGA[C/T]TATCACAGTGGAGGT | 92912 |
| rs371397429 | in-del | -/AGTC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896887 | TTTTGAAATGGAGAT[-/AGTC]AGTTTCCCATGTTCT | 92912 |
| rs371409115 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862389 | CATCTCTTTTTTCTT[C/T]AATAAATTTTTTTCT | 92912 |
| rs371481877 | snp | C/T | 0.000153988 | 0.00877327 | stop-gained, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883396 | GATCCTCCATTTGTT[C/T]GAGTGGTGTTACCTG | 92912 |
| rs371497031 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890223 | GAACCATTAGAAAAA[-/A]TTGACTAGAATTTCA | 92912 |
| rs371504999 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871484 | ATGGGGAGATACCTT[A/G]GACAATACCTGGCTT | 92912 |
| rs371713022 | in-del | -/TTA | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891318 | TTTACAGTTGTAAAC[-/TTA]TTATTAGTATGTATA | 92912 |
| rs371751797 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851266 | GGCTAATTTTTTGTA[C/T]TTTTTTGTAGAGACA | 92912 |
| rs371775487 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852894 | ATACAACTTATTCTT[A/G]AAAGAACATTTGGTA | 92912 |
| rs371786099 | snp | A/G | 1.65414e-05 | 0.00287583 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883367 | TATTTGCTTTTTAGG[A/G]TAACTTTCCATTTGA | 92912 |
| rs371805905 | snp | C/G/T | 0.000132401 | 0.00813538 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873471 | TGAAGGAAGAAGAGC[C/G/T]TATTAGTGGGAAAAA | 92912 |
| rs371812398 | snp | C/T | 0.000439903 | 0.0148242 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844471 | GAAAGGAGCATAGTA[C/T]CGTCGTTGCGGCAGG | 92912 |
| rs371822682 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885023 | TCTTAATTTTATTTT[C/T]TTCAGTATTGTTTCT | 92912 |
| rs371826723 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845795 | CACTGGTGCCCCATC[A/G]AGAACCATATTGAAG | 92912 |
| rs371827385 | snp | C/G | 5.06521e-05 | 0.00503225 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896954 | TGTAATAATTTTCAC[C/G]TAATTACACTTTTGA | 92912 |
| rs371872080 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861042 | CCCTTGGGCTGATTC[C/T]CTAATTGCTCTATGC | 92912 |
| rs371888054 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879481 | GTGGGACAAGATGGG[G/T]GGATCTTGAACACAG | 92912 |
| rs371925486 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844978 | TTTCAAAAAAAAAAA[-/A]GACAAGTGCTGTACT | 92912 |
| rs371925946 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883760 | GTTCTGGGGCCCACA[C/T]CTAGAACCATTAGTT | 92912 |
| rs371938023 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851533 | ACAAGTTTTCAAAAA[G/T]TCTAATTTTTTGTTC | 92912 |
| rs372089370 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866366 | AATTTTTTTGTAGAG[-/A]TGTGTTTTCACCATG | 92912 |
| rs372129900 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877917 | CCATAGTAATAGTTA[C/T]ATGATGAAATGAAGA | 92912 |
| rs372242696 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870274 | GTCTTGCTGTTTTGT[C/T]CAGGTTCATCTCGTG | 92912 |
| rs372324439 | in-del | -/GA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865201 | ACTCATCTTTCCTTA[-/GA]CATTTCTCTAGTGTT | 92912 |
| rs372325632 | snp | A/T | 8.27739e-05 | 0.00643274 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890873 | GCCTTCCCAAGTGGG[A/T]ATCAGAAATACTACT | 92912 |
| rs372427677 | snp | A/C | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843006 | CGTCTCCCACGAGGT[A/C]CCCCCAGTGAGGTTA | 92912 |
| rs372445323 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845075 | GTGAAGTCGTCCTCG[C/T]TCTCAGAACTCAGTC | 92912 |
| rs372464787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897470 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTAC | 92912 |
| rs372523622 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885645 | GAGTGATTCCCATGT[A/G]TTTTCTGCTGCAGAG | 92912 |
| rs372759645 | snp | C/T | 1.64939e-05 | 0.0028717 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868924 | ATTTGTTCTGTATAG[C/T]CCTGGCAGATTCTTT | 92912 |
| rs372764233 | snp | A/G | 0.000100408 | 0.00708478 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897076 | GGTATGTTTAATTCA[A/G]TAAGTGTTTATTGCC | 92912 |
| rs372868686 | in-del | -/AAAAA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879048 | AGTTTAGTTAAAAAA[-/AAAAA]TCTCTAACTTTTTAT | 92912 |
| rs372904742 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868445 | TAGTGAGGTGGTAAT[C/T]ATTTCATAATTCTTA | 92912 |
| rs372924006 | snp | A/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841725 | GGATCATAGCTTTTA[A/T]TAGATTCTCAAAGGG | 92912 |
| rs372924107 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886915 | TGATTATAAAATTGG[C/G]CAGTATAGCTTTTCA | 92912 |
| rs372932907 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879374 | AGGAATGTTCAGAGC[A/G]GCATCGTTTATAATA | 92912 |
| rs372939427 | snp | G/T | 0.000148732 | 0.00862229 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876312 | CTTTATGATTCTTCT[G/T]CTCTTTTCTATTGTC | 92912 |
| rs372963292 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856670 | AACAGAAGGCTGGGC[A/G]TGATGGCTCACGCCT | 92912 |
| rs372966764 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894412 | TCTCTGTAAAAAAAA[A/C]AAAACAAAACAAAAC | 92912 |
| rs372973199 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853705 | TTGTGCAATTTACCT[G/T]GGGTTCACTGGCTTG | 92912 |
| rs373102975 | snp | A/C/T | 0.000183506 | 0.00957729 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891050 | ACATAAACCATAAGA[A/C/T]ACATTTTATATTACT | 92912 |
| rs373137889 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899253 | GCACTCCAGCCTAGG[G/T]AACAGAGTGAAACTC | 92912 |
| rs373180024 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874543 | CCTGCCTTGGCCTCC[C/T]GAAGTGCTGGGATTA | 92912 |
| rs373277569 | snp | A/C/T | 4.96359e-05 | 0.00498155 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854434 | GTGGATTCTGAAGAC[A/C/T]CAAATCTGACATCAG | 92912 |
| rs373320091 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893185 | TAAAGTTACCAGTTA[C/G]ATTGAATTAATAAAA | 92912 |
| rs373334367 | in-del | -/AAATTGAA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881185 | ATCTTTCTTTTTAAA[-/AAATTGAA]TTATATGTCCTTATG | 92912 |
| rs373434921 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873005 | TGGCTGCAAGGTTGA[A/T]ATAGGTATCCTTATG | 92912 |
| rs373508585 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845903 | AGTGAATGAGACACT[C/T]TCAGTACAAGGAGGA | 92912 |
| rs373526760 | snp | A/T | 1.65195e-05 | 0.00287393 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859899 | CAGCAATTGAAGTGG[A/T]TGATATGTGAACTCT | 92912 |
| rs373551553 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888536 | ACTTAGATCATTAAT[A/G]TTTTTTTCCTTAGTA | 92912 |
| rs373673466 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895117 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 92912 |
| rs373695991 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884308 | TGATCATTTCTATGG[C/T]TGAGATAGTAATAGT | 92912 |
| rs374039324 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899897 | TTAGGAAATTTAAGG[C/G]CTTCTAAATCATAAT | 92912 |
| rs374099581 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872533 | TTTGTTTTCTTTTCC[-/T]TTTTTTTTTTTTTTT | 92912 |
| rs374128319 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858110 | TCTCCTCTGATCTCT[C/T]CTCCCTTGGCCTACT | 92912 |
| rs374163563 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895915 | GATATACGTACAAGG[A/T]TGCTCTTGGCAACAT | 92912 |
| rs374170512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855806 | ACAATTTTGCTGAGT[G/T]GAAGGAAAGATTTGC | 92912 |
| rs374172432 | snp | C/T | 0.00141821 | 0.0265912 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843642 | GCTCCCCTTCCGCGC[C/T]CCTCCCGCCGGAGAT | 92912 |
| rs374277641 | snp | A/G | 0.000108996 | 0.00738146 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843718 | CTGGCGTCCATCTTC[A/G]ACAAGAACCACGAGC | 92912 |
| rs374332459 | in-del | -/CTTTT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864794 | TAAATCTAGTGTTTT[-/CTTTT]TCATTTTTTGCTTAT | 92912 |
| rs374352758 | snp | A/C/G | 0.000120105 | 0.00774855 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843818 | CGCACTCGCTGCCGC[A/C/G]GCCACTCACGCTCCA | 92912 |
| rs374534171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858761 | CTCTGCCTCATCTTC[A/C]TTATGCACTTAGCAC | 92912 |
| rs374555420 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876628 | AATAATTGCCAAGTT[G/T]ATTTTTATGATTCCC | 92912 |
| rs374600941 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866416 | ACTTCTGGGCTCAAG[G/T]GATCCTCCTGCCTTG | 92912 |
| rs374641931 | in-del | -/GG | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881404 | GTAGAACTTCAGGGA[-/GG]GGGGACGATCTGGGA | 92912 |
| rs374780683 | snp | A/G | 0.000155988 | 0.00883004 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75897002 | TCTTTCAGAATCAAT[A/G]TAATCTAGCAAGAGC | 92912 |
| rs374827064 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856403 | GAATAGACTTGTTCA[A/G]CCAGATGTTCAATAA | 92912 |
| rs374922551 | in-del | -/TTTAT | 0.0372196 | 0.131242 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897222 | TTATTTATTTATTTA[-/TTTAT]TTTATTTTATTTTAT | 92912 |
| rs374927430 | snp | C/G | 4.92732e-05 | 0.00496328 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869038 | TATAAAAGAAGAGTT[C/G]ATAAATTTCTTCATT | 92912 |
| rs374934953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846386 | GGGATTACAGGTTTC[C/T]GCCGCCACACCCGGC | 92912 |
| rs374967786 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892179 | ATTGTGCAAGATGGT[-/A]AAAGTGGTCTCATGT | 92912 |
| rs375000930 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868323 | CCTAAAACCCCATCA[A/G]ATTCATTTCTGAACT | 92912 |
| rs375072111 | snp | C/T | 0.000100641 | 0.00709297 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873574 | CCATTTAAATGTAAG[C/T]GTGTGTAGATATCTA | 92912 |
| rs375079084 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887582 | TTTTTTTTTTTTTTT[-/C]CCCCTCTGCTAAGTA | 92912 |
| rs375081087 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851691 | ACATCGTCAGTTATC[C/T]TTTCAAGTAAAAATG | 92912 |
| rs375206857 | snp | A/G | 1.65636e-05 | 0.00287776 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883433 | CAGGAGGGTAAGTTT[A/G]AGTGACTACTTAAAA | 92912 |
| rs375207480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874485 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 92912 |
| rs375235245 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850543 | CTTAGCCCACCTGAC[A/C]GCTAATCACTGGAAA | 92912 |
| rs375366129 | snp | C/G | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844283 | TAACGCCTCATTTTT[C/G]AGTCGGATTTTCCTT | 92912 |
| rs375429666 | snp | C/G | 1.64955e-05 | 0.00287184 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876290 | AGGATCTCTGGATCC[C/G]TGCTCTCTTTATGAT | 92912 |
| rs375482664 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887515 | GAGTTTTAGGAAATA[C/G]TGCTGATGTAATATC | 92912 |
| rs375525674 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848857 | AGTGTTATGTGATCT[A/C]TTCTAGAAGATTCTG | 92912 |
| rs375545385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850003 | ACCTTATCAAAATTA[C/T]AAAACTTAAAGCATG | 92912 |
| rs375591727 | snp | A/G | 1.68533e-05 | 0.00290282 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854475 | TCTAGAAGATACTAA[A/G]AACAACAATTTGGTA | 92912 |
| rs375668268 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897528 | CACAAAACCTTAACA[G/T]TGTACTTCAGTCAAA | 92912 |
| rs375680457 | snp | A/G | 3.35514e-05 | 0.00409568 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878063 | CTCTTTGCAATGGTA[A/G]ACTATCACAGTGGAG | 92912 |
| rs375728782 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862764 | AGGCTGCAGTGGGCT[A/G]TGATCATGCCAGTGT | 92912 |
| rs375745495 | in-del | -/AAA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877159 | GAGTGAGACTCTGTC[-/AAA]AAAAAAAAAAAAAAA | 92912 |
| rs375800715 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879428 | TTCATTCCAATAAAA[C/T]GGAGAATTGTGGTGT | 92912 |
| rs375822830 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865553 | GGGGCATGAGGATCA[A/G]TTTCTTCTTTTACTC | 92912 |
| rs375905506 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872522 | GTATTCAAATTCTTT[G/T]TTTTCTTTTCCTTTT | 92912 |
| rs375922929 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898110 | CTTGGCATATTCATA[C/T]TATTCTAAAGTTTCA | 92912 |
| rs376003226 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877756 | AACTCATTAAAGAAT[-/T]CTTCTCAGTTGATGG | 92912 |
| rs376041531 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895016 | ACGGTGAAACCCTGT[C/G]TCTACTAAAAATACA | 92912 |
| rs376042960 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853184 | TTGTGTTTTAAAAAA[G/T]ATATGGGCCTGGCTT | 92912 |
| rs376052554 | snp | A/C | 3.3507e-05 | 0.00409297 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873572 | GACCATTTAAATGTA[A/C]GTGTGTGTAGATATC | 92912 |
| rs376082263 | snp | C/G | 2.54288e-05 | 0.00356563 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843809 | AGGGCAGCCCGCACT[C/G]GCTGCCGCCGCCACT | 92912 |
| rs376216396 | snp | C/G | 0.000153988 | 0.00877327 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876152 | TTAAATCTTAGCTCA[C/G]CAGACCCTGGTAAAC | 92912 |
| rs376318809 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886834 | GGAGGTTGCAGTCCA[G/T]CCTGGGCAATAGGGC | 92912 |
| rs376318944 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848073 | TTAGTAGTTAGGAGC[C/T]TAAGTAAGTCACTTC | 92912 |
| rs376366723 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883221 | CTTTGGTTTTCATTT[-/T]GGTTTTGGGTACTAA | 92912 |
| rs376414279 | snp | C/T | 0.000604473 | 0.0173744 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844475 | GGAGCATAGTACCGT[C/T]GTTGCGGCAGGTGGT | 92912 |
| rs376415843 | snp | C/T | 6.63317e-05 | 0.0057586 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854413 | TCTTCTTCACCGATA[C/T]GGTTTGTGGATTCTG | 92912 |
| rs376429875 | snp | C/T | 3.30202e-05 | 0.00406313 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859905 | TTGAAGTGGTTGATA[C/T]GTGAACTCTGCAGTT | 92912 |
| rs376520827 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865158 | AGAAACCTTCTGCAG[C/G]CTTCTTCCTGATCAC | 92912 |
| rs376715550 | snp | A/T | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844227 | CGCAGCTCCGGCTGT[A/T]GTTTGAGCCCAGGCC | 92912 |
| rs376756345 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885129 | GTGGGGTTTTTTTTT[-/T]ATTTGTTTTTTGAGA | 92912 |
| rs376758645 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845714 | GTGCTAGGAGTACAG[A/G]GATACCAAATGTTTT | 92912 |
| rs376807071 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899562 | AGCAGTACCGAAGAT[A/G]TTAGTTAATAGATAT | 92912 |
| rs376830163 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871404 | AGCACAGACCCTTTA[C/T]GGGTGTCAGGCTGGG | 92912 |
| rs376835471 | snp | A/G | 1.71784e-05 | 0.00293069 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854483 | ATACTAAGAACAACA[A/G]TTTGGTAAGAAAATA | 92912 |
| rs376956847 | snp | A/G | 0.000409261 | 0.0142991 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843627 | CCCCTTCCGCGCCCG[A/G]CTCCCCTTCCGCGCC | 92912 |
| rs376978746 | in-del | -/TTTAG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890587 | CTCCTACTCTTAAAT[-/TTTAG]TTTATTTTTAAAATA | 92912 |
| rs377122346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857602 | CAAAACTAGCGGCTC[C/T]TCTCTTAGTCCCCAA | 92912 |
| rs377165471 | snp | A/G | 6.70185e-05 | 0.00578833 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877949 | TAGCTAACATGCTCT[A/G]TATCTTAACAGGGAT | 92912 |
| rs377218054 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891154 | TTGTTACAAAAGTGA[A/T]CTATAGAAAATATGG | 92912 |
| rs377259052 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887424 | ACAATCAGTTATCTA[A/G]GAAAGAGAATGAGAT | 92912 |
| rs377275824 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871562 | GTACTTGAGATTAGG[A/G]AGTGGTGATGACTCT | 92912 |
| rs377411819 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876734 | TTTAAAGTTTTCATT[G/T]CCTTGTTTGACGAGT | 92912 |
| rs377457052 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876417 | TCAAATGCAATCAAG[C/T]TCCAAAAGATGTAGG | 92912 |
| rs377464786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852017 | AGCTGGGACTACAGG[C/T]GTGCAACCACCATGC | 92912 |
| rs377529933 | snp | A/G | 0.000155988 | 0.00883004 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897092 | TAAGTGTTTATTGCC[A/G]TTTAAGAAGTTTTAG | 92912 |
| rs377559315 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850006 | TTATCAAAATTACAA[A/T]ACTTAAAGCATGTGA | 92912 |
| rs377638158 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892588 | AATGTAGATGGGTAT[A/G]GTGGCTCACGCCTGT | 92912 |
| rs377709192 | snp | C/T | 1.87958e-05 | 0.00306554 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879232 | ACTTCCAGTGGGGTG[C/T]GTATATTTGTACAAG | 92912 |
| rs386364598 | in-del | -/A/C/CA | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878428 | AGACTTCATCTCTAC[-/A/C/CA]AAAAAAAAAAAAATT | 92912 |
| rs386383506 | in-del | -/AAA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877160 | AGTGAGACTCTGTCA[-/AAA]AAAAAAAAAAAAAAA | 92912 |
| rs386785462 | multinucleotide-polymorphism | GA/TT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896362 | ATAATATAGTGGATA[GA/TT]TGGGTACCACTATGG | 92912 |
| rs386785463 | multinucleotide-polymorphism | CTCCTGGGCTGATGTGATCCTCCTGCCTCAGTCTCCC/TTCCTGGGCTGATGTGATCCTCCTGCCTCAGTCTCCT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897759 | GACTGCAGCCTCAAG[lengthTooLong]CAGTAGCTTGGACTG | 92912 |
| rs397694357 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864624 | AAAAAAAAAAAAAAA[-/A]GGATCGCTTCATGTA | 92912 |
| rs397695822 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857771 | CAAAAAAAAAAAAAA[-/A]TGCAGCCATTTTTTC | 92912 |
| rs397724749 | in-del | -/G/T/TC | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875300 | GGAAACTTGATTTTT[-/G/T/TC]CCCCCCTTCAAAGTA | 92912 |
| rs397781769 | in-del | -/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884707 | TTTGTTGCTCAGGCT[-/T]GGAGTGCAGTGGTGC | 92912 |
| rs397853767 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872335 | GGGGAAAAAAAAAAA[-/A]GCCGAGATGCGTATA | 92912 |
| rs397854080 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860459 | TATTTATTTTTTTTT[-/T]ACTATAATACATGAT | 92912 |
| rs397854259 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877490 | TATAGAAAAAAAAAA[-/A]CAGATACTGGGTGGA | 92912 |
| rs398027975 | in-del | -/A | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862839 | AAAAAAAAAAAAAAA[-/A]GGACTGAAAGACTGA | 92912 |
| rs527317616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850658 | CTCAATGGAACTATG[C/T]AAGTTAATATAGAAT | 92912 |
| rs527413030 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879306 | TATGGTTCAGGAATC[C/T]CGTAGACATATTCTC | 92912 |
| rs527438252 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846326 | CACTGCAACCTCCGC[C/T]TCCCAGGTTCAAGCA | 92912 |
| rs527560509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872681 | ACCTGAGATAAAATT[A/C]TTTTTCTAACTTTTT | 92912 |
| rs527597792 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876352 | ATGTCATTTCTTAAA[A/G]CTGGACAGAAATGGA | 92912 |
| rs527727706 | snp | C/T | 1.7698e-05 | 0.00297468 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860026 | AGCTAAATAAATTGT[C/T]TCAAGCAAAAGTCAA | 92912 |
| rs527764278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876379 | TGGAAATGTTTACTA[A/G]CTTTATTTCAGGAAT | 92912 |
| rs527950590 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844126 | AGCCCCGAGGGGGGA[A/G]TCCGCGGCGGCCCAA | 92912 |
| rs527950602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889369 | GGACTTCTTTCCCTT[A/T]TTTTATTATTAAATA | 92912 |
| rs527963410 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889013 | GATGTTAACTCATCA[A/G]CCGATTATTAAGCTT | 92912 |
| rs527969743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882156 | GCGATTTGTAACTAT[G/T]TAGAGCCATTTGGTG | 92912 |
| rs528009272 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867184 | GGAAGAGGTGGAGTC[-/T]TAAGATTTTGCTGCT | 92912 |
| rs528134333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863505 | GTGGAGTGCAGTGGC[A/G]CGATCTCAACTCACT | 92912 |
| rs528136032 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871847 | AGGAAGGCCTTAAGC[A/G/T]GGGAATAGTGTGCTG | 92912 |
| rs528166867 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882504 | TAGTCACTCATTAGG[G/T]ATTCACATGTTTAAA | 92912 |
| rs528173671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879710 | AACATAAACAGATAT[A/G]CGATTTATCTATGGT | 92912 |
| rs528178847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871131 | ACAAAGGTCTTTGCA[C/T]CATAGACAAGGTAAA | 92912 |
| rs528190283 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884304 | CCTTTGATCATTTCT[A/G]TGGTTGAGATAGTAA | 92912 |
| rs528231693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885424 | CCCCACCTAGTGGTT[C/T]GTTAATAGATGTTTG | 92912 |
| rs528351985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847398 | TGAAAAAGACCAAAA[C/T]AGAGTAGATGTTTTA | 92912 |
| rs528431179 | snp | A/G | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880662 | TGTGCCACTATGTCC[A/G]CATAATTTTTGTATT | 92912 |
| rs528565706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895822 | TGTAGAGGGCAATTT[A/G]GCAATATCTCAGAAT | 92912 |
| rs528698733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848335 | GTAGTCCAGTCAAAG[C/T]TGTACAAAGGAAATA | 92912 |
| rs528720147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857672 | CCTTGTTGAAACATT[C/G]CTGCATTCTTAATGT | 92912 |
| rs528728673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895129 | AGGCGGAGCTTGCAG[C/T]GAGCCGAGATTGTGC | 92912 |
| rs528755427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856865 | GGAGAAGTGCTTCAA[C/T]CTGGGAGGCAGGTTG | 92912 |
| rs528828873 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862792 | TGTACTCCAGCCTGG[A/G]TGACAGAATGGAACC | 92912 |
| rs528963547 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866851 | ATGCAGTATCTTCCC[-/A]ATTACTGCTAAAGAT | 92912 |
| rs528978737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864207 | GGCTCTTATTTCAGT[A/G]TCAAGGGTATGCAGG | 92912 |
| rs529124294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894910 | TTGTGAAAGTACTAA[A/G]ACAAAAACTTTTTTG | 92912 |
| rs529177450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885822 | TTCTTTTGTTACCTT[C/T]AAAGCTTCCGTAGAC | 92912 |
| rs529201190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873234 | CCAGAGTCTAGATTT[C/T]AAATAAAATATAGGA | 92912 |
| rs529219910 | snp | C/G/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842712 | GCAAAATAAGGAAAG[C/G/T]GGGGAGAGAGAGACT | 92912 |
| rs529223282 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873706 | GATTCAGTCATGTGT[G/T]TTTTAAAACAGGGTC | 92912 |
| rs529256494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881882 | AGTACTTTAAGAAGG[A/G]TCTATTTAGATAAAC | 92912 |
| rs529367246 | snp | C/T | 2.73011e-05 | 0.00369457 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869047 | AGAGTTCATAAATTT[C/T]TTCATTTTTGAACAT | 92912 |
| rs529370292 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856856 | GCTGAGGCAGGAGAA[A/G]TGCTTCAACCTGGGA | 92912 |
| rs529433906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888654 | ATTTAATACAGAAGT[A/G]GAATCGGCCACTTTT | 92912 |
| rs529516899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849892 | ATTTTTGAGCACCAT[C/T]CACTGTTTAAAAACT | 92912 |
| rs529524239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849218 | ATTAAGGTACTATAT[C/G]CTAATTCTGTCAATT | 92912 |
| rs529576645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858448 | GGGAACTGTCTTAGC[A/G]TTCTTTTATATACTA | 92912 |
| rs529647166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877482 | ATTGTTTATATAGAA[A/G]AAAAAAAACAGATAC | 92912 |
| rs529691949 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855217 | ATTTACTGGCCAGGT[A/G]TGGTGGCTCACGCCT | 92912 |
| rs529734537 | in-del | -/T | 0.000306937 | 0.0123844 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869051 | TCATAAATTTCTTCA[-/T]TTTTTGAACATTTGA | 92912 |
| rs529786614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884251 | TATGTGACATAATCT[A/G]CATTATGGTGGTTAA | 92912 |
| rs529786623 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891998 | CTGCCCATAACCTCC[A/G]CTTATTCTCCCACAG | 92912 |
| rs529965663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852682 | AAAAATGGTCCAGAT[A/G]GTGTATTCCCAATGT | 92912 |
| rs530001144 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879520 | GAGACTGGACTCCAA[A/T]ACCTATTTTGTACAA | 92912 |
| rs530010646 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846659 | GATCGATGATTTGTT[A/G]TTCTCTAAAGTTGTA | 92912 |
| rs530019029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860604 | TTCTAGAATATTTAA[A/G]ATAGGATATTTCCTT | 92912 |
| rs530034444 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849917 | AAAACTGATATACCA[C/T]AGGTCATATTTATTT | 92912 |
| rs530067962 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847650 | ACACCGAAATGCAAA[A/C/G]CAGCTTGTTTTAAGC | 92912 |
| rs530071103 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894165 | TGCAATCATTACTTA[G/T]CAGAGACTAAAGGAG | 92912 |
| rs530139212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863316 | AGTTCTGGTCTGCCG[G/T]TAACCCCATTCCTTT | 92912 |
| rs530175532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846464 | GCTGGTCTTGAACTC[C/T]ACCTCAAGCTCCCAA | 92912 |
| rs530342986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878172 | TCTTAGATTGTTTAA[A/G]TGAGCTGTTGCTGAG | 92912 |
| rs530345461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869715 | CTTAAAGGTCCTACC[G/T]CTTAATAGCATCACA | 92912 |
| rs530359712 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870992 | GCGTTCAGCATATGG[A/T]GGATCCCGCCAGCCT | 92912 |
| rs530468580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879020 | TTTTAGCTGTCATAC[C/T]AGTTCATTTTTGAGT | 92912 |
| rs530575556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870497 | AAACATTAAACCTTT[G/T]TTGTGCGCCCAGTTT | 92912 |
| rs530608152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878238 | AGAGGGACCAGCTGC[A/G]GGATAAAGTGTTTTA | 92912 |
| rs530623917 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856698 | CCTGTAATCCCAGAA[C/G]TTTAGGAGGCCCAGG | 92912 |
| rs530770665 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893191 | TACCAGTTAGATTGA[A/G]TTAATAAAATCCAGC | 92912 |
| rs530774641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886637 | TCACGCCTGTAATCC[C/T]AGCACTTTCGGAGGC | 92912 |
| rs530793822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854227 | GGAGAATGGTTGTCT[C/G]AAAAGTCCAGCTCCT | 92912 |
| rs530797391 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900216 | AAGTTATTTAAAATA[C/G]TAAGTCATCTTACGT | 92912 |
| rs530831772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853441 | GTGCCATGCACTCCG[C/T]CTGGGCCACAGAGCA | 92912 |
| rs530879358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848270 | GTGGGAAATAAAGCA[A/G]TGCTGTTAACTTCAT | 92912 |
| rs530891262 | in-del | -/TCTT | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847589 | AGTATAGTTTTTCCA[-/TCTT]CAGTAAACTAACCTG | 92912 |
| rs530915350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847714 | GTTTTGAAGTATTTA[A/G]CATAACTTGGCAACT | 92912 |
| rs530915377 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856718 | GGAGGCCCAGGCAGG[C/T]GGATCAGTTGAGGTG | 92912 |
| rs530924527 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841758 | CTGTGAGAATCTTAG[C/T]CTTCTTAAAGGCTAG | 92912 |
| rs530973224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895601 | AAGGGGGTATAAAAA[A/G]TCTGTTTACAGAAAT | 92912 |
| rs531069587 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851066 | AACAAAATCCAACCT[A/T]ATACAGATACCTGGT | 92912 |
| rs531106346 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865594 | TAGGAAAAAAAAAAC[G/T]TTTTAAAAAGCATTT | 92912 |
| rs531196703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844726 | AAGCTATTCGTCGTG[A/C]AATTGATGTAGGATA | 92912 |
| rs531233385 | in-del | -/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842835 | CTTGGGTAAATGGAT[-/G]GGTTTGAGAGCAAAG | 92912 |
| rs531243791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890289 | TAAATTACCCATAGT[C/T]CTGTATCCCTAACAA | 92912 |
| rs531244664 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899301 | ATATAATATATATAT[A/T]TATTTTTTACGGTAG | 92912 |
| rs531269697 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851658 | GGAAAATGACTGCCA[A/C]AAACCCAAGTTGAAA | 92912 |
| rs531282230 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855559 | AAAAATAATCATCAT[C/T]ATTTTCAGCTGACAT | 92912 |
| rs531310264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850802 | TATTCAGCACTTAAG[A/G]GCTTTGGTTTATGTA | 92912 |
| rs531363033 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872116 | GAGAACAGAACGTTA[C/T]AGGGCTTGAAGAGAT | 92912 |
| rs531364223 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844171 | CATGGCCGCCCTCAG[C/T]CGGCCTGCTCCCGGG | 92912 |
| rs531444177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867234 | ACACTCTCTGTCTTT[C/T]CTGTCTGGTTTTGAC | 92912 |
| rs531463456 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886517 | GGTCATTTTTTGTTC[A/G]AAATCTTATTTGAGA | 92912 |
| rs531550698 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844776 | ATTCTCTTGGTTATA[A/G]TAGGCGTCAAGGTGG | 92912 |
| rs531610933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866632 | CTGTTCTCTTACTTA[C/T]ATCTCTTCTGTTTTC | 92912 |
| rs531615600 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897364 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 92912 |
| rs531649379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874563 | TGCTGGGATTACAGG[G/T]GTGAGCCACTGTGTC | 92912 |
| rs531769404 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889358 | GGAGATGAAAAGGAC[G/T]TCTTTCCCTTATTTT | 92912 |
| rs531778659 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861355 | GGCATTCTGAGTTTC[A/G]GTCATTTATGTATGG | 92912 |
| rs531816734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860643 | CAGCTTTTTGTTTTG[C/G]AGTGTCTTCCTCATA | 92912 |
| rs531848279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868516 | TCAAAATGTAAGGCA[A/G]TTGAATTTATGTAAA | 92912 |
| rs531872789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883628 | TTTTTTCTTCTAAAT[A/C]TAGTGTGCACCAGAA | 92912 |
| rs531883750 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876447 | GAGTAAAATAGGATG[A/C]GTTTACTTGTCTTTT | 92912 |
| rs531908377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883234 | TTTGGTTTTGGGTAC[C/T]AATTTTATGACTCTT | 92912 |
| rs531963870 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850253 | AGATATGATTCTACC[A/T]CTCAGAATATACCAC | 92912 |
| rs532016787 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848662 | CCCTTAGTATCTTGA[-/T]TTTTTTTTTTTAATT | 92912 |
| rs532071343 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845370 | TGAGAAGCCCACGAT[A/G]CAGGCTGGAGAAGGG | 92912 |
| rs532089579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883715 | AGTATTTACATTTTT[A/G]AGAAGTTTCCAGGTG | 92912 |
| rs532094388 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879938 | GGTGGGAGGTAGGGA[A/G]GTGTGAACTGAAAGG | 92912 |
| rs532137836 | in-del | -/GTT | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847623 | ATTGCCGTCTAATTA[-/GTT]GTTACAATCACACCG | 92912 |
| rs532168863 | snp | A/G | 0.00211406 | 0.0324432 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844333 | ATTGTTTTTAAGTTT[A/G]CGTTTAAGGAGAAAC | 92912 |
| rs532211654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899384 | CAGTTCTTCTAATTT[A/G]TTTAAGAATTATTTT | 92912 |
| rs532239435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891157 | TTACAAAAGTGATCT[A/G]TAGAAAATATGGAAT | 92912 |
| rs532283254 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849468 | TGCTTGAGATAGAGC[C/T]ACACAATGGTCTCAG | 92912 |
| rs532379144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898755 | TTTTGTTTGGGGAAA[G/T]AAGTACTTTCCATGA | 92912 |
| rs532432862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854366 | TGTAAATGTTTAACA[C/T]GTGTCTCTGTGTTAA | 92912 |
| rs532474871 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862353 | AGGAGCTATTTTGAT[A/T]CTCTTTGGCCCTCTC | 92912 |
| rs532611810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869612 | AAGGCAGAAGGGCAG[A/G]AGAGCAAGCTAGTCC | 92912 |
| rs532612672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853515 | ATATATATGTATGTA[C/T]GTATGTATGTGTGTA | 92912 |
| rs532644618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861553 | TTGTTAACTTTCTCC[C/T]TTCCATTTTATTTGT | 92912 |
| rs532708572 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858960 | CCTATGTCTTCTTTC[A/T]TTGTCCTTTGTAAAC | 92912 |
| rs532715930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884175 | TGAAATGTTCAGTAG[G/T]CCCTCAAAGTATGAG | 92912 |
| rs532873399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873303 | TTTTTCTCTCTCCCT[A/G]TAGGATAGTTACATT | 92912 |
| rs532874701 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857172 | CATGAAGGTAAGAGG[C/T]AAAAATTAAAAGCTA | 92912 |
| rs532874803 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887216 | AAAGTACTAAGTACT[C/T]CATTGATTATCAAAT | 92912 |
| rs532896295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865357 | CTATTGTGTGTAGCT[A/G]TAGTTCTTTTGCATT | 92912 |
| rs533005395 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872638 | AACTCCTGGGCCCAC[A/G]TGATCTTCCTATCTC | 92912 |
| rs533018265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866117 | TTTTATTTTTTCTTT[C/T]TGGTAGTTGGTATGA | 92912 |
| rs533079746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879909 | CATACAGGTTAGGGT[A/G]AGGAGTCCATCTAGG | 92912 |
| rs533219390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866651 | TCTTCTGTTTTCTCC[C/G]CCATCTCCTTTTTTT | 92912 |
| rs533228812 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893584 | GTGAACAGGCATGGT[A/G]TAATAGACAAATATA | 92912 |
| rs533264036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866462 | ACAGGCATGAGCCAC[C/T]GTGTCCGGCCTTCAG | 92912 |
| rs533314099 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868401 | AAGTATTTTGTTGTA[A/G]AATGTTTTTAAAAAG | 92912 |
| rs533324229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857788 | GCAGCCATTTTTTCC[A/G]TAAGAGCATGTGCAG | 92912 |
| rs533387449 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881837 | TGGTGTTTCGGGCAG[C/G]ATCTGAATTACTGAA | 92912 |
| rs533413322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875392 | TCTTATGATAAGATA[C/T]TGATGTGTTTTCATC | 92912 |
| rs533424369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896937 | TGCATTCATAAATTT[A/G]TTGTAATAATTTTCA | 92912 |
| rs533450381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874777 | TGCTCAGAGTAGGGA[A/G]ACATCAAATGATTGT | 92912 |
| rs533454734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888759 | ACTTGTCTTGTGTTC[A/G]ACAAACATTTGTGTA | 92912 |
| rs533556893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887926 | CTGACTTGGGAAGAA[A/G]TAAAAGCTTGCCATC | 92912 |
| rs533633803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850563 | ATCACTGGAAATGGG[G/T]TGGGCTGGTAGAGTC | 92912 |
| rs533748215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888806 | ACAAATGCACTTTTT[C/G]ACCTGAAAATCCAAA | 92912 |
| rs533807959 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843071 | GCCCCCAGGGGCTGG[C/T]GCTAGTCTGCAGCGG | 92912 |
| rs533876138 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867703 | TGGGCTGATGGTGAC[A/G]GACCCAGATGCATGT | 92912 |
| rs534059385 | snp | C/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841657 | CTAGTGCTGGGGTCA[C/T]GAATCCCCATAAGTA | 92912 |
| rs534087384 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895089 | TACTGGGGTGGCTGA[A/G]GCAGGAGAATGGCGT | 92912 |
| rs534143228 | in-del | -/CGGGGCGGGG | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844188 | GCCTGCTCCCGGGAC[-/CGGGGCGGGG]CGGGGCGGGGCGGGG | 92912 |
| rs534206734 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874034 | GATTACGTTTCTTAT[C/G]TATAGATAGCCACTT | 92912 |
| rs534207421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898265 | ATATTTATAGAAAAT[A/G]CTGTATTTGAGAGTG | 92912 |
| rs534369466 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854618 | ATTAAAGACTAGTTT[G/T]TTTGTTTTTTTTCCT | 92912 |
| rs534403408 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862955 | ATCTCCTGGTGCAAT[C/T]ATAAATGATGGCTGG | 92912 |
| rs534407981 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858866 | GGATCGTAATTTACC[A/G]TTCAACCTTCCTCAT | 92912 |
| rs534535295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881504 | TTTTCTGGGGTTGGA[C/G]TATTTCTTGAGAGGC | 92912 |
| rs534654926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872052 | CTGAAAGGTGCACAC[A/G]GGGAGAAGGGAGCTC | 92912 |
| rs534737071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861924 | GTGGAATGTCTGAGA[C/T]GACTTCTTCACCCAC | 92912 |
| rs534767507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878446 | AAAAAAAAAAATTAG[C/T]CAGGCATGGTGGAGT | 92912 |
| rs534767710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869881 | GCATTTAAATTCAAA[C/G]TTCAGAACAAAGATC | 92912 |
| rs534784366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871519 | AGGCAGAGGTCCCTG[C/T]GGCCTTCCGCAGTGT | 92912 |
| rs534873041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886078 | TTAAAATATCTTTAA[C/T]GAAGCCTTTACTGAT | 92912 |
| rs534977048 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858322 | TGACGTTTAAATTTG[A/C]GTTTACCCACCTCCT | 92912 |
| rs534996364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846758 | ATTCTACATGCTAGG[A/T]CTTGTTTTCTTTATA | 92912 |
| rs535104493 | snp | C/G | 1.66302e-05 | 0.00288355 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883346 | TTTAAATTAATTAAA[C/G]TTGCTTATTTGCTTT | 92912 |
| rs535137490 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841491 | CCTGTTAGGGTCCCA[A/G]GAAACTGGGGACTGA | 92912 |
| rs535148191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847879 | GAGCATAAATGATTA[C/T]CCTTTCTGCGTATAA | 92912 |
| rs535225467 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894407 | ACCAATCTCTGTAAA[A/C]AAAACAAAACAAAAC | 92912 |
| rs535294710 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893537 | CTACTAGTAAGATAA[A/G]CAGAATGCCCATATG | 92912 |
| rs535337262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855835 | GCATTCTGTGTTCCT[G/T]GATGAGCAGATTTCA | 92912 |
| rs535345390 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861164 | GTAAACCATTTAGAA[C/G]AGTGCCTGGTGCATA | 92912 |
| rs535373592 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891592 | CTGAAGCATACAGAA[A/G]TTAGTTAGATAACTT | 92912 |
| rs535409681 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864377 | CTGGTCATGGTAGGG[C/G]TGCTGTTGGCATTTC | 92912 |
| rs535411835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878483 | GTAGTCCCAGCTACT[C/G]GGGGTGGTGGGAGGC | 92912 |
| rs535468716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894440 | AACATGAAAATTAGC[G/T]GGGCATCGTGGCAGG | 92912 |
| rs535478339 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888839 | CTCCCTTTCTTCCCC[C/T]CACCTCTTAAGACTC | 92912 |
| rs535480942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856983 | GTTAAGGCTGAGGCT[C/T]GGCACAGTGGTTCAT | 92912 |
| rs535531604 | snp | A/C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861246 | TGATTGGTAGTTTGG[A/C/T]TGATTATATATTTCT | 92912 |
| rs535588134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871269 | CCTATCTCAGTAGAT[A/G]GAACGTACAATCGGG | 92912 |
| rs535602887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872201 | TCACTGTACTCCAGC[C/T]GGGGCAACGGAGCGA | 92912 |
| rs535638672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880091 | TGAATTTATGTGTTA[C/T]ATTTAATAAGGTTTT | 92912 |
| rs535719954 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897926 | CAAAGCAAACTTGTC[A/T]CTCTTTCAGTGATTG | 92912 |
| rs535801364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868753 | TTGAATTGTTCAAAA[C/T]TGTTTCATTTTTAAA | 92912 |
| rs535930781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867899 | AATTTAGGGAAATGA[A/G]AAAAGGGAGAATTAC | 92912 |
| rs535945420 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857414 | GTTTTTTAAAAGTGA[A/G]TATATTTACATGAAG | 92912 |
| rs535969628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880789 | CAGGCGTGATTTAAT[A/G]TGGATCTGGATGAGA | 92912 |
| rs536020580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887709 | GAAGAGAATATGAGA[C/T]ACATTGTGCTCACAG | 92912 |
| rs536118966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895244 | GCTGGAGTGCAATGG[C/T]ACGATCTCGGGCTCA | 92912 |
| rs536142046 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843856 | ATCACGGTGAGGCGC[C/T]CGGCCGCGGCCCCGC | 92912 |
| rs536159471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851977 | TTCTGGGCTCAATCA[A/G]TCCTTCTGCCTCAGC | 92912 |
| rs536191377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886242 | CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAC | 92912 |
| rs536210033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884918 | GCCTTGCAAAGTACT[A/G]GGATTACAAGTCTAA | 92912 |
| rs536243428 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893107 | AGAAAGTGAGAGAAA[A/T]AGAAGTTGTAAAGGT | 92912 |
| rs536248258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884472 | TTAAGAATCATTTCT[A/G]TGTAGTCAGAATACA | 92912 |
| rs536296499 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878146 | TTAGACTTTGTTTCT[A/G]TAGAAATAGTTCTTA | 92912 |
| rs536376832 | snp | C/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841873 | GTAGGCTGTGGGGAG[C/T]TACTAACTTACTGAG | 92912 |
| rs536447800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890605 | AGTTTATTTTTAAAA[C/T]AGCGTCTACTTTCAA | 92912 |
| rs536470768 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900483 | CATTTTATTGCCTTA[C/T]CTGAATCAGTCCTTT | 92912 |
| rs536485011 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853740 | CTCACCAGGCAGCGA[A/G]GTTGTTGGTGGCAGC | 92912 |
| rs536529272 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861647 | ATTTCTAAATTATTT[G/T]TCTTTAATTTTAAAA | 92912 |
| rs536566872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860972 | CCAGTGTTTGGTTTT[C/T]GGAGCCAGACCGTGA | 92912 |
| rs536592218 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847845 | ACAAATGAAACTTCA[-/T]TTTTTTATATTACTT | 92912 |
| rs536805075 | in-del | -/TTGT | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859569 | TTCTCTTGTCTGAAG[-/TTGT]AAGTTTCTCAGAAAA | 92912 |
| rs536839169 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899633 | CAGCCTTTGCATTTT[G/T]CTCATTTTAGATATC | 92912 |
| rs536888905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845250 | GACTACAATTTTGGA[A/T]GGCTGGCGGAAGGGC | 92912 |
| rs536911998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891405 | GTTATAGAACTAATT[C/G]CTGGTAAGCTTTTAT | 92912 |
| rs536927394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853102 | CAAAGTAACAGAGTA[A/G]ATGTCTGTTAGTGGG | 92912 |
| rs536949680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845070 | ATTGAGTGAAGTCGT[C/T]CTCGCTCTCAGAACT | 92912 |
| rs536976397 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851537 | GTTTTCAAAAATTCT[A/G]ATTTTTTGTTCAAAA | 92912 |
| rs537130996 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887849 | TGAAAGCTCATTGGA[A/G]GCAAAATCAAAATGG | 92912 |
| rs537143377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878675 | TATATATAGGACAGT[G/T]GTAGACAAATACAGG | 92912 |
| rs537167347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877524 | TGTTAAAGCATATCC[A/G]TAAAATAAACTACCA | 92912 |
| rs537170349 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860248 | GGTTTCCGTAAATGC[C/T]CTTGCTTCTTTCATA | 92912 |
| rs537275580 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893435 | CTATCAGAATAGCCT[C/T]AAAATACCCAGGAAA | 92912 |
| rs537280283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846631 | TGGGGTTGGATTTCA[A/G]ATGATTTGGTTTGAT | 92912 |
| rs537293357 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885770 | AGTGGAAATCCCAGG[C/T]TGGGTGTGAAATAGT | 92912 |
| rs537356404 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853888 | GGTCTGAGGCCTTTT[A/G]TAATACCTCGCCATG | 92912 |
| rs537511192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888879 | AAAGGAAGAGTGGGG[A/T]ACCTTAAAGGAAAGG | 92912 |
| rs537728249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849504 | TTATGGAGAAAAATA[G/T]ATACAGAAAGTTACT | 92912 |
| rs537728416 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867071 | TTGTCACTCTTTTCT[A/G]CTGTGGCCTCCCCCT | 92912 |
| rs537756150 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852048 | TAGCTAATTTTTTTA[-/T]TTTTTTTTTGTAGAG | 92912 |
| rs537759840 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862761 | TTAAGGCTGCAGTGG[G/T]CTGTGATCATGCCAG | 92912 |
| rs537881368 | snp | C/G | 0.000116294 | 0.00762452 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899522 | TTTCTAACATGCAGA[C/G]AAAAGCTTTGAGTGC | 92912 |
| rs537881984 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895046 | AAAAAATTAGCTGGG[A/C]GTGGTGGCGGGCGCC | 92912 |
| rs537888804 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864497 | AGGTTGAGAAACCAT[A/G]GTTTAAATAAAACTC | 92912 |
| rs537921357 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896614 | AAGTAATATTTTGTA[-/G]TTTTTTTAAAAATAG | 92912 |
| rs537945541 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892174 | CTCAGGATTGTGCAA[C/G]ATGGTAAAGTGGTCT | 92912 |
| rs537950038 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843215 | CCCCGAGCCTCCAGT[C/T]CGCGGGTGCGAAGAA | 92912 |
| rs538006044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867693 | GGATAGTAACTGGGC[C/T]GATGGTGACAGACCC | 92912 |
| rs538069291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897195 | AAAGAAACTTGTGCT[G/T]CATACAAAATCTTTA | 92912 |
| rs538087476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850161 | GGTTAAGTTTCCTGG[C/T]GTGGTGGATATTTTA | 92912 |
| rs538117469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898732 | CCTTGTATTCTAAAT[C/T]GCCAGGATTTTGTTT | 92912 |
| rs538145816 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875581 | CTTCTAGTATTTTCA[A/G]AAATTGCTGGGGTTT | 92912 |
| rs538192640 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875365 | CCAAAAAATAGTTCC[A/G]TTTGTATTTAGTCTT | 92912 |
| rs538203988 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875897 | AAATCCCGTCTCTAC[C/G]AAAAAAAAAAATACA | 92912 |
| rs538278887 | snp | C/G | 0.000101911 | 0.00713758 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844519 | TCGTGTGGCCCCTCC[C/G]TTGTGTGTAAGCCTC | 92912 |
| rs538320219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852060 | TTTATTTTTTTTTGT[A/G]GAGATGGGGTTTCAC | 92912 |
| rs538323126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890347 | TCATCCTTACTTGTG[C/T]GCATATTTTCTTGGT | 92912 |
| rs538331326 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845308 | AGAAGACACGGAGAT[G/T]TGAGAAAGTGTGGTT | 92912 |
| rs538479433 | snp | G/T | 1.94926e-05 | 0.00312185 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843767 | GGAAGCTGGACGAGC[G/T]GCACTGCCAGTTCCT | 92912 |
| rs538516165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850995 | TTCATTGATGTTTGC[G/T]CTGTCATTTGCTTTT | 92912 |
| rs538516201 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBE2Q2 | GRCh38.p7 | 15:75843425 | GTTGCCCTTTTAAGC[C/T]GCGGGGCCGCCGCCT | 92912 |
| rs538516645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866898 | AATTCTATTTATTTC[C/T]TTCATTAGTAATGCT | 92912 |
| rs538568897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859264 | CTTAAGAGCCTACTA[A/G]ATATCAAGTGTTACA | 92912 |
| rs538642108 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900258 | TAACGGGATGTTGCA[A/G]TCGTTTGTAAACTAA | 92912 |
| rs538651522 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841793 | AAGTTGGGGTAGAAG[A/G]TGGTAGAAGTTGGGG | 92912 |
| rs538688972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892305 | GAATTCACTCAAATC[A/G]TAGCATTCAAATAGT | 92912 |
| rs538701117 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851685 | GAAATAACATCGTCA[G/T]TTATCCTTTCAAGTA | 92912 |
| rs538741130 | in-del | -/CT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847497 | GAAGGGAAAAGAGTG[-/CT]CTTTTTCAACCTCGA | 92912 |
| rs538829341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898076 | AGAAACCTGTGTACT[A/G]CTTTGATACTTTATA | 92912 |
| rs538928935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868616 | AAATAAGCCATTGAT[A/C]TTATGCATATAGCCA | 92912 |
| rs538966426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867830 | ACTCTTTGGGAGTTT[C/T]AGGCTAGGTATATAG | 92912 |
| rs538991650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883959 | GTTACGATTAGAGAA[C/T]GGTCCCCACATGCCT | 92912 |
| rs538999030 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869544 | GGAAGTCCAAGATCA[A/G]GATACCAACATTGGG | 92912 |
| rs539082554 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892833 | CTGAGGCATGTTTGC[A/G]CACTCCAGCCTTGGT | 92912 |
| rs539294140 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854574 | TAATATGATATAAAA[A/G]CATGATTAATGATTA | 92912 |
| rs539339577 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863731 | CACTGCAGCCTCCGC[A/T]TCGTGGGTTCAAGCG | 92912 |
| rs539376112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871345 | ATGCCTTCCTCTTGT[C/T]TCAACTGCAAGAGGC | 92912 |
| rs539448778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896094 | AAAAGGGGCAGACCA[A/G]TGTCTGTAGCATGCA | 92912 |
| rs539510445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848605 | TGAAAGGAACAGATA[C/T]ATGAAGAGAAGACTT | 92912 |
| rs539513124 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875730 | ATATCCTCTTGAAAC[-/T]TCATAATGCTTCATT | 92912 |
| rs539546489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857094 | AGCAAGACCCTCTTT[C/T]TCTCTCTCTCTGTAC | 92912 |
| rs539560307 | in-del | -/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843142 | CTCCAGGCCGGGGGC[-/G]GGGGCGCGCGGGGGT | 92912 |
| rs539568867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865800 | CCCTGAATAATATCT[A/G]GTTGTTTTTTTTTTT | 92912 |
| rs539668658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864341 | TTTGGAAATATCTGG[A/G]GCCATTTCTGGTTTT | 92912 |
| rs539684049 | in-del | -/ATT | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891257 | TTGCTGTAGATAAAC[-/ATT]ATAAGTTTACAGTTG | 92912 |
| rs539706638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871992 | ATACAGGCTAAAGGC[A/G]TTTGTGAGAATTGTG | 92912 |
| rs539904124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866322 | GGGACTACAGGTGTG[C/T]ACTGCCACCGTGCAT | 92912 |
| rs539959411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873835 | CAAGTAGCTTGGACT[A/G]TAGGCACATGCCACC | 92912 |
| rs539994101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879824 | ACTGAGAAACACTTA[C/T]TTATGGATTCATACG | 92912 |
| rs539995732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872922 | AGGAGAAATTAGGCT[A/G]TGTTAGTATTTCAGT | 92912 |
| rs540025113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894847 | TTTGGGAGTTTCAGG[C/G]TATGTATAGTTTTTA | 92912 |
| rs540030783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886483 | TCAGTATTCCCATAA[A/G]CATGGGAAAAGGAAG | 92912 |
| rs540083595 | snp | A/G | 0.00288866 | 0.0378944 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879207 | AGAAAATAGTTACAG[A/G]ACCCCATATACTTCC | 92912 |
| rs540134058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880947 | TGCTTGGGGATATAT[C/T]TTATGATTGAACTTT | 92912 |
| rs540198696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872346 | AAAAAGCCGAGATGC[A/G]TATAAACTACTCCTT | 92912 |
| rs540271849 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBE2Q2 | GRCh38.p7 | 15:75843492 | CAGGCCGCCACACGC[C/T]GAGGCTTCCGCGCCC | 92912 |
| rs540280098 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871711 | GGTCAAAGATTAACA[A/G]AATCTCAAGGCAGAA | 92912 |
| rs540306444 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842562 | GACGATGTGACACAG[A/C/G]GTGACTATTTGAAAT | 92912 |
| rs540331765 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841296 | ATATATTTCTGGGAT[A/G]CAACTAGTAAAAACA | 92912 |
| rs540363146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887392 | AGGAAAATGATTTAC[A/C]TAGGTGAAAAGTAAA | 92912 |
| rs540391461 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853382 | AGGCTGAGGCAGGAG[A/T]ATCGCTTGAACCTAG | 92912 |
| rs540498135 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848083 | GGAGCTTAAGTAAGT[C/G]ACTTCTTTTACTGTG | 92912 |
| rs540507654 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842267 | TGCACTTACGATTGC[A/G]CACACTATTGTCTGC | 92912 |
| rs540534925 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856317 | CAGTACAAATCCCAG[C/T]AGATTTATTTTTGGA | 92912 |
| rs540546271 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845722 | AGTACAGGGATACCA[A/G]ATGTTTTGCAACGTT | 92912 |
| rs540618957 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897414 | TTAGTAGAGACCGGG[C/T]TTCCCTGTGTTAGCC | 92912 |
| rs540663944 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889503 | AACTGGAATGGAAGA[C/T]GTGCAGGCTAGAGTG | 92912 |
| rs540701060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845453 | GTGTTTTAAGGAGAC[C/G]GGCCTGAATGGCTTC | 92912 |
| rs540733133 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898988 | GAGTAGACTGGGTGC[A/G]GTGGCTCACACCTGT | 92912 |
| rs540735045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849767 | AAAGGACCTGAGTAA[A/T]TAGATGCTTAGATAA | 92912 |
| rs540771820 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858326 | GTTTAAATTTGCGTT[C/T]ACCCACCTCCTAGCA | 92912 |
| rs540779629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896607 | TATCTGAAAGTAATA[C/T]TTTGTAGTTTTTTTA | 92912 |
| rs540784474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853355 | ATGTGCTTGTTATCC[C/T]AGCTACTCGGGAGGC | 92912 |
| rs540791055 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854121 | GAATGCCAGGAGGTG[A/G]TGGTGATCGGGGCCA | 92912 |
| rs540862057 | in-del | -/TATG/TG | 0.00280448 | 0.0373413 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853504 | TTATATATATATATA[-/TATG/TG]TATGTATGTATGTAT | 92912 |
| rs540904356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862981 | GCTGGAACTACTCCA[C/T]TCCTCTGGAGATGAA | 92912 |
| rs540953299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864850 | TATTTTGCTTTTTCT[A/G]GTTTAGTGGATTAAT | 92912 |
| rs541006719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891955 | CTGACCTATTTCTAT[A/G]ATCAGGAAAGGCATC | 92912 |
| rs541049172 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892710 | ACAAAAAATACGCCC[C/T]CCACCCTAAAAAAAC | 92912 |
| rs541106833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854101 | CGGGAATTTTACAAG[G/T]GTGTGAATGCCAGGA | 92912 |
| rs541120247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863314 | TGAGTTCTGGTCTGC[C/T]GGTAACCCCATTCCT | 92912 |
| rs541159036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870945 | CACAGAGACAAAGTA[C/T]AGAGAAAGAAATAAG | 92912 |
| rs541175849 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899999 | AAACTTTTTAATGAC[A/T]ATGTGAAGATATGAA | 92912 |
| rs541195210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870317 | CAAGTGATCCACCAC[C/T]GGCCTCCCAAAGTGC | 92912 |
| rs541229832 | snp | C/G | 3.31785e-05 | 0.00407286 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75877978 | ATTTATTCAGTGGAA[C/G]TCATAAATGACAGTT | 92912 |
| rs541401437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884643 | TTCTGCCACATGGTA[A/G]AGCAATATAATTTAT | 92912 |
| rs541403933 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885648 | TGATTCCCATGTGTT[G/T]TCTGCTGCAGAGCAG | 92912 |
| rs541417341 | snp | A/G | 0.000202511 | 0.0100605 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844305 | ATTTTCCTTCTTCCC[A/G]CTTGTTCAGCCAATT | 92912 |
| rs541469691 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858827 | CTGGAGCTTGGTTTC[C/T]GTTTAAGCATGAAGA | 92912 |
| rs541520282 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852477 | TACAAGATTAAAAAC[A/G]TGATTTCAGTTAATT | 92912 |
| rs541614060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854181 | AAATCATTGACTTCT[A/G]TGAGCTGTAGCAACA | 92912 |
| rs541617460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885121 | CTAATAGTAGTGGGG[G/T]TTTTTTTTATTTGTT | 92912 |
| rs541775412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857452 | CAACTCACCTCCCAC[A/T]CTTGCAGCCTCTGCC | 92912 |
| rs541813519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848171 | CTCTTTGGCAATGAT[A/G]TTATGTTCTACAAAT | 92912 |
| rs541835633 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893715 | CAGTTGGTACCATAC[A/C]TACCATATAATTTAA | 92912 |
| rs541858143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884715 | CTCAGGCTGGAGTGC[A/G]GTGGTGCTGTCATGG | 92912 |
| rs541873082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894952 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 92912 |
| rs541878295 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884463 | AAAATCCTGTTAAGA[A/G]TCATTTCTGTGTAGT | 92912 |
| rs541890253 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846838 | GTTGTTTTTTACACA[A/C]GTGCATGCTAGTTCC | 92912 |
| rs541912200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856711 | AACTTTAGGAGGCCC[A/G]GGCAGGCGGATCAGT | 92912 |
| rs541979688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863358 | GTGTTTATTCTTCAC[C/T]GTAATTCTAGTGGAG | 92912 |
| rs542098988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853421 | GGTTGCAGTGAGCCG[A/G]GATTGTGCCATGCAC | 92912 |
| rs542135489 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869959 | TGATTTAAAAAAAAA[A/T]TTTTTTTTCTGTTTT | 92912 |
| rs542157504 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870999 | GCATATGGAGGATCC[C/T]GCCAGCCTCTGAGTT | 92912 |
| rs542167769 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864965 | ATCTGTTTTCTAAGT[A/T]AGTTTATTCCATCAT | 92912 |
| rs542194563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878976 | CAGCTTTAGACCTTC[C/T]CTTTCTGGAACTTGC | 92912 |
| rs542338670 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867215 | GCATTGAGTTATACT[A/G]AAAACACTCTCTGTC | 92912 |
| rs542369811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871575 | GGAAGTGGTGATGAC[G/T]CTTAAGGAGCATGCT | 92912 |
| rs542423362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875247 | CATATTTTAGAGATA[A/G]GAAAAACTTCTCATA | 92912 |
| rs542518924 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895866 | CTTTTGACACAGCAG[C/T]TCTACTCTAGGACAT | 92912 |
| rs542535615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888656 | TTAATACAGAAGTAG[A/G]ATCGGCCACTTTTAG | 92912 |
| rs542564051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851507 | GATATTCTTGGAAAA[C/T]GGTGGTGGATACAAG | 92912 |
| rs542656890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876977 | GCCTGGCCAACATGG[C/T]GAGCGAAGCCCCATC | 92912 |
| rs542720439 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871826 | CTTTTCCCCATAATT[A/G]TTGATAGGAAGGCCT | 92912 |
| rs542800961 | snp | A/G | 4.99663e-05 | 0.00499806 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891046 | TTTTACATAAACCAT[A/G]AGATACATTTTATAT | 92912 |
| rs542837646 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891648 | AGGATTGGAACTAGA[C/G]AGTCTGGCTGCCCTA | 92912 |
| rs542864420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899232 | GTGAGCTGAGTTTGC[A/G]CCATTGCACTCCAGC | 92912 |
| rs542930983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844721 | TCGTGAAGCTATTCG[C/T]CGTGAAATTGATGTA | 92912 |
| rs542936868 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848706 | TTAGACCTGGAAAAG[G/T]GTAGTATTTGATAAA | 92912 |
| rs542939615 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844764 | AAACTGCAGAATATT[C/G]TCTTGGTTATAATAG | 92912 |
| rs542946614 | in-del | -/AGCAC | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842540 | GCCCAACAAAAACTT[-/AGCAC]AGGACGATGTGACAC | 92912 |
| rs542969694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852402 | TGGGGGTCTGAGGTC[C/T]CCACTTTGGGAACCA | 92912 |
| rs543008743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869408 | AGTAGTGAAACTGTC[C/T]CTTGTTGAAAAATCA | 92912 |
| rs543055075 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845862 | GATGACCTGGATTAG[G/T]CAGTGGCAACAGAAA | 92912 |
| rs543060439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853254 | AGGTGGGCTGATCAC[A/G]AGATCAGGAGTTCAA | 92912 |
| rs543067596 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899865 | CAATACAGGTTTAAT[C/T]GATGTTCAATATTGG | 92912 |
| rs543095578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852524 | TAATATGGTTTTGAG[A/G]GGTTTCAGTCCAGAG | 92912 |
| rs543116326 | snp | A/C | | | intron-variant, utr-variant-3-prime | UBE2Q2 | GRCh38.p7 | 15:75874858 | TGAAATCTGAGTAGC[A/C]GTTACTTTGTCTTGG | 92912 |
| rs543146858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876395 | CTTTATTTCAGGAAT[A/G]TGAAACTCAAATGCA | 92912 |
| rs543175266 | snp | A/G | 1.75446e-05 | 0.00296176 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859848 | AGGGCTCTTTAACAT[A/G]ATGCTTATTTACTGA | 92912 |
| rs543214912 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868112 | ATTATTCCATCAGAG[C/T]GTCTAATAACAGATG | 92912 |
| rs543324122 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844148 | GCGGCCCAAGCCCTT[A/G]TGGGGTCCATGGCCG | 92912 |
| rs543349776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876021 | AGTGAACTGAGATTG[C/T]GCCACTGCACTCCAG | 92912 |
| rs543421444 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877720 | CTTTTTTTCAGTCAG[A/G]CTAAACGGTAAGCAG | 92912 |
| rs543490062 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861081 | TCCATTGGCAAAATG[C/G]GGGAACCAGTAATAA | 92912 |
| rs543547536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870137 | CAGTAGTGTGATCAC[A/G]GCTCACTGCAACCTC | 92912 |
| rs543614539 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849291 | AAAGTAATGTGTCCC[A/G]TAACTGGCCTTCAGA | 92912 |
| rs543624932 | in-del | -/TAAATTAGATTTAATTTACATAA | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868647 | ATAAGTAAAATGTTT[-/TAAATTAGATTTAATTTACATAA]TCTTATTTTAAATTA | 92912 |
| rs543669075 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882175 | AGCCATTTGGTGATG[C/T]AGTCTTTAAAATGTT | 92912 |
| rs543703319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852654 | GGAAAAGAAACCTAA[A/G]AACTAAAACAGTAAA | 92912 |
| rs543735717 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875363 | GACCAAAAAATAGTT[C/T]CGTTTGTATTTAGTC | 92912 |
| rs543762008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870828 | TTGAATTCGAGACAG[G/T]TGTGTTTCTATTTGG | 92912 |
| rs543774862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883502 | GGACGAGATCTCACT[A/G]TGTTGCCCTGGCTGG | 92912 |
| rs543820646 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874157 | TACCTTCCTCTCATG[A/G]GATCTGTATATTCAA | 92912 |
| rs543974856 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880516 | AGACAGAATCTTGCT[C/T]TGTTGCCCAGGCTGG | 92912 |
| rs543987981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892698 | GAACTCGTCTACACA[A/G]AAAATACGCCCCCCA | 92912 |
| rs544050677 | snp | C/T | | | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901138 | TGTTTGTAGGCTTTA[C/T]TGAGTTTCTGGAATA | 92912 |
| rs544121927 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842324 | GCTATCCAGACCTTT[A/C]TTCATTTTTTGAGCA | 92912 |
| rs544188716 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893202 | TTGAATTAATAAAAT[-/C]CAGCTGTTTTAATCT | 92912 |
| rs544263633 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858855 | AGATTTTTGTTGGAT[C/T]GTAATTTACCGTTCA | 92912 |
| rs544349081 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843909 | GGGGCGCTTCGAGTC[A/C]CGGGACAAAGGGGAG | 92912 |
| rs544446163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895502 | TTACTATTTTAAAGA[C/G]CTCTTAGATGTTGAA | 92912 |
| rs544476494 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841552 | GCTTAACCCAGCAAT[A/G]ATGCTAATACAGTAG | 92912 |
| rs544499139 | in-del | -/TGTT | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884569 | GAAACAAAAAGTGTG[-/TGTT]TGTTTGTTTTTTTAA | 92912 |
| rs544699521 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843580 | GGCCCCGCGGGGCGG[C/T]CGCGGCCGTGACGGC | 92912 |
| rs544703249 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880346 | TTGAATTCCTAACCT[C/T]AGGTGATCTGCCTGC | 92912 |
| rs544737151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874217 | AGTTCTTTCTCCTTC[A/G]TGAAGCTGACTTTGG | 92912 |
| rs544807305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897520 | CACTGCACCACAAAA[C/G]CTTAACATTGTACTT | 92912 |
| rs544888738 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871768 | GGAGTCTCCTATGTC[C/T]ACTTCTTTCTACACA | 92912 |
| rs545216158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899145 | GTGGGGCATAGTGGC[A/G]CATGCCTATAATCCC | 92912 |
| rs545388056 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884220 | AATGTTCCAACACTC[A/G]GGTGACTAATTCTAT | 92912 |
| rs545398103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859626 | CAATGTCTGGAACTT[C/T]CTTCCTCTGCCCTTA | 92912 |
| rs545421953 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884249 | ATTATGTGACATAAT[C/G]TACATTATGGTGGTT | 92912 |
| rs545464445 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869301 | TTAATCTGTATTTGG[-/T]TTATTTTTAGGAAGA | 92912 |
| rs545491955 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861475 | CATTGTGCTCAGTAC[A/T]CCAAATGGATAGGCC | 92912 |
| rs545504503 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882474 | AATTAAATCATACAT[A/T]ATGAAGAGGTTTTGT | 92912 |
| rs545530014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844625 | GACACTTTTAAAAAC[C/T]CACTCATTAAGCGGA | 92912 |
| rs545534631 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877755 | CAACTCATTAAAGAA[-/T]TCTTCTCAGTTGATG | 92912 |
| rs545624563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885385 | CCTCCCAAAGTGCTG[C/G]GATTACACGCATGAG | 92912 |
| rs545664644 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844112 | GGTCCCCGTCTCCTA[G/T]CCCCGAGGGGGGAGT | 92912 |
| rs545680529 | snp | C/T | 0.0166586 | 0.0897318 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843861 | GGTGAGGCGCCCGGC[C/T]GCGGCCCCGCGGGGC | 92912 |
| rs545698197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893787 | AACAAAAAGCTATGT[A/G]AATTTGGAAATTAAA | 92912 |
| rs545790106 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886350 | GTCTCAAACTCCTGG[C/G]CTGAAGTGATCCACC | 92912 |
| rs545838840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894580 | CAGAGCAAGACTCCA[C/T]CTCTTAAAAGAACCT | 92912 |
| rs546065014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847283 | AAGAATTTGTCAAAA[C/G]TGCAGAGATAACATC | 92912 |
| rs546143589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854235 | GTTGTCTCAAAAGTC[C/T]AGCTCCTCACAAGGT | 92912 |
| rs546175380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864095 | TTTGAATCATCCTTG[C/T]ATTTCTATAGTAAAC | 92912 |
| rs546198077 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896424 | AAGATATAGGTTGGT[C/T]GTACTTATGGTGACA | 92912 |
| rs546334826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864750 | GTTTTATTAGTCTTG[C/T]GAAAGAATCCTCTTT | 92912 |
| rs546421055 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864106 | CTTGCATTTCTATAG[A/G/T]AAACACCGTTAGAAT | 92912 |
| rs546489672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878447 | AAAAAAAAAATTAGC[A/C]AGGCATGGTGGAGTA | 92912 |
| rs546539349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894026 | TCTTAGTTAAATCTA[C/T]AAGTTAATAATAAAA | 92912 |
| rs546554081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880241 | CCTCAGCCTCCTGAG[G/T]AGCTGGGATTACAGG | 92912 |
| rs546582865 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864161 | GATTTTTACTTCTAT[A/T]TTAAGTAAGGTTATA | 92912 |
| rs546619633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871852 | GGCCTTAAGCAGGGA[A/G]TAGTGTGCTGAGGAT | 92912 |
| rs546619739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863590 | AGCTGGGATTACAGG[C/T]ACATGTCACTACGGC | 92912 |
| rs546652899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881262 | TATCCGTCCCTGTGG[C/T]CCCCTGTGTGCCCCT | 92912 |
| rs546703205 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842099 | GGGTAACTCTAGGTA[A/G]GACTGGAAAAGGAAA | 92912 |
| rs546755967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871142 | TGCATCATAGACAAG[A/G]TAAAGAATCAAGTGC | 92912 |
| rs546787414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885573 | TAGCATCTCAGAGGA[C/T]GGTGTCCTCTGGCTT | 92912 |
| rs546830586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849051 | TTTTATCATGGGTAT[A/G]TGAACATTTTTATTT | 92912 |
| rs546939790 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887137 | TGACCTACTCAAATA[A/G]ATCTTCTGATTCCTA | 92912 |
| rs546966136 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876565 | GGGGAAAGCATGAGC[A/G]ATATTGCTTGGAAAG | 92912 |
| rs547066644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887628 | TATTCATCTTTCTGT[A/G]TAACTGGTTGAGGAA | 92912 |
| rs547092545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883720 | TTACATTTTTAAGAA[G/T]TTTCCAGGTGAAGTT | 92912 |
| rs547104405 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844863 | TTGGTTGAGTCAGTG[G/T]GTACTCAAGTGCCTG | 92912 |
| rs547169241 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856432 | AAAATGTTGTATACT[A/G]ACTCTGTTCCAGACA | 92912 |
| rs547191469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895205 | AAAAAAATTTTGAGA[C/T]GGAGTTTTGTTCTTG | 92912 |
| rs547223620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891204 | ATACTAATTGATAAT[C/T]ACTTAATGATTTCGT | 92912 |
| rs547302051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856871 | GTGCTTCAACCTGGG[A/G]GGCAGGTTGCAGTGA | 92912 |
| rs547360830 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901472 | TGGGCTTTGCTCTGC[A/T]TCCTTGAGATTTTTC | 92912 |
| rs547363236 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899667 | GACTGAGCAGTGGGG[A/C]CTTTACTGTATTTTT | 92912 |
| rs547365613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851885 | ATAGACATTCTTTTT[A/G]TTTTTGAGACAGGGC | 92912 |
| rs547447729 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872842 | TTTTCTGTGCTTATT[A/T]CAGCGTAACTGAAAT | 92912 |
| rs547590172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869680 | TTAAGGAGGAAGGAG[C/T]CCTCTTGGCTTAATC | 92912 |
| rs547620075 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851143 | TATTCTTCTTTTTTT[A/T]TTTTTTGAGATGGGG | 92912 |
| rs547622796 | snp | A/G | 2.68482e-05 | 0.00366379 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899395 | ATTTATTTAAGAATT[A/G]TTTTAACTTTTTTTT | 92912 |
| rs547644644 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861585 | CATTTTGAAGTGTCC[A/G]TTAATGGGATTTTAG | 92912 |
| rs547683186 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876473 | CTTTTGGATTTTTAA[A/G]AAATGTTTTTATAGG | 92912 |
| rs547688992 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844854 | TAACTCCCTTTGGTT[G/T]AGTCAGTGGGTACTC | 92912 |
| rs547723786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868677 | AGATTATGTTTTAAC[A/G]TTTTTTTCTGTTTTG | 92912 |
| rs547723860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877360 | TGTGGGTGTCCTTAC[A/G]GTTTTTTGTGTAAGA | 92912 |
| rs547752812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850775 | CAGGACTCCTTTACA[C/T]TCTTGAAAATATATT | 92912 |
| rs547764376 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846410 | ACCCGGCTAATTTTT[G/T]TGTTTTTAGTAGAGA | 92912 |
| rs547886041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877498 | AAAAAAAACAGATAC[C/T]GGGTGGAATTTGTTA | 92912 |
| rs547900841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862435 | TTTTTTTTTTTTTAA[A/G]CCTTTCCTCAGGTAT | 92912 |
| rs547901233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845724 | TACAGGGATACCAAA[A/T]GTTTTGCAACGTTCA | 92912 |
| rs548143999 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878208 | ATAAGAAAGTGAGAA[A/G]GAGGAAGGACAGAAA | 92912 |
| rs548156853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894168 | AATCATTACTTATCA[C/G]AGACTAAAGGAGAGC | 92912 |
| rs548180576 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844967 | AAGGTGTGTTAATTT[A/C]AAAAAAAAAAAGACA | 92912 |
| rs548282955 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887758 | AGTAGTTGAGGGCCA[C/T]GCTGTTGTCTTAGAG | 92912 |
| rs548317782 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893361 | AACAGAAAGCATTAG[A/T]AACAATTTGATAATA | 92912 |
| rs548318891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845569 | GTGGGGAGCTACTAA[A/G]TTTACTCAGGTAAGT | 92912 |
| rs548414799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846486 | AGCTCCCAAAGTGCT[A/G]GGATTACAGGAGTGA | 92912 |
| rs548419884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892019 | TCTCCCACAGAATCC[C/T]CTAGACTGTGATCAC | 92912 |
| rs548453908 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846554 | GATGACTGTTTTGAT[A/G]AAATGACATGGCTTG | 92912 |
| rs548617250 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885262 | AGTAAGGACTACAGG[C/T]GTGCGCCACCATGTC | 92912 |
| rs548645986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847680 | CAGCCTTATTGGGAG[C/T]TAGTATATGGCTTTA | 92912 |
| rs548655819 | snp | A/T | 0.000100866 | 0.00710092 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843659 | CTCCCGCCGGAGATG[A/T]GGGGAAGATGTCCGT | 92912 |
| rs548734703 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858617 | GGAAAATTGAAATTC[G/T]TGGAGAGTGTACTAC | 92912 |
| rs548768441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866194 | CTTTTTTTTTTTGAA[A/G]CAGGGTCTTGCTCTC | 92912 |
| rs548836222 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863223 | TCTTGCTGTCAATAT[A/C]CCCCTAACCTCCACC | 92912 |
| rs548905652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865602 | AAAAAACTTTTTAAA[A/T]AGCATTTTCAGATGG | 92912 |
| rs549047645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873658 | ACATGCCCATCTCAG[C/T]TGCCCTCTTCCTCCA | 92912 |
| rs549093015 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843079 | GGGCTGGCGCTAGTC[G/T]GCAGCGGCGCCGACG | 92912 |
| rs549179373 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900011 | GACTATGTGAAGATA[C/T]GAATTGTTTCCTGAA | 92912 |
| rs549190463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869075 | CATTTGAGTAATTCT[C/T]AAATCTTTTTTATAG | 92912 |
| rs549347076 | snp | A/C/T | 3.35797e-05 | 0.00409743 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883326 | GTATAACACTAAGGA[A/C/T]GTTCTTTAAATTAAT | 92912 |
| rs549357809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889066 | CTAAATGAGTACCTG[A/G]ATCTTCTAATTCTGT | 92912 |
| rs549387235 | in-del | -/GGTGAGAAGGTCCTCACAGGAACCCAGGCT | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842868 | GGGAGCAGCGAGTCC[lengthTooLong]GGTGAGAAGGTCCTC | 92912 |
| rs549483596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851799 | TCATGTATACTTCCC[A/G]TTTCATCACTTGAAA | 92912 |
| rs549496514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860050 | AAGTCAAACTAGGAT[A/G]ATTTTTCTTTTTATT | 92912 |
| rs549535282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867635 | TTAAATTACTTCCCC[A/T]TTTTGAGGTGATGGG | 92912 |
| rs549538032 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859613 | GTGAGAAATTGGACA[A/G]TGTCTGGAACTTCCT | 92912 |
| rs549541216 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879651 | TTTAGAGTGAAAACA[A/G]TCTTAGCTATTAAAA | 92912 |
| rs549561664 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872938 | TGTTAGTATTTCAGT[A/G]GCCTCTTAATATTTT | 92912 |
| rs549566568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75874987 | ATTAATCTAATTTAT[A/G]ATTTTTAGTAGAGCA | 92912 |
| rs549699455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882216 | AATAACTTAGATGGC[C/T]AAGATGTTAAGATCT | 92912 |
| rs549701835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858662 | TGCTTGGTATGACTC[A/C]ACTACCCTGCTGCCT | 92912 |
| rs549744305 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876870 | TAATTTGAAAAGATA[A/G]CATTGGTTGGGTGCG | 92912 |
| rs549773327 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846878 | CTGTACAGGTGCTCT[A/G]CTGGCTTTTCCTTTC | 92912 |
| rs549891666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889416 | TATTAATGTTAGTGG[G/T]CTACAGTAAAAGTTT | 92912 |
| rs550040163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860684 | TTAATTTAAAAAATT[C/G]TGTTGTAGCCCTTTC | 92912 |
| rs550078940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868600 | TGGGAGATTTTATTT[C/T]AAATAAGCCATTGAT | 92912 |
| rs550104968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875682 | TTCACATGAGAAGAA[A/G]TAGGAAATGAACTAG | 92912 |
| rs550104969 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883629 | TTTTTCTTCTAAATA[C/T]AGTGTGCACCAGAAA | 92912 |
| rs550132848 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856745 | GGTGGGGAGTTCAAG[A/C]CCAGCCTGGCCAACA | 92912 |
| rs550280845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869554 | GATCAAGATACCAAC[A/G]TTGGGTGTCTGAGGA | 92912 |
| rs550295466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853046 | CTGAAGCTAATATAC[A/G]ATAATAATGGCTTTT | 92912 |
| rs550337404 | snp | C/T | 0.000383997 | 0.013851 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854521 | CTATTTTCTCTTTTC[C/T]TCATGAACATTACAT | 92912 |
| rs550376575 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887983 | TGTGATTCTAGATAG[A/G]TTATTGAGCAGTTTT | 92912 |
| rs550402297 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865234 | CACTTATGTATGCAT[A/C]CTTGAACAATACAGT | 92912 |
| rs550508055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886560 | CAAGGAAAAGATTTG[G/T]AAGAAATTTGCAAAT | 92912 |
| rs550510244 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871281 | GATGGAACGTACAAT[C/T]GGGTTTTATACCGAG | 92912 |
| rs550650179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889449 | AGATGCCTTGTCTGC[A/G]AAGTAATTTGGTTAG | 92912 |
| rs550689569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857001 | CACAGTGGTTCATGC[C/T]TGTAATCCCAGCACT | 92912 |
| rs550725183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871947 | ATTTCGTGGATGGGA[A/G]CATGACTGAGGTTGA | 92912 |
| rs550748380 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856976 | TTTAAGAGTTAAGGC[G/T]GAGGCTTGGCACAGT | 92912 |
| rs550761958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879864 | AAACTGCCCAAAGAG[C/G]AAAACTGTCCAAGAA | 92912 |
| rs550875091 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896802 | TTGGGGTACAATTTT[G/T]GTTTTGTTATTTTTA | 92912 |
| rs550922026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866260 | TCACTGCAGCCTCTA[C/T]CTTCCTGGGCATAAG | 92912 |
| rs550958853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873749 | CTAGGCTAGAGTGCA[G/T]TGGCACAATCATAGT | 92912 |
| rs550972003 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896940 | ATTCATAAATTTATT[G/T]TAATAATTTTCACCT | 92912 |
| rs550979058 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866039 | TCTTTACGCTTTTAT[A/C]TTCTGATATTTGTTA | 92912 |
| rs551142003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881320 | TCTTTACGGGAATAT[G/T]AAATATTGGCCAGGA | 92912 |
| rs551165876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872640 | CTCCTGGGCCCACAT[A/G]ATCTTCCTATCTCAG | 92912 |
| rs551216621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866139 | TTGGTATGATTTTCT[C/T]TGTAACTGTAAAGTG | 92912 |
| rs551239869 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842125 | GGAAAATGCGGAGCC[C/G]CTTTCTGAAAAATTA | 92912 |
| rs551305726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880573 | GTGGCACAATCTTGG[C/T]TCACTGCAACCTCTG | 92912 |
| rs551348868 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849952 | GAGAAATAGTAGGCA[A/G]ACTTATCTTTTCAAG | 92912 |
| rs551481060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857887 | TAATGTAAAAAAAAT[C/T]TATATGCTTGTTTAT | 92912 |
| rs551521524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865439 | GGATACAGACATGTG[C/G]GTTGTTTCCAGTGTT | 92912 |
| rs551527288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864112 | TTTCTATAGTAAACA[C/T]CGTTAGAATGGATAT | 92912 |
| rs551582347 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844642 | ACTCATTAAGCGGAA[A/G]TCTCATTAGAAACCC | 92912 |
| rs551591470 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872206 | GTACTCCAGCCGGGG[C/T]AACGGAGCGAGACTC | 92912 |
| rs551594731 | in-del | -/GAAAGATGTCCCT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877585 | ATGTATACTAACTTG[-/GAAAGATGTCCCT]GAAAGATGTCCCTGA | 92912 |
| rs551654986 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899514 | AGAAAATCTTTCTAA[C/T]ATGCAGACAAAAGCT | 92912 |
| rs551662031 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882069 | TTAGTTTTTATTTGC[A/T]TTTGGTGAATGCAGG | 92912 |
| rs551666443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889342 | GATTCTCCAGGATGG[A/G]GGAGATGAAAAGGAC | 92912 |
| rs551702360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897536 | CTTAACATTGTACTT[C/G]AGTCAAAATTTTTGT | 92912 |
| rs551719625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859332 | ATTTCTTTGTTTTAC[A/G]GATGGGTAGACTCAT | 92912 |
| rs551735538 | in-del | -/TCTCT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848854 | AACAGTGTTATGTGA[-/TCTCT]TCTAGAAGATTCTGA | 92912 |
| rs551802373 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875448 | ACTGAAACCAGTCGC[A/C]TGTAGGCAGATGTTT | 92912 |
| rs551806189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866656 | TGTTTTCTCCCCCAT[C/T]TCCTTTTTTTCTCTG | 92912 |
| rs551858661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862919 | CTGATTCCCAATTGT[C/T]ATTCCCTACCCCTCT | 92912 |
| rs551889361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870498 | AACATTAAACCTTTT[C/T]TGTGCGCCCAGTTTA | 92912 |
| rs551945951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, stop-lost | UBE2Q2 | GRCh38.p7 | 15:75874833 | GTGTTAGAGCTATTG[A/G]CCAACTCCGTGAAAT | 92912 |
| rs552004165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888760 | CTTGTCTTGTGTTCA[A/G]CAAACATTTGTGTAG | 92912 |
| rs552089197 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843621 | CCGGCTCCCCTTCCG[C/G]GCCCGGCTCCCCTTC | 92912 |
| rs552107417 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858510 | GTAATTTTCTAAGAC[C/T]TGTCCTTCTGAATGT | 92912 |
| rs552117414 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843026 | CAGTGAGGTTAGCGG[A/G]TGCCGCGCCGAGCGC | 92912 |
| rs552312995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847738 | GGCAACTCCATTACT[C/T]CTTTTATGGACTTTT | 92912 |
| rs552343860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878243 | GACCAGCTGCGGGAT[A/G]AAGTGTTTTATGGAG | 92912 |
| rs552380788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877573 | TGTGAATAGGTTTAT[A/G]TATACTAACTTGGAA | 92912 |
| rs552382552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884895 | CTGAAGCCATCTTAC[C/T]CGCCTCAGCCTTGCA | 92912 |
| rs552418251 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884317 | CTATGGTTGAGATAG[A/T]AATAGTTGCATTTAG | 92912 |
| rs552455959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856851 | TGGAGGCTGAGGCAG[G/T]AGAAGTGCTTCAACC | 92912 |
| rs552486036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846323 | GCCCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 92912 |
| rs552489691 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901383 | AGCATACCCATGGCC[G/T]CCTTGCACACAATTG | 92912 |
| rs552504834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894365 | CTGAGCTCAGGAGTT[C/T]GAGACCACCTTGGGC | 92912 |
| rs552527305 | in-del | -/AACAT | 0.00123077 | 0.0247764 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872012 | GAGAATTGTGAGGAA[-/AACAT]AACATGTAGGATGGA | 92912 |
| rs552557739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886746 | ACAAAAATTAGCTGG[C/G]CGTGGTGGTGGGTGC | 92912 |
| rs552570792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886329 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCAAACT | 92912 |
| rs552744413 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860745 | GGTTCCTCTGTGCCC[A/G]TCTTGGCAGGTTGTT | 92912 |
| rs552833517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854151 | ATTTTAGAGGCTGCC[C/T]ACCAGTGTTGAAGAA | 92912 |
| rs552959765 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863803 | GTGCACCACCACGCT[C/T]GGCTAATTTTTTGTA | 92912 |
| rs552959822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872069 | GGAGAAGGGAGCTCA[A/G]TGAAGTATGGAGTCA | 92912 |
| rs553005868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893585 | TGAACAGGCATGGTA[A/T]AATAGACAAATATAG | 92912 |
| rs553098611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871527 | GTCCCTGCGGCCTTC[C/T]GCAGTGTTTGTGTCC | 92912 |
| rs553181530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862002 | GCGTCTCATCCTCTC[C/G]GGCCTCTTCATGTGG | 92912 |
| rs553181658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870600 | CCGCAACATGGAGGG[A/G]AACCTAGAAAGGTAG | 92912 |
| rs553218301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869908 | GATCTTTGTTTCTGC[A/G]TTGACCAAATAGAGG | 92912 |
| rs553240335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880010 | TCTGGGCCAGGTTGA[G/T]GGTTACATGAGCACA | 92912 |
| rs553270790 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892686 | GGAACATGGTGAGAA[A/C]TCGTCTACACAAAAA | 92912 |
| rs553274247 | in-del | -/A | 0.303187 | 0.244277 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872324 | TTAGCCTGCTTGGGG[-/A]AAAAAAAAAAAGCCG | 92912 |
| rs553350741 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885141 | TTTTATTTGTTTTTT[C/G]AGACGGGGTCTCACT | 92912 |
| rs553362834 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888223 | TTCAAAAAGAAACCC[C/T]GTACTGATTAGCAGT | 92912 |
| rs553366669 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875911 | CCAAAAAAAAAAATA[A/C]AAAATTTAGCTGGGC | 92912 |
| rs553401339 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875198 | ATATCTTCACATTTA[C/G]TCTTCATAGCCACCG | 92912 |
| rs553519217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879487 | CAAGATGGGTGGATC[C/T]TGAACACAGTTGTAA | 92912 |
| rs553538678 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862419 | TAGTTTATTTTGGTC[-/T]TTTTTTTTTTTTTAA | 92912 |
| rs553555885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886108 | TTGGGGAGAAATGAC[A/G]TAACTATTGTGTTTT | 92912 |
| rs553658966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889564 | GCATTTGGAAGGGTA[A/G]GAAGCAGTAGGAATC | 92912 |
| rs553675626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851031 | TAATTTGTTGTATGC[C/T]ATTTGCTTGAAATAA | 92912 |
| rs553724821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892364 | AATAATAAATAATAG[A/G]TATGTTTCCCAAGGA | 92912 |
| rs553839905 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841828 | GCCAGGAAAAGTTAG[A/G]GCTGGTTTGAATGAT | 92912 |
| rs553862438 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867741 | ACCTCAGAGAGCTTT[G/T]GAAAAACAGATTCTC | 92912 |
| rs553972168 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880801 | AATATGGATCTGGAT[A/G]AGATGTAATGGTTTA | 92912 |
| rs553997849 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845748 | ACGTTCAGGCAGTCT[A/G]CCACAGCAAAGAATT | 92912 |
| rs554072212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889094 | TGTTAAATCAGTGAG[C/T]GCACATTATATACAA | 92912 |
| rs554115081 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75901019 | TAAACTTGCATCAAG[G/T]TTATGAATAAAGAAC | 92912 |
| rs554123433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884409 | CAGTTATTTTTAGTT[A/G]TATTTGCTTTACATG | 92912 |
| rs554124312 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877899 | TTAGTGTATACATTT[A/G]TACCATAGTAATAGT | 92912 |
| rs554146105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898133 | AAGTTTCATACTAAA[C/T]AGTACTTAGTCTAAT | 92912 |
| rs554311330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853062 | ATAATAATGGCTTTT[C/T]CCCAATTTATAATAG | 92912 |
| rs554338151 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845144 | GGTATCATCAGGAAA[A/G]CCAAAGCAACTAATT | 92912 |
| rs554344108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860903 | TCTCAGGTAAAACCC[C/T]AAGAAAGCATGGAGG | 92912 |
| rs554375147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844680 | GGTAAAGGAATTGAA[A/G]TATTAAGTTTCTCCA | 92912 |
| rs554602839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884490 | TAGTCAGAATACATA[C/G]TAACTTTGGTGTTGA | 92912 |
| rs554648867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869969 | AAAAATTTTTTTTTC[C/T]GTTTTGGGTCTTATA | 92912 |
| rs554687780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877764 | TAAAGAATCTTCTCA[G/T]TTGATGGCTGTAATT | 92912 |
| rs554711221 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891678 | AGGCCCAACCAAGAG[C/G]AGCTGAGAGCAAGCC | 92912 |
| rs554808101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882710 | TAATCTTACATTTCT[A/G]TTGCAAGTTAGAAAA | 92912 |
| rs554825317 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883490 | TTTTTTTTATAGGGA[C/T]GAGATCTCACTATGT | 92912 |
| rs554875040 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853208 | CTGGCTTAGTGGCTC[A/G]CGCCTGTAATCCCAG | 92912 |
| rs554933518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878488 | CCCAGCTACTGGGGG[C/T]GGTGGGAGGCTGAGG | 92912 |
| rs554966770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888843 | CTTTCTTCCCCCCAC[C/G]TCTTAAGACTCTGCA | 92912 |
| rs555086618 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861310 | GTCTATGCTGTTGTC[C/T]TCTAACCAGTCGTGG | 92912 |
| rs555237922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849389 | AATCCCTGAAGATAG[C/G]TGTGTCCTACATTTG | 92912 |
| rs555328438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873169 | GAGATTTAGAAGATG[A/G]CTTATTTGGTAATAG | 92912 |
| rs555333303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896402 | CCTGGTATATTAATT[C/T]GAAGCGAAGATATAG | 92912 |
| rs555358996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891757 | GAAGCATAGGCTGTA[A/T]TGTTAATTTTAGGAC | 92912 |
| rs555363563 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870504 | AAACCTTTTTTGTGC[G/T]CCCAGTTTACCATGA | 92912 |
| rs555364963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881088 | GAAGTTGCTAATGGC[C/T]ACATTTTTACTAATT | 92912 |
| rs555532346 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842271 | CTTACGATTGCACAC[A/G]CTATTGTCTGCCAAA | 92912 |
| rs555569195 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841310 | TACAACTAGTAAAAA[C/T]ACTTGCAATTTAAAA | 92912 |
| rs555574660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851117 | TAATGGCCATTTTAG[A/G]TAATCCTGGATATTC | 92912 |
| rs555631983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848815 | GAGTGATAAAGCAGG[A/G]GTCCCTTTTTCCAGA | 92912 |
| rs555658095 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867962 | AGTTTTTAGAAGACA[A/G]TGTGTCTAAAGAGAT | 92912 |
| rs555678085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896043 | CAGGTATGTTCTATA[C/T]TGATAAGGAACATTC | 92912 |
| rs555736918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898986 | TAGAGTAGACTGGGT[A/G]CAGTGGCTCACACCT | 92912 |
| rs555795212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881592 | AATTGCCAAGTTATT[A/G]GTATCGGGATTCACA | 92912 |
| rs555836891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874064 | TTTTACCCTGTTCAT[C/T]TGCTCTTCATATCCT | 92912 |
| rs555864024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850389 | TCACTCAACAATATT[A/G]TAGATCCGTGTTATA | 92912 |
| rs555946661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889001 | AAGATTGTGTTTGAT[G/T]TTAACTCATCAACCG | 92912 |
| rs555967420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858769 | CATCTTCATTATGCA[C/T]TTAGCACGCAATAGA | 92912 |
| rs555969417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866796 | TTATTTTTACTTTCT[A/G]GAATTGTGCTTGCAT | 92912 |
| rs556040285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850176 | CGTGGTGGATATTTT[A/G]TAATATGGAAAACAA | 92912 |
| rs556055712 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897245 | TATTTTATTTTATTT[G/T]ATTTGTTTTTTGAGA | 92912 |
| rs556074908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849506 | ATGGAGAAAAATAGA[C/T]ACAGAAAGTTACTTC | 92912 |
| rs556140758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874194 | CCTCTCCGACAAAAT[A/T]CAATTCAAGTTCTTT | 92912 |
| rs556179575 | snp | G/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842056 | GGATCTCTTGTAGAT[G/T]AGGAAGAAAGAGACA | 92912 |
| rs556379052 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844560 | AGGTGAAAGGAGATA[C/G]GCGCCAGGGCTGCTC | 92912 |
| rs556415797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899034 | GGGAGGTGGAGGTGG[A/G]TGGATCACCTGAGGT | 92912 |
| rs556420975 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842328 | TCCAGACCTTTATTC[A/G]TTTTTTGAGCACCTA | 92912 |
| rs556529313 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891463 | TTTTACTTTTTTTTT[C/T]CTCTGTGCCTATGCT | 92912 |
| rs556535047 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851548 | TTCTAATTTTTTGTT[A/C]AAAAACTTGCATTTT | 92912 |
| rs556589731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883507 | AGATCTCACTATGTT[G/T]CCCTGGCTGGTCTTG | 92912 |
| rs556630562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866981 | CAGCTCTCTGGTGAT[A/G]CCTGGTTATCTCCTC | 92912 |
| rs556654095 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843949 | GAGAGGCTCCGGCTC[C/T]CCGGGCGGGGCAGGC | 92912 |
| rs556688916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860193 | TATACAGGCAAACAA[G/T]TGCCCTTCTCTCTAC | 92912 |
| rs556720608 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862485 | ATTTGTAGTCTTTTA[A/G]TTCCCTTTTTTGTTC | 92912 |
| rs556730419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852182 | ATTCCCAGCCTTATC[A/G]TAGACATTCTTAAAT | 92912 |
| rs556816506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847073 | TATTTTTGCTTTGGT[C/G]ATGTTTTCTTATGCT | 92912 |
| rs556832238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875556 | GTAAATAATGTGTCA[C/T]CTTGAGTGTCTTCTA | 92912 |
| rs556885080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894477 | TAGTCCCAACTACTC[A/C]GGAGGCTGAGGTAGG | 92912 |
| rs556892416 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858698 | CCCAGCACTCCTGGA[A/G]CCCCTTCCGTGCCAG | 92912 |
| rs556895177 | snp | A/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842680 | TGGGGAGGGTTATCT[A/T]AAGCTTGGGAAACAA | 92912 |
| rs557014366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847895 | CCTTTCTGCGTATAA[C/G]TGGCTGTTTGCTAGG | 92912 |
| rs557033578 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852947 | TTCTGTGGCTTCAGC[A/T]ATAAATCAGATTATA | 92912 |
| rs557078202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866370 | TTTTTGTAGAGATGT[A/G]TTTTCACCATGTTGC | 92912 |
| rs557085778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865778 | GCTCCCTGCCCCTCA[A/G]GTATATCCCTGAATA | 92912 |
| rs557117019 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855359 | AACTGGGCATGGTGG[C/T]GCATGCTTGTAATCC | 92912 |
| rs557167436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854849 | AGAACTAGTATGAGG[A/G]AATTGCCTTTTCTTT | 92912 |
| rs557310089 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893469 | TGATAAAACCACAGG[A/G]AGAAGTTGACAAGTC | 92912 |
| rs557323389 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854137 | TGGTGATCGGGGCCA[-/T]TTTAGAGGCTGCCTA | 92912 |
| rs557441523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896187 | TAAAGAGGGACATAC[A/G]AGAAATTAGTAATAG | 92912 |
| rs557466193 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864528 | CAATCTGGAGGATGA[C/G]TCTTTGACTGTCTTT | 92912 |
| rs557515545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872209 | CTCCAGCCGGGGCAA[C/T]GGAGCGAGACTCCAT | 92912 |
| rs557592840 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855784 | CACGACTTTTATCAA[-/G]AACATGACAATTTTG | 92912 |
| rs557644579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887194 | CCAGCTATATAAGAG[G/T]GGATTAAAAGTACTA | 92912 |
| rs557644622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879600 | CATGCATTCTTAGTG[A/G]AGGCAATATCACCTG | 92912 |
| rs557649379 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875378 | CCGTTTGTATTTAGT[C/T]TTATGATAAGATATT | 92912 |
| rs557672192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864382 | CATGGTAGGGGTGCT[A/G]TTGGCATTTCTTAGG | 92912 |
| rs557694180 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850314 | GCTCATCTCTTTTCT[C/T]CGATGCTTATGTGTG | 92912 |
| rs557771967 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856349 | TTGACAAAATGACTC[-/T]TAACATTTGTTTAAA | 92912 |
| rs557777352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880273 | GCATGTCACCATGCC[C/T]GGCTAATTTTTTTAT | 92912 |
| rs557785488 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895173 | CCTGGGTGACAGAGC[A/G]AGACTCCGTCTCAAA | 92912 |
| rs557822232 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867077 | CTCTTTTCTACTGTG[A/G]CCTCCCCCTCCTGGT | 92912 |
| rs557846929 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892207 | TGTTAGTTGTATCCA[C/T]AGCTGTCATCAGAAG | 92912 |
| rs557914372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848705 | TTTAGACCTGGAAAA[A/G]GGTAGTATTTGATAA | 92912 |
| rs557927815 | in-del | -/C | 0.00244515 | 0.0348797 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873390 | ACTGCTGAAGAAAAA[-/C]TAGGTTGAATAAGCT | 92912 |
| rs557947306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848003 | CAGCAAGATACTAAA[C/T]TTTAAAAATGTTGGA | 92912 |
| rs558075589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863733 | CTGCAGCCTCCGCTT[C/T]GTGGGTTCAAGCGAT | 92912 |
| rs558095403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853897 | CCTTTTATAATACCT[C/T]GCCATGTAGGTCTCT | 92912 |
| rs558306730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865818 | TGTTTTTTTTTTTTT[C/T]AACCTAGAAAGGGTT | 92912 |
| rs558396955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873006 | GGCTGCAAGGTTGAA[A/G]TAGGTATCCTTATGC | 92912 |
| rs558452441 | snp | A/G | 0.000204009 | 0.0100977 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869041 | AAAAGAAGAGTTCAT[A/G]AATTTCTTCATTTTT | 92912 |
| rs558526774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861873 | CTATGTGGTTTAGAC[A/G]GTGGCAGGGACTGGT | 92912 |
| rs558546492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870868 | TTGAAGGGGTGGGTT[A/G]CCCCTCCACACCTGT | 92912 |
| rs558580914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878724 | TTTTCATAGTTCTGA[C/T]CATGGCAAACTTTTC | 92912 |
| rs558747273 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853468 | AGCAAGACTCTGTCT[C/T]GAGGAAAAAAAGAAA | 92912 |
| rs558774302 | snp | A/G | 5.83096e-05 | 0.0053992 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843765 | TTGGAAGCTGGACGA[A/G]CTGCACTGCCAGTTC | 92912 |
| rs558806066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876746 | ATTTCCTTGTTTGAC[A/G]AGTATTCTTACTCAA | 92912 |
| rs558822873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846729 | TTTCCTCTTTAGACA[A/G]TTCAAATATTTGAAT | 92912 |
| rs558842865 | snp | A/C | 1.64757e-05 | 0.00287012 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876209 | TGTCTGGGTCAGTGC[A/C]AGCTTCAGATAGACT | 92912 |
| rs558858048 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854583 | ATAAAAGCATGATTA[A/T]TGATTATAATCTTGT | 92912 |
| rs558907750 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884253 | TGTGACATAATCTAC[A/G]TTATGGTGGTTAAAA | 92912 |
| rs558944569 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855832 | TTTGCATTCTGTGTT[-/C]CTGGATGAGCAGATT | 92912 |
| rs558960912 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895290 | CCTGGGTTCAAGCGA[G/T]TCTCCTGCCTCAGCC | 92912 |
| rs558990641 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883093 | TACCTAGTCTATCAT[C/T]ATTGGAATGGTTCCT | 92912 |
| rs559021634 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892706 | CTACACAAAAAATAC[G/T]CCCCCCACCCTAAAA | 92912 |
| rs559030303 | in-del | -/GTTT | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854614 | AGGAATTAAAGACTA[-/GTTT]GTTTGTTTTTTTTCC | 92912 |
| rs559042018 | snp | G/T | 3.43826e-05 | 0.0041461 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854375 | TTAACATGTGTCTCT[G/T]TGTTAAACAGGAATC | 92912 |
| rs559068223 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882477 | TAAATCATACATAAT[A/G]AAGAGGTTTTGTAGT | 92912 |
| rs559098247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885054 | TAAGAGTTTACTTAC[C/T]TGACACCTGCAACCT | 92912 |
| rs559292460 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900795 | CATTTGTATAAAGTT[C/T]TGATTGCCAGTTGCT | 92912 |
| rs559356748 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892711 | CAAAAAATACGCCCC[A/C]CACCCTAAAAAAACA | 92912 |
| rs559435593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860567 | TAATTATCATTAGGA[C/T]TTTGTAGAGTAAAGC | 92912 |
| rs559468010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863315 | GAGTTCTGGTCTGCC[A/G]GTAACCCCATTCCTT | 92912 |
| rs559477667 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853402 | CTTGAACCTAGGAGG[A/C]GGAGGTTGCAGTGAG | 92912 |
| rs559490980 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887505 | TCATGTAGAAGAGTT[G/T]TAGGAAATAGTGCTG | 92912 |
| rs559504797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870978 | GACCCAGGAAACCAG[C/T]GTTCAGCATATGGAG | 92912 |
| rs559506876 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862436 | TTTTTTTTTTTTAAA[A/C]CTTTCCTCAGGTATC | 92912 |
| rs559514400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861254 | AGTTTGGTTGATTAT[A/G]TATTTCTAGGTTGAA | 92912 |
| rs559517766 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75901036 | TATGAATAAAGAACC[A/G]TTTAAAAATTTTGTT | 92912 |
| rs559518002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891985 | CTGTCTTTCCCTGCT[G/T]CCCATAACCTCCACT | 92912 |
| rs559545622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870357 | AGACATATAGACATG[C/T]GCCACTGTGCCTGGC | 92912 |
| rs559671564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847402 | AAAGACCAAAACAGA[C/G]TAGATGTTTTACTCT | 92912 |
| rs559732515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869172 | GGCTTTACCTCTAAC[G/T]AATGATATGCCTTTG | 92912 |
| rs559872307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850652 | ACTGGTCTCAATGGA[A/G]CTATGTAAGTTAATA | 92912 |
| rs559904927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874248 | TCTGTCCTGCTCTGA[C/G]CCAACCAAAAGTAAT | 92912 |
| rs559906514 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866141 | GGTATGATTTTCTCT[C/G]TAACTGTAAAGTGTG | 92912 |
| rs559941733 | snp | C/G | 1.66896e-05 | 0.00288869 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873424 | ATTTTTCGTCTCTTT[C/G]TAGGATATAGAAGAC | 92912 |
| rs560009944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864695 | GCCGTTTTCACTTCA[A/G]AAGTTTTCTTTATCT | 92912 |
| rs560035762 | in-del | -/AG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890044 | GTCAGTGTCATTGTC[-/AG]GGGAAAAACTCATGG | 92912 |
| rs560300373 | snp | A/G | 0.000117399 | 0.00766067 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896978 | CTTTTGATTTAAAAT[A/G]TGTAATTCTCTTTCA | 92912 |
| rs560320676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881813 | TATATTTTTAAGGAA[A/G]TCACTTTTTGGTGTT | 92912 |
| rs560439174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898586 | CCATGTTGTACAATA[C/G]CTCAAGATGGATTCT | 92912 |
| rs560444458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890173 | TAAGTTCTTAATTAC[G/T]GATATCATACAAATC | 92912 |
| rs560496894 | snp | G/T | 4.94907e-05 | 0.00497422 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876291 | GGATCTCTGGATCCC[G/T]GCTCTCTTTATGATT | 92912 |
| rs560595932 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883564 | ACCTTGGCCTCCCAA[A/C]GTGCTGGGATTACAG | 92912 |
| rs560674258 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844117 | CCGTCTCCTAGCCCC[A/G]AGGGGGGAGTCCGCG | 92912 |
| rs560695372 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844162 | TGTGGGGTCCATGGC[C/T]GCCCTCAGCCGGCCT | 92912 |
| rs560739008 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890931 | TAGGGCTGGAGCAGT[A/G]CCTACTCAATAGAAT | 92912 |
| rs560768742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866622 | TGTCCCTTAACTGTT[C/T]TCTTACTTACATCTC | 92912 |
| rs560800883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887469 | AGACCAGTTTGAGCT[A/G]TAACACAAGGAGGGT | 92912 |
| rs560881880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851408 | ATTTAGAAAATAGTG[A/G]TTCACCGAGATCTTC | 92912 |
| rs560998527 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886865 | AGAGTCCGTCTCAAA[-/T]TTTTTTTTTTTTTTA | 92912 |
| rs561039673 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849491 | GGTCTCAGTGGATTT[A/G]TGGAGAAAAATAGAT | 92912 |
| rs561078769 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852535 | TGAGGGGTTTCAGTC[A/C]AGAGTGAAGACATGT | 92912 |
| rs561141397 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884049 | TGGCTAATTACTCCT[A/G]GAGGTAATACTTGCA | 92912 |
| rs561158956 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876885 | GCATTGGTTGGGTGC[A/G/T]GTGGCTCACACTTAT | 92912 |
| rs561177959 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883622 | TTTTTTTTTTTTCTT[C/T]TAAATATAGTGTGCA | 92912 |
| rs561203554 | in-del | -/GTAAGCCTCGAAAATGGATAGGTGAAA | 0.00223941 | 0.033387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844526 | GCCCCTCCCTTGTGT[-/GTAAGCCTCGAAAATGGATAGGTGAAA]GGAGATACGCGCCAG | 92912 |
| rs561240100 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890268 | GCATGATAACATTAG[A/C]ATTTTTAAATTACCC | 92912 |
| rs561318301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876412 | GAAACTCAAATGCAA[C/T]CAAGTTCCAAAAGAT | 92912 |
| rs561323817 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884479 | TCATTTCTGTGTAGT[C/T]AGAATACATACTAAC | 92912 |
| rs561389899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877037 | TGGTGGCGCACGCCT[A/G]GTGATCCGAGCTACT | 92912 |
| rs561553762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872437 | TCTGCATAGATTTAT[A/G]TATGTGTAAGAACAG | 92912 |
| rs561580737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886489 | TTCCCATAAGCATGG[A/G]AAAAGGAAGACAGGT | 92912 |
| rs561640068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894123 | ATTTGAAATTAAAAC[C/T]GCAGAATATCTAGAG | 92912 |
| rs561654919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864995 | TTTGTTCACATTGCC[A/G]TACTATTAAAACTTT | 92912 |
| rs561657684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844722 | CGTGAAGCTATTCGT[C/T]GTGAAATTGATGTAG | 92912 |
| rs561675874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894855 | TTTCAGGGTATGTAT[A/G]GTTTTTACGTCCAGT | 92912 |
| rs561723523 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871881 | ATATTGTTTGAGAAA[C/G]ATAATGTTGAATTCT | 92912 |
| rs561859852 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886914 | GTGATTATAAAATTG[A/G]CCAGTATAGCTTTTC | 92912 |
| rs561898650 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890637 | AATGAAAAAGGTAAA[C/G]CAATAAAATGACATT | 92912 |
| rs561919236 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879350 | GTACTTAGGCGTACC[A/T]GGAGACACAGGAATG | 92912 |
| rs562048013 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899950 | TTTTATGATATTGCC[A/T]AAATGTGATAGGAAA | 92912 |
| rs562075269 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842593 | GGGTTGTGGTGGGGG[A/G]TGCCGGAGATGATAT | 92912 |
| rs562077406 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854281 | TTTTCCCCCCATACA[A/T]TTTGTTTAAATCCAT | 92912 |
| rs562110380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849776 | GAGTAATTAGATGCT[G/T]AGATAATTGTTCTGT | 92912 |
| rs562115503 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893088 | GAGATATTAGAATTA[C/T]ACTAGAAAGTGAGAG | 92912 |
| rs562134158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888637 | TTGACAAAATGAATG[C/T]AATTTAATACAGAAG | 92912 |
| rs562143624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881274 | TGGCCCCCTGTGTGC[C/T]CCTCCCTTGTCACTT | 92912 |
| rs562156624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896678 | ATCCAGATATAATCC[C/T]TTAACTTGATTCAGC | 92912 |
| rs562300238 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863026 | GCCTGAGGTAGATGT[A/G]TGTTTGCTTAGGTTC | 92912 |
| rs562372140 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880528 | GCTCTGTTGCCCAGG[C/G]TGGAGTGCAGTGGCC | 92912 |
| rs562416749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865964 | GTACACAGATAATGC[C/T]TCCTGTCTTGATGGA | 92912 |
| rs562444280 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865376 | TTCTTTTGCATTGCT[A/G]TATTTATTCCATTGT | 92912 |
| rs562719568 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845899 | AAGAAGTGAATGAGA[C/G]ACTTTCAGTACAAGG | 92912 |
| rs562819199 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897294 | CCCCAGCTGGAGTGC[A/T]GTGGCACTATCTCAG | 92912 |
| rs562861892 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856999 | GGCACAGTGGTTCAT[A/G]CCTGTAATCCCAGCA | 92912 |
| rs562881350 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875049 | TACTTAAAAAACAAA[A/G]TTTGTCATTTGAATT | 92912 |
| rs562898273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882823 | TTTGTTCTTCAGGGT[C/T]CCAACCTAAGGAGCC | 92912 |
| rs562901179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897521 | ACTGCACCACAAAAC[C/T]TTAACATTGTACTTC | 92912 |
| rs562905068 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843603 | GTGACGGCGGCTCCG[C/G]GCCCGGCTCCCCTTC | 92912 |
| rs562922906 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881084 | GACTGAAGTTGCTAA[A/T]GGCTACATTTTTACT | 92912 |
| rs562931367 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879709 | GAACATAAACAGATA[C/T]ACGATTTATCTATGG | 92912 |
| rs563033865 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889771 | AAATTTAAAATAACA[C/T]TGAAGGAGAAATGAA | 92912 |
| rs563076742 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850536 | TTCTTGGCTTAGCCC[A/T]CCTGACAGCTAATCA | 92912 |
| rs563097959 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842828 | ACCATCGTCTTGGGT[A/G]AATGGATGGTTTGAG | 92912 |
| rs563167920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878211 | AGAAAGTGAGAAAGA[A/G]GAAGGACAGAAAGAG | 92912 |
| rs563215530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849947 | TTAAAGAGAAATAGT[A/G]GGCAAACTTATCTTT | 92912 |
| rs563266504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879012 | GTGCTCTATTTTAGC[G/T]GTCATACTAGTTCAT | 92912 |
| rs563302945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885245 | CCTGCCTTAGCCTCC[C/T]GAGTAAGGACTACAG | 92912 |
| rs563316565 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849971 | TATCTTTTCAAGATA[C/G]ATATAAAGCTTAGTT | 92912 |
| rs563346984 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845617 | CATCCAGGATTAGAA[A/G]TGGTTCTCTACAGTG | 92912 |
| rs563395275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853050 | AGCTAATATACGATA[A/G]TAATGGCTTTTCCCC | 92912 |
| rs563455389 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901342 | TATCCTTAGTTCCCC[C/T]AGTGAAAATAATCTG | 92912 |
| rs563472081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846168 | GATTATTTTGAAGCA[G/T]ATTCCAGACAGATCA | 92912 |
| rs563485651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854207 | CAACAGACAGTGCTA[C/T]GCAAGGAGAATGGTT | 92912 |
| rs563518219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855550 | TCTTTATAGAAAAAT[A/C]ATCATCATTATTTTC | 92912 |
| rs563556350 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863459 | TTTGTTTTTCTTTTT[A/T]TTTTTTGACGGAGTC | 92912 |
| rs563571151 | in-del | -/CA | 0.288127 | 0.247076 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857756 | ATATTCTGTTGTAGG[-/CA]CAAAAAAAAAAAAAA | 92912 |
| rs563659489 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895045 | CAAAAAATTAGCTGG[A/G]CGTGGTGGCGGGCGC | 92912 |
| rs563714809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863904 | CTCGGCCTCCCAGAG[C/T]GCTGGGATTACAGGG | 92912 |
| rs563961221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871011 | TCCCGCCAGCCTCTG[A/G]GTTCCCTTAGTATTT | 92912 |
| rs563996153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846059 | TAACTTTTTATTATG[G/T]AAAATCATCAAATGT | 92912 |
| rs564019491 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884726 | GTGCAGTGGTGCTGT[C/T]ATGGCTCACTGCAAT | 92912 |
| rs564025112 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901389 | CCCATGGCCTCCTTG[C/G]ACACAATTGACAGAT | 92912 |
| rs564062433 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861838 | ACAGGTTTTCTGCTG[G/T]TCTCATTTGGCAGCT | 92912 |
| rs564098812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871111 | GTCAGCAGACAAACA[C/T]GTGAACAAAGGTCTT | 92912 |
| rs564106755 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842373 | TTGTGCTAGTGGTGG[C/G]GATTCCAGATAAGAG | 92912 |
| rs564145432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849685 | TAATGTTTATGGTAG[C/G]TTCACAGACAACTTC | 92912 |
| rs564168734 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861913 | GCTCAGCTGCAGTGG[-/A]ATGTCTGAGACGACT | 92912 |
| rs564209444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885405 | ACACGCATGAGCTAC[C/T]GCACCCCACCTAGTG | 92912 |
| rs564247337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893050 | AATGAGGTCTAAAAT[A/G]TGTCTTAGTGGAATC | 92912 |
| rs564269123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893985 | TCAAATACTGAAAAA[C/G]AGAAAAGGACAGTGT | 92912 |
| rs564321620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848301 | CTTGCATTTTTCTAG[C/T]CTTTACTATGATTAA | 92912 |
| rs564502650 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857629 | CCAAATTGACCCCTC[A/T]GCAGTATTTTGATAC | 92912 |
| rs564504313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880594 | GCAACCTCTGCCTCC[C/T]GGGTTTAAGCAGTTC | 92912 |
| rs564519416 | snp | C/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842186 | AAACCAAGCTCGAAG[C/T]CCTTCTAAGCTGGGA | 92912 |
| rs564541904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887537 | TGTAATATCTTGTAC[G/T]TAAACAGGTCTGTGG | 92912 |
| rs564687587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891155 | TGTTACAAAAGTGAT[C/G]TATAGAAAATATGGA | 92912 |
| rs564719994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872327 | AGCCTGCTTGGGGAA[A/G]AAAAAAAAGCCGAGA | 92912 |
| rs564720731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856852 | GGAGGCTGAGGCAGG[A/T]GAAGTGCTTCAACCT | 92912 |
| rs564855099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899305 | AATATATATATATAT[A/T]TTTTACGGTAGATTT | 92912 |
| rs564858189 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899866 | AATACAGGTTTAATC[G/T]ATGTTCAATATTGGT | 92912 |
| rs564883160 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899577 | GTTAGTTAATAGATA[C/T]TTTAGTGGATAATCT | 92912 |
| rs565070926 | snp | A/T | 0.089084 | 0.191327 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860454 | TTACCTATTTATTTT[A/T]TTTTTACTATAATAC | 92912 |
| rs565112360 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846281 | CTCGCTGTGTCGTCC[C/T]AGCTGGAGTGCAGTG | 92912 |
| rs565164841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877194 | AAAAAGGGTTATGAC[C/T]GATTCAATTCTAGCA | 92912 |
| rs565184411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861465 | TTTTTTCACTCATTG[C/T]GCTCAGTACACCAAA | 92912 |
| rs565239590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883683 | TTTCTGATTCAGTAG[A/G]TCTGTGGTGGGGCCT | 92912 |
| rs565260431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854308 | CCATGGTCATCTTGC[C/T]GTTTAGTGGTGTGGT | 92912 |
| rs565331565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868699 | TCTGTTTTGCTTTAT[A/G]TTTGATTGCTTTTCT | 92912 |
| rs565340655 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849271 | TTATTGAACAGCAAA[A/C]TATGAAAGTAATGTG | 92912 |
| rs565477779 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850458 | CCCCAAGGTGGCCAT[A/C]CTTGTCCCTGTGATT | 92912 |
| rs565538426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877409 | TAGAAACCTAATAAA[A/G]TACAAACATTTGAAT | 92912 |
| rs565569806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891848 | TGGTTTAAAGGCAAG[A/G]TGGTGCTTTATGAAG | 92912 |
| rs565645893 | snp | A/T | 0.000924537 | 0.0214805 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883474 | TTCAGTTAAAAAAAA[A/T]TTTTTTTTATAGGGA | 92912 |
| rs565692730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893105 | CTAGAAAGTGAGAGA[A/G]ATAGAAGTTGTAAAG | 92912 |
| rs565703308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876620 | TTACAGAGAATAATT[A/G]CCAAGTTGATTTTTA | 92912 |
| rs565740246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883748 | GTTGATGCTGTTGTT[C/G]TGGGGCCCACACCTA | 92912 |
| rs565815569 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900405 | CTTTTACATTGAAAG[A/C]TTAATAGAAACTCTA | 92912 |
| rs565834291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890573 | AAATTCTTTAATAGC[G/T]CCTACTCTTAAATTT | 92912 |
| rs565946329 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846446 | TTTCACCATGTTGGC[C/T]AGGCTGGTCTTGAAC | 92912 |
| rs565960245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898220 | TATCTTTGTTTTTAT[A/T]TCTTAACCATTACAA | 92912 |
| rs565989689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860909 | GTAAAACCCTAAGAA[A/G]GCATGGAGGAGTACA | 92912 |
| rs566033600 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885120 | CTAATAGTAGTGGGG[-/T]TTTTTTTTTATTTGT | 92912 |
| rs566039238 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887279 | AAGCAGCAAAGAGTT[A/G]CTGTGGCAATAGTGA | 92912 |
| rs566084326 | snp | A/C | 0.000149729 | 0.00865114 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75897022 | CTAGCAAGAGCCCAA[A/C]AATCCTATAATTCCA | 92912 |
| rs566207880 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883130 | AGTTCTAGTGAAGTG[A/G]AACCCCTTCATGTGT | 92912 |
| rs566245293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896227 | TGTGTGGAGGAAGGG[G/T]GATGAACGGGAGGAA | 92912 |
| rs566456558 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843035 | TAGCGGGTGCCGCGC[C/T]GAGCGCCAAGCTGAG | 92912 |
| rs566468114 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896043 | CAGGTATGTTCTATA[-/C]TGATAAGGAACATTC | 92912 |
| rs566479299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849959 | AGTAGGCAAACTTAT[A/C]TTTTCAAGATAGATA | 92912 |
| rs566480017 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895030 | TCTCTACTAAAAATA[C/T]AAAAAATTAGCTGGG | 92912 |
| rs566482287 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842218 | CACTGTGCAACTACA[C/T]AGGTTGGACGCATAT | 92912 |
| rs566508805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887914 | AGGAATTATTTGCTG[A/T]CTTGGGAAGAAGTAA | 92912 |
| rs566515126 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858569 | TTCTTCCTCCCATCC[C/T]TCAAATGCTTTTTTG | 92912 |
| rs566542471 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870029 | TTTTTAATCTAAAAT[A/G]TGCTTTTAGAATGCT | 92912 |
| rs566680018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857337 | AGTTATTTTTCAGTA[C/T]CTAAAATATTACATA | 92912 |
| rs566721202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864383 | ATGGTAGGGGTGCTG[C/T]TGGCATTTCTTAGGT | 92912 |
| rs566775665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859362 | TACTCAGGGAATTAG[A/G]TAGGATATCCAAGGT | 92912 |
| rs566879831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889395 | AAATATTGTCACTGT[A/G]ACAATTATTAATGTT | 92912 |
| rs567004080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897115 | AGTTTTAGATAATGT[A/G]TTAATACTTACCATT | 92912 |
| rs567004824 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879745 | AAATTCCATGGAGCA[-/G]GGGGGTAAAACTAGG | 92912 |
| rs567026942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881474 | CCATGGCTCCTGATA[A/C]CACAAAGAAGGGCCT | 92912 |
| rs567143807 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858720 | CCGTGCCAGAGGCCA[C/G]AGTGTCTAGGTCTGT | 92912 |
| rs567183422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857993 | GGCTCTGTGATAATT[G/T]AGTATAAAAGACAAG | 92912 |
| rs567209078 | in-del | -/TA | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899999 | AAACTTTTTAATGAC[-/TA]TGTGAAGATATGAAT | 92912 |
| rs567233506 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875243 | GCTTCATATTTTAGA[A/G]ATAGGAAAAACTTCT | 92912 |
| rs567264121 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843673 | GAGGGGAAGATGTCC[A/G]TGTCAGGGCTCAAGG | 92912 |
| rs567274910 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899785 | GAAGTTGAGGCTTTA[A/G]GGTAACTTTCCTATA | 92912 |
| rs567275915 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844951 | CAGACTATCTGGGCA[A/G]AAGGTGTGTTAATTT | 92912 |
| rs567297107 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843198 | GCCCGGGCGCCAGCT[G/T]GCCCCGAGCCTCCAG | 92912 |
| rs567373192 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897857 | CTTTACTTTGCTAGA[A/G]ATGTGTCAGTTTGTG | 92912 |
| rs567381098 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870213 | GCTGGGACTACAGGC[A/G]TGTGCCCCATGCCAA | 92912 |
| rs567403847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850786 | TACACTCTTGAAAAT[A/G]TATTCAGCACTTAAG | 92912 |
| rs567487229 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851516 | GGAAAACGGTGGTGG[A/G]TACAAGTTTTCAAAA | 92912 |
| rs567524675 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854069 | CTTTGTTAGAAGTGA[C/G]TCACTAGGTCCAGGG | 92912 |
| rs567586807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883115 | ATGGTTCCTTTATAT[A/C]GTTCTAGTGAAGTGG | 92912 |
| rs567609508 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846450 | ACCATGTTGGCCAGG[C/T]TGGTCTTGAACTCCA | 92912 |
| rs567685798 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852048 | TTAGCTAATTTTTTT[A/T]TTTTTTTTTGTAGAG | 92912 |
| rs567720998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860117 | CTATTGAATTGTTTT[A/G]TTTGTTCTGTTTTAG | 92912 |
| rs567802646 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890218 | TCTAAGAACCATTAG[-/A]AAAAATTGACTAGAA | 92912 |
| rs567812088 | in-del | -/TTAAGTTGGTATCTTGTGTCA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882654 | TTATAATAACTGTTG[-/TTAAGTTGGTATCTTGTGTCA]TTAAGTTGGTATCTT | 92912 |
| rs567830896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75874996 | ATTTATAATTTTTAG[A/T]AGAGCAAAGAAATTT | 92912 |
| rs567838417 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889236 | TTTTTGGAGAGTTTT[C/T]CTTTTAGATTTTCTT | 92912 |
| rs567840347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867680 | ATTTTAAAATGAGGG[A/G]TAGTAACTGGGCTGA | 92912 |
| rs567891120 | snp | A/C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880748 | TCATGGTACACTTCC[A/C/G]TTGGCCTTCCAAAGT | 92912 |
| rs567980448 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866195 | TTTTTTTTTTTGAAA[C/G]AGGGTCTTGCTCTCT | 92912 |
| rs568071946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855926 | TGTGTAGTGGCTCAT[C/G]CCTGTAATTCCAGAA | 92912 |
| rs568091307 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861099 | GAACCAGTAATAATA[C/T]TAGTACCTATGTTTT | 92912 |
| rs568110176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865641 | TTATTTTTAGTGCAT[C/T]AATATGGTCAGAGAA | 92912 |
| rs568255624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871222 | AGTATTGCTGCCCGC[A/G]TGTCCCACCTCCAGC | 92912 |
| rs568313447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878479 | ACCTGTAGTCCCAGC[C/T]ACTGGGGGTGGTGGG | 92912 |
| rs568408180 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860090 | ATTTAGAAGTTAGTT[G/T]CATTTTTGTTCCTAT | 92912 |
| rs568439288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873676 | CCCTCTTCCTCCATT[G/T]CTGCCTTAGTGGTGG | 92912 |
| rs568547832 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880063 | GTATATCTCTATATT[A/T]TATGTACTTTTCTGA | 92912 |
| rs568579240 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857028 | CACTTTGGGAGGCTG[A/G]GGTGGGAGGATTGCT | 92912 |
| rs568581643 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891299 | ACTTATTTGTAAACA[G/T]ATGTTTACAGTTGTA | 92912 |
| rs568625778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896031 | CAGTGTTTAAAACAG[G/T]TATGTTCTATACTGA | 92912 |
| rs568778330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879895 | CAAAGAGGTGATTAC[A/G]TACAGGTTAGGGTAA | 92912 |
| rs568789180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895240 | CCAGGCTGGAGTGCA[A/G]TGGTACGATCTCGGG | 92912 |
| rs568845645 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891902 | GGTAGTTGAGTTAAA[C/T]AGTGAAATCCTGGAG | 92912 |
| rs568880326 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894629 | GAAATTATTAAAGAT[A/G]TACAAGCAGAAATCA | 92912 |
| rs568884996 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857803 | ATAAGAGCATGTGCA[C/G]ATTTCTAAGATATAT | 92912 |
| rs568904891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858678 | ACTACCCTGCTGCCT[C/T]TCTCCCCAGCACTCC | 92912 |
| rs568923903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857008 | GTTCATGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 92912 |
| rs568942925 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869385 | CATTTTAGGGACTAC[C/T]CGCCAGAAGTAGTGA | 92912 |
| rs568987391 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871976 | GAAGGTATAGGAGGA[A/C]ATACAGGCTAAAGGC | 92912 |
| rs569005095 | in-del | -/AAAAC | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894407 | CCAATCTCTGTAAAA[-/AAAAC]AAAACAAAACAAAAC | 92912 |
| rs569020108 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873359 | AAGAATAATTTAATG[A/T]TATTTTGGCATAAGA | 92912 |
| rs569064341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863675 | CTGAGTTGGAGTCTC[A/G]CCTGTCGCCCAGGAT | 92912 |
| rs569081990 | in-del | -/TG | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900081 | AAAGCAGTGTAAAAC[-/TG]TATCAATTAAGGCTT | 92912 |
| rs569101102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871303 | TATACCGAGACATTC[C/T]ATTGCCCAGGGACGG | 92912 |
| rs569180549 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866917 | ATTAGTAATGCTTCA[A/G]ATCAATTGTGCTTAC | 92912 |
| rs569301587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861817 | GGCTTAACTGGGGCT[A/G]GTTGGACAGGTTTTC | 92912 |
| rs569335095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872883 | CTTTTTTGTATTGTT[C/T]TTCATTTTAAAGTTT | 92912 |
| rs569337546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873761 | GCAGTGGCACAATCA[G/T]AGTTCAGTGTAGTAG | 92912 |
| rs569375140 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881414 | CAGGGAGGGGACGAT[C/T]TGGGAGGTAAATGGC | 92912 |
| rs569446915 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873220 | TAAATCTGCTTTACC[C/T]AGAGTCTAGATTTTA | 92912 |
| rs569488309 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842166 | AATGGCGACACCAGA[A/C]TATTAAACCAAGCTC | 92912 |
| rs569548762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887775 | CTGTTGTCTTAGAGT[C/G]AAGTGAGGAGAACCT | 92912 |
| rs569702476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877517 | TGGAATTTGTTAAAG[C/T]ATATCCATAAAATAA | 92912 |
| rs569772045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884257 | ACATAATCTACATTA[C/T]GGTGGTTAAAATCTA | 92912 |
| rs569775928 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845126 | TAAGGTGACAGCTCC[G/T]GTGGTATCATCAGGA | 92912 |
| rs569930580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854563 | ATGTTAAGAGATAAT[A/G]TGATATAAAAGCATG | 92912 |
| rs569967005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853773 | TGATCATCCTAAGGC[A/G]GGATAGGGAGAGAAT | 92912 |
| rs570036352 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881093 | TGCTAATGGCTACAT[A/T]TTTACTAATTCATAT | 92912 |
| rs570209342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846487 | GCTCCCAAAGTGCTG[G/T]GATTACAGGAGTGAG | 92912 |
| rs570216309 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847661 | CAAAGCAGCTTGTTT[C/T]AAGCAGCCTTATTGG | 92912 |
| rs570219551 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856910 | TGTGCCACCGTACTC[C/T]AGCCTGGGCGACAGA | 92912 |
| rs570418093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854614 | AGGAATTAAAGACTA[A/G]TTTGTTTGTTTTTTT | 92912 |
| rs570454437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862948 | CTATCTTATCTCCTG[A/G]TGCAATCATAAATGA | 92912 |
| rs570526579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870503 | TAAACCTTTTTTGTG[C/T]GCCCAGTTTACCATG | 92912 |
| rs570584552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879421 | CCAAGTGTTCATTCC[A/G]ATAAAATGGAGAATT | 92912 |
| rs570657455 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863649 | CACCTGGCCAGTCTT[C/T]TTTTTTTTTTCTGAG | 92912 |
| rs570696323 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877588 | GTATACTAACTTGGA[A/G]AGATGTCCCTGAAAG | 92912 |
| rs570699789 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884319 | ATGGTTGAGATAGTA[A/G]TAGTTGCATTTAGGG | 92912 |
| rs570831373 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886833 | TGGAGGTTGCAGTCC[A/C]GCCTGGGCAATAGGG | 92912 |
| rs570845784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895118 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 92912 |
| rs570934335 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886044 | AAGTCATAGTTCTTA[C/G/T]GTTTTTCATAGTTTA | 92912 |
| rs570953902 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851798 | CTCATGTATACTTCC[C/T]GTTTCATCACTTGAA | 92912 |
| rs570977083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894366 | TGAGCTCAGGAGTTC[A/G]AGACCACCTTGGGCA | 92912 |
| rs570985995 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882592 | TATACCTTTCATTAT[A/G]TCTGTTAAATATAGA | 92912 |
| rs571086389 | snp | C/G | 0.000253059 | 0.0112457 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843766 | TGGAAGCTGGACGAG[C/G]TGCACTGCCAGTTCC | 92912 |
| rs571259048 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900234 | AGTCATCTTACGTTT[C/G]CATTTTATTAACGGG | 92912 |
| rs571272452 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869670 | CTTAATCCCATTAAG[A/G]AGGAAGGAGCCCTCT | 92912 |
| rs571608646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875826 | CAGCACTTTGGGAGG[C/T]CGAGGCAGGCAGACC | 92912 |
| rs571686339 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845077 | GAAGTCGTCCTCGCT[C/G]TCAGAACTCAGTCTT | 92912 |
| rs571741432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867840 | AGTTTTAGGCTAGGT[A/T]TATAGTCTTTAGATA | 92912 |
| rs571801202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860815 | TCATCTGCTCTCCTA[C/G]AGTAGATCCATTGTT | 92912 |
| rs571817227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875226 | CCGTGTGAAATAGGT[A/G]TGCTTCATATTTTAG | 92912 |
| rs571895320 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851345 | TGGTCTTTCTTGAAC[-/T]TTTGGATCTTTTACC | 92912 |
| rs571979066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859677 | ATCAGTTGTAGTGAT[G/T]ATACCCCAAGCCATA | 92912 |
| rs572001302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860257 | AAATGCTCTTGCTTC[G/T]TTCATAGTTTGTCTT | 92912 |
| rs572187829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891641 | CAGAACAAGGATTGG[A/T]ACTAGACAGTCTGGC | 92912 |
| rs572220923 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878928 | AAGGAGCTGGAACCT[A/G]TGGTGACCTCTATTT | 92912 |
| rs572229857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881831 | ACTTTTTGGTGTTTC[A/G]GGCAGCATCTGAATT | 92912 |
| rs572288303 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880911 | AAAGCTTCTTACGTA[A/G]CTTTTTTATGTGTGT | 92912 |
| rs572323023 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885744 | TTGATCACAAATATA[C/T]TATCACAGTGAGTGG | 92912 |
| rs572347573 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899628 | AGTTACAGCCTTTGC[A/C]TTTTGCTCATTTTAG | 92912 |
| rs572394391 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884443 | ATATATGTGTTTTGG[A/G]GGCTAAAATCCTGTT | 92912 |
| rs572449045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876889 | TGGTTGGGTGCGGTG[A/G]CTCACACTTATAATC | 92912 |
| rs572466976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883586 | GGATTACAGGCATGA[A/G]GCCACTGTGCCTGGC | 92912 |
| rs572483663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883986 | GCCTGTGATCCTAAT[A/T]GGTACTTTTAGGGAT | 92912 |
| rs572530101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845146 | TATCATCAGGAAAGC[C/T]AAAGCAACTAATTTT | 92912 |
| rs572565674 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849304 | CCATAACTGGCCTTC[A/G]GAAGAATTACAACTG | 92912 |
| rs572662263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852366 | CAACATGTTAGTATT[C/G]TTGTAAAAATAGTTT | 92912 |
| rs572702967 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850243 | CAAAACTAGGAGATA[C/T]GATTCTACCACTCAG | 92912 |
| rs572742249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894813 | GCAGTAGGGTTGGAA[A/G]GTGACTGCTTCACAG | 92912 |
| rs572787571 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875955 | CCTGTAGTCTCAGCT[A/C]CTTGGGAGGCTGAGG | 92912 |
| rs572796618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880362 | AGGTGATCTGCCTGC[C/G]TCGGCCTCCCAAAGT | 92912 |
| rs572885667 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBE2Q2 | GRCh38.p7 | 15:75843476 | CAAAGGAAGCGCCAC[C/T]CAGGCCGCCACACGC | 92912 |
| rs572915182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886457 | CTTGTTTATAAAATT[A/G]TGATGTTTACTCAGT | 92912 |
| rs573012346 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856312 | AATTTCAGTACAAAT[C/G]CCAGCAGATTTATTT | 92912 |
| rs573043041 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888551 | GTTTTTTTCCTTAGT[A/T]TTCTTGAACTGTCTC | 92912 |
| rs573102345 | in-del | -/GT | 0.00531042 | 0.0512544 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866755 | CTGGCCCTTCTACAA[-/GT]GGTTTTTTGGGGGTG | 92912 |
| rs573207793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850333 | TGCTTATGTGTGTTC[C/T]CTCTCCCTTAAAAAA | 92912 |
| rs573308891 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895786 | ACAGATGGCTGGTGG[A/G]CAGACACATTTGTGC | 92912 |
| rs573351118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858311 | ATTCAAAATGATGAC[A/G]TTTAAATTTGCGTTT | 92912 |
| rs573351886 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863647 | ATCACCTGGCCAGTC[-/T]TTTTTTTTTTTTCTG | 92912 |
| rs573380783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896543 | ATTCTTTAGATTTCT[A/G]ACTTAAAATGTCATT | 92912 |
| rs573418959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888118 | TTATATATGATAAAA[C/T]GCTTCGAAGTGTACA | 92912 |
| rs573427706 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864919 | TACATTTTCTTTGGG[C/T]GCTGTTTGAGTTTAT | 92912 |
| rs573495272 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892706 | TACACAAAAAATACG[-/C]CCCCCCACCCTAAAA | 92912 |
| rs573512858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865874 | CCTTGAATACTTGCT[A/G]TCTGTTATTTGTTCA | 92912 |
| rs573546418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864831 | CTTAATTATTTCCCC[A/T]TTTTATTTTGCTTTT | 92912 |
| rs573550669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873106 | ACTAGGAACACTTAA[A/G]GTTCTTGACACCTGC | 92912 |
| rs573585164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872338 | GGAAAAAAAAAAAGC[C/T]GAGATGCGTATAAAC | 92912 |
| rs573598177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873224 | TCTGCTTTACCCAGA[A/G]TCTAGATTTTAAATA | 92912 |
| rs573607590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895472 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCGGCTT | 92912 |
| rs573632906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881131 | CGAATAAAGCACCCA[A/G]GCCAAAAACAAAAAA | 92912 |
| rs573782577 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898888 | TGTGTTGAAAACTCA[C/G]GTACAATTTATTCAT | 92912 |
| rs573801065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849400 | ATAGCTGTGTCCTAC[A/C]TTTGGAAAGATACAA | 92912 |
| rs573813744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848849 | TTTGTAACAGTGTTA[C/T]GTGATCTCTTCTAGA | 92912 |
| rs573992861 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843873 | GGCCGCGGCCCCGCG[A/G]GGCAGGGCGAGGACG | 92912 |
| rs574000774 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843575 | AGGCCGGCCCCGCGG[A/G]GCGGTCGCGGCCGTG | 92912 |
| rs574022268 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848649 | GTGAATAGTATATCC[C/T]TTAGTATCTTGATTT | 92912 |
| rs574022967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897517 | AGCCACTGCACCACA[A/C]AACCTTAACATTGTA | 92912 |
| rs574031357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851146 | TCTTCTTTTTTTTTT[C/T]TTTGAGATGGGGGTT | 92912 |
| rs574092858 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880001 | GAATATATTTCTGGG[C/T]CAGGTTGATGGTTAC | 92912 |
| rs574129893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889646 | GTGGACTTGGTGTCC[A/G]CACAGACCTAATCAG | 92912 |
| rs574142659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850477 | GTCCCTGTGATTCCA[G/T]ATCTCCCAGAACTAG | 92912 |
| rs574265788 | in-del | -/AT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878099 | TTTCCTTCTAACTTG[-/AT]ACCTTTATACTATGG | 92912 |
| rs574278278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874109 | ATCCCTGTATTTGCC[C/G]CTTCCCGGCCTGTTT | 92912 |
| rs574295852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870665 | GAAAGAAGATATTCT[A/T]GGCTCCTAAAATAAT | 92912 |
| rs574373766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846789 | CTTACCAAGAAACAT[C/T]CTTATGCAGTTTCTC | 92912 |
| rs574411023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854672 | CTCTCTTTTATTTCC[C/T]ACATGTATAACCTTA | 92912 |
| rs574434058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846089 | TACAAAAGTTGAACA[A/G]TGTAATGTAGCCAGC | 92912 |
| rs574488835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857444 | GGAGAAAACAACTCA[C/T]CTCCCACTCTTGCAG | 92912 |
| rs574521203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856681 | GGGCATGATGGCTCA[C/T]GCCTGTAATCCCAGA | 92912 |
| rs574547046 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883697 | GGTCTGTGGTGGGGC[C/G]TGAGTATTTACATTT | 92912 |
| rs574558143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863810 | ACCACGCTCGGCTAA[C/T]TTTTTGTATTTTTTA | 92912 |
| rs574573521 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854153 | TTTAGAGGCTGCCTA[C/G]CAGTGTTGAAGAAAA | 92912 |
| rs574651047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877743 | GTAAGCAGTTTTTCA[A/G]CTCATTAAAGAATCT | 92912 |
| rs574679795 | in-del | -/AG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881635 | TAGCAGGTATGACTC[-/AG]AAAGATTTGCAGGAA | 92912 |
| rs574718502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862009 | ATCCTCTCGGGCCTC[C/T]TCATGTGGCTTCTCT | 92912 |
| rs574755936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861292 | TTACCTTAGAATTTC[A/G]AAGTCTATGCTGTTG | 92912 |
| rs574756023 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869958 | TTGATTTAAAAAAAA[A/T]TTTTTTTTTCTGTTT | 92912 |
| rs574841135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871528 | TCCCTGCGGCCTTCC[A/G]CAGTGTTTGTGTCCC | 92912 |
| rs574900787 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866773 | GTTTTTTGGGGGTGG[A/T]GGGGATCTTATTTTT | 92912 |
| rs575058038 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878877 | TTTACTAGATTAGAT[A/T]TAGAGTATTATGGTC | 92912 |
| rs575122535 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847507 | AGTGCTCTTTTTCAA[-/G]CCTCGAGTCCTTTTT | 92912 |
| rs575142251 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864473 | TGGCCCAATACGTCA[A/G]TATTGCTGAGGTTGA | 92912 |
| rs575166449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886145 | TTTTTTTTGAGACAG[A/G]GTCTCACTCTGTTGC | 92912 |
| rs575192447 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBE2Q2 | GRCh38.p7 | 15:75843364 | AGGGGGACGGGGGCG[A/G]GGTGGGGGCAGCCCT | 92912 |
| rs575255371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894575 | AGTGACAGAGCAAGA[C/T]TCCATCTCTTAAAAG | 92912 |
| rs575262244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886333 | CCATGTTGGCCAGGC[C/T]GGTCTCAAACTCCTG | 92912 |
| rs575264004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848979 | CTCAGTTTGCTTACA[A/G]TGATGTTCTCAGTAG | 92912 |
| rs575274981 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893756 | ATTAAGGTTAGAAGG[C/G]AATAATGAAGAGATT | 92912 |
| rs575361667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847921 | CTAGGCTGCTTTTAG[C/T]GGGACTTTGTTTTTG | 92912 |
| rs575411544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863188 | GAGCCTCTTCAGGGC[A/G]CTGTGAGATAAATTT | 92912 |
| rs575498340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856199 | CTCAAAAAAAAATGT[A/G]TATATATATGTGTGT | 92912 |
| rs575510564 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881236 | TTAAGAAATAGAACC[-/T]TTTTTTTTTTTATCC | 92912 |
| rs575587619 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859666 | TCTGCTAGGTATCAG[-/T]TTGTAGTGATTATAC | 92912 |
| rs575621390 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853240 | ACTTTGGGAGGCTGA[A/G]GTGGGCTGATCACGA | 92912 |
| rs575656530 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852492 | ATGATTTCAGTTAAT[G/T]GTTTTTGTAATTTTC | 92912 |
| rs575662466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861074 | TCAATTTTCCATTGG[C/T]AAAATGGGGGAACCA | 92912 |
| rs575719020 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870586 | TAATAAACAAGGGGC[C/T]GCAACATGGAGGGAA | 92912 |
| rs575788332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872216 | CGGGGCAACGGAGCG[A/G]GACTCCATCTCAAAA | 92912 |
| rs575871864 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871714 | CAAAGATTAACAGAA[G/T]CTCAAGGCAGAAGAA | 92912 |
| rs575926031 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868119 | CATCAGAGTGTCTAA[-/T]AACAGATGCTTAGAT | 92912 |
| rs576021574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879614 | GGAGGCAATATCACC[C/T]GCAGTGTAGTGAAAA | 92912 |
| rs576067148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878648 | GGGGAGGTGGGATTC[A/G]AATTAGACCTGTATA | 92912 |
| rs576092641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868101 | TTTTCTTGAGAATTA[C/T]TCCATCAGAGTGTCT | 92912 |
| rs576106298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877784 | TGGCTGTAATTATCT[A/G]TTAAGGGCATAAGAT | 92912 |
| rs576143110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884492 | GTCAGAATACATACT[A/G]ACTTTGGTGTTGATA | 92912 |
| rs576234221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875341 | TTTAAAATCTTTAAT[G/T]TCACGTGACCAAAAA | 92912 |
| rs576339481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891710 | TGGGACATAAGGATG[C/T]TGTTCAGGCTGGTTT | 92912 |
| rs576395638 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851619 | CTGTTGTTTTCCTTG[A/C]AATGACAGAATCTCA | 92912 |
| rs576412794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846033 | GGCAGCTGCTCAGTA[C/G]AAATGTCTGCTAACT | 92912 |
| rs576420218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882771 | AAAAATGAGATGATT[A/G]AAGCTGGCTGTCATT | 92912 |
| rs576576615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845930 | AGGATTTAGTGAGGA[C/G]TAGTGTAATGGCACC | 92912 |
| rs576606365 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875081 | ATGATGACTGTACTT[-/TA]TGTCTTGTGATCGAT | 92912 |
| rs576643981 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878487 | TCCCAGCTACTGGGG[A/G]TGGTGGGAGGCTGAG | 92912 |
| rs576649396 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899841 | GCAATATATTGTTCC[A/G]TTTACAGCCAATACA | 92912 |
| rs576673781 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900699 | TGTCATTTCTACATT[A/G]TGTGTGTTTAATTTC | 92912 |
| rs576823453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861897 | GACTGGTCATCTGGA[C/T]GCTCAGCTGCAGTGG | 92912 |
| rs576901164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870907 | CTCGTTAGGTGGAAC[A/G]AGAGACTTGGAAAAG | 92912 |
| rs576935716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878797 | CCTAAACTTTTTTTG[A/G]GTTCTTGAGAAAATT | 92912 |
| rs576965130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861108 | ATAATATTAGTACCT[A/G]TGTTTTGGGGGAACT | 92912 |
| rs577017542 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899884 | GTTCAATATTGGTTT[A/G]GGAAATTTAAGGCCT | 92912 |
| rs577035548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868260 | TAAACAGTGTCCTGG[C/T]GAGGGCTTACCTTTT | 92912 |
| rs577070838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877921 | AGTAATAGTTATATG[A/G]TGAAATGAAGAGTAG | 92912 |
| rs577074295 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883932 | TAAATTGTGATTGAG[G/T]GTTTAGAGAATGTTA | 92912 |
| rs577168188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863746 | TTCGTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 92912 |
| rs577222050 | snp | A/T | 1.64746e-05 | 0.00287002 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876226 | GCTTCAGATAGACTT[A/T]TGAAAGAGCTCAGGG | 92912 |
| rs577256380 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875126 | ATAGTCAAAACAACT[A/G]TAAGTTACTGAACAC | 92912 |
| rs577296303 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885501 | TTTACCAAAGGACTT[C/T]TTGGAGGCTTAATGC | 92912 |
| rs577315528 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868868 | TGACAGATGTTTGAG[A/G]GTTTGTGGCACCAGT | 92912 |
| rs577443790 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892708 | ACACAAAAAATACGC[C/T]CCCCACCCTAAAAAA | 92912 |
| rs577463711 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881247 | AACCTTTTTTTTTTT[A/T]ATCCGTCCCTGTGGC | 92912 |
| rs577466909 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889402 | GTCACTGTAACAATT[A/G]TTAATGTTAGTGGTC | 92912 |
| rs577602021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866526 | TCTAAAGTCTTTCTT[C/T]AGCTCAGCAGCACTT | 92912 |
| rs577694537 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899137 | AAAAATTAGTGGGGC[A/T]TAGTGGCGCATGCCT | 92912 |
| rs577785491 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | UBE2Q2 | GRCh38.p7 | 15:75843376 | GCGGGGTGGGGGCAG[C/T]CCTTTCCCAGGCGGT | 92912 |
| rs577804633 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862189 | ACTCACTGTGGGATG[A/G]GCCCATCCAAGGACG | 92912 |
| rs577815103 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842330 | CAGACCTTTATTCAT[G/T]TTTTGAGCACCTACA | 92912 |
| rs577883508 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897246 | ATTTTATTTTATTTT[A/T]TTTGTTTTTTGAGAC | 92912 |
| rs577915329 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898787 | GCTTACTTTCAAGTA[C/T]AGAACTGAAGTGGAA | 92912 |
| rs578017420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889842 | AGTAATGATTTTCTA[A/G]TGGGAGATTTGGTAC | 92912 |
| rs578034599 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881879 | GGTAGTACTTTAAGA[A/G]GGGTCTATTTAGATA | 92912 |
| rs578058927 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890753 | ACATTGGTTTGTTGT[G/T]TTTTTTTGTGAGATT | 92912 |
| rs578109515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844623 | AAGACACTTTTAAAA[A/G]CTCACTCATTAAGCG | 92912 |
| rs578189596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858836 | GGTTTCCGTTTAAGC[A/G]TGAAGATTTTTGTTG | 92912 |
| rs578198198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867013 | TTTATAGATGAGATA[C/T]ACCCTTGATCAGTAT | 92912 |
| rs578211505 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843966 | CGGGCGGGGCAGGCC[C/T]GCCCCTTTCCCCCGC | 92912 |
| rs578211561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852280 | CTAGTAGTTTGGTGT[C/T]ACCGCCTTTATTTGT | 92912 |
| rs745323345 | snp | C/T | | | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901376 | CTTCCTTAGCATACC[C/T]ATGGCCTCCTTGCAC | 92912 |
| rs745385479 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854678 | TTTATTTCCCACATG[C/T]ATAACCTTAATTTAG | 92912 |
| rs745473993 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855889 | CCATGTCTTCATATT[C/T]GTAAATGTAATTTCT | 92912 |
| rs745518803 | snp | C/G | 3.68922e-05 | 0.00429473 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843682 | ATGTCCGTGTCAGGG[C/G]TCAAGGCCGAGCTGA | 92912 |
| rs745527951 | snp | A/C/G | 3.30963e-05 | 0.00406783 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873473 | AAGGAAGAAGAGCCT[A/C/G]TTAGTGGGAAAAAGT | 92912 |
| rs745595268 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875364 | ACCAAAAAATAGTTC[C/T]GTTTGTATTTAGTCT | 92912 |
| rs745595286 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889978 | ACAGAATGGGTAAAA[A/C]CAATTTGAACCATAA | 92912 |
| rs745615700 | snp | C/T | 0.000100659 | 0.00709363 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844444 | GGCCTGGCTGCGCGC[C/T]GCTGTGTTCTGGAAA | 92912 |
| rs745632347 | in-del | -/AG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871710 | AGGTCAAAGATTAAC[-/AG]AATCTCAAGGCAGAA | 92912 |
| rs745679440 | snp | G/T | | | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883401 | TCCATTTGTTCGAGT[G/T]GTGTTACCTGTTCTC | 92912 |
| rs745702887 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862466 | CTATTCTATGTTGCT[C/T]ATCATTTGTAGTCTT | 92912 |
| rs745754543 | snp | A/C | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841297 | TATATTTCTGGGATA[A/C]AACTAGTAAAAACAC | 92912 |
| rs745777325 | in-del | -/TTC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887581 | TTTTTTTTTTTTTTT[-/TTC]CCCCCTCTGCTAAGT | 92912 |
| rs745918753 | in-del | -/C | 4.96112e-05 | 0.00498027 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899402 | TAAGAATTATTTTAA[-/C]TTTTTTTTTTTCATT | 92912 |
| rs745974053 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851379 | GTATGATATTATAAC[A/G]TCATGCATTGGTCAT | 92912 |
| rs745994608 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885097 | AGCTCTCAAAATGTT[C/T]TGTAAGCACTAATAG | 92912 |
| rs746061266 | snp | C/T | 1.77432e-05 | 0.00297847 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843869 | GCCCGGCCGCGGCCC[C/T]GCGGGGCAGGGCGAG | 92912 |
| rs746110323 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892624 | CAACACTTTGGGAGG[C/T]CGAGGCAGGAGGATG | 92912 |
| rs746171171 | snp | A/C | 1.65285e-05 | 0.00287471 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876310 | CTCTTTATGATTCTT[A/C]TGCTCTTTTCTATTG | 92912 |
| rs746186993 | snp | A/G | 8.35694e-05 | 0.00646357 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890405 | GAATAATTCTCGAGA[A/G]TTTTGTATGACTCCT | 92912 |
| rs746191595 | snp | A/G | 1.86465e-05 | 0.00305334 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854504 | TAAGAAAATAAGCCA[A/G]GCTATTTTCTCTTTT | 92912 |
| rs746217039 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872186 | TGAGCCGAGATCTTG[G/T]CACTGTACTCCAGCC | 92912 |
| rs746217617 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858294 | CTTACAGTGCCATGG[A/T]TATTCAAAATGATGA | 92912 |
| rs746237634 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859034 | GGAAACTGTTCCTGA[C/G]CGAGTTAAGTGAGTT | 92912 |
| rs746245774 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891797 | ACAGCCTTCCAAAGC[C/T]GGAGGTTTGTTACCA | 92912 |
| rs746323970 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846042 | TCAGTACAAATGTCT[C/G]CTAACTTTTTATTAT | 92912 |
| rs746364049 | snp | A/C | 1.65573e-05 | 0.00287721 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859885 | TTTTGTAGCTTCGTC[A/C]GCAATTGAAGTGGTT | 92912 |
| rs746445800 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890927 | TCTGTAGGGCTGGAG[C/T]AGTGCCTACTCAATA | 92912 |
| rs746487047 | in-del | -/TTC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847524 | CTCGAGTCCTTTTTA[-/TTC]TTTTCTGTGAAGCCA | 92912 |
| rs746537342 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842362 | TGTGCCAGGAATTGT[A/G]CTAGTGGTGGGGATT | 92912 |
| rs746572509 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874115 | GTATTTGCCCCTTCC[C/T]GGCCTGTTTATGCTG | 92912 |
| rs746591480 | in-del | -/GT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864370 | TCACAACTGGTCATG[-/GT]GTAGGGGTGCTGTTG | 92912 |
| rs746625240 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844745 | TGATGTAGGATATTG[G/T]TCCAAACTGCAGAAT | 92912 |
| rs746647440 | snp | G/T | 3.8771e-05 | 0.00440272 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869014 | GAGATGGCTGAAGTA[G/T]GTATTTTATATAAAA | 92912 |
| rs746726749 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891439 | CTAGGCTCTAGTCTT[C/T]TCATTTATTTTTACT | 92912 |
| rs746727245 | snp | A/T | 1.66815e-05 | 0.00288799 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891051 | CATAAACCATAAGAT[A/T]CATTTTATATTACTT | 92912 |
| rs746748719 | snp | G/T | 1.64993e-05 | 0.00287218 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876294 | TCTCTGGATCCCTGC[G/T]CTCTTTATGATTCTT | 92912 |
| rs746754829 | snp | A/G | 2.21007e-05 | 0.00332413 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843797 | TGGTGCCGCAGCAGG[A/G]CAGCCCGCACTCGCT | 92912 |
| rs746787481 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863861 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTG | 92912 |
| rs746804293 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864939 | TTTGAGTTTATTGCA[C/G]AAGTTTTAAAATCTG | 92912 |
| rs746885568 | in-del | -/AGGGCTCAAGGCCGAGCTGAAGTTCCTGGCG | 1.86694e-05 | 0.00305522 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843678 | GAAGATGTCCGTGTC[lengthTooLong]TCCATCTTCGACAAG | 92912 |
| rs746895902 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851521 | ACGGTGGTGGATACA[A/C]GTTTTCAAAAATTCT | 92912 |
| rs746904572 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893486 | GAAGTTGACAAGTCC[A/G]CCATCACAGTTGGAG | 92912 |
| rs746919306 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898689 | GTCATTGTGAAATGA[C/T]GTTATGGCTCCGATA | 92912 |
| rs746951462 | snp | A/C | 1.72329e-05 | 0.00293533 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843855 | CATCACGGTGAGGCG[A/C]CCGGCCGCGGCCCCG | 92912 |
| rs747010912 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885133 | GGGTTTTTTTTTATT[C/T]GTTTTTTGAGACGGG | 92912 |
| rs747066922 | snp | A/T | 1.69807e-05 | 0.00291377 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859861 | ATAATGCTTATTTAC[A/T]GAAATGTGTTTTGTA | 92912 |
| rs747172347 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866335 | GCACTGCCACCGTGC[-/A]ATGGCTACTTTTTAA | 92912 |
| rs747200655 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876195 | GTTTCAGGGTGCAGT[A/G]TCTGGGTCAGTGCAA | 92912 |
| rs747272542 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873894 | TAGAGATGAGGACTC[G/T]CTGTTGCCCAGGCTG | 92912 |
| rs747303604 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859106 | ACATTTTAAACAATG[A/G]ACACCATACTTGTGC | 92912 |
| rs747330809 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860208 | TTGCCCTTCTCTCTA[C/T]CACCACCTTTTTGTT | 92912 |
| rs747347036 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847564 | AAAGATTGCCTGTTA[C/T]ACAAACTTAAGTATA | 92912 |
| rs747372489 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846214 | TTTCTGCTTGTATCT[C/T]TTGAAGGTAAAAGAC | 92912 |
| rs747398046 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851652 | TTTTGAGGAAAATGA[C/T]TGCCAAAAACCCAAG | 92912 |
| rs747418974 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848155 | AGCATATAGAGGAAA[A/G]CTCTTTGGCAATGAT | 92912 |
| rs747436554 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894432 | CAAAACAAAACATGA[A/C]AATTAGCTGGGCATC | 92912 |
| rs747572225 | snp | C/G | 2.44993e-05 | 0.00349986 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843829 | CCGCCGCCACTCACG[C/G]TCCACTGCAACATCA | 92912 |
| rs747590068 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891707 | CCATGGGACATAAGG[A/G]TGTTGTTCAGGCTGG | 92912 |
| rs747601690 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881866 | AATTGAATTCTGAGG[C/T]AGTACTTTAAGAAGG | 92912 |
| rs747622178 | snp | C/T | 1.65946e-05 | 0.00288046 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854411 | CATCTTCTTCACCGA[C/T]ATGGTTTGTGGATTC | 92912 |
| rs747651538 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847059 | TCTTTAGTCCTTACT[A/G]TTTTTGCTTTGGTCA | 92912 |
| rs747672265 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845743 | TTGCAACGTTCAGGC[A/G]GTCTGCCACAGCAAA | 92912 |
| rs747780481 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859902 | CAATTGAAGTGGTTG[A/G]TATGTGAACTCTGCA | 92912 |
| rs747803667 | snp | A/G | 1.65329e-05 | 0.0028751 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890891 | CAGAAATACTACTGT[A/G]TTTTAGAGATACTTT | 92912 |
| rs747806524 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865135 | AGAAGGAACATTGCT[C/T]GCACTACAGAAACCT | 92912 |
| rs747822972 | snp | C/T | 3.32265e-05 | 0.0040758 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890426 | TATGACTCCTTTTTT[C/T]TTTTTAAGGTATGTA | 92912 |
| rs747839536 | snp | A/G | 1.65244e-05 | 0.00287436 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873515 | GGAATTGAAAAAGAA[A/G]ATTTGGCAATATTAG | 92912 |
| rs747871094 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879941 | GGGAGGTAGGGAGGT[A/G]TGAACTGAAAGGTAT | 92912 |
| rs747894322 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866601 | GTTAGATCTCTATAT[A/C]TTCAATGTCCCTTAA | 92912 |
| rs747916062 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900002 | CTTTTTAATGACTAT[A/G]TGAAGATATGAATTG | 92912 |
| rs747923360 | snp | A/G | | | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901053 | TTAAAAATTTTGTTT[A/G]TGCTGATCATGGCAA | 92912 |
| rs747973679 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866331 | GGTGTGCACTGCCAC[C/T]GTGCATGGCTACTTT | 92912 |
| rs747981142 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899152 | ATAGTGGCGCATGCC[C/T]ATAATCCCAGCTACT | 92912 |
| rs747985677 | snp | A/G | 3.36723e-05 | 0.00410305 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897096 | TGTTTATTGCCATTT[A/G]AGAAGTTTTAGATAA | 92912 |
| rs748004586 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886383 | CCTGGGCCTCCCAAA[G/T]TGCTAGGATTATGGC | 92912 |
| rs748038438 | in-del | -/GT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856247 | TATATGTGTATATAC[-/GT]GTGTGTGTGTGTGTG | 92912 |
| rs748047495 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863605 | CACATGTCACTACGG[C/G]CAGCTGATATTTTAT | 92912 |
| rs748178775 | snp | C/T | 1.6617e-05 | 0.00288239 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854407 | TATCCATCTTCTTCA[C/T]CGATATGGTTTGTGG | 92912 |
| rs748182365 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876190 | TTTGTGTTTCAGGGT[A/G]CAGTGTCTGGGTCAG | 92912 |
| rs748219757 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874025 | GTTGCTGTAGATTAC[A/G]TTTCTTATCTATAGA | 92912 |
| rs748233599 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860541 | TTATCTTTAGTCATA[C/T]AAGTAATCACTAATT | 92912 |
| rs748238147 | snp | A/T | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875070 | CATTTGAATTAATGA[A/T]GACTGTACTTTATGT | 92912 |
| rs748321970 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861890 | TGGCAGGGACTGGTC[A/G]TCTGGATGCTCAGCT | 92912 |
| rs748376950 | snp | A/G | 5.04562e-05 | 0.00502251 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854474 | GTCTAGAAGATACTA[A/G]GAACAACAATTTGGT | 92912 |
| rs748459456 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882066 | GCATTAGTTTTTATT[G/T]GCTTTTGGTGAATGC | 92912 |
| rs748543682 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883306 | CTTTTAAAATCTTCT[A/G]AATAGTATAACACTA | 92912 |
| rs748604960 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854724 | TCTCTTTTTCCCTGA[A/C]TTCTAACCATTAAGC | 92912 |
| rs748620392 | snp | A/G | 1.73634e-05 | 0.00294642 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879193 | TCTCTTTTAAGGTAA[A/G]AAAATAGTTACAGGA | 92912 |
| rs748692590 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852036 | CAACCACCATGCTTA[A/G]CTAATTTTTTTATTT | 92912 |
| rs748712041 | snp | A/C/T | 3.78711e-05 | 0.00435136 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879054 | GTTAAAAAAAAAAAT[A/C/T]TCTAACTTTTTATTT | 92912 |
| rs748754993 | snp | C/T | 3.63062e-05 | 0.00426049 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843710 | TGAAGTTCCTGGCGT[C/T]CATCTTCGACAAGAA | 92912 |
| rs748776281 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847341 | GGTCTCTAAGGGCTT[G/T]ATGGAAGTCTGTAAA | 92912 |
| rs748789639 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880364 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 92912 |
| rs748982307 | snp | C/T | 3.36717e-05 | 0.00410302 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896966 | CACCTAATTACACTT[C/T]TGATTTAAAATGTGT | 92912 |
| rs749005493 | snp | C/T | | | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901085 | CAAAAAAAAGATTAC[C/T]TTCTCATTTTTCCCT | 92912 |
| rs749114845 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888210 | ACATTTTCATGACTT[C/G]AAAAAGAAACCCCGT | 92912 |
| rs749124605 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870080 | TTGTAGGCTTGTTTT[-/G]TTTTTTTGAGACAGG | 92912 |
| rs749127821 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874070 | CCTGTTCATCTGCTC[C/T]TCATATCCTGGAACC | 92912 |
| rs749219491 | snp | G/T | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875172 | ACTATGCCAAGTACT[G/T]TATACTTCACATATC | 92912 |
| rs749229052 | snp | A/G | 1.65364e-05 | 0.0028754 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873483 | AGCCTATTAGTGGGA[A/G]AAAGTCAGAGGATGA | 92912 |
| rs749261396 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866969 | GCTAATTTTCTTCAG[C/G]TCTCTGGTGATACCT | 92912 |
| rs749315015 | snp | A/C/T | 3.34081e-05 | 0.00408695 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897072 | AAATGGTATGTTTAA[A/C/T]TCAATAAGTGTTTAT | 92912 |
| rs749318109 | snp | A/C | 1.88667e-05 | 0.00307132 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879050 | TTTAGTTAAAAAAAA[A/C]AATCTCTAACTTTTT | 92912 |
| rs749327830 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862121 | TCTGGAACAGGTCCA[A/G]TATAATTTCTACCAA | 92912 |
| rs749359841 | in-del | -/TT | 1.66482e-05 | 0.0028851 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890489 | CACAAAACAGGTGAC[-/TT]TTCTTACGATACTCC | 92912 |
| rs749387111 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849240 | CTGTCAATTTACTTC[A/G]TTCTCCACCCCACAT | 92912 |
| rs749412398 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896510 | GCTCCTTTAGTAAGC[A/T]TGGTGACAATTATGG | 92912 |
| rs749418119 | in-del | -/T | 1.67503e-05 | 0.00289393 | splice-donor-variant | UBE2Q2 | GRCh38.p7 | 15:75873569 | AAGACCATTTAAATG[-/T]TAAGTGTGTGTAGAT | 92912 |
| rs749460586 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850165 | AAGTTTCCTGGCGTG[A/G]TGGATATTTTATAAT | 92912 |
| rs749517809 | snp | A/G | 1.67156e-05 | 0.00289093 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879154 | TAAAAGAAAAAGAAG[A/G]CATAGAATATATTTT | 92912 |
| rs749520971 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898180 | AGCTTAGGTTTTTGC[A/G]GAACCTGGGACACAG | 92912 |
| rs749528873 | snp | A/C | 0.000100761 | 0.0070972 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844472 | AAAGGAGCATAGTAC[A/C]GTCGTTGCGGCAGGT | 92912 |
| rs749570448 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883741 | AGGTGAAGTTGATGC[C/T]GTTGTTCTGGGGCCC | 92912 |
| rs749620931 | snp | A/T | 1.74102e-05 | 0.00295039 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860017 | GTGTTCAAGAGCTAA[A/T]TAAATTGTCTCAAGC | 92912 |
| rs749681791 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870307 | CTCCTGACCTCAAGT[A/G]ATCCACCACTGGCCT | 92912 |
| rs749850311 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890568 | GTAGAAAATTCTTTA[A/G]TAGCTCCTACTCTTA | 92912 |
| rs749879697 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849650 | GGTGATGAACTTGTT[C/T]GAAATTTGTCCACTT | 92912 |
| rs749889373 | snp | A/G | 3.32817e-05 | 0.00407919 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75897045 | TAATTCCATTGTACA[A/G]ATACATGAGAAAAAT | 92912 |
| rs749937741 | in-del | -/AATT | 1.67438e-05 | 0.00289338 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883335 | TAAGGATGTTCTTTA[-/AATT]AATTAAACTTGCTTA | 92912 |
| rs750017651 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850747 | AAGGCAGCAGTTCTC[A/C]AAGTTTTGGGGTCAG | 92912 |
| rs750027309 | in-del | -/AG | 3.39524e-05 | 0.00412008 | frameshift-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75868997 | AGAGGAAGAAGAAGA[-/AG]AGAGATGGCTGAAGT | 92912 |
| rs750040078 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858495 | GCCCCCCGCAAACTA[G/T]TAATTTTCTAAGACC | 92912 |
| rs750084268 | snp | C/T | 1.65228e-05 | 0.00287422 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899510 | TTAAAGAAAATCTTT[C/T]TAACATGCAGACAAA | 92912 |
| rs750161479 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871790 | TTCTACACAGACACA[A/G]TAACAGGCTGATCTG | 92912 |
| rs750193694 | snp | C/T | 6.72246e-05 | 0.00579722 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879106 | TTCTTAGGGTTGACC[C/T]TGATAGTCCTTTGCA | 92912 |
| rs750252201 | snp | G/T | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844159 | CCTTGTGGGGTCCAT[G/T]GCCGCCCTCAGCCGG | 92912 |
| rs750274406 | snp | C/T | | | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844466 | TTCTGGAAAGGAGCA[C/T]AGTACCGTCGTTGCG | 92912 |
| rs750276402 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858689 | GCCTCTCTCCCCAGC[A/G]CTCCTGGAGCCCCTT | 92912 |
| rs750283987 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877186 | AAAAAAAAAAAAAGG[C/G]TTATGACCGATTCAA | 92912 |
| rs750294841 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845301 | CACCCAAAGAAGACA[C/T]GGAGATTTGAGAAAG | 92912 |
| rs750397409 | snp | A/G | 1.69137e-05 | 0.00290802 | splice-acceptor-variant | UBE2Q2 | GRCh38.p7 | 15:75854384 | GTCTCTGTGTTAAAC[A/G]GGAATCCTATCCATC | 92912 |
| rs750416255 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892563 | GAAATAGAACTTACA[A/G]AAATTAAAAAATGTA | 92912 |
| rs750427975 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878204 | TCTAATAAGAAAGTG[A/G]GAAAGAGGAAGGACA | 92912 |
| rs750511150 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864481 | TACGTCAATATTGCT[A/G]AGGTTGAGAAACCAT | 92912 |
| rs750518003 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879653 | TAGAGTGAAAACAAT[C/G]TTAGCTATTAAAATG | 92912 |
| rs750569536 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852686 | ATGGTCCAGATGGTG[C/T]ATTCCCAATGTGTGC | 92912 |
| rs750571272 | snp | A/T | 1.65179e-05 | 0.00287379 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75868964 | AGAATGGGACAACAG[A/T]AGAAGTGACTTCAGA | 92912 |
| rs750624386 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866883 | CCAATTAGGTTTTAA[A/G]ATTCTATTTATTTCC | 92912 |
| rs750653945 | snp | C/G | 5.37389e-05 | 0.0051833 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843637 | GCCCGGCTCCCCTTC[C/G]GCGCCCCTCCCGCCG | 92912 |
| rs750694247 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900372 | CTTACAGTAATTTTT[A/G]CCATGTCAAAACAAT | 92912 |
| rs750778688 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854081 | TGAGTCACTAGGTCC[A/G]GGGGCGGGAATTTTA | 92912 |
| rs750799242 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887120 | TTGAATAAGTCAGCT[G/T]GTGACCTACTCAAAT | 92912 |
| rs750815578 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873634 | TAGTTAATACCAGGC[A/G]ATTCATTAACATGCC | 92912 |
| rs750856983 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874680 | TCACTTTCCTCAGCT[C/T]TAAAATATGGCTAGA | 92912 |
| rs750876395 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868304 | AATGGATATGAAAGT[C/T]CTTCCTAAAACCCCA | 92912 |
| rs750889332 | in-del | -/TCTT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866518 | CTTAATATTCTAAAG[-/TCTT]TCTTTAGCTCAGCAG | 92912 |
| rs750889339 | snp | A/G | 0.000118091 | 0.00768319 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854386 | CTCTGTGTTAAACAG[A/G]AATCCTATCCATCTT | 92912 |
| rs750910279 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860092 | TTAGAAGTTAGTTTC[A/G]TTTTTGTTCCTATTG | 92912 |
| rs750951058 | snp | A/C | 1.69542e-05 | 0.0029115 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859993 | GTCAGGTAAAGTAAA[A/C]ATTCTCTAGTGTTCA | 92912 |
| rs750954836 | snp | C/T | 3.31153e-05 | 0.00406898 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891033 | CTTCTGTTAAGAATT[C/T]TACATAAACCATAAG | 92912 |
| rs750966082 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865796 | ATATCCCTGAATAAT[A/G]TCTGGTTGTTTTTTT | 92912 |
| rs751151952 | snp | C/T | 1.77599e-05 | 0.00297987 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854351 | TTGGGTTAGTCTGTA[C/T]GTAAATGTTTAACAT | 92912 |
| rs751189210 | snp | G/T | 1.66674e-05 | 0.00288676 | stop-gained, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75897003 | CTTTCAGAATCAATA[G/T]AATCTAGCAAGAGCC | 92912 |
| rs751276696 | in-del | -/CT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867222 | GTTATACTAAAAACA[-/CT]CTCTGTCTTTTCTGT | 92912 |
| rs751292650 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859697 | CCCAAGCCATAGTAA[C/T]TTTCTTACACTAGAG | 92912 |
| rs751304998 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892618 | TAATCTCAACACTTT[C/G]GGAGGCCGAGGCAGG | 92912 |
| rs751325248 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879749 | TCCATGGAGCAGGGG[C/G]GTAAAACTAGGAAGA | 92912 |
| rs751338461 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845603 | GAGAATGTATCTTTC[A/G]TCCAGGATTAGAAAT | 92912 |
| rs751448462 | in-del | -/A | 1.71434e-05 | 0.0029277 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883465 | AAATTTTTTTCAGTT[-/A]AAAAAAAATTTTTTT | 92912 |
| rs751476057 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883626 | TTTTTTTTCTTCTAA[A/G]TATAGTGTGCACCAG | 92912 |
| rs751506845 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895427 | GCCTCAGGTGATCTA[-/C]CTGCCTCAGCCTCTA | 92912 |
| rs751669049 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900452 | TATAGAACCTGACTC[A/G]AATCAAGGTACTCTC | 92912 |
| rs751740844 | snp | C/T | 1.65531e-05 | 0.00287686 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859966 | AGATGCTAGATCAAC[C/T]ACTACCCACGGGTCA | 92912 |
| rs751749345 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854229 | AGAATGGTTGTCTCA[A/G]AAGTCCAGCTCCTCA | 92912 |
| rs751803804 | snp | A/C | 1.64974e-05 | 0.00287201 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868936 | TAGCCCTGGCAGATT[A/C]TTTCTCTGTTTCAGA | 92912 |
| rs751817626 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887950 | TGCCATCTCAATCAG[G/T]GTAAAGCTTAAGCAT | 92912 |
| rs751824105 | in-del | -/CGGGG | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844193 | CTCCCGGGACCGGGG[-/CGGGG]CGGGGCGGGGCGGGG | 92912 |
| rs751834110 | snp | G/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841786 | TAGATAGAAGTTGGG[G/T]TAGAAGATGGTAGAA | 92912 |
| rs751906868 | snp | C/G | 1.94154e-05 | 0.00311566 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843763 | AGTTGGAAGCTGGAC[C/G]AGCTGCACTGCCAGT | 92912 |
| rs751923831 | snp | C/T | 3.29641e-05 | 0.00405968 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876170 | GACCCTGGTAAACAG[C/T]GGCTTTTGTGTTTCA | 92912 |
| rs751955547 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887324 | GAAGTAGGTGAGATC[A/C]CAGCTGGGCAGTGAA | 92912 |
| rs751962478 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876244 | AAAGAGCTCAGGGAC[A/G]TATACAGATCACAGA | 92912 |
| rs751972269 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863226 | TGCTGTCAATATCCC[A/C]CTAACCTCCACCTTT | 92912 |
| rs752066903 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848903 | TTGGAACCTAGGAAA[C/T]CACCCAGTGGGTTTC | 92912 |
| rs752089081 | snp | G/T | 1.84276e-05 | 0.00303537 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883475 | TCAGTTAAAAAAAAT[G/T]TTTTTTTATAGGGAC | 92912 |
| rs752104041 | in-del | -/ACTC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871918 | GATGTGCTGATTAAT[-/ACTC]AGAAAAAGAAATTTC | 92912 |
| rs752173385 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899200 | AGAATTGCTTGATCT[-/G]GGAGGTGGAGGTTGC | 92912 |
| rs752207945 | snp | A/G | 1.65828e-05 | 0.00287943 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75877981 | TATTCAGTGGAACTC[A/G]TAAATGACAGTTTAT | 92912 |
| rs752215519 | in-del | -/TA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856272 | GTGTGTGTGTGTGTA[-/TA]TATATATATATATAT | 92912 |
| rs752264156 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859957 | TGGATGTTGAGATGC[C/T]AGATCAACCACTACC | 92912 |
| rs752291201 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844525 | GGCCCCTCCCTTGTG[G/T]GTAAGCCTCGAAAAT | 92912 |
| rs752351077 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846993 | CCTGACCATCCGTCA[A/G]GGCTCTTCTGGGTCA | 92912 |
| rs752354216 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861180 | AGTGCCTGGTGCATA[A/G]CACATCCCCATCAAC | 92912 |
| rs752410379 | snp | C/G | 0.000100518 | 0.00708863 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844403 | AATGCAGACTCTGGT[C/G]CTGTTTGAGCGACCC | 92912 |
| rs752419734 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881220 | ATGCCTAACACCAAA[C/G]TTAAGAAATAGAACC | 92912 |
| rs752436199 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867466 | AGTTCACTAAGGGTA[C/T]TCTCCTTGTATTTGT | 92912 |
| rs752680424 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850418 | TAACTTACTCCTTAC[A/G]TGTAGGCAAGATGAA | 92912 |
| rs752781366 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859928 | CTGCAGTTTATATAA[C/T]CTTCCTAAGCACCTG | 92912 |
| rs752802836 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855407 | GAGGCAGGAGAATTG[C/T]TTGAATCTGGGAGAC | 92912 |
| rs752905633 | snp | G/T | 1.72868e-05 | 0.00293992 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859854 | CTTTAACATAATGCT[G/T]ATTTACTGAAATGTG | 92912 |
| rs752918059 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893705 | GATTTAAAAACAGTT[-/G]GTACCATACATACCA | 92912 |
| rs752959737 | snp | A/C | 1.65531e-05 | 0.00287686 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873468 | AGATGAAGGAAGAAG[A/C]GCCTATTAGTGGGAA | 92912 |
| rs752992363 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895054 | AGCTGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 92912 |
| rs753032204 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863262 | CTTTGCTCCATTAAT[G/T]AACTATTTTCCATTT | 92912 |
| rs753034134 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877947 | AGTAGCTAACATGCT[C/G]TATATCTTAACAGGG | 92912 |
| rs753050553 | in-del | -/C | 1.7849e-05 | 0.00298734 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859839 | TGTCTTCTAAGGGCT[-/C]TTTAACATAATGCTT | 92912 |
| rs753082162 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850799 | ATATATTCAGCACTT[A/C]AGGGCTTTGGTTTAT | 92912 |
| rs753130835 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898073 | CAAAGAAACCTGTGT[A/G]CTACTTTGATACTTT | 92912 |
| rs753161867 | snp | A/G | 4.35142e-05 | 0.00466425 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843652 | CGCGCCCCTCCCGCC[A/G]GAGATGAGGGGAAGA | 92912 |
| rs753162143 | in-del | -/CGGGG | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844189 | GCCTGCTCCCGGGAC[-/CGGGG]CGGGGCGGGGCGGGG | 92912 |
| rs753168449 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849940 | ATTTATTTTAAAGAG[A/G]AATAGTAGGCAAACT | 92912 |
| rs753192032 | in-del | -/TAGA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891248 | CTGTTATATTTGCTG[-/TAGA]TAAACATTATAAGTT | 92912 |
| rs753237407 | in-del | -/GA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886001 | AACCTTTCTCTTGCT[-/GA]GACACCACCAGTCTT | 92912 |
| rs753292392 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898945 | GCAAAATGCAGTGTT[C/T]CCAATCCAAGTGTAA | 92912 |
| rs753296373 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884857 | TTTTGCCATATTGCT[C/T]AGGCTGGTCTTGAAC | 92912 |
| rs753337876 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878748 | ACTTTTCTCCTTGAA[-/C]CCTTTGGCTAATAAT | 92912 |
| rs753353472 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854036 | TCAGAAGTGATGTTA[C/T]TACTTTTGCTGTATT | 92912 |
| rs753411693 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896191 | GAGGGACATACAAGA[A/G]ATTAGTAATAGTGGT | 92912 |
| rs753440437 | in-del | -/CAG | 3.31115e-05 | 0.00406874 | cds-indel, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75868976 | CAGAAGAAGTGACTT[-/CAG]AAGAAGAGGAAGAAG | 92912 |
| rs753455472 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848708 | AGACCTGGAAAAGGG[A/T]AGTATTTGATAAATG | 92912 |
| rs753532557 | snp | C/T | 6.59207e-05 | 0.00574073 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876264 | CAGATCACAGAGTTA[C/T]AAAACAGGTAAGGAT | 92912 |
| rs753585657 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855782 | TGCACGACTTTTATC[A/T]AGAACATGACAATTT | 92912 |
| rs753588931 | snp | A/G | 1.67524e-05 | 0.00289412 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883453 | ACTACTTAAAAAGAA[A/G]TTTTTTTCAGTTAAA | 92912 |
| rs753619881 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868439 | GCTTTTTAGTGAGGT[A/G]GTAATCATTTCATAA | 92912 |
| rs753629620 | snp | A/T | 3.33979e-05 | 0.0040863 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854465 | TTCTGGAACGTCTAG[A/T]AGATACTAAGAACAA | 92912 |
| rs753636255 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869813 | AGACATTGAGCTTAG[A/G]CCAGTTGTCAGTCAT | 92912 |
| rs753733933 | snp | C/T | 1.80631e-05 | 0.0030052 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859830 | CATTATTGATGTCTT[C/T]TAAGGGCTCTTTAAC | 92912 |
| rs753767591 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857440 | TGAAGGAGAAAACAA[C/T]TCACCTCCCACTCTT | 92912 |
| rs753877910 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889900 | GAATAGTCTTCAGGC[C/G]TAGAAAGAGCTTAAG | 92912 |
| rs753931999 | snp | A/C | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844181 | CTCAGCCGGCCTGCT[A/C]CCGGGACCGGGGCGG | 92912 |
| rs753967933 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842723 | AAAGGGGGGAGAGAG[A/G]GACTATATACGGCAG | 92912 |
| rs754013912 | snp | C/T | 2.33375e-05 | 0.00341588 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843647 | CCTTCCGCGCCCCTC[C/T]CGCCGGAGATGAGGG | 92912 |
| rs754022015 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863453 | GTTTGTTTGTTTTTC[-/T]TTTTTTTTTTTTGAC | 92912 |
| rs754138374 | snp | C/T | 1.83421e-05 | 0.00302832 | upstream-variant-2KB, stop-gained, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843733 | GACAAGAACCACGAG[C/T]GATTCCGCATCGTCA | 92912 |
| rs754165781 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851226 | ACCCTCAGTCTCCTG[C/G]GACTCAGGTGTAGGC | 92912 |
| rs754196805 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865700 | TCAGTAATCGTTTAG[A/G]CTTCACTATTGGTGT | 92912 |
| rs754254609 | in-del | -/AAAAG | 5.00371e-05 | 0.00500161 | frameshift-variant, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879140 | TGATCTTCAGATCTT[-/AAAAG]AAAAAGAAGGCATAG | 92912 |
| rs754256633 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898025 | CAAGGCCAGGTTTTC[A/G]TAATAATAATTTCTA | 92912 |
| rs754344575 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887037 | TCAGTTTTAAAATCT[C/G]TTACGTAGTTTCTTA | 92912 |
| rs754381683 | snp | C/T | 1.65858e-05 | 0.00287969 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873449 | GAAGACTTAGATCAC[C/T]ATGAGATGAAGGAAG | 92912 |
| rs754389597 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897629 | AGTAGATTAATGAAT[G/T]ACTCACTTTACTTAC | 92912 |
| rs754400005 | snp | A/T | 1.66402e-05 | 0.00288441 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75868979 | AAGAAGTGACTTCAG[A/T]AGAAGAGGAAGAAGA | 92912 |
| rs754440637 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876267 | ATCACAGAGTTATAA[A/G]ACAGGTAAGGATCTC | 92912 |
| rs754446024 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857903 | TATATGCTTGTTTAT[A/T]CTTTTTTCTTTCCTG | 92912 |
| rs754466511 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887566 | GACTGGCCACAGATC[-/T]TTTTTTTTTTTTTTT | 92912 |
| rs754477517 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871967 | ACTGAGGTTGAAGGT[A/G]TAGGAGGAAATACAG | 92912 |
| rs754480489 | snp | A/G | 1.96107e-05 | 0.00313129 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843770 | AGCTGGACGAGCTGC[A/G]CTGCCAGTTCCTGGT | 92912 |
| rs754547180 | in-del | -/AGG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864432 | CATCCTACAACACAC[-/AGG]AGAACCCTCCACAAA | 92912 |
| rs754630535 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845704 | CCGGCATTTAGTGCT[A/G]GGAGTACAGGGATAC | 92912 |
| rs754660141 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892721 | GCCCCCCACCCTAAA[A/G]AAACAATTAGCTGGG | 92912 |
| rs754674933 | snp | C/T | 2.44765e-05 | 0.00349824 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843827 | TGCCGCCGCCACTCA[C/T]GCTCCACTGCAACAT | 92912 |
| rs754689860 | in-del | -/T | 0.000361045 | 0.013431 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883473 | TTCAGTTAAAAAAAA[-/T]TTTTTTTTTATAGGG | 92912 |
| rs754691885 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898952 | GCAGTGTTCCCAATC[C/T]AAGTGTAAGTTTAAT | 92912 |
| rs754753061 | snp | A/G | 3.33962e-05 | 0.0040862 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854466 | TCTGGAACGTCTAGA[A/G]GATACTAAGAACAAC | 92912 |
| rs754791085 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846835 | TAAGTTGTTTTTTAC[A/G]CACGTGCATGCTAGT | 92912 |
| rs754794297 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850151 | TTGTGCTGAAGGTTA[A/G]GTTTCCTGGCGTGGT | 92912 |
| rs754888040 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900932 | AGACTGATAGCTGCA[C/T]ATTTGGCATGCTTTG | 92912 |
| rs754953542 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846461 | CAGGCTGGTCTTGAA[C/T]TCCACCTCAAGCTCC | 92912 |
| rs754984328 | snp | A/G | 3.32474e-05 | 0.00407708 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899527 | AACATGCAGACAAAA[A/G]CTTTGAGTGCCCCTA | 92912 |
| rs755013059 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887252 | CCATGGACTTAATTT[A/G]TCAGAGGTTTAAAGC | 92912 |
| rs755032877 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852862 | ACCAGGTATACTATT[A/G]ATGATGTCCTCCATC | 92912 |
| rs755053369 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854276 | TTGCCTTTTCCCCCC[A/G]TACATTTTGTTTAAA | 92912 |
| rs755142971 | snp | G/T | 2.27503e-05 | 0.00337263 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843649 | TTCCGCGCCCCTCCC[G/T]CCGGAGATGAGGGGA | 92912 |
| rs755155819 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868540 | ATGTAAATGATTCAG[C/G]CTTTCCAAAGTTAAA | 92912 |
| rs755170797 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873941 | TTCAAGTCATCCTCC[C/T]ATCTTGGCCTCCGAA | 92912 |
| rs755260348 | snp | A/C | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875045 | TGATTACTTAAAAAA[A/C]AAAGTTTGTCATTTG | 92912 |
| rs755302758 | snp | A/C | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841819 | TGGGGCATGGCCAGG[A/C]AAAGTTAGGGCTGGT | 92912 |
| rs755322449 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848943 | GGTGGTTCAGATCCT[C/T]ATCAGCACCTTTTTC | 92912 |
| rs755325595 | in-del | -/TAGT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854612 | GTAGGAATTAAAGAC[-/TAGT]TTGTTTGTTTTTTTT | 92912 |
| rs755437515 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887366 | GGGTTTGGTCAGCTG[A/G]TGGAGGTTGAAGGAA | 92912 |
| rs755514817 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883003 | ATCCTGCTCTCTGGT[G/T]TTCCCTTTTCTTAGC | 92912 |
| rs755549551 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849683 | AGTAATGTTTATGGT[A/G]GCTTCACAGACAACT | 92912 |
| rs755614652 | snp | C/T | 0.000148968 | 0.00862914 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859965 | GAGATGCTAGATCAA[C/T]CACTACCCACGGGTC | 92912 |
| rs755687269 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884055 | ATTACTCCTAGAGGT[A/G]ATACTTGCAGTTTAT | 92912 |
| rs755736565 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879962 | TGAAAGGTATATCTG[C/T]GCAGGCTTCTTGGAT | 92912 |
| rs755740309 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894269 | GTTAGAAAGGACAAT[A/T]AAAAAAACCTGAAGG | 92912 |
| rs755815825 | snp | G/T | 1.64955e-05 | 0.00287184 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876138 | CAGGTTGAAATATCT[G/T]AAATCTTAGCTCAGC | 92912 |
| rs755817242 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869324 | TAGGAAGAGGAACTA[C/T]TAAGTTTAAAAAATT | 92912 |
| rs755863121 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871316 | TCCATTGCCCAGGGA[C/T]GGGCAGGAGGCAGAT | 92912 |
| rs755876771 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867496 | TTTTTCTGCTACTGC[A/G]GCAGACCTACTCTTT | 92912 |
| rs755886332 | snp | C/T | 3.34018e-05 | 0.00408654 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879122 | TGATAGTCCTTTGCA[C/T]AGTGATCTTCAGATC | 92912 |
| rs755964007 | snp | A/G | 0.000370961 | 0.0136141 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854539 | ATGAACATTACATAT[A/G]GAAATTAAATGTTAA | 92912 |
| rs756008450 | snp | A/G/T | | | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901082 | AAGCAAAAAAAAGAT[A/G/T]ACTTTCTCATTTTTC | 92912 |
| rs756130730 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900595 | GAAGCACATTTTTCT[A/G]CACAAACAAGTTACA | 92912 |
| rs756166942 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889610 | GCATGGGCAGAGCCC[C/T]GGAGGACAGAACAAT | 92912 |
| rs756181629 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887795 | GAGGAGAACCTACAT[A/T]GGTTTGGTAGTCATG | 92912 |
| rs756201486 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842084 | ACAGGTGTCAGGGTT[A/G]GGTAACTCTAGGTAA | 92912 |
| rs756251796 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856592 | GAAGTTTGAGTCTCA[A/C]CTCTGATTTTTGTCA | 92912 |
| rs756285020 | snp | A/C | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75868968 | TGGGACAACAGAAGA[A/C]GTGACTTCAGAAGAA | 92912 |
| rs756309192 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861926 | GGAATGTCTGAGACG[A/G]CTTCTTCACCCACAG | 92912 |
| rs756324486 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876511 | GAATTTTGTCCTCTT[C/G]TTGATAAACAGTGAA | 92912 |
| rs756415843 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896449 | GTGACAAAATTAATC[C/T]TAGATTTGGCTCCTT | 92912 |
| rs756417384 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864345 | GAAATATCTGGAGCC[A/C]TTTCTGGTTTTCACA | 92912 |
| rs756490854 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850893 | CTTTAAAAACTCATC[A/T]CATATTATTATAAAT | 92912 |
| rs756515957 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861492 | CAAATGGATAGGCCT[A/G]TGGATAGGCTCTTTC | 92912 |
| rs756542831 | snp | G/T | 1.65389e-05 | 0.00287562 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890885 | GGGAATCAGAAATAC[G/T]ACTGTATTTTAGAGA | 92912 |
| rs756603792 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858757 | ATTGCTCTGCCTCAT[C/T]TTCATTATGCACTTA | 92912 |
| rs756658630 | in-del | -/AA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844685 | AGGAATTGAAGTATT[-/AA]GTTTCTCCATAAAAG | 92912 |
| rs756670016 | in-del | -/GAA | 0.000116889 | 0.007644 | cds-indel, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75868986 | ACTTCAGAAGAAGAG[-/GAA]GAAGAAGAAGAAGAG | 92912 |
| rs756725527 | snp | C/T | 1.65946e-05 | 0.00288046 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891036 | CTGTTAAGAATTTTA[C/T]ATAAACCATAAGATA | 92912 |
| rs756733004 | snp | A/C | 1.72835e-05 | 0.00293964 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860007 | AAATTCTCTAGTGTT[A/C]AAGAGCTAAATAAAT | 92912 |
| rs756735076 | in-del | -/GT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856248 | TATGTGTATATACGT[-/GT]GTGTGTGTGTGTGTG | 92912 |
| rs756744152 | snp | C/T | 1.6701e-05 | 0.00288968 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891052 | ATAAACCATAAGATA[C/T]ATTTTATATTACTTT | 92912 |
| rs756750990 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870259 | TTTTGTAGAGATTGG[G/T]TCTTGCTGTTTTGTC | 92912 |
| rs756862125 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887178 | TTCATTATACCAAAG[-/C]CCAGCTATATAAGAG | 92912 |
| rs756884827 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867754 | TTTGAAAAACAGATT[A/C]TCTGGGTAGGCTTTG | 92912 |
| rs756896699 | snp | A/G | 2.01534e-05 | 0.00317432 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869017 | ATGGCTGAAGTAGGT[A/G]TTTTATATAAAAGAA | 92912 |
| rs756940308 | snp | C/G | 1.66604e-05 | 0.00288616 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75897007 | CAGAATCAATATAAT[C/G]TAGCAAGAGCCCAAC | 92912 |
| rs756949104 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851393 | CATCATGCATTGGTC[A/G]TTTAGAAAATAGTGG | 92912 |
| rs757118522 | snp | C/T | 3.3355e-05 | 0.00408367 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878040 | AGTGGCTTTTTAATG[C/T]TCACCCACTCTTTGC | 92912 |
| rs757150358 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876564 | TGGGGAAAGCATGAG[C/T]GATATTGCTTGGAAA | 92912 |
| rs757240295 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863566 | CTCCTGCCTCTCAGC[C/T]TTCCAAGTAGCTGGG | 92912 |
| rs757249664 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889959 | GAACCATTTGATTCT[A/C]ACAACAGAATGGGTA | 92912 |
| rs757303545 | snp | G/T | 1.68165e-05 | 0.00289965 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859867 | CTTATTTACTGAAAT[G/T]TGTTTTGTAGCTTCG | 92912 |
| rs757306433 | snp | C/G | 0.000100619 | 0.0070922 | synonymous-codon, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844428 | CGACCCCTCTCCCCC[C/G]GGCCTGGCTGCGCGC | 92912 |
| rs757313372 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878182 | TTTAAATGAGCTGTT[A/G]CTGAGGTCTAATAAG | 92912 |
| rs757316106 | snp | A/C | 5.15521e-05 | 0.00507675 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879089 | TGTTTTTTGTTTTGT[A/C]ATTCTTAGGGTTGAC | 92912 |
| rs757399118 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891782 | TAGGACATTAGTGAG[A/G]CAGCCTTCCAAAGCC | 92912 |
| rs757437179 | in-del | -/GTAT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891327 | GTAAACTTATTATTA[-/GTAT]GTATAGTGTAGTAAA | 92912 |
| rs757438837 | snp | A/T | 1.68235e-05 | 0.00290026 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890519 | CCATTTTCACCCACA[A/T]TTTAGTGTTTTGATC | 92912 |
| rs757539027 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851291 | GAGACAGGGTTTTGC[C/T]ATGTTGCCTAGGCTT | 92912 |
| rs757596794 | in-del | -/TTG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897694 | TTACAGATGGAGTTC[-/TTG]TTGTTATAACTGGAG | 92912 |
| rs757696217 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865394 | TTTATTCCATTGTTT[A/G]AATACACCCTACCAT | 92912 |
| rs757719848 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861785 | ACAACAAATTTGCCT[A/G]TCTATCACTATTGTA | 92912 |
| rs757722862 | in-del | -/TT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859559 | TGCATTAATGTTCTC[-/TT]GTCTGAAGTTGTAAG | 92912 |
| rs757746673 | snp | A/C | 1.67832e-05 | 0.00289677 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890384 | ACTTAGAAATTGTTT[A/C]AGGAGGAATAATTCT | 92912 |
| rs757821560 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872023 | AGGAAAACATGTAGG[A/G]TGGAAGATCAGGGCT | 92912 |
| rs757945128 | snp | G/T | 1.64936e-05 | 0.00287168 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890914 | GATACTTTGTTCTTC[G/T]GTAGGGCTGGAGCAG | 92912 |
| rs757956973 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870131 | GGAGTGCAGTAGTGT[C/G]ATCACGGCTCACTGC | 92912 |
| rs758000174 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890040 | TAAGGTCAGTGTCAT[C/T]GTCAGGGGAAAAACT | 92912 |
| rs758001661 | snp | A/C | 1.65781e-05 | 0.00287902 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75877990 | GAACTCATAAATGAC[A/C]GTTTATATGACTGGC | 92912 |
| rs758172487 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891302 | TATTTGTAAACAGAT[A/G]TTTACAGTTGTAAAC | 92912 |
| rs758179154 | in-del | -/TG | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900080 | AAAGCAGTGTAAAAC[-/TG]TGTATCAATTAAGGC | 92912 |
| rs758189563 | in-del | -/T | 1.67524e-05 | 0.00289412 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883453 | CTACTTAAAAAGAAA[-/T]TTTTTTTCAGTTAAA | 92912 |
| rs758201253 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880805 | GGATCTGGATGAGAT[-/G]GTAATGGTTTAAAAT | 92912 |
| rs758221741 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845324 | TGAGAAAGTGTGGTT[C/T]CCTTAGAAGTAGAAA | 92912 |
| rs758279814 | in-del | -/AAG | 1.6531e-05 | 0.00287493 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869028 | AGGTATTTTATATAA[-/AAG]AAGAGTTCATAAATT | 92912 |
| rs758338864 | snp | C/T | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844260 | CAAGGGGAACGGCCC[C/T]TAAGTTTTAACGCCT | 92912 |
| rs758341481 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851466 | TATCAAAATACATTC[A/G]TCAATATTGCCATCA | 92912 |
| rs758356284 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877536 | TCCATAAAATAAACT[A/G]CCACAGAGTCATTAA | 92912 |
| rs758419380 | snp | C/T | 1.67553e-05 | 0.00289437 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883332 | CACTAAGGATGTTCT[C/T]TAAATTAATTAAACT | 92912 |
| rs758466316 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864682 | CATGTGGCTATATGC[C/T]GTTTTCACTTCAAAA | 92912 |
| rs758484713 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865911 | ATCTGACTCTGTATA[A/G]AGTATTCCACATTGG | 92912 |
| rs758501679 | in-del | -/TAAC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898469 | CTAAATCTAGCTAAT[-/TAAC]CTAGGCATCACCTTA | 92912 |
| rs758526419 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852838 | AAAATAGTAAATAAC[C/T]CATTATTGACCAGGT | 92912 |
| rs758534860 | in-del | -/AC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862639 | GGGCAACATATTGAG[-/AC]ACCCCATCTTTACAA | 92912 |
| rs758537353 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898668 | ACCTGCTGCGATGGC[C/T]TCCTTGTCATTGTGA | 92912 |
| rs758609672 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886154 | AGACAGAGTCTCACT[C/G]TGTTGCCCAGGCTGG | 92912 |
| rs758609695 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900825 | TCAGATAACAAGTGA[C/T]AAGGCAGAATTCTTT | 92912 |
| rs758627569 | snp | A/G | 1.68769e-05 | 0.00290485 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873589 | TGTGTGTAGATATCT[A/G]GAACCTGGACTTTTG | 92912 |
| rs758630080 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896210 | AGTAATAGTGGTTAA[A/C]TTGTGTGGAGGAAGG | 92912 |
| rs758641991 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873826 | TCAGCCTCCCAAGTA[G/T]CTTGGACTATAGGCA | 92912 |
| rs758672992 | snp | C/T | 1.72101e-05 | 0.00293338 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859856 | TTAACATAATGCTTA[C/T]TTACTGAAATGTGTT | 92912 |
| rs758739713 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865804 | AATAATATCTGGTTG[-/T]TTTTTTTTTTTTTTA | 92912 |
| rs758807607 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860130 | TTGTTTGTTCTGTTT[A/T]AGGTACTAAAAATAA | 92912 |
| rs758883067 | snp | C/T | 7.51753e-05 | 0.00613041 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843750 | ATTCCGCATCGTCAG[C/T]TGGAAGCTGGACGAG | 92912 |
| rs758959527 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894308 | GACAGTGGCTTACTC[C/T]TATAATCCTAGCACT | 92912 |
| rs759040555 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847483 | TGATCTTAAATAATG[A/G]AGGGAAAAGAGTGCT | 92912 |
| rs759191298 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861067 | CTATGCATCAATTTT[A/C]CATTGGCAAAATGGG | 92912 |
| rs759257690 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890488 | TCACAAAACAGGTGA[C/T]TTTTCTTACGATACT | 92912 |
| rs759267240 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895858 | TATATATCTTTTGAC[-/A]ACAGCAGCTCTACTC | 92912 |
| rs759273873 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894217 | CCAAATCCTTGTGCC[A/G]TTAAGAAAAGAATGA | 92912 |
| rs759277244 | snp | A/G | 1.65124e-05 | 0.00287331 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859904 | ATTGAAGTGGTTGAT[A/G]TGTGAACTCTGCAGT | 92912 |
| rs759277663 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848093 | TAAGTCACTTCTTTT[A/G]CTGTGTTTCTGTGTA | 92912 |
| rs759280934 | snp | G/T | 1.65954e-05 | 0.00288053 | stop-gained, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75877975 | GGGATTTATTCAGTG[G/T]AACTCATAAATGACA | 92912 |
| rs759323671 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874391 | CAGGTTCAAGCAGTT[C/T]TCCTGCCTCACCCTC | 92912 |
| rs759347544 | snp | C/T | 5.06504e-05 | 0.00503216 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883460 | AAAAAGAAATTTTTT[C/T]CAGTTAAAAAAAATT | 92912 |
| rs759384441 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886698 | TTGAGACCAGCCTGG[C/G]CAACATGGCAAAACC | 92912 |
| rs759531359 | snp | C/T | 1.64996e-05 | 0.0028722 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859930 | GCAGTTTATATAACC[C/T]TCCTAAGCACCTGGA | 92912 |
| rs759553334 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869714 | TCTTAAAGGTCCTAC[C/T]TCTTAATAGCATCAC | 92912 |
| rs759571481 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882476 | TTAAATCATACATAA[C/T]GAAGAGGTTTTGTAG | 92912 |
| rs759589989 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868216 | TGTGTTCTAACCTGA[A/G]CTGGCCTTCATGGTT | 92912 |
| rs759636097 | snp | A/G | 1.83555e-05 | 0.00302943 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843734 | ACAAGAACCACGAGC[A/G]ATTCCGCATCGTCAG | 92912 |
| rs759689809 | snp | A/G | 1.67959e-05 | 0.00289787 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873577 | TTTAAATGTAAGTGT[A/G]TGTAGATATCTAGAA | 92912 |
| rs759708761 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897598 | CAGAATCAAGATTTC[-/T]TTTTTTTTTTTTTTT | 92912 |
| rs759723290 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855289 | TGAGGCCAGGAGTTC[A/G]AGATCAGCCTGGCCA | 92912 |
| rs759750840 | in-del | -/TCGTT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852988 | CAGTGTTTCCTAAAA[-/TCGTT]TCTGTGAAATTGTTT | 92912 |
| rs759812353 | snp | A/T | 1.66829e-05 | 0.00288811 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75896999 | TTCTCTTTCAGAATC[A/T]ATATAATCTAGCAAG | 92912 |
| rs759815590 | in-del | -/T | 3.30077e-05 | 0.00406236 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876298 | TGGATCCCTGCTCTC[-/T]TTATGATTCTTCTGC | 92912 |
| rs759880883 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845035 | ATACGTCTGAGTGTT[C/T]TGGGCACTAGTGTTG | 92912 |
| rs759883434 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890725 | TCTAATTTGCTCATG[A/T]TGGGCACTTAGAACA | 92912 |
| rs759890314 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856644 | TTGGTTTAAACACAT[C/T]TATTCTTAAGAACAG | 92912 |
| rs759922031 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877825 | AGTAGTGTAATATTT[A/G]CTATATAGCTTAGTT | 92912 |
| rs759976365 | snp | C/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843236 | GTGCGAAGAACGGAG[C/T]AGATGGGTCGGGAAC | 92912 |
| rs759980326 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845000 | TGCTGTACTGAGGAG[A/G]TAATTCATTTATTGA | 92912 |
| rs760003369 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864114 | TCTATAGTAAACACC[A/G]TTAGAATGGATATGG | 92912 |
| rs760122560 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875426 | AGAGATGTCCCTGCA[C/G]TGAAAAACTGAAACC | 92912 |
| rs760134236 | snp | C/T | 1.65201e-05 | 0.00287398 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854538 | CATGAACATTACATA[C/T]AGAAATTAAATGTTA | 92912 |
| rs760135199 | snp | A/G | 3.32414e-05 | 0.00407671 | synonymous-codon, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899443 | CTGGTACACCCCTCC[A/G]AAGGAAGATGGCTAA | 92912 |
| rs760171417 | snp | C/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841374 | AAAATAAAGCTTAGA[C/G]AGATTAAATAGCTTG | 92912 |
| rs760208931 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874569 | GATTACAGGTGTGAG[C/T]CACTGTGTCCGGCCA | 92912 |
| rs760261723 | snp | C/T | 3.31142e-05 | 0.00406891 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890462 | TGGAGGAGCATTATG[C/T]ATGGAACTTCTCACA | 92912 |
| rs760282478 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861237 | CCTCACACTTGATTG[A/G]TAGTTTGGTTGATTA | 92912 |
| rs760294814 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875554 | TAGTAAATAATGTGT[C/T]ACCTTGAGTGTCTTC | 92912 |
| rs760374953 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849281 | GCAAACTATGAAAGT[A/G]ATGTGTCCCATAACT | 92912 |
| rs760442291 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862669 | AAAAATAAAAAATTA[A/G]GTGGGTATGGTGGCA | 92912 |
| rs760452081 | snp | A/C | 1.68289e-05 | 0.00290072 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883319 | CTAAATAGTATAACA[A/C]TAAGGATGTTCTTTA | 92912 |
| rs760541320 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856961 | AAAAAAAAAAGATAT[C/T]TTAAGAGTTAAGGCT | 92912 |
| rs760548622 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850530 | CAGATTTTCTTGGCT[C/T]AGCCCACCTGACAGC | 92912 |
| rs760577589 | snp | A/G | 1.65304e-05 | 0.00287488 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883424 | CTGTTCTCTCAGGAG[A/G]GTAAGTTTAAGTGAC | 92912 |
| rs760578254 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884098 | GTAATTGTATTGCTT[A/C]TTTTTATGGTTGGAA | 92912 |
| rs760608028 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870514 | TGTGCGCCCAGTTTA[C/T]CATGAAGCAGCCATT | 92912 |
| rs760649182 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842616 | GATGATATTTGAGCT[A/G]TGAGTTTAGTGAAAA | 92912 |
| rs760726673 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869787 | AGCAAATTTAGTAGA[A/G]TGCATTCCAAAGACA | 92912 |
| rs760747464 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857086 | GGCAACATAGCAAGA[C/T]CCTCTTTCTCTCTCT | 92912 |
| rs760775861 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880102 | TTATATTTAATAAGG[-/T]TTTTTTTTTGTTTGT | 92912 |
| rs760857275 | snp | C/T | 1.67061e-05 | 0.00289011 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896992 | TGTGTAATTCTCTTT[C/T]AGAATCAATATAATC | 92912 |
| rs760860726 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75877972 | ACAGGGATTTATTCA[C/G]TGGAACTCATAAATG | 92912 |
| rs760865221 | snp | A/T | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844065 | TTCCGGCTTCTCGCC[A/T]GGGGCTGGCTTGGGG | 92912 |
| rs760893236 | snp | C/T | 0.000101683 | 0.00712959 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844512 | TGTGTATTCGTGTGG[C/T]CCCTCCCTTGTGTGT | 92912 |
| rs760921017 | snp | A/T | 1.82088e-05 | 0.00301729 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843722 | CGTCCATCTTCGACA[A/T]GAACCACGAGCGATT | 92912 |
| rs760975216 | snp | C/G | 3.58134e-05 | 0.00423148 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879073 | AACTTTTTATTTGAA[C/G]TGTTTTTTGTTTTGT | 92912 |
| rs761009308 | in-del | -/T | 3.55929e-05 | 0.00421843 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879075 | TTTTTATTTGAACTG[-/T]TTTTTTGTTTTGTAA | 92912 |
| rs761012780 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862420 | TAGTTTATTTTGGTC[-/T]TTTTTTTTTTTTAAA | 92912 |
| rs761027076 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845081 | TCGTCCTCGCTCTCA[G/T]AACTCAGTCTTCTTG | 92912 |
| rs761028084 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891970 | GATCAGGAAAGGCAT[C/G]TGTCTTTCCCTGCTG | 92912 |
| rs761060364 | snp | C/T | 0.000100487 | 0.00708757 | synonymous-codon, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844369 | ATGAGAATGGACTCG[C/T]TGACGGAGGAAAAGT | 92912 |
| rs761151289 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900142 | AGTCTTGGCTGGGCT[C/G]AATCTGCTGCTTGTT | 92912 |
| rs761207828 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852206 | CTTAAATGAAACTGA[A/C]CTTTTGTTGCCCTTC | 92912 |
| rs761242285 | in-del | -/AT | 4.95454e-05 | 0.00497697 | frameshift-variant, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859902 | CAATTGAAGTGGTTG[-/AT]ATGTGAACTCTGCAG | 92912 |
| rs761367624 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858289 | TCTCACTTACAGTGC[C/T]ATGGATATTCAAAAT | 92912 |
| rs761388140 | in-del | -/AAAG | 1.66854e-05 | 0.00288833 | frameshift-variant, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879147 | CAGATCTTAAAAGAA[-/AAAG]AAGGCATAGAATATA | 92912 |
| rs761403582 | in-del | -/CATAT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893719 | TGGTACCATACATAC[-/CATAT]AATTTAAATATGAAG | 92912 |
| rs761440878 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849346 | GAACCTTCCAGAAGT[C/T]TGTGCATCAGTTTTA | 92912 |
| rs761459967 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885267 | GGACTACAGGCGTGC[A/G]CCACCATGTCCAGCT | 92912 |
| rs761508526 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897732 | TGGTTGTTTACAGGC[A/G]TGATCATAGTGGACT | 92912 |
| rs761609612 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850595 | TTTGGTCAGGTTTTG[A/T]GTCAAGAGAGGGAGG | 92912 |
| rs761624004 | snp | A/G | 2.10795e-05 | 0.00324643 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854526 | TTCTCTTTTCCTCAT[A/G]AACATTACATATAGA | 92912 |
| rs761628637 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870696 | ATGGGAACAGGCTCA[C/G]AACAACCTTGGACAT | 92912 |
| rs761723787 | snp | C/G | 1.81836e-05 | 0.00301521 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843717 | CCTGGCGTCCATCTT[C/G]GACAAGAACCACGAG | 92912 |
| rs761765096 | in-del | -/TAG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850950 | AGCCAAAAAATAGAA[-/TAG]TAGCACAGTCTTAAA | 92912 |
| rs761776757 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866470 | AGCCACCGTGTCCGG[-/A]CCTTCAGTATTCCTA | 92912 |
| rs761777973 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858614 | GGAGGAAAATTGAAA[C/T]TCGTGGAGAGTGTAC | 92912 |
| rs761805561 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846363 | CTGCCACCGCCTCCC[C/G]AGTAGCTGGGATTAC | 92912 |
| rs761856076 | in-del | -/GTAGAGAAAGT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890070 | CATGGCTGTAACATG[-/GTAGAGAAAGT]GTAGAGAAAGTTTCA | 92912 |
| rs761869662 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859254 | TATACAGACACTTAA[G/T]AGCCTACTAAATATC | 92912 |
| rs761918322 | snp | C/G | 1.65146e-05 | 0.0028735 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891021 | GCAAATAAGGTACTT[C/G]TGTTAAGAATTTTAC | 92912 |
| rs761937788 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845217 | GGCTGAGACAGTTAG[A/G]GATGAGCTTCCACAG | 92912 |
| rs761975588 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848818 | TGATAAAGCAGGGGT[C/G]CCTTTTTCCAGATCC | 92912 |
| rs761999912 | snp | C/T | 1.64988e-05 | 0.00287213 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868939 | CCCTGGCAGATTCTT[C/T]CTCTGTTTCAGAATG | 92912 |
| rs762005845 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865701 | CAGTAATCGTTTAGA[C/T]TTCACTATTGGTGTT | 92912 |
| rs762064715 | snp | G/T | 1.70423e-05 | 0.00291905 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873378 | TTTGGCATAAGAAAC[G/T]GCTGAAGAAAAATAG | 92912 |
| rs762107703 | snp | C/T | 3.34493e-05 | 0.00408944 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877952 | CTAACATGCTCTATA[C/T]CTTAACAGGGATTTA | 92912 |
| rs762186061 | snp | A/T | 0.00011764 | 0.00766852 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896973 | TTACACTTTTGATTT[A/T]AAATGTGTAATTCTC | 92912 |
| rs762197420 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876249 | GCTCAGGGACATATA[C/T]AGATCACAGAGTTAT | 92912 |
| rs762199187 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900247 | TTCCATTTTATTAAC[A/G]GGATGTTGCAATCGT | 92912 |
| rs762268681 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853899 | TTTTATAATACCTCG[C/T]CATGTAGGTCTCTCC | 92912 |
| rs762275507 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854980 | TTTTTTCTTGATTAT[A/G]AAACTCATGAGCAAG | 92912 |
| rs762277302 | snp | G/T | 0.0873444 | 0.18985 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844490 | CGTTGCGGCAGGTGG[G/T]GTTGAGTGTGTATTC | 92912 |
| rs762281731 | in-del | -/C | 3.33195e-05 | 0.0040815 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899536 | CAAAAGCTTTGAGTG[-/C]CCCCTATTACAGCAG | 92912 |
| rs762298171 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887788 | GTGAAGTGAGGAGAA[A/C]CTACATTGGTTTGGT | 92912 |
| rs762359617 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850749 | GGCAGCAGTTCTCAA[A/C]GTTTTGGGGTCAGGA | 92912 |
| rs762373302 | snp | G/T | 0.000100954 | 0.007104 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844319 | CGCTTGTTCAGCCAA[G/T]TGTTTTTAAGTTTGC | 92912 |
| rs762426200 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895253 | CAATGGTACGATCTC[-/G]GGCTCACTGCAAACT | 92912 |
| rs762440635 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865229 | GTTACCACTTATGTA[A/T]GCATCCTTGAACAAT | 92912 |
| rs762482413 | snp | A/T | 1.76328e-05 | 0.00296919 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879078 | TTTATTTGAACTGTT[A/T]TTTGTTTTGTAATTC | 92912 |
| rs762500888 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898747 | CGCCAGGATTTTGTT[A/T]GGGGAAATAAGTACT | 92912 |
| rs762527710 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864178 | TAAGTAAGGTTATAC[G/T]TTGTTTCCTTTTAGG | 92912 |
| rs762531986 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851855 | CAGATGTAGTAAAAT[C/T]TTCACTGCTTCATCA | 92912 |
| rs762571234 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886529 | TTCAAAATCTTATTT[A/G]AGAGAAAAAAAAGAT | 92912 |
| rs762610821 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897454 | TCGATCTCCTGACTT[A/T]GTGATCCGCCCGCCT | 92912 |
| rs762659908 | snp | A/G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900120 | GTGATTTCCACTGGG[A/G/T]CATCAGAGTCTTGGC | 92912 |
| rs762728478 | snp | A/T | 1.7871e-05 | 0.00298918 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854336 | GGTTTAATTGCATAT[A/T]TGGGTTAGTCTGTAT | 92912 |
| rs762764481 | snp | A/G | 1.65526e-05 | 0.00287681 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859964 | TGAGATGCTAGATCA[A/G]CCACTACCCACGGGT | 92912 |
| rs762779851 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892595 | ATGGGTATGGTGGCT[C/T]ACGCCTGTAATCTCA | 92912 |
| rs762841540 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890967 | ATCATGCAAATAAAT[A/G]CCACCTTAGTCAAAG | 92912 |
| rs762909279 | in-del | -/T | 0.000201877 | 0.0100448 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844321 | TTGTTCAGCCAATTG[-/T]TTTTTAAGTTTGCGT | 92912 |
| rs763011075 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893817 | ACACACTTGTAAATC[A/G]TAGTTTTAAAAAGTA | 92912 |
| rs763020587 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847913 | GCTGTTTGCTAGGCT[A/G]CTTTTAGTGGGACTT | 92912 |
| rs763124607 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854130 | GAGGTGATGGTGATC[A/G]GGGCCATTTTAGAGG | 92912 |
| rs763156406 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867029 | ACCCTTGATCAGTAT[A/C]CATTGTTGACCTGAG | 92912 |
| rs763313644 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867995 | AGATTTAAAGGAAAT[A/G]CAAGTTAATTCTGCA | 92912 |
| rs763317118 | in-del | -/GG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874230 | CGTGAAGCTGACTTT[-/GG]GGTCTGTCCTGCTCT | 92912 |
| rs763323361 | snp | C/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842582 | CTATTTGAAATGGGT[C/T]GTGGTGGGGGGTGCC | 92912 |
| rs763365409 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855211 | AAAAACATTTACTGG[A/C]CAGGTGTGGTGGCTC | 92912 |
| rs763381690 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841659 | AGTGCTGGGGTCATG[A/G]ATCCCCATAAGTACA | 92912 |
| rs763421692 | snp | A/G | 1.68709e-05 | 0.00290434 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877939 | AAATGAAGAGTAGCT[A/G]ACATGCTCTATATCT | 92912 |
| rs763429315 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875828 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGACCAC | 92912 |
| rs763482192 | snp | A/G | 0.000122302 | 0.00781894 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843806 | AGCAGGGCAGCCCGC[A/G]CTCGCTGCCGCCGCC | 92912 |
| rs763486443 | snp | C/T | 1.7829e-05 | 0.00298566 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854345 | GCATATTTGGGTTAG[C/T]CTGTATGTAAATGTT | 92912 |
| rs763538479 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853828 | ATGTTGGCAGGATTC[A/G]TCTCACAGGCTGTGG | 92912 |
| rs763575942 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876228 | TTCAGATAGACTTAT[C/G]AAAGAGCTCAGGGAC | 92912 |
| rs763590356 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890527 | ACCCACAATTTAGTG[G/T]TTTGATCATGTAAAT | 92912 |
| rs763598017 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896142 | GCCAGGGACAGTGGC[A/T]AATAACAGTGGGCTG | 92912 |
| rs763677413 | snp | C/G | 3.70824e-05 | 0.00430579 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879229 | TATACTTCCAGTGGG[C/G]TGCGTATATTTGTAC | 92912 |
| rs763767289 | snp | C/T | 1.75108e-05 | 0.0029589 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879081 | ATTTGAACTGTTTTT[C/T]GTTTTGTAATTCTTA | 92912 |
| rs763772537 | in-del | -/AAAAA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878601 | GGCACCCGGTCTCTT[-/AAAAA]AAAAAAAAAAAAAAA | 92912 |
| rs763797643 | snp | A/G | 1.65438e-05 | 0.00287605 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854432 | TTGTGGATTCTGAAG[A/G]CCCAAATCTGACATC | 92912 |
| rs763804375 | snp | A/G | 1.64953e-05 | 0.00287182 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868929 | TTCTGTATAGCCCTG[A/G]CAGATTCTTTCTCTG | 92912 |
| rs763833207 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848621 | ATGAAGAGAAGACTT[A/G]GGTTTCCCTTTTGTG | 92912 |
| rs763833231 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862702 | TGCCTGTAGTCCCAG[C/G]TACTCAAGAGGCTAA | 92912 |
| rs763838844 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897697 | CAGATGGAGTTCTTG[C/T]TGTTATAACTGGAGT | 92912 |
| rs763939976 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857224 | CCAGCAAGGGGGTTG[A/T]TGGGAAAGAGTGGTA | 92912 |
| rs763966537 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889872 | CATCCCCAGAAGTTA[C/T]CTTTTGTTCAGAGAA | 92912 |
| rs764027730 | snp | A/T | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844125 | TAGCCCCGAGGGGGG[A/T]GTCCGCGGCGGCCCA | 92912 |
| rs764177498 | snp | C/G | 1.64781e-05 | 0.00287033 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890978 | AAATGCCACCTTAGT[C/G]AAAGGCAAAGCCAGA | 92912 |
| rs764183151 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858482 | TTCTCTGACCCCCGC[A/C]CCCCGCAAACTAGTA | 92912 |
| rs764247146 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879525 | TGGACTCCAAAACCT[A/G]TTTTGTACAATTCCC | 92912 |
| rs764277034 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842706 | AACAAGGCAAAATAA[A/G]GAAAGGGGGGAGAGA | 92912 |
| rs764300691 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876339 | TGTCAGATTATAAAT[A/G]TCATTTCTTAAAACT | 92912 |
| rs764317362 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880112 | ATAAGGTTTTTTTTT[-/G]TTTGTTTGTTTGTTT | 92912 |
| rs764412484 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865643 | ATTTTTAGTGCATCA[A/G]TATGGTCAGAGAATA | 92912 |
| rs764421447 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876238 | CTTATGAAAGAGCTC[A/G]GGGACATATACAGAT | 92912 |
| rs764480114 | in-del | -/TC | 1.64988e-05 | 0.00287213 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868939 | CCCTGGCAGATTCTT[-/TC]TCTGTTTCAGAATGG | 92912 |
| rs764488792 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851028 | ATTTAATTTGTTGTA[A/T]GCTATTTGCTTGAAA | 92912 |
| rs764509740 | in-del | -/TCTCAGAGTCAGAATC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897575 | CACTTGGCCTAGGTA[-/TCTCAGAGTCAGAATC]AAGATTTCTTTTTTT | 92912 |
| rs764513081 | snp | C/T | 1.70069e-05 | 0.00291602 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873602 | CTAGAACCTGGACTT[C/T]TGTGGTTAAATAATT | 92912 |
| rs764576585 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852337 | CATTGTATCTGCACC[C/G]TTACAGCATATGTCA | 92912 |
| rs764590574 | in-del | -/TTTAAGGTAAGAAAATAG | 1.70857e-05 | 0.00292276 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879183 | TTGCTTAACTTCTCT[-/TTTAAGGTAAGAAAATAG]TTACAGGACCCCATA | 92912 |
| rs764593986 | snp | C/G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900229 | TACTAAGTCATCTTA[C/G/T]GTTTCCATTTTATTA | 92912 |
| rs764604782 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864039 | TTTTTCATGATTGTG[C/T]CCACGATTCTGTATA | 92912 |
| rs764680844 | in-del | -/G | 3.34169e-05 | 0.00408746 | frameshift-variant, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879119 | CCCTGATAGTCCTTT[-/G]CACAGTGATCTTCAG | 92912 |
| rs764718038 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887005 | TAGAGACAAATATTT[C/T]ATGCATAATGCCATT | 92912 |
| rs764742410 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861024 | CTACTTACTGGCTGT[A/G]TGCCCTTGGGCTGAT | 92912 |
| rs764751211 | snp | C/T | 0.000100487 | 0.00708757 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844373 | GAATGGACTCGTTGA[C/T]GGAGGAAAAGTTGGA | 92912 |
| rs764793745 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849397 | AAGATAGCTGTGTCC[A/T]ACATTTGGAAAGATA | 92912 |
| rs764892867 | snp | C/T | 1.773e-05 | 0.00297736 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879076 | TTTTTATTTGAACTG[C/T]TTTTTGTTTTGTAAT | 92912 |
| rs764893233 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870050 | TTAGAATGCTTCAGA[A/G]CTAAAGAAGCAGTGT | 92912 |
| rs764966564 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885293 | CAGCTAATTTTTGTG[G/T]TTTTAGTGGAGATGG | 92912 |
| rs764998674 | snp | A/C | 1.65015e-05 | 0.00287237 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859940 | TAACCTTCCTAAGCA[A/C]CTGGATGTTGAGATG | 92912 |
| rs765055259 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880809 | TCTGGATGAGATGTA[A/G]TGGTTTAAAATCTGT | 92912 |
| rs765066027 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857723 | AAATAAAAATCATAG[C/T]GTATAGTTTTATAAT | 92912 |
| rs765080262 | snp | C/T | 1.66563e-05 | 0.0028858 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890489 | CACAAAACAGGTGAC[C/T]TTTCTTACGATACTC | 92912 |
| rs765086621 | snp | C/T | 3.47802e-05 | 0.00417 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859852 | CTCTTTAACATAATG[C/T]TTATTTACTGAAATG | 92912 |
| rs765101560 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845292 | AGGAAACTCCACCCA[A/G]AGAAGACACGGAGAT | 92912 |
| rs765143346 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876986 | ACATGGCGAGCGAAG[C/G]CCCATCTCTACTAAA | 92912 |
| rs765212835 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891218 | TCACTTAATGATTTC[A/G]TATCTGTTTTTAGTC | 92912 |
| rs765225398 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879744 | AAAATTCCATGGAGC[-/A]GGGGGGTAAAACTAG | 92912 |
| rs765242021 | in-del | -/TG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898444 | TGAAGTATACATAAC[-/TG]TGGAATGACTAAATC | 92912 |
| rs765296818 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892447 | TGTGAGAAAATAGTT[A/G]TATGTGAAATCTAAT | 92912 |
| rs765322535 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846387 | GGATTACAGGTTTCC[A/G]CCGCCACACCCGGCT | 92912 |
| rs765382926 | snp | A/C | 1.72231e-05 | 0.0029345 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883466 | AAATTTTTTTCAGTT[A/C]AAAAAAATTTTTTTT | 92912 |
| rs765390586 | snp | A/G | 1.68451e-05 | 0.00290211 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843804 | GCAGCAGGGCAGCCC[A/G]CACTCGCTGCCGCCG | 92912 |
| rs765391786 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866868 | TTACTGCTAAAGATC[A/C]CAATTAGGTTTTAAA | 92912 |
| rs765414921 | snp | C/T | 5.54749e-05 | 0.00526634 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843741 | CCACGAGCGATTCCG[C/T]ATCGTCAGTTGGAAG | 92912 |
| rs765459444 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879566 | GTTCAAAAATAGGTA[A/C]AACTAATGTTGATTA | 92912 |
| rs765482320 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865709 | GTTTAGACTTCACTA[C/T]TGGTGTTACTGCTGT | 92912 |
| rs765500645 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852665 | CTAAAAACTAAAACA[C/G]TAAAAATGGTCCAGA | 92912 |
| rs765554507 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880856 | TTGATGGAAAAAGCA[A/G]TACTTCCTTTGTACT | 92912 |
| rs765556655 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846011 | ACTATCAGGAGATAA[C/T]TATCATGGCAGCTGC | 92912 |
| rs765582583 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887060 | GTTTCTTAATTGATT[C/G]TTTTTTGCCACAGTG | 92912 |
| rs765599047 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873586 | AAGTGTGTGTAGATA[C/T]CTAGAACCTGGACTT | 92912 |
| rs765602638 | snp | C/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873464 | TATGAGATGAAGGAA[C/G]AAGAGCCTATTAGTG | 92912 |
| rs765609658 | snp | A/C/T | 3.36736e-05 | 0.00410315 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873583 | TGTAAGTGTGTGTAG[A/C/T]TATCTAGAACCTGGA | 92912 |
| rs765687117 | snp | A/G | 1.66768e-05 | 0.00288758 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75897000 | TCTCTTTCAGAATCA[A/G]TATAATCTAGCAAGA | 92912 |
| rs765709434 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887809 | TTGGTTTGGTAGTCA[A/T]GGGAGTGGAAGGAGG | 92912 |
| rs765792519 | snp | G/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841392 | ATTAAATAGCTTGTT[G/T]AGGGAATTTTGTTTC | 92912 |
| rs765797422 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874579 | GTGAGCCACTGTGTC[C/T]GGCCACAACTTAATA | 92912 |
| rs765968391 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876250 | CTCAGGGACATATAC[A/G]GATCACAGAGTTATA | 92912 |
| rs765978909 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897201 | ACTTGTGCTGCATAC[A/G]AAATCTTTATTTATT | 92912 |
| rs766026233 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864254 | TTACATCTTTTTTCC[A/T]AAGATCTAGGGTGTA | 92912 |
| rs766028650 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849830 | GAGTGGTGCTAGAAG[C/T]ACTTAAACATTCTAT | 92912 |
| rs766057535 | snp | A/C | 1.66643e-05 | 0.0028865 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854463 | AGTTCTGGAACGTCT[A/C]GAAGATACTAAGAAC | 92912 |
| rs766066318 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873064 | GTTTCTTAGAATACA[A/G]TTCTAGAAGTTGAGT | 92912 |
| rs766112752 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883422 | ACCTGTTCTCTCAGG[A/G]GGGTAAGTTTAAGTG | 92912 |
| rs766120570 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886545 | AGAGAAAAAAAAGAT[A/C]AAGGAAAAGATTTGG | 92912 |
| rs766159686 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893888 | AATTACTAAAATTCT[A/G]TCTATTCCTTTCTCC | 92912 |
| rs766218663 | snp | A/G | 1.67913e-05 | 0.00289748 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883325 | AGTATAACACTAAGG[A/G]TGTTCTTTAAATTAA | 92912 |
| rs766224112 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846392 | ACAGGTTTCCGCCGC[C/T]ACACCCGGCTAATTT | 92912 |
| rs766247631 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881157 | AAAAACAAAACACAC[A/C]AAAAAGGAAGGTATC | 92912 |
| rs766252716 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892609 | TCACGCCTGTAATCT[C/T]AACACTTTGGGAGGC | 92912 |
| rs766306102 | in-del | -/TTG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891128 | TCATTTTCATTTGGT[-/TTG]TTTTCTTCTTGTTAC | 92912 |
| rs766352188 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879718 | CAGATATACGATTTA[C/T]CTATGGTGTTAAAAT | 92912 |
| rs766514333 | in-del | -/CA | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900123 | TTTCCACTGGGGCAT[-/CA]CAGAGTCTTGGCTGG | 92912 |
| rs766545751 | snp | C/T | 2.41929e-05 | 0.00347791 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843644 | TCCCCTTCCGCGCCC[C/T]TCCCGCCGGAGATGA | 92912 |
| rs766620866 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854156 | AGAGGCTGCCTACCA[G/T]TGTTGAAGAAAATCA | 92912 |
| rs766621648 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887885 | TCTTCATAGTCAACT[A/C]TTAAGTGAGGAGGAG | 92912 |
| rs766647378 | in-del | -/CT | 0.000100588 | 0.00709113 | frameshift-variant, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844419 | CTGTTTGAGCGACCC[-/CT]CTCCCCCGGGCCTGG | 92912 |
| rs766672110 | snp | C/T | 1.82493e-05 | 0.00302065 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843726 | CATCTTCGACAAGAA[C/T]CACGAGCGATTCCGC | 92912 |
| rs766692853 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868060 | ATCCAGAAGAGTTCT[A/G]ATACCCTCTGTGATC | 92912 |
| rs766703945 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874705 | GCTAGACAGTACATA[C/T]CTTTTGGATGATTGC | 92912 |
| rs766738526 | snp | A/G/T | 5.00691e-05 | 0.00500325 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75896996 | TAATTCTCTTTCAGA[A/G/T]TCAATATAATCTAGC | 92912 |
| rs766779560 | in-del | -/TGAT | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900287 | AATAAACTTATAAAG[-/TGAT]TGGCACAAAGACTCC | 92912 |
| rs766914961 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863143 | TTGCCTATCTGTCCC[A/G]CTTTCTGGGGTACCT | 92912 |
| rs766956744 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883907 | ATAAAAAAGCTAATG[-/T]TTTCAAATGTAAATT | 92912 |
| rs767076775 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859954 | ACCTGGATGTTGAGA[G/T]GCTAGATCAACCACT | 92912 |
| rs767078872 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846843 | TTTTTACACACGTGC[A/T]TGCTAGTTCCTGAAG | 92912 |
| rs767103823 | snp | A/C | 3.30371e-05 | 0.00406417 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899506 | TGCTTTAAAGAAAAT[A/C]TTTCTAACATGCAGA | 92912 |
| rs767121094 | snp | A/G | 0.000151033 | 0.00868871 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854527 | TCTCTTTTCCTCATG[A/G]ACATTACATATAGAA | 92912 |
| rs767139269 | snp | C/G | 1.66073e-05 | 0.00288156 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854455 | CTGACATCAGTTCTG[C/G]AACGTCTAGAAGATA | 92912 |
| rs767187845 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894230 | CCATTAAGAAAAGAA[A/T]GAAAATGAATCAAGC | 92912 |
| rs767189193 | snp | C/T | 1.70487e-05 | 0.0029196 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879093 | TTTTGTTTTGTAATT[C/T]TTAGGGTTGACCCTG | 92912 |
| rs767222055 | snp | C/T | 2.71713e-05 | 0.00368577 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843636 | CGCCCGGCTCCCCTT[C/T]CGCGCCCCTCCCGCC | 92912 |
| rs767256791 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853302 | TGGTGAAACCCCGTC[C/T]CTAATAAAAATACAA | 92912 |
| rs767348981 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882489 | AATGAAGAGGTTTTG[C/T]AGTCACTCATTAGGG | 92912 |
| rs767365341 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868243 | GGTTAAAGATGCATG[C/T]ATAAACAGTGTCCTG | 92912 |
| rs767391110 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881215 | TCCTTATGCCTAACA[C/T]CAAACTTAAGAAATA | 92912 |
| rs767430617 | in-del | -/T | 6.61441e-05 | 0.00575045 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876316 | ATGATTCTTCTGCTC[-/T]TTTCTATTGTCAGAT | 92912 |
| rs767439149 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886858 | ATAGGGCGAGAGTCC[A/G]TCTCAAATTTTTTTT | 92912 |
| rs767483100 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867319 | CTGTAGATGGGACAA[C/G]TACAGTAAAGAATGT | 92912 |
| rs767594318 | snp | A/G | 1.69697e-05 | 0.00291283 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873397 | GAAGAAAAATAGGTT[A/G]AATAAGCTAACATTT | 92912 |
| rs767613935 | snp | C/T | 1.65045e-05 | 0.00287263 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868948 | ATTCTTTCTCTGTTT[C/T]AGAATGGGACAACAG | 92912 |
| rs767651478 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890742 | GGGCACTTAGAACAT[G/T]GGTTTGTTGTTTTTT | 92912 |
| rs767659128 | in-del | -/AG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872560 | TTTTTTTTTTGAGAT[-/AG]AGTCTTGCTCTGTCA | 92912 |
| rs767745872 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876349 | TAAATGTCATTTCTT[A/G]AAACTGGACAGAAAT | 92912 |
| rs767774952 | snp | A/G | 3.30907e-05 | 0.00406746 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891029 | GGTACTTCTGTTAAG[A/G]ATTTTACATAAACCA | 92912 |
| rs767813244 | in-del | -/AT | 5.25362e-05 | 0.00512497 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854365 | ATGTAAATGTTTAAC[-/AT]GTGTCTCTGTGTTAA | 92912 |
| rs767813830 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899995 | TGTTAAACTTTTTAA[C/T]GACTATGTGAAGATA | 92912 |
| rs767819855 | snp | A/C | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841937 | GCTAAGGACTATAAC[A/C]TGATACAAAATCTCA | 92912 |
| rs767843375 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844967 | AGGTGTGTTAATTTC[-/A]AAAAAAAAAAAGACA | 92912 |
| rs767863287 | snp | C/G | 1.6825e-05 | 0.00290038 | upstream-variant-2KB, splice-donor-variant | UBE2Q2 | GRCh38.p7 | 15:75843847 | CACTGCAACATCACG[C/G]TGAGGCGCCCGGCCG | 92912 |
| rs767992490 | snp | A/G | 1.66771e-05 | 0.00288761 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877957 | ATGCTCTATATCTTA[A/G]CAGGGATTTATTCAG | 92912 |
| rs768006607 | in-del | -/A | 8.35778e-05 | 0.00646389 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897075 | TGGTATGTTTAATTC[-/A]ATAAGTGTTTATTGC | 92912 |
| rs768010263 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864235 | AGGGGTGACTTGGAA[A/C]GCTTTACATCTTTTT | 92912 |
| rs768025050 | in-del | -/TA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853492 | AAGAAAAAAAAATTA[-/TA]TATATATATATATAT | 92912 |
| rs768076051 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897994 | AGCAGAAGAGAGAAA[C/T]GATAAAATTTGAGGA | 92912 |
| rs768080264 | snp | C/T | 1.69378e-05 | 0.00291009 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890529 | CCACAATTTAGTGTT[C/T]TGATCATGTAAATTA | 92912 |
| rs768086749 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850774 | TCAGGACTCCTTTAC[A/G]CTCTTGAAAATATAT | 92912 |
| rs768093366 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875637 | GTTATTGTGGAATCC[A/G]TGGTGGTCTGGACAT | 92912 |
| rs768165982 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898769 | ATAAGTACTTTCCAT[A/G]AGGCTTACTTTCAAG | 92912 |
| rs768177552 | snp | C/T | 3.63042e-05 | 0.00426038 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843711 | GAAGTTCCTGGCGTC[C/T]ATCTTCGACAAGAAC | 92912 |
| rs768254473 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890461 | GTGGAGGAGCATTAT[A/G]TATGGAACTTCTCAC | 92912 |
| rs768258365 | snp | C/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842068 | GATTAGGAAGAAAGA[C/G]ACAGGTGTCAGGGTT | 92912 |
| rs768271605 | in-del | -/T | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875384 | TATTTAGTCTTATGA[-/T]TAAGATATTGATGTG | 92912 |
| rs768276066 | in-del | -/AA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855489 | AGTGATACTCCATCT[-/AA]CAAAAAAAAAAAAAA | 92912 |
| rs768342162 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876982 | GCCAACATGGCGAGC[A/G]AAGCCCCATCTCTAC | 92912 |
| rs768386689 | snp | A/T | 1.65258e-05 | 0.00287448 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883374 | TTTTTAGGATAACTT[A/T]CCATTTGATCCTCCA | 92912 |
| rs768435929 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863862 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTTGT | 92912 |
| rs768487140 | snp | C/T | 3.09181e-05 | 0.00393168 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869050 | GTTCATAAATTTCTT[C/T]ATTTTTGAACATTTG | 92912 |
| rs768503573 | snp | C/T | 1.68323e-05 | 0.00290101 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896967 | ACCTAATTACACTTT[C/T]GATTTAAAATGTGTA | 92912 |
| rs768516583 | snp | A/G | 8.26426e-05 | 0.00642763 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873500 | AAGTCAGAGGATGAA[A/G]GAATTGAAAAAGAAA | 92912 |
| rs768529480 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850546 | AGCCCACCTGACAGC[C/T]AATCACTGGAAATGG | 92912 |
| rs768576877 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885193 | GGCGTGATCTCAGCT[C/T]ACTGCAACCTCTGCC | 92912 |
| rs768596969 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886267 | TGGGACTATAGGCAT[A/G]CGCCACCATGCCCAG | 92912 |
| rs768597024 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870516 | TGCGCCCAGTTTACC[A/G]TGAAGCAGCCATTGT | 92912 |
| rs768619480 | snp | A/C | 3.02055e-05 | 0.00388611 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843618 | GGCCCGGCTCCCCTT[A/C]CGCGCCCGGCTCCCC | 92912 |
| rs768677651 | in-del | -/TT | 1.6612e-05 | 0.00288196 | frameshift-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873439 | TAGGATATAGAAGAC[-/TT]TTAGATCACTATGAG | 92912 |
| rs768683073 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872258 | AAACCCAAAAAGGAG[G/T]CCTATTGAATGGATA | 92912 |
| rs768701045 | in-del | -/AA | 3.62483e-05 | 0.00425709 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843697 | CTCAAGGCCGAGCTG[-/AA]GTTCCTGGCGTCCAT | 92912 |
| rs768729131 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859117 | AATGAACACCATACT[C/T]GTGCACATGATTTAC | 92912 |
| rs768762256 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849276 | GAACAGCAAACTATG[-/A]AAGTAATGTGTCCCA | 92912 |
| rs768793684 | snp | C/G | 0.000101333 | 0.0071173 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844306 | TTTTCCTTCTTCCCG[C/G]TTGTTCAGCCAATTG | 92912 |
| rs768813580 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882765 | TGCTTAAAAAATGAG[A/G]TGATTAAAGCTGGCT | 92912 |
| rs768831458 | in-del | -/TT | 0.000506286 | 0.0159024 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899403 | AAGAATTATTTTAAC[-/TT]TTTTTTTTTCATTCT | 92912 |
| rs768835505 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899798 | TAGGGTAACTTTCCT[A/G]TATTGAGCCCATGGG | 92912 |
| rs768923101 | in-del | -/ATA | | | cds-indel, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899908 | AAGGCCTTCTAAATC[-/ATA]ATAGCTCTTTCATGT | 92912 |
| rs768963484 | snp | C/T | 1.66538e-05 | 0.00288559 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854402 | AATCCTATCCATCTT[C/T]TTCACCGATATGGTT | 92912 |
| rs768963863 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851706 | CTTTCAAGTAAAAAT[A/G]GTATTCCATTTAAGT | 92912 |
| rs768981782 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860261 | GCTCTTGCTTCTTTC[A/G]TAGTTTGTCTTTGGT | 92912 |
| rs768998083 | in-del | -/AGTT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893701 | AGACGATTTAAAAAC[-/AGTT]GGTACCATACATACC | 92912 |
| rs769049844 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867801 | AATGCTCTTTCAATC[A/G]TTGATGCAACCAAAC | 92912 |
| rs769076438 | snp | A/G | | | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901447 | AGGACAACTCCAGGT[A/G]CTGTACATCTGGGCT | 92912 |
| rs769108594 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880713 | ACCATCTTGGCCAGG[A/C]TGGTTTTGAACTCCT | 92912 |
| rs769112520 | snp | G/T | 1.68111e-05 | 0.00289918 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877944 | AAGAGTAGCTAACAT[G/T]CTCTATATCTTAACA | 92912 |
| rs769156828 | snp | A/C/T | 8.78239e-05 | 0.0066261 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860023 | AAGAGCTAAATAAAT[A/C/T]GTCTCAAGCAAAAGT | 92912 |
| rs769187300 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894487 | TACTCAGGAGGCTGA[A/G]GTAGGAGAATTCCTT | 92912 |
| rs769251139 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879135 | CACAGTGATCTTCAG[A/C]TCTTAAAAGAAAAAG | 92912 |
| rs769324616 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894538 | GCAGTGAGCTGAGAT[-/C]CAGCCACTGCACTCT | 92912 |
| rs769365213 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897067 | GAGAAAAATGGTATG[C/T]TTAATTCAATAAGTG | 92912 |
| rs769458445 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865136 | GAAGGAACATTGCTC[A/G]CACTACAGAAACCTT | 92912 |
| rs769482354 | snp | C/T | 3.63412e-05 | 0.00426254 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843690 | GTCAGGGCTCAAGGC[C/T]GAGCTGAAGTTCCTG | 92912 |
| rs769482404 | in-del | -/AATTGAGTTG | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900039 | GAAGATAATACTCTT[-/AATTGAGTTG]TATTGTACTTCTTAG | 92912 |
| rs769495581 | in-del | -/TATA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856270 | GTGTGTGTGTGTGTG[-/TATA]TATATATATATATAT | 92912 |
| rs769550947 | snp | C/T | 1.64768e-05 | 0.00287021 | stop-gained, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890958 | GAATCGGTCATCATG[C/T]AAATAAATGCCACCT | 92912 |
| rs769552050 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851852 | ATTCAGATGTAGTAA[A/C]ATTTTCACTGCTTCA | 92912 |
| rs769610753 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863615 | TACGGCCAGCTGATA[C/T]TTTATAAACATCTAT | 92912 |
| rs769652174 | snp | A/T | 0.000100669 | 0.00709398 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844447 | CTGGCTGCGCGCTGC[A/T]GTGTTCTGGAAAGGA | 92912 |
| rs769683625 | snp | A/T | 1.64933e-05 | 0.00287165 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868917 | TGTGCATATTTGTTC[A/T]GTATAGCCCTGGCAG | 92912 |
| rs769736407 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859256 | TACAGACACTTAAGA[A/G]CCTACTAAATATCAA | 92912 |
| rs769755831 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887405 | ACATAGGTGAAAAGT[A/G]AACACAATCAGTTAT | 92912 |
| rs769757879 | in-del | -/T | 5.92522e-05 | 0.00544267 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899385 | AGTTCTTCTAATTTA[-/T]TTAAGAATTATTTTA | 92912 |
| rs769806617 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864898 | TAAACAAACATGTAA[-/G]GGGTATACATTTTCT | 92912 |
| rs769826360 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860562 | ATCACTAATTATCAT[G/T]AGGACTTTGTAGAGT | 92912 |
| rs769886766 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847746 | CATTACTCCTTTTAT[A/G]GACTTTTTGGCATCT | 92912 |
| rs769941370 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852264 | AAGAATACCATGACT[A/G]CTAGTAGTTTGGTGT | 92912 |
| rs770010084 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870532 | TGAAGCAGCCATTGT[A/G]CTAAAGTTCATGAAC | 92912 |
| rs770054185 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883091 | GTTACCTAGTCTATC[A/G]TTATTGGAATGGTTC | 92912 |
| rs770134168 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894889 | TTTCTTTTATTTTTG[A/T]CCTTTTTGTGAAAGT | 92912 |
| rs770152732 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882111 | GTAAGTCAAATTACA[A/G]AGAGGTGATTTTCAA | 92912 |
| rs770154435 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867842 | TTTTAGGCTAGGTAT[A/G]TAGTCTTTAGATACC | 92912 |
| rs770178068 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869386 | ATTTTAGGGACTACT[C/T]GCCAGAAGTAGTGAA | 92912 |
| rs770225483 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889062 | AAATCTAAATGAGTA[C/G]CTGGATCTTCTAATT | 92912 |
| rs770242412 | snp | A/C/T | 3.35555e-05 | 0.00409595 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883330 | AACACTAAGGATGTT[A/C/T]TTTAAATTAATTAAA | 92912 |
| rs770293759 | snp | C/T | 1.93845e-05 | 0.00311318 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854513 | AAGCCAAGCTATTTT[C/T]TCTTTTCCTCATGAA | 92912 |
| rs770297816 | snp | C/T | 1.67128e-05 | 0.00289069 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890406 | AATAATTCTCGAGAA[C/T]TTTGTATGACTCCTT | 92912 |
| rs770305260 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855147 | ATATACCTTTATACA[C/T]GTGTTTAAATAGTTG | 92912 |
| rs770354012 | snp | C/T | 3.30044e-05 | 0.00406216 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859921 | GTGAACTCTGCAGTT[C/T]ATATAACCTTCCTAA | 92912 |
| rs770426629 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854887 | CTGTAAGTCTGCAGT[A/G]AAAGAATAGAAAGTT | 92912 |
| rs770428989 | snp | C/T | 4.94287e-05 | 0.00497111 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890947 | CCTACTCAATAGAAT[C/T]GGTCATCATGCAAAT | 92912 |
| rs770458833 | snp | C/T | 1.64909e-05 | 0.00287144 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868901 | TCTAATGTACTCAGC[C/T]TGTGCATATTTGTTC | 92912 |
| rs770524912 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867025 | ATATACCCTTGATCA[C/G]TATCCATTGTTGACC | 92912 |
| rs770544338 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854603 | TATAATCTTGTAGGA[A/G]TTAAAGACTAGTTTG | 92912 |
| rs770568576 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866089 | CTATCTCATTCTTAA[-/T]TCTTTCTGTGTATTT | 92912 |
| rs770583567 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853299 | GCATGGTGAAACCCC[A/G]TCTCTAATAAAAATA | 92912 |
| rs770587265 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874368 | AGCTCACTGCAGCTT[C/T]CACCTCCCAGGTTCA | 92912 |
| rs770614382 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900121 | TGATTTCCACTGGGG[A/C]ATCAGAGTCTTGGCT | 92912 |
| rs770670266 | in-del | -/AAAA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878602 | GCACCCGGTCTCTTA[-/AAAA]AAAAAAAAAAAAAAA | 92912 |
| rs770702537 | snp | A/G | | | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901343 | ATCCTTAGTTCCCCC[A/G]GTGAAAATAATCTGC | 92912 |
| rs770746517 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860870 | TGGCTGACCCTTTCT[C/T]ATTTTGCCTGACTAT | 92912 |
| rs770805093 | snp | A/G | 1.65932e-05 | 0.00288034 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890478 | ATGGAACTTCTCACA[A/G]AACAGGTGACTTTTC | 92912 |
| rs770806805 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888252 | GTCACTCCCTGTACC[C/T]GTTTCCCCCACCATT | 92912 |
| rs770849544 | snp | C/T | 1.73087e-05 | 0.00294177 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843857 | TCACGGTGAGGCGCC[C/T]GGCCGCGGCCCCGCG | 92912 |
| rs770850933 | in-del | -/CAGA | 1.64893e-05 | 0.0028713 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876152 | TAAATCTTAGCTCAG[-/CAGA]CAGACCCTGGTAAAC | 92912 |
| rs770859720 | snp | G/T | 1.65053e-05 | 0.0028727 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876299 | GGATCCCTGCTCTCT[G/T]TATGATTCTTCTGCT | 92912 |
| rs770867886 | snp | C/T | 0.000133233 | 0.0081608 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843798 | GGTGCCGCAGCAGGG[C/T]AGCCCGCACTCGCTG | 92912 |
| rs770875667 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875183 | TACTTTATACTTCAC[A/G]TATCTTCACATTTAG | 92912 |
| rs770954640 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849254 | CGTTCTCCACCCCAC[A/G]TTTATTGAACAGCAA | 92912 |
| rs770956797 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896526 | TGGTGACAATTATGG[G/T]CATTCTTTAGATTTC | 92912 |
| rs770963572 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862234 | GTGGTTCATTGAGGA[C/T]CAACTCCCAAGATGA | 92912 |
| rs770964927 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855771 | CAACTTAGATGTGCA[C/T]GACTTTTATCAAGAA | 92912 |
| rs771040901 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883743 | GTGAAGTTGATGCTG[C/T]TGTTCTGGGGCCCAC | 92912 |
| rs771045063 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888239 | GTACTGATTAGCAGT[C/T]ACTCCCTGTACCCGT | 92912 |
| rs771104890 | snp | A/G | 1.78395e-05 | 0.00298654 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899415 | AACTTTTTTTTTTTC[A/G]TTCTATTTCAGGCTG | 92912 |
| rs771178211 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852694 | GATGGTGTATTCCCA[A/G]TGTGTGCTGAAGAAT | 92912 |
| rs771190221 | snp | A/G | 1.65869e-05 | 0.00287979 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854412 | ATCTTCTTCACCGAT[A/G]TGGTTTGTGGATTCT | 92912 |
| rs771234120 | snp | C/G | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876205 | GCAGTGTCTGGGTCA[C/G]TGCAAGCTTCAGATA | 92912 |
| rs771280744 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869591 | TGTTGCATCCTCACA[C/T]GGTAGAAGGCAGAAG | 92912 |
| rs771317262 | snp | G/T | 3.32491e-05 | 0.00407719 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883347 | TTAAATTAATTAAAC[G/T]TGCTTATTTGCTTTT | 92912 |
| rs771370696 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870313 | ACCTCAAGTGATCCA[C/G]CACTGGCCTCCCAAA | 92912 |
| rs771385151 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856433 | AAATGTTGTATACTA[A/C]CTCTGTTCCAGACAG | 92912 |
| rs771439049 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877630 | TTATAAAACAACATA[C/T]GTAGAAGGATTCCAT | 92912 |
| rs771450186 | snp | C/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842698 | GCTTGGGAAACAAGG[C/T]AAAATAAGGAAAGGG | 92912 |
| rs771488224 | snp | A/G | 1.65135e-05 | 0.00287341 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883407 | TGTTCGAGTGGTGTT[A/G]CCTGTTCTCTCAGGA | 92912 |
| rs771505219 | snp | C/T | 1.72276e-05 | 0.00293487 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854485 | ACTAAGAACAACAAT[C/T]TGGTAAGAAAATAAG | 92912 |
| rs771528820 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854684 | TCCCACATGTATAAC[C/T]TTAATTTAGATTACA | 92912 |
| rs771546730 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857963 | CACAATTAAGAAAAA[C/T]TGGCTTCTGTGTCAG | 92912 |
| rs771587281 | snp | A/G | 1.65564e-05 | 0.00287714 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890459 | GGGTGGAGGAGCATT[A/G]TGTATGGAACTTCTC | 92912 |
| rs771650390 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870349 | GGGATTATAGACATA[C/T]AGACATGCGCCACTG | 92912 |
| rs771690182 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855978 | AGGTTGCTTGAGCTC[A/T]TGAGTTTAAGACCAG | 92912 |
| rs771754698 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888344 | TATAAATAGAATCAT[A/G]TAAAATGTGGCTTTT | 92912 |
| rs771806725 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856499 | AAATGAGAATTTAGT[A/G]TAAGGTAAAGGTGGT | 92912 |
| rs771867446 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875482 | AGTGTCTTAATGTGC[C/G]AACTAGACCATCTGT | 92912 |
| rs771870437 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849273 | ATTGAACAGCAAACT[A/G]TGAAAGTAATGTGTC | 92912 |
| rs771904078 | snp | A/G | 6.6433e-05 | 0.00576299 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873552 | TTAGGAAGACTCAAA[A/G]GCAAGACCATTTAAA | 92912 |
| rs771944412 | snp | C/T | 2.16626e-05 | 0.00329102 | upstream-variant-2KB, stop-gained, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843793 | TTCCTGGTGCCGCAG[C/T]AGGGCAGCCCGCACT | 92912 |
| rs771978087 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876191 | TTGTGTTTCAGGGTG[C/T]AGTGTCTGGGTCAGT | 92912 |
| rs772102587 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863816 | CTCGGCTAATTTTTT[A/G]TATTTTTTAGTAGAG | 92912 |
| rs772104279 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850422 | TTACTCCTTACGTGT[A/G]GGCAAGATGAATTCT | 92912 |
| rs772151723 | snp | C/T | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841435 | CAACTTCTCAAGAGT[C/T]TGTTGCTCTTTGTCT | 92912 |
| rs772156143 | snp | C/T | 4.98277e-05 | 0.00499113 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854408 | ATCCATCTTCTTCAC[C/T]GATATGGTTTGTGGA | 92912 |
| rs772257924 | snp | A/G | 8.39553e-05 | 0.00647847 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896975 | ACACTTTTGATTTAA[A/G]ATGTGTAATTCTCTT | 92912 |
| rs772285737 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848074 | TAGTAGTTAGGAGCT[A/T]AAGTAAGTCACTTCT | 92912 |
| rs772287354 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859229 | TTCCTAGTGAATTAT[C/T]GTTATTTTTTATACA | 92912 |
| rs772334041 | in-del | -/T | 0.00478848 | 0.0486961 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899403 | AAGAATTATTTTAAC[-/T]TTTTTTTTTTCATTC | 92912 |
| rs772370196 | snp | G/T | 1.70603e-05 | 0.0029206 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897109 | TTAAGAAGTTTTAGA[G/T]AATGTATTAATACTT | 92912 |
| rs772434648 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858307 | GGATATTCAAAATGA[C/T]GACGTTTAAATTTGC | 92912 |
| rs772454915 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893414 | CAATTTTTGTATTTT[A/G]TGTACCTATCAGAAT | 92912 |
| rs772524596 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891896 | GGGAATGGTAGTTGA[C/G]TTAAATAGTGAAATC | 92912 |
| rs772584709 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865302 | TGTATGTATTTTTTC[A/G]TACCTTTGTTGTGCT | 92912 |
| rs772590071 | snp | A/G | 1.75225e-05 | 0.00295989 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879199 | TTAAGGTAAGAAAAT[A/G]GTTACAGGACCCCAT | 92912 |
| rs772618790 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879447 | GAATTGTGGTGTTTA[-/T]AAAGTGGTTTACAGC | 92912 |
| rs772667000 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865203 | CTCATCTTTCCTTAC[A/G]TTTCTCTAGTGTTAC | 92912 |
| rs772676262 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879145 | TTCAGATCTTAAAAG[A/G]AAAAGAAGGCATAGA | 92912 |
| rs772681381 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846050 | AATGTCTGCTAACTT[C/T]TTATTATGGAAAATC | 92912 |
| rs772757205 | in-del | -/CA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891918 | AGTGAAATCCTGGAG[-/CA]CACAGTCTTTAGGGC | 92912 |
| rs772827339 | snp | A/T | 6.9791e-05 | 0.00590683 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854533 | TTCCTCATGAACATT[A/T]CATATAGAAATTAAA | 92912 |
| rs772931800 | snp | C/G | 1.81836e-05 | 0.00301521 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843720 | GGCGTCCATCTTCGA[C/G]AAGAACCACGAGCGA | 92912 |
| rs773154769 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893701 | AGACGATTTAAAAAC[A/G]GTTGGTACCATACAT | 92912 |
| rs773156054 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846390 | TTACAGGTTTCCGCC[A/G]CCACACCCGGCTAAT | 92912 |
| rs773183098 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875897 | AATCCCGTCTCTACC[-/A]AAAAAAAAAAATACA | 92912 |
| rs773198143 | snp | C/T | 1.65151e-05 | 0.00287355 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883413 | AGTGGTGTTACCTGT[C/T]CTCTCAGGAGGGTAA | 92912 |
| rs773323985 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847752 | TCCTTTTATGGACTT[G/T]TTGGCATCTGGGCAT | 92912 |
| rs773351342 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883119 | TTCCTTTATATAGTT[A/C]TAGTGAAGTGGAACC | 92912 |
| rs773380150 | in-del | -/TACT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897120 | TAGATAATGTATTAA[-/TACT]TACCATTTTATTTTT | 92912 |
| rs773407065 | in-del | -/C | 1.82553e-05 | 0.00302115 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843729 | CTTCGACAAGAACCA[-/C]GAGCGATTCCGCATC | 92912 |
| rs773437730 | in-del | -/AC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885801 | TGTTTAGAATTGTGT[-/AC]AGTTTTCTTTTGTTA | 92912 |
| rs773516791 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882226 | ATGGCTAAGATGTTA[A/G]GATCTCAGATAACTT | 92912 |
| rs773563427 | snp | C/G | 1.66579e-05 | 0.00288595 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873559 | GACTCAAAGGCAAGA[C/G]CATTTAAATGTAAGT | 92912 |
| rs773578669 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899356 | AGAGACTGTAGCTAA[C/T]CTTATTACATGCCAG | 92912 |
| rs773581881 | snp | G/T | 3.36768e-05 | 0.00410333 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873410 | TTGAATAAGCTAACA[G/T]TTTTCGTCTCTTTGT | 92912 |
| rs773611179 | snp | A/G | 1.76558e-05 | 0.00297113 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879203 | GGTAAGAAAATAGTT[A/G]CAGGACCCCATATAC | 92912 |
| rs773664817 | snp | C/T | 1.88113e-05 | 0.00306681 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879056 | TAAAAAAAAAAATCT[C/T]TAACTTTTTATTTGA | 92912 |
| rs773826598 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851997 | TCTGCCTCAGCCTCC[C/G]TAGTAGCTGGGACTA | 92912 |
| rs773912815 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853338 | TAGCTTGGCGTGGTG[A/G]CATGTGCTTGTTATC | 92912 |
| rs773984802 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900124 | TTTCCACTGGGGCAT[C/T]AGAGTCTTGGCTGGG | 92912 |
| rs773998623 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886748 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGGTGCCT | 92912 |
| rs774002482 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867285 | TAGGGTTCCTATATA[A/G]GAGAGTGATCCTTAC | 92912 |
| rs774047636 | snp | C/T | 1.86855e-05 | 0.00305653 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879230 | ATACTTCCAGTGGGG[C/T]GCGTATATTTGTACA | 92912 |
| rs774064801 | snp | C/T | 0.000199475 | 0.00998487 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869060 | TTCTTCATTTTTGAA[C/T]ATTTGAGTAATTCTC | 92912 |
| rs774094996 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897627 | TTAGTAGATTAATGA[A/G]TGACTCACTTTACTT | 92912 |
| rs774116003 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895527 | GTTGAAAAAGACTAC[C/T]CTGTAGAAAAATAGG | 92912 |
| rs774147256 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886275 | TAGGCATGCGCCACC[A/G]TGCCCAGCTAATTTT | 92912 |
| rs774170325 | snp | C/T | 1.65168e-05 | 0.00287369 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883387 | TTTCCATTTGATCCT[C/T]CATTTGTTCGAGTGG | 92912 |
| rs774175382 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849265 | CCACATTTATTGAAC[A/G]GCAAACTATGAAAGT | 92912 |
| rs774214821 | snp | C/T | 1.81358e-05 | 0.00301124 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843714 | GTTCCTGGCGTCCAT[C/T]TTCGACAAGAACCAC | 92912 |
| rs774218891 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848051 | AAGTGAGAAGTTTAG[C/G]TTTTATTTAGTAGTT | 92912 |
| rs774274204 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860910 | TAAAACCCTAAGAAA[A/G]CATGGAGGAGTACAT | 92912 |
| rs774358661 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875245 | TTCATATTTTAGAGA[C/T]AGGAAAAACTTCTCA | 92912 |
| rs774378391 | snp | A/G | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873503 | TCAGAGGATGAAGGA[A/G]TTGAAAAAGAAAATT | 92912 |
| rs774398179 | in-del | -/G | 0.0001007 | 0.00709505 | frameshift-variant, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844460 | GCTGTGTTCTGGAAA[-/G]GAGCATAGTACCGTC | 92912 |
| rs774432630 | snp | A/T | 1.68105e-05 | 0.00289914 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896971 | AATTACACTTTTGAT[A/T]TAAAATGTGTAATTC | 92912 |
| rs774463514 | snp | G/T | 0.101265 | 0.200943 | splice-donor-variant, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844487 | CGTCGTTGCGGCAGG[G/T]GGTGTTGAGTGTGTA | 92912 |
| rs774494944 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852729 | AGAAGAAAATGCAGT[A/G]CTCAATAAGTGGTGT | 92912 |
| rs774636766 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868130 | CTAATAACAGATGCT[C/T]AGATACTGCCGAGAC | 92912 |
| rs774647955 | snp | A/G | 1.64906e-05 | 0.00287142 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75891006 | AGAGTGCAGTTTGGA[A/G]CAAATAAGGTACTTC | 92912 |
| rs774648075 | in-del | -/GT | 1.64846e-05 | 0.0028709 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876162 | GCTCAGCAGACCCTG[-/GT]AAACAGTGGCTTTTG | 92912 |
| rs774740974 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856610 | CTGATTTTTGTCAAA[A/G]TAAGTTATAGTTGTA | 92912 |
| rs774773977 | snp | A/G | 0.000302954 | 0.0123039 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844318 | CCGCTTGTTCAGCCA[A/G]TTGTTTTTAAGTTTG | 92912 |
| rs774786597 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891783 | AGGACATTAGTGAGA[C/T]AGCCTTCCAAAGCCG | 92912 |
| rs774860644 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844949 | ACCAGACTATCTGGG[A/C]AGAAGGTGTGTTAAT | 92912 |
| rs774871252 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888651 | GTAATTTAATACAGA[A/G]GTAGAATCGGCCACT | 92912 |
| rs774900305 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858005 | ATTGAGTATAAAAGA[A/C]AAGGCATGTCCCTGT | 92912 |
| rs775019381 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856941 | CAAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAG | 92912 |
| rs775147568 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874552 | GCCTCCCGAAGTGCT[C/G]GGATTACAGGTGTGA | 92912 |
| rs775192077 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890961 | TCGGTCATCATGCAA[A/G]TAAATGCCACCTTAG | 92912 |
| rs775237590 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875535 | TATGAATGGAACTCT[A/G]TTTTAGTAAATAATG | 92912 |
| rs775250477 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895954 | CAAAATATTGAGAAA[C/T]CCTGATGTCCACCAA | 92912 |
| rs775267252 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893307 | CATTAACTAGAAACA[A/C]ATGATGCAGCTTTAG | 92912 |
| rs775281059 | snp | C/T | 1.79806e-05 | 0.00299833 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879214 | AGTTACAGGACCCCA[C/T]ATACTTCCAGTGGGG | 92912 |
| rs775342878 | snp | A/G | 2.54806e-05 | 0.00356927 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869042 | AAAGAAGAGTTCATA[A/G]ATTTCTTCATTTTTG | 92912 |
| rs775369352 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884037 | GACCTATGGAACTGG[A/C]TAATTACTCCTAGAG | 92912 |
| rs775401577 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862612 | ACTTGAGCCCAAGAG[G/T]TAAGACCAGCCTGGG | 92912 |
| rs775421244 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849277 | AACAGCAAACTATGA[A/C]AGTAATGTGTCCCAT | 92912 |
| rs775478816 | snp | A/C | 1.69525e-05 | 0.00291135 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843805 | CAGCAGGGCAGCCCG[A/C]ACTCGCTGCCGCCGC | 92912 |
| rs775491635 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863842 | TAGAGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 92912 |
| rs775523500 | snp | C/T | 1.6857e-05 | 0.00290314 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896961 | ATTTTCACCTAATTA[C/T]ACTTTTGATTTAAAA | 92912 |
| rs775645240 | in-del | -/T/TT | 0.172732 | 0.237884 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899402 | AAGAATTATTTTAAC[-/T/TT]TTTTTTTTTTTCATT | 92912 |
| rs775653896 | in-del | -/GA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876446 | GGAGTAAAATAGGAT[-/GA]GTTTACTTGTCTTTT | 92912 |
| rs775690857 | snp | A/G | 1.70985e-05 | 0.00292386 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877916 | ACCATAGTAATAGTT[A/G]TATGATGAAATGAAG | 92912 |
| rs775693381 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891953 | TTCTGACCTATTTCT[A/G]TGATCAGGAAAGGCA | 92912 |
| rs775709245 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870447 | AGAGTTTAATGTTTT[C/T]ATGCAGTTTAGCTTA | 92912 |
| rs775711448 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858407 | ACAAAATGAAATAAT[C/T]AAACTAGTCACCCAT | 92912 |
| rs775737987 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890842 | GCTGCTGTTGAGTTA[G/T]ATACCATTTTGTTAG | 92912 |
| rs775764452 | snp | A/C/G/T | 0.000150353 | 0.00866942 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890497 | AGGTGACTTTTCTTA[A/C/G/T]GATACTCCATTTTCA | 92912 |
| rs775809531 | snp | A/G | 0.00016862 | 0.0091805 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843891 | CAGGGCGAGGACGGA[A/G]AGGGGGCGCTTCGAG | 92912 |
| rs775830288 | in-del | -/GGT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845113 | GGAAGAGTTCAATAA[-/GGT]GGTGACAGCTCCTGT | 92912 |
| rs775859186 | snp | C/T | 4.9423e-05 | 0.00497082 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876227 | CTTCAGATAGACTTA[C/T]GAAAGAGCTCAGGGA | 92912 |
| rs775876616 | in-del | -/T | 1.66988e-05 | 0.00288949 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878051 | AATGCTCACCCACTC[-/T]TTGCAATGGTAGACT | 92912 |
| rs775931658 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865487 | CTGTGATCATTCTTG[C/G]TTGTATTTCATGGTA | 92912 |
| rs776018151 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880465 | AGAATAGCAATGGAA[C/T]CTAGAAAAAATGTTA | 92912 |
| rs776051013 | snp | A/G | 1.64928e-05 | 0.00287161 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868907 | GTACTCAGCCTGTGC[A/G]TATTTGTTCTGTATA | 92912 |
| rs776071365 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877504 | AACAGATACTGGGTG[G/T]AATTTGTTAAAGCAT | 92912 |
| rs776081685 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863916 | GAGTGCTGGGATTAC[A/G]GGGGTGAGCCACTGC | 92912 |
| rs776095031 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890549 | CATGTAAATTAGATT[G/T]TAAGTAGAAAATTCT | 92912 |
| rs776112487 | snp | A/C | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842102 | TAACTCTAGGTAAGA[A/C]TGGAAAAGGAAAATG | 92912 |
| rs776183889 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875804 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 92912 |
| rs776338436 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862740 | GGATCAGTTGAGCCT[A/G]TGAGGTTAAGGCTGC | 92912 |
| rs776447570 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850567 | CTGGAAATGGGGTGG[A/G]CTGGTAGAGTCCTTT | 92912 |
| rs776504703 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886268 | GGGACTATAGGCATG[C/T]GCCACCATGCCCAGC | 92912 |
| rs776504773 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870668 | AGAAGATATTCTAGG[C/T]TCCTAAAATAATATG | 92912 |
| rs776560432 | snp | C/G | 1.66233e-05 | 0.00288295 | splice-donor-variant, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890484 | CTTCTCACAAAACAG[C/G]TGACTTTTCTTACGA | 92912 |
| rs776608944 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851717 | AAATGGTATTCCATT[C/T]AAGTGGTTAATTCAC | 92912 |
| rs776629131 | snp | C/G | 1.65004e-05 | 0.00287227 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859929 | TGCAGTTTATATAAC[C/G]TTCCTAAGCACCTGG | 92912 |
| rs776681271 | in-del | CACACACACACAC/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883841 | ATGTATTTATACATA[CACACACACACAC/T]ACACACACACACGTA | 92912 |
| rs776693180 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893590 | AGGCATGGTATAATA[A/G]ACAAATATAGACCTC | 92912 |
| rs776751293 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847665 | GCAGCTTGTTTTAAG[C/T]AGCCTTATTGGGAGC | 92912 |
| rs776868534 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892249 | ACTTTTTGTAGGAAA[A/G]CATCTCTAATTTAAG | 92912 |
| rs776875484 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879536 | ACCTATTTTGTACAA[G/T]TCCCTTTATATACAG | 92912 |
| rs776887394 | snp | A/G | 1.67804e-05 | 0.00289653 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873575 | CATTTAAATGTAAGT[A/G]TGTGTAGATATCTAG | 92912 |
| rs776929388 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866781 | GGGGTGGAGGGGATC[C/T]TATTTTTACTTTCTA | 92912 |
| rs776930429 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876206 | CAGTGTCTGGGTCAG[A/T]GCAAGCTTCAGATAG | 92912 |
| rs776956838 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893577 | ACAACCAGTGAACAG[C/G]CATGGTATAATAGAC | 92912 |
| rs776986667 | snp | A/G | 3.3552e-05 | 0.00409571 | missense, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899427 | TTCATTCTATTTCAG[A/G]CTGGTACACCCCTCC | 92912 |
| rs777031882 | snp | G/T | 1.76911e-05 | 0.0029741 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854492 | ACAACAATTTGGTAA[G/T]AAAATAAGCCAAGCT | 92912 |
| rs777067273 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899848 | ATTGTTCCATTTACA[A/G]CCAATACAGGTTTAA | 92912 |
| rs777139045 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867806 | TCTTTCAATCGTTGA[C/T]GCAACCAAACTCTTT | 92912 |
| rs777145514 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854899 | AGTAAAAGAATAGAA[A/G]GTTTTATTTTTGTTT | 92912 |
| rs777206393 | in-del | -/C | 1.81655e-05 | 0.0030137 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899413 | TAACTTTTTTTTTTT[-/C]CATTCTATTTCAGGC | 92912 |
| rs777229842 | in-del | -/AAA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878603 | CACCCGGTCTCTTAA[-/AAA]AAAAAAAAAAAAAAA | 92912 |
| rs777233369 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893079 | TCCCAGGAGGAGATA[C/T]TAGAATTACACTAGA | 92912 |
| rs777237120 | snp | C/T | | | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901466 | TACATCTGGGCTTTG[C/T]TCTGCTTCCTTGAGA | 92912 |
| rs777297003 | in-del | -/CAGAACTAGAGGT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850484 | TGATTCCAGATCTCC[-/CAGAACTAGAGGT]CTAGCTTCAGGGAAA | 92912 |
| rs777321252 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894277 | GGACAATAAAAAAAA[C/T]CTGAAGGAGGCCAGG | 92912 |
| rs777326072 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867531 | ATAAAATTCTGTCAT[C/T]TCAGTGGGGTTTTGA | 92912 |
| rs777348860 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848568 | TTTATGCTCCCTCAT[-/C]CCCCATTTTTATACC | 92912 |
| rs777413331 | snp | C/T | 0.000100568 | 0.00709042 | synonymous-codon, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844422 | TTTGAGCGACCCCTC[C/T]CCCCCGGGCCTGGCT | 92912 |
| rs777450771 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884080 | GTTTATTAGGGTCAA[A/T]TGGTAATTGTATTGC | 92912 |
| rs777469821 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847300 | GCAGAGATAACATCA[A/G]TAACTTGTCATGGAT | 92912 |
| rs777503824 | snp | C/T | 1.64923e-05 | 0.00287156 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890916 | TACTTTGTTCTTCTG[C/T]AGGGCTGGAGCAGTG | 92912 |
| rs777751057 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855650 | GGTTGAAAGCTCTGT[C/T]ACATAAAAGTCAATA | 92912 |
| rs777758016 | snp | A/G | 6.59065e-05 | 0.00574012 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876193 | GTGTTTCAGGGTGCA[A/G]TGTCTGGGTCAGTGC | 92912 |
| rs777760863 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876527 | TTGATAAACAGTGAA[C/G]TCTTACATGATTTTT | 92912 |
| rs777795212 | snp | C/T | 1.71211e-05 | 0.00292579 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859858 | AACATAATGCTTATT[C/T]ACTGAAATGTGTTTT | 92912 |
| rs777805879 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896473 | GCTCCTTAAAAAGAT[G/T]GTATATTTTTATCAA | 92912 |
| rs777874653 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861971 | TGTTTCTTCATCTGG[A/C]CTTTCTCTCTGCATA | 92912 |
| rs777880734 | snp | A/G | 1.64977e-05 | 0.00287203 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876292 | GATCTCTGGATCCCT[A/G]CTCTCTTTATGATTC | 92912 |
| rs777891630 | snp | A/G | 1.69804e-05 | 0.00291374 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854479 | GAAGATACTAAGAAC[A/G]ACAATTTGGTAAGAA | 92912 |
| rs777925388 | in-del | -/AG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899257 | TCCAGCCTAGGTAAC[-/AG]AGTGAAACTCTGTCT | 92912 |
| rs778062393 | snp | A/G | 7.91985e-05 | 0.0062923 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843662 | CCGCCGGAGATGAGG[A/G]GAAGATGTCCGTGTC | 92912 |
| rs778167434 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898179 | GAGCTTAGGTTTTTG[C/T]GGAACCTGGGACACA | 92912 |
| rs778258855 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881830 | CACTTTTTGGTGTTT[C/T]GGGCAGCATCTGAAT | 92912 |
| rs778271570 | snp | A/T | 1.66646e-05 | 0.00288652 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883342 | GTTCTTTAAATTAAT[A/T]AAACTTGCTTATTTG | 92912 |
| rs778344721 | snp | C/G | 1.99475e-05 | 0.00315806 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843777 | CGAGCTGCACTGCCA[C/G]TTCCTGGTGCCGCAG | 92912 |
| rs778355748 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870280 | CTGTTTTGTCCAGGT[G/T]CATCTCGTGAACTCC | 92912 |
| rs778365718 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866643 | CTTACATCTCTTCTG[-/T]TTTCTCCCCCATCTC | 92912 |
| rs778457434 | snp | A/G | 2.44879e-05 | 0.00349905 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843828 | GCCGCCGCCACTCAC[A/G]CTCCACTGCAACATC | 92912 |
| rs778541436 | snp | C/T | 1.64953e-05 | 0.00287182 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876289 | AAGGATCTCTGGATC[C/T]CTGCTCTCTTTATGA | 92912 |
| rs778543520 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882866 | GGGCCTGTCCTCGGT[A/G]GACGCTGAGCTCCAG | 92912 |
| rs778566580 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855872 | AAATATGTCACTTAT[C/T]GCCATGTCTTCATAT | 92912 |
| rs778640436 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870803 | AGAAAAGGCAGATGG[-/T]TTAAAAGTCTTGAAT | 92912 |
| rs778641907 | snp | A/G | 1.66974e-05 | 0.00288936 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890410 | ATTCTCGAGAATTTT[A/G]TATGACTCCTTTTTT | 92912 |
| rs778648982 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876176 | GGTAAACAGTGGCTT[C/T]TGTGTTTCAGGGTGC | 92912 |
| rs778655956 | in-del | -/GAA | 0.000116889 | 0.007644 | cds-indel, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75868987 | ACTTCAGAAGAAGAG[-/GAA]GAAGAAGAAGAGATG | 92912 |
| rs778795216 | snp | C/G | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844145 | GCGGCGGCCCAAGCC[C/G]TTGTGGGGTCCATGG | 92912 |
| rs778801708 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875451 | AAACCAGTCGCATGT[-/A]AGGCAGATGTTTCTC | 92912 |
| rs778831812 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888267 | CGTTTCCCCCACCAT[G/T]GATCCTGGCAACCTC | 92912 |
| rs778922016 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889962 | CCATTTGATTCTCAC[A/G]ACAGAATGGGTAAAA | 92912 |
| rs778924933 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898523 | TGAGACACTTTACAT[C/T]CACTCTTAACATTTT | 92912 |
| rs778929410 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863606 | ACATGTCACTACGGC[C/T]AGCTGATATTTTATA | 92912 |
| rs778941495 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885067 | ACCTGACACCTGCAA[A/C]CTAATCTTTGCCATA | 92912 |
| rs778960944 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873182 | TGGCTTATTTGGTAA[C/T]AGTTATGATTTTGTA | 92912 |
| rs778988536 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851306 | CATGTTGCCTAGGCT[G/T]CTTTTTTGATGCTCT | 92912 |
| rs778993915 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895483 | CCACCGTGCCTGGCC[A/G]GCTTTACTATTTTAA | 92912 |
| rs779012615 | snp | A/G | 0.000117532 | 0.00766498 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879163 | AAGAAGGCATAGAAT[A/G]TATTTTGCTTAACTT | 92912 |
| rs779015785 | snp | A/G | 1.66382e-05 | 0.00288424 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899532 | GCAGACAAAAGCTTT[A/G]AGTGCCCCTATTACA | 92912 |
| rs779028226 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878190 | AGCTGTTGCTGAGGT[C/T]TAATAAGAAAGTGAG | 92912 |
| rs779034816 | in-del | -/AGAATTATTTTAACT | 0.000114995 | 0.00758185 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899389 | CTTCTAATTTATTTA[-/AGAATTATTTTAACT]TTTTTTTTTTCATTC | 92912 |
| rs779050616 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870125 | CAGGCTGGAGTGCAG[C/T]AGTGTGATCACGGCT | 92912 |
| rs779085156 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850289 | GAATTTTGTATCTTT[C/G]CAGTTATCTGCTCAT | 92912 |
| rs779201306 | snp | A/G | 1.74136e-05 | 0.00295067 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75869000 | AGGAAGAAGAAGAAG[A/G]GATGGCTGAAGTAGG | 92912 |
| rs779306958 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886021 | CCACCAGTCTTTTAC[C/T]AGCCACCAAGTCATA | 92912 |
| rs779396485 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872167 | GGGGAGGTGAAGGCT[G/T]CAGTGAGCCGAGATC | 92912 |
| rs779470523 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857757 | TATTCTGTTGTAGGC[-/A]AAAAAAAAAAAAAAT | 92912 |
| rs779507056 | snp | C/T | 1.81158e-05 | 0.00300958 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843704 | CCGAGCTGAAGTTCC[C/T]GGCGTCCATCTTCGA | 92912 |
| rs779517777 | snp | C/T | 2.20359e-05 | 0.00331926 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843651 | CCGCGCCCCTCCCGC[C/T]GGAGATGAGGGGAAG | 92912 |
| rs779580597 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856089 | CTACTGAGGAGGCTG[A/T]GGTGGGAGGATTGCT | 92912 |
| rs779599112 | snp | A/G | 1.65405e-05 | 0.00287576 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873481 | AGAGCCTATTAGTGG[A/G]AAAAAGTCAGAGGAT | 92912 |
| rs779664211 | in-del | -/AC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881151 | AAAACAAAAAACAAA[-/AC]ACACAAAAAAGGAAG | 92912 |
| rs779673975 | snp | A/G | 1.66054e-05 | 0.00288139 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899519 | ATCTTTCTAACATGC[A/G]GACAAAAGCTTTGAG | 92912 |
| rs779684662 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891420 | CCTGGTAAGCTTTTA[C/T]GTGCTAGGCTCTAGT | 92912 |
| rs779687421 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844697 | ATTAAGTTTCTCCAT[A/G]AAAGTGTATCGTGAA | 92912 |
| rs779743732 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857798 | TTTCCATAAGAGCAT[C/G]TGCAGATTTCTAAGA | 92912 |
| rs779789289 | snp | A/G | 1.6684e-05 | 0.00288821 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897066 | TGAGAAAAATGGTAT[A/G]TTTAATTCAATAAGT | 92912 |
| rs779820998 | in-del | -/A | 1.71434e-05 | 0.0029277 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883466 | AAATTTTTTTCAGTT[-/A]AAAAAAATTTTTTTT | 92912 |
| rs779926785 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898686 | CTTGTCATTGTGAAA[C/T]GACGTTATGGCTCCG | 92912 |
| rs779964598 | snp | C/T | 3.35576e-05 | 0.00409606 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854391 | TGTTAAACAGGAATC[C/T]TATCCATCTTCTTCA | 92912 |
| rs779965922 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876801 | CTCTAACTAGAGGTA[A/C]AATTCTCATATTGTT | 92912 |
| rs780048602 | snp | A/C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852856 | TTATTGACCAGGTAT[A/C/G]CTATTAATGATGTCC | 92912 |
| rs780053703 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878492 | GCTACTGGGGGTGGT[A/G]GGAGGCTGAGGCAGG | 92912 |
| rs780080284 | snp | C/T | 0.00010069 | 0.0070947 | synonymous-codon, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844449 | GGCTGCGCGCTGCTG[C/T]GTTCTGGAAAGGAGC | 92912 |
| rs780089554 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899571 | GAAGATGTTAGTTAA[C/T]AGATATTTTAGTGGA | 92912 |
| rs780160271 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859076 | TCCCATTTGAGTCAC[A/G]TTATACATTGAAAAA | 92912 |
| rs780172496 | snp | C/T | 1.68724e-05 | 0.00290446 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878069 | GCAATGGTAGACTAT[C/T]ACAGTGGAGGTTATT | 92912 |
| rs780172656 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865965 | TACACAGATAATGCT[C/T]CCTGTCTTGATGGAG | 92912 |
| rs780175379 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886180 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAC | 92912 |
| rs780193113 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887185 | ATACCAAAGCCAGCT[A/G]TATAAGAGGGGATTA | 92912 |
| rs780235829 | in-del | -/TGAT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862852 | AAAGGACTGAAAGAC[-/TGAT]TGGGAGTTCTTTGTG | 92912 |
| rs780305926 | in-del | -/TTC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851130 | AGATAATCCTGGATA[-/TTC]TTCTTTTTTTTTTTT | 92912 |
| rs780341160 | snp | C/T | 1.65362e-05 | 0.00287538 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890888 | AATCAGAAATACTAC[C/T]GTATTTTAGAGATAC | 92912 |
| rs780401908 | in-del | -/TGGGCAGCCCTAGCTCCA | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842635 | GTTTAGTGAAAATAG[-/TGGGCAGCCCTAGCTCCA]TGGGGGTGTGGGTGG | 92912 |
| rs780500228 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846580 | GCTTGTTCATGTCGA[C/T]ACCATTTGCTTAGAA | 92912 |
| rs780619180 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844849 | GTTTTTAACTCCCTT[C/T]GGTTGAGTCAGTGGG | 92912 |
| rs780692002 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847541 | CTTTTCTGTGAAGCC[A/G]TGATATGAAAGATTG | 92912 |
| rs780710204 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848819 | GATAAAGCAGGGGTC[C/T]CTTTTTCCAGATCCT | 92912 |
| rs780714035 | in-del | -/CC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881272 | GTGGCCCCCTGTGTG[-/CC]CCCCTCCCTTGTCAC | 92912 |
| rs780726400 | snp | C/T | 1.68917e-05 | 0.00290613 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896947 | AATTTATTGTAATAA[C/T]TTTCACCTAATTACA | 92912 |
| rs780737608 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879906 | TTACATACAGGTTAG[A/G]GTAAGGAGTCCATCT | 92912 |
| rs780761077 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892731 | CTAAAAAAACAATTA[A/G]CTGGGTATGGGGTAC | 92912 |
| rs780772899 | snp | C/G | | | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844453 | GCGCGCTGCTGTGTT[C/G]TGGAAAGGAGCATAG | 92912 |
| rs780803745 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878073 | TGGTAGACTATCACA[C/G]TGGAGGTTATTTTCC | 92912 |
| rs780840048 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878888 | AGATTTAGAGTATTA[C/T]GGTCTCTTTTGGACA | 92912 |
| rs780850741 | snp | A/G | 2.14618e-05 | 0.00327573 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869024 | AAGTAGGTATTTTAT[A/G]TAAAAGAAGAGTTCA | 92912 |
| rs780921801 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864986 | ATTCCATCATTTGTT[C/T]ACATTGCCATACTAT | 92912 |
| rs780943865 | in-del | -/AGTC | 1.65343e-05 | 0.00287521 | frameshift-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873486 | CTATTAGTGGGAAAA[-/AGTC]AGAGGATGAAGGAAT | 92912 |
| rs781050596 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899077 | ACCAGCCTGACCAAC[A/C]TGGTGAAACCCTGTC | 92912 |
| rs781100761 | snp | C/G | 0.000100609 | 0.00709184 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844429 | GACCCCTCTCCCCCG[C/G]GCCTGGCTGCGCGCT | 92912 |
| rs781101881 | snp | A/G | 1.67108e-05 | 0.00289052 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878054 | GCTCACCCACTCTTT[A/G]CAATGGTAGACTATC | 92912 |
| rs781132450 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75901026 | GCATCAAGTTTATGA[A/G]TAAAGAACCATTTAA | 92912 |
| rs781185915 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888066 | TTCTTGACATAGCCA[A/G]ACATTTTTTAAATTA | 92912 |
| rs781193956 | snp | C/T | 1.66228e-05 | 0.0028829 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859975 | ATCAACCACTACCCA[C/T]GGGTCAGGTAAAGTA | 92912 |
| rs781208382 | snp | A/T | 1.65067e-05 | 0.00287282 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876301 | ATCCCTGCTCTCTTT[A/T]TGATTCTTCTGCTCT | 92912 |
| rs781224030 | snp | C/T | 1.69516e-05 | 0.00291127 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854383 | TGTCTCTGTGTTAAA[C/T]AGGAATCCTATCCAT | 92912 |
| rs781281478 | snp | A/G | 3.32138e-05 | 0.00407502 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854409 | TCCATCTTCTTCACC[A/G]ATATGGTTTGTGGAT | 92912 |
| rs781424915 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861627 | TGAGTCTTGTATCTC[A/G]TATTATTTCTAAATT | 92912 |
| rs781494964 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883015 | GGTGTTCCCTTTTCT[G/T]AGCCTTGAAATTATT | 92912 |
| rs781670591 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881951 | AGATTGATTGTATTC[C/G]GTGTCCTAGGATAGC | 92912 |
| rs781676043 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894508 | AGAATTCCTTGAACC[C/G]AGGAGGTGAAGGTTG | 92912 |
| rs781705136 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854641 | TTTTTCCTTCAAATT[C/T]TATTTACTACCTGGT | 92912 |
| rs781771907 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884837 | TATTTTTGGTAGAGA[C/T]GGTGTTTTGCCATAT | 92912 |
| rs781773130 | snp | A/G | 3.3493e-05 | 0.00409211 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890401 | GGAGGAATAATTCTC[A/G]AGAATTTTGTATGAC | 92912 |
| rs796074860 | in-del | -/TTAATC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893211 | TAAAATCCAGCTGTT[-/TTAATC]TATATATTTAAAATA | 92912 |
| rs796109982 | in-del | CACACACACAC/TAT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883843 | TATTTATACATACAC[CACACACACAC/TAT]CACACACACACGTAT | 92912 |
| rs796174241 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876520 | CCTCTTCTTGATAAA[C/T]AGTGAACTCTTACAT | 92912 |
| rs796188574 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850621 | GGAGGAGGAAAGATG[A/G]GAGGGAGGTAGCAAA | 92912 |
| rs796190747 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881033 | TTGTGGTTGTCAACT[-/G]GGTTGTCTTCCTAAA | 92912 |
| rs796226200 | in-del | -/TATAGTTG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856624 | AATAAGTTATAGTTG[-/TATAGTTG]GTTTAAACACATCTA | 92912 |
| rs796329151 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75843045 | CGCGCCGAGCGCCAA[A/G]CTGAGGAGCCGCCCC | 92912 |
| rs796350680 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886137 | TTAGttttttttttt[-/T]gagacagagtctcac | 92912 |
| rs796356866 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887334 | AGATCCCAGCTGGGC[A/G]GTGAAATGTGAGTGT | 92912 |
| rs796643709 | in-del | -/GTTTTTC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872895 | GTTTTTCATTTTAAA[-/GTTTTTC]GTTACAGGAGAAATT | 92912 |
| rs796686784 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889019 | AACTCATCAACCGAT[G/T]ATTAAGCTTTCAGCA | 92912 |
| rs796698970 | in-del | AC/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877893 | GCTATTTAGTGTATA[AC/T]TTTATACCATAGTAA | 92912 |
| rs796750949 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855615 | GGAACCAACTGAAAA[A/G]AAGAGTTTTTAAGAT | 92912 |
| rs796754775 | in-del | -/AC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883840 | CATGTATTTATACAT[-/AC]ACACACACACACACA | 92912 |
| rs796790081 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889180 | GAAATAGAATACACA[-/C]AAAAAAAATTTAATC | 92912 |
| rs796802086 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863646 | ATCACCTGGCCAGTC[-/T]TTTTTTTTTTTTTCT | 92912 |
| rs796837497 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888224 | TCAAAAAGAAACCCC[A/G]TACTGATTAGCAGTC | 92912 |
| rs796946462 | in-del | A/TT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860453 | TTACCTATTTATTTT[A/TT]TTTTACTATAATACA | 92912 |