SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs701537 | snp | A/T | 0.474992 | 0.108989 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386017 | TGAAATGGGATGGAG[A/T]AGAACAACAGCAGGC | 337867 |
rs723090 | snp | C/T | 0.431916 | 0.171483 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364851 | CAAATGCCCATCAAC[C/T]ATAGAATGGGTAAGT | 337867 |
rs727263 | snp | A/G | 0.299267 | 0.245097 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351854 | TGCCCGGTGTTAACT[A/G]GTTGATTATCACCTC | 337867 |
rs731150 | snp | A/G | 0.308414 | 0.24308 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355296 | ATTTCTGCATCGTAT[A/G]TTCTGTTTTCCCTTC | 337867 |
rs731955 | snp | A/T | 0.462472 | 0.13174 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218386 | TGAGCTGTAAAATTT[A/T]AAATCCTAGTCCTGA | 337867 |
rs747847 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383679 | TTCCGGGGAGGAGCA[C/T]GCTCACTGCGTGCAT | 337867 |
rs747848 | snp | C/T | 0.421684 | 0.181726 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383928 | GCACCTTCTTCCTCA[C/T]CTTGCTGAGTCCTTA | 337867 |
rs752820 | snp | C/T | 0.311859 | 0.242226 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217858 | GGTGGCAGCGTCCAC[C/T]GAGCTCGTGCCCACC | 337867 |
rs877856 | snp | C/T | 0.431916 | 0.171483 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341776 | CATTCTGATTTCTCA[C/T]ACCTTTCGCTCTTCT | 337867 |
rs912129 | snp | C/T | 0.393434 | 0.20476 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381398 | CACAAACGAATCCAT[C/T]TGCTGTCCACACTCA | 337867 |
rs912130 | snp | A/C | 0.498547 | 0.0269177 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380148 | tggcagtacaaatgg[A/C]aagttccacacctga | 337867 |
rs912131 | snp | C/T | 0.496314 | 0.0427728 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380092 | atgcaggccacaaca[C/T]gtagtttattcagtg | 337867 |
rs913464 | snp | A/G | 0.362523 | 0.223246 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337735 | GGCCTTGGCCTTCCC[A/G]ACCCACATGGACCCT | 337867 |
rs927988 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333024 | CCCAGCACTTGGGGA[A/G]GCCAAGATGGGAAGA | 337867 |
rs927989 | snp | C/G | 0.498503 | 0.0273153 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335452 | ACAGAGAATGCCTCT[C/G]CCTACCCCCTACCCT | 337867 |
rs984477 | snp | C/G | 0.495818 | 0.0455352 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220179 | TATAAAGTTATCATA[C/G]TTCCTTCTTATATAT | 337867 |
rs1042263 | snp | C/G/T | 3.33611e-05 | 0.00408405 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295900 | TATACTTTTTACCAC[C/G/T]GCTTTGCCTACACGA | 337867 |
rs1042273 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294936 | TTTCTTTCATTGGGC[A/G]CTTTCCCATCTCCAA | 337867 |
rs1051577 | snp | A/C | 0.0089417 | 0.0662638 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255044 | ACCTTCCTCATGAAC[A/C]TCAGCACGTGTCTGG | 337867 |
rs1058083 | snp | A/G | 0.475259 | 0.108435 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385979 | TTGCTCAGAGTATCC[A/G]GAGTTAGCCACTAGG | 337867 |
rs1058143 | snp | C/T | 0.474544 | 0.10991 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386082 | GTGGCTGGCCTGGCA[C/T]GGGCTCAGCCCAGGA | 337867 |
rs1060436 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335697 | CTGTGTTGTATGAAT[A/G]ACCCACTCTGCAGCT | 337867 |
rs1060437 | snp | G/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335782 | GCAGTGGAATGAGCC[G/T]CAAAGCTCTACTTGG | 337867 |
rs1060438 | snp | A/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335785 | GTGGAATGAGCCTCA[A/T]AGCTCTACTTGGTGT | 337867 |
rs1060440 | snp | A/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335786 | TGGAATGAGCCTCAA[A/T]GCTCTACTTGGTGTT | 337867 |
rs1134061 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325303 | AGAGACGGGGTTTCA[C/T]CGTGTTAGGCAGGAT | 337867 |
rs1160294 | snp | C/T | 0.498158 | 0.0302955 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281340 | AATGGATTATATGCT[C/T]CTCTCTTAGGTAAGA | 337867 |
rs1319132 | snp | C/G | 0.498813 | 0.0243321 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347347 | TATCATCTTCACTTG[C/G]CTTTTTTTTCCTGGG | 337867 |
rs1887701 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259774 | CATAGCTTAGGACTT[C/T]TCTAAAATTAAGTAT | 337867 |
rs1887702 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292569 | GAAAGGAAGATGTTA[C/T]ATAATATATGGACTG | 337867 |
rs1887703 | snp | C/T | 0.308166 | 0.243139 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297729 | GGTAAGTAGAAAACA[C/T]AAGAGGGTAGGGATG | 337867 |
rs1887704 | snp | C/G | 0.494315 | 0.0530107 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322238 | AATTCCACTAATTTT[C/G]TTACACATTAATACT | 337867 |
rs1923891 | snp | C/T | 0.119281 | 0.213102 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307691 | TAAGGTTTATTGCTT[C/T]AGTCTCTTTCAAAGA | 337867 |
rs1923894 | snp | A/G | 0.265453 | 0.249522 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370504 | CAATTTGTTTTGTTT[A/G]CTGAAAGGGAAAAAC | 337867 |
rs1923895 | snp | C/T | 0.498437 | 0.0279115 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366338 | ctcagaattcaaaac[C/T]acaaaatccacaagg | 337867 |
rs1923896 | snp | C/T | 0.322245 | 0.239334 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366033 | aaatcagagaaatac[C/T]aatcaaagaaagctg | 337867 |
rs1923897 | snp | A/G | 0.487368 | 0.0784625 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352087 | CATGATTGACAGGGC[A/G]GATCTGCCTCCTGGT | 337867 |
rs1927565 | snp | A/G | 0.49823 | 0.0296997 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198781 | TTTATGGTTCAAATT[A/G]ATCTTTTACCCACAT | 337867 |
rs1927724 | snp | A/C | 0.42357 | 0.179927 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340058 | ACAATCTTTTACCAG[A/C]ACTTTGAATACTAAA | 337867 |
rs1927725 | snp | C/T | 0.309154 | 0.242901 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340233 | AAATACCGTGTGCAG[C/T]GTCTGGAGGCTGCTG | 337867 |
rs1927726 | snp | A/G | 0.357238 | 0.225832 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260629 | AAAAGAAACTGCCCA[A/G]TCATTTGACAGCAAG | 337867 |
rs1927727 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302910 | CTTTGAGTCCTAAAT[C/T]GATAGCTATGTTTAT | 337867 |
rs1927728 | snp | C/T | 0.304937 | 0.243889 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303279 | GCTTTATATGTGTCC[C/T]GAACCCAGTGGATGT | 337867 |
rs1927729 | snp | A/G | 0.223522 | 0.248594 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303544 | GAAACTAAGAATCCC[A/G]CCATAATACTCATTT | 337867 |
rs1927730 | snp | C/T | 0.308908 | 0.242961 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306311 | GTTTTTTAGCACTTA[C/T]AATGAGAGGCAATGT | 337867 |
rs1927731 | snp | A/G | 0.42263 | 0.180829 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273618 | CTGTTGATGAATTTA[A/G]TGTTGATCTGATTAT | 337867 |
rs1927732 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226485 | AGCCTTCTAACTGGT[A/T]TACTATCTTCCACCA | 337867 |
rs1964897 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344929 | TGCTCATCTATTTCA[A/G]CTACAACTGCCTGAG | 337867 |
rs1964898 | snp | C/T | 0.422787 | 0.180679 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344927 | CTCATCTATTTCAGC[C/T]ACAACTGCCTGAGCT | 337867 |
rs1977252 | snp | A/C | 0.247053 | 0.249983 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382337 | ACATAAAATGCTGTC[A/C]AGTCAGGTCTCTCAA | 337867 |
rs1977253 | snp | C/T | 0.378174 | 0.214642 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382274 | catatctctgttaaa[C/T]tccatctgatcattt | 337867 |
rs1977254 | snp | C/G | 0.375996 | 0.215928 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382266 | tgttaaattccatct[C/G]atcattttccagtca | 337867 |
rs1998475 | snp | C/T | 0.349671 | 0.229272 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312121 | AACCAAACCAAAATA[C/T]AACACACACAAAACA | 337867 |
rs2004229 | snp | A/G | 0.305685 | 0.24372 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338300 | GAGGCCAAGGCGGGC[A/G]GATCACAAGAGGTCA | 337867 |
rs2038673 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365139 | ATAATGGCAGATTTT[A/T]AAAAAATCACAAGAA | 337867 |
rs2093642 | snp | A/G | 0.306431 | 0.243548 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379376 | ggtgagtttgccaag[A/G]tcattgctgacaaaa | 337867 |
rs2146676 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368852 | gaatccaccgttttc[C/T]taaataggcctggtt | 337867 |
rs2146677 | snp | A/T | 0.308908 | 0.242961 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359417 | TTTACTTGAATGAGT[A/T]AATGTAAAATCACAA | 337867 |
rs2146678 | snp | A/T | 0.307671 | 0.243257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331755 | TTTGTACATTCCCTA[A/T]TTTATTACCCCAAGA | 337867 |
rs2149261 | snp | C/T | 0.498253 | 0.0295011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277844 | ATCAAGCCTCTAATC[C/T]GGAGGTGGGTGGTGG | 337867 |
rs2149262 | snp | C/G | 0.445064 | 0.156365 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288417 | TAGCATGCAGATAGA[C/G]AACAGCTTTAAAATT | 337867 |
rs2149263 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299696 | CTTTTCAAAGCTTGC[C/T]GTTCAGTGTTCCTTT | 337867 |
rs2149264 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214730 | TCCTTAAGCAGATTG[C/T]CCCCCACCCCACCCT | 337867 |
rs2181500 | snp | C/T | 0.0295035 | 0.117819 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350540 | ccctgctccagcaca[C/T]attcagcaatctgga | 337867 |
rs2181501 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331103 | GAAGGATAAGAGATA[C/T]GTGATCTCAGCTGGA | 337867 |
rs2181502 | snp | C/T | 0.498059 | 0.0310896 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331065 | CTGGCTCAAATAAAA[C/T]GAACCTTCCCTTATG | 337867 |
rs2182885 | snp | A/G | 0.454784 | 0.1434 | intron-variant | UBAC2 | GRCh38.p7 | 13:99202870 | GGTGCTGGGAATGCA[A/G]CAACGAACAGGTCCT | 337867 |
rs2182886 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215020 | GGGATATGACCTTTA[C/T]TGAGCTTATCCACCA | 337867 |
rs2182954 | snp | C/T | 0.445724 | 0.155538 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284828 | CATATTCTAAGGCTG[C/T]TGGAAAATTAAAGTT | 337867 |
rs2225170 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219708 | atccctgtattaagc[A/C]gtcatgccctattac | 337867 |
rs2230341 | snp | A/G | 0.311859 | 0.242226 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295007 | ATGACAAACTTTGCA[A/G]GACTTCCCTTATAAA | 337867 |
rs2230342 | snp | G/T | 0.426238 | 0.177314 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295924 | TTCAACAAATTTGGT[G/T]ATTTCTGATATACTT | 337867 |
rs2230343 | snp | C/T | 0.112385 | 0.208715 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295843 | CTGGAGAATCGGAGA[C/T]GCCTTGTGTAGGATA | 337867 |
rs2296044 | snp | A/G | 0.41325 | 0.18934 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386571 | GTGCTACTTACAGGA[A/G]CAAAAGCACTTCACT | 337867 |
rs2296045 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385778 | AGTTTGAGAGAAAAA[A/G]CAGTAACTAAAAAAG | 337867 |
rs2296046 | snp | C/T | 0.371785 | 0.218331 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372616 | CTTTAGACTCAGAGC[C/T]GGTGACGCCACCTGT | 337867 |
rs2296860 | snp | A/G | 0.49823 | 0.0296997 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200499 | TCGGGAGAGATTAGA[A/G]GTGGCGCTCCTGCCC | 337867 |
rs2296911 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240059 | TGTGGTACAGGAAGC[A/G]TGCTTTGAGGCAAAC | 337867 |
rs2390236 | snp | A/T | 0.0607341 | 0.163335 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236666 | accagcctggccaac[A/T]tggtgaaaccccgtc | 337867 |
rs2390237 | snp | C/G | 0.470521 | 0.117772 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336050 | GAGCTTTACATTTTT[C/G]CCAGTTGCTGTATTT | 337867 |
rs2390238 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338047 | TTTTTTTCTTTTTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs2390239 | snp | G/T | 0.305685 | 0.24372 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341466 | GCAGAGTCTACAAGA[G/T]AAATAGAGAAGCAAA | 337867 |
rs2390240 | snp | A/T | 0.15698 | 0.23205 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345981 | CCCCTGACCTCATGA[A/T]CCACTTGCCTTGGCC | 337867 |
rs2390241 | snp | C/G | 0.00475057 | 0.0485048 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354481 | CTGTTCACTTGGCGG[C/G]TTGGCTGAGTTCTGT | 337867 |
rs2390276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383519 | TGAATCACCTGAGGG[C/T]GCCATAGTGTCCCAG | 337867 |
rs2892975 | snp | C/T | 0.308661 | 0.24302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373549 | CGGAATGTCCTGCCC[C/T]GAGGAGCTGTGAGCC | 337867 |
rs3031384 | in-del | -/GT | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216113 | TGTGTGTGTGTGTGT[-/GT]ATTTTTGAGACACAG | 337867 |
rs3031409 | in-del | -/A/AA | 0 | 0 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256723 | CCAAAAAAAAAAAAA[-/A/AA]CCGTCCATTTTAAAT | 337867 |
rs3031412 | in-del | -/T/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292729 | AGGGTTTTTTTTTTT[-/T/TT]AATGTGGTCAACTGC | 337867 |
rs3031415 | in-del | -/A/AA | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341032 | GTAGATAAAAAAAAA[-/A/AA]TGCTGTGTTTTCTCA | 337867 |
rs3031440 | in-del | -/TGTGTGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368720 | gtgtgtgtgtgtgtg[-/TGTGTGT]acacataccctcact | 337867 |
rs3181718 | snp | A/G | 0.201727 | 0.245295 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294599 | GTTTTGTTTTGTTTC[A/G]TTCTGGGTCATAAAA | 337867 |
rs3223410 | microsatellite | (CA)11/13/14/15/16/17/19 | 0.746112 | 0.121802 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216111 | tgtgtctcaaaaata[(CA)11/13/14/15/16/17/19]aaaTAtaggttggta | 337867 |
rs3742127 | snp | C/T | 0.164546 | 0.234942 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327198 | TTTTCTCTGAATGTT[C/T]CTTTACTTCAGATTG | 337867 |
rs3742130 | snp | C/T | 0.275128 | 0.248734 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255087 | GGGAACGGGGGAGAA[C/T]AGTTACAATCCCTGG | 337867 |
rs3759443 | snp | C/T | 0.165527 | 0.235296 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258068 | ATTTCATTTTAATAA[C/T]ACAGGCTGGGCGCAA | 337867 |
rs3759444 | snp | A/G | 0.320575 | 0.239832 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258009 | GGGAGGCCAAGGCAG[A/G]AGGATCAGTTGTGCC | 337867 |
rs3809367 | snp | A/G | 0.164546 | 0.234942 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260280 | TTGCATTGTTACTGC[A/G]TATTTACTTGCTTTT | 337867 |
rs3825426 | snp | C/G | 0.360421 | 0.224293 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326818 | ACTTTAAGAATAACT[C/G]TGTCTGTGCATCTCG | 337867 |
rs3839999 | in-del | -/T | 0.229136 | 0.249128 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385549 | TATTTTCTATCTATA[-/T]TTTTTATTGGGCATT | 337867 |
rs4462451 | snp | A/G | 0.493793 | 0.055364 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384619 | TAAGCCCCAGGCTGC[A/G]AGTGGCACAGCTGTC | 337867 |
rs4511390 | snp | A/G | 0.495174 | 0.0488838 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333774 | CGTCTGATTGTCATT[A/G]TGGGGGCAGGGAAGG | 337867 |
rs4517646 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248476 | tgctcactgcaacct[C/T]tgcctccctggttca | 337867 |
rs4630393 | snp | C/T | 0.266546 | 0.249452 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364718 | ATAGTCATACAAATG[C/T]ACTTTTTGTGTTTAT | 337867 |
rs4636771 | snp | G/T | 0.342134 | 0.232404 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369264 | TCCCTGACCTATAAT[G/T]GTCGAACTTTAACAA | 337867 |
rs4771326 | snp | A/G | 0.238171 | 0.24972 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243711 | GTTTTCCTTTGGTGT[A/G]TGCATTATGATTTTG | 337867 |
rs4771327 | snp | C/T | 0.139564 | 0.224285 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327480 | TTGGTTTTTCTCTCT[C/T]TCTCTGTGTGTGTGT | 337867 |
rs4771328 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334052 | TCTTGGGTCAAGTGA[C/T]CCTCCCACATCAGCC | 337867 |
rs4771329 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373668 | AGAGGAGGGGCCTGA[A/G]GACAAGTACATGGGA | 337867 |
rs4772180 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205200 | AGCCACTGTGCCCGG[C/T]TGGGGGAGTTTCTTT | 337867 |
rs4772181 | snp | C/G | 0.422315 | 0.181128 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208712 | TTGTGTCTGACTTCA[C/G]TAGTTTCTGGATTGA | 337867 |
rs4772182 | snp | G/T | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208716 | GTCTGACTTCACTAG[G/T]TTCTGGATTGAGTGG | 337867 |
rs4772183 | snp | C/T | 0.411746 | 0.190626 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209922 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCATTC | 337867 |
rs4772185 | snp | C/T | 0.231482 | 0.249313 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285687 | ATGAGCCACCATGCC[C/T]GGCCAGCTGGCTCAT | 337867 |
rs4772186 | snp | A/G | 0.40733 | 0.194287 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305733 | GCGATACATAAACAT[A/G]TGAGTGAACATTTTG | 337867 |
rs4772187 | snp | A/G | 0.230017 | 0.2492 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313841 | CTCCACTTTTCTCAC[A/G]CTTAGTAGGTGCTGA | 337867 |
rs4772189 | snp | C/T | 0.343254 | 0.231956 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342319 | TTACCTCCTTAAAGT[C/T]CCTACCTTTAAATAC | 337867 |
rs4772190 | snp | A/G | 0.359152 | 0.224913 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381862 | GAATTGAAGTTTCAC[A/G]TCTGGCAAAAGCTTA | 337867 |
rs5806101 | in-del | -/A/AA/AAA | 0 | 0 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256710 | TAAATTTCCATCACC[-/A/AA/AAA]AAAAAAAAAAAAACC | 337867 |
rs5806102 | in-del | -/A | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256717 | AAATTTCCATCACCA[-/A]AAAAAAAAAAAAACC | 337867 |
rs5806105 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290220 | ACAGCATTCTTGTGA[-/G]ATTTGAATGAGCACT | 337867 |
rs5806106 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292719 | AATAGCTTTGAGGGT[-/TT]TTTTTTTTTTAATGT | 337867 |
rs5806107 | in-del | -/G | 0 | 0 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303019 | CCTCCCCTGCCTCCT[-/G]GGGGGCTTGCTTTCT | 337867 |
rs5806108 | in-del | -/G | 0.313326 | 0.241847 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333096 | TGAAACCCCGTCTCT[-/G]GGGGGGGGAAGAAAG | 337867 |
rs5806110 | in-del | -/A/AA | 0.562068 | 0.176031 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341023 | GTAGATAAAAAAAAA[-/A/AA]TGCTGTGTTTTCTCA | 337867 |
rs5806111 | in-del | -/T | 0.497907 | 0.0322805 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366629 | GGCTTTTTAGTTTGA[-/T]TTTTTTTTCATCCCT | 337867 |
rs5806112 | in-del | -/C | 0.308908 | 0.242961 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383743 | ATGACATGGGCGGCA[-/C]CCCCCCGTTTGGAAA | 337867 |
rs6491493 | snp | C/G | 0.497855 | 0.0326773 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248166 | GTTTGCTTCCCAGCT[C/G]TCTATTTCCAACCCA | 337867 |
rs6491494 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292383 | TCCTGACCTCGTGAT[C/T]CACCCGCCTCGGCCT | 337867 |
rs6491495 | snp | G/T | 0.382402 | 0.213399 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292431 | ACAGGCATGAGCCAC[G/T]GCGCCCAGCTGGGGT | 337867 |
rs6491496 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308470 | ggacatagcttttgg[A/T]tcaaaagatgagagt | 337867 |
rs6491497 | snp | C/G | 0.346971 | 0.230427 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327484 | TTTTTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT | 337867 |
rs6491498 | snp | C/T | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384831 | CGAGCGTGGCAGTGA[C/T]GCCAGGAGTGCGATG | 337867 |
rs6491499 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384842 | GTGATGCCAGGAGTG[C/T]GATGCCAGGGCTGAG | 337867 |
rs7139522 | snp | A/C | 0.454182 | 0.144256 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323407 | AGAGTTCAACACCAG[A/C]CTGGCCAACATGGCA | 337867 |
rs7139654 | snp | G/T | 0.309401 | 0.24284 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240634 | TTCCTATGTGCTCTC[G/T]TGTACTGCCTCATTG | 337867 |
rs7139916 | snp | C/T | 0.307423 | 0.243316 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323644 | ACACACTCACATTCA[C/T]GTTGACTCATCCATA | 337867 |
rs7139964 | snp | A/G | 0.497613 | 0.0344622 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217960 | CTTGCCACTAACCAC[A/G]CATTTCCCCACTTGA | 337867 |
rs7140092 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372976 | AAAATAAAAATTAGC[C/T]GGGCATGGTGACGGG | 337867 |
rs7317547 | snp | C/T | 0.030278 | 0.119257 | intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99256356 | TAAATTATCATAGGT[C/T]GAGAAACAGCAATGT | 337867 |
rs7317555 | snp | A/G | 0.475525 | 0.107882 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381635 | TGGTCCTTAACTGGA[A/G]GGAACATCATACAGG | 337867 |
rs7318420 | snp | C/G | 0 | 0 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367818 | GGAATCGTCTTTTTC[C/G]TCCTTTACGTCAGCG | 337867 |
rs7318723 | snp | G/T | 0.155987 | 0.23165 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272761 | aattgcctcccaaag[G/T]tcctacctccaaata | 337867 |
rs7318947 | snp | A/G | 0.264327 | 0.249589 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367958 | CCATGTTTCAGAGTT[A/G]AAGCAGTTTCGATCA | 337867 |
rs7319473 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244816 | AATCAATTTTATATT[A/C]TTTCTTTAAAAttta | 337867 |
rs7320298 | snp | G/T | 0.387074 | 0.209071 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223412 | ttttattgatctcaa[G/T]aaccagctttgagtt | 337867 |
rs7320826 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244817 | ATCAATTTTATATTC[A/T]TTCTTTAAAAtttat | 337867 |
rs7322387 | snp | A/C | 0.31014 | 0.242659 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227209 | atctcaaaaaaaaaa[A/C]aacaacaaaaaaaGA | 337867 |
rs7322572 | snp | C/T | 0.462691 | 0.131387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227242 | GCACCCCTCCTTCCC[C/T]ggttatgctgcagta | 337867 |
rs7322759 | snp | C/G | 0.320575 | 0.239832 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257424 | CTCCCTTCACCTATC[C/G]TCATCCTTCAATTTT | 337867 |
rs7323101 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338996 | ttagtcctgttctct[A/C]ttctgctgtgtctcc | 337867 |
rs7323390 | snp | C/T | 0.424503 | 0.179021 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345714 | TGTCCCATCAGCTCT[C/T]GACAGGTACTGTTTC | 337867 |
rs7323484 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264612 | TCTTAACCATGTTAG[C/T]TCATTTCTCTGATGG | 337867 |
rs7323873 | snp | A/G | 0.309401 | 0.24284 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227750 | tattgctgtgcctca[A/G]gacctagaataatgc | 337867 |
rs7325242 | snp | C/T | 0.498673 | 0.0257246 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370249 | ggcttaggaataata[C/T]ctgtgcatgtcagta | 337867 |
rs7325572 | snp | A/G | 0.163236 | 0.234461 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370252 | ttaggaataatacct[A/G]tgcatgtcagtacat | 337867 |
rs7325747 | snp | C/T | 0.307919 | 0.243198 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377678 | GAATGTTATGCTCAC[C/T]ATTTAAAAAGATTGT | 337867 |
rs7325957 | snp | A/G | 0.426201 | 0.177351 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312901 | TGCCATCACATCTTT[A/G]TGAAGCATTTTATCT | 337867 |
rs7330165 | snp | C/T | 0.445855 | 0.155373 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237173 | CTTTGTTGTATACTT[C/T]CATCTTTATTGACTA | 337867 |
rs7330664 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318692 | tgggcgtggtggcag[A/G]cgcctgtagtcccag | 337867 |
rs7331703 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304800 | ATTCAGACCCAGGCA[G/T]TTTGGCTTCAGAAGT | 337867 |
rs7331894 | snp | C/T | 0.408871 | 0.193029 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200698 | CCTCCCCTACCGACG[C/T]ACTTCCCTTCCCCGG | 337867 |
rs7332161 | snp | A/G | 0.306431 | 0.243548 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371215 | AATGACAACAGCGAG[A/G]TTACTTCTTGTCAAC | 337867 |
rs7332358 | snp | A/G | 0.144632 | 0.226711 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371275 | CTCGCTCCGTGTTAC[A/G]AGAAGTTGTAAAAAC | 337867 |
rs7332472 | snp | C/G | 0.226188 | 0.248863 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292127 | ATTGGGGTTACATTC[C/G]TTTTTTTTTTCTTTT | 337867 |
rs7332516 | snp | C/G | 0.267703 | 0.249372 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200971 | GCCATCCTGGCTGCC[C/G]CCTACACGCCACCCT | 337867 |
rs7332672 | snp | C/T | 0.464203 | 0.128908 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225217 | cagtagtattaagta[C/T]gttcatattgtgcaa | 337867 |
rs7333055 | snp | A/G | 0.492775 | 0.059668 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248367 | tagctgtgactatag[A/G]tgtgccaccatgccc | 337867 |
rs7333266 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322676 | GCAGCCTTAGTGTGG[A/G]AAAAAAACAATCTGT | 337867 |
rs7334389 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248202 | CTCTCCTGATATTTC[G/T]TGAGTCTTAtttcct | 337867 |
rs7335185 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359742 | AAAGCCTTGGTCCAT[A/G]GCACACTGAGTAAGT | 337867 |
rs7335403 | snp | A/G | 0.495999 | 0.0445491 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243519 | CATTCTAGTTTACGT[A/G]TATAATTTTAAAAAA | 337867 |
rs7335579 | snp | C/G | 0.44546 | 0.155869 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287515 | CTGCAGCCTTGACTT[C/G]CTGAGCTCAGGTGAT | 337867 |
rs7336872 | snp | C/T | 0.275197 | 0.248727 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287647 | TTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs7337285 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384816 | GTGTGATGCCAGGGC[C/T]GAGCGTGGCAGTGAT | 337867 |
rs7337972 | snp | A/T | 0.350109 | 0.229081 | intron-variant | UBAC2 | GRCh38.p7 | 13:99356863 | CATCTCTTATCCAAG[A/T]GGTGAATGTGTTGCC | 337867 |
rs7338177 | snp | C/T | 0.462691 | 0.131387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217202 | CCACTTCAGCTAGGC[C/T]GTTGCTCAGCGTCAG | 337867 |
rs7338185 | snp | C/T | 0.309401 | 0.24284 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284256 | AATTGGGGGGAAGTG[C/T]CCCCATGAATGGGGC | 337867 |
rs7338593 | snp | C/T | 0.237882 | 0.249706 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344600 | ATTTTTTTTCAGTTA[C/T]TAACTGCTGTATGTT | 337867 |
rs7338709 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384854 | GTGCGATGCCAGGGC[C/T]GAGCATGGGTCACCA | 337867 |
rs7338726 | snp | A/G | 0.499859 | 0.0083854 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323079 | GGGATGGTAGGTGTG[A/G]GTTCCTCTGCGCCGC | 337867 |
rs7338843 | snp | C/T | 0.15698 | 0.23205 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344766 | TGCCACCCCCTGCCA[C/T]GTGCTCCTCGTGTGG | 337867 |
rs7338947 | snp | G/T | 0.0452246 | 0.143412 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201189 | GGTATCCCCAGGTGC[G/T]CTGCCCAGGAGTCTC | 337867 |
rs7339230 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323126 | CTCTCTCTTCTCTCC[A/G]TGCTTCCTTTTCTCC | 337867 |
rs7339337 | snp | A/C | 0.163236 | 0.234461 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353443 | TGACCTTGAGAAAAT[A/C]ATTTCTATTTTCCAT | 337867 |
rs7358849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315809 | GTAAATGTATTTCTT[A/G]TTTTGTTTTTGGCAT | 337867 |
rs7358855 | snp | C/T | 0.499035 | 0.0219437 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315544 | ATTGTGGAAAGTCTT[C/T]GGAGCCAGGTTGTTG | 337867 |
rs7358919 | snp | C/G | 0.447162 | 0.153712 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313206 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCAT | 337867 |
rs7490999 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338046 | CTTTTTTTCTTTTTT[C/T]CTTTTTTTTTTTTTT | 337867 |
rs7491404 | snp | G/T | 0.183886 | 0.241099 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216082 | tgtaccaacctaTAt[G/T]tgtgtgtgtgtgtgt | 337867 |
rs7982483 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228439 | ATTACAGGCTCCCCC[C/G]CACCCCACCACGCCC | 337867 |
rs7983491 | snp | A/G | 0.498133 | 0.030494 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214814 | ACTGGGATGGTGGTG[A/G]AAAGGCTGTTTGTAG | 337867 |
rs7985056 | snp | A/G | 0.309648 | 0.24278 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276732 | gctccatctgaggct[A/G]tccaggggctctacc | 337867 |
rs7990495 | snp | A/G | 0.159951 | 0.233219 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270084 | ACCACTGGTATAGCA[A/G]TTGTGAAACTCCTAT | 337867 |
rs7992045 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309236 | ctgcctcagcctccc[A/G]agtagctgggactac | 337867 |
rs7992856 | snp | A/G | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251353 | ctttcctatttgaat[A/G]ccttttctttctttc | 337867 |
rs7993014 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279667 | gacttataaacaacc[A/G]aaatttatttctcac | 337867 |
rs7993146 | snp | A/G | 0.495095 | 0.0492773 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251227 | ttctacattgatttg[A/G]catcccgaaactcta | 337867 |
rs7993615 | snp | G/T | 0.495445 | 0.0475058 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243030 | tcactttccagactg[G/T]gcagccagCAAAATT | 337867 |
rs7993715 | snp | C/G | 0.185472 | 0.241529 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356059 | GTAAGATCAGCTGTG[C/G]TAGGTATGTCAGGCC | 337867 |
rs7993927 | snp | A/G | 0.157311 | 0.232183 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334283 | TGTTGAGCTTTTAAG[A/G]TATATAGGTGTAAAA | 337867 |
rs7994322 | snp | G/T | 0.309401 | 0.24284 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242864 | gagacgctcctcacc[G/T]cccagacggggcggc | 337867 |
rs7994398 | snp | A/G | 0.373799 | 0.217195 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265896 | TGGGCAAGTTAAAAA[A/G]GTTTCGTATCAGAGA | 337867 |
rs7995524 | snp | A/G | 0.495521 | 0.0471118 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238069 | ATATGTATGAGTTTT[A/G]TGCATGCTCAGGAGC | 337867 |
rs7996326 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292393 | gtgattcacccgcct[C/T]ggcctcccaaagtgc | 337867 |
rs7996725 | snp | C/T | 0.248471 | 0.249995 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207995 | CCTCTCATCGTCTCT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs7997400 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216801 | TGGTGGTCTTCTTGG[A/T]TTTGTCGTTTTTGTT | 337867 |
rs7997823 | snp | C/T | 0.265727 | 0.249505 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366602 | GATTCCTGCTGTCTC[C/T]GGGGGAAGACAGGCT | 337867 |
rs7998034 | snp | C/T | 0.223819 | 0.248625 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366721 | GCTGCCTCTTTCAGA[C/T]CCAAGGCCGCATCTT | 337867 |
rs7998125 | snp | A/C | 0.157972 | 0.232445 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213112 | TACATATACATATAC[A/C]TATACATTTGATTTT | 337867 |
rs7999348 | snp | A/G | 0.504347 | 0.0802854 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280668 | CCTCAGCATGGAGTA[A/G]TGAAGAGTGTTCTTT | 337867 |
rs7999572 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252513 | TAGATGCTCATGACT[A/G]TGATTTAAACTCAGA | 337867 |
rs8000756 | snp | C/T | 0.306431 | 0.243548 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280832 | TCCTTCTTCTTTCCC[C/T]CTCTCTCTCTCTCTC | 337867 |
rs8000934 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280937 | ACGCCTGTAATCCCA[C/T]CACTTTGGGAGGCCG | 337867 |
rs8001476 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372202 | CCGGAAACCACAAGG[C/T]GAGATGTCTGCTCAT | 337867 |
rs8002409 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210697 | ggtcaggctggtctc[A/G]aactcccgacctctg | 337867 |
rs8181880 | snp | A/G | 0.208169 | 0.246476 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375703 | AGAAATCTCATTGGA[A/G]TGAATGTCCCATTTT | 337867 |
rs9284183 | snp | A/G | 0.496905 | 0.0392151 | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99294117 | CATTTTACTCGGATC[A/G]TATTTAGCAAGCAGC | 337867 |
rs9300536 | snp | C/T | 0.383632 | 0.211288 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273210 | TTTCCTAGTTGGTAA[C/T]ATTATTCAGTTTGTT | 337867 |
rs9300537 | snp | C/T | 0.225301 | 0.248777 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336237 | ATGTTCTGAATGCTG[C/T]CTTGGTTGGCTGTAT | 337867 |
rs9300538 | snp | A/G | 0.219349 | 0.248114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352859 | TCTGGAGGCAGCACC[A/G]TCGGAAACTCTCTAC | 337867 |
rs9300539 | snp | G/T | 0.234982 | 0.249549 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352915 | GTAGGGGCAGTGCAC[G/T]TGTGTTGCAAAGGAG | 337867 |
rs9300540 | snp | A/T | 0.409552 | 0.192466 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365971 | atccctaatactgcc[A/T]ttttttgccttcgag | 337867 |
rs9300541 | snp | A/C | 0.030278 | 0.119257 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386533 | TCGTCTTTCTTCAGA[A/C]GACTGGGTGCTCATT | 337867 |
rs9513579 | snp | A/G | 0.177503 | 0.239258 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202348 | TACCCTTTAGATAAA[A/G]AGCATTAGGACTGTA | 337867 |
rs9513580 | snp | A/C | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206893 | TGCTCCTTCCGCTTC[A/C]TGCTCCCTCTCTCTG | 337867 |
rs9513581 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209102 | TGTGCATGTGGGTCC[C/T]AGTGCTCAGCACGGC | 337867 |
rs9513582 | snp | C/T | 0.465683 | 0.126415 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213003 | TGATTCCCACGCCCA[C/T]GTAACCATTGTTGGT | 337867 |
rs9513584 | snp | A/G | 0.497933 | 0.032082 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224027 | tttttcaggtcttgt[A/G]tatccttactgattt | 337867 |
rs9513585 | snp | A/C | 0.495999 | 0.0445491 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229328 | GGGAGTATCTGTGCT[A/C]ATAAGGAAGGCATTG | 337867 |
rs9513586 | snp | G/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232405 | TAGTTGAGAGATATA[G/T]ATATATATATATATA | 337867 |
rs9513587 | snp | C/T | 0.452103 | 0.147154 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272114 | GGCTCAGTCCCAGCT[C/T]TCTTTCCTTGAGCTG | 337867 |
rs9513588 | snp | C/T | 0.309401 | 0.24284 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282859 | AAATAATCTCATACC[C/T]GTCTTAGGGTTGGAT | 337867 |
rs9513589 | snp | A/G | 0.312348 | 0.242101 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286540 | GGGGGGTACATATGC[A/G]GGTTTATTACATGGG | 337867 |
rs9513591 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294374 | TGCTAAGCAGAGGCC[C/T]TAAAAGACTGTGCTG | 337867 |
rs9513592 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297147 | CTTGTTATAAATAAT[A/G]TTAAAGCAGAAATTT | 337867 |
rs9513593 | snp | A/G | 0.450105 | 0.149859 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298006 | ATACAGAGGGTCACT[A/G]CAAAGGTTAAAAAGA | 337867 |
rs9513597 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324377 | ttgaagagccactgc[C/T]tggttccaccattgc | 337867 |
rs9513598 | snp | A/G | 0.307176 | 0.243374 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329849 | ctaagttactcccac[A/G]ttcctgcccccacag | 337867 |
rs9513600 | snp | A/G | 0.498927 | 0.0231381 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343761 | CTCAGCTGTGTCTCA[A/G]TTTTCTTCACATAAG | 337867 |
rs9513601 | snp | A/G | 0.428786 | 0.174744 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347880 | GGAGTGGGCTGCAGA[A/G]TATTAGCTGCAGCCT | 337867 |
rs9513602 | snp | A/G | 0.498133 | 0.030494 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350142 | aagctaatgattcat[A/G]atgtttataatgatt | 337867 |
rs9513603 | snp | C/T | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354216 | TTGGAGATAGGGGGT[C/T]GTACAGGTGACATTC | 337867 |
rs9513604 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364246 | tgaattttgtcaaat[G/T]gttttcatacctatt | 337867 |
rs9513605 | snp | C/T | 0.308661 | 0.24302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371334 | CTTATACATTGATTT[C/T]CTAAATCTTGTTTTT | 337867 |
rs9517648 | snp | A/G | 0.492237 | 0.0618148 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203059 | TTTATTTATTTATTG[A/G]GATGGAGTCTCACTG | 337867 |
rs9517649 | snp | C/T | 0.309648 | 0.24278 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211745 | ACTGCTTCTCAGCCT[C/T]AAAGAAGTTTATCTC | 337867 |
rs9517650 | snp | C/G | 0.465683 | 0.126415 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213025 | ATTGTTGGTAGTCTA[C/G]TGGTCATTCTTTTAG | 337867 |
rs9517651 | snp | A/T | 0.498133 | 0.030494 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215180 | CTTGAAGCCACAGTA[A/T]CACTTAAATATGGTT | 337867 |
rs9517652 | snp | C/T | 0.309648 | 0.24278 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218211 | TACATTTAATCATAG[C/T]GTTAATGTTTGTATA | 337867 |
rs9517653 | snp | C/T | 0.453939 | 0.144598 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229428 | AGGTAGTGAGCTGTG[C/T]GGTTTGATTGCAGCA | 337867 |
rs9517654 | snp | C/G | 0.464841 | 0.127841 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230509 | aataaatttattatc[C/G]tacagtttggaggcc | 337867 |
rs9517655 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233358 | cctcatgatctgctc[C/T]cctcggtctcccaaa | 337867 |
rs9517656 | snp | C/T | 0.179105 | 0.239737 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237671 | tttaagataattacc[C/T]gggctgggtgccgtg | 337867 |
rs9517657 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239342 | TGCTATAATGCAGTC[A/C]TTCTCAACCCCGGAC | 337867 |
rs9517658 | snp | C/T | 0.303187 | 0.244277 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242319 | gacggggcggctggc[C/T]gggcggggggctgac | 337867 |
rs9517660 | snp | G/T | 0.496279 | 0.0429702 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247205 | CTACTGTTTTTTTtt[G/T]tttgttttgttttgt | 337867 |
rs9517661 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247206 | TACTGTTTTTTTttt[G/T]ttgttttgttttgtt | 337867 |
rs9517662 | snp | C/G | 0.498369 | 0.0285077 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247308 | caagctccgcctccc[C/G]ggttcacgccattct | 337867 |
rs9517665 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259385 | ACCATAGTAAATCTG[G/T]GGCTTAGAAAAGTTA | 337867 |
rs9517667 | snp | A/G | 0.326741 | 0.23793 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262881 | TCTATAAGGTTGAGG[A/G]TTGTTGGTTTAAGAC | 337867 |
rs9517668 | snp | A/T | 0.390651 | 0.206682 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271586 | ATGTTGGCCTGTGCT[A/T]TCTTTTCATTGTTTC | 337867 |
rs9517669 | snp | A/G | 0.312104 | 0.242163 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275102 | gaaagcagaatcata[A/G]tgtatacatatgttt | 337867 |
rs9517670 | snp | A/G | 0.154661 | 0.231107 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281389 | ATATCTCCTTTCTCA[A/G]CCAAAAAGTTCTCAC | 337867 |
rs9517671 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285623 | tctcaaactcctggc[C/G]tcaagtgaccctcct | 337867 |
rs9517672 | snp | C/T | 0.31721 | 0.240796 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286652 | CAACCTCCATCACCC[C/T]ACACTCCCCCAACAA | 337867 |
rs9517673 | snp | A/T | 0.309401 | 0.24284 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291981 | AAGTTTATAATCTAT[A/T]CCTATTGTTGGGTTA | 337867 |
rs9517675 | snp | C/T | 0.0901694 | 0.192235 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296919 | GATCCATGCAATCTA[C/T]ACTTCTACCTTTGCA | 337867 |
rs9517676 | snp | A/G | 0.312837 | 0.241974 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297124 | TTTGGATTCTTTCCA[A/G]TTCTTTTCTTGTTAT | 337867 |
rs9517678 | snp | C/T | 0.313814 | 0.241719 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308805 | TCACTGTGTATAAAA[C/T]AAAGGTATTGAACTA | 337867 |
rs9517679 | snp | C/T | 0.307919 | 0.243198 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313279 | GTGAGACACTACGCC[C/T]GGCCGGAAGGAAGGG | 337867 |
rs9517680 | snp | A/C | 0.31357 | 0.241783 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313823 | CTGGGAAGAAAACAT[A/C]GCCTCCACTTTTCTC | 337867 |
rs9517681 | snp | A/G | 0.356824 | 0.239485 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314037 | TTACTTCAAAGATAC[A/G]TCTGCCATTTGTGTT | 337867 |
rs9517682 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314283 | TTTTTTTTTTTTTGG[G/T]CTTTTTCTCATTTGA | 337867 |
rs9517683 | snp | A/G | 0.495999 | 0.0445491 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315897 | CACAGCATGGCCTTC[A/G]TCACGGGGCCATTGT | 337867 |
rs9517684 | snp | A/C | 0.308414 | 0.24308 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322721 | AGATTTGGGACTTCA[A/C]ATGTGGTCTGAGTTT | 337867 |
rs9517685 | snp | C/T | 0.308166 | 0.243139 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325338 | ttgatctcctgacct[C/T]gCAGTTTCTTCCAAC | 337867 |
rs9517686 | snp | A/G | 0.499946 | 0.00519141 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325498 | CCCTTCTTCTAGGAA[A/G]TCTGACTTTATTTat | 337867 |
rs9517687 | snp | A/G | 0.324619 | 0.238604 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326313 | tgagcattttttcat[A/G]tacctattggccatt | 337867 |
rs9517690 | snp | A/C | 0.308414 | 0.24308 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334422 | AAATAATGTCATTTC[A/C]TTCAACGTCTTTTCA | 337867 |
rs9517691 | snp | C/G | 0.404035 | 0.196909 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336723 | ATCTGATAGGACTTA[C/G]GTTTCTTTAAAATTG | 337867 |
rs9517692 | snp | A/G | 0.312837 | 0.241974 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336792 | ACTCTTAATTGTGAT[A/G]TACAACACAAACTAA | 337867 |
rs9517693 | snp | A/G | 0.305436 | 0.243776 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337795 | CTTCTCTCTGTGGAG[A/G]GGAGAAAGGGTACAT | 337867 |
rs9517696 | snp | C/T | 0.0314385 | 0.121371 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349915 | ccctgactcctccaa[C/T]gaaaggagactccct | 337867 |
rs9517697 | snp | C/T | 0.308661 | 0.24302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360510 | ATTTGAGCCCAGTTA[C/T]TCTGGCTCTAGAGAC | 337867 |
rs9517698 | snp | A/G | 0.306927 | 0.243432 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362292 | CCCTCCTTAGGAACA[A/G]CTGAATTTTTTTCAT | 337867 |
rs9517699 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371026 | AGCAGTGAGTCACAT[C/T]CCTCATGGGGCAGCC | 337867 |
rs9517700 | snp | A/G | 0.306679 | 0.24349 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375558 | TCGCTTTCTGCAAGC[A/G]TCAGAATATGGGAAG | 337867 |
rs9517701 | snp | A/G | 0.307919 | 0.243198 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377286 | CTCATGCAAGTACCT[A/G]GTGCCAGTCCTTAGA | 337867 |
rs9517702 | snp | A/G | 0.308908 | 0.242961 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377955 | GGAGTCAGACCTAAG[A/G]CAGCATGCAGCTTCC | 337867 |
rs9517703 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378463 | acccaggaggtggag[G/T]ttgcagtgagccgag | 337867 |
rs9517704 | snp | A/T | 0.493925 | 0.054776 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380807 | TTGCTACTTAGCAAT[A/T]GTTTTTAATCTGGTG | 337867 |
rs9554571 | snp | C/T | 0.455024 | 0.143057 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216140 | ACAGTCTCACTCTGA[C/T]GCCTCAGCTGGAGTG | 337867 |
rs9554572 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232510 | CTTAATAAGTAGTTT[A/G]TTGTTTGTAATGATA | 337867 |
rs9554573 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234508 | GCTAGCCATTTCTAC[A/G]TGCATTACCTCACTT | 337867 |
rs9554574 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242751 | ccccacctctctccc[A/G]gacggggtggctgcc | 337867 |
rs9554575 | snp | C/T | 0.444444 | 0.157135 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242799 | acttcccagacgggg[C/T]ggctgccgggcggag | 337867 |
rs9554576 | snp | A/G | 0.222928 | 0.24853 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243010 | cggccgggcagagac[A/G]ctcctcactttccag | 337867 |
rs9554577 | snp | A/G | 0.205417 | 0.245993 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248453 | ctgcagtgcaatggc[A/G]tgatttctgctcact | 337867 |
rs9554578 | snp | C/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267349 | ttgtgtcctttgatg[C/G]AATTTTTGGAGCATA | 337867 |
rs9554579 | snp | A/G | 0.498673 | 0.0257246 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267651 | TCTTATGCTCTGAAA[A/G]GTATCTGCCTTTATT | 337867 |
rs9554580 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280773 | TAAATTATTGTGTCT[C/T]TGCTAATGTCCTTTt | 337867 |
rs9554581 | snp | C/T | 0.310632 | 0.242536 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310638 | ATGTGTATGTGTGGC[C/T]TAGTATTTAGTCATC | 337867 |
rs9554582 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317544 | CCATTGGACATAGAC[C/T]TAAGTAGGCTGGCAG | 337867 |
rs9554583 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333931 | TTTCattatattttt[C/G]ttaatttatttaaaa | 337867 |
rs9554584 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363865 | GCTCAATTCAGGAAC[A/G]TGCTGAATCTTTCCA | 337867 |
rs9557176 | snp | C/G | 0.20511 | 0.245937 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199550 | ACTGTGTTGATCTAC[C/G]AATCACAGATTTAGC | 337867 |
rs9557177 | snp | C/T | 0.478437 | 0.10157 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205730 | AGGGCGATCTGGCTG[C/T]GACATCTGTCACCCC | 337867 |
rs9557178 | snp | A/C | 0.205417 | 0.245993 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208107 | GGTTTGAGCAATTCT[A/C]CTGCCTCAGCCCCCC | 337867 |
rs9557179 | snp | A/G | 0.313082 | 0.241911 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223911 | cccagaatatagtct[A/G]ttttggtgaatgctc | 337867 |
rs9557180 | snp | A/G | 0.368529 | 0.220116 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235652 | aggtggcaagaacat[A/G]caatggagaaacgac | 337867 |
rs9557181 | snp | C/T | 0.222333 | 0.248464 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241905 | cgcagtgtttgtgtc[C/T]ctgggtacttgagat | 337867 |
rs9557182 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242770 | ggggtggctgccggg[C/T]ggagacgctcctcac | 337867 |
rs9557183 | snp | C/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242776 | gctgccgggcggaga[C/G]gctcctcacttccca | 337867 |
rs9557184 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242789 | gacgctcctcacttc[C/T]cagacggggtggctg | 337867 |
rs9557185 | snp | C/T | 0.311369 | 0.242351 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242853 | gcggccgggcagaga[C/T]gctcctcacctccca | 337867 |
rs9557186 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246172 | AATGTTTACAGTGTA[A/G]CTGCCTTTTGTGAAT | 337867 |
rs9557187 | snp | C/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259376 | TCAGACAAAACCATA[C/G]TAAATCTGTGGCTTA | 337867 |
rs9557188 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259540 | CAGTTACTTGCTTAA[A/G]AACTCAAGGTAAAGC | 337867 |
rs9557189 | snp | A/G | 0.19459 | 0.243782 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267626 | AGCCTTCCACTTGCT[A/G]CTGCTGCTTTCTTAT | 337867 |
rs9557190 | snp | A/T | 0.224965 | 0.248743 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271614 | TTCCCATTCTTTTTT[A/T]AAAAAGCACTTAATC | 337867 |
rs9557191 | snp | C/T | 0.205723 | 0.246048 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285162 | TAATATTATTTACTA[C/T]TGAAACTACTGTTTC | 337867 |
rs9557192 | snp | A/G | 0.209388 | 0.246679 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291911 | GTAGGTTCTATGGCA[A/G]TGCTGTATATATAAG | 337867 |
rs9557193 | snp | A/G | 0.264358 | 0.249587 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299767 | ATTGTGTCATCATGT[A/G]GAAACCTCACAGCAG | 337867 |
rs9557194 | snp | A/G | 0.205723 | 0.246048 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300036 | GTTTCAAAGTGGTCT[A/G]GGCTCTAAGGGCCAT | 337867 |
rs9557195 | snp | C/T | 0.202035 | 0.245356 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304368 | TCCTCTGAAAGGCAG[C/T]GTGGGTGTATTTGTG | 337867 |
rs9557196 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317175 | CTTGGTAAGTGTGCA[A/G]AACTTTGAGGTTTTC | 337867 |
rs9557197 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317196 | TGAGGTTTTCATCTA[A/G]CACAATGCCAGCGAT | 337867 |
rs9557198 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317207 | TCTAGCACAATGCCA[G/T]CGATGAACCTGGGCT | 337867 |
rs9557199 | snp | C/T | 0.365646 | 0.221644 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317252 | TCCTGCCTCTTCTTC[C/T]ACAATCAGAAGTAAA | 337867 |
rs9557201 | snp | A/G | 0.35809 | 0.225425 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337284 | TGCATCTTCCTATTC[A/G]TGGAACTGGTATCTT | 337867 |
rs9557202 | snp | A/G | 0.212122 | 0.247114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340026 | ACGGCTTTTTAAAAA[A/G]TGAAGACAGTGTCTT | 337867 |
rs9557203 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346491 | GTGTGCAAGCCCTTA[A/G]GCCAGCCATGCCTCA | 337867 |
rs9557204 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361532 | CCTTCCACTGTCCTG[A/G]AGTGGGTGTGTTGTG | 337867 |
rs9557205 | snp | C/G | 0.214239 | 0.247429 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383018 | TTCAAAGGGCAAAAT[C/G]AAGAGCTGTGGCATT | 337867 |
rs9557206 | snp | C/G | 0.375797 | 0.216044 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383959 | GGTTAATTTTGCTCA[C/G]AATATCCAGAGTTAG | 337867 |
rs9557207 | snp | A/G | 0.214239 | 0.247429 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384164 | CCACCATGTAGCACC[A/G]AGTAGCTCGCTCTCT | 337867 |
rs9582287 | snp | A/G | 0.23031 | 0.249223 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237406 | aaagacaaagattgc[A/G]tgttctcacacgtgg | 337867 |
rs9582289 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281066 | tggcgggcacctgta[A/G]tcccagctacttggg | 337867 |
rs9582290 | snp | A/G | 0.222928 | 0.24853 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284206 | GCTAAAATAAGAAGT[A/G]CAAATAAACACACAA | 337867 |
rs9582291 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367465 | ACTGGAGTTGGGACA[C/G]TCAGTGGCGTCACAG | 337867 |
rs9585021 | snp | C/T | 0.498277 | 0.0293024 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204226 | TTTAAAAAAGAACGT[C/T]TGTCCTCGGTGCTGT | 337867 |
rs9585023 | snp | C/T | 0.264084 | 0.249603 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218208 | TTTTACATTTAATCA[C/T]AGTGTTAATGTTTGT | 337867 |
rs9585024 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228334 | gctttgttgcccagg[A/C]tggagtgcaatggca | 337867 |
rs9585025 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228379 | tgcaacctccacctc[C/T]tgggttcaagcgatt | 337867 |
rs9585026 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230671 | catgacccaatttta[A/T]cttcgaagccaaggg | 337867 |
rs9585027 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237271 | atatatatatatata[C/T]acacacacacacaca | 337867 |
rs9585030 | snp | C/T | 0.222333 | 0.248464 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280105 | GTCACCATCTCAATG[C/T]CATCATCTGCACTGC | 337867 |
rs9585032 | snp | C/G | 0.207253 | 0.246318 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282927 | TAATGTGCTTGAAAT[C/G]TAATGTGCTTTTGTT | 337867 |
rs9585036 | snp | A/T | 0.217551 | 0.247885 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313074 | GCAAGCTCTGCCTCC[A/T]GGATTCACGCCATTC | 337867 |
rs9585037 | snp | A/T | 0.246485 | 0.249975 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348586 | CAGGACGGGTCTTCT[A/T]CCAAACTAAGAATTG | 337867 |
rs9585038 | snp | A/G | 0.245346 | 0.249957 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348598 | TCTACCAAACTAAGA[A/G]TTGCTGTTGTGTTCA | 337867 |
rs9585039 | snp | C/T | 0.227664 | 0.249 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363134 | GGACTGTATTCAGTA[C/T]GGGCTCATAACCAAG | 337867 |
rs9585040 | snp | C/T | 0.38821 | 0.208322 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363285 | AGAAATCCTTTCTTA[C/T]ATTTCTTCAAAATAG | 337867 |
rs9585041 | snp | C/T | 0.375598 | 0.21616 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365983 | GCCTTTTTTTGCCTT[C/T]GAGGTCTATTTATTT | 337867 |
rs9585042 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368688 | gtaaactcatgagag[A/T]gtgtgtgtgtgtgtg | 337867 |
rs9585043 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384690 | GTGACGCCAGGAGTG[C/T]GATGCCAGGGCCGAG | 337867 |
rs9585044 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384702 | GTGCGATGCCAGGGC[C/T]GAGCATGGCAGTGAC | 337867 |
rs9585045 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384707 | ATGCCAGGGCCGAGC[A/G]TGGCAGTGACGCCAG | 337867 |
rs9805153 | snp | C/T | 0.210909 | 0.246925 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336377 | CTAGTTTGTACCTTA[C/T]GTTTCTTAATTTAAA | 337867 |
rs9805233 | snp | C/T | 0.224116 | 0.248656 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361879 | GTGCACATCTATAGT[C/T]TCAGCTACTCAGGAG | 337867 |
rs10508037 | snp | A/C | 0.308908 | 0.242961 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374502 | TCCATTAGCCCAAGT[A/C]GAGAGAATGGCTTTA | 337867 |
rs10540867 | in-del | -/AT | 0.489434 | 0.0719116 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305292 | TCAGAGGATTCTCAC[-/AT]GTGTTATCTCATTTT | 337867 |
rs10622782 | in-del | -/CA | 0.375 | 0.216506 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299462 | GCACACACACACACA[-/CA]GAAAGATGTCTGTAT | 337867 |
rs10630757 | in-del | -/T/TT/TTT | 0.32885 | 0.23724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247873 | AATTCTCTCTCTCTC[-/T/TT/TTT]TTTTTTTTTTTACCT | 337867 |
rs10633287 | in-del | -/ATTT | 0.188644 | 0.244996 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305886 | CATAGACTCAGGGCC[-/ATTT]ATTTATTTATTTATT | 337867 |
rs10640542 | in-del | -/ATCT | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99258584 | CTTGAAGTCTGCATC[-/ATCT]ATCTATGGAAAGAGA | 337867 |
rs11069358 | snp | A/G | 0.205417 | 0.245993 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216644 | TCCCCAGGTCTTGGT[A/G]TTTGTTGATTCTTTC | 337867 |
rs11069359 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234205 | tttttttttttgaga[A/T]ggagtctcactctgt | 337867 |
rs11069362 | snp | C/G | 0 | 0 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352061 | GCCATTTGGTATCAT[C/G]TGAGATGTGCACCAG | 337867 |
rs11304203 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287664 | TTTTTTTTTTTTTTT[-/T]GGTAGAGACGAGGTT | 337867 |
rs11325868 | in-del | -/T | 0.357451 | 0.225731 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280834 | CTTCTTCTTTCCCTC[-/T]CTCTCTCTCTCTCTC | 337867 |
rs11338165 | in-del | -/T | 0.375 | 0.216506 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216835 | CTCTTTTCTTTTTTC[-/T]TTTTTTTTTTTTGAG | 337867 |
rs11406335 | in-del | -/G | 0.49681 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282225 | ATGACACTTGGGGGG[-/G]CAAAATCACCCATGA | 337867 |
rs11422677 | in-del | -/T/TT | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247884 | TCTCTTTTTTTTTTT[-/T/TT]ACCTCACCACTATAT | 337867 |
rs11428072 | in-del | -/A | 0.49334 | 0.057322 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353731 | TCCTCCCCAAAAAAA[-/A]GCCATCCTGATGGGT | 337867 |
rs11441292 | in-del | -/G | 0.0577344 | 0.159793 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306404 | TTGTGTGTGGGGGGG[-/G]CCACACAGCTTGTAA | 337867 |
rs11443091 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292309 | CCAGCTAATTTTTTT[-/T]TTTTTTGTATTTTTA | 337867 |
rs11451868 | in-del | -/A | 0.309648 | 0.24278 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363026 | GTTTGGCTTTCCACA[-/A]TTTAAATCTTTAATC | 337867 |
rs11551501 | snp | C/T | 0.00758275 | 0.0611062 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340506 | CAGAGAATGGAGCTG[C/T]TGGACCGGCAGCTGA | 337867 |
rs11551502 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386139 | CCTCCCTGTGGCAGG[A/G]CTAACTGCCTGGCCC | 337867 |
rs11557225 | snp | A/G | | | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258310 | GGAAACTACTTTTTA[A/G]AGCAACAAAAGAGTC | 337867 |
rs11617167 | snp | G/T | 0.163892 | 0.234703 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219444 | TAATTGCAGAACATT[G/T]TATCACGCCAGAAAG | 337867 |
rs11617711 | snp | C/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318512 | GGCTCAATGTTACTT[C/G]TGTGGTGATTAAAAA | 337867 |
rs11618451 | snp | C/G | 0.161924 | 0.233971 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285302 | CTTCCTCCTCTTCTT[C/G]CTCCCTTTGGTAGAG | 337867 |
rs11618564 | snp | A/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273491 | AAGCGGTTTCTTTAT[A/G]TGGTAGTTTGCCTGT | 337867 |
rs11618765 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316538 | GCCCTGTGCAATGGG[A/C]TATGACGTTGTGGGC | 337867 |
rs11618948 | snp | C/G | 0.223819 | 0.248625 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239128 | GGTATATGACTGCTA[C/G]CCTTTCTTTGCTAAG | 337867 |
rs11618955 | snp | C/T | 0.122758 | 0.215196 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362826 | TTGTAAACATTTTCT[C/T]TCAATCTGTAGTTTG | 337867 |
rs11620194 | snp | C/T | 0.19459 | 0.243782 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266212 | TTCTATATTATATTA[C/T]ATAATACTATATAAT | 337867 |
rs11620316 | snp | A/G | 0.130008 | 0.219321 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284285 | GCCTGAAGAAGCACT[A/G]TATGACACTCCAGTT | 337867 |
rs11620518 | snp | C/T | 0.157972 | 0.232445 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235316 | GGTATTCCATGCTTA[C/T]GGTTTGGAAGAATCA | 337867 |
rs11838457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373283 | TTTTTAAAACCAAAG[A/G]GGGAAAAACTCATCA | 337867 |
rs11838471 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257291 | TGTCATTCAAAGGAG[A/C]GTAATCTTGGAGGCT | 337867 |
rs11838488 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299527 | GAGTAATTTTGGGGC[C/T]TTACTCATATATTCT | 337867 |
rs11838527 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250249 | tgtatgtggtgcaag[A/G]taggggtacagtttc | 337867 |
rs11838656 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351243 | TTGTGGCTCTCAGGA[A/G]GTTTGAGAGAGTCCT | 337867 |
rs11838974 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274400 | gcagtggcatgatca[A/C]agcagcctcgacctc | 337867 |
rs11839133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217050 | tggccaggctggtct[C/T]gaacacctgaccttg | 337867 |
rs11839141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292657 | TATTCTATTTTTACT[A/G]TCCTCTCGCTGAATA | 337867 |
rs11839408 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306010 | aagggattctcctgc[C/T]tcaccctcttgagta | 337867 |
rs11839604 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228456 | accccaccacgcccg[A/G]ctaatttttgtattt | 337867 |
rs11839613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341332 | GCAAGAAGTAGGTCT[A/G]CAGATCTCACGATGG | 337867 |
rs11839876 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324605 | ctaagcactttacaa[A/G]cattattttaattag | 337867 |
rs11840204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277815 | CATCCCCTCTGTCAC[C/T]ACCCGCAAGCCTCAT | 337867 |
rs11840392 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200366 | CTCCGGCTCCCGTAC[C/T]CCTCTATCCGCATCT | 337867 |
rs11841085 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357643 | ATTTGTGGTTTCACC[A/G]GTTTCCCAGCATTGC | 337867 |
rs11841674 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203976 | ACCGGGTAAAAGTGC[A/G]TAGGATTAGTGATCA | 337867 |
rs11841930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209905 | gttgaacccaggagg[C/T]ggaggttgcagtgag | 337867 |
rs11842272 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240450 | CTCCATTTCCTTAAT[A/C]CTCAGATTTTCTTAG | 337867 |
rs11842400 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263823 | attgatgatacacag[C/G]gcagatagaacaaca | 337867 |
rs11842736 | snp | C/T | 0.498611 | 0.0263212 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324606 | taagcactttacaaa[C/T]attattttaattagc | 337867 |
rs11843501 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366917 | ATTTATCTATTAATA[A/G]CATTTTTAGGTGTTT | 337867 |
rs12019519 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250748 | atctttgattttttt[C/T]ttttttctttttttt | 337867 |
rs12020016 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250749 | tctttgatttttttc[C/T]tttttcttttttttt | 337867 |
rs12100212 | snp | C/T | 0.419776 | 0.18351 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314667 | GAGCTTTGGGGTTTT[C/T]AAGAAGCATTGTCAG | 337867 |
rs12232040 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374684 | CACCTTCTGAAAGCA[A/G]GGCTCTAATATTTAT | 337867 |
rs12232061 | snp | G/T | 0.224709 | 0.248717 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322738 | TGTGGTCTGAGTTTG[G/T]ATTGTTTTCTGTAAG | 337867 |
rs12428890 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200757 | GCACGCCCCTGACTG[A/C]GCATGCGCCGGGTGC | 337867 |
rs12429568 | snp | A/G | 0.155325 | 0.23138 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333644 | GAACACAAAAGCCCT[A/G]CTTCCCTGCCAGAAT | 337867 |
rs12430175 | snp | C/T | 0.413992 | 0.223693 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384522 | AAAAACAATGCATGC[C/T]TGTTCCTCCCTGCTT | 337867 |
rs12431275 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332885 | ACATATGGTCTTTTT[A/C]TAAAGCCTGCTTTTC | 337867 |
rs12561406 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242810 | ggggtggctgccggg[C/T]ggaggggctcctcac | 337867 |
rs12583270 | snp | G/T | 0.313326 | 0.241847 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309459 | AGAAGAGGTGATGGG[G/T]TCATTATCCTGTAAG | 337867 |
rs12583989 | snp | C/T | 0.309401 | 0.24284 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224490 | TTGTGGATTTATCTA[C/T]GTCCCATTTCAGTTC | 337867 |
rs12585056 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262894 | GGGTTGTTGGTTTAA[A/G]ACAAGTTACTTAGGA | 337867 |
rs12585062 | snp | A/G | 0.00956916 | 0.0685055 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262986 | CAGGCATGATTCTGA[A/G]AGCCTCACATGCTTG | 337867 |
rs12585224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263081 | TACTCATGACTCTCA[A/G]ATTGTATGTTCTTTC | 337867 |
rs12856660 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232401 | TCCTTAGTTGAGAGA[G/T]ATAGATATATATATA | 337867 |
rs12857217 | snp | C/T | 0.212122 | 0.247114 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264182 | TTTTCTTTTGAGAGA[C/T]GGTAAGCTTGAGGTT | 337867 |
rs12858044 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373172 | CTCTCttttttattg[G/T]ttttttttttttttt | 337867 |
rs12859788 | snp | A/G | 0.169435 | 0.236663 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303183 | AGGACCAAGTACAGA[A/G]AACTTCTTCAAGACA | 337867 |
rs12861519 | snp | A/C | 0.427423 | 0.176128 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377301 | AGTGCCAGTCCTTAG[A/C]GCAGAGGAGACCTGT | 337867 |
rs12863189 | snp | G/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228065 | tgagtcatgttgagt[G/T]gctcagaagctggca | 337867 |
rs12864373 | snp | A/T | 0.223522 | 0.248594 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236844 | gaaagagcaaaactc[A/T]gtctcaaaaacggca | 337867 |
rs12865617 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330477 | AAAAAAAAAAAAAAA[A/G]AAATACAGTTGATTT | 337867 |
rs12866777 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242699 | gaccccccccacctc[C/T]ctccccgacggggcg | 337867 |
rs12866783 | snp | C/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242705 | ccccacctccctccc[C/G]gacggggcggctggc | 337867 |
rs12866788 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242713 | ccctccccgacgggg[C/T]ggctggcctggccgg | 337867 |
rs12867203 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318537 | TAAAAAGGGCCAGTC[A/T]Cggccaggcgcagtg | 337867 |
rs12867344 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318546 | CCAGTCACggccagg[C/G]gcagtgactcacgcc | 337867 |
rs12869170 | snp | A/C | 0.205723 | 0.246048 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231061 | tcaaaaaaaaaagga[A/C]tcttgtgattgcata | 337867 |
rs12870206 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262740 | aaaaaaaaaaaaaaa[A/G]GGACTTGTGGAAGGT | 337867 |
rs12871250 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204828 | GAAAGTGCTTTCAAG[A/T]TCTCGGTTCTGAGAA | 337867 |
rs12872502 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204829 | AAAGTGCTTTCAAGA[C/T]CTCGGTTCTGAGAAT | 337867 |
rs12872667 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287667 | tttttttttttttgg[G/T]agagacgaggtttcg | 337867 |
rs12876116 | snp | G/T | 0.190205 | 0.242744 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256684 | GTAACTTGATGTGTA[G/T]GTAGAAACTTATAAA | 337867 |
rs12876124 | snp | C/T | 0.0371959 | 0.131204 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256696 | GTATGTAGAAACTTA[C/T]AAATTTCCATCACCA | 337867 |
rs12876442 | snp | C/G | 0.0810805 | 0.184299 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214312 | CTGGATCTTGCTTGG[C/G]CGTTCTTGTGCAGTC | 337867 |
rs12877371 | snp | A/C | 0.213635 | 0.247341 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350687 | gtcagtgtttccctg[A/C]gttctgtgagccatc | 337867 |
rs12877480 | snp | C/G | 0.247053 | 0.249983 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350564 | agcagggtgcagggg[C/G]tgccagagaggggca | 337867 |
rs12877831 | snp | C/T | 0.391397 | 0.206172 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336498 | TCCATTGCAAGTTTA[C/T]GTTTGGTGTCAGGAA | 337867 |
rs12877932 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232284 | ACTGAGAAAGGAGCA[A/C/G]ACTTTAATATTGAAT | 337867 |
rs12877943 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232304 | TAATATTGAATGTAA[A/C]CAGAAATAAACAAAT | 337867 |
rs13378347 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378862 | gtacttttatattta[C/T]ccttcattgatctaa | 337867 |
rs16956400 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216611 | GCCCTCAATTCTCCC[A/G]AAGATTGTTCATATT | 337867 |
rs16956405 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246617 | ATGGAATCGAATGAC[A/C]GTAGAACTTTCATAT | 337867 |
rs16956413 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279351 | TGAGAGAATAAACTG[C/G]CACCATTCAAGTGTT | 337867 |
rs16956420 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292092 | TGATTGAGTTGTCTT[C/G]TTTATGGCCAGGATA | 337867 |
rs16956428 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301364 | TTATTTTTATTGGTA[A/G]ACAAAGGAGACAATC | 337867 |
rs16956449 | snp | A/G | 0.423881 | 0.179625 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314351 | TTGGCTTCATGATCT[A/G]TATCAAATGTTTAAA | 337867 |
rs16956456 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315567 | GGTTGTTGAATTTCG[A/G]TTTAATGACTTGGTC | 337867 |
rs16956458 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316218 | ATCTAGGTCCTTAGC[A/G]TGAATGGCATGCAGG | 337867 |
rs16956459 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322794 | AGAAGAAACACTTTA[C/G]GATGGTGCAAGATTA | 337867 |
rs16956475 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363768 | TTTCCAAAGGGGGAA[A/G]ATGGATATTGGAAGT | 337867 |
rs17471994 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293661 | TGCCTATTTTTGACA[A/G]TGGCTTTAAAATCAG | 337867 |
rs17472050 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303144 | TCAGACCAGCTCCCA[A/G]TAGATCTGCGAAAGG | 337867 |
rs17472169 | snp | A/G | 0.341909 | 0.232492 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316258 | GACTGTCTGGTGTCA[A/G]CTCCCCCTGTGCCCA | 337867 |
rs17472302 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366879 | TCCACTTACTTCTTT[C/G]ATATTTAGCTGTGTA | 337867 |
rs17575181 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204676 | ACGGGCCTGAAGCGC[A/G]ACCTGTGGGAAAGAA | 337867 |
rs17575384 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282953 | TTGTTATCTGAACTA[A/G]AGGAAAAAGGCTTTG | 337867 |
rs17575643 | snp | C/T | 0.173643 | 0.238054 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332421 | GAACCGTGTAATTGA[C/T]GTCCATGTTTATTAG | 337867 |
rs17575699 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353491 | ATGAGAAAAAAGAGC[A/G]AGGTACAGTCTCATG | 337867 |
rs17575706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355163 | GTTTCTGTCAAAACA[C/T]TTACTGTAACAAGTA | 337867 |
rs17575748 | snp | G/T | 0.0139853 | 0.0824443 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372144 | AGTGCGCCCTGTGCT[G/T]CCTGGCCTGCTAGCT | 337867 |
rs17655647 | snp | A/G | 0.495559 | 0.0469148 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210128 | AAATAGAAAAAAAAC[A/G]GTCCTAGCATTTCAT | 337867 |
rs28394244 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285943 | CTCCCTGAAACTCCC[C/T]GATCCCTAGACTCTG | 337867 |
rs28454852 | snp | G/T | | | synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238530 | CTTTGTGTATGACCT[G/T]CACGCAGTCAAGAAC | 337867 |
rs28464652 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361315 | AAAGGAAACATTTCC[A/T]GTTTATAGAGGCTCA | 337867 |
rs28526763 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348629 | TCCTGCCAGAAGTGG[G/T]GGATCAGTGAGGCCT | 337867 |
rs28576575 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222684 | ACATTGATTTGCTTT[C/G]CATTCCCAGGATAAG | 337867 |
rs28600964 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228789 | TTAGATTTTAGATTC[C/T]GTGGAGCCTTGTTTG | 337867 |
rs28605076 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251820 | AGCTCAGTTTCTAGA[G/T]GACCCTCACATGTCA | 337867 |
rs28626604 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376617 | ATGTTACATTTGGGG[A/G]ATGTTAGTGTCTAGA | 337867 |
rs28669849 | snp | G/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259724 | GGACAGAAATCTGCC[G/T]GCATGCAGACCTAAT | 337867 |
rs28700111 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206726 | CAGCTAAGTTTCTGG[G/T]ATTCATTTCTCAGCT | 337867 |
rs33946546 | snp | C/T | 0.169435 | 0.236663 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259498 | ACCATAGCAACTATT[C/T]CTTGTGTGGATGAAG | 337867 |
rs34003948 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267933 | TAGGCAGGCTCTGTA[-/C]CCGGTAAGTCGTCAA | 337867 |
rs34012077 | in-del | -/T/TT | 0.616473 | 0.12875 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241726 | AGTTAAAATTTTAAC[-/T/TT]TTTTTTTTTTTTTCA | 337867 |
rs34018220 | in-del | -/G | | | intron-variant, frameshift-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99295563 | CCCAAGCAGAATCCA[-/G]GGGAAGAGATTTAGT | 337867 |
rs34026571 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264968 | TTTTTTTTTTTTTTT[-/T]AATTGTTCTTCAGTG | 337867 |
rs34031700 | in-del | -/CC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347334 | CCCCCCCCCCCCCCC[-/CC]AGGAAAAAAAAGGCA | 337867 |
rs34039955 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249162 | TAGTTAGTTTTTCAA[-/C]CCCTTGCTCCCCTCC | 337867 |
rs34075883 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268789 | ATATGCCCCTAGATG[-/C]CCATTTGTAGGATTA | 337867 |
rs34094820 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371470 | CAGTGGGTACTATAG[-/C]AGATTATAAAAGATA | 337867 |
rs34131091 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273334 | CAGATTAGGTTAAGA[-/G]GGGGCAGTGAGCACC | 337867 |
rs34164759 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375990 | TTTTTTTTTTTTTTT[-/T]GGTAGAGACAAGGGT | 337867 |
rs34166694 | snp | C/G | 0.021333 | 0.101051 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310951 | CTATAATCACCAAGA[C/G]AGCAGGCCATATTTT | 337867 |
rs34209917 | snp | C/T | 0.497907 | 0.0322805 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209940 | GATCATGCCATTCCA[C/T]TGCACTCCAGCCTGG | 337867 |
rs34232562 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276660 | TTCCTGGAGGCTGGT[-/G]GGGTGGTGCTGAAAG | 337867 |
rs34237437 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263547 | GGTATCGAGTAACAA[-/G]GGAACATTGCTGGTG | 337867 |
rs34246185 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265563 | CATGTGGGTACTGAT[-/C]CCCTGATTGCACTTT | 337867 |
rs34259893 | in-del | -/A | 0.495213 | 0.048687 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377210 | CTGGTGCCAGCCCTC[-/A]AGGGAGCTCACCGTC | 337867 |
rs34286895 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259730 | GGACAGATTAGGTCT[G/T]CATGCAGGCAGATTT | 337867 |
rs34291227 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325270 | ACCATGCCCAGCTAA[-/T]TTTTTTGTGTTTTTT | 337867 |
rs34297241 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311313 | GGTGCGGTTTGAAAT[-/G]GGGGCAGTCAGGGAG | 337867 |
rs34314551 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263989 | GTAAACCTTTTGGGT[-/G]GGGGTGTGGGCATGT | 337867 |
rs34318354 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375801 | CTTTTCCTTTTTCCC[-/T]TTTTTTTTTTTTTTT | 337867 |
rs34324109 | in-del | -/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99307491 | TCACCCTGTGACTGA[-/G]GCATGTAATGAGCAG | 337867 |
rs34326221 | in-del | -/A | 0.144296 | 0.226554 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370030 | GATTTTGTACTGGAG[-/A]AAAAATGTCTGATGA | 337867 |
rs34339709 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293722 | TCTGAATATACTAGT[-/A]AAATGGTGTTGAATC | 337867 |
rs34350028 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226914 | TAAGACCGGCACCCC[-/T]TTGGCTGGGCGCGGT | 337867 |
rs34354981 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213153 | GCATTCAAATACACA[-/T]TTTGATGTTCTTCCA | 337867 |
rs34378425 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214129 | GGCCTGATTGTGTAT[-/A]TTATTGTAGAGCCAG | 337867 |
rs34395953 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281024 | AACTCCATCTCTGCT[-/A]AAAATACAAAAATAA | 337867 |
rs34537761 | in-del | -/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259345 | GTTTGGGGTCCATCC[-/T]TTTTTTTTTTTTTTC | 337867 |
rs34600801 | snp | A/C | 0.188 | 0.24219 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331553 | TTTAGTATCATTTCT[A/C]TTCCCTCATATGAGA | 337867 |
rs34600991 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231407 | GCTTTGCTGTATACA[-/T]TTTTTTTTTTTTTTT | 337867 |
rs34624945 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223951 | TGAAAAAATGTGTAA[-/C]CTTGCCGTTGTTGGG | 337867 |
rs34647286 | snp | A/G | 0.204803 | 0.245881 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212998 | CATAATGATTCCCAC[A/G]CCCACGTAACCATTG | 337867 |
rs34647733 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324238 | AAATATGTTCTGCCC[C/T]TCTCTACTGAAGCCC | 337867 |
rs34731765 | in-del | -/T/TT/TTT | 0.245916 | 0.249967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292718 | AAATAGCTTTGAGGG[-/T/TT/TTT]TTTTTTTTTTTTTAA | 337867 |
rs34751916 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232506 | GGGCTTAATAAGTAG[-/T]TTTATTGTTTGTAAT | 337867 |
rs34777739 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386126 | CCCTTGCCTGCCCCT[-/A]CCCTGTGGCAGGGCT | 337867 |
rs34831043 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300037 | TTTCAAAGTGGTCTA[A/G]GCTCTAAGGGCCATC | 337867 |
rs34849046 | in-del | -/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256049 | AATTACTGTGAATGT[-/T]CAGTAGTTAACCAGT | 337867 |
rs34867310 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313703 | GTGCCATGGCGACAG[-/T]ATCACTGGACAGGGC | 337867 |
rs34874753 | in-del | -/ATT | 0.373598 | 0.21731 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364162 | TTGGTTTTTGTTCTC[-/ATT]ATGCTGTGACTTGTG | 337867 |
rs34906550 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315642 | CCCCATCTATCAAAT[-/G]GGGGATGATAATATC | 337867 |
rs34923467 | snp | A/G | 0.078151 | 0.181571 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307517 | AGCAGTTAGCCTCGT[A/G]TACGTGTGTGCACTT | 337867 |
rs34923520 | in-del | -/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368235 | GGAGGATGGGGAGGG[-/G]AGTGTGCCTTTGGCA | 337867 |
rs34924388 | in-del | -/AGTT | 0.455024 | 0.143057 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201659 | AGACTGCGTGTTAAC[-/AGTT]AGGCACGGGTACAGC | 337867 |
rs34925730 | snp | A/T | 0.496245 | 0.0431677 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208581 | TCTTCATTCAAAGAT[A/T]AGACTTTCCCCCCTT | 337867 |
rs34945610 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342260 | AAAATGGGGACCAGT[-/C]CCTGTTGGGTAAGTC | 337867 |
rs34949273 | in-del | -/TT | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214837 | TTTGTAGACTGTGGG[-/TT]TGGGGAAGGGTTTGA | 337867 |
rs34955321 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282990 | CAAGAGAATAGGCAT[-/C]CCCTGTTTTGGCTGG | 337867 |
rs35022784 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207893 | TTTTGTGTTCTCATG[-/A]AAGGAGCAAACCGTG | 337867 |
rs35053968 | in-del | -/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256087 | AGAGAGAATGGGAAC[-/T]TTTTCCTTTGTTACA | 337867 |
rs35055617 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273813 | CTCAGTTCTTTCTGG[-/T]AAATCCTATTACCTA | 337867 |
rs35060502 | in-del | -/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99307462 | TTTTATGGTGGTGAC[-/T]TTTTTTTTTCTCTGT | 337867 |
rs35078558 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258233 | CTATTTTAACAGAAG[A/C]AACTCAAAGATATCC | 337867 |
rs35079734 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223955 | AAAATGTGTAACTTG[-/C]CCGTTGTTGGGTGGA | 337867 |
rs35086120 | snp | G/T | 0.048067 | 0.147387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243988 | CTTTGCTACTTAGGC[G/T]GTAGAAAAAAATTTT | 337867 |
rs35088344 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233763 | AAATTATCATTATGT[-/A]AAACCCTAGTGTAAG | 337867 |
rs35107471 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371432 | CTGGCATTATTCATT[-/C]CTGCAGGCTCTTGGT | 337867 |
rs35122971 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345402 | AGGAGACAAATAGAA[-/G]GGAGGTTTCTAAAGC | 337867 |
rs35123648 | in-del | -/A | 0.375996 | 0.215928 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384332 | TTTTAATATAAGTAC[-/A]AAAAAAATGTATTCC | 337867 |
rs35132998 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314823 | CGAATGTCAATTGCT[-/C]CCCTGCTGGGCTCCA | 337867 |
rs35174102 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227904 | GAGGTTTGAGGAGAG[-/A]AGGAAGAGATAGTGT | 337867 |
rs35191508 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321352 | TCGCTGTGTCACTCA[-/G]GGCTGGAGTGTAGTG | 337867 |
rs35193753 | in-del | -/GTGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368689 | TAAACTCATGAGAGA[-/GTGT]GTGTGTGTGTGTGTG | 337867 |
rs35213725 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343590 | CAGAGCAGGACACCA[-/G]GCCCCTGGGCTCTTG | 337867 |
rs35278611 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99279404 | TTTTGCAGAAGCTGT[-/G]CTTTGACTACCCCCA | 337867 |
rs35291365 | in-del | -/C | | | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255905 | GCATGATACTTAGAA[-/C]ACTGTAAAAATAGTT | 337867 |
rs35298349 | snp | C/T | 0.167158 | 0.235875 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343483 | TGCATTCCCACCAGG[C/T]GCCTGTGAAGTGGCA | 337867 |
rs35300790 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320770 | GGAAGATTGTAAAAG[A/C]CAATATCAGTATTAT | 337867 |
rs35300879 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211912 | CATGGCAGCCTCCTT[-/A]CCTGGGTTCTACCAT | 337867 |
rs35309448 | snp | A/G | 0.17138 | 0.237316 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224201 | GCCTGCTGGCTTCTA[A/G]CTGTGTCATCACATG | 337867 |
rs35336464 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241265 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 337867 |
rs35343898 | in-del | -/A | 0.181022 | 0.240296 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290728 | CACCGTTTCACCACC[-/A]AAAAAAAAAAAAAAA | 337867 |
rs35353148 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311195 | AAGCTTCCATTCTAC[-/T]TTTTAAGATAGATAG | 337867 |
rs35362714 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220054 | ATCCTGTGTTTTCAG[-/T]TTTTCTTGGGTATAT | 337867 |
rs35362750 | in-del | -/G | 0.375797 | 0.216044 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384120 | CCCTGAGCAGAGGAA[-/G]GGGTGGTGATACTGG | 337867 |
rs35371140 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379980 | ATTGTGGGGAACCTG[-/C]CCCACTGGCATGTGC | 337867 |
rs35419383 | in-del | -/T | 0.366266 | 0.221319 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218495 | TTCTCTTTCCTGACC[-/T]TTTTTTTTTTTTCCC | 337867 |
rs35455438 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212663 | GGGACATAAAATATA[-/G]GGGAAAAAAACATAA | 337867 |
rs35494820 | in-del | -/A | 0.213635 | 0.247341 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332932 | CAAGAAAACTCGCTC[-/A]ATTCAGAAGACCTAG | 337867 |
rs35595586 | in-del | -/G | 0.223225 | 0.248562 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246499 | AGCCTACTGAGTGAT[-/G]GGGAGGTATGTGTGT | 337867 |
rs35605326 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253937 | ATTTATTTTACTTCC[-/C]ATAAGTATTCAGGAT | 337867 |
rs35626687 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345770 | TTTTTGAGACAGAGT[-/G]CTTGCTCTGTTGCCC | 337867 |
rs35640725 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248389 | ACCATGCCCACCTAA[-/T]TTTTTTTTTTTTTTT | 337867 |
rs35656558 | in-del | -/A | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256524 | GAAAGCAGCACCTTG[-/A]AAAAAGCTAGTGCCG | 337867 |
rs35656713 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289267 | AGATGGATGGCTTTG[-/C]AGTAGTCAAAGAAGG | 337867 |
rs35673982 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221963 | TAGGTAATGTACTCT[-/C]CCGAGTCACAGTTTT | 337867 |
rs35686257 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274491 | TGGCTAGTTTTTTTT[-/T]ATTTTTAGTAGAAAC | 337867 |
rs35694871 | snp | C/T | 0.211819 | 0.247067 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384701 | AGTGCGATGCCAGGG[C/T]CGAGCATGGCAGTGA | 337867 |
rs35715041 | snp | C/T | 0.223225 | 0.248562 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289767 | CAGTTGGGTGGGGCA[C/T]GGGGTGGGAGTTCTC | 337867 |
rs35729364 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244294 | TAAAAATTATGGCTG[G/T]TAATACATTTGAGCA | 337867 |
rs35763604 | in-del | -/A | 0.417196 | 0.185864 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347195 | AAGAGGGAAAAAAAA[-/A]GAACCCCCAGGGACC | 337867 |
rs35773388 | in-del | -/A | 1.84521e-05 | 0.00303738 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296168 | GGTCCAGGTGTCTAG[-/A]AAAAAACCAAGAAGG | 337867 |
rs35775451 | in-del | -/GGC | 0.207559 | 0.246371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352639 | TTCCTGTTGCCTCTT[-/GGC]CTCACCAGTGCTACC | 337867 |
rs35812595 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378698 | ACTGAACATAGCACA[A/G]GCCAGAGGTTGTGTC | 337867 |
rs35823326 | in-del | -/T | 0.232651 | 0.249397 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360107 | TTCTCCATTTTACTC[-/T]TTTTATGGGGCACCA | 337867 |
rs35837824 | in-del | -/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303007 | CTGTTTGGGGGACCT[-/C]CCCCTGCCTCCTGGG | 337867 |
rs35861217 | in-del | -/AC | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299466 | ACACACACACGCACA[-/AC]CACACACACAGAAAG | 337867 |
rs35884013 | in-del | -/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257531 | TGTCACCAATACTTA[-/T]ATTCATTTGCTGACG | 337867 |
rs35891357 | snp | G/T | 0.0810805 | 0.184299 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213979 | GTGCACCACCACACC[G/T]GGCTAATTTTTGTAT | 337867 |
rs35912802 | snp | A/C | 0.412249 | 0.190198 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233982 | TATTTTATTATTATT[A/C]TTATTCTTATTTTCA | 337867 |
rs35941591 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224874 | AGTAAAAGTACAAAT[-/C]CTTGAGTTGATGAGC | 337867 |
rs35963404 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355863 | CGCCCTGGTGCATGG[A/C]TGAGCCATGTGCATC | 337867 |
rs36039409 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385763 | TCCTTCTTCATGGAC[-/T]TTTTTTAGTTACTGT | 337867 |
rs36041704 | in-del | -/CT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280831 | TTCCTTCTTCTTTCC[-/CT]CTCTCTCTCTCTCTC | 337867 |
rs36042800 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213222 | CAATTTTTTTTTTTT[-/T]ATTTAAGATGGGATT | 337867 |
rs36051995 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322699 | CAATCTGTTACACCC[-/A]AAAGTAAGATTTGGG | 337867 |
rs36083848 | in-del | -/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300243 | CGACCGTTGTGCACT[-/G]GGAGGTGGCCAAAGA | 337867 |
rs36110013 | snp | A/G | 0.167158 | 0.235875 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344034 | TGGAGCTTAGGTCCT[A/G]TCTCTCTTGCAGAAT | 337867 |
rs41279138 | snp | G/T | 0.0063894 | 0.0561594 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255314 | GTCGAGTGAGGTTCA[G/T]CACGTTCACAGCTTT | 337867 |
rs41279140 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256020 | TCGAGAGCATTTAAT[C/T]AAGGAACGATTCAAC | 337867 |
rs41279142 | snp | C/T | 0.0566069 | 0.158427 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258610 | AGAGAAGATTTGATA[C/T]TGAGTAAAAGGGGGT | 337867 |
rs41280144 | snp | A/G | 0.000562392 | 0.0167595 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295777 | GTCAATACTCAGGCA[A/G]GTCATAAAGTTCACA | 337867 |
rs41280146 | snp | C/T | 0.000791039 | 0.0198719 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295867 | TCTCCAGTCAAAGCC[C/T]ATTGCATAGTAGGCT | 337867 |
rs41308570 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314669 | GCTTTGGGGTTTTCA[A/G]GAAGCATTGTCAGCT | 337867 |
rs41315058 | snp | C/T | 0.00240096 | 0.0345646 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201221 | TGGGGCCGCTGCAAG[C/T]GGGCAGGTGCCCTGG | 337867 |
rs55661380 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245990 | AGTATGAAATATAGA[C/T]ACCAGATATTTAAAA | 337867 |
rs55672515 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325120 | TTTTTTTTTTTTTTT[-/T]GATACGGAGTCTCTC | 337867 |
rs55689056 | snp | A/G | 0.347694 | 0.230122 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342895 | GGGGTTCCCCTGATC[A/G]CTGTCTTTCAAGATT | 337867 |
rs55760478 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335457 | GAATGCCTCTGCCTA[C/T]CCCCTACCCTGTCCC | 337867 |
rs55772696 | snp | C/T | 0.140581 | 0.224783 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223957 | AAATGTGTAACTTGC[C/T]GTTGTTGGGTGGAGT | 337867 |
rs55826332 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280428 | CAAACTTCTACCAAG[A/G]AAACAAGGAGAACTT | 337867 |
rs55907415 | snp | A/G | 0.161924 | 0.233971 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297392 | TATATTTAAAGAACT[A/G]TACAGTATTTCCTTA | 337867 |
rs55913986 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312334 | TCTTTTTTTTCTGGT[A/G]CCATTTTCCCAAAAG | 337867 |
rs55921446 | in-del | -/TGAGCGTGGCAGTGACGCCAGGAGTGTGATGCCAGGGC | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384815 | GTGTGATGCCAGGGC[lengthTooLong]CGAGCGTGGCAGTGA | 337867 |
rs55943303 | snp | C/G | 0.157311 | 0.232183 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384403 | TTAATTGGGAAAAAA[C/G]GTTGCAAATAAGCTT | 337867 |
rs55974901 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256094 | AATGGGAACTTTTCC[C/T]TTGTTACAGCTATAG | 337867 |
rs56134626 | in-del | -/AATT | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244815 | AATCAATTTTATATT[-/AATT]CTTTCTTTAAAATTT | 337867 |
rs56162973 | snp | A/T | 0.157642 | 0.232314 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339793 | GGTGAGGATTTTAAA[A/T]GTCTAGAAAAATCAG | 337867 |
rs56176137 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226476 | TTCCCTAACAGCCTT[C/T]TAACTGGTTTACTAT | 337867 |
rs56192948 | in-del | -/TT | 0.164873 | 0.23506 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277808 | TTGCCCCATCCCCTC[-/TT]TGTCACCACCCGCAA | 337867 |
rs56222963 | snp | A/G | 0.144296 | 0.226554 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357268 | CACATCTAGGTTTCT[A/G]TAAGTACACAGCAAC | 337867 |
rs56315294 | in-del | -/ATG | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325069 | GACAGGATTCAAATG[-/ATG]TAGGTAGCATAACTT | 337867 |
rs56386226 | in-del | -/TTAT | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305908 | TATTTATTTATTTAT[-/TTAT]CTATCGAGACAGAGT | 337867 |
rs56695114 | in-del | -/T | 0.0596104 | 0.162024 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318176 | ACTGTCTCACCATTC[-/T]TTTTTTTTGAGACAG | 337867 |
rs56732866 | snp | G/T | 0.28052 | 0.24813 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232399 | CATCCTTAGTTGAGA[G/T]ATATAGATATATATA | 337867 |
rs56785191 | in-del | -/CAAGAATGCAGTGAGC | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262651 | GAGGTTGCAGTGAGC[-/CAAGAATGCAGTGAGC]TGAGGCTGAACTCCA | 337867 |
rs57005833 | in-del | -/TT | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314280 | TTTTTTTTTTTTTTT[-/TT]GGTCTTTTTCTCATT | 337867 |
rs57125709 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357909 | GTTATCCATTTTGCA[A/G]CTGTTTCTTGAGTGC | 337867 |
rs57174182 | in-del | -/GTGC/GTGTGC/GTGTGT/GTGTGTGTGT | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368726 | TGTGTGTGTGTGTGT[lengthTooLong]ACACATACCCTCACT | 337867 |
rs57203383 | in-del | -/C/CTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338045 | CTTTTTTTCTTTTTT[-/C/CTT]TCTTTTTTTTTTTTT | 337867 |
rs57466771 | in-del | -/CA/CACACAC/CACACACACACA | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237298 | ACACACACACACACA[-/CA/CACACAC/CACACACACACA]GTGGAATATTATTCA | 337867 |
rs57530761 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372721 | AAGAAGATAAATAGA[A/T]ACTGTTTGTCAACAA | 337867 |
rs57546006 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277805 | ACTCTTGCCCCATCC[C/T]CTCTGTCACCACCCG | 337867 |
rs57779407 | in-del | -/TTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375990 | TTTTTTTTTTTTTTT[-/TTT]GGTAGAGACAAGGGT | 337867 |
rs57796820 | snp | A/T | 0.5 | 0 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254461 | CAACATAATTTCTTA[A/T]ATAGGAATTCTGGAA | 337867 |
rs57840599 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219515 | CCCATGGGCCATATG[C/G]GACCCAAGACAGCTT | 337867 |
rs57922081 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381753 | CCTCTCCCTGCACAA[C/G]CTGATGGAGGCTTGA | 337867 |
rs58033174 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366428 | CTCCAGAGTAATTTT[-/T]ACATTTGCTTTTGCT | 337867 |
rs58095792 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242693 | GGGGCTGACCCCCCC[-/C]ACCTCCCTCCCCGAC | 337867 |
rs58103279 | in-del | -/TATT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203054 | ATTTATTTATTTATT[-/TATT]GAGATGGAGTCTCAC | 337867 |
rs58112188 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223958 | AATGTGTAACTTGCC[A/G/T]TTGTTGGGTGGAGTG | 337867 |
rs58113819 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219655 | CCCAAGATAATTCTT[C/T]TTTTCCAGTGTGGCC | 337867 |
rs58126781 | snp | A/C | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351074 | AAGAACAAGAATGGG[A/C]AGTTAGGGACTCAAT | 337867 |
rs58140652 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259145 | CAGCAGAAAGGGAAG[C/T]GAGCAACGAATCGCT | 337867 |
rs58182971 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330677 | TATTATACTAGCTAG[A/G]ACCTCTAATAGAATA | 337867 |
rs58199058 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325748 | TCTGATTCTGTGAAA[C/T]TGACTATCTTATATA | 337867 |
rs58212310 | snp | C/G | 0.0399052 | 0.1355 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308120 | AACCAACTAACGTGT[C/G]TGTCAGAATGCAGTT | 337867 |
rs58218583 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253462 | TTATTAGACTTTTTG[C/T]GTTTATCTTTTTTTT | 337867 |
rs58282002 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303198 | GAACTTCTTCAAGAC[A/G]GAAAAAGACAGAAAA | 337867 |
rs58290528 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373172 | CTCTCTTTTTTATTG[-/TT]TTTTTTTTTTTTTTT | 337867 |
rs58304241 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227624 | CCTAGTTCATTTCTC[A/T]TAGGATTTATTTCCA | 337867 |
rs58313297 | in-del | -/A/ACC | 0.375 | 0.216506 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343379 | ACGGTGTCTTTCCCC[-/A/ACC]CCAGATACTTGGAAC | 337867 |
rs58403451 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278780 | ATCTGTTTTACTGGT[A/G]CGAAAACATTTTTAG | 337867 |
rs58662292 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335877 | TCAGTTCCCTCCATC[C/G]TTACCAAAACCTCAC | 337867 |
rs58673326 | in-del | -/TTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373172 | CTCTCTTTTTTATTG[-/TTT]TTTTTTTTTTTTTTA | 337867 |
rs58716363 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294955 | CAATGAAAGAAATAT[A/G]AAAGAATACTAATTG | 337867 |
rs58739511 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301300 | TCGGCCTTCAAGGCT[C/G]CTGTACCTTCTGCTG | 337867 |
rs58776228 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345918 | CGGCTAATTTTTGTA[A/T]TTTTAGTAAAGACGG | 337867 |
rs58944134 | in-del | -/C | 0.308414 | 0.24308 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352798 | GTGATGGTCACTCTT[-/C]CTGGGAGAAATGTGT | 337867 |
rs58955687 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271156 | AAAATAAAAATTTGT[A/T]ATATATATATGCCAG | 337867 |
rs59020204 | snp | G/T | 0.498632 | 0.0261223 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247224 | GTTTTGTTTTGTTTT[G/T]TTTTTCTTGAGACGG | 337867 |
rs59056819 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215358 | CCTGAGATAACAAGG[A/C]ATCCAGGCATACATT | 337867 |
rs59113998 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289018 | AAATAATAGACCATA[G/T]ACCGTACGATGGCTG | 337867 |
rs59168010 | in-del | -/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287644 | TTTTTTTTTTTTTTT[-/T]GGTAGAGACGAGGTT | 337867 |
rs59174527 | in-del | -/GT | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327503 | TGTGTGTGTGTGTGT[-/GT]TTAAGTGTCCAGTGT | 337867 |
rs59186511 | snp | C/T | 0.304438 | 0.244001 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333984 | AACAAGATCTTGCTC[C/T]GTCACCCAGGCTGGA | 337867 |
rs59217154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349680 | TTCTTCTATGCACTT[A/G]TAAGAAAGATCAAAG | 337867 |
rs59240606 | snp | A/G | 0.308661 | 0.24302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382521 | GAGGGCAGTGGCCTC[A/G]CTGCCCTGGTGAGAC | 337867 |
rs59409181 | in-del | -/AAAAAAAA | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330476 | AAAAAAAAAAAAAAA[-/AAAAAAAA]GAAATACAGTTGATT | 337867 |
rs59451553 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215329 | CACTGGACAGCTGTT[A/C]TTTTATTTAGAGTCC | 337867 |
rs59470419 | in-del | -/CA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237281 | TATATACACACACAC[-/CA]ACACACACACACACA | 337867 |
rs59495343 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308951 | AGGCTGCAGAGTACT[A/T]GAAGAAGACACTGTT | 337867 |
rs59511908 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308950 | TAGGCTGCAGAGTAC[A/T]TGAAGAAGACACTGT | 337867 |
rs59517637 | in-del | -/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375821 | TTTTTTTTTTTTTTT[-/T]GAGACATGGTCTTGC | 337867 |
rs59523743 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364605 | CATTAAAGATTTCAT[-/A]CACTTCACCTGTAGG | 337867 |
rs59585161 | in-del | -/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231430 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCTC | 337867 |
rs59654298 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99296715 | AAGTCTGAGAAATAG[A/G]CTTAGTCCATGTTAG | 337867 |
rs59704974 | in-del | -/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341427 | TATATCAGGGGGGGG[-/G]AGGAAGGGGGCAGCT | 337867 |
rs59722139 | snp | A/C/G | 0.00634314 | 0.055959 | stop-gained, synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254964 | TCGAAGGTAATTACG[A/C/G]TATAGCATGACACTA | 337867 |
rs59728258 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221637 | TTCTTTTCTATGGCC[A/T]CTCTAGACCATTGAG | 337867 |
rs59763441 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336041 | TGTTAGAGGAGCTTT[-/T]ACATTTTTGCCAGTT | 337867 |
rs59832604 | snp | G/T | 0.140581 | 0.224783 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247196 | GAGAGAAAACTACTG[G/T]TTTTTTTTTTTTGTT | 337867 |
rs60219325 | in-del | -/CT | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280853 | TCTCTCTCTCTCTCT[-/CT]TTCTCACTCAGTAAG | 337867 |
rs60331560 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254678 | ATCTGTGTGAACAAG[A/G]CTTGACTAGGAAAGA | 337867 |
rs60367498 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296776 | GAAGAAGACGACGAC[C/T]GCAACAACCATGACT | 337867 |
rs60467106 | in-del | -/A | 0.429238 | 0.174281 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347122 | CATCTCTATTTAAAG[-/A]AAAAAAAAGATCTAC | 337867 |
rs60486141 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243255 | TTTTTTTTTTTTTTT[-/TT]GTATGTCCCCTTATA | 337867 |
rs60548478 | in-del | -/CTAT | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258590 | GTCTGCATCATCTAT[-/CTAT]GGAAAGAGAAGATTT | 337867 |
rs60558451 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280911 | AAAATGTAGGCTGGG[C/T]GTGGTGGCTCACGCC | 337867 |
rs60595385 | snp | A/G | 0.0399052 | 0.1355 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308116 | TTTAAACCAACTAAC[A/G]TGTCTGTCAGAATGC | 337867 |
rs60700966 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318674 | AAATACAGAAAAATT[A/T]GCTGGGCGTGGTGGC | 337867 |
rs60706378 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329976 | GAGTTCTCCAATGCA[C/T]GAACGTGATAAGTCT | 337867 |
rs60715890 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270373 | CACTAGAATGCACAT[A/G]TATGTAAATGTTAAT | 337867 |
rs60731470 | snp | C/G | 0.030278 | 0.119257 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254615 | CCCCCCTACTGACTT[C/G]ATTAACACACATGTG | 337867 |
rs60842957 | in-del | -/CC/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347321 | CTATCCCCGGGCGCC[-/CC/G]CCCCCCCCCCCCCAG | 337867 |
rs60996118 | in-del | -/A/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339652 | GATTTTTTTTTTTTT[-/A/T]ACAAAGGAATAGCCA | 337867 |
rs61016589 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241833 | GAGGGAAGGTCAGCA[A/G]ATAAACAAGTGAACA | 337867 |
rs61061929 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241733 | ATTTTAACTTTTTTT[-/T]TTTTTTCAACTTTTT | 337867 |
rs61063734 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241918 | TCCCTGGGTACTTGA[A/G]ATTAGGGAGTGGTGA | 337867 |
rs61261612 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260732 | TTTTTTTTTCCCCAA[A/G]CAGAGGAACTTATTC | 337867 |
rs61314371 | in-del | -/ATATATATATATATATATATATATAT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232421 | TATATATATATATAT[-/ATATATATATATATATATATATATAT]TCACACACACATACT | 337867 |
rs61432643 | in-del | -/GTT | | | intron-variant, cds-indel | UBAC2 | GRCh38.p7 | 13:99328833 | CTTGATTAATTCATT[-/GTT]AACTGGTTTTTAAAA | 337867 |
rs61466370 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342891 | ATAGGGGGTTCCCCT[C/G]ATCGCTGTCTTTCAA | 337867 |
rs61499852 | snp | C/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341420 | CAGAGTTTATATCAG[C/G]GGGGGGGAGGAAGGG | 337867 |
rs61600056 | snp | A/C | 0.021333 | 0.101051 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380272 | CACGTCTGCGCAGGC[A/C]TCAATTTCGTCTTTC | 337867 |
rs61627160 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262739 | AAAAAAAAAAAAAAA[-/AA]GGACTTGTGGAAGGT | 337867 |
rs61736137 | snp | C/G/T | 0.000346092 | 0.0131501 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254986 | ATGACACTAATGACT[C/G/T]GAGCCTGAAATTGTT | 337867 |
rs61968336 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209510 | TGTGGGCCAGGAACT[A/G]TTTGGCTCTCTTCTT | 337867 |
rs61968337 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209866 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 337867 |
rs61968338 | snp | C/G | 0.227664 | 0.249 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213111 | ATACATATACATATA[C/G]CTATACATTTGATTT | 337867 |
rs61968339 | snp | A/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215417 | AATCAGAGATTTGTG[A/G]ATGTGTGGAATGACA | 337867 |
rs61968340 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224791 | TTCTCTAAACACTTA[A/C]ATGTGCATTGTTATT | 337867 |
rs61968341 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226634 | GGTTAAAGTCCTCAT[A/G]ATGGCCTGTAGGGCT | 337867 |
rs61968342 | snp | G/T | 0.220246 | 0.248223 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233004 | GAATTGGAAATATCA[G/T]TATGAATCATGATTT | 337867 |
rs61968344 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237269 | GTATATATATATATA[C/T]ATACACACACACACA | 337867 |
rs61968345 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237594 | TCTGTAGTTGACACT[A/G]ATCTATCGTACGTTT | 337867 |
rs61970275 | snp | A/C | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248384 | GTGCCACCATGCCCA[A/C]CTAATTTTTTTTTTT | 337867 |
rs61970276 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249509 | ATGAACATGTGAGTG[C/T]GTGTGTCTTTTTGGT | 337867 |
rs61970277 | snp | G/T | 0.5 | 0 | stop-gained, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255465 | CGCCAGCACGGCTTT[G/T]CACGTGTTTTTAAGT | 337867 |
rs61970278 | snp | C/T | 0.227369 | 0.248974 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256051 | TGGTTAACTACTGAA[C/T]ATTCACAGTAATTCT | 337867 |
rs61970279 | snp | C/T | 0.0569829 | 0.158885 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258280 | TGTATTTAAGAAATG[C/T]TGTATTTTGTTTTAG | 337867 |
rs61970281 | snp | A/G | 0.0566069 | 0.158427 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259117 | TGTTTTCACCTAAGA[A/G]GGGAAATGAAACCAG | 337867 |
rs61970282 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260729 | ATTTTTTTTTTTCCC[C/T]AAACAGAGGAACTTA | 337867 |
rs61970283 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262067 | CCTCCCCAGGACATG[A/C]GTCCTCCCTTTGCCC | 337867 |
rs61970284 | snp | C/T | 0.490007 | 0.0699769 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266517 | TGTAGACCATTTCTG[C/T]CCTCTTTGGAAGCAT | 337867 |
rs61970285 | snp | A/G | 0.107694 | 0.205546 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267552 | ACCTTTGCCTTGTCC[A/G]GGAGGATATAAGTAA | 337867 |
rs61970286 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271869 | GTTGCCTGGATTAGC[C/T]TTTATATTATTTTCT | 337867 |
rs61970287 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273017 | CTTTTTTTTTTTTTG[G/T]TTCATCTTTTCAAGA | 337867 |
rs61970288 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275695 | TGTTTCTTCTGAGTT[C/G]CTTTTTACCTCTTTG | 337867 |
rs61970290 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291614 | CCTCTTGAAATATAA[A/G]ATTATTTCTGTATTT | 337867 |
rs61970291 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291659 | TTGTTGGCTAATTAG[C/T]GCTCTCCTTTAATGT | 337867 |
rs61970292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300096 | ATTGCCCAGCTGCTC[C/T]AGAGCAAAGGGACAA | 337867 |
rs61970293 | snp | C/T | 0.223819 | 0.248625 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300578 | ATATCTTCCTTTAAT[C/T]ATCTTAAGGATTCCT | 337867 |
rs61970294 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302118 | CCACAGTGGATGTAC[C/T]AAAGAGGAACTTCCA | 337867 |
rs61970296 | snp | G/T | 0.0771755 | 0.180648 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318113 | TTCTCTCTCTCTCCT[G/T]TAAAAACATTAGGAA | 337867 |
rs61970297 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318454 | TTACAGGCATGAGCC[A/G]CTGCACCCGGCTCTC | 337867 |
rs61970331 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319301 | ATAAATTTTAACTAG[C/T]GGTTATAGAGCATAG | 337867 |
rs61970332 | snp | C/G | 0.0569829 | 0.158885 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323559 | TTCTTAAGAAGCATC[C/G]AAATTTGGAGGGTGC | 337867 |
rs61970333 | snp | A/C | 0.225597 | 0.248806 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324408 | TCTGTCCCCTTTGCC[A/C]TGAGAAAAGCAGGGC | 337867 |
rs61970334 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329950 | GCTACTACAACAATC[C/T]TAACAGTATTGAGTT | 337867 |
rs61970335 | snp | C/G | 0.0554779 | 0.157039 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334811 | TGAATAATAGCTAAA[C/G]ACTCCAATCAAAAGG | 337867 |
rs61970337 | snp | A/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337189 | CATTTACATTCCAAC[A/T]AAACACCCTGTTAAG | 337867 |
rs61970338 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337783 | CACAGCTTTTCCCTT[C/G]TCTCTGTGGAGGGGA | 337867 |
rs61970339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339471 | TCTTTGCTGTATTCT[A/G]AGTTCCCAGAACAGT | 337867 |
rs61970340 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341903 | TGGCCTAGATAATCT[G/T]AGATAGATGACTGAT | 337867 |
rs61970341 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342006 | GGAGGAGATTCTCCA[C/T]TGGAGAGCTTTGAAT | 337867 |
rs61972460 | snp | A/C | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386748 | CGCCATCTCGGGTTG[A/C]AAGGAACAGTTGATG | 337867 |
rs61974212 | snp | C/T | 0.2462 | 0.249971 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349681 | TCTTCTATGCACTTA[C/T]AAGAAAGATCAAAGA | 337867 |
rs61974213 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364387 | AGAATTATTTTGAAA[A/G]CATTGTTGGATTGAA | 337867 |
rs61974214 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369287 | TTTAACAATTTTTCA[A/G]TTTTACAGTGGTGCA | 337867 |
rs61974215 | snp | A/C | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380480 | CTGCTAGTTTTTGCT[A/C]CAGTTCTTACTGTCT | 337867 |
rs61974229 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382631 | GAACTGGATCCTGAA[A/G]CACAGGAATGAGCAA | 337867 |
rs61974230 | snp | A/G | 0.0566069 | 0.158427 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386039 | ACAGCAGGCTTCCTG[A/G]AGCCACATGGGCTGA | 337867 |
rs61974231 | snp | A/G | 0.0569829 | 0.158885 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386435 | TGTGTTTTACTCTTC[A/G]GTATTTTTCTATCAG | 337867 |
rs62620186 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215445 | ACACCACCACCAGCA[A/G]TTGTAGCCTTGATGA | 337867 |
rs62637588 | snp | A/G | 0.00212344 | 0.0325148 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295296 | AAATCTGGAACGAAT[A/G]TCTTTGGCTACATTC | 337867 |
rs62637605 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215604 | GCTGCGCTGTACACA[A/G]CGGCAGTTGCACCCA | 337867 |
rs66462714 | in-del | -/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259352 | GTCCATCCTTTTTTT[-/T]TTTTTTTCTCAGACA | 337867 |
rs66511421 | in-del | -/ATTA/TTAT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244813 | AGAATCAATTTTATA[-/ATTA/TTAT]TTCTTTCTTTAAAAT | 337867 |
rs66520914 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339640 | CATCAAGATTTTTTT[-/T]TTTTTTACAAAGGAA | 337867 |
rs66593945 | in-del | -/ACC/CCA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343378 | CACGGTGTCTTTCCC[-/ACC/CCA]CCCAGATACTTGGAA | 337867 |
rs66626478 | in-del | -/A | 0.347914 | 0.230028 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383353 | ATTTTCCAGCCAACC[-/A]AAATGAATTCTTTTC | 337867 |
rs66906559 | in-del | -/G | 0.499551 | 0.0149693 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341419 | CCAGAGTTTATATCA[-/G]GGGGGGGGAGGAAGG | 337867 |
rs67072178 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315207 | CCGTTACACGCCCCC[-/T]GATCCTACCTGATAT | 337867 |
rs67182900 | in-del | -/ATA | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364164 | AGCACAAGTCACAGC[-/ATA]ATGAGAACAAAAACC | 337867 |
rs67297884 | in-del | -/T | 0.0995161 | 0.199636 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247210 | GTTTTTTTTTTTTTG[-/T]TTTGTTTTGTTTTGT | 337867 |
rs67434891 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373172 | CTCTCTTTTTTATTG[-/T]TTTTTTTTTTTTTTT | 337867 |
rs67452504 | in-del | -/ATGAGCAAAT | 0.245631 | 0.249962 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346906 | GAACTGTGGGAATTA[-/ATGAGCAAAT]ATGAGCATAATAAAT | 337867 |
rs67548612 | in-del | -/C | 0.375 | 0.216506 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256289 | CCACTTTAAAAAAAA[-/C]AAAAAGTTTAATAGC | 337867 |
rs67614616 | in-del | -/T | 0.357451 | 0.225731 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280832 | TCCTTCTTCTTTCCC[-/T]CTCTCTCTCTCTCTC | 337867 |
rs67744400 | in-del | -/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210479 | TTTCTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 337867 |
rs67805172 | in-del | -/T | 0.0966517 | 0.197444 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205009 | CCTGGGTTCAAGCAA[-/T]TCTTCTGCCTCAGCA | 337867 |
rs68068527 | in-del | -/TGCAGTGAGCCAAGAA | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262641 | CCGGGAGATGGAGGT[-/TGCAGTGAGCCAAGAA]TGCAGTGAGCTGAGG | 337867 |
rs71118464 | in-del | -/CTAA | 0 | 0 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201661 | TTGCTGTACCCGTGC[-/CTAA]CTGTTAACACGCAGT | 337867 |
rs71118465 | in-del | -/AATAAATA/AATAAATAAATA/AATTAAATAAATA | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203057 | GTGAGACTCCATCTC[lengthTooLong]AATAAATAAATAAAT | 337867 |
rs71118469 | in-del | -/C | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268635 | TTACCTTTTGTGCTT[-/C]TTTTTTTTTTTTTTT | 337867 |
rs71118470 | in-del | -/AAAAAAAAAAA | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283742 | GCAAGACTCAGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA | 337867 |
rs71118473 | in-del | -/C | 0 | 0 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350364 | AATCACTTATTAGTT[-/C]CCCCTGGTAACCAGC | 337867 |
rs71203425 | in-del | CTTTTTTTTTT/TTTC | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268638 | TCTTTACCTTTTGTG[CTTTTTTTTTT/TTTC]TTTTTTTTTTTTTTT | 337867 |
rs71203426 | multinucleotide-polymorphism | ATATATATA/GTGTGTGTG | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237273 | TGTGTGTGTGTGTGT[ATATATATA/GTGTGTGTG]TATATATATATACGC | 337867 |
rs71215516 | in-del | -/T | 0.296364 | 0.245663 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335379 | TCCAATTCATTACTG[-/T]TTTTTTTTTTCCATA | 337867 |
rs71292858 | in-del | -/AC/TACA/TACACA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368725 | GTGAGGGTATGTGTA[-/AC/TACA/TACACA]CACACACACACACAC | 337867 |
rs71437996 | snp | C/T | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200610 | TCGGGAGCTACGCCT[C/T]CGCTTCCCCAGTGCC | 337867 |
rs71437997 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205849 | GCTGCGTGCTCGGTC[A/G]AAGAGGACGACCATC | 337867 |
rs71437998 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262536 | GGCAAAACCCTGTCT[C/T]TACTAAAAATACAAA | 337867 |
rs71437999 | snp | A/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330569 | TCTGTGGATTCCTTA[A/G]AGTTTTCAACATAGG | 337867 |
rs71438000 | snp | A/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330601 | GGTCTGTGTCATCCA[A/G]AAATAAGTTTTATGT | 337867 |
rs71438001 | snp | C/G | 0.14933 | 0.228835 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338426 | TCCTGGGCCACATGT[C/G]GCCCACAGGCCTCAG | 337867 |
rs71438002 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352628 | CCTTAGGAAGCTTCC[C/T]GTTGCCTCTTGGCCT | 337867 |
rs71697202 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268641 | AAAAAAAAAGAAACA[-/C]AAAAGGTAAAGAAGG | 337867 |
rs71740121 | in-del | -/C | 0.294064 | 0.246086 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345744 | TTTTTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 337867 |
rs71959491 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336005 | CAAAATGGAAAAAAA[-/A]AAAAAAAGAGATAAA | 337867 |
rs72271450 | in-del | -/TC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280842 | TTCCCTCTCTCTCTC[-/TC]TCTCTCTCTCTTTCT | 337867 |
rs72473264 | in-del | -/AATATGAGCA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346913 | GGGAATTAATGAGCA[-/AATATGAGCA]TAATAAATAGATACA | 337867 |
rs72648069 | snp | C/T | 0.31014 | 0.242659 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206009 | AGCTGATTGGATCTG[C/T]GGCGAGGGAGGAGTT | 337867 |
rs72648071 | snp | C/T | 0.181022 | 0.240296 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211076 | AACTTTTAGTACGTA[C/T]TGCCAAATTCCAATC | 337867 |
rs72648072 | snp | C/G | 0.180702 | 0.240204 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211223 | TTCCCCTCCACAAAC[C/G]AGTCTTTTCACGCTC | 337867 |
rs72648073 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214227 | ATCTTTGGTTTGTTT[G/T]TTTTTTTTTTTTTCC | 337867 |
rs72648075 | snp | A/G | 0.119978 | 0.213528 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216603 | TGAGAAATGCCCTCA[A/G]TTCTCCCGAAGATTG | 337867 |
rs72648076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217939 | CTTGAATTTACAACA[C/T]GTTTTCTTGCCACTA | 337867 |
rs72648082 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236988 | CTTAAAAAAAAAAAA[A/T]AAAACTACCATATGA | 337867 |
rs72648086 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248862 | TTTATAGACTCAAAG[A/C]AAACTCATGTTCAGA | 337867 |
rs72648087 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250007 | TTCTCCCATTTTATA[A/G]GTTGTTTGTTTACTC | 337867 |
rs72648088 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252419 | GTAGCCCCAGTAAGA[C/T]TGTAAGGGAAGGCCT | 337867 |
rs72648091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257040 | AATTAACTTGAGCAA[C/T]TGCTGTGGTTAAACA | 337867 |
rs72648093 | snp | C/T | 0.162253 | 0.234095 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258780 | CTAAACCAGAAAGAT[C/T]CCAAGTGCTTAATAG | 337867 |
rs72648094 | snp | A/G | 0.309401 | 0.24284 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268342 | AGGAGGCCAGGCATG[A/G]TGGCTCTCACCTGTA | 337867 |
rs72648096 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270352 | ATATGAACCACAGAC[G/T]GTTTTCACTAGAATG | 337867 |
rs72648098 | snp | A/G | 0.141596 | 0.225274 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276644 | ATCTCCCACCACCCC[A/G]CTTCCTGGAGGCTGG | 337867 |
rs72648099 | snp | A/T | 0.155987 | 0.23165 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285846 | GTGGCTCTTGAATTC[A/T]GTATGAGCCAAGGCA | 337867 |
rs72648100 | snp | A/T | 0.312348 | 0.242101 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291082 | TCTGGGACCGGAGAG[A/T]GTGGGATTAAACCGG | 337867 |
rs72649510 | snp | C/T | 0.313082 | 0.241911 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305367 | CTGGAGAACACCACG[C/T]GTCCTCTACACAGGC | 337867 |
rs72649512 | snp | C/T | 0.308414 | 0.24308 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310324 | GTGACTGACAGATAC[C/T]GGTGTCTCAAGAAAA | 337867 |
rs72649515 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316026 | AGTGTTACACAGCTC[A/C]CCATGAGGGATCCCC | 337867 |
rs72649581 | snp | C/T | 0.158962 | 0.232835 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327778 | AATTTAAAAGATTTA[C/T]GTATCTATTTGAGAT | 337867 |
rs72649582 | snp | G/T | 0.124144 | 0.21601 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332521 | GGCATATGGGGGGCT[G/T]CTCCCTCTGACCTGG | 337867 |
rs72649591 | snp | C/T | 0.164219 | 0.234823 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342600 | CCATGGCCATCCATT[C/T]GTGTGCCAGCGCTGG | 337867 |
rs72649595 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352619 | GGCCAGCTTCCTTAG[A/G]AAGCTTCCTGTTGCC | 337867 |
rs72649597 | snp | A/G | 0.0409646 | 0.137128 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356086 | GGCCTCTGAAAAGAA[A/G]TGTCATTAAAGTAAA | 337867 |
rs72649600 | snp | C/T | 0.187369 | 0.242028 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359564 | AAGCTTCCCAGCCAC[C/T]GTGCCATGGTCATAG | 337867 |
rs72651006 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368108 | GGCATTATTGGTTGG[A/G]GGGCGGCGGGTGGGA | 337867 |
rs72651008 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368507 | CAAGGTTTAGTTTTC[A/G]TAAAGGTATGAGTAT | 337867 |
rs72651010 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370732 | CCACTGTCACGTGCC[C/T]ATTGACTTGATCCAG | 337867 |
rs72651012 | snp | A/C | 0.157642 | 0.232314 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373348 | AATGACTGTTAGGTA[A/C]AATCAGACAAGAAAG | 337867 |
rs72651013 | snp | A/C | 0.167158 | 0.235875 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374935 | AAACTTCCCTTTCAG[A/C]ACTCTTGTTTTCACA | 337867 |
rs72651021 | snp | C/T | 0.138207 | 0.223612 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386733 | CTTGAATCTGAATTG[C/T]GCCATCTCGGGTTGC | 337867 |
rs73563979 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203689 | ATGATTCACATAGTG[A/C]TAAGTGACATGAAGA | 337867 |
rs73563985 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206582 | CTGGAACCTGTAGTT[C/G]ATTACTGGAGCCATG | 337867 |
rs73563986 | snp | A/C/G | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207781 | GGCCTGCACTCTCCA[A/C/G]CTTCGTTCCAGCTTA | 337867 |
rs73563990 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209627 | CACTCTTCCCCACCA[A/G]TCTTAAGTTTTTGGG | 337867 |
rs73564000 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212348 | TGTAAATGAGAATTA[C/T]AAAGTAATCCTTATT | 337867 |
rs73565907 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213088 | CTTTTTTTTTCTGAC[A/G]CATGTATATACATAT | 337867 |
rs73565912 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216729 | TTGAAACAACTTTGG[A/C]AGGGCGGGAACGTGG | 337867 |
rs73565915 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221945 | GACATTTTCTAGTCA[C/T]GGATAGGTAATGTAC | 337867 |
rs73565920 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225641 | GTTTAACAAACACTC[C/T]TGACTGCCTTTATGT | 337867 |
rs73565924 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229410 | GAAAGCAACATGTTC[A/G]GGAGGTAGTGAGCTG | 337867 |
rs73565931 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236856 | CTCTGTCTCAAAAAC[A/G]GCAACAACTACCAAA | 337867 |
rs73565932 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237354 | ATTTGCAGCCACATG[A/G]ATGGAACTAGAAGAC | 337867 |
rs73565933 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237418 | TGCATGTTCTCACAC[A/G]TGGAAGCTAAAATAG | 337867 |
rs73565964 | snp | C/T | 0.0232847 | 0.105357 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254380 | GCTGATGGGGATGGC[C/T]GTAACAGGCCCCTTG | 337867 |
rs73565974 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263746 | CAACCTGAATGTTCA[A/G]CTATAGCATGAATAA | 337867 |
rs73565982 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264433 | CTATTTAAAAACTGC[C/T]TTATAGCTTGTGTAA | 337867 |
rs73565992 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270667 | GTTGATGGTGTGGAC[A/T]TGCACATGAGTTCTG | 337867 |
rs73565995 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271793 | CCATGTCCCCCAGCT[C/T]ACAAAAGTATCTCTG | 337867 |
rs73565997 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272071 | TTTTTAGTCTTCTCT[C/G]TAAAAGACAGTGATC | 337867 |
rs73566000 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272844 | ACAAAGTTCAGTGCA[C/G]AGCAGCATGTATATT | 337867 |
rs73566002 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275930 | ACCACCAATGGGTTG[A/G]TCAGATTCCCCAGAT | 337867 |
rs73568003 | snp | C/T | 0.021333 | 0.101051 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276530 | AGTGCACGGAGCTCT[C/T]GTGCCTTCTGTGGGC | 337867 |
rs73568008 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280150 | TTTATCTACAAAGGA[G/T]ATCTGGTCTTATTCC | 337867 |
rs73568016 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285906 | CTACACATCCAACGG[A/G]GTGCCAGAGTTCACA | 337867 |
rs73568025 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291667 | TAATTAGCGCTCTCC[G/T]TTAATGTGTCTAATT | 337867 |
rs73568039 | snp | C/T | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297439 | TGATCAAAAGCACTG[C/T]CTGCAAATCTGCTTC | 337867 |
rs73568043 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299051 | ACTGTAGAGTCTGCA[A/G]ATCCTCCATATGAAT | 337867 |
rs73568050 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300385 | TTCCGCTAGCTGGCC[C/T]TAATATGTCACTTTA | 337867 |
rs73568054 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303898 | GGCGCCCAGGACTCC[A/G]TGTTCTCCCTCACCT | 337867 |
rs73568057 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311038 | GGCTTTTTAAAACAA[A/G]AGGCAAGTTCTGCTG | 337867 |
rs73568067 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315214 | ACGCCCCCTGATCCT[A/G]CCTGATATCCATGTA | 337867 |
rs73568073 | snp | A/C | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323876 | TTTAAATGCTCAGTG[A/C]AGAATAAATGAAATG | 337867 |
rs73568081 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328654 | CTTTTGTGAAATATC[C/T]GTTCAAATCTTTTAT | 337867 |
rs73568082 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, missense | UBAC2 | GRCh38.p7 | 13:99329163 | ATATGTCTGTCCTTA[C/T]GCCAATACCACACTG | 337867 |
rs73568084 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329265 | TTTAAAACTGGTTTG[C/T]TTATTTTAGGACACT | 337867 |
rs73568087 | snp | A/G | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332575 | GACTCTCAGCTGGAC[A/G]TGGGCCAGGGGTTCT | 337867 |
rs73568089 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332962 | GTGTAAAAAAGGTTT[A/G]TGAGATCATGAAAAT | 337867 |
rs73568096 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334313 | ATATGACAGAAGTAA[C/T]GCAGTGGATGGGAAG | 337867 |
rs73568097 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334818 | TAGCTAAACACTCCA[A/G]TCAAAAGGTAGAGAT | 337867 |
rs73568099 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335169 | ATCACAGTTGAATAC[C/T]TTGAGACCGAAAAAT | 337867 |
rs73568101 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336672 | AGATAAAGACCACAC[C/T]GTTTTAGGTAGCCAA | 337867 |
rs73570103 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337536 | TGTAAATTTCGTTTT[A/G]GCATTCTTTTAGGGA | 337867 |
rs73570105 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337977 | CACACATAATATACA[C/T]TAACACTGAAGATAG | 337867 |
rs73570107 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339889 | TGATAAATTGATCGT[A/G]TGACTGGGTCAGCTG | 337867 |
rs73570115 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348042 | CAGAGCTGCCTTCTC[C/T]AAAGCAGGTGGCATC | 337867 |
rs73570128 | snp | C/T | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354887 | CAGCAAGGACCTAAA[C/T]GGGCAGATCCTCTCC | 337867 |
rs73570130 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355919 | CCTGCACCTCCAGGG[C/T]CTCCCCAGATGGAAC | 337867 |
rs73570137 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363077 | GTGGTGTGAAGTAAG[A/G]GCCTAGTTTTATCTT | 337867 |
rs73570141 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365576 | GTTTTTTGTTTTAGT[A/T]ATTATTTTGATGTTG | 337867 |
rs73570149 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367152 | TCAGTCTTCAGGATC[C/T]GTGGAGCCACCCTCA | 337867 |
rs73570152 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369321 | GTGATACATACTCAG[C/T]AGAAGCCATACATCA | 337867 |
rs73570159 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371687 | AAATATCAGAGCCAC[A/G]TAATTTTAATGCATT | 337867 |
rs73570162 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372782 | TTGATAAAACTCCTT[C/T]GAGTAATCAAATACG | 337867 |
rs73570164 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374754 | CAAGCATGGCAGCAC[A/G]TTGGGTATTGGGTTA | 337867 |
rs73570168 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379143 | TCTGGTAAGAAATTC[A/G]CTGCTTGAAAACAGC | 337867 |
rs73570170 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379240 | CAGCAAAGTTGTTCT[A/G]CCCTTGATGTCCTCA | 337867 |
rs74112018 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221832 | TCTGTTTCGCTCCCC[G/T]TGTCCTTCACTACTG | 337867 |
rs74112022 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228796 | TTAGATTCCGTGGAG[A/C]CTTGTTTGCATTTTG | 337867 |
rs74112032 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305484 | AGCTCTTTTAAATGT[A/C]AGCTTCTTGAGGATG | 337867 |
rs74112033 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305839 | AAGAAGTGTGCAGTC[C/T]TACCAGTAAGCACAG | 337867 |
rs74112050 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334590 | AACTCCAAATATATT[A/G]TGCTCAATTTTGAAT | 337867 |
rs74112056 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359512 | TTAAATCAACCTGTT[A/T]CCTAAATGTGTAAGT | 337867 |
rs74243328 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368204 | GTTCTCTGTGAAGGA[A/T]CGGGGACAAGGAGGT | 337867 |
rs74437874 | snp | C/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242655 | CCCCACCTCCCTCCC[C/G]GACGGGGCGGCTGGC | 337867 |
rs74451935 | in-del | -/CCTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231704 | ATGTGAGCCACCACG[-/CCTG]GCTCTCTTTTTGTAT | 337867 |
rs74489844 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345761 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT | 337867 |
rs74498945 | snp | C/G | 0.00716266 | 0.059414 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254817 | TACAGAATATCCATT[C/G]ACGCCAGAGTAGTTA | 337867 |
rs74507059 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378151 | ATCACTGTTGTCACA[G/T]TCACCTTGACTCAGA | 337867 |
rs74529235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300081 | TGGCACATGCGCAAC[A/G]TTGCCCAGCTGCTCC | 337867 |
rs74547352 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269504 | GTGATTGATTTTTTG[C/G]TTTCTTATAAGCAAG | 337867 |
rs74559579 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324072 | CACTCCAACTACACA[A/C]AATCCATTCCCAAAC | 337867 |
rs74560760 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365512 | TATTCATTCTTAGCT[A/G]TCTTCTAATTTCCAT | 337867 |
rs74577432 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344604 | TTTTTCAGTTACTAA[C/T]TGCTGTATGTTACAC | 337867 |
rs74584042 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201855 | GGTGGGCGGATCACG[A/G]GGTCAGGAGATCGAG | 337867 |
rs74589347 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362747 | ATAAGTTCATAAGTG[C/T]CATTGATTTATTAAG | 337867 |
rs74638649 | snp | A/C | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345977 | TGAACCCCTGACCTC[A/C]TGATCCACTTGCCTT | 337867 |
rs74642775 | snp | A/C/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292422 | GCAGGGATTACAGGC[A/C/G]TGAGCCACTGCGCCC | 337867 |
rs74684097 | snp | A/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314393 | AGAACAAGAACATCA[A/G]GGTATAGAAGATACT | 337867 |
rs74730437 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362082 | TAGTATTACATTTTA[C/T]TTATATTATTTACAT | 337867 |
rs74740318 | snp | C/T | 0.046775 | 0.145601 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223132 | TATGGGCGTAAAGTA[C/T]TTCCTAACATTCCCT | 337867 |
rs74747457 | snp | A/G | 0.021333 | 0.101051 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256889 | GTAATATGGAGGTGG[A/G]TGAAAAGTTTCCTTC | 337867 |
rs74809430 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206944 | AGCTTTGTTCCTTTC[C/T]TCCAATCCAGAAGAA | 337867 |
rs74860258 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251334 | TAAAGAGAGATAGTT[C/T]GGGCTTTCCTATTTG | 337867 |
rs74895076 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222950 | GCTTGGTAGAATTCT[A/C]CCCTGAAGCCATCAG | 337867 |
rs74898814 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292902 | GTTCTGTAACAGAAT[A/G]TAACAATTATACAGC | 337867 |
rs74960551 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217913 | CACTGCCTGCCTGGC[A/C]TCTGTAGGCACTTGA | 337867 |
rs75002535 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341737 | TCGTATTTAGCAGGA[A/G]GTAAATCCTTCAAGG | 337867 |
rs75015335 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209067 | CAGCCTGGCTGGGAC[G/T]GCGTGTTCCTTGCCC | 337867 |
rs75118041 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202187 | CACAGGCATAATTTT[A/G]AATCTTCCTCACTTC | 337867 |
rs75141278 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241740 | ACTTTTTTTTTTTTT[C/T]AACTTTTTTTTTTTT | 337867 |
rs75163487 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275286 | TGCTGTTGGCAGGAA[A/G]CCTCAGCTCCTCACC | 337867 |
rs75180218 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270439 | ATGGTCACATTTATA[G/T]TCATCAGCTTTTGTC | 337867 |
rs75220226 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338076 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 337867 |
rs75233255 | snp | C/T | 0.470715 | 0.117409 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237273 | ATATATATATATATA[C/T]ACACACACACACACA | 337867 |
rs75261568 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207485 | CTTATTTTTTCCCTG[C/T]TCTCATCTCCCTTCA | 337867 |
rs75273995 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240027 | AGGAAGTAACATGAA[C/T]TTCAGACCCTTAGGA | 337867 |
rs75343460 | snp | A/C | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268639 | AAAAAAAAAAAGAAA[A/C]ACAAAAGGTAAAGAA | 337867 |
rs75346908 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338053 | TCTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs75373843 | snp | A/G | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323457 | AACAAACAAACAAAC[A/G]AACAAAAATTTCAAG | 337867 |
rs75378353 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372256 | GGAGGAAGATCAGAA[A/G]AAAACCCCACAAGTT | 337867 |
rs75412252 | in-del | -/GTTA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244735 | AAACTTCTAGATATA[-/GTTA]AATTGATTTTATATG | 337867 |
rs75425017 | snp | C/T | 0.0763149 | 0.179815 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350331 | ATGTCCAGGCTCTCC[C/T]GGATAGCCTCAGATG | 337867 |
rs75435514 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299639 | TTAATGGGAAAAAAT[G/T]TTAGTTCCCCTTTTC | 337867 |
rs75449415 | snp | A/G | 0.0252325 | 0.109451 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352231 | ATAACTCACCCCCTC[A/G]AAGTGTACAGTTCGG | 337867 |
rs75455261 | snp | C/T | 0.133435 | 0.221162 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290055 | AGAGAGAAAATACGA[C/T]GATGAAGAGTGCAGA | 337867 |
rs75535500 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208015 | TTTTTTTTTTTTTTT[G/T]AGGTGGAGTTTCGCT | 337867 |
rs75556235 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297981 | CAAGGCAAATTCAAT[A/G]TTAATAGGAATACAG | 337867 |
rs75562771 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380596 | CCCTCCACTGGGGAG[C/T]ATTGGGTAAGCACCC | 337867 |
rs75612227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266106 | TTCACCTTTACCCCT[C/T]CTAAAGTCTCTTTGA | 337867 |
rs75613290 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344144 | TATCTCATTTATGCC[C/T]GGTGTACGCCTAGAG | 337867 |
rs75653253 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386031 | GAAGAACAACAGCAG[A/G]CTTCCTGGAGCCACA | 337867 |
rs75667683 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246976 | GTAAACTTTGTGTAA[C/T]GTAAATATATCTCTT | 337867 |
rs75686119 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262045 | ATCTCTCACTGTCCC[A/G]CTCCTTCCTCCCCAG | 337867 |
rs75707602 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287100 | CTTTTAATCATTTTT[C/T]CAAACACACAAACTT | 337867 |
rs75721036 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301769 | TGGTCCTAATTTACT[C/T]GTTCAAGTAATTAAA | 337867 |
rs75812859 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269927 | ATAAATAACAGAATG[G/T]TATTATACTTTATAC | 337867 |
rs75821566 | snp | A/G | 0.0364509 | 0.129988 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231043 | ACAGAGGGAGACTCC[A/G]TCTCAAAAAAAAAAG | 337867 |
rs75838686 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367997 | CAAAAGTAATCAAGC[A/G]TGTAAATACAAAGAT | 337867 |
rs75879053 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357349 | CACGTGACTACAGTT[C/T]TAAGTCTAACAAGAT | 337867 |
rs75887366 | in-del | -/TTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283710 | TAATGCCTTAATGCC[-/TTT]ACCTTTTTTTTTTTT | 337867 |
rs75888208 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296505 | GCAGAAATTCCCCTT[C/T]CCTTTTTTGAATCAT | 337867 |
rs75914990 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373999 | TTTGGTGCATTAATA[A/T]TAATAATACATTTAT | 337867 |
rs75930770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367776 | ATAACTGTGTGTTGA[C/T]CTCTTTTTAGGGAGG | 337867 |
rs75931719 | snp | A/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292303 | ACCACGCCCAGCTAA[A/T]TTTTTTTTTTTTGTA | 337867 |
rs75988157 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241299 | GAAAAGAGTTACTAT[C/T]ACCAATGTTCGCAGC | 337867 |
rs76045544 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374308 | TTAGAAAAAGCAGGT[C/G]TTCTTGTTTTGGGAT | 337867 |
rs76081348 | snp | C/T | 0.269809 | 0.249214 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237275 | ATATATATATATACA[C/T]ACACACACACACACA | 337867 |
rs76143419 | in-del | -/TCAAGGA/TCAAGGACCTG | 0.437118 | 0.165792 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341386 | AGGTCCTTAGAGTCC[-/TCAAGGA/TCAAGGACCTG]CATTGGAGATGCAGG | 337867 |
rs76167596 | snp | A/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228291 | TCTCTATATTCATTC[A/T]TTTTTTTTTTTTTTG | 337867 |
rs76179601 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283023 | TGTTAGTTGAAGTAA[C/T]AGAATGAATTCTGGC | 337867 |
rs76188325 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377563 | GAGAGATGGGCTGAC[A/C]ATCTATAATACCATT | 337867 |
rs76190203 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380489 | TTTGCTCCAGTTCTT[A/G]CTGTCTATATGGTGA | 337867 |
rs76268846 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280662 | CAGCTCCCTCAGCAT[G/T]GAGTAGTGAAGAGTG | 337867 |
rs76291015 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274736 | CTTTTTTTTTTTTTT[G/T]AGACAGGGTTTCACT | 337867 |
rs76307858 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233801 | TGTAAACTTTTTCAC[A/G]GTAAAAGGATGGGAG | 337867 |
rs76323503 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310569 | TGAAGTCTGTGTGTG[C/T]AGAAATAGCAACGGA | 337867 |
rs76355106 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366637 | AGTTTGATTTTTTTT[C/T]CATCCCTTTCGCTGA | 337867 |
rs76381801 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260826 | TTCACTTGCAAAAGA[G/T]GGATTTTACTTATTC | 337867 |
rs76389840 | in-del | -/CAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241264 | AGTGAGACCCTGTCT[-/CAA]AAAAAAAAAAAAAAA | 337867 |
rs76436899 | snp | C/T | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297094 | TAATTTGCTTAGCTA[C/T]TCCCTTGATGAACTT | 337867 |
rs76439338 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238172 | CTATGGAAGTTCTGG[C/T]TGTAAACTTGGTCTC | 337867 |
rs76510902 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332314 | TCAAGAGTGTTTTGC[A/C]TGTTTTCTACCCAGC | 337867 |
rs76552170 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280481 | TGCTCCACGAAACCC[C/T]GCTCCAGCCAGAGTT | 337867 |
rs76577576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351036 | AGCCATGCTCACAAT[A/G]GAAAGCAGCGTAATA | 337867 |
rs76578713 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329672 | CACATGGCCAACAAT[C/T]GTGGCCTCCTGCCAA | 337867 |
rs76598410 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303367 | CTTGAGCACGGGAAT[C/T]CTTTGGTTGAACACC | 337867 |
rs76606211 | snp | G/T | 0.0379877 | 0.132479 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325585 | CTTAAATTTTTAAGT[G/T]ACAGTTTATAATTGT | 337867 |
rs76611498 | snp | G/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208013 | TTTTTTTTTTTTTTT[G/T]TGAGGTGGAGTTTCG | 337867 |
rs76617964 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303073 | AGGGGCTTAGTAGAG[A/G]CAGCCTTATTGAGGA | 337867 |
rs76657225 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325115 | TTTTTTTTTTTTTTT[G/T]TTTTTGATACGGAGT | 337867 |
rs76682947 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222115 | CATTCTGGCTATGGG[G/T]ATATGGCAGTGAGCA | 337867 |
rs76693341 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322245 | CTAATTTTCTTACAC[A/T]TTAATACTTTTCCTT | 337867 |
rs76719678 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319472 | TGTGTCATCCTGTAC[A/G]CCTGCTTACCCCTCT | 337867 |
rs76739507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372009 | TGGTGAGTAAACCCA[C/T]GGCACCTCTGCCAAT | 337867 |
rs76778832 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273575 | TTGGTAGGTACCTAC[A/C]TCTTAAGGTAGGTAC | 337867 |
rs76819420 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314818 | CCTCAGCGAATGTCA[A/G]TTGCTCCCTGCTGGG | 337867 |
rs76819734 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319994 | CAAAAGCATTCAAAT[A/G]TTGAAGTACCTTATT | 337867 |
rs76868633 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310233 | TCTGGAGGCTGAGGC[A/G]AGAAGATTGCTTGAG | 337867 |
rs76897258 | snp | A/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235977 | TGTCTCAAAAAAAAA[A/T]TTGTGCTGGTAAAAC | 337867 |
rs76974202 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207518 | TTTTAGCCTTGTGCA[A/G]TTAGTCTGCTACTCT | 337867 |
rs76997935 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257109 | CCTTCCCTTCCCTTT[C/T]TTCCCTTCTTCTCCT | 337867 |
rs77032765 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243546 | AAAATCTTACTAAAC[A/G]TGATCCTGAAATTTC | 337867 |
rs77053523 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290970 | GCCCTGGAGGACATA[A/G]GACAGGGAGGAATGG | 337867 |
rs77091832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204278 | CTGGTTGTGGGGAGG[C/T]ACAGTTAAGGAAGAC | 337867 |
rs77108018 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274280 | GTAGTTAATTTTTTT[C/T]CCATTATTGGTATAG | 337867 |
rs77114638 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322244 | ACTAATTTTCTTACA[C/G]ATTAATACTTTTCCT | 337867 |
rs77119690 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233540 | GGTAGGTGGAGCAGC[C/T]AGAGCAGGCGTTGAG | 337867 |
rs77121709 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322700 | AATCTGTTACACCCA[A/G]AAGTAAGATTTGGGA | 337867 |
rs77123877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221098 | TCCCATTTTTATGGA[C/T]AGAACATAATTTACC | 337867 |
rs77128154 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314607 | ATTGAATACAGTGTC[A/G]CAAATAAAGCTCTGA | 337867 |
rs77170492 | snp | A/C | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235968 | GTGAGACCCTGTCTC[A/C]AAAAAAAAATTGTGC | 337867 |
rs77177193 | snp | A/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250387 | TCATGTGGATTTATT[A/T]CTGTGTTCTGTATTC | 337867 |
rs77295741 | snp | A/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368690 | AAACTCATGAGAGAG[A/T]GTGTGTGTGTGTGTG | 337867 |
rs77318962 | snp | A/G | 0.179105 | 0.239737 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205149 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAGA | 337867 |
rs77321496 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319745 | ACTTGTGGTGGCTTA[A/G]GGCCATCCTGGGGTT | 337867 |
rs77361373 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342089 | GGAAGATTTTTATAC[A/G]AAGAGTTTATGAGAG | 337867 |