SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs77372753 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348707 | AGTCATAATATGAAC[A/G]TTGTCTGAAGGGATG | 337867 |
rs77374309 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249669 | ACCAACAGTGTATAA[A/G]TGTTCCCTTTTCTCA | 337867 |
rs77379791 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208894 | GACCTGGGGGTTTGC[A/G]TCTTTATTTTGGTCG | 337867 |
rs77428433 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216848 | TCTTTTTTTTTTTTT[G/T]AGACGAAGTCTTGCC | 337867 |
rs77461533 | snp | A/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278592 | GTGTCTTTAAAAGTG[A/G]AAAAAAGTGATATTT | 337867 |
rs77469374 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340044 | AAGACAGTGTCTTGA[A/C]AATCTTTTACCAGAA | 337867 |
rs77475159 | snp | A/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213181 | CCAACATCTCAGATA[A/T]TAAAAAACGTGAGTT | 337867 |
rs77539420 | snp | C/T | 0.0271762 | 0.113356 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254737 | CACAAAAATGTTTTA[C/T]ATAAGTTTTTAAAAT | 337867 |
rs77558949 | snp | C/G | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324876 | AGAACACTTGATTTT[C/G]TGTATGAAAAAATAT | 337867 |
rs77602421 | snp | A/C | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347335 | CCCCCCCCCCCCCCC[A/C]GGAAAAAAAAGGCAA | 337867 |
rs77615948 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224396 | ATTTTAGGAGGAAAC[A/G]TTCAGTCCATAACAG | 337867 |
rs77635998 | snp | A/C | | | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295379 | TGGTAAGGTGTGAAA[A/C]AGAGAACAAACACAA | 337867 |
rs77654077 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374698 | AGGGCTCTAATATTT[A/C]TTGGTTTTGAGACAC | 337867 |
rs77661338 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310152 | GGGAACACAGCGAGA[A/C]CCTGTTTCTAAAAAA | 337867 |
rs77667628 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304529 | ATTCAATAAATACCC[A/G]TTAGTTAAAGAATAG | 337867 |
rs77720066 | snp | A/C/G | 0.0472437 | 0.146695 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350941 | GGGGTATGAAGCCCC[A/C/G]CAGCACATCTGGTGT | 337867 |
rs77789462 | snp | A/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285409 | TTTTTTTTTTTTTTA[A/G]GAGACAATTGTCTTG | 337867 |
rs77825727 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358741 | AGACAGTGGCGGGGG[A/G]GTTCCAGTGGACAGA | 337867 |
rs77914076 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331861 | TTTTTCTGTTTTGCT[C/T]CTTACTATGTTTCAG | 337867 |
rs78016823 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336171 | TGAAATTACCTTTTC[A/G]TATGCTTTTAAAACT | 337867 |
rs78068484 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212432 | CCATTGTTTCAGTCA[G/T]TTCCCAGAATTTAGT | 337867 |
rs78074322 | snp | A/C | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268615 | AGACTCTGTCTCAAA[A/C]AAAAAAAAAAAAAAA | 337867 |
rs78077018 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371763 | TTTGAGTTTTTTCTG[C/T]TGTAAACAGATACTT | 337867 |
rs78131897 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281687 | GCTTTTCTTGTCTCA[C/T]TTATGTCTTGACATT | 337867 |
rs78132684 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247076 | CCTGGGCTCAAGTGA[A/T]CCTCCTTTCTTGGCC | 337867 |
rs78183359 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222294 | CCACTCTGAGGAGGT[G/T]CTCTTAGAAATGAGG | 337867 |
rs78185716 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235067 | TGACTGCTTTTAGTA[C/G]AAGGCAGAGGTCACA | 337867 |
rs78210037 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362568 | TTGTGGGTATAAAAT[A/T]ACTTGTTTTCATTTG | 337867 |
rs78272224 | snp | G/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242672 | ACGGGGCGGCTGGCC[G/T]GGCGGGGGGCTGACC | 337867 |
rs78291444 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228638 | TCTCGTAACACTTTT[C/G]AGGTAGGTTCTCATC | 337867 |
rs78325979 | snp | C/T | 0.0349115 | 0.127424 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200061 | GTTTTCAGGCTCACA[C/T]ATTTAAAAACCGTGA | 337867 |
rs78355062 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234601 | TACTGTGTCCAATGA[C/T]AAGCATCAGTAAGTG | 337867 |
rs78434948 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245458 | TATGCTTTCATATTG[C/T]GTTGATCTTCTTTAA | 337867 |
rs78522968 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320733 | ATGAAATATTTACTG[C/T]GATGTGGCATACTTT | 337867 |
rs78538526 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348844 | TTTTGCCTTTTAGTA[A/G]AAAGGGGGTTTCACC | 337867 |
rs78564539 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243131 | TCTCATAAGGTCATT[G/T]TGAAGGGGAAATAAG | 337867 |
rs78566377 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334595 | CAAATATATTATGCT[C/T]AATTTTGAATGCATA | 337867 |
rs78574209 | snp | A/C | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202734 | TGTCTTGGCCTGTTT[A/C]TAAAATTAAGTGCTT | 337867 |
rs78596209 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313380 | ATGGATTAGAGAGAA[A/G]CAAGACTGTAAGTAG | 337867 |
rs78623879 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201845 | GGGAGGCCGAGGTGG[A/G]CGGATCACGAGGTCA | 337867 |
rs78657815 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359784 | CCCTGCCTCGCCTCC[C/T]GTGTGCCCAAGCACA | 337867 |
rs78698370 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209745 | TTGGGAGGCCAAGGC[A/G]GGTGGATCATCTGAG | 337867 |
rs78698476 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341421 | AGAGTTTATATCAGG[C/G/T]GGGGGGAGGAAGGGG | 337867 |
rs78702138 | snp | A/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241755 | CAACTTTTTTTTTTT[A/T]TATTGATCATTCTTG | 337867 |
rs78720707 | snp | G/T | 0.306927 | 0.243432 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199643 | CCCTTTCATTTAGCT[G/T]GGTAGTGTGGTCAAT | 337867 |
rs78739367 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227348 | CCTAGGAGGGGTCCA[C/G]TCCACACTGTCGTCA | 337867 |
rs78790107 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292827 | ATGTATCACCCGATT[C/T]ATGGAGAAAATACTT | 337867 |
rs78811985 | in-del | -/TCC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382638 | TCCTGAAACACAGGA[-/TCC]ATGAGCAAAGGCAGC | 337867 |
rs78828681 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273880 | TTTTTTTTTTTTTTC[C/T]TGCTTTCTTTCTCTG | 337867 |
rs78970264 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283098 | TTAGGAAGGCAAATA[A/G]TCAGTCATGGGTACA | 337867 |
rs78983110 | snp | A/G | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230695 | CCAAGGGTGACTGGT[A/G]GACTCTTTCTTACAC | 337867 |
rs78987394 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297957 | TTAACATCAGAAAAA[-/A]ATAGAATTCAAGGCA | 337867 |
rs79016676 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319955 | TTAGCAGTAATGGTT[C/T]TGAGTTCTGTTTTAA | 337867 |
rs79048693 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375591 | AAAACCCAAAAAAAA[A/C]ATTTGTTTTTGACGC | 337867 |
rs79101016 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333098 | GAAACCCCGTCTCTG[A/G]GGGGGGAAGAAAGAG | 337867 |
rs79140207 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274305 | GTATAGTATTTTGGT[G/T]TGTGAATACCACCAT | 337867 |
rs79145601 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327400 | TCACATTGTCTTTTT[A/G]TCAGGAAATTAAAAT | 337867 |
rs79166560 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277972 | TTTCCTCATGGTCTC[C/G]CCATAGAAGGGCCTT | 337867 |
rs79175617 | snp | G/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287662 | TTTTTTTTTTTTTTT[G/T]TTGGTAGAGACGAGG | 337867 |
rs79199942 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352776 | GAAAGCGTCAGTTAC[A/G]GTGAAATGTGATGGT | 337867 |
rs79201331 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344121 | TATAGTAAGTACTCA[A/G]TATATGTTATCTCAT | 337867 |
rs79204134 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247204 | ACTACTGTTTTTTTT[G/T]TTTTGTTTTGTTTTG | 337867 |
rs79237042 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270743 | ATTTTCAGTACATTG[C/G]GTACTTTTATTAACT | 337867 |
rs79293354 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218928 | GTGGAAGTGCAAGGT[A/G]TCTCTTGCAAGGCAT | 337867 |
rs79331702 | snp | A/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235818 | TTTCTCCAAAAAAAA[A/T]TTAGCCAGGTGTGGT | 337867 |
rs79378470 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371262 | ACTTAATTTCTTCCT[C/T]GCTCCGTGTTACGAG | 337867 |
rs79432737 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239152 | TGCTAAGCACTTGGT[C/T]AGCCCATTTTAAGCA | 337867 |
rs79502098 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229380 | CTGGAAAAATTTTCC[A/G]AAGGCATTGAAACAG | 337867 |
rs79536795 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267567 | AGGAGGATATAAGTA[A/G]GGAAGGAAGAAACTA | 337867 |
rs79559909 | snp | A/G | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350812 | TGAAGTAGGGGAGCA[A/G]TCTTGTGGGAGTGGG | 337867 |
rs79573169 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345405 | GAGACAAATAGAAGG[A/C]GGTTTCTAAAGCCCG | 337867 |
rs79644438 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209433 | GGTGGCAGCAGCCCT[G/T]CTCTTTTGGTACCTT | 337867 |
rs79648564 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352711 | CAGGCTCTGGTGAGT[C/T]CCACAGTGACCAAGG | 337867 |
rs79696635 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267873 | GCTGACACAGTGGCT[C/T]AAAGAGCGCAGATGT | 337867 |
rs79708491 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221899 | TGGAAGCCTTTGTCT[C/T]ACCTTTTACTCTTAG | 337867 |
rs79722430 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273015 | CTCTTTTTTTTTTTT[G/T]GGTTCATCTTTTCAA | 337867 |
rs79817944 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338060 | TTCTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs79826018 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277066 | TGCCAAGATAGCTAC[A/C]CTGTATAGTGTTGCT | 337867 |
rs79826314 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281938 | CCAGTTTAAAAGGGC[A/G]TGTAAGCTGTTGCCA | 337867 |
rs79888798 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273962 | TCTAATTAATATTTT[A/T]AAATAAATTTTTATT | 337867 |
rs79918079 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273878 | CTTTTTTTTTTTTTT[C/T]CCTGCTTTCTTTCTC | 337867 |
rs80063222 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358703 | GACTGTGGTCTCACA[C/T]GGGGCAGTGAGAGTG | 337867 |
rs80109706 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385461 | AAGAGGGAGGTTCCA[C/T]CGCACCCCTGCCCTC | 337867 |
rs80113139 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274734 | TTCTTTTTTTTTTTT[G/T]TGAGACAGGGTTTCA | 337867 |
rs80135501 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300660 | TAGTGCCTCCATGTG[C/G]TAGATGCTGGGAATA | 337867 |
rs80138729 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325982 | ATGTTGGCTATTGCA[A/G]ATAACATGGTGATGA | 337867 |
rs80149313 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199180 | CCTGACCTTGTGATC[C/T]GCCCACCTCGGCCTC | 337867 |
rs80175291 | in-del | -/AA | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301652 | GCAAAAGGAAAAAAA[-/AA]TAAAAGGCCCCCCAA | 337867 |
rs80193525 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208393 | ATGCTTTAATTAACT[A/G]ATTCAGCAGATACTT | 337867 |
rs80200505 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201078 | CGCGTCCGAACCCTG[C/T]TAGTTCCCGGTCTTG | 337867 |
rs80255898 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360089 | AATGCCCCCTCTGTA[A/T]TTGTTCTCCATTTTA | 337867 |
rs80272484 | snp | A/C | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353731 | GAAGTTTTTCCTCCC[A/C]AAAAAAAGCCATCCT | 337867 |
rs80305728 | snp | A/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235820 | TCTCCAAAAAAAAAT[A/T]AGCCAGGTGTGGTGG | 337867 |
rs80317548 | snp | A/C | 0.5 | 0 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301264 | TCCTTATTCAGGTTC[A/C]ACCTGTGGAACAGGG | 337867 |
rs111237135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341175 | ACATCAGGCTAAAAC[C/T]TCAGGCCTGATCTTT | 337867 |
rs111239052 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286067 | GTAGACCAGTCCTTA[C/T]GTGTTCCAGGAGTCT | 337867 |
rs111276652 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377297 | ACCTAGTGCCAGTCC[G/T]TAGAGCAGAGGAGAC | 337867 |
rs111287787 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346390 | TTCACTCCAGCTATC[A/G]TCCTTCAGGGCCTCT | 337867 |
rs111340127 | snp | A/G | 0 | 0 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256205 | ATGAGATGATTCACA[A/G]CAACTCTACTTTGCT | 337867 |
rs111432572 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242566 | AGGGGCTCCTCACTT[C/G]CCAGTAGGGGCGGCC | 337867 |
rs111462497 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251724 | GTCTTTGCCATCAGA[C/T]CAGATTTGAGATTCC | 337867 |
rs111527943 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349644 | GAAGCTGAGAGAGAG[A/G]AGGCACCATACGTCA | 337867 |
rs111537409 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335293 | TTCTGCTGAATCAGC[A/G]TAATGCTGATATACA | 337867 |
rs111639337 | snp | C/T | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350836 | GAGTGGGCCCTTAAC[C/T]TGTGGGCTCTGATGT | 337867 |
rs111654062 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264183 | TTTCTTTTGAGAGAC[A/G]GTAAGCTTGAGGTTC | 337867 |
rs111666221 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325206 | CTCCCGGGTTCACAC[C/G]ATTCTCCTGCCTCAG | 337867 |
rs111677102 | in-del | -/TG | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216082 | GTACCAACCTATATT[-/TG]TGTGTGTGTGTGTGT | 337867 |
rs111681873 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290608 | TGGGCACCTGTAATC[C/T]CAGCTGCTCAGGAGG | 337867 |
rs111697314 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238836 | AGGGAATTAAAAACA[A/G]TGTTTAATCTTTTTT | 337867 |
rs111714850 | snp | C/T | 0.0189856 | 0.0955633 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259163 | GCAACGAATCGCTGC[C/T]TGCCTTGTTAGGTTA | 337867 |
rs111779134 | snp | A/G/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319829 | AGTTAGAACTGTTGC[A/G/T]TGACTGAGGAAGACT | 337867 |
rs111787954 | snp | A/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215783 | TGCTGAAGCTCAAGC[A/T]AGGCAGAGAAAGGGC | 337867 |
rs111819140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247360 | GCTGGGACTACAGGC[A/G]CCCGCTACCACGCCC | 337867 |
rs111828813 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280833 | CCTTCTTCTTTCCCT[C/T]TCTCTCTCTCTCTCT | 337867 |
rs111849791 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204896 | GTAAGGGGGAGTTTC[A/G]TTTCCTTTTTTTTTT | 337867 |
rs111923197 | snp | C/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311843 | CTGTCCTGGGGTGCT[C/G]AGCCTGGGAAGAAGG | 337867 |
rs111938999 | snp | A/G | 1.64798e-05 | 0.00287047 | stop-gained, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255500 | TGGCGTACTTCGGCT[A/G]TACAATGGCCATGTA | 337867 |
rs111980174 | snp | A/C | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314925 | TTTTGATGTAGTTTT[A/C]TTCTACAGCTTCCTG | 337867 |
rs112002792 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242390 | AGGGGCTCCTCACTT[C/G]CCAGTAGGGGCGGCC | 337867 |
rs112022334 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287643 | CTTTTTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs112026030 | in-del | -/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214988 | GTTCTTTTCTTTTTG[-/T]TTTTTTTTTTTCTTG | 337867 |
rs112027403 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290797 | CATTTAAGAGGAGAG[A/C]ACCCAGGTAGGGATT | 337867 |
rs112077589 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360964 | CGAGGTCAGCCACCC[A/G]TGAGCTCTTCTGGCT | 337867 |
rs112108603 | snp | C/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361822 | CAGAGTCACCATGAC[C/G]ATATATCCATCTAAA | 337867 |
rs112139613 | snp | A/G | 0.000270934 | 0.0116359 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385365 | CACTGGGACCGGACC[A/G]GCAGCCGAGTGACAG | 337867 |
rs112239164 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317570 | GGCAGGGTTCTTCCC[A/G]TCTAAATTTAGGGTG | 337867 |
rs112281493 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202699 | CAGGGAGAGGCGTAG[A/G]TCTGGAGCCCCTCTG | 337867 |
rs112324324 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299159 | ATGCGTGTCTGACTG[C/T]ATCACCAAATAAGAT | 337867 |
rs112342415 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244936 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 337867 |
rs112372555 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283025 | TTAGTTGAAGTAATA[A/G]AATGAATTCTGGCTG | 337867 |
rs112385818 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287655 | TTTCTTTTTTTTTTT[C/T]TTTTTTTTTGGTAGA | 337867 |
rs112468881 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369769 | GGTTATCAAAATTAA[C/T]ATCACCAATTATGGA | 337867 |
rs112471195 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99307080 | TTGTGAGTTTATACA[A/G]TAGTACATGAAGTGA | 337867 |
rs112488929 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205902 | TTGGTCAAGGGTATA[C/G]GAGTAGCTGCGCTCC | 337867 |
rs112494789 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250827 | TCTTGGCTCACTGCA[G/T]CCTCCGCCTCCCAGG | 337867 |
rs112520636 | snp | A/C | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315116 | TGTTATCAATGGCTC[A/C]TCTGGGGCGTTTTCT | 337867 |
rs112562385 | snp | G/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318514 | CTCAATGTTACTTCT[G/T]TGGTGATTAAAAAGG | 337867 |
rs112651213 | snp | A/G | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262556 | AAAAATACAAAAATT[A/G]GCTGGGCATGGTGGT | 337867 |
rs112664575 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300234 | CCTTAACTGACGACC[A/G]TTGTGCACTGGAGGT | 337867 |
rs112673324 | snp | A/G | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367508 | TAGGAGTGTCTGTAC[A/G]GTGTCTTTCACTGCC | 337867 |
rs112680808 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228933 | TACAATAACCACAGT[C/G]TCAACTGTAACTGGT | 337867 |
rs112722541 | snp | A/C | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343256 | GGCACTTCATGGTGC[A/C]GCAGCAGTTTATGCA | 337867 |
rs112736006 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242667 | CCCGGACGGGGCGGC[G/T]GGCCGGGCGGGGGGC | 337867 |
rs112740998 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245080 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 337867 |
rs112759777 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249665 | TCCCACCAACAGTGT[A/G]TAAGTGTTCCCTTTT | 337867 |
rs112759907 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346709 | CAGGGAGGCCTTCCC[C/T]AGCTTCCTGGGGGGC | 337867 |
rs112770353 | in-del | -/A | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278923 | GGCTTATGGTTCCTC[-/A]ATGATCATCAGTTTG | 337867 |
rs112788225 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245783 | GAGGTTGCAGTGAGC[A/G]GAGATCGCTCCACTG | 337867 |
rs112808371 | snp | A/T | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99294108 | GTAAGTTTGCATTTT[A/T]CTCGGATCGTATTTA | 337867 |
rs112919246 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375943 | TGAGTAACTGGGACT[A/G]CAGGCACATGCCACC | 337867 |
rs112971737 | snp | A/C | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347321 | ACTATCCCCGGGCGC[A/C]CCCCCCCCCCCCCAG | 337867 |
rs113037568 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341649 | ATGAGAGCTGAGAGC[C/T]GAAAGCAAAGAAGTA | 337867 |
rs113052273 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259003 | TCTGCTTTTCTAGTG[C/T]GTGGAAGTCTAGAAA | 337867 |
rs113082622 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347333 | CGCCCCCCCCCCCCC[C/G]CAGGAAAAAAAAGGC | 337867 |
rs113126449 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376977 | TGCAGTATGCAGCGC[C/T]GTGCCTCGCCTCGCC | 337867 |
rs113131301 | in-del | -/AC | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268638 | AAAAAAAAAAAAGAA[-/AC]ACAAAAGGTAAAGAA | 337867 |
rs113157550 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208865 | CTCCCGACTTCTATC[C/G]CTTTTGCCTCCTTGA | 337867 |
rs113197573 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292099 | GTTGTCTTCTTTATG[A/G]CCAGGATACAGAATT | 337867 |
rs113235552 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225437 | ACCGGCTTATTTCAC[A/G]TAGCATAATGTCCTC | 337867 |
rs113263460 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284010 | AGTGCTGGGATAACA[A/G]GCGTGAGCCACCACG | 337867 |
rs113275758 | snp | A/G | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203440 | CTACCCCCATGGGTG[A/G]TGAATAACAGTCCCT | 337867 |
rs113300618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240577 | GGTGTTCTGAGGAGA[C/T]GACAGTCATCATCAT | 337867 |
rs113304325 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254526 | ATTCCATTCCTAGTG[C/T]AAATTAGACCTAAGG | 337867 |
rs113314787 | snp | A/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268631 | AAAAAAAAAAAAAAA[A/G]AAAGAAACACAAAAG | 337867 |
rs113323581 | snp | C/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345745 | TTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs113423187 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365770 | TATGTCCATTCAGAA[A/G]TAAACTTGTTATTTT | 337867 |
rs113426130 | in-del | -/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332156 | AGCTTGCCTTGTGGG[-/T]TTTTTGTTCAGCCAC | 337867 |
rs113440376 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378505 | GCACTCCAACCTGGG[C/T]GACTGAGCAAGACTC | 337867 |
rs113454189 | snp | C/T | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351298 | TATTACTCGTAAAAG[C/T]TTGTAACCTCTAGAG | 337867 |
rs113510604 | snp | C/T | 0.140581 | 0.224783 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236950 | AAATTAGTACAGTCA[C/T]GATGGAAAACAGTAT | 337867 |
rs113526169 | in-del | -/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265897 | GGGCAAGTTAAAAAG[-/G]TTTCGTATCAGAGAA | 337867 |
rs113575252 | snp | C/G | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262606 | TACTCAGGAGGCTGA[C/G]GCAGGAGAATCGCTT | 337867 |
rs113618557 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339021 | GTCTCCTCCTCCCCC[C/G]CATTTTATCTCCTCT | 337867 |
rs113642813 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364962 | ATTTCTTTTATTCAG[A/G]AGTGGAATTGCTGAG | 337867 |
rs113696529 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203021 | TGATTTCCTTTGTTT[C/T]ATTTTATTTATTTAT | 337867 |
rs113843686 | snp | A/G | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279804 | TTCCCTTTTATAAGG[A/G]CACTAATCCTATTTG | 337867 |
rs113860034 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201016 | GGAGGCTGGGGCAGC[A/G]GGGACCCTCGGGTTT | 337867 |
rs113865163 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203149 | TCAAGCGATTCTCCC[A/G]CCTCAGCCTCCCAAG | 337867 |
rs113868732 | snp | A/G | 0.176861 | 0.239062 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349936 | GAGACTCCCTTTCGC[A/G]GTCTGCTAAGTAATG | 337867 |
rs113886917 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313157 | GCCCGGCTAATTTTA[C/T]GTATTTTTAGTAGAG | 337867 |
rs113914077 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239971 | AAAAAGAAGGGATGA[C/T]TGTTAATTAGCAATG | 337867 |
rs113930625 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227336 | CACTGCAAGTTACCT[A/G]GGAGGGGTCCACTCC | 337867 |
rs113931258 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220293 | GTTATTTAGCCTTTC[G/T]TAGTTTATTTCTTCA | 337867 |
rs114014993 | snp | A/C/T | 0.0189929 | 0.095638 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200659 | CGGTTCTGACCGCCA[A/C/T]CGTTTCAACCTGGAG | 337867 |
rs114047048 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205449 | GCTGCAAAAAAATCA[A/G]TCACGGTGTTTTCTG | 337867 |
rs114076133 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367731 | AAAGCTCTTCCAAGC[A/C]TTATGATGATTCTGC | 337867 |
rs114174757 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302755 | CATAGTCAGAGCCTC[A/C]TGGTGCTTCATTAGT | 337867 |
rs114175883 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366430 | TCCAGAGTAATTTTA[A/C]ATTTGCTTTTGCTTG | 337867 |
rs114187552 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282619 | ATGATGGAAGTTTAA[C/T]GCTGGTTAAGTGAGA | 337867 |
rs114192594 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284764 | CAGTCTGTCTTGGGC[A/G]ACCTTGGCATTTTTG | 337867 |
rs114193848 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312485 | GATTTCCGTCCTGTG[A/T]TGAGTTCCTTGAGGT | 337867 |
rs114208266 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378809 | TGTTGAAAATCTTCC[A/G]TACCCATTCATTTGT | 337867 |
rs114235144 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364072 | CACTCTTGGATTTTC[G/T]AGGTAGACAGTCATC | 337867 |
rs114270874 | snp | A/C | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199759 | CATCTAATCAGGGTA[A/C]TTAGCACATCCATCA | 337867 |
rs114278138 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321686 | AACTTTAAAATATTC[A/C]ACTGATTAAAATAGA | 337867 |
rs114283029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256970 | TCTTTAAGGAAAACT[A/G]TGGGGGAGATTTGCT | 337867 |
rs114318773 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248438 | CTCTTGCCGCCCAGG[C/G]TGCAGTGCAATGGCG | 337867 |
rs114346424 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380431 | GTAATTGTTAGTGTC[C/T]ACCAAAGAGCCCTAC | 337867 |
rs114355128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356704 | CTGTTTTTATAGCAC[A/G]ACACAAAGATCATGG | 337867 |
rs114360200 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334871 | AAAAATTGCTATATG[A/G/T]TATCTACAAGACACA | 337867 |
rs114399580 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325645 | TCTCTGGAGCTTATC[A/G/T]CTCTTGCTTAACTGA | 337867 |
rs114419399 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270041 | GTGTGTTAATTTTTC[C/T]TAAACAACACAATAA | 337867 |
rs114432580 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357916 | ATTTTGCAACTGTTT[C/T]TTGAGTGCTTGCATA | 337867 |
rs114433536 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324095 | TCCCAAACATCCACT[C/T]TCAGGATTCTGTATG | 337867 |
rs114435006 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380991 | AGACGCTCTCTTCTG[C/T]CAAGACCTGTGAAAA | 337867 |
rs114439792 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343598 | GGACACCAGCCCCTG[G/T]GCTCTTGCTGGGCTT | 337867 |
rs114466672 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99329124 | ATAGGTTTATTTCTT[A/G]ACTCTTTTCTTTCCC | 337867 |
rs114468645 | snp | C/T | 0.00132773 | 0.0257313 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351853 | CTGCCCGGTGTTAAC[C/T]GGTTGATTATCACCT | 337867 |
rs114485760 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341422 | GAGTTTATATCAGGG[C/G]GGGGGAGGAAGGGGG | 337867 |
rs114513391 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374957 | GTTTTCACATAAAAA[A/T]TGTGCTAGAGAGTGG | 337867 |
rs114562238 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214714 | AACCCCCTCATTGTT[C/T]TCCTTAAGCAGATTG | 337867 |
rs114594673 | snp | G/T | 0.440746 | 0.161604 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341423 | AGTTTATATCAGGGG[G/T]GGGGAGGAAGGGGGC | 337867 |
rs114619148 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318853 | AAAAGGCCAGTCACA[G/T]GGAAAATTGAGACAA | 337867 |
rs114635193 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205594 | ATCCCCCCACCCCAG[C/G]ACATTTTAATGGACA | 337867 |
rs114688567 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243692 | CAGAGAACATACATA[C/T]ATAGTTTTCCTTTGG | 337867 |
rs114701598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311395 | GGAGATTCAGGGCCT[A/G]GGACGTCTTTGTCAT | 337867 |
rs114706094 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250116 | TTGCTTTTGAGGACT[C/T]AGTCACAAATTCTTC | 337867 |
rs114706101 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284043 | TGGCCAATGCCACTT[C/T]ATTTTTAAAGGTAAA | 337867 |
rs114717608 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370042 | GAGAAAAAATGTCTG[A/T]TGAAAGGCCATTTTA | 337867 |
rs114742285 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316454 | ATGAAGACTTGAATC[A/G]TAATCGGAAGAGCCA | 337867 |
rs114763803 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306801 | CAAAGATTGGTACTC[A/T]TTGCTGGCGGGAGGG | 337867 |
rs114822695 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213372 | TAACTTTTTTTTTGT[A/T]TTTTTTGAGACAAGG | 337867 |
rs114871295 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211855 | CATTGGAAACTGCAT[C/T]ATTGTGTCCTGGCAG | 337867 |
rs114890611 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382602 | TGCACAAATGGGAGG[C/G]GATGGGCTGAAAGGA | 337867 |
rs114934223 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322861 | GGGTAGGGAAAATGA[A/G]CCATCTGGAGGGAGT | 337867 |
rs114949002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210934 | TTCCCTTTGTCATAA[A/G]CATTCCCCTAGGATG | 337867 |
rs114990939 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364237 | AATGGGTATTGAATT[G/T]TGTCAAATTGTTTTC | 337867 |
rs114993006 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271581 | AAGTCATGTTGGCCT[A/G]TGCTTTCTTTTCATT | 337867 |
rs115038753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240227 | TTGCTGAGTGCAAGC[C/T]GGTAGCCAGTTACCA | 337867 |
rs115062436 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375432 | GCCAGTTGCTATGAC[A/C]GCAGTGGGCGAGGCA | 337867 |
rs115115825 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289951 | TGCTCTTCCTCCCCA[C/T]CCCCAAGGAACTTGA | 337867 |
rs115171946 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309560 | ACCAGGGTTTCTTGA[C/G]TTGTGATTGTACTGT | 337867 |
rs115181737 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324426 | AGAAAAGCAGGGCCC[A/G]GAGAGGGGCAGCTCC | 337867 |
rs115244728 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216401 | TGAGCCACCGTGCCC[A/G]GCCCAGTGTGTTTAT | 337867 |
rs115264600 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251075 | ATTTTTTTCAGCAGT[A/G]TTTTGTAGTTCTTGT | 337867 |
rs115297360 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331702 | ATGTATGACAAATGG[A/C]AGAAATAACTTTGGG | 337867 |
rs115305850 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211854 | TCATTGGAAACTGCA[A/T]CATTGTGTCCTGGCA | 337867 |
rs115307678 | snp | G/T | 0.0349115 | 0.127424 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200706 | ACCGACGCACTTCCC[G/T]TCCCCGGCAGGAAGG | 337867 |
rs115308847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380266 | TGACTGCACGTCTGC[A/G]CAGGCCTCAATTTCG | 337867 |
rs115340384 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367171 | GAGCCACCCTCAGAA[A/G]GATGGTTACTGATGC | 337867 |
rs115348566 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291168 | TGATAGTCATACCAT[A/G]TCTTAAGGTAGTGAG | 337867 |
rs115368218 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344124 | AGTAAGTACTCAGTA[C/T]ATGTTATCTCATTTA | 337867 |
rs115414046 | snp | A/C | 0.0168055 | 0.0901129 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351948 | GCTTTCAGTTACTTT[A/C]GCAGCATTTGGTTAA | 337867 |
rs115416400 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375437 | TTGCTATGACAGCAG[A/T]GGGCGAGGCAGGCCC | 337867 |
rs115460505 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306256 | TTCACCCTCTGGTAC[A/G]TCAGTGGCCAGAGAG | 337867 |
rs115479151 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226509 | TCCACCATTGCCTTA[C/G]TGTAATTTCTTCTCA | 337867 |
rs115487896 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228162 | TGGATCAAGCTGCCC[A/G]TTGCACTTACATCAC | 337867 |
rs115537808 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213087 | TCTTTTTTTTTCTGA[C/T]GCATGTATATACATA | 337867 |
rs115544151 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236357 | TAAGGAGCTCAAACA[A/G]CTCAATAGCAAAAAC | 337867 |
rs115556014 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369718 | TAAAGGAAAACCGTA[A/G]TTCTACAGAAGAGAA | 337867 |
rs115584582 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214354 | GATTCCTAAGTACCT[A/G]GTGTGGGTTTCCTCT | 337867 |
rs115632367 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210037 | CTAGGGAGGGACAAG[C/T]TTAAGAGAGGATGCT | 337867 |
rs115634819 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204833 | TGCTTTCAAGATCTC[C/G]GTTCTGAGAATCAAG | 337867 |
rs115686596 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314519 | CGTACTTTTTAACAA[C/T]CATAGTATGAAGTGG | 337867 |
rs115696676 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247671 | GATGGGTCGATACGT[A/G]CAGCAAACCACCATG | 337867 |
rs115754415 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302525 | CAATTATTTGAAAAC[A/G]CCTTCTTGTTCAAAC | 337867 |
rs115761685 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331038 | AGTTGCCTTCCAGTA[A/T]ATTTTTTCCTTCATA | 337867 |
rs115767977 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221924 | TCTTAGAGGAACCCC[A/G]GCTAAGACATTTTCT | 337867 |
rs115773909 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215285 | AAAATTGTGTTTTTC[A/T]CAGAAATATAGTCCA | 337867 |
rs115793797 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382569 | ACTCAGTTCTGGGCG[C/T]GGTGTTCTGAGACGG | 337867 |
rs115823114 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354236 | AGGTGACATTCATGA[A/G]CAGTGTGAGCCGGGT | 337867 |
rs115823816 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369441 | TTTCACTTGCAGCAC[A/G]ATACTCAATAATTAC | 337867 |
rs115826004 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331391 | ATGATTTCCCAAAAG[A/G]AAAAGCCTAGAGCAG | 337867 |
rs115826969 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321685 | TAACTTTAAAATATT[C/G]CACTGATTAAAATAG | 337867 |
rs115896962 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355008 | CCTGCCACGGTGAAC[A/G]CAGATAGGCAAGTGC | 337867 |
rs115904729 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269537 | GTATTTTTAAATTTT[G/T]AAGTACGTACTTCCA | 337867 |
rs115929404 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234760 | GAAGGCATGAAAACA[A/C]AAAGGTGGAACCAAG | 337867 |
rs115944980 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301001 | TTTATATAAACTAAG[G/T]TATACTAGAAAGTAT | 337867 |
rs115948348 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229107 | TTTATGGTGGATGTA[A/G]CGAAGGGTAAGGCAT | 337867 |
rs115965492 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294403 | TGGCAGCTCCAGGAA[A/C]AGCTCAGTGCTTTCA | 337867 |
rs115995095 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287437 | CTGTTCTTTTTTTTT[A/T]AAATTTTGAGACAGG | 337867 |
rs115999812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279495 | AGCACTCATCACTAT[A/G]GATAGTAAATAAGAT | 337867 |
rs116000171 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327881 | ACATACAATAGAACT[C/T]ACCAATTTTAAGTGT | 337867 |
rs116001128 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271161 | AAAAATTTGTAATAT[A/G]TATATGCCAGATCAT | 337867 |
rs116040737 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339805 | AAATGTCTAGAAAAA[C/T]CAGTAGTTGAAAAAC | 337867 |
rs116072402 | snp | C/T | 0.029116 | 0.117091 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370007 | GTGGAAAATGTGATC[C/T]TGGACTGGATTTTGT | 337867 |
rs116077564 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293180 | GATAAAATCATTTAT[A/G]TAGATTTGTGGTATA | 337867 |
rs116115728 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293721 | AATCTGAATATACTA[A/G]TAAATGGTGTTGAAT | 337867 |
rs116220744 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275218 | GTGGTTGTACTCAGG[A/G]TGTCAGGGACCACAG | 337867 |
rs116235650 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374692 | GAAAGCAGGGCTCTA[A/G]TATTTATTGGTTTTG | 337867 |
rs116291642 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343303 | GTTTGCGCACGCCCT[C/T]GCTCCAGGATTCTAC | 337867 |
rs116307012 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271572 | TGGGAGATGAAGTCA[C/T]GTTGGCCTGTGCTTT | 337867 |
rs116328390 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328359 | TATGTTTTCCTTCTT[C/T]AGGAACGGAATTGCT | 337867 |
rs116377678 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339773 | TTATAAATGGAACTA[A/G]TATTGGTGAGGATTT | 337867 |
rs116398056 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282557 | GTCTAATAGGAAATA[C/T]GTTTTGTTCAAAAAG | 337867 |
rs116429797 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267205 | TATTCAAGTTCTTTG[C/T]CCATTTGTTAATCTT | 337867 |
rs116430810 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256301 | TTTGTTTTTTTTAAA[A/G]TGGAAACACTTCATA | 337867 |
rs116482066 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354991 | TGGGAAGTGGACATC[C/T]GCCTGCCACGGTGAA | 337867 |
rs116483695 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347486 | ATATCACTCTGTTCT[C/G]ACTGGCTGCCCTCAT | 337867 |
rs116536516 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258112 | CAGTACATAAAGCAT[C/T]ACTTTTGACAATAAT | 337867 |
rs116588080 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330796 | AAATCCACAAATCTT[C/T]TAGAGCTTCACATTC | 337867 |
rs116686588 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343597 | AGGACACCAGCCCCT[C/G]GGCTCTTGCTGGGCT | 337867 |
rs116689578 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292610 | TATTGAGCTCTTCAC[A/G]TATACATGATGCCAT | 337867 |
rs116740777 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319198 | CGTTTGTCCTAAATT[A/C]TCTGTGAGGTATTAA | 337867 |
rs116744265 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208702 | CTCAGATTTCTTGTG[C/T]CTGACTTCACTAGTT | 337867 |
rs116749830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376745 | ATTTCGATTTGGGGG[C/T]TAGAAACCAAGCTGC | 337867 |
rs116760906 | snp | C/T | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356076 | AGGTATGTCAGGCCT[C/T]TGAAAAGAAATGTCA | 337867 |
rs116779152 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235349 | ATTGTTAAAATGGCA[A/G]TACTACCCAAAGCAA | 337867 |
rs116817284 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218409 | ACAGCTCACTCTTTC[C/T]TCCCCTCTAATTCAC | 337867 |
rs116888429 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308948 | CTTAGGCTGCAGAGT[A/G]CTTGAAGAAGACACT | 337867 |
rs116906133 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371651 | TACTTTTTCAATTAA[A/G]TGTTTGTATTTTCTT | 337867 |
rs116915317 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224464 | AAGAGTGCTGAATTC[C/T]CCAACTATATTTGTG | 337867 |
rs116915753 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206529 | CCTTGTCTCCAGTGT[A/G]TCAGCCCATTTGTGG | 337867 |
rs116916489 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282376 | AGAATATTTCTAGTA[C/G]TTGACTGAAATAGCT | 337867 |
rs117051265 | snp | C/G | 0.0798611 | 0.183174 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218339 | TTGAAACACTTTTCT[C/G]TGGCATGCAGGCCTC | 337867 |
rs117075673 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303165 | CTGCGAAAGGCCATT[C/T]ATAGGACCAAGTACA | 337867 |
rs117078742 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383631 | CTAGCCAGGGCTGTG[C/T]GTCAGTCCCCGTGCT | 337867 |
rs117105631 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293477 | TGGTTCCTCTTTAGA[A/G]ATCCAACTCAGATGA | 337867 |
rs117110686 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330967 | AATGGATATTAGAAG[C/G]TGTTTGTTTACATAT | 337867 |
rs117140656 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353633 | AGTTTTTGAAAGGAC[A/G]AATGAATTTAGAGAT | 337867 |
rs117181777 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207577 | TTGTGGCCTGCTTCC[A/G]TCCCGCTATACCATT | 337867 |
rs117271780 | snp | C/T | 0.021333 | 0.101051 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335552 | CACAAACGGCATAGA[C/T]TATTATTTTGTTGTC | 337867 |
rs117339283 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329438 | AGATTCTTTTACACA[A/T]CAAGAGGTGGAGCTT | 337867 |
rs117346369 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305227 | AATATTTTTATTCTT[C/T]TCTTTGGGCTTCCAA | 337867 |
rs117391072 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259570 | CCAGGTCCAGTTTCT[C/T]CCGCTGTAATAACTT | 337867 |
rs117405531 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286059 | TTCTCCTGGTAGACC[A/T]GTCCTTATGTGTTCC | 337867 |
rs117416561 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324508 | GCATGAACAGGAAAG[A/G]AATCTTTGTTATAAG | 337867 |
rs117450104 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303547 | ACTAAGAATCCCACC[A/T]TAATACTCATTTTAG | 337867 |
rs117451083 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248582 | AGGACAGGGTTTCAC[C/T]GTATTGGTCAGGCTG | 337867 |
rs117451628 | snp | A/C | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227218 | AAAAAAAAACAACAA[A/C]AAAAGACGGCACCCC | 337867 |
rs117463218 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210956 | CCTAGGATGCTGCAG[A/T]ATTAGGTTGTTTCTC | 337867 |
rs117528727 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333078 | ACCAGCCTGAGCAAC[A/G]TGGTGAAACCCCGTC | 337867 |
rs117546184 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372800 | GTAATCAAATACGCT[C/G]AATGTCTGCTATCTT | 337867 |
rs117556900 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273356 | GTGAGCACCCAGGAT[A/G]GAGAATCCACAGCCA | 337867 |
rs117631409 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276314 | CAGATGCCAGTCACA[C/G/T]GTTTCAGGACATCTG | 337867 |
rs117648842 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301786 | TTCAAGTAATTAAAG[C/T]GTTTTCTTAGCCTTT | 337867 |
rs117651102 | snp | C/G | 0.0585207 | 0.160895 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330391 | TTGAACCTGGGACGC[C/G]GAGGTTGTAGTGAGC | 337867 |
rs117757082 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359435 | TCATTCAAGTAAAAC[G/T]ATCTAGTCTTTTTCT | 337867 |
rs117759201 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312952 | AAGGAAGGGTTTTTT[G/T]GTTTTGTTTTTTATT | 337867 |
rs117807058 | snp | G/T | 0.0724559 | 0.176006 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200865 | GCTCGCACTTCAGCT[G/T]CCCCTCCCCCGGCGC | 337867 |
rs117839943 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207472 | AAGGTGATCTTCCCT[C/T]ATTTTTTCCCTGTTC | 337867 |
rs117880027 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207996 | CCTCTCATCGTCTCT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs117908129 | snp | G/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258762 | AGTAGGATTGTAGGG[G/T]CCCTAAACCAGAAAG | 337867 |
rs117940009 | snp | A/T | 0.113334 | 0.209338 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226416 | CCTCCCTCTTCATCT[A/T]CACCTCCACCCTGCT | 337867 |
rs117974538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347528 | ACTGTGGTCACGCTG[A/G]TCCCCGTTCAAGTTA | 337867 |
rs118077233 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336643 | TTGTTCTCTTGGTCT[A/G]TTTAAGTAACCCTAG | 337867 |
rs118105675 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272193 | CAACTCCAGGGGCTT[G/T]TATCTAGGTCAAGTG | 337867 |
rs118110221 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230175 | TGGTTTAAAACAAAA[G/T]AAATATGGCCAGGCA | 337867 |
rs118142402 | snp | A/G | 0.039522 | 0.134904 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292869 | ATTTTCAAACAGTAT[A/G]TTATATAATAAAGTC | 337867 |
rs118158470 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249534 | TTTGGTAGAATGATT[C/T]ATTTTCTTTTGGCTA | 337867 |
rs118167355 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370626 | GTAGCAAAACTTTGT[C/T]CTCATTTTTCCCAAA | 337867 |
rs118168446 | snp | A/T | 0.0214469 | 0.101309 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314260 | CTTTTCTTTAACCAG[A/T]TCTTTTTTTTTTTTT | 337867 |
rs118169878 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303710 | GTTTCTGGAAATAAT[A/G]TGTACCTTTTCTCTT | 337867 |
rs118173657 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343466 | CCTGCCCTGCTGGAG[C/T]GTGCATTCCCACCAG | 337867 |
rs118180118 | snp | C/T | 0.234982 | 0.249549 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203095 | CAGGCTGGAGTGCAG[C/T]GGTGGATCTCCGCTC | 337867 |
rs137873801 | in-del | -/TG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383153 | CATTAGTAGTGTGCA[-/TG]TGTGTGTGTGTGCCT | 337867 |
rs137897825 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319531 | TTTTCTGTGTTCATT[C/G]TTTGCTTAAAATTCA | 337867 |
rs137922433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350828 | TCTTGTGGGAGTGGG[C/T]CCTTAACCTGTGGGC | 337867 |
rs137933235 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205857 | CTCGGTCGAAGAGGA[C/T]GACCATCCCCGATAG | 337867 |
rs137933725 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273474 | TTAGCAGTATTGAGA[A/G]TAAGCGGTTTCTTTA | 337867 |
rs137935053 | snp | A/G | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323616 | GTCAGTGCTTGTCCA[A/G]TGTACACCCCACACA | 337867 |
rs137943843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239090 | GGTTCTTGTCTATGA[A/G]TTGGAGTGTTCATGC | 337867 |
rs137952665 | snp | C/T | 3.30677e-05 | 0.00406605 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201551 | TGTTTTCCTGGCGTG[C/T]TAGCGGTGGTCAGCA | 337867 |
rs137962062 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359819 | CCCTAAAGAGTCACA[G/T]CGCCCTTCGCTGCCT | 337867 |
rs138015901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314743 | TTTGCTAAATGGTTT[A/G]CTGTGAAGACTACTA | 337867 |
rs138016388 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263737 | AATTAGGAACAACCT[G/T]AATGTTCAACTATAG | 337867 |
rs138045086 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347253 | TGGCCAGGGAGCCTG[C/T]GGAGTAGAATGTTTC | 337867 |
rs138056208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267314 | CTCTTACTCCGTAGG[A/G]TGCCTCTTTTCTTTG | 337867 |
rs138068048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227768 | CCTAGAATAATGCAT[A/G]GTACAGCGTGGATGC | 337867 |
rs138085628 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309826 | TATGTTGCCCAGGCT[C/G]GTCTCAAACTCCTGA | 337867 |
rs138105159 | in-del | -/CCA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343377 | GCACGGTGTCTTTCC[-/CCA]CCCCAGATACTTGGA | 337867 |
rs138108915 | snp | C/T | 0.000197755 | 0.00994176 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255365 | TCTTGAGGCAGGTGG[C/T]GGGAGTGGAGTCTTT | 337867 |
rs138125059 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377987 | CTGCATTTTTATTTC[A/T]CGGAAGCATGAACCT | 337867 |
rs138165560 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385891 | TACCTTCTCCTACAT[C/G]TAGTAACAAAGAATG | 337867 |
rs138173026 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278127 | AGCTAAGAAATAGCT[A/G]TGATGGTGACACCAA | 337867 |
rs138183914 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343255 | AGGCACTTCATGGTG[C/T]AGCAGCAGTTTATGC | 337867 |
rs138188303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263481 | TCGCCAGAATGCCTA[C/T]GATGAAAAAGACGGA | 337867 |
rs138228577 | in-del | -/AA | 0.0279526 | 0.114869 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304730 | CATTGACAGAAGGTG[-/AA]ACGGAGGCACCAGGG | 337867 |
rs138256015 | snp | A/C | 0.000428258 | 0.0146269 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314167 | CAAGTGGCACAAATT[A/C]TGGGTCCGTTGTCCA | 337867 |
rs138264693 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324544 | GAAATTTGATAATTT[C/G]TTACCACAGTATAAC | 337867 |
rs138277867 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377289 | ATGCAAGTACCTAGT[A/G]CCAGTCCTTAGAGCA | 337867 |
rs138284467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279784 | AAAGCAGAGAGTTCA[A/G]TGGGTTCCCTTTTAT | 337867 |
rs138287243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297066 | TTCTACAGTCTTCCA[A/G]TGTGTCAATGCATAA | 337867 |
rs138304355 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338427 | CCTGGGCCACATGTG[G/T]CCCACAGGCCTCAGG | 337867 |
rs138322102 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302276 | GGTTAAGACTGAGGA[A/G]AAATTTCTGGAGCAG | 337867 |
rs138322454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251471 | TTCTACTGTCATTAT[C/T]ATCCCAGTCTAAACT | 337867 |
rs138325978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212124 | TTTTCCAACTTTTTC[C/T]GTTCTCAACCTGTCT | 337867 |
rs138394107 | snp | C/G/T | 5.14929e-05 | 0.00507383 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255821 | TTTTGTATTCATCTG[C/G/T]ATGTGAGCTGTTAAA | 337867 |
rs138395730 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315168 | TCATGAAATCTTTTT[A/G]TTCTCCATCTCTCAA | 337867 |
rs138403399 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370672 | CTGGGCAGGGATCTC[A/G]TAGCCACCCATGGGT | 337867 |
rs138407691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241011 | ACACCTGTCATTTCA[G/T]CACCTTGGGAGGCCA | 337867 |
rs138435721 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99329053 | TTCCATTACCAGTTA[C/T]TGAAAAGACCCTTTT | 337867 |
rs138436079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372810 | ACGCTCAATGTCTGC[C/T]ATCTTAGAAATAAGT | 337867 |
rs138459102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244984 | ACTACAGGCACGTGC[C/T]ACCATGCCTGGCTAA | 337867 |
rs138485475 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355748 | CCTGTGGCTCAGCCC[A/G]CAGCGTGCTTGGTGC | 337867 |
rs138502977 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367376 | CAGATTTCTGGCTGC[C/G]CTCAGTGATTTAGCC | 337867 |
rs138518957 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99256502 | TGCTCTACTTCAGTG[A/G]TTCACAGAAAGCAGC | 337867 |
rs138599225 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385767 | TTCTTCATGGACTTT[C/T]TTAGTTACTGTTTTT | 337867 |
rs138609331 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210597 | ATTCTTCTGCCTCAG[A/C]CTCCTGAGTAGCTGG | 337867 |
rs138646599 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354888 | AGCAAGGACCTAAAC[A/G]GGCAGATCCTCTCCC | 337867 |
rs138652713 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279574 | TGCCAGGAGGAGACT[C/G]TGTTAGTTTGTCTCA | 337867 |
rs138660274 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303802 | ATTAAATATCATTAT[A/T]TTATGGATAAACTGA | 337867 |
rs138660550 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350411 | CAGCCCCACCCCCAA[C/T]CTCTGTGATTAGGGA | 337867 |
rs138673822 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223207 | AGAAATACATAACAT[A/T]AAACTTACTGTTTTA | 337867 |
rs138685814 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231600 | ATTTTTAGTAGAGAC[A/G]GGGTTTTGCCATGTT | 337867 |
rs138690866 | in-del | -/AGAA | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322459 | TGGCATGATTAAAAT[-/AGAA]AGAGCCTTCTTTTGC | 337867 |
rs138692541 | snp | G/T | 8.27917e-05 | 0.00643343 | intron-variant, stop-gained, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201491 | CAAGTGGAGGGAAGT[G/T]AGGAAGTCGTGGCGA | 337867 |
rs138696587 | snp | A/G | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308722 | TAAAGTGCTGTGAGT[A/G]TGGAGGAACATTGTC | 337867 |
rs138706866 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226537 | TCAATTTAGCAACCA[A/G]AGTGATCATTCAAAA | 337867 |
rs138725918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348706 | TAGTCATAATATGAA[C/T]GTTGTCTGAAGGGAT | 337867 |
rs138764148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303181 | ATAGGACCAAGTACA[G/T]AGAACTTCTTCAAGA | 337867 |
rs138773615 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351046 | ACAATAGAAAGCAGC[A/G]TAATATAATGAAAAG | 337867 |
rs138808622 | in-del | -/GCCT | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231703 | GATGTGAGCCACCAC[-/GCCT]GGCTCTCTTTTTGTA | 337867 |
rs138817519 | in-del | -/ATTA | 0.497959 | 0.0318836 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244812 | TAGAATCAATTTTAT[-/ATTA]ATTCTTTCTTTAAAA | 337867 |
rs138839064 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221931 | GGAACCCCGGCTAAG[A/G]CATTTTCTAGTCATG | 337867 |
rs138864766 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226083 | AGTATGTTGATTCAC[A/T]TTTGGCACAAACTCT | 337867 |
rs138883833 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360212 | TTCCATCCATCACAG[A/C]CCTCCAGGATCCTGT | 337867 |
rs138887932 | in-del | -/T | 0.380138 | 0.213458 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228292 | CTCTATATTCATTCA[-/T]TTTTTTTTTTTTTGA | 337867 |
rs138891830 | snp | G/T | 0.029116 | 0.117091 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250872 | CTGCCTCAGCCTCCC[G/T]AGTAGCTGGGATTAC | 337867 |
rs138903552 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320089 | AGTAACTCTTATGTG[A/G]CTCAGTTTTTTAAAA | 337867 |
rs138918610 | snp | C/T | 0.031825 | 0.122064 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375441 | TATGACAGCAGTGGG[C/T]GAGGCAGGCCCAGCA | 337867 |
rs138924564 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99296672 | GAAATATGAACTTAC[A/C]ACAGTGATCTGATTT | 337867 |
rs138930528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206189 | CGGTCAGAGGTACTC[A/G]GGACACTTGGGGAAA | 337867 |
rs138956239 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333879 | AAGAGCTTCTACCAA[A/G]TTGTGAACTCCTTAA | 337867 |
rs138958242 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283545 | TTAAATGAATAGCCA[C/T]AAGCAGACTTGCAAG | 337867 |
rs138964526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202647 | TATCTATGGCACATG[G/T]TGGTGAGTGTTGAAT | 337867 |
rs138990085 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331368 | AGTTGACCTAATCCT[C/T]CTGATGCATGATTTC | 337867 |
rs138998162 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282854 | CACAAAAATAATCTC[-/A]TACCTGTCTTAGGGT | 337867 |
rs139000673 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212369 | AATCCTTATTTAAAT[A/C]ATGATTTTCCCCCCA | 337867 |
rs139019415 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338874 | GCTTCAGTGATAACT[A/T]AACTCTATTTCCCTT | 337867 |
rs139044979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219033 | AAGTTACTTTATGAG[A/T]CACCAAGTCACCCCA | 337867 |
rs139066988 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378586 | GCTTACTGACAGACT[C/T]GAAGGTATATTTTTT | 337867 |
rs139068036 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264837 | CTGAATGCGTCCAGG[A/G]TGCATTTCCTAAGTC | 337867 |
rs139071706 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262849 | ACAGCCATTTGTATA[G/T]TAAAAGTAAACATGT | 337867 |
rs139073025 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299393 | ACTGGGAATTATGTT[A/G]AGTGAGGAAAGCAGA | 337867 |
rs139085787 | snp | A/C | | | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352043 | TATCCTCCCCCAGCA[A/C]CAGCCATTTGGTATC | 337867 |
rs139112601 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303930 | CTGCCTCTGGTCAGC[A/G]AGCAGTCCCTGTGCC | 337867 |
rs139112781 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99254121 | AAAATCAATTAACTT[C/G]TTTTGTAAAAATGGT | 337867 |
rs139118243 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344775 | CTGCCACGTGCTCCT[C/T]GTGTGGCTCTGGGGG | 337867 |
rs139150621 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213422 | CTGGAGTGCAATGGT[A/G]TGATCTCGGCTTACT | 337867 |
rs139190098 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381110 | AAGCTTTCGTTCTTA[C/T]TCTAGGATGTCACCT | 337867 |
rs139191844 | snp | A/C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335177 | TGAATACTTTGAGAC[A/C/T]GAAAAATAAAAATGT | 337867 |
rs139223843 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339966 | CCAACAAAGGTAACC[A/G]CAGAGTCAGTACAGT | 337867 |
rs139243700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331732 | GAATCCCTAATTTGC[A/G]TTCACATTCTTGGGG | 337867 |
rs139259594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317425 | GGAAGAATTTCATGA[C/G]ATCTAATTCTAATTA | 337867 |
rs139309689 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345284 | TTGGACATTGGCTGT[-/G]GAAAAATTGTTTATT | 337867 |
rs139363590 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386418 | TACAATAAAGTTTTT[A/C]ATGTGTTTTACTCTT | 337867 |
rs139363944 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259763 | TGCCTTATTCACATA[A/G]CTTAGGACTTTTCTA | 337867 |
rs139381006 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215846 | CTCCTTCATCGCACC[A/G]TGATTCAAACTGCCC | 337867 |
rs139436322 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269617 | ACCATTAAGGTAAGA[A/G]CTAAATAATGAGTTG | 337867 |
rs139455385 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260682 | ACTTGTATAATGTAG[A/T]CACAAGTTTCTTTAA | 337867 |
rs139484990 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357424 | TACGTTTGTTTTGTT[A/G]TCTCAGCCAAACTCT | 337867 |
rs139511118 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315709 | TTTAGTGTAATCTGA[A/G]CAGATAATAAGAGTT | 337867 |
rs139522463 | in-del | -/A | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277145 | TGGGCTTATACCTTT[-/A]AAAAAAATCCTTTTA | 337867 |
rs139527409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360383 | TTTGATTCTCATACT[C/T]TCCATGTGAGGTGGG | 337867 |
rs139537315 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383685 | GGAGGAGCACGCTCA[A/C]TGCGTGCATTTGTAA | 337867 |
rs139537759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235083 | AAGGCAGAGGTCACA[C/G]TAGTCTCTCCTGGAA | 337867 |
rs139537934 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283914 | TAATTTTTGTATTTT[C/T]AATAGAGACGGTGTT | 337867 |
rs139553483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361921 | AGATTGCTTGGGTCC[A/G]GGAGTTCAGGACTGC | 337867 |
rs139555764 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208537 | ATTTAAAAATTAAAA[C/G]TGTCCAGTTCAATAT | 337867 |
rs139641542 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326047 | TCATTTCTTTTGGAT[A/G]TATACCCAATAGTGG | 337867 |
rs139641627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373622 | CGGGTGCTGCTGAGG[C/G]CAAGAAAGGCCGTCA | 337867 |
rs139660300 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378179 | AGAACCATCTCAGCT[A/G]TTTCACCATGGGTCA | 337867 |
rs139679900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332320 | GTGTTTTGCATGTTT[C/T]CTACCCAGCAAATTA | 337867 |
rs139685493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286862 | GCGTCCCATTCTCCT[A/G]TGATTTGAATTGCTG | 337867 |
rs139686282 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248636 | GATCGACCTGCCTTG[A/G]CCTCCCAAAGTGCTG | 337867 |
rs139703129 | in-del | -/AGTTGCC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317996 | TTGAATTTTATTTTT[-/AGTTGCC]TTTTTTTTTTCTTTT | 337867 |
rs139705830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241318 | AATGTTCGCAGCAGC[A/G]TTATTCACAATAGCA | 337867 |
rs139755385 | snp | C/T | 0.000181538 | 0.00952554 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385308 | CAATGACCTCAATGT[C/T]GCCACCAACTTCCTG | 337867 |
rs139800985 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213744 | ATCTTTGTAACTAAG[G/T]TATTGATTGCATCTT | 337867 |
rs139820586 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343902 | TAATACCAGGAGAAA[A/G]GTTTATTTTCATTTA | 337867 |
rs139886216 | in-del | -/TCTAGGTATAGAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251294 | GAGTCTTTAGGGTTT[-/TCTAGGTATAGAA]TCATATTGTCAGTAA | 337867 |
rs139927532 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293247 | AATGTTATTCTGTTG[C/T]CAAATGCCATAGGTA | 337867 |
rs139945409 | snp | A/G | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298619 | CAAGTGGAAGAAAAC[A/G]ATAGAGATAACTGCA | 337867 |
rs139993013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217318 | TGCTCGGATCTCTTA[C/T]GCTTTTCTCCCAGGG | 337867 |
rs140014290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321583 | GCTGGGATTATAGGC[A/G]TGAGCCACCGTGTCT | 337867 |
rs140032557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275952 | TCCCCAGATCATACT[C/G]TCCACTCTAATACCT | 337867 |
rs140035378 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312934 | GGATACTGGAGCCTA[C/T]GGAAGGAAGGGTTTT | 337867 |
rs140057816 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352112 | ATCATGAGAGTTCCT[A/G]TCATTAATCAAGTAT | 337867 |
rs140061829 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307541 | TGCACTTTGTGTTTT[C/T]TTTTGTTTTAAATGG | 337867 |
rs140066990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333384 | TTTATCTTTTATCAT[A/G]TGGGAAAGTATAAAC | 337867 |
rs140093886 | snp | G/T | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319144 | TATGTTTGCTGGAAT[G/T]TTTTCATCTTGTCTA | 337867 |
rs140097159 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312375 | AAACACAGACTGAGT[A/G]ATTAAGCCAAGTGTT | 337867 |
rs140099208 | in-del | -/A | 0.102726 | 0.202016 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334904 | TAAATACAAAGACAC[-/A]AAAAAAAGCCTGAAA | 337867 |
rs140101247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285474 | TGTAGCTCACTGTAA[C/T]GTCAAACTTCTGGGC | 337867 |
rs140108355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229157 | CTTTATTGTGGTTGG[C/G]ATAGCAAAACTGTAC | 337867 |
rs140120491 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255061 | TTCATGAGGAAGGTG[A/G]TAAAGGCTCCCCAGG | 337867 |
rs140129959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378783 | GTGTGGCATCCTTCA[C/T]GCTAAACGCCTGTTG | 337867 |
rs140157853 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280446 | ACAAGGAGAACTTCA[A/G]GTGTCCCCTTGGGTA | 337867 |
rs140189830 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250756 | TTTTTTTCTTTTTTC[-/T]TTTTTTTTGAGACGG | 337867 |
rs140231715 | in-del | -/AGAGATAT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232396 | GTCCATCCTTAGTTG[-/AGAGATAT]AGATATATATATATA | 337867 |
rs140233484 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223596 | CACCATTATGTGAGA[-/C]CTTTTTTCTTCCTAA | 337867 |
rs140288301 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370134 | CAGGACTTGGTACAT[A/G]CCGACCGTGGTTAGG | 337867 |
rs140290146 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228493 | GTGACGGGGCTTCAC[C/G]ATGTTGGCCAGGCTA | 337867 |
rs140308170 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374719 | TTTGAGACACATCTC[A/G]TGCTTCTGCTCTGAG | 337867 |
rs140309574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281421 | CTTTGGGCTCAGTTC[A/T]GTATTTGGGTGTTGG | 337867 |
rs140312850 | snp | A/G | 0.000401218 | 0.014158 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295032 | TGTCATACAGTTTAC[A/G]TCACTATAAACCAAA | 337867 |
rs140321779 | snp | A/G | 1.65231e-05 | 0.00287424 | intron-variant, synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201516 | TGGCGAGGGAGCGCA[A/G]CTGTGCTGCTGGATG | 337867 |
rs140344261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313927 | TTCATAAAGTGTTCT[A/G]TAAGTACAAATTATT | 337867 |
rs140433464 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263273 | TATTCTCAAGGAAAG[A/G]TTTTATAGCTGGATC | 337867 |
rs140436180 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350563 | GAGCAGGGTGCAGGG[G/T]GTGCCAGAGAGGGGC | 337867 |
rs140445463 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224544 | TCCTTTCTCAGCTCT[C/T]AGATTCTATGATTCA | 337867 |
rs140494301 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230128 | CTATTTTAGTGTACT[A/G]TTGCTTCTCTAACAA | 337867 |
rs140514159 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385622 | AAATGCATTAAAATG[C/G]AAGATTTCTGCAGGC | 337867 |
rs140518866 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308652 | CTCCAGGATTCTGTA[A/G]AAATAGTCGAGTAGC | 337867 |
rs140525496 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288221 | AAACCAGAAATAAAT[A/G]TTTTAACACTCTGAG | 337867 |
rs140532589 | in-del | -/C | 0.166832 | 0.235761 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343286 | AAGTGGGATTCTTGG[-/C]TGTTTGCGCACGCCC | 337867 |
rs140536323 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338304 | CTCTTGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 337867 |
rs140539549 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255740 | TACAACTGAAAACCC[A/G]TAATGCAGTGATGTT | 337867 |
rs140567398 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226144 | GACTGGTTATTTTGA[A/G]TGGCACTGGTAGAGA | 337867 |
rs140632275 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353328 | CTGCTGTGTTTCCAG[G/T]GCTTTTGTAGTTGAT | 337867 |
rs140635455 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276937 | TGCAGTGCTCTGCCT[C/T]CCTCTTAGCACTTCT | 337867 |
rs140636933 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380040 | AAAGGCATGTCACAG[C/G]TGAAGGAGGGTGAGA | 337867 |
rs140652585 | snp | A/C | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332956 | GACCTAGTGTAAAAA[A/C]GGTTTATGAGATCAT | 337867 |
rs140668170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291941 | GAGAAGAGGCACTTG[C/T]CCTCACCGAGCCCAC | 337867 |
rs140671553 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368753 | CACTCTGACCGAGAG[A/G]GCTCAGAAGCAGTGG | 337867 |
rs140682952 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234374 | TTTGTATTTTTAGTA[A/G]AGATGGGGTTTCGCC | 337867 |
rs140717469 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207791 | CTCCACCTTCGTTCC[A/G]GCTTAGGATCCTGCC | 337867 |
rs140722120 | snp | A/G | 0.00272405 | 0.0368049 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243964 | GCAGTAAGTTTTTAT[A/G]TATTTTGTCTTTGCT | 337867 |
rs140769802 | snp | C/T | 0.000164742 | 0.00907435 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255146 | AGGGCATAAAGCAGA[C/T]GAGCACCTGCACCAG | 337867 |
rs140772906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252076 | CTCTTCTTTCCTTTC[A/G]GAGTCCTCCTCATCT | 337867 |
rs140834147 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322412 | ATGCACCCTAATTCT[C/G]AAAAGCCGAGGTCTC | 337867 |
rs140839417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237819 | AATTAGCCAGGCATG[A/G]TGGCACGTGCCTGTA | 337867 |
rs140859469 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203972 | TATGACCGGGTAAAA[A/G]TGCGTAGGATTAGTG | 337867 |
rs140932972 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349728 | ATTTCTTCTACTGCT[A/G]TCTACTACGAACTTC | 337867 |
rs140940961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268754 | GAAATGGCATCATGG[A/G]GTGACTGCCAGTTGA | 337867 |
rs140947040 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221481 | ATTATCAGAGCTTGA[A/G]TTCTGGTTCTGCTGC | 337867 |
rs140955383 | snp | A/G | 0.00187762 | 0.0305824 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254961 | GCTTCGAAGGTAATT[A/G]CGGTATAGCATGACA | 337867 |
rs140964017 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235655 | TGGCAAGAACATACA[A/C]TGGAGAAACGACAGT | 337867 |
rs141012985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350404 | AGACTTTCAGCCCCA[C/T]CCCCAACCTCTGTGA | 337867 |
rs141021102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270632 | TTGTACTTAGAAACA[A/T]AGTTAGATAGAAATT | 337867 |
rs141030009 | snp | A/G | 3.3305e-05 | 0.00408061 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99296035 | GAAGACGAGGCTGTA[A/G]TGCAGAGGCATTACT | 337867 |
rs141052734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215532 | CACTTTACCTTTAAG[A/T]CTTTTGATGCATTTC | 337867 |
rs141056313 | snp | C/G | 0.00159617 | 0.0282053 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386882 | TCCACTCTCTGTGTT[C/G]CCCGTGCAAAGGAGC | 337867 |
rs141073361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229545 | GACTTGTCATTTGAG[C/T]TTGAAGGTCATACCA | 337867 |
rs141086199 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358736 | GGTGGAGACAGTGGC[A/C/G]GGGGAGTTCCAGTGG | 337867 |
rs141090390 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220032 | TGTAGGTTTTTGTGG[-/A]AAAAAAAATCCTGTG | 337867 |
rs141117277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342729 | ATGCTGTTCCTTTAG[C/G]TGGATCCTCCTTGTT | 337867 |
rs141126049 | snp | G/T | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362251 | TAATGGTCTTTTATA[G/T]AATAGAACCACTTAT | 337867 |
rs141197211 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270204 | CACACTACTTGGCCC[G/T]AATAGTAACATTAAA | 337867 |
rs141202447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324141 | ATTTTTCTTTAACAA[A/G]CACACAGCACTTAGT | 337867 |
rs141215183 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386369 | AAAATGAGCAACGAT[A/G]TATCAAATTGATGCA | 337867 |
rs141220022 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312063 | TCTAGCATTTGCTGC[A/G]TTTGTGTTGATAGCA | 337867 |
rs141255314 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212979 | GTAGAAGGGATTAGT[C/T]CCACATAATGATTCC | 337867 |
rs141310117 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199546 | AGGGACTGTGTTGAT[A/C]TACGAATCACAGATT | 337867 |
rs141317785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243141 | TCATTGTGAAGGGGA[A/G]ATAAGATTAGGATGT | 337867 |
rs141320365 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317872 | TAAGTAACAGTTGAT[A/G]TTTACTAATTTTCCA | 337867 |
rs141333448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375285 | GAGATGTGAAAGGAG[C/G]GGGGATCTGCAGTTC | 337867 |
rs141350597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333737 | CTGAAATTGAATACA[C/T]AGTTTTGTGAGTGTA | 337867 |
rs141373407 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382933 | CAGTGGGTTGAGGGA[A/G]GAAGGAGAGGGCTGT | 337867 |
rs141383378 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272818 | ACATATGAATTTAGG[G/T]GTGGGGGGAGACAAA | 337867 |
rs141391779 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372216 | GCGAGATGTCTGCTC[A/G]TGCCTTCCCTGTGCA | 337867 |
rs141459253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370676 | GCAGGGATCTCATAG[A/C]CACCCATGGGTAAGG | 337867 |
rs141478546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322921 | GCCTTTCTCTCTTCC[C/T]TCTGTAGTACTTTTA | 337867 |
rs141487000 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344497 | AATCTCATGCTGTGT[A/G]TTTCATTTAAAATAC | 337867 |
rs141489837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238817 | AGTGTAATTTATAAC[C/T]TCAAGGGAATTAAAA | 337867 |
rs141512164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343007 | CTTGGTCATGAGGGG[C/T]CCACCAGCTGTGGTA | 337867 |
rs141513075 | in-del | -/AA | | | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99296755 | TTAGATTTTCTTTTT[-/AA]AAAAAGAAGAAGACG | 337867 |
rs141547707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296949 | ACATAGTAGCAAGCA[C/T]CACACTTTATATTTT | 337867 |
rs141549663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346106 | TGATGAAAAGCACCC[A/G]TTGTTTACCCGAAAG | 337867 |
rs141572912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331431 | ACAGTATGTGAGAAA[C/T]GAATAATCTGTGATT | 337867 |
rs141594545 | snp | C/G/T | 0.00016602 | 0.00910973 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296025 | GCCCAATGATGAAGA[C/G/T]GAGGCTGTAATGCAG | 337867 |
rs141677756 | in-del | -/GTGACGCCAGGAGTGTGATGCCAGGGCTGAGCGTGGCA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384751 | GGCTGAGCGTGGCAG[lengthTooLong]TGACGCCAGGAGTGT | 337867 |
rs141680363 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359869 | AACCTTCCCTGCATG[G/T]TGGCCTGCAGGGGGC | 337867 |
rs141693898 | snp | G/T | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349560 | GGAGGGTGAATCTTC[G/T]AAGTGATTGACAAGG | 337867 |
rs141704005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237050 | AAATCAGTATTTCAA[A/G]GACATATCTGCACTT | 337867 |
rs141710847 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378018 | GGTTTTCTGTCCCTA[C/T]AAGTTGAGTATCCCT | 337867 |
rs141710927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308967 | GAAGAAGACACTGTT[A/G]ATAAATTTTTCAGTT | 337867 |
rs141764466 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225235 | TCATATTGTGCAACC[A/G]ATGTCTATAACTCTT | 337867 |
rs141806197 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315101 | CAGTCTGCTGTCATG[C/T]GTTATCAATGGCTCA | 337867 |
rs141808699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223221 | TAAAACTTACTGTTT[C/T]AACTATTTTTAAGTG | 337867 |
rs141811120 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231130 | ACATCTGATTAGCAA[A/C]CTCAATTCTGTCTGC | 337867 |
rs141821654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334442 | ACGTCTTTTCATTAC[A/G]GCATTGAGGAGACAA | 337867 |
rs141835771 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206887 | CCTGGGTGCTCCTTC[C/T]GCTTCCTGCTCCCTC | 337867 |
rs141840574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286704 | GTTGTTCCTATCTTC[A/G]TGTCCATGTGTATTC | 337867 |
rs141847876 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349004 | ACACTAGAGGAAGAA[A/G]ACCAGGTGGGAGACA | 337867 |
rs141860525 | in-del | -/TAGT | 0.0562307 | 0.157967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244733 | TTAAACTTCTAGATA[-/TAGT]TAAATTGATTTTATA | 337867 |
rs141864081 | snp | C/T | 8.25948e-05 | 0.00642577 | synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238485 | CCTCTCCCTCCTGCT[C/T]GCCCTCCTCCTGCCT | 337867 |
rs141885137 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303886 | AGGGGTCGTGAAGGC[C/G]CCCAGGACTCCGTGT | 337867 |
rs141901848 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301156 | CGTGGCCCCTCAGCC[A/G]TCCTTCGTGCTGCCC | 337867 |
rs141910184 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221274 | GTGTTGCAACCTCCA[C/G]AAACTGCAGTCTTTT | 337867 |
rs141913193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324997 | GAATGTGTCCTTATC[A/T]TTAAGCAACACATGA | 337867 |
rs141915591 | in-del | -/TTTA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203024 | TTTCCTTTGTTTTAT[-/TTTA]TTTATTTATTTATTT | 337867 |
rs141931004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323621 | TGCTTGTCCAATGTA[C/T]ACCCCACACACACTC | 337867 |
rs141947371 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283314 | TATAAATAAATGACA[A/G]TACCAAGGATAGGTT | 337867 |
rs141963841 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327312 | TGCCAAGAAACACCC[A/G]TACTTTTACATTGTA | 337867 |
rs141967623 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278298 | ACATTATTAATACAT[A/G]TGGCAATAGAGTTGG | 337867 |
rs141994406 | in-del | -/TGTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99254164 | ATAAGAAGAGCAAAC[-/TGTT]TGTATTGGAGAATGG | 337867 |
rs142043053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264607 | GGTTGTCTTAACCAT[A/G]TTAGCTCATTTCTCT | 337867 |
rs142101763 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364887 | TTCCCGTCTTTGACT[G/T]TTGGAAATAATGCTG | 337867 |
rs142113843 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286426 | TTTCTGGTATAACCT[A/G]TTCTTTGCTGGTGAC | 337867 |
rs142149791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284795 | AAGACTGTAAGCCAG[A/G]ACTTACAGAAAACGA | 337867 |
rs142152487 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240460 | TTAATCCTCAGATTT[C/T]CTTAGTGGCTCTCAG | 337867 |
rs142202138 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205501 | CCTCCCCAGAGGGTC[A/T]GATTCAGAAGAGCTA | 337867 |
rs142212387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333317 | TGCAGTAGCACTTTA[C/T]TTGACAACTTGAGGT | 337867 |
rs142217628 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249402 | CTGCATAATATTCCA[C/T]GGTGTGTATGTACCA | 337867 |
rs142297948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383680 | TCCGGGGAGGAGCAC[A/G]CTCACTGCGTGCATT | 337867 |
rs142311934 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281973 | TCTACATGAAGCCAC[A/G]TGATAAGTGATTTTG | 337867 |
rs142315009 | snp | C/G | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200151 | AAGCTCGCCAGGGCA[C/G]AAGCGCAGGGTCGCT | 337867 |
rs142327104 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302650 | ATCATCTGAGGGATT[A/G]TGGGTGTTGTTTGCC | 337867 |
rs142332399 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361617 | ACCTAAACACCATTG[A/G]CATTTTGATCCAGAC | 337867 |
rs142336861 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284525 | TATCATTTTCTCTCT[A/G]CACAGTATTTTTTCT | 337867 |
rs142347160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308164 | AATTACCAGATATGT[A/G]GCACTCAGATCAGGA | 337867 |
rs142379045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300250 | TTGTGCACTGGAGGT[A/G]GCCAAAGAAAGGCAT | 337867 |
rs142437132 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255106 | TCCCCCGTTCCCAGC[A/G]TCAGGAAAGCGAAAC | 337867 |
rs142451597 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357340 | GTTAAGCGACACGTG[A/G]CTACAGTTTTAAGTC | 337867 |
rs142471196 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316742 | ATGACAAAATGATAC[A/G]CTCTTTTTACTTGCG | 337867 |
rs142475329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234824 | GTCTCACAATAGTGT[C/G]CATTTTGATTAAATG | 337867 |
rs142486423 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337602 | CTTTATTCTAGAAAA[C/G]TCTCAGCTGTTTATC | 337867 |
rs142517074 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219954 | ACATTTTGTTCATTT[A/G]TTGATGGACATTGGT | 337867 |
rs142519269 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265521 | AACTGGAGTTTGAAG[A/T]ATCTGTGACACATCT | 337867 |
rs142525199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347375 | ATACTGGAAGACCAC[C/T]ACTGGATTCAGCAGA | 337867 |
rs142525959 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224271 | CTTTTCTTAAAAGAC[A/G]TGTCACATTGAATTA | 337867 |
rs142531925 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267363 | GCAATTTTTGGAGCA[C/T]ATTTTAGGCTTGCTC | 337867 |
rs142541591 | snp | A/G | 8.38638e-05 | 0.00647494 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295823 | ATGTAAAACACTAGC[A/G]CAGTTATCCTACACA | 337867 |
rs142551140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222437 | TGATGCTAATACCTC[C/T]ACTTCCTAAGTGCTT | 337867 |
rs142568689 | in-del | -/TATATA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237255 | AGAAAATTTTATGCG[-/TATATA]TATATATATATACAC | 337867 |
rs142590935 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217110 | TGCTGGGATCACAGG[C/T]GTGAGCCACGGCGCC | 337867 |
rs142636614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385131 | TTTTGTAAACAGTTT[C/T]GACCTTTGCCACAAG | 337867 |
rs142683139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290204 | AAATAGAACAAGCCT[C/T]ACAGCATTCTTGTGA | 337867 |
rs142684001 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232526 | TTGTTTGTAATGATA[C/T]TGATACTGTAATATT | 337867 |
rs142687799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343618 | TTGCTGGGCTTTTAC[A/G]TTGAGTGGTCTGCTG | 337867 |
rs142704028 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236694 | GTCTCTACTAAAAAT[A/G]CAGAAATTAGCTGGG | 337867 |
rs142717404 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360469 | GAAAATGCATCTAAG[A/G]TGTTACAATAAGAGG | 337867 |
rs142751231 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274560 | TGAATTCATGAGCTC[A/C]AGTGATCCTCCTGCC | 337867 |
rs142765529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355077 | GGATGAACTCTCCAC[A/G]GAGGAAATGTAAGAA | 337867 |
rs142771606 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279731 | ACTGGCAGATTTGGT[A/G]TTTGGGGCTGTCTTT | 337867 |
rs142852597 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198895 | TGTACAGTTGTCCAA[C/T]TGTACAATGGAAAAC | 337867 |
rs142898390 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342611 | CATTCGTGTGCCAGC[A/G]CTGGGTTATCTGGTG | 337867 |
rs142906356 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229199 | GCTCATAGTAGTGTG[C/T]GGGAACGAGGGTGCA | 337867 |
rs142924074 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329352 | GAGTTAAGATTTTGC[G/T]TGTAATTGCGTTGAA | 337867 |
rs142930478 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245939 | ACCTCCAAGCATCTG[A/C]ATGAAGTATCTGAGA | 337867 |
rs142943764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201620 | TTTTCTCACTGAGTG[C/T]GTGGAATTGACTTTC | 337867 |
rs142965224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292892 | ATAAAGTCATGTTCT[C/G]TAACAGAATATAACA | 337867 |
rs142983150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385065 | ATTGAAAAATTTGTA[C/T]CTGGTATAACTTTTA | 337867 |
rs142984439 | snp | A/G | 1.648e-05 | 0.0028705 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255523 | GCCATGTATCTGTCA[A/G]CACTAATAAAGGCAA | 337867 |
rs142985001 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352544 | AAGATCTGCCTAGTA[C/G]AGCTTTATGTGTGCA | 337867 |
rs142986475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215958 | CTATTTTCCTATTGT[A/G]ACAAAAAGAGCAGGA | 337867 |
rs142991630 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274893 | CAGCTAATTTTTGTA[G/T]TCTTTGTAGAGATGA | 337867 |
rs143024622 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212638 | TTAACTCTGTTTCTA[A/G]GATTTATTGGGGGAC | 337867 |
rs143052672 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367414 | CATGCCTTCCTTCCT[A/G]TCACACCCTGCAAAG | 337867 |
rs143067657 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364058 | GAGACATTTGTAAAC[A/C]CTCTTGGATTTTCTA | 337867 |
rs143074994 | snp | C/G/T | 0.00880064 | 0.0658183 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255096 | GTAACTGTTCTCCCC[C/G/T]GTTCCCAGCATCAGG | 337867 |
rs143087060 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323702 | CTCCCTCTCTATGCT[A/G]CCTTTCCCACTCCTG | 337867 |
rs143090464 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239629 | GAGTTAATTTGGTTC[A/G]TTTGGCTAAGCCCAC | 337867 |
rs143093022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324742 | ATCAACAACAGAGTG[C/T]GTATTCAGTGGTGGC | 337867 |
rs143100166 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241226 | GATGTGATCACATCA[C/T]TGCACTACAGCCTGG | 337867 |
rs143101199 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335178 | GAATACTTTGAGACC[A/G]AAAAATAAAAATGTT | 337867 |
rs143120358 | snp | C/T | 0.0298908 | 0.118541 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294503 | TGACACTCCCACTGA[C/T]AGTTGACAGGGAGCA | 337867 |
rs143138028 | snp | A/G | 0.000201069 | 0.0100247 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295501 | GCAGATCTGAGAATA[A/G]CAGATGAGAATGATT | 337867 |
rs143161108 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217605 | GCCAGCTGTTACCCG[C/T]GCTCGCCCTGGCATG | 337867 |
rs143171650 | snp | A/C/T | 0.000428427 | 0.0146301 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255468 | CAGCACGGCTTTGCA[A/C/T]GTGTTTTTAAGTTCT | 337867 |
rs143192583 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319050 | CGAGGGAAAAAAATA[A/T]TGCCAACTGGAAAGT | 337867 |
rs143196588 | in-del | -/A | 0.0271762 | 0.113356 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375582 | GGGAAGTAAAAACCC[-/A]AAAAAAAACATTTGT | 337867 |
rs143213155 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308432 | ACTCCAGAGACTAGC[A/G]GGAGGGTCAGTAAGA | 337867 |
rs143250374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338278 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCTT | 337867 |
rs143258128 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225977 | TGTTAAGTGCTATGA[A/G]AAAAGCAGGACAAAG | 337867 |
rs143276182 | snp | A/G | 0.000362456 | 0.0134572 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340338 | TCCGGTCTGTGCTAC[A/G]ACAGCAAAATGTTCC | 337867 |
rs143283188 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255224 | GCTTAGACGTCCTGC[C/T]GTGAAGGAGATTATG | 337867 |
rs143296748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350294 | GCCCACAGTGAGAAG[C/T]GTCTTTTCACATGGA | 337867 |
rs143309777 | in-del | -/A | 0.308414 | 0.24308 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297952 | CAGTATTAACATCAG[-/A]AAAAAATAGAATTCA | 337867 |
rs143380938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370677 | CAGGGATCTCATAGC[C/T]ACCCATGGGTAAGGC | 337867 |
rs143383399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292577 | GATGTTACATAATAT[A/G]TGGACTGTTTTATAA | 337867 |
rs143386931 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273708 | CCATTTGGGTTGTAC[A/T]CTTGGTGTGGGCCCT | 337867 |
rs143401786 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214224 | GGCATCTTTGGTTTG[-/T]TTTTTTTTTTTTTTT | 337867 |
rs143479521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299144 | CCAGTTTGTATACAA[A/G]TGCGTGTCTGACTGC | 337867 |
rs143484553 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201244 | TGCCCTGGTGTTCTC[G/T]TGGGCCGGCCCCAGG | 337867 |
rs143488298 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328942 | TCAAGAATTTAATAG[C/T]TTCTGCTATTACATT | 337867 |
rs143499844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214678 | TACCCCAAGCTCTCT[C/T]CTACTTTTTTGCAGA | 337867 |
rs143521632 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315902 | CATGGCCTTCATCAC[A/G]GGGCCATTGTAGTAG | 337867 |
rs143528211 | snp | A/G | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230801 | CACGCTTGTAATCCT[A/G]GCGCTTTGGGAGGCC | 337867 |
rs143546517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276238 | TCTGACACTTTCTAC[C/T]TGGAGTTAGTATCAG | 337867 |
rs143557998 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268554 | CCGAGGCTGCAGTGA[G/T]CCATGATCCTGTCAC | 337867 |
rs143571069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343268 | TGCAGCAGCAGTTTA[C/T]GCAAGTGGGATTCTT | 337867 |
rs143608361 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353947 | AGGAATTTTCAGAGT[C/G/T]GTGAGTCACGATCTC | 337867 |
rs143612853 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277976 | CTCATGGTCTCCCCA[C/T]AGAAGGGCCTTTCCT | 337867 |
rs143632196 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266586 | GTGTATTCCTGGGCT[A/G]GGGCCTTGAGAAGAT | 337867 |
rs143677600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377231 | GCTCACCGTCTATGA[A/G]GGAGACCAGATCCAT | 337867 |
rs143721003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322004 | GTGTTACCTTTTTCC[G/T]CATTTGACAGTTCTG | 337867 |
rs143748837 | in-del | -/C | 0.0566069 | 0.158427 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337751 | ACCCACATGGACCCT[-/C]CTTGGTTCATGCCCT | 337867 |
rs143806394 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251611 | GGCTTAACCACACTA[A/G]TTCTTTTAAAAACCC | 337867 |
rs143806582 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334022 | GTGCAATCATAGCTC[A/G]CTACAACCTCGAATT | 337867 |
rs143811198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251133 | GTATTCCTAGGTATC[C/T]TTTTGTGTGTGTTGT | 337867 |
rs143842731 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256754 | GGAAAGGAGGTTATT[C/T]GGGGTTGCAAATATC | 337867 |
rs143845900 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228482 | TATTTTTAGTAGTGA[C/T]GGGGCTTCACGATGT | 337867 |
rs143896293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280459 | CAAGTGTCCCCTTGG[A/G]TAGCTCTGCTCCACG | 337867 |
rs143901332 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310876 | CTATGAATTAAGCGC[C/G]TCCAAGGGCATGTTC | 337867 |
rs143908754 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372896 | GAGGCGGACGGATCA[C/T]GAGGTCAGGAGATCG | 337867 |
rs143912952 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293307 | ATTGACTCCCTTAGC[A/C]CAGAGAGGACTCTTG | 337867 |
rs143917027 | snp | A/G | 0.000115322 | 0.00759261 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314175 | ACAAATTCTGGGTCC[A/G]TTGTCCATCACAAAC | 337867 |
rs143928037 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377469 | GACAGGAAGCAGCCT[A/G]CAGAGAAAATGAAGT | 337867 |
rs143932174 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297111 | CCCTTGATGAACTTT[C/T]GGATTCTTTCCAATT | 337867 |
rs143955123 | snp | C/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350950 | AGCCCCCCAGCACAT[C/G]TGGTGTCAGAATATT | 337867 |
rs143965754 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254346 | TGTTTTTAAAAGAAT[G/T]AATTCAGAGTAGGGA | 337867 |
rs144031573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374736 | GCTTCTGCTCTGAGT[A/G]GCCAAGCATGGCAGC | 337867 |
rs144035947 | snp | A/G | 0.000619283 | 0.0175857 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295447 | TACACCAGATTTCTC[A/G]GTGAGTGGGTTTTGT | 337867 |
rs144039046 | snp | C/G | 0.0084658 | 0.0645076 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295276 | GCATACTGTAAAGTG[C/G]AGAGAAATCTGGAAC | 337867 |
rs144051944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378635 | CATCATTTTATCCTC[A/G]TTTGACATGTGGAAT | 337867 |
rs144101533 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373867 | CAAGAAACACCATCA[C/T]TGGGTTTCCCAAGAG | 337867 |
rs144130595 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213518 | GGCACCTGCCATCAT[A/G]CCCAGCTAATTTTTG | 337867 |
rs144143922 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340022 | TTTTACGGCTTTTTA[A/G]AAAATGAAGACAGTG | 337867 |
rs144149003 | snp | C/T | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260116 | TGATGGCATGGCCTG[C/T]TGCTCTTTGTTCTTG | 337867 |
rs144178890 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317558 | CCTAAGTAGGCTGGC[A/G]GGGTTCTTCCCATCT | 337867 |
rs144183700 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235216 | AACACCCAGGAATCA[A/G]TTAACCAAAGATGTG | 337867 |
rs144203184 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237353 | CATTTGCAGCCACAT[A/G]GATGGAACTAGAAGA | 337867 |
rs144270484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353510 | TACAGTCTCATGATA[C/G]CTCAGAAAACAAGCA | 337867 |
rs144271574 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332170 | GGTTTTTGTTCAGCC[A/G]CAGTTGGCCAAAGAA | 337867 |
rs144273970 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297205 | TCCTACAATAAAGTT[A/C]TGTAGATGAGGGTAA | 337867 |
rs144277923 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203667 | TCAAACAGGCTAACA[A/T]GTCAGTATGATTCAC | 337867 |
rs144281094 | in-del | -/TTC | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331228 | GTCGCCTTTTGTCCT[-/TTC]TTATTTTTTTTCTTC | 337867 |
rs144293307 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216688 | GAAAGGACACATTTC[A/G]CTGGTGTTTTGAGGG | 337867 |
rs144319206 | in-del | -/ACC | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259733 | TCTGCCTGCATGCAG[-/ACC]TAATCTGTCCTTTGC | 337867 |
rs144344568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228504 | TCACGATGTTGGCCA[G/T]GCTAGTCTCAAACTC | 337867 |
rs144355505 | in-del | -/CTGGG | 0.0221229 | 0.10282 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204673 | AAACGGGCCTGAAGC[-/CTGGG]GCGACCTGTGGGAAA | 337867 |
rs144360478 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368348 | AAACTGAAAAGAAAC[A/G]AACAAATGCTCTAAC | 337867 |
rs144362480 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234483 | GCGTGAGCCACTGCG[C/T]CCTGCCTGTGCTAGC | 337867 |
rs144367897 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288357 | GTTTTCAGTTGAGTG[A/G]ACAGGATGTCTAAGA | 337867 |
rs144369683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238074 | TATGAGTTTTGTGCA[C/T]GCTCAGGAGCTAACT | 337867 |
rs144392553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356467 | CCTGATCGTATTGCC[A/G]TGGAAACTGCCTTCT | 337867 |
rs144397301 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280298 | CCTTGTACTCTGCAT[A/G]TCAGCTAAATTGCAT | 337867 |
rs144400645 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246543 | AACTTTGGAGATGGA[C/T]AGTAACTTAGCATTA | 337867 |
rs144408985 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287635 | TCTTTCTTCTTTTTT[C/T]TTTCTTTCTTTTTTT | 337867 |
rs144461236 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349417 | TAAATAAAGACACAA[A/G]ACAAAGAGATAAAGA | 337867 |
rs144467294 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268063 | ATGCAGGAGGAGGGA[C/T]TGCCTTTCCCCAGGT | 337867 |
rs144497125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320815 | TTTACACACCACTGA[C/G]TATAGGATCCAAGCC | 337867 |
rs144530244 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361942 | TCAGGACTGCAGTGC[C/G]CCATGATTGTGCCTG | 337867 |
rs144542056 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284855 | AGTTTGTGAAGGTGA[A/C]GCAGTAGATGAAAAT | 337867 |
rs144628337 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223802 | TTTGGGGGATTTTCC[A/G]TCTTTCTGCTGTTGG | 337867 |
rs144632306 | snp | A/G | 1.66062e-05 | 0.00288146 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201481 | AGAGTGCTTTCAAGT[A/G]GAGGGAAGTTAGGAA | 337867 |
rs144643379 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210173 | TTTTCTTTTTCTATA[C/T]ACTTATGTTCTTGTT | 337867 |
rs144657408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285792 | CTCCCTTGCCTGGAG[C/T]TCTGGATATGATTTA | 337867 |
rs144680829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206010 | GCTGATTGGATCTGC[A/G]GCGAGGGAGGAGTTG | 337867 |
rs144712434 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367996 | TCAAAAGTAATCAAG[C/T]GTGTAAATACAAAGA | 337867 |
rs144723805 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258757 | TATCCAGTAGGATTG[C/T]AGGGGCCCTAAACCA | 337867 |
rs144726676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271065 | CTGGGCTCTGAGGAT[C/T]CTGCACTGATCAAAG | 337867 |
rs144778864 | snp | C/T | 0.0295035 | 0.117819 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349790 | AAAGTGGACAAGGAG[C/T]GTGACCGTTGAAGCA | 337867 |
rs144786763 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268927 | AGAGAAGAAACTGGG[A/G]CAGAACTGTCTTCCA | 337867 |
rs144808865 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274587 | TGCCTTGGCCTTCCA[A/G]AGTGTTAGGATTACA | 337867 |
rs144820165 | snp | A/T | 0.00019799 | 0.00994766 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295345 | AAGCTTCTTAATCAT[A/T]TGTTGAATAATTGCA | 337867 |
rs144821826 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224722 | CCCTTTATTTATTTG[A/G]TCAGTACCATATGAT | 337867 |
rs144826738 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350405 | GACTTTCAGCCCCAC[C/T]CCCAACCTCTGTGAT | 337867 |
rs144828154 | snp | C/T | 0.031825 | 0.122064 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206613 | GTCTCATCCAGACTC[C/T]CGGAGACCTGGCACG | 337867 |
rs144884307 | in-del | -/TC | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219573 | ACTTTCTTAAAACAT[-/TC]TGAGATTTTTTTCAA | 337867 |
rs144887456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362551 | GTGTATTTTTGCGAG[C/T]CTTGTGGGTATAAAA | 337867 |
rs144893041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348505 | GCAAGGAATTGCATT[C/T]GCCTGAGATTGAGGT | 337867 |
rs144902189 | in-del | -/GT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216092 | ATATTTGTGTGTGTG[-/GT]TGTGTGTGTGTGTGT | 337867 |
rs144912146 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264861 | CTAAGTCCTCATCCC[-/A]GGGAGGAAAACCAAG | 337867 |
rs144931247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299742 | TGACTTACTAGTTGT[A/G]TACCTTTGCATTGTG | 337867 |
rs144952827 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265643 | GGACCTGGCACGTGC[A/G]TCTTCAAACGTTTCA | 337867 |
rs144959573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219733 | TATTACCTTCTCCCA[A/G]CTGTCCCTGACAAAC | 337867 |
rs144996530 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358222 | TAAGAAATTTCTGTC[A/G]GATTCTGAAAGCAAC | 337867 |
rs145019459 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318602 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATCG | 337867 |
rs145026469 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235745 | TTTGGGAGGCTGAGG[C/T]GAGAGGATCACTTGA | 337867 |
rs145047547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267003 | CCTATCTTGGCTCGC[A/C]GGCACACCTCTCTCA | 337867 |
rs145062428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294469 | GCAGTTCAAAGTCTA[C/T]TGCCAATTATCTTTT | 337867 |
rs145066961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270531 | TACTTTTTACATTTC[C/T]ATATCAATGTCCAAG | 337867 |
rs145100086 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248799 | CCCAAAGGGCTGGGA[G/T]TATAGGCGTGACCAC | 337867 |
rs145127508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264941 | CCCTGATGGGGTCAC[A/G]TTAGTTCCTGATCTT | 337867 |
rs145132565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333760 | TGAGTGTATACTCAC[A/G]TCTGATTGTCATTGT | 337867 |
rs145143990 | in-del | -/TTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223543 | CTTTCTCTTTTTCTG[-/TTT]TTTTTTTTTTTTTTT | 337867 |
rs145144700 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99229112 | GGTGGATGTAGCGAA[A/G]GGTAAGGCATGTGGC | 337867 |
rs145192008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332414 | ATCTGAAGAACCGTG[C/T]AATTGACGTCCATGT | 337867 |
rs145200086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248679 | TGAGCCACTGTATCC[A/G]GCCATTTTTTGTTTG | 337867 |
rs145263565 | in-del | -/AGAAA | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324411 | GTCCCCTTTGCCATG[-/AGAAA]AGCAGGGCCCGGAGA | 337867 |
rs145308079 | snp | C/G/T | 0.0349115 | 0.127424 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326974 | ACTTTTTGCAGCCTT[C/G/T]TGTGTGCTGACCAAT | 337867 |
rs145308189 | snp | C/T | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373838 | GACACCAAGGAACCA[C/T]GCGGGATCTTACACA | 337867 |
rs145311407 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243437 | TTTTTGAGTTTATAC[A/C]TAAGTTGTTTTTCAG | 337867 |
rs145334174 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245203 | CTATTCTGATCCTGA[G/T]AGAATTAGTTTTGTG | 337867 |
rs145368676 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345346 | AAATGTCATTTTATT[A/G]CACAGTGTAAGATGG | 337867 |
rs145414279 | in-del | -/ATG | 0.145642 | 0.227177 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325066 | GGAGACAGGATTCAA[-/ATG]ATGTAGGTAGCATAA | 337867 |
rs145421823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225339 | CTGCCTCTGGCAACC[A/G]CTTTTCTACTTTCTG | 337867 |
rs145449053 | snp | A/G | 0.000131813 | 0.00811721 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255318 | AGTGAGGTTCAGCAC[A/G]TTCACAGCTTTTAGA | 337867 |
rs145455774 | snp | C/T | 0.0349115 | 0.127424 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328307 | TATTATGAATAATGC[C/T]GCTGTGAACATCTGT | 337867 |
rs145485385 | snp | G/T | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248458 | GTGCAATGGCGTGAT[G/T]TCTGCTCACTGCAAC | 337867 |
rs145498062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261691 | AAATCAGTCCTGGAA[C/G]CACTGAAGTCCCATG | 337867 |
rs145507019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313955 | ATTTTGGACATGAAT[C/G]ATATTTGAAAATCAA | 337867 |
rs145510039 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312416 | CAGGTGCAAGCTTGT[A/G]CCCAAACCACTCTAC | 337867 |
rs145561760 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385864 | GCTGTTCCAGGCCAG[A/G]GGACTCTGCAGTACC | 337867 |
rs145562033 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322877 | CCATCTGGAGGGAGT[C/T]AAGACAGCGCATTTG | 337867 |
rs145582730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277616 | GTTGTGAAATCATTT[A/T]TTTCTCCATTGATAG | 337867 |
rs145605184 | snp | A/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386483 | CTTGTTCCAGGCTAT[A/T]CATATTTACCAGTCA | 337867 |
rs145606686 | snp | C/G | 0.000379842 | 0.0137759 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295995 | TGACGACCAAGGCTA[C/G]TAAGTTTCCCACGAG | 337867 |
rs145683683 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307763 | TTGCATGTAAAAGTA[C/T]GGGTTTTTAAATGTT | 337867 |
rs145702855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226200 | GCTTGGGGGAGCATA[C/T]TGCAAGATGGGCCCA | 337867 |
rs145711034 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313264 | GCTGGGATTACAGGC[A/G]TGAGACACTACGCCC | 337867 |
rs145721308 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230425 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 337867 |
rs145817810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278318 | AATAGAGTTGGTACC[A/G]GGCAGTGGTATTCAC | 337867 |
rs145827468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384260 | CGCAAGTGGCTAAAA[A/C]ACTCAACATGTACAA | 337867 |
rs145840529 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370331 | TATGGCCAAATAACA[A/G]TTGGTGAATCTGGTT | 337867 |
rs145868043 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232405 | AGTTGAGAGATATAG[-/AT]ATATATATATATATA | 337867 |
rs145898012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367065 | TTTTAAAGCAGCATG[C/T]GATGCATTTTTCTTC | 337867 |
rs145902748 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286530 | TTTTAGGTTCGGGGG[G/T]TACATATGCAGGTTT | 337867 |
rs145938475 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383681 | CCGGGGAGGAGCACG[C/G]TCACTGCGTGCATTT | 337867 |
rs145952109 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260163 | GAAGCTTTCTCTGCC[A/C]TCCGAAGCTGGGCTG | 337867 |
rs146013998 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223118 | TAAGTTATCAAATTT[A/G]TGGGCGTAAAGTATT | 337867 |
rs146020941 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343753 | CTTCTTCACTCAGCT[A/G]TGTCTCAGTTTTCTT | 337867 |
rs146024590 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264484 | AGCACTAGTTCTCTT[G/T]GCTTCGTTTGTCCCC | 337867 |
rs146059805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360477 | ATCTAAGGTGTTACA[A/G]TAAGAGGCAGAGCTG | 337867 |
rs146073124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321147 | TAATGTGGTTTTTAA[G/T]AAAAAGAGTATTTTT | 337867 |
rs146105671 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358564 | CTTGTGATTGTTAAT[A/G]AGTTATTAAATATTT | 337867 |
rs146120180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282022 | AGTGGCATCATTGAC[C/T]TAAGCTAGAGTTTCC | 337867 |
rs146136441 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202382 | GAAGCTGACAGTTCA[A/G]GAAGGCAATGTGGTT | 337867 |
rs146137467 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283427 | TTTTTTGACAGCAGG[A/T]TTTACCCTTTCTCTT | 337867 |
rs146145562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324771 | GCCCTGTGGATTCTA[A/G]TGGAGCATAGGTAGA | 337867 |
rs146147581 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241248 | ACAGCCTGGGCAACA[C/G]AGTGAGACCCTGTCT | 337867 |
rs146208469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236585 | TGCTGGGCACGGTGG[C/T]TCATGCCTGTAATCC | 337867 |
rs146257206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263669 | AAACACATGCTGCGT[A/T]CCAGGAGACATGGAC | 337867 |
rs146262870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382986 | TAGGAAAAGAGAATA[A/G]GGTTGTTCTCGGTTA | 337867 |
rs146264828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303897 | AGGCGCCCAGGACTC[C/T]GTGTTCTCCCTCACC | 337867 |
rs146271975 | snp | C/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256813 | CCCCATGATGCAACA[C/G]CAACAACAGACTTCA | 337867 |
rs146276520 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259359 | CCTTTTTTTTTTTTT[C/T]CTCAGACAAAACCAT | 337867 |
rs146312426 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357371 | TAACAAGATGCCTCT[C/T]GTTCAGTCCTGAAGT | 337867 |
rs146314490 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280498 | CTCCAGCCAGAGTTG[A/G]AATTAACCTCTCCTT | 337867 |
rs146383930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360375 | TTAACTCTTTTGATT[C/G]TCATACTCTCCATGT | 337867 |
rs146387043 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283632 | GTCACTAAGTGACGG[C/T]TACTTAAGTGGCAAG | 337867 |
rs146409182 | in-del | -/TATATACACACATATGCATGTGTG | 0.117188 | 0.211804 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244371 | AAATAATTTCAAATA[-/TATATACACACATATGCATGTGTG]TATATACACACATAT | 337867 |
rs146421615 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337762 | CCCTCCTTGGTTCAT[A/G]CCCTACACAGCTTTT | 337867 |
rs146440940 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378705 | ATAGCACAGGCCAGA[A/G]GTTGTGTCAGGCTTG | 337867 |
rs146442598 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333677 | GCAGTCCTATTTTTG[C/T]TTATTACTGGGTGGG | 337867 |
rs146444449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250292 | TGACTAGCCAGCTAT[C/T]CTAGCACCATTTATT | 337867 |
rs146447212 | snp | A/G | 1.66007e-05 | 0.00288098 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385183 | GGCCCAGGGATAAGC[A/G]GCAATGTCAGCGCCC | 337867 |
rs146455146 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254819 | CAGAATATCCATTGA[C/T]GCCAGAGTAGTTAGT | 337867 |
rs146486628 | in-del | -/AA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370309 | CAGAGACAGAGAGAG[-/AA]AGCAGCTATGGCCAA | 337867 |
rs146523338 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213603 | GACCTCAGGTGATCC[C/G]CACGACTCAGCCTCC | 337867 |
rs146534122 | in-del | -/C | 0.0283406 | 0.115616 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375591 | AAAACCCAAAAAAAA[-/C]ATTTGTTTTTGACGC | 337867 |
rs146556669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381043 | CAGCACCGCGGCACA[C/T]GTCGTTCATGTCTGA | 337867 |
rs146560243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237374 | AACTAGAAGACATGT[A/G]AGTGAAATAAGAACA | 337867 |
rs146565476 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357849 | CTAAGAAAACCCCAT[A/G]CGCCTTAACTCAGCA | 337867 |
rs146565735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313512 | TCTTAGCCCAAGCTA[G/T]AGAAAGGGTTGAGAT | 337867 |
rs146568632 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230575 | AGGTGTCAGCAGGGC[A/T]GCATTTCTTTTGGAA | 337867 |
rs146579185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235378 | AATTTACAGATTCAA[A/T]GCAATCCTCTCAAAA | 337867 |
rs146614165 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375273 | GAGTTCAACCAAGAG[A/C/G]TGTGAAAGGAGGGGG | 337867 |
rs146685151 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291710 | TCTTCAAGGGCATAC[A/G]CTCTATATTGTGTAA | 337867 |
rs146685218 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341848 | AGAGGCACAGAGCTT[A/T]TGAGGGAGAGAAAGA | 337867 |
rs146690022 | snp | A/T | 1.64743e-05 | 0.00287 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255236 | TGCCGTGAAGGAGAT[A/T]ATGAATAATGACCAA | 337867 |
rs146692266 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214618 | ATTACCCTCCTTGTC[C/T]GTTCCCCGTCACCTG | 337867 |
rs146695518 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294918 | CTTGGGCTTACTTCC[A/G]AGTTGGAGATGGGAA | 337867 |
rs146709613 | snp | A/G | 8.33563e-05 | 0.00645532 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295531 | TATAAGTGGAAGTAC[A/G]TATCCTATGAAACAT | 337867 |
rs146732973 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353559 | GGCTTTTTGAAGATG[G/T]AAAAGTTATCAGTAA | 337867 |
rs146748361 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253757 | GACCTCAAGTGATCC[A/G]TCCACCTCAGCCTCC | 337867 |
rs146785681 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352791 | AGTGAAATGTGATGG[A/T]CACTCTTCTGGGAGA | 337867 |
rs146799206 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230106 | TTCCTCAGGGACATG[A/G]TAATCACTATTTTAG | 337867 |
rs146806412 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270538 | TACATTTCTATATCA[A/G]TGTCCAAGATTATAG | 337867 |
rs146817503 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276446 | ATTTTACTTACGTTT[A/C]TTGGTTTATTATAAA | 337867 |
rs146846751 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220138 | GGAACCAAAAAGATA[C/T]ATCTTAAGTATTAAA | 337867 |
rs146871706 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235081 | ACAAGGCAGAGGTCA[C/T]ACTAGTCTCTCCTGG | 337867 |
rs146896952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215548 | CTTTTGATGCATTTC[C/T]TGCCAGTTCAAGTCC | 337867 |
rs146898238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342817 | CACACGTGTAATTGC[C/G]TCAGGCCACTTCTCT | 337867 |
rs146907202 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212354 | TGAGAATTATAAAGT[A/T]ATCCTTATTTAAATC | 337867 |
rs146919028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236891 | ACAGAGGCTGGCCAG[C/G]ATGTGGAGAAAGGAG | 337867 |
rs146942965 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362315 | TTTTTCATTTTCTTA[C/G]TTAATATTACAACCA | 337867 |
rs146959257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359124 | GGCGTAGCTAGAGGG[C/G]TAGAAAGAAAGCGGG | 337867 |
rs146992910 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199652 | TTAGCTGGGTAGTGT[A/G]GTCAATTTTCCCCAT | 337867 |
rs147005918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323183 | CTTCTCCATTGACCA[A/G]AGAGTGGTATAGGTA | 337867 |
rs147034568 | snp | C/T | 4.94295e-05 | 0.00497115 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314112 | CCTGGCACCTGTGTT[C/T]GCTCTGTTTGTACCA | 337867 |
rs147047570 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215967 | TATTGTAACAAAAAG[A/T]GCAGGAAGTAATATT | 337867 |
rs147048609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296965 | CACACTTTATATTTT[A/G]TTTCTTGCTTTATTC | 337867 |
rs147049039 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346266 | GTTCAGGCCACCGGC[A/G/T]CCATTTGCCTGGATT | 337867 |
rs147059415 | in-del | -/GT | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377499 | TAGTCCAGGGTTTCA[-/GT]GTGAGTTAATGTGTG | 337867 |
rs147065473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343231 | ATGCTCACTTTGTGG[C/T]CTACAGACAGGCACT | 337867 |
rs147115820 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221305 | TATATTTCGTTCACA[A/G]TTACATTTACTTTTG | 337867 |
rs147160185 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268728 | CTGAATGATAGAGTT[C/G]TTTGGCTTGTGAAAT | 337867 |
rs147160440 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320037 | ATTGTGTTAGTTACT[A/G]TTAATTCTTTTACTC | 337867 |
rs147170172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273765 | CTTCTTGAATTTTTC[C/T]TGAATTATTTTGATC | 337867 |
rs147264359 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377869 | AGGAAACAGAGAGTC[A/G]GAGCCTGGTCCCCTG | 337867 |
rs147274650 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335099 | TCCACAAACAGGAAC[A/G]GCTTCTAGATATATG | 337867 |
rs147276678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251714 | AAATAGCATGGTCTT[A/T]GCCATCAGACCAGAT | 337867 |
rs147296705 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386687 | GAGGTGACTTTCTTG[A/G]AGCCCAGCTGGTCCC | 337867 |
rs147309209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316133 | TTTTGTAATATTTCC[A/G]GTAACTTTGAGAGGG | 337867 |
rs147370743 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355671 | GTCCCTGGAGGAAAA[A/C/G]TTCCCCATGAGGAGT | 337867 |
rs147370794 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312212 | AAGGATGAGAAATTG[C/T]GCAAGAGGCCAGGAG | 337867 |
rs147380829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315663 | TGATAATATCTACCT[C/T]ACAGAGGTATTTTAA | 337867 |
rs147383157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233065 | AAAGAGCTAGAAGCA[C/T]TGGGACCCAGAAAAT | 337867 |
rs147403838 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368421 | ATGGATTTCAGTAAC[A/G]TTTGTACCGGATATA | 337867 |
rs147413655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373099 | GCACTCCAGCCTGGG[A/T]GACAGAGCAAGACTC | 337867 |
rs147465089 | in-del | -/TGTTTTTTTTTGTTTGTT/TGTTTTTTTTTGTTTGTTTGTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247193 | AAGAGAGAAAACTAC[lengthTooLong]TGTTTTTTTTTTTTT | 337867 |
rs147474658 | snp | C/T | 0.000510906 | 0.0159747 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254970 | GTAATTACGGTATAG[C/T]ATGACACTAATGACT | 337867 |
rs147476787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339252 | ACGGGCACCGCATCA[A/T]CCTTAAGATCTTCGC | 337867 |
rs147476848 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287561 | TCAGTTCTTTCTGAA[C/T]CCATCCCTGAACTTC | 337867 |
rs147478310 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212788 | ATTTTTAAAGGAAAG[G/T]TCAGCCTATCTACAG | 337867 |
rs147485996 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293138 | GATTAGAGTTTACCT[C/T]TTTGGCAGTATGGTT | 337867 |
rs147487984 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208503 | TCTTAGGTGATAGAA[G/T]TCTTGAAATGTAGGC | 337867 |
rs147490848 | snp | A/G | 0.000428611 | 0.0146329 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255693 | TGCCACATTCATCAT[A/G]TAGATGGTTACCGTG | 337867 |
rs147518716 | snp | A/G | 0.000859476 | 0.0207123 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351819 | GCTCTTCTTTTAACT[A/G]CCTCCTCATCTCATT | 337867 |
rs147614491 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332480 | CCTTACATTCTCAGA[C/T]TTACAGGGTCACAGC | 337867 |
rs147624557 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284665 | GCAAAAAGGAAAATC[A/G]AAATTCTAGTCCATC | 337867 |
rs147631989 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327080 | TTCTCTTCTAAAATC[A/T]TCAAGATATTTAACT | 337867 |
rs147638870 | snp | C/T | 0.0275645 | 0.114116 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199707 | TGTATTTCTGGGGTA[C/T]AGTGTGATGGTTCCA | 337867 |
rs147641553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281607 | TCAGAAACCTTCAGC[A/G]CTATTTTCTATAAAT | 337867 |
rs147673127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380435 | TTGTTAGTGTCCACC[A/G]AAGAGCCCTACAGAC | 337867 |
rs147729719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265417 | GTTCTCAGACTGTGT[C/T]GGCTTACATCTTTCT | 337867 |
rs147733305 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385092 | TTTAAGTATCAGATT[A/C]CATATTGAAATGAAA | 337867 |
rs147736177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308063 | GCACAGGGTGAAAGA[A/G]ACTCATGCCATTCAC | 337867 |
rs147745816 | snp | A/G | 0.030278 | 0.119257 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262275 | ATGTATGTACAGGAA[A/G]AAAATAGTAAGTATA | 337867 |
rs147746086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312913 | TTTATGAAGCATTTT[A/G]TCTTTGGATACTGGA | 337867 |
rs147776560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358617 | AGGAGCCAGCAAAGG[A/G]TTTCTAAGTAGAGGA | 337867 |
rs147812053 | in-del | -/A | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324284 | GCATGCCCTGTTGAC[-/A]ATCAGGTTTTGTTGT | 337867 |
rs147839082 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362127 | TTATGTAAATGGTAT[A/G]TGTATATGTTGTATA | 337867 |
rs147841426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285444 | GTCACCCAGGCTGGA[A/G]TGCAGTGGTGCGATT | 337867 |
rs147851224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289189 | TTTTTTCTTCCTTTG[C/T]TGTAAGATCTAAATT | 337867 |
rs147851454 | snp | C/G/T | 0.00262263 | 0.0361183 | missense, synonymous-codon, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238471 | CTGGTCCCCAGTGCC[C/G/T]TCTCCCTCCTGCTCG | 337867 |
rs147872761 | in-del | -/CCAGGGCTGAGCGTGGCAGTGACGCCAGGAGTGTGATG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384733 | CCAGGAGTGTGATGC[lengthTooLong]CAGGGCTGAGCGTGG | 337867 |
rs147872916 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385511 | TTTTAGTGTGGAGAT[A/G]AGTTTGCCATTACAT | 337867 |
rs147918436 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225044 | TCAGATCTGTATTTT[C/T]AGGGGTTTGTTTGGT | 337867 |
rs147946809 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346017 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCGC | 337867 |
rs147955072 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220728 | TGCTTGGGTTCTGTG[C/T]GTATGAACCACTTCC | 337867 |
rs147980884 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236925 | CCTGGTACACTGTTG[A/G]TGGGAATGTAAATTA | 337867 |
rs147996908 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283184 | TACTTAATGTTTAAT[A/T]TTGGCTTCTAGGATG | 337867 |
rs148029516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343294 | TTCTTGGCTGTTTGC[A/G]CACGCCCTCGCTCCA | 337867 |
rs148039645 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297970 | AAAATAGAATTCAAG[A/G]CAAATTCAATATTAA | 337867 |
rs148048769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99354044 | GAGGTGTGTGCACAC[A/G]TGCAGTGCCTGTTCA | 337867 |
rs148054594 | snp | C/T | 1.65173e-05 | 0.00287374 | missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238475 | TCCCCAGTGCCCTCT[C/T]CCTCCTGCTCGCCCT | 337867 |
rs148060564 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230944 | GTCCCAGCTACTCAG[C/G]GGGCTGAGGCAGGAG | 337867 |
rs148077199 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221346 | CACTACTTTGATTTC[C/T]ATTAGTGCTGTTTGT | 337867 |
rs148082492 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252641 | CCTTATATACCTATT[-/A]TTTTTTGTTAGTATT | 337867 |
rs148086884 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266699 | AATATATATATATAT[A/G]TATTAGACAATTTAT | 337867 |
rs148092521 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334275 | CATTGTATTGTTGAG[A/C]TTTTAAGGTATATAG | 337867 |
rs148155282 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286687 | TCCCCAGTGTCTATT[C/G]TGTTGTTCCTATCTT | 337867 |
rs148157258 | in-del | -/T | 0.0554779 | 0.157039 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328100 | CTTAGTATTGTATAA[-/T]ATGAAGTATTTTGTG | 337867 |
rs148176169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206791 | CTCTATTTTGTCTTC[A/G]GCTCAAGGCTATTCT | 337867 |
rs148210951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239875 | TACATGACATCCTTG[A/G]GGGGTGATCAAGGAA | 337867 |
rs148245410 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272785 | CCAAATACCACCACA[C/T]TGGGGGCTAGTGCTT | 337867 |
rs148251554 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339625 | CTAATCCTAAGAATC[A/G]AATTCACATCAAGAT | 337867 |
rs148261798 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319072 | CTGGAAAGTCAGGTG[G/T]GTTGGACCTGACCAA | 337867 |
rs148302452 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372133 | CCAAGCCACACAGTG[C/T]GCCCTGTGCTGCCTG | 337867 |
rs148305418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292844 | TGGAGAAAATACTTA[C/T]AGGGTTGTGATTTTC | 337867 |
rs148309260 | in-del | -/TTG | 0.465892 | 0.126058 | intron-variant, cds-indel | UBAC2 | GRCh38.p7 | 13:99328831 | ATCTTGATTAATTCA[-/TTG]TTAACTGGTTTTTAA | 337867 |
rs148354473 | snp | A/G | 3.29881e-05 | 0.00406115 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340496 | CCAGAGACAGCAGAG[A/G]ATGGAGCTGCTGGAC | 337867 |
rs148355068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364659 | TACTGTTTCAATTAC[A/G]TTAAAGTATGATATA | 337867 |
rs148366806 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246604 | TTTCCTGCTGCACAT[A/G]GAATCGAATGACAGT | 337867 |
rs148395698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224264 | TCCCTCCCTTTTCTT[A/G]AAAGACATGTCACAT | 337867 |
rs148397372 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349531 | ATTGCATACAAGACC[A/G]GGGGTCAGGGTAAGG | 337867 |
rs148400082 | snp | G/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268547 | TGGAGGGCCGAGGCT[G/T]CAGTGAGCCATGATC | 337867 |
rs148405905 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337588 | GATTTATATTCTTTC[C/T]TTATTCTAGAAAACT | 337867 |
rs148447559 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216839 | TTTCTTTTTTCTTTT[C/T]TTTTTTTTGAGACGA | 337867 |
rs148494542 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289628 | GGTCTTTTTTTTTTC[A/G]TTCCAAGTAGGTTAA | 337867 |
rs148510199 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198585 | AAAACCTGGCTTCAC[C/T]TAGATACACCCCCAC | 337867 |
rs148543663 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212817 | AGTTTCATATTCTGC[C/T]TTTTTCATTTACTCT | 337867 |
rs148556456 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287643 | CTTTTTTTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 337867 |
rs148556710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274874 | AGGTGCGCACCACCA[C/T]TCCCAGCTAATTTTT | 337867 |
rs148561647 | in-del | -/AGCCTA | 0.0225045 | 0.103662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207676 | TAGAGAAGTTTGATG[-/AGCCTA]AGGTCCACTGGTGTC | 337867 |
rs148598008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320688 | TAAGGAACATTTTCT[G/T]TCTTTGTCTAGAAAA | 337867 |
rs148607942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311010 | TCCCATTAAAAATGA[C/T]AAAAAGGAAGGGGGC | 337867 |
rs148612664 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374056 | GCAAATTTAGTGACA[C/G]ATCTATTTGGCTTTT | 337867 |
rs148615814 | snp | C/T | 0.0298908 | 0.118541 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294493 | ATCTTTTCCCTGACA[C/T]TCCCACTGATAGTTG | 337867 |
rs148617491 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264510 | TCCCCTTTTTTTCTT[C/T]GTAGCTTATTTAAAT | 337867 |
rs148666432 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368264 | CATGGTTTCACTTTT[A/G]TATGGTTTTGAGTCA | 337867 |
rs148670950 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259132 | AGGGAAATGAAACCA[A/G]CAGAAAGGGAAGTGA | 337867 |
rs148678061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249217 | CTCTAATAGTCTTCC[A/G]TGTCTGTTGCTGCCA | 337867 |
rs148713997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237381 | AGACATGTAAGTGAA[A/G]TAAGAACAAAAAGAC | 337867 |
rs148730744 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284080 | TAGTTAATGGTCACT[A/G]TAGCAGGAAGCAACT | 337867 |
rs148755055 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361387 | CTAGAACCTAGAGCC[A/G]TAACTTTCTGCTTTT | 337867 |
rs148765658 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316442 | ATGAATGAATGAATG[A/C]AGACTTGAATCATAA | 337867 |
rs148767971 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234779 | GGTGGAACCAAGGAA[G/T]ACCAGAGGGAGAGAA | 337867 |
rs148779334 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262932 | TTATATCTGCCATTA[-/TTC]TTAACTAAATTATGA | 337867 |
rs148795491 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255104 | TCTCCCCCGTTCCCA[A/G]CATCAGGAAAGCGAA | 337867 |
rs148809798 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357315 | ACATTTCTCAGAATG[A/C]AGCCCTGTTGTTAAG | 337867 |
rs148817092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282670 | GGAGATACTTTAATA[A/G]TGAAGGGAACTTGAA | 337867 |
rs148859462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328681 | TTATCCATTTTGTTC[A/G]TTGGGCTATTTATCT | 337867 |
rs148862700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214619 | TTACCCTCCTTGTCC[A/G]TTCCCCGTCACCTGT | 337867 |
rs148867627 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353662 | ATGTACTCTGGAGCA[A/G]TATCATGTTAAACCA | 337867 |
rs148870282 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277627 | ATTTTTTTCTCCATT[C/G]ATAGTTACCTCTACA | 337867 |
rs148914448 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209374 | GGGGACTGCCTTGCA[A/G]TCACTCTTGGAAAGT | 337867 |
rs148932418 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265804 | AGATACAATTACAAA[C/G]ACGTACCAAATAAAA | 337867 |
rs148983107 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342286 | AAGTCCCATGCGTAC[A/G]ACCTCTTTGAACCTT | 337867 |
rs148985243 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261924 | GGCTTCAGTTACCTT[C/G]AGTTACCTTCAGTCA | 337867 |
rs149005667 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376900 | AAATTTCTTTGAGAC[A/C]TTTTTAAAATTTTCC | 337867 |
rs149027392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239316 | TAGTGTAGCTTCTGT[A/G]TTATTTCAGTTGCTA | 337867 |
rs149062267 | snp | C/T | 5.05617e-05 | 0.00502775 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201464 | ACAAACACACACTGA[C/T]GAGAGTGCTTTCAAG | 337867 |
rs149068372 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363697 | CAACATGGAAAGATA[A/C]TGAGAAAGGTAGCAA | 337867 |
rs149069813 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285729 | GGGTTCTCCTAGTGT[A/G]CTTCCCATAAAGCAG | 337867 |
rs149080690 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235948 | ACTCCAGCTTGGGCA[A/G]TAGAGTGAGACCCTG | 337867 |
rs149090712 | in-del | -/A | 0.167158 | 0.235875 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231047 | GGGAGACTCCGTCTC[-/A]AAAAAAAAAAGGACT | 337867 |
rs149093679 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285894 | CCTGGTGCAGTTCTA[-/C]ACATCCAACGGGGTG | 337867 |
rs149113944 | snp | C/T | 0.00011536 | 0.00759387 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255458 | CCACACACGCCAGCA[C/T]GGCTTTGCACGTGTT | 337867 |
rs149130191 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350260 | TCAGTTTCTTACCTC[A/G]GCACCTAGGTAATCC | 337867 |
rs149133898 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225454 | AGCATAATGTCCTCA[A/C]GGTTCATGCATGTTG | 337867 |
rs149194891 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299772 | GTCATCATGTAGAAA[C/T]CTCACAGCAGCCCTA | 337867 |
rs149235639 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315311 | TAAAGTTGTTGTGAC[A/C]GAGGCCATGTGGAAT | 337867 |
rs149245745 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267650 | TTCTTATGCTCTGAA[A/G]GGTATCTGCCTTTAT | 337867 |
rs149267941 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366629 | GGCTTTTTAGTTTGA[A/T]TTTTTTTTCATCCCT | 337867 |
rs149299264 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263494 | TACGATGAAAAAGAC[A/G]GACAGTGCAAAGTGC | 337867 |
rs149320388 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378308 | GAGGTGGGCAGATCA[C/T]TTGAGGTCAGGAGTT | 337867 |
rs149374896 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381383 | AGATCTCCAAATTGC[C/T]GAGTGTGGACAGCAA | 337867 |
rs149385152 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287453 | AAATTTTGAGACAGG[A/G]TCTCACTCTCACCCA | 337867 |
rs149387371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257691 | GATACCATGATTATC[C/T]GTAGCTTTTCTTTTC | 337867 |
rs149393440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320127 | CATTTTCTTTCTTTA[A/T]TCTTTTTTTAGACTC | 337867 |
rs149409673 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206405 | GGAGTTGCGTCTCTT[C/T]CCCTAGTCCAGCGGA | 337867 |
rs149436945 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360321 | GCTGCAATAAGCTTA[C/T]AGATGGCTTTACGTT | 337867 |
rs149439323 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333985 | ACAAGATCTTGCTCC[A/G]TCACCCAGGCTGGAT | 337867 |
rs149442047 | snp | G/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251048 | ATGAGCCACCAAGCC[G/T]GGCCATCTTTGATTT | 337867 |
rs149459502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227847 | TTATTCATTTGGTGC[A/G]TGTGTTGGGAGTTTG | 337867 |
rs149510228 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303745 | GTTCAAGGAGTTTCA[A/G]TTTTGTTTTTGTCTC | 337867 |
rs149535784 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310467 | AGGTCAAACTGAATT[A/G]CTGTTGACAGTATAG | 337867 |
rs149577289 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216687 | TGAAAGGACACATTT[C/T]GCTGGTGTTTTGAGG | 337867 |
rs149595963 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332109 | GTCCCAGTAGATGGT[C/T]GGTTTCTTGAATGTG | 337867 |
rs149603414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356018 | AAACCAACTGAACCT[A/G]TTTGTAAAATTGTAC | 337867 |
rs149605818 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280162 | GGAGATCTGGTCTTA[C/T]TCCTTTACACCTTGA | 337867 |
rs149615763 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233644 | GCAACTGATTGTGAC[A/G]CATTGACTAAGTAAA | 337867 |
rs149628464 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212297 | AATGGTACTATGAGG[A/C]GCTCCTGAAGTTTTA | 337867 |
rs149628682 | in-del | -/TTAAA | 0.0146672 | 0.084371 | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99293796 | GGTAAGATGAGAACT[-/TTAAA]TAAAATATTTTCAGG | 337867 |
rs149690394 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305927 | TCGAGACAGAGTCTC[A/G]CATGGTCGCCCAGGC | 337867 |
rs149695257 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369648 | CTTAACTCCATCGTA[G/T]GTTGAGGAGCGCTTG | 337867 |
rs149700571 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261385 | GGTGTAGGGGAGATA[C/T]GTTGAATAGTAAGAG | 337867 |
rs149706248 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322493 | CAATTTTCTTTTTAC[A/G]GTTCACACATTTATC | 337867 |
rs149727242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208921 | GTCGATTTATTTTGG[C/G]CAGTTTATTTTGGTG | 337867 |
rs149751935 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337448 | GTTTATTTTTTCTTT[C/G]TAAACAGTCTGTATT | 337867 |
rs149851016 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229786 | TTCTCTTATAAATGT[A/G]TAGTTATAAATGCAT | 337867 |
rs149857139 | snp | C/T | 1.64811e-05 | 0.00287059 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295304 | AACGAATGTCTTTGG[C/T]TACATTCCAGGAAAT | 337867 |
rs149896083 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219426 | TTAACAGCAACCACA[A/G]TTTAATTGCAGAACA | 337867 |
rs149911175 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299701 | CAAAGCTTGCTGTTC[A/G]GTGTTCCTTTTTCAG | 337867 |
rs149973744 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283925 | TTTTTAATAGAGACG[A/G]TGTTTCACCATGTAG | 337867 |
rs149990739 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203389 | ATTCTGATCCTGAGC[A/G]AGAATCTGAAAGAAG | 337867 |
rs150053856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225256 | TATAACTCTTCTCAT[C/T]TTGCAGAAATGAAAC | 337867 |
rs150057167 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349973 | TTCGCAGACACTGGC[A/G]TTACCGCTTGACCAA | 337867 |
rs150059701 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269724 | TTCTTACAGAACTTC[A/G]ATCTAGACTGTAAGC | 337867 |
rs150084817 | snp | C/T | 0.132409 | 0.220618 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280834 | CTTCTTCTTTCCCTC[C/T]CTCTCTCTCTCTCTC | 337867 |
rs150099153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354870 | ATAATCTCGGAGTGC[A/G]ACAGCAAGGACCTAA | 337867 |
rs150100658 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327707 | TTTTCAAAGCAGCAG[A/C]AGTTTTTTGTTGTTA | 337867 |
rs150127397 | in-del | -/GTG | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319734 | GTATTCTTGAGACTT[-/GTG]GTGGCTTAGGGCCAT | 337867 |
rs150163628 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99231461 | CCTGTCGTCCAGGCT[A/G]GAGTACAATGGTGTG | 337867 |
rs150168054 | snp | C/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200204 | GACCCCCCAGCCACC[C/T]GCCACCACGGCGGGG | 337867 |
rs150201902 | in-del | -/AC | 0.00398564 | 0.0444627 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306524 | CGCCCCCCTCCCCCA[-/AC]ACACACACACAAACA | 337867 |
rs150212800 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346546 | GCTCATATTGTTTCA[C/T]GCAGTCTCACCTTTA | 337867 |
rs150217744 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235743 | CCTTTGGGAGGCTGA[C/G]GCGAGAGGATCACTT | 337867 |
rs150223201 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302983 | CAGCATAGAGTTGAC[A/T]GTGGTCCGTCTGTTT | 337867 |
rs150233589 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250847 | CGCCTCCCAGGTTCA[A/C]GCAATTCTCCTGCCT | 337867 |
rs150255753 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359888 | CCTGCAGGGGGCCAC[C/T]GATTGTAGACTGGAG | 337867 |
rs150272775 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375317 | CCCAAGGAAGAGAGT[A/G]GTCAGACAGGGAGAG | 337867 |
rs150275827 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296430 | CTGGCAAAGGAAACA[A/G]AACCATTTAAATAGG | 337867 |
rs150328288 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333643 | TGAACACAAAAGCCC[A/T]ACTTCCCTGCCAGAA | 337867 |
rs150369216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350786 | GCAGGTTAGGTCTGG[C/T]GATTGCCATCTGAAG | 337867 |
rs150371999 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273338 | ATTAGGTTAAGAGGG[A/G]CAGTGAGCACCCAGG | 337867 |
rs150422263 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385702 | CATGTCATCTCCTGC[A/G]TCGTGATGGGGAGAG | 337867 |
rs150424464 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308654 | CCAGGATTCTGTAAA[A/C]ATAGTCGAGTAGCTT | 337867 |
rs150426294 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277037 | GGTGGCTTAGTATTT[C/G]GTTTTCTCAGGTTTG | 337867 |
rs150434375 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263299 | GGATCCTGGCAGCTC[A/G]TACATGTAATTGTGG | 337867 |
rs150466889 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211543 | TACGTGTTAGGCACT[C/G]TTCTAAGCAGTTTAC | 337867 |
rs150476753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380068 | AGAGGGTCTCTTTTC[C/T]CTTGGAGACACTGAA | 337867 |
rs150487001 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338417 | TGAAAGCTGTCCTGG[A/G]CCACATGTGGCCCAC | 337867 |
rs150488971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255970 | TAAATGCTTAACATT[C/T]TCCCACTCAGCTTGA | 337867 |
rs150523279 | in-del | -/TCA | | | intron-variant, cds-indel | UBAC2, GPR183 | GRCh38.p7 | 13:99294428 | CTTTCATTGCCTCAG[-/TCA]TCATCATCATCATTT | 337867 |
rs150531989 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237175 | TTGTTGTATACTTCC[A/G]TCTTTATTGACTAGT | 337867 |
rs150532581 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224338 | ATTACCTCTTTAAAG[G/T]GCCTATCTCCAAACT | 337867 |
rs150537714 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305556 | CAGAACCAACCTACA[A/G]TAGATATCTAGTAAA | 337867 |
rs150561898 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378094 | TATTTTCTCTGTGTC[A/G]TCTGTAGACACTTTT | 337867 |
rs150574378 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252836 | AGAATCACAGCATAC[A/G]TTTTCACTTTCTTGA | 337867 |
rs150591350 | snp | C/G | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298505 | AGGCAATCTGAGATA[C/G]ATATAAAGCCTTGAA | 337867 |
rs150598370 | in-del | -/GTT | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246794 | TGAATAAATTGAAAA[-/GTT]GTAGCATCCCCTTTG | 337867 |
rs150612287 | snp | A/C/T | 6.60737e-05 | 0.00574746 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254926 | CGTAGACTACCAGAT[A/C/T]GGAAACTTTTTCTGC | 337867 |
rs150626747 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286848 | AATGTGGCCAGTGCG[C/T]GTCCCATTCTCCTAT | 337867 |
rs150670001 | snp | A/T | 3.29554e-05 | 0.00405914 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295290 | GCAGAGAAATCTGGA[A/T]CGAATGTCTTTGGCT | 337867 |
rs150683288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352545 | AGATCTGCCTAGTAG[A/G]GCTTTATGTGTGCAA | 337867 |
rs150735815 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386406 | GATGTTGATACTTAC[A/G]ATAAAGTTTTTAATG | 337867 |
rs150739999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279738 | GATTTGGTGTTTGGG[A/G]CTGTCTTTTCGTGGT | 337867 |
rs150745630 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344725 | GCTTATGCCAGAGTT[C/T]ATCCTGCCATCTGGC | 337867 |
rs150747480 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264682 | GGGGTCATCCACTTC[C/T]GGCCTTGTGTGATTT | 337867 |
rs150758541 | snp | A/C | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213411 | TGTCGTCCAGCCTGG[A/C]GTGCAATGGTGTGAT | 337867 |
rs150782701 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293374 | GAAGGCGTCTCTACT[C/T]CAGTGTAGTCACAGA | 337867 |
rs150803460 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227422 | GGCAGGTGAAAAGAA[A/C]AAGAATGATTCCCTG | 337867 |
rs150827094 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338071 | TTTTTTTTTTTTTTT[A/T]TTTTGAGACAGAGTC | 337867 |
rs150834755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331655 | CAAAGGCACATGGTT[C/G]TGTCTGTCATGAAAA | 337867 |
rs150851648 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372708 | GAGGAGGAGGAAGAA[G/T]AAGATAAATAGAAAC | 337867 |
rs150854501 | in-del | -/TTTATTTA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203024 | TTTCCTTTGTTTTAT[-/TTTATTTA]TTTATTTATTTATTT | 337867 |
rs150888953 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324256 | TCTACTGAAGCCCTC[C/T]CTATAGGGCCTCTGC | 337867 |
rs150896814 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316970 | AAAATATTTGTCTAC[A/C/G]TGGTTCCATCCTTAT | 337867 |
rs150908222 | in-del | -/TATA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237255 | AGAAAATTTTATGCG[-/TATA]TATATATATATATAC | 337867 |
rs150911743 | snp | A/G | 6.58989e-05 | 0.00573978 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367856 | GTAAACTATCAGGGC[A/G]GTCGGCAGTCTGAGC | 337867 |
rs150932589 | snp | A/G | 0.000461209 | 0.0151787 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255136 | CAGATGTGGAAGGGC[A/G]TAAAGCAGACGAGCA | 337867 |
rs150940144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290261 | AGTGCTTAAAGCACT[A/G]TGCTATATAATTGTT | 337867 |
rs150991889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361920 | AAGATTGCTTGGGTC[C/T]GGGAGTTCAGGACTG | 337867 |
rs151002480 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243746 | GGACATTAAAAATAG[G/T]CAGTGTAAACATAAC | 337867 |
rs151033492 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346328 | CCCTCCTGAGCCTGC[C/T]CCACAGCCTCCACCA | 337867 |
rs151068919 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199384 | TCCAGCTGGGGAGAG[C/T]GAGACTCCGTCTCAA | 337867 |
rs151087669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342654 | TCATTCTGTCCACCT[C/T]CCATTTGGTGCCTTT | 337867 |
rs151109049 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275732 | GCTTTTGATGTCAGG[A/C]GTTTTCCTTACATAT | 337867 |
rs151119372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229403 | TGAAACAGAAAGCAA[C/T]ATGTTCAGGAGGTAG | 337867 |
rs151130815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218145 | TAAAATTATTATTTC[A/G]TTATAATTACATTTC | 337867 |
rs151140947 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374294 | GGGATCTCCTATTTT[G/T]AGAAAAAGCAGGTCT | 337867 |
rs151151390 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333342 | TGAGGTCATGCTGGC[A/C/G]TGCCAGTGACATGGA | 337867 |
rs151204686 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325373 | CTCCCAAATTGCTGG[G/T]ATTACAGACATGAGC | 337867 |
rs151263530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350343 | TCCTGGATAGCCTCA[C/G]ATGGGGGCTGGTTAC | 337867 |
rs151265733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322079 | AAATGTTGCAAAATT[A/G]TAATTGGAAAGCTTG | 337867 |
rs151267592 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237734 | CCAAGGCAGAAGGAT[C/T]GCTTGAGCCCAGGAG | 337867 |
rs151297376 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380008 | TGCTTGCGTGGGGGA[A/G]TCGGGGCATGTGCAG | 337867 |
rs151299654 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300983 | CATGTTATTTAAGAT[A/G]TATTTATATAAACTA | 337867 |
rs151309537 | snp | C/T | 0.00250193 | 0.0352804 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255474 | GGCTTTGCACGTGTT[C/T]TTAAGTTCTTTGGCG | 337867 |
rs151322129 | in-del | -/GCCTC | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376979 | AGTATGCAGCGCCGT[-/GCCTC]GCCTCGCCTCGCCTC | 337867 |
rs151327539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269345 | TCCAGCCAAGGGACC[A/G]CATTTCCCAGGATGT | 337867 |
rs180780693 | snp | A/C/T | 0.00239401 | 0.0345304 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203697 | CATAGTGATAAGTGA[A/C/T]ATGAAGACAATGAGA | 337867 |
rs180785538 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250532 | CTTTTTTTTCCCTTA[A/G]GATTGCTTTGGCTAT | 337867 |
rs180793625 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229707 | AATCAATGGGGAAAA[A/T]TTGGATTGTTCTGTG | 337867 |
rs180801088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223514 | TCTGCTTGCTTAGGT[A/T]TTAATTTGCTCTTCT | 337867 |
rs180802494 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267880 | CAGTGGCTCAAAGAG[A/C]GCAGATGTTCATTTC | 337867 |
rs180809708 | snp | C/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260683 | CTTGTATAATGTAGA[C/G]ACAAGTTTCTTTAAT | 337867 |
rs180814260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213453 | GCAACTGCTGCCTCC[C/T]GGGTTCAAGTGATTC | 337867 |
rs180819155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285858 | TTCAGTATGAGCCAA[A/G]GCATATGAGATAGCC | 337867 |
rs180831627 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298372 | AGGATAAGTTTGGAA[A/G]TGAAAAAATACACTT | 337867 |
rs180836876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373052 | TGTGAACCCGAGAGG[C/T]AGAGCTTGCAGTGAG | 337867 |
rs180843178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240096 | TTAGATTGGAGAAGT[C/G]CAGGAGGGCTCAGTT | 337867 |
rs180843525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335844 | GCTTCACCTTCCCTC[A/G]GGACTGTGTGAGAGT | 337867 |
rs180853670 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277927 | AACGTTCTTCTAATA[A/T]CTGCAGATACCCAGT | 337867 |
rs180857876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274779 | GGAGTGTGGTGGCAC[A/G]CAGTCATGGTTCACT | 337867 |
rs180861824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283092 | GAATATTTAGGAAGG[C/T]AAATAATCAGTCATG | 337867 |
rs180862786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256637 | AAAAAAGGAGTATCT[A/G]AGACAAGTAGATATT | 337867 |
rs180864727 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315938 | TGCAAAAGTAATTGC[A/G]GTTTTTGCCATTAAA | 337867 |
rs180864895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292863 | GTTGTGATTTTCAAA[C/G]AGTATGTTATATAAT | 337867 |
rs180878883 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313281 | GAGACACTACGCCCG[G/T]CCGGAAGGAAGGGTT | 337867 |
rs180882959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357587 | GCAGCTTCCACAGAG[C/G]ACAGGGAATTGCAAA | 337867 |
rs180884243 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332496 | TTACAGGGTCACAGC[C/T]TCTGCTGTTGGCATA | 337867 |
rs180887885 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319251 | AGTTTTATTCTTCAT[C/T]CATGACTTAAATTTA | 337867 |
rs180893579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352320 | CCCAAAAGAAACTGC[A/G]CCCCATTAGCAGTCA | 337867 |
rs180906682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233802 | GTAAACTTTTTCACG[A/G]TAAAAGGATGGGAGA | 337867 |
rs180909490 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370447 | TAAAAGAAAGTTAAG[A/C]GTGTTGCCATCATAA | 337867 |
rs180924234 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301479 | AGCAAAATATCTTCC[A/G]AAGTATTTTTACTTA | 337867 |
rs180940675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342696 | TGCCCGTGGTGGGCA[C/T]GACCTGCAAGACACT | 337867 |
rs180984166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328013 | TGCTCTTTCCCCACA[C/T]CCAGCTGCCAGCCGC | 337867 |
rs181029153 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208933 | TGGCCAGTTTATTTT[A/G]GTGACTCCTCAGCAC | 337867 |
rs181054682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218645 | GACCTGTATGAGGAG[C/G]GGTCAGTGTGGCAGG | 337867 |
rs181060611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226906 | CAGGTTGGATAAGAC[C/T]GGCACCCCTTGGCTG | 337867 |
rs181064777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214108 | ACAGGCGTGAGCCAC[C/T]GCACCTGGCCTGATT | 337867 |
rs181066059 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199474 | AATAAAAGTCATACT[C/T]TTGCCTTCTATAATC | 337867 |
rs181080382 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263493 | CTACGATGAAAAAGA[C/T]GGACAGTGCAAAGTG | 337867 |
rs181082469 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245289 | GTTTAATTAGATTAG[A/G]AAACAAAATTAATTT | 337867 |
rs181088395 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297284 | TTTTAAAAGAAAAAT[A/C]ATTCCTCTGATAGAA | 337867 |
rs181089461 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251317 | TAGAATCATATTGTC[A/G]GTAAAGAGAGATAGT | 337867 |
rs181091314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277252 | ATATTAAGGCCAGGT[A/G]CAGTGGCTCATGCCT | 337867 |
rs181101052 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269870 | TTTAACTCCTCTAAA[A/G]TAAGTTATTAAATGG | 337867 |
rs181119434 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99202797 | CTCAGAAGGCTGTGT[A/C]TTACATGCTCATTTT | 337867 |
rs181124688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222921 | CAGAGTTTGTATAGA[A/G]TTGGTATTTAAATGC | 337867 |
rs181142253 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238115 | ATAGAAACACACTTC[C/T]CTATTTCTTTACACT | 337867 |
rs181155944 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260166 | GCTTTCTCTGCCATC[C/T]GAAGCTGGGCTGGTT | 337867 |
rs181181484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287168 | GTTTCCATTTTTCAT[C/T]TTACCATGTGGTTCC | 337867 |
rs181278637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335470 | TACCCCCTACCCTGT[C/T]CCCCATCACCCCTCT | 337867 |
rs181283054 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356526 | GAAGTATCTCATCCA[C/T]CAACACTGGTCACTG | 337867 |
rs181294892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372736 | AACTGTTTGTCAACA[A/G]CAACAGCAAAAATGC | 337867 |
rs181322164 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372626 | TCACCGGCTCTGAGT[C/T]TAAAGGGAAAATGGG | 337867 |
rs181368699 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309398 | ACAGGTGTGAGCCAC[C/T]GTGCCCAGCCCCTTT | 337867 |
rs181405955 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347432 | GGTGGAGAGATGGGG[A/C/T]TGAGAAGCGCTGCAT | 337867 |
rs181419188 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382956 | AGGGCTGTCACACCC[A/G]CAAAGTGCTTTATGT | 337867 |
rs181436508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362080 | AATAGTATTACATTT[C/T]ATTTATATTATTTAC | 337867 |
rs181445961 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379329 | AAACAGTGATGTTCC[A/G]TCAGCATTATAGACT | 337867 |
rs181456658 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218380 | GCTGTTTCAGGACTA[A/G]GATTTTAAATTTTAC | 337867 |
rs181470388 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199385 | CCAGCTGGGGAGAGC[A/G]AGACTCCGTCTCAAA | 337867 |
rs181476087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256137 | TTGAGCATGTAATAG[A/G]TACTCAATAAATAAA | 337867 |
rs181484862 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233550 | GCAGCCAGAGCAGGC[A/G]TTGAGGGCCCTGGTT | 337867 |
rs181497055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274565 | TCATGAGCTCAAGTG[A/G]TCCTCCTGCCTTGGC | 337867 |
rs181510379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327271 | TTACTGAATAAAGGA[A/G]AAAGAAGTAGAGATA | 337867 |
rs181532456 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366595 | GGACCAAGATTCCTG[C/T]TGTCTCCGGGGGAAG | 337867 |
rs181586731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321946 | CTCTTGTACTTAAAG[A/G]TGACTGTAAGATTAT | 337867 |
rs181592690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343849 | CCGTATTTGTGTGCA[C/T]GCACGAGTACCGTAC | 337867 |
rs181621941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278578 | TTGAAAAATGATCAG[C/T]GTCTTTAAAAGTGAA | 337867 |
rs181627977 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299496 | GATGTCTGTATGCCA[A/C]AACATAATTTTGTAT | 337867 |
rs181636333 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347196 | AGAGTGCAAAGAGGG[A/G]AAAAAAAGAACCCCC | 337867 |
rs181642276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316520 | GAGAGCCCATAACAT[C/G]ATGCCCTGTGCAATG | 337867 |
rs181645747 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366358 | TGAATTCTGAGTTTT[A/C/T]CCCCACTGGAGCTTT | 337867 |
rs181651714 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382570 | CTCAGTTCTGGGCGC[A/G]GTGTTCTGAGACGGT | 337867 |
rs181683545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227286 | AAATATCAGGAACCC[A/G]AGACAAGGCTTGCAT | 337867 |
rs181686691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264465 | GTGCATGCTGTAGAC[A/C]CTAAGCACTAGTTCT | 337867 |
rs181692714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291985 | TTATAATCTATACCT[A/G]TTGTTGGGTTATTTG | 337867 |
rs181703373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331105 | CAGCTGAGATCACGT[A/G]TCTCTTATCCTTCGC | 337867 |
rs181710226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303313 | GCAAAGACCCACTTC[A/G]GCTTCATAGACGCGC | 337867 |
rs181713321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370268 | TGCATGTCAGTACAT[A/T]GTGTGTGATTGTGTG | 337867 |
rs181731414 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250833 | CTCACTGCAGCCTCC[A/G]CCTCCCAGGTTCAAG | 337867 |
rs181732609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286487 | CTTCTTTTTTTTAAT[A/G]TTTATTTATTTTTAA | 337867 |
rs181774690 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246211 | GTGTGAATATCCATG[A/C]ATGTTGACCTTTAGC | 337867 |
rs181789632 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313109 | GCCTCAGCCTCCCGA[A/G]TAGTAGCTGGGACTA | 337867 |
rs181794403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358155 | AGAGAATGTGAGGGC[A/G]GTGTTGTGAGAAAGT | 337867 |
rs181809431 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226990 | GATCACCTGAGGCCA[A/G]GAGTTCAAGACCAGC | 337867 |
rs181819295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284243 | GAAAAAAAGTTCCAA[C/T]TGGGGGGAAGTGCCC | 337867 |
rs181820843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209189 | AGATTTAGCACATGA[A/G]ATAGGCCATCGAGCC | 337867 |
rs181821735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245606 | TGCCACCTTTGGGAG[A/G]CCGAGGTGGGCGGAT | 337867 |
rs181829273 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283969 | CAAACTCCTGACCTC[A/G]TGATCTGTCTGCCTT | 337867 |
rs181834148 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264026 | ATAAGGAAGGGTCCC[C/T]CATCATCTGTATGGC | 337867 |
rs181835403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303224 | GAAAAACATCTTCAA[C/G]ACTGAAAAAGGGTTT | 337867 |
rs181837759 | snp | C/T | 0.000495295 | 0.015729 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351856 | CCCGGTGTTAACTGG[C/T]TGATTATCACCTCTG | 337867 |
rs181914538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213677 | TTATAACATTTTATC[A/G]TACTAAAATAAGTTT | 337867 |
rs181927538 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269027 | ACGGGGACATGCTAC[A/G]GGATATAGCTTTGGG | 337867 |
rs181969920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308577 | TTTTGAGGGATGATG[C/T]AAACAGAATTGAATC | 337867 |
rs181996152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371306 | ATGAGGGGTTGTTTT[C/T]AACATACACTTTCTT | 337867 |
rs181997016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320528 | TACTATGACAAAAAA[C/T]CTGATAAATCTTCAT | 337867 |
rs182013546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343329 | TCTACGGACCCCCAT[G/T]GTGGTTCTCCTTTCC | 337867 |
rs182038104 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336725 | CTGATAGGACTTACG[A/T]TTCTTTAAAATTGCC | 337867 |
rs182045261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348158 | CATCCCCAGTAGAAT[A/G]TGAGCTCTTGGAGGA | 337867 |
rs182054041 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366926 | TTAATAGCATTTTTA[A/G]GTGTTTGTAGTAGGA | 337867 |
rs182058667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374187 | AGCAATAGAAAAATA[A/T]CTGATAGGTTAACAT | 337867 |
rs182162037 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252153 | TTTCTTCGCTTGCTA[C/T]GCATTTGCATTCTCA | 337867 |
rs182179481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224902 | AGCGAATCTTGTTGT[C/T]TATAATGATACTATA | 337867 |
rs182182491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205471 | TGTTTTCTGAATGTA[C/T]ACCTTCCTGGGTCTC | 337867 |
rs182191189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287535 | GCTCAGGTGATTCTC[C/T]CACACCAGCCTCAGT | 337867 |
rs182191445 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229877 | GAGAATTAAAGGGTT[G/T]TATTTCTTTGTAAGA | 337867 |
rs182194670 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242877 | CCTCCCAGACGGGGC[A/G]GCGGGGCAGAGGTGC | 337867 |
rs182199784 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309783 | TTTTTGTATTTTTTT[G/T]TGTGTGTGTGTGGAG | 337867 |
rs182203173 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327821 | TCACATTCTTTTTTA[A/T]TAAAAGATTCTTTTT | 337867 |
rs182217482 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227567 | TGTTTGGGAAGAGAC[A/G]GGAAATATGTGGTGA | 337867 |
rs182222829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210904 | GGTGTGAGCCACCAT[A/G]CTGGGCCCCGCTTTT | 337867 |
rs182228834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247603 | GGTAAGGGGCAAGGG[A/G]AGGGAGAGCATTAGG | 337867 |
rs182235571 | snp | A/C/G | 0.0150606 | 0.0854603 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217714 | CTCTGTGGAGGTTGT[A/C/G]GGGGGCAGGTTGGAG | 337867 |
rs182247679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379085 | AGACCAATCAGAAAA[G/T]ATATCCCTAGTTAAA | 337867 |
rs182255177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353547 | GATGATGTACTTGGC[C/T]TTTTGAAGATGTAAA | 337867 |
rs182350912 | snp | A/G | | | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295476 | GTTTGGCAGTTCTGA[A/G]GAGTTTGCAGCAGAT | 337867 |
rs182355046 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300470 | TGATCCCAAATTGAG[A/G]GGAAAATCCTTTCAT | 337867 |
rs182360802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314650 | GTGTGCTCTACCAAC[C/G]CGAGCTTTGGGGTTT | 337867 |
rs182370826 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339238 | CAGTTCATCAAGTCA[C/T]GGGCACCGCATCATC | 337867 |
rs182374260 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333561 | GGCCAAGTAGTGATC[A/G]AAAGCAACCCAAATC | 337867 |
rs182381973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354929 | CAGTAGTCCTTCAGC[A/G]TTGGCTGGGTTTGAT | 337867 |
rs182388080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376764 | AAACCAAGCTGCACT[C/G]TAATCTGATATTTTG | 337867 |
rs182506610 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361720 | TGCCGACAGCACCAC[C/T]ATCCTGTCCCCCCTC | 337867 |
rs182508606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332857 | TCCCCCAGCCCCCTG[A/G]CACACAAATCCAACA | 337867 |
rs182535891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231557 | AGCTGGGACTACAGG[C/T]GTGCCACCACGCCCA | 337867 |
rs182551692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262288 | AAAAAAATAGTAAGT[A/T]TAGGGTTTGGTACTA | 337867 |
rs182588181 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372012 | TGAGTAAACCCACGG[C/T]ACCTCTGCCAATTCA | 337867 |
rs182611905 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317351 | TTTCAGAGTCCTTAT[A/G]ATTTTTTTTTAATTA | 337867 |
rs182615320 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284498 | GTTATTAACATTTTC[C/T]GCATTTGCTGTTATC | 337867 |
rs182622127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220308 | TTAGTTTATTTCTTC[A/G]CCTAGAGAATGCTGA | 337867 |
rs182627642 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258951 | CTTCTGCTTTGCCAC[A/G]TACATTTATCCACTT | 337867 |
rs182630690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383096 | CTCAGCCACCTGGCA[A/G]TGAGGCCAGGGCACT | 337867 |
rs182636169 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322747 | AGTTTGGATTGTTTT[A/C]TGTAAGGAGTGGGGA | 337867 |
rs182638195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359785 | CCTGCCTCGCCTCCC[A/G]TGTGCCCAAGCACAG | 337867 |
rs182654332 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362630 | TTTTCATATGTTTCT[C/T]GACTTGGGATTTCCC | 337867 |
rs182742175 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345887 | AGCTGGGATTACAGG[C/T]GCTCACCACCACATC | 337867 |
rs182747379 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364476 | GTATAATTTTTCTTG[C/T]TCATAATGGCCTTGT | 337867 |
rs182752164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380878 | ACTTGTCTTCTCACC[C/T]ATAAAAATCACTTAA | 337867 |
rs182764813 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214859 | AGGGTTTGAGGCCCC[A/G]CTGCTGTCATGCTTG | 337867 |
rs182781978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299787 | CCTCACAGCAGCCCT[A/G]TGAGCTTGAGCATTG | 337867 |
rs182784259 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253605 | TGCAGCCTCCGCCTC[A/C]TGGGTTCAAGCTATT | 337867 |
rs182797683 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271909 | GCTCCCAGACCATTC[A/C]AGTGGGGGTAAATCT | 337867 |
rs182799194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317015 | TTTCCACTGAACAAA[C/T]GTCCGTGCTACATCA | 337867 |
rs182799284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338613 | ATGGACCTTGGAGTT[C/T]GTTTCTGTTTTCATT | 337867 |
rs182803943 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289653 | GGTTAAACACTGTTT[C/T]AATCAGAACAGGTTA | 337867 |
rs182806708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358810 | GTCACACCCCAAGAC[A/G]GGGGACACAGCAAGA | 337867 |
rs182815334 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375618 | ACGCACTTAGCTAAA[A/G]GGGAAGTTAAAGAAA | 337867 |
rs182842101 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281192 | AGACTCCATCTCAAA[A/C]AAAACAAAACAAAAC | 337867 |
rs182856007 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241635 | GTCTAGGATGATGAA[G/T]AGTTCTGGAAATAGA | 337867 |
rs182858975 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314439 | TCTTTAGAAATCTGA[A/T]AAGAGCTTTCACTGT | 337867 |
rs182866435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205197 | GTGAGCCACTGTGCC[C/T]GGTTGGGGGAGTTTC | 337867 |
rs182889692 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200752 | CGGGCGCACGCCCCT[A/G]ACTGCGCATGCGCCG | 337867 |
rs182892655 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236667 | CCAGCCTGGCCAACT[G/T]GGTGAAACCCCGTCT | 337867 |
rs182894246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265545 | CACATCTCTCTTTGA[C/T]AGTCATGTGGGTACT | 337867 |
rs182902541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276295 | CAGAAGACTGTCTCC[A/T]CTTCAGATGCCAGTC | 337867 |
rs182910547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303498 | TATGGAAGTTATTGA[A/G]GATGAAGATGACATA | 337867 |
rs182920699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344200 | CGGAGGCTCAGGGGA[A/G]TGCTTGCTTGTCCAG | 337867 |
rs182941754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379728 | TCAGATCCTATATGG[C/T]GGTCACTCCAACACC | 337867 |
rs182957649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348548 | GAGGCAATGAAAGAC[A/C]TGGTTGGGAAGAGAG | 337867 |
rs182967010 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367286 | TCCTCCACTGTGTGC[A/G]CTCAGGATTTACTTC | 337867 |
rs182978112 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200394 | TCTGAGTGACCAGAT[C/T]CCACTGCAGTCAACA | 337867 |
rs183004800 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258056 | AGGCGTGGGCCATTG[C/T]GCCCAGCCTGTATTA | 337867 |
rs183013678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219471 | AAAGAAACGGAGTGC[C/G]CATTAAGCCAGGCTT | 337867 |
rs183017727 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235746 | TTGGGAGGCTGAGGC[A/G]AGAGGATCACTTGAG | 337867 |
rs183020976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276042 | ATTTTGATTTTTAGT[A/G]TTGTATTTGTACTGT | 337867 |
rs183036417 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294371 | TATTGCTAAGCAGAG[A/G]CCCTAAAAGACTGTG | 337867 |
rs183041079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224038 | TTGTGTATCCTTACT[C/G]ATTTTACTGGTCAGC | 337867 |
rs183049218 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204853 | TGAGAATCAAGAGAG[G/T]GAGTTGTGGTTAGAG | 337867 |
rs183055325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241094 | CATGGCAAAACACCA[C/T]CTCTACAAAAAATAC | 337867 |
rs183065439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261772 | ATCCAGAGTCGCCAA[C/G]GCAGCAGATTGAGCA | 337867 |
rs183124088 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280377 | TCATTTATTACGACA[A/G]TTGTGGTTACAACAT | 337867 |
rs183147846 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311265 | GTCAGGAAGAGAGTA[A/G]AGAATGCAGAGGGGG | 337867 |
rs183157246 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383907 | CCACCTGCCTCTCTA[C/T]TCTCTGCACCTTCTT | 337867 |
rs183170282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224436 | GTTTGCTTGTATTAT[C/T]GATTACTGTGAGAAG | 337867 |
rs183177681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349329 | AAGCCCTTGGAATCT[C/G]CACAGTGAGCATAGG | 337867 |
rs183210650 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384478 | AAGTACAGGAAATCT[C/G/T]CGTATTCACAGAATC | 337867 |
rs183238509 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333102 | CCCCGTCTCTGGGGG[G/T]GGAAGAAAGAGAGAG | 337867 |
rs183248660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371460 | GGTGTTCTTTGCAGT[A/G]GGTACTATAGAGATT | 337867 |
rs183260432 | snp | A/C/G | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199571 | CAGATTTAGCACACT[A/C/G]GCTGGCACTTATGAG | 337867 |
rs183370603 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248148 | CTACAGTGAACGTGT[A/G]TTGTTTGCTTCCCAG | 337867 |
rs183378452 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261891 | AGTAGTCCCCTTATC[C/T]GCAATTTTGCTGTCT | 337867 |
rs183386156 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228250 | AGCCCGGGGTGTTGT[A/G]ATGGTGCTGGTGGTA | 337867 |
rs183393785 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265902 | AGTTAAAAAGGTTTC[A/G]TATCAGAGAAGTTAG | 337867 |
rs183400454 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304716 | AACTTTCACAAGTCC[A/T]TTGACAGAAGGTGAA | 337867 |
rs183400671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284832 | TTCTAAGGCTGCTGG[A/G]AAATTAAAGTTTGTG | 337867 |
rs183415166 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323898 | AATGAAATGATGCCA[C/T]TGTCTTAATAAAGCT | 337867 |
rs183416472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345065 | AGGACGGGTGGAATT[C/T]GGATGGGTGGAGAGG | 337867 |
rs183424688 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363214 | TTGCCTAACTTCCAC[C/T]AATACCACATGACTT | 337867 |
rs183428464 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328673 | CAAATCTTTTATCCA[C/T]TTTGTTCATTGGGCT | 337867 |
rs183436395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367970 | GTTGAAGCAGTTTCG[A/G]TCAACAGGACTCAAA | 337867 |
rs183439061 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215208 | GTTAAGACTCAAATG[C/G]AGAAATTTGGTTGGA | 337867 |
rs183479692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354454 | GGAAACCCAGACTCA[A/G]GGTTTTATTCTCTGT | 337867 |
rs183482189 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252674 | TATGTGGATGTTACA[C/T]CGTTTTCCAGAATAC | 337867 |
rs183487637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288835 | ACAAATCATATAATC[C/T]CCTCAGCTAATATTT | 337867 |
rs183522798 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328027 | ATCCAGCTGCCAGCC[A/G]CAGGTAACCACTGAT | 337867 |
rs183601931 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272599 | TCAAGTTCTGGTGAG[A/G]GCCTGCCGTCTTCCT | 337867 |
rs183606012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209803 | ACATGGTGAAACCCT[A/C]TCTCTACTAAAAATA | 337867 |
rs183612448 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290302 | TATTATTGTTAATCT[C/G/T]CTGGCTTCTGGTACA | 337867 |
rs183616975 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245462 | CTTTCATATTGCGTT[A/G]ATCTTCTTTAAAAAA | 337867 |
rs183624776 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312344 | CTGGTGCCATTTTCC[A/C]AAAAGTGGGAAAATA | 337867 |
rs183631758 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263757 | TTCAACTATAGCATG[A/G]ATAAGTCACTTGTGG | 337867 |
rs183633916 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329819 | CATGAGAGACCTTGA[A/G]CCATAACCACTCAGC | 337867 |
rs183647914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350976 | ATATTGTGTTGAGTC[A/G]TGTGTGAGTGTAGAA | 337867 |
rs183656145 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368755 | CTCTGACCGAGAGGG[C/T]TCAGAAGCAGTGGCC | 337867 |
rs183665961 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385496 | GCAAGACTGTTGCCG[G/T]TTTAGTGTGGAGATA | 337867 |
rs183705654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232162 | TATGGGAGTGGGTTT[A/G]GGGGTATGGGATAGA | 337867 |
rs183719893 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234359 | CGCCCGGGTAATTTT[G/T]TTGTATTTTTAGTAG | 337867 |
rs183720163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211254 | AGAAAATGATTTGTC[A/G]AAGACCACATAGCTA | 337867 |
rs183733528 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271223 | GGAAGGGAATGCCAG[G/T]GTGTGAGTGGGATTG | 337867 |
rs183737209 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310349 | AGAAAAAAAGAAAGG[A/G]TGGATGAAATGTTTA | 337867 |
rs183842438 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229464 | TCCTGAGAACAAAGC[A/C]ATGGATGTTGTGCTG | 337867 |
rs183855360 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213092 | TTTTTTCTGACGCAT[A/G]TATATACATATACAT | 337867 |
rs183856819 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249261 | GTGTACCCAGTGTTT[A/G]GCTCCCACTTTTAAG | 337867 |
rs183870026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285584 | TTTTATAGAGACAAC[A/G]TCTCGTTATGTTGCC | 337867 |
rs183870312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267437 | ATTTCTAAATGGTGA[A/G]GGGAAGGGAGGGGAG | 337867 |
rs183909606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315821 | CTTGTTTTGTTTTTG[A/G]CATAAAGCAAGTAGT | 337867 |
rs183911182 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335679 | CTGGATGGCTGTATA[A/G]TACTGTGTTGTATGA | 337867 |
rs183917915 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99356748 | TGACAGGGTTAGATT[C/T]AGTCTTCTGAGTTTT | 337867 |
rs183939620 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372966 | AAAAAATAAAAAAAT[A/T]AAAATTAGCCGGGCA | 337867 |
rs183942090 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219228 | TTTCTGGGTTGCTCC[C/T]CTACCTGTCTGTCTT | 337867 |
rs183944141 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257713 | TTTCTTTTCTTAAAA[A/T]CCATTAAGTTATTTC | 337867 |
rs183974612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377592 | TTATTTATATAGTCA[C/T]CAGAGTTGTGTATTT | 337867 |
rs184000534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275051 | TCTTTTGTTGCATAT[A/G]TGTATGCATTTCTGC | 337867 |
rs184022549 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313980 | AATCAATATGTATAT[C/G]TAAGACCATGCTTTC | 337867 |
rs184072986 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380368 | GAGATGTGTGGGGAC[G/T]GGGCGTGCTGGGCTT | 337867 |
rs184141323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319180 | TTGTATTTTAATAAT[A/G]AGCGTTTGTCCTAAA | 337867 |
rs184144502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341935 | GTTCCATTTCACCAA[C/T]ATCAAAAGAGCAGAT | 337867 |
rs184152630 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361355 | CTACGTAAAGAGCAG[A/G]TTCATGTCAAAACAT | 337867 |
rs184157646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301895 | GCTGAAATGTCACCT[C/T]TGCCCTCTAATATTT | 337867 |
rs184157805 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293376 | AGGCGTCTCTACTCC[A/T]GTGTAGTCACAGAAC | 337867 |
rs184164816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343027 | CAGCTGTGGTAGTCG[A/G]TGTTAGCTGGGAAGA | 337867 |
rs184165670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378223 | TGGAGCCCCCTTATC[A/G]ATATTAAAAACTTCA | 337867 |
rs184175325 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237788 | GGTGAAACATGGTCT[C/G]TACTAAGAATACAAA | 337867 |
rs184181524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378654 | GACATGTGGAATCCT[C/T]CAAAGTCACCACCTT | 337867 |
rs184183102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276912 | GTGGGTAGAGTTCAG[C/G]GGGTGGCTGTGCAGT | 337867 |
rs184187434 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259817 | CCATTGCTGCTAAAA[C/T]CAACAGATACATTGA | 337867 |
rs184197959 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297170 | AGAAATTTTAAGTAC[C/T]AAATTGAAAAATGGA | 337867 |
rs184202014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315344 | GAAGAGCACTCCAGA[C/T]CTCCCTCAGGAGACC | 337867 |
rs184259353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254473 | TTATATAGGAATTCT[A/G]GAAGTCAGTGTTTGG | 337867 |
rs184274029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283251 | AGCTGTTATTCCAGT[A/G]TGTAGAATAGCAGCT | 337867 |
rs184279861 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215694 | TGCAAGCCGGCTCTC[A/T]GCGAGCGGGAAACCG | 337867 |
rs184299775 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320209 | AGTGCACTAAAATTG[A/G]AGGTTGCATTTTTCA | 337867 |
rs184321281 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361582 | ATCTTTACTACATAC[A/C]TACTTATCAGGGTTT | 337867 |
rs184326101 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222785 | TTGCATCTGTTAATA[C/T]GTTCATAAAGTATAT | 337867 |
rs184332472 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202004 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGCGAG | 337867 |
rs184343067 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232758 | AAAACCCTGTCTCTA[C/T]ACACACAAAAAAACA | 337867 |
rs184371100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225655 | CTTGACTGCCTTTAT[A/G]TGTCAGGTCCTATTG | 337867 |
rs184381759 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218033 | GAACTTTCTGTAAGC[A/G]TCCTGATTTACTTTA | 337867 |
rs184393507 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198662 | TTTTTGATACTATAC[A/G]ATAACTTAGCAAGTG | 337867 |
rs184393678 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281468 | ATTGTACTTGGTACT[A/T]TGTCACCTTGGTAGT | 337867 |
rs184400276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262824 | TGTGTGTGGTTGAGG[A/G]TTTTAGTACACAGCC | 337867 |
rs184403399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300682 | CTGGGAATACAGAGA[C/T]GGTACCTTTTTGTAT | 337867 |
rs184414772 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319010 | GAGAGATAGTCTGCT[C/T]ATTTTGTAAAAAGAC | 337867 |
rs184471879 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217139 | CCTGGCCTCTTTCCT[C/T]GTTTTCGAATTAATT | 337867 |
rs184577800 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99307085 | AGTTTATACAGTAGT[A/T]CATGAAGTGAGCCCT | 337867 |
rs184613431 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340801 | ATTCTTGTTCCACCT[A/G]TATTAGATAAGCATG | 337867 |
rs184648681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324790 | AGCATAGGTAGAAAC[C/T]TGGTGTATGGCACTC | 337867 |
rs184650610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297777 | ATGGGTTGAGCTTGC[C/T]TATTACAGGACAGAG | 337867 |
rs184668346 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365207 | CCTTCCTTTGTCTTT[A/T]CATCAAGCTTGCCAG | 337867 |
rs184775525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351910 | CTACTGACACCCAGA[A/G]TGGCTCAGCGATACT | 337867 |
rs184806791 | snp | C/T | 2.47216e-05 | 0.0035157 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201407 | GACCTCTCAGTTTCA[C/T]TTGGATGTGTTTCTT | 337867 |
rs184807783 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346117 | ACCCATTGTTTACCC[C/G]AAAGTCCAAACCTAG | 337867 |
rs184817900 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381604 | GTTTGGCCTGAGTTA[C/T]CTCCACCAATGACAA | 337867 |
rs184845429 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369458 | TACTCAATAATTACA[G/T]GAGATAGTCAATACT | 337867 |
rs184859853 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386019 | AAATGGGATGGAGAA[C/G]AACAACAGCAGGCTT | 337867 |
rs184883168 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207923 | GTTCCTACTGACATT[C/T]TTTCTTAAGTATGCA | 337867 |
rs184897774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370287 | TGTGATTGTGTGTAT[A/G]TGTGACAGAGACAGA | 337867 |
rs184902762 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244979 | CTGGGACTACAGGCA[C/T]GTGCCACCATGCCTG | 337867 |
rs184917189 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365922 | TGCCATTGTGTTACA[A/T]ATAAATATGATATTC | 337867 |
rs184923496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382050 | GTGCAATGAAGTGGG[C/T]TTGAAACTGATTAAA | 337867 |
rs184933942 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292959 | CTGGTTAGGAGAATG[C/T]CCCGGAAATAAATGT | 337867 |
rs184938549 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282649 | ACTCAGGTAACAGAC[A/C]GCAAAGGAGATACTT | 337867 |
rs184946516 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313315 | AAGCAAGGGAGTGTT[A/G]TGATCAGAGTTGTAT | 337867 |
rs184960458 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332578 | TCTCAGCTGGACGTG[A/G]GCCAGGGGTTCTCTG | 337867 |
rs184968764 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352634 | GAAGCTTCCTGTTGC[A/C]TCTTGGCCTCACCAG | 337867 |
rs184973711 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370459 | AAGAGTGTTGCCATC[A/G]TAATACTTTGAAGTT | 337867 |
rs184989577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305750 | GAGTGAACATTTTGT[A/G]GAGTAGCATATTCTT | 337867 |
rs185017546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226055 | ATAGCAGGACTTCAT[C/T]CCTGAAGGAGGCAGT | 337867 |
rs185040409 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372349 | AGAAGTCTAAATCTG[A/G]TGAAAGGACAAAGGT | 337867 |
rs185050717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250644 | GAATAGCCTTAAATC[C/T]GTAGATTGCTTTGGT | 337867 |
rs185052276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301069 | AGAAATGTTAGTTCT[A/T]AATCTTTTTTCTTTA | 337867 |
rs185064881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268426 | ATCCTGGGCAACATA[G/T]CAAAACCTTGTGTTT | 337867 |
rs185084067 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285372 | AGATTAACTGGCTCA[C/T]TATTTATTATTACCT | 337867 |
rs185085236 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286094 | GTCTATTCCTGGAGG[C/T]GCTGGATCTGGCCTT | 337867 |
rs185095069 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307617 | CCTTGGAATTTATGA[A/G]TTGTTGATATCTGTG | 337867 |
rs185101507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325269 | CACCATGCCCAGCTA[A/G]TTTTTTTGTGTTTTT | 337867 |
rs185103826 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346572 | CTTTACATCTTCCCT[G/T]TCCTCTCTGCCCAGA | 337867 |
rs185118613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226926 | CCCCTTGGCTGGGCG[C/T]GGTGGCTCATGCCTG | 337867 |
rs185140049 | snp | G/T | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356315 | ATGCACAGGCAAGGC[G/T]TGTGGCCTTTGGGAC | 337867 |
rs185151131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229038 | TGAGGCTTTTCTGTG[A/G]TCTTGGCTGTTAATG | 337867 |
rs185154484 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214313 | TGGATCTTGCTTGGC[C/G]GTTCTTGTGCAGTCC | 337867 |
rs185163141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266645 | ATTATACTAAGATAT[G/T]AAACATAAATGTGGC | 337867 |
rs185164183 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231282 | CACTGAGTTTCTCTA[A/C/G]CTGCCCACCTTGAAT | 337867 |
rs185243048 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212258 | CTCATCAATAATTTA[A/G]CATTTTTGAAGTGTG | 337867 |
rs185252466 | snp | C/T | 0.00255196 | 0.0356296 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255442 | GTCATTATCCAGACT[C/T]CCACACACGCCAGCA | 337867 |
rs185262983 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291504 | AAAAAGTAACCAAAA[C/T]AGACCATTTTAAGGG | 337867 |
rs185284267 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249064 | GGGGGTACATGTGAA[A/G]GTTTGTTTTATGAGT | 337867 |
rs185298985 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209071 | CTGGCTGGGACTGCG[C/T]GTTCCTTGCCCTGGC | 337867 |
rs185312818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207322 | TAGAATTTTGCCATA[A/G]TAACTACTCAGGTTT | 337867 |
rs185349357 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233193 | TCTCGGCTCACTGCA[A/G]CCTCCACTACCCGGG | 337867 |
rs185372449 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251421 | AGTCTTAGTAATTCA[A/G]AGTCCTAAATGAATA | 337867 |
rs185379979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272922 | CTCTATTCCATTGGT[A/C]CGTGTGTCTGTTCAT | 337867 |
rs185391737 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270285 | TAAGCAGATATTTTT[A/T]TCAAGGGCATATGGT | 337867 |
rs185399916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287372 | TTGATCTCTTGTCAC[A/G]TGTGTATCAGGCCTG | 337867 |
rs185402027 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309632 | TGGAGACAGGGTCTC[A/G]CTCTGTTGCCCAGGC | 337867 |
rs185469454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360520 | AGTTATTCTGGCTCT[A/G]GAGACTGTTCTTAAC | 337867 |
rs185471457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330666 | TTATTTTTCTTTATT[A/G]TACTAGCTAGGACCT | 337867 |
rs185598718 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312995 | TGTTTGTTTGTTTGT[G/T]TTTTGAGACGGAGTC | 337867 |
rs185602507 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218507 | ACCTTTTTTTTTTTT[C/T]CCCTGGAAACTTCTT | 337867 |
rs185610173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351556 | ACCTTTTACCTGGAA[A/G]TGTGAATTCTCTCTT | 337867 |
rs185617551 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199391 | GGGGAGAGCGAGACT[C/T]CGTCTCAAAACAAAC | 337867 |
rs185621454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256198 | ACTTTTGATGAGATG[A/T]TTCACAGCAACTCTA | 337867 |
rs185629479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233687 | TAGAGTGATACCGAG[A/G]TACAAGGAGAATGAA | 337867 |
rs185634960 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274610 | GGATTACAGGCATGA[G/T]GCACGTGCCTGGCCT | 337867 |
rs185652378 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313227 | CTGACCTCATGATCC[A/G]CCCGCCTCGGCCTCC | 337867 |
rs185654777 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292148 | TTTTTCTTTTCTTTT[C/T]TTTTTGAGACAGTCT | 337867 |
rs185666096 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237498 | AGGGTAGGAGGGAGA[A/G]GGGGATAAAAAGAGG | 337867 |
rs185697068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213454 | CAACTGCTGCCTCCC[A/G]GGTTCAAGTGATTCT | 337867 |
rs185701430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276501 | TGGAAGGGCAAGGTG[C/T]GAGGGTGGGTGAGAG | 337867 |
rs185712288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315109 | TGTCATGTGTTATCA[A/G]TGGCTCATCTGGGGC | 337867 |
rs185726166 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344108 | ATTTTGCCAGTCCTA[C/T]AGTAAGTACTCAGTA | 337867 |
rs185730541 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355760 | CCCGCAGCGTGCTTG[C/G]TGCCACAAGCCCCCC | 337867 |
rs185731825 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362450 | TGTTGCTCTCCAAAA[C/G]GGTTGTGTCAGTTTA | 337867 |
rs185739509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379372 | AGATTTTTGTCAGCA[A/G]TGACCTTGGCAAACT | 337867 |
rs185753919 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199484 | ATACTTTTGCCTTCT[A/G]TAATCAGTGTTAACA | 337867 |
rs185785411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233867 | CGTAAGTATTTCATT[A/C]TTTGATGGAAATCTC | 337867 |
rs185795262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274964 | CTCAAGCAGTCCTCC[C/T]ACCTCCACCTCCCAA | 337867 |
rs185816279 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259274 | GTTATGCATGGTTTG[A/T]CAACTTTTTAAAGGG | 337867 |
rs185833817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229712 | ATGGGGAAAATTTGG[A/G]TTGTTCTGTGACTTT | 337867 |
rs185844556 | snp | A/G | 1.88397e-05 | 0.00306912 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296183 | AAAAAAACCAAGAAG[A/G]ATCATATAAGTAAAA | 337867 |
rs185850888 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333910 | ATACTGGCAAAAACT[A/G]TGCATTTTCATTATA | 337867 |
rs185851739 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344286 | GAGGTCTCTGTTTCT[C/G]ATCCCTAACTCATAT | 337867 |
rs185873812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372188 | GGCAACAGCGATCCC[C/T]GGAAACCACAAGGCG | 337867 |
rs185896045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218743 | GTTTTACTTCTAAAC[A/C]CTGTAGGGAAACAGC | 337867 |
rs185923816 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224045 | TCCTTACTGATTTTA[C/G]TGGTCAGCTTGGGCT | 337867 |
rs185929838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256887 | TTGTAATATGGAGGT[A/G]GATGAAAAGTTTCCT | 337867 |
rs185939245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241426 | TTCAACTATAAATGA[A/G]AATGAGATTGATACA | 337867 |
rs185951824 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278612 | AAGTGATATTTCTCA[A/G]CCTAAAAATAGGACT | 337867 |
rs185959565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261830 | AGCCTTCTGCTGCAC[A/G]TTCTGATCTCACAGT | 337867 |
rs185961660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299541 | CTTTACTCATATATT[C/T]TAGATTTTTAATGCT | 337867 |
rs185973183 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323396 | GCTTGAGCCCAAGAG[C/T]TCAACACCAGCCTGG | 337867 |
rs185974096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316589 | AAATCAGTATCACCC[A/G]CTGGGTGAGATGTAG | 337867 |
rs185975942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366406 | AACCCCAAGGCAAGA[G/T]AATATCTCTCCAGAG | 337867 |
rs185986241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382645 | AACACAGGAATGAGC[A/G]AAGGCAGCCACAGCC | 337867 |
rs185986500 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337120 | GCTTCTTTCTCCCAA[C/T]ATGGTGTTTTTAAAA | 337867 |
rs185990378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358233 | TGTCGGATTCTGAAA[A/G]CAACAGGGATGCATT | 337867 |
rs186041289 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223220 | ATAAAACTTACTGTT[G/T]TAACTATTTTTAAGT | 337867 |
rs186050256 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260346 | ATGTGTTGCATATGT[A/G]TGTAGAGAAGAGGCA | 337867 |
rs186071924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379942 | CAGTGAGTGACGCAC[A/G]TGGGTTTTGGCCCCA | 337867 |
rs186139360 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203148 | TTCAAGCGATTCTCC[C/T]GCCTCAGCCTCCCAA | 337867 |
rs186161959 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239502 | GGTGGTGGCGCCTGG[A/G]CATTGCTGTACATTT | 337867 |
rs186183847 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245790 | CAGTGAGCGGAGATC[A/G]CTCCACTGCACTTCA | 337867 |
rs186191944 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362887 | TAATACAAAAGTTCT[C/T]ACAGGTAAAGTAATT | 337867 |
rs186268597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287674 | TTTTTTGGTAGAGAC[A/G]AGGTTTCGCCATGTT | 337867 |
rs186271837 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310238 | AGGCTGAGGCGAGAA[C/G]ATTGCTTGAGCCTAG | 337867 |
rs186274461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327849 | TTTCCCTTTTTTTGT[A/T]TATTAAGATGTTATT | 337867 |
rs186290737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348236 | GCCCTGAGGGATTAA[A/C]TAAGACGCCGCCTGC | 337867 |
rs186293576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327605 | TAAAATTAACATGTC[A/G]TTTTGAATTTATTTA | 337867 |
rs186303772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367114 | TGTTGGTGACATAGA[C/T]TAAGCCAGGAACGGC | 337867 |
rs186310232 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383157 | AGTAGTGTGCATGTG[C/T]GTGTGTGTGCCTGTG | 337867 |
rs186313946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366685 | GATTGTATCTTTAGA[C/T]AGATAATTGAGCTCA | 337867 |
rs186354238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322036 | TTTTTAATGCAAACA[C/T]TTAGTATTTAAAATA | 337867 |
rs186357947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234481 | AGGCGTGAGCCACTG[C/T]GCCCTGCCTGTGCTA | 337867 |
rs186367348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264035 | GGTCCCCCATCATCT[A/G]TATGGCAGGATCCTG | 337867 |
rs186370244 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219313 | TTAGTGTCTCCAGTA[C/T]CCAAAAGATACATAT | 337867 |
rs186371445 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303286 | ATGTGTCCTGAACCC[A/G]GTGGATGTGCAGCAA | 337867 |
rs186373056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284013 | GCTGGGATAACAGGC[A/G]TGAGCCACCACGCCT | 337867 |
rs186389014 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320542 | ATCTGATAAATCTTC[A/C]TATTAACCTTGTTCT | 337867 |
rs186393864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343625 | GCTTTTACGTTGAGT[A/G]GTCTGCTGGGCAGCA | 337867 |
rs186396283 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361728 | GCACCACCATCCTGT[A/C]CCCCCTCCCCTCCTT | 337867 |
rs186421054 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277291 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTAGATCA | 337867 |
rs186480316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210986 | CCCCTCCTTTATTTT[A/G]GTAATGCCAAGAGCA | 337867 |
rs186481495 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347649 | GAACAGTGACCAGGG[A/T]GATGGCTCTATAGAT | 337867 |
rs186500271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227833 | AGCAAACCGTTCATT[C/T]ATTCATTTGGTGCAT | 337867 |
rs186503918 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383070 | GGGCAGAACACCAGG[A/G]TGGCAGCATTCTCAG | 337867 |
rs186516732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210563 | GCTTGCTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 337867 |
rs186525348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246263 | TGAATAATGTTTGAA[A/T]GGAGGCATAAAGTTC | 337867 |
rs186528417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284326 | TACTTGTATTTTCAT[G/T]TAATAGACTGAAGAA | 337867 |
rs186536435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247660 | AAAACCTAGATGATG[A/G]GTCGATACGTGCAGC | 337867 |
rs186537302 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203773 | TGCATGGTCACGGAG[A/G/T]GTAGCCGGGAAGGTG | 337867 |
rs186547645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284681 | AAATTCTAGTCCATC[A/G]TCTGGTTCAGTATTA | 337867 |
rs186547841 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265603 | TCTTCTTCTTGTTCT[C/T]GTTTTGTGTGTGCCT | 337867 |
rs186550057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229947 | CTGTTGTGTAACTTA[C/T]GGGGAGTATCTATCT | 337867 |
rs186564888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260712 | ATACTTGAACCTAAT[G/T]AATTTTTTTTTTTCC | 337867 |
rs186565167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303326 | TCGGCTTCATAGACG[C/T]GCTCCTTGGAAATGA | 337867 |
rs186582015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204986 | TCAGCTCACTGCAAC[C/T]TCTGCCTCCTGGGTT | 337867 |
rs186586529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269126 | GAATTTGACACTGAG[A/G]ATACTCAGGCTGTGG | 337867 |
rs186590414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308660 | TTCTGTAAAAATAGT[C/T]GAGTAGCTTTTGCCT | 337867 |
rs186608071 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347302 | AGGAACAGATTCAGA[C/T]GTTACTATCCCCGGG | 337867 |
rs186734247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227395 | GATAGAGTAACCACC[A/G]TCTTGCACGTTGGCA | 337867 |
rs186744028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264490 | AGTTCTCTTGGCTTC[A/G]TTTGTCCCCTTTTTT | 337867 |
rs186766604 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331294 | CTTTTTAAATATGAA[A/G]GTGAAATAAACTTCT | 337867 |
rs186791027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213818 | ATCAAAAGATAAGAA[C/T]ATTTTATTTTATTTT | 337867 |
rs186810035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251234 | TTGATTTGGCATCCC[A/G]AAACTCTAGTGAAGT | 337867 |
rs186815743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286576 | TGTGTGTCACTCAGG[C/T]TTGGGGTACAAATGA | 337867 |
rs186839211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327052 | TATGAAGAATGTGGC[C/T]TATAGCTATGCTTTC | 337867 |
rs186869738 | snp | A/G/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227186 | CCGGACAACAAGAGC[A/G/T]AAACTCCATCTCAAA | 337867 |
rs186878511 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374271 | TATTATGCTGACTTG[G/T]GTAGTCTGGGATCTC | 337867 |
rs186902695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314903 | ACTTTTCTTTTACTC[C/T]CACGGCTTTTGATGT | 337867 |
rs186907141 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333691 | GTTTATTACTGGGTG[A/G]GGTATCCATATTCTT | 337867 |
rs186912096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354960 | GGACAGAGGAGAGCT[G/T]AGTCCAGACATGAGC | 337867 |
rs186920277 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372181 | TCAGGATGGCAACAG[C/T]GATCCCCGGAAACCA | 337867 |
rs187056088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209595 | AAACCTGAACAGCTC[A/G]TTTACTCTTGGGGAC | 337867 |
rs187075476 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364705 | ATGCTATATAATAAT[A/T]GTCATACAAATGTAC | 337867 |
rs187082083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381542 | TGTTTGGGGGCCATG[A/G]CATCATGGTGGTGGA | 337867 |
rs187105893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253706 | TTTAGTAGAGATGAG[G/T]TTTCACCATATTGGC | 337867 |
rs187110183 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215710 | GCGAGCGGGAAACCG[A/C]CTTTGTCTTGGCCTT | 337867 |
rs187113723 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232603 | TATTTAAGAGAGAAA[A/C/T]GACAGAAATGCAAAG | 337867 |
rs187114824 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257800 | ACCATAAACATTTTC[A/T]TTCCTTAAGTTGAAA | 337867 |
rs187118665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272361 | TTTCAACACTGATCA[A/G]CTCATGGCCACCTTG | 337867 |
rs187126090 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339145 | CCCACTCAGTAGCCC[A/C]CCAAGATATCTAATA | 337867 |
rs187129264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311293 | GGGAAGGCTGTGAGG[G/T]CGGGAGGTGCGGTTT | 337867 |
rs187130737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290051 | TTTAAGAGAGAAAAT[A/T]CGATGATGAAGAGTG | 337867 |
rs187135343 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359137 | GGCTAGAAAGAAAGC[A/G]GGATGCCACAAAGCC | 337867 |
rs187139105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99293942 | TTGGTGTCATTGCCA[A/C]CAGAGAATACTGCAT | 337867 |
rs187140748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375730 | TTTTACTTATGTCAA[A/G]GAGGAGTTGAATTGC | 337867 |
rs187143498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329325 | TGTAATTTCTTCAAA[A/G]AAAGGGGAAAAGAGT | 337867 |
rs187145632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332902 | AAAGCCTGCTTTTCA[G/T]AGGGTCTATGGATTT | 337867 |
rs187159857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371369 | TTTCTTGATTATCCT[G/T]CAAATAGCTGTTATA | 337867 |
rs187177014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276119 | TGCTTCTAAATAATA[A/C]ATCTCCAGCCATCTG | 337867 |
rs187195674 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294468 | TGCAGTTCAAAGTCT[A/G]TTGCCAATTATCTTT | 337867 |
rs187196126 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357777 | CACCCCTTCCACCCC[A/G]CCTTCATTAGTAACC | 337867 |
rs187198225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314453 | ATAAGAGCTTTCACT[A/G]TAATTTGTATCTGTG | 337867 |
rs187199842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333119 | GAAGAAAGAGAGAGA[G/T]AATGAAAATTAAAAT | 337867 |
rs187284986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262830 | TGGTTGAGGATTTTA[A/G]TACACAGCCATTTGT | 337867 |
rs187328529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275225 | TACTCAGGATGTCAG[A/G]GACCACAGTCATCTT | 337867 |
rs187334879 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313999 | GACCATGCTTTCAGA[C/G]TGAAATAAAATTATA | 337867 |
rs187336906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212291 | TTGTGAAATGGTACT[A/G]TGAGGAGCTCCTGAA | 337867 |
rs187343199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379100 | GATATCCCTAGTTAA[A/G]CATGCCTTTTTGTTA | 337867 |
rs187343587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219700 | GATTAGACATCCCTG[C/T]ATTAAGCCGTCATGC | 337867 |
rs187343723 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236232 | ACTAAAAAGCTCCAG[G/T]TGCACAGCAAAAGAA | 337867 |
rs187356706 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353786 | AGCTCTTAATGAGGA[A/G]CAGACCACTGGAGTA | 337867 |
rs187392787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232317 | AAACAGAAATAAACA[A/T]ATCTCTGTGTTATAA | 337867 |
rs187402768 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215346 | TTTATTTAGAGTCCT[A/G]AGATAACAAGGAATC | 337867 |
rs187406229 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336105 | AGTCCTAAAAACAAG[G/T]GAGGATAAACATCTT | 337867 |
rs187416795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316038 | CTCACCATGAGGGAT[A/C]CCCCTTAGCCCTGCC | 337867 |
rs187419137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373436 | CTTCCTCTCTTCGAT[G/T]CATGTCTTTCTTTCC | 337867 |
rs187468086 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300692 | AGAGATGGTACCTTT[G/T]TGTATTAGAGGGTCT | 337867 |
rs187472357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281782 | GATCTGTGCCTTCTG[A/T]ATCAAAGTGGCGTGC | 337867 |
rs187475562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319066 | TGCCAACTGGAAAGT[C/T]AGGTGGGTTGGACCT | 337867 |
rs187483668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384013 | GATAGAGAGGAAGAA[C/G]AGCAGGCTTTCTGGA | 337867 |
rs187485031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341550 | AGATGCCCATGGTGT[A/T]TTTAAAGCTGGAGGA | 337867 |
rs187487062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360893 | TGGGGCGCTCTTCGG[A/G]AGCAAGGATGAGACC | 337867 |
rs187489387 | snp | A/G | 0.000560643 | 0.0167334 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200903 | GGCTCCGAGCCCGGC[A/G]GGACCATGTTCACCA | 337867 |
rs187489672 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237088 | TATTGCAGCACTATT[C/T]ACAATAGCCAAAATG | 337867 |
rs187491884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377901 | ATGTGGTCACACGGG[G/T]CCAACTCCAAAGCTC | 337867 |
rs187500620 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303825 | TAAACTGAATTCCAG[A/G]TCAACTCGGTCATTC | 337867 |
rs187514324 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276408 | ATACATTTGCAGGAA[C/T]GTCTCACAGAACTCA | 337867 |
rs187589264 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200020 | ATCAACTTAAAAAAA[A/C]ACTTTTTAAAACGAC | 337867 |
rs187670336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270532 | ACTTTTTACATTTCT[A/G]TATCAATGTCCAAGA | 337867 |
rs187672646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298544 | TTTAAAAAAGGAAAG[A/G]TTTAAAATATATGTT | 337867 |
rs187704310 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266156 | AAAAGCTATTAATTG[A/G]TAGAATATTATAAAA | 337867 |
rs187723307 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305304 | CACATGTGTTATCTC[A/G]TTTTATACAATGCCC | 337867 |
rs187726351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284839 | GCTGCTGGAAAATTA[A/C]AGTTTGTGAAGGTGA | 337867 |
rs187727860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220333 | TGCTGATAATTAATT[C/T]GTGCTTCAGGGCTAT | 337867 |
rs187736513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324077 | CAACTACACACAATC[C/T]ATTCCCAAACATCCA | 337867 |
rs187739611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345457 | CTGGGCTGATGCTGT[A/G]CTCTGGATCGAGCTC | 337867 |
rs187750109 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363728 | GTCACACGTATATAC[A/C]CACCCAAGAAAACCA | 337867 |
rs187754905 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259018 | CGTGGAAGTCTAGAA[A/G]TAATTTCTTTTGCAT | 337867 |
rs187755446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380373 | GTGTGGGGACTGGGC[A/G]TGCTGGGCTTCTCTG | 337867 |
rs187762944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243434 | ATATTTTTGAGTTTA[C/T]ACCTAAGTTGTTTTT | 337867 |
rs187769153 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281217 | CAAAACAAAACAAAA[A/C]AAAACAACAGCAACA | 337867 |
rs187777342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262448 | TGGCTCATGCCTGTA[A/T]TCCCAGCACTTTGGG | 337867 |
rs187786461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368547 | AAAATTATGCTGTGT[A/G]TATTATAGATTTGAG | 337867 |
rs187903391 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224590 | CCAATGTTTTAATTA[G/T]GAAAAATTTCAAACA | 337867 |
rs187909380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262181 | AGTGCTTGTGTTCCA[A/G]TAACCCTTATTTAAT | 337867 |
rs187936987 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300272 | GAAAGGCATTTGCAG[A/G]ATGTGGACGTGTAAG | 337867 |
rs187946536 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225102 | AATAGGGTCAGTTAT[C/T]AGTTCAGTAAATATT | 337867 |
rs187953556 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205695 | AGAGAAGATAGAAGA[C/T]AGAAGGATTCTTGGA | 337867 |
rs187973271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369183 | AAATTTGCAAGCATC[A/G]TAATAAAAATCCATT | 337867 |
rs187982591 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385547 | TGTATTTTCTATCTA[C/T]ATTTTTTATTGGGCA | 337867 |
rs188000119 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249105 | ATGCTGAGGTTTGGG[A/G]TACAGATGATCCTGT | 337867 |
rs188008198 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285416 | TTTTTTTAAGAGACA[A/G]TTGTCTTGCTCTGTC | 337867 |
rs188027760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354846 | CATGTCATCCAAGAA[A/G]TTGTTGGCATAATCT | 337867 |
rs188034987 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324543 | TGAAATTTGATAATT[G/T]GTTACCACAGTATAA | 337867 |
rs188162222 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229599 | TTTAGGAAAGAGTAT[A/G]TACAAACACACACAG | 337867 |
rs188177997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213429 | GCAATGGTGTGATCT[C/T]GGCTTACTGCAACTG | 337867 |
rs188179841 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242714 | CCTCCCCGACGGGGC[G/T]GCTGGCCTGGCCGGG | 337867 |
rs188180620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249938 | TGCTTGTTGAATCAA[G/T]TTCCTTACAGATTCT | 337867 |
rs188184173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205198 | TGAGCCACTGTGCCC[G/T]GTTGGGGGAGTTTCT | 337867 |
rs188211845 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281047 | AAAAATAAGCCAGGT[G/T]TGTTGGCGGGCACCT | 337867 |
rs188224834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317290 | TCTGAAGTTCTAAAA[A/G]TTAACCAACAATAAC | 337867 |
rs188256177 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349530 | TATTGCATACAAGAC[C/G/T]GGGGGTCAGGGTAAG | 337867 |
rs188257500 | snp | C/T | 3.3869e-05 | 0.00411502 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99244563 | TTATTTGACTTTCTC[C/T]TCATTGAAGCTATGC | 337867 |
rs188259625 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271530 | TGGCCTTTAATCAGG[G/T]CATTCGGGAGCCATT | 337867 |
rs188268376 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229229 | AGAGTGGGGGAAAAG[C/T]CCTTCAGGCTAAAAT | 337867 |
rs188278229 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266805 | CATTTTCATCTTCCC[A/G]GACTGAAAGCCTGTA | 337867 |
rs188302900 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305965 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAACCTC | 337867 |
rs188304610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335775 | CAGGGCTGCAGTGGA[A/G]TGAGCCTCAAAGCTC | 337867 |
rs188315261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371620 | ATAACTTGAATTAAC[A/G]AAAGCTTTTTTTGCT | 337867 |
rs188316249 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357389 | TCAGTCCTGAAGTGC[G/T]TCTTGTTTAGTTTTT | 337867 |
rs188319431 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345888 | GCTGGGATTACAGGC[A/G]CTCACCACCACATCC | 337867 |
rs188362346 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292389 | CCTCGTGATTCACCC[G/T]CCTCGGCCTCCCAAA | 337867 |
rs188368817 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361386 | CCTAGAACCTAGAGC[C/T]GTAACTTTCTGCTTT | 337867 |
rs188368872 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313236 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 337867 |
rs188370914 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331787 | TTCCCTTATGCTTTC[G/T]CTAACATTTTCATTG | 337867 |
rs188383503 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352268 | TTAGTATTTTTTAAT[C/T]GCACAAATACCGTAA | 337867 |
rs188393308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267857 | GCTTCTGTAACAAAC[C/T]GCTGACACAGTGGCT | 337867 |
rs188401359 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285822 | AGGTTCCATTATTCA[C/G]AAAAACGTGTGGCTC | 337867 |
rs188403352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99307356 | TATCAGTGACTCGTT[C/T]GGGTCTCTGTGTAGT | 337867 |
rs188426699 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200486 | CGGGCGTCCAGTCTC[C/G]GGAGAGATTAGAAGT | 337867 |
rs188485819 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349091 | CATCACAGTGAAGGA[C/G/T]GAGGGCAGGCTTTGC | 337867 |
rs188529082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233759 | TATCAAAATTATCAT[G/T]ATGTAAACCCTAGTG | 337867 |
rs188534555 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252891 | TGTGCTTTTTGCTCT[A/G]AGACTAAACTCTTCT | 337867 |
rs188535127 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274716 | ATCCTTTTTCCTTTT[A/C]TTTTCTTTTTTTTTT | 337867 |
rs188540896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289049 | GCAAAGAGCTTGCCT[A/G]TTATCTAACACTTAC | 337867 |
rs188543330 | snp | C/T | | | intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99256458 | TGGGAGTACGTAAAG[C/T]CAAGTCTTCCAGGTT | 337867 |
rs188575372 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237911 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 337867 |
rs188585835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276993 | GGGAAGTCAAATGTT[A/G]ATCAGGTTGCCTCTC | 337867 |
rs188591774 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372203 | CGGAAACCACAAGGC[G/T]AGATGTCTGCTCATG | 337867 |
rs188593562 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259968 | CCATAGGCCTGGCTT[C/T]AGGTTGGGGTGAGCT | 337867 |
rs188595410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297274 | GTGTGATTATTTTTA[A/G]AAGAAAAATAATTCC | 337867 |
rs188607905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315508 | TGTTTTATTAATTGT[C/G]GAGTAGGAGTTCAGT | 337867 |
rs188613084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208316 | CTGTCTCTTTAAAAT[A/T]CACTCAGTTGGGGAG | 337867 |
rs188625991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356381 | CGGGGCAGAGGGCAG[C/T]CGATAGTTGGAAACT | 337867 |
rs188635983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372552 | TGTGGAATCAGTGAC[C/T]GTGAGAAGCAGCCTT | 337867 |
rs188711815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228807 | GGAGCCTTGTTTGCA[A/T]TTTGGTCATGAAGAA | 337867 |
rs188760358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328096 | TATACTTAGTATTGT[A/G]TAATATGAAGTATTT | 337867 |
rs188772550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334245 | GGATTACAGGCGTGA[A/G]CACAGAAAAACCAAC | 337867 |
rs188778095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367402 | TAGCCTCGTCTCCAT[A/G]CCTTCCTTCCTATCA | 337867 |
rs188818954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218083 | TTAACTGATTTATCC[A/C]ATATTTGTGTGTTAC | 337867 |
rs188819545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318151 | CTATTTAGATTGTGC[A/G]TCATATTCAACTGTC | 337867 |
rs188829034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233441 | AAAGACCATTTCCCA[A/G]CATTCCCTAACAGGG | 337867 |
rs188834112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359947 | AAACCTGGCATGCTG[A/C]TAAAGGCTTTCTGAG | 337867 |
rs188837139 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199194 | CGGATCACGAGGTCA[A/G]GAGTTCGAGACCAGC | 337867 |
rs188861832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356088 | CCTCTGAAAAGAAAT[A/G]TCATTAAAGTAAACA | 337867 |
rs188934305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214966 | TCAGGTCATGACTCC[C/T]TTTTCAGTTCTTTTC | 337867 |
rs188959972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211544 | ACGTGTTAGGCACTG[C/T]TCTAAGCAGTTTACC | 337867 |
rs188970496 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252408 | TTGATTACAGTGTAG[A/C]CCCAGTAAGACTGTA | 337867 |
rs188981828 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248170 | GCTTCCCAGCTGTCT[A/C]TTTCCAACCCACACT | 337867 |
rs189025341 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311356 | AAGGTGCTGTCCTGC[A/G]GAGCACAGGATCAGA | 337867 |
rs189037501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315266 | TTTGATTCTTATGAG[C/T]AGGATTTGCTATAGC | 337867 |
rs189039762 | snp | A/G | 0.000609841 | 0.0174513 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255645 | ATAAAACATTCGAAA[A/G]GGTAAAGTCATTATA | 337867 |
rs189052762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203407 | AATCTGAAAGAAGGA[C/T]GACACGTGTACCTAG | 337867 |
rs189090288 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300514 | ACTATCCCATTCTTA[C/T]ATCAGCCAGTCCCAA | 337867 |
rs189098381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339404 | TGATTACTGCCTGTT[C/T]TCCACATTGACTGCT | 337867 |
rs189118204 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377527 | TGTGTTGTGGCTAAA[A/G]TGTGGTGCTTTCGAT | 337867 |
rs189233140 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343795 | GATAAATCACCACGT[A/G]GAGAACTCTTTTGTT | 337867 |
rs189240307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231580 | CACGCCCAGCTACTT[C/T]TTATATTTTTAGTAG | 337867 |
rs189245645 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361835 | ACCATATATCCATCT[A/T]AAAAAGTTAAAATAG | 337867 |
rs189253472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379303 | TGTGTCTTTCTGGAG[C/T]AATAAAACCAAAACA | 337867 |
rs189271360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201811 | GCGCGGTGGCTCACG[C/G]CTGTAATCCCAGCAC | 337867 |
rs189272178 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239663 | GTGGGCATCTGTGCT[G/T]TAAAGGTGGTGACCT | 337867 |
rs189274415 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308459 | AAGAAGTTACTGGAC[A/G]TAGCTTTTGGATCAA | 337867 |
rs189275228 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259338 | TTTAGACAGTTTGGG[A/G]TCCATCCTTTTTTTT | 337867 |
rs189276542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325350 | CCTCGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 337867 |
rs189287319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237697 | CCGTGGCCCATGCCT[A/G]TAATCCCAGCACTTT | 337867 |
rs189291157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346686 | ATTCCTGACAAATAT[C/T]GCCTCCTCAGGGAGG | 337867 |
rs189295226 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366211 | AGGTCCTCCTGTGAC[A/G]TCCTAGTCTTTTTGA | 337867 |
rs189306539 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382372 | ATTCCTGAGTGTTTT[C/T]AGCAGGCCCAGCTTA | 337867 |
rs189316264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346229 | CCTTGATGTAAGTCC[A/G]TCATTCATCTCCAGT | 337867 |
rs189320458 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315869 | GAAAGGGGGTCTTAG[G/T]TGGATGAAGAGGCAC | 337867 |
rs189330000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381989 | CTTTGACAACATCTC[A/G]TCAGCTTATGAGAGA | 337867 |
rs189382114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342111 | TTATGAGAGAACACC[A/G]TCAGCATCAGTATCT | 337867 |
rs189410221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370323 | AAAGCAGCTATGGCC[A/G]AATAACAATTGGTGA | 337867 |
rs189466508 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286483 | AGGACTTCTTTTTTT[A/T]AATATTTATTTATTT | 337867 |
rs189492982 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226927 | CCCTTGGCTGGGCGC[A/G]GTGGCTCATGCCTGT | 337867 |
rs189504781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209168 | CACTGTACCCTTGCT[A/G]GTCACAGATTTAGCA | 337867 |
rs189510288 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245538 | TAGAGTTGACAGAAC[A/G]AGACTCCATCTCAAA | 337867 |
rs189516387 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312434 | CAAACCACTCTACTC[A/T]TTCATATTACCTGCC | 337867 |
rs189520553 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283788 | TACCCAGGCCAGAGT[A/G]CAGTGGTGCTATCTC | 337867 |
rs189522406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263867 | TGAATCTAGTGTTAA[G/T]TTGAAAAAGCCAGAC | 337867 |
rs189527200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226636 | TTAAAGTCCTCATAA[C/T]GGCCTGTAGGGCTCT | 337867 |
rs189528508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302878 | TGTACACTGTAAGGT[A/G]ACTTTTTCCCAGCCA | 337867 |
rs189530260 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329990 | ACGAACGTGATAAGT[C/G]TCTACGTTTATTTAG | 337867 |
rs189533965 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351007 | AGGAAGAAAACAGTG[G/T]TGTTTTTCTTCAGAG | 337867 |
rs189539184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263278 | TCAAGGAAAGGTTTT[A/G]TAGCTGGATCCTGGC | 337867 |
rs189566964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223506 | TCTTTATATCTGCTT[A/G]CTTAGGTTTTAATTT | 337867 |
rs189567397 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301155 | ACGTGGCCCCTCAGC[C/T]GTCCTTCGTGCTGCC | 337867 |
rs189573094 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260511 | GGCAAGGGCCTGAGG[G/T]CTGTCGTCCTCCCCT | 337867 |
rs189582661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324949 | CACTCTGTAATGTTC[A/G]CACGATGACCAGATC | 337867 |
rs189585940 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222790 | TCTGTTAATACGTTC[A/G]TAAAGTATATTGGTC | 337867 |
rs189586406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298331 | CTACAGTGCAGCTAA[A/G]TTATAAACCAATGAT | 337867 |
rs189604351 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365615 | TTTAATTGCATTATG[A/G]TGAGAATATAATCTG | 337867 |
rs189619104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303927 | CTGCTGCCTCTGGTC[A/G]GCGAGCAGTCCCTGT | 337867 |
rs189621170 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332843 | CTCCTTGGTAGAGTT[C/T]CCCCAGCCCCCTGAC | 337867 |
rs189624850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284737 | CCTTACTGTTTAATC[C/T]GGACTGTTCCTCAGT | 337867 |
rs189627668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353352 | AGTTGATCATACTGA[C/T]CTTTTTGACAAAATT | 337867 |
rs189629803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323504 | AGGGTGATGGGACTT[A/G]TGAAAGGACCACATG | 337867 |
rs189635905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371007 | GTTACTGTTTACTTG[A/G]TACAGCAGTGAGTCA | 337867 |
rs189647628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286714 | TCTTCGTGTCCATGT[A/G]TATTCAATGTTTAGC | 337867 |
rs189675063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327154 | CCTTCAGCAAACTCA[C/G]TGTCTTGTATTTCTT | 337867 |
rs189817041 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214517 | GTGGTGGTGGGGGAA[A/G]CAGGACTGTGAGAAC | 337867 |
rs189817876 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245210 | GATCCTGATAGAATT[A/T]GTTTTGTGTGTTTTT | 337867 |
rs189831309 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282650 | CTCAGGTAACAGACA[C/G]CAAAGGAGATACTTT | 337867 |
rs189836372 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251557 | TGAATTTGAAAGCAT[A/T]CCATACAATGCTGTC | 337867 |
rs189839528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319184 | ATTTTAATAATAAGC[A/G]TTTGTCCTAAATTCT | 337867 |
rs189845299 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207382 | GCCTATTCTTAAAAA[C/T]GCAAAAGTATAACCC | 337867 |
rs189845639 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202009 | ACCCGGGAGGCGGAG[C/G]TTGCAGCGAGCCGAG | 337867 |
rs189848933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99231486 | GGTGTGATCTCGGCT[C/T]ACTGCAGTCTCTGTC | 337867 |
rs189852754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270312 | TGGTAATATTGTTTG[C/T]CATTTTGTGTCTCTT | 337867 |
rs189858448 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376105 | AATAAGGAAAGAGAA[A/G]CTGGTACAGATTTAT | 337867 |
rs189870252 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309707 | CTGGGCTCAAGTGAT[C/T]CTCCCACCTCAGCTT | 337867 |
rs189870443 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287487 | TGAAGTGCAGTGGCA[C/T]GATCATGACTAACTG | 337867 |
rs189883651 | snp | A/C | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327690 | ATTGATAGCTGAGAA[A/C]ATTTTCAAAGCAGCA | 337867 |
rs189887676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348156 | TTCATCCCCAGTAGA[A/G]TATGAGCTCTTGGAG | 337867 |
rs189896093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366529 | ATATAACAACATATG[C/T]ATAGTATAACTTGAA | 337867 |
rs189932589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309204 | CAACCTCCACCTCCC[A/G]GCTTCAAGCAATTCT | 337867 |
rs189941348 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347318 | GTTACTATCCCCGGG[C/T]GCCCCCCCCCCCCCC | 337867 |
rs190098842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227545 | GGTGGGGAGCAGTCC[C/T]ACCATGTGTTTGGGA | 337867 |
rs190102750 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210677 | AGACGGGGTTTCTCC[A/T]TTTTGGTCAGGCTGG | 337867 |
rs190103991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333503 | ACCATTCACCCAGGA[A/G]ATACTTACAGTACTA | 337867 |
rs190106789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225760 | AGACTGAAGATGGGC[A/G]GATGGACAATAGACC | 337867 |
rs190110236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379598 | ACCAAGGGATCCATC[C/T]TCGGTACATGATCAG | 337867 |
rs190112518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272986 | TATGTATTGATATCT[A/G]GTAGAACAGGTTACT | 337867 |
rs190116137 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354882 | TGCAACAGCAAGGAC[C/T]TAAACGGGCAGATCC | 337867 |
rs190122659 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313024 | TCTCGCTCTGTCGCC[C/G]AGGCTGGAGTGCAGT | 337867 |
rs190124346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371864 | TATTCTAAGAAGAAT[A/G]TGCATCCTTTAATAA | 337867 |
rs190129103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214048 | GGTCTCGAACTCCCA[A/G]CCTCAAGTGATCTGC | 337867 |
rs190139547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351639 | GATGAGAATTCTGTT[A/G]TATACCACAACACAA | 337867 |
rs190144954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230816 | AGCGCTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 337867 |
rs190156658 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386873 | AAACCAAAATCCACT[C/T]TCTGTGTTCCCCGTG | 337867 |
rs190159388 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382850 | CAGGCTCAGGGCAGA[C/G]GGCAGAGACAGCAAC | 337867 |
rs190328034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261847 | TCTGATCTCACAGTT[A/G]CCAGAGGTGCAAATG | 337867 |
rs190336226 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299678 | ACCTTGTTATCTGAC[A/G]TGCTTTTCAAAGCTT | 337867 |
rs190340463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279880 | CTCCTAAGAGCATCA[C/T]ACTGGGGGTTAGGAT | 337867 |
rs190357137 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229827 | AAAAATAGTAAAACA[A/G]TATACTGTAATTTAT | 337867 |
rs190361385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268485 | TGGTGGCATGTGCCT[A/G]TAGTCTCAGCTACCT | 337867 |
rs190369184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296416 | ACTTTGGCAAAGCTC[C/T]GGCAAAGGAAACAGA | 337867 |
rs190370006 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291554 | TCCCCTTCTAAAATC[A/G]CATGCCACCTTGTAC | 337867 |
rs190377008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330703 | GAATATTAAATAAAA[A/G]TGGTGAATGGATATC | 337867 |
rs190397809 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369611 | CTTATGATATTTTCA[A/G]CGTACAGTGGATTTA | 337867 |
rs190408778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217582 | ACAGGGAGGCACCCC[A/G]GCTTGGGGCCAGCTG | 337867 |
rs190422476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254607 | CTCGATTTCCCCCCT[A/G]CTGACTTGATTAACA | 337867 |
rs190426820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290492 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 337867 |
rs190465062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320321 | GGTACCTGTTTTAAC[C/T]TTTTAAAAGGAATCA | 337867 |
rs190479482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361602 | TATCAGGGTTTCTCA[A/G]CCTAAACACCATTGA | 337867 |
rs190538840 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316809 | GCCAGTCCTGGATAC[A/G]CTCCAGCCCACCACC | 337867 |
rs190556543 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337809 | GGGGAGAAAGGGTAC[A/G]TGGAGCATGAGGAGG | 337867 |
rs190562741 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358332 | TCTAACTGTGTATCT[A/G]TGTGGCTGGATTTGC | 337867 |
rs190569945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375534 | GTGGGGGCCGTCTTC[A/G]GGTGGGCATCGCTTT | 337867 |
rs190601578 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276662 | TCCTGGAGGCTGGTG[G/T]GTGGTGCTGAAAGTT | 337867 |
rs190607738 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213621 | CGACTCAGCCTCCCA[G/T]AGTGCTGGGATTACA | 337867 |
rs190623125 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250781 | AGACGGAGTCTCACT[C/T]TGTCACCCAGGCTGG | 337867 |
rs190654527 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232779 | CAAAAAAACAAAAAC[A/T]ACGAAAAAAAAACCT | 337867 |
rs190665213 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272821 | TATGAATTTAGGGGT[G/T]GGGGGAGACAAAGTT | 337867 |
rs190718844 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362936 | TGTGATTTATACTTC[A/G]TATTTCTGTTTTAGA | 337867 |
rs190720136 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343301 | CTGTTTGCGCACGCC[C/G]TCGCTCCAGGATTCT | 337867 |
rs190736238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310341 | GTGTCTCAAGAAAAA[A/G]AGAAAGGATGGATGA | 337867 |
rs190741222 | snp | C/G | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200128 | AAATTTAAATGGCCT[C/G]AGTCCGGAAGCTCGC | 337867 |
rs190749010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327875 | TTATTTACATACAAT[A/G]GAACTCACCAATTTT | 337867 |
rs190752662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348469 | AAAAACGCACAGGGG[C/T]TCAAAACAGCTGTGG | 337867 |
rs190761022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367161 | AGGATCCGTGGAGCC[A/G]CCCTCAGAAAGATGG | 337867 |
rs190771315 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383367 | CCAAATGAATTCTTT[C/T]CAATTCTAGTTTTGT | 337867 |
rs190772761 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257832 | AAATTACATTTAGTA[C/T]TAATGTAAAGCAATA | 337867 |
rs190776992 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219418 | TTGTGCAATTAACAG[C/G]AACCACAATTTAATT | 337867 |
rs190778711 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303312 | AGCAAAGACCCACTT[C/T]GGCTTCATAGACGCG | 337867 |
rs190782559 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359166 | CCTGGGGAAGAGAAT[A/G]TCGAGGAAGAGTGGT | 337867 |
rs190783105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284139 | TGTGTATTTCAACTT[C/T]AGCAATGTAAATGTC | 337867 |
rs190784872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234973 | GAGAGAAGACATTTA[C/T]AGTTTCTAAAATACC | 337867 |
rs190795551 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321784 | TCACAGAAAATAACT[A/C]AATCATTTTTCTGAG | 337867 |
rs190795782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275480 | TTCATTTATTGGTTT[A/G]TTGTTTTGGTTTTCT | 337867 |
rs190835286 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278108 | AGGCACAGATAATTT[C/T]GGAAGCTAAGAAATA | 337867 |
rs190941266 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211060 | AAGTGTATTCTCGTA[A/T]AACTTTTAGTACGTA | 337867 |
rs190949680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281141 | TTGCAGTGAGATGAG[A/G]TCACACCATGGTACT | 337867 |
rs190956414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228097 | GGAAGAGGAAGGACT[A/G]ACGGGGCCCATTGCA | 337867 |
rs190961012 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317319 | ACCCACAAATCATTT[A/C]TTTGTTGCAGGAACA | 337867 |
rs190963456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344521 | AAAATACAACTGTTA[C/T]TTATTTAAAAACTTG | 337867 |
rs190970337 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247740 | ACATGTATCCCCGGA[A/G]CTTAAAATAAAAATA | 337867 |
rs190975242 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380281 | GCAGGCCTCAATTTC[A/G/T]TCTTTCTGTAATTTG | 337867 |
rs190975786 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383095 | TCTCAGCCACCTGGC[A/G]GTGAGGCCAGGGCAC | 337867 |
rs190981769 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264570 | GCTGTGCAGGAGCCC[A/T]GCATGTGCCACTAAC | 337867 |
rs190988080 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265807 | TACAATTACAAAGAC[G/T]TACCAAATAAAATAA | 337867 |
rs190998391 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204677 | CGGGCCTGAAGCGCG[A/G]CCTGTGGGAAAGAAA | 337867 |
rs191015710 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303484 | TTTATATTGAAAAGT[A/G]TGGAAGTTATTGAAG | 337867 |
rs191017151 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223987 | TGTTCTATAAATGTC[A/T]ATCAGGCCAAATTGG | 337867 |
rs191026716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261330 | TCCCCTCCTTTCTGT[G/T]TCTCAAACTTGTATC | 337867 |
rs191029908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344131 | ACTCAGTATATGTTA[C/T]CTCATTTATGCCCGG | 337867 |
rs191032664 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240328 | TGTCCTTGAGTATGA[C/T]TGCAACACATAAATT | 337867 |
rs191154645 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199436 | TGTGAAAATGAACTT[C/T]ACGAATAAAGCCTAA | 337867 |
rs191181801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262237 | TACTGAGCCTAATGT[A/G]TAAGTTAAACTTTAT | 337867 |
rs191209442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300281 | TTGCAGAATGTGGAC[A/G]TGTAAGTGGGATGGC | 337867 |
rs191215560 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366837 | GGCTCTGCTTCCCAC[G/T]CCCACTTGTTCCTGA | 337867 |
rs191223664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339237 | CCAGTTCATCAAGTC[A/G]CGGGCACCGCATCAT | 337867 |
rs191234693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224288 | GTCACATTGAATTAG[A/G]GCTCCATCTATCCTT | 337867 |
rs191237878 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247552 | TGTACTTCATGGACA[C/T]AGGGAGGGGAACGTC | 337867 |
rs191242000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284383 | AAATGCTGCCACTTA[C/T]GTTTTATACTTTTTG | 337867 |
rs191242964 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251247 | CCGAAACTCTAGTGA[A/T]GTTGTTTCTCGATTC | 337867 |
rs191267560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322286 | TTACTTACTGAACTT[C/T]ATTTAAATTCTTCTT | 337867 |
rs191277883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362454 | GCTCTCCAAAAGGGT[G/T]GTGTCAGTTTATACT | 337867 |
rs191373302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99307392 | TGAGTAGTTGTCCAA[A/G]CTGAAGTAAGTTTTA | 337867 |
rs191380271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218628 | CTGCCCGGTTGTCTG[G/T]GGACCTGTATGAGGA | 337867 |
rs191381269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355633 | AAACACAGGAAAAGG[C/T]TGGGACACCTCTGGT | 337867 |
rs191388273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372185 | GATGGCAACAGCGAT[A/C]CCCGGAAACCACAAG | 337867 |
rs191390144 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324970 | TGACCAGATCACATA[A/G]CACATTTCTCAGAAT | 337867 |
rs191392457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346534 | CAGTTAACTGCTGCT[C/T]ATATTGTTTCACGCA | 337867 |
rs191427018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205438 | CTCCTGTCCCAGCTG[C/T]AAAAAAATCAATCAC | 337867 |
rs191433506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311567 | AAAAACTGCTTTGTT[A/C]ATTTTAAAAAATCCA | 337867 |
rs191435203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329554 | AGAGCAGATCATAAA[A/G]GACACAGCTAGTCCT | 337867 |
rs191443411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349844 | GACTTCGGATGACTG[C/T]GGGCAGACTGGGATA | 337867 |
rs191453623 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368713 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTAC | 337867 |
rs191487955 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205162 | CCGCCTCGGCCTCCC[A/G]GAGTGCTGGGATTAT | 337867 |
rs191488299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241560 | TCATAGAGACATTAA[C/G]TAGAATAGTGTTTCC | 337867 |
rs191490181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269478 | TTTGATATTTTTTCT[A/G]TATAATCTAAGTGAT | 337867 |
rs191587552 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253792 | GTGCTGGGATTACAG[A/G]CGTGAGCCACCACGC | 337867 |
rs191592554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232636 | CTTAGGAAAAAGCAC[C/T]GTAGGCCAGGCATGG | 337867 |
rs191597464 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272398 | CTATATCCTTAATCT[C/T]AAGCCATTCTCATGG | 337867 |
rs191614926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290182 | TCATCTGGAAAGTGC[A/G]ACTGATAAATAGAAC | 337867 |
rs191636828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229350 | AAGGCATTGATGATA[C/T]TTGGGGATTTAAGTC | 337867 |
rs191638536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276236 | GTTCTGACACTTTCT[A/G]CCTGGAGTTAGTATC | 337867 |
rs191642874 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99258514 | TGAAATGATGGCATA[C/T]ATTTAAGATAATTAT | 337867 |
rs191644440 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212396 | CCCAGATTTTTCCCT[A/G]AGGCTTTCTAAGTTA | 337867 |
rs191644641 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295002 | TTTGCTTTATAAGGG[A/C]AGTCCTGCAAAGTTT | 337867 |
rs191649404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249153 | TGGTATCCAGTAGTT[A/G]GTTTTTCAACCCTTG | 337867 |
rs191656169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314582 | AGAAAATCAGTGTCA[A/G]AATTAATTTATTGAA | 337867 |
rs191702295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246090 | ATGTATCTTGATTCA[A/C]ATTCACTTTGGATCC | 337867 |
rs191707061 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209633 | TCCCCACCAGTCTTA[A/C]GTTTTTGGGGGCTGT | 337867 |
rs191755170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314307 | CATTTGATCTCCTTG[A/G]AAACAATGGTTTTTT | 337867 |
rs191780050 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353799 | GAACAGACCACTGGA[A/G]TACCCATGAGCATCT | 337867 |
rs191792106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231786 | AAAATGTCACATGAA[C/T]TTATCATTGGAAGAT | 337867 |
rs191795389 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384363 | TGTGGCAATCTGGGG[A/C]CATGAATATTTTTGT | 337867 |
rs191803641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270645 | CATAGTTAGATAGAA[A/G]TTGATGGTTGATGGT | 337867 |
rs191808803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299319 | GAATACAGGAATACA[A/G]CCATGCAGTGAATAC | 337867 |
rs191818626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336679 | GACCACACTGTTTTA[A/G]GTAGCCAAACTTTAT | 337867 |
rs191836633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374031 | ATGCATGTCAAACGA[C/T]AGAATTACAGCAAAT | 337867 |
rs191854769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215483 | ATTCTTCATCTGCAC[A/G]AATAGCAAGTTGCAA | 337867 |
rs191856179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253199 | TGTGTTTTTCTCTTT[A/G]TTGAGAAACTGCATC | 337867 |
rs191994504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218844 | TCATTCCTCCTTAAC[A/G]TGGTCACCGAATCTA | 337867 |
rs192005138 | snp | A/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227205 | CTCCATCTCAAAAAA[A/T]AAAAAACAACAAAAA | 337867 |
rs192009895 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264230 | CAGGGAAATGTACAC[G/T]GTGACCTCAGGTTCC | 337867 |
rs192019699 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300972 | GCAGCTTCTGACATG[G/T]TATTTAAGATATATT | 337867 |
rs192021741 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257331 | TTTTTAACTGGAATG[C/T]ATTCTTATTAAATAG | 337867 |
rs192022243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282089 | CCTTTGCGGTGGGGG[C/T]GGTCCCGTGCACTGC | 337867 |
rs192027905 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292993 | GCTAACTAATAACAA[C/G]ACAGTGAGAGGATGC | 337867 |
rs192040277 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319103 | AGTCTCATCATGGAA[A/G]AAGGGAATGAACCAA | 337867 |
rs192042740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341744 | TAGCAGGAGGTAAAT[C/T]CTTCAAGGAAACTGA | 337867 |
rs192058311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294318 | TTTAGCAAGCAGACC[C/T]TCCTCCCAATGGGCA | 337867 |
rs192060437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361298 | TTTGAAGAAGACAAA[A/G]TAAAGGAAACATTTC | 337867 |
rs192066565 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378131 | GCGTTAGCATCATCT[C/G]CATCATCACTGTTGT | 337867 |
rs192085195 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371374 | TGATTATCCTGCAAA[C/T]AGCTGTTATAAACCA | 337867 |
rs192105776 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345725 | CTCTTGACAGGTACT[A/G]TTTCTTTTTTTCTTT | 337867 |
rs192106013 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99296769 | TTAAAAAGAAGAAGA[C/T]GACGACCGCAACAAC | 337867 |
rs192110878 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252485 | CTTTGCTTAGAAATT[A/G]TAGCTGACATGATAG | 337867 |
rs192111345 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288404 | GAAGCCACACAGTTA[A/G]CATGCAGATAGACAA | 337867 |
rs192117323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316426 | ATGAATGGATGAATG[A/G]ATGAATGAATGAATG | 337867 |
rs192120118 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380678 | CGCATACCCAAGCCC[A/G]AGCATGCAGTTTCAG | 337867 |
rs192127399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358154 | TAGAGAATGTGAGGG[C/T]GGTGTTGTGAGAAAG | 337867 |
rs192225223 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259152 | AAGGGAAGTGAGCAA[C/T]GAATCGCTGCCTGCC | 337867 |
rs192239624 | snp | A/C/G | 3.35109e-05 | 0.00409321 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296051 | TGCAGAGGCATTACT[A/C/G]TCCTGGCCGTGCTGT | 337867 |
rs192255202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222727 | ATGATGTATTCTTTT[A/T]ATATAATGCTAGGTT | 337867 |
rs192255759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333724 | CAGAATGGTCCTGCT[A/G]AAATTGAATACATAG | 337867 |
rs192269669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201899 | ACACGGTGAAACCCC[A/G]TCTCTCTACTAAAAA | 337867 |
rs192284795 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237770 | GACCAGTCTGGCCAA[C/G]ATGGTGAAACATGGT | 337867 |
rs192286883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276711 | GGTCTTCCTGCTGGT[C/T]GGCCAGCTCCATCTG | 337867 |
rs192290037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365774 | TCCATTCAGAAATAA[A/C]CTTGTTATTTTTTAT | 337867 |
rs192290470 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305717 | TACCATTGTCACTAA[C/T]GCGATACATAAACAT | 337867 |
rs192294436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324178 | CAGACACTTGTGGTA[G/T]ATTTTTTACTCTAGT | 337867 |
rs192299937 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207192 | TTGCATCCTTATTTG[G/T]TGAGAGGGCAGAGTA | 337867 |
rs192313765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225413 | TCATATAATATTTAT[A/C]TTTTTGTGACCGGCT | 337867 |
rs192322807 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199521 | CCCACTGGAACCTCT[C/G]TTTGAGGGTAGGGAC | 337867 |
rs192332922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243496 | AAAATGAACATTTGT[C/T]AGCCTTTCATTCTAG | 337867 |
rs192342406 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281459 | GTGTCCGGCATTGTA[C/G]TTGGTACTATGTCAC | 337867 |
rs192346718 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262747 | AAAAAAAAAGGACTT[A/G]TGGAAGGTAAAGGAA | 337867 |
rs192347850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300676 | TAGATGCTGGGAATA[C/T]AGAGATGGTACCTTT | 337867 |
rs192351133 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234049 | TACAAAGGGAGGTAC[A/G]GGGTTATTATATAAA | 337867 |
rs192357623 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384856 | GCGATGCCAGGGCTG[A/G]GCATGGGTCACCACC | 337867 |
rs192364547 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361567 | TTTGCATGTTTTTGT[A/G]TCTTTACTACATACA | 337867 |
rs192381527 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274969 | GCAGTCCTCCCACCT[C/G]CACCTCCCAAAGTGC | 337867 |
rs192385643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313830 | GAAAACATAGCCTCC[A/G]CTTTTCTCACACTTA | 337867 |
rs192439545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351266 | AGAGTCCTAATTTAG[A/G]AGCCAACCTTGATAG | 337867 |
rs192537681 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200653 | CTCAGGCGGTTCTGA[C/T]CGCCATCGTTTCAAC | 337867 |
rs192543491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236615 | CTAGTACTTTGGGAG[G/T]CCGAGGTGGGTATCA | 337867 |
rs192577395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266979 | CAGCAACACAATGCC[C/T]AGTTTCTCCCTATCT | 337867 |
rs192583596 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306404 | TAGGTAACTTGTGTG[G/T]GGGGGGGCCACACAG | 337867 |
rs192598190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201192 | ATCCCCAGGTGCTCT[A/G]CCCAGGAGTCTCTTG | 337867 |
rs192604468 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345927 | TTTGTATTTTTAGTA[A/C]AGACGGGGTTTCACC | 337867 |
rs192607580 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386013 | CGGGTGAAATGGGAT[A/G]GAGAAGAACAACAGC | 337867 |
rs192654317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276442 | ACGTATTTTACTTAC[A/G]TTTATTGGTTTATTA | 337867 |
rs192664882 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314906 | TTTCTTTTACTCTCA[C/T]GGCTTTTGATGTAGT | 337867 |
rs192706348 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382042 | TAATGATAGTGCAAT[G/T]AAGTGGGTTTGAAAC | 337867 |
rs192740890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378542 | AAAAATAAAATAAAA[A/C]ATAAAAACTTCAATA | 337867 |
rs192756470 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381589 | GGCAGGCCAGCTCCC[A/G]TTTGGCCTGAGTTAT | 337867 |
rs192787808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224857 | GAGTTAAAATTTTTA[A/C]GTAGTAAAAGTACAA | 337867 |
rs192825677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219870 | AATGTTTTTGAGGTT[A/C]ATCTATGTTGTAGCA | 337867 |
rs192841236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285559 | CACCACGCCCAGCTA[A/G]TTCTTAATTTTTTAT | 337867 |
rs192856368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289202 | TGTTGTAAGATCTAA[A/G]TTAAAACTATGTGGC | 337867 |
rs192859386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225885 | ATTATATTTGGCAGC[A/G]TTTATTTTTTAGTGG | 337867 |
rs192861364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262906 | TAAGACAAGTTACTT[A/G]GGATTTTTTATTATA | 337867 |
rs192861984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364784 | GTTGCATGTCATTCT[A/G]GTTCATTCATTCAAA | 337867 |
rs192867539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328322 | TGCTGTGAACATCTG[C/T]GTACACATTTGTGTG | 337867 |
rs192877877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367449 | GAGCTCCTAAGAGTT[A/G]ACTGGAGTTGGGACA | 337867 |
rs192911639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315329 | GGCCATGTGGAATTC[A/G]AAGAGCACTCCAGAC | 337867 |
rs192917405 | snp | A/G/T | 0.00123979 | 0.0248671 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356197 | GTGCTGGAGCTTCCC[A/G/T]ATGTACTCTGTAGAT | 337867 |
rs192952904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207696 | AAGGTCCACTGGTGT[C/T]AGCCTGTGGTGTGGA | 337867 |
rs192968596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211914 | ATGGCAGCCTCCTTC[C/G]TGGGTTCTACCATGC | 337867 |
rs192988921 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248326 | ACTCCTGGGTTCAAG[C/T]AGTCCTCCCAGCTCA | 337867 |
rs192995454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285058 | TCCAGACATCATAAT[A/G]TCATATTTCATATTT | 337867 |
rs193021994 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233136 | TTTTTTTTCTGAGAC[A/G]AAGTCTTACTCTGTT | 337867 |
rs193037448 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272882 | TATGTGTACATTGTG[A/G]GTCTGTGTGTGTATC | 337867 |
rs193037480 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340036 | AAAAAATGAAGACAG[C/T]GTCTTGACAATCTTT | 337867 |
rs193039632 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312562 | GGCATCTTACCGTGA[A/C]ATCCTTGGCACGCAT | 337867 |
rs193047680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377589 | CCATTATTTATATAG[C/T]CATCAGAGTTGTGTA | 337867 |
rs193060139 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244902 | CATTGGCACGATCTC[A/G]GCTCACTACAACCTC | 337867 |
rs193065444 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271658 | TTAGAGTTTTTAAAT[A/T]GTTTTTCACTTCTGC | 337867 |
rs193070535 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311223 | TAGGCAGTGATGAGA[A/C]GGCTGTAAGTGCTGT | 337867 |
rs193079413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349233 | TCCCTCCCTTTGCTC[A/G]CTGTAGCAAAGAAGC | 337867 |
rs193118649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221618 | TGTGTTCCTCCCATG[C/G]GGCTTCTTTTCTATG | 337867 |
rs193160556 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334412 | AACATCATTCAAATA[A/G]TGTCATTTCATTCAA | 337867 |
rs193164846 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372219 | AGATGTCTGCTCATG[C/T]CTTCCCTGTGCAGAC | 337867 |
rs193193878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228871 | AGATGCTCACAAGAC[A/C]TTACCAGAGAGGAAA | 337867 |
rs193195192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266201 | TTTATGAATATTTCT[A/T]TATTATATTACATAA | 337867 |
rs193218266 | snp | A/G/T | 0.000115358 | 0.00759392 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255097 | TAACTGTTCTCCCCC[A/G/T]TTCCCAGCATCAGGA | 337867 |
rs193220513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291391 | TTGTCACCGGGTCAC[G/T]TGTAATCCACATGCT | 337867 |
rs193220546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318854 | AAAGGCCAGTCACAG[A/G]GAAAATTGAGACAAA | 337867 |
rs193224386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360245 | TCTAGTTGGGAAGAC[A/G]AGAAACAATACTGTA | 337867 |
rs193227122 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329995 | CGTGATAAGTCTCTA[C/T]GTTTATTTAGCTCTT | 337867 |
rs193275864 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237254 | AAGAAAATTTTATGC[A/G]TATATATATATATAT | 337867 |
rs199500318 | snp | C/T | 0.00622225 | 0.0554293 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318013 | TTGCCTTTTTTTTTT[C/T]TTTTATAGCTTTTCA | 337867 |
rs199523206 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348954 | GGAGGTCAAGGTGCA[A/G]TCACGGCTCAAAAAG | 337867 |
rs199571345 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247204 | CTACTGTTTTTTTTT[-/G]TTTTGTTTTGTTTTG | 337867 |
rs199582904 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247224 | GTTTTGTTTTGTTTT[-/G]TTTTTCTTGAGACGG | 337867 |
rs199626458 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247953 | TTTCTAAAGCCACTG[C/G]CCATCCTCTTTAACC | 337867 |
rs199631215 | in-del | -/TATT | 0.0158469 | 0.0875917 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282582 | AAAAAGAAATAAAGA[-/TATT]TATAACTGTTGGGCT | 337867 |
rs199649179 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363028 | GTTTGGCTTTCCACA[A/T]TTAAATCTTTAATCT | 337867 |
rs199652984 | in-del | -/ATG | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353527 | TCAGAAAACAAGCAA[-/ATG]ATGATGATGTACTTG | 337867 |
rs199681759 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349882 | GCCTCCCACAAGAAG[C/G]TGGTGGAGCAGAGTG | 337867 |
rs199687530 | in-del | -/GA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368682 | TCATCGTAAACTCAT[-/GA]GAGAGAGTGTGTGTG | 337867 |
rs199704027 | snp | A/G | 4.9498e-05 | 0.00497459 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99318028 | CTTTTATAGCTTTTC[A/G]CCTCTGGTTCCTACA | 337867 |
rs199762287 | snp | A/G | 9.88484e-05 | 0.00702954 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255140 | TGTGGAAGGGCATAA[A/G]GCAGACGAGCACCTG | 337867 |
rs199769746 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235829 | AAAATTAGCCAGGTG[-/T]TGGTGGCTTGTGCCT | 337867 |
rs199829772 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315381 | CTAGTCCTAGCATGG[C/T]TGTCTCCAGCCATGA | 337867 |
rs199843492 | in-del | -/GT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214836 | GTTTGTAGACTGTGG[-/GT]GTGGGGAAGGGTTTG | 337867 |
rs199875385 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273878 | TTTTTTTTTTTTTTT[-/T]CCTGCTTTCTTTCTC | 337867 |
rs199911860 | in-del | -/AG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341418 | CCCAGAGTTTATATC[-/AG]GGGGGGGGAGGAAGG | 337867 |
rs199952291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344052 | TCTCTTGCAGAATTA[A/G]CATGTTTCACTCTTT | 337867 |
rs200031537 | in-del | -/ATG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337217 | AAGATTTTATTTTGA[-/ATG]ATATTTAATTTATGT | 337867 |
rs200042342 | snp | A/C | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256708 | TTATAAATTTCCATC[A/C]CCAAAAAAAAAAAAA | 337867 |
rs200057657 | snp | C/T | 0.000857505 | 0.0206886 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295695 | AGACAAATATGCACA[C/T]GCCTTTTGCATGTTC | 337867 |
rs200066003 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203058 | ATTTATTTATTTATT[G/T]AGATGGAGTCTCACT | 337867 |
rs200069112 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264986 | TTTTTTTTTTTTTTA[A/T]TTGTTCTTCAGTGTG | 337867 |
rs200070184 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382237 | AATGAGAATTGAAAA[G/T]AATTCATTTTGGTTG | 337867 |
rs200103186 | in-del | -/CT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280854 | TCTCTCTCTCTCTCT[-/CT]TTCTCACTCAGTAAG | 337867 |
rs200119357 | in-del | -/TGTGTGTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216083 | GTACCAACCTATATT[-/TGTGTGTG]TGTGTGTGTGTGTGT | 337867 |
rs200137156 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232449 | ACTCTAAGGACCAAA[A/G]GAAAAAAAAAAATCT | 337867 |
rs200208251 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210662 | TTGTGTTTTTAGTAG[A/G]GACGGGGTTTCTCCA | 337867 |
rs200227025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314231 | TGCAGGTACAGTATG[C/T]ATTTTTATGTTCACT | 337867 |
rs200269342 | in-del | -/TC | 0.49306 | 0.0584955 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207989 | TTTTGCCTCTCATCG[-/TC]TCTCTTTTTTTTTTT | 337867 |
rs200285046 | snp | G/T | 0.000161878 | 0.00899515 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243808 | TTACTCTTGTTTATT[G/T]TTCTTTTTTAAATCC | 337867 |
rs200303270 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228439 | ATTACAGGCTCCCCC[-/G]CACCCCACCACGCCC | 337867 |
rs200339558 | in-del | -/T/TT | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241739 | ACTTTTTTTTTTTTT[-/T/TT]CAACTTTTTTTTTTT | 337867 |
rs200374704 | snp | A/G/T | 0.000303065 | 0.0123064 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296060 | ATTACTATCCTGGCC[A/G/T]TGCTGTGATGTGCAT | 337867 |
rs200413364 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276180 | TTCCAACGCTAACAA[A/G]TAGTACTCCAGTTCT | 337867 |
rs200432720 | snp | A/G | 0.00199804 | 0.0315441 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296184 | AAAAAACCAAGAAGG[A/G]TCATATAAGTAAAAG | 337867 |
rs200483232 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285621 | GGTCTCAAACTCCTG[A/G]CCTCAAGTGACCCTC | 337867 |
rs200525385 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247128 | GGTGTGAGCCACTGC[A/C]CCCAGCCACAAATAT | 337867 |
rs200539103 | in-del | -/T | 0.0322114 | 0.122752 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307536 | TGTGTGCACTTTGTG[-/T]TTTTTTTTTGTTTTA | 337867 |
rs200598447 | in-del | -/AC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368727 | TGTGTGTGTGTGTGT[-/AC]ACATACCCTCACTCT | 337867 |
rs200620224 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334129 | TTCTTTTTATTTATT[-/C]TTATTTTTTTTTTAG | 337867 |
rs200647652 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356224 | AGATGTCTTTGCACC[C/T]TCTGTCCTCATTGCC | 337867 |
rs200669857 | snp | C/T | 3.29533e-05 | 0.00405901 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295182 | CTTGCCGTTTCAGCA[C/T]CCTCATAACCTTTCT | 337867 |
rs200683203 | snp | G/T | 0.000132778 | 0.00814686 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295574 | ATCCAGGGAAGAGAT[G/T]TAGTTTCTTCAAAGT | 337867 |
rs200720452 | snp | A/G | 0.000774179 | 0.0196593 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340443 | TCTTCAGAACCCACC[A/G]GCGAAGCCAGAATTG | 337867 |
rs200721643 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289401 | AAACCAACTAGACAA[A/C]CTTGAAAGGCCCATA | 337867 |
rs200730909 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303025 | CCTGCCTCCTGGGGG[C/G]TTGCTTTCTGGCTTA | 337867 |
rs200731624 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282230 | AATGACACTTGGGGG[-/A]GCAAAATCACCCATG | 337867 |
rs200755088 | in-del | -/TG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237262 | TTATGCGTATATATA[-/TG]TATATATATACACAC | 337867 |
rs200763660 | snp | A/G | 4.95585e-05 | 0.00497763 | missense, synonymous-codon, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238486 | CTCTCCCTCCTGCTC[A/G]CCCTCCTCCTGCCTC | 337867 |
rs200769929 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318100 | CTTTTACACCCAATT[C/T]TCTCTCTCTCCTGTA | 337867 |
rs200830529 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364325 | TGTTGCTAGTTTTTC[C/T]AAGATTTTTGAGATA | 337867 |
rs200832981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274409 | TGATCACAGCAGCCT[C/T]GACCTCCTGGGCTCA | 337867 |
rs200834301 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247209 | TGTTTTTTTTTTTTT[G/T]TTTTGTTTTGTTTTG | 337867 |
rs200850577 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249365 | GTTCCTGCAAAGGAC[A/C]TGATTTCATTCTTTT | 337867 |
rs200867882 | in-del | -/TTC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345742 | TCTTTTTTTCTTTCT[-/TTC]TTTTTTTTTTTTTTT | 337867 |
rs200887360 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268635 | AAAAAAAAAAAAAAA[A/G]AAACACAAAAGGTAA | 337867 |
rs200900247 | snp | C/T | 0.00199806 | 0.0315443 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295346 | AGCTTCTTAATCATA[C/T]GTTGAATAATTGCAA | 337867 |
rs200908851 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347192 | TAGAGAGTGCAAAGA[-/G]GGGAAAAAAAAGAAC | 337867 |
rs200931038 | in-del | -/A | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301645 | TCTAGCCGCAAAAGG[-/A]AAAAAAAATAAAAGG | 337867 |
rs200951517 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292730 | AGGGTTTTTTTTTTT[A/T]ATGTGGTCAACTGCC | 337867 |
rs200952492 | snp | A/G | 0.000197896 | 0.00994528 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295944 | AATTTGTTGAATAGA[A/G]GGTGGTAGAGTTGAT | 337867 |
rs201001697 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296593 | TTAATTTCAGTTGGA[-/T]TTTTTTTTTAACCAA | 337867 |
rs201004761 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210478 | TTTTCTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs201028910 | snp | A/G | 0.00176534 | 0.0296573 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385211 | CCCTCAGGTTTCTGC[A/G]TTTTCTCTGCCTGCA | 337867 |
rs201039765 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232450 | CTCTAAGGACCAAAA[A/G]AAAAAAAAAAATCTT | 337867 |
rs201071651 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242195 | CCCCACCTTTCCCCC[A/C]CTTCTATTCCACAAA | 337867 |
rs201108037 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232451 | AAAGAAAAAAAAAAA[-/A]TCTTCAAAGGTATCT | 337867 |
rs201170460 | snp | A/G | 6.58957e-05 | 0.00573964 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255225 | CTTAGACGTCCTGCC[A/G]TGAAGGAGATTATGA | 337867 |
rs201205227 | in-del | -/AG/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268630 | AAAAAAAAAAAAAAA[-/AG/G]AAAAGAAACACAAAA | 337867 |
rs201273165 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258788 | GAAAGATCCCAAGTG[C/T]TTAATAGTACCTGGC | 337867 |
rs201307900 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292718 | TAAATAGCTTTGAGG[G/T]TTTTTTTTTTTAATG | 337867 |
rs201350547 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346263 | GTAGTTCAGGCCACC[A/G]GCGCCATTTGCCTGG | 337867 |
rs201376219 | snp | G/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256710 | ATAAATTTCCATCAC[G/T]AAAAAAAAAAAAACC | 337867 |
rs201377496 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213221 | ATAACTTTTTTTTTC[-/A]ATTTTTTTTTTTTAT | 337867 |
rs201390013 | in-del | -/TC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345743 | CTTTTTTTCTTTCTT[-/TC]TTTTTTTTTTTTTTT | 337867 |
rs201394149 | in-del | -/AC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237272 | TATATATATATATAT[-/AC]ACACACACACACACA | 337867 |
rs201415219 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274500 | TGGCTAGTTTTTTTT[A/T]TTTTTAGTAGAAACA | 337867 |
rs201415603 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247214 | TTTTTTTTTTGTTTT[G/T]TTTTGTTTTGTTTTT | 337867 |
rs201462641 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305292 | TCAGAGGATTCTCAC[A/G]TGTGTTATCTCATTT | 337867 |
rs201543366 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317352 | TCAGAGTCCTTATGA[-/T]TTTTTTTTTAATTAC | 337867 |
rs201552661 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218510 | TTTTTTTTTTTTTCC[A/G]TGGAAACTTCTTAGC | 337867 |
rs201554689 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252330 | GGCTGTTTGAGGGGG[C/T]ACCAAGTTTTACTTT | 337867 |
rs201584591 | snp | C/G/T | 3.29692e-05 | 0.00406001 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255082 | GCTCCCCAGGGATTG[C/G/T]AACTGTTCTCCCCCG | 337867 |
rs201594389 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245760 | GAATCACTTGAACCC[C/G]GGAGGCAGAGGTTGC | 337867 |
rs201609724 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337020 | TCATCATCTTTGCGC[-/T]TTCCTGTCTCGTTTT | 337867 |
rs201620105 | snp | A/T | 5.05055e-05 | 0.00502496 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295851 | ACAAGGCATCTCCGA[A/T]TCTCCAGTCAAAGCC | 337867 |
rs201628121 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341418 | CCCAGAGTTTATATC[A/G]GGGGGGGGGAGGAAG | 337867 |
rs201631345 | in-del | -/A | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307709 | CAATAAACCTTAACC[-/A]AAAAAAAAGACCAAG | 337867 |
rs201659138 | snp | A/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303019 | AGAAAGCAAGCCCCC[A/C]GGAGGCAGGGGAGGT | 337867 |
rs201671130 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268637 | AAAAAAAAAAAAAGA[A/G]ACACAAAAGGTAAAG | 337867 |
rs201680506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201635 | TGTGGAATTGACTTT[C/T]GGTAAGGTAGACTGC | 337867 |
rs201712233 | snp | C/T | 0.00211429 | 0.0324449 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99244567 | TTGACTTTCTCCTCA[C/T]TGAAGCTATGCAGTA | 337867 |
rs201744264 | in-del | -/T | 0.187053 | 0.241946 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242152 | TTTCTACACAGAGAC[-/T]GGCAACCATCCGATT | 337867 |
rs201755595 | snp | C/T | 0.000298374 | 0.0122106 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295395 | AGAGAACAAACACAA[C/T]AATAATAAGAATAAT | 337867 |
rs201760336 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341387 | AGGTCCTTAGAGTCC[C/T]ATTGGAGATGCAGGT | 337867 |
rs201807572 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247205 | TACTGTTTTTTTTTT[-/G]TTTGTTTTGTTTTGT | 337867 |
rs201809418 | snp | A/G | 0.000774472 | 0.0196631 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99318043 | ACCTCTGGTTCCTAC[A/G]TCTGGATTGTAGCCA | 337867 |
rs201858255 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214839 | TTGTAGACTGTGGGT[G/T]GGGAAGGGTTTGAGG | 337867 |
rs201880129 | snp | A/G | 4.94246e-05 | 0.0049709 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367860 | ACTATCAGGGCGGTC[A/G]GCAGTCTGAGCCAGC | 337867 |
rs201898192 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305293 | CAGAGGATTCTCACA[C/T]GTGTTATCTCATTTT | 337867 |
rs201905018 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273003 | TAGAACAGGTTACTC[-/T]TTTTTTTTTTTTGGT | 337867 |
rs201953194 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345741 | TTTCTTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs201970091 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287427 | TCTTAACTGCTGTTC[-/T]TTTTTTTTTTAAATT | 337867 |
rs201976833 | in-del | -/TTTCTTTTTTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287640 | CTTCTTTTTTTTTTC[-/TTTCTTTTTTTTTTTT]TTTTTTTTTGGTAGA | 337867 |
rs201978913 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203060 | TTATTTATTTATTGA[G/T]ATGGAGTCTCACTGT | 337867 |
rs202049006 | snp | C/G | 1.66649e-05 | 0.00288655 | stop-gained, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254908 | TTTATATTGCTTAGT[C/G]ACCGTAGACTACCAG | 337867 |
rs202060909 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349729 | TTTCTTCTACTGCTA[C/T]CTACTACGAACTTCA | 337867 |
rs202068254 | snp | C/T | 0.00299544 | 0.0385843 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367707 | CTATAGATGTAACTG[C/T]ATTGAGAGAAAGCTC | 337867 |
rs202099334 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247873 | TAATTCTCTCTCTCT[A/G]TTTTTTTTTTTACCT | 337867 |
rs202121468 | snp | A/T | 1.89328e-05 | 0.00307669 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296189 | ACCAAGAAGGATCAT[A/T]TAAGTAAAAGCATAT | 337867 |
rs202148578 | in-del | -/TA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235806 | TGGCAAGACTATTTC[-/TA]TCCAAAAAAAAATTA | 337867 |
rs202154292 | snp | A/T | 0.000430437 | 0.014664 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254887 | ATTATTCATAACATT[A/T]CACTGTTTATATTGC | 337867 |
rs202199802 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383405 | GTTTTTTGTTTTTTG[-/T]TTTTTTTTATCTACG | 337867 |
rs202220209 | snp | A/G | 0.00023892 | 0.0109272 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201380 | CAAAGTTCAGCCTCC[A/G]CTTTAGAAGCTGACC | 337867 |
rs207474305 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362703 | TTGAGTCACTTATTT[C/T]TTTCTCATTGATTTA | 337867 |
rs367589490 | in-del | -/CAAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245562 | TCTCAAACAAACAAA[-/CAAA]AAAACAGGCCGGGCG | 337867 |
rs367603189 | snp | A/G/T | 4.94534e-05 | 0.00497239 | missense, synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254969 | GGTAATTACGGTATA[A/G/T]CATGACACTAATGAC | 337867 |
rs367609501 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320111 | TTTTTAAAACACATT[C/G]CATTTTCTTTCTTTA | 337867 |
rs367617257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299316 | GTAGAATACAGGAAT[A/G]CAGCCATGCAGTGAA | 337867 |
rs367630089 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200529 | CAGCGCCGGCAATCC[A/G]GGGGAATCCGCGGCC | 337867 |
rs367645175 | snp | G/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340444 | CTTCAGAACCCACCA[G/T]CGAAGCCAGAATTGG | 337867 |
rs367651389 | snp | A/G/T | 8.23953e-05 | 0.00641807 | stop-gained, synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255489 | TTTAAGTTCTTTGGC[A/G/T]TACTTCGGCTGTACA | 337867 |
rs367659001 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243516 | TTTCATTCTAGTTTA[C/T]GTATATAATTTTAAA | 337867 |
rs367670011 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316270 | TCAACTCCCCCTGTG[C/T]CCACCTTGAAGGAGT | 337867 |
rs367670849 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265550 | CTCTCTTTGACAGTC[A/T]TGTGGGTACTGATCC | 337867 |
rs367700017 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335247 | GTACTACATTTTTAA[A/T]ATTTTGTTATGTTTA | 337867 |
rs367739224 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238198 | GTCTCATTTAAGAGC[C/T]AACTGGCAATGAAGC | 337867 |
rs367763416 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214603 | GAAGCTGCCTTTCTT[A/C]TTACCCTCCTTGTCC | 337867 |
rs367782408 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321807 | TTTCTGAGTTGAGGG[A/G]AGACAGTTTTTAGCT | 337867 |
rs367791975 | snp | A/G | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351726 | AGCAGAACTAAGGTG[A/G]AGCCCAGTGTGAATG | 337867 |
rs367795735 | snp | A/C/T | 3.29719e-05 | 0.00406018 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255640 | GCATAATAAAACATT[A/C/T]GAAAGGGTAAAGTCA | 337867 |
rs367799941 | in-del | -/CA | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305918 | ATTTATCTATCGAGA[-/CA]GAGTCTCGCATGGTC | 337867 |
rs367850704 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345712 | ACTGTCCCATCAGCT[C/G]TTGACAGGTACTGTT | 337867 |
rs367889098 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99254135 | TCTTTTGTAAAAATG[G/T]TATCTTCAACCACAT | 337867 |
rs367902368 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217852 | TAGGTGGGTGGCAGC[A/G]TCCACCGAGCTCGTG | 337867 |
rs368015812 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272662 | TTACATGGCTGAGAG[A/C]GCTCACTTTGGTCTC | 337867 |
rs368050221 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283968 | TCAAACTCCTGACCT[C/T]GTGATCTGTCTGCCT | 337867 |
rs368054886 | in-del | -/GT | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353167 | TTCAAGAGTTTATAA[-/GT]ATATAGCATCAGATG | 337867 |
rs368089393 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320380 | AAAAATCCCTTGTTT[C/T]AGAAGGGTGAATAGA | 337867 |
rs368107105 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332054 | TCATGCAGAGGCAAT[A/G]TCATGCCCCTGGGAA | 337867 |
rs368124948 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366655 | TCCCTTTCGCTGAGG[A/G]TGCTGCCATTTGAAG | 337867 |
rs368138868 | in-del | A/GG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341423 | AGTTTATATCAGGGG[A/GG]GGGAGGAAGGGGGCA | 337867 |
rs368153146 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281054 | AGCCAGGTGTGTTGG[C/T]GGGCACCTGTAATCC | 337867 |
rs368166968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226840 | ATATCTGCAAGGCCT[A/G]CATCTTCAGGTCTCT | 337867 |
rs368169438 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239008 | TTCTCTTGAGTTTCT[G/T]CTGTGGGAAAGAGCA | 337867 |
rs368183230 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352689 | TTCCGCAGAATACAC[A/G]CAGTGCCAGGCTCTG | 337867 |
rs368247102 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229986 | GTGAATTGTCATACA[C/G]CTTTCTGAGTTTGGC | 337867 |
rs368270365 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344443 | TTATGTTTCAAATAC[A/G]TGTTTTTGTTGTTTG | 337867 |
rs368278575 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247219 | TTTTTGTTTTGTTTT[G/T]TTTTGTTTTTCTTGA | 337867 |
rs368306557 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261629 | ACACTTAACCTCACA[A/G]CAAACAAGTTGAATC | 337867 |
rs368351318 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327102 | TATTTAACTGGTCCT[C/G]TCTCCATGCTTGGTT | 337867 |
rs368358584 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337910 | TCTAGTCCAGGGGTA[C/T]CTAGTCTTTTGAACT | 337867 |
rs368378847 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350110 | TATATTAGTAATGCA[A/G]CAAAGAGTAATATTA | 337867 |
rs368386095 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309781 | AATTTTTGTATTTTT[G/T]TGTGTGTGTGTGTGG | 337867 |
rs368418472 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284970 | AATGAGCCCTATTAC[C/G]CAGATTCAGTAATTA | 337867 |
rs368428676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240360 | TTTAAAACTGTAGCT[A/G]GCAGCTTTATTTTCA | 337867 |
rs368461325 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380495 | CCAGTTCTTACTGTC[C/T]ATATGGTGAACCTCT | 337867 |
rs368466610 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378086 | CCATCACATATTTTC[C/T]CTGTGTCGTCTGTAG | 337867 |
rs368541419 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242708 | CACCTCCCTCCCCGA[C/T]GGGGCGGCTGGCCTG | 337867 |
rs368551471 | in-del | -/T | 0.030665 | 0.119967 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312966 | TTTTTTATTTTTTTT[-/T]GTTTTTGTTTGTTTG | 337867 |
rs368551795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303892 | CGTGAAGGCGCCCAG[G/T]ACTCCGTGTTCTCCC | 337867 |
rs368578745 | in-del | -/CC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204900 | GGGGGAGTTTCGTTT[-/CC]TTTTTTTTTTTTTTT | 337867 |
rs368602296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334594 | CCAAATATATTATGC[C/T]CAATTTTGAATGCAT | 337867 |
rs368629370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357341 | TTAAGCGACACGTGA[C/T]TACAGTTTTAAGTCT | 337867 |
rs368632904 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337754 | CACATGGACCCTCCT[G/T]GGTTCATGCCCTACA | 337867 |
rs368659305 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209664 | ATTATTGAAACTTCC[A/G]AGGAATATACTCTTC | 337867 |
rs368662275 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289064 | ATTATCTAACACTTA[C/T]TTCACTGACAAGACA | 337867 |
rs368666458 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342686 | CTGTGGTGGATGCCC[A/G]TGGTGGGCACGACCT | 337867 |
rs368675351 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340307 | ACAATCACATTGGAC[A/G]TTTTTCTTCTAGATG | 337867 |
rs368679575 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358686 | GAGCCACCCCGGCCA[A/T]GGACTGTGGTCTCAC | 337867 |
rs368694271 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374250 | TTAAAGCAGAGGGGA[A/G]TTCCTTATTATGCTG | 337867 |
rs368694443 | in-del | -/CA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268641 | AAAAAAAAAGAAACA[-/CA]AAAGGTAAAGAAGGT | 337867 |
rs368709386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384819 | TGATGCCAGGGCCGA[A/G]CGTGGCAGTGATGCC | 337867 |
rs368716317 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250712 | CATGAGAATGGAATG[C/T]TTTTTCCATTTGTTT | 337867 |
rs368723592 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223368 | CTTCTCTCTTTTTGT[A/C]CTGATCATTTCTGCT | 337867 |
rs368745279 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259892 | CACGGTGCACAGGGG[C/T]ATTCTTGTTTCTGAA | 337867 |
rs368759384 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286130 | TTTTCAGCAATTGTA[-/A]TAAGCACCGAATTCT | 337867 |
rs368770523 | snp | A/T | | | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352441 | TATGTAGCTGATCTT[A/T]ATGACTGGCTTCTTT | 337867 |
rs368779969 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202049 | CTGCACTTTGGCCTG[G/T]GCGACAAAGCGAGAC | 337867 |
rs368786123 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257254 | ATGAGGAAAGTGCTA[C/T]AGAGAAAAATTATAT | 337867 |
rs368791023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328213 | AATAGATTAAGTATT[A/C]ATCTATAGTATGGAT | 337867 |
rs368791975 | in-del | -/GA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237494 | GGGAAGGGTAGGAGG[-/GA]GAGGGGGATAAAAAG | 337867 |
rs368815046 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199670 | CAATTTTCCCCATAA[C/T]ATGCGTTCTCACATA | 337867 |
rs368834775 | snp | A/G | 3.31225e-05 | 0.00406941 | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356247 | TCATTGCCATCCCCA[A/G]TCAGTCCCTGGAACA | 337867 |
rs368836074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247245 | CTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 337867 |
rs368859180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336152 | CCATTTGAGTTTTCT[C/T]TTCTGAAATTACCTT | 337867 |
rs368868428 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341723 | CTACAGATGAAGCCT[C/T]GTATTTAGCAGGAGG | 337867 |
rs368870276 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309191 | TGTCGGCTCACTGCA[A/G]CCTCCACCTCCCGGC | 337867 |
rs368886705 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377820 | TCACTGTTCTGGGCT[G/T]CTCACATGCATCCCT | 337867 |
rs368934456 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359936 | TTCACACTTCAAAAC[C/G]TGGCATGCTGATAAA | 337867 |
rs368955362 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319257 | ATTCTTCATCCATGA[C/G]TTAAATTTAAACCTC | 337867 |
rs368956198 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323416 | CACCAGCCTGGCCAA[C/T]ATGGCAAAACCCTGT | 337867 |
rs368965405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306112 | TGTTGGCCAGGCTGG[C/T]CTCGAACTCCTGATC | 337867 |
rs368971706 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338717 | TCTTCAGCCTACTAC[A/T]GTCTGTCTTTGGTAC | 337867 |
rs368990134 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383844 | AGGCTTTTGGGGGAG[A/G]AGGGTCTGGGTGTCT | 337867 |
rs369028428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272924 | CTATTCCATTGGTCC[A/G]TGTGTCTGTTCATGC | 337867 |
rs369037314 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368681 | TATCATCGTAAACTC[A/G]TGAGAGAGTGTGTGT | 337867 |
rs369068641 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210640 | GCACCACCACGTCCG[C/G]CTAATTTTGTGTTTT | 337867 |
rs369076377 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313605 | AGTGGTGTAAGAAAT[C/G]ACTGGGCAACCACTG | 337867 |
rs369080392 | snp | A/G | 3.3065e-05 | 0.00406588 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367945 | ACTCATTCTAAATCC[A/G]TGTTTCAGAGTTGAA | 337867 |
rs369099228 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218715 | AGGAGCTGATTGATG[A/G]ATGGCTTCCAGTGTT | 337867 |
rs369102336 | snp | C/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201086 | AACCCTGCTAGTTCC[C/G]GGTCTTGGGGGTCAG | 337867 |
rs369170599 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382648 | ACAGGAATGAGCAAA[A/G]GCAGCCACAGCCCTC | 337867 |
rs369180907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206816 | TATTCTCAGTCTCTC[C/T]CCATCTCTTCACCCA | 337867 |
rs369182254 | snp | A/T | 0.0748431 | 0.178382 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213222 | TAACTTTTTTTTTCA[A/T]TTTTTTTTTTTTATT | 337867 |
rs369203911 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237217 | AGTTTCCAATGAATG[A/G]GAAAAAAATGGATGA | 337867 |
rs369221388 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261465 | TCTTAAGTCCCAACA[A/G]TTTACAGCTATAATC | 337867 |
rs369232404 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311304 | GAGGGCGGGAGGTGC[G/T]GTTTGAAATGGGGCA | 337867 |
rs369235637 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240875 | TTTGACAGTTGATAT[A/G]CTCAGACTTCTCATT | 337867 |
rs369239487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261940 | AGTTACCTTCAGTCA[A/G]ATATGGTCTGAAAAT | 337867 |
rs369256359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305497 | GTAAGCTTCTTGAGG[A/G]TGATGACTTGATCTC | 337867 |
rs369256528 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323061 | TGGCCTGCTTCTGGG[C/T]GAGGGATGGTAGGTG | 337867 |
rs369257399 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371094 | TTTGGGCACTTCAGG[-/A]AAAAAAAAGTGTCAA | 337867 |
rs369303917 | snp | C/G | 3.5197e-05 | 0.00419491 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255854 | GGACAGGTTGATCTT[C/G]ATTGTTCAGGGTGAT | 337867 |
rs369313889 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215809 | AGGGCTAATCAGACC[C/T]GTGGTGAGATCCCAC | 337867 |
rs369336452 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295050 | ACTATAAACCAAAAT[A/G]CAATCCATTTCACTT | 337867 |
rs369342839 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203023 | ATTTCCTTTGTTTTA[-/T]TTTATTTATTTATTT | 337867 |
rs369364227 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198762 | CTAAAGTTTACTGGT[A/G]TATTTTATGGTTCAA | 337867 |
rs369384308 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313870 | GAACCACTTCTTTGC[A/G]GTGGTTTCAGGAGGG | 337867 |
rs369389101 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336913 | ATGGTGCCCCCCTTC[C/G]TTCCCACCTCTCTTC | 337867 |
rs369443935 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99307359 | CAGTGACTCGTTCGG[G/T]TCTCTGTGTAGTAGC | 337867 |
rs369475888 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234332 | AAGTGGGATTATAGG[C/T]GCTTGCCACCACGCC | 337867 |
rs369486895 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376412 | GACACCTCCAAGAGG[A/G]TCTTCATCCCTGTGG | 337867 |
rs369499931 | in-del | -/TG/TGTG | 0.263128 | 0.255491 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327484 | TTTTCTCTCTCTCTC[-/TG/TGTG]TGTGTGTGTGTGTGT | 337867 |
rs369517206 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294564 | CCTGCTCTTTATTCC[A/G]AAAGAGTTCCTTAAC | 337867 |
rs369522853 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347043 | AGCACTTTGGGAAGC[C/G]CAGGCGGGCAGATTG | 337867 |
rs369537134 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289022 | AATAGACCATAGACC[A/G]TACGATGGCTGGCAA | 337867 |
rs369542909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263772 | AATAAGTCACTTGTG[A/G]TGTAGGCATAGAGTG | 337867 |
rs369545447 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355481 | GGCATGCTCTTCCTG[C/T]GCTGATGTCCCTGAC | 337867 |
rs369547058 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236253 | AGCAAAAGAAACAGT[C/T]AACAAAGAGATAACC | 337867 |
rs369556566 | snp | A/C/G | 0.000153988 | 0.00877328 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201452 | AAGAGTTTTTAGACA[A/C/G]ACACACACTGATGAG | 337867 |
rs369562259 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368686 | TCGTAAACTCATGAG[A/T]GAGTGTGTGTGTGTG | 337867 |
rs369611878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276531 | GTGCACGGAGCTCTC[A/G]TGCCTTCTGTGGGCA | 337867 |
rs369614491 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244259 | TGTTTTACTTGTTAA[A/G]AATATATCTTCAACA | 337867 |
rs369636634 | in-del | GGG/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341421 | AGAGTTTATATCAGG[GGG/T]GGGGAGGAAGGGGGC | 337867 |
rs369637540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312006 | TCCCCAGTCCTGACA[C/T]AGTGCCTGCACTTAG | 337867 |
rs369646056 | snp | A/G | 1.83448e-05 | 0.00302854 | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99296162 | GGTGGTGGTCCAGGT[A/G]TCTAGAAAAAAACCA | 337867 |
rs369652694 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355537 | ACCCTGTGGTCCCCC[C/T]ACGCCACCCTCTCAC | 337867 |
rs369656328 | in-del | -/C | 0.000525708 | 0.0162043 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314262 | TTTCTTTAACCAGAT[-/C]TTTTTTTTTTTTTTT | 337867 |
rs369661782 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343757 | TTCACTCAGCTGTGT[C/T]TCAGTTTTCTTCACA | 337867 |
rs369665605 | snp | A/T | 1.65952e-05 | 0.00288051 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295580 | GGAAGAGATTTAGTT[A/T]CTTCAAAGTTTGGAT | 337867 |
rs369678412 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281914 | TACCAGGGAGCAGAC[C/T]TAATGTATCCAGTTT | 337867 |
rs369741053 | snp | A/G | 4.98741e-05 | 0.00499345 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356094 | AAAAGAAATGTCATT[A/G]AAGTAAACAAGACTT | 337867 |
rs369747931 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214811 | CCAACTGGGATGGTG[A/G]TGAAAAGGCTGTTTG | 337867 |
rs369776304 | snp | C/T | 3.31093e-05 | 0.00406861 | intron-variant, stop-gained, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201562 | CGTGTTAGCGGTGGT[C/T]AGCAGGTAGGGGGCG | 337867 |
rs369781239 | snp | A/C | 4.96389e-05 | 0.00498166 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356146 | GTACACAGTAGAAGC[A/C]TCCCTTGCAGGGGCT | 337867 |
rs369781516 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314109 | TAGCCTGGCACCTGT[A/G]TTTGCTCTGTTTGTA | 337867 |
rs369791446 | in-del | C/GGG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341420 | CAGAGTTTATATCAG[C/GGG]GGGGGAGGAAGGGGG | 337867 |
rs369809735 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248870 | CTCAAAGAAAACTCA[C/T]GTTCAGAAGCTCTCT | 337867 |
rs369831242 | in-del | -/AAT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219665 | TCTTCTTTTCCAGTG[-/AAT]TGGCCCAGGGAAACC | 337867 |
rs369846618 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371667 | TGTTTGTATTTTCTT[C/T]ATTTAAATATCAGAG | 337867 |
rs369860759 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207994 | GCCTCTCATCGTCTC[-/T]TTTTTTTTTTTTTTT | 337867 |
rs369861060 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99356878 | TGGTGAATGTGTTGC[C/T]AGTTTGTGTGTGGTT | 337867 |
rs369879817 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228646 | CACTTTTGAGGTAGG[G/T]TCTCATCTCCATTTT | 337867 |
rs369889090 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300389 | GCTAGCTGGCCCTAA[A/T]ATGTCACTTTAGTTC | 337867 |
rs369893966 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268362 | TCTCACCTGTAATCT[C/T]GGCATTTTGGGAGGC | 337867 |
rs369896954 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335909 | CCTGGAATCCCAGCA[C/T]TTAGGGAGGCAGAGG | 337867 |
rs369903981 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375570 | AGCGTCAGAATATGG[A/G]AAGTAAAAACCCAAA | 337867 |
rs369951570 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291582 | TACTCAATGGTAGGA[A/G]CCACTGTCTGCCCTT | 337867 |
rs369959344 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328577 | TGGTTTTAATTTGCA[G/T]TTCTCTAATGATTAG | 337867 |
rs369995186 | snp | A/C/G/T | 8.23646e-05 | 0.00641694 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255182 | TGATGATGATCCTTA[A/C/G/T]GGACTTCTCCTTGAC | 337867 |
rs370006065 | snp | C/T | 0.000214163 | 0.0103458 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367859 | AACTATCAGGGCGGT[C/T]GGCAGTCTGAGCCAG | 337867 |
rs370008781 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222783 | TTTTGCATCTGTTAA[C/T]ACGTTCATAAAGTAT | 337867 |
rs370025197 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378710 | ACAGGCCAGAGGTTG[A/T]GTCAGGCTTGCATAG | 337867 |
rs370039128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321471 | ACGCCACCAAGCCCG[G/T]CTACTTTTTTTGTAT | 337867 |
rs370049415 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379665 | TTTTCATTAATTTCT[C/G]TTTATCACTTTTAGC | 337867 |
rs370064261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249820 | TTTGCATTTCTTGAT[A/G]ATTACCTTTGAGCAT | 337867 |
rs370067010 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269699 | ACATTTTTCATATTA[C/T]TACTACGAATTCTTA | 337867 |
rs370106352 | snp | G/T | 0.00398564 | 0.0444627 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200792 | TTCGTCAGCGGCGAG[G/T]GGCCTCGCGGCGCCG | 337867 |
rs370118227 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373338 | AAGCTTAGAAAATGA[C/G]TGTTAGGTAAAATCA | 337867 |
rs370150616 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377580 | TCTATAATACCATTA[C/T]TTATATAGTCATCAG | 337867 |
rs370156548 | snp | G/T | 0.0114868 | 0.0749095 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356120 | GACTTGGGACACATG[G/T]CTGTCAGACTGTACA | 337867 |
rs370176443 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214837 | GTTTGTAGACTGTGG[G/T]TGGGGAAGGGTTTGA | 337867 |
rs370198611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277358 | TGGAGAAACCCCGTC[C/T]CTACTAAAAATACAA | 337867 |
rs370272167 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267218 | TGCCCATTTGTTAAT[C/G]TTTCTTGGTTGTTGA | 337867 |
rs370286403 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351305 | CGTAAAAGCTTGTAA[A/C]CTCTAGAGCAACAGT | 337867 |
rs370292225 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341554 | GCCCATGGTGTATTT[A/T]AAGCTGGAGGATGGA | 337867 |
rs370310695 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209304 | CTTCACGGGAGGGAA[C/T]CCTCACATTCCACTG | 337867 |
rs370330640 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242402 | CTTCCCAGTAGGGGC[A/G]GCCGGGCAGAGGCGC | 337867 |
rs370331461 | snp | C/T | 3.29701e-05 | 0.00406005 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255446 | TTATCCAGACTCCCA[C/T]ACACGCCAGCACGGC | 337867 |
rs370340638 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326150 | TTTGCATTTCTGCCA[A/G]CTGTGCACAGGGGTT | 337867 |
rs370364634 | snp | A/G | 0.000121182 | 0.00778307 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385384 | GCCGAGTGACAGTGC[A/G]TGGTCCCCACCATCA | 337867 |
rs370380272 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324734 | ACGTTTTGATCAACA[A/G]CAGAGTGCGTATTCA | 337867 |
rs370390118 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355904 | CTCCAGAGTCCCTTC[C/G]CTGCACCTCCAGGGC | 337867 |
rs370396713 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198589 | CCTGGCTTCACCTAG[A/C]TACACCCCCACGGTT | 337867 |
rs370488292 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324430 | AAGCAGGGCCCGGAG[A/G]GGGGCAGCTCCTCAG | 337867 |
rs370491199 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242288 | GTGGCCGGGCAGAGG[C/T]GCCCCTCACCTCCCG | 337867 |
rs370498237 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225691 | ATGAGGGATGCTGCA[A/G]CAAGGAATGTACCAG | 337867 |
rs370509504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308004 | TTGAATAACAGGGAA[A/G]CAGTTGAAGGGAGGC | 337867 |
rs370514601 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265012 | GTGTGTATGTTTTTT[A/G]CCATATTTTAAATTT | 337867 |
rs370547441 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334150 | TTTTTTTTAGAGATG[A/G]GGGTCTTGCTCTGTT | 337867 |
rs370551534 | snp | C/G | 0.000708419 | 0.0188071 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318108 | CCCAATTCTCTCTCT[C/G]TCCTGTAAAAACATT | 337867 |
rs370562281 | in-del | -/TTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223543 | CTTTCTCTTTTTCTG[-/TTTTT]TTTTTTTTTTTTTTT | 337867 |
rs370593541 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209607 | CTCGTTTACTCTTGG[A/G]GACACACTCTTCCCC | 337867 |
rs370617291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384498 | TTCACAGAATCAGGA[C/T]TTGTGGTCAAAAACA | 337867 |
rs370619291 | in-del | -/ATGGATT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281813 | AGAGGTACTTACCTT[-/ATGGATT]GCTGGCTAATTGTGA | 337867 |
rs370652520 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202095 | AAAAAAAAAAAAAAA[-/G]ATCTGTTGGGAATGT | 337867 |
rs370672393 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316213 | ATAAAATCTAGGTCC[C/T]TAGCATGAATGGCAT | 337867 |
rs370676779 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297247 | AGCAGGAAGAACAGA[A/G]CAATAAATCCTGTGT | 337867 |
rs370686759 | snp | G/T | 0.000153988 | 0.00877328 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255891 | ACAGCTTGTTGGTAG[G/T]CATGATACTTAGAAA | 337867 |
rs370699755 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348958 | GTCAAGGTGCAATCA[C/T]GGCTCAAAAAGAAAA | 337867 |
rs370728716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318558 | AGGCGCAGTGACTCA[C/T]GCCTGTAATCCCAGC | 337867 |
rs370729217 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242196 | CCCACCTTTCCCCCC[C/T]TTCTATTCCACAAAA | 337867 |
rs370735266 | snp | C/G/T | 0.000165196 | 0.00908702 | missense, synonymous-codon, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238492 | CTCCTGCTCGCCCTC[C/G/T]TCCTGCCTCACTGCC | 337867 |
rs370758689 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245562 | TCTCAAACAAACAAA[A/C]AAAAAAACAGGCCGG | 337867 |
rs370791897 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371313 | GTTGTTTTTAACATA[C/T]ACTTTCTTATACATT | 337867 |
rs370794732 | snp | A/G/T | 0.000182181 | 0.00954266 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238393 | TAAATCTTAGGAACA[A/G/T]TCATTCTGAAAGTGC | 337867 |
rs370836811 | in-del | -/TA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223905 | TTTATGCCCAGAATA[-/TA]GTCTATTTTGGTGAA | 337867 |
rs370897782 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211670 | AGTAACTTTCCTGCT[C/G]AGGAGCAGGTCTAGG | 337867 |
rs370928373 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283557 | CCACAAGCAGACTTG[C/G]AAGAGTAGATGTTGC | 337867 |
rs370935252 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253519 | TTTCCAGAAATTAAT[C/T]TCTTTTTTTTTTGAG | 337867 |
rs371014489 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217487 | GTGTGGCCTGGGGAC[A/G]TTCCAGCACCATCTT | 337867 |
rs371016326 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259738 | CTGCATGCAGACCTA[A/G]TCTGTCCTTTGCCTT | 337867 |
rs371101437 | in-del | -/TAA | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291014 | GGTGGAACCTCTTAC[-/TAA]TAACCAAGTTTCAGT | 337867 |
rs371104353 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253427 | TCTAAGGGACCTTCT[A/G]GTGCAAAAATGCCAT | 337867 |
rs371163027 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302960 | GAAGGATTGAGAACA[A/T]TGATATTCAGCATAG | 337867 |
rs371174116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217510 | ACCATCTTTGTAGCT[C/T]GGGCAGCCTTACTTG | 337867 |
rs371176615 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239121 | AAATTCTGGTATATG[A/T]CTGCTACCCTTTCTT | 337867 |
rs371189661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265303 | CGCTCAGCAAGCCAC[A/G]GTCTAAAGAGAGTCT | 337867 |
rs371189899 | snp | C/G/T | 0.000149224 | 0.00863663 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340299 | ACATTTAAACAATCA[C/G/T]ATTGGACGTTTTTCT | 337867 |
rs371193541 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336277 | ATACTTTCTTCAGGC[C/G]TCTTGTGTTTTCATT | 337867 |
rs371195004 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292316 | AATTTTTTTTTTTTT[A/G]TATTTTTAGTAGAGA | 337867 |
rs371284241 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230821 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCATGAGG | 337867 |
rs371286261 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205766 | TCGCCAGAGTTGATT[C/T]GGCTGATCTGGCTGG | 337867 |
rs371298203 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272754 | TAAACCTAATTGCCT[C/G]CCAAAGGTCCTACCT | 337867 |
rs371322556 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270526 | ATTACTACTTTTTAC[A/C]TTTCTATATCAATGT | 337867 |
rs371324993 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302887 | TAAGGTGACTTTTTC[C/G]CAGCCAACTTTGAGT | 337867 |
rs371330260 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316412 | TGTTGAATGAATGAA[C/T]GAATGGATGAATGAA | 337867 |
rs371336722 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301868 | GTGCTAGAATAACAG[C/T]TTTTGGTTTTTGCTG | 337867 |
rs371349117 | in-del | -/AC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247370 | CAGGCGCCCGCTACC[-/AC]GCCCGGCTAATTTTT | 337867 |
rs371360790 | snp | C/T | 3.30006e-05 | 0.00406192 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295108 | CATCTGCGTTTCTGT[C/T]ATTTCACGTGAATTT | 337867 |
rs371398228 | snp | A/G | 6.60502e-05 | 0.00574637 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255769 | TTAACAAATAATCCA[A/G]TTATGAAGATACAGC | 337867 |
rs371418292 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291244 | AGTCAGTGATCAGCA[A/G]GGTCTTAATCGAATA | 337867 |
rs371420997 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99349320 | CAGCACCTAAAGCCC[G/T]TGGAATCTCCACAGT | 337867 |
rs371441036 | snp | A/G | 0.0114144 | 0.0746788 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255786 | TATGAAGATACAGCT[A/G]TAGAAGACAAGGGCT | 337867 |
rs371444985 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218063 | ATTTAGAGTTATTCC[A/G]ACTGTTAACTGATTT | 337867 |
rs371446743 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245213 | CCTGATAGAATTAGT[A/T]TTGTGTGTTTTTATA | 337867 |
rs371529573 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363515 | TGGGCAGCCCAGGCC[A/G]GCGGGGCAGTGTCCT | 337867 |
rs371541337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243168 | ATGTTTGAGATGTCA[C/T]TGGGATTATCTTTAA | 337867 |
rs371561274 | snp | A/G | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325093 | ATAACTTTAGTGTCT[A/G]TGCTCTTTTTTTTTT | 337867 |
rs371570537 | snp | A/C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283026 | TAGTTGAAGTAATAG[A/C/G]ATGAATTCTGGCTGA | 337867 |
rs371593828 | snp | A/G | 0.000134714 | 0.00820603 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295849 | ACACAAGGCATCTCC[A/G]ATTCTCCAGTCAAAG | 337867 |
rs371621046 | snp | C/T | 2.14654e-05 | 0.00327601 | intron-variant, synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201423 | TTGGATGTGTTTCTT[C/T]TTCAGTCTCCAAGAA | 337867 |
rs371657972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270928 | GCATGAATGAATGAG[A/G]GAATTCTACCTCATA | 337867 |
rs371678311 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227112 | CTGAGACAGGAGAAT[C/T]GCTTGAACCCAGGAG | 337867 |
rs371687232 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359383 | AGTATTACCAGGTAC[A/G]TTAGTAGATGTGATA | 337867 |
rs371704108 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293286 | CTTGTTTGTAGGATC[C/T]TAAGAATTGACTCCC | 337867 |
rs371728608 | in-del | -/T | 0.349671 | 0.229272 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244838 | TAAAATTTATTTTAC[-/T]TTTTTTTTTTTTGAG | 337867 |
rs371749068 | snp | A/G | 5.14911e-05 | 0.00507375 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340577 | GCAGGTAAAAGTGAT[A/G]ATAATCACTAAAAAT | 337867 |
rs371765611 | snp | A/G | | | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254738 | ACAAAAATGTTTTAT[A/G]TAAGTTTTTAAAATG | 337867 |
rs371781090 | snp | A/G | 9.88419e-05 | 0.00702931 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367827 | TTTTTCCTCCTTTAC[A/G]TCAGCGACAAAACGT | 337867 |
rs371801276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310765 | ATTTTTTTTAGTTTA[C/G]GTTGAAATGTAACCT | 337867 |
rs371821392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342767 | TTCCAGTCCCCTGAC[C/T]GACCAACCAGGTGAT | 337867 |
rs371823544 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369369 | TTTTCCCAGGCCAGC[A/G]ATACGTGGTACGAGA | 337867 |
rs371852181 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335460 | TGCCTCTGCCTACCC[C/G]CTACCCTGTCCCCCA | 337867 |
rs371872214 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247885 | TCTCTTTTTTTTTTT[A/T]CCTCACCACTATATA | 337867 |
rs371876214 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237151 | GTGAGCCATCAGGCC[C/G]GGCCTTCTTTGTTGT | 337867 |
rs371886416 | in-del | -/TA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216077 | ACTTTTGTACCAACC[-/TA]TATTTGTGTGTGTGT | 337867 |
rs371899461 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309227 | GCAATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC | 337867 |
rs371913614 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328833 | CTTGATTAATTCATT[A/G]TTAACTGGTTTTTAA | 337867 |
rs371915078 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355215 | ACTTTTACTTTATAA[G/T]TTGTGTGTAGAGCCA | 337867 |
rs371919034 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377898 | TGCATGTGGTCACAC[A/G]GGGCCAACTCCAAAG | 337867 |
rs371928947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267713 | TTTATCTTTTTGTAG[A/C]ATTCTTGGTCCCTGC | 337867 |
rs372005948 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290494 | ACTTTGGGAGGCCGA[A/G]GCAGGTGGATCACTT | 337867 |
rs372030900 | in-del | -/C | 0.0008567 | 0.0206789 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318104 | TACACCCAATTCTCT[-/C]TCTCTCCTGTAAAAA | 337867 |
rs372031693 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357464 | CATAGGAAATTAGTC[A/G]TTTCTCTGTGTCACA | 337867 |
rs372041492 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303327 | CGGCTTCATAGACGC[A/G]CTCCTTGGAAATGAT | 337867 |
rs372078311 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206053 | CTTTACTGCCTGGGC[A/C]GCTGGGTGGATAGGT | 337867 |
rs372086125 | snp | G/T | 1.68607e-05 | 0.00290346 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254899 | ATTTCACTGTTTATA[G/T]TGCTTAGTGACCGTA | 337867 |
rs372110443 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247815 | TTTCTTTCCCATCAG[C/T]ACCAAATTTATCTGC | 337867 |
rs372122462 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374265 | GTTCCTTATTATGCT[G/T]ACTTGTGTAGTCTGG | 337867 |
rs372132716 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285012 | ATCCTCTTTCCATTC[C/T]CTGGCATTTTAAAAG | 337867 |
rs372168628 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325279 | GCTAATTTTTTTGTG[-/T]TTTTTTGTAGAGACG | 337867 |
rs372171431 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214510 | GGAGTAGGTGGTGGT[C/G]GGGGAAGCAGGACTG | 337867 |
rs372194157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373649 | GTCAGGGCAGTGGTG[C/T]TGCAGAGGAGGGGCC | 337867 |
rs372200353 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247315 | CGCCTCCCCGGTTCA[C/T]GCCATTCTCCTGCCT | 337867 |
rs372231429 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287648 | TTTTTTCTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs372232392 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304289 | GGCCCCTATCCTGTA[A/T]CCTTAGCTCTTACTT | 337867 |
rs372241522 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261726 | CCCAGGCCCAGAGTT[C/T]GCAGTGTGACATTTT | 337867 |
rs372252279 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289194 | TCTTCCTTTGTTGTA[A/G]GATCTAAATTAAAAC | 337867 |
rs372269335 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275219 | TGGTTGTACTCAGGA[C/T]GTCAGGGACCACAGT | 337867 |
rs372303318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370144 | TACATACCGACCGTG[G/T]TTAGGAAAGAGAATA | 337867 |
rs372311398 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218227 | GTTAATGTTTGTATA[A/C]AATCTCCCTAAGAAG | 337867 |
rs372329866 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99256430 | ATAGATGAGCTGTTT[C/T]CTAGTGCACAATTGG | 337867 |
rs372349804 | in-del | -/CTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223540 | CTTCTTTCTCTTTTT[-/CTG]TTTTTTTTTTTTTTT | 337867 |
rs372413471 | snp | A/G | 3.29522e-05 | 0.00405894 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255132 | GAAACAGATGTGGAA[A/G]GGCATAAAGCAGACG | 337867 |
rs372421029 | snp | C/T | 0.000247099 | 0.0111125 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367840 | ACGTCAGCGACAAAA[C/T]GTAAACTATCAGGGC | 337867 |
rs372452610 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338116 | AGGCTGGAGTGCAGC[A/G]GCACAATCTCGACTT | 337867 |
rs372454825 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304919 | AACCTTAACGTACAC[A/T]AACTCATACCTATCT | 337867 |
rs372481605 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206701 | AGTCTGGGCCCTTGG[C/T]ACCGTTTCTCAGCTA | 337867 |
rs372518197 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276359 | CCGCTGTAAATTGGG[G/T]GTTCCCACAAGGTCT | 337867 |
rs372531844 | snp | A/T | 9.93526e-05 | 0.00704744 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238396 | ATCTTAGGAACAATC[A/T]TTCTGAAAGTGCTTT | 337867 |
rs372561771 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313231 | CCTCATGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 337867 |
rs372591764 | snp | A/C/T | 4.57229e-05 | 0.00478119 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244480 | TATTTTTAGGAGACT[A/C/T]ATCTCTATCATTTTT | 337867 |
rs372667220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310265 | CTAGGAATTAGAGGC[C/T]ACAGTGAGCCGTGAT | 337867 |
rs372687154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379469 | TTTTCTTAAATTTCT[A/G]CAGCCAACATGTTGA | 337867 |
rs372689137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361518 | TCAAAGCCCATTCCC[C/T]TTCCACTGTCCTGGA | 337867 |
rs372739338 | snp | C/G | 3.57647e-05 | 0.0042286 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255883 | ATCATTTTACAGCTT[C/G]TTGGTAGGCATGATA | 337867 |
rs372786166 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377604 | TCATCAGAGTTGTGT[A/G]TTTGCTAAACTTTAT | 337867 |
rs372806680 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292012 | TTTGTCCTATTTAAG[G/T]ATTATGAAGTCGGCT | 337867 |
rs372827815 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328260 | ATCCATTCACCAATT[G/T]GTGGACATTTGAGTT | 337867 |
rs372831753 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312112 | TATCACATTTGTTTT[C/G]TGTGTGTTGTATTTT | 337867 |
rs372843504 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300489 | AAATCCTTTCATATG[C/T]GTGACTGTTACTATC | 337867 |
rs372858987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239863 | AGGTCACAGGTGTAC[A/T]TGACATCCTTGGGGG | 337867 |
rs372866249 | snp | A/C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238122 | CACACTTCTCTATTT[A/C/T]TTTACACTTGGGTAG | 337867 |
rs372946578 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382922 | CCGAGAAAAGCCAGT[A/G]GGTTGAGGGAGGAAG | 337867 |
rs373001460 | snp | C/T | 9.94893e-05 | 0.00705229 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385194 | AAGCGGCAATGTCAG[C/T]GCCCTCAGGTTTCTG | 337867 |
rs373019872 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372239 | CCTGTGCAGACGTGC[A/G]GGGAGGAAGATCAGA | 337867 |
rs373025732 | snp | C/T | 0.000166403 | 0.00911997 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243783 | GCTAAGGAAGAGACC[C/T]GAACAAATTTTACTC | 337867 |
rs373028030 | in-del | -/GT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368689 | TAAACTCATGAGAGA[-/GT]GTGTGTGTGTGTGTG | 337867 |
rs373034392 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228757 | ACTTTTGAATTACGA[A/G]GCAATGAGGAACTCG | 337867 |
rs373044787 | snp | A/C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311026 | AAAAAGGAAGGGGGC[A/C/T]TTTTAAAACAAAAGG | 337867 |
rs373050743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268405 | ATCGTTTGAGTCCTG[A/G]AGACCATCCTGGGCA | 337867 |
rs373062126 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261754 | TTTACTATTGGAAGA[A/G]AGATCCAGAGTCGCC | 337867 |
rs373070680 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238268 | CACTTACATCCCCAG[G/T]TCGATGTTTTGAAAG | 337867 |
rs373087776 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241235 | ACATCACTGCACTAC[A/T]GCCTGGGCAACAGAG | 337867 |
rs373092915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303788 | AAATAATGATATTTA[A/G]TGTTCCTCCCTAATT | 337867 |
rs373108220 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285325 | TGGTAGAGTATTTTT[G/T]TACTTTATTAGAATG | 337867 |
rs373116156 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305594 | AGAATAAATAAATGA[A/G]TTAAAGTCATATAGA | 337867 |
rs373135063 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242248 | GTTCTCAATGAGCTG[C/T]TGGGCACACCTCCCA | 337867 |
rs373146623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208143 | GCTGGGATTACAGGC[A/G]TGTACCACCACGCCT | 337867 |
rs373148694 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225219 | GTAGTATTAAGTACG[A/T]TCATATTGTGCAACC | 337867 |
rs373153510 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250719 | ATGGAATGCTTTTTC[C/T]ATTTGTTTGTATCAT | 337867 |
rs373160006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346547 | CTCATATTGTTTCAC[A/G]CAGTCTCACCTTTAC | 337867 |
rs373167817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286122 | CTTCTAGCCTTTTCA[A/G]CAATTGTATAAGCAC | 337867 |
rs373174545 | snp | C/T | 1.64939e-05 | 0.0028717 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295697 | ACAAATATGCACACG[C/T]CTTTTGCATGTTCAA | 337867 |
rs373180956 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382555 | ACCCGTGGTGTCACA[C/T]TCAGTTCTGGGCGCG | 337867 |
rs373187318 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355600 | TTCTCATTCTCTACC[A/C]AAACCAAAACCAAAC | 337867 |
rs373233662 | snp | A/G/T | 1.65976e-05 | 0.00288072 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201572 | GTGGTCAGCAGGTAG[A/G/T]GGGCGGAGTATTTTT | 337867 |
rs373245027 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282892 | TTTGGTATATGTTAT[A/G/T]TGTTGAGTTCTGAAA | 337867 |
rs373246421 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302722 | GAGGAACCTGCACTG[C/T]TGTGGAGCTGTGACC | 337867 |
rs373261228 | in-del | -/AACT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278273 | ATGCTATTATTAATT[-/AACT]GTTACCACATTATTA | 337867 |
rs373273400 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368682 | ATCATCGTAAACTCA[A/T]GAGAGAGTGTGTGTG | 337867 |
rs373276231 | in-del | -/TTTA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203023 | TTTCCTTTGTTTTAT[-/TTTA]TTTATTTATTTATTT | 337867 |
rs373277279 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341418 | CCCAGAGTTTATATC[-/A]GGGGGGGGGAGGAAG | 337867 |
rs373278251 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268630 | AAAAAAAAAAAAAAA[A/G]AAAAGAAACACAAAA | 337867 |
rs373305963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244798 | ATTATGTTCTTGAAA[C/T]AGAATCAATTTTATA | 337867 |
rs373318009 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318245 | CGATCTCAGCTCACC[A/G]CAACCTCTGCCTCCC | 337867 |
rs373318603 | in-del | -/TG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377502 | TCCAGGGTTTCAGTG[-/TG]AGTTAATGTGTGTTG | 337867 |
rs373350242 | snp | C/G | 0.000198465 | 0.00995958 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356165 | CTTGCAGGGGCTGTT[C/G]GGTTGCATCCTAAGC | 337867 |
rs373364683 | snp | C/T | 0.000384541 | 0.0138608 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200863 | GGGCTCGCACTTCAG[C/T]TTCCCCTCCCCCGGC | 337867 |
rs373388818 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288636 | GTGGTGCTCCTCTTA[C/T]ACTCTCAACAGAAAA | 337867 |
rs373392982 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306148 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 337867 |
rs373399371 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235851 | CTTGTGCCTGTAGTC[C/G]CAGCTACTAGGGAGG | 337867 |
rs373418764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346160 | GACATTTCCCACTTA[C/T]ACATCCATGTCCTTC | 337867 |
rs373435446 | snp | A/C | 3.72398e-05 | 0.00431492 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296175 | GTGTCTAGAAAAAAA[A/C]CAAGAAGGATCATAT | 337867 |
rs373438091 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330395 | ACCTGGGACGCCGAG[G/T]TTGTAGTGAGCTGAG | 337867 |
rs373441585 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329218 | AAGTCTTGCAATCAG[A/G]CAATATAAGTCCTCC | 337867 |
rs373443522 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316540 | CCTGTGCAATGGGCT[A/C]TGACGTTGTGGGCTC | 337867 |
rs373445647 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243273 | ATGTCCCCTTATATG[C/T]TTTTTATGCAGCCAG | 337867 |
rs373460595 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216469 | TGTTTTCCATTTACC[A/G]TAGTGATATCAAATT | 337867 |
rs373470471 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215646 | CCCGTCGTCCTAGAT[C/T]TCAGGTGTTGATGAA | 337867 |
rs373505649 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319253 | TTTTATTCTTCATCC[A/G]TGACTTAAATTTAAA | 337867 |
rs373601112 | snp | C/T | 0.000287491 | 0.0119859 | synonymous-codon, intron-variant, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99244610 | CACTGCAGCTAGTAA[C/T]TTGCCTTCTGGATTG | 337867 |
rs373608782 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242366 | CGGACGGGGCGGCTG[G/T]CCGGGCAGAGGGGCT | 337867 |
rs373651784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274865 | TGGGATTACAGGTGC[A/G]CACCACCACTCCCAG | 337867 |
rs373668814 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339953 | TGATGGCCATCTGCC[A/G]ACAAAGGTAACCGCA | 337867 |
rs373692023 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376420 | CAAGAGGGTCTTCAT[C/T]CCTGTGGGGGCTCTG | 337867 |
rs373715311 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292205 | CAGTGGTGCAATCTC[G/T]GCTCACTGCAAGCTC | 337867 |
rs373718246 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247277 | TGGAGTGCAGTGGCG[C/G]GATCTCGGCTCACTG | 337867 |
rs373731487 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324555 | ATTTGTTACCACAGT[A/G]TAACTTAGAAAAAGC | 337867 |
rs373742106 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99279492 | TATAGCACTCATCAC[C/T]ATAGATAGTAAATAA | 337867 |
rs373742313 | snp | C/T | 3.29853e-05 | 0.00406098 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295115 | GTTTCTGTCATTTCA[C/T]GTGAATTTTCTTCAG | 337867 |
rs373767362 | snp | A/C/G | 4.94241e-05 | 0.00497092 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340372 | TGCATCAGGTGCTCT[A/C/G]CATCCCCAGCTGGAT | 337867 |
rs373776094 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259801 | GTATTGATTAGCTTC[C/T]CCATTGCTGCTAAAA | 337867 |
rs373776628 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348106 | TCTTTACACTGCCAG[A/G]GCCATTACATAACTT | 337867 |
rs373782349 | in-del | -/CCTACCTCA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209213 | CGAGCCCCTACCTCA[-/CCTACCTCA]GCTTGGTATGAAGGT | 337867 |
rs373789570 | snp | A/G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321593 | TAGGCGTGAGCCACC[A/G/T]TGTCTGGCCTAGGCT | 337867 |
rs373798603 | snp | A/G | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351514 | TCCCTGCTGTAGAAG[A/G]TTATATAGCCAGCAG | 337867 |
rs373815033 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383269 | AAATGCTCTCGAGTC[A/C]GGTCTCTCAAATCCT | 337867 |
rs373820892 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275679 | TTCTCTACACAGTTT[A/G]TGTTTCTTCTGAGTT | 337867 |
rs373842419 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265353 | GGAGGCAGGCAGGAC[C/T]ACCCTGAGACCCACA | 337867 |
rs373855208 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372497 | CAAATCCATAGACCC[C/T]GGGATTGCTTTTGGA | 337867 |
rs373860989 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242018 | ATTTAACCCTGAGTG[G/T]ACACAGCACATGTTT | 337867 |
rs373929105 | snp | A/G | 9.93098e-05 | 0.00704592 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238403 | GAACAATCATTCTGA[A/G]AGTGCTTTCCTTTTT | 337867 |
rs373958250 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203408 | ATCTGAAAGAAGGAC[A/G]ACACGTGTACCTAGC | 337867 |
rs373965776 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240711 | CGGTACTGTTTCTCC[G/T]TGAGCCCAGCTATGG | 337867 |
rs373974695 | in-del | -/TAG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383141 | GTGCATATGATGCAT[-/TAG]TAGTGTGCATGTGTG | 337867 |
rs373977770 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238970 | GATAACTTTTACAGT[A/G]GTGGTTAAACGAAGT | 337867 |
rs373978485 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199312 | GAGGCTGAGGCAGGA[C/G]AATCGCTTGAACCGG | 337867 |
rs373985587 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222272 | AGCAAAAAATCACGA[C/T]GGAAGGCCACTCTGA | 337867 |
rs374000246 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329207 | AGCTTTATGGTAAGT[C/G]TTGCAATCAGGCAAT | 337867 |
rs374002364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267497 | TTGGAACCTTTCCTC[A/G]TGACTTAAGCCGAAG | 337867 |
rs374003672 | snp | A/C | | | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254674 | AATTATCTGTGTGAA[A/C]AAGGCTTGACTAGGA | 337867 |
rs374009609 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359828 | GTCACATCGCCCTTC[A/G]CTGCCTACCCCATGG | 337867 |
rs374014333 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283853 | TATTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG | 337867 |
rs374039428 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247218 | TTTTTTGTTTTGTTT[G/T]GTTTTGTTTTTCTTG | 337867 |
rs374072536 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236151 | TGGTCTGGGCAAAGA[A/C]TTTTTGTGTAAGATC | 337867 |
rs374082583 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265391 | TGCCGCTGTGCTTCT[C/T]TGGAAAAAAGGTTCT | 337867 |
rs374082786 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217884 | CCACCTTCTTGCCAT[C/T]GACTCCCCCATTTCA | 337867 |
rs374102574 | snp | A/G | 1.80094e-05 | 0.00300073 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255896 | TTGTTGGTAGGCATG[A/G]TACTTAGAAACTGTA | 337867 |
rs374108017 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348984 | GAAAAAGAAAAGAAA[A/T]GGTGACACTAGAGGA | 337867 |
rs374123651 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377211 | TGGTGCCAGCCCTCA[A/G]GGGAGCTCACCGTCT | 337867 |
rs374158355 | in-del | -/CAGT | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215121 | ACAGTTTTTTAAAAA[-/CAGT]CAGCTCAATCAAAGC | 337867 |
rs374180692 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203282 | CTCAAGTGGTCCTCC[C/T]GCCTCGGCCTCCAAA | 337867 |
rs374195543 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233193 | CTCGGCTCACTGCAA[-/C]CCTCCACTACCCGGG | 337867 |
rs374222791 | snp | A/G | 6.69165e-05 | 0.00578392 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295510 | AGAATAGCAGATGAG[A/G]ATGATTATAAGTGGA | 337867 |
rs374293433 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253544 | TTTGAGACGGAGTCT[C/T]GCTTTGTCACCCAGG | 337867 |
rs374299759 | snp | A/G/T | 3.29621e-05 | 0.00405958 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255459 | CACACACGCCAGCAC[A/G/T]GCTTTGCACGTGTTT | 337867 |
rs374302490 | snp | C/T | 3.30033e-05 | 0.00406209 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385218 | GTTTCTGCGTTTTCT[C/T]TGCCTGCAGGTCGCC | 337867 |
rs374323225 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377141 | TCAGCCTTCTCTAAC[G/T]GGTGCTGGGCACCGG | 337867 |
rs374331780 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255266 | AGTAGCACCCAATCA[C/T]GATGAACAAAGGAAT | 337867 |
rs374342081 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367882 | TGAGCCAGCAGCGCC[C/T]CCTCTAGAAGTTTCT | 337867 |
rs374343123 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327094 | CATCAAGATATTTAA[C/G]TGGTCCTCTCTCCAT | 337867 |
rs374349786 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229659 | ACCGTAAAAATGACC[A/G]TGCAAGTTGAAACCG | 337867 |
rs374361203 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325276 | CCAGCTAATTTTTTT[-/T]GTGTTTTTTGTAGAG | 337867 |
rs374380378 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204989 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 337867 |
rs374388592 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312628 | ATAGCTTGGGGGCCA[C/T]GAGGAGAGCCACCAG | 337867 |
rs374398623 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250041 | TGATAGTTTATTTTG[C/T]TGTGCAGAAGCTCTT | 337867 |
rs374416624 | snp | A/G/T | 4.94858e-05 | 0.00497398 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254942 | GGAAACTTTTTCTGC[A/G/T]CATGCTTCGAAGGTA | 337867 |
rs374421049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360678 | TTCTCCATCGTTGAA[A/G]TCATTCTCTTTTAAT | 337867 |
rs374443265 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339185 | AAGCTCGGGCTGCGC[A/G]GCATCTGCTGCTTTC | 337867 |
rs374452807 | snp | A/C | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356443 | TGAGCAACAGGATGT[A/C]TTGTGTCTCCTGATC | 337867 |
rs374460117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296943 | CTTTGCACATAGTAG[C/T]AAGCATCACACTTTA | 337867 |
rs374480618 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226348 | TCTGCCCATGCACCC[A/G]GTTAGTCAGCATATC | 337867 |
rs374485400 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205676 | GGAGTCTGGTGCGCT[C/G]ATGAGAGAAGATAGA | 337867 |
rs374489272 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230996 | GAGGTTGCAGTGAGC[A/T]GAGATTGTGCCACTG | 337867 |
rs374546166 | snp | A/G | 0.000115347 | 0.00759343 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255504 | GTACTTCGGCTGTAC[A/G]ATGGCCATGTATCTG | 337867 |
rs374560491 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350975 | AATATTGTGTTGAGT[C/T]GTGTGTGAGTGTAGA | 337867 |
rs374575554 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347328 | CGGGCGCCCCCCCCC[-/G]CCCCCCAGGAAAAAA | 337867 |
rs374583538 | in-del | -/CTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344426 | TGCTTCCATCTTCTT[-/CTT]TATGTTTCAAATACA | 337867 |
rs374584432 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201496 | GGAGGGAAGTTAGGA[A/G]GTCGTGGCGAGGGAG | 337867 |
rs374595745 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336318 | TAGCTTTTGGCATAC[G/T]ACAGCTTTTAAATTG | 337867 |
rs374606214 | snp | A/T | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261063 | ATGCTTCTATGTTAG[A/T]CATTTGTCTATGCCA | 337867 |
rs374608032 | snp | C/T | 5.03005e-05 | 0.00501475 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340269 | TGAGTCGTGTACATT[C/T]TTTAAAATAATACTA | 337867 |
rs374613982 | snp | G/T | 0.0023933 | 0.0345097 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386719 | CGCACAAGCCCCTCC[G/T]TGAATCTGAATTGCG | 337867 |
rs374624325 | snp | C/T | 3.37302e-05 | 0.00410658 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238589 | CCCCTGAGAGGAGAG[C/T]GGACAGTTTTTTTTT | 337867 |
rs374625597 | snp | A/G | 1.65682e-05 | 0.00287817 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340300 | CATTTAAACAATCAC[A/G]TTGGACGTTTTTCTT | 337867 |
rs374683969 | in-del | -/ACACACAC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237271 | TATATATATATATAT[-/ACACACAC]ACACACACACACACA | 337867 |
rs374726403 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344180 | CAGGTATTCCCTCAT[G/T]ACCCCGGAGGCTCAG | 337867 |
rs374734989 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271341 | GGAGATATTGGGGAA[A/G]GTATTCCAGATATCA | 337867 |
rs374773211 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248494 | CCTCCCTGGTTCAAG[C/T]GATTCTTCTGCCTTA | 337867 |
rs374777916 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99231452 | GAGTTTCTCCCTGTC[A/G]TCCAGGCTGGAGTAC | 337867 |
rs374845632 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242775 | GGCTGCCGGGCGGAG[A/G]CGCTCCTCACTTCCC | 337867 |
rs374854407 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361622 | AACACCATTGACATT[C/T]TGATCCAGACCATTC | 337867 |
rs374870437 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212559 | GTTTTTTGACATTGA[C/T]GATGCAGATTAACAC | 337867 |
rs374873259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276034 | GTGGACAAATTTTGA[C/T]TTTTAGTATTGTATT | 337867 |
rs374881529 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346614 | TGTACCAACCCCTTC[A/T]CCCCACCCCTCCCAC | 337867 |
rs374887641 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355220 | TACTTTATAATTTGT[A/G]TGTAGAGCCAATGCT | 337867 |
rs374897515 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298353 | ACCAATGATAAAAAG[A/G]TAAAGGATAAGTTTG | 337867 |
rs374901678 | in-del | -/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290744 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 337867 |
rs374916208 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315258 | TTTCTGCATTTGATT[C/G]TTATGAGTAGGATTT | 337867 |
rs374920639 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227851 | TCATTTGGTGCATGT[A/G]TTGGGAGTTTGGTAT | 337867 |
rs374925642 | snp | C/T | 1.76024e-05 | 0.00296663 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340604 | AAATTTAGAAATTCT[C/T]AGTGGCCCAAGCAAA | 337867 |
rs374936656 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335196 | AAATAAAAATGTTTA[A/G]TTTTGTACTTCATTC | 337867 |
rs374972490 | snp | C/G | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383363 | CCAACCAAATGAATT[C/G]TTTTCAATTCTAGTT | 337867 |
rs375004591 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261901 | TTATCCGCAATTTTG[C/T]TGTCTGAGGCTTCAG | 337867 |
rs375015837 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310603 | TTTCTGCAGAACAGC[C/T]CATATAATTTTGGTC | 337867 |
rs375022075 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293317 | TTAGCCCAGAGAGGA[C/T]TCTTGCCTACCCTAA | 337867 |
rs375061757 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332015 | CAGTTGCAAGGGGAC[A/G]TTTATTCCTTTGGCT | 337867 |
rs375078561 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221923 | CTCTTAGAGGAACCC[C/T]GGCTAAGACATTTTC | 337867 |
rs375104785 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381177 | AAGGGGTTCTTCCCT[C/T]TCCAGGGCAGGGCCT | 337867 |
rs375124614 | in-del | -/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198818 | TCATAACATTATGCA[-/T]CGGTCAACTGGAAAA | 337867 |
rs375131776 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288891 | TTTGGAGCACTGTCT[A/T]TGTTCAGGGTGTCAT | 337867 |
rs375133866 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373535 | TAAGATGGATAAGGC[C/G]GAATGTCCTGCCCTG | 337867 |
rs375134758 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349791 | AAGTGGACAAGGAGC[A/G]TGACCGTTGAAGCAC | 337867 |
rs375136729 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385112 | TTGAAATGAAAATTG[G/T]TTTTTTTGTAAACAG | 337867 |
rs375155045 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228291 | CTCTATATTCATTCA[-/T]TTTTTTTTTTTTTTG | 337867 |
rs375174547 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202056 | TTGGCCTGGGCGACA[A/G]AGCGAGACTCCATCT | 337867 |
rs375193612 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379066 | CAGGTCCAAAATGTT[G/T]GTGAGACCAATCAGA | 337867 |
rs375197939 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247213 | TTTTTTTTTTTGTTT[G/T]GTTTTGTTTTGTTTT | 337867 |
rs375208806 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337531 | CTAGATGTAAATTTC[A/G]TTTTAGCATTCTTTT | 337867 |
rs375241093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279497 | CACTCATCACTATAG[A/G]TAGTAAATAAGATGT | 337867 |
rs375249249 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247886 | CTCTTTTTTTTTTTA[A/C]CTCACCACTATATAG | 337867 |
rs375287293 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337752 | CCCACATGGACCCTC[C/T]TTGGTTCATGCCCTA | 337867 |
rs375297206 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316780 | CCTGGAAGAGTGGAG[A/C]GCATGGCTGTAGAGC | 337867 |
rs375336082 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209976 | AGACTGTCTCAAAAA[A/G]CAAAACAAAAAACAA | 337867 |
rs375403795 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210626 | GGGATTATAGGCATG[C/T]ACCACCACGTCCGGC | 337867 |
rs375406376 | snp | A/G | 0.000132501 | 0.00813836 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296015 | TTTCCCACGAGCCCA[A/G]TGATGAAGACGAGGC | 337867 |
rs375428714 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384755 | TGAGCGTGGCAGTGA[C/T]GCCAGGAGTGTGATG | 337867 |
rs375518972 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242542 | CGGACGGGGCGGCTG[G/T]CCGGGCAGAGGGGCT | 337867 |
rs375520188 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322829 | AGCCTTATCAGGGTT[C/T]GTAGATCATAGGACA | 337867 |
rs375523714 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249110 | GAGGTTTGGGGTACA[C/G]ATGATCCTGTCACCC | 337867 |
rs375526452 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277323 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTAACC | 337867 |
rs375543364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247036 | AGAAAAGGTTTTGCT[A/G]TGTTGTCTAGGCTGG | 337867 |
rs375575166 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384176 | ACCAAGTAGCTCGCT[C/G]TCTTTCGGAAAGAAA | 337867 |
rs375590153 | snp | G/T | 1.71314e-05 | 0.00292667 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296100 | AGTCATTTCCCTGAG[G/T]AGTTGCAGAGGGCGG | 337867 |
rs375609220 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300300 | AAGTGGGATGGCTTG[A/G]AAATGATCTTAGGTA | 337867 |
rs375638410 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349629 | CCCTCTTAGGTAGCC[A/G]AAGCTGAGAGAGAGA | 337867 |
rs375643508 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310126 | GATGCCAGGAGTCTG[A/C]GATCACTGTGGGGAA | 337867 |
rs375651118 | in-del | -/A | 0.0314385 | 0.121371 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230942 | TAGTCCCAGCTACTC[-/A]GGGGGCTGAGGCAGG | 337867 |
rs375707010 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266776 | TCACACTGCTGTGCA[C/G]CCAACCTCCAGGACA | 337867 |
rs375721828 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352668 | TACCATTTTCATTAC[A/C]GTCTATTCCGCAGAA | 337867 |
rs375730423 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310875 | TCTATGAATTAAGCG[C/T]CTCCAAGGGCATGTT | 337867 |
rs375744336 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334504 | TTCCAAGAACCTATC[A/G]GTGAGTTAAGTGAGG | 337867 |
rs375744561 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368281 | ATGGTTTTGAGTCAT[A/G]TTAATGTTTTACATA | 337867 |
rs375759290 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353109 | TTCCTTGTCAACAAA[A/G]CAGTCTAATCAGTTA | 337867 |
rs375817398 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237950 | ACAAAGTGAGACTCT[C/T]TCTGGATATGATTAT | 337867 |
rs375850908 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242253 | CAATGAGCTGCTGGG[C/T]ACACCTCCCAGACGG | 337867 |
rs375852830 | snp | C/T | 0.0402515 | 0.136035 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200770 | TGCGCATGCGCCGGG[C/T]GCGCCGTTCGTCAGC | 337867 |
rs375859097 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225659 | ACTGCCTTTATGTGT[C/T]AGGTCCTATTGGAGG | 337867 |
rs375859232 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208372 | AGGCCTTGTGACTTA[C/T]CCTTTATGCTTTAAT | 337867 |
rs375878347 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286475 | CTCTTATTAGGACTT[A/C]TTTTTTTTAATATTT | 337867 |
rs375909658 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313536 | TTGAGATTGTATGAG[A/G]AGATGAGAGAGCAAG | 337867 |
rs375911307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241787 | GTGTTTCTCGCACAG[A/G]GGGATTTGGCAGGGT | 337867 |
rs375923342 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287682 | TAGAGACGAGGTTTC[A/G]CCATGTTGCCCAGGC | 337867 |
rs375949865 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284872 | CAGTAGATGAAAATA[A/G]TGTGTAGTTTTCGTA | 337867 |
rs375951956 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352038 | CTCTTTATCCTCCCC[C/T]AGCAACAGCCATTTG | 337867 |
rs375958897 | snp | A/G | 0.000387925 | 0.0139216 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356128 | ACACATGTCTGTCAG[A/G]CTGTACACAGTAGAA | 337867 |
rs375967936 | in-del | -/GTTGGGA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367456 | TAAGAGTTAACTGGA[-/GTTGGGA]CAGTCAGTGGCGTCA | 337867 |
rs375969903 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330389 | GCTTGAACCTGGGAC[A/G]CCGAGGTTGTAGTGA | 337867 |
rs375973476 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322472 | ATAGAAAGAGCCTTC[C/T]TTTGCCAATTTTCTT | 337867 |
rs375993080 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361857 | TTAAAATAGACCAGA[C/T]GCAATGGTGCACATC | 337867 |
rs375998626 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379540 | TAGATCCTTGCTTGT[C/T]TCCTGACCCACATAG | 337867 |
rs376002841 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323004 | GAAACAGCATAACCT[G/T]CTGTGGAAGCATAAG | 337867 |
rs376073973 | snp | G/T | 3.34801e-05 | 0.00409132 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201597 | ATTTTTACAGCCAGT[G/T]AAACGGCTTTTCTCA | 337867 |
rs376085431 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234908 | TGGGAAAAAAAGTGA[A/G]CTTGAAGAAAACATA | 337867 |
rs376086651 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364164 | GGTTTTTGTTCTCAT[G/T]ATGCTGTGACTTGTG | 337867 |
rs376087942 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252318 | GGCTACCCACTGGCT[-/G]GTTTGAGGGGGAACC | 337867 |
rs376092952 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385829 | GTGAGGGAGAAACAG[A/G]GAGCTGAATCCTCCC | 337867 |
rs376093417 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252538 | CTCAGAAAATGTAAC[C/T]ATTAGGTTTTGAAAG | 337867 |
rs376116842 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367839 | TACGTCAGCGACAAA[A/G]CGTAAACTATCAGGG | 337867 |
rs376123667 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372098 | GCTGTGCAGGCAGGC[-/G]GGTGGGAGGCTGCAG | 337867 |
rs376159827 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255467 | CCAGCACGGCTTTGC[A/C]CGTGTTTTTAAGTTC | 337867 |
rs376236253 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266970 | CAGCTGCACCAGCAA[C/T]ACAATGCCCAGTTTC | 337867 |
rs376237200 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270661 | TTGATGGTTGATGGT[A/G]TGGACATGCACATGA | 337867 |
rs376248947 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212973 | TGTAGTGTAGAAGGG[A/G]TTAGTCCCACATAAT | 337867 |
rs376252686 | snp | C/T | 8.80282e-05 | 0.00663373 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244489 | GAGACTCATCTCTAT[C/T]ATTTTTCTGCTGTTT | 337867 |
rs376253816 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229932 | GTGTTTGCCTTCTTC[C/G]TGTTGTGTAACTTAT | 337867 |
rs376254263 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247340 | CTGCCTCAGCCTCCC[C/G]AGTAGCTGGGACTAC | 337867 |
rs376260432 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203301 | TCGGCCTCCAAAAGT[G/T]CTGGGATTACAGGCG | 337867 |
rs376264097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228932 | GTACAATAACCACAG[C/T]GTCAACTGTAACTGG | 337867 |
rs376269818 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258761 | CAGTAGGATTGTAGG[A/G]GCCCTAAACCAGAAA | 337867 |
rs376292485 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336102 | CAGAGTCCTAAAAAC[A/G]AGTGAGGATAAACAT | 337867 |
rs376348477 | snp | C/T | 3.31923e-05 | 0.0040737 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295575 | TCCAGGGAAGAGATT[C/T]AGTTTCTTCAAAGTT | 337867 |
rs376388109 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317589 | AAATTTAGGGTGACA[A/G]TGTTAAGAAATTAAA | 337867 |
rs376407460 | in-del | -/TTGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99254167 | AGAAGAGCAAACTGT[-/TTGT]ATTGGAGAATGGCAT | 337867 |
rs376428638 | in-del | -/TGTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216083 | GTACCAACCTATATT[-/TGTG]TGTGTGTGTGTGTGT | 337867 |
rs376431180 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368684 | CATCGTAAACTCATG[A/T]GAGAGTGTGTGTGTG | 337867 |
rs376476131 | snp | A/G/T | 0.000115386 | 0.00759479 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255418 | AGCAGAGGGGTGGTC[A/G/T]TGGTCAGGGTCATTA | 337867 |
rs376502594 | snp | C/T | 0.000393922 | 0.0140288 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200882 | CCCTCCCCCGGCGCC[C/T]TCTGGGGCTCCGAGC | 337867 |
rs376504981 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338486 | TTTTCTGAGTCCCAC[A/G]GGACTCTCTGCAGGC | 337867 |
rs376506613 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207642 | AACATTTGGTAGGGA[A/G]CCTTGGGCCAGATGC | 337867 |
rs376512484 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337054 | GCTTAGTGTGTGGTT[-/T]AGGTTCATTCATTCA | 337867 |
rs376512829 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375047 | GATCCCAAAGTTAGA[C/T]GTGTTACAATGAAAT | 337867 |
rs376529283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348536 | TCCTATAAGAAAGAG[A/G]CAATGAAAGACATGG | 337867 |
rs376546201 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281610 | GAAACCTTCAGCGCT[A/G]TTTTCTATAAATTGA | 337867 |
rs376565110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281877 | GGAATTTCAAACTGC[A/G]GTCTCAGTGGCCAGA | 337867 |
rs376611082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243358 | TAGCAGCAGTTGCCA[C/T]AAATTACTTTGCATA | 337867 |
rs376613539 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335366 | CTACTTCCTTGCCTC[C/G]AATTCATTACTGTTT | 337867 |
rs376613634 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211958 | TGCCAGTGCACAAGT[C/G]TGCCTCTCCCCACAT | 337867 |
rs376627659 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245921 | TGTTAGCACATGTAA[A/G]TGACCTCCAAGCATC | 337867 |
rs376637548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291559 | TTCTAAAATCGCATG[C/T]CACCTTGTACTCAAT | 337867 |
rs376645960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328533 | TGTTTTAGCTTTAGC[C/T]GCTCTATTGGGTGTG | 337867 |
rs376656979 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214204 | CTTGTATCATTTTTT[A/G]CCTTGGCATCTTTGG | 337867 |
rs376705146 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302689 | GGACAGTGGGAAACA[C/T]GCATTCCTGGTGTGC | 337867 |
rs376712479 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261386 | GTGTAGGGGAGATAT[A/G]TTGAATAGTAAGAGT | 337867 |
rs376718786 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240784 | CTGGCAGGTGAGGTG[A/T]ACTCTGGTGGCCAGT | 337867 |
rs376739193 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305387 | TCTACACAGGCCACG[C/T]CCAGGGCTGCCTAAC | 337867 |
rs376775893 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347323 | TATCCCCGGGCGCCC[C/T]CCCCCCCCCCCAGGA | 337867 |
rs376776065 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306207 | AGCCTGATTCAGGGT[C/T]TTTATGTAAAATATC | 337867 |
rs376801378 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376725 | TGAAGTTAGAGGAAG[C/G]AATCATTTCGATTTG | 337867 |
rs376805617 | snp | C/T | 0.000117315 | 0.00765791 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340270 | GAGTCGTGTACATTT[C/T]TTAAAATAATACTAC | 337867 |
rs376820135 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260435 | GAGGAATGGATAAAT[A/G]TCTGGGCCTTGAGTC | 337867 |
rs376847587 | snp | C/T | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386545 | AGACGACTGGGTGCT[C/T]ATTTGAAGTGAGTGA | 337867 |
rs376868191 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241255 | GGGCAACAGAGTGAG[A/C]CCCTGTCTCAAAAAA | 337867 |
rs376874405 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270520 | ATTTTAATTACTACT[G/T]TTTACATTTCTATAT | 337867 |
rs376933391 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310342 | TGTCTCAAGAAAAAA[A/G]GAAAGGATGGATGAA | 337867 |
rs376942836 | snp | C/T | 1.74717e-05 | 0.00295559 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295031 | TTGTCATACAGTTTA[C/T]GTCACTATAAACCAA | 337867 |
rs376946101 | snp | C/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256915 | CCTTCAAAAATGTCA[C/G]TTTGCAGAGTGGGCT | 337867 |
rs376956169 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347840 | CCTTTGGAGGCTTGT[C/G]TCATGGGCCTGTGGC | 337867 |
rs376958459 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378199 | ACCATGGGTCAGTTA[A/T]TGAACAGCTGGAGCC | 337867 |
rs376959902 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357826 | ATCCCAACTAACTAC[A/G]GTCTTGGCTAAGAAA | 337867 |
rs376966351 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255165 | CACCTGCACCAGCAG[C/T]GTGATGATGATCCTT | 337867 |
rs376969228 | snp | C/T | 6.58989e-05 | 0.00573978 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367855 | CGTAAACTATCAGGG[C/T]GGTCGGCAGTCTGAG | 337867 |
rs377052097 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237267 | GCGTATATATATATA[C/T]ATATACACACACACA | 337867 |
rs377052146 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242127 | AATGAAAAGTCTCCC[A/G]TGTCTACTTCTTTCT | 337867 |
rs377064623 | snp | C/G/T | 6.59091e-05 | 0.00574028 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255301 | AAAAAAAATGTCAGT[C/G/T]GAGTGAGGTTCAGCA | 337867 |
rs377065284 | in-del | -/C | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231972 | GCTGGTGTTGTTTTA[-/C]CAAATCATGGTAACT | 337867 |
rs377076527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286027 | TCCCAGCTGCCTCAG[C/T]GTGTCAGAGGAAACA | 337867 |
rs377080324 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262060 | GCTCCTTCCTCCCCA[C/G]GACATGAGTCCTCCC | 337867 |
rs377107627 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224388 | ACATACAAATTTTAG[A/G]AGGAAACGTTCAGTC | 337867 |
rs377131740 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355743 | GCAGGCCTGTGGCTC[A/G]GCCCGCAGCGTGCTT | 337867 |
rs377138443 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206291 | GAGGTGGGGGGACAG[C/T]TGGAAGCTGAGGACA | 337867 |
rs377163523 | snp | C/T | 1.6557e-05 | 0.00287719 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385197 | CGGCAATGTCAGCGC[C/T]CTCAGGTTTCTGCGT | 337867 |
rs377175213 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304506 | TCTCTAGGTGATGTA[G/T]GATCGATATTCAATA | 337867 |
rs377177547 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283157 | CTCTCTCCTAAAATT[A/G]TTTTGTTTACTTACT | 337867 |
rs377182203 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227314 | CATCTCACTGGTGTT[C/G]CATCTCCACTGCAAG | 337867 |
rs377214854 | in-del | -/GCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285251 | GGTGTGTCTTAAGTA[-/GCT]GCTGCTGCTGCTGCT | 337867 |
rs377279422 | in-del | -/TTCTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223538 | CTCTTCTTTCTCTTT[-/TTCTG]TTTTTTTTTTTTTTT | 337867 |
rs377287560 | snp | C/T | 4.94434e-05 | 0.00497184 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295733 | TTTATCTTGTTGTAG[C/T]GTAGAGGGTGCACCA | 337867 |
rs377289845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277145 | TGGGCTTATACCTTT[A/T]AAAAAAATCCTTTTA | 337867 |
rs377300076 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344044 | GTCCTGTCTCTCTTG[A/C]AGAATTAGCATGTTT | 337867 |
rs377303947 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282822 | ATGTCTTGGTAACTA[-/T]AGCAAAATATACAGC | 337867 |
rs377313062 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319991 | TTCCAAAAGCATTCA[A/T]ATATTGAAGTACCTT | 337867 |
rs377314250 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283513 | CATATGTTCCTGATT[G/T]AAATGAATAGCCAGA | 337867 |
rs377350801 | in-del | -/AG | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284944 | TTCAGTGACACAAGC[-/AG]AGAGAATAAAATGAG | 337867 |
rs377361851 | in-del | -/TC | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327473 | TTGGTTTTTGGTTTT[-/TC]TCTCTCTCTCTGTGT | 337867 |
rs377365350 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234416 | GCTGGTCTCAAACTC[C/T]TGACCTCAGGTGATC | 337867 |
rs377380322 | snp | C/G/T | 6.61741e-05 | 0.00575181 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238414 | CTGAAAGTGCTTTCC[C/G/T]TTTTCCCTCCAGACA | 337867 |
rs377415457 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375318 | CCAAGGAAGAGAGTG[G/T]TCAGACAGGGAGAGG | 337867 |
rs377419804 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221323 | ACATTTACTTTTGTT[A/G]CACAGGGCACTACTT | 337867 |
rs377431553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216430 | ATTTTTATAGTTACC[A/G]CCTATTAATGAGAAA | 337867 |
rs377433575 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277824 | TGTCACCACCCGCAA[C/G]CCTCATCAAGCCTCT | 337867 |
rs377435916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250375 | AGATGGCTGTAGTTA[C/T]GAGGCTTTATTTCTG | 337867 |
rs377441012 | snp | C/T | 0.000151097 | 0.00869054 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295822 | GATGTAAAACACTAG[C/T]GCAGTTATCCTACAC | 337867 |
rs377442433 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292297 | CCCACCACCACGCCC[A/G]GCTAATTTTTTTTTT | 337867 |
rs377475694 | in-del | -/AAAAACAAAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281192 | AGACTCCATCTCAAA[-/AAAAACAAAA]CAAAACAAAACAAAA | 337867 |
rs377494891 | snp | C/T | 9.43192e-05 | 0.00686664 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296185 | AAAAACCAAGAAGGA[C/T]CATATAAGTAAAAGC | 337867 |
rs377543666 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343813 | AACTCTTTTGTTAAA[-/C]CCACCACTGGAAATT | 337867 |
rs377573304 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235041 | GACTAGATCAAGGAG[A/G]AAGAGGGGCGTGACT | 337867 |
rs377595958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201341 | GGCTTGGGGGACCGA[A/T]CTAACTCCCCCCGCC | 337867 |
rs377605288 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324008 | AAAAATCTAGCCTCC[G/T]TTCAAAATGCGACCT | 337867 |
rs377640448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372032 | CTGCCAATTCATCAC[C/T]CCTCAGAGATGCCAC | 337867 |
rs377650908 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380417 | TGAGAGCCACAGCAG[C/T]AATTGTTAGTGTCCA | 337867 |
rs377652787 | snp | A/G | 6.26521e-05 | 0.00559662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244642 | AAGTAGCACTTAAAG[A/G]TTGACTTAATTTAGA | 337867 |
rs377655328 | snp | A/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318714 | TAGTCCCAGCTACTC[A/T]GGAGGCTGAGGCAGG | 337867 |
rs377656760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252226 | GGATTAATTGTCCTT[A/T]TATGTGTATTACAAC | 337867 |
rs377694102 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229673 | CGTGCAAGTTGAAAC[C/T]GGGCAAAGCTATTTT | 337867 |
rs377701168 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319062 | ATAATGCCAACTGGA[A/C]AGTCAGGTGGGTTGG | 337867 |
rs377701888 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247300 | GCTCACTGCAAGCTC[C/T]GCCTCCCCGGTTCAC | 337867 |
rs377718691 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314067 | TTAAAATTCACTATT[A/G]TAGTGATTTTTTTTT | 337867 |
rs377730318 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334287 | GAGCTTTTAAGGTAT[A/G]TAGGTGTAAAATATG | 337867 |
rs377731900 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315494 | GAGAATGAAAACACT[A/G]TTTTATTAATTGTGG | 337867 |
rs377732648 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348276 | AAGTTTGCAGCCAGC[A/G/T]AGGGGAAGACATGAG | 337867 |
rs377763189 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252769 | TTTAAAAAATAACTT[C/T]TAAGTGATCTACAAT | 337867 |
rs386773814 | in-del | AC/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256050 | CTGGTTAACTACTGA[AC/T]ATTCACAGTAATTCT | 337867 |
rs386773815 | multinucleotide-polymorphism | CCA/TCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293374 | GAAGGCGTCTCTACT[CCA/TCT]GTGTAGTCACAGAAC | 337867 |
rs386773816 | multinucleotide-polymorphism | CC/GA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321685 | TAACTTTAAAATATT[CC/GA]ACTGATTAAAATAGA | 337867 |
rs386773817 | in-del | ATGAGAAA/CGG | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324408 | TCTGTCCCCTTTGCC[ATGAGAAA/CGG]AGCAGGGCCCGGAGA | 337867 |
rs386773818 | multinucleotide-polymorphism | AC/GT | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324605 | CTAAGCACTTTACAA[AC/GT]ATTATTTTAATTAGC | 337867 |
rs386773819 | multinucleotide-polymorphism | AGC/GGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344927 | AGCTCAGGCAGTTGT[AGC/GGT]TGAAATAGATGAGCA | 337867 |
rs397689720 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347203 | AAGAGGGAAAAAAAA[-/A]GAACCCCCAGGGACC | 337867 |
rs397716281 | in-del | -/A | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353738 | TCCTCCCCAAAAAAA[-/A]GCCATCCTGATGGGT | 337867 |
rs397763791 | in-del | -/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246502 | CTACTGAGTGATGGG[-/G]AGGTATGTGTGTCTG | 337867 |
rs397768169 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214838 | TTGTAGACTGTGGGT[-/TT]GGGGAAGGGTTTGAG | 337867 |
rs397774171 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259359 | ATGGTTTTGTCTGAG[-/A]AAAAAAAAAAAAAAG | 337867 |
rs397787039 | in-del | -/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282231 | ATGACACTTGGGGGG[-/G]CAAAATCACCCATGA | 337867 |
rs397794424 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352799 | TGATGGTCACTCTTC[-/C]TGGGAGAAATGTGTA | 337867 |
rs397801956 | in-del | -/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303024 | CCTGCCTCCTGGGGG[-/G]CTTGCTTTCTGGCTT | 337867 |
rs397841540 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385554 | TCTATCTATATTTTT[-/T]ATTGGGCATTTTCCC | 337867 |
rs397851336 | in-del | -/T | 0.451856 | 0.147493 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375971 | ACCAAGCCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 337867 |
rs397851352 | in-del | -/A | 0.499846 | 0.00878459 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318822 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 337867 |
rs397936691 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277809 | TGCCCCATCCCCTCT[-/TT]GTCACCACCCGCAAG | 337867 |
rs397947831 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247208 | TGTTTTTTTTTTTTT[-/T]GTTTTGTTTTGTTTT | 337867 |
rs397952560 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386093 | GCATGGGCTCAGCCC[-/C]AGGAAGAGGAGAAAC | 337867 |
rs397953916 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360111 | CCATTTTACTCTTTT[-/T]ATGGGGCACCAACTT | 337867 |
rs397955698 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363027 | GTTTGGCTTTCCACA[-/A]TTTAAATCTTTAATC | 337867 |
rs397960483 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264984 | TTTTTTTTTTTTTTT[-/T]AATTGTTCTTCAGTG | 337867 |
rs397961108 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287664 | TTTTTTTTTTTTTTT[-/T]GGTAGAGACGAGGTT | 337867 |
rs398024137 | in-del | -/A | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318184 | GTGAAATTCTGTCTC[-/A]AAAAAAAAGAATGGT | 337867 |
rs398037828 | in-del | -/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213234 | CAATTTTTTTTTTTT[-/T]ATTTAAGATGGGATT | 337867 |
rs398037829 | in-del | -/T | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335389 | TACTGTTTTTTTTTT[-/T]CCATATTGACTTCAT | 337867 |
rs398077531 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318183 | CACCATTCTTTTTTT[-/T]TGAGACAGAATTTCA | 337867 |
rs398077532 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347129 | ATTTAAAGAAAAAAA[-/A]AGATCTACGGATACT | 337867 |
rs398077533 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366636 | TAGTTTGATTTTTTT[-/T]TCATCCCTTTCGCTG | 337867 |
rs398117807 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383356 | TTCCAGCCAACCAAA[-/A]TGAATTCTTTTCAAT | 337867 |
rs527240945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374128 | CAGAATGTGAGCTCC[C/T]GCCAGGCAGTACTGG | 337867 |
rs527252403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277768 | TCTGGGCCTACTTAC[C/T]GGGGCTTTGAGTATT | 337867 |
rs527265777 | snp | C/T | 7.0039e-05 | 0.00591731 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295019 | GTCCTGCAAAGTTTG[C/T]CATACAGTTTACGTC | 337867 |
rs527271278 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326780 | GCACATCTCAAGGCT[C/G]TCATCCATGTCTCTT | 337867 |
rs527306081 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360065 | GCTTTTCTAAAACAT[C/T]GCATTCATAATGCCC | 337867 |
rs527314388 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249450 | CCATTGCTGATGGGC[A/T]CTTAGGTTGATTCCA | 337867 |
rs527318156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228437 | GGATTACAGGCTCCC[C/T]CGCACCCCACCACGC | 337867 |
rs527344423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321019 | TATAGATGATATTCA[A/G]TGTTTTGGGGAATGT | 337867 |
rs527380347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205726 | TGTGAGGGCGATCTG[C/G]CTGTGACATCTGTCA | 337867 |
rs527391604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368007 | CAAGCGTGTAAATAC[A/G]AAGATGGTGACAGCA | 337867 |
rs527399885 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321890 | CTATTTTGTTATCCA[C/G]TAGAGACTCCAGCTG | 337867 |
rs527417038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264642 | GTCACTCTCCCCAGG[A/G]GCAGTTGGGTGAGGC | 337867 |
rs527420516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272701 | CTCTTACAAGGGCAC[G/T]AATCTCATCATGGGG | 337867 |
rs527452560 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385502 | CTGTTGCCGTTTTAG[C/T]GTGGAGATAAGTTTG | 337867 |
rs527462872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248492 | TGCCTCCCTGGTTCA[A/G]GCGATTCTTCTGCCT | 337867 |
rs527467991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206900 | TCCGCTTCCTGCTCC[C/T]TCTCTCTGACTTGTT | 337867 |
rs527469998 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200370 | GGCTCCCGTACCCCT[C/G]TATCCGCATCTGAGT | 337867 |
rs527490935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340178 | TTCTGCAGTGTGGTA[A/G]AGGATTTTGCTTATT | 337867 |
rs527510196 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283966 | TCTCAAACTCCTGAC[C/T]TCGTGATCTGTCTGC | 337867 |
rs527514024 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385892 | ACCTTCTCCTACATC[C/T]AGTAACAAAGAATGG | 337867 |
rs527531328 | snp | C/G | 0.0289792 | 0.116832 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200747 | CCCAGCGGGCGCACG[C/G]CCCTGACTGCGCATG | 337867 |
rs527533820 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285003 | ATTTTTGCTATCCTC[G/T]TTCCATTCCCTGGCA | 337867 |
rs527554917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332987 | GAAAATTAGGTCAGG[C/T]ATGGTGGCTCACACC | 337867 |
rs527558544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284942 | ATTTCAGTGACACAA[A/G]CAGAGAGAATAAAAT | 337867 |
rs527565408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341295 | ACCTCTGCCATCTCT[C/G]TGTCTTCCACTAGCA | 337867 |
rs527569426 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293149 | ACCTTTTTGGCAGTA[A/T]GGTTGCTGATGACTG | 337867 |
rs527584161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373608 | CTTGTGGAAGTGTTC[A/G]GGTGCTGCTGAGGCC | 337867 |
rs527596201 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241882 | AGGCAGAGGACCCTG[C/T]GGCCTTCCGCAGTGT | 337867 |
rs527618908 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325754 | TCTGTGAAATTGACT[A/G]TCTTATATACCTCAT | 337867 |
rs527663619 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302059 | TGTAGGTCAAGTCTT[C/G]TCTAGAGTCAGCTTA | 337867 |
rs527681592 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330327 | AGCCAGGCTTGGTGG[C/T]GGATGCCTGTAATCC | 337867 |
rs527683889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219193 | ATTTTTACATGCGTG[A/G]CTTGTGGAGGCAGGC | 337867 |
rs527700500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263174 | AATAGAGAATCATCA[C/T]AAATGGTAATTTGAC | 337867 |
rs527701260 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303964 | GCCTTGTGCTCTGCT[C/G]CACATCCGTGTCTGT | 337867 |
rs527706932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359464 | CTGCCCTTGATCTCC[A/G]TGGTAGGTCATCCCC | 337867 |
rs527708249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313921 | AGAGTTTTCATAAAG[A/T]GTTCTATAAGTACAA | 337867 |
rs527722967 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346264 | TAGTTCAGGCCACCG[A/G]CGCCATTTGCCTGGA | 337867 |
rs527734360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263754 | ATGTTCAACTATAGC[A/G]TGAATAAGTCACTTG | 337867 |
rs527754694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206174 | GGGGTTTGCAGAGTC[A/C]GGTCAGAGGTACTCG | 337867 |
rs527760575 | in-del | -/TTAA | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223482 | CATTGATTTCTACTC[-/TTAA]TTATTTCTTTATATC | 337867 |
rs527768547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345891 | GGGATTACAGGCGCT[C/T]ACCACCACATCCGGC | 337867 |
rs527772232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352688 | ATTCCGCAGAATACA[C/T]GCAGTGCCAGGCTCT | 337867 |
rs527772291 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343589 | TCCAGAGCAGGACAC[C/G]AGCCCCTGGGCTCTT | 337867 |
rs527795953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299078 | GAATAATTATTATTG[C/T]AGAAATTAGGAAAGT | 337867 |
rs527797454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306385 | AGCAGCTGAAGCCAG[A/G]TATTAGGTAACTTGT | 337867 |
rs527829583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248078 | TGACTTAGTTACTGC[A/G]TGCAGCTCTTTTCTC | 337867 |
rs527853933 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283630 | GAGTCACTAAGTGAC[A/G]GCTACTTAAGTGGCA | 337867 |
rs527875447 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214346 | AATGACTGGATTCCT[A/C/G]AGTACCTAGTGTGGG | 337867 |
rs527877808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232554 | ATTAAAATTTTATGT[A/G]TAACCTAGGATAAAG | 337867 |
rs527880036 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247457 | CTGACCTCGTGATCC[G/T]CCCGCCTCGGCCTCC | 337867 |
rs527880267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276470 | TTATAAAGGATACAA[C/T]GCAGGAACAGCCAAA | 337867 |
rs527883949 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332103 | CCTGTTGTCCCAGTA[C/G]ATGGTCGGTTTCTTG | 337867 |
rs527907738 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225126 | AAATATTTGCTTATA[C/T]TTAGTTTTAATTTTT | 337867 |
rs527914795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233237 | CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGACTG | 337867 |
rs527916304 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223749 | CTTCCTCTTTGACCC[A/C]GATATTGTTTAGAAA | 337867 |
rs527916448 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266806 | ATTTTCATCTTCCCA[C/G]ACTGAAAGCCTGTAC | 337867 |
rs527916489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226649 | AATGGCCTGTAGGGC[G/T]CTGGACCATTCCCCT | 337867 |
rs527953399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325188 | GTTCACCGCAAGCTC[C/T]ACCTCCCGGGTTCAC | 337867 |
rs527966917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277039 | TGGCTTAGTATTTGG[C/T]TTTCTCAGGTTTGCC | 337867 |
rs527968147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269401 | CAGAACTTGTTCCAG[A/G]ACATAATTCACTGCA | 337867 |
rs527978131 | snp | C/T | 0.0555102 | 0.157079 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200782 | GGGTGCGCCGTTCGT[C/T]AGCGGCGAGTGGCCT | 337867 |
rs527983190 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366000 | AGGTCTATTTATTTG[A/C/G]CATGAATGTAGCAAC | 337867 |
rs527994213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319091 | GGACCTGACCAAAGT[C/T]TCATCATGGAAGAAG | 337867 |
rs528027534 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297083 | GTGTCAATGCATAAT[G/T]TGCTTAGCTACTCCC | 337867 |
rs528049724 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287993 | GCAGTAACCTTATAC[A/G]TTTTTACTATGTAGC | 337867 |
rs528051036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305120 | TTAGACTGAAATTTC[A/G]ATTGAAAAAAGATGG | 337867 |
rs528054035 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320340 | TAAAAGGAATCAGAC[A/G]TTTAAAATAAAATTC | 337867 |
rs528095416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205686 | GCGCTGATGAGAGAA[A/G]ATAGAAGATAGAAGG | 337867 |
rs528102569 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290649 | TGAATCATTTAAACC[C/G]AGGAGGTGGAGGTTG | 337867 |
rs528103499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337953 | ATTGGAAGAAGAATT[C/G]TCTTGGGCCACACAT | 337867 |
rs528112997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290451 | ACAGGCAAGGCCGGG[C/T]GCAGTGGTTTACGCT | 337867 |
rs528114325 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310851 | TTACTAAATGTAAAC[-/AGA]AGAACTTCTATGAAT | 337867 |
rs528140678 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264044 | TCATCTGTATGGCAG[A/G]ATCCTGGAGCTGTTG | 337867 |
rs528151630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247117 | CTGGAATTGCAGGTG[G/T]GAGCCACTGCACCCA | 337867 |
rs528159389 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199397 | AGCGAGACTCCGTCT[C/G]AAAACAAACGAACAA | 337867 |
rs528223003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225460 | ATGTCCTCAAGGTTC[A/G]TGCATGTTGTTCCAT | 337867 |
rs528264409 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266169 | TGGTAGAATATTATA[A/C]AATATTTTAATGTTA | 337867 |
rs528283409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260503 | GAGACTTAGGCAAGG[A/G]CCTGAGGTCTGTCGT | 337867 |
rs528284331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236429 | ACATTCTCAAAAGAA[A/G]ACATACAAATGGCCA | 337867 |
rs528302173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217210 | GCTAGGCCGTTGCTC[A/G]GCGTCAGTGGCTGGA | 337867 |
rs528323330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312133 | GTTGTATTTTGGTTT[C/G]GTTTTGTTTTTAACA | 337867 |
rs528337071 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318339 | CGCCTGGATAATTTT[G/T]TATTTTTAGTAGAGA | 337867 |
rs528360835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350644 | CATCTGTATCCCTTG[A/C]AATATCCTTTCTAAT | 337867 |
rs528367676 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291683 | TTAATGTGTCTAATT[G/T]AAATTACAGGATCTT | 337867 |
rs528395029 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216608 | AATGCCCTCAATTCT[C/T]CCGAAGATTGTTCAT | 337867 |
rs528407980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253835 | AAATTTCTAACCAAT[A/G]CATGTATTTGGTTCT | 337867 |
rs528409980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304389 | TGTATTTGTGAGAGT[A/G]CTGTGCTCTGTCATA | 337867 |
rs528416796 | snp | C/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259387 | CATAGTAAATCTGTG[C/G]CTTAGAAAAGTTACT | 337867 |
rs528423221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344168 | CCTAGAGAGATGCAG[G/T]TATTCCCTCATGACC | 337867 |
rs528431445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351045 | CACAATAGAAAGCAG[C/T]GTAATATAATGAAAA | 337867 |
rs528438778 | in-del | -/TC | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99231494 | CTCGGCTCACTGCAG[-/TC]TCTGTCTCCTGGGTT | 337867 |
rs528457518 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227173 | ATTGCACTCCAGCCC[A/G]GACAACAAGAGCGAA | 337867 |
rs528457704 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230356 | CTGTAGTCCCAGCTG[C/G]TTGGGAGGCTGAGGG | 337867 |
rs528466993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289280 | TTGAGTAGTCAAAGA[A/G]GGATTAAGGGAGGCG | 337867 |
rs528476785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237554 | TTAGAAGAAATAAGA[C/T]GGTGTTCAGTAGGTC | 337867 |
rs528507387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370486 | AGTTTCCCTCTGCCT[A/G]TTGTTTTTCCCTTTC | 337867 |
rs528544486 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359893 | AGGGGGCCACCGATT[A/G]TAGACTGGAGGTGCC | 337867 |
rs528546165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323642 | ACACACACTCACATT[C/T]ACGTTGACTCATCCA | 337867 |
rs528591470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324244 | GTTCTGCCCCTCTCT[A/G]CTGAAGCCCTCCCTA | 337867 |
rs528606512 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345292 | TTGGCTGTGAAAAAT[G/T]GTTTATTCAGTAACA | 337867 |
rs528614479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275812 | GCTGATTGGAGTCTC[A/G]GGATGAGGTCCTCGA | 337867 |
rs528625593 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364137 | CTTTATGTGAGATTT[C/T]TGTTTGGGTTTGGTT | 337867 |
rs528638996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302963 | GGATTGAGAACAATG[A/T]TATTCAGCATAGAGT | 337867 |
rs528647725 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366590 | AGGCAGGACCAAGAT[G/T]CCTGCTGTCTCCGGG | 337867 |
rs528650789 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209594 | CAAACCTGAACAGCT[C/T]GTTTACTCTTGGGGA | 337867 |
rs528651085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203083 | CTCACTGTTGCCCAG[A/G]CTGGAGTGCAGTGGT | 337867 |
rs528657796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251935 | CCCTTCCATGTATTG[C/T]TTTTCTTAAGAGACA | 337867 |
rs528688032 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343291 | GGATTCTTGGCTGTT[A/T]GCGCACGCCCTCGCT | 337867 |
rs528727129 | snp | C/G/T | 1.67427e-05 | 0.00289328 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295818 | TGTTGATGTAAAACA[C/G/T]TAGCGCAGTTATCCT | 337867 |
rs528743570 | snp | G/T | 7.96559e-05 | 0.00631044 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244501 | TATCATTTTTCTGCT[G/T]TTTTATTTTGTAGTC | 337867 |
rs528783516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245305 | AAACAAAATTAATTT[A/G]TACGAAGTTAAGCTT | 337867 |
rs528789229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376477 | TGGGTCTTCATCCCC[A/G]TGAGGGCGGAGCTGG | 337867 |
rs528797216 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316460 | ACTTGAATCATAATC[A/G]GAAGAGCCAAAATGC | 337867 |
rs528802346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383224 | CCAGTTAAGCTGGGC[C/T]TGCTGAAAACACTCA | 337867 |
rs528839492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291254 | CAGCAAGGTCTTAAT[C/T]GAATAGAAATTTGGG | 337867 |
rs528840078 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239326 | TCTGTATTATTTCAG[C/T]TGCTATAATGCAGTC | 337867 |
rs528841999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247712 | ACCTCTGTAACAAAC[C/G]TGCACGTTCTGCACA | 337867 |
rs528843473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285235 | TTTTGCATTCGATTG[C/T]GGTGTGTCTTAAGTA | 337867 |
rs528854685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384907 | GAGTCGTGTGTCCTC[A/G]CAGTGAGCCTGGGCA | 337867 |
rs528865435 | in-del | -/CC | 0.0240643 | 0.107019 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280829 | CCTTCCTTCTTCTTT[-/CC]CTCTCTCTCTCTCTC | 337867 |
rs528883873 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378715 | CCAGAGGTTGTGTCA[A/G]GCTTGCATAGCTGTG | 337867 |
rs528901688 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316000 | AACCTAATATCTAGT[A/G]CCGTTTCCACAGTGT | 337867 |
rs528907830 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258032 | GGCCTCCCAAAGTGT[A/T]GGAGTTACAGGCGTG | 337867 |
rs528915202 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214133 | CTGATTGTGTATTTA[C/T]TGTAGAGCCAGGGTT | 337867 |
rs528934329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332233 | ATAGTTTCTAACCTT[A/T]GCCTGTTGTGGTTTC | 337867 |
rs528990676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233274 | CGCACCACCATGCCC[A/G]GCTAATTTTTGTATT | 337867 |
rs529009901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325216 | CACACCATTCTCCTG[A/C]CTCAGCCTCCCAAGT | 337867 |
rs529054617 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351092 | TTAGGGACTCAATCC[G/T]GGGTTGACAGGGACA | 337867 |
rs529074709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312615 | TGGTGAAACTGACAT[A/C]GCTTGGGGGCCACGA | 337867 |
rs529094209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290042 | GTTTATTTGTTTAAG[A/G]GAGAAAATACGATGA | 337867 |
rs529098337 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305817 | GAGAGAAAACATGCT[-/A]AAATATAAGAAGTGT | 337867 |
rs529109883 | in-del | -/A | 0.499999 | 0.000798721 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232450 | TCTAAGGACCAAAAG[-/A]AAAAAAAAAAATCTT | 337867 |
rs529110047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262022 | GCCATTCTGAGCAGC[A/C]GGATGAAATCTCTCA | 337867 |
rs529118453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344881 | GAAGAACATGTCCTT[C/T]CCCTCCGTGAGTTTG | 337867 |
rs529134464 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263477 | CCATTCGCCAGAATG[C/T]CTACGATGAAAAAGA | 337867 |
rs529158395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205704 | AGAAGATAGAAGGAT[G/T]CTTGGATGTGAGGGC | 337867 |
rs529177449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345702 | TCTCCACTTCACTGT[C/G]CCATCAGCTCTTGAC | 337867 |
rs529198117 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212005 | TTTACCTTTGGTAGA[C/T]ATGTTTTATGTCCTG | 337867 |
rs529220551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297847 | TTGCTGCTTAGAAGA[C/G]ATACAGCTCAAAGTG | 337867 |
rs529225886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324349 | GTGACAAATGCTTCA[C/T]CCAAGCAGAAGCTTG | 337867 |
rs529253265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282691 | GGAACTTGAAGTCTG[A/G]TTGTATTCAAGATTC | 337867 |
rs529260437 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371295 | GTTGTAAAAACATGA[G/T]GGGTTGTTTTTAACA | 337867 |
rs529288870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364174 | CTCATTATGCTGTGA[C/T]TTGTGCTGAATGCAA | 337867 |
rs529311481 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324667 | TTCTCCCTATTATAG[A/T]TGAAGAAACTGAGGC | 337867 |
rs529317559 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256571 | CCTCATTCCATCTAG[A/G]TTCAGAAGCTTCAAT | 337867 |
rs529321444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371813 | CAAGAAAACCTGGTA[A/G]ACATGAAATGTATGC | 337867 |
rs529340704 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227436 | ACAAGAATGATTCCC[C/T]GGCTCTTAAAGGGTC | 337867 |
rs529363742 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317011 | GTCATTTCCACTGAA[A/C]AAACGTCCGTGCTAC | 337867 |
rs529370646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324645 | AAACCTGAGGAACTA[C/T]GGAATATTCTCCCTA | 337867 |
rs529371537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312270 | CAAGGACAGTTCTTT[G/T]TAGAAGTGAAACATA | 337867 |
rs529378134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217337 | TTTCTCCCAGGGAGA[A/G]GTCCCGTGGCTCATC | 337867 |
rs529384277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350724 | AATTAACTGAACCCA[A/G]GGAGTGGACCACGGG | 337867 |
rs529392147 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384548 | TGCTTCTGGTGGCTT[A/T]CACTGCCTCCTTCCT | 337867 |
rs529402549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296239 | ATTAGTTTTAAAAAA[A/G]TTTAAATAATGTATC | 337867 |
rs529403856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268502 | AGTCTCAGCTACCTA[C/G]GAGGCTGAGGTGGGA | 337867 |
rs529404273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261458 | TGGTTTTTCTTAAGT[A/C]CCAACAATTTACAGC | 337867 |
rs529429207 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204447 | TGGAGTGAGCAGTTC[A/G]TAAGAGATGTGTGGT | 337867 |
rs529431853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383311 | TAAGTCTAGGACAGT[A/G]CATATCTCTGTTAAA | 337867 |
rs529452748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336797 | TAATTGTGATATACA[A/G]CACAAACTAACTGTC | 337867 |
rs529504849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289585 | CTGGATAGTGTCTGC[A/G]TTTTTCTTTTCTTAC | 337867 |
rs529519025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330042 | CAATTTTTAAATTTT[C/T]AATGTACAGGTCTTG | 337867 |
rs529531780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237599 | AGTTGACACTAATCT[A/G]TCGTACGTTTCAAAA | 337867 |
rs529554748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323836 | TTGTTAACACAGGGA[A/G]GTAGCGACCAGTTGA | 337867 |
rs529567796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290259 | AAAGTGCTTAAAGCA[C/G]TATGCTATATAATTG | 337867 |
rs529568112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231019 | TGCCACTGTACTCCA[A/G]CCTGGGCGACAGAGG | 337867 |
rs529577089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245978 | GGGAAATGAGATAGT[A/G]TGAAATATAGATACC | 337867 |
rs529581366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330411 | TTGTAGTGAGCTGAG[A/G]TCATGCCACTGCACT | 337867 |
rs529594981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238054 | AAAATGTATTTTTAT[A/G]TATGTATGAGTTTTG | 337867 |
rs529601295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370566 | CACGCCATCGCCTCC[C/G]CATTCCCTGTCCCCA | 337867 |
rs529603626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377620 | TTTGCTAAACTTTAT[A/G]AATACATAAAGTGTA | 337867 |
rs529652695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215886 | CTTACTATTCCTGAT[C/T]GGATCAAAGAGAAAA | 337867 |
rs529666338 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328020 | TCCCCACATCCAGCT[A/G]CCAGCCGCAGGTAAC | 337867 |
rs529669426 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241490 | AGTGAAATGAGCAAA[C/T]GCAAAAGGACAAATA | 337867 |
rs529679056 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259632 | AGATAGGACTTCTTA[C/T]GGCTGAATCACATTC | 337867 |
rs529703567 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362653 | GATTTCCCCTTCTGT[A/G]AATGGAGTATTCATA | 337867 |
rs529708187 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242978 | AAGAGGCGCTCCTCA[C/G]TTCCTAGATGGGATG | 337867 |
rs529710212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203713 | ATGAAGACAATGAGA[A/G]GGTAACTGCAAAGAC | 337867 |
rs529716949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267565 | CCAGGAGGATATAAG[C/T]AAGGAAGGAAGAAAC | 337867 |
rs529766033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210154 | TTCATTTAATTTATT[C/T]GTCTTTTCTTTTTCT | 337867 |
rs529774777 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252010 | AAGCCCAGTCCTCCC[A/G]CCTCAGCCTCCTGAG | 337867 |
rs529848943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273620 | GTTGATGAATTTAGT[A/G]TTGATCTGATTATTA | 337867 |
rs529853711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369128 | CTAAATGGAATGTCA[A/C]GTAATAAATATACAA | 337867 |
rs529860109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287811 | TCTTTTAACAAACCA[A/G]TAATGTTCAACTTTA | 337867 |
rs529861696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252914 | ACTCTTCTTATCAAG[A/G]CAAGCTATGGCAGAG | 337867 |
rs529864113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369777 | AAATTAACATCACCA[A/G]TTATGGAACAAAGAA | 337867 |
rs529872090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341923 | AGATGACTGATAGTT[C/T]CATTTCACCAATATC | 337867 |
rs529892075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | UBAC2 | GRCh38.p7 | 13:99329176 | TACGCCAATACCACA[C/T]TGCACTGATGACTAC | 337867 |
rs529908479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229469 | AGAACAAAGCAATGG[A/G]TGTTGTGCTGGAGAG | 337867 |
rs529925601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362096 | ATTTATATTATTTAC[A/T]TAAACTACATACAAT | 337867 |
rs529970053 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352799 | GTGATGGTCACTCTT[C/T]TGGGAGAAATGTGTA | 337867 |
rs529981020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266895 | TGAAAGTGAAATTGC[C/T]GGATCGTGTGGTAAT | 337867 |
rs530014222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251042 | ATAGGCATGAGCCAC[C/G]AAGCCTGGCCATCTT | 337867 |
rs530054637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294390 | TAAAAGACTGTGCTG[C/G]CAGCTCCAGGAAAAG | 337867 |
rs530068264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302029 | GAGATGATCACCAAT[A/T]GGAGGTGACTTCTCT | 337867 |
rs530084222 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243001 | ATGGGATGGCGGCCG[A/G]GCAGAGACGCTCCTC | 337867 |
rs530085687 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214017 | AGAGATGGGGTTTCA[C/T]CATGTTGGCCAGGCT | 337867 |
rs530115302 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287133 | AATAATTTGACAGTT[G/T]GATCCCTAATGGGAC | 337867 |
rs530125262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375484 | CCCAACAGGGTGTGC[A/C]TGCTACCCTGCACCC | 337867 |
rs530137107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342437 | TGGAAAGGGCCCAGC[A/G]TAGTCTCGGCGCTGA | 337867 |
rs530185547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222041 | TTTTGAGGTTTAAAC[C/T]GTGTAAGTAATTCAT | 337867 |
rs530191295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360994 | TTCTCTAATGTAGAC[A/G]CTGCCTGACCATCCC | 337867 |
rs530191535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335201 | AAAATGTTTAATTTT[A/G]TACTTCATTCAAATC | 337867 |
rs530224005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315188 | CCATCTCTCAACCCC[C/T]GTACCGTTACACGCC | 337867 |
rs530238308 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325433 | AAAAGATAGCTTTGC[A/G]TAACCACATGCAGTT | 337867 |
rs530242157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214854 | GGGGAAGGGTTTGAG[A/G]CCCCACTGCTGTCAT | 337867 |
rs530252971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257352 | TATTAAATAGTAGCA[A/C]TTATAATATAAATGA | 337867 |
rs530256021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328343 | CATTTGTGTGTGGAC[A/G]TATGTTTTCCTTCTT | 337867 |
rs530283540 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266678 | TAGAACAAATTTGAC[-/AT]GTTAAATATATATAT | 337867 |
rs530285244 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297659 | AGCAAAAATGGAAAT[A/C]AAACATTTTATTATC | 337867 |
rs530303056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208185 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 337867 |
rs530305349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307896 | ACAGGTTTCTGTGGC[A/G]TGGGGGTGAGTGACA | 337867 |
rs530311208 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323217 | GCTCAGATAACTCCT[C/G]TGATGCACAAGCCTC | 337867 |
rs530311295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214394 | GGTACAGCCTTTTCC[C/T]GCAAGAGGCTCAAAC | 337867 |
rs530312642 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382593 | GAGACGGTGTGCACA[A/G]ATGGGAGGGGATGGG | 337867 |
rs530320572 | in-del | -/TCTCATTGTGGTTTTGATTTGC | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249788 | TGGTGTGAGATGGTA[-/TCTCATTGTGGTTTTGATTTGC]ATTTCTTGATGATTA | 337867 |
rs530365493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250399 | ATTTCTGGGTTCTCT[A/C]TTCTGTTCCACTGGT | 337867 |
rs530365558 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258660 | CTTTATAAGCTATGT[A/G]ACTTTGTCTAGTTAC | 337867 |
rs530366033 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376666 | GTGGAAGACAGGAAA[A/G/T]CAAAGCATGCTGGAG | 337867 |
rs530373359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348454 | CGGGGGGCCTTATGA[A/G]AAAACGCACAGGGGC | 337867 |
rs530404901 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348088 | TACTTGCAGCTGTGA[A/T]CATCTTTACACTGCC | 337867 |
rs530422259 | snp | C/G | | | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99294245 | GAAAAGAGAAATGAT[C/G]CCCTAGTGATCCCAA | 337867 |
rs530429351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301272 | CAGGTTCCACCTGTG[G/T]AACAGGGCCCTGTCG | 337867 |
rs530430597 | snp | C/G/T | 0.0221141 | 0.102801 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204675 | AACGGGCCTGAAGCG[C/G/T]GACCTGTGGGAAAGA | 337867 |
rs530432168 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386513 | AACCAAATCCTCCGC[A/G]CTGCTCGTCTTTCTT | 337867 |
rs530435233 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309070 | ATAGTGAAGGACTCA[C/G]CTAGTTCAAGTAATT | 337867 |
rs530446110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261078 | ACATTTGTCTATGCC[A/G]CAGGTAAAATAATAT | 337867 |
rs530471987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367445 | CCCTGAGCTCCTAAG[A/G]GTTAACTGGAGTTGG | 337867 |
rs530474036 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342121 | ACACCGTCAGCATCA[A/G]TATCTATGGGGGCGG | 337867 |
rs530486024 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359971 | TTCTGAGCACCAAAG[A/G]CTGAGAAGAAAGGGT | 337867 |
rs530487017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312004 | TGTCCCCAGTCCTGA[C/T]ACAGTGCCTGCACTT | 337867 |
rs530511240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210299 | AGGAAGAAATAAAAT[A/G]GCATTTATTGATATT | 337867 |
rs530532783 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241100 | AAACACCATCTCTAC[-/A]AAAAAATACAAAAAT | 337867 |
rs530563122 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266280 | AAAACAAGGTGGCCA[A/G]TCTTCTGGCTTCCCT | 337867 |
rs530572082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370444 | CTATAAAAGAAAGTT[A/G]AGAGTGTTGCCATCA | 337867 |
rs530573234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304265 | TCTTCCCTCTGTTTG[A/G]TGTCCTCTGGCCCCT | 337867 |
rs530581173 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245480 | CTTCTTTAAAAAAAA[A/C]AAAAACCATGTATTA | 337867 |
rs530587192 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250557 | GGCTATTTGGGGCTC[-/T]TTTTTTGGTTCTATA | 337867 |
rs530615570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224203 | CTGCTGGCTTCTAGC[C/T]GTGTCATCACATGGT | 337867 |
rs530634283 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373634 | AGGCCAAGAAAGGCC[A/G]TCAGGGCAGTGGTGT | 337867 |
rs530723883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323588 | GCCTTATAATTAAAA[C/T]AGCAAGTGTGATGTC | 337867 |
rs530728038 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298133 | GTGGGAGATCTTAAC[A/G]CATTTCTATTATGAT | 337867 |
rs530739823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275014 | TGAGCCACTGCATGC[A/G]GCTTGAATGTCTTTG | 337867 |
rs530742278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215945 | TCTCTAATAAAGGCT[A/G]TTTTCCTATTGTAAC | 337867 |
rs530745299 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377012 | CTCACCATTGCCTCC[A/T]CTCACGCCAGAACAA | 337867 |
rs530754123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350080 | TGACCCTATGCCCGC[A/C]GGTTATTCCTAGGTT | 337867 |
rs530763137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317019 | CACTGAACAAACGTC[C/T]GTGCTACATCAAAGG | 337867 |
rs530775488 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217012 | ATTTTTGTATTTTTA[A/G]TAGAAACGGGGTTTC | 337867 |
rs530801209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244350 | TAAAGTCTATTTTAA[C/T]AAAAACAAATAATTT | 337867 |
rs530812154 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364271 | CCTATTGAGATGAGC[A/G]TTTGATTTTTCTCCT | 337867 |
rs530836582 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376235 | GACAGTGACAGTGCT[C/T]TTGTGGCAACGCCTA | 337867 |
rs530856717 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216610 | TGCCCTCAATTCTCC[C/T]GAAGATTGTTCATAT | 337867 |
rs530859370 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208819 | AAGCTGACCCTGTGT[C/T]CTGCAGGTGCTTCAG | 337867 |
rs530864920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320809 | GTTTGATTTACACAC[C/T]ACTGACTATAGGATC | 337867 |
rs530866361 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347624 | CATATTCCCATTCCA[C/G]AGCTCTGATGAACAG | 337867 |
rs530882224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329243 | TCCTCCCACCTTGTT[G/T]TTCTTTTTTAAAACT | 337867 |
rs530887364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237061 | TCAAGGACATATCTG[C/T]ACTTCCATGCTTATT | 337867 |
rs530890552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281374 | TCTTATATTCACAAG[A/G]TATCTCCTTTCTCAA | 337867 |
rs530895471 | in-del | -/TTA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211501 | ACTAATAAGTGTGAG[-/TTA]TTATTGGTTTTAATG | 337867 |
rs530898155 | snp | C/T | 0.00143279 | 0.0267272 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295735 | TATCTTGTTGTAGCG[C/T]AGAGGGTGCACCACA | 337867 |
rs530901423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369958 | AAAATACGATGTTCC[A/G]GATTAAAGGAGACTT | 337867 |
rs530904134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287313 | GGTACCAGGTTTCAA[A/G]TAGAGCTCATAGGAG | 337867 |
rs531012854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321126 | ATTTTATTTCATTCT[A/G]GCAATTAATGTGGTT | 337867 |
rs531014973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348535 | TTCCTATAAGAAAGA[C/G]GCAATGAAAGACATG | 337867 |
rs531018127 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208792 | TGGCTCCCTGAGCCT[C/T]GCACGTAGTTAAAGC | 337867 |
rs531023457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376909 | TGAGACATTTTTAAA[A/G]TTTTCCAGACCAATG | 337867 |
rs531038077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323198 | AAGAGTGGTATAGGT[A/G]GCAGCTCAGATAACT | 337867 |
rs531069266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251090 | GTTTTGTAGTTCTTG[C/T]AGAGATCTTTTACCT | 337867 |
rs531072534 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380050 | CACAGCTGAAGGAGG[A/G]TGAGAGGGTCTCTTT | 337867 |
rs531076038 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323067 | GCTTCTGGGCGAGGG[A/G]TGGTAGGTGTGAGTT | 337867 |
rs531076318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342692 | TGGATGCCCGTGGTG[A/G]GCACGACCTGCAAGA | 337867 |
rs531079486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99202937 | CAGTTTTCCAGGACT[G/T]GTCATTAGAAAAGGC | 337867 |
rs531123821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208204 | GTTTCTCCATGTTGG[C/T]CAGGCTGGTCTTGAA | 337867 |
rs531158552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243650 | TGCCACTGTTGGGAG[A/G]AATTTTTACTATGAG | 337867 |
rs531174998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279726 | AAGGCACTGGCAGAT[C/T]TGGTGTTTGGGGCTG | 337867 |
rs531176040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302070 | TCTTCTCTAGAGTCA[C/G]CTTATACAGAGAGGT | 337867 |
rs531204886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228880 | CAAGACCTTACCAGA[C/G]AGGAAATAGTTGGGC | 337867 |
rs531214121 | snp | A/G | 3.4205e-05 | 0.00413537 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295053 | ATAAACCAAAATACA[A/G]TCCATTTCACTTTCC | 337867 |
rs531243652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322694 | AAAAACAATCTGTTA[A/C]ACCCAAAAGTAAGAT | 337867 |
rs531248235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381911 | AGATGGTTTGTGAAC[A/G]TTGAAAAGACAGCTG | 337867 |
rs531280252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251730 | GCCATCAGACCAGAT[A/T]TGAGATTCCAGCTCT | 337867 |
rs531285557 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368123 | GGGGCGGCGGGTGGG[A/T]ATGTATTATGGTAGC | 337867 |
rs531324711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222914 | GTTGTAACAGAGTTT[G/T]TATAGAATTGGTATT | 337867 |
rs531327295 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374221 | GTTACTTCAGGTTGC[-/T]TTTTTTTTAAGGGTT | 337867 |
rs531336011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214880 | GTCATGCTTGTTCGG[C/T]GGCATTTGCACCACT | 337867 |
rs531346102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368904 | ACAGGATAGCCCTGG[A/G]TCATCGTGTGCCAGG | 337867 |
rs531350042 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382288 | AATTTAACAGAGATA[C/T]GTAGAGTCCTAGACT | 337867 |
rs531350949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361292 | ATTGCTTTTGAAGAA[A/G]ACAAAGTAAAGGAAA | 337867 |
rs531372339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315277 | TGAGTAGGATTTGCT[A/G]TAGCAGATTTAATAT | 337867 |
rs531386758 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224491 | TGTGGATTTATCTAC[A/G]TCCCATTTCAGTTCT | 337867 |
rs531389491 | snp | C/T | 0.00166113 | 0.0287716 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201206 | TGCCCAGGAGTCTCT[C/T]GGGGCCGCTGCAAGT | 337867 |
rs531422460 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306983 | TCTATATTAAAATAA[C/G]TTTGTTCCTTTTCCT | 337867 |
rs531432397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380681 | ATACCCAAGCCCAAG[C/T]ATGCAGTTTCAGTTT | 337867 |
rs531453179 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289771 | TGGGTGGGGCATGGG[A/G]TGGGAGTTCTCACTT | 337867 |
rs531459173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308586 | ATGATGTAAACAGAA[A/T]TGAATCATTTGGTAG | 337867 |
rs531475251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326869 | GGATGAGGCCCCATT[A/C]ATCAGCAATGGAGAC | 337867 |
rs531496324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380293 | TTCGTCTTTCTGTAA[C/T]TTGAGCACAGGAGTT | 337867 |
rs531514079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235479 | AGTAGCCAAAATAAT[C/G]CTGAGCAAAAAGAAC | 337867 |
rs531517075 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241948 | ATGACTCTTAAGGAG[C/T]ATGCTGCCTTCAAGC | 337867 |
rs531562447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374197 | AAATAACTGATAGGT[C/T]AACATTGAGTTACTT | 337867 |
rs531568972 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202255 | GATTTCCTTTGTTTC[A/G]TAATTAATTTGATTT | 337867 |
rs531598205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314572 | AGTAGAAAGTAGAAA[A/G]TCAGTGTCAAAATTA | 337867 |
rs531605026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234847 | ATTAAATGACATACT[C/T]GGGGGAAATGTTCCT | 337867 |
rs531612812 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327671 | GTCTTCCATGTTAGC[G/T]TATATTGATAGCTGA | 337867 |
rs531613425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278545 | CTAAATAGCCAACAT[A/G]TAAATAATCATCATA | 337867 |
rs531652271 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338015 | CTTTAAAAAAATTGC[-/A]AAAAAAATCTCCTAA | 337867 |
rs531673883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256972 | TTTAAGGAAAACTAT[C/G]GGGGAGATTTGCTGT | 337867 |
rs531691236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306543 | CACACACAAACACAC[A/G]TATATAAAACCCTCA | 337867 |
rs531724917 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326128 | ACTGTTTTCCATAGT[G/T]GCATCATTTGCATTT | 337867 |
rs531729904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213643 | GGGATTACAGGCATT[A/G]GTCACTGCACCCGGT | 337867 |
rs531735425 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206983 | CCTTCTCCTGAGGCC[C/T]ACCCTCCACCGATTC | 337867 |
rs531775847 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381495 | TAGCTTTTCCAAGCC[A/G]TTTAAATAAACGTCA | 337867 |
rs531795160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248635 | TGATCGACCTGCCTT[A/G]GCCTCCCAAAGTGCT | 337867 |
rs531796109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270174 | TCCAAATTTTAACTA[C/T]GTAAGGTGAGGCAAC | 337867 |
rs531797275 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301543 | CTAGAATGTATTTCA[C/T]TGCTAATAGAGTTGC | 337867 |
rs531797959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277640 | TTGATAGTTACCTCT[A/G]CAATCATTCAGACAT | 337867 |
rs531804172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347214 | AAAAAGAACCCCCAG[A/G]GACCAAGGAGAAAAC | 337867 |
rs531859121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341394 | TAGAGTCCCATTGGA[A/G]ATGCAGGTCCCAGAG | 337867 |
rs531902249 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201324 | CATGCCCCATTCTTT[C/T]AGGCTTGGGGGACCG | 337867 |
rs531942069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325644 | ATCTCTGGAGCTTAT[C/T]GCTCTTGCTTAACTG | 337867 |
rs531964160 | snp | A/G | 9.80633e-05 | 0.00700157 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243980 | TATTTTGTCTTTGCT[A/G]CTTAGGCTGTAGAAA | 337867 |
rs531972720 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306760 | TTTTTCACTTATCTA[A/G]TTAGTAGTATTTAGC | 337867 |
rs531977399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315891 | AAGAGGCACAGCATG[A/G]CCTTCATCACGGGGC | 337867 |
rs531978892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319848 | CTGAGGAAGACTTAA[C/T]CAGCCTGAGAACAGC | 337867 |
rs532007144 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219869 | TAATGTTTTTGAGGT[A/T]CATCTATGTTGTAGC | 337867 |
rs532007560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359534 | TGTGTAAGTATTTCC[C/T]TATGGCCTGGGGTAA | 337867 |
rs532012988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316286 | CCACCTTGAAGGAGT[A/G]TAACTGAACTCCTTT | 337867 |
rs532014599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309285 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA | 337867 |
rs532024058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215421 | AGAGATTTGTGGATG[C/T]GTGGAATGACACCAC | 337867 |
rs532058327 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332498 | ACAGGGTCACAGCTT[A/C]TGCTGTTGGCATATG | 337867 |
rs532061554 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303509 | TTGAAGATGAAGATG[A/G]CATATGTTTAGAGAA | 337867 |
rs532075926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219931 | ATAATATTCTATTGT[A/G]TGGATATACATTTTG | 337867 |
rs532098401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309986 | TTTTATGTTTTCTAT[C/T]GAGTGCGATCATGAA | 337867 |
rs532104473 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289548 | TGAAAGTGGGATTAA[A/G]GAAGATTGTTTGCCA | 337867 |
rs532108105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361645 | GACCATTCTTTGTTA[C/T]AGCGGCTGCCCTGTA | 337867 |
rs532133378 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379724 | TTCTTCAGATCCTAT[A/G]TGGTGGTCACTCCAA | 337867 |
rs532148354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286204 | TATCTATAACTGAAC[C/T]TTGGCTGACAGAACT | 337867 |
rs532151776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349286 | ATGTATCTGTTCTCT[A/G]CCACTGGCCCCTGAC | 337867 |
rs532152688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355015 | CGGTGAACGCAGATA[C/G]GCAAGTGCGGGAATG | 337867 |
rs532157505 | in-del | -/TATTTATT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203050 | ATTTATTTATTTATT[-/TATTTATT]GAGATGGAGTCTCAC | 337867 |
rs532187329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266809 | TTCATCTTCCCAGAC[A/T]GAAAGCCTGTACCCA | 337867 |
rs532227894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355640 | GGAAAAGGTTGGGAC[A/T]CCTCTGGTCCTGACG | 337867 |
rs532235228 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304508 | TCTAGGTGATGTATG[A/G]TCGATATTCAATAAA | 337867 |
rs532260186 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215732 | CTTGGCCTTTCCGGA[C/G]TCCTTCCCAGCCTTA | 337867 |
rs532275059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328284 | TTGAGTTGCTTCCAG[A/G]TTTGGATTATTATGA | 337867 |
rs532289512 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259556 | AACTCAAGGTAAAGC[C/T]AGGTCCAGTTTCTCC | 337867 |
rs532301219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280474 | GTAGCTCTGCTCCAC[A/G]AAACCCTGCTCCAGC | 337867 |
rs532304277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374888 | GCCCCAGCATCGGTC[A/G]GAGAAGGGTTGAACA | 337867 |
rs532304883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369029 | GGGGATCAGAATAAA[C/T]AAAGGATAGTAAGAA | 337867 |
rs532335405 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355577 | CTCCTCACAGAGCAG[C/G]CTTAGCATTCTCATT | 337867 |
rs532335774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235653 | GGTGGCAAGAACATA[C/G]AATGGAGAAACGACA | 337867 |
rs532360224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308347 | TGCTTTGTAGGCATA[A/G]GGTCATTATCCTTAT | 337867 |
rs532380731 | in-del | -/TC | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327472 | TTGGTTTTTGGTTTT[-/TC]TCTCTCTCTCTCTGT | 337867 |
rs532380986 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368148 | GGTAGCTTGTTTTAG[A/G]TGCTCTTACACTTCA | 337867 |
rs532390640 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373290 | AACCAAAGGGGGAAA[A/G]ACTCATCAAGTGTAT | 337867 |
rs532410674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347993 | AAGCTGCTCTCAGTA[A/G]TTCCTTGCCCGCTGA | 337867 |
rs532421929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236180 | TCTCAAAAGCACAGA[C/T]AGCCAAAGGAAAAAT | 337867 |
rs532450073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222216 | AATTTCAAGTAGTAA[A/G]GAATGCCACAGAGTA | 337867 |
rs532457642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99294148 | AGCTATATTTTTCAC[G/T]GCTCATCATGCACCA | 337867 |
rs532459561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229412 | AAGCAACATGTTCAG[A/G]AGGTAGTGAGCTGTG | 337867 |
rs532529612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359649 | AGCCACTGGGCCAGC[G/T]GTAAACAGTTTTGGC | 337867 |
rs532546567 | in-del | -/AC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244400 | TGCATGTGTGTATAT[-/AC]ACACACACACACATA | 337867 |
rs532554010 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373480 | GACCAGCTGTCTGCT[C/G]TGCACCGGGGCTAAG | 337867 |
rs532557928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341461 | TAGGGGCAGAGTCTA[C/T]AAGAGAAATAGAGAA | 337867 |
rs532585693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263998 | TTTGGGTGGGGTGTG[A/G]GCATGTGTAATAATA | 337867 |
rs532591510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360110 | CTCCATTTTACTCTT[C/T]TATGGGGCACCAACT | 337867 |
rs532604361 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242232 | ATTGTCATCATGGCC[C/G]GTTCTCAATGAGCTG | 337867 |
rs532611104 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221103 | TTTTTATGGATAGAA[A/C]ATAATTTACCCATTT | 337867 |
rs532614247 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325501 | TTCTTCTAGGAAGTC[C/T]TACTCATTTAAGTCC | 337867 |
rs532623354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264584 | CAGCATGTGCCACTA[A/C]CTGACCAGGTTGTCT | 337867 |
rs532647391 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273217 | GTTGGTAATATTATT[C/G]AGTTTGTTTCTTTTT | 337867 |
rs532657260 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341428 | ATATCAGGGGGGGGG[-/A]GGAAGGGGGCAGCTT | 337867 |
rs532679224 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338107 | GTGTCGCCCAGGCTG[G/T]AGTGCAGCGGCACAA | 337867 |
rs532708259 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257200 | AAACATATTAAATTT[A/T]CCAAATATTGGTGTG | 337867 |
rs532739955 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354140 | GCACCTGCTCCCTCA[C/T]GTGGACACTGTCCAC | 337867 |
rs532752283 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327486 | TTTCTCTCTCTCTCT[C/G/T]TGTGTGTGTGTGTGT | 337867 |
rs532752722 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233350 | ACTCCTGACCTCATG[A/T]TCTGCTCTCCTCGGT | 337867 |
rs532758708 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384150 | GGCCCCTTCTCTTTC[C/T]ACCATGTAGCACCAA | 337867 |
rs532788841 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342109 | GTTTATGAGAGAACA[C/T]CGTCAGCATCAGTAT | 337867 |
rs532838453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233938 | TTCTCAAGACTAGTC[G/T]TTTGATACTATGAAT | 337867 |
rs532840513 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253534 | TTCTTTTTTTTTTGA[G/T]ACGGAGTCTCGCTTT | 337867 |
rs532863263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366819 | AGGCTGCTCACAGTG[G/T]GCGGCTCTGCTTCCC | 337867 |
rs532887631 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254789 | TCAAGAGAAAAGGGA[C/G/T]TTGATAGTATTATAC | 337867 |
rs532892434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326762 | AGTCCAGCACCTTAC[A/G]CTGCACATCTCAAGG | 337867 |
rs532901999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228647 | ACTTTTGAGGTAGGT[G/T]CTCATCTCCATTTTA | 337867 |
rs532918594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278294 | TACCACATTATTAAT[A/G]CATGTGGCAATAGAG | 337867 |
rs532928952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284359 | TGCTGTTTCTTTTCA[A/G]TAGCTACCAAATGCT | 337867 |
rs532932881 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346960 | TTTAAGCAAGCTGAA[C/T]ACAGATGAATAATCA | 337867 |
rs532953393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213082 | TGCATTCTTTTTTTT[C/T]CTGACGCATGTATAT | 337867 |
rs532965079 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385919 | ATGGTGATAACCATG[C/T]ACTGGTTCAAGGTTC | 337867 |
rs532965207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345842 | CTGTCTCCTGGCTTC[A/G]AGCAATTCTCCTGCC | 337867 |
rs532965351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206069 | GCTGGGTGGATAGGT[A/G]ACGTTCCCAGTCACT | 337867 |
rs532978182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373526 | TGAAAACACTAAGAT[A/G]GATAAGGCGGAATGT | 337867 |
rs533016286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325668 | TTAACTGAAACTTTA[C/T]GCCTGTTGATTTTTA | 337867 |
rs533019456 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313247 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 337867 |
rs533026368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339370 | CAGAACTTGCCAGAA[A/G]TAGTTTTATGTGTTG | 337867 |
rs533087658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340082 | TACTAAATGATTAGA[A/G]TTTTGCTAGCTCTTC | 337867 |
rs533105869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305913 | TATTTATTTATCTAT[C/T]GAGACAGAGTCTCGC | 337867 |
rs533174058 | snp | A/T | 0.000263604 | 0.0114775 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255294 | AATCAAGAAAAAAAA[A/T]GTCAGTCGAGTGAGG | 337867 |
rs533186169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312738 | GAAAGCAGAACCTGC[A/G]TCAGTGGAGAGTCAA | 337867 |
rs533194666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358199 | GACAGGAGTCTGGTA[A/G]GCCCAGGTAAGAAAT | 337867 |
rs533197975 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99298993 | TTTCTAAGCAGATTC[A/T]TGGGAATTGCCTTTA | 337867 |
rs533198070 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286963 | GCCTCTACCCCCGAT[-/G]TAACAAGAGTAAGGG | 337867 |
rs533213975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247900 | ACCTCACCACTATAT[A/G]GGAACTTCTCTTATA | 337867 |
rs533226903 | snp | A/C | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259452 | TTGTTACAACCTGCC[A/C]GAATGATGGGTTTTA | 337867 |
rs533242069 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249964 | ATTCTGGACATTAGA[A/C]CTTTGTCAGATGCAG | 337867 |
rs533247420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292074 | ACCTTTTCAGGGGCC[A/G]CATGATTGAGTTGTC | 337867 |
rs533274558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313209 | CAGGATGGTCTCCAT[C/T]TCCTGACCTCATGAT | 337867 |
rs533290379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305344 | GAGAAGGTGATAAAC[C/T]CCCCAGACTGGAGAA | 337867 |
rs533294217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218835 | AGGAGGCACTCATTC[C/T]TCCTTAACGTGGTCA | 337867 |
rs533326066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364818 | CTTTATTAGATTACA[C/G]TATGTGAATGCACCA | 337867 |
rs533338770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377737 | ACCACACACCTGGCC[C/T]CGCTGCCCTCCATAG | 337867 |
rs533346423 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330495 | ATACAGTTGATTTCT[G/T]TATTTCGTTCTTGTG | 337867 |
rs533362256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277689 | CATTGTGTCATCCTC[C/T]AGCATCACTCTCTTA | 337867 |
rs533369763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282883 | GTTGGATTTTTTGGT[A/G]TATGTTATGTGTTGA | 337867 |
rs533383052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269200 | TGGTAGGTACCACAA[A/G]TGGAGTGCCTATGAA | 337867 |
rs533421362 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270024 | AAACTGGTATTGTGT[A/C]TGTGTGTTAATTTTT | 337867 |
rs533449967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358643 | GAGGAGGGGCTTGAC[A/G]AGATTTGTATCTTAG | 337867 |
rs533474904 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225224 | ATTAAGTACGTTCAT[A/G]TTGTGCAACCGATGT | 337867 |
rs533478154 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253080 | TTAAATATATGTAAG[-/A]TATACAAATAATATA | 337867 |
rs533500215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359112 | GGACACTGAGAAGGC[A/G]TAGCTAGAGGGCTAG | 337867 |
rs533509056 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99352002 | ACTTGGTAACATTCT[G/T]TGGCTGTGAAAATTG | 337867 |
rs533509297 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366853 | CCCACTTGTTCCTGA[A/G]GCCTTGCAACTCCAC | 337867 |
rs533523803 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382745 | ACAGAAGGCAGTGGG[G/T]CAATGAGGACTTCGC | 337867 |
rs533532137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384365 | TGGCAATCTGGGGCC[A/G]TGAATATTTTTGTAA | 337867 |
rs533554227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238111 | TTTGATAGAAACACA[C/T]TTCTCTATTTCTTTA | 337867 |
rs533554879 | in-del | -/TG | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305293 | CAGAGGATTCTCACA[-/TG]TGTTATCTCATTTTA | 337867 |
rs533557960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352364 | TGTCCTAGGCAGCCA[C/G]TTAATCTACTTTCTG | 337867 |
rs533559475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359783 | GCCCTGCCTCGCCTC[C/T]CGTGTGCCCAAGCAC | 337867 |
rs533563597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220259 | AGCCCCTCTACTAAC[G/T]AGCTGTGACCTTCAG | 337867 |
rs533601859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371361 | TTTTGGTGTTTCTTG[A/G]TTATCCTGCAAATAG | 337867 |
rs533620821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352871 | ACCGTCGGAAACTCT[A/C]TACCTCCGTCTCCAC | 337867 |
rs533640164 | snp | A/G/T | 0.000132372 | 0.0081345 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255778 | AATCCAATTATGAAG[A/G/T]TACAGCTATAGAAGA | 337867 |
rs533641967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238964 | ATTTTTGATAACTTT[G/T]ACAGTGGTGGTTAAA | 337867 |
rs533647524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331344 | TGTTTGAAGTTTTCT[A/G]CTTAGCATAGTTGAC | 337867 |
rs533672163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283503 | CCTTGTTTGACATAT[A/G]TTCCTGATTTAAATG | 337867 |
rs533674751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99256438 | GCTGTTTTCTAGTGC[A/G]CAATTGGGAGTACGT | 337867 |
rs533677170 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232409 | TGAGAGATATAGATA[G/T]ATATATATATATTCA | 337867 |
rs533684006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213858 | AGAGTCTTGCTTTGT[C/T]GCTCAGGCTGGAGTA | 337867 |
rs533719511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233029 | TGATTTCAAAAATAT[A/G]TTTTCTAGCTCTGAT | 337867 |
rs533726704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240162 | AGATTTTGGCAGTGA[A/T]TGCAGAGGTACAGTC | 337867 |
rs533740057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219451 | AGAACATTTTATCAC[G/T]CCAGAAAGAAACGGA | 337867 |
rs533758233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313697 | CGTGCCAGTGCCATG[A/G]CGACAGATCACTGGA | 337867 |
rs533787654 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226033 | CATGTTTAGTTGATA[A/C/T]GTTTTCATAGCAGGA | 337867 |
rs533792181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263506 | GACGGACAGTGCAAA[A/G]TGCTGGCAAGGATGT | 337867 |
rs533835660 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306139 | GATCTCAGGTGATCC[A/G]CCTGCCTCGGCCTCC | 337867 |
rs533889850 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362857 | CTTATTTAATTCAGT[-/A]AACAATTGAACTTTT | 337867 |
rs533902491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344449 | TTCAAATACATGTTT[C/T]TGTTGTTTGCTCCTG | 337867 |
rs533920561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305413 | CTAACAACTCCAGCA[A/G]GTCTTAACCATAGCA | 337867 |
rs533927512 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346840 | CTCCGGATGGAGCAG[A/G]CTTGTTTTCTGTATA | 337867 |
rs533931958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205487 | ACCTTCCTGGGTCTC[C/G]TCCCCAGAGGGTCAG | 337867 |
rs533939189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212622 | AATCTGTTTGACTTT[A/G]TTAACTCTGTTTCTA | 337867 |
rs533956387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246777 | AGCAAGAGTTACAAA[C/T]TTGAATAAATTGAAA | 337867 |
rs533995623 | in-del | -/AGTT | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278488 | TTAGCAATAAGTGAC[-/AGTT]AGCTTTCTAAATTAT | 337867 |
rs534005724 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211289 | TATGTGGAAGAGCTG[A/C]GATTTGACTCCGATT | 337867 |
rs534018480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284499 | TTATTAACATTTTCC[A/G]CATTTGCTGTTATCA | 337867 |
rs534027636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276763 | TAAATAACCCATTAG[A/G]GTAAATTCAGATGTG | 337867 |
rs534065674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277324 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTAACCA | 337867 |
rs534092434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216979 | GGGATTACAGGCGCC[C/T]GCCACCATGACCGGC | 337867 |
rs534106311 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268137 | CAAGAACTTGGTCAC[A/G]TGGCCACACCTAATC | 337867 |
rs534213658 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318355 | ATTTTTAGTAGAGAT[-/G]GGGGTTTCTCCATGT | 337867 |
rs534221202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345109 | TTCCAGAGGAGAGGA[C/G]CAGCAAGAGTGAGGC | 337867 |
rs534225709 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298144 | TAACACATTTCTATT[A/T]TGATGTGCTAGATAG | 337867 |
rs534254377 | in-del | -/TTG | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240128 | ATGAAGGGCTTTATT[-/TTG]TAAGTTCTGAACCTC | 337867 |
rs534271063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289831 | TGCCACCATCTAGAA[C/T]ATTGCCAAACACTGT | 337867 |
rs534285448 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338970 | TATTTGTGCACTCCT[A/G]GATTCAGTCCTTAGT | 337867 |
rs534286754 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350842 | GCCCTTAACCTGTGG[G/T]CTCTGATGTTATCTC | 337867 |
rs534290996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377435 | CTGATGCTTCTCATC[C/T]CAGTAGCTGGACTAC | 337867 |
rs534292058 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378504 | TGCACTCCAACCTGG[G/T]TGACTGAGCAAGACT | 337867 |
rs534295877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385035 | ATGCATATATATTGG[C/G]TACACATAGTGAACA | 337867 |
rs534305294 | in-del | -/GTTCGTCAGCGGCGA | 0.0116955 | 0.0755709 | cds-indel, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200776 | TGCGCCGGGTGCGCC[-/GTTCGTCAGCGGCGA]GTGGCCTCGCGGCGC | 337867 |
rs534343100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239563 | GGCTGGCTTTGAGGA[C/T]CACTAATGTAAGGGC | 337867 |
rs534354770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282336 | CTCATGACCTAGGAA[A/G]CTTGTTGAGAACTTT | 337867 |
rs534357567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364477 | TATAATTTTTCTTGC[C/T]CATAATGGCCTTGTC | 337867 |
rs534372956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324006 | GCAAAAATCTAGCCT[C/T]CTTTCAAAATGCGAC | 337867 |
rs534378582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276127 | AATAATAAATCTCCA[A/G]CCATCTGCCAAGATG | 337867 |
rs534415698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268712 | ATCAGCTGTAGAGGC[A/G]CTGAATGATAGAGTT | 337867 |
rs534429267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357561 | GCATATTCATACTTA[C/T]ACCAAAAGCTGCAGC | 337867 |
rs534446834 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383986 | TTAGCCACTAGGCTG[C/T]GGGTGAAGTGGGATA | 337867 |
rs534458367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317378 | ATTACCCTGAGCACA[A/G]CTCTAAGATATAAAC | 337867 |
rs534491214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380314 | CACAGGAGTTGATGC[G/T]TCACATGCCGAGTAA | 337867 |
rs534492635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358242 | CTGAAAGCAACAGGG[A/T]TGCATTGAGTAGCAT | 337867 |
rs534522871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208671 | GGCTTCTGGTGCGTT[C/T]GGCTCCTCTCTGTCC | 337867 |
rs534523643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252274 | CTGTTAGTATTTATT[A/C]TATTACGTTGTCATG | 337867 |
rs534524464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99254203 | CACCATATAGTAGAA[A/G]CCTCAAATGATAGAA | 337867 |
rs534533507 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368979 | CACTGGAGCCAGCTG[C/T]GGGATCCCACTGGCC | 337867 |
rs534553154 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268552 | GGCCGAGGCTGCAGT[A/G]AGCCATGATCCTGTC | 337867 |
rs534556675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253353 | CTGAGCAAGTCACAT[A/G]ACCTCTTCAGACCTC | 337867 |
rs534582842 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309663 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 337867 |
rs534616747 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330220 | AATCCCAGCACTTTG[C/G]GAGGCCAAGGTGGGC | 337867 |
rs534651019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358976 | TTGGGAGTCTCTACC[C/G]CATGAAGCCCTAGGA | 337867 |
rs534657242 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233915 | CAAATCTGCTGGTAC[C/G]ACTTGAGTTCTCAAG | 337867 |
rs534685920 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228310 | TTTTTTTTTTTGATA[C/T]GGAATCTCGCTTTGT | 337867 |
rs534698114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363535 | GGCAGTGTCCTGAAG[A/G]TGTCAGCCCCCGGCT | 337867 |
rs534698772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223532 | AATTTGCTCTTCTTT[A/C]TCTTTTTCTGTTTTT | 337867 |
rs534703078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331083 | TTATTTGAGCCAGCA[A/G]TGCCTCCAGCTGAGA | 337867 |
rs534708265 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371497 | GATAAAAAAGATACT[G/T]TTGTTGCCCTCAAGA | 337867 |
rs534711016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225218 | AGTAGTATTAAGTAC[A/G]TTCATATTGTGCAAC | 337867 |
rs534711136 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361259 | CTGTTTCCTTCTTCA[C/G/T]TTTTAAAATATGTGG | 337867 |
rs534731972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355349 | TGCACTTCCATTCTT[A/T]TGTCTTCAAGGCCAC | 337867 |
rs534732283 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215687 | TGGGAACTGCAAGCC[A/G]GCTCTCTGCGAGCGG | 337867 |
rs534790317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355877 | GCTGAGCCATGTGCA[C/T]CCCATGGCTCTCTCC | 337867 |
rs534817483 | in-del | -/TCTCCACAAAA | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335985 | ATGGCAACACCTCAT[-/TCTCCACAAAA]TGGAAAAAAAAAAAA | 337867 |
rs534819627 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259813 | TTCCCCATTGCTGCT[A/G]AAATCAACAGATACA | 337867 |
rs534820278 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234972 | AGAGAGAAGACATTT[A/G]TAGTTTCTAAAATAC | 337867 |
rs534822919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203948 | TGAAACTATATTGCT[C/G]TCTGCAATTATGACC | 337867 |
rs534842747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350173 | GATAATGTCCATGAT[C/T]ATCTCTATATCTAAT | 337867 |
rs534887696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204695 | TGTGGGAAAGAAAGA[C/G]GCCCCCCCAGAACCT | 337867 |
rs534900086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336568 | GCCCCTTCCCTCCCA[A/G]TTTACCCATGTCTGC | 337867 |
rs534932690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296451 | TTTAAATAGGGCAAA[C/T]GCACTTTTGTGACAG | 337867 |
rs534949595 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236660 | TTCAAGACCAGCCTG[G/T]CCAACTTGGTGAAAC | 337867 |
rs534951182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375566 | TGCAAGCGTCAGAAT[A/G]TGGGAAGTAAAAACC | 337867 |
rs534951384 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229319 | TTTAGATAAGGGAGT[A/G]TCTGTGCTAATAAGG | 337867 |
rs534953541 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307697 | AAAGAGACTGAAGCA[A/G]TAAACCTTAACCAAA | 337867 |
rs534960237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245554 | AGACTCCATCTCAAA[C/T]AAACAAACAAAAAAA | 337867 |
rs534961024 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328565 | AGTGGTATCTTGTGG[C/G/T]TTTAATTTGCATTTC | 337867 |
rs534964878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337031 | GCGCTTTCCTGTCTC[A/G]TTTTACTGCTTAGTG | 337867 |
rs534968620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384984 | ACCCTCAGAAGCCCT[A/G]TGTCCTTGTCTGTAG | 337867 |
rs534988157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229739 | CTTTTAAAAATCTTC[A/G]TTGAAAGAATGCTTT | 337867 |
rs535018561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274631 | TGCCTGGCCTCATAA[C/T]ACTGTTAATGTTAAT | 337867 |
rs535048662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322920 | TGCCTTTCTCTCTTC[C/G]CTCTGTAGTACTTTT | 337867 |
rs535088518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309691 | CTGCAACCTCTGCCT[C/G]CTGGGCTCAAGTGAT | 337867 |
rs535123480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276170 | GAGGGGTGTTTTCCA[A/G]CGCTAACAAGTAGTA | 337867 |
rs535131900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364541 | AAATTAGGTGGGAAA[C/T]TCTCCTTCCTTTTCT | 337867 |
rs535155222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216017 | TTGTTATAGGTTGGT[A/G]CAAAAGTAATTGCGG | 337867 |
rs535161608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276521 | GTGGGTGAGAGTGCA[C/T]GGAGCTCTCGTGCCT | 337867 |
rs535192176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357705 | GAGGATGCTATGTCC[A/G]TGAAGAATGTAGGTA | 337867 |
rs535194469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243696 | GAACATACATATATA[A/G]TTTTCCTTTGGTGTG | 337867 |
rs535202874 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375226 | TCAGAGCAGCCCAGA[A/T]CGCTGGCAGGGTCTG | 337867 |
rs535208704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312459 | CCTGCCTAGCACTTG[C/T]AGGAATGTAAGATTT | 337867 |
rs535229150 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319916 | TGAGGATGTACTGTT[C/T]GTTCCATGGCATATT | 337867 |
rs535237069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327968 | TATGGAAAGCAGTCT[C/T]CTGACCATGAATGGT | 337867 |
rs535269089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383642 | TGTGCGTCAGTCCCC[A/G]TGCTAAGGGTTGAAA | 337867 |
rs535285948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245617 | GGAGGCCGAGGTGGG[C/T]GGATCACGAGGTCAG | 337867 |
rs535286081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280277 | CCTCATTTTCTGTCA[C/T]TCCTTCCTTGTACTC | 337867 |
rs535291117 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253909 | TTTAGCAGAGAGGAA[G/T]TTATAGTTGAATCAT | 337867 |
rs535294252 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337146 | TAAAATGCAAACCTT[A/C]AATATTCCGCATGAA | 337867 |
rs535299954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205399 | GGTTACTCTTGGTCA[C/T]GGAGCGGTGGTTGTC | 337867 |
rs535304656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377489 | GAAAATGAAGTAGTC[C/T]AGGGTTTCAGTGTGA | 337867 |
rs535318777 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357058 | AATATGTTTTGGTCA[A/G]TGACAGATTGCATGT | 337867 |
rs535320044 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289982 | GGATATTTGGTGAGC[A/C]GTGTGTGTCTCTTTT | 337867 |
rs535322631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246433 | GCATTGCCAAATCAT[C/T]AGTTTTCCCCAAAAC | 337867 |
rs535342052 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347984 | GACACACATAAGCTG[C/T]TCTCAGTAGTTCCTT | 337867 |
rs535345194 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277350 | ACCAACATGGAGAAA[-/C]CCCCGTCTCTACTAA | 337867 |
rs535346958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237807 | TAAGAATACAAAAAT[C/T]AGCCAGGCATGGTGG | 337867 |
rs535373440 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233517 | GCCTAAAGCAAGGAA[G/T]ATGAGTGGGTAGGTG | 337867 |
rs535414918 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231924 | CTGATCATAATGCAC[A/G]TCTTACTGACATAAT | 337867 |
rs535428277 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381006 | CCAAGACCTGTGAAA[A/G]GCCAGTCTTAGTTGT | 337867 |
rs535451579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225000 | ATGTGATTTTTGCTC[A/G]TTTTGAGAGGAATAC | 337867 |
rs535452765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267164 | TTCTTGGCCATTTAT[A/G]TATATTTCTTCTTTA | 337867 |
rs535458557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254575 | AAATAATTTAATCAA[A/G]TTATTTTGTATGGTA | 337867 |
rs535462334 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285427 | GACAATTGTCTTGCT[C/G]TGTCACCCAGGCTGG | 337867 |
rs535475884 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216733 | AACAACTTTGGAAGG[A/G]CGGGAACGTGGACAG | 337867 |
rs535489536 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259897 | TGCACAGGGGCATTC[C/T]TGTTTCTGAATTGCC | 337867 |
rs535497235 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257768 | GTGATGAACATTCCT[A/G]AATATACATATGATT | 337867 |
rs535517190 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324846 | GGGAAATGACTGATA[C/T]TCAGTCATGGTGCCA | 337867 |
rs535531948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350265 | TTCTTACCTCGGCAC[C/T]TAGGTAATCCTTCGC | 337867 |
rs535551884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226800 | GTACTTGCTTTTTTT[C/T]CCTCCAGAATCACCC | 337867 |
rs535553973 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318796 | CATTGCTCTCCAGCC[G/T]GGGCGACAGAGTGAG | 337867 |
rs535599358 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358538 | CTATATTTATGTTAG[C/T]AAGTAATAGGCTTGT | 337867 |
rs535611955 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361037 | TTCAATGCCTGTAGA[A/G]CATGGATTTCTGTTC | 337867 |
rs535615190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343932 | ACTTTTCAACAAATA[A/G]GTACTTAGTGCTTAT | 337867 |
rs535618648 | in-del | -/CTG | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276967 | TGGAAAGCCCTGGCC[-/CTG]CAACCTTTGGGAAGT | 337867 |
rs535619484 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304897 | GTAAAATAGGAAGGC[A/G]TCTCAAAACCTTAAC | 337867 |
rs535631050 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230952 | TACTCAGGGGGCTGA[A/G]GCAGGAGAATCGCTA | 337867 |
rs535637611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304510 | TAGGTGATGTATGAT[C/T]GATATTCAATAAATA | 337867 |
rs535640299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323003 | GGAAACAGCATAACC[C/T]GCTGTGGAAGCATAA | 337867 |
rs535640371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329401 | AAGGATTGCCATGGT[G/T]ATGGTTTTTAAATGT | 337867 |
rs535653864 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229839 | ACAGTATACTGTAAT[G/T]TATTAAAAACTTCAG | 337867 |
rs535667031 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207490 | TTTTTCCCTGTTCTC[A/G]TCTCCCTTCACTTTT | 337867 |
rs535696464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370202 | AGTATGAAGGAAAAC[A/G]GCACCATGATGTGTG | 337867 |
rs535705224 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338109 | GTCGCCCAGGCTGGA[A/G]TGCAGCGGCACAATC | 337867 |
rs535707860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330343 | GGATGCCTGTAATCC[C/T]AGCTATTCAGGAGGC | 337867 |
rs535717759 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198622 | AAAAGGAAGCATTTT[A/C]ATAGCCTTTCAGGTG | 337867 |
rs535718214 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223813 | TTCCATCTTTCTGCT[G/T]TTGGCTTCTGATTTT | 337867 |
rs535721663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323408 | GAGTTCAACACCAGC[C/T]TGGCCAACATGGCAA | 337867 |
rs535731570 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364648 | AGATTTTTAAGTACT[A/G]TTTCAATTACATTAA | 337867 |
rs535785467 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238330 | GACTTTGTCTTCATT[C/G]TGATTTAAAAGAAGT | 337867 |
rs535785707 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208381 | GACTTACCCTTTATG[A/C]TTTAATTAACTGATT | 337867 |
rs535796753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330935 | TAACTTTTAAAGGAG[A/G]ATGGTCCGCTTGTTA | 337867 |
rs535798105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363215 | TGCCTAACTTCCACT[A/C]ATACCACATGACTTT | 337867 |
rs535818591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317296 | GTTCTAAAAATTAAC[A/C]AACAATAACCCACAA | 337867 |
rs535837306 | snp | A/G | 0.000101271 | 0.00711514 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238590 | CCCTGAGAGGAGAGC[A/G]GACAGTTTTTTTTTT | 337867 |
rs535837727 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250548 | GATTGCTTTGGCTAT[C/T]TGGGGCTCTTTTTTT | 337867 |
rs535841283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202401 | GGCAATGTGGTTTTC[C/T]TGGGATCACACAGTG | 337867 |
rs535848039 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270227 | ACATTAAAGAAAAAA[A/G]TAATCATTATCTGAA | 337867 |
rs535884782 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303243 | GAAAAAGGGTTTAGC[A/C]GTCTACTGTTTCCTC | 337867 |
rs535898143 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215457 | GCAATTGTAGCCTTG[A/G]TGAGAATCCAATTCT | 337867 |
rs535908637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311300 | CTGTGAGGGCGGGAG[C/G]TGCGGTTTGAAATGG | 337867 |
rs535930494 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371830 | CATGAAATGTATGCC[A/G]TGTACTTTGAAAGCA | 337867 |
rs535944182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260540 | CTGCAACCCATGAGC[C/G]CTATAGCATTGACCC | 337867 |
rs535977521 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210689 | TCCATTTTGGTCAGG[C/T]TGGTCTCAAACTCCC | 337867 |
rs535998770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288451 | GAGGAAGGTGAACTC[C/T]TGAAACAAAAAGGAA | 337867 |
rs536037759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315387 | CTAGCATGGCTGTCT[C/G]CAGCCATGAGACTTG | 337867 |
rs536058336 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352669 | ACCATTTTCATTACC[A/G]TCTATTCCGCAGAAT | 337867 |
rs536065750 | in-del | -/GG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341426 | TTATATCAGGGGGGG[-/GG]AGGAAGGGGGCAGCT | 337867 |
rs536066761 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335717 | ACTCTGCAGCTGTTC[C/T]CCTCTTGGGGATGAT | 337867 |
rs536079876 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326498 | ACTTGATACACATTC[C/T]AAAAATAATTTTTTA | 337867 |
rs536096818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281556 | TTAGAACAGCCCTGG[A/G]AGGTGAGAACTCGCA | 337867 |
rs536102634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273999 | TAAATGTATATATCT[A/T]GAGTCCAGAGCTCAC | 337867 |
rs536106026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308723 | AAAGTGCTGTGAGTA[C/T]GGAGGAACATTGTCA | 337867 |
rs536116294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230410 | GGCGTCAGAGGTTGC[A/G]GTGAGCTGAGATCAC | 337867 |
rs536139748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274757 | GGGTTTCACTGTTGC[C/T]CAGGCTGGAGTGTGG | 337867 |
rs536143997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309470 | TGGGGTCATTATCCT[A/G]TAAGAGGCCGCTGAA | 337867 |
rs536146201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301604 | TTTGCATAACCGGAC[A/G]TGTTGACATGAACTG | 337867 |
rs536155620 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258333 | TAGTTTCCAGTGTAA[C/T]GCTTGGCGTCGGAGT | 337867 |
rs536185317 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208383 | CTTACCCTTTATGCT[C/T]TAATTAACTGATTCA | 337867 |
rs536196106 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221814 | CCTTCTTTGGACTCT[C/T]CCTCTGTTTCGCTCC | 337867 |
rs536212243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374367 | ATTGTGTGGCATTTA[A/G]CATGAGTGACTCCAT | 337867 |
rs536232688 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213139 | TTTTATACAGAAATG[A/G]CATTCAAATACACAT | 337867 |
rs536236523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294603 | ATGACCCAGAACGAA[A/G]CAAAACAAAACATTG | 337867 |
rs536276566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251254 | TCTAGTGAAGTTGTT[G/T]CTCGATTCCTGGAGC | 337867 |
rs536287313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278868 | ACTTGAATCTAAAAC[C/T]GCCATGCCTCCAAGT | 337867 |
rs536292833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382209 | GAGGGAGATGATTAA[A/C]AGTAGATAACAAAAT | 337867 |
rs536316271 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336115 | ACAAGTGAGGATAAA[C/T]ATCTTTTCATGAGTT | 337867 |
rs536324204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279888 | AGCATCACACTGGGG[A/G]TTAGGATTTTAACAT | 337867 |
rs536332200 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272385 | CACCTTGTTTTATCT[A/G]TATCCTTAATCTTAA | 337867 |
rs536341573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368262 | GGCATGGTTTCACTT[C/T]TGTATGGTTTTGAGT | 337867 |
rs536356092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382678 | CATACTGGGAGTTCA[A/C]AGTGGTGGGGAGAAG | 337867 |
rs536372114 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336223 | TAGGGTTTCTTGATA[G/T]GTTCTGAATGCTGCC | 337867 |
rs536380031 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321512 | GACGAGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 337867 |
rs536398023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244723 | AAATAATATTTTAAA[C/T]TTCTAGATATAGTTA | 337867 |
rs536406940 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324059 | TCTGTGAACCATACA[C/T]TCCAACTACACACAA | 337867 |
rs536419357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264975 | CATCGCTGTTTTTTT[G/T]TTTTTTTTTAATTGT | 337867 |
rs536443630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222406 | GTGGCAGGAGCAAAG[A/T]AGCACACATAAAGTG | 337867 |
rs536454987 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350837 | AGTGGGCCCTTAACC[C/T]GTGGGCTCTGATGTT | 337867 |
rs536464188 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354675 | TTAGAGAAGTAATTT[A/G]CGATGGGGCTGGTTT | 337867 |
rs536466994 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264683 | GGGTCATCCACTTCC[A/G]GCCTTGTGTGATTTG | 337867 |
rs536469311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248765 | CTCCTGGCCTCCAGC[A/G]ATCCTCCTGCCTTGG | 337867 |
rs536486133 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290902 | AGAGAAATTCAGGGG[C/T]TTGAGGGGAAAGGTG | 337867 |
rs536509422 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341605 | GGAAGCTACATATAT[A/T]TATAGGTGATGGAGT | 337867 |
rs536523510 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333473 | TATTTATTTTTGTGG[A/G]GCATTTGTTAATTCA | 337867 |
rs536526805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348239 | CTGAGGGATTAAATA[A/G]GACGCCGCCTGCGCC | 337867 |
rs536551914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380390 | GCTGGGCTTCTCTGA[A/G]CAGAGGAATAGTGAG | 337867 |
rs536564931 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285350 | AGAATGGTATGGTGG[A/G]TATACTAGATTAACT | 337867 |
rs536571446 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386787 | GATGTCCCTGACTTC[A/T]TTCCCTAACTAGGCC | 337867 |
rs536580347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215504 | CAAGTTGCAAGTGAC[A/G]AGGGGTAATATACAC | 337867 |
rs536584766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242270 | CACCTCCCAGACGGG[A/G]TGGTGGCCGGGCAGA | 337867 |
rs536585935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250769 | TCTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 337867 |
rs536590097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342499 | AGGCACACACAGTCT[C/G]TGTGGATGCCAGGTT | 337867 |
rs536637007 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264440 | AAAACTGCCTTATAG[C/T]TTGTGTAAAGTGCAT | 337867 |
rs536649010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336464 | TTTACAATTTCATGA[A/G]TTCTATTTGAGTTCT | 337867 |
rs536681044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367613 | TGCCAATTTTGTGCT[A/G]TTGACTGAAGGATGT | 337867 |
rs536694725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327762 | ATCCTACCTCTTATA[A/G]AATTTAAAAGATTTA | 337867 |
rs536695260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376709 | AGAGCTGGCTTCTCA[A/G]TGAAGTTAGAGGAAG | 337867 |
rs536701890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321392 | TGGCTCACTGCAACC[A/G]CTGCCTCCCGGGTTC | 337867 |
rs536732074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289685 | CTTATGTTGCAGCCA[C/T]GAAATAACCCTGAAA | 337867 |
rs536787067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221778 | ATCTGTCACTCATGG[C/T]GATCGCCTACTTGAC | 337867 |
rs536793492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315026 | TAACCGGATACTGGC[A/G]TCACTTCAGAATGCC | 337867 |
rs536794875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323483 | TCAAGGCTGACCAAA[G/T]CCATGAGGGTGATGG | 337867 |
rs536794974 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369215 | AGGGAAAAATGATCA[A/G]TATATGAAGACTAGG | 337867 |
rs536833596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299978 | TTCAGTCCTTAGCAC[A/G]GGCAGCTGTTTCATG | 337867 |
rs536855438 | snp | C/G/T | 0.000134621 | 0.00820341 | missense, stop-gained, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340563 | CGACAGAGACAGCAG[C/G/T]AGGTAAAAGTGATAA | 337867 |
rs536869673 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344901 | CCGTGAGTTTGTGGC[A/C]AACTTCAGGGAGCTC | 337867 |
rs536877947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300490 | AATCCTTTCATATGC[A/G]TGACTGTTACTATCC | 337867 |
rs536880606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292913 | GAATATAACAATTAT[A/G]CAGCCCTGTCCTGTT | 337867 |
rs536908735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241481 | ATTATGCAAAGTGAA[A/G]TGAGCAAATGCAAAA | 337867 |
rs536916227 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201321 | TACCATGCCCCATTC[A/T]TTTAGGCTTGGGGGA | 337867 |
rs536929130 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273968 | TAATATTTTAAAATA[A/C]ATTTTTATTGAGGTA | 337867 |
rs536971645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203275 | TCCTGACCTCAAGTG[A/G]TCCTCCCGCCTCGGC | 337867 |
rs536972084 | snp | G/T | 0.000452614 | 0.0150367 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295461 | CAGTGAGTGGGTTTT[G/T]TTTGGCAGTTCTGAA | 337867 |
rs537002071 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336281 | TTTCTTCAGGCCTCT[C/T]GTGTTTTCATTTCAT | 337867 |
rs537006448 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269733 | AACTTCAATCTAGAC[C/T]GTAAGCTTCCATGTT | 337867 |
rs537035835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229206 | GTAGTGTGTGGGAAC[A/G]AGGGTGCAGAGTGGG | 337867 |
rs537043463 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203800 | GGTGACATTGAGCTG[A/T]GGCTCAGATGGTGTG | 337867 |
rs537065682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244864 | TTGAGACGGAGTCTC[G/T]CTCTGTCACCCAGGC | 337867 |
rs537117024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336930 | TCCCACCTCTCTTCC[G/T]CCTTCCCACCTCCCT | 337867 |
rs537123102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222532 | GATCAAAGGGGTAGC[C/G]CATTGGTAATTACAT | 337867 |
rs537141261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265787 | GGCTAATGTTTCTAG[A/G]TAGATACAATTACAA | 337867 |
rs537145884 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361796 | TATCTCCTGGATTGG[A/G]GGTAGGAGAACAGAG | 337867 |
rs537178409 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339933 | GTTTTCTGCTGGTGT[C/G]TCTGTGATGGCCATC | 337867 |
rs537189966 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237669 | TATTTAAGATAATTA[C/G]CCGGGCTGGGTGCCG | 337867 |
rs537195137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330050 | AAATTTTCAATGTAC[A/G]GGTCTTGCACATCTT | 337867 |
rs537223598 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386665 | ACTAGCTGCTCAGAG[G/T]GGGGTCGAGGTGACT | 337867 |
rs537230736 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316623 | CTGTCCTCAAGGAGC[A/C]CAGCCATGAGAAAAC | 337867 |
rs537258459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209125 | AGCACGGCTTTTCCA[C/G]CTCTCTAGATTTCCC | 337867 |
rs537264722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348840 | ACATAGTGAGACCTC[C/T]TCTCTACAAAAAAAT | 337867 |
rs537266005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355815 | ACTCTGTGCAGGGGG[C/T]CTGGAGGGCAGCGGC | 337867 |
rs537269824 | in-del | -/CT | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288230 | ATAAATGTTTTAACA[-/CT]CTGAGAAAATGGATA | 337867 |
rs537270157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242306 | CCCTCACCTCCCGGA[A/C]GGGGCGGCTGGCCGG | 337867 |
rs537285535 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351002 | AGAAAGGAAGAAAAC[-/A]AGTGTTGTTTTTCTT | 337867 |
rs537289209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310293 | GATTATGCCACTGCA[C/T]TCTACTCCAGCCTGG | 337867 |
rs537295799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381046 | CACCGCGGCACATGT[C/T]GTTCATGTCTGAGAG | 337867 |
rs537306899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235205 | TTTAAAAACAAAACA[A/C]CCAGGAATCAATTAA | 337867 |
rs537308930 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243081 | ACCACAATAAAAATA[A/C]AAAGAAAAGTTGGAA | 337867 |
rs537314158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334706 | ATAGCACAAAAGAAC[A/G]TAGGAAAGGGGGAGT | 337867 |
rs537314362 | in-del | -/GCCATTCTGACTGGTGTGAGAT | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249762 | TTTGGCTTTTTAGTA[-/GCCATTCTGACTGGTGTGAGAT]GGTATCTCATTGTGG | 337867 |
rs537322011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349623 | GCCCTTCCCTCTTAG[C/G]TAGCCGAAGCTGAGA | 337867 |
rs537326014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342927 | AGCCATCATGCAGCC[A/G]TTTCTTTCAGCTGCC | 337867 |
rs537327046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286525 | CCCACTTTTAGGTTC[A/G]GGGGGTACATATGCA | 337867 |
rs537331588 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364229 | TCTTCATGAATGGGT[A/G]TTGAATTTTGTCAAA | 337867 |
rs537333889 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346854 | GACTTGTTTTCTGTA[C/T]ATCTCCAGTGTGTGA | 337867 |
rs537360370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375019 | AGTAGATTGGAAATA[C/T]GTTTTCTAACAAGAT | 337867 |
rs537371398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303153 | CTCCCAATAGATCTG[C/T]GAAAGGCCATTTATA | 337867 |
rs537383321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243986 | GTCTTTGCTACTTAG[A/G]CTGTAGAAAAAAATT | 337867 |
rs537395309 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335137 | AATAGCTAATGGGAG[C/T]AATGAACAAATCAAC | 337867 |
rs537397423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235724 | TCATGCCTATCATCC[C/T]AACCCTTTGGGAGGC | 337867 |
rs537403641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221547 | TCAGCCTCACCTTTT[A/G]TTTTATTTCTACAGA | 337867 |
rs537437207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328529 | CAGTTGTTTTAGCTT[C/T]AGCCGCTCTATTGGG | 337867 |
rs537453056 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372843 | ATCCAGGCCGGGCGC[A/G]GTGGCCCACACCTGT | 337867 |
rs537464458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214544 | GAACCCCCTGCAGTC[A/G]TCAAAGGGTGGCTCA | 337867 |
rs537527244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347459 | GCATGAGCTGGAAGT[A/G]GGGGAAGGTCAATAT | 337867 |
rs537550035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316002 | CCTAATATCTAGTGC[C/T]GTTTCCACAGTGTTA | 337867 |
rs537561955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223442 | TTCATTGATTTGTCT[C/G]TATTATAGTTTGTTT | 337867 |
rs537574838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207885 | GGCTCTTTTTTTTGT[G/T]TTCTCATGAAGGAGC | 337867 |
rs537580865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215179 | CCTTGAAGCCACAGT[A/T]TCACTTAAATATGGT | 337867 |
rs537592448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341650 | TGAGAGCTGAGAGCC[A/G]AAAGCAAAGAAGTAG | 337867 |
rs537592567 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348157 | TCATCCCCAGTAGAA[C/T]ATGAGCTCTTGGAGG | 337867 |
rs537599018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293643 | AGATGTTACAAAGAC[C/G]AGTGCCTATTTTTGA | 337867 |
rs537599466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285155 | AATTCTGTAATATTA[G/T]TTACTACTGAAACTA | 337867 |
rs537600974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301377 | TAAACAAAGGAGACA[A/G]TCCCAGTTTTGCCTC | 337867 |
rs537629853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275507 | TTCTTAAAAATATTT[A/G]TAACCTATTTTAAAT | 337867 |
rs537629950 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304774 | CAAAGACCTAGCTGT[G/T]AAATGTTAGGATTCA | 337867 |
rs537634038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326038 | GATCCTGATTCATTT[A/C]TTTTGGATGTATACC | 337867 |
rs537652438 | in-del | -/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256289 | CTATTAAACTTTTTG[-/T]TTTTTTTTAAAGTGG | 337867 |
rs537666689 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277830 | CACCCGCAAGCCTCA[C/T]CAAGCCTCTAATCTG | 337867 |
rs537671678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250457 | ATGCTGTTTTGCTTA[C/T]TGTAGCCTTATAATC | 337867 |
rs537696548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285907 | TACACATCCAACGGG[G/T]TGCCAGAGTTCACAG | 337867 |
rs537706788 | snp | C/T | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260890 | ATAGTGTGTTTTAGC[C/T]GCAGTTTTGGGTTTT | 337867 |
rs537720341 | snp | G/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320330 | TTTAACTTTTTAAAA[G/T]GAATCAGACGTTTAA | 337867 |
rs537720804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227780 | CATGGTACAGCGTGG[A/T]TGCCTACTCATATTT | 337867 |
rs537788355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220307 | CTTAGTTTATTTCTT[C/T]ACCTAGAGAATGCTG | 337867 |
rs537807809 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245678 | AAACCCCATCTCTAC[G/T]AGAAATACAAAAATT | 337867 |
rs537811606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272147 | TAAGGTCACCTCTTT[C/T]AGCTCTACTAGACCT | 337867 |
rs537841510 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199590 | GGCACTTATGAGCAC[C/T]GAAAATGCTTTTTTT | 337867 |
rs537847318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264729 | CCAACTCTTTGCATT[A/G]CAGAGAGTATTTTAC | 337867 |
rs537866051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207324 | GAATTTTGCCATAGT[A/C]ACTACTCAGGTTTAA | 337867 |
rs537873092 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207003 | TCCACCGATTCTGAA[-/CT]CTTTCTTCCCTGTCT | 337867 |
rs537902174 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385518 | GTGGAGATAAGTTTG[C/T]CATTACATTAGCATG | 337867 |
rs537918225 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340276 | TGTACATTTTTTAAA[A/T]TAATACTACATTTAA | 337867 |
rs537954492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379941 | ACAGTGAGTGACGCA[C/T]GTGGGTTTTGGCCCC | 337867 |
rs537992942 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386236 | GGCGACAGGAGGCAG[A/G]GCAGACTGTGGAGGA | 337867 |
rs538008108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277454 | CGCTTGAACCTGGGA[A/G]GCGGAGGTTACAGTG | 337867 |
rs538012274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366512 | GGGTTCTGAGACCAT[A/G]AATATAACAACATAT | 337867 |
rs538029801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227364 | TCCACACTGTCGTCA[A/G]CCCCGGGAGCTGGCT | 337867 |
rs538068690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358945 | GAGACACAGTGTTTG[A/G]GTTGGAGGTTCGAGT | 337867 |
rs538088567 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217761 | AGCACTTTAAAATTG[C/G]CTTATTTCAGACCTA | 337867 |
rs538090502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313284 | ACACTACGCCCGGCC[A/G]GAAGGAAGGGTTTTT | 337867 |
rs538128801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367473 | TGGGACAGTCAGTGG[C/T]GTCACAGTCGGGCTG | 337867 |
rs538151908 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263296 | GCTGGATCCTGGCAG[C/G/T]TCGTACATGTAATTG | 337867 |
rs538153195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314344 | CATAATCTTGGCTTC[A/G]TGATCTATATCAAAT | 337867 |
rs538168991 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384763 | GCAGTGACGCCAGGA[A/G]TGTGATGCCAGGGCT | 337867 |
rs538169191 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298341 | GCTAAATTATAAACC[A/C]ATGATAAAAAGATAA | 337867 |
rs538177171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305982 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 337867 |
rs538186904 | snp | A/G | 3.29587e-05 | 0.00405934 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255542 | TAATAAAGGCAAGAA[A/G]CCATAAAGCAATGCT | 337867 |
rs538194118 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299643 | TGGGAAAAAATTTTA[C/G]TTCCCCTTTTCTTGT | 337867 |
rs538196996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339020 | TGTCTCCTCCTCCCC[C/T]CCATTTTATCTCCTC | 337867 |
rs538219174 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354588 | TTGGGCCCTATGCAA[A/G]TGGAAGGGACCAGGG | 337867 |
rs538236987 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217229 | TCAGTGGCTGGAGAT[A/G]TTGGCAGAGTCAGTC | 337867 |
rs538244966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207926 | CCTACTGACATTCTT[C/T]CTTAAGTATGCATTC | 337867 |
rs538262770 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298295 | TTCAGAAAATAGTTA[C/T]TTTCTGATCACATTG | 337867 |
rs538267062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248191 | AACCCACACTACTCT[C/T]CTGATATTTCTTGAG | 337867 |
rs538270120 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348827 | ACCAGCCTGGGCAAC[A/C]TAGTGAGACCTCTTC | 337867 |
rs538280019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348182 | TGGAGGACAGGAGCT[A/G]TTGTACTTCTTTGTC | 337867 |
rs538280529 | in-del | -/AGAGAATAA | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279338 | AGAATGAAGGATGTG[-/AGAGAATAA]ACTGCCACCATTCAA | 337867 |
rs538284072 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301555 | TCATTGCTAATAGAG[A/T]TGCTAACACTTCTTG | 337867 |
rs538287031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379132 | CATAATAATGGTCTG[A/G]TAAGAAATTCGCTGC | 337867 |
rs538295115 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239361 | TCAACCCCGGACACA[C/T]ATTAGAATCACCTGA | 337867 |
rs538299447 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270660 | ATTGATGGTTGATGG[C/T]GTGGACATGCACATG | 337867 |
rs538303282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332562 | GGTCTTTGGCCTAGA[C/T]TCTCAGCTGGACGTG | 337867 |
rs538306573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250591 | ATTTTAGAATAATTT[C/T]TTCTAATTCTGTGAA | 337867 |
rs538332659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342462 | CGCTGAGTGACTGTT[C/G]TGCTTGCAGACGGTA | 337867 |
rs538353005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373006 | GCGCCTGTAGTCCCA[C/T]CTACTTGGGAGGCTG | 337867 |
rs538369999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294513 | ACTGATAGTTGACAG[G/T]GAGCATTGAGGGACA | 337867 |
rs538384727 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233576 | TGGTTGAAAGGCCGC[A/C]GGAGCTGGTCAGAGG | 337867 |
rs538387061 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358295 | CATCCGAAAAGGCCC[C/T]TAATGTACTCTCCCT | 337867 |
rs538394050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334825 | ACACTCCAATCAAAA[A/G]GTAGAGATTGTCAGA | 337867 |
rs538436052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321198 | AAACATGAGTAATTT[G/T]TTATTTGCTGTCATA | 337867 |
rs538436915 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327903 | TTTAAGTGTATAGTT[C/G]GTTGAACTTTGGTAG | 337867 |
rs538456723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272247 | CATATTTTAATTTCT[A/G]TCTTTGTTTCTGATA | 337867 |
rs538459025 | snp | A/G | 0.000162324 | 0.00900755 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351627 | CTGTTGGCTGATGAT[A/G]AGAATTCTGTTATAT | 337867 |
rs538469760 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302978 | ATATTCAGCATAGAG[C/T]TGACTGTGGTCCGTC | 337867 |
rs538500537 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220707 | CTTAACCTTCTGTTT[C/G]ATCTCTGCTTGGGTT | 337867 |
rs538519592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345363 | ACAGTGTAAGATGGA[C/T]GGGGGAAAGGAGAAA | 337867 |
rs538521218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352181 | TTACTGGTCCTTGAT[A/G]TATTTTTTAGCAGCT | 337867 |
rs538521271 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375157 | AGCTCAGCCAGCCTT[A/G]ACTAAAGACCTGCTC | 337867 |
rs538558241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205822 | CACCGTTCCATGTGC[A/G]TCCCTCCCGAAGCTG | 337867 |
rs538569280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213150 | AATGGCATTCAAATA[C/T]ACATTTGATGTTCTT | 337867 |
rs538574482 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99349313 | TGACACACAGCACCT[A/G]AAGCCCTTGGAATCT | 337867 |
rs538575507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247446 | GTCTCGATCTCCTGA[C/T]CTCGTGATCCGCCCG | 337867 |
rs538582443 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345950 | GTTTCACCATGTTGG[-/C]CAGGCTGGTCTTGAA | 337867 |
rs538585560 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378063 | GCTGCTCTAGTCCTT[C/G]AGTAAGCCCATCACA | 337867 |
rs538619008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300706 | TTTGTATTAGAGGGT[C/G]TGGAACTGAAGGGTG | 337867 |
rs538627372 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214964 | AGTCAGGTCATGACT[A/C]CCTTTTCAGTTCTTT | 337867 |
rs538641498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249923 | AATGGGGTTGTTTTG[C/T]GCTTGTTGAATCAAG | 337867 |
rs538685647 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225015 | ATTTTGAGAGGAATA[C/T]TTAATGGTAATTATC | 337867 |
rs538696656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285237 | TTGCATTCGATTGTG[A/G]TGTGTCTTAAGTAGC | 337867 |
rs538701942 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369600 | ATGCATTTCAACTTA[C/T]GATATTTTCAACGTA | 337867 |
rs538723579 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281324 | AAAATCATTTCCAGC[A/G]TCTTACCTAAGAGAG | 337867 |
rs538763694 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99354021 | AAAATCATTCTGTCT[A/G]AGCAATGGAGGTGTG | 337867 |
rs538787523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220377 | TGAGATGGTATTACA[C/T]GTAAAGTGCTTTTAT | 337867 |
rs538790224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271404 | ATGGGACCATCCCGT[A/G]CGTGGACAGCTGGAG | 337867 |
rs538805193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367511 | GAGTGTCTGTACAGT[A/G]TCTTTCACTGCCTTC | 337867 |
rs538825428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228535 | CTGACCTCAAGCGAT[C/T]TGCCCGACTTGGCCT | 337867 |
rs538829127 | in-del | -/CTTT | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248216 | CTTGAGTCTTATTTC[-/CTTT]CTTTCTTTTATTTTA | 337867 |
rs538846211 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237255 | AGAAAATTTTATGCG[G/T]ATATATATATATATA | 337867 |
rs538857012 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267558 | GCCTTGTCCAGGAGG[A/G]TATAAGTAAGGAAGG | 337867 |
rs538881181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352815 | TGGGAGAAATGTGTA[A/G]TGCAGTCAGGAAGAG | 337867 |
rs538887712 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335813 | TGTTGCCACATTGCT[-/C]CCCAGAGGCGCCATA | 337867 |
rs538895113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306665 | CTGCATAGAATTCAT[C/T]GTGATTTTTTCCCCT | 337867 |
rs538902501 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385169 | TGAAGAACATTTGGG[A/G]CCCAGGGATAAGCGG | 337867 |
rs538918839 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215767 | CAGCCATTTCGAGTT[C/T]TGCTGAAGCTCAAGC | 337867 |
rs538923869 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353856 | CTTGATTTCGTGCAA[A/C]CCCCAAGGTTTCAGA | 337867 |
rs538925499 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264814 | GAGCTTGGAGGCTGC[A/T]TGGAAGCCTGAATGC | 337867 |
rs538925639 | in-del | -/CCC/CCCCA | 0.499104 | 0.0211472 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343375 | CCGCACGGTGTCTTT[-/CCC/CCCCA]CCCCCCAGATACTTG | 337867 |
rs538929483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361325 | TTTCCTGTTTATAGA[A/G]GCTCATATTTAACCC | 337867 |
rs538945093 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346638 | CTCCCACATACACAT[C/G]ATTTTCACTTGTCTA | 337867 |
rs538961798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265551 | TCTCTTTGACAGTCA[G/T]GTGGGTACTGATCCC | 337867 |
rs538970678 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292296 | GCCCACCACCACGCC[C/T]AGCTAATTTTTTTTT | 337867 |
rs538995434 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336363 | GTGTGTTTTCTTTTC[C/T]AGTTTGTACCTTATG | 337867 |
rs539005831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380033 | GTGCAGAAAAGGCAT[C/G]TCACAGCTGAAGGAG | 337867 |
rs539017332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365685 | AGGATCTAGTACACA[A/G]TTACTTTGTAAATAC | 337867 |
rs539023349 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322117 | CAGCCAAGTGACATA[C/T]ATCAGTTTAAACAAA | 337867 |
rs539043382 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333086 | GAGCAACATGGTGAA[A/C]CCCCGTCTCTGGGGG | 337867 |
rs539048054 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207203 | TTTGGTGAGAGGGCA[A/G]AGTATAGAGGTGTAG | 337867 |
rs539048427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269706 | TCATATTATTACTAC[A/G]AATTCTTACAGAACT | 337867 |
rs539067193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373771 | AGCTGGACAGAAAGG[A/C]GGCCAGACAGGCTCG | 337867 |
rs539077300 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326302 | ATTAGTGACATTGAG[C/G]ATTTTTTCATGTACC | 337867 |
rs539118899 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251338 | GAGAGATAGTTTGGG[C/G]TTTCCTATTTGAATA | 337867 |
rs539135651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234962 | ATCAGAGGGAAGAGA[A/G]AAGACATTTATAGTT | 337867 |
rs539146406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358978 | GGGAGTCTCTACCCC[A/G]TGAAGCCCTAGGAAT | 337867 |
rs539163763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320521 | GGCCTTCTACTATGA[C/G]AAAAAATCTGATAAA | 337867 |
rs539170970 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203253 | GTTGACCAGGCTGGT[C/T]TTGAGCTCCTGACCT | 337867 |
rs539180000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352305 | AACATTTTTCATCAC[C/T]CCAAAAGAAACTGCG | 337867 |
rs539235038 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247276 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 337867 |
rs539240344 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255684 | GTCCACTAATGCCAC[A/G]TTCATCATATAGATG | 337867 |
rs539240550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346143 | CCTAGGGTTTCACCC[C/T]AGACATTTCCCACTT | 337867 |
rs539243023 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226349 | CTGCCCATGCACCCG[A/G]TTAGTCAGCATATCC | 337867 |
rs539250044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206536 | TCCAGTGTATCAGCC[C/G]ATTTGTGGCATCTCT | 337867 |
rs539255376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338831 | GCATTAGATATAGCT[A/G]ACCATCCCTATTTTA | 337867 |
rs539256840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299261 | AACAGTTCAAATATC[C/T]TTCATTAGGGGATTA | 337867 |
rs539257554 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199524 | ACTGGAACCTCTCTT[C/T]GAGGGTAGGGACTGT | 337867 |
rs539270746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248306 | ATAGCTCACTGTCAC[C/G]TCAAACTCCTGGGTT | 337867 |
rs539285032 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228974 | CCAGGGAATTTCTTA[G/T]GAATAAGATGAAGGT | 337867 |
rs539311438 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232143 | ACTATTAGAAGTGTG[A/T]ATCTATGGGAGTGGG | 337867 |
rs539313362 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239413 | CCATATCTATACTTA[A/C/T]GTGAAGGTATAATTT | 337867 |
rs539317607 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204432 | AGGGGTGGTTATGGC[C/T]GGAGTGAGCAGTTCG | 337867 |
rs539347042 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200533 | GCCGGCAATCCAGGG[C/G]AATCCGCGGCCATCG | 337867 |
rs539356296 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207026 | TCCCTGTCTTTTCTA[A/G]CACCACTCTTGCTTT | 337867 |
rs539369049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207135 | TAGTGGCACCCCTCC[C/T]TGAGTTGGGAGTCTT | 337867 |
rs539394565 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361732 | CACCATCCTGTCCCC[C/G]CTCCCCTCCTTCACA | 337867 |
rs539398010 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210713 | AACTCCCGACCTCTG[A/G]TGATCTGCCTGCCTT | 337867 |
rs539399845 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235968 | GTGAGACCCTGTCTC[-/A]AAAAAAAAATTGTGC | 337867 |
rs539401618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217404 | GCAGGCGTGTGTTCT[A/G]CCTGCCCTCTTTCTC | 337867 |
rs539407210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350335 | CCAGGCTCTCCTGGA[C/T]AGCCTCAGATGGGGG | 337867 |
rs539420658 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318914 | TTGATGAAAGTTTTA[C/G]CTGGGCTTGTCAGTG | 337867 |
rs539444558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218416 | ACTCTTTCCTCCCCT[C/T]TAATTCACACTGTTT | 337867 |
rs539461297 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311501 | CAGCTGTTTTAATCA[G/T]TTGTGCTTGGGTTTA | 337867 |
rs539464338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204945 | AGTCTTGCTCTGTCG[C/T]CAGGCTGGAGTGCAG | 337867 |
rs539465095 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378055 | AATGCATGCTGCTCT[-/A]AGTCCTTCAGTAAGC | 337867 |
rs539492868 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262291 | AAAATAGTAAGTATA[C/G]GGTTTGGTACTATCT | 337867 |
rs539506650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313013 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 337867 |
rs539566800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383976 | ATATCCAGAGTTAGC[C/T]ACTAGGCTGCGGGTG | 337867 |
rs539577811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212890 | CCAACTTTTACCATT[A/T]TCTTTGTTTTGCCTT | 337867 |
rs539579798 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281188 | GCGAGACTCCATCTC[-/A]AAAAAAAACAAAACA | 337867 |
rs539589473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345033 | TGATGCTGCCAAAAA[A/C]GATTTCAGGAAGTAG | 337867 |
rs539589515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338143 | ACTTACTGTAACCTC[C/T]ACCACCCAGGTTCAA | 337867 |
rs539599678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99354083 | GCAGGCAGATCGTGG[A/G]TTTAGGATGGGGGAG | 337867 |
rs539604069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290691 | GATTGCGCCACTGCA[C/T]TCCAGCCTGGGTGAC | 337867 |
rs539622536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384614 | CTGCGTAAGCCCCAG[A/G]CTGCAAGTGGCACAG | 337867 |
rs539666487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378387 | CAAAAATTAGCCAGG[C/T]ATGGTGGCACATGCC | 337867 |
rs539693052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291489 | AAATTACAATGGTCC[A/C]AAAAGTAACCAAAAT | 337867 |
rs539704480 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283907 | GCCCAGCTAATTTTT[G/T]TATTTTTAATAGAGA | 337867 |
rs539739584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99356898 | TGTGTGTGGTTCTGG[C/T]GGTGGGCTTTGTTTG | 337867 |
rs539750857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317952 | TCATGACTATAGTTA[C/T]GTAAAAATAAGTGTG | 337867 |
rs539763707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324925 | ATCCCATCTAGGTTT[A/G]TGTAAGTACACTCTG | 337867 |
rs539784659 | in-del | -/G | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386664 | CACTAGCTGCTCAGA[-/G]GGGGGTCGAGGTGAC | 337867 |
rs539801082 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212435 | TTGTTTCAGTCATTT[C/T]CCAGAATTTAGTCCC | 337867 |
rs539815340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312337 | TTTTTTTCTGGTGCC[A/G]TTTTCCCAAAAGTGG | 337867 |
rs539829362 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273065 | CTGTATAAATTTTAG[A/G]GTAAGTTAATCAGTT | 337867 |
rs539856841 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261569 | TCTTGTCTTTAGCAA[A/T]TTTTGTGTGTAGTTT | 337867 |
rs539857724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304621 | GATGAATAATAATCA[A/G]TTAAAATTACTAAGC | 337867 |
rs539877199 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221575 | AGAGTCCCATTTGGT[A/G]TGTAAGCTGGTTTTT | 337867 |
rs539887338 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208968 | GAACTTAGATCCCCC[G/T]ATAGTTTCCTCCTGC | 337867 |
rs539905732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262352 | AATGTATCCTCTGAG[A/C]ATAAGGGGGAACCAC | 337867 |
rs539927818 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346186 | CCTTCCTGCCTTCCC[C/G]ACCAGTTCAGCCCCA | 337867 |
rs539947197 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199325 | GAGAATCGCTTGAAC[A/C]GGGGAGGCAGAGGTA | 337867 |
rs539962336 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246609 | TGCTGCACATGGAAT[A/C/T]GAATGACAGTAGAAC | 337867 |
rs539972091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248412 | TTTTTTTTTTTTGAG[A/T]CAGATTTTCACTCTT | 337867 |
rs539978197 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246456 | CCCAAAACATCTCCT[A/G]TCAGGCCAGTTCTTT | 337867 |
rs539987282 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241279 | CAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAGTTA | 337867 |
rs539993269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282116 | CTGCAGGGTGGCTGG[A/C]AGCATCACTGGCCTC | 337867 |
rs540013895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370661 | AAAAGGTGCCCCTGG[A/G]CAGGGATCTCATAGC | 337867 |
rs540016724 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379309 | TTTCTGGAGCAATAA[A/G]ACCAAAACAGTGATG | 337867 |
rs540019334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226297 | AGTTCTTCCAGTTGT[C/T]CAGAACAAAACTTAA | 337867 |
rs540039769 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357847 | GGCTAAGAAAACCCC[A/G]TACGCCTTAACTCAG | 337867 |
rs540048075 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357851 | AAGAAAACCCCATAC[A/G]CCTTAACTCAGCAAT | 337867 |
rs540063569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358052 | AGTGAAATGGGATGT[A/G]CTGAGAGCTGTCCTG | 337867 |
rs540075713 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363441 | ACATGACAGATAACA[A/C]AACATAGCAGAAACT | 337867 |
rs540085482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365790 | CTTGTTATTTTTTAT[A/G]TTATTTTTTGTCTGG | 337867 |
rs540099047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225046 | AGATCTGTATTTTTA[A/G]GGGTTTGTTTGGTCC | 337867 |
rs540113664 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352812 | TTCTGGGAGAAATGT[A/G]TAGTGCAGTCAGGAA | 337867 |
rs540128104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268054 | AGAAGGGGCATGCAG[A/G]AGGAGGGATTGCCTT | 337867 |
rs540129329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358499 | TCTGTTTGGGAAAAC[A/T]TGGTTATTTTTTATT | 337867 |
rs540141246 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269763 | TAAAGCTGTTTTCCC[C/G]TTTCTGAAATGAGCA | 337867 |
rs540146513 | in-del | -/AG | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385827 | GAGTGAGGGAGAAAC[-/AG]GGAGCTGAATCCTCC | 337867 |
rs540166447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268583 | ACTGCACTCCATTCA[A/G]CCTGGGCTACAGAGT | 337867 |
rs540166534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260667 | TGGGTCAAGGATTCA[A/T]CTTGTATAATGTAGA | 337867 |
rs540180800 | snp | C/G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305644 | TCCATTAACTGACTG[C/G/T]TCATGGTACTAATTA | 337867 |
rs540194719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205694 | GAGAGAAGATAGAAG[A/G]TAGAAGGATTCTTGG | 337867 |
rs540203167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218618 | GCCAGGCACTCTGCC[C/T]GGTTGTCTGGGGACC | 337867 |
rs540224613 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275842 | ATGACCATGGGCTCT[C/G]TCATAAGGTCCCCTG | 337867 |
rs540236222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345614 | TGGCTCCCATGAGTC[A/C]CTCAAGATCTAGAGA | 337867 |
rs540282316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216487 | GTGATATCAAATTTC[A/G]TTTAAAATATTTATG | 337867 |
rs540287688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231573 | GTGCCACCACGCCCA[A/G]CTACTTTTTATATTT | 337867 |
rs540294735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290778 | GAAAAGATAGGGAAG[A/G]GTGCATTTAAGAGGA | 337867 |
rs540306959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371267 | ATTTCTTCCTCGCTC[C/T]GTGTTACGAGAAGTT | 337867 |
rs540323089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238722 | TATTGATTTTTCAGC[A/G]AAACAGATAATAATG | 337867 |
rs540363452 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212544 | TTGTTGGCCATATTG[-/T]TTTTTTGACATTGAC | 337867 |
rs540363492 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199885 | ACGTGCAAGAGAATA[C/T]CAAAACTTATTCCTT | 337867 |
rs540372048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225523 | AAATTCCATTATATG[C/T]GTATGCCACATTTTG | 337867 |
rs540388302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276278 | GTCAAAGAGCTCAGT[C/T]TCAGAAGACTGTCTC | 337867 |
rs540389845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364704 | CATGCTATATAATAA[C/T]AGTCATACAAATGTA | 337867 |
rs540436837 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292377 | TCAATCTCCTGACCT[C/T]GTGATTCACCCGCCT | 337867 |
rs540437915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318458 | AGGCATGAGCCGCTG[C/T]ACCCGGCTCTCAACA | 337867 |
rs540445443 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204324 | TATTTGGGCTGACTT[C/T]TGAGAGTTTGGCAGG | 337867 |
rs540457420 | snp | A/G | | | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255077 | TAAAGGCTCCCCAGG[A/G]ATTGTAACTGTTCTC | 337867 |
rs540469330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269072 | TAACTTTGCAGCACT[C/T]ACTGTCTCAAGATGA | 337867 |
rs540484010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343610 | CTGGGCTCTTGCTGG[A/G]CTTTTACGTTGAGTG | 337867 |
rs540484899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312573 | GTGACATCCTTGGCA[C/T]GCATTTGATTCACTG | 337867 |
rs540493325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303912 | CGTGTTCTCCCTCAC[C/T]TGCTGCCTCTGGTCA | 337867 |
rs540496020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381660 | TACAGGTTATTTCCA[C/T]CCAAGATTGGAAAGA | 337867 |
rs540508040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261948 | TCAGTCAAATATGGT[A/C]TGAAAATATTAAATG | 337867 |
rs540520205 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334587 | ATTAACTCCAAATAT[A/G]TTATGCTCAATTTTG | 337867 |
rs540525013 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376673 | ACAGGAAAGCAAAGC[A/G]TGCTGGAGGCGAACC | 337867 |
rs540539335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296201 | CATATAAGTAAAAGC[A/G]TATGTATTCAGTTTG | 337867 |
rs540551290 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375545 | CTTCAGGTGGGCATC[A/G]CTTTCTGCAAGCGTC | 337867 |
rs540565946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245322 | ACGAAGTTAAGCTTC[G/T]GAAGAATAATTTTTT | 337867 |
rs540574590 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305127 | GAAATTTCGATTGAA[A/G]AAAGATGGTGAATAT | 337867 |
rs540604195 | snp | C/T | 0.000231279 | 0.0107511 | synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238488 | CTCCCTCCTGCTCGC[C/T]CTCCTCCTGCCTCAC | 337867 |
rs540615202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384046 | CACATGCCCAGGCCC[A/G]TGCCCGGCCCCTCCT | 337867 |
rs540630249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274366 | AGATAGGGTCTTGCT[C/G]TGTTGCCCAGGCTGG | 337867 |
rs540635102 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305720 | CATTGTCACTAACGC[A/G]ATACATAAACATGTG | 337867 |
rs540666951 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202387 | TGACAGTTCAAGAAG[A/G]CAATGTGGTTTTCCT | 337867 |
rs540671806 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378016 | CTGGTTTTCTGTCCC[C/T]ACAAGTTGAGTATCC | 337867 |
rs540685663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316322 | AAAATGTCTGTCCTC[C/T]ACCTGCCTCCCTCCC | 337867 |
rs540708526 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373046 | GAATGGTGTGAACCC[A/G]AGAGGCAGAGCTTGC | 337867 |
rs540716595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246979 | AACTTTGTGTAATGT[A/C]AATATATCTCTTAAA | 337867 |
rs540717431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266824 | TGAAAGCCTGTACCC[A/G]TCATACAGCAAATAT | 337867 |
rs540724940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371764 | TTGAGTTTTTTCTGC[C/T]GTAAACAGATACTTT | 337867 |
rs540747300 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324623 | TTATTTTAATTAGCC[C/G]TCATAAAAACCTGAG | 337867 |
rs540751249 | snp | G/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198869 | CAGTGGAAAATCCAG[G/T]TACGTAGCTCTGTAC | 337867 |
rs540751885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215844 | TACTCCTTCATCGCA[C/T]CGTGATTCAAACTGC | 337867 |
rs540752716 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275822 | GTCTCGGGATGAGGT[C/T]CTCGATGACCATGGG | 337867 |
rs540764859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310938 | CCCAAATAGGGTTCT[A/G]TAATCACCAAGAGAG | 337867 |
rs540771927 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325445 | TGCATAACCACATGC[A/G]GTTTCTTCCAACTAT | 337867 |
rs540781781 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357104 | TAAGATTATGATGCC[A/G]TATTTTTGCTATGTC | 337867 |
rs540808900 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365556 | TTGGTTTCCAAATGT[G/T]TGAGGTTTTTTGTTT | 337867 |
rs540837024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350385 | ATAAGTGATTAGAGG[G/T]TTGAGACTTTCAGCC | 337867 |
rs540840625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252757 | CTAAGTAAATTATTT[A/C]AAAAATAACTTTTAA | 337867 |
rs540847012 | in-del | -/ACAATGCAGTTGAA | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203890 | AATACAGTTTCAGAC[-/ACAATGCAGTTGAA]AACACCCTGCCATGC | 337867 |
rs540854811 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287720 | CAATTCCTGGGCTCA[A/G]GTGAGCCTCCTGTCT | 337867 |
rs540896731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344068 | CATGTTTCACTCTTT[A/T]TCAGTAAGAAGACCA | 337867 |
rs540909266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375857 | ATCCCAAGCTGGAGT[G/T]CAGTGGTGCTATCAT | 337867 |
rs540919224 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318946 | GTTTTTAAATCATAG[-/A]AAAAAAAAAAAGCCT | 337867 |
rs540926954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296882 | AAATTTTAAAACTCT[A/G]TCAATCTGCAAGTAC | 337867 |
rs540942368 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281212 | CAAAACAAAACAAAA[A/C]AAAAAAAAACAACAG | 337867 |
rs540955627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245786 | GTTGCAGTGAGCGGA[A/G]ATCGCTCCACTGCAC | 337867 |
rs540974459 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369743 | AGAGAAATTGGACAC[C/T]ACCTTAACCAGGTTA | 337867 |
rs540993125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323093 | GAGTTCCTCTGCGCC[A/G]CCTTTGCTTGTGCCC | 337867 |
rs540999666 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354879 | GAGTGCAACAGCAAG[G/T]ACCTAAACGGGCAGA | 337867 |
rs541006285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230641 | GCTTTCTGAGGCAGC[A/T]CACATTTCTTGACTC | 337867 |
rs541024928 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229537 | GGGACAGTGACTTGT[C/T]ATTTGAGCTTGAAGG | 337867 |
rs541028540 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99258522 | TGGCATATATTTAAG[A/T]TAATTATATACAAAG | 337867 |
rs541035716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323510 | ATGGGACTTGTGAAA[A/G]GACCACATGTAGAAG | 337867 |
rs541057286 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362574 | GTATAAAATAACTTG[G/T]TTTCATTTGCCTTTC | 337867 |
rs541077057 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306114 | TTGGCCAGGCTGGTC[A/T]CGAACTCCTGATCTC | 337867 |
rs541085588 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386951 | TGCTACCCCTTTAAA[C/T]AGCACCTAGCCAAGT | 337867 |
rs541101574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348442 | GTGTTTCAGTCACGG[A/G]GGGCCTTATGAAAAA | 337867 |
rs541129969 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301907 | CCTTTGCCCTCTAAT[A/T]TTTATTTATTTTAAT | 337867 |
rs541154234 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341998 | GAATCCTGGGAGGAG[A/T]TTCTCCATTGGAGAG | 337867 |
rs541156666 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250971 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 337867 |
rs541180223 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338323 | TTGGCCTCCCAAAGT[G/T]CAGGGATGACAGGTG | 337867 |
rs541182594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342990 | TGTTTTCCCCTCTGT[C/T]ACTTGGTCATGAGGG | 337867 |
rs541205835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228771 | AGGCAATGAGGAACT[C/T]GGTTAGATTTTAGAT | 337867 |
rs541209030 | snp | A/C | 3.31384e-05 | 0.00407039 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295620 | ATGTAATCCTTTCAG[A/C]CTCCTGCTTTGACAT | 337867 |
rs541227187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203287 | GTGGTCCTCCCGCCT[C/T]GGCCTCCAAAAGTGC | 337867 |
rs541238735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244032 | TTATTTTGTTAAACT[C/T]GGTGTTGTTATTTAC | 337867 |
rs541251544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335731 | CCCCTCTTGGGGATG[A/G]TTTGTTTCTGCTTCC | 337867 |
rs541273343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236910 | TGGAGAAAGGAGAAC[A/C]CTGGTACACTGTTGG | 337867 |
rs541312844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265229 | TTCTTATTGCTAATA[C/T]CATTTGTATGGGTAG | 337867 |
rs541313360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272651 | TTGCTGTGTCCTTAC[A/G]TGGCTGAGAGAGCTC | 337867 |
rs541324498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376766 | ACCAAGCTGCACTCT[A/C]ATCTGATATTTTGTG | 337867 |
rs541345844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221966 | GGTAATGTACTCTCC[A/G]AGTCACAGTTTTGTC | 337867 |
rs541351473 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276757 | TCTACCTAAATAACC[C/T]ATTAGGGTAAATTCA | 337867 |
rs541364865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329737 | CCACCTTGGAAGGTT[A/T]TCCTCCAGTGCCAGT | 337867 |
rs541380398 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265875 | GTAGAGGTTTTAAGG[G/T]AAAAGTGGGCAAGTT | 337867 |
rs541381302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229984 | TTGTGAATTGTCATA[C/T]ACCTTTCTGAGTTTG | 337867 |
rs541381940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275589 | TCATTTTGTGGATGC[A/G]ATATTTTTTATCCCT | 337867 |
rs541407321 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214836 | TGTTTGTAGACTGTG[G/T]GTGGGGAAGGGTTTG | 337867 |
rs541418298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308999 | GTTGAAAGACCATTC[C/T]GGTGGGGTTTTGCCT | 337867 |
rs541435686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350180 | TCCATGATCATCTCT[A/G]TATCTAATTTGTATT | 337867 |
rs541448306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310969 | CAGGCCATATTTTGA[A/G]CTACATATGAAACCA | 337867 |
rs541460968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208647 | TCTGTCCGAAAAAGC[A/G]GTGTGACAGGCTTCT | 337867 |
rs541469804 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268279 | AACACATTAGCTGCC[A/T]CAGCAAGCTGGAGTT | 337867 |
rs541507441 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260190 | GCTGGTTTCTCTGCC[A/C]TCCGAAGCTGGGCTG | 337867 |
rs541531735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304186 | GGCCTGGCTCCAGGC[A/G]TGCAAAATTACTTAG | 337867 |
rs541582045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281357 | GCATATAATCCATTC[A/G]TTCTTATATTCACAA | 337867 |
rs541601167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250466 | TGCTTACTGTAGCCT[C/T]ATAATCTGAAGTCAG | 337867 |
rs541649028 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205078 | CCGGCTAATTTTTGT[A/G]TTTTTGCTAGAGACA | 337867 |
rs541668059 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252563 | TGAAAGTAGAAATAA[C/T]TCCATTATTAAAAGC | 337867 |
rs541669850 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370397 | AACTTTTCTAAGTTT[C/G]AAATTATTTCAAACT | 337867 |
rs541696806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315147 | TACCACTTTTACAAC[A/C]GTTTCTCATGAAATC | 337867 |
rs541700452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354210 | ATCTTATTGGAGATA[A/G]GGGGTTGTACAGGTG | 337867 |
rs541714464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222680 | AATTACATTGATTTG[C/T]TTTGCATTCCCAGGA | 337867 |
rs541724119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370914 | AACCTGCCATGTGTA[A/G]AATCTTCCTATAACA | 337867 |
rs541777534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349106 | CGAGGGCAGGCTTTG[C/T]AGAGCCTCCTTGTCT | 337867 |
rs541796381 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317462 | CCATTAATTAACTTT[C/G]TTCTGTTATTTAGTT | 337867 |
rs541800322 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228201 | ATCTGCAGTCCTGTC[-/AA]AGAGTCACAAAGGAG | 337867 |
rs541811327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216568 | CAGAAACTGGTGCTG[C/T]AGTGGTAATGCCTGC | 337867 |
rs541827014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227185 | CCCGGACAACAAGAG[C/T]GAAACTCCATCTCAA | 337867 |
rs541827500 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252276 | GTTAGTATTTATTAT[A/T]TTACGTTGTCATGGT | 337867 |
rs541839118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357245 | AGCCTTGGTGTGTAG[G/T]AGGCGATCACATCTA | 337867 |
rs541861602 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202206 | CTTCCTCACTTCTCA[A/G]CTTCTCAGGTTTTGA | 337867 |
rs541874948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343134 | CCACCTATGCTGAGC[C/T]CAGATGCCCGTGTCC | 337867 |
rs541892442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260970 | CCAGTTTTTGAGTGA[A/T]TATAATTCAGTTAAG | 337867 |
rs541904142 | in-del | -/ATA | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354368 | CAGATGTTCTTTAAT[-/ATA]ATGATTGGGAAGAGA | 337867 |
rs541918711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244248 | TTAGTGGTTTGTGTT[G/T]TACTTGTTAAAAATA | 337867 |
rs541945037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375995 | TTTTTTTTTTTGGTA[A/G]AGACAAGGGTTGCCC | 337867 |
rs541957179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245125 | TGTGTGAGCCACCTT[C/G]CCCAGGCACCTTCTT | 337867 |
rs541977343 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287871 | GGAAAATAATAAGCA[A/G]TAATACATGAAATGG | 337867 |
rs541995581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236984 | GGTTCTTAAAAAAAA[A/T]AAATAAAACTACCAT | 337867 |
rs542017739 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362290 | TTCCCTCCTTAGGAA[C/G]AACTGAATTTTTTTC | 337867 |
rs542022355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361589 | CTACATACATACTTA[C/T]CAGGGTTTCTCAACC | 337867 |
rs542092779 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336547 | TTCCTTGTGTATAGC[C/T]CATGTGCCCCTTCCC | 337867 |
rs542092947 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384201 | AAGAAAAATTGGAAA[-/CT]CTGACTAAGTCCTCA | 337867 |
rs542101948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265961 | ACACAGTTTATTTGA[A/G]TATGAAATAGATCCA | 337867 |
rs542103642 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323543 | GAAGACAAGTAGCAG[C/G]TTCTTAAGAAGCATC | 337867 |
rs542110563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355471 | ACAAGGCCTTGGCAT[A/G]CTCTTCCTGCGCTGA | 337867 |
rs542130356 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248443 | GCCGCCCAGGCTGCA[C/G]TGCAATGGCGTGATT | 337867 |
rs542137385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215337 | AGCTGTTCTTTTATT[C/T]AGAGTCCTGAGATAA | 337867 |
rs542143164 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258748 | ATAATACTATATCCA[C/G]TAGGATTGTAGGGGC | 337867 |
rs542162409 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209301 | TGTCTTCACGGGAGG[A/G]AACCCTCACATTCCA | 337867 |
rs542191617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224702 | TGGCTTTAGCAAATA[C/T]CAATCCCTTTATTTA | 337867 |
rs542193443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324064 | GAACCATACACTCCA[A/G]CTACACACAATCCAT | 337867 |
rs542239950 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302842 | CAGTACATGCCTCTG[A/T]GGCCTGGTTAAATAC | 337867 |
rs542273177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228850 | CTTTACTAATGGTTC[C/T]AGTTTAGATGCTCAC | 337867 |
rs542275282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328075 | TTTGCCTTTGCTGGA[A/G]TTTCATATACTTAGT | 337867 |
rs542276935 | snp | C/T | 0.00131941 | 0.0256508 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295689 | GAATCCAGACAAATA[C/T]GCACACGCCTTTTGC | 337867 |
rs542278166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235359 | TGGCAATACTACCCA[A/G]AGCAATTTACAGATT | 337867 |
rs542288217 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343497 | GCGCCTGTGAAGTGG[C/T]ACAGGCCTTTATGGC | 337867 |
rs542301816 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343258 | CACTTCATGGTGCAG[C/T]AGCAGTTTATGCAAG | 337867 |
rs542333435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270610 | TAAGTAAGTAGGGAA[C/T]GAGAGTTTGTACTTA | 337867 |
rs542355460 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332080 | GGGAAAGCAGCCCCT[A/C]GGTTTGTCCTGTTGT | 337867 |
rs542360819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222042 | TTTGAGGTTTAAACC[A/G]TGTAAGTAATTCATT | 337867 |
rs542360913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229354 | CATTGATGATATTTG[C/G]GGATTTAAGTCTGGA | 337867 |
rs542361044 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322629 | GTTACTTGTCATGTA[A/C]AGTATATCAGACTTT | 337867 |
rs542364510 | snp | C/T | 0.000403158 | 0.0141921 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99296059 | CATTACTATCCTGGC[C/T]GTGCTGTGATGTGCA | 337867 |
rs542375706 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305854 | CTACCAGTAAGCACA[G/T]TTAGATGTGTGATCA | 337867 |
rs542386669 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313926 | TTTCATAAAGTGTTC[C/T]ATAAGTACAAATTAT | 337867 |
rs542391605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308237 | CAGCCACTTCTGGGT[A/G]CTGCTTTTTACGAAG | 337867 |
rs542399369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273396 | CTTTGTGATCCACTC[A/C]TGTTTGGTGAGGTTC | 337867 |
rs542479602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300753 | CATGTGCTGTTATCT[C/G]AGTGAGGTGTTCCTC | 337867 |
rs542481933 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316243 | TGCAGGGTTCTTCTT[C/G]ACTGTCTGGTGTCAA | 337867 |
rs542492581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266676 | CTTAGAACAAATTTG[A/T]CATGTTAAATATATA | 337867 |
rs542515640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309169 | AGGCTGGAGTGCAGG[A/G]GTGTGCTGTCGGCTC | 337867 |
rs542519489 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386291 | AGGCAGGGGTGGACC[A/G]CCATGAGCATGAAAA | 337867 |
rs542533835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341872 | AGAAAGAAGTAGGGG[A/T]TGGTTCTGATGTTTC | 337867 |
rs542543287 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219632 | GTGTTAGTGTACTTT[A/T]TGTGTGGCCCAAGAT | 337867 |
rs542562669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99293838 | GTCCAATAAAAATTT[A/G]AAGTGTAACAGAGTG | 337867 |
rs542567281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277957 | TTTCTGCAGGATAAA[G/T]TTCCTCATGGTCTCC | 337867 |
rs542579015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284878 | ATGAAAATAATGTGT[A/G]GTTTTCGTATTTCTC | 337867 |
rs542586180 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282668 | AAGGAGATACTTTAA[C/T]AGTGAAGGGAACTTG | 337867 |
rs542587343 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242839 | ACTTCTCAGACGGGG[A/C]GGCCGGGCAGAGACG | 337867 |
rs542599214 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287707 | CCAGGCTGATCTCCA[A/G]TTCCTGGGCTCAAGT | 337867 |
rs542611202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334942 | GATGAAGATATATTA[C/T]GGAGACAGTAACCAT | 337867 |
rs542612893 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256606 | TTTAAATTTTAACAA[C/T]TTTCAAAGTAAATCC | 337867 |
rs542620095 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367197 | GATGCTCACTTCTCA[A/C]CTTTTTGCTGTTTGT | 337867 |
rs542620679 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381430 | TGGCTGGGTGCAAAG[A/C]AGCAGCCAGTCCTCA | 337867 |
rs542625047 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325622 | TAGGTATGGGGTTGT[G/T]CAGCGAATCTCTGGA | 337867 |
rs542626045 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362008 | AAGACCCTCATCCCC[-/A]AAAAAAAGTTAAAAT | 337867 |
rs542642517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320551 | ATCTTCATATTAACC[A/T]TGTTCTTTATTACTA | 337867 |
rs542664412 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235881 | GCTGAGGTGGGAGGA[G/T]CACTTGAGCCCAGGA | 337867 |
rs542675668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279622 | CCTTAGCCTGTTCAG[C/G]CTCCTCTAACAAAAT | 337867 |
rs542685087 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214135 | GATTGTGTATTTATT[A/G]TAGAGCCAGGGTTAG | 337867 |
rs542695291 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319946 | TTGTTTCACTTAGCA[A/G]TAATGGTTTTGAGTT | 337867 |
rs542711125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322505 | TACAGTTCACACATT[C/T]ATCTTTACTTGACCC | 337867 |
rs542761609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280334 | ACTACTGCCTGTCAC[A/G]CATACATCATTACAG | 337867 |
rs542762633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347174 | AGAAAGCAAGACCCA[A/T]GTCTAGAGAGTGCAA | 337867 |
rs542781362 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358221 | GTAAGAAATTTCTGT[C/G]GGATTCTGAAAGCAA | 337867 |
rs542794510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353978 | CCACCCAAGATTAGA[A/G]CACAGATTAGCCATA | 337867 |
rs542796150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214197 | CTTCAATCTTGTATC[A/G]TTTTTTGCCTTGGCA | 337867 |
rs542805281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284242 | AGAAAAAAAGTTCCA[A/G]TTGGGGGGAAGTGCC | 337867 |
rs542812918 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256945 | TGTCTTGAAATCAGC[C/G]CAGAATTTCTCTTTA | 337867 |
rs542842029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284824 | GATACATATTCTAAG[G/T]CTGCTGGAAAATTAA | 337867 |
rs542843583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265998 | TTATGTATGGTCTCC[A/G]GTTTTCCATACCGAT | 337867 |
rs542855618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257848 | TAATGTAAAGCAATA[C/T]TGAAAATAAATGTAA | 337867 |
rs542857607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347669 | GCTCTATAGATCTCA[C/T]TTCAACTGAGACATG | 337867 |
rs542871300 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235064 | GCGTGACTGCTTTTA[A/G]TACAAGGCAGAGGTC | 337867 |
rs542873641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240588 | GAGATGACAGTCATC[A/G]TCATCGGACATTGGT | 337867 |
rs542875961 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344299 | TGATCCCTAACTCAT[-/A]ATACCTCCCAATATG | 337867 |
rs542890723 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366528 | AATATAACAACATAT[A/G]TATAGTATAACTTGA | 337867 |
rs542908469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233731 | CTAAGAAATAGAAAA[G/T]TAATGACAGAATTAT | 337867 |
rs542923868 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368116 | TGGTTGGGGGGCGGC[A/G]GGTGGGAATGTATTA | 337867 |
rs542943436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249973 | ATTAGACCTTTGTCA[C/G]ATGCAGTTTGTGAGT | 337867 |
rs542956027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380666 | GCTGGTTGTCATCGC[A/C]TACCCAAGCCCAAGC | 337867 |
rs542966830 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213756 | AAGTTATTGATTGCA[C/T]CTTTAACCCCATTTT | 337867 |
rs542967160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270658 | AAATTGATGGTTGAT[A/G]GTGTGGACATGCACA | 337867 |
rs542984350 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267943 | TCTGTACCGGTAAGT[A/C]GTCAAGGGCCTGGTC | 337867 |
rs543006965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359505 | ACTCCTGTTAAATCA[A/G]CCTGTTTCCTAAATG | 337867 |
rs543011123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219912 | CCATTCCTCTTATGA[A/C]TGAATAATATTCTAT | 337867 |
rs543025279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227993 | GGAGAGTGTCACCTT[A/G]AGACTTGAGACCAAG | 337867 |
rs543089011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281364 | ATCCATTCATTCTTA[C/T]ATTCACAAGATATCT | 337867 |
rs543089553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213606 | CTCAGGTGATCCGCA[C/T]GACTCAGCCTCCCAG | 337867 |
rs543092251 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265642 | AGGACCTGGCACGTG[C/T]GTCTTCAAACGTTTC | 337867 |
rs543123457 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375820 | TTTTTTTTTTTTTTT[-/TT]GAGACATGGTCTTGC | 337867 |
rs543133659 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367599 | CACCTACTGCAGGCT[G/T]CCAATTTTGTGCTAT | 337867 |
rs543149825 | snp | C/G | 0.000873082 | 0.0208753 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255354 | GATGTCAGAAATCTT[C/G]AGGCAGGTGGCGGGA | 337867 |
rs543158361 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316263 | TCTGGTGTCAACTCC[C/G]CCTGTGCCCACCTTG | 337867 |
rs543182519 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232378 | TTTTGAACACAAGAC[C/G]CTGTCCATCCTTAGT | 337867 |
rs543196606 | in-del | -/ATATAT | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341599 | AAATGTGGAAGCTAC[-/ATATAT]ATATAGGTGATGGAG | 337867 |
rs543204520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201759 | CTGGAGGACAGAAAC[A/G]TCTGACATTTCCAAA | 337867 |
rs543205587 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386837 | TGCTGAGCAAAGCCG[C/T]GTGTGTCTGACCTCT | 337867 |
rs543223815 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208479 | GTAAAAGGCCACATA[A/C]GGTGATGATCTTAGG | 337867 |
rs543227652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233264 | ACTGCAGGCACGCAC[C/T]ACCATGCCCAGCTAA | 337867 |
rs543238763 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, splice-donor-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200637 | TGCCACCCGTTTTTA[C/T]CTCAGGCGGTTCTGA | 337867 |
rs543246040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373197 | TTTTTTTAAACAGGT[A/G]TCTTTATACTACTAT | 337867 |
rs543250577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294813 | GGAGTTATTAAGAGC[A/G]CCTCCTTTTGGTGTA | 337867 |
rs543304446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325595 | TAAGTGACAGTTTAT[A/G]ATTGTTGACTATAGG | 337867 |
rs543305965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366622 | GAAGACAGGCTTTTT[A/G]GTTTGATTTTTTTTT | 337867 |
rs543333550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335151 | GCAATGAACAAATCA[A/G]CAATCACAGTTGAAT | 337867 |
rs543336005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286776 | AGTTTGCTGTTGCCA[C/T]GTTATTCTTAGGACT | 337867 |
rs543355511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319682 | ACAGAGCTAAACCCT[A/G]TTGTGAAGTCTTCAA | 337867 |
rs543378857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272587 | ATGTTGGCATGGTCA[A/G]GTTCTGGTGAGGGCC | 337867 |
rs543381057 | in-del | -/AGGCTG | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310088 | TCTCAGCAATTCAGA[-/AGGCTG]AGGCAGGAGGATTGC | 337867 |
rs543382716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328133 | TTACTTCTTTCACTT[C/G]AACATGAAAATTTCA | 337867 |
rs543385186 | in-del | -/AA | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370308 | CAGAGACAGAGAGAG[-/AA]AGCAGCTATGGCCAA | 337867 |
rs543391918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326353 | TCTTTGGAGAAATGT[C/T]TGTTTAGGTCCTTAG | 337867 |
rs543424541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368915 | CTGGATCATCGTGTG[C/T]CAGGAAAGTAAGGAA | 337867 |
rs543424747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328968 | ACATTTAGGTCTGTG[A/T]TCCAGTTTGAGTATA | 337867 |
rs543482939 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273479 | AGTATTGAGAGTAAG[C/T]GGTTTCTTTATATGG | 337867 |
rs543483640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274318 | GTGTGTGAATACCAC[C/T]ATCTATCCATTCTAC | 337867 |
rs543487587 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338949 | CTACTCTGTCTGTCC[A/G]TAGAATATTTGTGCA | 337867 |
rs543488718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369617 | ATATTTTCAACGTAC[A/G]GTGGATTTATTGGGA | 337867 |
rs543521586 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300986 | GTTATTTAAGATATA[G/T]TTATATAAACTAAGG | 337867 |
rs543522832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308291 | GAGGGGCCTGGATAG[C/T]AGGTCTTAGGAGAAC | 337867 |
rs543540254 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386375 | AGCAACGATGTATCA[A/G]ATTGATGCAAATTTA | 337867 |
rs543554295 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362009 | AAGACCCTCATCCCC[A/C]AAAAAAGTTAAAATA | 337867 |
rs543572606 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315635 | CCCCATTTCCCCATC[C/T]ATCAAATGGGGATGA | 337867 |
rs543590495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208070 | TGGCGTGATCTTGGC[C/T]CACTGCAGCCTCTGC | 337867 |
rs543595549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374013 | ATTAATAATACATTT[A/G]TAATGCATGTCAAAC | 337867 |
rs543598379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380723 | TTAGTTTTGGACACT[A/G]TGGGAAACCTTCAGG | 337867 |
rs543598547 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253288 | TATTATTGAAAAATT[A/G]GTGTTTGACATGAAA | 337867 |
rs543602270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301838 | AAACCTTTACCATAT[G/T]CGGGGATTTAGTTGG | 337867 |
rs543611263 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318816 | GACAGAGTGAGACTC[C/T]ATCTCAAAAAAAAAA | 337867 |
rs543611363 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287118 | AACACACAAACTTCA[A/G]ATAATTTGACAGTTG | 337867 |
rs543616399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202605 | CAAATTTGATACAGG[A/G]CAACTGTGGGGAAGA | 337867 |
rs543621532 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309184 | GGTGTGCTGTCGGCT[C/T]ACTGCAACCTCCACC | 337867 |
rs543656150 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242916 | TCTCAGACGATGGGC[A/G]GCCGGGTAGAGACGC | 337867 |
rs543658497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367347 | GAGCATTTTAAGGGC[C/T]GTGATGGAAACACCA | 337867 |
rs543661826 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342543 | TGGCAGGAGATAGGT[C/T]GGCCTAGGTGAGGGG | 337867 |
rs543687333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271777 | TTTGCTCTTCGAGTC[C/T]CCATGTCCCCCAGCT | 337867 |
rs543719489 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228107 | GGACTGACGGGGCCC[A/G]TTGCACAAGGACAGG | 337867 |
rs543743913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335497 | CTCTACAGCAAAGAC[G/T]GCTTTCTGTGATTCT | 337867 |
rs543779190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236101 | GAAACTATGAAACTA[C/G]TAGCAGAAAATGTTG | 337867 |
rs543801236 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214271 | GGAGTAAATTTTTTT[C/T]GTGTAAGGACACGAG | 337867 |
rs543807908 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268862 | GATGGGGTGGAGATG[A/G]AGATTGGCCATGGGA | 337867 |
rs543812340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206748 | TTCTCAGCTAAGTTT[C/T]TGGGATTCAGTCATC | 337867 |
rs543821898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347017 | GTGCAGTGGTTCACG[C/T]CTGTAATCCCAGCAC | 337867 |
rs543884157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340765 | AAATAAATTGCAGCT[A/G]AAAGATTGGTCAAAC | 337867 |
rs543901561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240667 | CATATTGATGGAGGT[A/G]TATGCTGCCTAAAGT | 337867 |
rs543908004 | in-del | -/TCT | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344419 | GAACTTTTGCTTCCA[-/TCT]TCTTCTTTATGTTTC | 337867 |
rs543924530 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99258470 | ACAAATGATTTGTTT[A/G]TGAAGTCACACTTAG | 337867 |
rs543968446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218739 | CAGTGTTTTACTTCT[A/G]AACACTGTAGGGAAA | 337867 |
rs543979966 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256056 | AACTACTGAACATTC[A/G]CAGTAATTCTCATTT | 337867 |
rs544048562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326443 | GTTTATAGGAATTCT[A/G]TGTTATTCTTCATAA | 337867 |
rs544055095 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242880 | CCCAGACGGGGCGGC[A/G]GGGCAGAGGTGCTCC | 337867 |
rs544076698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279233 | TTTGGTTAGCCCTAC[C/T]GGGGATTTTAGTAAA | 337867 |
rs544093242 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218812 | CAGTCTTTGTTGAGA[C/T]GATCACCAGGAGGCA | 337867 |
rs544111337 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378663 | AATCCTTCAAAGTCA[C/T]CACCTTGTTCGTCAT | 337867 |
rs544113579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359277 | AACCTGGAAGAAAAA[A/G]GAAAAAGTGTTTCAT | 337867 |
rs544144345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228651 | TTGAGGTAGGTTCTC[A/G]TCTCCATTTTACAGG | 337867 |
rs544171425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263630 | CCATGACTCAGAGTC[A/C]ACTCCTAGGTCTATA | 337867 |
rs544185739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306217 | AGGGTCTTTATGTAA[A/G]ATATCCATAACATAT | 337867 |
rs544187145 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385427 | GACCGAGCATCTCTG[C/G]TGCTGATGTTCTTGT | 337867 |
rs544191744 | in-del | -/TG | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327482 | GTTTTTCTCTCTCTC[-/TG]TCTGTGTGTGTGTGT | 337867 |
rs544209264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255942 | AATAAGAATAAAATC[A/G]TTGGTTAAAAAATAA | 337867 |
rs544213182 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341342 | GGTCTGCAGATCTCA[C/T]GATGGTTTGGAGAAG | 337867 |
rs544213747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340046 | GACAGTGTCTTGACA[A/G]TCTTTTACCAGAACT | 337867 |
rs544220923 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324668 | TCTCCCTATTATAGA[G/T]GAAGAAACTGAGGCA | 337867 |
rs544226598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299516 | TAATTTTGTATGAGT[A/G]ATTTTGGGGCTTTAC | 337867 |
rs544240761 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215699 | CCGGCTCTCTGCGAG[-/C]CGGGAAACCGCCTTT | 337867 |
rs544255355 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379413 | TTTCTTTGCTGCTTC[A/G]TGATGCTTTGTCACC | 337867 |
rs544256036 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300084 | CACATGCGCAACATT[A/G]CCCAGCTGCTCCAGA | 337867 |
rs544256305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318559 | GGCGCAGTGACTCAC[A/G]CCTGTAATCCCAGCA | 337867 |
rs544257868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292430 | TACAGGCATGAGCCA[C/T]TGCGCCCAGCTGGGG | 337867 |
rs544258534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325007 | TTATCATTAAGCAAC[A/G]CATGACTGTAATTTG | 337867 |
rs544258629 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213881 | CTGGAGTATAGTGGC[A/G]TGATCTCAGCTCACT | 337867 |
rs544262984 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265637 | GAACAAGGACCTGGC[A/C]CGTGCGTCTTCAAAC | 337867 |
rs544275120 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382232 | AACAAAATGAGAATT[A/G]AAAATAATTCATTTT | 337867 |
rs544275952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332910 | CTTTTCAGAGGGTCT[A/G]TGGATTTCAAGAAAA | 337867 |
rs544326107 | snp | C/T | 0.000606171 | 0.0173988 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200892 | GCGCCCTCTGGGGCT[C/T]CGAGCCCGGCGGGAC | 337867 |
rs544378410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313193 | GTTTCACCGTGTTAG[C/T]CAGGATGGTCTCCAT | 337867 |
rs544389420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269959 | AACACCTTTAACAGT[C/T]TGATACCCTGTGACT | 337867 |
rs544411905 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245579 | AAAAAACAGGCCGGG[C/T]GCGGTGGCTCATGCC | 337867 |
rs544427207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227035 | GAAACTCAGTCTCTA[A/C]TAAAAATACAAAATT | 337867 |
rs544434823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297504 | TAACTTCATTCTAAC[A/G]ACCTTAAAACTGAGA | 337867 |
rs544449779 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221965 | AGGTAATGTACTCTC[C/T]GAGTCACAGTTTTGT | 337867 |
rs544468502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355992 | CTCTCTTGGGTTTGC[A/G]GCTGCTGTTGAAACC | 337867 |
rs544488240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254330 | TTGAATGACTATTCT[C/T]TGTTTTTAAAAGAAT | 337867 |
rs544496761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205575 | GTATTTTTAAAGTCT[C/T]CACATCCCCCCACCC | 337867 |
rs544507695 | snp | A/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327644 | AAACAACAGCATAGG[A/T]TGTTATCAAAGGTCT | 337867 |
rs544528418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298715 | GTGGTTCTTAAATAG[A/C]AAATCATAGGGATTT | 337867 |
rs544552953 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362589 | TTTTCATTTGCCTTT[C/T]CCTAACACTAGTGAG | 337867 |
rs544603842 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378537 | GTCTCAAAAATAAAA[A/T]AAAAAATAAAAACTT | 337867 |
rs544619486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232324 | AATAAACAAATCTCT[A/G]TGTTATAACCACTAG | 337867 |
rs544640898 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTTTT | 0.494187 | 0.0535994 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283714 | TGCCTTAATGCCACC[-/TTTTTTTTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTGAGA | 337867 |
rs544642587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239808 | GCAGTTCTGCCTTGG[G/T]AAATCTAAACACACG | 337867 |
rs544657631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234754 | AGAGAGGAAGGCATG[A/G]AAACACAAAGGTGGA | 337867 |
rs544676429 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200993 | CGCCACCCTAGGCAC[C/T]TCTTTGAGGAGGCTG | 337867 |
rs544688315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334086 | CAAGTATCTGGGACT[A/G]CAGGCATGCACCACC | 337867 |
rs544697968 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276884 | TTTGTAGAATACCAC[A/G]GCCAGCCAGCAGGTG | 337867 |
rs544698087 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269175 | GGGGTGTTGCAGGAA[G/T]TCCACTCATTGGTAG | 337867 |
rs544701634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365921 | ATGCCATTGTGTTAC[A/G]TATAAATATGATATT | 337867 |
rs544746010 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228290 | TTCTCTATATTCATT[A/C]ATTTTTTTTTTTTTT | 337867 |
rs544747762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235295 | GAGGACATAAAAAAA[C/T]GAAAGGGTATTCCAT | 337867 |
rs544764722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213556 | GTAGAGACAGGGTTT[A/T]ACCATGTTGGCCAGG | 337867 |
rs544772546 | in-del | -/TGTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216078 | TTTTGTACCAACCTA[-/TGTG]TATTTGTGTGTGTGT | 337867 |
rs544782285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374540 | AAGGTGCTTTCACTC[G/T]TAGCTGATAAATAGC | 337867 |
rs544786699 | in-del | -/GAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372701 | AAAGAGGAGGAGGAG[-/GAA]GAAGAAGAAGATAAA | 337867 |
rs544803760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327372 | GCAGGACAGAACATT[C/T]TCCCATGGGTCTTCA | 337867 |
rs544827364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206883 | ATCACCTGGGTGCTC[C/T]TTCCGCTTCCTGCTC | 337867 |
rs544838257 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309775 | CAGCTAATTTTTGTA[-/T]TTTTTTTGTGTGTGT | 337867 |
rs544900250 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281848 | AAAGGAGACTCAGGC[-/T]TTTTAACACTGCAGG | 337867 |
rs544911805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290878 | ACAGAGAATGCAGGT[A/C]GAGTTTGTAGAGAAA | 337867 |
rs544922226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331122 | CTCTTATCCTTCGCC[C/T]CTCAGTCTGACCACT | 337867 |
rs544963424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284763 | TCAGTCTGTCTTGGG[C/T]GACCTTGGCATTTTT | 337867 |
rs544969389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380238 | GGAATGCTTAACGTG[A/T]GTTTTGCTTACCTGA | 337867 |
rs544973729 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234217 | AGATGGAGTCTCACT[C/G]TGTCGCCCAGGCTGG | 337867 |
rs544976973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300213 | CAAGGGTAGCCTGTT[C/G]AGGGTCCTTAACTGA | 337867 |
rs544997934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293675 | AATGGCTTTAAAATC[A/G]GGTGGCTCTTTGTGA | 337867 |
rs545002827 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386239 | GACAGGAGGCAGGGC[A/G]GACTGTGGAGGACAG | 337867 |
rs545011156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293122 | CATTAATTGGAGATA[A/G]GATTAGAGTTTACCT | 337867 |
rs545011202 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337734 | AGGCCTTGGCCTTCC[C/T]AACCCACATGGACCC | 337867 |
rs545024868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232702 | CGAGGCGGGCAGATC[A/G]CTTGAGCTCAGGAGT | 337867 |
rs545032040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374052 | TACAGCAAATTTAGT[A/G]ACAGATCTATTTGGC | 337867 |
rs545044373 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242352 | CCCCACCTCCCTCCC[G/T]GACGGGGCGGCTGTC | 337867 |
rs545047898 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285519 | TGCCTTAGCCTCCTG[A/T]GTAGCTAGGACTACA | 337867 |
rs545054785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319576 | ACAGCTGATATGCTT[G/T]CAGCCAATATTCTGG | 337867 |
rs545059530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289076 | TTACTTCACTGACAA[A/G]ACAATTGAAGTCTAG | 337867 |
rs545061313 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235425 | CACAGAAATAGAAAA[A/G]AAAATCCTAAGATTT | 337867 |
rs545072917 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378293 | GCAAGTTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 337867 |
rs545076185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326764 | TCCAGCACCTTACAC[C/T]GCACATCTCAAGGCT | 337867 |
rs545090608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325474 | ATATCCCCTATTTCA[C/G]TCACATATCCCTTCT | 337867 |
rs545096608 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262298 | TAAGTATAGGGTTTG[A/G]TACTATCTGCAGTTT | 337867 |
rs545106370 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222913 | TGTTGTAACAGAGTT[C/T]GTATAGAATTGGTAT | 337867 |
rs545110823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277461 | ACCTGGGAGGCGGAG[A/G]TTACAGTGAGCCGAG | 337867 |
rs545134022 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361403 | TAACTTTCTGCTTTT[G/T]AAGCACTTTTCTACT | 337867 |
rs545147411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270631 | TTTGTACTTAGAAAC[A/G]TAGTTAGATAGAAAT | 337867 |
rs545160556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352644 | GTTGCCTCTTGGCCT[C/T]ACCAGTGCTACCATT | 337867 |
rs545185422 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291000 | GAGCTCAGGCTACAG[C/G]GTGGAACCTCTTACT | 337867 |
rs545223583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346456 | TGCCTGCTATGTGGC[C/T]GCATCTCCTTTCTGC | 337867 |
rs545232516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291799 | TTCATTGAGAATTAA[C/G]AACTTCACAGATATT | 337867 |
rs545247358 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240548 | TGGAGCTGCCTCTTA[C/T]GGTTTTTGAATCTGG | 337867 |
rs545252256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299612 | GGAATGAATAAATAG[A/G]TAAAAAAAATTTTAA | 337867 |
rs545270097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298419 | TTAAAGAAGAAATCA[C/G]AGTGGAAATTTCGAA | 337867 |
rs545275312 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341948 | AATATCAAAAGAGCA[A/G]ATTTGGGGGAAATAT | 337867 |
rs545275816 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318947 | GTTTTTAAATCATAG[A/G]AAAAAAAAAAGCCTG | 337867 |
rs545311947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256829 | CAACAACAGACTTCA[A/G]AAATAGACTTTGCTG | 337867 |
rs545322501 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200712 | GCACTTCCCTTCCCC[A/G]GCAGGAAGGAGGGCG | 337867 |
rs545341927 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385875 | CCAGAGGACTCTGCA[A/G]TACCTTCTCCTACAT | 337867 |
rs545355729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261318 | CTCCAACCTTTGTCC[C/T]CTCCTTTCTGTTTCT | 337867 |
rs545357684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268983 | GAGGAGTTAAATAAG[C/G]GGGGAATGGCCTGTG | 337867 |
rs545363322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227084 | ATGCCTGTAATCCCA[A/G]CTACTCGGGAGGCTG | 337867 |
rs545423513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270034 | TGTGTATGTGTGTTA[A/G]TTTTTCCTAAACAAC | 337867 |
rs545443578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217857 | GGGTGGCAGCGTCCA[C/T]CGAGCTCGTGCCCAC | 337867 |
rs545448751 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224479 | TCCAACTATATTTGT[A/G]GATTTATCTACGTCC | 337867 |
rs545479532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331504 | AATCAGAAGGATATC[C/T]AGCATTTTAATTGGG | 337867 |
rs545512948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384386 | ATTTTTGTAATATAT[C/T]CTTAATTGGGAAAAA | 337867 |
rs545527514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359434 | CTCATTCAAGTAAAA[C/T]GATCTAGTCTTTTTC | 337867 |
rs545536587 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208765 | AGGTGAGGCTCTCAG[-/A]TTGTTCTTCTGTGGC | 337867 |
rs545569916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231536 | TCCCACCTCAGCCTC[C/T]CGAGTAGCTGGGACT | 337867 |
rs545576700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345491 | TTCCTCTGTTCACTC[C/G]CTAAATAGGTTGTTT | 337867 |
rs545578703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338451 | CCTCAGGTTGAACAA[G/T]CTTGCTCTAGTCCCT | 337867 |
rs545579839 | snp | A/G | 0.000164921 | 0.00907929 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351802 | GCCCAGGAGTCCTTG[A/G]TGCTCTTCTTTTAAC | 337867 |
rs545631212 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201848 | AGGCCGAGGTGGGCG[G/T]ATCACGAGGTCAGGA | 337867 |
rs545639549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371703 | TAATTTTAATGCATT[A/C]AGAAACTTAGTAATT | 337867 |
rs545649386 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355597 | GCATTCTCATTCTCT[A/G]CCAAAACCAAAACCA | 337867 |
rs545667426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331945 | AATAAATGAGGTCTC[G/T]GTGGGTCTGGTTACC | 337867 |
rs545698822 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364616 | TCATACACTTCACCT[G/T]TAGGTTTTTGGTGGG | 337867 |
rs545713975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325125 | TTTTTTTTTTTGATA[C/T]GGAGTCTCTCACTGT | 337867 |
rs545735291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324590 | TAATAGTACTCTTTT[C/T]TAAGCACTTTACAAA | 337867 |
rs545750253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343565 | ATGGTCTCACTAACA[G/T]ATCTGAAGTCCAGAG | 337867 |
rs545754748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233205 | GCAACCTCCACTACC[C/T]GGGTTCAAGTGATTC | 337867 |
rs545761504 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332802 | GTTTGCTCTTTGGCT[G/T]ACCCAGGTCTGAGGG | 337867 |
rs545767507 | in-del | -/TAAC | 0.00517822 | 0.0506191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278272 | TATGCTATTATTAAT[-/TAAC]TGTTACCACATTATT | 337867 |
rs545778932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211020 | TAACTTTCAGATATT[C/T]ATAGAAGTGAAAGAA | 337867 |
rs545790286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357291 | ACAGCAACAAAGTCA[C/G]CCAACAGCACATTTC | 337867 |
rs545793581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312489 | TCCGTCCTGTGATGA[C/G]TTCCTTGAGGTCAAG | 337867 |
rs545804055 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249042 | GAAATTTCAACTTTC[A/G]GATTCAGGGGGTACA | 337867 |
rs545813426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336699 | CCAAACTTTATAGTA[C/T]GTCTTGAAATCTGAT | 337867 |
rs545815223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344019 | CAGTCCTTTTTCTTA[C/T]GGAGCTTAGGTCCTG | 337867 |
rs545838001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212051 | AGCAGTTAGTGCTCT[A/G]CAGTTGTTTTTATTT | 337867 |
rs545844300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237431 | ACGTGGAAGCTAAAA[C/T]AGTGGATCTCATGAA | 337867 |
rs545848955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305055 | GTAAGTAAAGGTTTT[A/G]TAAATGGATTTAGAG | 337867 |
rs545871548 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254395 | TGTAACAGGCCCCTT[A/G]GGTTCTTGTTGCTAT | 337867 |
rs545872184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383172 | TGTGTGTGTGCCTGT[A/G]CACGCTCTTGTGTAA | 337867 |
rs545929160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245734 | CAGCTGCTCAGGAGG[C/T]TGAGGCAGAAGAATC | 337867 |
rs545933571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376940 | AATGACTGCAAGCCC[A/G]TGAAGCCAACACTGA | 337867 |
rs545934228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237858 | TACTCAGGAGGCTGA[G/T]GCAGGAGAATCGCTT | 337867 |
rs545934303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230803 | CGCTTGTAATCCTAG[C/T]GCTTTGGGAGGCCGA | 337867 |
rs545943347 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282620 | TGATGGAAGTTTAAC[A/G/T]CTGGTTAAGTGAGAC | 337867 |
rs545951729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215701 | CGGCTCTCTGCGAGC[A/G]GGAAACCGCCTTTGT | 337867 |
rs545956465 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205613 | TTTTAATGGACAAAC[A/G]GATTGAGATGGAGGC | 337867 |
rs545962112 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350213 | GACTACTCTTACTCT[A/G]TTTTCTTTTTTATAC | 337867 |
rs545972415 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329968 | ACAGTATTGAGTTCT[C/T]CAATGCACGAACGTG | 337867 |
rs545991306 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251789 | GCAAGTTGCTTCTCT[C/G]AAGCTCCATTTCCTG | 337867 |
rs545991325 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383777 | CCTGGCTGGACTCCA[G/T]CTTCTGAGCAGTGTC | 337867 |
rs546004919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281896 | TCAGTGGCCAGAGTG[C/T]CTTACCAGGGAGCAG | 337867 |
rs546028210 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248300 | GAGATCATAGCTCAC[C/T]GTCACCTCAAACTCC | 337867 |
rs546049867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355590 | AGCCTTAGCATTCTC[A/G]TTCTCTACCAAAACC | 337867 |
rs546063697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216254 | GGATTATAGATGCCC[A/G]CCACCACACCTGGCT | 337867 |
rs546065544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209448 | TCTCTTTTGGTACCT[C/T]AGTGGAAATTCCTGT | 337867 |
rs546113592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349208 | TCTCCACAGCTTCAC[C/G]GTGCATGTCTCCCTC | 337867 |
rs546122431 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334505 | TCCAAGAACCTATCA[A/G]TGAGTTAAGTGAGGA | 337867 |
rs546128522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217197 | GTTCCCCACTTCAGC[C/T]AGGCCGTTGCTCAGC | 337867 |
rs546160042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318376 | TTCTCCATGTTGGTC[A/T]GGCTGGTCTCAAACT | 337867 |
rs546173238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251892 | AAAGAAGGTCTCTTA[C/T]GCCAAGCTTCTAGGA | 337867 |
rs546174591 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241670 | GGTGATGGGTGTACA[A/G]TATTGTGAATTTGCT | 337867 |
rs546176770 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377879 | GAGTCAGAGCCTGGT[A/C]CCCTGCATGTGGTCA | 337867 |
rs546187110 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384479 | AGTACAGGAAATCTC[C/T]GTATTCACAGAATCA | 337867 |
rs546216959 | snp | G/T | 0.000201209 | 0.0100282 | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99296160 | TTGGTGGTGGTCCAG[G/T]TGTCTAGAAAAAAAC | 337867 |
rs546219387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203588 | GTCTGTTGGGTACCC[A/G]TATCAGCCACACACT | 337867 |
rs546225753 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276339 | CATCTGTTCTTCTGA[A/C]TGACCCGCTGTAAAT | 337867 |
rs546229252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214799 | ATAAATTTCTTTCCA[A/G]CTGGGATGGTGGTGA | 337867 |
rs546236624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383663 | AGGGTTGAAAGCAAC[A/G]TTCCGGGGAGGAGCA | 337867 |
rs546241007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378187 | CTCAGCTATTTCACC[A/G]TGGGTCAGTTAATGA | 337867 |
rs546258427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297809 | CTATCGGTTTAGATT[A/T]AAAAAAAAAAAATTC | 337867 |
rs546294990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338626 | TTTGTTTCTGTTTTC[A/G]TTTTCTTTGTCTTGT | 337867 |
rs546299805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377549 | GCTTTCGATAGGGAG[A/G]GAGATGGGCTGACCA | 337867 |
rs546301240 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217159 | TCGAATTAATTTTAG[C/T]GTTTGGGGTTTTAGT | 337867 |
rs546308120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330365 | TCAGGAGGCTGAGGC[A/G]GGAGAATCGCTTGAA | 337867 |
rs546346333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291132 | CTTGTTGCTATAGTT[G/T]CCTCATCAGCAAGAT | 337867 |
rs546362187 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327527 | CCAGTGTTTGTCTTC[A/G]GGGACTGACTGTGTT | 337867 |
rs546370896 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374448 | TTTTGGTCAATTCAC[A/G]TGACACGTCGTGTGG | 337867 |
rs546372973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239170 | CCCATTTTAAGCATA[A/G]TAATCCATTTCTTGA | 337867 |
rs546386656 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266777 | CACACTGCTGTGCAG[C/G]CAACCTCCAGGACAT | 337867 |
rs546394791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362548 | GCTGTGTATTTTTGC[A/G]AGTCTTGTGGGTATA | 337867 |
rs546410014 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356040 | AAATTGTACCTATGT[C/T]ACAGTAAGATCAGCT | 337867 |
rs546419146 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350670 | CTAATAAATGGGTAG[A/T]TGTCAGTGTTTCCCT | 337867 |
rs546419748 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360613 | GGCGGTATAAACCCA[C/G]TTAGGCCCCTTTCTT | 337867 |
rs546425302 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345583 | AGCCCCTGTCCTCAC[A/C]ACTTTATTGAGCTCA | 337867 |
rs546436332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268487 | GTGGCATGTGCCTGT[A/G]GTCTCAGCTACCTAG | 337867 |
rs546446422 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217264 | CATCCATTAGGTGCT[A/G]AAGGGCCACTCAGAA | 337867 |
rs546448887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310777 | TTACGTTGAAATGTA[A/T]CCTCAAAAAAGAACT | 337867 |
rs546469737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349834 | AGGGGTTTAGGACTT[C/T]GGATGACTGCGGGCA | 337867 |
rs546476346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253884 | ATCATGTTAAGAGTG[A/G]TAAAGGTAATTTAGC | 337867 |
rs546492801 | snp | A/G | 0.0120915 | 0.0768083 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200825 | TTCGTCGCTCCGCCA[A/G]GAGTGCGCCTGCGCG | 337867 |
rs546511551 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259972 | AGGCCTGGCTTCAGG[C/T]TGGGGTGAGCTCTCA | 337867 |
rs546527221 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383890 | CTGGGAGGTTCCCTC[C/T]CCCACCTGCCTCTCT | 337867 |
rs546528614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337967 | TGTCTTGGGCCACAC[A/G]TAATATACACTAACA | 337867 |
rs546529311 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330369 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCTG | 337867 |
rs546544995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246297 | GTCATAATTAGCATG[C/T]AGTTTGAATTCCACA | 337867 |
rs546558837 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211078 | CTTTTAGTACGTACT[G/T]CCAAATTCCAATCCC | 337867 |
rs546578827 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198542 | TTCAGTTTGTTGGGA[C/T]ACATTGCTTTGGTTG | 337867 |
rs546613869 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302336 | GAAGATGAAAGCTCA[A/G]GGTTAATTGAAATTT | 337867 |
rs546640406 | snp | A/C | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328237 | TATGGATGCACCATA[A/C]TTTGTTTATCCATTC | 337867 |
rs546647589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224904 | CGAATCTTGTTGTCT[A/G]TAATGATACTATATA | 337867 |
rs546673436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274715 | TATCCTTTTTCCTTT[C/T]CTTTTCTTTTTTTTT | 337867 |
rs546675970 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377375 | TTACATTGAAACTTT[C/G]TCTTCCTGTGGATGT | 337867 |
rs546713745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231824 | CACAACTACATACTT[A/T]ACTGTCTGTGCATGA | 337867 |
rs546714242 | in-del | -/TA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237254 | AGAAAATTTTATGCG[-/TA]TATATATATATATAT | 337867 |
rs546714955 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219562 | CAAATTTGTAAACTT[C/T]CTTAAAACATTCTGA | 337867 |
rs546801355 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312184 | CATTTTTTAAAATAA[A/C]GTAGTCTCTATCAAG | 337867 |
rs546802669 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267114 | TTTCATTTCCATTTC[C/T]GATGATGAGTGACTT | 337867 |
rs546804761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336181 | TTTTCATATGCTTTT[A/T]AAACTGGGCTCTTTC | 337867 |
rs546826860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317685 | TATGTTGTTAATTCT[A/C]ATAATTTCTTTATAT | 337867 |
rs546853426 | snp | A/G | | | splice-donor-variant | UBAC2 | GRCh38.p7 | 13:99367907 | GTTTCTGAGGAACAG[A/G]TAATTAATCAGTAAT | 337867 |
rs546862774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344185 | ATTCCCTCATGACCC[C/T]GGAGGCTCAGGGGAG | 337867 |
rs546866044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336753 | GCCTTGCCTTTTCTG[A/G]GTTTTTTATTTCTTT | 337867 |
rs546888416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329342 | AAGGGGAAAAGAGTT[A/C]AGATTTTGCTTGTAA | 337867 |
rs546888862 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304393 | TTTGTGAGAGTGCTG[C/T]GCTCTGTCATAGTGT | 337867 |
rs546897024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204716 | CCCAGAACCTTTCCA[C/G]AAAAGCTCATCCAGT | 337867 |
rs546921174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230373 | TGGGAGGCTGAGGGA[C/T]GAGAATTGCTTGAAC | 337867 |
rs546930765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376485 | CATCCCCGTGAGGGC[A/G]GAGCTGGAGTTTGCC | 337867 |
rs546935764 | in-del | -/AG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238727 | ATTTTTCAGCAAAAC[-/AG]ATAATAATGAAGCAA | 337867 |
rs546978962 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370686 | CATAGCCACCCATGG[A/G]TAAGGCTGTGACAGG | 337867 |
rs546981220 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342498 | CAGGCACACACAGTC[C/T]CTGTGGATGCCAGGT | 337867 |
rs546981968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289370 | AGAACCAAACATTTT[A/G]TCCACAGGACAGACA | 337867 |
rs546990338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370143 | GTACATACCGACCGT[A/G]GTTAGGAAAGAGAAT | 337867 |
rs547008215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281952 | CGTGTAAGCTGTTGC[C/T]AGAAGTCTACATGAA | 337867 |
rs547012537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237576 | CAGTAGGTCAGGAGC[A/G]TGTCTGTAGTTGACA | 337867 |
rs547014821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323399 | TGAGCCCAAGAGTTC[A/G]ACACCAGCCTGGCCA | 337867 |
rs547031666 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317268 | ACAATCAGAAGTAAA[C/T]CCCCAATCTGAAGTT | 337867 |
rs547042255 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309987 | TTTATGTTTTCTATC[A/G]AGTGCGATCATGAAT | 337867 |
rs547071693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208908 | CATCTTTATTTTGGT[C/T]GATTTATTTTGGCCA | 337867 |
rs547091387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344085 | CAGTAAGAAGACCAC[C/T]ACCATTTATTTTGCC | 337867 |
rs547092709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267737 | TCCCTGCTGTTCTGA[C/T]TAATATTTTATCAGT | 337867 |
rs547123821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343292 | GATTCTTGGCTGTTT[A/G]CGCACGCCCTCGCTC | 337867 |
rs547127324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225954 | TGATGGATCACTATT[A/T]AATCCACTGTTAAGT | 337867 |
rs547131394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302475 | AAATCATTCATTACT[A/T]CTTCCTCTGGTTACC | 337867 |
rs547162945 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311239 | GGCTGTAAGTGCTGT[G/T]GGGGAGGACAGTCAG | 337867 |
rs547166037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342754 | CTTGTTCCCTCCCTT[C/G]CAGTCCCCTGACCGA | 337867 |
rs547172139 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307696 | GAAAGAGACTGAAGC[A/G]ATAAACCTTAACCAA | 337867 |
rs547179882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279815 | AAGGGCACTAATCCT[A/G]TTTGTGAAGACTCTA | 337867 |
rs547189589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251958 | AAGAGACAAGGTCTT[A/G]CCATGTTATCCAGGC | 337867 |
rs547197953 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253932 | TGAATCATTTATTTT[A/C]CTTCCATAAGTATTC | 337867 |
rs547217462 | snp | C/T | 3.29549e-05 | 0.00405911 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295291 | CAGAGAAATCTGGAA[C/T]GAATGTCTTTGGCTA | 337867 |
rs547252182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368206 | TCTCTGTGAAGGATC[A/G]GGGACAAGGAGGTGG | 337867 |
rs547267185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383264 | ACATAAAATGCTCTC[A/G]AGTCAGGTCTCTCAA | 337867 |
rs547276222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322153 | CAACATTTCAGTGAC[C/T]GTATCAACTGTTCTT | 337867 |
rs547284641 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285102 | AATGGCATTTCTTAT[-/A]TAACCATAATGTTAC | 337867 |
rs547321456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281472 | TACTTGGTACTATGT[C/G]ACCTTGGTAGTCAGC | 337867 |
rs547330723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222269 | AAAAGCAAAAAATCA[C/T]GATGGAAGGCCACTC | 337867 |
rs547330851 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266183 | AAAATATTTTAATGT[G/T]ACTTTATGAATATTT | 337867 |
rs547331662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383798 | GAGCAGTGTCCACTG[C/T]GTGTCCCTGTTGGCC | 337867 |
rs547332079 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228795 | TTTAGATTCCGTGGA[A/G]CCTTGTTTGCATTTT | 337867 |
rs547333394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377146 | CTTCTCTAACTGGTG[C/T]TGGGCACCGGGTGTG | 337867 |
rs547380513 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355024 | CAGATAGGCAAGTGC[A/G]GGAATGAGACTCAGG | 337867 |
rs547398874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265589 | ACTTTCACCCCTTTT[C/G]TTCTTCTTGTTCTCG | 337867 |
rs547443261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355654 | CACCTCTGGTCCTGA[C/T]GGTCCCTGGAGGAAA | 337867 |
rs547447250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249444 | TCCAGTCCATTGCTG[A/G]TGGGCACTTAGGTTG | 337867 |
rs547455288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293438 | GAAGCTTTCTTTTTG[A/G]TTTTCCTTTAGTAGT | 337867 |
rs547462914 | in-del | -/AAAG | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296817 | AAAAAGAAGAAAGAT[-/AAAG]AAAATGAGAGAGAAA | 337867 |
rs547465205 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258810 | GTACCTGGCACTTAG[C/T]AGGTACTCCTAAATG | 337867 |
rs547484223 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242236 | TCATCATGGCCCGTT[C/G]TCAATGAGCTGCTGG | 337867 |
rs547485333 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206083 | TAACGTTCCCAGTCA[C/T]TAGAGAGGGAATGCA | 337867 |
rs547489159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286234 | TGCTAATCAAAAGAA[C/T]GTAACATTTATATTT | 337867 |
rs547494036 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335381 | CAATTCATTACTGTT[G/T]TTTTTTTTCCATATT | 337867 |
rs547502175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251237 | ATTTGGCATCCCGAA[A/G]CTCTAGTGAAGTTGT | 337867 |
rs547502223 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259559 | TCAAGGTAAAGCCAG[A/G]TCCAGTTTCTCCCGC | 337867 |
rs547527319 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385857 | CCCCCAAGCTGTTCC[A/G]GGCCAGAGGACTCTG | 337867 |
rs547547748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264013 | GGCATGTGTAATAAT[A/G]AGGAAGGGTCCCCCA | 337867 |
rs547589181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374905 | AGAAGGGTTGAACAC[A/G]AAGGTGTGGCCAGTA | 337867 |
rs547613392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369064 | TGCATTATAATAGTA[A/G]ATAAATATTTATATA | 337867 |
rs547644889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213815 | AGAATCAAAAGATAA[C/G]AATATTTTATTTTAT | 337867 |
rs547656374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361346 | TATTTAACCCTACGT[A/G]AAGAGCAGATTCATG | 337867 |
rs547658098 | in-del | -/ATG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367734 | GCTCTTCCAAGCATT[-/ATG]ATGATTCTGCTCCTT | 337867 |
rs547658231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322742 | GTCTGAGTTTGGATT[A/G]TTTTCTGTAAGGAGT | 337867 |
rs547692279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273591 | TCTTAAGGTAGGTAC[C/T]TTGCAGTGTGGCTGT | 337867 |
rs547692979 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198778 | TATTTTATGGTTCAA[A/C]TTAATCTTTTACCCA | 337867 |
rs547697285 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346816 | ACTGCCCTTTCTCCA[-/C]CAGTGTGTCTCCGGA | 337867 |
rs547719627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361662 | GCGGCTGCCCTGTAC[A/C]TTGTAGGATGTTTAG | 337867 |
rs547742970 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304308 | TAGCTCTTACTTTCC[A/T]TCAAGCCTTAGTTCT | 337867 |
rs547760424 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375164 | CCAGCCTTAACTAAA[-/G]ACCTGCTCCATACAA | 337867 |
rs547770368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303113 | CCAGCCTGCCAACCC[C/T]ATTGCATATCCTGGG | 337867 |
rs547771778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201316 | CCCCTTACCATGCCC[C/T]ATTCTTTTAGGCTTG | 337867 |
rs547837328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99294220 | GTAGAGTACTAACAG[C/T]TTGGGGGAAGAAAAG | 337867 |
rs547866025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242986 | CTCCTCACTTCCTAG[A/G]TGGGATGGCGGCCGG | 337867 |
rs547889372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296328 | TTTAACAGTTTATAA[G/T]TATAATATGGTTACA | 337867 |
rs547914288 | in-del | -/CTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338047 | TTTTTTTCTTTTTTT[-/CTTTTTTT]TTTTTTTTTTTTTTT | 337867 |
rs547936721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273649 | TAATACTTTGTGACA[A/G]TTTTGATGAGGTGCT | 337867 |
rs547948513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382709 | CTATCACCCCACAGA[C/T]ACAGCTGCAGGGAGC | 337867 |
rs547952979 | in-del | -/A | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257550 | ATTTGCTGACGTTTG[-/A]AAAAAAAATGAGTGA | 337867 |
rs547961871 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247521 | GCCCGGCCTGTGTTG[-/T]TTTTTTTTAAATCAA | 337867 |
rs547967805 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369882 | AACTTTGATCGTAAG[C/G]GAAAATAAGATAAAC | 337867 |
rs547979978 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331552 | ATTTAGTATCATTTC[C/T]ATTCCCTCATATGAG | 337867 |
rs547990232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288535 | ATTGCCAGGATTTCT[C/T]TCCATTTGGATATGC | 337867 |
rs547995744 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249627 | TCCAAACTGCTTTCT[A/G]TAGTGGCTGAACTAA | 337867 |
rs548015580 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335999 | TTCTCCACAAAATGG[-/A]AAAAAAAAAAAAAGA | 337867 |
rs548018147 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214533 | CAGGACTGTGAGAAC[A/C]CCCTGCAGTCGTCAA | 337867 |
rs548022612 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314633 | TCTGAAGAAGAAACC[C/T]GGTGTGCTCTACCAA | 337867 |
rs548022858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204671 | TCAAAACGGGCCTGA[A/G]GCGCGACCTGTGGGA | 337867 |
rs548024435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306708 | AAAGATACGTTTAGT[C/G]TAAGTAAACACAAGT | 337867 |
rs548027687 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200787 | CGCCGTTCGTCAGCG[A/G]CGAGTGGCCTCGCGG | 337867 |
rs548034431 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225182 | AAAATGTACAATCTT[-/A]ACTATTTTTGTGTAT | 337867 |
rs548091029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207176 | TGCGTTGACCTGGGG[A/G]TTGCATCCTTATTTG | 337867 |
rs548102831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266992 | CCCAGTTTCTCCCTA[C/T]CTTGGCTCGCAGGCA | 337867 |
rs548104215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315926 | GTAGTAGGTTGGTGC[A/G]AAAGTAATTGCGGTT | 337867 |
rs548104959 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283437 | GCAGGATTTACCCTT[C/T]CTCTTAAGAAATCTT | 337867 |
rs548133738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209692 | TTCATAAATTTTAGC[A/G]GCTGGGCATAGTGGC | 337867 |
rs548141709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309480 | ATCCTGTAAGAGGCC[A/G]CTGAAGCTGTATATT | 337867 |
rs548153371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207581 | GGCCTGCTTCCGTCC[C/T]GCTATACCATTGAGC | 337867 |
rs548166516 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258989 | CTGTATTTTGTAAGT[C/G]TGCTTTTCTAGTGCG | 337867 |
rs548234720 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382592 | TGAGACGGTGTGCAC[-/A]AATGGGAGGGGATGG | 337867 |
rs548236250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349979 | GACACTGGCATTACC[A/G]CTTGACCAAGGAGCC | 337867 |
rs548239056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375489 | CAGGGTGTGCATGCT[A/C]CCCTGCACCCAGTGT | 337867 |
rs548243740 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353490 | CATGAGAAAAAAGAG[C/T]GAGGTACAGTCTCAT | 337867 |
rs548244519 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203740 | AGACCGAAGTTATGG[G/T]GGAGGACCACTTTAG | 337867 |
rs548278398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332988 | AAAATTAGGTCAGGC[A/G]TGGTGGCTCACACCT | 337867 |
rs548291485 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252921 | TTATCAAGACAAGCT[A/G]TGGCAGAGAACTTTT | 337867 |
rs548298099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343654 | CACAGACCAGACTCT[A/T]GATTTTTTCCTAAGC | 337867 |
rs548300431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383315 | TCTAGGACAGTACAT[A/G]TCTCTGTTAAATTCC | 337867 |
rs548302774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235697 | AATTGTGCTGGGGCC[A/G]GGTGCAGTGGCTCAT | 337867 |
rs548316750 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307514 | ATGAGCAGTTAGCCT[C/T]GTGTACGTGTGTGCA | 337867 |
rs548325000 | in-del | -/AAGGA | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376093 | TTAAAAATAAAAAAT[-/AAGGA]AAGAGAAACTGGTAC | 337867 |
rs548341787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354419 | AGGCTATCTAGTCCA[G/T]CTTTCCATTTTACAG | 337867 |
rs548403070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348110 | TACACTGCCAGGGCC[A/G]TTACATAACTTTTCA | 337867 |
rs548426008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323133 | TTCTCTCCGTGCTTC[C/T]TTTTCTCCTATTTAA | 337867 |
rs548445034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266896 | GAAAGTGAAATTGCC[A/G]GATCGTGTGGTAATT | 337867 |
rs548450529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355095 | GGAAATGTAAGAAGA[A/G]GGGAAACCTTGAGTA | 337867 |
rs548455980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250407 | GTTCTCTATTCTGTT[C/T]CACTGGTCTGTATGT | 337867 |
rs548464950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224158 | TCAGGGTTTTGGCGG[A/G]TTTGGTTTCTCCTGG | 337867 |
rs548488122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203851 | GTTTGTTGAAAACTC[C/T]TCATTTTGAAGAAAG | 337867 |
rs548492753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215521 | GGGGTAATATACACT[C/T]TACCTTTAAGTCTTT | 337867 |
rs548517631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342639 | GTGATGGAGCCACAG[G/T]CATTCTGTCCACCTT | 337867 |
rs548536740 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327675 | TCCATGTTAGCTTAT[A/G]TTGATAGCTGAGAAC | 337867 |
rs548555063 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298432 | CACAGTGGAAATTTC[A/G]AAATGCTTAGAACTA | 337867 |
rs548559580 | snp | A/C/G | 3.50019e-05 | 0.00418329 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295021 | CCTGCAAAGTTTGTC[A/C/G]TACAGTTTACGTCAC | 337867 |
rs548561615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381776 | AGGCTTGAGAAAGCA[C/T]AGGGAGGAACACTTA | 337867 |
rs548580588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335290 | ATCTTCTGCTGAATC[A/G]GCGTAATGCTGATAT | 337867 |
rs548595514 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342224 | GCACAGTGAAGCTGG[A/G]AGAGCCCTTCTGAGT | 337867 |
rs548596323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220279 | GTGACCTTCAGTGAG[C/T]TATTTAGCCTTTCTT | 337867 |
rs548626158 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343351 | CTCCTTTCCTGCCTT[G/T]CTGTAAACTCCGCAC | 337867 |
rs548662916 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338910 | CACTGGCAGCCCTGT[C/G]TCAGATTTCCTTACT | 337867 |
rs548676617 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316132 | TTTTTGTAATATTTC[C/T]GGTAACTTTGAGAGG | 337867 |
rs548691277 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301671 | AAAGGCCCCCCAAAA[C/T]TCATTTATTTAGCAT | 337867 |
rs548726074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321038 | TTTGGGGAATGTTAC[A/G]AAACCTGTTGATGAG | 337867 |
rs548735034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322795 | GAAGAAACACTTTAC[A/G]ATGGTGCAAGATTAC | 337867 |
rs548786915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308555 | GATGCTTGAGTAAAC[C/T]TGATGATTTTGAGGG | 337867 |
rs548808496 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214492 | TATAGGTTGCAGAGG[G/T]GGGGAGTAGGTGGTG | 337867 |
rs548844580 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208186 | ATTTTTAGTAGAGAC[C/G]GGGTTTCTCCATGTT | 337867 |
rs548859447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340221 | TATGACTAAGAAAAA[A/T]ACCGTGTGCAGTGTC | 337867 |
rs548862080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325859 | TCCATGTTGTTGCAT[A/G]TTACAAAATGCCCTT | 337867 |
rs548901221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227766 | GACCTAGAATAATGC[A/G]TGGTACAGCGTGGAT | 337867 |
rs548901292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326787 | TCAAGGCTCTCATCC[A/G]TGTCTCTTCCAGCCA | 337867 |
rs548901783 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223498 | TAATTATTTCTTTAT[A/G]TCTGCTTGCTTAGGT | 337867 |
rs548916601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241027 | CACCTTGGGAGGCCA[A/G]CGTTTGTGGATGGAT | 337867 |
rs548931883 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253575 | CTGGAGTGCAATGGC[A/G]CAATCTCGGCTCACT | 337867 |
rs548941780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202162 | TCTGACAGTGAGTTA[C/G]TATCAGCGCCACAGG | 337867 |
rs548948438 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305974 | AATCTCGGCTCACTG[C/T]AACCTCCGCCTCCCA | 337867 |
rs548959395 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350736 | CCAAGGAGTGGACCA[C/T]GGGAACCCTCATTTA | 337867 |
rs548961864 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258057 | GGCGTGGGCCATTGC[A/G]CCCAGCCTGTATTAT | 337867 |
rs548992978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278340 | GGTATTCACTTTCTC[A/G]GGCGCGTGAAGGGAT | 337867 |
rs549038067 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299102 | GGAAAGTAACACTTA[C/T]GTGACACTCAGAGGT | 337867 |
rs549051582 | snp | A/C | 3.41326e-05 | 0.004131 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295055 | AAACCAAAATACAAT[A/C]CATTTCACTTTCCAT | 337867 |
rs549062784 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272311 | TAAGAAAGGAGAGAA[C/T]ACTGTAATGAACCCC | 337867 |
rs549066703 | in-del | -/TAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361203 | AATCTTCTTACAAAC[-/TAA]TAATAAGTATTTCAT | 337867 |
rs549107720 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200379 | ACCCCTCTATCCGCA[A/T]CTGAGTGACCAGATC | 337867 |
rs549130104 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363546 | GAAGGTGTCAGCCCC[C/T]GGCTCTTTGCTGCTG | 337867 |
rs549135507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240205 | GTTGAGTTGCAGAAG[A/C]AGTGCTTTGCTGAGT | 337867 |
rs549149969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307921 | GTGACAGTCCAGGAT[A/G]TGGAGTGGACTGGAT | 337867 |
rs549160777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276499 | AATGGAAGGGCAAGG[C/T]GCGAGGGTGGGTGAG | 337867 |
rs549164448 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233749 | ATGACAGAATTATCA[A/G]AATTATCATTATGTA | 337867 |
rs549197825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277045 | AGTATTTGGTTTTCT[C/T]AGGTTTGCCAAGATA | 337867 |
rs549199143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379765 | TCCTGTAAGACGTTT[C/T]ACACTTACACTGCTC | 337867 |
rs549212637 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386243 | GGAGGCAGGGCAGAC[-/T]GTGGAGGACAGGATG | 337867 |
rs549226951 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327751 | GTTCTGCTAAAATCC[C/T]ACCTCTTATAAAATT | 337867 |
rs549235226 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385507 | GCCGTTTTAGTGTGG[A/G]GATAAGTTTGCCATT | 337867 |
rs549240734 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337655 | CCCCATATTCCCTCT[C/G]TTGTCTTCTTCTGGA | 337867 |
rs549278404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233988 | ATTATTATTATTATT[A/C]TTATTTTCAGTTGCA | 337867 |
rs549278638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285598 | CGTCTCGTTATGTTG[C/T]CCAGGCTGGTCTCAA | 337867 |
rs549292740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320235 | TTTCATCTCTTTATA[C/G]TCTTTTTAAAATCTA | 337867 |
rs549299373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368858 | GCCTATTTAGGAAAA[C/T]GGTGGATTCCAGGCC | 337867 |
rs549304167 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339022 | TCTCCTCCTCCCCCC[C/G]ATTTTATCTCCTCTA | 337867 |
rs549306898 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348394 | TCCCTAAGGGATACA[G/T]CGAGGGTAATCTTGA | 337867 |
rs549311708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374129 | AGAATGTGAGCTCCC[A/G]CCAGGCAGTACTGGA | 337867 |
rs549315877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277804 | CACTCTTGCCCCATC[C/T]CCTCTGTCACCACCC | 337867 |
rs549344941 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242516 | GGGGCTGCCCCCCCC[-/A]ACCTCCCTCCCGGAC | 337867 |
rs549351598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366032 | ACAGCTTTCTTTGAT[G/T]AGTATTTCTCTGATT | 337867 |
rs549361087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230156 | CAAATTATCACAAAC[A/G]TGGTGGTTTAAAACA | 337867 |
rs549366630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352097 | AGATCTGCCCTGTCA[A/G]TCATGAGAGTTCCTA | 337867 |
rs549413294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344017 | CCCAGTCCTTTTTCT[C/T]ATGGAGCTTAGGTCC | 337867 |
rs549420069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315850 | GTATGTTTCATCTCT[C/T]GGGGAAAGGGGGTCT | 337867 |
rs549431251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270110 | CCTATGATGTAAACC[C/T]AAGAATGATTTTTAG | 337867 |
rs549443596 | snp | A/C | 3.29701e-05 | 0.00406005 | stop-gained, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255443 | TCATTATCCAGACTC[A/C]CACACACGCCAGCAC | 337867 |
rs549448114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339730 | ACCATACATTATAAA[C/T]GACCTTCAAGATGAA | 337867 |
rs549452464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214891 | TCGGTGGCATTTGCA[C/T]CACTGGAGATGATTT | 337867 |
rs549456106 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215230 | TTGGTTGGAAAGCTA[A/G]TTAAACTTCCAACTT | 337867 |
rs549481964 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337254 | ATTTGATGAAAATTG[A/G]TATCTTAAAAGTTTT | 337867 |
rs549512167 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208207 | TCTCCATGTTGGTCA[A/G]GCTGGTCTTGAACTC | 337867 |
rs549514265 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215396 | CTTCTGTTGTCCTTT[A/C/T]TTCCCAATCAGAGAT | 337867 |
rs549532119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365056 | CTGTTTTCTCTAGAA[A/T]AAGTTTTAATAAGTT | 337867 |
rs549559632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354506 | TTCTGTGGAAGTTCA[A/G]CAGAGCAGGGGAACA | 337867 |
rs549565589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308607 | CATTTGGTAGGAATT[C/T]GTAACTCTGTGATCT | 337867 |
rs549578751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318731 | GAGGCTGAGGCAGGA[G/T]AATGGCGTGGAACCC | 337867 |
rs549579531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347276 | AATGTTTCAGGAAGA[A/G]TAGGTGTTTCAGGAA | 337867 |
rs549586196 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258138 | ATAATCATGAAGTTA[A/C]TTAAATGCTGCTTAC | 337867 |
rs549619260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226774 | GAGCATGTTTTCATC[C/T]CAAAGCATGTGTACT | 337867 |
rs549621347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325190 | TCACCGCAAGCTCCA[C/T]CTCCCGGGTTCACAC | 337867 |
rs549622177 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207932 | GACATTCTTTCTTAA[A/G]TATGCATTCAGTGTG | 337867 |
rs549637786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358247 | AGCAACAGGGATGCA[C/T]TGAGTAGCATCAAAG | 337867 |
rs549649475 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301387 | AGACAATCCCAGTTT[A/T]GCCTCTGTAATGCAG | 337867 |
rs549655241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321173 | TTTTTTAAACAAAGA[A/T]ATTTGTATGAAACAT | 337867 |
rs549687320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313280 | TGAGACACTACGCCC[A/G]GCCGGAAGGAAGGGT | 337867 |
rs549695695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314833 | ATTGCTCCCTGCTGG[A/G]CTCCAGGTCTGTGGT | 337867 |
rs549695857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322056 | TATTTAAAATAGGAC[C/T]TTTCATGAAATGTTG | 337867 |
rs549700852 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358890 | TCTCCTTAACATTTA[C/G]ATGAAAGTGTGTTCA | 337867 |
rs549714594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326903 | ATTCTGGAGGGCAAT[A/C]TTGGGTATGAAGAGG | 337867 |
rs549726247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222136 | GCAGTGAGCAAGACA[A/G]CTAGGACCCTGTCTT | 337867 |
rs549746045 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278577 | CTTGAAAAATGATCA[C/G]TGTCTTTAAAAGTGA | 337867 |
rs549747603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264768 | TTCCTCTGAATTTCT[A/G]TAGGACTGTGGATAG | 337867 |
rs549751560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311826 | GGACTGCCTCTTCTT[C/T]CCTGTCCTGGGGTGC | 337867 |
rs549816468 | in-del | -/AT | 0.000611282 | 0.0174719 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367945 | ACTCATTCTAAATCC[-/AT]GTTTCAGAGTTGAAG | 337867 |
rs549817617 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221561 | TATTTTATTTCTACA[C/G]AGTCCCATTTGGTGT | 337867 |
rs549842905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265531 | TGAAGTATCTGTGAC[A/T]CATCTCTCTTTGACA | 337867 |
rs549872354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293305 | GAATTGACTCCCTTA[A/G]CCCAGAGAGGACTCT | 337867 |
rs549872557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207020 | CTTTCTTCCCTGTCT[C/T]TTCTAGCACCACTCT | 337867 |
rs549872857 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248246 | TTTATTTTTAGAAAT[A/G]AGGTCTTATTCAGTT | 337867 |
rs549874977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256236 | AAAAAACTCTAGTTT[A/G]TAATTCTCTAGTTTG | 337867 |
rs549879786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266006 | GGTCTCCGGTTTTCC[A/G]TACCGATTGATAGTT | 337867 |
rs549886593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382867 | GCAGAGACAGCAACA[C/T]AGCAGAACAAGCCAC | 337867 |
rs549894193 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313261 | AGTGCTGGGATTACA[A/G]GCGTGAGACACTACG | 337867 |
rs549894211 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284220 | TACAAATAAACACAC[A/C]ATGCAAAGAAAAAAA | 337867 |
rs549914980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270195 | GTGAGGCAACACACT[A/G]CTTGGCCCTAATAGT | 337867 |
rs549930911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285273 | CTGCTGCTGCTGCTC[C/T]TCCTGCTCCTCCTCT | 337867 |
rs549949718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366692 | TCTTTAGACAGATAA[C/T]TGAGCTCAAAATTGC | 337867 |
rs549953085 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230813 | CCTAGCGCTTTGGGA[A/G]GCCGAGGCGGGTGGA | 337867 |
rs549985156 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200788 | GCCGTTCGTCAGCGG[C/T]GAGTGGCCTCGCGGC | 337867 |
rs549995646 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374208 | AGGTTAACATTGAGT[A/T]ACTTCAGGTTGCTTT | 337867 |
rs550002707 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270775 | AGAAAATATGCTAAT[C/G]TTTTATGGTAAATTA | 337867 |
rs550016324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234886 | GAAAGCTGATATTTT[G/T]TTCTATTGGGAAAAA | 337867 |
rs550042020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327538 | CTTCGGGGACTGACT[A/G]TGTTGATATTTTCCT | 337867 |
rs550053149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235534 | CTTCAAAATATACTA[C/T]AGAGTAACCAAATCA | 337867 |
rs550059206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374803 | TCTCCCTGTGGACAG[C/T]GAGCTTCCTGAGGGC | 337867 |
rs550059220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367482 | CAGTGGCGTCACAGT[C/T]GGGCTGAAATTAGGA | 337867 |
rs550086906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228908 | GGCTATTTTTATATG[C/T]TTAGACAAGTACAAT | 337867 |
rs550118240 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368125 | GGCGGCGGGTGGGAA[C/T]GTATTATGGTAGCTT | 337867 |
rs550127290 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266454 | GTCCTGGGCCCATGT[A/G]GCCCATGGGCTGCAG | 337867 |
rs550154356 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385525 | TAAGTTTGCCATTAC[A/G]TTAGCATGTATTTTC | 337867 |
rs550174447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240034 | AACATGAATTTCAGA[C/T]CCTTAGGAGTGTGGT | 337867 |
rs550214469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352790 | CAGTGAAATGTGATG[A/G]TCACTCTTCTGGGAG | 337867 |
rs550219335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372827 | TCTTAGAAATAAGTG[G/T]ATCCAGGCCGGGCGC | 337867 |
rs550225978 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207509 | CCCTTCACTTTTTAG[A/C]CTTGTGCAATTAGTC | 337867 |
rs550236286 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262292 | AAATAGTAAGTATAG[G/T]GTTTGGTACTATCTG | 337867 |
rs550237902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249274 | TTAGCTCCCACTTTT[A/G]AGTGAGTTCATGTGG | 337867 |
rs550244466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333037 | GAGGCCAAGATGGGA[A/G]GATCACTTGAAGCCA | 337867 |
rs550253568 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306554 | ACACATATATAAAAC[C/G]CTCACTGCCCTTTAA | 337867 |
rs550257261 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299688 | CTGACATGCTTTTCA[A/G]AGCTTGCTGTTCAGT | 337867 |
rs550265555 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339265 | CATCCTTAAGATCTT[C/G]GCTCAAGTATCACTT | 337867 |
rs550276886 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308749 | TGTCAGACACAAGAA[A/G]GAGCATCAAGCAAGT | 337867 |
rs550280609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366232 | GTCTTTTTGAAGTGT[A/G]TAATCATTTTCAGAT | 337867 |
rs550284415 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371368 | GTTTCTTGATTATCC[A/T]GCAAATAGCTGTTAT | 337867 |
rs550302553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277662 | TTCAGACATTTTATT[A/G]AGGCCATTTTACATT | 337867 |
rs550310299 | snp | C/T | | | missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238433 | TCCCTCCAGACAAGG[C/T]GCCTCTGTCGAAGAG | 337867 |
rs550325862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234285 | CCTTCCAGGTTCAAG[C/T]GATTCAAGTGATTCT | 337867 |
rs550330995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358957 | TTGGGTTGGAGGTTC[A/G]AGTTTGGGAGTCTCT | 337867 |
rs550333420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351140 | GAATACTGTTGTCAT[C/T]GGGGATAAAAAAAAT | 337867 |
rs550333468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344263 | GAGACCCAGCTGTGT[C/T]TGACTCTGAGGTCTC | 337867 |
rs550355272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233278 | CCACCATGCCCAGCT[A/G]ATTTTTGTATTTTTA | 337867 |
rs550374006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227610 | CAGGTTTTATTTTCC[C/G]TAGTTCATTTCTCAT | 337867 |
rs550402698 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305987 | TGCAACCTCCGCCTC[A/C]CAGGTTCAAGGGATT | 337867 |
rs550417822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319937 | ATGGCATATTTGTTT[C/G]ACTTAGCAGTAATGG | 337867 |
rs550418610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277184 | CTTATGAGATTTTAG[A/G]AAAGAACAGAGGAGA | 337867 |
rs550482350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213184 | ACATCTCAGATATTA[A/G]AAAACGTGAGTTAGA | 337867 |
rs550488087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305233 | TTTATTCTTCTCTTT[C/G]GGCTTCCAAAACACC | 337867 |
rs550499093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206507 | TGCTCACCAGCCTCT[A/G]ATCCCTCCTTGTCTC | 337867 |
rs550504384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224552 | CAGCTCTCAGATTCT[A/G]TGATTCACTGTGCAC | 337867 |
rs550548432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283827 | GCAGCCTCTGCCTCC[C/T]GGGTTCAAGCTATTC | 337867 |
rs550562843 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232701 | CCGAGGCGGGCAGAT[A/C/T]GCTTGAGCTCAGGAG | 337867 |
rs550583376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317941 | TATATAAATGGTCAT[A/G]ACTATAGTTATGTAA | 337867 |
rs550585846 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216762 | AGGTGTCCTGGGTCT[C/G]CTGTCTTAGACTGGA | 337867 |
rs550592878 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292024 | AAGGATTATGAAGTC[A/G]GCTAGCATGTAATAA | 337867 |
rs550607267 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318878 | AGACAAAGGAGGCCA[A/G]TTTGTGCTTTCAAGG | 337867 |
rs550612542 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326195 | ATCCTAACCAACACT[C/T]GTCTTTTGGTGTTTT | 337867 |
rs550619699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359974 | TGAGCACCAAAGACT[A/G]AGAAGAAAGGGTGCA | 337867 |
rs550629261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384932 | TGGGCAGCTCATGCC[A/G]ACCTGCTTCCAAGGC | 337867 |
rs550649146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217394 | TCTCCACCATGCAGG[C/T]GTGTGTTCTGCCTGC | 337867 |
rs550667393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350742 | AGTGGACCACGGGAA[C/T]CCTCATTTATAGCAC | 337867 |
rs550694380 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241120 | AATACAAAAATTAGA[C/T]GGGTGTGGTGGTGCA | 337867 |
rs550716688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205404 | CTCTTGGTCACGGAG[C/T]GGTGGTTGTCAAACG | 337867 |
rs550719018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253940 | TTATTTTACTTCCAT[A/G]AGTATTCAGGATAAT | 337867 |
rs550731274 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217017 | TGTATTTTTAGTAGA[A/G]ACGGGGTTTCACCAT | 337867 |
rs550753803 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283534 | AATAGCCAGATTTAA[A/G]TGAATAGCCACAAGC | 337867 |
rs550760824 | in-del | -/ATTA | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234832 | ATAGTGTGCATTTTG[-/ATTA]AATGACATACTTGGG | 337867 |
rs550767733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330044 | ATTTTTAAATTTTCA[A/G]TGTACAGGTCTTGCA | 337867 |
rs550780695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297128 | GATTCTTTCCAATTC[C/T]TTTCTTGTTATAAAT | 337867 |
rs550789156 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320832 | ATAGGATCCAAGCCT[C/G]AGATTCACAAAGCCA | 337867 |
rs550806017 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342052 | AACCAGAGAAGTTGC[A/G]TTTCTCAGATTGGCC | 337867 |
rs550812460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368017 | AATACAAAGATGGTG[A/T]CAGCAGTCCATCTGC | 337867 |
rs550840419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312618 | TGAAACTGACATAGC[C/T]TGGGGGCCACGAGGA | 337867 |
rs550846400 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338814 | TGTCTTACTTATCAG[C/G]TGCATTAGATATAGC | 337867 |
rs550857428 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323841 | AACACAGGGAGGTAG[C/T]GACCAGTTGACGTGT | 337867 |
rs550867113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321339 | TTTTGGAGACAGGCT[C/T]GCTGTGTCACTCAGG | 337867 |
rs550890290 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294278 | AAACCAATCATATAG[G/T]CATGTCTTTTATTCT | 337867 |
rs550894165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324383 | AGCCACTGCCTGGTT[C/T]CACCATTGCTCTGTC | 337867 |
rs550898540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225040 | ATTATCAGATCTGTA[G/T]TTTTAGGGGTTTGTT | 337867 |
rs550903082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291289 | GTCTTTTAAGCAACC[C/T]GCTTTTCTGAGTTTA | 337867 |
rs550948118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267936 | GGCAGGCTCTGTACC[A/G]GTAAGTCGTCAAGGG | 337867 |
rs550979990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227243 | CACCCCTCCTTCCCC[A/G]GTTATGCTGCAGTAG | 337867 |
rs550980229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233946 | ACTAGTCTTTTGATA[C/T]TATGAATATTACAGG | 337867 |
rs550985917 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330420 | GCTGAGATCATGCCA[C/T]TGCACTCCAGCCTGG | 337867 |
rs550997612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357372 | AACAAGATGCCTCTC[A/G]TTCAGTCCTGAAGTG | 337867 |
rs551008216 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348115 | TGCCAGGGCCATTAC[A/G]TAACTTTTCATGGGT | 337867 |
rs551011680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312303 | TTTTGCATTTTTCTC[A/G]TGATAATGAAATAAT | 337867 |
rs551012140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282809 | CAAAATGCTAACCAT[A/G]TCTTGGTAACTATAG | 337867 |
rs551017035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227704 | CCTGTCTACACTCCA[A/G]ACCACAAGGCTAGGG | 337867 |
rs551024445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317318 | AACCCACAAATCATT[C/T]CTTTGTTGCAGGAAC | 337867 |
rs551028459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231625 | CATGTTGACCAGGCT[C/G]GTCTCAAACTCCTGA | 337867 |
rs551029665 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366770 | AGAACCCAAGTGGTC[C/T]TGGGTGAGCAGGGCC | 337867 |
rs551061368 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290773 | AAAAAGAAAAGATAG[A/G]GAAGAGTGCATTTAA | 337867 |
rs551068997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316863 | ATTGCTTAACCACTC[A/G]GTTTTACTGAAGTGC | 337867 |
rs551093173 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368748 | ACCCTCACTCTGACC[A/G]AGAGGGCTCAGAAGC | 337867 |
rs551109824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336897 | GCCAGCCCCGCAGCC[C/T]ATGGTGCCCCCCTTC | 337867 |
rs551123135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206098 | CTAGAGAGGGAATGC[A/G]GAGAAGCAGGAGCTC | 337867 |
rs551126525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277706 | GCATCACTCTCTTAC[G/T]TGAAATAAAATAGGC | 337867 |
rs551165077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237631 | AGCTAGAAGAGAATA[A/T]TTCAGCCTAAAGAAA | 337867 |
rs551188765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282048 | TTTCCTCACCCTCAG[A/C]ACTTTTGACATTTTA | 337867 |
rs551193757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377241 | TATGAGGGAGACCAG[A/T]TCCATGCAAGGCCCT | 337867 |
rs551214945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366350 | TGTGGTTTTGAATTC[C/T]GAGTTTTTCCCCACT | 337867 |
rs551255106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377626 | AAACTTTATAAATAC[A/G]TAAAGTGTATTTTAG | 337867 |
rs551255928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231020 | GCCACTGTACTCCAG[C/T]CTGGGCGACAGAGGG | 337867 |
rs551257070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370605 | AAATGCCACGCACCT[A/G]CCTCTGTAGCAAAAC | 337867 |
rs551262495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340100 | TTGCTAGCTCTTCTA[A/G]TTCAATAAAAAACAA | 337867 |
rs551290231 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247937 | ACCAGTGGCCACCTA[A/T]TTTCTAAAGCCACTG | 337867 |
rs551312286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275265 | CTGGGATTGGAAGAC[G/T]CACAGTGCTGTTGGC | 337867 |
rs551319432 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325304 | GAGACGGGGTTTCAC[A/C]GTGTTAGGCAGGATG | 337867 |
rs551329397 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260807 | ATGAGTGAAGGAGAA[A/G]TGTTTCACTTGCAAA | 337867 |
rs551354238 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277302 | AGGCCGAGGCAGGTA[G/T]ATCACCTGAGGTCAG | 337867 |
rs551358747 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346241 | TCCGTCATTCATCTC[C/T]AGTGCTGTAGTTCAG | 337867 |
rs551374984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312816 | CTTGTGTGTGTTGGG[C/T]CAGATGAGGGGAAGC | 337867 |
rs551385864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284884 | ATAATGTGTAGTTTT[C/T]GTATTTCTCTTGGAA | 337867 |
rs551405936 | in-del | -/AAAA | 0.0401523 | 0.135882 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236976 | AGTATGGAGGTTCTT[-/AAAA]AAAAAAAATAAAACT | 337867 |
rs551418871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354832 | ATCTTACTGGCAGTC[A/G]TGTCATCCAAGAAGT | 337867 |
rs551419839 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208633 | AGTTGGCAACCATCT[C/T]TGTCCGAAAAAGCGG | 337867 |
rs551444617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212451 | CCAGAATTTAGTCCC[C/T]TCAGTGGACGTGATA | 337867 |
rs551447795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269287 | CTCTTCTTTATTGTG[A/T]GATTCATAAGTAGGC | 337867 |
rs551458006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218134 | ATTTTGGCTTTTAAA[A/G]TTATTATTTCATTAT | 337867 |
rs551504513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205742 | CTGTGACATCTGTCA[C/T]CCCATTGATCGCCAG | 337867 |
rs551509727 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199535 | TCTTTGAGGGTAGGG[A/G]CTGTGTTGATCTACG | 337867 |
rs551526970 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339767 | GTTGGTTTATAAATG[G/T]AACTAATATTGGTGA | 337867 |
rs551584600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283506 | TGTTTGACATATGTT[C/T]CTGATTTAAATGAAT | 337867 |
rs551586185 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369014 | CTAGGGCATCGGCTT[A/G]GGGATCAGAATAAAT | 337867 |
rs551593879 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99352011 | CATTCTGTGGCTGTG[A/G]AAATTGTTTCTCTCT | 337867 |
rs551597562 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384992 | AAGCCCTGTGTCCTT[C/G]TCTGTAGAATGAGGG | 337867 |
rs551599475 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259489 | TTGGAGACAACCATA[C/G]CAACTATTTCTTGTG | 337867 |
rs551604768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378874 | TTATCCTTCATTGAT[C/G]TAAGAATACCTTGGC | 337867 |
rs551620805 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333759 | GTGAGTGTATACTCA[C/T]GTCTGATTGTCATTG | 337867 |
rs551645655 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317959 | TATAGTTATGTAAAA[A/G]TAAGTGTGCTGTGAC | 337867 |
rs551653454 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316537 | TGCCCTGTGCAATGG[A/G]CTATGACGTTGTGGG | 337867 |
rs551659450 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385481 | CCCCTGCCCTCAACC[G/T]CAAGACTGTTGCCGT | 337867 |
rs551664225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378170 | CCTTGACTCAGAACC[A/G]TCTCAGCTATTTCAC | 337867 |
rs551670145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372903 | ACGGATCACGAGGTC[A/G]GGAGATCGAGACCAT | 337867 |
rs551682319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240922 | TTGGCAAGAGCACAG[G/T]TTGTATGACTTTACA | 337867 |
rs551683761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318688 | TTGCTGGGCGTGGTG[G/T]CAGGCGCCTGTAGTC | 337867 |
rs551714294 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293455 | TTTCCTTTAGTAGTC[G/T]TCACGATGGTTCCTC | 337867 |
rs551731303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296417 | CTTTGGCAAAGCTCT[G/T]GCAAAGGAAACAGAA | 337867 |
rs551739259 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219991 | CCACTTTTTGTGTTA[C/T]GATAATGCTACTATG | 337867 |
rs551777081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324743 | TCAACAACAGAGTGC[A/G]TATTCAGTGGTGGCC | 337867 |
rs551809256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305365 | GACTGGAGAACACCA[C/T]GCGTCCTCTACACAG | 337867 |
rs551810881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383799 | AGCAGTGTCCACTGC[A/G]TGTCCCTGTTGGCCC | 337867 |
rs551821146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289693 | GCAGCCACGAAATAA[A/C]CCTGAAATCACAGTG | 337867 |
rs551842046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345061 | TAGAAGGACGGGTGG[A/G]ATTTGGATGGGTGGA | 337867 |
rs551847334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262075 | GGACATGAGTCCTCC[C/T]TTTGCCCAGTGTCTC | 337867 |
rs551856096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290392 | TGTAATTAGGTGTGC[A/C]AAGGCCAGTGTCTGG | 337867 |
rs551864052 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328026 | CATCCAGCTGCCAGC[C/T]GCAGGTAACCACTGA | 337867 |
rs551882568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263106 | TCTTTCTGTATTTTG[C/T]ATTATAATATTATAC | 337867 |
rs551893774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298080 | AACAGCAAAATTTGA[C/G]GGAATTTGAAGGAGA | 337867 |
rs551916183 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330501 | TTGATTTCTGTATTT[C/T]GTTCTTGTGTCCTGC | 337867 |
rs551922911 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330992 | ACATATAAGAACCTG[A/G]TGATGGTTTTCTCCA | 337867 |
rs551936983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362968 | ATCCTTTCCTATCCT[A/G]ATGACATGAAAATAA | 337867 |
rs551950709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297058 | GATAGATATTCTACA[A/G]TCTTCCAATGTGTCA | 337867 |
rs551954870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324422 | CATGAGAAAAGCAGG[G/T]CCCGGAGAGGGGCAG | 337867 |
rs551977033 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284567 | AAGCAAGTTGTAGAC[A/C]TAATGTCCCTTTGAC | 337867 |
rs551983006 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351373 | TGTACAATCTGAAGC[G/T]AGGAACAGGTTTTAC | 337867 |
rs552005940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225831 | ACGTTTTAATGATTC[C/T]AAAATTGGAACGTGC | 337867 |
rs552019566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231663 | TGATCTACCCGTCTC[A/G]GCCTCCCAAAGTGCT | 337867 |
rs552031127 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260313 | TCCTCCACTAAATTG[C/T]ATTCCTTGAGAGTTG | 337867 |
rs552045527 | in-del | -/AATC | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304616 | CCCTTGATGAATAAT[-/AATC]AATTAAAATTACTAA | 337867 |
rs552058268 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232427 | ATATATATATTCACA[C/T]ACACATACTCTAAGG | 337867 |
rs552059342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217486 | TGTGTGGCCTGGGGA[C/T]GTTCCAGCACCATCT | 337867 |
rs552071166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355831 | CTGGAGGGCAGCGGC[A/G]GCACAGACCCACTGG | 337867 |
rs552083817 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306677 | CATTGTGATTTTTTC[C/T]CCTCAGGCACATAGA | 337867 |
rs552084130 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288111 | TGTTACTTTTTTTAG[A/G]TTAGGTCTCAAACCT | 337867 |
rs552107336 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364828 | TTACAGTATGTGAAT[A/G]CACCATAACTTACCC | 337867 |
rs552127798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268653 | ACACAAAAGGTAAAG[A/C]AGGTAAGAGAGAGAA | 337867 |
rs552154063 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245489 | AAAAAACAAAAACCA[C/T]GTATTAGTGTGTGAA | 337867 |
rs552177075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343782 | TTCACATAAGTATGA[C/T]AAATCACCACGTAGA | 337867 |
rs552224070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205182 | GCTGGGATTATAGGC[A/G]TGAGCCACTGTGCCC | 337867 |
rs552238253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336946 | CCTTCCCACCTCCCT[C/G]CTGTGACCCCTTCCC | 337867 |
rs552245114 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245294 | ATTAGATTAGGAAAC[-/AA]AATTAATTTGTACGA | 337867 |
rs552245997 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379751 | CCAACACCATACTCT[C/T]CTGTAAGACGTTTCA | 337867 |
rs552262727 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384362 | CTGTGGCAATCTGGG[A/G]CCATGAATATTTTTG | 337867 |
rs552268215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377782 | TGAGAGGTCATGTTT[A/G]TTGAGCGCTGGTCAT | 337867 |
rs552275829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362255 | GGTCTTTTATATAAT[A/G]GAACCACTTATTAAT | 337867 |
rs552314724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208822 | CTGACCCTGTGTCCT[A/G]CAGGTGCTTCAGTGG | 337867 |
rs552325011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342368 | GGGCTTCAGCGTGTG[A/G]ATTTGGGGCAGGGGC | 337867 |
rs552395792 | snp | A/G | 1.65633e-05 | 0.00287774 | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356251 | TGCCATCCCCAATCA[A/G]TCCCTGGAACACCAG | 337867 |
rs552419959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317040 | ACATCAAAGGTTCAG[A/G]TTTAAAGTTGCAGCC | 337867 |
rs552444837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243659 | TGGGAGGAATTTTTA[C/T]TATGAGAGACTTGAG | 337867 |
rs552455901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202290 | CATCTTTCATGGATT[G/T]GTCCCGGAGTATGTT | 337867 |
rs552476926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244356 | CTATTTTAATAAAAA[A/C]AAATAATTTCAAATA | 337867 |
rs552485836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209834 | CAAAATTAACTGGGC[A/G]TGGTGGTTGGCGCCT | 337867 |
rs552497367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217664 | TGGGTGCCCACCCCG[C/T]GGTGCTTCTCCAGGC | 337867 |
rs552538130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376334 | CTGCTGACGCCTGTG[A/G]TTCAGAAGCTCGTGA | 337867 |
rs552544201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282351 | GCTTGTTGAGAACTT[G/T]TGACTAGGTAGAATA | 337867 |
rs552552716 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210508 | TTGAGATGGAGTTTC[C/G]CTCTTGTTGCCCATG | 337867 |
rs552592772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335307 | CGTAATGCTGATATA[A/C]ACCCTATTTTCTGTT | 337867 |
rs552604150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288293 | TTTTGGATCAGTTGC[A/G]GTAGGTGCCATGTGG | 337867 |
rs552640987 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345796 | TGCCCAGGCTGGAGT[G/T]CAGTGGCGTGATCTT | 337867 |
rs552679216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224237 | TCCTTTGTGTGTGCA[A/T]GCATCCCTGGGTCCC | 337867 |
rs552681773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311641 | AAACCTAGATAAAAT[A/G]TGATGCTTTCTCTCA | 337867 |
rs552708165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252326 | CACTGGCTGTTTGAG[A/G]GGGAACCAAGTTTTA | 337867 |
rs552715885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302095 | AGAGGTGACCTAAAT[A/C]AATGTGCCCACAGTG | 337867 |
rs552716258 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326777 | ACTGCACATCTCAAG[C/G]CTCTCATCCATGTCT | 337867 |
rs552735660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316501 | TTTAAGTATCCAATG[A/G]CTTGAGAGCCCATAA | 337867 |
rs552735936 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297962 | CATCAGAAAAAATAG[A/G]ATTCAAGGCAAATTC | 337867 |
rs552745546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371570 | GGCCAGTTTGTTTAA[C/T]CACTGTCTAAAATAT | 337867 |
rs552790691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324444 | GAGGGGCAGCTCCTC[A/T]GACTCCAGAATGAAG | 337867 |
rs552794756 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336272 | TCTGAATACTTTCTT[C/T]AGGCCTCTTGTGTTT | 337867 |
rs552808816 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364502 | CTTGTCTAGTTTTGG[A/G]AACAGTGTTATGCTA | 337867 |
rs552822414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383580 | CCTCCCCACCGCAAG[A/G]CATTTGGAAGACACC | 337867 |
rs552822433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376874 | GAATGTTGAAAGAAC[A/G]CCTTTTTAGAAAATT | 337867 |
rs552827001 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99298963 | TCCAAAAATCTAAAT[C/G]TATATTTTTGAGTAT | 337867 |
rs552849941 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99296708 | AACCTAAAAGTCTGA[A/G]AAATAGGCTTAGTCC | 337867 |
rs552855167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281697 | TCTCACTTATGTCTT[G/T]ACATTGCCTGAGGAC | 337867 |
rs552868630 | snp | C/T | 6.60567e-05 | 0.00574665 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295099 | ATGTATCATCATCTG[C/T]GTTTCTGTCATTTCA | 337867 |
rs552915631 | snp | A/G | 1.64879e-05 | 0.00287118 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295756 | GTGCACCACAGCAAT[A/G]AAGCGGTCAATACTC | 337867 |
rs552918481 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215606 | TGCGCTGTACACAGC[A/G]GCAGTTGCACCCACA | 337867 |
rs552924973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362331 | TTAATATTACAACCA[A/G]TGCTTCACAGAAGAT | 337867 |
rs552929040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355380 | TGTCTCAGTCCTCGC[C/T]GTGTGGCCCTTACCG | 337867 |
rs552975274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330240 | CCAAGGTGGGCTGAT[C/G]ATGAGGTCAGGAGTT | 337867 |
rs552977039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230642 | CTTTCTGAGGCAGCT[C/T]ACATTTCTTGACTCA | 337867 |
rs552980410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245582 | AAACAGGCCGGGCGC[A/G]GTGGCTCATGCCACC | 337867 |
rs552992088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363647 | TGGTCGGCCCATATT[A/C]CCTTTCTGCTGACAT | 337867 |
rs552992267 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355911 | GTCCCTTCCCTGCAC[C/G]TCCAGGGCCTCCCCA | 337867 |
rs552999144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289909 | ACGCGTCTTTTGCCC[A/C]CAACCCATTGGTCAG | 337867 |
rs553028553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317393 | ACTCTAAGATATAAA[C/G]GATTTGGAAAACAAA | 337867 |
rs553047185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216992 | CCTGCCACCATGACC[A/G]GCTAATTTTTGTATT | 337867 |
rs553050943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268183 | GATGTAATCTTACCT[A/G]GGCAGTTGTGTCCCT | 337867 |
rs553052176 | in-del | -/TTTTAC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317707 | TCTTTATATGTAGTA[-/TTTTAC]TTTAAGTCAGTTGAA | 337867 |
rs553070327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251498 | AACTCTTAAATCTTT[C/T]CTTGTCTACTTTTTT | 337867 |
rs553098336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343467 | CTGCCCTGCTGGAGC[A/G]TGCATTCCCACCAGG | 337867 |
rs553101530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225228 | AGTACGTTCATATTG[G/T]GCAACCGATGTCTAT | 337867 |
rs553126018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267132 | TGATGAGTGACTTCA[A/G]GAATCTTTTCATGGG | 337867 |
rs553133892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349074 | CTAGAGCATGCTTAG[C/T]TCATCACAGTGAAGG | 337867 |
rs553148195 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325720 | CCAGCCCCTAGCAAC[C/G]ACCATTTTACTCTCT | 337867 |
rs553148521 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270821 | TCAGTCATGTTTTAG[G/T]AGAAGAAAGAATTTC | 337867 |
rs553148954 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319385 | ACACATTTCACTGCA[A/C]TCACTGTACACATTT | 337867 |
rs553162117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237152 | TGAGCCATCAGGCCC[A/G]GCCTTCTTTGTTGTA | 337867 |
rs553169461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203958 | TTGCTGTCTGCAATT[A/G]TGACCGGGTAAAAGT | 337867 |
rs553182090 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201256 | TCGTGGGCCGGCCCC[-/A]AGGCCCTTTGCGGAG | 337867 |
rs553184972 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216078 | CTTTTGTACCAACCT[A/G]TATTTGTGTGTGTGT | 337867 |
rs553189327 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289026 | GACCATAGACCGTAC[A/G]ATGGCTGGCAAAGAG | 337867 |
rs553197366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209879 | TCGGGAGGCTGAGGC[A/G]GGGAGAATCAGTTGA | 337867 |
rs553202357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288954 | AGCTAGTGTCTCTTC[C/T]CCAATGGAGTTTATG | 337867 |
rs553228944 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299336 | CATGCAGTGAATACA[A/G]TGCAGCTCTGAAAAT | 337867 |
rs553234379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336620 | CTGAGGATCCTATTT[C/T]TAGGCTCTTGTTCTC | 337867 |
rs553265767 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271241 | GTGAGTGGGATTGCA[A/G]TTTTAATAATTCTAG | 337867 |
rs553284805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223774 | TAGAAATGTGTTGTT[A/G]AGTTTTCACATATTT | 337867 |
rs553287719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329784 | TGCAGATAGGCTGAC[A/G]CCTTGACTGACTACA | 337867 |
rs553295709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337082 | TCACAGAAGTGGAAT[C/T]GTGTTTTCAGGCTTT | 337867 |
rs553296974 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285665 | CCAGAGTGTTGGGAT[A/T]ATAGGCATGAGCCAC | 337867 |
rs553300091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268223 | GGAACAGTGGGTTTT[C/T]GGGGAGCTGCTAGCA | 337867 |
rs553359460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273351 | GGGCAGTGAGCACCC[A/G]GGATAGAGAATCCAC | 337867 |
rs553361690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215691 | AACTGCAAGCCGGCT[C/G]TCTGCGAGCGGGAAA | 337867 |
rs553387687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222724 | GTCATGATGTATTCT[G/T]TTTATATAATGCTAG | 337867 |
rs553423186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209205 | ATAGGCCATCGAGCC[A/C]CTACCTCAGCTTGGT | 337867 |
rs553461008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302802 | TTCTATTAATAATAC[A/G]CTGCTAACCAACTGT | 337867 |
rs553502676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235765 | GGATCACTTGAGGCT[A/G]GGAGTTTGAGACCAG | 337867 |
rs553510010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203304 | GCCTCCAAAAGTGCT[A/G]GGATTACAGGCGTGA | 337867 |
rs553514609 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266684 | AATTTGACATGTTAA[-/AT]ATATATATATATATG | 337867 |
rs553519312 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375579 | ATATGGGAAGTAAAA[A/C]CCCAAAAAAAACATT | 337867 |
rs553537074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242496 | ACGGGGCGGCTGGCC[A/G]GGCGGGGGGCTGCCC | 337867 |
rs553537999 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376975 | GTTGCAGTATGCAGC[A/G]CCGTGCCTCGCCTCG | 337867 |
rs553572138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353382 | TCAGAACAGAAAGAT[A/G]GGATCAATCTAAAGT | 337867 |
rs553584404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369396 | GAGACTCTTTTGCGA[A/T]GCTGGGCAGCGACTG | 337867 |
rs553609827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308145 | GCAGTTTATTTGTAG[A/G]CTAAATTACCAGATA | 337867 |
rs553637179 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273835 | TATTACCTAGATGTT[C/T]AGTCTCCTGGACAGG | 337867 |
rs553665809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316139 | AATATTTCCGGTAAC[A/T]TTGAGAGGGAGAAGT | 337867 |
rs553670653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280891 | CAAATCTGTTACTTA[A/G]GAGAAAAATGTAGGC | 337867 |
rs553692519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348206 | CTTTGTCTTTTGGCT[C/G]TAATGCAGTGTACTG | 337867 |
rs553715800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214138 | TGTGTATTTATTGTA[A/G]AGCCAGGGTTAGAAC | 337867 |
rs553745779 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301556 | CATTGCTAATAGAGT[G/T]GCTAACACTTCTTGA | 337867 |
rs553757788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342474 | GTTCTGCTTGCAGAC[A/G]GTAGTTATCAGGCAC | 337867 |
rs553784591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294559 | AGCATCCTGCTCTTT[A/G]TTCCAAAAGAGTTCC | 337867 |
rs553787426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347639 | CAGCTCTGATGAACA[A/G]TGACCAGGGTGATGG | 337867 |
rs553801968 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99385016 | ATGAGGGTTATGTGC[A/G]ATCATGCATATATAT | 337867 |
rs553813025 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243228 | AAATAGGCCTTTGAG[A/T]AGCTCTTTTTTTTTT | 337867 |
rs553816622 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277882 | GCAAGAGGGAACTTG[C/G]TTAGTCTCGGGATCC | 337867 |
rs553828150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300730 | AAGGGTGAATATATA[A/G]CGTTGAACATGTGCT | 337867 |
rs553883915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314461 | TTTCACTGTAATTTG[C/T]ATCTGTGGAAAATAT | 337867 |
rs553909988 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255727 | CTCTTCTTGGTGGTA[C/T]AACTGAAAACCCATA | 337867 |
rs553933708 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375516 | GTGTGAGCTCAGGAT[C/T]GGGTGGGGGCCGTCT | 337867 |
rs553935978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382206 | TTTGAGGGAGATGAT[A/T]AACAGTAGATAACAA | 337867 |
rs553952488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286645 | GGCTTTTCAACCTCC[A/G]TCACCCCACACTCCC | 337867 |
rs553982719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271470 | AGGAGATGAGGCCAG[G/T]GAGGTAAGAGTGGTC | 337867 |
rs553985215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360515 | AGCCCAGTTATTCTG[G/T]CTCTAGAGACTGTTC | 337867 |
rs553987973 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337489 | TTGCTTTTAAGGATT[C/T]CTTTCTTTTGTTTCA | 337867 |
rs553992698 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220419 | CTGGCATAAAATAAT[C/G]CACATATACTGTAAT | 337867 |
rs554008178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379252 | TCTGCCCTTGATGTC[C/T]TCAGTTCCTGGAGGG | 337867 |
rs554018238 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385629 | TTAAAATGGAAGATT[G/T]CTGCAGGCAGTTGAA | 337867 |
rs554052814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353905 | TGGTTGACAGACGTG[A/G]TTTTGTGGAGAAAGC | 337867 |
rs554053964 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359021 | AGAACACGGAAGAAG[C/G]AGAGAAACACTCCCC | 337867 |
rs554071548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380035 | GCAGAAAAGGCATGT[A/C]ACAGCTGAAGGAGGG | 337867 |
rs554080399 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374711 | TTATTGGTTTTGAGA[C/T]ACATCTCGTGCTTCT | 337867 |
rs554084445 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201774 | ATCTGACATTTCCAA[A/G]TATTAAAGATCTGTT | 337867 |
rs554109278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354621 | GGCACTTTAGGTGGC[A/G]GGGACAGTTTGAGCC | 337867 |
rs554119925 | in-del | -/CCTACCTCA | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209204 | ATAGGCCATCGAGCC[-/CCTACCTCA]CCTACCTCAGCTTGG | 337867 |
rs554128064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257809 | ATTTTCTTTCCTTAA[C/G]TTGAAAAAAATTACA | 337867 |
rs554130871 | snp | A/T | 4.95094e-05 | 0.00497517 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295351 | CTTAATCATATGTTG[A/T]ATAATTGCAACATGG | 337867 |
rs554152890 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200542 | CCAGGGGAATCCGCG[A/G]CCATCGCGGATCCAC | 337867 |
rs554215619 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234436 | CTCAGGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 337867 |
rs554224740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328774 | TATGAAAATTGTATT[A/C]TAATTTGTGGCTTGT | 337867 |
rs554239710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327067 | CTATAGCTATGCTTT[C/G]TCTTCTAAAATCATC | 337867 |
rs554248971 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386261 | GGAGGACAGGATGCA[A/G]GTCAGGGAGAGGGAA | 337867 |
rs554254206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367512 | AGTGTCTGTACAGTG[C/T]CTTTCACTGCCTTCC | 337867 |
rs554268638 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235696 | AAATTGTGCTGGGGC[C/T]GGGTGCAGTGGCTCA | 337867 |
rs554303383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227863 | TGTGTTGGGAGTTTG[G/T]TATTCAAGTTGGGAG | 337867 |
rs554338503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228540 | CTCAAGCGATCTGCC[A/C]GACTTGGCCTCTCAA | 337867 |
rs554356697 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221145 | ATTCATATTGTTTCT[A/G]GTCTTTTCACTATTA | 337867 |
rs554377459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206550 | CCATTTGTGGCATCT[C/T]TTTCTTCATATCCAG | 337867 |
rs554422719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257869 | ATAAATGTAAAATCA[C/T]ATTAATGTGGAAAGA | 337867 |
rs554429805 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248691 | TCCGGCCATTTTTTG[G/T]TTGTTTGTTTGTTTT | 337867 |
rs554434465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339952 | GTGATGGCCATCTGC[C/T]AACAAAGGTAACCGC | 337867 |
rs554445043 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373721 | GGCTGGAGTAGAGGG[G/T]ACTGGAGGGCCGGGG | 337867 |
rs554477809 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221994 | GTCTTCTGTATAAAT[C/G]TGAGAAGAGTGATGT | 337867 |
rs554490519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294640 | TTGAGGGAATTAAAT[C/T]TAACATTGAGAGAAA | 337867 |
rs554490866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302540 | GCCTTCTTGTTCAAA[C/T]AGGGGCATCTAAATT | 337867 |
rs554493779 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340508 | GAGAATGGAGCTGCT[A/G]GACCGGCAGCTGATG | 337867 |
rs554494449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208047 | TTGTTGCCCAGGCTG[C/G]AGTGCAATGGCGTGA | 337867 |
rs554495596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332599 | GGGTTCTCTGGTTGC[A/G]TGACCATGTGTCCCC | 337867 |
rs554499653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329210 | TTTATGGTAAGTCTT[G/T]CAATCAGGCAATATA | 337867 |
rs554539739 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279152 | TTCCCCCTTTTCTTA[C/T]CCCTTTATCTCCCCT | 337867 |
rs554547451 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386808 | TAACTAGGCCACAGT[C/G]AACACCTCCTGAGTG | 337867 |
rs554549141 | in-del | -/AAAAAAAACA | 0.0146672 | 0.084371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281189 | GCGAGACTCCATCTC[-/AAAAAAAACA]AAACAAAACAAAACA | 337867 |
rs554550718 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200832 | CTCCGCCAAGAGTGC[G/T]CCTGCGCGGTCGCTG | 337867 |
rs554558473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382224 | CAGTAGATAACAAAA[C/T]GAGAATTGAAAATAA | 337867 |
rs554569147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243371 | CATAAATTACTTTGC[A/G]TAGTTGCTATGAAGT | 337867 |
rs554569239 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297287 | AAAAGAAAAATAATT[-/C]CCTCTGATAGAACTG | 337867 |
rs554572044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357144 | TTTAGATACACAACT[A/G]CCATTGTGTTACAGC | 337867 |
rs554576050 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342520 | ATGCCAGGTTGGATG[C/T]TCCATAGTGGCAGGA | 337867 |
rs554591160 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372910 | ACGAGGTCAGGAGAT[C/G/T]GAGACCATCCCGGCT | 337867 |
rs554612744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381446 | AGCAGCCAGTCCTCA[G/T]CTGCACTTGAAGTAC | 337867 |
rs554638544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236717 | TAGCTGGGCATGGTG[A/G]TGGGTGCCTGTAATC | 337867 |
rs554659028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280960 | GGAGGCCGAGGCAGG[A/C]AGATCACTTGAGGTC | 337867 |
rs554660318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272998 | TCTAGTAGAACAGGT[C/T]ACTCTTTTTTTTTTT | 337867 |
rs554676311 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375632 | AAGGGAAGTTAAAGA[A/C]AACCACACTCTAGTT | 337867 |
rs554728606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360570 | TGTCCCTCTGCCGTT[A/G]TTCCTTAGCATTGCT | 337867 |
rs554737709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376684 | AAGCATGCTGGAGGC[A/G]AACCCAACTAGAGCT | 337867 |
rs554755556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240002 | AAGAGAGGGAAGGGC[A/G]TTTTACTTCAGGAAG | 337867 |
rs554761502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315037 | TGGCGTCACTTCAGA[A/T]TGCCTTCCTCCCTCC | 337867 |
rs554769243 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308735 | GTATGGAGGAACATT[G/T]TCAGACACAAGAAAG | 337867 |
rs554781450 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264984 | TTTTTTTTTTTTTTT[A/T]AATTGTTCTTCAGTG | 337867 |
rs554786590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354707 | GGCAGACCTGCAAAA[C/T]AGGACAGACTCAGAC | 337867 |
rs554791731 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99258437 | ATGACTTTACCCTGG[A/G]TGTGGTTTTTCTCTT | 337867 |
rs554792244 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216059 | AAAGGTAAAATGGCA[A/G]TTACTTTTGTACCAA | 337867 |
rs554798490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308276 | AACACCTGTGGCAGT[A/G]AGGGGCCTGGATAGC | 337867 |
rs554813416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373959 | AGGAAACATGGTGCA[A/G]CTGCCCAGACAAGAG | 337867 |
rs554813774 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380430 | AGTAATTGTTAGTGT[A/C]CACCAAAGAGCCCTA | 337867 |
rs554827779 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242287 | GGTGGCCGGGCAGAG[A/G]TGCCCCTCACCTCCC | 337867 |
rs554829580 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215132 | AAAACAGTCAGCTCA[A/G]TCAAAGCCCAGTACT | 337867 |
rs554834964 | snp | A/C | 1.72338e-05 | 0.00293541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340583 | AAAAGTGATAATAAT[A/C]ACTAAAAATTTAGAA | 337867 |
rs554850943 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202520 | GTACATATAAAAAAA[A/T]AAAGGGCAAGAGAAA | 337867 |
rs554878761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374409 | TTCTGGTTTGTTGGA[A/G]CCCAAAACAATGGCG | 337867 |
rs554880389 | in-del | -/T | 0.221141 | 0.248329 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292302 | ACCACGCCCAGCTAA[-/T]TTTTTTTTTTTTTGT | 337867 |
rs554926020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352526 | CTCTGTGGTTTAGAT[A/G]GCAAGATCTGCCTAG | 337867 |
rs554953553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234482 | GGCGTGAGCCACTGC[A/G]CCCTGCCTGTGCTAG | 337867 |
rs554960504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228641 | CGTAACACTTTTGAG[A/G]TAGGTTCTCATCTCC | 337867 |
rs554961841 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205031 | GCCTCAGCATCCTGA[C/G]TAGCAGGGACTATAG | 337867 |
rs554990376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352885 | TCTACCTCCGTCTCC[A/G]CCCCTGTGTCCGGGG | 337867 |
rs555010021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321457 | GGAATTGCAGGTGCA[C/T]GCCACCAAGCCCGGC | 337867 |
rs555016546 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263534 | TGTTGAGTGATGAGG[A/C/G]TATCGAGTAACAAGG | 337867 |
rs555021645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248424 | GAGACAGATTTTCAC[A/T]CTTGCCGCCCAGGCT | 337867 |
rs555051309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346890 | GCCTGGCAGATGTTA[A/G]GAACTGTGGGAATTA | 337867 |
rs555060733 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296261 | TAATGTATCAAAGCA[A/G]TCCAAACTGTCTTTT | 337867 |
rs555070771 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242723 | CGGGGCGGCTGGCCT[G/T]GCCGGGGCTGACCCC | 337867 |
rs555078963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315485 | AGAATCTTTGAGAAT[G/T]AAAACACTGTTTTAT | 337867 |
rs555091531 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270672 | TGGTGTGGACATGCA[C/G]ATGAGTTCTGAAGAA | 337867 |
rs555098005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332513 | CTGCTGTTGGCATAT[C/G]GGGGGCTGCTCCCTC | 337867 |
rs555112556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324991 | TTCTCAGAATGTGTC[C/T]TTATCATTAAGCAAC | 337867 |
rs555148236 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386086 | CTGGCCTGGCATGGG[C/G]TCAGCCCAGGAAGAG | 337867 |
rs555148743 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336743 | CTTTAAAATTGCCTT[A/G]CCTTTTCTGGGTTTT | 337867 |
rs555151287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325339 | TGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 337867 |
rs555153650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226971 | TGGGAGGCCAAGGAG[A/G]GTGGATCACCTGAGG | 337867 |
rs555157961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206628 | TCGGAGACCTGGCAC[A/G]TCTGTTCTGTGGTGC | 337867 |
rs555163358 | snp | A/C/T | 0.000500403 | 0.0158112 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200880 | TCCCCTCCCCCGGCG[A/C/T]CCTCTGGGGCTCCGA | 337867 |
rs555174846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341620 | ATATAGGTGATGGAG[A/T]CACCTCTGTAGGGAT | 337867 |
rs555213836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293545 | GCCCTTTCTTTTCCT[C/T]CACTTGGGAAAGTTT | 337867 |
rs555219094 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230973 | AGAATCGCTAAACCC[A/G]GTAGGCGGAGGTTGC | 337867 |
rs555230365 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375367 | CCTTGCAAGGGTCTC[A/C/G]GCCATGCGTCAGCAT | 337867 |
rs555236410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333932 | TTCATTATATTTTTC[C/T]TAATTTATTTAAAAA | 337867 |
rs555246086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233042 | ATATTTTCTAGCTCT[C/G]ATTACTGAAAGAGCT | 337867 |
rs555252051 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209688 | ACTCTTCATAAATTT[C/T]AGCGGCTGGGCATAG | 337867 |
rs555281844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326383 | GCCCATTTTTAAAAC[C/T]AGGTTATTAGTTTTT | 337867 |
rs555309472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205792 | GCTGGCTAGGCGGGT[A/G]TCCCCTTCCTCCCTC | 337867 |
rs555309512 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199143 | GGCCCAGAGGCTCAC[A/G]CCTGTAATCCCAACA | 337867 |
rs555326855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228094 | CAAGGAAGAGGAAGG[A/C]CTGACGGGGCCCATT | 337867 |
rs555361129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314303 | TTCTCATTTGATCTC[C/T]TTGAAAACAATGGTT | 337867 |
rs555366579 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383520 | GAATCACCTGAGGGC[A/G]CCATAGTGTCCCAGG | 337867 |
rs555370201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319372 | GATTCATAATAATAC[A/G]CATTTCACTGCAATC | 337867 |
rs555373867 | in-del | -/AT | | | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254626 | ACTTGATTAACACAC[-/AT]GTGTCGCTTGCACAT | 337867 |
rs555383314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264048 | CTGTATGGCAGGATC[C/T]TGGAGCTGTTGCTTT | 337867 |
rs555392705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270506 | AGATCAAGTGTTAGA[C/T]TTTAATTACTACTTT | 337867 |
rs555397584 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385854 | CCTCCCCCAAGCTGT[C/T]CCAGGCCAGAGGACT | 337867 |
rs555406640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313703 | AGTGCCATGGCGACA[G/T]ATCACTGGACAGGGC | 337867 |
rs555412523 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257957 | TTAATTAAATATATT[G/T]TTTTAATAGAGACGG | 337867 |
rs555422536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306147 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 337867 |
rs555423817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331754 | TTCTTGGGGTAATAA[A/G]TTAGGGAATGTACAA | 337867 |
rs555430411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213923 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGTCTCAG | 337867 |
rs555439678 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225305 | CTTCCCATTTCCCCC[G/T]TCCTCCGCCCACTGT | 337867 |
rs555441671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345177 | CCAGGAGCCCTGTGA[C/T]TGACATGTGGGCAGA | 337867 |
rs555442454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207242 | CCTGGAAGTGAGACT[A/G]CCTGTACTTCAGATG | 337867 |
rs555459352 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306881 | AAGCTTTAGAAAATA[C/T]ACCCTTTGCCCTAGG | 337867 |
rs555465407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299471 | ACACACGCACACACA[C/T]ACACAGAAAGATGTC | 337867 |
rs555478631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384717 | CGAGCATGGCAGTGA[C/T]GCCAGGAGTGTGATG | 337867 |
rs555517016 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270903 | AGTAAATGTTTGGGT[A/G]TTTATGCATGCATGA | 337867 |
rs555538004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365908 | TTTCTGTGTTTTGAT[A/G]CCATTGTGTTACATA | 337867 |
rs555546556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319011 | AGAGATAGTCTGCTC[A/G]TTTTGTAAAAAGACA | 337867 |
rs555556708 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209693 | TCATAAATTTTAGCG[A/G]CTGGGCATAGTGGCT | 337867 |
rs555565801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312422 | CAAGCTTGTGCCCAA[A/C]CCACTCTACTCATTC | 337867 |
rs555566572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269772 | TTTCCCCTTTCTGAA[A/G]TGAGCATGCTCAGCA | 337867 |
rs555570328 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332132 | TGAATGTGGGACCGG[C/T]GGTTGGCACAGCTTG | 337867 |
rs555593763 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276804 | GCTCATTATGAAGAA[A/G]AAAAGGCACTTCTGT | 337867 |
rs555596705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304754 | CACCAGGGCACTTAA[A/G]TGACCAAAGACCTAG | 337867 |
rs555644093 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335805 | CTACTTGGTGTTGCC[A/G]CATTGCTCCCCAGAG | 337867 |
rs555684945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305452 | AGTATCCCTGTAAAC[A/G]GCTTTATTAGGTGCG | 337867 |
rs555691452 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338133 | CACAATCTCGACTTA[C/T]TGTAACCTCCACCAC | 337867 |
rs555702081 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338357 | GCCACTGCGCCCAAC[C/G]TTGTAATGTTTTAAG | 337867 |
rs555708484 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304918 | AAACCTTAACGTACA[C/G]TAACTCATACCTATC | 337867 |
rs555725530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347029 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAAGCCC | 337867 |
rs555751845 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352678 | ATTACCGTCTATTCC[A/G]CAGAATACACGCAGT | 337867 |
rs555756794 | snp | A/G | 1.69398e-05 | 0.00291026 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254896 | AACATTTCACTGTTT[A/G]TATTGCTTAGTGACC | 337867 |
rs555758868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246876 | TCTCTTCCTTTTCAA[A/G]TCACAAAACATTATA | 337867 |
rs555776388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211762 | AAGAAGTTTATCTCC[A/G]TGTGTCTCCCAACCA | 337867 |
rs555779923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238743 | GATAATAATGAAGCA[A/G]TGGCAGTATTTCCTT | 337867 |
rs555787119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347471 | AGTGGGGGAAGGTCA[A/G]TATCACTCTGTTCTG | 337867 |
rs555789285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340798 | GACATTCTTGTTCCA[C/G]CTATATTAGATAAGC | 337867 |
rs555827928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207904 | TCATGAAGGAGCAAA[C/T]CGTGTTCCTACTGAC | 337867 |
rs555846663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247375 | GCCCGCTACCACGCC[C/T]GGCTAATTTTTTGTA | 337867 |
rs555850395 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341734 | GCCTCGTATTTAGCA[A/G]GAGGTAAATCCTTCA | 337867 |
rs555859851 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207343 | ACTCAGGTTTAAGTA[G/T]TATTAACTGGATCCT | 337867 |
rs555864282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372438 | GAGAAGGCCCCTAAT[A/G]CCCCCCAAAGACCAC | 337867 |
rs555884462 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260733 | TTTTTTTTCCCCAAA[C/T]AGAGGAACTTATTCA | 337867 |
rs555903412 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201967 | ATTCCCAGCTACTCG[C/G]GAGGCTGAGGCAGGA | 337867 |
rs555907591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319477 | CATCCTGTACGCCTG[C/T]TTACCCCTCTTCTTC | 337867 |
rs555927206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249036 | TTTTTTGAAATTTCA[A/G]CTTTCAGATTCAGGG | 337867 |
rs555934506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379105 | CCCTAGTTAAACATG[C/T]CTTTTTGTTAGCATA | 337867 |
rs555944395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320384 | ATCCCTTGTTTCAGA[A/G]GGGTGAATAGAATTA | 337867 |
rs555954208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210914 | ACCATGCTGGGCCCC[A/G]CTTTTTCCCTTTGTC | 337867 |
rs556015065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380467 | ACTGTTCTCTGTGCT[G/T]CTAGTTTTTGCTCCA | 337867 |
rs556015198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254302 | TTGGTGCATAGTAGG[C/T]TCTCAGTGTTTGTTG | 337867 |
rs556038773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350841 | GGCCCTTAACCTGTG[A/G]GCTCTGATGTTATCT | 337867 |
rs556052009 | in-del | -/GTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99229194 | TGGCTGCTCATAGTA[-/GTG]TGTGGGAACGAGGGT | 337867 |
rs556069359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297414 | ATTTCCTTAAAGACT[A/G]TCTCTACCCTGATCA | 337867 |
rs556092375 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282916 | TCTGAAATATCTAAT[A/G]TGCTTGAAATCTAAT | 337867 |
rs556100241 | snp | A/G | 0.00301788 | 0.0387277 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351443 | ATCTCTTGCCTCTTT[A/G]TCTTCCAAACCTAAA | 337867 |
rs556100684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304689 | GTGTGTTTACTCATT[A/G]AATCCTCTCAGAACT | 337867 |
rs556110000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353796 | GAGGAACAGACCACT[A/G]GAGTACCCATGAGCA | 337867 |
rs556115490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292275 | TGAGTAGCTGGGACT[A/G]CAGGCGCCCACCACC | 337867 |
rs556116873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254292 | TAAATAGGGTTTGGT[G/T]CATAGTAGGCTCTCA | 337867 |
rs556142466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308082 | CATGCCATTCACCTC[A/G]TAGTTGTAGTTGACT | 337867 |
rs556143486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359823 | AAAGAGTCACATCGC[A/C]CTTCGCTGCCTACCC | 337867 |
rs556149449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282587 | GAAATAAAGATATTT[A/G]TAACTGTTGGGCTAG | 337867 |
rs556189062 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378475 | GAGGTTGCAGTGAGC[C/T]GAGATCACATCACTG | 337867 |
rs556200174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249835 | GATTACCTTTGAGCA[C/T]TTTTTCTTGTGTGTT | 337867 |
rs556204329 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385843 | GGGAGCTGAATCCTC[A/C]CCCAAGCTGTTCCAG | 337867 |
rs556206969 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364432 | ATTTAGGATTATTGT[A/G]TCTACCCAAGAAAAA | 337867 |
rs556215226 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99307135 | TCTGGTGGACCCATC[A/G]CTTTCAGTCAACTTT | 337867 |
rs556217966 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325365 | GCCTCGGCCTCCCAA[A/G]TTGCTGGGATTACAG | 337867 |
rs556244955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293017 | AGGATGCCCACAGCC[A/G]TGTATGAACAGTGGC | 337867 |
rs556265118 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386168 | CCTCCTGGCTCGCAG[C/T]CAGCCAGCCCCCTGG | 337867 |
rs556300180 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281275 | ATTTGGGTTCAGTGA[-/T]TTTTTTTTTTTAAGG | 337867 |
rs556317479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332573 | TAGACTCTCAGCTGG[A/G]CGTGGGCCAGGGGTT | 337867 |
rs556320943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359327 | GAGCTTCTAAAAGGC[A/G]GGGAGGTTGTCTTAA | 337867 |
rs556329154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313828 | AAGAAAACATAGCCT[C/T]CACTTTTCTCACACT | 337867 |
rs556334742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293660 | GTGCCTATTTTTGAC[A/G]ATGGCTTTAAAATCA | 337867 |
rs556339284 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252154 | TTCTTCGCTTGCTAC[A/G]CATTTGCATTCTCAT | 337867 |
rs556339445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227789 | GCGTGGATGCCTACT[C/T]ATATTTAGAGAATGA | 337867 |
rs556372493 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233615 | CTGGACCATCTGAAC[A/G]TTGGAAAAAGAATGC | 337867 |
rs556382803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277456 | CTTGAACCTGGGAGG[C/T]GGAGGTTACAGTGAG | 337867 |
rs556409577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227366 | CACACTGTCGTCAGC[C/G]CCGGGAGCTGGCTGA | 337867 |
rs556420077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271363 | CAGATATCAGAGACT[G/T]CCAGTGCCAAGGCCC | 337867 |
rs556477119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291709 | ATCTTCAAGGGCATA[C/T]GCTCTATATTGTGTA | 337867 |
rs556478985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299148 | TTTGTATACAAATGC[A/G]TGTCTGACTGCATCA | 337867 |
rs556494512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305488 | CTTTTAAATGTAAGC[C/T]TCTTGAGGATGATGA | 337867 |
rs556512182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264271 | AATCTCCCCTGAGGC[G/T]CCTGTTAGCAGGAAG | 337867 |
rs556528005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276230 | AATTCAGTTCTGACA[C/G]TTTCTACCTGGAGTT | 337867 |
rs556563451 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221662 | ATTGAGGATGGAAGC[C/T]GATGGATAAAAATGC | 337867 |
rs556563952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205848 | AGCTGCGTGCTCGGT[C/G]GAAGAGGACGACCAT | 337867 |
rs556565179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239826 | ATCTAAACACACGCA[C/T]ACACATAAGAACGTG | 337867 |
rs556565489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248198 | ACTACTCTCCTGATA[C/T]TTCTTGAGTCTTATT | 337867 |
rs556566773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268853 | TGGCATCAGGATGGG[A/G]TGGAGATGGAGATTG | 337867 |
rs556575971 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333655 | CCCTACTTCCCTGCC[A/G]GAATTTGCAGTCCTA | 337867 |
rs556581478 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245686 | TCTCTACTAGAAATA[C/T]AAAAATTAGTTGGGC | 337867 |
rs556601784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240334 | TGAGTATGATTGCAA[C/T]ACATAAATTATTTAA | 337867 |
rs556610656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385129 | TTTTTTGTAAACAGT[C/T]TTGACCTTTGCCACA | 337867 |
rs556641805 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354256 | GTGAGCCGGGTGACA[C/T]GGGGGTGTCAACCCA | 337867 |
rs556653667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269554 | AGTACGTACTTCCAG[A/G]AAGTCTTTATAAATA | 337867 |
rs556683308 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209047 | CCTCTGCTGGCTCTC[A/G]CGCACAGCCTGGCTG | 337867 |
rs556716062 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265598 | CCTTTTCTTCTTCTT[C/G]TTCTCGTTTTGTGTG | 337867 |
rs556726504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373678 | CCTGAAGACAAGTAC[A/G]TGGGAGGTGGGGAGC | 337867 |
rs556728319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366524 | CATGAATATAACAAC[A/G]TATGTATAGTATAAC | 337867 |
rs556750525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331899 | AACATAGGCTGGCAC[A/G]TATTAGCATTGAGTA | 337867 |
rs556769339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212800 | AAGGTCAGCCTATCT[A/G]CAGTTTCATATTCTG | 337867 |
rs556781705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349207 | GTCTCCACAGCTTCA[C/T]GGTGCATGTCTCCCT | 337867 |
rs556785222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384794 | GAGCGTGGCAGTGAC[A/G]CCAGGAGTGTGATGC | 337867 |
rs556800139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358324 | CTTTCTTTTCTAACT[C/G]TGTATCTATGTGGCT | 337867 |
rs556804232 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343142 | GCTGAGCCCAGATGC[C/T]CGTGTCCATCTGATG | 337867 |
rs556807089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377936 | CTCCCTGCCACCCTG[C/T]GCTGGAGTCAGACCT | 337867 |
rs556808595 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312965 | TTTGTTTTGTTTTTT[A/T]TTTTTTTTTGTTTTT | 337867 |
rs556808976 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370929 | AAATCTTCCTATAAC[A/G/T]TGTTTAAAAAATAAG | 337867 |
rs556837899 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275599 | GATGCGATATTTTTT[A/T]TCCCTCTCATATTGA | 337867 |
rs556862832 | in-del | -/CTTTTTTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338047 | TTTTTTTCTTTTTTT[-/CTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 337867 |
rs556877303 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247466 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 337867 |
rs556910404 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278655 | AAATTTGAAGCGATC[A/T]CATTAACATGTTTGG | 337867 |
rs556910603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338115 | CAGGCTGGAGTGCAG[C/T]GGCACAATCTCGACT | 337867 |
rs556911979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364564 | CCTTTTCTGTACTCT[A/G]GAGCAGTTTATATAA | 337867 |
rs556923497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349803 | AGCGTGACCGTTGAA[A/G]CACAGCATCACAGGG | 337867 |
rs556951470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290628 | TGCTCAGGAGGCTGA[A/G]GCAGGTGAATCATTT | 337867 |
rs556955694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330942 | TAAAGGAGGATGGTC[A/C]GCTTGTTAAAATGGA | 337867 |
rs556974713 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312932 | TTGGATACTGGAGCC[C/T]ATGGAAGGAAGGGTT | 337867 |
rs556979613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357824 | ATATCCCAACTAACT[A/G]CAGTCTTGGCTAAGA | 337867 |
rs556980960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343543 | CAGACTCCTCCACTT[C/T]CATAGGATGGTCTCA | 337867 |
rs556999359 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357952 | GGTCGTACAGGAGGC[C/T]AGGTCTACAAACAGG | 337867 |
rs557001856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318280 | TCGAGTGATTCTCCT[C/G]CCTTAGCCTCCAGAG | 337867 |
rs557002651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231964 | ACTGAAGAGCTGGTG[G/T]TGTTTTACCAAATCA | 337867 |
rs557010403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312477 | GAATGTAAGATTTCC[A/G]TCCTGTGATGAGTTC | 337867 |
rs557011299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245143 | CAGGCACCTTCTTTT[C/T]TTAGCTTTGAAAGTT | 337867 |
rs557031085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261781 | CGCCAAGGCAGCAGA[A/T]TGAGCAGAACTCCAT | 337867 |
rs557044130 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343946 | AAGTACTTAGTGCTT[A/T]TTATATGGTAGGCCT | 337867 |
rs557046955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304850 | TTTATCTCCTATTTC[C/T]GACGTGATCTGCTAT | 337867 |
rs557070936 | in-del | -/AATAGC | 0.00398564 | 0.0444627 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304539 | ACCCATTAGTTAAAG[-/AATAGC]AATAGCAACATTGCA | 337867 |
rs557091688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217758 | GCCAGCACTTTAAAA[C/T]TGGCTTATTTCAGAC | 337867 |
rs557112420 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338013 | GAGCTTTAAAAAAAT[C/T]GCAAAAAAATCTCCT | 337867 |
rs557138152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323449 | CTACAAAAAACAAAC[A/C]AACAAACAAACAAAA | 337867 |
rs557162040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330353 | AATCCCAGCTATTCA[C/G]GAGGCTGAGGCAGGA | 337867 |
rs557232055 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215696 | CAAGCCGGCTCTCTG[A/C]GAGCGGGAAACCGCC | 337867 |
rs557248106 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274868 | GATTACAGGTGCGCA[C/T]CACCACTCCCAGCTA | 337867 |
rs557250005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225280 | ATGAAACTCTGTATC[C/T]ATTAAACAACTTCCC | 337867 |
rs557266093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361935 | CGGGAGTTCAGGACT[A/G]CAGTGCGCCATGATT | 337867 |
rs557269225 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293227 | GAAAACTGAACAGAT[A/G]AAAGAATGTTATTCT | 337867 |
rs557269920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281569 | GGAAGGTGAGAACTC[A/G]CATCTACTTTGAGGA | 337867 |
rs557274435 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259915 | TTTCTGAATTGCCAG[A/C]CTCTTAGAGGAGGCA | 337867 |
rs557286111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230413 | GTCAGAGGTTGCAGT[G/T]AGCTGAGATCACGCC | 337867 |
rs557311893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358456 | GAGATTTGCAAAAAT[A/G]GAAAACAGTGCCACT | 337867 |
rs557313248 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309529 | ACAAACCTTGTTTTT[A/G]TTGCTGTTGAAAGTT | 337867 |
rs557333773 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282269 | TCATGACATGCATGA[C/T]GCTGGGTGGTAGATA | 337867 |
rs557358563 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261201 | CATGTATCCCAGCAG[A/G]GGGACAGTCAGCACA | 337867 |
rs557374996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359052 | ACATGGAACCTTCAA[A/G]AACACCCGTGTCTGA | 337867 |
rs557417528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204043 | TGTCACTCAGCTCTA[C/T]GTTGAGTAATATGTG | 337867 |
rs557473081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383650 | AGTCCCCGTGCTAAG[A/G]GTTGAAAGCAACGTT | 337867 |
rs557484734 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310026 | GTAGATGCTCAGTAA[A/C]TATTAGTGATTTTAA | 337867 |
rs557509665 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335190 | ACCGAAAAATAAAAA[A/T]GTTTAATTTTGTACT | 337867 |
rs557534956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239478 | CAGAACAACTGAGTC[A/C]CAGAGTCTGGTGGTG | 337867 |
rs557535055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215887 | TTACTATTCCTGATC[A/G]GATCAAAGAGAAAAT | 337867 |
rs557578962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274075 | AACAGAATGTGACCC[A/C]CTCCCTAAAAGGTCC | 337867 |
rs557581669 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364627 | ACCTGTAGGTTTTTG[G/T]TGGGTAGATTTTTAA | 337867 |
rs557583394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370208 | AAGGAAAACGGCACC[A/G]TGATGTGTGCAACCT | 337867 |
rs557612989 | in-del | -/A | 0.226779 | 0.248919 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324411 | GTCCCCTTTGCCATG[-/A]GAAAAGCAGGGCCCG | 337867 |
rs557621763 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231831 | ACATACTTTACTGTC[G/T]GTGCATGAATGGAAT | 337867 |
rs557622451 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213655 | ATTAGTCACTGCACC[A/C]GGTCGATTATAACAT | 337867 |
rs557622748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232799 | AAAAAAAACCTGGCC[A/G]GTCATGGGGCCTTGC | 337867 |
rs557625617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316646 | GAGAAAACACACAGA[C/T]ACTGTGAAGACATAG | 337867 |
rs557647328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365746 | TCTAAATATTAAATG[C/T]AAGGTATATATGTCC | 337867 |
rs557659167 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264450 | TATAGCTTGTGTAAA[G/T]TGCATGCTGTAGACA | 337867 |
rs557660244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356009 | CTGCTGTTGAAACCA[A/G]CTGAACCTGTTTGTA | 337867 |
rs557700228 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204964 | GCTGGAGTGCAGCGG[G/T]GTGATCTCAGCTCAC | 337867 |
rs557744147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324943 | TAAGTACACTCTGTA[A/T]TGTTCACACGATGAC | 337867 |
rs557755558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344312 | CATATACCTCCCAAT[A/G]TGAGAGCTCCTTGGT | 337867 |
rs557755579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337456 | TTTCTTTCTAAACAG[A/T]CTGTATTTTATCCCT | 337867 |
rs557761563 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334370 | TAACCTTGTCAGTAG[A/G]TTCTTGGAAATTCCA | 337867 |
rs557789674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313015 | GAGACGGAGTCTCGC[C/T]CTGTCGCCCAGGCTG | 337867 |
rs557792800 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365839 | AGTTATATGCTGAAA[A/G]TTAAATATATGTCTG | 337867 |
rs557795778 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233921 | TGCTGGTACCACTTG[A/C]GTTCTCAAGACTAGT | 337867 |
rs557797563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226924 | CACCCCTTGGCTGGG[C/T]GCGGTGGCTCATGCC | 337867 |
rs557825402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305647 | ATTAACTGACTGGTC[A/G]TGGTACTAATTAGCT | 337867 |
rs557829484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219435 | ACCACAATTTAATTG[C/T]AGAACATTTTATCAC | 337867 |
rs557830291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350824 | GCAGTCTTGTGGGAG[A/T]GGGCCCTTAACCTGT | 337867 |
rs557877437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313682 | GGGCCAGAGGTGAAC[C/T]GTGCCAGTGCCATGG | 337867 |
rs557881575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212944 | AAAAGTTCAAAAATT[A/T]TACAAATATTTTATG | 337867 |
rs557885215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304642 | ATTACTAAGCAGAGA[C/G]TGTGTTCCAGGCACT | 337867 |
rs557893754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213234 | TCAATTTTTTTTTTT[A/T]ATTTAAGATGGGATT | 337867 |
rs557895754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205867 | GAGGACGACCATCCC[C/T]GATAGAGGAGGACCG | 337867 |
rs557898942 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361709 | TACCTACTAAATGCC[A/G]ACAGCACCACCATCC | 337867 |
rs557913294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99254151 | TATCTTCAACCACAT[A/G]AGAAGAGCAAACTGT | 337867 |
rs557917091 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277381 | AAATACAAAATTAGC[C/T]GAGCATGGTGGCACA | 337867 |
rs557923501 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371762 | ATTTGAGTTTTTTCT[C/G]CTGTAAACAGATACT | 337867 |
rs557929782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317352 | TTCAGAGTCCTTATG[A/T]TTTTTTTTTAATTAC | 337867 |
rs558003682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276244 | ACTTTCTACCTGGAG[G/T]TAGTATCAGATCCTA | 337867 |
rs558016853 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340878 | CTGTTTTTATAATCT[A/T]GTAAAAGCCACAGTG | 337867 |
rs558017715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311400 | TTCAGGGCCTGGGAC[A/G]TCTTTGTCATGACTG | 337867 |
rs558026749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226234 | CTTGTAGGTAGGAAA[A/G]ACAACATGTCAGTAA | 337867 |
rs558026760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342624 | GCGCTGGGTTATCTG[A/G]TGATGGAGCCACAGT | 337867 |
rs558034346 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323932 | AGATAGAATTGCCTT[A/G]TAAAATTTATAAAAA | 337867 |
rs558039863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210768 | AGGCTTGAACCACCA[C/T]GCCTGACCTATTTTT | 337867 |
rs558051176 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289080 | TTCACTGACAAGACA[A/G]TTGAAGTCTAGAAAG | 337867 |
rs558054220 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307723 | CCAAAAAAAAGACCA[A/T]GTTACTGATGATTTT | 337867 |
rs558090773 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322175 | ACTGTTCTTCTAGAT[G/T]TCTGGTGAGAGACCT | 337867 |
rs558092350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253553 | GAGTCTCGCTTTGTC[A/T]CCCAGGCTGGAGTGC | 337867 |
rs558107667 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288750 | AGTACCAAGCAAGTA[G/T]TAGTTATCTGTTGCT | 337867 |
rs558143944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261649 | CAAGTTGAATCCATA[C/T]CTAACCATATATAAG | 337867 |
rs558163095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285903 | GTTCTACACATCCAA[C/T]GGGGTGCCAGAGTTC | 337867 |
rs558163257 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216842 | CTTTTTTCTTTTTTT[A/T]TTTTTGAGACGAAGT | 337867 |
rs558184820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383667 | TTGAAAGCAACGTTC[C/T]GGGGAGGAGCACGCT | 337867 |
rs558226171 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327045 | TTCGTAATATGAAGA[A/G]TGTGGCCTATAGCTA | 337867 |
rs558245225 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281163 | CATGGTACTCCAGCC[G/T]GGGTGACAGAGCGAG | 337867 |
rs558246742 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299720 | TTCCTTTTTCAGATT[G/T]CTGCATTGACTTACT | 337867 |
rs558283188 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259040 | CTTTTGCATAAAAAT[G/T]TCTGCAAATCTTAGC | 337867 |
rs558288474 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284680 | AAAATTCTAGTCCAT[C/T]GTCTGGTTCAGTATT | 337867 |
rs558325585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290741 | ACCAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 337867 |
rs558345369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330057 | CAATGTACAGGTCTT[A/G]CACATCTTTCATTAG | 337867 |
rs558351189 | in-del | -/TCTGTTTCTGTCAAAACAT | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355145 | ATTAGGAGTTTCACC[-/TCTGTTTCTGTCAAAACAT]TTACTGTAACAAGTA | 337867 |
rs558362629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216303 | AGAAACAGGTTTTCA[C/T]CATGTTGGCCAGGCT | 337867 |
rs558368853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99356938 | TTTTGGGCTTTGTTT[A/G]GTTTTTCCCCAGTTT | 337867 |
rs558371635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282253 | CACCCATGATGGAGA[A/G]TCATGACATGCATGA | 337867 |
rs558382187 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267379 | ATTTTAGGCTTGCTC[A/G]TTTATCATATTTTGA | 337867 |
rs558426847 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268061 | GCATGCAGGAGGAGG[G/T]ATTGCCTTTCCCCAG | 337867 |
rs558462208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287677 | TTTGGTAGAGACGAG[A/G]TTTCGCCATGTTGCC | 337867 |
rs558489626 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351375 | TACAATCTGAAGCTA[-/G]GAACAGGTTTTACAT | 337867 |
rs558492214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357411 | TTAGTTTTTAATGTA[C/T]GTTTGTTTTGTTATC | 337867 |
rs558507587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361416 | TTTAAGCACTTTTCT[A/G]CTATCACAGGAGTAG | 337867 |
rs558520152 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349634 | TTAGGTAGCCGAAGC[G/T]GAGAGAGAGAAGGCA | 337867 |
rs558549662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252195 | CTTGCTTTCTGCTTC[C/G]TCTTGCCCTTTGGCA | 337867 |
rs558556972 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348828 | CCAGCCTGGGCAACA[C/T]AGTGAGACCTCTTCT | 337867 |
rs558561466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329653 | GCAGACCTGTGGAGA[C/G]GTCCACATGGCCAAC | 337867 |
rs558569842 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99354079 | GGATGCAGGCAGATC[A/G]TGGGTTTAGGATGGG | 337867 |
rs558591621 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229967 | AGTATCTATCTTAAA[C/T]CTTGTGAATTGTCAT | 337867 |
rs558631036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274885 | ACCACTCCCAGCTAA[C/T]TTTTGTATTCTTTGT | 337867 |
rs558649265 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99258508 | TCCCCTTGAAATGAT[A/G]GCATATATTTAAGAT | 337867 |
rs558649413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266313 | GCCACATTGGGAGAA[C/T]TGTCTTGGGCCACAC | 337867 |
rs558649650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224494 | GGATTTATCTACGTC[C/G]CATTTCAGTTCTATT | 337867 |
rs558691330 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213519 | GCACCTGCCATCATG[C/T]CCAGCTAATTTTTGT | 337867 |
rs558702461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348917 | ACTCAGGAGGCTGAG[A/T]TGGAACGATCACTTG | 337867 |
rs558706002 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370423 | AAACTACAACCTTTT[C/G]AAAATCTATAAAAGA | 337867 |
rs558716257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231087 | GCATAGAATCCAGCT[A/G]GATATCTTAGGTAGT | 337867 |
rs558718967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273707 | TCCATTTGGGTTGTA[C/T]ACTTGGTGTGGGCCC | 337867 |
rs558730705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302691 | ACAGTGGGAAACATG[C/G]ATTCCTGGTGTGCAA | 337867 |
rs558735994 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215841 | ATCTACTCCTTCATC[A/G]CACCGTGATTCAAAC | 337867 |
rs558758920 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209140 | GCTCTCTAGATTTCC[C/G]AGGTTGGAGATCCAC | 337867 |
rs558776249 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265110 | GGTAATAAAACTGCA[C/T]TGATTTTGGTTACTC | 337867 |
rs558779182 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367877 | CAGTCTGAGCCAGCA[A/G]CGCCCCCTCTAGAAG | 337867 |
rs558784754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348318 | CACTAGGTTTCTACA[G/T]GAGTCTGTGCAAAGA | 337867 |
rs558807681 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275195 | GATTCTGGCCTAGAG[C/G/T]CTCTCATGTGGTTGT | 337867 |
rs558812846 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244121 | AAGAAAATTTTAAAA[C/T]GTAAGACATTAGCAT | 337867 |
rs558815186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301840 | ACCTTTACCATATTC[A/G]GGGATTTAGTTGGTG | 337867 |
rs558838656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342982 | CATTTGGCTGTTTTC[A/C]CCTCTGTCACTTGGT | 337867 |
rs558840211 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368431 | GTAACGTTTGTACCG[G/T]ATATACCCTCAGTCT | 337867 |
rs558902283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343379 | CACGGTGTCTTTCCC[C/T]CCAGATACTTGGAAC | 337867 |
rs558910812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273238 | GTTTCTTTTTTGTTG[C/T]GACTGTGTTCTAAGG | 337867 |
rs558915958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274944 | GCTGGTCTCAAACTC[C/T]TGTGCTCAAGCAGTC | 337867 |
rs558925066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327345 | GATTACTGGTAGATT[A/T]TCATGTCCGTTGCAG | 337867 |
rs558926600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222587 | TATGGATTGATGACA[A/G]ATTGGTTTCATAGAA | 337867 |
rs558943071 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372401 | GAAAATGAAGGATGA[C/T]GGACCAGCTAAGGGA | 337867 |
rs558948202 | in-del | -/CTCACTGCAAGCTCCGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292207 | GTGGTGCAATCTCTG[-/CTCACTGCAAGCTCCGT]CTCCCAGGTTCACGC | 337867 |
rs558956394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322476 | AAAGAGCCTTCTTTT[A/G]CCAATTTTCTTTTTA | 337867 |
rs558977953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228694 | AGGCTGAAATGGCTC[A/G]AGAAAGGATTTAGGT | 337867 |
rs558992757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315553 | AGTCTTTGGAGCCAG[A/G]TTGTTGAATTTCGGT | 337867 |
rs559017916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310945 | AGGGTTCTATAATCA[C/G]CAAGAGAGCAGGCCA | 337867 |
rs559039544 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267586 | AGGAAGAAACTAGCT[C/G]TGTTCCAGAGTCTGC | 337867 |
rs559058750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323512 | GGGACTTGTGAAAGG[A/T]CCACATGTAGAAGTT | 337867 |
rs559059781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303475 | TTGGTGGCTTTTATA[C/T]TGAAAAGTATGGAAG | 337867 |
rs559073941 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239279 | TTTAGTTATTTATCC[A/G]TATTACTGATTTGTC | 337867 |
rs559093597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316932 | GTCTGTTATTCTTTC[C/T]ATTTTTAGAAGAAAA | 337867 |
rs559100221 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381080 | GAACTCAGAAGGAAG[G/T]CTCGTGTACATAGAA | 337867 |
rs559105580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280491 | AACCCTGCTCCAGCC[A/G]GAGTTGGAATTAACC | 337867 |
rs559132194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375868 | GAGTGCAGTGGTGCT[A/G]TCATGGCTCACCGCA | 337867 |
rs559133442 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289874 | TGCCACTCCCTCTCA[C/T]CTCGGGCTGGAAGTG | 337867 |
rs559161238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375183 | TGCTCCATACAAGAC[C/T]CTGACGAGGCTCTAG | 337867 |
rs559165766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290344 | AAAGGCTAAAGTTTC[C/T]GACTCTCATCAAGAG | 337867 |
rs559171340 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285928 | GAGTTCACAGTTCAA[C/T]TCCCTGAAACTCCCT | 337867 |
rs559198018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210146 | CCTAGCATTTCATTT[A/C]ATTTATTCGTCTTTT | 337867 |
rs559203314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280201 | CTATGGCTTCCTCCT[C/G]CTGTTTTATAAAGTT | 337867 |
rs559244280 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244089 | GTATCTGATTTGAGG[A/C]ACATGGACATTAACC | 337867 |
rs559266918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287765 | GCTGGGATTATAGGC[A/G]TGAGCCACCACGTGC | 337867 |
rs559270575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316327 | GTCTGTCCTCCACCT[G/T]CCTCCCTCCCCTCCA | 337867 |
rs559286899 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314623 | CAAATAAAGCTCTGA[A/G]GAAGAAACCCGGTGT | 337867 |
rs559294932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266870 | TTTCAGTTCTTTTGG[C/G]TTATATCCCTGAAAG | 337867 |
rs559303989 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282727 | CTGTTCTTGTTTATC[A/G]CTGGAAAGTTGCACC | 337867 |
rs559355678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250981 | GTCTCGATCTCCTGA[C/T]CTCGTGATCAGCCTG | 337867 |
rs559386921 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355655 | ACCTCTGGTCCTGAC[A/G]GTCCCTGGAGGAAAA | 337867 |
rs559391571 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322564 | CAGGCCTATATTCCT[C/T]AGACTTCTCCCTTCA | 337867 |
rs559414774 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230524 | CTACAGTTTGGAGGC[C/T]AGAAGTCCAAAATGG | 337867 |
rs559459161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236267 | TCAACAAAGAGATAA[A/C]CCACAGAATGGGAGA | 337867 |
rs559467671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286976 | ATGTAACAAGAGTAA[C/G]GGCATGTGTTAGAGA | 337867 |
rs559467810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375480 | CTCCCCCAACAGGGT[A/G]TGCATGCTACCCTGC | 337867 |
rs559518720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360987 | TTCTGGCTTCTCTAA[C/T]GTAGACACTGCCTGA | 337867 |
rs559548156 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266087 | TTAGTGGGTCTTGGA[A/G]CTCTTCACCTTTACC | 337867 |
rs559556397 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335762 | TCTCTCTCTCATGCA[A/G]GGCTGCAGTGGAATG | 337867 |
rs559572003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361543 | CCTGGAGTGGGTGTG[C/T]TGTGTGCCTTTGCAT | 337867 |
rs559572203 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368153 | CTTGTTTTAGATGCT[C/T]TTACACTTCATATAT | 337867 |
rs559574213 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339188 | CTCGGGCTGCGCAGC[A/G]TCTGCTGCTTTCTCT | 337867 |
rs559582667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323105 | GCCGCCTTTGCTTGT[A/G]CCCAGCTCTCTCTTC | 337867 |
rs559603314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274368 | ATAGGGTCTTGCTCT[A/G]TTGCCCAGGCTGGAG | 337867 |
rs559603910 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344755 | CAGGTGCTCGCTGCC[A/G]CCCCCTGCCACGTGC | 337867 |
rs559634925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362091 | ATTTTATTTATATTA[G/T]TTACATAAACTACAT | 337867 |
rs559635351 | snp | A/G | 1.65247e-05 | 0.00287438 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295666 | TGGGAGTGTCTGAGC[A/G]AATACTAGAATCCAG | 337867 |
rs559669189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221277 | TTGCAACCTCCACAA[A/G]CTGCAGTCTTTTTAT | 337867 |
rs559672359 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229995 | CATACACCTTTCTGA[G/T]TTTGGCTGAGTTTCC | 337867 |
rs559679629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348444 | GTTTCAGTCACGGGG[G/T]GCCTTATGAAAAAAC | 337867 |
rs559680329 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237654 | TAAAGAAAAGAGAGA[G/T]ATTTAAGATAATTAC | 337867 |
rs559685194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333548 | TTCTAAGTGCAGAGG[A/C]CAAGTAGTGATCAAA | 337867 |
rs559712534 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386980 | GTAAAACCAAACCAG[A/T]GGCAAAGGTATCCCT | 337867 |
rs559717055 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240137 | TTTATTTTGTAAGTT[C/G]TGAACCTCCAGATTT | 337867 |
rs559742056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342619 | TGCCAGCGCTGGGTT[A/G]TCTGGTGATGGAGCC | 337867 |
rs559743987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334186 | GGCTGGTCTTGAACT[C/T]CTGGCCTCTAGTGAT | 337867 |
rs559769183 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386311 | GAGCATGAAAAGACC[C/T]GAAGCAAGTTGACTC | 337867 |
rs559793904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315627 | TTCTGAGCCCCCATT[G/T]CCCCATCTATCAAAT | 337867 |
rs559800420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228395 | TGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCCTC | 337867 |
rs559803764 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301965 | GCTTACCTAGGAATT[A/C]TGTTTAATTGTAGCC | 337867 |
rs559812236 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348074 | CAGAGTCATTTTGCT[A/C]CTTGCAGCTGTGATC | 337867 |
rs559812537 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219810 | CATATAAGTGGAGTC[A/G]TATAGTACATAACTT | 337867 |
rs559815446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201905 | TGAAACCCCGTCTCT[A/C]TACTAAAAACACAAA | 337867 |
rs559821714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243517 | TTCATTCTAGTTTAC[A/G]TATATAATTTTAAAA | 337867 |
rs559826640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301228 | GGGCATGGATAATGA[C/G]TGGGCCACAGGAAGC | 337867 |
rs559850679 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275897 | GTCAGGATCTGTGCA[A/T]TTGTTTCTTCCCTGC | 337867 |
rs559857277 | in-del | -/GGCTGGCCGGGCGGGG | 0.0170251 | 0.090679 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242664 | CCTCCCGGACGGGGC[-/GGCTGGCCGGGCGGGG]GGCTGACCCCCCCCA | 337867 |
rs559879014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202701 | GGGAGAGGCGTAGGT[C/T]TGGAGCCCCTCTGCA | 337867 |
rs559890109 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272682 | ACTTTGGTCTCTCTT[A/C]CTCCTCTTACAAGGG | 337867 |
rs559904169 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210858 | CTCAGGTGATCCACC[C/T]ACCTCGGCCTCACAA | 337867 |
rs559936964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221987 | CAGTTTTGTCTTCTG[C/T]ATAAATCTGAGAAGA | 337867 |
rs559939276 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307499 | GTGACTGAGCATGTA[A/G]TGAGCAGTTAGCCTC | 337867 |
rs559939768 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326770 | ACCTTACACTGCACA[G/T]CTCAAGGCTCTCATC | 337867 |
rs559956037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340120 | ATAAAAAACAATTTT[A/G]TTTTACTAAGTTCAA | 337867 |
rs559962046 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352817 | GGAGAAATGTGTAGT[A/G]CAGTCAGGAAGAGTC | 337867 |
rs559962081 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358385 | GTAACAGAACAAAAT[C/T]GAATGCAGAAGCAGA | 337867 |
rs559996885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272065 | GGAATATTTTTAGTC[C/T]TCTCTCTAAAAGACA | 337867 |
rs560006354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207411 | CCATCCAACAACTCT[A/G]TCATGTACCTTCCCA | 337867 |
rs560006493 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200721 | TTCCCCGGCAGGAAG[A/G]AGGGCGCTGACCCAG | 337867 |
rs560019676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341235 | GGCTCCCCATTTTTC[A/G]CCTCCACCTTCTTTA | 337867 |
rs560021528 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201069 | CTCCAGACCCGCGTC[C/G]GAACCCTGCTAGTTC | 337867 |
rs560057755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241811 | GCAGGGTCATAGGAC[A/G]ATAGTGGAGGGAAGG | 337867 |
rs560067367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346515 | TGCCTCACCGGGTTA[C/T]TCACAGTTAACTGCT | 337867 |
rs560089024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308457 | GTAAGAAGTTACTGG[A/G]CATAGCTTTTGGATC | 337867 |
rs560105762 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208172 | CTGGCTAATTTTGTA[G/T]TTTTAGTAGAGACGG | 337867 |
rs560124955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248488 | CCTCTGCCTCCCTGG[G/T]TCAAGCGATTCTTCT | 337867 |
rs560126028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309056 | TAAAACATTTTTATA[C/T]AGTGAAGGACTCAGC | 337867 |
rs560201840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380559 | TTGGCTAACTTGCAC[A/G]GCTGTGAGCACTGCA | 337867 |
rs560212689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240942 | ATGACTTTACAAACT[A/T]TAGTTTCTCTGTGCC | 337867 |
rs560213205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313885 | AGTGGTTTCAGGAGG[A/G]TCAATAAGGATAGAA | 337867 |
rs560249551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306351 | TTGGCAGTAGTAATA[C/T]TCCCCATTTTACAGG | 337867 |
rs560259655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278305 | TAATACATGTGGCAA[C/T]AGAGTTGGTACCAGG | 337867 |
rs560261048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319083 | GGTGGGTTGGACCTG[A/G]CCAAAGTCTCATCAT | 337867 |
rs560271121 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370727 | AGAAACCACTGTCAC[A/G]TGCCCATTGACTTGA | 337867 |
rs560273375 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198872 | TGGAAAATCCAGTTA[C/T]GTAGCTCTGTACAGT | 337867 |
rs560325932 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322676 | GCAGCCTTAGTGTGG[-/A]AAAAAAACAATCTGT | 337867 |
rs560332187 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291835 | AGGGCTTTAGAATTT[C/T]ATTAGTAATAATACA | 337867 |
rs560338403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347148 | TCTACGGATACTCTT[G/T]AGAGAACAGTAGAAA | 337867 |
rs560352989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300233 | TCCTTAACTGACGAC[C/T]GTTGTGCACTGGAGG | 337867 |
rs560462284 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379713 | TATCCTTCTGTTTCT[A/T]CAGATCCTATATGGT | 337867 |
rs560477714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380265 | CTGACTGCACGTCTG[C/T]GCAGGCCTCAATTTC | 337867 |
rs560492515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227427 | GTGAAAAGAACAAGA[A/G]TGATTCCCTGGCTCT | 337867 |
rs560511072 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268919 | TACCCCAGAGAGAAG[-/A]AACTGGGGCAGAACT | 337867 |
rs560517982 | in-del | -/ACACACACACAC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237267 | CGTATATATATATAT[-/ACACACACACAC]ATATACACACACACA | 337867 |
rs560520911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378587 | CTTACTGACAGACTC[A/G]AAGGTATATTTTTTA | 337867 |
rs560521784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277467 | GAGGCGGAGGTTACA[A/G]TGAGCCGAGATCACA | 337867 |
rs560528654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347138 | AAAAAAAAGATCTAC[A/G]GATACTCTTGAGAGA | 337867 |
rs560543266 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263139 | CGTTTTAGTAATTTT[C/T]GTTGAAGTTGGCCCT | 337867 |
rs560546558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319607 | GGCTCCAAGTCACTT[A/T]GTTTTCTCCTCCCTA | 337867 |
rs560579799 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373050 | GGTGTGAACCCGAGA[A/G]GCAGAGCTTGCAGTG | 337867 |
rs560586400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350002 | AAGGAGCCCTCATGC[C/T]GGCGTGACAGAGGGC | 337867 |
rs560586877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372631 | GGCTCTGAGTCTAAA[G/T]GGAAAATGGGTGGCA | 337867 |
rs560588040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219828 | TAGTACATAACTTTA[C/T]ATGACTGGCTTTTTT | 337867 |
rs560591737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328089 | AATTTCATATACTTA[A/G]TATTGTATAATATGA | 337867 |
rs560604568 | in-del | -/ATTT | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328172 | TAAAATTAATTTTTC[-/ATTT]ATTATTGTATTAAGT | 337867 |
rs560609304 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325160 | CAGGCTGGAGTGCTG[G/T]GGCGCGATCTTGGTT | 337867 |
rs560627859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331386 | GATGCATGATTTCCC[A/T]AAAGGAAAAGCCTAG | 337867 |
rs560633767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339176 | GACACTCCCAAGCTC[A/G]GGCTGCGCAGCATCT | 337867 |
rs560637939 | in-del | -/AC | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280636 | AAAGAGCAGGATCTT[-/AC]TCTCTCTTACAGCTC | 337867 |
rs560638750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222079 | ATAGTTACTGAAAGG[C/T]AACTGTGTGCTAAGT | 337867 |
rs560651352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213568 | TTTTACCATGTTGGC[C/T]AGGCTGGTCTTGAAC | 337867 |
rs560671439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214877 | GCTGTCATGCTTGTT[C/T]GGTGGCATTTGCACC | 337867 |
rs560692406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247565 | CACAGGGAGGGGAAC[A/G]TCACACACTGGGGCT | 337867 |
rs560694817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332078 | CTGGGAAAGCAGCCC[C/T]TAGGTTTGTCCTGTT | 337867 |
rs560708520 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199735 | CCATACATATACACA[C/T]TGTGCAACCATCTAA | 337867 |
rs560739128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372170 | TAGCTAGACAGTCAG[A/G]ATGGCAACAGCGATC | 337867 |
rs560750084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233219 | CCGGGTTCAAGTGAT[C/T]CTCCTGCCTCAGCCT | 337867 |
rs560772661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300971 | AGCAGCTTCTGACAT[A/G]TTATTTAAGATATAT | 337867 |
rs560785781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324767 | GGTGGCCCTGTGGAT[C/T]CTAATGGAGCATAGG | 337867 |
rs560794667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365984 | CCTTTTTTTGCCTTC[A/G]AGGTCTATTTATTTG | 337867 |
rs560804991 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378784 | TGTGGCATCCTTCAC[A/G]CTAAACGCCTGTTGA | 337867 |
rs560817967 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241365 | AATGTCTATTAACAG[A/T]TACATGGATAAACAA | 337867 |
rs560820131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265425 | ACTGTGTTGGCTTAC[A/G]TCTTTCTGCCTCTGG | 337867 |
rs560820628 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300373 | CTTGAAGGATGATTC[C/T]GCTAGCTGGCCCTAA | 337867 |
rs560855955 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217019 | TATTTTTAGTAGAAA[C/T]GGGGTTTCACCATGT | 337867 |
rs560865498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373176 | CTTTTTTATTGTTTT[G/T]TTTTTTTTTTTTAAA | 337867 |
rs560876394 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385990 | ATCCAGAGTTAGCCA[C/T]TAGGCTGCGGGTGAA | 337867 |
rs560909325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341375 | AAATCAGGTTTGAGG[C/T]CCTTAGAGTCCCATT | 337867 |
rs560948352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293182 | TAAAATCATTTATAT[A/G]GATTTGTGGTATAGT | 337867 |
rs560949912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306510 | AAAAACAAAATACCA[C/T]GCCCCCCTCCCCCAA | 337867 |
rs560952121 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324438 | CCCGGAGAGGGGCAG[A/C]TCCTCAGACTCCAGA | 337867 |
rs560967129 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273459 | TTAAACTCTCAGAAA[C/T]TAGCAGTATTGAGAG | 337867 |
rs561002651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234837 | GTGCATTTTGATTAA[A/G]TGACATACTTGGGGG | 337867 |
rs561042677 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327768 | CCTCTTATAAAATTT[A/G]AAAGATTTATGTATC | 337867 |
rs561044126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307605 | TATCCAAAAGCCCCT[G/T]GGAATTTATGAATTG | 337867 |
rs561045340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347689 | ACTGAGACATGAGAC[C/G]TAGGTGCTGACAGGG | 337867 |
rs561047222 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286607 | GCCCATCACCCAGGT[A/G]GTGACCATAGTACCC | 337867 |
rs561071569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361598 | TACTTATCAGGGTTT[C/G]TCAACCTAAACACCA | 337867 |
rs561073704 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242881 | CCAGACGGGGCGGCG[A/G]GGCAGAGGTGCTCCC | 337867 |
rs561080581 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211775 | CCGTGTGTCTCCCAA[C/T]CACTGGGATCGTCTC | 337867 |
rs561101488 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341469 | GAGTCTACAAGAGAA[A/G]TAGAGAAGCAAAAGT | 337867 |
rs561105465 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241944 | GGTGATGACTCTTAA[G/T]GAGCATGCTGCCTTC | 337867 |
rs561151086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256165 | AAATATTTACTGAAT[A/T]GATGAATAAATGAAG | 337867 |
rs561153784 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373243 | TTAACAAATGATTAA[A/T]TTTTTCTCATATTTG | 337867 |
rs561154138 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386339 | CTCTTGCAATGTGCA[A/G]CTGTTATGTTCTGCA | 337867 |
rs561182815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341875 | AAGAAGTAGGGGATG[A/G]TTCTGATGTTTCTGG | 337867 |
rs561187582 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238873 | CCAGTAGGCATACTT[A/G]GCTTTGCCAAAACCT | 337867 |
rs561196951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99293939 | AAATTGGTGTCATTG[C/T]CAACAGAGAATACTG | 337867 |
rs561224358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206959 | CTCCAATCCAGAAGA[A/C]TGAAGCAGCCTTCTC | 337867 |
rs561241061 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343925 | TTCATTTACTTTTCA[A/G]CAAATAAGTACTTAG | 337867 |
rs561266974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352767 | CTTAGAGTAGAAAGC[A/G]TCAGTTACAGTGAAA | 337867 |
rs561286219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286083 | GTGTTCCAGGAGTCT[A/G]TTCCTGGAGGCGCTG | 337867 |
rs561287893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233266 | TGCAGGCACGCACCA[C/T]CATGCCCAGCTAATT | 337867 |
rs561303422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220874 | CTAATTGTCAAAATC[A/G]ATTTTTTTTTGGTAA | 337867 |
rs561306234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320588 | CATAATTAGATGACT[A/G]TTTATTTAAAATAAT | 337867 |
rs561321945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353467 | TTTCCATCCTGCCTT[C/G]GTGTCTTCATGAGAA | 337867 |
rs561331528 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301146 | AAAAGATGCACGTGG[C/T]CCCTCAGCCGTCCTT | 337867 |
rs561342719 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314563 | CAATCAAAAAGTAGA[A/C]AGTAGAAAATCAGTG | 337867 |
rs561359109 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382458 | ACACATATGCACACT[A/G]CTAATGCATTCCTCT | 337867 |
rs561369923 | in-del | -/T | 0.424348 | 0.179172 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325099 | TTAGTGTCTATGCTC[-/T]TTTTTTTTTTTTTTT | 337867 |
rs561383788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214210 | TCATTTTTTGCCTTG[G/T]CATCTTTGGTTTGTT | 337867 |
rs561418566 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297685 | TTATCCAGAAAAGAG[A/G]CAATGGGAAAAAAAC | 337867 |
rs561423242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325215 | TCACACCATTCTCCT[A/G]CCTCAGCCTCCCAAG | 337867 |
rs561447123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207482 | TCCCTTATTTTTTCC[C/T]TGTTCTCATCTCCCT | 337867 |
rs561467350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227194 | CAAGAGCGAAACTCC[A/G]TCTCAAAAAAAAAAA | 337867 |
rs561476789 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235454 | TTATATGGAAACACA[A/G]AAGATTCTGAGTAGC | 337867 |
rs561497003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240624 | CCTTGGCAGTTTCCT[A/G]TGTGCTCTCGTGTAC | 337867 |
rs561509646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325604 | GTTTATAATTGTTGA[C/T]TATAGGTATGGGGTT | 337867 |
rs561510999 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345651 | CTCCCTCTCTCCTGG[A/G/T]GCTCCAGACCGAAAT | 337867 |
rs561518677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226354 | CATGCACCCGGTTAG[G/T]CAGCATATCCTGCCT | 337867 |
rs561535447 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202272 | AATTAATTTGATTTA[C/T]GGCATCTTTCATGGA | 337867 |
rs561540320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358106 | AGCACGCAGAGGAGT[A/G]CAGGGTGGTGAGAGC | 337867 |
rs561547477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384906 | TGAGTCGTGTGTCCT[C/T]GCAGTGAGCCTGGGC | 337867 |
rs561552285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227566 | GTGTTTGGGAAGAGA[C/T]GGGAAATATGTGGTG | 337867 |
rs561556476 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346606 | AACTTCCCTGTACCA[A/G]CCCCTTCACCCCACC | 337867 |
rs561572483 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383979 | TCCAGAGTTAGCCAC[G/T]AGGCTGCGGGTGAAG | 337867 |
rs561593304 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227198 | GCGAAACTCCATCTC[-/A]AAAAAAAAAAAAACA | 337867 |
rs561593315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219922 | TATGACTGAATAATA[C/T]TCTATTGTATGGATA | 337867 |
rs561605380 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351081 | AGAATGGGCAGTTAG[A/G]GACTCAATCCTGGGT | 337867 |
rs561615127 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325354 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAATTGC | 337867 |
rs561644669 | in-del | -/ATTTTTGT | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213527 | CATCATGCCCAGCTA[-/ATTTTTGT]ATTTTTGTAGAGACA | 337867 |
rs561683980 | in-del | -/T | 0.310853 | 0.242481 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314263 | TTCTTTAACCAGATC[-/T]TTTTTTTTTTTTTTT | 337867 |
rs561691162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298607 | GTTTGTCCAAAGCAA[A/G]TGGAAGAAAACAATA | 337867 |
rs561693385 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199465 | AAAGAAGCAAATAAA[A/G]GTCATACTTTTGCCT | 337867 |
rs561703129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318476 | CCGGCTCTCAACATT[C/G]TTTTAACCCATGGCA | 337867 |
rs561719380 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359906 | TTGTAGACTGGAGGT[A/G]CCCCTGCTGTGTGCT | 337867 |
rs561723947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269105 | TGATCTCCCTTGGGA[C/G]CTGCTGAATTTGACA | 337867 |
rs561742023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312574 | TGACATCCTTGGCAC[A/G]CATTTGATTCACTGA | 337867 |
rs561748998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205948 | AAACAAGCTCTCAAG[A/G]TAGAAGGATTCTAAA | 337867 |
rs561755840 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199951 | CCCATCTTCCTCCCC[A/C]CTAACTCTCCTCTGT | 337867 |
rs561764717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261991 | AAATAAACAATTCAT[A/C]AGTTTTCTGTTGCAT | 337867 |
rs561790454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324319 | CTTACACTAGCCACT[A/G]AAATATGAACAGCAG | 337867 |
rs561833807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225576 | TGCCAGTGGACACTT[A/G]GGTTCCTCCCGCCAG | 337867 |
rs561962293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305209 | TTTGCAGAGATTTAA[C/T]AAAATATTTTTATTC | 337867 |
rs561963156 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310433 | GGCTTCCAGAAGGTA[G/T]TTCTTCACAGTATGA | 337867 |
rs561970634 | snp | A/G | 6.74923e-05 | 0.00580875 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385360 | GCCAACACTGGGACC[A/G]GACCGGCAGCCGAGT | 337867 |
rs561971557 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204446 | CTGGAGTGAGCAGTT[C/G/T]GTAAGAGATGTGTGG | 337867 |
rs561996971 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297842 | GCTGTTTGCTGCTTA[C/G]AAGAGATACAGCTCA | 337867 |
rs561998832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305748 | GTGAGTGAACATTTT[A/G]TGGAGTAGCATATTC | 337867 |
rs561999517 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283769 | AGACTGAGTCTTGCT[C/G]TTTTACCCAGGCCAG | 337867 |
rs562014073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371779 | TGTAAACAGATACTT[C/T]AGGAATTTAGTGAGA | 337867 |
rs562045533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282685 | GTGAAGGGAACTTGA[A/G]GTCTGGTTGTATTCA | 337867 |
rs562060386 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202694 | TTGCCCAGGGAGAGG[C/T]GTAGGTCTGGAGCCC | 337867 |
rs562102514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240039 | GAATTTCAGACCCTT[A/C]GGAGTGTGGTACAGG | 337867 |
rs562107944 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221787 | TCATGGTGATCGCCT[A/C]CTTGACAGTGCCCTT | 337867 |
rs562130100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275860 | ATAAGGTCCCCTGGT[A/G]AGGATGTTTGGGAAT | 337867 |
rs562186327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364147 | GATTTTTGTTTGGGT[A/T]TGGTTTTTGTTCTCA | 337867 |
rs562186807 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240697 | TTTCAGTGTGACTCC[C/G]GTACTGTTTCTCCTT | 337867 |
rs562194591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317743 | ATTTGTAAATAACAT[C/T]ATACTTGGGTTTCAT | 337867 |
rs562198504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232294 | GAGCAAACTTTAATA[C/T]TGAATGTAAACAGAA | 337867 |
rs562215138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268500 | GTAGTCTCAGCTACC[G/T]AGGAGGCTGAGGTGG | 337867 |
rs562250294 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266659 | TTAAACATAAATGTG[A/G]CCTTAGAACAAATTT | 337867 |
rs562271723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374029 | TAATGCATGTCAAAC[A/G]ACAGAATTACAGCAA | 337867 |
rs562273713 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200476 | TGGAAGGCGCCGGGC[A/G]TCCAGTCTCGGGAGA | 337867 |
rs562289883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383307 | CTTTTAAGTCTAGGA[C/T]AGTACATATCTCTGT | 337867 |
rs562310768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253638 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGATTA | 337867 |
rs562331726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296211 | AAAGCATATGTATTC[A/G]GTTTGATTACTCATT | 337867 |
rs562334121 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205454 | AAAAAAATCAATCAC[A/G]GTGTTTTCTGAATGT | 337867 |
rs562348059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245384 | AACATAAAACAAAGC[C/T]GGTGTATAGGTTATA | 337867 |
rs562348605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379439 | TCACCACATTAAAAA[A/G]TTTGGTTTCATGTTT | 337867 |
rs562366864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289397 | GACAAAACCAACTAG[A/G]CAAACTTGAAAGGCC | 337867 |
rs562376424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213039 | AGTGGTCATTCTTTT[A/G]GACTTTTTCTGTGTA | 337867 |
rs562382504 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345770 | TTTTTTGAGACAGAG[C/T]CTTGCTCTGTTGCCC | 337867 |
rs562394195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332946 | TCATTCAGAAGACCT[A/G]GTGTAAAAAAGGTTT | 337867 |
rs562406341 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252324 | CCCACTGGCTGTTTG[A/C]GGGGGAACCAAGTTT | 337867 |
rs562407734 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249443 | ATCCAGTCCATTGCT[A/G]ATGGGCACTTAGGTT | 337867 |
rs562429586 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306756 | CTTTTTTTTCACTTA[C/T]CTAATTAGTAGTATT | 337867 |
rs562442076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224861 | TAAAATTTTTACGTA[A/G]TAAAAGTACAAATCT | 337867 |
rs562443829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339326 | GCCCCCAGAGTAGGT[C/T]CGTGCCCCATGTCAC | 337867 |
rs562466195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346295 | TTTCTTCCCTCCCAT[C/T]TCCATCACCGACTGC | 337867 |
rs562491392 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292782 | AGATTAGTTTTTCTA[A/G]CTCCCAATTATTATT | 337867 |
rs562492166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277671 | TTTATTAAGGCCATT[G/T]TACATTGTGTCATCC | 337867 |
rs562495116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324712 | TACAGTCATGCACTG[C/T]GTAACAACGTTTTGA | 337867 |
rs562520695 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351930 | TCAGCGATACTCACA[C/T]GTGCTTTCAGTTACT | 337867 |
rs562547692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305905 | TATTTATTTATTTAT[C/T]TATCTATCGAGACAG | 337867 |
rs562575938 | snp | A/G | 0.000115328 | 0.0075928 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255284 | TGAACAAAGGAATCA[A/G]GAAAAAAAATGTCAG | 337867 |
rs562580801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318574 | GCCTGTAATCCCAGC[A/T]CTCTGGGAGGCTGAG | 337867 |
rs562601393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218077 | CAACTGTTAACTGAT[A/T]TATCCCATATTTGTG | 337867 |
rs562603785 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334759 | CAGACAGAAACCAAA[C/T]TGCAAAATCCAGCTA | 337867 |
rs562662436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247855 | AGTTCTTTACTTCCT[A/G]TTTAATTCTCTCTCT | 337867 |
rs562664169 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334132 | TTTTATTTATTCTTA[-/T]TTTTTTTTTTAGAGA | 337867 |
rs562671174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262963 | GAAAGGTAATCAGAG[G/T]TGACTGTCAGGCATG | 337867 |
rs562686935 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385450 | GTTCTTGTGGGAAGA[A/G]GGAGGTTCCACCGCA | 337867 |
rs562726051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276428 | CACAGAACTCAGGAA[C/T]GTATTTTACTTACGT | 337867 |
rs562758117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297550 | AGGGTTAGCAGAGGA[C/T]TGTGGTCATGTTATG | 337867 |
rs562759080 | in-del | -/G | 0.110167 | 0.207236 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216081 | TGTACCAACCTATAT[-/G]TTGTGTGTGTGTGTG | 337867 |
rs562764676 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99298939 | AAGTTCTTTGAAAAT[A/C/G]TATTTTTTTCCAAAA | 337867 |
rs562787031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384980 | CTTTACCCTCAGAAG[A/C]CCTGTGTCCTTGTCT | 337867 |
rs562792441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290928 | AGGTGAATTGAATTC[A/G]GATGTGGTGATGGGG | 337867 |
rs562795324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306238 | CATAACATATCTGTT[A/G]GATTCACCCTCTGGT | 337867 |
rs562800943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292036 | GTCGGCTAGCATGTA[A/G]TAAAGCAGTCGAGGC | 337867 |
rs562857415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358627 | AAAGGGTTTCTAAGT[A/G]GAGGAGGGGCTTGAC | 337867 |
rs562861770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364786 | TGCATGTCATTCTGG[C/T]TCATTCATTCAAACT | 337867 |
rs562863743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372610 | AGAAAGACAGGTGGC[A/G]TCACCGGCTCTGAGT | 337867 |
rs562865325 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329755 | CTCCAGTGCCAGTCA[A/G]GTCTTGAGATGAGTG | 337867 |
rs562912449 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215697 | AAGCCGGCTCTCTGC[A/G]AGCGGGAAACCGCCT | 337867 |
rs562912834 | snp | A/G | | | intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99256357 | AAATTATCATAGGTT[A/G]AGAAACAGCAATGTT | 337867 |
rs562930978 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327643 | TAAACAACAGCATAG[G/T]ATGTTATCAAAGGTC | 337867 |
rs562945269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269180 | GTTGCAGGAAGTCCA[A/C]TCATTGGTAGGTACC | 337867 |
rs562954903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358163 | TGAGGGCGGTGTTGT[A/G]AGAAAGTGACTCCAG | 337867 |
rs562971703 | in-del | -/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301384 | AGGAGACAATCCCAG[-/T]TTTGCCTCTGTAATG | 337867 |
rs562977137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312622 | ACTGACATAGCTTGG[A/G]GGCCACGAGGAGAGC | 337867 |
rs562978695 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273417 | GGTGAGGTTCCAGAG[G/T]TGTCTTGGCTAGTGA | 337867 |
rs562981999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269988 | CTATTTCATAAAGGC[A/G]TGTGCTGTAGTTAGA | 337867 |
rs562989852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227050 | ATAAAAATACAAAAT[A/T]AGCCAGTTGTGGTGG | 337867 |
rs562998110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205753 | GTCACCCCATTGATC[A/G]CCAGAGTTGATTCGG | 337867 |
rs563005099 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210359 | AAATGAATATCTAAA[A/T]AATAGGTAAAAATAA | 337867 |
rs563026081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246085 | ACTGTATGTATCTTG[A/G]TTCAAATTCACTTTG | 337867 |
rs563049624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284512 | CCGCATTTGCTGTTA[C/T]CATTTTCTCTCTACA | 337867 |
rs563069303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296958 | CAAGCATCACACTTT[A/G]TATTTTGTTTCTTGC | 337867 |
rs563076626 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283462 | AATCTTAATAAATTT[A/T]TATTGAACAATTTTG | 337867 |
rs563107492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237414 | AGATTGCATGTTCTC[A/G]CACGTGGAAGCTAAA | 337867 |
rs563124331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330451 | GTGACAGAGTGAGAC[A/G]TCATCTCAAAAAAAA | 337867 |
rs563129623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274445 | TTCTCCTGCCTCAGC[C/T]TCCCCAGTAGCTGAG | 337867 |
rs563135307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357258 | AGTAGGCGATCACAT[C/G]TAGGTTTCTGTAAGT | 337867 |
rs563143178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311906 | TGGGGGTAGGAACCC[A/G]CTGTGCCGTGCACCT | 337867 |
rs563150262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370409 | TTTGAAATTATTTCA[A/G]ACTACAACCTTTTCA | 337867 |
rs563164054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260998 | AAGCCAGTTTTTAAT[C/G]AGAAAGAATGTAGTT | 337867 |
rs563173775 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276378 | CCCACAAGGTCTGTA[C/T]CCCCACCAGGTCTGA | 337867 |
rs563177589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231652 | CTGACCTTAAGTGAT[A/C]TACCCGTCTCGGCCT | 337867 |
rs563179034 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201273 | GGCCCTTTGCGGAGC[A/G]TGTGCCGCGCTGAAG | 337867 |
rs563181918 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199281 | GTGTCAGGTGCCTGT[A/G]GTCCCAGCTACTTGG | 337867 |
rs563204893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274997 | TGCTGGGATTATAGA[A/T]GTGAGCCACTGCATG | 337867 |
rs563226049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304264 | TTCTTCCCTCTGTTT[C/G]ATGTCCTCTGGCCCC | 337867 |
rs563243435 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317464 | ATTAATTAACTTTGT[A/T]CTGTTATTTAGTTTG | 337867 |
rs563250754 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205154 | TGATCCGCCCGCCTC[A/G]GCCTCCCAGAGTGCT | 337867 |
rs563252724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253749 | GAACTCCTGACCTCA[A/G]GTGATCCGTCCACCT | 337867 |
rs563263545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310983 | AGCTACATATGAAAC[C/T]ATGTGTTTTAATCCC | 337867 |
rs563284101 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260193 | GGTTTCTCTGCCCTC[C/T]GAAGCTGGGCTGGTT | 337867 |
rs563293417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329863 | CATTCCTGCCCCCAC[A/G]GAAATTGGATAATAG | 337867 |
rs563296191 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303514 | GATGAAGATGACATA[C/T]GTTTAGAGAACTAAG | 337867 |
rs563297434 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243637 | CAAGTACCTTTCGTG[C/G]CACTGTTGGGAGGAA | 337867 |
rs563308856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217128 | GAGCCACGGCGCCTG[G/T]CCTCTTTCCTCGTTT | 337867 |
rs563322937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253075 | ATATGTTAAATATAT[G/T]TAAGATATACAAATA | 337867 |
rs563326154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281840 | CTAATTGTGAAAGGA[C/G]ACTCAGGCTTTTAAC | 337867 |
rs563331015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210179 | TTTTCTATACACTTA[C/T]GTTCTTGTTTTGAAA | 337867 |
rs563331718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350526 | GGGTTTAGAGAACTT[C/T]CAGATTGCTGAATGT | 337867 |
rs563381535 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283348 | TAATATCAGTGACAA[C/T]ATGAAGGAAAAATAT | 337867 |
rs563385760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244257 | TGTGTTTTACTTGTT[A/G]AAAATATATCTTCAA | 337867 |
rs563396131 | snp | C/T | 0.000807428 | 0.0200764 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204673 | AAAACGGGCCTGAAG[C/T]GCGACCTGTGGGAAA | 337867 |
rs563413680 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316657 | CAGATACTGTGAAGA[C/T]ATAGGCAGACATAAT | 337867 |
rs563417684 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284808 | AGGACTTACAGAAAA[C/T]GATACATATTCTAAG | 337867 |
rs563439309 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383743 | CATGACATGGGCGGC[A/G]CCCCCCGTTTGGAAA | 337867 |
rs563463930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230138 | GTACTGTTGCTTCTC[C/T]AACAAATTATCACAA | 337867 |
rs563468282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363726 | AAGTCACACGTATAT[A/G]CACACCCAAGAAAAC | 337867 |
rs563471434 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369949 | TGTTCTTCAAAAATA[C/T]GATGTTCCAGATTAA | 337867 |
rs563485520 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376905 | TCTTTGAGACATTTT[A/T]AAAATTTTCCAGACC | 337867 |
rs563554695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317016 | TTCCACTGAACAAAC[A/G]TCCGTGCTACATCAA | 337867 |
rs563578649 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386093 | GGCATGGGCTCAGCC[C/G]AGGAAGAGGAGAAAC | 337867 |
rs563662606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349127 | CTCCTTGTCTTCAGA[C/T]CTCCAGATCAATTAC | 337867 |
rs563683906 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230070 | GAGTTTCCTTAATAT[A/G]TAGATTTTTGCCAGC | 337867 |
rs563731008 | in-del | -/TT | 0.276267 | 0.248616 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375802 | CTTTTCCTTTTTCCC[-/TT]TTTTTTTTTTTTTTT | 337867 |
rs563734087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253794 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 337867 |
rs563753256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287964 | TTTGCATTTATTTTT[A/G]TAGGCTAATATAGGC | 337867 |
rs563758463 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207287 | AGGAAGATCAGAAAA[C/G]TTAGTATGTGTGGAG | 337867 |
rs563779732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253486 | TTTTTTTTAAGGAAT[A/G]TGAATTTACCTATGT | 337867 |
rs563792173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355539 | CCTGTGGTCCCCCCA[C/T]GCCACCCTCTCACCA | 337867 |
rs563820816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329223 | TTGCAATCAGGCAAT[A/G]TAAGTCCTCCCACCT | 337867 |
rs563838553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209380 | TGCCTTGCAATCACT[A/C]TTGGAAAGTTCTGCA | 337867 |
rs563844250 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226699 | TTAGCTCCCTCCCTG[C/T]CTGCCTTGTGCTCAT | 337867 |
rs563884643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99291055 | ATGAATGCTCCAAGT[C/T]AGGCCACAGGTTCTG | 337867 |
rs563888803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384821 | ATGCCAGGGCCGAGC[A/G]TGGCAGTGATGCCAG | 337867 |
rs563897917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265997 | CTTATGTATGGTCTC[C/T]GGTTTTCCATACCGA | 337867 |
rs563912252 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309170 | GGCTGGAGTGCAGGG[C/G]TGTGCTGTCGGCTCA | 337867 |
rs563932817 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258751 | ATACTATATCCAGTA[A/G]GATTGTAGGGGCCCT | 337867 |
rs563938424 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385918 | AATGGTGATAACCAT[G/T]CACTGGTTCAAGGTT | 337867 |
rs563946379 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305807 | TGAACCCGCAGAGAG[-/A]AAACATGCTAAAATA | 337867 |
rs563947995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305059 | GTAAAGGTTTTATAA[A/G]TGGATTTAGAGTACT | 337867 |
rs563961913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302063 | GGTCAAGTCTTCTCT[A/G]GAGTCAGCTTATACA | 337867 |
rs563968453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344746 | GCCATCTGGCAGGTG[C/T]TCGCTGCCACCCCCT | 337867 |
rs563969265 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223638 | TTATGCTACATTTTC[C/T]CCTCTAAGCATTGCT | 337867 |
rs563998935 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302844 | GTACATGCCTCTGTG[G/T]CCTGGTTAAATACAT | 337867 |
rs564001025 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208121 | TCCTGCCTCAGCCCC[C/G]CAAGTAGCTGGGATT | 337867 |
rs564043555 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205593 | CATCCCCCCACCCCA[A/C/G]GACATTTTAATGGAC | 337867 |
rs564050611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247061 | GGCTGGTCTTGAATT[C/T]CTGGGCTCAAGTGAT | 337867 |
rs564057116 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277562 | AAATAAAAGGCAATA[C/T]TGGTTTTTAAAAAGG | 337867 |
rs564057734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357910 | TTATCCATTTTGCAA[C/T]TGTTTCTTGAGTGCT | 337867 |
rs564067090 | in-del | -/TGT | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310491 | AGTATAGAGAACAGA[-/TGT]TGTCATAAAATAAGG | 337867 |
rs564089079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344151 | TTTATGCCCGGTGTA[C/T]GCCTAGAGAGATGCA | 337867 |
rs564110181 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275758 | CATATCTCTAAGCCT[A/T]TGATTATCTGTTTGG | 337867 |
rs564129646 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337012 | ACACATAGTCATCAT[C/T]TTTGCGCTTTCCTGT | 337867 |
rs564162253 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205666 | CAGAGAGAACGGAGT[C/G]TGGTGCGCTGATGAG | 337867 |
rs564174970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338558 | TCACTTGATAAGCTT[C/T]CTATTTTGTTAGCAT | 337867 |
rs564182228 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306115 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGATCTCA | 337867 |
rs564190419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338395 | ATGAATTTGTGTTGG[A/C]CCACATTGAAAGCTG | 337867 |
rs564203717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286960 | TCTGCCTCTACCCCC[A/G]ATGTAACAAGAGTAA | 337867 |
rs564209443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345511 | ATAGGTTGTTTCCCA[A/G]GACTCAGTTCTCTGC | 337867 |
rs564223870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237889 | GAACCTGGGAGGTGG[A/G]GGTTGCAGTGAGCCG | 337867 |
rs564242836 | snp | C/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259258 | ATTATCTTTATGTTT[C/G]GTTATGCATGGTTTG | 337867 |
rs564245707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317088 | GAGCCTATCACTAGA[A/G]CAAAGCTTGCCAGCC | 337867 |
rs564256700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378171 | CTTGACTCAGAACCA[C/T]CTCAGCTATTTCACC | 337867 |
rs564268428 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363012 | CAAAAAAATTTTCAC[A/C]GTTTGGCTTTCCACA | 337867 |
rs564305388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309975 | TGTCTCTGTTATTTT[A/G]TGTTTTCTATCGAGT | 337867 |
rs564315043 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315242 | GTAACCAAATAGCCC[G/T]TTTCTGCATTTGATT | 337867 |
rs564348681 | in-del | -/TAT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285150 | TTCATAATTCTGTAA[-/TAT]TATTTACTACTGAAA | 337867 |
rs564369960 | in-del | -/TTT | 0.493925 | 0.054776 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231407 | GCTTTGCTGTATACA[-/TTT]TTTTTTTTTTTTTTT | 337867 |
rs564370027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318414 | TCAGGTGTTCTGCCC[A/G]CCTCAGCCTCCCAAA | 337867 |
rs564384642 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253374 | TTCAGACCTCAGTTT[G/T]TTATATTTCGAACAG | 337867 |
rs564407676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312558 | GCTGGGCATCTTACC[A/G]TGACATCCTTGGCAC | 337867 |
rs564433921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210123 | TTGGAAAATAGAAAA[A/G]AAACGGTCCTAGCAT | 337867 |
rs564506312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377081 | TCCTACCAGCATTCT[C/G]ATTTTGTCCTCCACA | 337867 |
rs564525334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290071 | GATGAAGAGTGCAGA[A/C]CATGGAGCCAGACCC | 337867 |
rs564527236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281912 | CTTACCAGGGAGCAG[A/T]CCTAATGTATCCAGT | 337867 |
rs564586648 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249818 | GATTTGCATTTCTTG[A/G]TGATTACCTTTGAGC | 337867 |
rs564593670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215413 | TCCCAATCAGAGATT[G/T]GTGGATGTGTGGAAT | 337867 |
rs564605561 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346879 | GTGTGAATAATGCCT[G/T]GCAGATGTTAGGAAC | 337867 |
rs564647435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275093 | CTAGGAGTGGAAAGC[A/G]GAATCATAGTGTATA | 337867 |
rs564648476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252675 | ATGTGGATGTTACAT[C/T]GTTTTCCAGAATACA | 337867 |
rs564707500 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260003 | CTTTTTCCTCATCTT[G/T]CTCTCCATTCCAGCC | 337867 |
rs564738803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251922 | AGCAAGCGTATACCC[C/T]TTCCATGTATTGCTT | 337867 |
rs564753549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286139 | AATTGTATAAGCACC[G/T]AATTCTGTGTACTAA | 337867 |
rs564755633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294872 | ATTTGCATTTTTATT[G/T]TGCTTTATGTTGTTT | 337867 |
rs564766539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323074 | GGCGAGGGATGGTAG[A/G]TGTGAGTTCCTCTGC | 337867 |
rs564775552 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384182 | TAGCTCGCTCTCTTT[C/T]GGAAAGAAAAATTGG | 337867 |
rs564797702 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99202841 | GCATCTCCTCTGGGC[C/G]ATGAACTGGGCTAGG | 337867 |
rs564801027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274323 | TGAATACCACCATCT[A/G]TCCATTCTACTGCTT | 337867 |
rs564803752 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229698 | TATTTTAATAATCAA[C/T]GGGGAAAATTTGGAT | 337867 |
rs564805308 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266222 | TATTACATAATACTA[C/T]ATAATATGTAGCTTT | 337867 |
rs564809578 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383214 | ACTGGTGTGGCCAGT[G/T]AAGCTGGGCCTGCTG | 337867 |
rs564820531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244384 | ATATATATACACACA[C/T]ATGCATGTGTGTATA | 337867 |
rs564826293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309270 | CATATGCCACCATGC[C/T]CAGCTAATTTTTGTA | 337867 |
rs564866869 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369645 | GGACTTAACTCCATC[A/G]TAGGTTGAGGAGCGC | 337867 |
rs564881034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273501 | TTTATATGGTAGTTT[A/G]CCTGTCCTGGGGGAA | 337867 |
rs564902786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361922 | GATTGCTTGGGTCCG[A/G]GAGTTCAGGACTGCA | 337867 |
rs564917651 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339798 | GGATTTTAAATGTCT[A/G]GAAAAATCAGTAGTT | 337867 |
rs564934989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374881 | CACAGGTGCCCCAGC[A/G]TCGGTCGGAGAAGGG | 337867 |
rs564936540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265143 | ACAAGGTATTTACCA[G/T]AACTCTCCCTTGTAT | 337867 |
rs564982304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327544 | GGACTGACTGTGTTG[A/G]TATTTTCCTTCTGTC | 337867 |
rs565007746 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268720 | TAGAGGCACTGAATG[A/G]TAGAGTTGTTTGGCT | 337867 |
rs565030535 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235574 | TCACATAAAAACAGA[C/T]ACATAGACCAGTGGA | 337867 |
rs565031028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242955 | TCCTAGATGGGATGG[C/T]GGCCGGGAAGAGGCG | 337867 |
rs565046693 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378767 | GCATTGGCAACAGCA[C/T]GTGTGGCATCCTTCA | 337867 |
rs565101561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335166 | ACAATCACAGTTGAA[C/T]ACTTTGAGACCGAAA | 337867 |
rs565124330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243444 | GTTTATACCTAAGTT[A/G]TTTTTCAGTTACAAC | 337867 |
rs565130310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367351 | ATTTTAAGGGCCGTG[A/G]TGGAAACACCAGATT | 337867 |
rs565135146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257063 | GTTAAACACAAGAAA[C/T]GTGCCTGTCTGCCTT | 337867 |
rs565151144 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362403 | TGAAGTTGCCAGGTC[A/G]TAGACTAGAATAGTT | 337867 |
rs565152094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375433 | CCAGTTGCTATGACA[A/G]CAGTGGGCGAGGCAG | 337867 |
rs565160052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236155 | CTGGGCAAAGACTTT[C/T]TGTGTAAGATCTCAA | 337867 |
rs565167666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249344 | ATGGCCTCCAGCTGC[A/G]TCCATGTTCCTGCAA | 337867 |
rs565187453 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319683 | CAGAGCTAAACCCTA[C/T]TGTGAAGTCTTCAAA | 337867 |
rs565188205 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285900 | GCAGTTCTACACATC[C/T]AACGGGGTGCCAGAG | 337867 |
rs565205192 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364472 | TATTGTATAATTTTT[-/C]TTGCTCATAATGGCC | 337867 |
rs565205561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369008 | CCACATCTAGGGCAT[C/T]GGCTTGGGGATCAGA | 337867 |
rs565208065 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218394 | AGGATTTTAAATTTT[A/G]CAGCTCACTCTTTCC | 337867 |
rs565254490 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347254 | GGCCAGGGAGCCTGC[A/G]GAGTAGAATGTTTCA | 337867 |
rs565275776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380768 | GTAATTGTTTATTCT[C/T]TTTAAAGAACTGTGC | 337867 |
rs565282856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308310 | TCTTAGGAGAACTGA[G/T]TAAATAAGCTGGGGA | 337867 |
rs565304601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227623 | CCCTAGTTCATTTCT[C/G]ATAGGATTTATTTCC | 337867 |
rs565310666 | in-del | -/CA | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247369 | ACAGGCGCCCGCTAC[-/CA]CGCCCGGCTAATTTT | 337867 |
rs565311959 | in-del | -/CAAA | 0.0232847 | 0.105357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242045 | TTTCAGAGAGCACAG[-/CAAA]GGTTGGGGGTAAGGT | 337867 |
rs565315641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257967 | ATATTTTTTTAATAG[A/G]GACGGGGTCTCACTA | 337867 |
rs565318395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347957 | CTTTTGTAAACTCGG[A/G]ACACTATGCTGGACA | 337867 |
rs565324725 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368491 | ATCTTAAACATTTCT[C/T]CAAGGTTTAGTTTTC | 337867 |
rs565373208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208096 | TCTGCCTCCTGGGTT[G/T]GAGCAATTCTCCTGC | 337867 |
rs565383942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220115 | TAATTCTGTGCTTGA[C/T]GTTTTGTGGAACCAA | 337867 |
rs565386168 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341992 | CCTTTGGAATCCTGG[A/G]AGGAGATTCTCCATT | 337867 |
rs565387078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201799 | TCTGTTGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 337867 |
rs565390548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203140 | CTCCCGAGTTCAAGC[A/G]ATTCTCCCGCCTCAG | 337867 |
rs565401086 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250220 | ATATCTTTAATCCAT[C/T]TTGAATTAATTTTTG | 337867 |
rs565429485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326534 | AAAACTTAATATTAT[A/C]AAAAAATAATTTCTG | 337867 |
rs565436280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303072 | GAGGGGCTTAGTAGA[A/G]GCAGCCTTATTGAGG | 337867 |
rs565459110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335446 | TTTGTTACAGAGAAT[A/G]CCTCTGCCTACCCCC | 337867 |
rs565518759 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268461 | AAAATACAAAAAATT[A/C]GCCAGGCGTGGTGGC | 337867 |
rs565534711 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343675 | TTTCCTAAGCTTCCT[A/G]AGTTCTCTTCTAGGG | 337867 |
rs565556322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314606 | TATTGAATACAGTGT[C/T]GCAAATAAAGCTCTG | 337867 |
rs565597579 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214272 | GAGTAAATTTTTTTC[A/G]TGTAAGGACACGAGT | 337867 |
rs565646324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208360 | TGAAAAGCTGTCAGG[C/T]CTTGTGACTTACCCT | 337867 |
rs565664745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348680 | AGATTTATTTTTAAG[A/G]AAGCTCACTTTAGTC | 337867 |
rs565673315 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258851 | TTTTACTACCAAGTT[A/C]TTAAAAATCATAGAA | 337867 |
rs565690535 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386510 | GTCAACCAAATCCTC[C/T]GCACTGCTCGTCTTT | 337867 |
rs565691530 | in-del | -/CC | 0.46014 | 0.13543 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347320 | TACTATCCCCGGGCG[-/CC]CCCCCCCCCCCCCAG | 337867 |
rs565695067 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380374 | TGTGGGGACTGGGCG[A/T]GCTGGGCTTCTCTGA | 337867 |
rs565698178 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209683 | AATATACTCTTCATA[A/T]ATTTTAGCGGCTGGG | 337867 |
rs565712491 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234062 | ACAGGGTTATTATAT[A/G]AAGTAATTATTTCCA | 337867 |
rs565713917 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287856 | TTGCTCCCTTACTGG[A/G]GAAAATAATAAGCAA | 337867 |
rs565720645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257982 | AGACGGGGTCTCACT[A/G]TGGTGCTCCTGGGCA | 337867 |
rs565739593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99349386 | GTTCTCCCCATGTGC[A/G]GAGATGAGATTGTAA | 337867 |
rs565744999 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367292 | ACTGTGTGCGCTCAG[A/C/G]ATTTACTTCAGTCAT | 337867 |
rs565748913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369086 | ATTTATATAAATACA[C/T]ACACTGGAGGGAAGG | 337867 |
rs565758312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380879 | CTTGTCTTCTCACCC[A/G]TAAAAATCACTTAAA | 337867 |
rs565775292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382208 | TGAGGGAGATGATTA[A/C]CAGTAGATAACAAAA | 337867 |
rs565781983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243715 | TCCTTTGGTGTGTGC[A/G]TTATGATTTTGTTTA | 337867 |
rs565794870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286368 | GTTCCTCAAAGAACA[G/T]TGTGTGTGTGTTTAT | 337867 |
rs565795215 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278782 | CTGTTTTACTGGTAC[A/G]AAAACATTTTTAGAG | 337867 |
rs565801806 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233796 | TTAATTGTAAACTTT[G/T]TCACGGTAAAAGGAT | 337867 |
rs565805301 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361226 | AGTATTTCATAAAAC[A/G]CCTGTTCAAACTGCA | 337867 |
rs565820612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315901 | GCATGGCCTTCATCA[C/T]GGGGCCATTGTAGTA | 337867 |
rs565825148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322221 | AGTCTTTACATATTC[A/G]TAATTCCACTAATTT | 337867 |
rs565838383 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236197 | GCCAAAGGAAAAATA[A/G]ACAAGTGGGATTAAA | 337867 |
rs565840690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229081 | CATCTGTGCAAGGGA[C/T]GGTGCTAGGCTTTAT | 337867 |
rs565912082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315376 | AAGTTCTAGTCCTAG[C/T]ATGGCTGTCTCCAGC | 337867 |
rs565928525 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214988 | GTTCTTTTCTTTTTG[G/T]TTTTTTTTTTTCTTG | 337867 |
rs565931433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353654 | ATTTAGAGATGTACT[C/G]TGGAGCAGTATCATG | 337867 |
rs565933638 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368901 | CGTACAGGATAGCCC[C/T]GGATCATCGTGTGCC | 337867 |
rs565944797 | in-del | -/T | 0.490508 | 0.0682328 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339639 | AAATTCACATCAAGA[-/T]TTTTTTTTTTTTTAC | 337867 |
rs565949701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354649 | GCCGACATAGTAATT[C/T]AGGATGTAATTTAGA | 337867 |
rs565953893 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361718 | AATGCCGACAGCACC[A/G]CCATCCTGTCCCCCC | 337867 |
rs565960846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248742 | ATTTTGCCCAGGCTG[C/G]TCTCAAACTCCTGGC | 337867 |
rs565962966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257308 | TAATCTTGGAGGCTT[A/C]AATCTTATTTTTAAC | 337867 |
rs565972053 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350770 | CACGTTGGTTAGAAC[C/T]GCAGGTTAGGTCTGG | 337867 |
rs565972791 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99307279 | CTTTTACCTTAAAAC[C/T]TAGGCTTTTAAAGTT | 337867 |
rs565974362 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259158 | AGTGAGCAACGAATC[A/G]CTGCCTGCCTTGTTA | 337867 |
rs565974939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242997 | CTAGATGGGATGGCG[A/G]CCGGGCAGAGACGCT | 337867 |
rs565977398 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337658 | CATATTCCCTCTGTT[G/T]TCTTCTTCTGGAACC | 337867 |
rs566012094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355037 | GCGGGAATGAGACTC[A/G]GGTGGTCACTGAAGA | 337867 |
rs566017205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242266 | GGCACACCTCCCAGA[C/T]GGGGTGGTGGCCGGG | 337867 |
rs566022597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367586 | CTTTTCTCCTGAGCA[C/T]CTACTGCAGGCTGCC | 337867 |
rs566024818 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386046 | GCTTCCTGGAGCCAC[A/G]TGGGCTGACTAGGGC | 337867 |
rs566039634 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328677 | TCTTTTATCCATTTT[A/G]TTCATTGGGCTATTT | 337867 |
rs566065064 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235683 | AGTCCCTTCAAAAAA[A/T]TTGTGCTGGGGCCGG | 337867 |
rs566090551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233976 | GGTTATTATTTTATT[A/C]TTATTATTATTCTTA | 337867 |
rs566122238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334490 | GTTAAAGTTGGAGTT[G/T]CCAAGAACCTATCAG | 337867 |
rs566135250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264630 | ATTTCTCTGATGGTC[A/G]CTCTCCCCAGGGGCA | 337867 |
rs566139195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346783 | TGGCACCGCAAACCC[A/G]ATGTTCACTGGTGAT | 337867 |
rs566142908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359060 | CCTTCAAGAACACCC[A/G]TGTCTGAAGGACAGG | 337867 |
rs566150167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374906 | GAAGGGTTGAACACG[A/C]AGGTGTGGCCAGTAA | 337867 |
rs566153614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299820 | ACCCCTTATCTACTT[C/T]GCAGGTGATAAAACT | 337867 |
rs566154627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228599 | GTGCCCAGCCCCTAT[A/G]TTTATTCTTTTATTT | 337867 |
rs566177931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227714 | CTCCAAACCACAAGG[C/T]TAGGGACTTTGTCCA | 337867 |
rs566178047 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357038 | GTAGTCATGCACCAC[A/C]TAACAATATGTTTTG | 337867 |
rs566197658 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327750 | TGTTCTGCTAAAATC[C/G]TACCTCTTATAAAAT | 337867 |
rs566198791 | snp | C/T | 0.000399281 | 0.0141238 | stop-gained, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340548 | TTTGCACAAGGGAGG[C/T]GACAGAGACAGCAGC | 337867 |
rs566204154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359772 | TCCTTGTGTGGGCCC[C/T]GCCTCGCCTCCCGTG | 337867 |
rs566213607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368245 | GGAGGGAGTGTGCCT[C/T]TGGCATGGTTTCACT | 337867 |
rs566246429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306718 | TTAGTCTAAGTAAAC[A/T]CAAGTATAAACCACA | 337867 |
rs566263928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352861 | TGGAGGCAGCACCGT[C/T]GGAAACTCTCTACCT | 337867 |
rs566265958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360244 | GTCTAGTTGGGAAGA[C/T]GAGAAACAATACTGT | 337867 |
rs566283144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307779 | GGGTTTTTAAATGTT[G/T]TAAGGAAAATAGTGT | 337867 |
rs566293636 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312213 | AGGATGAGAAATTGC[A/G]CAAGAGGCCAGGAGG | 337867 |
rs566313253 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351051 | AGAAAGCAGCGTAAT[A/G]TAATGAAAAGAACAA | 337867 |
rs566325207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331703 | TGTATGACAAATGGC[A/G]GAAATAACTTTGGGA | 337867 |
rs566328001 | snp | A/G | 0.00126662 | 0.0251338 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200841 | GAGTGCGCCTGCGCG[A/G]TCGCTGGGGCTCGCA | 337867 |
rs566363120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300488 | AAAATCCTTTCATAT[A/G]CGTGACTGTTACTAT | 337867 |
rs566372027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332447 | ATTAGTGGACTAAGA[A/G]AAAATCATTTCCTCT | 337867 |
rs566376063 | snp | A/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327868 | TAAGATGTTATTTAC[A/T]TACAATAGAACTCAC | 337867 |
rs566389185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201320 | TTACCATGCCCCATT[C/T]TTTTAGGCTTGGGGG | 337867 |
rs566435044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332982 | ATCATGAAAATTAGG[C/T]CAGGCATGGTGGCTC | 337867 |
rs566454940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277748 | TGTGCTCTATTGTCT[C/T]ACTTTCTGGGCCTAC | 337867 |
rs566456576 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224913 | TTGTCTATAATGATA[C/T]TATATACTTATCCTG | 337867 |
rs566473100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366845 | TTCCCACGCCCACTT[A/G]TTCCTGAGGCCTTGC | 337867 |
rs566503713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312851 | AGGAGGACAGTGGTG[G/T]CAGACTCCAGTGATG | 337867 |
rs566505239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211581 | GACTCACTTAATTCT[C/T]ATAACAGCCCTGTTA | 337867 |
rs566519978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313683 | GGCCAGAGGTGAACC[A/G]TGCCAGTGCCATGGC | 337867 |
rs566526506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220183 | AAGTTATCATAGTTC[C/T]TTCTTATATATTAGA | 337867 |
rs566536641 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280992 | GGAGTTTGAGACCAG[C/G]GTGGCCAACATAGTG | 337867 |
rs566548032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239495 | AGAGTCTGGTGGTGG[C/T]GCCTGGGCATTGCTG | 337867 |
rs566554795 | snp | A/G/T | 4.94306e-05 | 0.00497124 | synonymous-codon, missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314199 | CACAAACAAGACATT[A/G/T]ATTTATATATTGGGA | 337867 |
rs566565576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205474 | TTTCTGAATGTACAC[C/T]TTCCTGGGTCTCCTC | 337867 |
rs566568920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212482 | CAATGGGAAGAGCAT[C/G]ACACTAATCTTTGGA | 337867 |
rs566586162 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220888 | CGATTTTTTTTTGGT[-/A]AAAAATTAAGATCTC | 337867 |
rs566621162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305962 | GTGCAGTGGCGCAAT[C/T]TCGGCTCACTGCAAC | 337867 |
rs566621733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385015 | AATGAGGGTTATGTG[C/T]GATCATGCATATATA | 337867 |
rs566630799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378476 | AGGTTGCAGTGAGCC[A/G]AGATCACATCACTGC | 337867 |
rs566642293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206166 | AGTGTTGAGGGGTTT[A/G]CAGAGTCCGGTCAGA | 337867 |
rs566642317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338929 | GATTTCCTTACTGGC[A/G]TTTCCTACTCTGTCT | 337867 |
rs566657866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248036 | TGCTCTCTTGAGTCC[C/T]ACACACTACTCCCTC | 337867 |
rs566673399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325332 | ATGGTCTTGATCTCC[C/T]GACCTCGTGATCCAC | 337867 |
rs566694182 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240158 | CTCCAGATTTTGGCA[A/G]TGAATGCAGAGGTAC | 337867 |
rs566694733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283923 | TATTTTTAATAGAGA[C/T]GGTGTTTCACCATGT | 337867 |
rs566699102 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243549 | ATCTTACTAAACGTG[A/G]TCCTGAAATTTCTTA | 337867 |
rs566725490 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302535 | AAAACGCCTTCTTGT[G/T]CAAACAGGGGCATCT | 337867 |
rs566744694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351291 | TGATAGTTATTACTC[C/G]TAAAAGCTTGTAACC | 337867 |
rs566761987 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274928 | TCTCCATGTTGCCCC[A/G]GCTGGTCTCAAACTC | 337867 |
rs566768509 | snp | A/T | 1.69821e-05 | 0.00291389 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317985 | GTGACTGGCAGTTGA[A/T]TTTTATTTTTAGTTG | 337867 |
rs566792532 | snp | C/T | 0.000347887 | 0.0131842 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356125 | GGGACACATGTCTGT[C/T]AGACTGTACACAGTA | 337867 |
rs566808179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373557 | CCTGCCCTGAGGAGC[G/T]GTGAGCCCAGGGCAG | 337867 |
rs566813437 | in-del | -/A | 0.494962 | 0.0499384 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236979 | ATGGAGGTTCTTAAA[-/A]AAAAAAAATAAAACT | 337867 |
rs566817822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284885 | TAATGTGTAGTTTTC[A/G]TATTTCTCTTGGAAT | 337867 |
rs566840088 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241839 | AGGTCAGCAGATAAA[C/G]AAGTGAACAAAGGTC | 337867 |
rs566861375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247355 | GAGTAGCTGGGACTA[C/T]AGGCGCCCGCTACCA | 337867 |
rs566863097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99254192 | GAATGGCATTTCACC[A/G]TATAGTAGAAACCTC | 337867 |
rs566928064 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323457 | AACAAACAAACAAAC[-/A]AACAAAAATTTCAAG | 337867 |
rs566960753 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384648 | TCAAAGTAGTCTGAG[C/G]ACCCAAAGGCAGGCA | 337867 |
rs566961130 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294996 | AATTATTTTGCTTTA[C/T]AAGGGAAGTCCTGCA | 337867 |
rs566986551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299072 | CCATATGAATAATTA[C/T]TATTGTAGAAATTAG | 337867 |
rs566994504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353784 | AAAGCTCTTAATGAG[C/G]AACAGACCACTGGAG | 337867 |
rs567020871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268687 | TAGGTCTTTCTCTTG[A/T]GTCTTAAAAATCAGC | 337867 |
rs567030320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231765 | CTTTTGATGATCTAT[C/T]TTTGTAAAATGTCAC | 337867 |
rs567040557 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383955 | CTTAGGTTAATTTTG[C/T]TCAGAATATCCAGAG | 337867 |
rs567101338 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369277 | ATTGTCGAACTTTAA[C/T]AATTTTTCAATTTTA | 337867 |
rs567104309 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345531 | CAGTTCTCTGCCTAC[C/T]GAGCTTTTCACGTTA | 337867 |
rs567104395 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373841 | ACCAAGGAACCATGC[A/G]GGATCTTACACAAGA | 337867 |
rs567110709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276463 | TGGTTTATTATAAAG[G/T]ATACAACGCAGGAAC | 337867 |
rs567116118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228454 | GCACCCCACCACGCC[C/T]GGCTAATTTTTGTAT | 337867 |
rs567164955 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348242 | AGGGATTAAATAAGA[C/T]GCCGCCTGCGCCTTC | 337867 |
rs567175821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261667 | AACCATATATAAGTG[A/G]TGGCAGTGAAATCAG | 337867 |
rs567197396 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213951 | CAGCCTTCTAGTAGC[G/T]GGGATTACAGGTGTG | 337867 |
rs567215238 | snp | C/T | | | missense, stop-gained, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238442 | ACAAGGCGCCTCTGT[C/T]GAAGAGCCTTCTGCT | 337867 |
rs567245443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272134 | TCCTTGAGCTGCTTA[A/G]GGTCACCTCTTTTAG | 337867 |
rs567287528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305975 | ATCTCGGCTCACTGC[A/C]ACCTCCGCCTCCCAG | 337867 |
rs567300344 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360207 | AGGTCTTCCATCCAT[C/T]ACAGCCCTCCAGGAT | 337867 |
rs567303345 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233569 | AGGGCCCTGGTTGAA[A/G]GGCCGCAGGAGCTGG | 337867 |
rs567317887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264702 | TTGTGTGATTTGAAG[A/G]CATTCCTCTCCCCAA | 337867 |
rs567325084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299123 | ACTCAGAGGTGCCAT[C/T]GCTTGCCAGTTTGTA | 337867 |
rs567356608 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257545 | ATATTCATTTGCTGA[C/G/T]GTTTGAAAAAAAATG | 337867 |
rs567379096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207855 | GCTAAAATGGACACC[A/G]ACATTGACTCCTGAG | 337867 |
rs567390953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324018 | CCTCCTTTCAAAATG[C/T]GACCTCCTCACCTAC | 337867 |
rs567424442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241064 | AGCCCAGGAGTTCAA[A/G]ACCAGCCTGGGCAAC | 337867 |
rs567429309 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288373 | ACAGGATGTCTAAGA[A/G]CATTACTAACTACGA | 337867 |
rs567439447 | in-del | -/AAATTTTAGGAGGAAACGTTCAGTCCATA | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224379 | AGAGCTTCAACATAC[lengthTooLong]ACAGTGATTTTCTGT | 337867 |
rs567440171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333017 | CTGTAACCCCAGCAC[A/T]TGGGGAGGCCAAGAT | 337867 |
rs567514590 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290073 | TGAAGAGTGCAGACC[A/G]TGGAGCCAGACCCCA | 337867 |
rs567568682 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291704 | ACAGGATCTTCAAGG[C/G]CATACGCTCTATATT | 337867 |
rs567584623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270170 | CAGTTCCAAATTTTA[A/G]CTACGTAAGGTGAGG | 337867 |
rs567594213 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340034 | TTAAAAAATGAAGAC[A/T]GTGTCTTGACAATCT | 337867 |
rs567596573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305463 | AAACGGCTTTATTAG[A/G]TGCGAAGCTCTTTTA | 337867 |
rs567605146 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264681 | AGGGGTCATCCACTT[-/C]CGGCCTTGTGTGATT | 337867 |
rs567614442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271179 | TATGCCAGATCATGA[C/T]CTGTGTTGTACAAAA | 337867 |
rs567614561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99278501 | ACAGTTAGCTTTCTA[A/C]ATTATTGTGTCTCTG | 337867 |
rs567642350 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292167 | TTGAGACAGTCTCTC[A/G]CACTGTCACCCAGAC | 337867 |
rs567709824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318747 | AATGGCGTGGAACCC[G/T]AGAGGTGGAGCTTGC | 337867 |
rs567739265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99371595 | AAATATTTGTTAATA[A/G]CATGTTAAGATAACT | 337867 |
rs567742435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379115 | ACATGCCTTTTTGTT[A/G]GCATAATAATGGTCT | 337867 |
rs567763890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321500 | ATTTTTAGTAGAGAC[A/G]AGGTTTCACCATGTT | 337867 |
rs567766564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276148 | TGCCAAGATGGGGAG[A/G]GGCAGTGAGGGGTGT | 337867 |
rs567771917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358249 | CAACAGGGATGCATT[A/G]AGTAGCATCAAAGGG | 337867 |
rs567774925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292665 | TTTTACTATCCTCTC[A/G]CTGAATAGTCAGTGA | 337867 |
rs567802922 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379815 | TGACTTTCTGTGCTA[C/T]AGATAAACATAAATC | 337867 |
rs567821864 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277907 | GGATCCATCTGTAGG[A/G]ACATAACGTTCTTCT | 337867 |
rs567822770 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212662 | GGGGGACATAAAATA[A/T]AGGGAAAAAAACATA | 337867 |
rs567825084 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226792 | AAGCATGTGTACTTG[A/C]TTTTTTTTCCTCCAG | 337867 |
rs567853375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366378 | ACTGGAGCTTTAACT[A/G]TAAATCCCATGTAAC | 337867 |
rs567889111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205821 | TCACCGTTCCATGTG[C/T]GTCCCTCCCGAAGCT | 337867 |
rs567889688 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319168 | TTGTCTATGCTATTG[G/T]ATTTTAATAATAAGC | 337867 |
rs567906533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218290 | GGACCAAAATGAACA[C/T]TTAGGTGCCCAGTGC | 337867 |
rs567915245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238286 | GATGTTTTGAAAGTG[C/G]ATATTAGAACCAAAT | 337867 |
rs567918338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358939 | GGCTCTGAGACACAG[C/T]GTTTGGGTTGGAGGT | 337867 |
rs567920582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219301 | CAAGGCCTGTGGTTA[A/G]TGTCTCCAGTACCCA | 337867 |
rs567945672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253889 | GTTAAGAGTGATAAA[A/G]GTAATTTAGCAGAGA | 337867 |
rs567958163 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282124 | TGGCTGGCAGCATCA[C/G]TGGCCTCCACCCAGT | 337867 |
rs567962939 | snp | A/G | 0.000135044 | 0.00821606 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254898 | CATTTCACTGTTTAT[A/G]TTGCTTAGTGACCGT | 337867 |
rs567974696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213133 | ATTTGATTTTATACA[G/T]AAATGGCATTCAAAT | 337867 |
rs568004312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231892 | ACTTAGAAAGAAGTG[A/G]CATACATGATTGGTT | 337867 |
rs568018852 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333053 | GATCACTTGAAGCCA[C/G]GAGTTTGAGACCAGC | 337867 |
rs568027610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246304 | TTAGCATGCAGTTTG[A/G]ATTCCACAGGTGGTC | 337867 |
rs568031569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338703 | TGTCCACCATTCACT[C/T]TTCAGCCTACTACAG | 337867 |
rs568033112 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253600 | CTCACTGCAGCCTCC[A/G]CCTCCTGGGTTCAAG | 337867 |
rs568034151 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243463 | TTCAGTTACAACTTT[G/T]TCTTATTCAATAACA | 337867 |
rs568077697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230964 | TGAGGCAGGAGAATC[A/G]CTAAACCCGGTAGGC | 337867 |
rs568084391 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386666 | CTAGCTGCTCAGAGG[G/T]GGGTCGAGGTGACTT | 337867 |
rs568092755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331462 | AGTGTTATTACTTCT[G/T]TCTCTATTCCAATTT | 337867 |
rs568092822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324466 | AGAATGAAGAAGTCA[A/G]ATGGAGCAGGGCTGT | 337867 |
rs568108956 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283758 | TTTTTTTTTTGAGAC[G/T]GAGTCTTGCTCTTTT | 337867 |
rs568114551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224972 | ATTATTGCTTTCCAC[A/G]TAGGTTTCTGAGATG | 337867 |
rs568125355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232621 | CAGAAATGCAAAGTC[C/T]TTAGGAAAAAGCACT | 337867 |
rs568158133 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378239 | ATATTAAAAACTTCA[A/G]TATCTGGCTGGGCTC | 337867 |
rs568178113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324831 | CTGCAGATCAAGTAG[A/G]GGAAATGACTGATAT | 337867 |
rs568190961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356697 | CAATACACTGTTTTT[A/G]TAGCACGACACAAAG | 337867 |
rs568222413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344195 | GACCCCGGAGGCTCA[C/G]GGGAGTGCTTGCTTG | 337867 |
rs568223593 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344585 | TTAGTCAGAAAGTCA[-/T]TTTTTTTTCAGTTAC | 337867 |
rs568226850 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303777 | TATCAGATGGAAATT[A/C/G]GGGAGGAACATTAAA | 337867 |
rs568238127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261446 | TGTCTAAATGTGTGG[C/T]TTTTCTTAAGTCCCA | 337867 |
rs568244260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343930 | TTACTTTTCAACAAA[C/T]AAGTACTTAGTGCTT | 337867 |
rs568248265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296612 | TTTTTTAACCAAATG[C/T]ATATCACTGCCAGGA | 337867 |
rs568257178 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383893 | GGAGGTTCCCTCCCC[A/C]ACCTGCCTCTCTACT | 337867 |
rs568279051 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373821 | CATGTGGTTATACTC[C/T]AGACACCAAGGAACC | 337867 |
rs568279330 | in-del | -/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259346 | TTTGGGGTCCATCCT[-/T]TTTTTTTTTTTTTCT | 337867 |
rs568285042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211160 | GCTTTTCTTAAGTTA[C/T]TACATTTCGTATTCA | 337867 |
rs568297570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336210 | TCTTACACATTCCTA[A/G]GGTTTCTTGATATGT | 337867 |
rs568300096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290572 | TCCACTAAAAATACA[A/G]AAATTAGCTGGGTGC | 337867 |
rs568312841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205390 | AAGAGGAGGGGTTAC[C/T]CTTGGTCACGGAGCG | 337867 |
rs568389467 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230398 | TTGAACCTGGGAGGC[A/G]TCAGAGGTTGCAGTG | 337867 |
rs568396090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316582 | AATACTTAAATCAGT[A/G]TCACCCACTGGGTGA | 337867 |
rs568408921 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301872 | TAGAATAACAGCTTT[G/T]GGTTTTTGCTGAAAT | 337867 |
rs568420853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267137 | AGTGACTTCAAGAAT[C/T]TTTTCATGGGCTTCT | 337867 |
rs568432317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330020 | GCTCTTCTTTAATTC[C/T]CCTTTGCAATTTTTA | 337867 |
rs568463294 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260517 | GGCCTGAGGTCTGTC[A/G]TCCTCCCCTGCAACC | 337867 |
rs568490497 | snp | A/G | 0.145305 | 0.227022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216080 | TTTGTACCAACCTAT[A/G]TTTGTGTGTGTGTGT | 337867 |
rs568513469 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99270915 | GGTATTTATGCATGC[A/G]TGAATGAATGAGAGA | 337867 |
rs568513912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244695 | TGTTATTATTATTAT[G/T]TGAAAGTCAGTAAAA | 337867 |
rs568514543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372890 | GAGGCTGAGGCGGAC[A/G]GATCACGAGGTCAGG | 337867 |
rs568550286 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274563 | ATTCATGAGCTCAAG[G/T]GATCCTCCTGCCTTG | 337867 |
rs568557522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233282 | CATGCCCAGCTAATT[G/T]TTGTATTTTTAGTAG | 337867 |
rs568573345 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339216 | TCTGCCCAAAATGTT[A/G]TTTCCCCAGTTCATC | 337867 |
rs568580065 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366299 | GTGTGTTTTGTGTGC[C/T]GACTTGCTCATCATG | 337867 |
rs568582943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288449 | TTGAGGAAGGTGAAC[C/T]CTTGAAACAAAAAGG | 337867 |
rs568588199 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244437 | AATACACACCTCTGA[A/G]CTGATTCTAGCTGAA | 337867 |
rs568596764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221039 | AACATCTTTCCAAGG[C/T]ACAAAATATTTTTCT | 337867 |
rs568601296 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237264 | TATGCGTATATATAT[A/G]TATATATACACACAC | 337867 |
rs568614997 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208603 | TCCCCCCTTTTTTTC[C/T]CAGTTAAGACTTGTA | 337867 |
rs568627894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382664 | GCAGCCACAGCCCTC[A/G]TACTGGGAGTTCACA | 337867 |
rs568678905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378127 | TGCAGCGTTAGCATC[A/G]TCTCCATCATCACTG | 337867 |
rs568691587 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376523 | CAGCACCAGCTGCAC[C/T]TTGGTGTCCTCTGAG | 337867 |
rs568704994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370554 | GACCACACCATCCAC[A/G]CCATCGCCTCCCCAT | 337867 |
rs568721304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324920 | TATATATCCCATCTA[C/G]GTTTGTGTAAGTACA | 337867 |
rs568730346 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281496 | AGTCAGCAAGCACAC[G/T]CCAGGCTCATCCCAG | 337867 |
rs568739881 | snp | C/T | | | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352044 | ATCCTCCCCCAGCAA[C/T]AGCCATTTGGTATCA | 337867 |
rs568745524 | snp | A/G/T | 0.000264264 | 0.011492 | synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238443 | CAAGGCGCCTCTGTC[A/G/T]AAGAGCCTTCTGCTG | 337867 |
rs568751394 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338823 | TATCAGCTGCATTAG[A/G]TATAGCTGACCATCC | 337867 |
rs568754072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377176 | GTCAGGCTCTGTGTT[A/G]GGGGGAAGCAAGCCA | 337867 |
rs568781078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362357 | AAGATCCTCATACAT[A/G]ACCCCTTCAGCATTC | 337867 |
rs568798482 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277819 | CCCTCTGTCACCACC[C/T]GCAAGCCTCATCAAG | 337867 |
rs568804159 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226871 | GCTCAAATCCACATT[A/G]CAAGAAGGTTTTCCC | 337867 |
rs568825629 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372693 | GTAGACAAGAAAGAG[C/G]AGGAGGAGGAAGAAG | 337867 |
rs568833181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239406 | TCTGTCTCCATATCT[A/G]TACTTACGTGAAGGT | 337867 |
rs568864790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317945 | TAAATGGTCATGACT[A/G]TAGTTATGTAAAAAT | 337867 |
rs568873203 | snp | A/C | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351668 | AAACTTGGGGATAAA[A/C]CTTTCCATTAGGCAT | 337867 |
rs568883639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325277 | CCAGCTAATTTTTTT[A/G]TGTTTTTTGTAGAGA | 337867 |
rs568945810 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284696 | GTCTGGTTCAGTATT[A/G]CATGTTGCATTTCAT | 337867 |
rs568955325 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210704 | CTGGTCTCAAACTCC[C/T]GACCTCTGGTGATCT | 337867 |
rs568955482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217395 | CTCCACCATGCAGGC[A/G]TGTGTTCTGCCTGCC | 337867 |
rs568962794 | in-del | -/TGAA | 0.0146672 | 0.084371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316399 | AACCAGGGACATTGT[-/TGAA]TGAATGAATGAATGA | 337867 |
rs568965133 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385463 | GAGGGAGGTTCCACC[A/G]CACCCCTGCCCTCAA | 337867 |
rs568969910 | in-del | -/CAAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245550 | AACGAGACTCCATCT[-/CAAA]CAAACAAACAAAAAA | 337867 |
rs568987772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319187 | TTAATAATAAGCGTT[C/T]GTCCTAAATTCTCTG | 337867 |
rs568989404 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198728 | GAAACCATATGAATG[A/G]ACATTTTGGACTGTT | 337867 |
rs569022908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344269 | CAGCTGTGTCTGACT[C/T]TGAGGTCTCTGTTTC | 337867 |
rs569036027 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378352 | GCCAACATAGTGAAA[C/G]CCCATCTCTACTAAA | 337867 |
rs569066184 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205727 | GTGAGGGCGATCTGG[C/T]TGTGACATCTGTCAC | 337867 |
rs569076278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290682 | GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC | 337867 |
rs569081265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331627 | AAAGAATAGCAAGTC[G/T]CAGAGTAACTGCCAA | 337867 |
rs569085317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283839 | TCCCGGGTTCAAGCT[A/G]TTCTCCTGCCTCAGC | 337867 |
rs569095850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204207 | GTCTATTGGGGCAAA[A/G]CTTTTTAAAAAAGAA | 337867 |
rs569184519 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311365 | TCCTGCGGAGCACAG[G/T]ATCAGAATGGGGATG | 337867 |
rs569185289 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217745 | AGGAGAGTTACTTGC[C/T]AGCACTTTAAAATTG | 337867 |
rs569201698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99225718 | CCAGACAAAGCTGAT[A/G]CCCTAAGTAAGCTTG | 337867 |
rs569217591 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99267614 | TGCTCACTTCAGAGC[C/T]TTCCACTTGCTACTG | 337867 |
rs569221871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324392 | CTGGTTCCACCATTG[C/T]TCTGTCCCCTTTGCC | 337867 |
rs569227492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261483 | TACAGCTATAATCTT[C/G]TAACCCAGTTAGTAT | 337867 |
rs569232901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304608 | CCAGTAAGCCCTTGA[C/T]GAATAATAATCAATT | 337867 |
rs569263057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99254003 | CTTTTAGATGGATAA[A/G]TTACTTGGTTTGTTA | 337867 |
rs569299105 | snp | A/G | | | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295761 | CCACAGCAATGAAGC[A/G]GTCAATACTCAGGCA | 337867 |
rs569315680 | snp | C/G | 1.66535e-05 | 0.00288556 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295904 | GTAGGCAAAGCGGTG[C/G]TAAAAAGTATATCAG | 337867 |
rs569340406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231657 | CTTAAGTGATCTACC[C/T]GTCTCGGCCTCCCAA | 337867 |
rs569340708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330045 | TTTTTAAATTTTCAA[C/T]GTACAGGTCTTGCAC | 337867 |
rs569349059 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351155 | TGGGGATAAAAAAAA[A/T]TATACAAAATTACCT | 337867 |
rs569401068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296371 | GGAAGAACAGAATAA[A/C]ATTTGTGTTTTTACT | 337867 |
rs569423734 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250197 | TTATAGTTTGAAGTC[C/T]TACATTTATATCTTT | 337867 |
rs569425610 | snp | A/G | | | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99243949 | GGAAGCAGAAAATTT[A/G]CAGTAAGTTTTTATG | 337867 |
rs569429030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237634 | TAGAAGAGAATAATT[C/T]AGCCTAAAGAAAAGA | 337867 |
rs569500842 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363298 | TATATTTCTTCAAAA[C/T]AGTCATGCCTAGTTT | 337867 |
rs569502215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266261 | GATATGAATGTATTC[C/T]TCTAAAACAAGGTGG | 337867 |
rs569532454 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275267 | GGGATTGGAAGACTC[A/T]CAGTGCTGTTGGCAG | 337867 |
rs569548110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252085 | CCTTTCAGAGTCCTC[C/T]TCATCTGACCACCAG | 337867 |
rs569582507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275969 | CCACTCTAATACCTG[C/T]AGGGTGTAAGCCTGG | 337867 |
rs569588115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266930 | GTTTTAGTTTGTTGG[A/G]GAATGGCTGTATCGT | 337867 |
rs569596111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302643 | AACAGCCATCATCTG[A/G]GGGATTATGGGTGTT | 337867 |
rs569604793 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208232 | GAACTCCTGACCTCA[A/G/T]GTGATCCGCCCTCCT | 337867 |
rs569618222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268016 | AGGCTCCATGGCTTC[C/T]GCTTCCAGCTGGTGT | 337867 |
rs569629941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383347 | TCTGATCATTTTCCA[G/T]CCAACCAAATGAATT | 337867 |
rs569646308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343321 | TCCAGGATTCTACGG[A/G]CCCCCATTGTGGTTC | 337867 |
rs569675550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336907 | CAGCCCATGGTGCCC[C/G]CCTTCCTTCCCACCT | 337867 |
rs569703006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244806 | CTTGAAATAGAATCA[A/G]TTTTATATTCTTTCT | 337867 |
rs569714940 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284229 | ACACACAATGCAAAG[-/A]AAAAAAGTTCCAATT | 337867 |
rs569721822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375528 | GATCGGGTGGGGGCC[A/G]TCTTCAGGTGGGCAT | 337867 |
rs569722498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288626 | GGAAAAGCTAGTGGT[C/G]CTCCTCTTATACTCT | 337867 |
rs569731965 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349602 | ACGTAATCACAGGAC[-/A]GGGGGGCCCTTCCCT | 337867 |
rs569732767 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329450 | ACATCAAGAGGTGGA[A/G]CTTATTTTTCCTCTG | 337867 |
rs569741624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362242 | CTGCTTTTATAATGG[G/T]CTTTTATATAATAGA | 337867 |
rs569747892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376708 | TAGAGCTGGCTTCTC[A/G]ATGAAGTTAGAGGAA | 337867 |
rs569759547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281571 | AAGGTGAGAACTCGC[A/G]TCTACTTTGAGGAAA | 337867 |
rs569772649 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204902 | GGGAGTTTCGTTTCC[-/TT]TTTTTTTTTTTTTTT | 337867 |
rs569776562 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273133 | TTTTCTTTTATCTCT[C/T]CTATTAGTATACCTA | 337867 |
rs569780757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369250 | TTATATATAGATGGT[C/G]CCTGACCTATAATTG | 337867 |
rs569784161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245471 | TGCGTTGATCTTCTT[A/T]AAAAAAAACAAAAAC | 337867 |
rs569784426 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237345 | AATCCTGTCATTTGC[A/T]GCCACATGGATGGAA | 337867 |
rs569789100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316445 | AATGAATGAATGAAG[A/G]CTTGAATCATAATCG | 337867 |
rs569822808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355143 | TAATTAGGAGTTTCA[A/C]CTCTGTTTCTGTCAA | 337867 |
rs569863253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273686 | TGATGAATCCAAGCA[G/T]ATTCATCCATTTGGG | 337867 |
rs569869923 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309519 | TCATGAGCTCACAAA[C/T]CTTGTTTTTATTGCT | 337867 |
rs569872603 | snp | G/T | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386946 | CTCCATGCTACCCCT[G/T]TAAACAGCACCTAGC | 337867 |
rs569904351 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269799 | AGCAGTTCAGTAGGC[A/G]TTGCCTGCAGTAACA | 337867 |
rs569906774 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259015 | GTGCGTGGAAGTCTA[C/G]AAATAATTTCTTTTG | 337867 |
rs569917350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348764 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAG | 337867 |
rs569925318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215935 | CTGAAAGACCTCTCT[A/C]ATAAAGGCTATTTTC | 337867 |
rs569930015 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233554 | CCAGAGCAGGCGTTG[A/G]GGGCCCTGGTTGAAA | 337867 |
rs569931688 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364457 | GAAAAATTAACTATA[C/T]ATTGTATAATTTTTC | 337867 |
rs569935340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335292 | CTTCTGCTGAATCAG[C/T]GTAATGCTGATATAC | 337867 |
rs569942499 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251322 | TCATATTGTCAGTAA[A/G]GAGAGATAGTTTGGG | 337867 |
rs569942705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250432 | GTATGTCTGTTTTTG[A/T]ACCAGTACCATGCTG | 337867 |
rs569944942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242302 | GTGCCCCTCACCTCC[C/T]GGACGGGGCGGCTGG | 337867 |
rs569953223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203245 | TTTGCCATGTTGACC[A/G]GGCTGGTCTTGAGCT | 337867 |
rs569963559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99287178 | TTCATTTTACCATGT[A/G]GTTCCTAAAATCTGC | 337867 |
rs569967368 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209260 | CCCCTCAAGGATTCA[C/T]TTCACAAAGCCCCCT | 337867 |
rs569987561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235699 | TTGTGCTGGGGCCGG[A/G]TGCAGTGGCTCATGC | 337867 |
rs569991198 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250467 | CTTACTGTAGCCTTA[-/T]TAATCTGAAGTCAGG | 337867 |
rs569995289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236474 | ATGTGCTCAACATTA[C/T]TGATCATCAGAGAAA | 337867 |
rs570029311 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225254 | TCTATAACTCTTCTC[A/G]TCTTGCAGAAATGAA | 337867 |
rs570055149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374990 | TTATGCCAGGTTTTT[C/G]CATTGCTTGCTCTAG | 337867 |
rs570075590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383475 | CTGCCTTTGCTCTAC[A/G]CTGTCCACCAGCCCT | 337867 |
rs570085900 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206243 | GGACATGAGTAGGTG[A/C]GAGTTAGGTTGTGGG | 337867 |
rs570092493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328496 | ATTCTCTACACCCTT[G/T]TCAACACTTGGTATT | 337867 |
rs570092754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322398 | TCATTACCACAGGGA[C/T]GCACCCTAATTCTCA | 337867 |
rs570108810 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386130 | TTGCCTGCCCCTCCC[A/T]GTGGCAGGGCTAACT | 337867 |
rs570122712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300732 | GGGTGAATATATAGC[A/G]TTGAACATGTGCTGT | 337867 |
rs570137864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383841 | CTAAGGCTTTTGGGG[A/G]AGGAGGGTCTGGGTG | 337867 |
rs570145024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222522 | ATTGAGGTTAGATCA[A/G]AGGGGTAGCCCATTG | 337867 |
rs570160725 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361747 | CCTCCCCTCCTTCAC[A/T]TAACAACCAAAACTG | 337867 |
rs570169681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282335 | GCTCATGACCTAGGA[A/C]GCTTGTTGAGAACTT | 337867 |
rs570169760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290410 | GGCCAGTGTCTGGAC[C/T]AGGATGATGGTAGTG | 337867 |
rs570180220 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201035 | ACCCTCGGGTTTGCC[A/G]GAGGTGGTGGGGCCG | 337867 |
rs570191582 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208190 | TTAGTAGAGACGGGG[G/T]TTCTCCATGTTGGTC | 337867 |
rs570193869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360673 | CTCTCTTCTCCATCG[C/T]TGAAATCATTCTCTT | 337867 |
rs570205873 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335591 | TGCAGGAAGATGAGC[G/T]CAACATGTGATACCT | 337867 |
rs570207681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358534 | AAATCTATATTTATG[A/T]TAGCAAGTAATAGGC | 337867 |
rs570257314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99282896 | GTATATGTTATGTGT[C/T]GAGTTCTGAAATATC | 337867 |
rs570264156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293604 | ATTTGGGCTTTCATC[C/T]GTGTTGTCTCACCTG | 337867 |
rs570268580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201328 | CCCCATTCTTTTAGG[C/T]TTGGGGGACCGAACT | 337867 |
rs570291503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342257 | TCCCAAAATGGGGAC[C/T]AGTCCTGTTGGGTAA | 337867 |
rs570296943 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259805 | TGATTAGCTTCCCCA[C/T]TGCTGCTAAAATCAA | 337867 |
rs570374462 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311867 | AAGAAGGACTGATAC[A/G]TGAGGAATTCTAGAC | 337867 |
rs570431469 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230782 | TGGGCCGGTTGCAGC[G/T]GCTCACGCTTGTAAT | 337867 |
rs570440736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337026 | TCTTTGCGCTTTCCT[A/G]TCTCGTTTTACTGCT | 337867 |
rs570440794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377849 | CTCTCATCTCCCAAA[C/G]TGCGAGGAAACAGAG | 337867 |
rs570455466 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284203 | GCTGCTAAAATAAGA[A/G]GTACAAATAAACACA | 337867 |
rs570460394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330180 | AAATACAGCTGATTG[G/T]CTGGGTGTGGTGGCT | 337867 |
rs570464482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246225 | GAATGTTGACCTTTA[A/G]CTCTTTTAATAATGT | 337867 |
rs570489617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307746 | ATGATTTTATATTGA[C/T]TTTGCATGTAAAAGT | 337867 |
rs570499732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237685 | CCGGGCTGGGTGCCG[G/T]GGCCCATGCCTGTAA | 337867 |
rs570515063 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361860 | AAATAGACCAGACGC[A/G]ATGGTGCACATCTAT | 337867 |
rs570548009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323972 | AATTTTATTATTGCA[A/G]CTTATGTTCTACCTG | 337867 |
rs570557681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230338 | GGGCATGGTGGCAAG[C/T]GCCTGTAGTCCCAGC | 337867 |
rs570569723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275407 | AGCAGATGTGTGGTG[A/G]TATATTTTTGTGATT | 337867 |
rs570570206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99266419 | AGTGTACTAATTTGT[G/T]TTGGACTGCATTCAA | 337867 |
rs570583795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231089 | ATAGAATCCAGCTGG[A/G]TATCTTAGGTAGTCT | 337867 |
rs570585618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238153 | CCATTTTCTGAAAGG[G/T]GTTCTATGGAAGTTC | 337867 |
rs570598166 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99254070 | TCCAAGGTTCCTACT[A/G]GTACTATTTATACTG | 337867 |
rs570610651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350168 | TGATTGATAATGTCC[A/G]TGATCATCTCTATAT | 337867 |
rs570610857 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373173 | TCTCTTTTTTATTGT[-/TT]TTTTTTTTTTTTTTA | 337867 |
rs570633775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310338 | CCGGTGTCTCAAGAA[A/G]AAAAGAAAGGATGGA | 337867 |
rs570650704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303608 | GCATGATTTGTAGGA[C/T]GCAGCATGTGGGAAA | 337867 |
rs570662847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253290 | TTATTGAAAAATTGG[G/T]GTTTGACATGAAAGA | 337867 |
rs570670063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311150 | AGACAGTGGGAATAA[A/C]ACAAAACAGACCAAA | 337867 |
rs570700213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209850 | TGGTGGTTGGCGCCT[A/G]TAATCCCAGCTACTC | 337867 |
rs570716217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203927 | GCCATGCCTGTTTCA[A/G]GTGCTTGAAACTATA | 337867 |
rs570716233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343465 | CCCTGCCCTGCTGGA[A/G]CGTGCATTCCCACCA | 337867 |
rs570716999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329308 | ACACTCTACAATCAG[C/G]CTGTAATTTCTTCAA | 337867 |
rs570750788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335323 | ACCCTATTTTCTGTT[G/T]TATATCAGATCTTCA | 337867 |
rs570785631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322908 | CGGGCTGTGATTTGC[C/T]TTTCTCTCTTCCCTC | 337867 |
rs570804732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323392 | GATCGCTTGAGCCCA[A/G]GAGTTCAACACCAGC | 337867 |
rs570829957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236617 | AGTACTTTGGGAGGC[C/T]GAGGTGGGTATCACC | 337867 |
rs570848363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369320 | AGTGATACATACTCA[A/G]TAGAAGCCATACATC | 337867 |
rs570857799 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304375 | AAAGGCAGTGTGGGT[A/G]TATTTGTGAGAGTGC | 337867 |
rs570883981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315328 | AGGCCATGTGGAATT[C/T]GAAGAGCACTCCAGA | 337867 |
rs570887296 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308643 | GCCTTTCTGCTCCAG[C/G]ATTCTGTAAAAATAG | 337867 |
rs570891005 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215659 | ATTTCAGGTGTTGAT[G/T]AATACAGCCCTCTGG | 337867 |
rs570907969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316131 | ATTTTTGTAATATTT[C/T]CGGTAACTTTGAGAG | 337867 |
rs570923341 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302097 | AGGTGACCTAAATCA[A/G]TGTGCCCACAGTGGA | 337867 |
rs570938744 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247875 | ATTCTCTCTCTCTCT[C/T]TTTTTTTTTACCTCA | 337867 |
rs570944866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316512 | AATGACTTGAGAGCC[C/T]ATAACATCATGCCCT | 337867 |
rs570952761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355848 | CACAGACCCACTGGA[C/T]GCCCTGGTGCATGGC | 337867 |
rs570953625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214943 | AGTAAACATCATTGA[A/G]ATAGAAGTCAGGTCA | 337867 |
rs570963901 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208208 | CTCCATGTTGGTCAG[C/G/T]CTGGTCTTGAACTCC | 337867 |
rs570975458 | in-del | -/AT | 0.00597247 | 0.0543191 | intron-variant | UBAC2 | GRCh38.p7 | 13:99223902 | TCTTTTATGCCCAGA[-/AT]ATAGTCTATTTTGGT | 337867 |
rs571024180 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380542 | AGGACAGCAGGGGCC[A/G]CTTGGCTAACTTGCA | 337867 |
rs571034303 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353848 | CGAGAAGCCTTGATT[C/T]CGTGCAACCCCCAAG | 337867 |
rs571045666 | snp | C/G | 0.000130738 | 0.00808404 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200801 | GGCGAGTGGCCTCGC[C/G]GCGCCGGATTCGTCG | 337867 |
rs571060900 | snp | C/G/T | 8.23803e-05 | 0.00641749 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295247 | GGGTCCATGCAGCAA[C/G/T]TGAAGTTCATCAGGC | 337867 |
rs571095727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376415 | ACCTCCAAGAGGGTC[C/T]TCATCCCTGTGGGGG | 337867 |
rs571126152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222181 | TCTGATGAAGGAGAC[A/G]GACAAAGAAGCAAAC | 337867 |
rs571145354 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328534 | GTTTTAGCTTTAGCC[A/G]CTCTATTGGGTGTGT | 337867 |
rs571159297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321175 | TTTTAAACAAAGATA[C/T]TTGTATGAAACATGA | 337867 |
rs571192414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314893 | ACTACCTGTCACTTT[C/T]CTTTTACTCTCACGG | 337867 |
rs571196022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322078 | GAAATGTTGCAAAAT[C/T]GTAATTGGAAAGCTT | 337867 |
rs571215686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354523 | AGAGCAGGGGAACAG[C/G]AGGGTTTGGGTTGCA | 337867 |
rs571218523 | in-del | -/TGCGGCCTTCCGCAGTG | 0.00636936 | 0.0560724 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241880 | CTAGGCAGAGGACCC[-/TGCGGCCTTCCGCAGTG]TTTGTGTCCCTGGGT | 337867 |
rs571245619 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257716 | CTTTTCTTAAAAACC[A/G]TTAAGTTATTTCATG | 337867 |
rs571257299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99206666 | GCAAAACCCTAACTT[C/T]GCATTGATTTATGGG | 337867 |
rs571276823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348176 | AGCTCTTGGAGGACA[A/G]GAGCTGTTGTACTTC | 337867 |
rs571295606 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236704 | AAAATACAGAAATTA[C/G]CTGGGCATGGTGGTG | 337867 |
rs571326473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250524 | TTCCTTTTCTTTTTT[C/T]TCCCTTAGGATTGCT | 337867 |
rs571331996 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369091 | TATAAATACATACAC[C/T]GGAGGGAAGGAAATG | 337867 |
rs571334916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202315 | TATGTTACAACTACT[A/G]AGTAATCTTCCCCAA | 337867 |
rs571335438 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346539 | AACTGCTGCTCATAT[C/T]GTTTCACGCAGTCTC | 337867 |
rs571335689 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258162 | TGCTTACCTCCTGTC[C/G]ATCAAAAGTCTGTGT | 337867 |
rs571391321 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342704 | GTGGGCACGACCTGC[A/C]AGACACTTGATGCTG | 337867 |
rs571423969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234940 | TTTGCTTCTTTTTTT[C/T]TCTCATATCAGAGGG | 337867 |
rs571436304 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285760 | AGGTTGGAAAGCTGA[A/G]TGCTCTATTTCTTAA | 337867 |
rs571438886 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297699 | GACAATGGGAAAAAA[A/G]CAAAGAATGAGGATG | 337867 |
rs571462264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268826 | AACAAGGATGTTGCT[C/G]GTGGTCCAGGTTGGC | 337867 |
rs571478173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272195 | ACTCCAGGGGCTTGT[A/G]TCTAGGTCAAGTGCC | 337867 |
rs571486464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221574 | CAGAGTCCCATTTGG[C/T]GTGTAAGCTGGTTTT | 337867 |
rs571494165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263468 | GGGTATTATCCATTC[A/G]CCAGAATGCCTACGA | 337867 |
rs571495872 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260660 | TAAACAATGGGTCAA[A/G]GATTCAACTTGTATA | 337867 |
rs571503748 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362780 | TCATTGATTTGTAAC[-/TT]TTGAATTTTGAGCAT | 337867 |
rs571516134 | in-del | -/TAGT | 0.0134861 | 0.0810011 | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356594 | AAACTAGCCTGGGAC[-/TAGT]TTTGTTCAAGCGATC | 337867 |
rs571529160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368129 | GCGGGTGGGAATGTA[C/T]TATGGTAGCTTGTTT | 337867 |
rs571534826 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316621 | CCCTGTCCTCAAGGA[A/G]CCCAGCCATGAGAAA | 337867 |
rs571562769 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364259 | ATTGTTTTCATACCT[A/G]TTGAGATGAGCGTTT | 337867 |
rs571574159 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288207 | TCATTCTTGTACAGA[A/G]ACCAGAAATAAATGT | 337867 |
rs571583164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263935 | ATTTCAAAAAGCAGA[C/T]GAAATGAAAATACAG | 337867 |
rs571591207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361312 | AGTAAAGGAAACATT[A/T]CCTGTTTATAGAGGC | 337867 |
rs571599013 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335136 | AAATAGCTAATGGGA[A/G]CAATGAACAAATCAA | 337867 |
rs571609802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248678 | GTGAGCCACTGTATC[C/T]GGCCATTTTTTGTTT | 337867 |
rs571614890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264783 | GTAGGACTGTGGATA[A/G]GAGCCGGCAGGATAG | 337867 |
rs571625692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373710 | ACGGATGGGTGGGCT[A/G]GAGTAGAGGGGACTG | 337867 |
rs571666101 | snp | C/T | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386622 | GTGCAAACCTGGAAG[C/T]TCGGCCTCACTGAGG | 337867 |
rs571672658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326281 | TTGATTTGCATTTCC[C/T]TGATGATTAGTGACA | 337867 |
rs571679741 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301557 | ATTGCTAATAGAGTT[G/T]CTAACACTTCTTGAG | 337867 |
rs571685624 | snp | C/G/T | 3.30678e-05 | 0.00406608 | intron-variant, synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201552 | GTTTTCCTGGCGTGT[C/G/T]AGCGGTGGTCAGCAG | 337867 |
rs571691471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380354 | GGAGAGACCGTAATG[A/G]GATGTGTGGGGACTG | 337867 |
rs571704282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99334240 | TGCTGGGATTACAGG[A/C]GTGAGCACAGAAAAA | 337867 |
rs571735348 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302153 | CTCACTTTCAAAAAC[A/G]GCCAGGGGAGCCACC | 337867 |
rs571749504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202395 | CAAGAAGGCAATGTG[A/G]TTTTCCTGGGATCAC | 337867 |
rs571774302 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327421 | AAATTAAAATTTTTT[A/C]ATCAGTTTTGATTAT | 337867 |
rs571790211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234334 | GTGGGATTATAGGCG[C/T]TTGCCACCACGCCCG | 337867 |
rs571793254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219419 | TGTGCAATTAACAGC[A/C]ACCACAATTTAATTG | 337867 |
rs571805317 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359570 | CCCAGCCACTGTGCC[A/T]TGGTCATAGATGGGC | 337867 |
rs571822303 | snp | C/T | 0.000346195 | 0.0131521 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255659 | AGGGTAAAGTCATTA[C/T]AAATATCAAGTCCAC | 337867 |
rs571828123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299179 | CCAAATAAGATGCAG[C/G]ATCTAGCAGAGCCAG | 337867 |
rs571854301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248296 | TGGTGAGATCATAGC[G/T]CACTGTCACCTCAAA | 337867 |
rs571879130 | in-del | -/GCCACCT | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339122 | TTCTAGAATTACATA[-/GCCACCT]GCCCACTCAGTAGCC | 337867 |
rs571886752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306557 | CATATATAAAACCCT[A/C]ACTGCCCTTTAAAGG | 337867 |
rs571914300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213198 | AAAAAACGTGAGTTA[A/G]AATGATTATAACTTT | 337867 |
rs571915615 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386741 | TGAATTGCGCCATCT[C/T]GGGTTGCAAGGAACA | 337867 |
rs571919361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256255 | TTCTCTAGTTTGAAA[A/G]TGAAGACTTGTGTAG | 337867 |
rs571928284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213700 | ATAAGTTTTTTTTGC[A/G]GTATTTTCCCGTTAG | 337867 |
rs571942275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342494 | TTATCAGGCACACAC[A/G]GTCTCTGTGGATGCC | 337867 |
rs571957637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207445 | GCTGACCACCTTCTT[C/T]CCAGCTCTTAAAAGG | 337867 |
rs571971017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243321 | GATTTAAATAAACTA[A/G]TATTTCAAACCTAGT | 337867 |
rs571980784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99293829 | GGATATAAAGTCCAA[C/T]AAAAATTTAAAGTGT | 337867 |
rs571991786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207043 | ACCACTCTTGCTTTT[A/T]CTTTACCTTCATTCT | 337867 |
rs571995151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242500 | GGCGGCTGGCCGGGC[A/G]GGGGGCTGCCCCCCC | 337867 |
rs572035751 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344887 | CATGTCCTTTCCCTC[C/T]GTGAGTTTGTGGCCA | 337867 |
rs572063500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99250688 | TTAATGATATTGATT[A/G]TTTCAGACCATGAGA | 337867 |
rs572082381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99286066 | GGTAGACCAGTCCTT[A/G]TGTGTTCCAGGAGTC | 337867 |
rs572099379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314919 | CACGGCTTTTGATGT[A/C]GTTTTATTCTACAGC | 337867 |
rs572102864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381406 | GACAGCAAATGGATT[C/T]GTTTGTGCTGGCTGG | 337867 |
rs572116040 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332327 | GCATGTTTTCTACCC[A/G]GCAAATTAAATTATT | 337867 |
rs572127466 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207576 | ATTGTGGCCTGCTTC[C/T]GTCCCGCTATACCAT | 337867 |
rs572158515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347155 | ATACTCTTGAGAGAA[A/C]AGTAGAAAGCAAGAC | 337867 |
rs572171609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279603 | CACTAATGATGCCTC[A/G]CTGCCTTAGCCTGTT | 337867 |
rs572190911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214187 | CCTGCTGTTTCTTCA[A/G]TCTTGTATCATTTTT | 337867 |
rs572195501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214691 | CTTCTACTTTTTTGC[A/G]GACCTCCAACCCCCT | 337867 |
rs572206563 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362511 | ATTTCTTTCACATCA[C/T]TCCCACACTCAGTAT | 337867 |
rs572208338 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280326 | CATTACTCACTACTG[A/C]CTGTCACGCATACAT | 337867 |
rs572224409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314504 | GTACAATTGCATGTG[C/T]GTACTTTTTAACAAT | 337867 |
rs572240757 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210415 | CTTTTTTCCACCCAA[A/G]AGAATCTTTTAAAAT | 337867 |
rs572256319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99221681 | GGATAAAAATGCTGC[C/T]CTGTTCCACCTGGGA | 337867 |
rs572275282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347650 | AACAGTGACCAGGGT[A/G]ATGGCTCTATAGATC | 337867 |
rs572307598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366609 | GCTGTCTCCGGGGGA[A/G]GACAGGCTTTTTAGT | 337867 |
rs572310404 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386283 | GAGAGGGAAGGCAGG[A/G]GTGGACCGCCATGAG | 337867 |
rs572334189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257835 | TTACATTTAGTATTA[A/G]TGTAAAGCAATATTG | 337867 |
rs572338464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249150 | GCGTGGTATCCAGTA[A/G]TTAGTTTTTCAACCC | 337867 |
rs572343778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319639 | AAATTTTCACATCTA[C/T]CCAGATACCTGATTT | 337867 |
rs572364065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373840 | CACCAAGGAACCATG[C/T]GGGATCTTACACAAG | 337867 |
rs572402057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380037 | AGAAAAGGCATGTCA[C/T]AGCTGAAGGAGGGTG | 337867 |
rs572421415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234469 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 337867 |
rs572421468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227505 | GCAAGTCACACTGCC[A/G]TGCCTCACTTCATTT | 337867 |
rs572433176 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277544 | AAATAAATAAATAAA[A/G]TAAAATAAAAGGCAA | 337867 |
rs572457405 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305977 | CTCGGCTCACTGCAA[C/T]CTCCGCCTCCCAGGT | 337867 |
rs572464006 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326339 | CCATTTGTATGTCTT[A/C]TTTGGAGAAATGTCT | 337867 |
rs572465220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321390 | CTTGGCTCACTGCAA[C/G]CACTGCCTCCCGGGT | 337867 |
rs572477705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220482 | CCTGATTAGTATTTA[C/T]TGCCTCAAAGAAATG | 337867 |
rs572482234 | in-del | -/AAA | 0.226779 | 0.248919 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324413 | CCCCTTTGCCATGAG[-/AAA]AGCAGGGCCCGGAGA | 337867 |
rs572487115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272373 | TCAACTCATGGCCAC[C/T]TTGTTTTATCTATAT | 337867 |
rs572503625 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249549 | TATTTTCTTTTGGCT[A/G]CGTACTCAGTAGTGG | 337867 |
rs572512373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227901 | TAGGGAGGTTTGAGG[A/G]GAGAGGAAGAGATAG | 337867 |
rs572515314 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322624 | CATTCGTTACTTGTC[A/T]TGTACAGTATATCAG | 337867 |
rs572515412 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345827 | GCTCACTGCAACCTC[-/T]TGTCTCCTGGCTTCA | 337867 |
rs572536043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239960 | CAGTTTGGTCCAAAA[A/G]GAAGGGATGACTGTT | 337867 |
rs572538222 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319430 | CTATCCTTGTTTCTT[A/G]GGTGAATGACTGGTA | 337867 |
rs572540236 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309069 | TATAGTGAAGGACTC[A/G]GCTAGTTCAAGTAAT | 337867 |
rs572540748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264459 | TGTAAAGTGCATGCT[A/G]TAGACACTAAGCACT | 337867 |
rs572572636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352345 | CAGTCATTCCCATCC[A/G]CCCTGTCCTAGGCAG | 337867 |
rs572615545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360518 | CCAGTTATTCTGGCT[C/T]TAGAGACTGTTCTTA | 337867 |
rs572647276 | snp | A/T | 0.116838 | 0.211584 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373188 | TTTTTTTTTTTTTTT[A/T]AAACAGGTATCTTTA | 337867 |
rs572652748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232188 | ATAGAGGGGATAAAT[A/G]ACTGAAGTGAAAGTA | 337867 |
rs572665772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241454 | ACATGCTTTACCATG[A/C]ACCTTGAAAATATTA | 337867 |
rs572667330 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270849 | TTCCAAAGTGAGGAA[A/G]AGAATAGCTTGACAC | 337867 |
rs572694376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273698 | GCAGATTCATCCATT[A/T]GGGTTGTACACTTGG | 337867 |
rs572717844 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200612 | GGGAGCTACGCCTCC[A/G]CTTCCCCAGTGCCAC | 337867 |
rs572736187 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99332706 | CTCTTTGTTCCTTTT[G/T]GCTTTATCTGATCGT | 337867 |
rs572739785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226238 | TAGGTAGGAAAGACA[A/G]CATGTCAGTAAACTT | 337867 |
rs572749310 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372023 | ACGGCACCTCTGCCA[A/G]TTCATCACCCCTCAG | 337867 |
rs572757183 | snp | C/G/T | 0.000566554 | 0.0168229 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351834 | GCCTCCTCATCTCAT[C/G/T]GGGCTGCCCGGTGTT | 337867 |
rs572771442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316776 | GAGACCTGGAAGAGT[A/G]GAGAGCATGGCTGTA | 337867 |
rs572780872 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227187 | CGGACAACAAGAGCG[A/T]AACTCCATCTCAAAA | 337867 |
rs572780975 | snp | C/T | 0.00478085 | 0.0486577 | splice-donor-variant, intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254712 | ATCAGATGCTTTTCT[C/T]TGAATAATTCACAAA | 337867 |
rs572786252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218535 | CTTAGCACTTTCTCC[G/T]GCTTATTTTCCTGAT | 337867 |
rs572789144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233696 | ACCGAGATACAAGGA[A/G]AATGAAGACAGAAGG | 337867 |
rs572796977 | snp | A/G/T | 0.00279242 | 0.0372774 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333099 | AAACCCCGTCTCTGG[A/G/T]GGGGGAAGAAAGAGA | 337867 |
rs572798163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99212964 | AATATTTTATGTAGT[A/G]TAGAAGGGATTAGTC | 337867 |
rs572814948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99213348 | GCATGAGCCACCACG[C/T]CCTATCCATAACTTT | 337867 |
rs572821110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345589 | TGTCCTCACCACTTT[A/G]TTGAGCTCATGGCTC | 337867 |
rs572835700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298507 | GCAATCTGAGATAGA[C/T]ATAAAGCCTTGAATG | 337867 |
rs572835877 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337689 | CCTATGCTGACAGCC[A/G]CATGAGATGCACATA | 337867 |
rs572850885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99358492 | CAGTAATTCTGTTTG[A/G]GAAAACATGGTTATT | 337867 |
rs572886160 | in-del | -/TTTCT | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210064 | TGCTTTTAGAAAATG[-/TTTCT]TTTCATCGTAAAAGT | 337867 |
rs572924988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346176 | ACATCCATGTCCTTC[C/G]TGCCTTCCCCACCAG | 337867 |
rs572928333 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282835 | TATAGCAAAATATAC[A/G]GCACACAAAAATAAT | 337867 |
rs572932469 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258906 | TTTAAACATTTCTAA[A/G]TGCTTAAAAGTAGGA | 337867 |
rs572939634 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222689 | GATTTGCTTTGCATT[C/G]CCAGGATAAGCATTA | 337867 |
rs572939918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205882 | CGATAGAGGAGGACC[A/G]GTCTTTGGTCAAGGG | 337867 |
rs572955662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362017 | CATCCCCAAAAAAAG[C/T]TAAAATAGTATATAT | 337867 |
rs572960360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306138 | TGATCTCAGGTGATC[C/T]GCCTGCCTCGGCCTC | 337867 |
rs572968556 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353699 | TATTAGAAAAATCAT[C/T]CTCATAATCATTCTG | 337867 |
rs572968796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276256 | GAGTTAGTATCAGAT[C/G]CTACAAGTCAAAGAG | 337867 |
rs572969570 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330375 | GAGGCAGGAGAATCG[A/C]TTGAACCTGGGACGC | 337867 |
rs572984650 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99296766 | TTTTTAAAAAGAAGA[A/C]GACGACGACCGCAAC | 337867 |
rs573008233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269049 | AGCTTTGGGCTTGGC[A/G]TAAGGAGTAACTTTG | 337867 |
rs573008835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339197 | CGCAGCATCTGCTGC[G/T]TTCTCTGCCCAAAAT | 337867 |
rs573015261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231567 | ACAGGCGTGCCACCA[C/T]GCCCAGCTACTTTTT | 337867 |
rs573016141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372275 | ACCCCACAAGTTCCT[A/G]TCAATTTCACAGAAC | 337867 |
rs573058306 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317367 | ATTTTTTTTTAATTA[C/T]CCTGAGCACAACTCT | 337867 |
rs573060172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310883 | TTAAGCGCCTCCAAG[A/G]GCATGTTCTGTGGTA | 337867 |
rs573105173 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210127 | AAAATAGAAAAAAAA[A/C]GGTCCTAGCATTTCA | 337867 |
rs573113368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319001 | AAAAATAAGGAGAGA[C/T]AGTCTGCTCATTTTG | 337867 |
rs573130725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296822 | GAAGAAAGATAAAGA[A/T]AATGAGAGAGAAAAA | 337867 |
rs573133960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99269730 | CAGAACTTCAATCTA[A/G]ACTGTAAGCTTCCAT | 337867 |
rs573138598 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240545 | ACTTGGAGCTGCCTC[G/T]TATGGTTTTTGAATC | 337867 |
rs573145954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311504 | CTGTTTTAATCAGTT[A/G]TGCTTGGGTTTATAA | 337867 |
rs573165740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210873 | CACCTCGGCCTCACA[A/G]AGTGCTGGGATTACA | 337867 |
rs573184376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237890 | AACCTGGGAGGTGGA[C/G]GTTGCAGTGAGCCGA | 337867 |
rs573185226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344418 | AGAACTTTTGCTTCC[A/G]TCTTCTTCTTTATGT | 337867 |
rs573217679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246698 | TCAATTTTGAAGTTG[G/T]TGGGAATACTTTTGC | 337867 |
rs573221956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377574 | TGACCATCTATAATA[C/T]CATTATTTATATAGT | 337867 |
rs573245075 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383668 | TGAAAGCAACGTTCC[A/G]GGGAGGAGCACGCTC | 337867 |
rs573253822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377996 | TATTTCACGGAAGCA[C/T]GAACCTGGTTTTCTG | 337867 |
rs573285516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290159 | AACCTCTCTGGAGCA[C/T]AGTTTCATCATCTGG | 337867 |
rs573291040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346265 | AGTTCAGGCCACCGG[C/T]GCCATTTGCCTGGAT | 337867 |
rs573301628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238671 | AATTTGTAAGAAATA[C/T]TTATTATTAATATTT | 337867 |
rs573302256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384033 | GGCTTTCTGGAGCCA[C/T]ATGCCCAGGCCCATG | 337867 |
rs573311423 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99352899 | CACCCCTGTGTCCGG[G/T]GTAGGGGCAGTGCAC | 337867 |
rs573345213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216375 | CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC | 337867 |
rs573372244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290759 | AGAAAGAAAGAAAGA[A/G]AAAGAAAAGATAGGG | 337867 |
rs573372809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248430 | GATTTTCACTCTTGC[C/T]GCCCAGGCTGCAGTG | 337867 |
rs573374882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99346939 | AATAAATAGATACAG[A/G]AAGACTTTAAGCAAG | 337867 |
rs573387292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216855 | TTTTTTTTGAGACGA[A/G]GTCTTGCCCTTGTCC | 337867 |
rs573393619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349854 | GACTGCGGGCAGACT[A/G]GGATAATATCCAGCC | 337867 |
rs573404832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248837 | GGTCCAGAGTCTCAT[C/T]TCCTGATGATTTATA | 337867 |
rs573409428 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283196 | AATATTGGCTTCTAG[A/G]ATGTAGGATTCAGAG | 337867 |
rs573430717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350384 | AATAAGTGATTAGAG[G/T]GTTGAGACTTTCAGC | 337867 |
rs573456292 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260032 | CCCTCTGGACTGGCT[A/G]CATTTGCTCTTCCTG | 337867 |
rs573484654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357012 | TTTCTCTCTGTATTG[C/T]GCTCACTCTTGTAGT | 337867 |
rs573524967 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243181 | ATTGGGATTATCTTT[-/A]AAAAATCTGAAAAAT | 337867 |
rs573541193 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227353 | GAGGGGTCCACTCCA[C/T]ACTGTCGTCAGCCCC | 337867 |
rs573544385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252733 | GTTTAAATGTATTTG[A/G]TTATAATGCTAAGTA | 337867 |
rs573566392 | snp | C/T | 0.000236409 | 0.0108696 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255919 | AAACTGTAAAAATAG[C/T]TAAGAAAAATAAGAA | 337867 |
rs573571227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219481 | AGTGCCCATTAAGCC[A/G]GGCTTGTCCACCCTG | 337867 |
rs573582958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253582 | GCAATGGCGCAATCT[C/T]GGCTCACTGCAGCCT | 337867 |
rs573589974 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385416 | ATCAGCCCGGGGACC[A/G]AGCATCTCTGGTGCT | 337867 |
rs573598220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306894 | TATACCCTTTGCCCT[A/C]GGAATTCTACCCCTG | 337867 |
rs573620316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256585 | GATTCAGAAGCTTCA[A/G]TATTATTTAAATTTT | 337867 |
rs573629787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306159 | CCTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 337867 |
rs573651619 | in-del | -/TTATGGA | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281811 | GCAGAGGTACTTACC[-/TTATGGA]TTGCTGGCTAATTGT | 337867 |
rs573675392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331113 | ATCACGTATCTCTTA[C/T]CCTTCGCCTCTCAGT | 337867 |
rs573676333 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385795 | TTTTCTCTCAAACTT[A/G]TTTTCGAATCTCCTG | 337867 |
rs573678058 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310898 | GGCATGTTCTGTGGT[A/G]AGAGACCTCTGGTGC | 337867 |
rs573716984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340644 | TGTGATTGCATGTGA[A/G]ATAGAGACTACATTT | 337867 |
rs573726962 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322494 | AATTTTCTTTTTACA[G/T]TTCACACATTTATCT | 337867 |
rs573732897 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199587 | GCTGGCACTTATGAG[C/T]ACTGAAAATGCTTTT | 337867 |
rs573742609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319031 | GTAAAAAGACATTGT[C/T]ACACGAGGGAAAAAA | 337867 |
rs573760069 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322312 | TTCTTGTGGTTCTGC[A/G]GAGAGCTTTTGAGCC | 337867 |
rs573800077 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314652 | GTGCTCTACCAACCC[A/G]AGCTTTGGGGTTTTC | 337867 |
rs573804464 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200890 | CGGCGCCCTCTGGGG[C/T]TCCGAGCCCGGCGGG | 337867 |
rs573806987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99319417 | AAATAAATTATCACT[A/G]TCCTTGTTTCTTGGG | 337867 |
rs573846778 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304017 | TCCCGCCCTTCTGCC[C/T]GCAGCCACGGCAGCA | 337867 |
rs573893314 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99313771 | ATGTTTGCTGCTTTC[A/G/T]ATTTGTCTAGTTTCT | 337867 |
rs573916399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99290836 | ACCTGAATCCCATGA[A/G]TGAGAGAAAAGTATC | 337867 |
rs573925688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263539 | AGTGATGAGGGTATC[A/G]AGTAACAAGGAACAT | 337867 |
rs573935101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304764 | CTTAAGTGACCAAAG[A/T]CCTAGCTGTTAAATG | 337867 |
rs573935845 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384725 | GCAGTGACGCCAGGA[A/G]TGTGATGCCAGGGCT | 337867 |
rs573942408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238759 | TGGCAGTATTTCCTT[C/T]TATTAGGCACATTTG | 337867 |
rs573957690 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338088 | TTTGAGACAGAGTCT[C/G]ACTGTGTCGCCCAGG | 337867 |
rs573976116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339018 | TGTGTCTCCTCCTCC[C/T]CCCCATTTTATCTCC | 337867 |
rs574009378 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239694 | GCTTGGATGGAAGAA[C/G]ACCACTCTTCTGTCC | 337867 |
rs574011613 | in-del | -/TATA | 0.00358779 | 0.0422022 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314395 | ACAAGAACATCAAGG[-/TATA]TATAGAAGATACTAG | 337867 |
rs574018119 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199162 | GTAATCCCAACACTT[C/T]GGGAGGCCAAGGCGG | 337867 |
rs574068441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99283987 | ATCTGTCTGCCTTGG[C/G]CTCCCAAAGTGCTGG | 337867 |
rs574075239 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247376 | CCCGCTACCACGCCC[A/G]GCTAATTTTTTGTAT | 337867 |
rs574092410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365911 | CTGTGTTTTGATGCC[A/G]TTGTGTTACATATAA | 337867 |
rs574095263 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233047 | TTCTAGCTCTGATTA[C/T]TGAAAGAGCTAGAAG | 337867 |
rs574101676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378519 | GTGACTGAGCAAGAC[C/T]CTGTCTCAAAAATAA | 337867 |
rs574108273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275519 | TTTATAACCTATTTT[A/G]AATTTTTATTAGCTC | 337867 |
rs574132870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312448 | CATTCATATTACCTG[C/T]CTAGCACTTGTAGGA | 337867 |
rs574138444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99210916 | CATGCTGGGCCCCGC[C/T]TTTTCCCTTTGTCAT | 337867 |
rs574155443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261767 | GAGAGATCCAGAGTC[A/G]CCAAGGCAGCAGATT | 337867 |
rs574162712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372504 | ATAGACCCTGGGATT[C/G]CTTTTGGAGATGGGT | 337867 |
rs574187689 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336044 | TTAGAGGAGCTTTAC[A/G]TTTTTGCCAGTTGCT | 337867 |
rs574195951 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231911 | ACATGATTGGTTGCT[A/G]ATCATAATGCACGTC | 337867 |
rs574195979 | snp | A/G | | | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254973 | ATTACGGTATAGCAT[A/G]ACACTAATGACTCGA | 337867 |
rs574201860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205145 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 337867 |
rs574202924 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246378 | GGGGAAAATAGTGTA[A/G]TCATCAGGAATGATT | 337867 |
rs574221880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276866 | CCAAACACCAAATAC[A/G]TTTTTGTAGAATACC | 337867 |
rs574222775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99211837 | TAGAGCTTGAGCCCT[A/G]GTCATTGGAAACTGC | 337867 |
rs574228081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372979 | ATAAAAATTAGCCGG[G/T]CATGGTGACGGGCGC | 337867 |
rs574237179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205525 | AGAGCTAGCATGAGT[A/G]TCAGAAACCTGTTAT | 337867 |
rs574237896 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208467 | ATTCAATAGGAAGTA[A/G]AAGGCCACATAAGGT | 337867 |
rs574247745 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384225 | AGTCCTCAGGTGAAC[C/T]CACAAAAGCCTCTTT | 337867 |
rs574248888 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383006 | GTTCTCGGTTACTTC[A/T]AAGGGCAAAATCAAG | 337867 |
rs574262241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99253654 | GAGTAGCTGGGATTA[C/T]AGGAACCTGCCATCA | 337867 |
rs574287470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338379 | TGTTTTAAGAAAGTT[G/T]ATGAATTTGTGTTGG | 337867 |
rs574300540 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210419 | TTTCCACCCAAGAGA[A/G]TCTTTTAAAATGTAA | 337867 |
rs574309730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99376875 | AATGTTGAAAGAACA[A/C]CTTTTTAGAAAATTT | 337867 |
rs574327174 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231283 | ACTGAGTTTCTCTAG[C/T]TGCCCACCTTGAATG | 337867 |
rs574333542 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366336 | TTCCTTGTGGATTTT[G/T]TGGTTTTGAATTCTG | 337867 |
rs574338159 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC2 | GRCh38.p7 | 13:99248583 | GGACAGGGTTTCACC[A/G]TATTGGTCAGGCTGG | 337867 |
rs574367183 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300059 | AGGGCCATCCTCAAC[C/T]ATATCATGGCACATG | 337867 |
rs574369782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363684 | GTCAGAACCTAGTCA[A/C]CATGGAAAGATACTG | 337867 |
rs574370335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377483 | TGCAGAGAAAATGAA[A/G]TAGTCCAGGGTTTCA | 337867 |
rs574378398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281759 | ACAAGATTTTAGTAA[A/T]GTTTGAAGATCTGTG | 337867 |
rs574390171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99246917 | TTTTTAAATCTTCAG[C/G]CTTTCTCAAACATAG | 337867 |
rs574440410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224617 | AACATGCCACAAAGT[A/G]GAAAGAGGGGTACAC | 337867 |
rs574458554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364510 | GTTTTGGAAACAGTG[C/T]TATGCTAGTCCCAAA | 337867 |
rs574465793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99311696 | TTTGAGAACTCTGTA[G/T]AGTCAATTCAAATGT | 337867 |
rs574476924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324036 | CCTCCTCACCTACCC[C/T]TGTCACTTCTGTGAA | 337867 |
rs574510867 | snp | A/G | 3.3461e-05 | 0.00409016 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296048 | TAATGCAGAGGCATT[A/G]CTATCCTGGCCGTGC | 337867 |
rs574536735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357380 | GCCTCTCGTTCAGTC[C/T]TGAAGTGCTTCTTGT | 337867 |
rs574543488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336621 | TGAGGATCCTATTTC[G/T]AGGCTCTTGTTCTCT | 337867 |
rs574547466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288995 | GGGATACAAGAATAT[C/T]GCACATGAAATAATA | 337867 |
rs574567014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349739 | TGCTATCTACTACGA[A/G]CTTCAAAGAGGAACC | 337867 |
rs574568503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99357211 | GTTTGTAGCCTGGTC[A/G]CCATAGGCTACACCA | 337867 |
rs574576076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237396 | ATAAGAACAAAAAGA[C/G]AAAGATTGCATGTTC | 337867 |
rs574584678 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382434 | CAAGTGCATGCACAG[A/G]CACACACAACACATA | 337867 |
rs574593084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252407 | CTTGATTACAGTGTA[A/G]CCCCAGTAAGACTGT | 337867 |
rs574595311 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379170 | AGCAAGGACACAAAC[-/T]TTTTGCCTGTCATGC | 337867 |
rs574598812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244177 | TGTAGTATTAGTTGT[A/G]AACACTAATACAAAT | 337867 |
rs574622463 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222270 | AAAGCAAAAAATCAC[A/G]ATGGAAGGCCACTCT | 337867 |
rs574641463 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374500 | TATCCATTAGCCCAA[A/G]TAGAGAGAATGGCTT | 337867 |
rs574655682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370357 | TGGTTAAGGAGGAAT[C/G]AAGAGTTCCAGGTAC | 337867 |
rs574664147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99289949 | CCTGCTCTTCCTCCC[C/T]ACCCCCAAGGAACTT | 337867 |
rs574667369 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199701 | ATTGCATGTATTTCT[A/G]GGGTACAGTGTGATG | 337867 |
rs574728297 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215692 | ACTGCAAGCCGGCTC[G/T]CTGCGAGCGGGAAAC | 337867 |
rs574749848 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99329833 | AGCCATAACCACTCA[A/G]CTAAGTTACTCCCAC | 337867 |
rs574786448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323532 | ATGTAGAAGTTGAAG[A/G]CAAGTAGCAGGTTCT | 337867 |
rs574788443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330275 | ACCAGCCTGACCAAC[A/G]TGGTGAAACCCCATC | 337867 |
rs574789683 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209295 | CTGTCCTGTCTTCAC[G/T]GGAGGGAACCCTCAC | 337867 |
rs574811058 | in-del | -/ACCTTAAGATATATACCTAAGATACCTTAG | 0.030278 | 0.119257 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300986 | TTATTTAAGATATAT[lengthTooLong]TTATATAAACTAAGG | 337867 |
rs574819981 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240057 | AGTGTGGTACAGGAA[C/G]CGTGCTTTGAGGCAA | 337867 |
rs574838388 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259879 | GACTTGAATTCTTCA[C/T]GGTGCACAGGGGCAT | 337867 |
rs574840504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309729 | CCTCAGCTTCCTAAG[C/T]AGCTGGGGCTACAGG | 337867 |
rs574843532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355466 | GCAAGACAAGGCCTT[A/G]GCATGCTCTTCCTGC | 337867 |
rs574854449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295672 | TGTCTGAGCAAATAC[C/T]AGAATCCAGACAAAT | 337867 |
rs574894620 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380259 | GCTTACCTGACTGCA[C/T]GTCTGCGCAGGCCTC | 337867 |
rs574926448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302839 | AGTCAGTACATGCCT[C/T]TGTGGCCTGGTTAAA | 337867 |
rs574928267 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297238 | TTTGATTAAAGCAGG[A/G]AGAACAGAGCAATAA | 337867 |
rs574928544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99310514 | TAAAATAAGGAAAAG[A/G]AAAAGACTGGTCAGT | 337867 |
rs574946885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203314 | GTGCTGGGATTACAG[A/G]CGTGAGCCACTGCCT | 337867 |
rs574955645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99369407 | GCGATGCTGGGCAGC[G/T]ACTGTGAACCGTTCT | 337867 |
rs574961894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322949 | TTAAAGACAAACAAA[A/G]AAACCCAAACCACTG | 337867 |
rs574968349 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322625 | ATTCGTTACTTGTCA[G/T]GTACAGTATATCAGA | 337867 |
rs574979150 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201647 | TTCGGTAAGGTAGAC[-/T]TGCGTGTTAACAGTT | 337867 |
rs575020320 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372802 | AATCAAATACGCTCA[A/G]TGTCTGCTATCTTAG | 337867 |
rs575024699 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204921 | TTTTTTTTTTTTTTT[-/TT]GCGACGGAGTCTTGC | 337867 |
rs575042752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375605 | ACATTTGTTTTTGAC[A/G]CACTTAGCTAAAAGG | 337867 |
rs575049901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215336 | CAGCTGTTCTTTTAT[G/T]TAGAGTCCTGAGATA | 337867 |
rs575061257 | in-del | -/T/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314263 | TCTTTAACCAGATCT[-/T/TT]TTTTTTTTTTTTTTT | 337867 |
rs575080749 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346668 | AGCTGCTATTTACTC[A/G]GCATTCCTGACAAAT | 337867 |
rs575089767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237827 | AGGCATGGTGGCACG[C/T]GCCTGTAATCCCAGC | 337867 |
rs575109356 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99349025 | GTGGGAGACAGTGAA[A/G]ATTCTGTGTGCTCAG | 337867 |
rs575119998 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99205064 | GTGTGATGCCACACC[C/G/T]GGCTAATTTTTGTAT | 337867 |
rs575145291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99275322 | GCTGCCTCCTGACAT[A/G]GCAGCTATTACAGCT | 337867 |
rs575170790 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327060 | ATGTGGCCTATAGCT[A/G]TGCTTTCTCTTCTAA | 337867 |
rs575173680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363735 | GTATATACACACCCA[A/G]GAAAACCAAAACTGT | 337867 |
rs575188840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99268404 | GATCGTTTGAGTCCT[A/G]GAGACCATCCTGGGC | 337867 |
rs575190593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364580 | GAGCAGTTTATATAA[G/T]ATAAGGAGTCATTAA | 337867 |
rs575216810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99209943 | CATGCCATTCCACTG[C/T]ACTCCAGCCTGGGTG | 337867 |
rs575223172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99343557 | TTCATAGGATGGTCT[C/T]ACTAACAGATCTGAA | 337867 |
rs575232273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304943 | CCTATCTGAACAAGA[A/G]AGACTAGGAGAACTG | 337867 |
rs575270661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318324 | AGGTGTGTGCCACCA[C/T]GCCTGGATAATTTTG | 337867 |
rs575296077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377542 | ATGTGGTGCTTTCGA[C/T]AGGGAGAGAGATGGG | 337867 |
rs575303688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245153 | CTTTTTTTAGCTTTG[A/C]AAGTTTGTGTTTTAG | 337867 |
rs575317410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217817 | AGGCGGATGATCTGG[C/T]AGCCTCAGGGCCGAG | 337867 |
rs575325690 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354432 | CAGCTTTCCATTTTA[C/T]AGCTGGGGAAACCCA | 337867 |
rs575329102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351796 | AGCAAAGCCCAGGAG[A/T]CCTTGGTGCTCTTCT | 337867 |
rs575342474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99245702 | AAAAATTAGTTGGGC[A/G]TGGTGGCACGTAGTC | 337867 |
rs575343270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99330356 | CCCAGCTATTCAGGA[C/G]GCTGAGGCAGGAGAA | 337867 |
rs575355664 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213690 | TCGTACTAAAATAAG[-/T]TTTTTTTGCAGTATT | 337867 |
rs575382805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99231532 | AGTCTCCCACCTCAG[C/T]CTCCCGAGTAGCTGG | 337867 |
rs575394425 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316261 | TGTCTGGTGTCAACT[C/G]CCCCTGTGCCCACCT | 337867 |
rs575410169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99377951 | CGCTGGAGTCAGACC[C/T]AAGACAGCATGCAGC | 337867 |
rs575439709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344686 | CTTGATTCAGTGTTG[G/T]ATTTCTTTAGATTTC | 337867 |
rs575444780 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242865 | AGACGCTCCTCACCT[C/T]CCAGACGGGGCGGCG | 337867 |
rs575459546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99316671 | ACATAGGCAGACATA[A/G]TGGGGACCACACAGG | 337867 |
rs575469534 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331586 | GAAAAGCTATAGAAA[A/G]TTCAATCTGAATCAC | 337867 |
rs575472559 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215845 | ACTCCTTCATCGCAC[C/T]GTGATTCAAACTGCC | 337867 |
rs575503331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216225 | TCATTCCTCAGCCTC[C/T]GAAGTAGTAGCTAGG | 337867 |
rs575513281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99232056 | TTTTTGTACCATGTC[G/T]ACATGTGTATTTATA | 337867 |
rs575536990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99252614 | AGTAACTCATTCCTG[C/T]CACACATCTGGCCTT | 337867 |
rs575558393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349816 | AAGCACAGCATCACA[A/G]GGAGGGGTTTAGGAC | 337867 |
rs575585735 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340013 | AATCAGATCTTTTAC[A/G]GCTTTTTAAAAAATG | 337867 |
rs575594637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204044 | GTCACTCAGCTCTAC[A/G]TTGAGTAATATGTGT | 337867 |
rs575596065 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218511 | TTTTTTTTTTTTCCC[C/T]GGAAACTTCTTAGCA | 337867 |
rs575619979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383150 | ATGCATTAGTAGTGT[G/T]CATGTGTGTGTGTGT | 337867 |
rs575634724 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324581 | AAAGCTGACTAATAG[A/T]ACTCTTTTCTAAGCA | 337867 |
rs575634862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317543 | ACCATTGGACATAGA[C/T]CTAAGTAGGCTGGCA | 337867 |
rs575637584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383662 | AAGGGTTGAAAGCAA[A/C]GTTCCGGGGAGGAGC | 337867 |
rs575651672 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239347 | TAATGCAGTCCTTCT[C/T]AACCCCGGACACACA | 337867 |
rs575652878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99204943 | GGAGTCTTGCTCTGT[C/T]GCCAGGCTGGAGTGC | 337867 |
rs575663865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337316 | ATTATCACTAGGGTT[A/G]GTTTTGAAAAAATAT | 337867 |
rs575677074 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337684 | GAACCCCTATGCTGA[C/T]AGCCGCATGAGATGC | 337867 |
rs575715321 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286021 | GTGATTTCCCAGCTG[C/T]CTCAGTGTGTCAGAG | 337867 |
rs575731252 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354583 | GGAGTTGGGCCCTAT[-/AG]GCAAATGGAAGGGAC | 337867 |
rs575741588 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370285 | TGTGTGATTGTGTGT[A/G]TGTGTGACAGAGACA | 337867 |
rs575750369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296120 | GCAGAGGGCGGAGTA[A/G]AATTGTTTGCCATTT | 337867 |
rs575754094 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99362547 | GGCTGTGTATTTTTG[C/T]GAGTCTTGTGGGTAT | 337867 |
rs575755498 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323030 | ATAAGCATCTTTAGA[A/G]TATGTTTTGAGGCCC | 337867 |
rs575787106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99296724 | AAATAGGCTTAGTCC[A/G]TGTTAGGAACTGAAA | 337867 |
rs575800605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355548 | CCCCCACGCCACCCT[C/G]TCACCACCACCTCCT | 337867 |
rs575829853 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334256 | GTGAGCACAGAAAAA[A/C]CAACATTGTATTGTT | 337867 |
rs575841375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99309798 | GTGTGTGTGTGTGGA[G/T]ACAAGGTCTCATTAT | 337867 |
rs575859498 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346305 | CCCATCTCCATCACC[A/G]ACTGCCTCCCTCCTG | 337867 |
rs575880282 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227527 | ACTTCATTTGGGAGT[-/G]GGGGTGGGGAGCAGT | 337867 |
rs575894855 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207993 | TGCCTCTCATCGTCT[-/C]TTTTTTTTTTTTTTT | 337867 |
rs575899686 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382257 | CATTTTGGTTGACTG[A/G]AAAATGATCAGATGG | 337867 |
rs575912761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294712 | TATTAACATCTGGCA[A/G]TATATAATCTATTCA | 337867 |
rs575985603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236100 | TGAAACTATGAAACT[A/G]CTAGCAGAAAATGTT | 337867 |
rs575991050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328918 | CAAAGATTTTCTCCT[A/G]TATGTTCTTCAAGAA | 337867 |
rs576003331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99251973 | GCCATGTTATCCAGG[C/T]TGGCCTTGAACTCCT | 337867 |
rs576019178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229383 | GAAAAATTTTCCAAA[C/G]GCATTGAAACAGAAA | 337867 |
rs576034181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380952 | CAGAGGATGAAGAGC[A/G]AGCCCGCTGCAAGCT | 337867 |
rs576047315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281005 | AGCGTGGCCAACATA[A/G]TGAAACTCCATCTCT | 337867 |
rs576050958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272525 | TGGGTGGCTTACACA[C/G]AAATTTATTTTCTCA | 337867 |
rs576060519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375413 | GTGCCAACAGGTAAC[C/T]GGTGCCAGTTGCTAT | 337867 |
rs576075970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229925 | TTGAACAGTGTTTGC[C/T]TTCTTCCTGTTGTGT | 337867 |
rs576108010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308783 | CTGAATTCTTTGGGC[C/T]GCCACCTCACTGTGT | 337867 |
rs576111182 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99229282 | AAAGTAGAAACAACT[A/G]TAATTTGAAGGCTGC | 337867 |
rs576121654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375680 | GTCTTTCACTGAGGG[G/T]AGTTGCTAGAAATCT | 337867 |
rs576140143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236777 | ATCACTTGAATCCGG[G/T]GGGCAGAGGTTGCAG | 337867 |
rs576142589 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99258450 | GGATGTGGTTTTTCT[C/T]TTTCACAAATGATTT | 337867 |
rs576169900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208054 | CCAGGCTGGAGTGCA[A/G]TGGCGTGATCTTGGC | 337867 |
rs576178701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265786 | TGGCTAATGTTTCTA[A/G]GTAGATACAATTACA | 337867 |
rs576191784 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252156 | CTTCGCTTGCTACGC[A/G]TTTGCATTCTCATGC | 337867 |
rs576204075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99208432 | CTCCTGTGGGCCAGC[C/T]GGTCTCCTAGGTTCT | 337867 |
rs576214306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202531 | AAAATAAAGGGCAAG[A/G]GAAATCTTATTGGTT | 337867 |
rs576221325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241587 | TTCCTGGGGCTAAGG[A/G]GAGAGGGAACAGGAA | 337867 |
rs576221844 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386835 | AGTGCTGAGCAAAGC[C/T]GTGTGTGTCTGACCT | 337867 |
rs576232648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201703 | AGCTCTAATTTTGCA[A/G]TTGCTTGTCACTGTT | 337867 |
rs576275701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381536 | CCAAGTTGTTTGGGG[A/G]CCATGGCATCATGGT | 337867 |
rs576288167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215137 | AGTCAGCTCAATCAA[A/G]GCCCAGTACTTCAGA | 337867 |
rs576294985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348247 | TTAAATAAGACGCCG[C/T]CTGCGCCTTCAAGAA | 337867 |
rs576299905 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335149 | GAGCAATGAACAAAT[C/G]AACAATCACAGTTGA | 337867 |
rs576306887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374424 | GCCCAAAACAATGGC[A/G]TCCCATAATTTTGGT | 337867 |
rs576355023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342525 | AGGTTGGATGCTCCA[C/T]AGTGGCAGGAGATAG | 337867 |
rs576378444 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374765 | GCACATTGGGTATTG[G/T]GTTAGCCTCCCATGG | 337867 |
rs576388100 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352745 | CACGATCCCTCCTCT[A/C]CCTGAGCTTAGAGTA | 337867 |
rs576390092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360601 | TTGCTCCTTGAAGGC[A/G]GTATAAACCCACTTA | 337867 |
rs576411965 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315091 | CTCACTTCTCCAGTC[A/T]GCTGTCATGTGTTAT | 337867 |
rs576425508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361399 | GCCGTAACTTTCTGC[C/T]TTTTAAGCACTTTTC | 337867 |
rs576427133 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354300 | AGCTCCTCCTGCAGC[A/G]GCTCTGGCAGGTGGC | 337867 |
rs576442173 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99264996 | TTTTAATTGTTCTTC[A/G]GTGTGTATGTTTTTT | 337867 |
rs576448359 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329778 | GATGAGTGCAGATAG[C/G]CTGACACCTTGACTG | 337867 |
rs576451257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281617 | TCAGCGCTATTTTCT[A/G]TAAATTGATAAAAGA | 337867 |
rs576486879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354732 | TCAGACAGGATGCCC[C/G]AGGGTTTTTGGTTGA | 337867 |
rs576494149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99321458 | GAATTGCAGGTGCAC[A/G]CCACCAAGCCCGGCT | 337867 |
rs576495464 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308290 | TGAGGGGCCTGGATA[C/G]CAGGTCTTAGGAGAA | 337867 |
rs576500217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220988 | ATTATTTTTGTATAA[C/T]AATACCACTAGAATA | 337867 |
rs576520142 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247366 | ACTACAGGCGCCCGC[C/T]ACCACGCCCGGCTAA | 337867 |
rs576530076 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257899 | ATGATTATATAGCCT[A/G]TTTCAAGGTCTTTCA | 337867 |
rs576534178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380080 | TTCCCTTGGAGACAC[C/T]GAATAAACTACATGT | 337867 |
rs576539221 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331981 | CCTTGAGGGCACATG[A/C]AGTCTATGTGCTGGG | 337867 |
rs576544280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292963 | TTAGGAGAATGCCCC[A/G]GAAATAAATGTAAAG | 337867 |
rs576574255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214762 | TTTGGAGAGTTTCTA[A/G]GATTTTATTTTGGGG | 337867 |
rs576579069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333157 | AATGTGTGAATGTAA[C/T]ATAGTATTATAATAA | 337867 |
rs576581221 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285388 | TATTTATTATTACCT[G/T]TCTTCTTTTTTTTTT | 337867 |
rs576635722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347751 | AGCACAGGCATGTGA[C/T]AACGTCATCTAGTGT | 337867 |
rs576644652 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378168 | CACCTTGACTCAGAA[C/T]CATCTCAGCTATTTC | 337867 |
rs576662740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382302 | ATGTAGAGTCCTAGA[C/G]TTAAAAGGTCAGGTA | 337867 |
rs576664952 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226261 | GTAAACTTAGTCAGG[G/T]CCATCTCAGTAACTG | 337867 |
rs576669165 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199792 | AAAACACTTGTCATT[C/T]CTTTGTGGTGAGAAT | 337867 |
rs576681972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235085 | GGCAGAGGTCACACT[A/C]GTCTCTCCTGGAAAA | 337867 |
rs576685042 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249186 | CCCCTCCGTCCTTCC[C/G]CCTCCCTTCTTCCCC | 337867 |
rs576691962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99279157 | CCTTTTCTTACCCCT[G/T]TATCTCCCCTGCTTT | 337867 |
rs576707714 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201797 | GATCTGTTGGCCGGG[C/T]GCGGTGGCTCACGCC | 337867 |
rs576724334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382955 | GAGGGCTGTCACACC[C/T]GCAAAGTGCTTTATG | 337867 |
rs576760559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99276128 | ATAATAAATCTCCAG[C/T]CATCTGCCAAGATGG | 337867 |
rs576761447 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288771 | ATCTGTTGCTGCCTA[A/G]CAAATTATGACATGT | 337867 |
rs576774089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326389 | TTTTAAAACTAGGTT[A/G]TTAGTTTTTTGGTAT | 337867 |
rs576789246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274346 | TACTGCTTTTTTTTT[C/T]CTTGAGATAGGGTCT | 337867 |
rs576792598 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278222 | TGTAATATTTTTCTT[A/G]AATTTGTAGTCCTGT | 337867 |
rs576795034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323506 | GGTGATGGGACTTGT[G/T]AAAGGACCACATGTA | 337867 |
rs576806187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265806 | ATACAATTACAAAGA[C/T]GTACCAAATAAAATA | 337867 |
rs576806695 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218455 | TAGATGTGGAGCACA[A/T]TTTTTGTATCTAGAG | 337867 |
rs576809409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99224015 | TGGTTGATAATGTTT[A/T]TCAGGTCTTGTGTAT | 337867 |
rs576810536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320680 | TTTGAACCTAAGGAA[C/T]ATTTTCTTTCTTTGT | 337867 |
rs576817473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99274891 | CCCAGCTAATTTTTG[G/T]ATTCTTTGTAGAGAT | 337867 |
rs576827313 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248879 | AACTCATGTTCAGAA[A/G]CTCTCTTCTCTTCTG | 337867 |
rs576897554 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305615 | GTCATATAGAAACCT[C/G]AGTTAATATTTATTC | 337867 |
rs576905423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99237363 | CACATGGATGGAACT[A/G]GAAGACATGTAAGTG | 337867 |
rs576905847 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229972 | CTATCTTAAACCTTG[C/T]GAATTGTCATACACC | 337867 |
rs576945383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202659 | ATGGTGGTGAGTGTT[A/G]AATTCTAGGAACCAA | 337867 |
rs576950613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230596 | TCTTTTGGAAGCTCT[A/G]AGAAGGAATCTGTTT | 337867 |
rs576959188 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382051 | TGCAATGAAGTGGGT[A/T]TGAAACTGATTAAAA | 337867 |
rs576965712 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383756 | GCACCCCCCGTTTGG[A/C]AAAGCCCTGGCTGGA | 337867 |
rs576971706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295586 | GATTTAGTTTCTTCA[A/G]AGTTTGGATACTCCA | 337867 |
rs577022967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99235221 | CCAGGAATCAATTAA[A/C]CAAAGATGTGCAATA | 337867 |
rs577035471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244004 | GTAGAAAAAAATTTT[G/T]TTTAAATGGATTTTA | 337867 |
rs577060958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99363517 | GGCAGCCCAGGCCGG[C/T]GGGGCAGTGTCCTGA | 337867 |
rs577065639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375828 | TTTTTTTTTGAGACA[C/T]GGTCTTGCTCTGTAT | 337867 |
rs577073891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99329064 | GTTATTGAAAAGACC[C/T]TTTTCTCATTGCATG | 337867 |
rs577105765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342986 | TGGCTGTTTTCCCCT[C/T]TGTCACTTGGTCATG | 337867 |
rs577107127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99360870 | TATCTTGCCTTCCCC[C/T]GAGGAGATGGGGCGC | 337867 |
rs577123688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99222660 | TTTAACTTGTTGATA[C/T]GGTAAATTACATTGA | 337867 |
rs577140848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99229277 | GGAGGAAAGTAGAAA[A/C]AACTGTAATTTGAAG | 337867 |
rs577151544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99203283 | TCAAGTGGTCCTCCC[G/T]CCTCGGCCTCCAAAA | 337867 |
rs577161136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99265191 | AGTACTCCATTCAGT[G/T]GAATATTTGCAGCAA | 337867 |
rs577165345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361491 | ACTCTCTTGTAAGAA[A/G]TGAAATGGAACTCAA | 337867 |
rs577165595 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335695 | TACTGTGTTGTATGA[A/C]TAACCCACTCTGCAG | 337867 |
rs577198201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207346 | CAGGTTTAAGTAGTA[C/T]TAACTGGATCCTTCT | 337867 |
rs577210888 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340998 | GAAGGCAAGAAGATT[G/T]TCAGTGGAACAACCA | 337867 |
rs577215546 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264795 | ATAGGAGCCGGCAGG[A/G]TAGGAGCTTGGAGGC | 337867 |
rs577228038 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336516 | TTGGTGTCAGGAAGG[A/G]GCCCTGTTCTGTCTC | 337867 |
rs577233642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355300 | GGAAAACAGAATATA[C/T]GATGCAGAAATGGAT | 337867 |
rs577238473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348415 | GTAATCTTGAGGCCA[C/G]CATTGGGGCAGGTGT | 337867 |
rs577263491 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213430 | CAATGGTGTGATCTC[A/G]GCTTACTGCAACTGC | 337867 |
rs577267366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99315565 | CAGGTTGTTGAATTT[C/T]GGTTTAATGACTTGG | 337867 |
rs577291411 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | UBAC2 | GRCh38.p7 | 13:99241756 | AACTTTTTTTTTTTT[A/T]ATTGATCATTCTTGG | 337867 |
rs577296495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99348959 | TCAAGGTGCAATCAC[A/G]GCTCAAAAAGAAAAA | 337867 |
rs577300329 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214834 | GCTGTTTGTAGACTG[G/T]GGGTGGGGAAGGGTT | 337867 |
rs577327339 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345293 | TGGCTGTGAAAAATT[C/G]TTTATTCAGTAACAA | 337867 |
rs577329854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99374536 | CCACAAGGTGCTTTC[A/G]CTCTTAGCTGATAAA | 337867 |
rs577330544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234707 | GGATTAGCTCAGCAA[A/G]TAGCTTCAGGGGCTT | 337867 |
rs577364482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327349 | ACTGGTAGATTATCA[C/T]GTCCGTTGCAGGACA | 337867 |
rs577377611 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205259 | AAGGTGTTGGGAAAA[A/C]CCCAGTGGGAAGGGT | 337867 |
rs577378182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99320506 | TCAGCCAAAGTTACC[A/G]GCCTTCTACTATGAC | 337867 |
rs577390332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99375188 | CATACAAGACCCTGA[C/T]GAGGCTCTAGACACA | 337867 |
rs577392577 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221356 | ATTTCTATTAGTGCT[A/G]TTTGTGATTGTGTAT | 337867 |
rs577403641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99228754 | TCTACTTTTGAATTA[C/T]GAGGCAATGAGGAAC | 337867 |
rs577409302 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237467 | AGAGTAGGTTGGTGG[C/T]TATCAGAGGCTGGGA | 337867 |
rs577417296 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251602 | TAAAATGCAGGCTTA[A/T]CCACACTAGTTCTTT | 337867 |
rs577421710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99272646 | CCCTCTTGCTGTGTC[C/T]TTACATGGCTGAGAG | 337867 |
rs577446404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99342601 | CATGGCCATCCATTC[A/G]TGTGCCAGCGCTGGG | 337867 |
rs577481970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214098 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 337867 |
rs577509781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273314 | GTTAAACCACTTTGG[C/G]AGAGTCAGATTAGGT | 337867 |
rs577535418 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300210 | CTCCAAGGGTAGCCT[G/T]TTGAGGGTCCTTAAC | 337867 |
rs577563547 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303280 | CTTTATATGTGTCCT[A/G]AACCCAGTGGATGTG | 337867 |
rs577574515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300697 | TGGTACCTTTTTGTA[C/T]TAGAGGGTCTGGAAC | 337867 |
rs577583278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292280 | AGCTGGGACTACAGG[C/T]GCCCACCACCACGCC | 337867 |
rs577585509 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331788 | TCCCTTATGCTTTCT[C/G]TAACATTTTCATTGG | 337867 |
rs577602132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380164 | CCATTTGTACTGCCA[C/T]GTTGGTACTCAAAAA | 337867 |
rs577620505 | snp | C/T | 5.53725e-05 | 0.00526148 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201394 | CGCTTTAGAAGCTGA[C/T]CTCTCAGTTTCACTT | 337867 |
rs577631045 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367515 | GTCTGTACAGTGTCT[C/T]TCACTGCCTTCCAGA | 337867 |
rs577634469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99249860 | TGTGTTGGCCGCTTG[C/T]GTGTCTTCTTTTGAA | 337867 |
rs577657112 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353010 | GGCACGTGGCACCCT[C/T]CTCAGCACTTTTCCT | 337867 |
rs577665539 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312862 | GGTGGCAGACTCCAG[C/T]GATGAAAGCGAACTG | 337867 |
rs577675378 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | UBAC2 | GRCh38.p7 | 13:99242337 | GCGGGGGGCTGACCC[A/C]CCCACCTCCCTCCCG | 337867 |
rs577692374 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348812 | GCCTAGGAGTTTGAG[A/G]CCAGCCTGGGCAACA | 337867 |
rs577717903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99293030 | CCGTGTATGAACAGT[A/G]GCTTGATGAGTAGAA | 337867 |
rs577739590 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386224 | TCTTCAACCTGTGGC[A/G]ACAGGAGGCAGGGCA | 337867 |
rs577753459 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337052 | CTGCTTAGTGTGTGG[-/T]TTAGGTTCATTCATT | 337867 |
rs577754900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99207956 | CAGTGTGTGGGAGAT[A/G]ATGCAAATAAATCTT | 337867 |
rs577772081 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308838 | TGATCTCCAAGGTAA[G/T]TCCTAGTACAAAAAT | 337867 |
rs577780982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99271401 | GAGATGGGACCATCC[C/T]GTACGTGGACAGCTG | 337867 |
rs577786873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297575 | GTTATGTTAGAGGTA[A/T]GCATTCTGTACAGTG | 337867 |
rs577819461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255979 | AACATTCTCCCACTC[A/C]GCTTGACTGCCAGTG | 337867 |
rs577824097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298401 | TTCTAAGGAACTCAT[A/G]GGTTAAAGAAGAAAT | 337867 |
rs577834148 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99280215 | TGCTGTTTTATAAAG[A/T]TTAACTTGCTTGTGA | 337867 |
rs577834843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99353198 | GTGGAATAAGTTACT[A/G]GTGCTTAGTTGATAA | 337867 |
rs577843608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99285972 | TGCCAAAGTGGTTTG[A/G]CCTTGGAGCTCACAG | 337867 |
rs577870264 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262627 | AGAATCGCTTGAACC[C/T]GGGAGATGGAGGTTG | 337867 |
rs577897347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347123 | ATCTCTATTTAAAGA[A/G]AAAAAAAGATCTACG | 337867 |
rs577919885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379199 | GCAAGTTTACGCTTA[G/T]GCATGCCTGCTGCAT | 337867 |
rs577933286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263709 | CACGGTAACATTATT[A/T]ACAACAACTCCAAAT | 337867 |
rs577954272 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325112 | TCTTTTTTTTTTTTT[C/T]TTTTTTTTGATACGG | 337867 |
rs577960687 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99361122 | AACCATCATGTATGT[-/A]ATGTATGAATATATA | 337867 |
rs577962685 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322184 | CTAGATGTCTGGTGA[C/G]AGACCTTCAAAAATT | 337867 |
rs577969108 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361711 | CCTACTAAATGCCGA[A/C]AGCACCACCATCCTG | 337867 |
rs577969368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264361 | AGGCTAGGGAAGGGA[A/G]AAGAAGCAAATGGAT | 337867 |
rs577980403 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289224 | CTATGTGGCATATAC[C/T]GTAAAAGCCAGATAA | 337867 |
rs577981622 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373078 | GTGAGCTGAGATCAC[A/G]CCACTGCACTCCAGC | 337867 |
rs577985643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99227080 | GTGCATGCCTGTAAT[C/G]CCAGCTACTCGGGAG | 337867 |
rs578042090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372615 | GACAGGTGGCGTCAC[A/C]GGCTCTGAGTCTAAA | 337867 |
rs578044634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277457 | TTGAACCTGGGAGGC[A/G]GAGGTTACAGTGAGC | 337867 |
rs578095377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99233643 | TGCAACTGATTGTGA[C/T]ACATTGACTAAGTAA | 337867 |
rs578100518 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247013 | ATTTTTATTATTATT[A/T]TTGGTAGAGAAAAGG | 337867 |
rs578102184 | in-del | -/CATC | 0.00119737 | 0.0244387 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284716 | TGCATTTCATTGGTA[-/CATC]CATCCCCTTACTGTT | 337867 |
rs578115769 | in-del | -/GC | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99323087 | GGTGTGAGTTCCTCT[-/GC]GCGCCGCCTTTGCTT | 337867 |
rs578128391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99384813 | GGAGTGTGATGCCAG[A/G]GCCGAGCGTGGCAGT | 337867 |
rs578140466 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199293 | TGTAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 337867 |
rs578170644 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258230 | AAGGGATATCTTTGA[G/T]TTGCTTCTGTTAAAA | 337867 |
rs578178230 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC2 | GRCh38.p7 | 13:99247503 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTGTGT | 337867 |
rs578186645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99378555 | AAAATAAAAACTTCA[A/G]TATCCACTTCTTCTG | 337867 |
rs578194135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331935 | TTGTGGAATGAATAA[A/G]TGAGGTCTCGGTGGG | 337867 |
rs578213505 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320726 | TTTTATTATGAAATA[C/T]TTACTGTGATGTGGC | 337867 |
rs578238461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99339142 | CTGCCCACTCAGTAG[C/T]CCCCCAAGATATCTA | 337867 |
rs578253012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99239838 | GCATACACATAAGAA[C/T]GTGATCTGTAGGTCA | 337867 |
rs745326847 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384923 | CAGTGAGCCTGGGCA[G/T]CTCATGCCGACCTGC | 337867 |
rs745332552 | in-del | -/CT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280833 | CCTTCTTCTTTCCCT[-/CT]CTCTCTCTCTCTCTC | 337867 |
rs745336132 | in-del | -/AA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318821 | GTGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 337867 |
rs745340696 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372889 | GGAGGCTGAGGCGGA[C/T]GGATCACGAGGTCAG | 337867 |
rs745347743 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216383 | GTGCTGGGATTACAG[A/G]TGTGAGCCACCGTGC | 337867 |
rs745356452 | snp | C/T | 8.24165e-05 | 0.00641883 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255450 | CCAGACTCCCACACA[C/T]GCCAGCACGGCTTTG | 337867 |
rs745372398 | snp | G/T | 1.65029e-05 | 0.00287248 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367918 | ACAGGTAATTAATCA[G/T]TAATACCTGGTACTC | 337867 |
rs745374536 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249671 | CAACAGTGTATAAGT[C/G]TTCCCTTTTCTCACT | 337867 |
rs745377931 | snp | A/C | 0.000197948 | 0.0099466 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385221 | TCTGCGTTTTCTCTG[A/C]CTGCAGGTCGCCCGG | 337867 |
rs745382033 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250909 | CCACCACCATGCCTG[C/G]CTACTTTCTTTTGTA | 337867 |
rs745389807 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314101 | TGTTTGCATAGCCTG[A/G]CACCTGTGTTTGCTC | 337867 |
rs745393785 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374163 | GTGCATTTTGTAAGA[A/T]GGAAACAGAGCAATA | 337867 |
rs745395705 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361420 | AGCACTTTTCTACTA[G/T]CACAGGAGTAGAGGG | 337867 |
rs745472844 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99229022 | AGAATGTCCCCATCA[A/G]TGAGGCTTTTCTGTG | 337867 |
rs745476205 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314197 | ATCACAAACAAGACA[C/T]TGATTTATATATTGG | 337867 |
rs745500683 | in-del | -/AAG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367308 | ATTTACTTCAGTCAT[-/AAG]AAGAAGAAAGGTAGA | 337867 |
rs745508876 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384156 | TTCTCTTTCCACCAT[A/G]TAGCACCAAGTAGCT | 337867 |
rs745511388 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344421 | ACTTTTGCTTCCATC[A/T]TCTTCTTTATGTTTC | 337867 |
rs745544413 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275296 | AGGAAGCCTCAGCTC[C/T]TCACCACGGAGCTGC | 337867 |
rs745564121 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236810 | AGCCGAGATGGCACC[A/G]CTTCACTCCAGCCTG | 337867 |
rs745566697 | snp | A/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262160 | GGTTTACTGTCACAG[A/T]GTCACAGTGCTTGTG | 337867 |
rs745568495 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345068 | ACGGGTGGAATTTGG[A/T]TGGGTGGAGAGGGTA | 337867 |
rs745602534 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304815 | GTTTGGCTTCAGAAG[G/T]CACATTCAGTACAAT | 337867 |
rs745610853 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379723 | TTTCTTCAGATCCTA[A/T]ATGGTGGTCACTCCA | 337867 |
rs745633739 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223685 | AATTTTGCTTGGTTG[C/T]GCTTCATTTTTTTAT | 337867 |
rs745654917 | snp | C/G | 3.35284e-05 | 0.00409427 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295068 | ATCCATTTCACTTTC[C/G]ATTTGAAGACTTGGA | 337867 |
rs745660446 | snp | A/T | 1.7795e-05 | 0.00298282 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340617 | CTCAGTGGCCCAAGC[A/T]AATCTTTCCTCTGTG | 337867 |
rs745674362 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270019 | ATTAAAAACTGGTAT[C/T]GTGTATGTGTGTTAA | 337867 |
rs745721043 | snp | A/G | 3.2969e-05 | 0.00405998 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255063 | CATGAGGAAGGTGGT[A/G]AAGGCTCCCCAGGGA | 337867 |
rs745723065 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338998 | AGTCCTGTTCTCTCT[C/T]CTGCTGTGTCTCCTC | 337867 |
rs745727782 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211794 | TGGGATCGTCTCAGG[C/T]GAGTGATGTTAGTAG | 337867 |
rs745748389 | snp | C/G | 0.0012576 | 0.0250443 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351844 | CTCATTGGGCTGCCC[C/G]GTGTTAACTGGTTGA | 337867 |
rs745762461 | snp | A/C | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294296 | TGTCTTTTATTCTCA[A/C]GATGAATTTAGCAAG | 337867 |
rs745776686 | snp | A/C | 8.21389e-05 | 0.00640802 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201181 | CCCCACCTGGTATCC[A/C]CAGGTGCTCTGCCCA | 337867 |
rs745802609 | snp | G/T | 4.36176e-05 | 0.00466979 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201421 | ACTTGGATGTGTTTC[G/T]TCTTCAGTCTCCAAG | 337867 |
rs745817932 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282401 | ATAGCTTTGGTTGAG[A/G]CTATTAGTAAAAATT | 337867 |
rs745846929 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227892 | AGTGTGAATTAGGGA[-/G]GTTTGAGGAGAGAGG | 337867 |
rs745858693 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339653 | ATTTTTTTTTTTTTA[-/A]CAAAGGAATAGCCAT | 337867 |
rs745867741 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265754 | AAGAAAGGTTATGCC[A/G]TGTCTCAAAAAATGA | 337867 |
rs745872731 | in-del | -/GCCTC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376980 | AGTATGCAGCGCCGT[-/GCCTC]GCCTCGCCTCGCCTC | 337867 |
rs745900708 | snp | C/G | 1.68303e-05 | 0.00290084 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295841 | GTTATCCTACACAAG[C/G]CATCTCCGATTCTCC | 337867 |
rs745952926 | snp | A/G | 0.000939834 | 0.0216572 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255539 | CACTAATAAAGGCAA[A/G]AAGCCATAAAGCAAT | 337867 |
rs745978084 | snp | A/T | 1.64936e-05 | 0.00287168 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295940 | ACCAAATTTGTTGAA[A/T]AGAGGGTGGTAGAGT | 337867 |
rs745980556 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266853 | ATCTCTTCAGTCCCT[A/G]CTTTCAGTTCTTTTG | 337867 |
rs745989260 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326796 | TCATCCATGTCTCTT[C/G]CAGCCACGAGATGCA | 337867 |
rs746010255 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332329 | ATGTTTTCTACCCAG[C/T]AAATTAAATTATTTG | 337867 |
rs746015328 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377337 | TTCATTCCTGTACTT[C/T]AACAACTTGACATCA | 337867 |
rs746017784 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220374 | CACTGAGATGGTATT[A/T]CATGTAAAGTGCTTT | 337867 |
rs746039141 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248279 | CCAGGCCTAGAGTAC[A/C]GTGGTGAGATCATAG | 337867 |
rs746050359 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289897 | TGGAAGTGACACACG[C/T]GTCTTTTGCCCCCAA | 337867 |
rs746067503 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358527 | ATTTCAAAAATCTAT[A/C]TTTATGTTAGCAAGT | 337867 |
rs746079490 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371049 | GGGCAGCCGTTAAGA[C/T]GAGGTATTTAAAGGT | 337867 |
rs746079951 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273162 | TATTAATATATTTTA[C/T]AACTTGAGGTTCATC | 337867 |
rs746085181 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380062 | GGGTGAGAGGGTCTC[-/T]TTTTCCCTTGGAGAC | 337867 |
rs746104805 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291081 | TTCTGGGACCGGAGA[C/G]TGTGGGATTAAACCG | 337867 |
rs746124492 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207649 | GGTAGGGAGCCTTGG[C/G]CCAGATGCAGTTAGA | 337867 |
rs746135103 | in-del | -/ATTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203055 | TTTATTTATTTATTT[-/ATTG]AGATGGAGTCTCACT | 337867 |
rs746146526 | snp | A/T | 1.71059e-05 | 0.00292449 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385375 | GGACCGGCAGCCGAG[A/T]GACAGTGCGTGGTCC | 337867 |
rs746161237 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217088 | TGCCTGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 337867 |
rs746186380 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315497 | AATGAAAACACTGTT[C/T]TATTAATTGTGGAGT | 337867 |
rs746201999 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328101 | TTAGTATTGTATAAT[A/G]TGAAGTATTTTGTGT | 337867 |
rs746209995 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371176 | TTTTTTGTTTAATGA[A/G]TCATTTTTCCTTGAT | 337867 |
rs746216180 | snp | A/T | 3.38513e-05 | 0.00411394 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99244559 | AGCCTTATTTGACTT[A/T]CTCCTCATTGAAGCT | 337867 |
rs746217690 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239509 | GCGCCTGGGCATTGC[C/T]GTACATTTAAAAACA | 337867 |
rs746227347 | snp | C/T | 1.66048e-05 | 0.00288134 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340297 | CTACATTTAAACAAT[C/T]ACATTGGACGTTTTT | 337867 |
rs746227780 | snp | A/C | 3.29544e-05 | 0.00405908 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318084 | TGTAAGTGTGACTAC[A/C]CTTTTACACCCAATT | 337867 |
rs746237524 | in-del | -/C | 0.000130959 | 0.00809087 | utr-variant-5-prime, upstream-variant-2KB, frameshift-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200890 | CGGCGCCCTCTGGGG[-/C]TCCGAGCCCGGCGGG | 337867 |
rs746239552 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373350 | TGACTGTTAGGTAAA[A/G]TCAGACAAGAAAGTT | 337867 |
rs746241287 | in-del | -/TG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358691 | ACCCCGGCCATGGAC[-/TG]TGGTCTCACACGGGG | 337867 |
rs746273742 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274541 | ATGTTGCCCAGGCAG[G/T]TCTTGAATTCATGAG | 337867 |
rs746312442 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208938 | AGTTTATTTTGGTGA[C/T]TCCTCAGCACCTAGG | 337867 |
rs746313675 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295343 | CGAAGCTTCTTAATC[A/G]TATGTTGAATAATTG | 337867 |
rs746329960 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309984 | TATTTTATGTTTTCT[A/G]TCGAGTGCGATCATG | 337867 |
rs746352536 | in-del | -/TTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283910 | CAGCTAATTTTTGTA[-/TTT]TTAATAGAGACGGTG | 337867 |
rs746354702 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365295 | TGTTTCTTTGTTTTC[C/T]GTTTTACTGACATTT | 337867 |
rs746366329 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298081 | ACAGCAAAATTTGAC[A/G]GAATTTGAAGGAGAA | 337867 |
rs746392645 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99229233 | TGGGGGAAAAGCCCT[G/T]CAGGCTAAAATGGTT | 337867 |
rs746393700 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284296 | CACTATATGACACTC[C/T]AGTTATTTAGCTATT | 337867 |
rs746402582 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210087 | CATCGTAAAAGTAAC[A/G]TTAACCACACTATAG | 337867 |
rs746414354 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198546 | GTTTGTTGGGATACA[C/T]TGCTTTGGTTGAAGC | 337867 |
rs746416420 | in-del | -/TAAC | | | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258330 | AAGTAGTTTCCAGTG[-/TAAC]GCTTGGCGTCGGAGT | 337867 |
rs746424593 | snp | A/G | 0.00013182 | 0.00811742 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255295 | ATCAAGAAAAAAAAT[A/G]TCAGTCGAGTGAGGT | 337867 |
rs746434946 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338895 | TATTTCCCTTCTCTT[C/T]ACTGGCAGCCCTGTC | 337867 |
rs746445200 | in-del | -/ATGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289307 | GGCGGTGTGATTTGG[-/ATGT]AAGTGTAAACAAGAA | 337867 |
rs746470006 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362740 | TTGTCTTATAAGTTC[A/G]TAAGTGTCATTGATT | 337867 |
rs746491301 | snp | A/G | 1.67742e-05 | 0.002896 | intron-variant, stop-gained | UBAC2, GPR183 | GRCh38.p7 | 13:99295494 | GTTTGCAGCAGATCT[A/G]AGAATAGCAGATGAG | 337867 |
rs746522982 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367826 | CTTTTTCCTCCTTTA[C/T]GTCAGCGACAAAACG | 337867 |
rs746523107 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363676 | ATACCATTGTCAGAA[C/G]CTAGTCAACATGGAA | 337867 |
rs746531773 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324652 | AGGAACTACGGAATA[G/T]TCTCCCTATTATAGA | 337867 |
rs746539150 | snp | A/T | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351452 | CTCTTTATCTTCCAA[A/T]CCTAAAATGTTTACC | 337867 |
rs746542167 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283186 | CTTAATGTTTAATAT[C/T]GGCTTCTAGGATGTA | 337867 |
rs746552132 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331857 | GGGATTTTTCTGTTT[C/T]GCTCCTTACTATGTT | 337867 |
rs746564668 | snp | C/T | 8.2392e-05 | 0.00641788 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255334 | TTCACAGCTTTTAGA[C/T]AGATGATGTCAGAAA | 337867 |
rs746571500 | snp | A/G | | | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201531 | GCTGTGCTGCTGGAT[A/G]TTGCTGTTTTCCTGG | 337867 |
rs746579679 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358435 | TCTAGTAAGTCAGAC[A/G]TTAAAGAGATTTGCA | 337867 |
rs746590981 | snp | A/G | 8.71878e-05 | 0.00660199 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296115 | GAGTTGCAGAGGGCG[A/G]AGTAAAATTGTTTGC | 337867 |
rs746597832 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273864 | GGTCCAGTTTTCATC[-/T]TTTTTTTTTTTTTTC | 337867 |
rs746601024 | snp | A/G | 1.65707e-05 | 0.00287838 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238386 | GGTTTTTTAAATCTT[A/G]GGAACAATCATTCTG | 337867 |
rs746618914 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305825 | ACATGCTAAAATATA[A/G]GAAGTGTGCAGTCCT | 337867 |
rs746640755 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312104 | CTGCCATTTATCACA[-/T]TTGTTTTGTGTGTGT | 337867 |
rs746667383 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346509 | CAGCCATGCCTCACC[G/T]GGTTACTCACAGTTA | 337867 |
rs746682387 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215501 | TAGCAAGTTGCAAGT[C/G]ACGAGGGGTAATATA | 337867 |
rs746706224 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206888 | CTGGGTGCTCCTTCC[G/T]CTTCCTGCTCCCTCT | 337867 |
rs746716504 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264418 | TATGTGTTACCTTTC[C/G]TATTTAAAAACTGCC | 337867 |
rs746723010 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323871 | TGATTTTTAAATGCT[C/T]AGTGCAGAATAAATG | 337867 |
rs746740039 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241740 | CTTTTTTTTTTTTTC[-/T]AACTTTTTTTTTTTT | 337867 |
rs746746536 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213099 | TGACGCATGTATATA[C/T]ATATACATATACCTA | 337867 |
rs746759064 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369393 | TACGAGACTCTTTTG[C/T]GATGCTGGGCAGCGA | 337867 |
rs746778970 | snp | G/T | 1.65968e-05 | 0.00288065 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255785 | TTATGAAGATACAGC[G/T]ATAGAAGACAAGGGC | 337867 |
rs746786038 | snp | A/G | 1.89777e-05 | 0.00308034 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296193 | AGAAGGATCATATAA[A/G]TAAAAGCATATGTAT | 337867 |
rs746790451 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225634 | CCCTTTTGTTTAACA[A/G]ACACTCTTGACTGCC | 337867 |
rs746790527 | in-del | -/GGCTGACCCCCCCACCTCCCTCCCGGACGGGGC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242630 | GCTGGCCAGGCGGGG[lengthTooLong]GGCTGACCCCCCCAC | 337867 |
rs746791766 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341792 | TGAGAAATCAGAATG[A/G]TCAAGGTCAGAAAAA | 337867 |
rs746795774 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259008 | TTTTCTAGTGCGTGG[A/G]AGTCTAGAAATAATT | 337867 |
rs746810291 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370408 | GTTTGAAATTATTTC[A/C]AACTACAACCTTTTC | 337867 |
rs746814333 | snp | C/T | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260609 | GTTGGCAGGGAATTA[C/T]AGTGAAAAGAAACTG | 337867 |
rs746832986 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246515 | GGGAGGTATGTGTGT[A/C]TGTGTTAGAATGAAC | 337867 |
rs746864955 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313275 | AGGCGTGAGACACTA[C/T]GCCCGGCCGGAAGGA | 337867 |
rs746873928 | snp | C/T | 1.79855e-05 | 0.00299873 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255894 | GCTTGTTGGTAGGCA[C/T]GATACTTAGAAACTG | 337867 |
rs746875061 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224780 | ATAGTCACATTTTCT[C/G]TAAACACTTAAATGT | 337867 |
rs746882174 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253344 | GTTCTTGAGCTGAGC[A/G]AGTCACATAACCTCT | 337867 |
rs746883930 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325524 | TTAAGTCCTGGCCCA[A/G]CCCTTTTCCTGAGTC | 337867 |
rs746892767 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381615 | GTTATCTCCACCAAT[C/G]ACAATGGTCCTTAAC | 337867 |
rs746948384 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352560 | AGCTTTATGTGTGCA[A/C]GTGCCACTCCACCAG | 337867 |
rs746957543 | snp | A/C | 0.000171189 | 0.00925014 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200908 | CGAGCCCGGCGGGAC[A/C]ATGTTCACCAGCACC | 337867 |
rs746959412 | snp | G/T | 1.64844e-05 | 0.00287087 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255037 | ATCACATCCAGACAC[G/T]TGCTGAGGTTCATGA | 337867 |
rs746965706 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271364 | AGATATCAGAGACTG[C/T]CAGTGCCAAGGCCCT | 337867 |
rs747017010 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300731 | AGGGTGAATATATAG[C/T]GTTGAACATGTGCTG | 337867 |
rs747030435 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221767 | CTGTCAGAAACATCT[A/G]TCACTCATGGTGATC | 337867 |
rs747065867 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298250 | TATGCAAATTTGACC[A/G]TGTGCTAGGTCACCA | 337867 |
rs747091685 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253181 | CTATTGAAACTAAAA[-/AT]ACTGTGTTTTTCTCT | 337867 |
rs747092838 | in-del | -/AATT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291793 | TTTCTTTTCATTGAG[-/AATT]AAGAACTTCACAGAT | 337867 |
rs747102868 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378842 | CTAGCATGTTGTTCA[A/G]GAAGGTACTTTTATA | 337867 |
rs747113659 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338256 | AGAGACGGGTTTTTA[-/C]CATGTTGGCCAGGCT | 337867 |
rs747134357 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366122 | GGGGAGGAGGTGAGA[A/G]GTGAGAGTGGCTTCT | 337867 |
rs747151096 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235263 | AAAACTATCAAACAC[C/T]GATGAAAGAACTTGA | 337867 |
rs747155396 | snp | A/G | 1.83572e-05 | 0.00302957 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200982 | TGCCCCCTACACGCC[A/G]CCCTAGGCACCTCTT | 337867 |
rs747156351 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273307 | GAAAGGTGTTAAACC[A/T]CTTTGGCAGAGTCAG | 337867 |
rs747199458 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309007 | ACCATTCTGGTGGGG[A/T]TTTGCCTGTTAATTT | 337867 |
rs747218813 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349473 | CTGCCATCAAGATGC[A/G]GAGACCAGTAGTGGC | 337867 |
rs747233282 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361026 | TCCAGAAACCTTTCA[A/G]TGCCTGTAGAACATG | 337867 |
rs747263675 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310085 | TAATCTCAGCAATTC[A/G]GAAGGCTGAGGCAGG | 337867 |
rs747280949 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267178 | TATATATTTCTTCTT[C/T]AGAGAATTGCCTATT | 337867 |
rs747317037 | in-del | -/GA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368683 | TCATCGTAAACTCAT[-/GA]GAGAGTGTGTGTGTG | 337867 |
rs747319192 | in-del | -/T | 3.30508e-05 | 0.00406501 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254925 | CCGTAGACTACCAGA[-/T]CGGAAACTTTTTCTG | 337867 |
rs747330996 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275615 | TCCCTCTCATATTGA[G/T]GATAGTTTCTTCACT | 337867 |
rs747340193 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318325 | GGTGTGTGCCACCAC[A/G]CCTGGATAATTTTGT | 337867 |
rs747344397 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304870 | TGATCTGCTATTATG[A/G]GTAGAAAACAAGTAA | 337867 |
rs747357350 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263467 | AGGGTATTATCCATT[C/T]GCCAGAATGCCTACG | 337867 |
rs747363898 | snp | A/G | 4.94972e-05 | 0.00497455 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385304 | CAAACAATGACCTCA[A/G]TGTCGCCACCAACTT | 337867 |
rs747364454 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255526 | ATGTATCTGTCAGCA[C/T]TAATAAAGGCAAGAA | 337867 |
rs747376431 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376114 | AGAGAAACTGGTACA[G/T]ATTTATTTCCATCTC | 337867 |
rs747377756 | snp | C/T | 1.73063e-05 | 0.00294157 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99243933 | ATTTGAAAGAAGATA[C/T]GGAAGCAGAAAATTT | 337867 |
rs747382265 | snp | C/T | 1.64898e-05 | 0.00287135 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314237 | TACAGTATGCATTTT[C/T]ATGTTCACTTTTCTT | 337867 |
rs747388623 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345437 | CTCTCAGAGGAGTGC[C/G]TTGGCTGGGCTGATG | 337867 |
rs747404946 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369837 | TCAGTTATGTCCTTG[-/T]TAACATATGCAGTTA | 337867 |
rs747441881 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216468 | TTGTTTTCCATTTAC[C/T]GTAGTGATATCAAAT | 337867 |
rs747446027 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230660 | ATTTCTTGACTCATG[A/G]CCCAATTTTATCTTC | 337867 |
rs747448589 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211238 | GAGTCTTTTCACGCT[C/G]AGAAAATGATTTGTC | 337867 |
rs747449163 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276619 | TGCAGAAGAGTTTTT[A/G]TAGGGCTCCATCTCC | 337867 |
rs747464698 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99385125 | TGGTTTTTTTGTAAA[C/T]AGTTTTGACCTTTGC | 337867 |
rs747480609 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285479 | CTCACTGTAACGTCA[A/G]ACTTCTGGGCTCAAG | 337867 |
rs747482441 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299476 | CGCACACACACACAC[A/G]GAAAGATGTCTGTAT | 337867 |
rs747505430 | snp | C/T | 1.69562e-05 | 0.00291167 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99244547 | CTGGGTTTTGTCAGC[C/T]TTATTTGACTTTCTC | 337867 |
rs747514037 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241176 | GGCTGAGCTGCGAGT[A/G]TTGATTCAGTCTCAG | 337867 |
rs747533790 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286357 | TAGGAGATCAAGTTC[C/T]TCAAAGAACATTGTG | 337867 |
rs747534851 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200676 | GTTTCAACCTGGAGA[A/G]GTGAGCCCTCCCCTA | 337867 |
rs747565086 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274637 | GCCTCATAATACTGT[C/T]AATGTTAATGGACAT | 337867 |
rs747571445 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316650 | AAACACACAGATACT[G/T]TGAAGACATAGGCAG | 337867 |
rs747592554 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215624 | AGTTGCACCCACATG[C/T]CTGTGACCCGTCGTC | 337867 |
rs747635180 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238325 | TTCTGGACTTTGTCT[G/T]CATTCTGATTTAAAA | 337867 |
rs747659754 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272543 | ATTTATTTTCTCACA[A/G]TTTTGGAGGCTAGAA | 337867 |
rs747663821 | snp | A/C | 1.64857e-05 | 0.00287099 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295323 | ATTCCAGGAAATTAG[A/C]GAAACGAAGCTTCTT | 337867 |
rs747667539 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342234 | GCTGGGAGAGCCCTT[C/G]TGAGTTGTCCCAAAA | 337867 |
rs747674086 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243136 | TAAGGTCATTGTGAA[C/G]GGGAAATAAGATTAG | 337867 |
rs747688899 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271517 | ATTGTACTAATTTTG[A/G]CCTTTAATCAGGGCA | 337867 |
rs747691054 | snp | A/C | 1.64776e-05 | 0.00287028 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295204 | AACCTTTCTCTTATA[A/C]CCTTTACATGCAAAG | 337867 |
rs747698022 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336598 | CTGAATACCAGGTGC[C/G]CTTACACTGAGGATC | 337867 |
rs747706361 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282475 | GAGTTGCTTTGCTGC[A/T]CAATTCCTTTTATTT | 337867 |
rs747716613 | snp | A/G/T | 3.29491e-05 | 0.00405877 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255222 | CAGCTTAGACGTCCT[A/G/T]CCGTGAAGGAGATTA | 337867 |
rs747733676 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324917 | AAATATATATCCCAT[C/G]TAGGTTTGTGTAAGT | 337867 |
rs747755230 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295706 | CACACGCCTTTTGCA[C/T]GTTCAATCCTTTTTA | 337867 |
rs747809534 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363797 | GTGAACCAGCAGTCT[G/T]CTAGACTGGAGTTGG | 337867 |
rs747841558 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201219 | CTTGGGGCCGCTGCA[A/G]GTGGGCAGGTGCCCT | 337867 |
rs747848399 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283322 | AATGACAATACCAAG[A/G]ATAGGTTTGTTAATA | 337867 |
rs747858005 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325633 | TTGTGCAGCGAATCT[C/G]TGGAGCTTATCGCTC | 337867 |
rs747867840 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381971 | GCAAGAGATCACCAA[A/G]ACCTTTGACAACATC | 337867 |
rs747892266 | snp | C/T | 0.000115832 | 0.00760937 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296007 | CTAGTAAGTTTCCCA[C/T]GAGCCCAATGATGAA | 337867 |
rs747905404 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338046 | CTTTTTTTCTTTTTT[-/T]CTTTTTTTTTTTTTT | 337867 |
rs747906490 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215192 | GTATCACTTAAATAT[G/T]GTTAAGACTCAAATG | 337867 |
rs747919834 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228391 | CTCCTGGGTTCAAGC[-/G]ATTCTCCTGCCTCAG | 337867 |
rs747938799 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371268 | TTTCTTCCTCGCTCC[A/G]TGTTACGAGAAGTTG | 337867 |
rs747959649 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291357 | TCATGTAGTCCTCCC[C/T]GGGTTCAAAATAATG | 337867 |
rs747964079 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333401 | GGGAAAGTATAAACT[C/T]GGGACCAAAAAGAAT | 337867 |
rs747969657 | snp | A/G | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367809 | TGATCAATTGGAATC[A/G]TCTTTTTCCTCCTTT | 337867 |
rs747980078 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233760 | ATCAAAATTATCATT[A/C]TGTAAACCCTAGTGT | 337867 |
rs747987963 | snp | C/G | 1.70667e-05 | 0.00292114 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296095 | GTCACAGTCATTTCC[C/G]TGAGGAGTTGCAGAG | 337867 |
rs748004268 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322480 | AGCCTTCTTTTGCCA[A/G]TTTTCTTTTTACAGT | 337867 |
rs748029280 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227403 | AACCACCATCTTGCA[C/T]GTTGGCAGGTGAAAA | 337867 |
rs748032389 | snp | C/T | 3.30464e-05 | 0.00406474 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255773 | CAAATAATCCAATTA[C/T]GAAGATACAGCTATA | 337867 |
rs748044947 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315173 | AAATCTTTTTATTCT[C/G]CATCTCTCAACCCCC | 337867 |
rs748066627 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203595 | GGGTACCCATATCAG[C/G]CACACACTGTTGATA | 337867 |
rs748118719 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303512 | AAGATGAAGATGACA[A/T]ATGTTTAGAGAACTA | 337867 |
rs748148321 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211657 | GCACAGACACTTAAG[A/T]AACTTTCCTGCTGAG | 337867 |
rs748188853 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367735 | CTCTTCCAAGCATTA[C/T]GATGATTCTGCTCCT | 337867 |
rs748201402 | in-del | -/A | 1.64804e-05 | 0.00287053 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255286 | AACAAAGGAATCAAG[-/A]AAAAAAATGTCAGTC | 337867 |
rs748217364 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257687 | TATAGATACCATGAT[C/T]ATCTGTAGCTTTTCT | 337867 |
rs748219045 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380223 | TGAATTTTCAGATTA[C/G]GAATGCTTAACGTGT | 337867 |
rs748236156 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200780 | CCGGGTGCGCCGTTC[C/G]TCAGCGGCGAGTGGC | 337867 |
rs748241864 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368960 | CTGGGGCCTGTCAGA[A/C]GGACACTGGAGCCAG | 337867 |
rs748257890 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368756 | TCTGACCGAGAGGGC[C/T]CAGAAGCAGTGGCCT | 337867 |
rs748273932 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288140 | CTTTTGTAGCCTCCA[C/T]GTAGTTTCATTCTGA | 337867 |
rs748281263 | in-del | -/TTGTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227661 | TAATGTATATCTACC[-/TTGTT]TTGTTTTGTTTGTTG | 337867 |
rs748299735 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379030 | CATCCAGCCCAGCTT[C/T]CCTGCAGTGAGCACA | 337867 |
rs748321111 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212971 | TATGTAGTGTAGAAG[A/G]GATTAGTCCCACATA | 337867 |
rs748348291 | in-del | -/CCC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253554 | AGTCTCGCTTTGTCA[-/CCC]AGGCTGGAGTGCAAT | 337867 |
rs748357810 | snp | A/C | 1.79496e-05 | 0.00299574 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200902 | GGGCTCCGAGCCCGG[A/C]GGGACCATGTTCACC | 337867 |
rs748375828 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339131 | TACATAGCCACCTGC[C/T]CACTCAGTAGCCCCC | 337867 |
rs748375915 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351156 | GGGGATAAAAAAAAT[G/T]ATACAAAATTACCTT | 337867 |
rs748394395 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290957 | GGAGATGTCCAAGGC[A/C]CTGGAGGACATAGGA | 337867 |
rs748413757 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256565 | TCATATCCTCATTCC[A/G]TCTAGATTCAGAAGC | 337867 |
rs748436853 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231909 | ATACATGATTGGTTG[C/G]TGATCATAATGCACG | 337867 |
rs748459802 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374467 | CACGTCGTGTGGATT[C/T]TGTTTATGTCTCTGA | 337867 |
rs748479648 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335703 | TGTATGAATAACCCA[C/G]TCTGCAGCTGTTCCC | 337867 |
rs748508269 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328365 | TTCCTTCTTTAGGAA[C/T]GGAATTGCTGGGTCA | 337867 |
rs748515166 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217526 | GGGCAGCCTTACTTG[C/T]CACCCTGTTTGGTTG | 337867 |
rs748534540 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236743 | TAATCCCAGGTACTT[-/G]GTAGGCTGAGGCAGG | 337867 |
rs748540061 | in-del | -/TG | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327480 | TGGTTTTTCTCTCTC[-/TG]TCTCTGTGTGTGTGT | 337867 |
rs748541807 | snp | C/T | 3.2963e-05 | 0.00405961 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255380 | CGGGAGTGGAGTCTT[C/T]ATCTGGGTCTTTATA | 337867 |
rs748566382 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347763 | TGATAACGTCATCTA[A/G]TGTGCTTTGACCTCC | 337867 |
rs748573755 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236446 | CATACAAATGGCCAA[C/T]AGGCATATGAAAATG | 337867 |
rs748584289 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375297 | GAGGGGGGATCTGCA[A/G]TTCTCCCAAGGAAGA | 337867 |
rs748590745 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207097 | CACGTGGTTACAGCT[A/G]ATGCTTTCTCCTGCG | 337867 |
rs748625862 | snp | A/T | | | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201431 | GTTTCTTCTTCAGTC[A/T]CCAAGAAGAGTTTTT | 337867 |
rs748637338 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210665 | TGTTTTTAGTAGAGA[C/T]GGGGTTTCTCCATTT | 337867 |
rs748638687 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357150 | TACACAACTACCATT[G/T]TGTTACAGCTGCCTC | 337867 |
rs748641623 | snp | C/T | 3.29728e-05 | 0.00406021 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385234 | TGCCTGCAGGTCGCC[C/T]GGCTCATGGAGATGG | 337867 |
rs748642989 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346735 | GGGGCTCCCAGGGCT[C/G]TCTCTGCCCCTGTAG | 337867 |
rs748646123 | in-del | -/CTTCAGTTAC | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261911 | TTTTGCTGTCTGAGG[-/CTTCAGTTAC]CTTCAGTTACCTTCA | 337867 |
rs748648382 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255512 | GCTGTACAATGGCCA[C/T]GTATCTGTCAGCACT | 337867 |
rs748660556 | in-del | -/AGAC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370296 | GTGTATGTGTGACAG[-/AGAC]AGAGAGAGAAAGCAG | 337867 |
rs748663801 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379195 | CATGCAAGTTTACGC[-/T]TTATGCATGCCTGCT | 337867 |
rs748667371 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275965 | CTCTCCACTCTAATA[C/T]CTGTAGGGTGTAAGC | 337867 |
rs748673900 | snp | A/C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320353 | ACGTTTAAAATAAAA[A/C/T]TCTTGACCAAAAAAA | 337867 |
rs748684446 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276700 | TCTAGTCACTTGGTC[A/T]TCCTGCTGGTCGGCC | 337867 |
rs748690151 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220615 | CTTTTAGATTAATGC[A/G]TTGTCTGTTATTCTC | 337867 |
rs748724429 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305964 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT | 337867 |
rs748730396 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382659 | CAAAGGCAGCCACAG[C/T]CCTCATACTGGGAGT | 337867 |
rs748740025 | snp | A/G | 3.29734e-05 | 0.00406025 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385235 | GCCTGCAGGTCGCCC[A/G]GCTCATGGAGATGGG | 337867 |
rs748767644 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262048 | TCTCACTGTCCCGCT[C/T]CTTCCTCCCCAGGAC | 337867 |
rs748772033 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344191 | TCATGACCCCGGAGG[C/G]TCAGGGGAGTGCTTG | 337867 |
rs748796033 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274190 | ACTTTACATAATAGA[G/T]ATGTGGACTCTTCTG | 337867 |
rs748798359 | in-del | -/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199599 | GAGCACTGAAAATGC[-/T]TTTTTTTTTTTAGTA | 337867 |
rs748807717 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227735 | ACTTTGTCCACAGTT[C/T]ATTGCTGTGCCTCAG | 337867 |
rs748810760 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371337 | ATACATTGATTTTCT[A/G]AATCTTGTTTTTGGT | 337867 |
rs748818180 | snp | C/T | 1.66294e-05 | 0.00288347 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295078 | CTTTCCATTTGAAGA[C/T]TTGGAATGTATCATC | 337867 |
rs748828348 | snp | C/T | 1.64817e-05 | 0.00287064 | splice-donor-variant | UBAC2 | GRCh38.p7 | 13:99314222 | TATTGGGACTGCAGG[C/T]ACAGTATGCATTTTT | 337867 |
rs748833605 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376687 | CATGCTGGAGGCGAA[C/T]CCAACTAGAGCTGGC | 337867 |
rs748851717 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226332 | ATTCTTGACTTCTCC[A/C]TCTGCCCATGCACCC | 337867 |
rs748863803 | in-del | -/TG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99349278 | TGAGAAAGATGTATC[-/TG]TTCTCTACCACTGGC | 337867 |
rs748871057 | in-del | -/TA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237260 | TTTTATGCGTATATA[-/TA]TATATATATATACAC | 337867 |
rs748873391 | snp | A/C | 1.64844e-05 | 0.00287087 | stop-gained, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255071 | AGGTGGTAAAGGCTC[A/C]CCAGGGATTGTAACT | 337867 |
rs748888818 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314532 | AATCATAGTATGAAG[C/T]GGAAACAAATGAGAA | 337867 |
rs748915908 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267142 | CTTCAAGAATCTTTT[-/C]ATGGGCTTCTTGGCC | 337867 |
rs748916017 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326883 | TCATCAGCAATGGAG[A/G]CATGATTCTGGAGGG | 337867 |
rs748944354 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366249 | AATCATTTTCAGATC[C/T]TCCTATATTCAGGTC | 337867 |
rs748956911 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353637 | TTTGAAAGGACGAAT[A/G]AATTTAGAGATGTAC | 337867 |
rs748957626 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272626 | TCCTGACTTGCAGAT[A/G]GCCACCCTCTTGCTG | 337867 |
rs748968651 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199357 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 337867 |
rs749008201 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343485 | CATTCCCACCAGGCG[C/T]CTGTGAAGTGGCACA | 337867 |
rs749018144 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198594 | CTTCACCTAGATACA[A/C]CCCCACGGTTGGAAA | 337867 |
rs749028529 | in-del | -/A | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356545 | ACTGGTCACTGTGAG[-/A]AAACCACAAAGGAAA | 337867 |
rs749063351 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361066 | TCCATGGAACTTCTG[C/T]TTAATAAAATGTCAG | 337867 |
rs749098697 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236309 | ATACTTGCAGATTAA[A/T]CCATCTGACAAGGGA | 337867 |
rs749100505 | snp | A/G | 1.65397e-05 | 0.00287569 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356184 | TGCATCCTAAGCTGT[A/G]CTGGAGCTTCCCGAT | 337867 |
rs749101483 | in-del | -/TATGAAGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335111 | AACAGCTTCTAGATA[-/TATGAAGT]TAAAATAGCTAATGG | 337867 |
rs749106721 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350629 | TTCCATCTGACTGTT[A/C]ATCTGTATCCCTTGC | 337867 |
rs749127348 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362596 | TTGCCTTTCCCTAAC[A/G]CTAGTGAGATTGAAT | 337867 |
rs749145977 | snp | A/G | 1.91232e-05 | 0.00309212 | intron-variant, synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201435 | CTTCTTCAGTCTCCA[A/G]GAAGAGTTTTTAGAC | 337867 |
rs749151270 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360140 | TTGTACGAGCAGTCA[C/G]CTCAGGCTGCAGTGA | 337867 |
rs749168986 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216195 | CAACCTCTGCCTCCC[C/T]GGTTCAAGGGGTTCT | 337867 |
rs749177375 | snp | A/G | 3.30606e-05 | 0.00406561 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201506 | TAGGAAGTCGTGGCG[A/G]GGGAGCGCAGCTGTG | 337867 |
rs749190085 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295957 | GAGGGTGGTAGAGTT[A/G]ATTTTTTTCCTGTTT | 337867 |
rs749197933 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304672 | TGCCCTGGGCACTCT[A/G]TGTGTGTTTACTCAT | 337867 |
rs749216581 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243475 | TTTGTCTTATTCAAT[A/C]ACATAAAAATGAACA | 337867 |
rs749220370 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272053 | CAGACTATAAATGGA[A/G]TATTTTTAGTCTTCT | 337867 |
rs749221546 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249582 | TTGCTGAGTGGAATG[A/G]TAGTCCTGTTTTAAG | 337867 |
rs749258869 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205757 | CCCCATTGATCGCCA[C/G]AGTTGATTCGGCTGA | 337867 |
rs749285422 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334366 | GTCTTAACCTTGTCA[A/G]TAGGTTCTTGGAAAT | 337867 |
rs749285554 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323092 | TGAGTTCCTCTGCGC[C/T]GCCTTTGCTTGTGCC | 337867 |
rs749319825 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276835 | CACTTAGGTGATGCC[A/G]AAGATTTTTTGGGAG | 337867 |
rs749323566 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255655 | CGAAAGGGTAAAGTC[A/G]TTATAAATATCAAGT | 337867 |
rs749348020 | snp | A/G | 1.68403e-05 | 0.0029017 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99296062 | TACTATCCTGGCCGT[A/G]CTGTGATGTGCATAG | 337867 |
rs749349858 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320604 | TTTATTTAAAATAAT[G/T]AATATTCATGAATCA | 337867 |
rs749356549 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246363 | GAGTATTCTGTTATT[A/G]GGGAAAATAGTGTAG | 337867 |
rs749370883 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231978 | GTTGTTTTACCAAAT[C/T]ATGGTAACTGAAGTC | 337867 |
rs749376030 | snp | A/G | 3.40414e-05 | 0.00412547 | missense, intron-variant, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99244579 | TCATTGAAGCTATGC[A/G]GTATTTCTTTGGCAT | 337867 |
rs749382941 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346818 | TGCCCTTTCTCCACC[A/G]GTGTGTCTCCGGATG | 337867 |
rs749400001 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358328 | CTTTTCTAACTGTGT[A/G]TCTATGTGGCTGGAT | 337867 |
rs749401473 | in-del | -/CTTCTGTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379702 | CTTCAACAGTTTATC[-/CTTCTGTTT]CTTCAGATCCTATAT | 337867 |
rs749434511 | snp | A/G | 1.64925e-05 | 0.00287158 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255750 | AACCCATAATGCAGT[A/G]ATGTTAACAAATAAT | 337867 |
rs749470980 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300629 | CCATTCTTTCATTCA[G/T]CAGGAAAATGGTTTT | 337867 |
rs749482439 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288322 | GGGGCAGAAAGTAAC[A/G]TGGCCCCTGCTCTGG | 337867 |
rs749523426 | in-del | -/AG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284946 | CAGTGACACAAGCAG[-/AG]AGAATAAAATGAGCC | 337867 |
rs749523896 | snp | G/T | 0.000622859 | 0.0176364 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200854 | CGGTCGCTGGGGCTC[G/T]CACTTCAGCTTCCCC | 337867 |
rs749557744 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238624 | TTTCTAGATTTGCTT[G/T]TTCTTCCTGCTGTTA | 337867 |
rs749579391 | in-del | -/TG | 1.64798e-05 | 0.00287047 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255570 | GCTTGGGTAAAACAC[-/TG]TGAGAGCTCCAAGAA | 337867 |
rs749600903 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297020 | ATGTATATATTTGTC[A/G]TGTATATTTTATATA | 337867 |
rs749601072 | in-del | -/C | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349993 | CGCTTGACCAAGGAG[-/C]CCTCATGCCGGCGTG | 337867 |
rs749614151 | snp | A/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340431 | CCCATCTTCTCTTCT[A/T]CAGAACCCACCAGCG | 337867 |
rs749629581 | snp | A/G | 1.65105e-05 | 0.00287315 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295361 | TGTTGAATAATTGCA[A/G]CATGGTAAGGTGTGA | 337867 |
rs749630082 | snp | A/G | 1.67136e-05 | 0.00289076 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295517 | CAGATGAGAATGATT[A/G]TAAGTGGAAGTACAT | 337867 |
rs749663566 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99254136 | CTTTTGTAAAAATGG[C/T]ATCTTCAACCACATA | 337867 |
rs749684258 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364936 | ATGTCTTTTGATGAA[C/G]ATGTGTTTGAATTTC | 337867 |
rs749706550 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305879 | TGATCATCCATAGAC[C/T]CAGGGCCATTTATTT | 337867 |
rs749713385 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278623 | CTCAACCTAAAAATA[G/T]GACTACCTGGATCTC | 337867 |
rs749722415 | snp | A/G | 0.000231241 | 0.0107502 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200894 | GCCCTCTGGGGCTCC[A/G]AGCCCGGCGGGACCA | 337867 |
rs749743204 | snp | G/T | 1.64789e-05 | 0.0028704 | stop-gained, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255357 | GTCAGAAATCTTGAG[G/T]CAGGTGGCGGGAGTG | 337867 |
rs749752276 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215248 | AAACTTCCAACTTGC[C/T]CAAATAGAATTACAA | 337867 |
rs749752556 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307767 | ATGTAAAAGTATGGG[G/T]TTTTAAATGTTTTAA | 337867 |
rs749765725 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321974 | TATTCACATGTATCA[C/T]TGATAAATGTTTTTG | 337867 |
rs749766483 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253806 | GGCGTGAGCCACCAC[A/G]CCCAGCCAGAAATAA | 337867 |
rs749779203 | in-del | -/AAAC | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323441 | CCCTGTTTCTACAAA[-/AAAC]AAACAAACAAACAAA | 337867 |
rs749793792 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347954 | ATTCTTTTGTAAACT[C/T]GGGACACTATGCTGG | 337867 |
rs749814538 | in-del | -/GGC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352638 | TTCCTGTTGCCTCTT[-/GGC]GGCCTCACCAGTGCT | 337867 |
rs749818477 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331777 | ATGTACAAAGTTCCC[-/T]TATGCTTTCTCTAAC | 337867 |
rs749872494 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280821 | CCTTCTTCCTTCCTT[-/C]CTTCTTTCCCTCTCT | 337867 |
rs749880572 | snp | A/G | | | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255796 | CAGCTATAGAAGACA[A/G]GGGCTGCAATTTTGT | 337867 |
rs749920503 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274957 | CCTGTGCTCAAGCAG[-/T]TCCTCCCACCTCCAC | 337867 |
rs749923064 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245612 | CTTTGGGAGGCCGAG[C/G]TGGGCGGATCACGAG | 337867 |
rs749925488 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230473 | GACTCTGTCTCCTCA[A/G]TAAATAAATAAATAA | 337867 |
rs749925552 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319913 | GCCTGAGGATGTACT[C/G]TTTGTTCCATGGCAT | 337867 |
rs749937280 | in-del | -/ATA | 3.72398e-05 | 0.00431492 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296175 | TGTCTAGAAAAAAAC[-/ATA]CAAGAAGGATCATAT | 337867 |
rs749955749 | in-del | -/AAAT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376639 | GTGTCTAGAAATAAG[-/AAAT]AAGTAGATGTGGAAG | 337867 |
rs749975339 | in-del | -/AAAC | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323444 | GTTTCTACAAAAAAC[-/AAAC]AAACAAACAAACAAA | 337867 |
rs749975900 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382895 | CACGGTACCCACAGG[C/G]CTGGGTGGGGGCCGA | 337867 |
rs749986669 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346406 | TCCTTCAGGGCCTCT[A/C]CATAGCTTTCAGGGT | 337867 |
rs749996354 | snp | G/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258145 | TGAAGTTAATTAAAT[G/T]CTGCTTACCTCCTGT | 337867 |
rs750007704 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277261 | CCAGGTGCAGTGGCT[C/T]ATGCCTGTAATCCCA | 337867 |
rs750015297 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231565 | CTACAGGCGTGCCAC[C/G]ACGCCCAGCTACTTT | 337867 |
rs750018249 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329497 | ACTTGGTGATACTTA[C/T]AATGAATAGAATGTG | 337867 |
rs750019559 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321748 | ACTAGGTAAGTTGAC[A/C]ACTTTTTATCTTCAG | 337867 |
rs750044310 | snp | G/T | 1.64806e-05 | 0.00287054 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255601 | ATCTGGCAGAAGTAC[G/T]CTCCAAATGGCCATT | 337867 |
rs750045874 | snp | A/G | 0.000166085 | 0.00911126 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243784 | CTAAGGAAGAGACCC[A/G]AACAAATTTTACTCT | 337867 |
rs750048232 | snp | A/G | 1.66843e-05 | 0.00288823 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385349 | GATAGTCCCAGGCCA[A/G]CACTGGGACCGGACC | 337867 |
rs750050061 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243977 | ATGTATTTTGTCTTT[C/G]CTACTTAGGCTGTAG | 337867 |
rs750071835 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212529 | AGTTAGGTTGGGAAT[A/G]TTGTTGGCCATATTG | 337867 |
rs750089951 | in-del | -/TAG | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257344 | TGCATTCTTATTAAA[-/TAG]TAGCAATTATAATAT | 337867 |
rs750104794 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294507 | ACTCCCACTGATAGT[G/T]GACAGGGAGCATTGA | 337867 |
rs750107011 | snp | A/T | 2.26303e-05 | 0.00336373 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244482 | TTTTTAGGAGACTCA[A/T]CTCTATCATTTTTCT | 337867 |
rs750126175 | in-del | -/TAGT | 1.79696e-05 | 0.00299741 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254827 | CCATTGACGCCAGAG[-/TAGT]TAGTGAAGTGAATTT | 337867 |
rs750143224 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330962 | GTTAAAATGGATATT[A/G]GAAGGTGTTTGTTTA | 337867 |
rs750153145 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325478 | CCCCTATTTCACTCA[C/G]ATATCCCTTCTTCTA | 337867 |
rs750153959 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99356730 | CATGGGTGGCACTTC[A/C]CATGACAGGGTTAGA | 337867 |
rs750255236 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238092 | TCAGGAGCTAACTGG[C/T]TGATTTGATAGAAAC | 337867 |
rs750266033 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295165 | AGAAATCGATACACT[A/G]ACTTGCCGTTTCAGC | 337867 |
rs750278250 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304858 | CTATTTCCGACGTGA[A/T]CTGCTATTATGGGTA | 337867 |
rs750278397 | snp | G/T | 1.64821e-05 | 0.00287067 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318114 | TCTCTCTCTCTCCTG[G/T]AAAAACATTAGGAAA | 337867 |
rs750293068 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283962 | CTGGTCTCAAACTCC[C/T]GACCTCGTGATCTGT | 337867 |
rs750305729 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243528 | TACGTATATAATTTT[-/A]AAAAAATCTTACTAA | 337867 |
rs750310230 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218032 | AGAACTTTCTGTAAG[C/T]GTCCTGATTTACTTT | 337867 |
rs750318185 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335427 | TCTTCATTAAAAATA[C/T]ATATTTGTTACAGAG | 337867 |
rs750319071 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252120 | TCTCTCAAACCACTT[A/C]CCAACTGGTCATCCA | 337867 |
rs750336592 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306971 | GCATAGGAATATTCT[A/G]TATTAAAATAACTTT | 337867 |
rs750343499 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308249 | GGTGCTGCTTTTTAC[A/G]AAGACATAGATAACA | 337867 |
rs750355797 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375020 | GTAGATTGGAAATAC[A/G]TTTTCTAACAAGATC | 337867 |
rs750387704 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255172 | ACCAGCAGCGTGATG[A/G]TGATCCTTATGGACT | 337867 |
rs750393822 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207535 | TAGTCTGCTACTCTT[C/T]GATGGCGGGGCCCTG | 337867 |
rs750406883 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376398 | ACTGGGGCACCCTGG[A/C]CACCTCCAAGAGGGT | 337867 |
rs750407321 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363610 | TCTAAGAAGGGCGAG[C/T]CCCTGCCTCTGAGGA | 337867 |
rs750439076 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334142 | TTCTTATTTTTTTTT[A/T]AGAGATGGGGGTCTT | 337867 |
rs750453679 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252640 | CCTTATATACCTATT[-/A]ATTTTTTGTTAGTAT | 337867 |
rs750457740 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377758 | CCCTCCATAGGAGAA[C/T]AGTGGTCCTGAGAGG | 337867 |
rs750494988 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249226 | TCTTCCGTGTCTGTT[A/G]CTGCCATCTTTATGT | 337867 |
rs750496075 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360857 | TTCCATTTCTGGGTA[C/T]CTTGCCTTCCCCCGA | 337867 |
rs750509921 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262802 | TAAACATAAACCTAT[A/G]TAATAGTGTGTGTGG | 337867 |
rs750535103 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250209 | GTCTTACATTTATAT[C/T]TTTAATCCATCTTGA | 337867 |
rs750538391 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373819 | GGCATGTGGTTATAC[G/T]CTAGACACCAAGGAA | 337867 |
rs750546152 | in-del | -/TGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216083 | GTACCAACCTATATT[-/TGT]GTGTGTGTGTGTGTG | 337867 |
rs750548697 | snp | A/G/T | 4.94192e-05 | 0.00497067 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367769 | GTGTCTGATAACTGT[A/G/T]TGTTGATCTCTTTTT | 337867 |
rs750551756 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281040 | AAAATACAAAAATAA[A/G]CCAGGTGTGTTGGCG | 337867 |
rs750574083 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343949 | TACTTAGTGCTTATT[A/G]TATGGTAGGCCTAGA | 337867 |
rs750580203 | in-del | -/AGGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346095 | ACTCCCTACCTGATG[-/AGGT]AAAAGCACCCATTGT | 337867 |
rs750582643 | in-del | -/AAAAA | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200013 | TCACGAGATCAACTT[-/AAAAA]AAAACTTTTTAAAAC | 337867 |
rs750636310 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261670 | CATATATAAGTGATG[A/G]CAGTGAAATCAGTCC | 337867 |
rs750644629 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263638 | CAGAGTCCACTCCTA[C/G]GTCTATAACCAGTAA | 337867 |
rs750664339 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301613 | CCGGACATGTTGACA[C/T]GAACTGACAGGTTCT | 337867 |
rs750674322 | snp | A/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304455 | TGAGCCTGTGAAGTA[A/C]TGTGAGTGGGGACCC | 337867 |
rs750715232 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333276 | GCACTTTATATTTTA[A/G]TCCTTTGTGAAAATC | 337867 |
rs750736365 | snp | G/T | 1.64909e-05 | 0.00287144 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255744 | ACTGAAAACCCATAA[G/T]GCAGTGATGTTAACA | 337867 |
rs750741692 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269231 | ATCCCTTTAAACCGT[C/G]AGCATTCTGTGGTTT | 337867 |
rs750746122 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378749 | TCAGTCACTGTGTTC[C/T]ATGCATTGGCAACAG | 337867 |
rs750807050 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257257 | AGGAAAGTGCTACAG[A/G]GAAAAATTATATCTC | 337867 |
rs750821911 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311113 | ATTTATTGAAACCTT[A/G]CTCTATGCCAGGCAC | 337867 |
rs750822967 | snp | C/T | 1.76508e-05 | 0.00297071 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254873 | AATGAAAGAACCTTA[C/T]TATTCATAACATTTC | 337867 |
rs750837913 | snp | A/G | 1.72922e-05 | 0.00294038 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255831 | ATCTGGATGTGAGCT[A/G]TTAAAAGGGACAGGT | 337867 |
rs750844347 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323478 | AAATTTCAAGGCTGA[C/T]CAAAGCCATGAGGGT | 337867 |
rs750861553 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300041 | AAAGTGGTCTAGGCT[C/T]TAAGGGCCATCCTCA | 337867 |
rs750876497 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375840 | ACATGGTCTTGCTCT[A/G]TATCCCAAGCTGGAG | 337867 |
rs750897095 | snp | C/T | 3.29511e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340403 | GGCAAAATTCTTTTC[C/T]TGGACACTTGAACCC | 337867 |
rs750929509 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200889 | CCGGCGCCCTCTGGG[A/G]CTCCGAGCCCGGCGG | 337867 |
rs750958025 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281709 | CTTGACATTGCCTGA[A/G]GACTGATTAGGAACT | 337867 |
rs750961981 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223123 | TATCAAATTTATGGG[C/T]GTAAAGTATTTCCTA | 337867 |
rs750963025 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206281 | GAGGACTCCAGAGGT[C/G]GGGGGACAGTTGGAA | 337867 |
rs750984475 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350985 | TGAGTCGTGTGTGAG[C/T]GTAGAAAGGAAGAAA | 337867 |
rs751004148 | snp | C/T | 1.65529e-05 | 0.00287683 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340526 | CCGGCAGCTGATGTT[C/T]TCTCAGTTTGCACAA | 337867 |
rs751021284 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278640 | ACTACCTGGATCTCC[A/G]AATTTGAAGCGATCA | 337867 |
rs751022260 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265395 | GCTGTGCTTCTTTGG[A/G]AAAAAGGTTCTCAGA | 337867 |
rs751060441 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308335 | TGGGGATGTGTATGC[A/T]TTGTAGGCATAGGGT | 337867 |
rs751062440 | snp | C/G | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386662 | GCCACTAGCTGCTCA[C/G]AGGGGGGTCGAGGTG | 337867 |
rs751066792 | in-del | -/CT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383110 | AGTGAGGCCAGGGCA[-/CT]CAGCCACAGCTGATG | 337867 |
rs751096163 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376700 | AACCCAACTAGAGCT[A/G]GCTTCTCAATGAAGT | 337867 |
rs751124248 | snp | A/G | 0.00014881 | 0.00862454 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200956 | TGAGTACCGGCCTCC[A/G]CCATCCTGGCTGCCC | 337867 |
rs751145918 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336296 | TGTGTTTTCATTTCA[C/T]TTATGGTAGCTTTTG | 337867 |
rs751161268 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215145 | CAATCAAAGCCCAGT[A/C]CTTCAGAATCAATAG | 337867 |
rs751164038 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357941 | TGCATATGCCAGGTC[A/G]TACAGGAGGCCAGGT | 337867 |
rs751176615 | snp | A/G | 1.65274e-05 | 0.00287462 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295664 | AGTGGGAGTGTCTGA[A/G]CAAATACTAGAATCC | 337867 |
rs751184581 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336357 | ACCAGTGTGTGTTTT[C/T]TTTTCTAGTTTGTAC | 337867 |
rs751191912 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269014 | GTGAATGAAGACCAC[A/G]GGGACATGCTACGGG | 337867 |
rs751193051 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295759 | CACCACAGCAATGAA[A/G]CGGTCAATACTCAGG | 337867 |
rs751200595 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277343 | CCAGCCTAACCAACA[C/T]GGAGAAACCCCGTCT | 337867 |
rs751201262 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231758 | GTTCCCTCTTTTGAT[G/T]ATCTATTTTTGTAAA | 337867 |
rs751202786 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271270 | AGTAAGGAAAAGCTT[A/C]AGAAATCAGGTAATA | 337867 |
rs751209676 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202601 | TATTCAAATTTGATA[C/T]AGGGCAACTGTGGGG | 337867 |
rs751213941 | snp | C/G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321469 | GCACGCCACCAAGCC[C/G/T]GGCTACTTTTTTTGT | 337867 |
rs751222136 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99307397 | AGTTGTCCAAACTGA[A/G]GTAAGTTTTAACTGT | 337867 |
rs751271927 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359180 | TGTCGAGGAAGAGTG[A/G]TCAGTAAGACCTGGT | 337867 |
rs751289142 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218308 | AGGTGCCCAGTGCCT[C/T]TGCTGACTTGCAGAT | 337867 |
rs751292679 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314940 | ATTCTACAGCTTCCT[A/G]TGTCACCATGTGTCG | 337867 |
rs751312881 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354209 | TATCTTATTGGAGAT[-/A]GGGGGTTGTACAGGT | 337867 |
rs751319660 | in-del | -/GGAATATAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320410 | AATTACAGTGTGTTT[-/GGAATATAA]TTCAAAGATAATGTA | 337867 |
rs751322292 | snp | C/T | 1.65146e-05 | 0.0028735 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385210 | GCCCTCAGGTTTCTG[C/T]GTTTTCTCTGCCTGC | 337867 |
rs751352051 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199012 | GGGTCAGGGTGTAGT[C/T]CATCAACAGCTTCTG | 337867 |
rs751359780 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370371 | TCAAGAGTTCCAGGT[A/G]CTATTCTAGAAACTT | 337867 |
rs751410268 | snp | G/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314176 | CAAATTCTGGGTCCG[G/T]TGTCCATCACAAACA | 337867 |
rs751413542 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382401 | TAACTGGCCACACCA[A/G]TGATGCAGCTCCTTA | 337867 |
rs751414315 | in-del | -/CT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280599 | TTACCTAATTGACCA[-/CT]CTCTCAACTGGATGC | 337867 |
rs751416107 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240578 | GTGTTCTGAGGAGAT[A/G]ACAGTCATCATCATC | 337867 |
rs751417236 | snp | A/T | 3.41664e-05 | 0.00413304 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295054 | TAAACCAAAATACAA[A/T]CCATTTCACTTTCCA | 337867 |
rs751447663 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208646 | CTCTGTCCGAAAAAG[C/T]GGTGTGACAGGCTTC | 337867 |
rs751456737 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273369 | ATAGAGAATCCACAG[C/T]CACTGCAGGACCTTT | 337867 |
rs751483185 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322684 | AGTGTGGAAAAAAAA[-/C]AATCTGTTACACCCA | 337867 |
rs751495447 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344759 | TGCTCGCTGCCACCC[C/T]CTGCCACGTGCTCCT | 337867 |
rs751495569 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322180 | TCTTCTAGATGTCTG[G/T]TGAGAGACCTTCAAA | 337867 |
rs751498083 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364623 | CTTCACCTGTAGGTT[A/T]TTGGTGGGTAGATTT | 337867 |
rs751499299 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286524 | CCCACTTTTAGGTTC[-/G]GGGGGGTACATATGC | 337867 |
rs751534788 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353296 | TTATCTCAATCTGTA[A/C]CTCCTTGCAGAAGCT | 337867 |
rs751535635 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284029 | TGAGCCACCACGCCT[A/G]GCCAATGCCACTTTA | 337867 |
rs751537691 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257467 | CTGTACTTACAAACC[A/G]TCTTGAGTCTTTTTT | 337867 |
rs751610777 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326232 | TTTTATAATAGCCAT[C/T]CCAGCAGGTGTGAGG | 337867 |
rs751628083 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236097 | ACCTGAAACTATGAA[A/G]CTACTAGCAGAAAAT | 337867 |
rs751628655 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330490 | AAGAAATACAGTTGA[C/T]TTCTGTATTTCGTTC | 337867 |
rs751635253 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265784 | AATGGCTAATGTTTC[C/T]AGGTAGATACAATTA | 337867 |
rs751642017 | snp | C/G | 1.64814e-05 | 0.00287061 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295132 | TGAATTTTCTTCAGG[C/G]GCTGACTTCACAGCA | 337867 |
rs751665414 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205714 | AGGATTCTTGGATGT[C/G]AGGGCGATCTGGCTG | 337867 |
rs751715458 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216868 | GAAGTCTTGCCCTTG[A/T]CCCCCAGGCTGGAGT | 337867 |
rs751721076 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363155 | CATAACCAAGTGCCC[A/G]TGTTTACTGTTGATT | 337867 |
rs751723695 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345980 | ACCCCTGACCTCATG[A/T]TCCACTTGCCTTGGC | 337867 |
rs751729206 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343285 | AAGTGGGATTCTTGG[-/C]CTGTTTGCGCACGCC | 337867 |
rs751739612 | in-del | -/CA | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305289 | CTTTCAGAGGATTCT[-/CA]CATGTGTTATCTCAT | 337867 |
rs751754578 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333072 | TTTGAGACCAGCCTG[A/G]GCAACATGGTGAAAC | 337867 |
rs751782083 | snp | C/T | 0.000191904 | 0.00979364 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201395 | GCTTTAGAAGCTGAC[C/T]TCTCAGTTTCACTTG | 337867 |
rs751784495 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250397 | TTATTTCTGGGTTCT[C/G]TATTCTGTTCCACTG | 337867 |
rs751784671 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99307131 | TATTTCTGGTGGACC[C/T]ATCGCTTTCAGTCAA | 337867 |
rs751805709 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373939 | AATTTTCTCTATCCA[A/G]GCCCAGGAAACATGG | 337867 |
rs751824336 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293571 | AGTTTAGAGGTGGAG[G/T]GAAGGAAAGGCAGTA | 337867 |
rs751830343 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206400 | TAGGAGGAGTTGCGT[C/T]TCTTCCCCTAGTCCA | 337867 |
rs751835279 | snp | A/C | 3.31543e-05 | 0.00407137 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201487 | CTTTCAAGTGGAGGG[A/C]AGTTAGGAAGTCGTG | 337867 |
rs751838846 | in-del | -/CAGGTGCCTGTAGTCC | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199270 | TAGCCAGGGTGGTGT[-/CAGGTGCCTGTAGTCC]CAGCTACTTGGGAGG | 337867 |
rs751848237 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335082 | TGTGCCTAATAACAG[C/T]GTCCACAAACAGGAA | 337867 |
rs751854491 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222775 | GTTGAGAATTTTGCA[C/T]CTGTTAATACGTTCA | 337867 |
rs751876675 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380661 | TGCTGGCTGGTTGTC[A/G]TCGCATACCCAAGCC | 337867 |
rs751895248 | snp | A/G | 3.32618e-05 | 0.00407797 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295906 | AGGCAAAGCGGTGGT[A/G]AAAAGTATATCAGAA | 337867 |
rs751908710 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337834 | AGGAGGAACTGGGGT[A/G]CCTCTTACCCAGACT | 337867 |
rs751943901 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340256 | GGCTGCTGATTTTTG[A/G]GTCGTGTACATTTTT | 337867 |
rs751949979 | in-del | -/TTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232511 | TTAATAAGTAGTTTA[-/TTG]TTTGTAATGATACTG | 337867 |
rs751963137 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357023 | ATTGTGCTCACTCTT[A/G]TAGTCATGCACCACA | 337867 |
rs751963667 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301718 | ATACCCACTTGGAGG[A/G]ATTTGTGATTTTTCA | 337867 |
rs751964738 | snp | A/G | 1.64844e-05 | 0.00287087 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255630 | TTCATCTTTTGCATA[A/G]TAAAACATTCGAAAG | 337867 |
rs751966260 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312800 | GGATTTTTGAGAGGG[C/T]CTTGTGTGTGTTGGG | 337867 |
rs752002335 | in-del | -/A | 7.69838e-05 | 0.00620371 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314260 | CTTTTCTTTAACCAG[-/A]TCTTTTTTTTTTTTT | 337867 |
rs752017507 | snp | G/T | 1.79548e-05 | 0.00299617 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254840 | AGTAGTTAGTGAAGT[G/T]AATTTTGATGGGATT | 337867 |
rs752026004 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315665 | ATAATATCTACCTTA[C/G]AGAGGTATTTTAAAG | 337867 |
rs752026714 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270781 | TATGCTAATCTTTTA[C/T]GGTAAATTATGGAGG | 337867 |
rs752032038 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245673 | TGGTGAAACCCCATC[C/T]CTACTAGAAATACAA | 337867 |
rs752037812 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212654 | GATTTATTGGGGGAC[A/G]TAAAATATAGGGAAA | 337867 |
rs752117916 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313549 | AGGAGATGAGAGAGC[A/C]AGAAGAAAAGGCTAT | 337867 |
rs752123122 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300205 | TTGAGCTCCAAGGGT[A/G]GCCTGTTGAGGGTCC | 337867 |
rs752143673 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264037 | TCCCCCATCATCTGT[A/G]TGGCAGGATCCTGGA | 337867 |
rs752198336 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297596 | CTGTACAGTGTTGAT[A/G]GGTTAGTCATTATAA | 337867 |
rs752206636 | snp | A/G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377937 | TCCCTGCCACCCTGC[A/G/T]CTGGAGTCAGACCTA | 337867 |
rs752213731 | snp | A/C | 0.00296296 | 0.0383758 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200820 | CCGGATTCGTCGCTC[A/C]GCCAAGAGTGCGCCT | 337867 |
rs752223006 | snp | A/G | 1.67128e-05 | 0.00289069 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340286 | TTAAAATAATACTAC[A/G]TTTAAACAATCACAT | 337867 |
rs752223699 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348779 | GCTTTGGGAGGCCAA[A/G]GCAGGAGGATAGCAT | 337867 |
rs752227287 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326554 | AATAATTTCTGTACT[A/G]TAAAACATTATACTA | 337867 |
rs752229789 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234349 | CTTGCCACCACGCCC[A/G]GGTAATTTTTTTGTA | 337867 |
rs752238071 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347331 | GGCGCCCCCCCCCCC[C/G]CCCAGGAAAAAAAAG | 337867 |
rs752239795 | in-del | -/TTTTTTTTTTCTTTCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287629 | TATCTTTCTTTCTTC[-/TTTTTTTTTTCTTTCT]TTTTTTTTTTTTTTT | 337867 |
rs752251476 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298755 | ATAAAAGTAGAAAAA[G/T]ATTTTTCCATTTAGT | 337867 |
rs752253836 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297809 | CTATCGGTTTAGATT[-/A]AAAAAAAAAAAATTC | 337867 |
rs752254335 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322672 | TCCAGCAGCCTTAGT[A/G]TGGAAAAAAAACAAT | 337867 |
rs752254725 | snp | A/C | 1.7065e-05 | 0.00292099 | stop-gained, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255815 | CTGCAATTTTGTATT[A/C]ATCTGGATGTGAGCT | 337867 |
rs752257092 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366065 | TTTCCATCTCTTTAC[A/T]TCAACTTGTGTACGT | 337867 |
rs752261855 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378490 | CGAGATCACATCACT[C/G]CACTCCAACCTGGGT | 337867 |
rs752282024 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203059 | TTATTTATTTATTGA[-/TT]GATGGAGTCTCACTG | 337867 |
rs752302677 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308460 | AGAAGTTACTGGACA[C/T]AGCTTTTGGATCAAA | 337867 |
rs752303695 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309605 | CCTTTACAGTTTTTT[G/T]GTTTGTTTGTTTGGA | 337867 |
rs752311419 | snp | A/C/G | 3.30974e-05 | 0.0040679 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295638 | CCTGCTTTGACATAG[A/C/G]GTTGATGAGGAGTGG | 337867 |
rs752317974 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248977 | AAGCTGGAAATCTTT[C/T]ATTTTGCTTGTCAGT | 337867 |
rs752321774 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221308 | ATTTCGTTCACAATT[A/T]CATTTACTTTTGTTA | 337867 |
rs752327711 | snp | A/G | 4.95806e-05 | 0.00497874 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340513 | TGGAGCTGCTGGACC[A/G]GCAGCTGATGTTCTC | 337867 |
rs752334617 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219887 | TCTATGTTGTAGCAT[G/T]TATCAGGATCCATTC | 337867 |
rs752348316 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337193 | TACATTCCAACAAAA[C/T]ACCCTGTTAAGATTT | 337867 |
rs752357194 | snp | A/G | 1.6764e-05 | 0.00289512 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295455 | ATTTCTCAGTGAGTG[A/G]GTTTTGTTTGGCAGT | 337867 |
rs752362147 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266291 | GCCAATCTTCTGGCT[G/T]CCCTTGGCCACATTG | 337867 |
rs752367491 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246062 | TATGTTTTGAGAACT[A/G]TTAAGCTACTGTATG | 337867 |
rs752370347 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376923 | AATTTTCCAGACCAA[C/T]GAATGACTGCAAGCC | 337867 |
rs752371279 | snp | C/T | 0.000160424 | 0.00895466 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200881 | CCCCTCCCCCGGCGC[C/T]CTCTGGGGCTCCGAG | 337867 |
rs752395460 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383804 | TGTCCACTGCGTGTC[C/T]CTGTTGGCCCTCAAC | 337867 |
rs752412207 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255317 | GAGTGAGGTTCAGCA[C/T]GTTCACAGCTTTTAG | 337867 |
rs752435160 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257807 | ACATTTTCTTTCCTT[A/G]AGTTGAAAAAAATTA | 337867 |
rs752444306 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262988 | GGCATGATTCTGAGA[A/G]CCTCACATGCTTGAG | 337867 |
rs752452738 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372379 | TGGATAAAGTAGGCT[A/G]TGGGGGGAAAATGAA | 337867 |
rs752453088 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349962 | TAATGGGTGTCTTCG[C/G]AGACACTGGCATTAC | 337867 |
rs752480921 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286165 | ACTAAATCTGCTGCC[C/T]AAAATAGCTGACAAG | 337867 |
rs752488447 | in-del | -/GAG | 1.66704e-05 | 0.00288703 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238581 | CTCATTGGCCCCTGA[-/GAG]GAGAGCGGACAGTTT | 337867 |
rs752505629 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255419 | GCAGAGGGGTGGTCG[C/T]GGTCAGGGTCATTAT | 337867 |
rs752529736 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261865 | AGAGGTGCAAATGGA[G/T]ATGGGTATACAGTAG | 337867 |
rs752547695 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215830 | GAGATCCCACCATCT[A/G]CTCCTTCATCGCACC | 337867 |
rs752555976 | snp | A/G | 0.000420256 | 0.0144897 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234362 | CCGGGTAATTTTTTT[A/G]TATTTTTAGTAGAGA | 337867 |
rs752564901 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366975 | CTATAATTTTGTCAG[G/T]ACTAGAAGACTTCTA | 337867 |
rs752573805 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305510 | GGATGATGACTTGAT[C/T]TCATCCAACATTTTA | 337867 |
rs752584767 | in-del | -/GTGT/GTGTGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368692 | CTCATGAGAGAGTGT[-/GTGT/GTGTGT]GTGTGTGTGTGTGTG | 337867 |
rs752611174 | snp | C/T | 6.60622e-05 | 0.00574689 | missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238469 | TGCTGGTCCCCAGTG[C/T]CCTCTCCCTCCTGCT | 337867 |
rs752630875 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240633 | TTTCCTATGTGCTCT[C/G]GTGTACTGCCTCATT | 337867 |
rs752633440 | snp | A/C | 1.66266e-05 | 0.00288323 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238574 | GCTCTGCCTCATTGG[A/C]CCCTGAGAGGAGAGC | 337867 |
rs752635953 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327728 | TTTGTTGTTAAAAGC[C/T]TGTTTTTGTTCTGCT | 337867 |
rs752651061 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240492 | GCTTATCCCTGAGTA[A/G]AGTATTTTCATTGTA | 337867 |
rs752678537 | snp | A/C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232615 | AAACGACAGAAATGC[A/C/G]AAGTCCTTAGGAAAA | 337867 |
rs752681136 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210909 | GAGCCACCATGCTGG[A/G]CCCCGCTTTTTCCCT | 337867 |
rs752683045 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316152 | ACTTTGAGAGGGAGA[A/G]GTTGAGATCAGAAAA | 337867 |
rs752697567 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200179 | GCTCCGCCGGGCTCG[C/G]CGGGCCGGGGACCCC | 337867 |
rs752734537 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380957 | GATGAAGAGCGAGCC[C/T]GCTGCAAGCTGTGAC | 337867 |
rs752759295 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301842 | CTTTACCATATTCGG[G/T]GATTTAGTTGGTGCT | 337867 |
rs752759800 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271133 | ATTGAGGGTAAAAGA[C/G]AGTAAACAAAATAAA | 337867 |
rs752779562 | snp | C/T | | | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99293902 | AACTCAGAATTAACA[C/T]TTTCTTTATCTACCA | 337867 |
rs752781548 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272108 | GGTCTGGGCTCAGTC[C/G]CAGCTCTCTTTCCTT | 337867 |
rs752784594 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99258523 | GGCATATATTTAAGA[G/T]AATTATATACAAAGG | 337867 |
rs752843037 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280923 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCATC | 337867 |
rs752857041 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341793 | GAGAAATCAGAATGA[C/T]CAAGGTCAGAAAAAC | 337867 |
rs752867105 | snp | A/G | 1.73682e-05 | 0.00294683 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295038 | ACAGTTTACGTCACT[A/G]TAAACCAAAATACAA | 337867 |
rs752870654 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324535 | TAAGCTACTGAAATT[C/T]GATAATTTGTTACCA | 337867 |
rs752876970 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273502 | TTATATGGTAGTTTG[-/C]CTGTCCTGGGGGAAA | 337867 |
rs752879458 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225241 | TGTGCAACCGATGTC[C/T]ATAACTCTTCTCATC | 337867 |
rs752892823 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372707 | GGAGGAGGAGGAAGA[A/C]GAAGATAAATAGAAA | 337867 |
rs752922006 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325399 | TGAGCCACAGTGCCC[A/G]GCCTATGTCTATGCT | 337867 |
rs752922229 | snp | A/G | 1.64844e-05 | 0.00287087 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255022 | ACGATGTAGTAGAGA[A/G]TCACATCCAGACACG | 337867 |
rs752950078 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363411 | GAATAGGAATAATAA[A/T]AGGAATCTGACTCCA | 337867 |
rs752951291 | in-del | -/TTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223545 | TTCTCTTTTTCTGTT[-/TTT]TTTTTTTTTTTTTTT | 337867 |
rs752988727 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282991 | CAAGAGAATAGGCAT[C/T]CCTGTTTTGGCTGGA | 337867 |
rs752992246 | in-del | -/A | 1.72776e-05 | 0.00293913 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340587 | GTGATAATAATCACT[-/A]AAAATTTAGAAATTC | 337867 |
rs753027904 | snp | A/C | 0.00210919 | 0.032406 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351760 | CCTGCTTGTTGGTAC[A/C]AGCCAAGTGGGACAT | 337867 |
rs753034175 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247836 | ATTTATCTGCACTCT[C/G]TATAGTTCTTTACTT | 337867 |
rs753035824 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290612 | CACCTGTAATCCCAG[C/T]TGCTCAGGAGGCTGA | 337867 |
rs753040641 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277611 | TTGCAGTTGTGAAAT[C/T]ATTTTTTTCTCCATT | 337867 |
rs753082169 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213765 | ATTGCATCTTTAACC[C/T]CATTTTAAAGAAATA | 337867 |
rs753117807 | snp | C/T | 1.66565e-05 | 0.00288583 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295801 | GTTCACACCTGCATA[C/T]GTGTTGATGTAAAAC | 337867 |
rs753139847 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266686 | TTTGACATGTTAAAT[-/AT]ATATATATATATGTA | 337867 |
rs753148361 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204239 | GTTTGTCCTCGGTGC[C/T]GTGGGTTTATTGCAG | 337867 |
rs753159106 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245955 | ATGAAGTATCTGAGA[C/T]ACTATTTGGGAAATG | 337867 |
rs753159651 | snp | G/T | 1.64836e-05 | 0.0028708 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255624 | TGGCCATTCATCTTT[G/T]GCATAATAAAACATT | 337867 |
rs753160778 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260194 | GTTTCTCTGCCCTCC[A/G]AAGCTGGGCTGGTTG | 337867 |
rs753163751 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289092 | ACAATTGAAGTCTAG[A/G]AAGGCTCAAAGACTG | 337867 |
rs753164630 | snp | G/T | 2.86086e-05 | 0.003782 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201389 | GCCTCCGCTTTAGAA[G/T]CTGACCTCTCAGTTT | 337867 |
rs753171614 | snp | A/G | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386836 | GTGCTGAGCAAAGCC[A/G]TGTGTGTCTGACCTC | 337867 |
rs753198231 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342688 | GTGGTGGATGCCCGT[A/G]GTGGGCACGACCTGC | 337867 |
rs753214399 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306549 | CAAACACACATATAT[A/G]AAACCCTCACTGCCC | 337867 |
rs753214712 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99356904 | TGGTTCTGGTGGTGG[A/G]CTTTGTTTGGTTTTC | 337867 |
rs753245990 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382088 | ATTAACCCCTTGAAC[A/C]CAGAGTTCTGGGCTC | 337867 |
rs753261876 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240717 | TGTTTCTCCTTGAGC[A/C]CAGCTATGGCCTCAA | 337867 |
rs753288447 | in-del | -/GCGGCCTTCC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241881 | TAGGCAGAGGACCCT[-/GCGGCCTTCC]GCAGTGTTTGTGTCC | 337867 |
rs753317944 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332130 | CTTGAATGTGGGACC[A/G]GTGGTTGGCACAGCT | 337867 |
rs753374485 | in-del | -/ACAC/ACACAC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237263 | TATGCGTATATATAT[-/ACAC/ACACAC]ATATATATACACACA | 337867 |
rs753393070 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311119 | TGAAACCTTACTCTA[C/T]GCCAGGCACAATTCT | 337867 |
rs753395910 | snp | C/T | 6.74195e-05 | 0.00580562 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385359 | GGCCAACACTGGGAC[C/T]GGACCGGCAGCCGAG | 337867 |
rs753398640 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275249 | TCATCTTCAGGCTTT[A/G]CTGGGATTGGAAGAC | 337867 |
rs753400325 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286980 | AACAAGAGTAAGGGC[A/G]TGTGTTAGAGAACAT | 337867 |
rs753425256 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222774 | TGTTGAGAATTTTGC[A/G]TCTGTTAATACGTTC | 337867 |
rs753425884 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341142 | TTCCATGGGCAGTGA[C/G]AGAAGGAGGGTTAGT | 337867 |
rs753428711 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368319 | AGCAAACCAAAAGGA[C/T]AGGGACAAATGTAAA | 337867 |
rs753435309 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338513 | AGGCATTTGGACTTA[C/T]ATGCTGCTTATATGC | 337867 |
rs753438229 | in-del | -/TC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207990 | TTTTGCCTCTCATCG[-/TC]TCTTTTTTTTTTTTT | 337867 |
rs753448119 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99298839 | GAGAGAGGTGAAAAT[C/T]CCAGGCAAGGGTTGC | 337867 |
rs753452437 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243642 | ACCTTTCGTGCCACT[A/G]TTGGGAGGAATTTTT | 337867 |
rs753458670 | snp | A/G | 1.64874e-05 | 0.00287113 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255706 | ATATAGATGGTTACC[A/G]TGGTTCTCTTCTTGG | 337867 |
rs753481408 | in-del | -/TTTCTTTTTTTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287640 | CTTCTTTTTTTTTTC[-/TTTCTTTTTTTTTTTTT]TTTTTTTTGGTAGAG | 337867 |
rs753489347 | snp | A/T | 5.02904e-05 | 0.00501425 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340272 | GTCGTGTACATTTTT[A/T]AAAATAATACTACAT | 337867 |
rs753500305 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255930 | ATAGTTAAGAAAAAT[A/G]AGAATAAAATCGTTG | 337867 |
rs753501325 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327859 | TTTGTTTATTAAGAT[G/T]TTATTTACATACAAT | 337867 |
rs753510035 | snp | A/G | 2.26925e-05 | 0.00336834 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244656 | GATTGACTTAATTTA[A/G]AACTACTTGAATCTG | 337867 |
rs753529789 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374060 | ATTTAGTGACAGATC[C/T]ATTTGGCTTTTATTT | 337867 |
rs753532962 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252861 | TCTTGATTTTGTATC[A/G]ATAGAATCTTTTGTT | 337867 |
rs753550102 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335289 | TATCTTCTGCTGAAT[C/T]AGCGTAATGCTGATA | 337867 |
rs753556663 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340012 | TAATCAGATCTTTTA[C/T]GGCTTTTTAAAAAAT | 337867 |
rs753575557 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251950 | CTTTTCTTAAGAGAC[A/G]AGGTCTTGCCATGTT | 337867 |
rs753594079 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367249 | TAGCCTGTTGCTGAG[G/T]TTTTATCACAGTCTG | 337867 |
rs753616430 | snp | A/G | 1.672e-05 | 0.00289132 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295438 | CTTTTTGTTTACACC[A/G]GATTTCTCAGTGAGT | 337867 |
rs753622319 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282249 | AAATCACCCATGATG[A/G]AGAGTCATGACATGC | 337867 |
rs753647559 | in-del | -/TGAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316400 | AACCAGGGACATTGT[-/TGAA]TGAATGAATGAATGG | 337867 |
rs753669542 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374909 | GGGTTGAACACGAAG[A/G]TGTGGCCAGTAAACT | 337867 |
rs753673096 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306511 | AAAACAAAATACCAC[A/G]CCCCCCTCCCCCAAC | 337867 |
rs753680852 | snp | A/T | | | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99293809 | CTTTAAATAAAATAT[A/T]TTCAGGATATAAAGT | 337867 |
rs753684351 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206448 | CTTCCACGGAATCAC[A/G]CGTCCCGCAGCCGCT | 337867 |
rs753730427 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298399 | ACTTCTAAGGAACTC[A/C]TGGGTTAAAGAAGAA | 337867 |
rs753744772 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344910 | TGTGGCCAACTTCAG[A/G]GAGCTCAGGCAGTTG | 337867 |
rs753747097 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230160 | TTATCACAAACGTGG[C/T]GGTTTAAAACAAAAG | 337867 |
rs753764690 | snp | C/G | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356527 | AAGTATCTCATCCAT[C/G]AACACTGGTCACTGT | 337867 |
rs753781033 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367797 | TTTAGGGAGGAATGA[G/T]CAATTGGAATCGTCT | 337867 |
rs753808729 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217083 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 337867 |
rs753811033 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212356 | AGAATTATAAAGTAA[C/T]CCTTATTTAAATCAT | 337867 |
rs753839575 | in-del | -/ATTT | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305887 | CATAGACTCAGGGCC[-/ATTT]ATTTATTTATTTATT | 337867 |
rs753850180 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263252 | TGTTTCTTGCTAATG[A/T]GTTGATATTCTCAAG | 337867 |
rs753865190 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371018 | CTTGATACAGCAGTG[A/G]GTCACATCCCTCATG | 337867 |
rs753867005 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261156 | GCCTCCCATCAGTGC[A/G]GGGACCAGGGGTCCA | 337867 |
rs753884366 | in-del | -/CTT | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199898 | TACCAAAACTTATTC[-/CTT]CTAACTATAACTTTG | 337867 |
rs753900997 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303196 | GAGAACTTCTTCAAG[A/G]CAGAAAAAGACAGAA | 337867 |
rs753908963 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373112 | GGTGACAGAGCAAGA[C/G]TCTGTCTCAAAATAA | 337867 |
rs753919018 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248180 | TGTCTATTTCCAACC[C/T]ACACTACTCTCCTGA | 337867 |
rs753938253 | snp | C/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260448 | ATGTCTGGGCCTTGA[C/G]TCAGCAGGCAGGGAC | 337867 |
rs753939039 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332289 | GACAGTTGAAGTTTA[C/T]TCTCTATAATCAAGA | 337867 |
rs753954480 | in-del | -/GACTTGG | 3.32231e-05 | 0.00407559 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356105 | CATTAAAGTAAACAA[-/GACTTGG]GACACATGTCTGTCA | 337867 |
rs754010421 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313941 | TATAAGTACAAATTA[C/T]TTTGGACATGAATCA | 337867 |
rs754017717 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215068 | GTACAAAGCCAAATG[G/T]TTGTTACTATAACTT | 337867 |
rs754027225 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353021 | CCCTCCTCAGCACTT[C/T]TCCTTTTTGGCTATG | 337867 |
rs754037204 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238874 | CAGTAGGCATACTTA[C/G]CTTTGCCAAAACCTT | 337867 |
rs754043235 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326153 | GCATTTCTGCCAACT[A/G]TGCACAGGGGTTCCA | 337867 |
rs754046548 | snp | C/T | 3.29484e-05 | 0.00405871 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314139 | ACCATTTTACTGCTC[C/T]ATACCAAGAGTCCAA | 337867 |
rs754065360 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314862 | GTAGGAGAATGATTT[C/T]CAGTTTTCTATCTGT | 337867 |
rs754081003 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381037 | CAAAACCAGCACCGC[A/G]GCACATGTCGTTCAT | 337867 |
rs754089285 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346156 | CCAGACATTTCCCAC[-/T]TTATACATCCATGTC | 337867 |
rs754128013 | snp | C/G | 1.74811e-05 | 0.00295639 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295026 | AAAGTTTGTCATACA[C/G]TTTACGTCACTATAA | 337867 |
rs754140368 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213880 | GCTGGAGTATAGTGG[C/T]GTGATCTCAGCTCAC | 337867 |
rs754151617 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342839 | CACTTCTCTTCACAC[A/T]GAGTTGATGACCAAA | 337867 |
rs754153729 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353025 | CCTCAGCACTTTTCC[-/T]TTTTGGCTATGCTCT | 337867 |
rs754216969 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309766 | CCACCACGCCCAGCT[A/G]ATTTTTGTATTTTTT | 337867 |
rs754220079 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205457 | AAAATCAATCACGGT[A/G]TTTTCTGAATGTACA | 337867 |
rs754228120 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287644 | TTTTTTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 337867 |
rs754243770 | snp | A/G | 1.67287e-05 | 0.00289207 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340554 | CAAGGGAGGCGACAG[A/G]GACAGCAGCAGGTAA | 337867 |
rs754244344 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380222 | TTGAATTTTCAGATT[A/G]GGAATGCTTAACGTG | 337867 |
rs754246997 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266725 | TTTATCGTCTTAACC[A/G]TGTTTAAATGTGCAG | 337867 |
rs754269449 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377988 | TGCATTTTTATTTCA[C/T]GGAAGCATGAACCTG | 337867 |
rs754282727 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221506 | TGCTGCTCACTAGCT[G/T]CTTCTTGCACACTGT | 337867 |
rs754292251 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249065 | GGGGTACATGTGAAG[A/G]TTTGTTTTATGAGTA | 337867 |
rs754297101 | snp | C/T | 3.29696e-05 | 0.00406001 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255008 | GAAATTGTTTTGAAA[C/T]GATGTAGTAGAGAAT | 337867 |
rs754326199 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99279658 | AGACTGTGTGACTTA[C/T]AAACAACCGAAATTT | 337867 |
rs754331726 | snp | A/G | 1.65116e-05 | 0.00287324 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295681 | AAATACTAGAATCCA[A/G]ACAAATATGCACACG | 337867 |
rs754338158 | snp | C/T | 0.000296235 | 0.0121667 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201381 | AAAGTTCAGCCTCCG[C/T]TTTAGAAGCTGACCT | 337867 |
rs754349070 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333261 | AGACTAGGGTTTTAA[A/G]CACTTTATATTTTAA | 337867 |
rs754350232 | snp | A/C | 7.45073e-05 | 0.00610312 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200961 | ACCGGCCTCCGCCAT[A/C]CTGGCTGCCCCCTAC | 337867 |
rs754387916 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204431 | TAGGGGTGGTTATGG[C/T]TGGAGTGAGCAGTTC | 337867 |
rs754392406 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99349161 | AGTCTCCTGTAGTAA[C/T]GATCATCCGAATGGT | 337867 |
rs754407143 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360706 | AATATTCAGCCCCAG[A/C]CCCATCCTCTTGGAA | 337867 |
rs754408457 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205439 | TCCTGTCCCAGCTGC[A/T]AAAAAATCAATCACG | 337867 |
rs754436141 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376735 | GGAAGGAATCATTTC[A/G]ATTTGGGGGCTAGAA | 337867 |
rs754443875 | snp | C/T | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99318030 | TTTATAGCTTTTCAC[C/T]TCTGGTTCCTACATC | 337867 |
rs754456404 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253793 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 337867 |
rs754468993 | snp | A/T | 1.6797e-05 | 0.00289797 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340273 | TCGTGTACATTTTTT[A/T]AAATAATACTACATT | 337867 |
rs754481541 | snp | A/G | | | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254759 | TTTTAAAATGAAGAT[A/G]ATGAATTTATTTTTT | 337867 |
rs754484818 | snp | C/T | 1.93425e-05 | 0.00310981 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244504 | CATTTTTCTGCTGTT[C/T]TATTTTGTAGTCCTT | 337867 |
rs754489720 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364626 | CACCTGTAGGTTTTT[A/G]GTGGGTAGATTTTTA | 337867 |
rs754513232 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206000 | TGTCAATAAAGCTGA[C/T]TGGATCTGCGGCGAG | 337867 |
rs754514134 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238218 | GGCAATGAAGCCCTG[C/T]TAGGGCATTCTGCTT | 337867 |
rs754530880 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219818 | TGGAGTCATATAGTA[C/T]ATAACTTTATATGAC | 337867 |
rs754536955 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337155 | AACCTTAAATATTCC[A/G]CATGAATTTGAGGCT | 337867 |
rs754549354 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208667 | GACAGGCTTCTGGTG[C/T]GTTCGGCTCCTCTCT | 337867 |
rs754553558 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281934 | GTATCCAGTTTAAAA[-/G]GGCGTGTAAGCTGTT | 337867 |
rs754556701 | in-del | -/T | 1.71737e-05 | 0.00293028 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318113 | TCTCTCTCTCTCCTG[-/T]TAAAAACATTAGGAA | 337867 |
rs754594727 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271535 | TTTAATCAGGGCATT[C/T]GGGAGCCATTGCATG | 337867 |
rs754612679 | snp | C/T | 2.56328e-05 | 0.00357991 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200803 | CGAGTGGCCTCGCGG[C/T]GCCGGATTCGTCGCT | 337867 |
rs754625117 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277440 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 337867 |
rs754627408 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347699 | GAGACCTAGGTGCTG[A/T]CAGGGGCAGGGTACA | 337867 |
rs754649709 | in-del | -/CT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383424 | TTTTTATCTACGACA[-/CT]CTCTCCTCTGGTGGG | 337867 |
rs754662469 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349975 | CGCAGACACTGGCAT[C/T]ACCGCTTGACCAAGG | 337867 |
rs754670866 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308403 | TGTTTACATTGCTTG[C/T]GTCAGTCTTCCTAAC | 337867 |
rs754684282 | snp | A/G | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386705 | CCCAGCTGGTCCCAC[A/G]CACAAGCCCCTCCTT | 337867 |
rs754688558 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375228 | AGAGCAGCCCAGAAC[A/G]CTGGCAGGGTCTGTA | 337867 |
rs754707546 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343157 | CCGTGTCCATCTGAT[A/G]ATGGGTTTCTGTCGG | 337867 |
rs754707751 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354239 | TGACATTCATGAGCA[A/G]TGTGAGCCGGGTGAC | 337867 |
rs754711229 | snp | C/T | | | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295660 | GAGGAGTGGGAGTGT[C/T]TGAGCAAATACTAGA | 337867 |
rs754729562 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265419 | TCTCAGACTGTGTTG[A/G]CTTACATCTTTCTGC | 337867 |
rs754746735 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255216 | GGGTTTCAGCTTAGA[C/T]GTCCTGCCGTGAAGG | 337867 |
rs754780793 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199068 | CGTTTTCCTGAAAAA[C/T]AACTCGAACGAACCT | 337867 |
rs754781012 | snp | C/G | 1.67184e-05 | 0.00289118 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295439 | TTTTTGTTTACACCA[C/G]ATTTCTCAGTGAGTG | 337867 |
rs754796505 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273549 | AGAAATGATTAAGGA[A/T]ATGCTATCTCTTGGT | 337867 |
rs754801857 | snp | G/T | 1.65266e-05 | 0.00287455 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201509 | GAAGTCGTGGCGAGG[G/T]AGCGCAGCTGTGCTG | 337867 |
rs754812364 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284042 | CTGGCCAATGCCACT[G/T]TATTTTTAAAGGTAA | 337867 |
rs754815399 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215153 | GCCCAGTACTTCAGA[A/G]TCAATAGCTTCCTTG | 337867 |
rs754848022 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298253 | CAAATTTGACCATGT[-/G]GCTAGGTCACCAGAA | 337867 |
rs754856752 | snp | A/G | 8.4416e-05 | 0.00649622 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201612 | TAAACGGCTTTTCTC[A/G]CTGAGTGTGTGGAAT | 337867 |
rs754861363 | snp | A/G | | | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314140 | CCATTTTACTGCTCC[A/G]TACCAAGAGTCCAAG | 337867 |
rs754874855 | in-del | -/TTTTTTTC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338032 | AAAAAATCTCCTAAC[-/TTTTTTTC]TTTTTTTCTTTTTTT | 337867 |
rs754886024 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230050 | ATGTGACAAAATATC[C/T]CTGAGAGTTTCCTTA | 337867 |
rs754922890 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367800 | AGGGAGGAATGATCA[A/G]TTGGAATCGTCTTTT | 337867 |
rs754935586 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353380 | ATTCAGAACAGAAAG[A/G]TAGGATCAATCTAAA | 337867 |
rs754936072 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367872 | GTCGGCAGTCTGAGC[C/T]AGCAGCGCCCCCTCT | 337867 |
rs754958343 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239190 | CCATTTCTTGAACAC[A/T]GACACCTTTTCTTCA | 337867 |
rs755010475 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284819 | AAAACGATACATATT[C/T]TAAGGCTGCTGGAAA | 337867 |
rs755025611 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269705 | TTCATATTATTACTA[C/T]GAATTCTTACAGAAC | 337867 |
rs755032636 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272495 | GTGTCTTAGTAAACT[C/T]GTGCTGTCATAGAGT | 337867 |
rs755032788 | snp | G/T | 1.70061e-05 | 0.00291595 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296087 | GCATAGAGGTCACAG[G/T]CATTTCCCTGAGGAG | 337867 |
rs755048166 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378967 | ATGAGATGTCAGCTG[A/G]AGGATGAACAGAAAA | 337867 |
rs755049040 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351089 | CAGTTAGGGACTCAA[C/T]CCTGGGTTGACAGGG | 337867 |
rs755050839 | snp | C/T | 3.73888e-05 | 0.00432354 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296176 | TGTCTAGAAAAAAAC[C/T]AAGAAGGATCATATA | 337867 |
rs755059165 | snp | C/T | 1.65042e-05 | 0.0028726 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255765 | GATGTTAACAAATAA[C/T]CCAATTATGAAGATA | 337867 |
rs755097376 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99307208 | TTACATTATTAATAT[A/G]ATTTTTGTTAGAAGT | 337867 |
rs755103227 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380169 | TGTACTGCCATGTTG[A/G]TACTCAAAAAGTTTC | 337867 |
rs755104602 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312882 | AAAGCGAACTGGGGA[A/G]CTTTGCCATCACATC | 337867 |
rs755112652 | snp | A/G | 1.77193e-05 | 0.00297647 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255865 | TCTTGATTGTTCAGG[A/G]TGATCATTTTACAGC | 337867 |
rs755119891 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206422 | CCTAGTCCAGCGGAT[A/G]GATGTGCCTTCTTCC | 337867 |
rs755146439 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323518 | TGTGAAAGGACCACA[C/T]GTAGAAGTTGAAGAC | 337867 |
rs755191527 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311837 | TCTTCCCTGTCCTGG[A/G]GTGCTCAGCCTGGGA | 337867 |
rs755192636 | in-del | -/TAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216269 | GCCACCACACCTGGC[-/TAA]TTTTTGTATTTTTAG | 337867 |
rs755202426 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215003 | TTTTTTTTTTTTCTT[A/G]GGGGATATGACCTTT | 337867 |
rs755218218 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282011 | ACATGAAGGGCAGTG[A/G]CATCATTGACCTAAG | 337867 |
rs755228176 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357097 | GGTCTCATAAGATTA[C/T]GATGCCATATTTTTG | 337867 |
rs755237935 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324505 | GTAGCATGAACAGGA[A/G]AGAAATCTTTGTTAT | 337867 |
rs755255011 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331060 | TCCTTCATAAGGGAA[G/T]GTTCGTTTTATTTGA | 337867 |
rs755265219 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276623 | GAAGAGTTTTTATAG[G/T]GCTCCATCTCCCACC | 337867 |
rs755267322 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255011 | ATTGTTTTGAAACGA[C/T]GTAGTAGAGAATCAC | 337867 |
rs755273048 | in-del | -/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260845 | TTTTACTTATTCCCA[-/G]AGACTGCAAGATTCC | 337867 |
rs755275777 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361984 | TGCTCTCCAGTCTGG[A/G]CAATGTAGCAAGACC | 337867 |
rs755286750 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254962 | CTTCGAAGGTAATTA[C/T]GGTATAGCATGACAC | 337867 |
rs755308407 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236134 | GAAATGCTCCAGGAC[A/G]TTGGTCTGGGCAAAG | 337867 |
rs755322265 | snp | A/G | 8.2513e-05 | 0.00642259 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295688 | AGAATCCAGACAAAT[A/G]TGCACACGCCTTTTG | 337867 |
rs755322367 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231809 | TGGAAGATGAGGCAA[C/T]ACAACTACATACTTT | 337867 |
rs755324448 | snp | A/G | 1.82563e-05 | 0.00302123 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200965 | GCCTCCGCCATCCTG[A/G]CTGCCCCCTACACGC | 337867 |
rs755341903 | snp | C/G | 0.000333259 | 0.0129042 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200896 | CCTCTGGGGCTCCGA[C/G]CCCGGCGGGACCATG | 337867 |
rs755346251 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320044 | TAGTTACTATTAATT[A/C]TTTTACTCTCCATAT | 337867 |
rs755347303 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314259 | CTTTTCTTTAACCAG[-/AT]ATCTTTTTTTTTTTT | 337867 |
rs755360539 | snp | A/G | 0.000162324 | 0.00900755 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351665 | CACAAACTTGGGGAT[A/G]AAACTTTCCATTAGG | 337867 |
rs755367999 | in-del | -/TTTA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203028 | CTTTGTTTTATTTTA[-/TTTA]TTTATTTATTTATTT | 337867 |
rs755425766 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358024 | TTGTGAGATTCAGGC[C/T]GGTTAGCCTGCAAGT | 337867 |
rs755441320 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385983 | TCAGAGTATCCAGAG[G/T]TAGCCACTAGGCTGC | 337867 |
rs755448856 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257531 | TGTCACCAATACTTA[C/T]ATTCATTTGCTGACG | 337867 |
rs755457756 | in-del | -/TTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223544 | TTTCTCTTTTTCTGT[-/TTTT]TTTTTTTTTTTTTTT | 337867 |
rs755496363 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328102 | TAGTATTGTATAATA[C/T]GAAGTATTTTGTGTT | 337867 |
rs755502855 | snp | C/G | 1.6483e-05 | 0.00287076 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255452 | AGACTCCCACACACG[C/G]CAGCACGGCTTTGCA | 337867 |
rs755527399 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364466 | ACTATATATTGTATA[A/C]TTTTTCTTGCTCATA | 337867 |
rs755540362 | snp | C/G | | | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258334 | AGTTTCCAGTGTAAC[C/G]CTTGGCGTCGGAGTT | 337867 |
rs755549294 | snp | A/G | 3.31246e-05 | 0.00406955 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295781 | ATACTCAGGCAGGTC[A/G]TAAAGTTCACACCTG | 337867 |
rs755591625 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239389 | TGAAAAAACTTCAAA[G/T]ATCTGTCTCCATATC | 337867 |
rs755614190 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326596 | GGATGCTTACAATGT[A/G]TACTGCCTTACTAGG | 337867 |
rs755614282 | snp | A/G | 3.29788e-05 | 0.00406058 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385231 | CTCTGCCTGCAGGTC[A/G]CCCGGCTCATGGAGA | 337867 |
rs755626668 | snp | A/C/T | 6.59124e-05 | 0.00574042 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255506 | ACTTCGGCTGTACAA[A/C/T]GGCCATGTATCTGTC | 337867 |
rs755629503 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366184 | TCTCATAATACCTTA[C/T]TCTTTTCTTTAAGGT | 337867 |
rs755632968 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246367 | ATTCTGTTATTGGGG[A/G]AAATAGTGTAGTCAT | 337867 |
rs755674600 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209845 | GGGCGTGGTGGTTGG[C/T]GCCTGTAATCCCAGC | 337867 |
rs755684536 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272024 | ATGTAAGCTAACTTT[-/C]TTTGTTGTTTCAGCA | 337867 |
rs755693077 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199175 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGG | 337867 |
rs755695020 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315184 | TTCTCCATCTCTCAA[C/G]CCCCGTACCGTTACA | 337867 |
rs755700594 | snp | C/G | 1.67711e-05 | 0.00289573 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385354 | TCCCAGGCCAACACT[C/G]GGACCGGACCGGCAG | 337867 |
rs755715199 | snp | A/T | 0.000165385 | 0.00909204 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243789 | GAAGAGACCCGAACA[A/T]ATTTTACTCTTGTTT | 337867 |
rs755724340 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309610 | ACAGTTTTTTTGTTT[A/G]TTTGTTTGGAGACAG | 337867 |
rs755772428 | snp | A/G | 2.21924e-05 | 0.00333102 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244487 | AGGAGACTCATCTCT[A/G]TCATTTTTCTGCTGT | 337867 |
rs755790561 | snp | A/G/T | 0.00114219 | 0.0238712 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318018 | TTTTTTTTTTCTTTT[A/G/T]TAGCTTTTCACCTCT | 337867 |
rs755816501 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231408 | CTTTGCTGTATACAT[-/TT]TTTTTTTTTTTTTTT | 337867 |
rs755818118 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284205 | TGCTAAAATAAGAAG[C/T]ACAAATAAACACACA | 337867 |
rs755820166 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313638 | AGCAGGGTTTCAGAC[-/A]AAAGGGAGGAAGGAA | 337867 |
rs755822067 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297672 | ATAAAACATTTTATT[A/T]TCCAGAAAAGAGACA | 337867 |
rs755824613 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364911 | AATGCTGCTGAGAAC[A/G]TTCTAGTCCATGTCT | 337867 |
rs755851435 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333512 | CCAGGAAATACTTAC[A/G]GTACTATGTGCCAGA | 337867 |
rs755853228 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295167 | AAATCGATACACTGA[C/T]TTGCCGTTTCAGCAT | 337867 |
rs755884901 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263026 | AACCTTCATGCTGAC[C/T]GCAAAGTATGTAGTT | 337867 |
rs755887296 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344846 | AATACTGGTGGCTTC[A/G]CTGTGGGCACAAAAT | 337867 |
rs755902953 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373962 | AAACATGGTGCAACT[A/G]CCCAGACAAGAGATG | 337867 |
rs755906669 | snp | A/G | 3.2956e-05 | 0.00405918 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295292 | AGAGAAATCTGGAAC[A/G]AATGTCTTTGGCTAC | 337867 |
rs755906704 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255103 | TTCTCCCCCGTTCCC[A/G]GCATCAGGAAAGCGA | 337867 |
rs755918313 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249533 | TTTTGGTAGAATGAT[G/T]TATTTTCTTTTGGCT | 337867 |
rs755918882 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216894 | GGAGTGCAGTGGTGC[A/G]ATCTTGGCTCACTGC | 337867 |
rs755945264 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230199 | CCAGGCACAGTGGCT[C/T]ATGCCTGTAATCATA | 337867 |
rs755952549 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273655 | TTTGTGACAGTTTTG[A/G]TGAGGTGCTTTGGAG | 337867 |
rs755968285 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292616 | GCTCTTCACATATAC[A/C]TGATGCCATTTCTAA | 337867 |
rs755977204 | in-del | -/GCTGGACGGCCCA | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200306 | GGGAACAAAGAGGCG[-/GCTGGACGGCCCA]GCTCTCCGCACCCGG | 337867 |
rs756002307 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305563 | AACCTACAATAGATA[C/T]CTAGTAAATATCTAT | 337867 |
rs756009692 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208854 | CTCTTCAGAGACTCC[C/T]GACTTCTATCCCTTT | 337867 |
rs756018610 | snp | A/G | 3.31082e-05 | 0.00406854 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295388 | GTGAAACAGAGAACA[A/G]ACACAACAATAATAA | 337867 |
rs756055188 | in-del | -/AAAAA | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298015 | GTCACTGCAAAGGTT[-/AAAAA]GAACAGTCTACAAAG | 337867 |
rs756078322 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275128 | TGTTTAGATTTGGAA[C/G]ATACTGCTAGTTTTC | 337867 |
rs756081982 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383839 | CCCTAAGGCTTTTGG[A/G]GGAGGAGGGTCTGGG | 337867 |
rs756113990 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362384 | ATTCACAGCTCCCTA[A/G]AGGTGAAGTTGCCAG | 337867 |
rs756114358 | snp | A/G/T | 0.000198457 | 0.00995948 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201500 | GGAAGTTAGGAAGTC[A/G/T]TGGCGAGGGAGCGCA | 337867 |
rs756182912 | snp | A/G | 1.654e-05 | 0.00287571 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356172 | GGGCTGTTGGGTTGC[A/G]TCCTAAGCTGTGCTG | 337867 |
rs756206172 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381035 | GTCAAAACCAGCACC[A/G]CGGCACATGTCGTTC | 337867 |
rs756215611 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341841 | TAAAGGTAGAGGCAC[A/C]GAGCTTATGAGGGAG | 337867 |
rs756221929 | in-del | -/GCC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346038 | GAGCCACCGCACACA[-/GCC]GACATGTACTGTTTC | 337867 |
rs756227129 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283215 | TAGGATTCAGAGAGC[-/A]ACTTGGTCTGTGTGG | 337867 |
rs756242753 | snp | C/T | 1.66571e-05 | 0.00288587 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201583 | GTAGGGGGCGGAGTA[C/T]TTTTACAGCCAGTTA | 337867 |
rs756244665 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280969 | GGCAGGCAGATCACT[C/T]GAGGTCAGGAGTTTG | 337867 |
rs756258948 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370231 | TGCAACCTGCTCTCA[A/C]ATGGCTTAGGAATAA | 337867 |
rs756259667 | snp | C/G | | | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352121 | GTTCCTATCATTAAT[C/G]AAGTATTTTGAATTC | 337867 |
rs756270996 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331260 | CTGGCTGCTTTGACT[A/G]CAGTTAAGATGTTTG | 337867 |
rs756279099 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213795 | AATCATAAATGTTGA[A/C]TTATAGAATCAAAAG | 337867 |
rs756325325 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325410 | GCCCGGCCTATGTCT[A/G]TGCTCTTAAAAGATA | 337867 |
rs756327832 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216557 | ATCAGGGCAGGCAGA[A/C]ACTGGTGCTGTAGTG | 337867 |
rs756337208 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237985 | ATGTATCAGATTATC[A/G]TATGTACTCCCAAAA | 337867 |
rs756339437 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300517 | ATCCCATTCTTATAT[C/T]AGCCAGTCCCAATTT | 337867 |
rs756408986 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204281 | GTTGTGGGGAGGCAC[A/G]GTTAAGGAAGACTTC | 337867 |
rs756410859 | snp | A/G | 1.73318e-05 | 0.00294374 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255834 | TGGATGTGAGCTGTT[A/G]AAAGGGACAGGTTGA | 337867 |
rs756411331 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347848 | GGCTTGTCTCATGGG[C/T]CTGTGGCAGTGAAGA | 337867 |
rs756424491 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255745 | CTGAAAACCCATAAT[A/G]CAGTGATGTTAACAA | 337867 |
rs756448167 | snp | C/T | 1.75422e-05 | 0.00296155 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254878 | AAGAACCTTATTATT[C/T]ATAACATTTCACTGT | 337867 |
rs756455656 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220068 | AGTTTTCTTGGGTAT[A/T]TTCCTCAGAGTGGAA | 337867 |
rs756455854 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308468 | CTGGACATAGCTTTT[A/G]GATCAAAAGATGAGA | 337867 |
rs756466021 | snp | A/T | 1.64931e-05 | 0.00287163 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254944 | AAACTTTTTCTGCGC[A/T]TGCTTCGAAGGTAAT | 337867 |
rs756470111 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206840 | CACCCACCATCTCAC[-/T]TCTTCACCCATCCAA | 337867 |
rs756499102 | snp | C/T | 1.81618e-05 | 0.0030134 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200845 | GCGCCTGCGCGGTCG[C/T]TGGGGCTCGCACTTC | 337867 |
rs756514794 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215446 | CACCACCACCAGCAA[C/T]TGTAGCCTTGATGAG | 337867 |
rs756520190 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99279450 | ACAGTCTCTTGTGAT[A/G]TGCTTTCTTAGAACA | 337867 |
rs756553337 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236466 | ATATGAAAATGTGCT[C/T]AACATTATTGATCAT | 337867 |
rs756559919 | snp | A/G | 1.64762e-05 | 0.00287016 | stop-gained, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340406 | AAAATTCTTTTCTTG[A/G]ACACTTGAACCCATC | 337867 |
rs756576373 | in-del | -/TCT | 4.19701e-05 | 0.00458075 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314261 | TTTTCTTTAACCAGA[-/TCT]TTTTTTTTTTTTTTT | 337867 |
rs756576871 | in-del | -/AAAAAAAA/AAAAAAAAAAAAAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330458 | GTGAGACGTCATCTC[-/AAAAAAAA/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 337867 |
rs756600857 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370746 | CCATTGACTTGATCC[A/C]GCCCCTCCCGCTTGC | 337867 |
rs756621605 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321626 | TTTTTAATCTCTCCT[C/T]GGTGTCCCTTATTCT | 337867 |
rs756635473 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305718 | ACCATTGTCACTAAC[A/G]CGATACATAAACATG | 337867 |
rs756639868 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290924 | GGAAAGGTGAATTGA[A/T]TTCAGATGTGGTGAT | 337867 |
rs756660020 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379532 | CATCCTGATAGATCC[-/T]TGCTTGTTTCCTGAC | 337867 |
rs756660412 | in-del | -/GAG | 0.000162298 | 0.00900682 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351627 | CTGTTGGCTGATGAT[-/GAG]AATTCTGTTATATAC | 337867 |
rs756666997 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248122 | TATCTTGCCCACTTT[A/C]TTGATTTCAACTACA | 337867 |
rs756701353 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231949 | CATAATGATCTATGT[A/G]CTGAAGAGCTGGTGT | 337867 |
rs756715322 | snp | A/C | 1.65913e-05 | 0.00288017 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340538 | GTTCTCTCAGTTTGC[A/C]CAAGGGAGGCGACAG | 337867 |
rs756737187 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230181 | AAAACAAAAGAAATA[C/T]GGCCAGGCACAGTGG | 337867 |
rs756738652 | in-del | -/TT | 0.000242891 | 0.0110176 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238596 | GAGGAGAGCGGACAG[-/TT]TTTTTTTTTTCTTTC | 337867 |
rs756748972 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277639 | ATTGATAGTTACCTC[A/T]ACAATCATTCAGACA | 337867 |
rs756757511 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243674 | CTATGAGAGACTTGA[A/G]CTCAGAGAACATACA | 337867 |
rs756771434 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355830 | CCTGGAGGGCAGCGG[C/T]GGCACAGACCCACTG | 337867 |
rs756787056 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317194 | TTTGAGGTTTTCATC[C/T]AGCACAATGCCAGCG | 337867 |
rs756809133 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198736 | ATGAATGAACATTTT[A/G]GACTGTTACACTAAA | 337867 |
rs756818032 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216211 | GGTTCAAGGGGTTCT[C/T]ATTCCTCAGCCTCCG | 337867 |
rs756827927 | in-del | -/AA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268620 | TGTCTCAAAAAAAAA[-/AA]AAAAAAAAAAAAAAG | 337867 |
rs756838281 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285076 | ATATTTCATATTTCA[C/G]AAAGCTCTAAAATGG | 337867 |
rs756850144 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289141 | TGGGTTGGAGTCTGA[C/T]AGAACCAGGCCACCC | 337867 |
rs756860068 | in-del | -/TC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247861 | TACTTCCTATTTAAT[-/TC]TCTCTCTCTCTCTTT | 337867 |
rs756863639 | in-del | -/AA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253029 | CTACATATCCAATAC[-/AA]GAGTTGTTTTTCTTG | 337867 |
rs756878728 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367898 | CCTCTAGAAGTTTCT[A/G]AGGAACAGGTAATTA | 337867 |
rs756891669 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211102 | CAATCCCAAAGGGTA[A/G]TACCAATTTAAACTC | 337867 |
rs756896525 | snp | A/G | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356559 | AGAAACCACAAAGGA[A/G]AAGTGAAACCGAGAG | 337867 |
rs756920534 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327955 | CCACCATAATCAATA[C/T]GGAAAGCAGTCTCCT | 337867 |
rs756923885 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318823 | TGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 337867 |
rs756971401 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380598 | CTCCACTGGGGAGTA[C/T]TGGGTAAGCACCCAT | 337867 |
rs756980934 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266759 | AGTAGTGTTAAGTTC[-/A]TTCACACTGCTGTGC | 337867 |
rs756983185 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314182 | CTGGGTCCGTTGTCC[A/G]TCACAAACAAGACAT | 337867 |
rs756990360 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367283 | TCTTCCTCCACTGTG[G/T]GCGCTCAGGATTTAC | 337867 |
rs757018585 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362087 | TTACATTTTATTTAT[A/G]TTATTTACATAAACT | 337867 |
rs757025009 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240796 | GTGAACTCTGGTGGC[C/T]AGTACAGTCATGACA | 337867 |
rs757027038 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255498 | TTTGGCGTACTTCGG[C/G]TGTACAATGGCCATG | 337867 |
rs757036261 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206455 | GGAATCACGCGTCCC[A/G]CAGCCGCTTCCCTGG | 337867 |
rs757036923 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335325 | CCTATTTTCTGTTTT[A/G]TATCAGATCTTCAGA | 337867 |
rs757045113 | snp | C/T | 1.69298e-05 | 0.0029094 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238598 | GGAGAGCGGACAGTT[C/T]TTTTTTTTTCTTTCT | 337867 |
rs757048921 | snp | A/C | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327742 | CTTGTTTTTGTTCTG[A/C]TAAAATCCTACCTCT | 337867 |
rs757066436 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363462 | AGCAGAAACTTAACC[A/G]AGGTAGTTTATTTCT | 337867 |
rs757070933 | snp | A/T | 0.000255156 | 0.0112922 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317990 | TGGCAGTTGAATTTT[A/T]TTTTTAGTTGCCTTT | 337867 |
rs757107809 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209699 | ATTTTAGCGGCTGGG[C/T]ATAGTGGCTCACGCC | 337867 |
rs757135284 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351193 | CAGAGGCTCTATCAG[A/T]TATTAGTTATTATCA | 337867 |
rs757138652 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276471 | TATAAAGGATACAAC[G/T]CAGGAACAGCCAAAT | 337867 |
rs757151234 | snp | C/T | | | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295191 | TCAGCATCCTCATAA[C/T]CTTTCTCTTATACCC | 337867 |
rs757186898 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217085 | ATCTGCCTGCCTCGG[C/T]CTCCCAAAGTGCTGG | 337867 |
rs757190073 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275035 | AATGTCTTTGAACAT[A/G]TCTTTTGTTGCATAT | 337867 |
rs757205479 | snp | A/G | 1.64803e-05 | 0.00287052 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295142 | TCAGGGGCTGACTTC[A/G]CAGCACTAGAAATCG | 337867 |
rs757218352 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374076 | ATTTGGCTTTTATTT[A/G]CAACTTATGAATTAG | 337867 |
rs757281675 | in-del | -/AA | 1.65411e-05 | 0.00287581 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356208 | CCCGATGTACTCTGT[-/AA]AGATGTCTTTGCACC | 337867 |
rs757282650 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255040 | ACATCCAGACACGTG[C/T]TGAGGTTCATGAGGA | 337867 |
rs757299328 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207054 | TTTTTCTTTACCTTC[A/G]TTCTCTCTCCTGCAG | 337867 |
rs757305096 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261478 | CAATTTACAGCTATA[A/G]TCTTCTAACCCAGTT | 337867 |
rs757360538 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333270 | TTTTAAGCACTTTAT[A/G]TTTTAATCCTTTGTG | 337867 |
rs757362935 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290980 | ACATAGGACAGGGAG[G/T]AATGGAGCTCAGGCT | 337867 |
rs757373733 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332294 | TTGAAGTTTACTCTC[C/T]ATAATCAAGAGTGTT | 337867 |
rs757376877 | snp | C/T | 1.6543e-05 | 0.00287597 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356154 | TAGAAGCATCCCTTG[C/T]AGGGGCTGTTGGGTT | 337867 |
rs757396305 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215075 | GCCAAATGTTTGTTA[C/G]TATAACTTCTGCATT | 337867 |
rs757404491 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283362 | ATATGAAGGAAAAAT[A/G]TGGAGTAACATTATG | 337867 |
rs757429382 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232798 | AAAAAAAAACCTGGC[C/T]GGTCATGGGGCCTTG | 337867 |
rs757430201 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230665 | TTGACTCATGACCCA[A/G]TTTTATCTTCGAAGC | 337867 |
rs757443201 | snp | A/T | 5.2651e-05 | 0.00513057 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201400 | AGAAGCTGACCTCTC[A/T]GTTTCACTTGGATGT | 337867 |
rs757465904 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354478 | TCTCTGTTCACTTGG[C/T]GGCTTGGCTGAGTTC | 337867 |
rs757468937 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302172 | AGGGGAGCCACCCAG[A/G]TGCAGCCACACAGAT | 337867 |
rs757476079 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326233 | TTTATAATAGCCATC[C/G]CAGCAGGTGTGAGGT | 337867 |
rs757486682 | snp | G/T | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260467 | GCAGGCAGGGACACT[G/T]TGACCAGCTTATGAG | 337867 |
rs757496271 | snp | A/G | 1.65715e-05 | 0.00287845 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201488 | TTTCAAGTGGAGGGA[A/G]GTTAGGAAGTCGTGG | 337867 |
rs757528716 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289639 | TTTCATTCCAAGTAG[A/G]TTAAACACTGTTTTA | 337867 |
rs757571720 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350284 | GTAATCCTTCGCCCA[A/C]AGTGAGAAGTGTCTT | 337867 |
rs757587144 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297899 | AGGCAAGAGAAAATA[C/T]ATACCAGGCAAATCC | 337867 |
rs757600315 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255636 | TTTTGCATAATAAAA[C/T]ATTCGAAAGGGTAAA | 337867 |
rs757600538 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238709 | TAACTTTTCTAGTTA[C/T]TGATTTTTCAGCAAA | 337867 |
rs757604553 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268879 | GATTGGCCATGGGAG[A/G]AACAGGTGGAGAACA | 337867 |
rs757618699 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221510 | GCTCACTAGCTTCTT[C/T]TTGCACACTGTTTCA | 337867 |
rs757618760 | snp | A/G | 3.29734e-05 | 0.00406025 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255735 | GGTGGTACAACTGAA[A/G]ACCCATAATGCAGTG | 337867 |
rs757626940 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338740 | TTTGGTACCAAAACT[A/G]TTCTTGTAAACACCT | 337867 |
rs757635219 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222912 | GTGTTGTAACAGAGT[C/T]TGTATAGAATTGGTA | 337867 |
rs757646007 | snp | A/G | 3.29554e-05 | 0.00405914 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255117 | CAGCATCAGGAAAGC[A/G]AAACAGATGTGGAAG | 337867 |
rs757651803 | snp | G/T | 1.69504e-05 | 0.00291117 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99244548 | TGGGTTTTGTCAGCC[G/T]TATTTGACTTTCTCC | 337867 |
rs757679739 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378559 | TAAAAACTTCAATAT[A/C]CACTTCTTCTGGCTT | 337867 |
rs757680967 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360735 | AAGTCTTACCCCTGT[A/G]CTTTGGCCGCAGTGG | 337867 |
rs757719765 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311156 | TGGGAATAAAACAAA[A/G]CAGACCAAAATCCCC | 337867 |
rs757736022 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366328 | TGGGTGATTTCCTTG[G/T]GGATTTTGTGGTTTT | 337867 |
rs757753361 | in-del | -/TTCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207921 | GTGTTCCTACTGACA[-/TTCT]TTCTTAAGTATGCAT | 337867 |
rs757773188 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280951 | ATCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 337867 |
rs757784128 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266822 | ACTGAAAGCCTGTAC[C/T]CATCATACAGCAAAT | 337867 |
rs757798890 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373157 | TCCATTATTCCATCT[C/G]TCTCTTTTTTATTGT | 337867 |
rs757806105 | in-del | -/ATG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381547 | GGGGGCCATGGCATC[-/ATG]GTGGTGGATAGTAGG | 337867 |
rs757813230 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234695 | GTTCTTTCCCATGGA[G/T]TAGCTCAGCAAGTAG | 337867 |
rs757815333 | snp | A/G | 7.14107e-05 | 0.00597497 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254859 | TTTGATGGGATTGAA[A/G]TGAAAGAACCTTATT | 337867 |
rs757832596 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385889 | AGTACCTTCTCCTAC[A/G]TCTAGTAACAAAGAA | 337867 |
rs757854115 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264297 | GGAAGCCAGGGGCCC[A/G]TGAGCCTTTGCATAG | 337867 |
rs757857220 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354525 | AGCAGGGGAACAGGA[C/G]GGTTTGGGTTGCAGA | 337867 |
rs757869105 | snp | A/C/G | 0.000133342 | 0.00816415 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200888 | CCCGGCGCCCTCTGG[A/C/G]GCTCCGAGCCCGGCG | 337867 |
rs757871445 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99307101 | CATGAAGTGAGCCCT[A/G]TTTTTTGACAAAGAT | 337867 |
rs757890665 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374202 | ACTGATAGGTTAACA[C/T]TGAGTTACTTCAGGT | 337867 |
rs757903372 | snp | A/G | 3.33267e-05 | 0.00408194 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340292 | TAATACTACATTTAA[A/G]CAATCACATTGGACG | 337867 |
rs757918774 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217162 | AATTAATTTTAGTGT[C/T]TGGGGTTTTAGTGGG | 337867 |
rs757921805 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340383 | CTCTGCATCCCCAGC[C/T]GGATGGCAAAATTCT | 337867 |
rs757936050 | snp | A/C | 3.29777e-05 | 0.00406051 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295328 | AGGAAATTAGAGAAA[A/C]GAAGCTTCTTAATCA | 337867 |
rs757936070 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346432 | AGGGTGGTTCCAACA[C/T]AAGGCTCCTGCCTGC | 337867 |
rs757939834 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375061 | ATGTGTTACAATGAA[A/G]TACTAGATGGTACTC | 337867 |
rs757994968 | snp | G/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201280 | TGCGGAGCGTGTGCC[G/T]CGCTGAAGGAAGGGG | 337867 |
rs758012978 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287506 | CATGACTAACTGCAG[C/T]CTTGACTTGCTGAGC | 337867 |
rs758025892 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227328 | TCCATCTCCACTGCA[A/G]GTTACCTAGGAGGGG | 337867 |
rs758044713 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200785 | TGCGCCGTTCGTCAG[A/C]GGCGAGTGGCCTCGC | 337867 |
rs758070225 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384953 | CTTCCAAGGCCTGGT[C/G]CCAGTAGGCCACTTT | 337867 |
rs758079282 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202466 | AATTCTTCAATTTCA[A/G]TTGTTCTTTAGCATT | 337867 |
rs758111123 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305758 | ATTTTGTGGAGTAGC[A/G]TATTCTTTGTGGTTT | 337867 |
rs758115946 | in-del | -/AGTGA | 1.7968e-05 | 0.00299728 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254832 | GACGCCAGAGTAGTT[-/AGTGA]AGTGAATTTTGATGG | 337867 |
rs758121913 | snp | A/G | 3.29571e-05 | 0.00405924 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367879 | GTCTGAGCCAGCAGC[A/G]CCCCCTCTAGAAGTT | 337867 |
rs758136586 | in-del | -/T | 0.000336222 | 0.0129614 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314074 | TCACTATTATAGTGA[-/T]TTTTTTTTATTTGTT | 337867 |
rs758137581 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276532 | TGCACGGAGCTCTCG[G/T]GCCTTCTGTGGGCAC | 337867 |
rs758139379 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357992 | AGAATCACAGTCCCC[C/G]TGGAGCTAATAGGCT | 337867 |
rs758141427 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266434 | GTTGGACTGCATTCA[A/G]AGCTGTCCTGGGCCC | 337867 |
rs758151814 | in-del | -/AAAC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281194 | ACTCCATCTCAAAAA[-/AAAC]AAAACAAAACAAAAC | 337867 |
rs758157897 | snp | A/G | | | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352328 | AAACTGCGCCCCATT[A/G]GCAGTCATTCCCATC | 337867 |
rs758172153 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325489 | CTCACATATCCCTTC[C/T]TCTAGGAAGTCTTAC | 337867 |
rs758185216 | snp | A/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305182 | ATTGATTTTTAAACT[A/C]CTTTTTAGATATTTG | 337867 |
rs758186651 | snp | C/G | 1.64836e-05 | 0.0028708 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255426 | GGTGGTCGTGGTCAG[C/G]GTCATTATCCAGACT | 337867 |
rs758190568 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208617 | CCCAGTTAAGACTTG[G/T]AGTTGGCAACCATCT | 337867 |
rs758206571 | snp | A/G | | | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295358 | ATATGTTGAATAATT[A/G]CAACATGGTAAGGTG | 337867 |
rs758227068 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207545 | CTCTTCGATGGCGGG[A/G]CCCTGTTCTGGGCTC | 337867 |
rs758227453 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314009 | TCAGACTGAAATAAA[A/G]TTATAAGCAGTGTTA | 337867 |
rs758238649 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271296 | TAATATTTGAGCAAA[C/G]ACCTGAAGGGGTCAA | 337867 |
rs758251803 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346509 | CAGCCATGCCTCACC[-/G]GGTTACTCACAGTTA | 337867 |
rs758262211 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277620 | TGAAATCATTTTTTT[C/T]TCCATTGATAGTTAC | 337867 |
rs758284503 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341917 | TTAGATAGATGACTG[A/G]TAGTTCCATTTCACC | 337867 |
rs758301601 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265129 | TTTTGGTTACTCAGA[C/G]AAGGTATTTACCAGA | 337867 |
rs758304848 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314174 | CACAAATTCTGGGTC[C/T]GTTGTCCATCACAAA | 337867 |
rs758315181 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253108 | ATATAAAGATATAAT[A/G]TCTATAAAGGTACTT | 337867 |
rs758352522 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363631 | CCTCTGAGGATCTTC[C/T]TGGTCGGCCCATATT | 337867 |
rs758381056 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376411 | GGACACCTCCAAGAG[G/T]GTCTTCATCCCTGTG | 337867 |
rs758389041 | snp | A/G | 5.13554e-05 | 0.00506705 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295052 | TATAAACCAAAATAC[A/G]ATCCATTTCACTTTC | 337867 |
rs758393007 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248388 | ACCATGCCCACCTAA[-/T]TTTTTTTTTTTTTTT | 337867 |
rs758396937 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205682 | TGGTGCGCTGATGAG[A/G]GAAGATAGAAGATAG | 337867 |
rs758422146 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296514 | CCCCTTCCCTTTTTT[A/G]AATCATTGTCTGGTT | 337867 |
rs758441020 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281155 | GATCACACCATGGTA[C/T]TCCAGCCTGGGTGAC | 337867 |
rs758460772 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334176 | CTGTTGCCCAGGCTG[A/G]TCTTGAACTCCTGGC | 337867 |
rs758472213 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343144 | TGAGCCCAGATGCCC[A/G]TGTCCATCTGATGAT | 337867 |
rs758478426 | snp | C/G | 1.79114e-05 | 0.00299255 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255886 | ATTTTACAGCTTGTT[C/G]GTAGGCATGATACTT | 337867 |
rs758486873 | snp | A/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304468 | TACTGTGAGTGGGGA[A/C]CCTATGGTGTTAATT | 337867 |
rs758487416 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351158 | GGATAAAAAAAATTA[C/T]ACAAAATTACCTTAG | 337867 |
rs758490453 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250257 | GTGCAAGGTAGGGGT[A/G]CAGTTTCATTTTCTG | 337867 |
rs758498785 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360950 | GACGCTCGAGTGCCC[A/G]AGGTCAGCCACCCGT | 337867 |
rs758528279 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236011 | TTAACCATATGCACA[A/T]AAATGAAAGACCCAT | 337867 |
rs758559274 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350363 | GGGCTGGTTACCAGG[A/G]GAACTAATAAGTGAT | 337867 |
rs758585811 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255033 | GAGAATCACATCCAG[A/G]CACGTGCTGAGGTTC | 337867 |
rs758604615 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204532 | GAACATTTTAAACTT[C/T]AAAGAGGGAGAAGAG | 337867 |
rs758636662 | snp | C/G | 7.67607e-05 | 0.00619471 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200972 | CCATCCTGGCTGCCC[C/G]CTACACGCCACCCTA | 337867 |
rs758637803 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340135 | GTTTTACTAAGTTCA[A/G]TTTTGTGTTGATTTG | 337867 |
rs758638842 | snp | C/G/T | 8.24078e-05 | 0.00641859 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255092 | GATTGTAACTGTTCT[C/G/T]CCCCGTTCCCAGCAT | 337867 |
rs758663536 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261673 | ATATAAGTGATGGCA[A/G]TGAAATCAGTCCTGG | 337867 |
rs758677359 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280124 | CATCTGCACTGCCCC[A/G]CTCCCCTAATTTTAT | 337867 |
rs758685480 | snp | C/G | 0.000489436 | 0.0156358 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351790 | TTTGGCAGCAAAGCC[C/G]AGGAGTCCTTGGTGC | 337867 |
rs758693215 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200642 | CCCGTTTTTACCTCA[A/G]GCGGTTCTGACCGCC | 337867 |
rs758696917 | snp | C/T | 6.59163e-05 | 0.00574054 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255516 | TACAATGGCCATGTA[C/T]CTGTCAGCACTAATA | 337867 |
rs758699387 | in-del | -/AATTT | | | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99293833 | ATAAAGTCCAATAAA[-/AATTT]AAAGTGTAACAGAGT | 337867 |
rs758705164 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375858 | TCCCAAGCTGGAGTG[C/T]AGTGGTGCTATCATG | 337867 |
rs758711847 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328120 | AGTATTTTGTGTTTT[A/G]CTTCTTTCACTTGAA | 337867 |
rs758721629 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286095 | TCTATTCCTGGAGGC[A/G]CTGGATCTGGCCTTC | 337867 |
rs758728739 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372265 | TCAGAAGAAAACCCC[A/C]CAAGTTCCTATCAAT | 337867 |
rs758728838 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359898 | GCCACCGATTGTAGA[C/T]TGGAGGTGCCCCTGC | 337867 |
rs758765196 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212561 | TTTTTGACATTGACG[A/T]TGCAGATTAACACTT | 337867 |
rs758766966 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329500 | TGGTGATACTTATAA[C/T]GAATAGAATGTGGCA | 337867 |
rs758780054 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241121 | ATACAAAAATTAGAC[A/G]GGTGTGGTGGTGCAC | 337867 |
rs758791519 | snp | A/G | 1.66735e-05 | 0.00288729 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295901 | CGTGTAGGCAAAGCG[A/G]TGGTAAAAAGTATAT | 337867 |
rs758797384 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351023 | TGTTTTTCTTCAGAG[C/T]CATGCTCACAATAGA | 337867 |
rs758828401 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205953 | AGCTCTCAAGATAGA[A/G]GGATTCTAAAGATGT | 337867 |
rs758831638 | snp | C/T | 2.84475e-05 | 0.00377133 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201390 | CCTCCGCTTTAGAAG[C/T]TGACCTCTCAGTTTC | 337867 |
rs758832108 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269344 | GTCCAGCCAAGGGAC[C/T]GCATTTCCCAGGATG | 337867 |
rs758851090 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281765 | TTTTAGTAATGTTTG[A/T]AGATCTGTGCCTTCT | 337867 |
rs758887216 | snp | A/G | 0.000129049 | 0.00803167 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99243846 | GATTTGGAGGTTGAT[A/G]TGTGGAAGAATAATT | 337867 |
rs758896142 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99349397 | GTGCGGAGATGAGAT[C/T]GTAATAAATAAAGAC | 337867 |
rs758932436 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378825 | TACCCATTCATTTGT[A/T]GCTAGCATGTTGTTC | 337867 |
rs758991760 | in-del | -/AT | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305291 | TCAGAGGATTCTCAC[-/AT]ATGTGTTATCTCATT | 337867 |
rs758993071 | snp | A/G | 1.79677e-05 | 0.00299725 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254833 | ACGCCAGAGTAGTTA[A/G]TGAAGTGAATTTTGA | 337867 |
rs759004749 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255627 | CCATTCATCTTTTGC[A/G]TAATAAAACATTCGA | 337867 |
rs759012726 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256187 | TAAATGAAGGAACTT[C/T]TGATGAGATGATTCA | 337867 |
rs759018484 | snp | A/C | 3.29745e-05 | 0.00406031 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255712 | ATGGTTACCGTGGTT[A/C]TCTTCTTGGTGGTAC | 337867 |
rs759038989 | snp | A/C | 1.75308e-05 | 0.00296059 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296121 | CAGAGGGCGGAGTAA[A/C]ATTGTTTGCCATTTG | 337867 |
rs759047482 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360334 | TATAGATGGCTTTAC[A/G]TTCTATTTTAAATGT | 337867 |
rs759055077 | in-del | -/TGTCA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214915 | TGATTTTAGACAGGG[-/TGTCA]TGTCAGCCCAGCAGT | 337867 |
rs759055241 | snp | C/T | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386839 | CTGAGCAAAGCCGTG[C/T]GTGTCTGACCTCTGA | 337867 |
rs759060225 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303836 | CCAGGTCAACTCGGT[C/G]ATTCGCTCAGGGATC | 337867 |
rs759073439 | snp | C/G | 1.68032e-05 | 0.0028985 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255799 | CTATAGAAGACAAGG[C/G]CTGCAATTTTGTATT | 337867 |
rs759078732 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359361 | TCTTTCTACTTTTGT[C/T]GCTGAAAGTATTACC | 337867 |
rs759107060 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297773 | TTAAATGGGTTGAGC[C/T]TGCCTATTACAGGAC | 337867 |
rs759119389 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323196 | CAAAGAGTGGTATAG[A/G]TAGCAGCTCAGATAA | 337867 |
rs759121169 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267489 | GAGTCCTTTTGGAAC[C/T]TTTCCTCATGACTTA | 337867 |
rs759128579 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221298 | GTCTTTTTATATTTC[C/G]TTCACAATTACATTT | 337867 |
rs759129487 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377884 | AGAGCCTGGTCCCCT[G/T]CATGTGGTCACACGG | 337867 |
rs759153965 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232413 | AGATATAGATATATA[G/T]ATATATATTCACACA | 337867 |
rs759156556 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248662 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTATC | 337867 |
rs759164125 | snp | C/T | 1.65545e-05 | 0.00287697 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254918 | TTAGTGACCGTAGAC[C/T]ACCAGATCGGAAACT | 337867 |
rs759188971 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366870 | CCTTGCAACTCCACT[C/T]ACTTCTTTCATATTT | 337867 |
rs759196638 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299813 | CATTGCTACCCCTTA[G/T]CTACTTCGCAGGTGA | 337867 |
rs759244925 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254982 | TAGCATGACACTAAT[A/G]ACTCGAGCCTGAAAT | 337867 |
rs759248607 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205471 | GTTTTCTGAATGTAC[-/G]ACCTTCCTGGGTCTC | 337867 |
rs759264321 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278952 | TGCAGAGAATTATAT[A/T]TCTGAGTATTGATTA | 337867 |
rs759271113 | snp | C/G | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340340 | CGGTCTGTGCTACGA[C/G]AGCAAAATGTTCCAG | 337867 |
rs759275749 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316032 | ACACAGCTCACCATG[A/T]GGGATCCCCCTTAGC | 337867 |
rs759297846 | snp | C/T | 0.000145486 | 0.00852772 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200947 | TGGGCTCTGTGAGTA[C/T]CGGCCTCCGCCATCC | 337867 |
rs759320353 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199851 | GAAGTTAACATTATC[G/T]TTGAGTATAGTCATC | 337867 |
rs759324888 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240593 | GACAGTCATCATCAT[C/T]GGACATTGGTAAAGT | 337867 |
rs759347462 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243430 | ATGCATATTTTTGAG[A/T]TTATACCTAAGTTGT | 337867 |
rs759379593 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350759 | CTCATTTATAGCACG[A/T]TGGTTAGAACCGCAG | 337867 |
rs759386705 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210800 | TACTTGTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 337867 |
rs759407022 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297501 | AGCTAACTTCATTCT[A/C]ACAACCTTAAAACTG | 337867 |
rs759429751 | snp | A/C | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328715 | AACTGACTTAAAATA[A/C]TTCTTTATATATTCT | 337867 |
rs759503644 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222571 | GTGGTCAGTTTAGCC[A/T]TATGGATTGATGACA | 337867 |
rs759531825 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338325 | GGCCTCCCAAAGTGC[A/G]GGGATGACAGGTGTG | 337867 |
rs759577971 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267885 | GCTCAAAGAGCGCAG[A/T]TGTTCATTTCACTTT | 337867 |
rs759592271 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364119 | TTGTTTCTCTTTTTC[C/T]ATCTTTATGTGAGAT | 337867 |
rs759601966 | snp | C/G | 3.31554e-05 | 0.00407144 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385193 | TAAGCGGCAATGTCA[C/G]CGCCCTCAGGTTTCT | 337867 |
rs759603515 | in-del | -/GAAAG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292554 | TTTCACAGGATTGTA[-/GAAAG]GAAGATGTTACATAA | 337867 |
rs759611365 | snp | C/G | 1.65168e-05 | 0.00287369 | missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238446 | GGCGCCTCTGTCGAA[C/G]AGCCTTCTGCTGGTC | 337867 |
rs759619794 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252632 | CACATCTGGCCTTAT[A/G]TACCTATTATTTTTT | 337867 |
rs759643235 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264030 | GGAAGGGTCCCCCAT[C/T]ATCTGTATGGCAGGA | 337867 |
rs759649634 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274722 | TTTCCTTTTCTTTTC[-/TTTTTTTTTTTTT]TGAGACAGGGTTTCA | 337867 |
rs759661276 | snp | G/T | 1.64787e-05 | 0.00287038 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255473 | CGGCTTTGCACGTGT[G/T]TTTAAGTTCTTTGGC | 337867 |
rs759664371 | snp | A/G | 1.66125e-05 | 0.00288201 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238569 | GGTAAGCTCTGCCTC[A/G]TTGGCCCCTGAGAGG | 337867 |
rs759711711 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237878 | GAGAATCGCTTGAAC[C/G]TGGGAGGTGGAGGTT | 337867 |
rs759713334 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237265 | ATGCGTATATATATA[C/T]ATATATACACACACA | 337867 |
rs759718136 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314158 | CCAAGAGTCCAAGTG[A/G]CACAAATTCTGGGTC | 337867 |
rs759768628 | in-del | -/AAAAAAA | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262710 | GCAGAACTCCCTCTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 337867 |
rs759778929 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386346 | AATGTGCAACTGTTA[C/T]GTTCTGCAAAATGAG | 337867 |
rs759791561 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347104 | GCCACATGGTGAGAC[C/T]CCCATCTCTATTTAA | 337867 |
rs759799070 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335934 | CAGAGGCAGGAGGAT[C/T]GCTTGAGCCCAGGAG | 337867 |
rs759808461 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213602 | TGACCTCAGGTGATC[C/T]GCACGACTCAGCCTC | 337867 |
rs759827986 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374862 | CTATGAAAAGCCTGA[A/T]ACACACAGGTGCCCC | 337867 |
rs759833878 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259880 | ACTTGAATTCTTCAC[A/G]GTGCACAGGGGCATT | 337867 |
rs759841114 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243681 | AGACTTGAGCTCAGA[A/G]AACATACATATATAG | 337867 |
rs759843341 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216286 | ATTTTTGTATTTTTA[A/G]TAGAAACAGGTTTTC | 337867 |
rs759857123 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264775 | GAATTTCTGTAGGAC[C/T]GTGGATAGGAGCCGG | 337867 |
rs759867511 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294934 | AGTTGGAGATGGGAA[A/G]GTGCCCAATGAAAGA | 337867 |
rs759884377 | snp | C/T | 3.3077e-05 | 0.00406662 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314245 | GCATTTTTATGTTCA[C/T]TTTTCTTTAACCAGA | 337867 |
rs759890936 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313609 | GTGTAAGAAATCACT[A/G]GGCAACCACTGAGAA | 337867 |
rs759892484 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251670 | GTCAGATTCCTCCAA[G/T]ATGCTATCTAGGCAG | 337867 |
rs759904368 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308027 | AGGGAGGCCCATTAT[A/G]GATAAAATCCAGCCT | 337867 |
rs759915142 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283544 | TTTAAATGAATAGCC[A/G]CAAGCAGACTTGCAA | 337867 |
rs759921734 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260875 | CCTTTGCTTTATCAA[A/G]TAGTGTGTTTTAGCT | 337867 |
rs759949737 | snp | C/T | 1.65233e-05 | 0.00287426 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295095 | TGGAATGTATCATCA[C/T]CTGCGTTTCTGTCAT | 337867 |
rs759953071 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214717 | CCCCTCATTGTTCTC[C/G]TTAAGCAGATTGTCC | 337867 |
rs759970982 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325838 | CATATAGGTCCTCAT[G/T]TTTCATCCATGTTGT | 337867 |
rs759973681 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246799 | AAATTGAAAAGTTGT[A/G]GCATCCCCTTTGAAA | 337867 |
rs760004618 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295225 | ACATGCAAAGAAGTA[A/G]ATAAAAGGGTCCATG | 337867 |
rs760015477 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301745 | TTCACAGAGGACATG[C/T]ACCTTCCATGGTCCT | 337867 |
rs760022462 | snp | A/G | 2.91864e-05 | 0.00382 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201385 | TTCAGCCTCCGCTTT[A/G]GAAGCTGACCTCTCA | 337867 |
rs760042502 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232406 | AGTTGAGAGATATAG[-/AT]ATATATATATATATT | 337867 |
rs760044708 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272037 | TTCTTTGTTGTTTCA[A/G]CAGACTATAAATGGA | 337867 |
rs760065132 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201944 | TGGGCGTGGTGGCGG[G/T]TGCCTGTATTCCCAG | 337867 |
rs760071206 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380778 | ATTCTTTTTAAAGAA[C/T]TGTGCTAACATTATT | 337867 |
rs760075171 | snp | A/G | 3.31972e-05 | 0.004074 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356110 | AAGTAAACAAGACTT[A/G]GGACACATGTCTGTC | 337867 |
rs760089153 | snp | A/C/T | 6.68308e-05 | 0.00578027 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295899 | TTCGTGTAGGCAAAG[A/C/T]GGTGGTAAAAAGTAT | 337867 |
rs760098772 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352896 | CTCCACCCCTGTGTC[C/T]GGGGTAGGGGCAGTG | 337867 |
rs760111455 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210982 | TTCTCCCCTCCTTTA[C/T]TTTAGTAATGCCAAG | 337867 |
rs760134164 | snp | A/G | 1.64819e-05 | 0.00287066 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255614 | ACTCTCCAAATGGCC[A/G]TTCATCTTTTGCATA | 337867 |
rs760137593 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250756 | TTTTTTCTTTTTTCT[-/T]TTTTTTTTGAGACGG | 337867 |
rs760144772 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99298795 | CTTCATGTGAAAAGC[A/G]GCTTTTCAGGAACTA | 337867 |
rs760165040 | snp | A/G | 1.65416e-05 | 0.00287586 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356210 | CCGATGTACTCTGTA[A/G]ATGTCTTTGCACCTT | 337867 |
rs760178958 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323381 | TGAGGCAGGTGGATC[A/G]CTTGAGCCCAAGAGT | 337867 |
rs760183576 | snp | A/C | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351565 | CTGGAAATGTGAATT[A/C]TCTCTTAGTTCTGGT | 337867 |
rs760197229 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293034 | GTATGAACAGTGGCT[C/T]GATGAGTAGAATGGG | 337867 |
rs760202981 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269043 | GGATATAGCTTTGGG[C/T]TTGGCATAAGGAGTA | 337867 |
rs760211495 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214038 | TGGCCAGGCTGGTCT[C/G]GAACTCCCAACCTCA | 337867 |
rs760233130 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367126 | AGACTAAGCCAGGAA[C/T]GGCATTGCTGTCAGT | 337867 |
rs760235308 | snp | C/T | 1.6582e-05 | 0.00287936 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296019 | CCACGAGCCCAATGA[C/T]GAAGACGAGGCTGTA | 337867 |
rs760241293 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223923 | TCTATTTTGGTGAAT[A/G]CTCCATATGCACTTG | 337867 |
rs760257428 | in-del | -/AATTCTTTT | | | cds-indel, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340392 | CCAGCTGGATGGCAA[-/AATTCTTTT]AATTCTTTTCTTGGA | 337867 |
rs760287763 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361649 | ATTCTTTGTTATAGC[A/G]GCTGCCCTGTACATT | 337867 |
rs760301777 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369726 | AACCGTAATTCTACA[A/G]AAGAGAAATTGGACA | 337867 |
rs760303465 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311025 | TAAAAAGGAAGGGGG[A/C]TTTTTAAAACAAAAG | 337867 |
rs760307065 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304232 | CACGTTCCCTCACAA[C/T]TCTGTGCCCGGTAAC | 337867 |
rs760313803 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219687 | AGGGAAACCAAAAGA[-/T]TAGACATCCCTGTAT | 337867 |
rs760315191 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274775 | GGCTGGAGTGTGGTG[A/G]CACGCAGTCATGGTT | 337867 |
rs760329641 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366982 | TTTGTCAGGACTAGA[A/C]GACTTCTAGAAATAG | 337867 |
rs760338661 | snp | A/G | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356514 | ATAGTACTGTTTGAA[A/G]TATCTCATCCATCAA | 337867 |
rs760347013 | in-del | -/TTG | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328830 | ATCTTGATTAATTCA[-/TTG]TTGTTAACTGGTTTT | 337867 |
rs760353744 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215798 | AGGCAGAGAAAGGGC[-/T]TAATCAGACCCGTGG | 337867 |
rs760356537 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280717 | AAAGCTGACTGGGAT[C/T]GGTCTGCCACATGCT | 337867 |
rs760398254 | in-del | -/G | 4.94621e-05 | 0.00497279 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255678 | ATCAAGTCCACTAAT[-/G]GCCACATTCATCATA | 337867 |
rs760417906 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350611 | CCTTGCCCTGTGCAT[C/T]TCTTCCATCTGACTG | 337867 |
rs760420083 | snp | C/G | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340331 | CTAGATGTCCGGTCT[C/G]TGCTACGACAGCAAA | 337867 |
rs760424233 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287237 | CCTGCCCTTGCCTCA[G/T]ATTTGCCAGTATCTC | 337867 |
rs760439002 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377222 | CTCAAGGGAGCTCAC[A/C]GTCTATGAGGGAGAC | 337867 |
rs760455511 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230115 | GACATGATAATCACT[A/G]TTTTAGTGTACTGTT | 337867 |
rs760471872 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231144 | ACCTCAATTCTGTCT[G/T]CAACCTTAACTCCCC | 337867 |
rs760496604 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348194 | GCTGTTGTACTTCTT[C/T]GTCTTTTGGCTCTAA | 337867 |
rs760500488 | in-del | -/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260292 | TGCATATTTACTTGC[-/T]TTTTCTCCTCCACTA | 337867 |
rs760506455 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385506 | TGCCGTTTTAGTGTG[G/T]AGATAAGTTTGCCAT | 337867 |
rs760525352 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357412 | TAGTTTTTAATGTAC[A/G]TTTGTTTTGTTATCT | 337867 |
rs760528552 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341234 | GGGCTCCCCATTTTT[C/T]GCCTCCACCTTCTTT | 337867 |
rs760542343 | snp | C/T | 2.09888e-05 | 0.00323944 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244643 | AGTAGCACTTAAAGA[C/T]TGACTTAATTTAGAA | 337867 |
rs760549456 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299847 | AACTGACAATAAATA[C/T]CAATTTTATATTTTG | 337867 |
rs760553460 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262785 | TGTGTTATCAGGTTA[-/T]TTAAACATAAACCTA | 337867 |
rs760553725 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285904 | TTCTACACATCCAAC[A/G]GGGTGCCAGAGTTCA | 337867 |
rs760601362 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202274 | TTAATTTGATTTATG[A/G]CATCTTTCATGGATT | 337867 |
rs760609128 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211882 | GCAGTGTGCTTTTCC[C/G]TCATCCCCTTGGGAC | 337867 |
rs760610716 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234746 | GATCTATGAGAGAGG[A/C]AGGCATGAAAACACA | 337867 |
rs760628775 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365534 | AATTTCCATTATGAG[G/T]ATTTTTTTGGTTTCC | 337867 |
rs760650640 | snp | C/T | 0.000251099 | 0.0112021 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200871 | ACTTCAGCTTCCCCT[C/T]CCCCGGCGCCCTCTG | 337867 |
rs760663891 | snp | C/T | 1.6703e-05 | 0.00288985 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295434 | GAGCCTTTTTGTTTA[C/T]ACCAGATTTCTCAGT | 337867 |
rs760664366 | in-del | -/AAAAAAAAAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330464 | CGTCATCTCAAAAAA[-/AAAAAAAAAA]AAAAAAAAAAAAGAA | 337867 |
rs760667932 | in-del | -/T/TT | 0.0709413 | 0.1745 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238595 | GAGGAGAGCGGACAG[-/T/TT]TTTTTTTTTTTTCTT | 337867 |
rs760677889 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353902 | CTGTGGTTGACAGAC[A/G]TGGTTTTGTGGAGAA | 337867 |
rs760707250 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382154 | AACTTGAACAAAGTT[G/T]TAGAGGTTTACTAAT | 337867 |
rs760714062 | snp | C/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340471 | TTGGGATGGGAGCCA[C/T]GCTGGACATCCAGAG | 337867 |
rs760729614 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244205 | AATTTTAATACTTTG[A/T]CTTTAATAAAATTAT | 337867 |
rs760739327 | snp | C/G/T | 0.00016591 | 0.00910656 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295589 | TTAGTTTCTTCAAAG[C/G/T]TTGGATACTCCATGC | 337867 |
rs760742349 | snp | C/T | 1.65195e-05 | 0.00287393 | missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238439 | CAGACAAGGCGCCTC[C/T]GTCGAAGAGCCTTCT | 337867 |
rs760761342 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352953 | GGAATCCAAAGGGAG[C/T]GAATTCTCATGTGTC | 337867 |
rs760766191 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255395 | TATCTGGGTCTTTAT[A/G]GAGCAGTAGCAGAGG | 337867 |
rs760766242 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314706 | TTTCCTTGTTTGTGA[A/C]GCTGTGATGGTAGCG | 337867 |
rs760801082 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198592 | GGCTTCACCTAGATA[C/T]ACCCCCACGGTTGGA | 337867 |
rs760807935 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363399 | ATAGCAGTTAGGGAA[C/T]AGGAATAATAATAGG | 337867 |
rs760816325 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284714 | TGTTGCATTTCATTG[G/T]TACATCCCCTTACTG | 337867 |
rs760854957 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226925 | ACCCCTTGGCTGGGC[A/G]CGGTGGCTCATGCCT | 337867 |
rs760860208 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377480 | GCCTGCAGAGAAAAT[G/T]AAGTAGTCCAGGGTT | 337867 |
rs760862997 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337428 | CTTGCTGTTATTTGC[C/T]AACAGTTTATTTTTT | 337867 |
rs760922629 | snp | A/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296293 | TATATCTAAGTTTTA[A/C]AATTTCATGACATGC | 337867 |
rs760928894 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248070 | TTCTTTCTGACTTAG[-/T]TTACTGCGTGCAGCT | 337867 |
rs760937759 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326006 | GTGATGACATGAGAG[G/T]GCCGAGACCTCTTTG | 337867 |
rs760949483 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336935 | CCTCTCTTCCTCCTT[C/T]CCACCTCCCTCCTGT | 337867 |
rs760962258 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248951 | TTAGTAGCATCTACT[C/T]AGAGTCATGCAAGCT | 337867 |
rs761005623 | snp | A/G | | | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254533 | TCCTAGTGCAAATTA[A/G]ACCTAAGGGAGCTGC | 337867 |
rs761019209 | snp | C/T | 4.98567e-05 | 0.00499258 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385182 | GGGCCCAGGGATAAG[C/T]GGCAATGTCAGCGCC | 337867 |
rs761027749 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323150 | TTTCTCCTATTTAAC[C/T]TTTTTTCCCTTAGAT | 337867 |
rs761030594 | snp | C/T | 1.65608e-05 | 0.00287752 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295087 | TGAAGACTTGGAATG[C/T]ATCATCATCTGCGTT | 337867 |
rs761034149 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262280 | TGTACAGGAAAAAAA[C/T]AGTAAGTATAGGGTT | 337867 |
rs761039081 | in-del | -/CA | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199554 | TGTTGATCTACGAAT[-/CA]CAGATTTAGCACACT | 337867 |
rs761048418 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249855 | TCTTGTGTGTTGGCC[A/G]CTTGCGTGTCTTCTT | 337867 |
rs761049502 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283892 | GGCGTGTGCCACCAC[A/G]CCCAGCTAATTTTTG | 337867 |
rs761049595 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297213 | TAAAGTTCTGTAGAT[G/T]AGGGTAAACTTTGAT | 337867 |
rs761073205 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291784 | TTTGGGTTGTTTCTT[C/T]TCATTGAGAATTAAG | 337867 |
rs761087609 | snp | G/T | 1.65395e-05 | 0.00287567 | missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238514 | CTCACTGCCAGAAGC[G/T]CTTTGTGTATGACCT | 337867 |
rs761094881 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215593 | ACTCCAGGATGGCTG[C/T]GCTGTACACAGCGGC | 337867 |
rs761097486 | in-del | -/TATC | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262864 | GTAAAAGTAAACATG[-/TATC]TATAAGGTTGAGGGT | 337867 |
rs761108920 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314135 | TTGTACCATTTTACT[A/G]CTCCATACCAAGAGT | 337867 |
rs761133860 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297084 | TGTCAATGCATAATT[C/T]GCTTAGCTACTCCCT | 337867 |
rs761141371 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261084 | GTCTATGCCACAGGT[A/G]AAATAATATTTCCTG | 337867 |
rs761159178 | in-del | -/TGAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316403 | AGGGACATTGTTGAA[-/TGAA]TGAATGAATGAATGG | 337867 |
rs761164970 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205394 | GGAGGGGTTACTCTT[A/G]GTCACGGAGCGGTGG | 337867 |
rs761171717 | snp | A/G | 0.000162668 | 0.00901706 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351525 | GAAGGTTATATAGCC[A/G]GCAGCTTTCAAAGTA | 337867 |
rs761185561 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254996 | TGACTCGAGCCTGAA[A/G]TTGTTTTGAAACGAT | 337867 |
rs761198368 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287026 | AAATTTATTACAGAA[A/G]TTTTCAAATATACAT | 337867 |
rs761227740 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227949 | TAGAGCAGATATACT[A/G]GAGAAAATCAGTGGA | 337867 |
rs761231164 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203240 | GGGGTTTTGCCATGT[A/T]GACCAGGCTGGTCTT | 337867 |
rs761254083 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343793 | ATGATAAATCACCAC[A/G]TAGAGAACTCTTTTG | 337867 |
rs761257236 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240594 | ACAGTCATCATCATC[A/G]GACATTGGTAAAGTC | 337867 |
rs761261823 | in-del | -/AGG | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257286 | TCTAGTGTCATTCAA[-/AGG]AGAGTAATCTTGGAG | 337867 |
rs761263414 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383309 | TTTAAGTCTAGGACA[G/T]TACATATCTCTGTTA | 337867 |
rs761293256 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224905 | GAATCTTGTTGTCTA[C/T]AATGATACTATATAC | 337867 |
rs761305716 | snp | C/T | 7.33057e-05 | 0.00605372 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200957 | GAGTACCGGCCTCCG[C/T]CATCCTGGCTGCCCC | 337867 |
rs761307203 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344554 | TTTTAGATGCTTTTC[A/G]TAGAATCTGAGTTTA | 337867 |
rs761316470 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380536 | AAAGAAAGGACAGCA[A/G]GGGCCACTTGGCTAA | 337867 |
rs761337812 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368354 | AAAAGAAACAAACAA[A/G]TGCTCTAACTGCATT | 337867 |
rs761359431 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301144 | TGAAAAGATGCACGT[A/G]GCCCCTCAGCCGTCC | 337867 |
rs761365026 | snp | C/T | 3.01983e-05 | 0.00388564 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201376 | CTTGCAAAGTTCAGC[C/T]TCCGCTTTAGAAGCT | 337867 |
rs761394601 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379879 | CACACCTTTTAGATA[C/T]TTTAACAACATTTTT | 337867 |
rs761417687 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223944 | TATGCACTTGAAAAA[A/G]TGTGTAACTTGCCGT | 337867 |
rs761418484 | snp | C/G | 8.31788e-05 | 0.00644845 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356083 | TCAGGCCTCTGAAAA[C/G]AAATGTCATTAAAGT | 337867 |
rs761420584 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342807 | CCAGCAGATCCACAC[A/G]TGTAATTGCCTCAGG | 337867 |
rs761431344 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299910 | CCACGCTGGGCTTAA[A/G]TGCCATGCTAGATCC | 337867 |
rs761432452 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245588 | GCCGGGCGCGGTGGC[C/T]CATGCCACCTTTGGG | 337867 |
rs761442453 | snp | A/G | 3.30136e-05 | 0.00406273 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295766 | GCAATGAAGCGGTCA[A/G]TACTCAGGCAGGTCA | 337867 |
rs761444270 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340025 | TACGGCTTTTTAAAA[A/T]ATGAAGACAGTGTCT | 337867 |
rs761445595 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381241 | CCTGTGTGTAGCCAG[-/C]CCCATTATCAGCATC | 337867 |
rs761465035 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369486 | ACTCTAGATTTGTGA[A/G]AGATGATTTTGCCCA | 337867 |
rs761493082 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312563 | GCATCTTACCGTGAC[A/C]TCCTTGGCACGCATT | 337867 |
rs761514261 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313146 | CCCACCACCAAGCCC[A/G]GCTAATTTTATGTAT | 337867 |
rs761521184 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219416 | TGTTGTGCAATTAAC[A/G]GCAACCACAATTTAA | 337867 |
rs761527706 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336069 | GTTGCTGTATTTAAG[A/G]TTGCTCATTTTAGAT | 337867 |
rs761532728 | snp | C/T | 1.66007e-05 | 0.00288098 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385342 | CAGCACTGATAGTCC[C/T]AGGCCAACACTGGGA | 337867 |
rs761534823 | snp | A/G | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386511 | TCAACCAAATCCTCC[A/G]CACTGCTCGTCTTTC | 337867 |
rs761538552 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265058 | TCTTGGAGACATTAT[A/T]ATCAACCTTTAGAGG | 337867 |
rs761539589 | in-del | -/TTTA | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325549 | TGAGTCAGTCCTGAC[-/TTTA]TTTATGAGAGCTCTC | 337867 |
rs761541993 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253375 | TCAGACCTCAGTTTT[C/T]TATATTTCGAACAGA | 337867 |
rs761558466 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227146 | GAGGTTGCAATGAGC[C/T]GAGATTGTGCCATTG | 337867 |
rs761560719 | in-del | -/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256871 | ATCTGTGGCATCCCC[-/T]TTGTAATATGGAGGT | 337867 |
rs761565469 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353022 | CCTCCTCAGCACTTT[C/T]CCTTTTTGGCTATGC | 337867 |
rs761576193 | snp | A/G | 3.36576e-05 | 0.00410215 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295868 | CTCCAGTCAAAGCCC[A/G]TTGCATAGTAGGCTA | 337867 |
rs761613992 | snp | G/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257132 | CTTCTCCTTCTTTCC[G/T]TCTCAAATATTTAGG | 337867 |
rs761619782 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313283 | GACACTACGCCCGGC[C/T]GGAAGGAAGGGTTTT | 337867 |
rs761631737 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237111 | CCAAAATGTGGAATC[A/G]ACTGAAGTGTCCATC | 337867 |
rs761659721 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217940 | TTGAATTTACAACAC[A/G]TTTTCTTGCCACTAA | 337867 |
rs761664900 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358681 | CTCTGGAGCCACCCC[A/G]GCCATGGACTGTGGT | 337867 |
rs761669083 | snp | C/G | 1.64795e-05 | 0.00287045 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255588 | GAGAGCTCCAAGAAT[C/G]TGGCAGAAGTACTCT | 337867 |
rs761722169 | snp | A/G | 1.64874e-05 | 0.00287113 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255662 | GTAAAGTCATTATAA[A/G]TATCAAGTCCACTAA | 337867 |
rs761745263 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277068 | CCAAGATAGCTACCC[G/T]GTATAGTGTTGCTGT | 337867 |
rs761773459 | snp | A/G | 1.73003e-05 | 0.00294106 | missense, intron-variant, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99244591 | TGCAGTATTTCTTTG[A/G]CATCACTGCAGCTAG | 337867 |
rs761794986 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375971 | ACCAAGCCCAGCTAA[-/TT]TTTTTTTTTTTTTTT | 337867 |
rs761822588 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357477 | TCATTTCTCTGTGTC[A/T]CAGCCTCCTTATCTG | 337867 |
rs761828911 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355295 | GGAAGGGAAAACAGA[A/G]TATACGATGCAGAAA | 337867 |
rs761853792 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231558 | GCTGGGACTACAGGC[A/G]TGCCACCACGCCCAG | 337867 |
rs761864458 | in-del | -/T | 0.0030888 | 0.0391773 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318002 | TTATTTTTAGTTGCC[-/T]TTTTTTTTTTCTTTT | 337867 |
rs761868756 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221612 | TATTTCTGTGTTCCT[C/G]CCATGGGGCTTCTTT | 337867 |
rs761869836 | snp | C/T | 1.65318e-05 | 0.002875 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340306 | AACAATCACATTGGA[C/T]GTTTTTCTTCTAGAT | 337867 |
rs761882430 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361303 | AGAAGACAAAGTAAA[-/G]GAAACATTTCCTGTT | 337867 |
rs761883130 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255271 | CACCCAATCATGATG[A/T]ACAAAGGAATCAAGA | 337867 |
rs761884610 | in-del | -/GTC | 1.65452e-05 | 0.00287616 | intron-variant, cds-indel, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201497 | GAGGGAAGTTAGGAA[-/GTC]GTGGCGAGGGAGCGC | 337867 |
rs761891767 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306528 | CCCCCTCCCCCAACA[C/T]ACACACAAACACACA | 337867 |
rs761916790 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304301 | GTATCCTTAGCTCTT[A/G]CTTTCCTTCAAGCCT | 337867 |
rs761926425 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383575 | ACAGCCCTCCCCACC[A/G]CAAGGCATTTGGAAG | 337867 |
rs761941749 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228172 | TGCCCGTTGCACTTA[A/C]ATCACCCCTGCTCCA | 337867 |
rs761969684 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274822 | ACCTGGCCTCAGGTG[A/G]TCCTCCCACCTCAGC | 337867 |
rs761980710 | snp | A/G | 0.000181197 | 0.00951659 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255166 | ACCTGCACCAGCAGC[A/G]TGATGATGATCCTTA | 337867 |
rs761987691 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215656 | TAGATTTCAGGTGTT[A/G]ATGAATACAGCCCTC | 337867 |
rs762004758 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366821 | GCTGCTCACAGTGTG[C/T]GGCTCTGCTTCCCAC | 337867 |
rs762011784 | snp | A/T | 4.94189e-05 | 0.00497062 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367763 | CCTTCTGTGTCTGAT[A/T]ACTGTGTGTTGATCT | 337867 |
rs762042289 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298443 | TTTCGAAATGCTTAG[A/G]ACTAAATGATGAAAG | 337867 |
rs762046220 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210683 | GGTTTCTCCATTTTG[A/G]TCAGGCTGGTCTCAA | 337867 |
rs762077015 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224362 | CCAAACTTAGTCAGC[A/G]TAGAGCTTCAACATA | 337867 |
rs762079842 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284738 | CTTACTGTTTAATCC[A/G]GACTGTTCCTCAGTC | 337867 |
rs762088870 | in-del | -/TTCT | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199899 | ACCAAAACTTATTCC[-/TTCT]AACTATAACTTTGTG | 337867 |
rs762104839 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233116 | CCCAGATTTGGTTTC[-/T]TTTTTTTTTTTTCTG | 337867 |
rs762108786 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216080 | TTTGTACCAACCTAT[-/AT]TTGTGTGTGTGTGTG | 337867 |
rs762108823 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263504 | AAGACGGACAGTGCA[A/C]AGTGCTGGCAAGGAT | 337867 |
rs762128920 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285555 | GTGCCACCACGCCCA[A/G]CTAATTCTTAATTTT | 337867 |
rs762134106 | in-del | -/CCCC/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347322 | TATCCCCGGGCGCCC[-/CCCC/T]CCCCCCCCCCCCAGG | 337867 |
rs762135690 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240382 | TTATTTTCATTAACT[A/G]AAAAAATGGGGTTCT | 337867 |
rs762146735 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362921 | AACCACTTTTTTCAT[C/T]GTGATTTATACTTCG | 337867 |
rs762155856 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379433 | GCTTTGTCACCACAT[G/T]AAAAAATTTGGTTTC | 337867 |
rs762164828 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235769 | CACTTGAGGCTAGGA[C/G]TTTGAGACCAGCCTG | 337867 |
rs762182992 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236794 | GGCAGAGGTTGCAGT[A/G]AGCCGAGATGGCACC | 337867 |
rs762212171 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334079 | AGCCTTCCAAGTATC[G/T]GGGACTACAGGCATG | 337867 |
rs762222102 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375972 | CCAAGCCCAGCTAAT[-/T]TTTTTTTTTTTTTTT | 337867 |
rs762235340 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206182 | CAGAGTCCGGTCAGA[C/G]GTACTCGGGACACTT | 337867 |
rs762241637 | in-del | -/GTCATGAT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222709 | GATAAGCATTATTTG[-/GTCATGAT]GTATTCTTTTTATAT | 337867 |
rs762254571 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305249 | GGCTTCCAAAACACC[A/G]CAGCCATCTGTGTTA | 337867 |
rs762259955 | snp | A/G | 1.65449e-05 | 0.00287614 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201557 | CCTGGCGTGTTAGCG[A/G]TGGTCAGCAGGTAGG | 337867 |
rs762268933 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273723 | ACTTGGTGTGGGCCC[C/T]GTCAAACAGGTGATC | 337867 |
rs762272405 | snp | A/G | 3.58905e-05 | 0.00423603 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296144 | GCCATTTGTATATCC[A/G]TTGGTGGTGGTCCAG | 337867 |
rs762277659 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250200 | TAGTTTGAAGTCTTA[A/C]ATTTATATCTTTAAT | 337867 |
rs762308224 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357776 | TCACCCCTTCCACCC[C/T]GCCTTCATTAGTAAC | 337867 |
rs762360156 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205455 | AAAAAATCAATCACG[C/G]TGTTTTCTGAATGTA | 337867 |
rs762369439 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246697 | TTCAATTTTGAAGTT[A/G]GTGGGAATACTTTTG | 337867 |
rs762415931 | snp | C/G | 1.65108e-05 | 0.00287317 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254928 | TAGACTACCAGATCG[C/G]AAACTTTTTCTGCGC | 337867 |
rs762416389 | snp | A/G | 1.82022e-05 | 0.00301675 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255921 | ACTGTAAAAATAGTT[A/G]AGAAAAATAAGAATA | 337867 |
rs762430205 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214494 | TAGGTTGCAGAGGTG[A/G]GGAGTAGGTGGTGGT | 337867 |
rs762434008 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263643 | TCCACTCCTAGGTCT[A/C]TAACCAGTAAAAACA | 337867 |
rs762447971 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323417 | ACCAGCCTGGCCAAC[A/G]TGGCAAAACCCTGTT | 337867 |
rs762449119 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325305 | AGACGGGGTTTCACC[A/G]TGTTAGGCAGGATGG | 337867 |
rs762469386 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321282 | GCTTATTTTATTTAG[C/G]TAGGTACTGGTTGAT | 337867 |
rs762471452 | snp | A/G | 1.64844e-05 | 0.00287087 | stop-gained, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254987 | TGACACTAATGACTC[A/G]AGCCTGAAATTGTTT | 337867 |
rs762501540 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290187 | TGGAAAGTGCGACTG[A/G]TAAATAGAACAAGCC | 337867 |
rs762513032 | in-del | -/TC | 0.152778 | 0.230321 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318099 | CCTTTTACACCCAAT[-/TC]TCTCTCTCTCCTGTA | 337867 |
rs762518104 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203707 | AGTGACATGAAGACA[A/G]TGAGAGGGTAACTGC | 337867 |
rs762539309 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369741 | GAAGAGAAATTGGAC[A/G]CCACCTTAACCAGGT | 337867 |
rs762540403 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248543 | TTTGCCACCATGCCT[A/G]GCTATTTTTTTTGTA | 337867 |
rs762564613 | snp | A/G | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386598 | GCACTGCCCACAGTG[A/G]CATTACCTGTGCAAA | 337867 |
rs762565690 | snp | A/C | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259539 | CCAGTTACTTGCTTA[A/C]GAACTCAAGGTAAAG | 337867 |
rs762577494 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288782 | CCTAACAAATTATGA[A/C]ATGTAATAATATCAA | 337867 |
rs762580191 | snp | A/G | 1.65321e-05 | 0.00287502 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340516 | AGCTGCTGGACCGGC[A/G]GCTGATGTTCTCTCA | 337867 |
rs762587467 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359013 | GGGCACCCAGAACAC[A/G]GAAGAAGGAGAGAAA | 337867 |
rs762593929 | in-del | -/CCACCTCTCTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336917 | TGCCCCCCTTCCTTC[-/CCACCTCTCTT]CCTCCTTCCCACCTC | 337867 |
rs762595604 | snp | C/T | 7.30007e-05 | 0.00604111 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200953 | CTGTGAGTACCGGCC[C/T]CCGCCATCCTGGCTG | 337867 |
rs762604732 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382061 | TGGGTTTGAAACTGA[-/T]TAAAAATGTTGATTA | 337867 |
rs762618789 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320795 | TATTATTTGTGAGTG[-/T]TTGATTTACACACCA | 337867 |
rs762619526 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381671 | TCCACCCAAGATTGG[A/T]AAGACCACCTTGATC | 337867 |
rs762629726 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331747 | ATTCACATTCTTGGG[A/G]TAATAAATTAGGGAA | 337867 |
rs762633324 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301600 | CATTTTTGCATAACC[A/G]GACATGTTGACATGA | 337867 |
rs762667621 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326187 | TTCCCCACATCCTAA[C/T]CAACACTTGTCTTTT | 337867 |
rs762670401 | snp | A/T | | | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254700 | TAGGAAAGAAAAATC[A/T]GATGCTTTTCTCTGA | 337867 |
rs762672475 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267292 | AGATGATTTGCAAAT[A/G]TTTTTTCTCTTACTC | 337867 |
rs762683707 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239124 | TTCTGGTATATGACT[A/G]CTACCCTTTCTTTGC | 337867 |
rs762683808 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255488 | TTTTAAGTTCTTTGG[C/T]GTACTTCGGCTGTAC | 337867 |
rs762706743 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338040 | TCCTAACTTTTTTTC[-/T]TTTTTTCTTTTTTTT | 337867 |
rs762722615 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209355 | GAGAGGACTGTGGGA[A/G]TCAGGGGACTGCCTT | 337867 |
rs762722891 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239390 | GAAAAAACTTCAAAG[A/C]TCTGTCTCCATATCT | 337867 |
rs762733965 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332773 | CTGCTGCCTTCTTTT[G/T]CAGTGGCCCCTCCGT | 337867 |
rs762737470 | snp | C/T | 0.00024567 | 0.0110804 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351464 | CAAACCTAAAATGTT[C/T]ACCACCTGGCCCTTT | 337867 |
rs762738895 | snp | A/G | 1.67337e-05 | 0.00289251 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238584 | ATTGGCCCCTGAGAG[A/G]AGAGCGGACAGTTTT | 337867 |
rs762791089 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365933 | TACATATAAATATGA[C/T]ATTCATGTATTCTAT | 337867 |
rs762794904 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349627 | TTCCCTCTTAGGTAG[C/T]CGAAGCTGAGAGAGA | 337867 |
rs762796614 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337017 | TAGTCATCATCTTTG[C/T]GCTTTCCTGTCTCGT | 337867 |
rs762806096 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322561 | TAACAGGCCTATATT[C/T]CTCAGACTTCTCCCT | 337867 |
rs762820291 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221207 | AGAATCTTTGTGCAC[A/C]TTTATGATAATTACT | 337867 |
rs762835836 | in-del | -/ATATAC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213094 | TTTTCTGACGCATGT[-/ATATAC]ATATACATATACCTA | 337867 |
rs762884246 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308282 | TGTGGCAGTGAGGGG[C/T]CTGGATAGCAGGTCT | 337867 |
rs762906458 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278354 | CGGGCGCGTGAAGGG[A/T]TTGCCTGTCTGGAGG | 337867 |
rs762908875 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219719 | AAGCCGTCATGCCCT[A/G]TTACCTTCTCCCAAC | 337867 |
rs762916180 | snp | C/T | 1.65181e-05 | 0.00287381 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385319 | ATGTCGCCACCAACT[C/T]CCTGCTGCAGCACTG | 337867 |
rs762935828 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319183 | TATTTTAATAATAAG[C/T]GTTTGTCCTAAATTC | 337867 |
rs762937021 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266118 | CCTTCTAAAGTCTCT[C/T]TGAAATTGAAATAAT | 337867 |
rs762939422 | in-del | -/ACAC | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326815 | CCACGAGATGCACAG[-/ACAC]AGTTATTCTTAAAGT | 337867 |
rs762946306 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233965 | GAATATTACAGGGTT[A/G]TTATTTTATTATTAT | 337867 |
rs762952383 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335040 | CAGCAGAATGCTTTG[G/T]TATGACGAAAGGGTC | 337867 |
rs762965379 | snp | C/T | 1.72973e-05 | 0.00294081 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385383 | AGCCGAGTGACAGTG[C/T]GTGGTCCCCACCATC | 337867 |
rs762977351 | snp | A/C/G | 1.64773e-05 | 0.00287026 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318097 | ACCCTTTTACACCCA[A/C/G]TTCTCTCTCTCTCCT | 337867 |
rs762977979 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345943 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 337867 |
rs763046112 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372031 | TCTGCCAATTCATCA[A/C]CCCTCAGAGATGCCA | 337867 |
rs763064393 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263926 | TTTGTATAAATTTCA[A/G]AAAGCAGATGAAATG | 337867 |
rs763070467 | snp | C/T | 1.70662e-05 | 0.00292109 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317971 | AAAATAAGTGTGCTG[C/T]GACTGGCAGTTGAAT | 337867 |
rs763100391 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206299 | GGGACAGTTGGAAGC[C/T]GAGGACAGACCTTCA | 337867 |
rs763120033 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288252 | AAAATGGATAAAAGC[C/T]AATCAGAAAAGCACT | 337867 |
rs763131413 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201601 | TTACAGCCAGTTAAA[C/T]GGCTTTTCTCACTGA | 337867 |
rs763138632 | snp | G/T | 3.29538e-05 | 0.00405904 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295267 | GTTCATCAGGCATAC[G/T]GTAAAGTGCAGAGAA | 337867 |
rs763139493 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344729 | ATGCCAGAGTTCATC[C/T]TGCCATCTGGCAGGT | 337867 |
rs763139517 | snp | A/G | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356459 | TTGTGTCTCCTGATC[A/G]TATTGCCATGGAAAC | 337867 |
rs763139783 | in-del | -/T | 0.00233372 | 0.0340795 | intron-variant | UBAC2 | GRCh38.p7 | 13:99234355 | ACCACGCCCGGGTAA[-/T]TTTTTTGTATTTTTA | 337867 |
rs763160138 | in-del | -/TGTA/TGTGTC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368713 | GTGTGTGTGTGTGTG[-/TGTA/TGTGTC]TGTGTGTGTGTGTAC | 337867 |
rs763175140 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291303 | CTGCTTTTCTGAGTT[C/T]AATGAAAACCTTCCA | 337867 |
rs763181920 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200798 | AGCGGCGAGTGGCCT[A/C]GCGGCGCCGGATTCG | 337867 |
rs763190507 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286658 | CCATCACCCCACACT[A/C]CCCCAACAAGCAGTC | 337867 |
rs763195511 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374656 | GAAAACCCACCGAAA[C/T]TCCTAAAATGCTCAC | 337867 |
rs763195535 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361870 | GACGCAATGGTGCAC[A/T]TCTATAGTCTCAGCT | 337867 |
rs763208777 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247195 | GAGAGAAAACTACTG[-/T]TTTTTTTTTTTTTGT | 337867 |
rs763315151 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294824 | GAGCGCCTCCTTTTG[A/G]TGTATTCGTTTACAA | 337867 |
rs763320996 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207141 | CACCCCTCCCTGAGT[G/T]GGGAGTCTTTACCTG | 337867 |
rs763324858 | snp | C/G | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351852 | GCTGCCCGGTGTTAA[C/G]TGGTTGATTATCACC | 337867 |
rs763327814 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319159 | TTTTTCATCTTGTCT[A/G]TGCTATTGTATTTTA | 337867 |
rs763372547 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363915 | GATCTTTTGTTTGAT[G/T]TTATTCTTAACTACC | 337867 |
rs763400434 | in-del | -/AGTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344802 | GGGGCACAGTTAGAC[-/AGTT]AGACTGCTTGGGAAG | 337867 |
rs763402456 | snp | C/G | 3.30994e-05 | 0.004068 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356228 | GTCTTTGCACCTTCT[C/G]TCCTCATTGCCATCC | 337867 |
rs763404593 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340662 | AGAGACTACATTTTA[C/T]TCCAGTGCCTTGCAA | 337867 |
rs763418540 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276364 | GTAAATTGGGGGTTC[C/T]CACAAGGTCTGTACC | 337867 |
rs763438606 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313392 | GAAGCAAGACTGTAA[A/G]TAGAAAGACACATAA | 337867 |
rs763466431 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304242 | CACAACTCTGTGCCC[A/G]GTAACATTCTTCCCT | 337867 |
rs763471924 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252106 | TGACCACCAGCTAGT[C/G]TCTCAAACCACTTCC | 337867 |
rs763497376 | snp | A/G | 3.32088e-05 | 0.00407471 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99296026 | CCCAATGATGAAGAC[A/G]AGGCTGTAATGCAGA | 337867 |
rs763519161 | snp | A/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299895 | AGTGGTTCTTAAAAG[A/C]CACGCTGGGCTTAAA | 337867 |
rs763539814 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212020 | CATGTTTTATGTCCT[G/T]ATTAGGATCTTTTGT | 337867 |
rs763554698 | snp | G/T | 1.64827e-05 | 0.00287073 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254989 | ACACTAATGACTCGA[G/T]CCTGAAATTGTTTTG | 337867 |
rs763567971 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325294 | GTTTTTTGTAGAGAC[A/G]GGGTTTCACCGTGTT | 337867 |
rs763570549 | snp | A/G | | | intron-variant, synonymous-codon | UBAC2 | GRCh38.p7 | 13:99329164 | TATGTCTGTCCTTAC[A/G]CCAATACCACACTGC | 337867 |
rs763586943 | in-del | -/GAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212304 | CTATGAGGAGCTCCT[-/GAA]GTTTTAACCCTCATT | 337867 |
rs763601496 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252454 | ACCACAGACCTGTTC[A/C]TTTCTTTTTCTAGTG | 337867 |
rs763603437 | snp | C/T | 7.27352e-05 | 0.00603012 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200954 | TGTGAGTACCGGCCT[C/T]CGCCATCCTGGCTGC | 337867 |
rs763607713 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312699 | GCAGTGTTGCACAAG[A/C]TGAGTTTCCTAGGCA | 337867 |
rs763612892 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99298820 | GAACTAGGACTAGAC[A/G]CAAGAGAGAGGTGAA | 337867 |
rs763628733 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221379 | TTGTGTATGTCTTTC[A/G]CTTGAAATCCACCAT | 337867 |
rs763653418 | snp | G/T | 0.000175208 | 0.00935806 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351483 | ACCTGGCCCTTTACA[G/T]AAAAATATTTGCCAG | 337867 |
rs763665016 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379786 | TACACTGCTCTCCAC[C/T]TTCTCCAACAGCTTG | 337867 |
rs763665223 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367067 | TTAAAGCAGCATGTG[A/T]TGCATTTTTCTTCCC | 337867 |
rs763697750 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276969 | GAAAGCCCTGGCCCT[G/T]CAACCTTTGGGAAGT | 337867 |
rs763724917 | in-del | -/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326213 | TTTTGGTGTTTTTTG[-/T]TTTTTTTATAATAGC | 337867 |
rs763726266 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200261 | ACGACAGTCGGCCCC[G/T]GTGGTGGGGATTCCG | 337867 |
rs763736622 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256922 | AAATGTCACTTTGCA[A/G]AGTGGGCTGTCTTGA | 337867 |
rs763748913 | snp | C/G | 1.65416e-05 | 0.00287586 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340520 | GCTGGACCGGCAGCT[C/G]ATGTTCTCTCAGTTT | 337867 |
rs763762370 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350860 | CTGATGTTATCTCCT[A/G]GGAGACAGTGTGGGG | 337867 |
rs763767311 | in-del | -/GAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250799 | CACCCAGGCTGGAGT[-/GAA]GAAGTGGTGTGATCT | 337867 |
rs763771061 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267621 | TTCAGAGCCTTCCAC[G/T]TGCTACTGCTGCTTT | 337867 |
rs763790707 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221912 | TCACCTTTTACTCTT[-/A]AGAGGAACCCCGGCT | 337867 |
rs763799105 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281603 | AGGCTCAGAAACCTT[C/G]AGCGCTATTTTCTAT | 337867 |
rs763808654 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350674 | TAAATGGGTAGATGT[A/C]AGTGTTTCCCTGAGT | 337867 |
rs763830277 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216955 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 337867 |
rs763839031 | snp | A/G | 1.65479e-05 | 0.0028764 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295642 | CTTTGACATAGGGTT[A/G]ATGAGGAGTGGGAGT | 337867 |
rs763840669 | in-del | -/CTTTTTTTC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338031 | AAAAAAATCTCCTAA[-/CTTTTTTTC]TTTTTTTCTTTTTTT | 337867 |
rs763856755 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385591 | GGAGAGTCAGCACTC[A/G]TTTTGAATGTGTTTA | 337867 |
rs763857769 | snp | A/C/T | 3.62143e-05 | 0.00425513 | splice-acceptor-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255907 | CATGATACTTAGAAA[A/C/T]TGTAAAAATAGTTAA | 337867 |
rs763859000 | in-del | -/AAAAAAAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268613 | TGAGACTCTGTCTCA[-/AAAAAAAA]AAAAAAAAAAAAAAG | 337867 |
rs763859711 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269068 | GGAGTAACTTTGCAG[C/T]ACTCACTGTCTCAAG | 337867 |
rs763877650 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222754 | GGTTTGATTTACTGA[A/T]GTTTTGTTGAGAATT | 337867 |
rs763901955 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319563 | GCCTTTGTTCCCCAC[A/G]GCTGATATGCTTGCA | 337867 |
rs763921448 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243634 | ATTCAAGTACCTTTC[A/G]TGCCACTGTTGGGAG | 337867 |
rs763922274 | snp | C/G | 1.65395e-05 | 0.00287567 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385202 | ATGTCAGCGCCCTCA[C/G]GTTTCTGCGTTTTCT | 337867 |
rs763930044 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335277 | ATAACATTTTGCTAT[C/T]TTCTGCTGAATCAGC | 337867 |
rs763948173 | snp | G/T | 0.000222072 | 0.010535 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317981 | TGCTGTGACTGGCAG[G/T]TGAATTTTATTTTTA | 337867 |
rs763958593 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234947 | CTTTTTTTCTCTCAT[A/G]TCAGAGGGAAGAGAG | 337867 |
rs763972706 | in-del | -/AT | 1.81734e-05 | 0.00301436 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255915 | TTAGAAACTGTAAAA[-/AT]AGTTAAGAAAAATAA | 337867 |
rs763978714 | snp | A/G | 0.000103697 | 0.00719984 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243989 | TTTGCTACTTAGGCT[A/G]TAGAAAAAAATTTTG | 337867 |
rs763981020 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332618 | CCATGTGTCCCCTTT[C/T]CTAGCCAGGGTTCCT | 337867 |
rs763984491 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306471 | TGCTCTTATTACACT[A/G]TATTGTACTCAGAGT | 337867 |
rs763996021 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264088 | CACCACACTTAGGCC[C/G]AAAGAGATCAAGGAA | 337867 |
rs764012022 | snp | A/G/T | 8.272e-05 | 0.00643074 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385331 | ACTTCCTGCTGCAGC[A/G/T]CTGATAGTCCCAGGC | 337867 |
rs764017668 | snp | C/T | 1.64871e-05 | 0.00287111 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295124 | ATTTCACGTGAATTT[C/T]CTTCAGGGGCTGACT | 337867 |
rs764036979 | in-del | -/T | 0.00633478 | 0.0559219 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238596 | GAGGAGAGCGGACAG[-/T]TTTTTTTTTTTCTTT | 337867 |
rs764061145 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276462 | TTGGTTTATTATAAA[A/G]GATACAACGCAGGAA | 337867 |
rs764063514 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330586 | GTTTTCAACATAGGT[A/G]GTCTGTGTCATCCAG | 337867 |
rs764092943 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317467 | AATTAACTTTGTTCT[G/T]TTATTTAGTTTGCTC | 337867 |
rs764103904 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314755 | TTTGCTGTGAAGACT[A/G]CTAGAGTACTACTGT | 337867 |
rs764128251 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260359 | GTGTGTAGAGAAGAG[A/G]CATTTAATATTGGTT | 337867 |
rs764153594 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198661 | TTTTTTGATACTATA[C/T]GATAACTTAGCAAGT | 337867 |
rs764225459 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227044 | TCTCTAATAAAAATA[A/C]AAAATTAGCCAGTTG | 337867 |
rs764227100 | snp | A/C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315566 | AGGTTGTTGAATTTC[A/C/G]GTTTAATGACTTGGT | 337867 |
rs764238941 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352970 | AATTCTCATGTGTCC[C/T]GAGCATCCTCAGAGA | 337867 |
rs764249449 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364277 | GAGATGAGCGTTTGA[A/T]TTTTCTCCTTCAAAC | 337867 |
rs764253262 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326056 | TTGGATGTATACCCA[A/G]TAGTGGGATTGCTGG | 337867 |
rs764258639 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273122 | AGATATTAATATTTT[C/T]TTTTATCTCTTCTAT | 337867 |
rs764265446 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272149 | AGGTCACCTCTTTTA[A/G]CTCTACTAGACCTAA | 337867 |
rs764268743 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342823 | TGTAATTGCCTCAGG[A/C]CACTTCTCTTCACAC | 337867 |
rs764269994 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313850 | TCTCACACTTAGTAG[A/G]TGCTGAACCACTTCT | 337867 |
rs764285619 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343861 | GCATGCACGAGTACC[A/G]TACAGGGTGCAGTTG | 337867 |
rs764295873 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205418 | GCGGTGGTTGTCAAA[C/T]GCTGCTCCTGTCCCA | 337867 |
rs764306532 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384439 | ACATTGCCAATTTCA[A/G]TACTGGAGACTGCCT | 337867 |
rs764327970 | in-del | -/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296589 | TAAATTTAATTTCAG[-/T]TGGATTTTTTTTTAA | 337867 |
rs764363585 | in-del | -/ATGA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316422 | TGAATGAATGGATGA[-/ATGA]ATGAATGAATGAATG | 337867 |
rs764369165 | snp | A/G | 8.23852e-05 | 0.00641762 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295270 | CATCAGGCATACTGT[A/G]AAGTGCAGAGAAATC | 337867 |
rs764377396 | snp | C/T | 1.6554e-05 | 0.00287693 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356139 | TCAGACTGTACACAG[C/T]AGAAGCATCCCTTGC | 337867 |
rs764382132 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280888 | CCTCAAATCTGTTAC[C/T]TAAGAGAAAAATGTA | 337867 |
rs764398987 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234561 | ATTAGGTCAGATGAA[A/G]TGACTGAAGCTCAGA | 337867 |
rs764433035 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309674 | GGCACGATCTTGGCT[C/T]ACTGCAACCTCTGCC | 337867 |
rs764443672 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268780 | GTTGACACTAATATG[C/G]CCCTAGATGCCATTT | 337867 |
rs764452278 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284718 | GCATTTCATTGGTAC[A/G]TCCCCTTACTGTTTA | 337867 |
rs764458382 | snp | A/G/T | 6.58957e-05 | 0.00573964 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255147 | GGGCATAAAGCAGAC[A/G/T]AGCACCTGCACCAGC | 337867 |
rs764484533 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350003 | AGGAGCCCTCATGCC[A/G]GCGTGACAGAGGGCT | 337867 |
rs764506479 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360512 | TTGAGCCCAGTTATT[C/T]TGGCTCTAGAGACTG | 337867 |
rs764511915 | snp | A/G | 1.65968e-05 | 0.00288065 | intron-variant, synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201483 | AGTGCTTTCAAGTGG[A/G]GGGAAGTTAGGAAGT | 337867 |
rs764550178 | snp | G/T | 1.6636e-05 | 0.00288405 | intron-variant, stop-gained | UBAC2, GPR183 | GRCh38.p7 | 13:99296032 | GATGAAGACGAGGCT[G/T]TAATGCAGAGGCATT | 337867 |
rs764562565 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303972 | CTCTGCTGCACATCC[A/G]TGTCTGTCTGTCTGC | 337867 |
rs764567740 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240617 | GTAAAGTCCTTGGCA[C/G]TTTCCTATGTGCTCT | 337867 |
rs764615078 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301224 | TGGAGGGCATGGATA[A/G]TGACTGGGCCACAGG | 337867 |
rs764638150 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255714 | GGTTACCGTGGTTCT[C/T]TTCTTGGTGGTACAA | 337867 |
rs764643123 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290946 | TGTGGTGATGGGGAG[A/T]TGTCCAAGGCCCTGG | 337867 |
rs764645470 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369595 | ACTAAATGCATTTCA[A/T]CTTATGATATTTTCA | 337867 |
rs764657443 | snp | G/T | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261098 | TAAAATAATATTTCC[G/T]GTTCTGTTAGCATAG | 337867 |
rs764658155 | snp | C/G | 1.68539e-05 | 0.00290287 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255802 | TAGAAGACAAGGGCT[C/G]CAATTTTGTATTCAT | 337867 |
rs764660348 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213313 | GCCTTTCTTGGCCTC[C/T]CAAGTTGCTGGGATT | 337867 |
rs764667251 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227976 | TGGAAATGCTGGTCA[C/G]TGGAGAGTGTCACCT | 337867 |
rs764673689 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202386 | CTGACAGTTCAAGAA[A/G]GCAATGTGGTTTTCC | 337867 |
rs764710507 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319871 | AGAACAGCAAAGAAG[G/T]AGCTCATTGCTTTGA | 337867 |
rs764717567 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204344 | AGTTTGGCAGGCATC[A/G]TAGTGTGGAGAAGGC | 337867 |
rs764729503 | in-del | -/CTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338031 | AAAAAAATCTCCTAA[-/CTTTTTTT]CTTTTTTTCTTTTTT | 337867 |
rs764730599 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333163 | TGAATGTAACATAGT[A/G]TTATAATAACTGATG | 337867 |
rs764741908 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276502 | GGAAGGGCAAGGTGC[C/G]AGGGTGGGTGAGAGT | 337867 |
rs764749040 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335868 | TGAGAGTTCTCAGTT[C/T]CCTCCATCCTTACCA | 337867 |
rs764761836 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211145 | AAGGGAGAAAAGATT[G/T]CTTTTCTTAAGTTAT | 337867 |
rs764764889 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287044 | TTCAAATATACATAA[A/G]TACAGAGAGAATGGT | 337867 |
rs764766723 | snp | A/G | 1.7967e-05 | 0.0029972 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254835 | GCCAGAGTAGTTAGT[A/G]AAGTGAATTTTGATG | 337867 |
rs764801832 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245608 | CCACCTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 337867 |
rs764817547 | snp | C/G | 0.00449436 | 0.0471909 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200808 | GGCCTCGCGGCGCCG[C/G]ATTCGTCGCTCCGCC | 337867 |
rs764818263 | in-del | -/TCTTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253041 | TACAAGAGTTGTTTT[-/TCTTG]TTTTAGAAATAATTA | 337867 |
rs764830487 | snp | A/G | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356562 | AACCACAAAGGAAAA[A/G]TGAAACCGAGAGCTG | 337867 |
rs764864531 | in-del | -/G | 3.71768e-05 | 0.00431127 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296174 | GTGTCTAGAAAAAAA[-/G]CCAAGAAGGATCATA | 337867 |
rs764883750 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357484 | TCTGTGTCACAGCCT[C/T]CTTATCTGGCCCCAG | 337867 |
rs764889201 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341611 | TACATATATATATAG[A/G]TGATGGAGTCACCTC | 337867 |
rs764926180 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212401 | ATTTTTCCCTAAGGC[G/T]TTCTAAGTTACATTG | 337867 |
rs764933754 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344323 | CAATATGAGAGCTCC[C/T]TGGTGATTTGTTTTC | 337867 |
rs764954115 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368392 | AATAACATAATCACA[C/T]TGAAGGAGGGAAAAT | 337867 |
rs764977941 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257191 | TATATTTAAAAACAT[A/G]TTAAATTTTCCAAAT | 337867 |
rs764980448 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329780 | TGAGTGCAGATAGGC[C/T]GACACCTTGACTGAC | 337867 |
rs764988834 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336938 | CTCTTCCTCCTTCCC[A/G]CCTCCCTCCTGTGAC | 337867 |
rs764990278 | snp | C/T | 3.30447e-05 | 0.00406464 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340512 | ATGGAGCTGCTGGAC[C/T]GGCAGCTGATGTTCT | 337867 |
rs764995966 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258139 | TAATCATGAAGTTAA[C/T]TAAATGCTGCTTACC | 337867 |
rs765018066 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336075 | GTATTTAAGATTGCT[A/C]ATTTTAGATTTCAGA | 337867 |
rs765023840 | in-del | -/TTTTC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338041 | CTAACTTTTTTTCTT[-/TTTTC]TTTTTCTTTTTTTTT | 337867 |
rs765025666 | in-del | -/TT | 4.98834e-05 | 0.00499392 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318003 | TTATTTTTAGTTGCC[-/TT]TTTTTTTTCTTTTAT | 337867 |
rs765034577 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308180 | GCACTCAGATCAGGA[A/G]AGGTGATGTTTACAC | 337867 |
rs765035538 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212519 | TCTGTAGCCAAGTTA[G/T]GTTGGGAATGTTGTT | 337867 |
rs765038589 | snp | C/G | 4.96528e-05 | 0.00498236 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295637 | TCCTGCTTTGACATA[C/G]GGTTGATGAGGAGTG | 337867 |
rs765045993 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208549 | AAAGTGTCCAGTTCA[A/G]TATATTAACACTTCA | 337867 |
rs765056201 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266054 | AAATACTGTGCTTCT[A/G]CTGCCACCTACAGAT | 337867 |
rs765056521 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306809 | GGTACTCTTTGCTGG[C/T]GGGAGGGTAAATTGG | 337867 |
rs765068550 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231563 | GACTACAGGCGTGCC[A/G]CCACGCCCAGCTACT | 337867 |
rs765076091 | snp | A/G | 3.29544e-05 | 0.00405908 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295220 | CCTTTACATGCAAAG[A/G]AGTAGATAAAAGGGT | 337867 |
rs765086542 | in-del | -/TCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280834 | CTTCTTCTTTCCCTC[-/TCT]CTCTCTCTCTCTCTC | 337867 |
rs765090796 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264194 | AGACGGTAAGCTTGA[C/G]GTTCCCTTACAGGAA | 337867 |
rs765104174 | in-del | -/GTGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368688 | TAAACTCATGAGAGA[-/GTGT]GTGTGTGTGTGTGTG | 337867 |
rs765116810 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348296 | GAAGACATGAGGCTG[C/T]ACTAGGCACTAGGTT | 337867 |
rs765118516 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253422 | GATTGTCTAAGGGAC[C/T]TTCTAGTGCAAAAAT | 337867 |
rs765120090 | in-del | -/ATGA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316419 | TGAATGAATGAATGG[-/ATGA]ATGAATGAATGAATG | 337867 |
rs765129014 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296461 | GCAAACGCACTTTTG[A/T]GACAGAAGGGAATGC | 337867 |
rs765155939 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277193 | TTTTAGGAAAGAACA[C/G]AGGAGATAAATATGT | 337867 |
rs765156525 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306353 | GGCAGTAGTAATACT[C/T]CCCATTTTACAGGTA | 337867 |
rs765180870 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265070 | TATAATCAACCTTTA[G/T]AGGAAGACGTGTTGT | 337867 |
rs765181006 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314160 | AAGAGTCCAAGTGGC[A/G]CAAATTCTGGGTCCG | 337867 |
rs765188000 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321172 | ATTTTTTAAACAAAG[A/T]TATTTGTATGAAACA | 337867 |
rs765202949 | snp | A/T | 1.65173e-05 | 0.00287374 | missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238447 | GCGCCTCTGTCGAAG[A/T]GCCTTCTGCTGGTCC | 337867 |
rs765206228 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367875 | GGCAGTCTGAGCCAG[C/T]AGCGCCCCCTCTAGA | 337867 |
rs765225941 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333271 | TTTAAGCACTTTATA[G/T]TTTAATCCTTTGTGA | 337867 |
rs765235078 | snp | A/G | | | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367841 | CGTCAGCGACAAAAC[A/G]TAAACTATCAGGGCG | 337867 |
rs765247147 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381503 | CCAAGCCGTTTAAAT[-/A]AACGTCATTAAGAGT | 337867 |
rs765254250 | snp | G/T | 1.66131e-05 | 0.00288206 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238570 | GTAAGCTCTGCCTCA[G/T]TGGCCCCTGAGAGGA | 337867 |
rs765272474 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221917 | CTTTTACTCTTAGAG[C/G]AACCCCGGCTAAGAC | 337867 |
rs765274986 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249220 | TAATAGTCTTCCGTG[C/T]CTGTTGCTGCCATCT | 337867 |
rs765348930 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315620 | TTACTTTTTCTGAGC[C/G]CCCATTTCCCCATCT | 337867 |
rs765351220 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344641 | TGTCTGCAGTTTTTC[A/C]TTTCAGGTATTCCAA | 337867 |
rs765360810 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249486 | TTGCTATTGTGAATA[-/G]TTCTGGAATGAACAT | 337867 |
rs765374388 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372238 | CCCTGTGCAGACGTG[C/T]GGGGAGGAAGATCAG | 337867 |
rs765375206 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379477 | AATTTCTGCAGCCAA[A/C]ATGTTGAATATTCAT | 337867 |
rs765387752 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343934 | TTTTCAACAAATAAG[G/T]ACTTAGTGCTTATTA | 337867 |
rs765400081 | snp | C/T | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261544 | ATTGTAAATTTAATA[C/T]TCCCAAATTTCTTGT | 337867 |
rs765401155 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99354113 | GGCCACCGCACCCCC[C/T]TTCACTGCTCTGCAC | 337867 |
rs765406518 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334095 | GGGACTACAGGCATG[C/T]ACCACCATGCCCAGC | 337867 |
rs765423992 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240477 | TTAGTGGCTCTCAGA[A/G]CTTATCCCTGAGTAG | 337867 |
rs765427434 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199729 | ATGGTTCCATACATA[C/T]ACACATTGTGCAACC | 337867 |
rs765433612 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263547 | GGGTATCGAGTAACA[A/G]GGAACATTGCTGGTG | 337867 |
rs765449556 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262794 | AGGTTATTTAAACAT[A/G]AACCTATATAATAGT | 337867 |
rs765465237 | snp | C/T | 0.000209118 | 0.0102233 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314256 | TTCACTTTTCTTTAA[C/T]CAGATCTTTTTTTTT | 337867 |
rs765470477 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236840 | GGGCGAAAGAGCAAA[A/C]CTCTGTCTCAAAAAC | 337867 |
rs765476244 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227231 | AAAAAAAGACGGCAC[C/G]CCTCCTTCCCCGGTT | 337867 |
rs765492087 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353084 | AACGATTCTTTTCAA[G/T]TTGCTATGCTTCCTT | 337867 |
rs765533939 | snp | A/T | 2.8823e-05 | 0.00379614 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201387 | CAGCCTCCGCTTTAG[A/T]AGCTGACCTCTCAGT | 337867 |
rs765559105 | in-del | -/TTTTTTTCTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338040 | TCCTAACTTTTTTTC[-/TTTTTTTCTTT]TTTTTTTTTTTTTTT | 337867 |
rs765588803 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299065 | AAATCCTCCATATGA[A/G]TAATTATTATTGTAG | 337867 |
rs765592145 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244980 | TGGGACTACAGGCAC[A/G]TGCCACCATGCCTGG | 337867 |
rs765603878 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274864 | CTGGGATTACAGGTG[C/T]GCACCACCACTCCCA | 337867 |
rs765605928 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255015 | TTTTGAAACGATGTA[A/G]TAGAGAATCACATCC | 337867 |
rs765637210 | snp | C/T | 0.000162324 | 0.00900755 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351672 | TTGGGGATAAAACTT[C/T]CCATTAGGCATTTCT | 337867 |
rs765637231 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324187 | GTGGTAGATTTTTTA[C/T]TCTAGTATTTTTGTT | 337867 |
rs765641579 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311189 | CTATGTGAAGCTTCC[A/G]TTCTACTTTTAAGAT | 337867 |
rs765661875 | snp | A/G | 1.64844e-05 | 0.00287087 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255084 | TCCCCAGGGATTGTA[A/G]CTGTTCTCCCCCGTT | 337867 |
rs765670480 | snp | C/G | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351718 | ATTTTAGAAGCAGAA[C/G]TAAGGTGAAGCCCAG | 337867 |
rs765671178 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251258 | GTGAAGTTGTTTCTC[A/G]ATTCCTGGAGCCTTT | 337867 |
rs765704118 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281691 | TTCTTGTCTCACTTA[C/T]GTCTTGACATTGCCT | 337867 |
rs765723600 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360764 | GGGTTGATGTCCACT[C/G]TGAGCTTTTCTAGTC | 337867 |
rs765726940 | snp | C/T | 0.000116081 | 0.00761756 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356116 | ACAAGACTTGGGACA[C/T]ATGTCTGTCAGACTG | 337867 |
rs765760828 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281002 | ACCAGCGTGGCCAAC[A/G]TAGTGAAACTCCATC | 337867 |
rs765762575 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250205 | TGAAGTCTTACATTT[A/G]TATCTTTAATCCATC | 337867 |
rs765786821 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373748 | GGGGCACTTCTTGGG[A/G]TTCTAGAAGCTGGAC | 337867 |
rs765810582 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203779 | GTCACGGAGGGTAGC[C/T]GGGAAGGTGACATTG | 337867 |
rs765814634 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321289 | TTATTTAGCTAGGTA[C/T]TGGTTGATTTATTTT | 337867 |
rs765816111 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371155 | AAGTCTTCAGGGTTG[-/T]TTTTTTTTTTTGTTT | 337867 |
rs765840483 | snp | A/G | 1.67638e-05 | 0.0028951 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201469 | CACACACTGATGAGA[A/G]TGCTTTCAAGTGGAG | 337867 |
rs765842851 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229713 | TGGGGAAAATTTGGA[G/T]TGTTCTGTGACTTTT | 337867 |
rs765849879 | in-del | -/ACAGAGA | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264337 | CCACCAGCCTCTGGG[-/ACAGAGA]ACAGGCTAGGGAAGG | 337867 |
rs765850458 | snp | C/T | 1.64827e-05 | 0.00287073 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255615 | CTCTCCAAATGGCCA[C/T]TCATCTTTTGCATAA | 337867 |
rs765851965 | in-del | -/TATATT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216077 | ACTTTTGTACCAACC[-/TATATT]TGTGTGTGTGTGTGT | 337867 |
rs765875727 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308299 | TGGATAGCAGGTCTT[A/T]GGAGAACTGATTAAA | 337867 |
rs765936310 | snp | C/T | 4.94654e-05 | 0.00497295 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255705 | CATATAGATGGTTAC[C/T]GTGGTTCTCTTCTTG | 337867 |
rs765938430 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245658 | CCAGCCTGGTCAATA[G/T]GGTGAAACCCCATCT | 337867 |
rs765939679 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232692 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCGCTTGA | 337867 |
rs765949786 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347189 | TGTCTAGAGAGTGCA[A/C]AGAGGGAAAAAAAAG | 337867 |
rs765963735 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265289 | CATACAGCTTCTTGC[A/G]CTCAGCAAGCCACAG | 337867 |
rs765964851 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370655 | AAACTCAAAAGGTGC[C/T]CCTGGGCAGGGATCT | 337867 |
rs765973902 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242686 | CGGGCGGGGGGCTGA[-/C]CCCCCCCACCTCCCT | 337867 |
rs765991691 | snp | A/G | 2.11598e-05 | 0.0032526 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244646 | AGCACTTAAAGATTG[A/G]CTTAATTTAGAACTA | 337867 |
rs766019278 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369745 | AGAAATTGGACACCA[C/T]CTTAACCAGGTTATC | 337867 |
rs766040826 | in-del | -/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327002 | AATAGCCAAGGAAAA[-/T]TTTTTCTCATTAGCA | 337867 |
rs766048270 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320027 | ATACGATTTCATTGT[A/G]TTAGTTACTATTAAT | 337867 |
rs766062269 | snp | A/C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246775 | GTAGCAAGAGTTACA[A/C/G]ACTTGAATAAATTGA | 337867 |
rs766078657 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361423 | ACTTTTCTACTATCA[C/T]AGGAGTAGAGGGATT | 337867 |
rs766079215 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202472 | TCAATTTCAATTGTT[A/C]TTTAGCATTTTGATC | 337867 |
rs766094970 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277331 | AGGAGTTCGAGACCA[A/G]CCTAACCAACATGGA | 337867 |
rs766105400 | snp | A/C | 4.94336e-05 | 0.00497135 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295293 | GAGAAATCTGGAACG[A/C]ATGTCTTTGGCTACA | 337867 |
rs766114459 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289025 | AGACCATAGACCGTA[C/T]GATGGCTGGCAAAGA | 337867 |
rs766123220 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297704 | TGGGAAAAAAACAAA[A/G]AATGAGGATGGTAAG | 337867 |
rs766126078 | snp | G/T | | | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255641 | CATAATAAAACATTC[G/T]AAAGGGTAAAGTCAT | 337867 |
rs766127707 | snp | A/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326226 | TTGTTTTTTTATAAT[A/T]GCCATCCCAGCAGGT | 337867 |
rs766134685 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231689 | GTGCTGGGATTATAG[A/G]TGTGAGCCACCACGC | 337867 |
rs766148059 | snp | C/T | 4.94344e-05 | 0.00497139 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340337 | GTCCGGTCTGTGCTA[C/T]GACAGCAAAATGTTC | 337867 |
rs766151040 | in-del | -/TC | 0.152778 | 0.230321 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318098 | CCTTTTACACCCAAT[-/TC]TCTCTCTCTCTCCTG | 337867 |
rs766154550 | in-del | -/TA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369931 | GTAAAATACCTGGTC[-/TA]TATGTTCTTCAAAAA | 337867 |
rs766206838 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296560 | CATTTCAGACAGGCA[G/T]TAAGCTTTGCTTTTA | 337867 |
rs766230191 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198820 | ATAACATTATGCATC[A/G]GTCAACTGGAAAATC | 337867 |
rs766237939 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284026 | GCGTGAGCCACCACG[A/C]CTGGCCAATGCCACT | 337867 |
rs766256931 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314938 | TTATTCTACAGCTTC[C/G]TGTGTCACCATGTGT | 337867 |
rs766282657 | snp | C/T | 0.000222643 | 0.0105485 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200873 | TTCAGCTTCCCCTCC[C/T]CCGGCGCCCTCTGGG | 337867 |
rs766300242 | snp | A/C | 1.67142e-05 | 0.00289081 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295436 | GCCTTTTTGTTTACA[A/C]CAGATTTCTCAGTGA | 337867 |
rs766312614 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364595 | GATAAGGAGTCATTA[A/G]AGATTTCATACACTT | 337867 |
rs766312940 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206397 | CTGTAGGAGGAGTTG[C/T]GTCTCTTCCCCTAGT | 337867 |
rs766333231 | snp | C/T | 1.66854e-05 | 0.00288833 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201586 | GGGGGCGGAGTATTT[C/T]TACAGCCAGTTAAAC | 337867 |
rs766355278 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255298 | AAGAAAAAAAATGTC[A/G]GTCGAGTGAGGTTCA | 337867 |
rs766377712 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335047 | ATGCTTTGTTATGAC[A/G]AAAGGGTCAGTTGTG | 337867 |
rs766399945 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377738 | CCACACACCTGGCCC[C/T]GCTGCCCTCCATAGG | 337867 |
rs766408007 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255941 | AAATAAGAATAAAAT[C/T]GTTGGTTAAAAAATA | 337867 |
rs766408447 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255405 | TTTATAGAGCAGTAG[C/T]AGAGGGGTGGTCGTG | 337867 |
rs766419702 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372134 | CAAGCCACACAGTGC[A/G]CCCTGTGCTGCCTGG | 337867 |
rs766421969 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233817 | GTAAAAGGATGGGAG[A/G]AAAAAAAAGGCAGTG | 337867 |
rs766434766 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291482 | GAATAAGAAATTACA[A/G]TGGTCCAAAAAGTAA | 337867 |
rs766441711 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276188 | CTAACAAGTAGTACT[C/T]CAGTTCTTCTGAGTG | 337867 |
rs766442144 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337092 | GGAATCGTGTTTTCA[A/G]GCTTTGGGTCTGGCT | 337867 |
rs766443264 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200433 | GGTAGCCAGCTTCGA[C/G]GGACCGCCCGGAAAG | 337867 |
rs766445756 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384576 | CCTCAGTTGCTGCCC[C/T]AGGCTCAGCCCCACT | 337867 |
rs766459799 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281887 | ACTGCGGTCTCAGTG[A/G]CCAGAGTGTCTTACC | 337867 |
rs766485339 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305507 | TGAGGATGATGACTT[A/G]ATCTCATCCAACATT | 337867 |
rs766490574 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221253 | AGAAATGGATTTCTT[A/G]GATCTGTGTTGCAAC | 337867 |
rs766493948 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294871 | TATTTGCATTTTTAT[C/T]GTGCTTTATGTTGTT | 337867 |
rs766514502 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207144 | CCCTCCCTGAGTTGG[C/G]AGTCTTTACCTGCTG | 337867 |
rs766518679 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271660 | AGAGTTTTTAAATTG[-/T]TTTTCACTTCTGCTT | 337867 |
rs766534830 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324316 | TGACTTACACTAGCC[A/C]CTAAAATATGAACAG | 337867 |
rs766559613 | in-del | -/T/TTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247210 | TTTTTTTTTTTTTGT[-/T/TTG]TTTGTTTTGTTTTGT | 337867 |
rs766564225 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229800 | TATAGTTATAAATGC[A/G]TAGGGAAATGAAAAA | 337867 |
rs766587215 | snp | A/G | 3.49883e-05 | 0.00418245 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295023 | TGCAAAGTTTGTCAT[A/G]CAGTTTACGTCACTA | 337867 |
rs766602578 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224304 | GCTCCATCTATCCTT[-/A]TGACCTCACTTAACC | 337867 |
rs766609415 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345967 | AGGCTGGTCTTGAAC[C/G]CCTGACCTCATGATC | 337867 |
rs766632532 | in-del | -/TT/TTTCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345741 | TTCTTTTTTTCTTTC[-/TT/TTTCT]TTTTTTTTTTTTTTT | 337867 |
rs766645228 | snp | C/T | 5.26903e-05 | 0.00513248 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255851 | AAGGGACAGGTTGAT[C/T]TTGATTGTTCAGGGT | 337867 |
rs766648655 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341735 | CCTCGTATTTAGCAG[A/G]AGGTAAATCCTTCAA | 337867 |
rs766662351 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340697 | ATTTTGACATTTCCA[A/G]AGAGATTGTAGGTCT | 337867 |
rs766681086 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212595 | AGATCCTTTGCAGCC[A/G]TACAACAGAGAAATC | 337867 |
rs766697559 | snp | A/G | | | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258331 | AGTAGTTTCCAGTGT[A/G]ACGCTTGGCGTCGGA | 337867 |
rs766704850 | snp | A/G | 1.85259e-05 | 0.00304345 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296170 | TCCAGGTGTCTAGAA[A/G]AAAACCAAGAAGGAT | 337867 |
rs766707024 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262957 | AATTATGAAAGGTAA[A/T]CAGAGGTGACTGTCA | 337867 |
rs766711455 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380650 | CTTCTCGTCCTTGCT[A/G]GCTGGTTGTCATCGC | 337867 |
rs766721251 | snp | C/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314136 | TGTACCATTTTACTG[C/G]TCCATACCAAGAGTC | 337867 |
rs766725416 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250343 | ACTGTTTAGTTTTGT[A/G]AACTTTGTTGAATAT | 337867 |
rs766725528 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263992 | AAACCTTTTGGGTGG[A/G]GTGTGGGCATGTGTA | 337867 |
rs766775080 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331015 | TTTCTCCATGTGCTA[C/G]AGACTCTAGTTGCCT | 337867 |
rs766783804 | snp | G/T | 3.29669e-05 | 0.00405984 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254997 | GACTCGAGCCTGAAA[G/T]TGTTTTGAAACGATG | 337867 |
rs766785849 | snp | A/G | 1.66671e-05 | 0.00288674 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340549 | TTGCACAAGGGAGGC[A/G]ACAGAGACAGCAGCA | 337867 |
rs766797178 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300194 | GCCACACATCATTGA[C/G]CTCCAAGGGTAGCCT | 337867 |
rs766799920 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237786 | ATGGTGAAACATGGT[A/C]TCTACTAAGAATACA | 337867 |
rs766851327 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301662 | AAAAAAATAAAAGGC[C/G]CCCCAAAACTCATTT | 337867 |
rs766863033 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282913 | AGTTCTGAAATATCT[A/G]ATGTGCTTGAAATCT | 337867 |
rs766865025 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269544 | TAAATTTTGAAGTAC[A/G]TACTTCCAGAAAGTC | 337867 |
rs766882329 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312770 | GCAGCCAGCGTGTTC[A/G]GGGAGCAGCTGTGTG | 337867 |
rs766914013 | snp | A/T | 7.34889e-05 | 0.00606127 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200960 | TACCGGCCTCCGCCA[A/T]CCTGGCTGCCCCCTA | 337867 |
rs766914839 | snp | C/T | 0.000162324 | 0.00900755 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351557 | CCTTTTACCTGGAAA[C/T]GTGAATTCTCTCTTA | 337867 |
rs766947867 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319244 | GAAGTGGAGTTTTAT[G/T]CTTCATCCATGACTT | 337867 |
rs766951793 | snp | C/T | 8.24165e-05 | 0.00641883 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255079 | AAGGCTCCCCAGGGA[C/T]TGTAACTGTTCTCCC | 337867 |
rs766976518 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224040 | GTGTATCCTTACTGA[C/T]TTTACTGGTCAGCTT | 337867 |
rs767005016 | snp | C/T | 3.30469e-05 | 0.00406477 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295771 | GAAGCGGTCAATACT[C/T]AGGCAGGTCATAAAG | 337867 |
rs767014328 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297506 | ACTTCATTCTAACAA[C/T]CTTAAAACTGAGATG | 337867 |
rs767039294 | in-del | -/TTTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216835 | TCTTTTCTTTTTTCT[-/TTTTTTTTT]TTTTTTTTTTTTGAG | 337867 |
rs767040986 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235420 | TCTTCACAGAAATAG[-/A]AAAAAAAAATCCTAA | 337867 |
rs767046031 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337187 | GGCATTTACATTCCA[A/G]CAAAACACCCTGTTA | 337867 |
rs767046352 | snp | A/G/T | 3.35302e-05 | 0.00409441 | intron-variant, synonymous-codon, stop-gained | UBAC2, GPR183 | GRCh38.p7 | 13:99295887 | CATAGTAGGCTATTC[A/G/T]TGTAGGCAAAGCGGT | 337867 |
rs767096993 | snp | A/C/T | 1.64977e-05 | 0.00287203 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254941 | CGGAAACTTTTTCTG[A/C/T]GCATGCTTCGAAGGT | 337867 |
rs767108143 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225010 | TGCTCATTTTGAGAG[A/G]AATACTTAATGGTAA | 337867 |
rs767111486 | snp | A/G | 1.66338e-05 | 0.00288386 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385345 | CACTGATAGTCCCAG[A/G]CCAACACTGGGACCG | 337867 |
rs767117054 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377916 | GCCAACTCCAAAGCT[C/T]GGGTCTCCCTGCCAC | 337867 |
rs767131476 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211469 | TCTATATGGTTCTTA[C/T]ACCTTTTCAATCAAC | 337867 |
rs767147360 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299881 | AGGAAAAAAATTGGA[G/T]TGGTTCTTAAAAGCC | 337867 |
rs767161326 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360339 | ATGGCTTTACGTTCT[A/G]TTTTAAATGTTTCAC | 337867 |
rs767170313 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322659 | TGATTATCTCTGATC[C/T]AGCAGCCTTAGTGTG | 337867 |
rs767173472 | in-del | -/GGG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206281 | GAGGACTCCAGAGGT[-/GGG]GGGACAGTTGGAAGC | 337867 |
rs767177401 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367062 | TTTTTTTAAAGCAGC[A/G]TGTGATGCATTTTTC | 337867 |
rs767203040 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234333 | AGTGGGATTATAGGC[A/G]CTTGCCACCACGCCC | 337867 |
rs767271623 | in-del | -/ATG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363984 | TACTTACATTCTCTA[-/ATG]ATTTCAATAGAGGGA | 337867 |
rs767308339 | snp | G/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257784 | AATATACATATGATT[G/T]ACCATAAACATTTTC | 337867 |
rs767320274 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366064 | TTTTCCATCTCTTTA[C/T]ATCAACTTGTGTACG | 337867 |
rs767322493 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222595 | GATGACAAATTGGTT[C/T]CATAGAATAAGCAGT | 337867 |
rs767327161 | snp | C/T | | | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255592 | GCTCCAAGAATCTGG[C/T]AGAAGTACTCTCCAA | 337867 |
rs767339317 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344749 | ATCTGGCAGGTGCTC[A/G]CTGCCACCCCCTGCC | 337867 |
rs767341178 | in-del | -/CCT | 3.30382e-05 | 0.00406423 | cds-indel, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99238488 | CTCCCTCCTGCTCGC[-/CCT]CCTCCTGCCTCACTG | 337867 |
rs767351496 | snp | A/T | 0.000169107 | 0.00919375 | intron-variant | UBAC2 | GRCh38.p7 | 13:99317996 | TTGAATTTTATTTTT[A/T]GTTGCCTTTTTTTTT | 337867 |
rs767357894 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199859 | CATTATCGTTGAGTA[C/T]AGTCATCCAAACGTG | 337867 |
rs767359819 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316120 | AAATTTCCAATATTT[C/T]TGTAATATTTCCGGT | 337867 |
rs767364485 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275049 | TGTCTTTTGTTGCAT[A/G]TATGTATGCATTTCT | 337867 |
rs767368073 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328938 | TTCTTCAAGAATTTA[A/G]TAGTTTCTGCTATTA | 337867 |
rs767409790 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304498 | TTCTTGTATCTCTAG[A/G]TGATGTATGATCGAT | 337867 |
rs767412353 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199124 | AGACTGTGAAAATGG[G/T]CTGGGCCCAGAGGCT | 337867 |
rs767424226 | snp | G/T | 6.50005e-05 | 0.00570053 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200786 | GCGCCGTTCGTCAGC[G/T]GCGAGTGGCCTCGCG | 337867 |
rs767428640 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255171 | CACCAGCAGCGTGAT[C/G]ATGATCCTTATGGAC | 337867 |
rs767428805 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298742 | ATTTCATTGTGGAAT[A/G]AAAGTAGAAAAAGAT | 337867 |
rs767453792 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240623 | TCCTTGGCAGTTTCC[C/T]ATGTGCTCTCGTGTA | 337867 |
rs767490637 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317110 | TTGCCAGCCTCTTTA[C/T]CTGAGTGTGTCAACT | 337867 |
rs767504574 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259925 | GCCAGACTCTTAGAG[A/G]AGGCATCCAGGAGCA | 337867 |
rs767514888 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208302 | ATGCCCCACCTTCAC[G/T]GTCTCTTTAAAATAC | 337867 |
rs767517085 | snp | C/T | 1.66593e-05 | 0.00288607 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295424 | ATTGTGTTGAGAGCC[C/T]TTTTGTTTACACCAG | 337867 |
rs767548818 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230103 | CACTTCCTCAGGGAC[A/G]TGATAATCACTATTT | 337867 |
rs767616627 | snp | A/T | 1.65638e-05 | 0.00287778 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201490 | TCAAGTGGAGGGAAG[A/T]TAGGAAGTCGTGGCG | 337867 |
rs767616768 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335604 | GCGCAACATGTGATA[C/T]CTTCTATGTGTATTT | 337867 |
rs767618741 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294954 | CCAATGAAAGAAATA[C/T]AAAAGAATACTAATT | 337867 |
rs767630194 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364120 | TGTTTCTCTTTTTCT[A/G]TCTTTATGTGAGATT | 337867 |
rs767647265 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363307 | TCAAAATAGTCATGC[C/G]TAGTTTTGAGCTTTA | 337867 |
rs767651002 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283558 | CACAAGCAGACTTGC[A/G]AGAGTAGATGTTGCT | 337867 |
rs767666705 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296206 | AAGTAAAAGCATATG[C/T]ATTCAGTTTGATTAC | 337867 |
rs767669752 | in-del | -/AGA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309923 | AGTGACCTTTTCTAT[-/AGA]AGAAGTGAAATGGAC | 337867 |
rs767679614 | in-del | -/AAAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241265 | GTGAGACCCTGTCTC[-/AAAA]AAAAAAAAAAAAAAA | 337867 |
rs767691194 | snp | C/T | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351989 | GCTGCACATCCTCAC[C/T]TGGTAACATTCTGTG | 337867 |
rs767710502 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332014 | TCAGTTGCAAGGGGA[C/T]ATTTATTCCTTTGGC | 337867 |
rs767720662 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214726 | GTTCTCCTTAAGCAG[A/T]TTGTCCCCCACCCCA | 337867 |
rs767728850 | snp | C/T | 1.79648e-05 | 0.00299701 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296145 | CCATTTGTATATCCA[C/T]TGGTGGTGGTCCAGG | 337867 |
rs767731282 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303056 | TGGAGTGTGACTAGC[C/T]GAGGGGCTTAGTAGA | 337867 |
rs767733371 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272650 | CTTGCTGTGTCCTTA[-/C]ATGGCTGAGAGAGCT | 337867 |
rs767758132 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336017 | AAAAAAAAAAAGAGA[G/T]AAAACTGGATGTTAG | 337867 |
rs767760205 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324507 | AGCATGAACAGGAAA[G/T]AAATCTTTGTTATAA | 337867 |
rs767765176 | in-del | -/TAAA | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99307240 | ATGGTAGCTTGTTCT[-/TAAA]TAGATTGTTTTCCTT | 337867 |
rs767770243 | in-del | -/CC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280828 | CCTTCCTTCTTCTTT[-/CC]CCCTCTCTCTCTCTC | 337867 |
rs767771375 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251727 | TTTGCCATCAGACCA[G/T]ATTTGAGATTCCAGC | 337867 |
rs767789433 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216400 | GTGAGCCACCGTGCC[C/T]GGCCCAGTGTGTTTA | 337867 |
rs767790336 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291660 | TGTTGGCTAATTAGC[A/G]CTCTCCTTTAATGTG | 337867 |
rs767794391 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226736 | TTTGCCAGTTGGCAG[C/T]CTTATCATCTCTTAA | 337867 |
rs767808801 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247051 | ATGTTGTCTAGGCTG[A/G]TCTTGAATTCCTGGG | 337867 |
rs767809276 | snp | A/T | 1.64906e-05 | 0.00287142 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255743 | AACTGAAAACCCATA[A/T]TGCAGTGATGTTAAC | 337867 |
rs767831693 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321541 | GTCTCGAACTCCTGA[C/T]GTCAGGGGATCCATC | 337867 |
rs767841085 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367767 | CTGTGTCTGATAACT[A/G]TGTGTTGATCTCTTT | 337867 |
rs767861313 | snp | A/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367848 | GACAAAACGTAAACT[A/G]TCAGGGCGGTCGGCA | 337867 |
rs767889622 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200668 | CCGCCATCGTTTCAA[C/T]CTGGAGAGGTGAGCC | 337867 |
rs767890449 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224664 | CACCACCTAGATTCT[A/G]CACAATTAACATTTT | 337867 |
rs767907610 | snp | C/T | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260978 | TGAGTGAATATAATT[C/T]AGTTAAGCCAGTTTT | 337867 |
rs767928570 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343691 | AGTTCTCTTCTAGGG[G/T]CCGCACATGGGTACA | 337867 |
rs767968594 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381926 | GTTGAAAAGACAGCT[A/G]TGGTCTAGGACACCA | 337867 |
rs767994519 | in-del | -/A | 1.64821e-05 | 0.00287067 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318114 | CTCTCTCTCTCCTGT[-/A]AAAAACATTAGGAAA | 337867 |
rs767997247 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223924 | CTATTTTGGTGAATG[C/T]TCCATATGCACTTGA | 337867 |
rs767998124 | snp | C/T | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261137 | AGGGCAGCTTATCCT[C/T]GTTGCCTCCCATCAG | 337867 |
rs768003345 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312479 | ATGTAAGATTTCCGT[C/T]CTGTGATGAGTTCCT | 337867 |
rs768004390 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290607 | GTGGGCACCTGTAAT[C/T]CCAGCTGCTCAGGAG | 337867 |
rs768009744 | snp | G/T | 1.65721e-05 | 0.0028785 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295085 | TTTGAAGACTTGGAA[G/T]GTATCATCATCTGCG | 337867 |
rs768045727 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301830 | ACAGAACAAAACCTT[C/T]ACCATATTCGGGGAT | 337867 |
rs768068260 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272084 | CTCTAAAAGACAGTG[A/G]TCTTTGATGGTCTGG | 337867 |
rs768071537 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370128 | CATTTCCAGGACTTG[A/G]TACATACCGACCGTG | 337867 |
rs768091976 | snp | C/T | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351518 | TGCTGTAGAAGGTTA[C/T]ATAGCCAGCAGCTTT | 337867 |
rs768104392 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353850 | AGAAGCCTTGATTTC[A/G]TGCAACCCCCAAGGT | 337867 |
rs768112733 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225239 | ATTGTGCAACCGATG[A/T]CTATAACTCTTCTCA | 337867 |
rs768113252 | in-del | -/ATTT | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305890 | GACTCAGGGCCATTT[-/ATTT]ATTTATTTATTTATT | 337867 |
rs768146874 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237015 | ATGATCCACTACTGG[A/G]TATATATTCAAAAGA | 337867 |
rs768166670 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331996 | AAGTCTATGTGCTGG[G/T]GCTCAGTTGCAAGGG | 337867 |
rs768167198 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255075 | GGTAAAGGCTCCCCA[A/G]GGATTGTAACTGTTC | 337867 |
rs768169939 | in-del | -/AA | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351665 | CACAAACTTGGGGAT[-/AA]AACTTTCCATTAGGC | 337867 |
rs768216402 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341264 | TACCCCTGGGGTAGT[G/T]GTAAACCGTACAGTT | 337867 |
rs768219680 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306205 | CCAGCCTGATTCAGG[G/T]TCTTTATGTAAAATA | 337867 |
rs768225706 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295184 | TGCCGTTTCAGCATC[C/T]TCATAACCTTTCTCT | 337867 |
rs768231263 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324761 | TTCAGTGGTGGCCCT[A/G]TGGATTCTAATGGAG | 337867 |
rs768234044 | in-del | -/ACACACAG/ACACAG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237297 | CACACACACACACAC[-/ACACACAG/ACACAG]AGTGGAATATTATTC | 337867 |
rs768253462 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215637 | TGTCTGTGACCCGTC[A/G]TCCTAGATTTCAGGT | 337867 |
rs768277086 | snp | A/C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331541 | AAAATCTTTTAATTT[A/C/G]GTATCATTTCTATTC | 337867 |
rs768277576 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251094 | TGTAGTTCTTGTAGA[A/G]ATCTTTTACCTTCGT | 337867 |
rs768295811 | snp | A/T | 1.65403e-05 | 0.00287574 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356189 | CCTAAGCTGTGCTGG[A/T]GCTTCCCGATGTACT | 337867 |
rs768334423 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357450 | ACTCTTTTCAGGGCC[A/G]TAGGAAATTAGTCAT | 337867 |
rs768361644 | snp | C/T | 9.02731e-05 | 0.00671777 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201231 | GCAAGTGGGCAGGTG[C/T]CCTGGTGTTCTCGTG | 337867 |
rs768363815 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252346 | ACCAAGTTTTACTTT[A/G]TGTACTCTTTGCCCT | 337867 |
rs768365421 | in-del | -/AAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290750 | AAAAAAAAAAGAAAG[-/AAA]GAAAGAAAAAGAAAA | 337867 |
rs768365665 | snp | A/T | 6.59109e-05 | 0.0057403 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255112 | GTTCCCAGCATCAGG[A/T]AAGCGAAACAGATGT | 337867 |
rs768372702 | snp | G/T | 0.000304275 | 0.0123307 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351872 | TGATTATCACCTCTG[G/T]GTTTTGCCTGCAAGG | 337867 |
rs768373905 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379223 | GCTGCATTAGCACAT[-/C]CCAGCAAAGTTGTTC | 337867 |
rs768391786 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380997 | TCTCTTCTGCCAAGA[-/C]CTGTGAAAAGCCAGT | 337867 |
rs768402117 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320888 | TGCTCAACATGACTT[C/T]CCCTCTTCCTTTATA | 337867 |
rs768420163 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264771 | CTCTGAATTTCTGTA[A/G]GACTGTGGATAGGAG | 337867 |
rs768420803 | snp | A/G | 1.83266e-05 | 0.00302704 | intron-variant, synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201441 | CAGTCTCCAAGAAGA[A/G]TTTTTAGACAAACAC | 337867 |
rs768460491 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206994 | GGCCCACCCTCCACC[A/G]ATTCTGAACTCTTTC | 337867 |
rs768463679 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289940 | AGGTAGTCACCTGCT[C/G]TTCCTCCCCACCCCC | 337867 |
rs768478672 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99279435 | CCTCAGACTAGGTCA[-/C]CAGTCTCTTGTGATA | 337867 |
rs768520341 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302349 | CAGGGTTAATTGAAA[C/T]TTCAAAGATATGGTT | 337867 |
rs768555703 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370427 | TACAACCTTTTCAAA[A/G]TCTATAAAAGAAAGT | 337867 |
rs768557105 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339035 | CCCATTTTATCTCCT[A/C]TAGTCCTGTTACCCT | 337867 |
rs768570401 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352862 | GGAGGCAGCACCGTC[A/G]GAAACTCTCTACCTC | 337867 |
rs768584608 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203504 | CTGCATGTTTCCCAC[A/G]TTTTGTGGTTAGTAG | 337867 |
rs768609379 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342134 | CAGTATCTATGGGGG[C/T]GGGCTGGCGAAGGCA | 337867 |
rs768620730 | snp | C/G | 1.70478e-05 | 0.00291952 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254892 | TCATAACATTTCACT[C/G]TTTATATTGCTTAGT | 337867 |
rs768623980 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288395 | TAACTACGAGAAGCC[A/G]CACAGTTAGCATGCA | 337867 |
rs768639160 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248077 | CTGACTTAGTTACTG[C/T]GTGCAGCTCTTTTCT | 337867 |
rs768656206 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271402 | AGATGGGACCATCCC[A/G]TACGTGGACAGCTGG | 337867 |
rs768671767 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355232 | TGTGTGTAGAGCCAA[C/T]GCTGGGAAGGAAAAA | 337867 |
rs768674842 | snp | A/G | | | intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99256452 | CACAATTGGGAGTAC[A/G]TAAAGCCAAGTCTTC | 337867 |
rs768684074 | snp | A/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328346 | TTGTGTGTGGACATA[A/T]GTTTTCCTTCTTTAG | 337867 |
rs768692039 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221408 | ATGAAGGTGAAAATT[C/T]GTTTGAACCGTGGCA | 337867 |
rs768694635 | snp | A/G | 1.64999e-05 | 0.00287222 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295978 | TTTCCTGTTTTGAAC[A/G]ATGACGACCAAGGCT | 337867 |
rs768700715 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255556 | AGCCATAAAGCAATG[C/T]TTGGGTAAAACACTG | 337867 |
rs768705603 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366605 | TCCTGCTGTCTCCGG[A/G]GGAAGACAGGCTTTT | 337867 |
rs768717491 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369418 | CAGCGACTGTGAACC[A/G]TTCTGTTTTTCACTT | 337867 |
rs768719527 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259013 | TAGTGCGTGGAAGTC[C/T]AGAAATAATTTCTTT | 337867 |
rs768732475 | snp | A/G | 1.70528e-05 | 0.00291995 | synonymous-codon, intron-variant, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99244580 | CATTGAAGCTATGCA[A/G]TATTTCTTTGGCATC | 337867 |
rs768736587 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240118 | GGCTCAGTTGATGAA[A/G]GGCTTTATTTTGTAA | 337867 |
rs768738777 | in-del | -/AC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292157 | TCTTTTTTTTTTGAG[-/AC]AGTCTCTCGCACTGT | 337867 |
rs768752139 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255657 | AAAGGGTAAAGTCAT[C/T]ATAAATATCAAGTCC | 337867 |
rs768771112 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249048 | TCAACTTTCAGATTC[-/A]GGGGGTACATGTGAA | 337867 |
rs768776863 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367559 | AAGAGCTTTTACACT[G/T]CCTATTACTTTCTTT | 337867 |
rs768783605 | snp | C/T | 8.67152e-05 | 0.00658408 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200772 | CGCATGCGCCGGGTG[C/T]GCCGTTCGTCAGCGG | 337867 |
rs768806901 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209216 | AGCCCCTACCTCAGC[A/T]TGGTATGAAGGTGTG | 337867 |
rs768815068 | snp | A/G | 1.77461e-05 | 0.00297871 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200856 | GTCGCTGGGGCTCGC[A/G]CTTCAGCTTCCCCTC | 337867 |
rs768838568 | in-del | -/ATATAT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232397 | CCATCCTTAGTTGAG[-/ATATAT]AGATATAGATATATA | 337867 |
rs768872977 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268251 | GCAGTCTTCTCAGAA[A/G]AACAATAGCTCTAAC | 337867 |
rs768880759 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285485 | GTAACGTCAAACTTC[C/T]GGGCTCAAGGGATCC | 337867 |
rs768883120 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285015 | CTCTTTCCATTCCCT[-/G]GCATTTTAAAAGTAT | 337867 |
rs768914454 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310135 | AGTCTGAGATCACTG[C/T]GGGGAACACAGCGAG | 337867 |
rs768924484 | snp | C/T | 4.94311e-05 | 0.00497123 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340437 | TTCTCTTCTTCAGAA[C/T]CCACCAGCGAAGCCA | 337867 |
rs768947900 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374361 | AATTTGATTGTGTGG[C/G]ATTTAGCATGAGTGA | 337867 |
rs768971461 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304995 | GAGGAAGAGATGTTG[A/T]TTCAAATGAAGGAGT | 337867 |
rs768978291 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274652 | TAATGTTAATGGACA[A/T]TGGGATTGTTTATAA | 337867 |
rs768990971 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297235 | AACTTTGATTAAAGC[A/G]GGAAGAACAGAGCAA | 337867 |
rs768996275 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345479 | ATCGAGCTCTCCTTC[C/T]TCTGTTCACTCCCTA | 337867 |
rs769027974 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350557 | GTGCTGGAGCAGGGT[G/T]CAGGGGGTGCCAGAG | 337867 |
rs769056103 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262431 | AGGAGGGCTGGGCAC[A/G]GTGGCTCATGCCTGT | 337867 |
rs769057446 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373561 | CCCTGAGGAGCTGTG[A/C]GCCCAGGGCAGGGAA | 337867 |
rs769060123 | snp | C/G | 1.65072e-05 | 0.00287286 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367925 | ATTAATCAGTAATAC[C/G]TGGTACTCATTCTAA | 337867 |
rs769082273 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293040 | ACAGTGGCTTGATGA[A/G]TAGAATGGGCAGCCT | 337867 |
rs769082415 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375803 | TTTCCTTTTTCCCTT[-/T]TTTTTTTTTTTTTTT | 337867 |
rs769097676 | snp | C/G | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255246 | GAGATTATGAATAAT[C/G]ACCAAGTAGCACCCA | 337867 |
rs769108525 | in-del | -/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262282 | ACAGGAAAAAAATAG[-/T]TAAGTATAGGGTTTG | 337867 |
rs769113719 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258621 | GATATTGAGTAAAAG[A/G]GGGTTTAAAGTCTAG | 337867 |
rs769126721 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316719 | ACCCAGAGGAAATTA[C/G]TTTTTCAATGACAAA | 337867 |
rs769138130 | snp | A/G | 1.65748e-05 | 0.00287874 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385195 | AGCGGCAATGTCAGC[A/G]CCCTCAGGTTTCTGC | 337867 |
rs769148105 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259165 | AACGAATCGCTGCCT[A/G]CCTTGTTAGGTTAAT | 337867 |
rs769155938 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341604 | GGAAGCTACATATAT[-/AT]ATATAGGTGATGGAG | 337867 |
rs769164712 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217270 | TTAGGTGCTGAAGGG[A/C]CACTCAGAAGCCCAA | 337867 |
rs769169278 | snp | C/T | 1.77012e-05 | 0.00297494 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296130 | GAGTAAAATTGTTTG[C/T]CATTTGTATATCCAT | 337867 |
rs769190986 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311866 | GAAGAAGGACTGATA[C/G]GTGAGGAATTCTAGA | 337867 |
rs769199739 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334611 | AATTTTGAATGCATA[A/T]TATAACCTCTAGGGC | 337867 |
rs769202760 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386332 | AAGTTGACTCTTGCA[A/G]TGTGCAACTGTTATG | 337867 |
rs769210449 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299572 | GAACGTTTCTATTCA[G/T]AATGTTCATTTCTAG | 337867 |
rs769216247 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286361 | AGATCAAGTTCCTCA[A/G]AGAACATTGTGTGTG | 337867 |
rs769257531 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314106 | GCATAGCCTGGCACC[C/T]GTGTTTGCTCTGTTT | 337867 |
rs769262213 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275624 | TATTGAGGATAGTTT[C/G]TTCACTACCTGCCTC | 337867 |
rs769271390 | in-del | -/ACAA | 3.53707e-05 | 0.00420525 | intron-variant, frameshift-variant, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201449 | AAGAAGAGTTTTTAG[-/ACAA]ACACACACTGATGAG | 337867 |
rs769280319 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353623 | CTTATTAATCAGTTT[C/T]TGAAAGGACGAATGA | 337867 |
rs769289500 | in-del | -/TT | 3.30071e-05 | 0.00406232 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254933 | TACCAGATCGGAAAC[-/TT]TTTCTGCGCATGCTT | 337867 |
rs769292053 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215826 | TGGTGAGATCCCACC[-/A]TCTACTCCTTCATCG | 337867 |
rs769299863 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384442 | TTGCCAATTTCAATA[C/T]TGGAGACTGCCTGTA | 337867 |
rs769303356 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253999 | TTTTCTTTTAGATGG[A/G]TAAGTTACTTGGTTT | 337867 |
rs769313352 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272571 | GAAGTCCAAGATCAG[C/G]ATGTTGGCATGGTCA | 337867 |
rs769322073 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349759 | AAGAGGAACCAGGAG[-/T]TACGGGAGGAACATG | 337867 |
rs769324995 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214330 | TTCTTGTGCAGTCCT[A/G]AATGACTGGATTCCT | 337867 |
rs769342102 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380553 | GGCCACTTGGCTAAC[C/T]TGCACGGCTGTGAGC | 337867 |
rs769351228 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331678 | CATGAAAAGAATAAT[C/T]TTTTCAAAATGTATG | 337867 |
rs769367469 | in-del | -/ATA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244135 | ATGTAAGACATTAGC[-/ATA]ATAATAATAGTGATA | 337867 |
rs769376842 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347012 | GTTGAGTGCAGTGGT[A/T]CACGCCTGTAATCCC | 337867 |
rs769377006 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318640 | CTGGCTGACATGATG[-/A]AAACCCCATCTCTGC | 337867 |
rs769391499 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238364 | TTCTCTTGCTTTTCA[C/T]GCATGTGGTTTTTTA | 337867 |
rs769393637 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314438 | GTCTTTAGAAATCTG[A/T]TAAGAGCTTTCACTG | 337867 |
rs769398828 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217255 | CAGTCCCTCCATCCA[C/T]TAGGTGCTGAAGGGC | 337867 |
rs769405857 | snp | C/G | 1.65201e-05 | 0.00287398 | missense, synonymous-codon, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238489 | TCCCTCCTGCTCGCC[C/G]TCCTCCTGCCTCACT | 337867 |
rs769423816 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255067 | AGGAAGGTGGTAAAG[A/G]CTCCCCAGGGATTGT | 337867 |
rs769474011 | snp | C/G/T | 5.01202e-05 | 0.00500579 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295071 | CATTTCACTTTCCAT[C/G/T]TGAAGACTTGGAATG | 337867 |
rs769507813 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280322 | ATTGCATTACTCACT[A/G]CTGCCTGTCACGCAT | 337867 |
rs769518066 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203799 | AGGTGACATTGAGCT[A/G]AGGCTCAGATGGTGT | 337867 |
rs769523403 | snp | G/T | 3.29679e-05 | 0.00405991 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254985 | CATGACACTAATGAC[G/T]CGAGCCTGAAATTGT | 337867 |
rs769551746 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99313354 | GAGAGTACTGCCAAC[A/G]ATGTTAAGAAATGGA | 337867 |
rs769559976 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373597 | TGGACAAAGAGCTTG[C/T]GGAAGTGTTCGGGTG | 337867 |
rs769563598 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239166 | TTAGCCCATTTTAAG[C/G]ATAATAATCCATTTC | 337867 |
rs769564645 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204696 | TGGGAAAGAAAGAGG[-/C]CCCCCCCAGAACCTT | 337867 |
rs769582705 | snp | C/T | 7.27934e-05 | 0.00603253 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200948 | GGGCTCTGTGAGTAC[C/T]GGCCTCCGCCATCCT | 337867 |
rs769611405 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265078 | ACCTTTAGAGGAAGA[C/T]GTGTTGTTTTTTTCT | 337867 |
rs769629509 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237555 | TAGAAGAAATAAGAC[A/G]GTGTTCAGTAGGTCA | 337867 |
rs769655819 | snp | A/G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233774 | TATGTAAACCCTAGT[A/G/T]TAAGTCTTAATTGTA | 337867 |
rs769659661 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324409 | CTGTCCCCTTTGCCA[G/T]GAGAAAAGCAGGGCC | 337867 |
rs769667705 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291396 | ACCGGGTCACTTGTA[A/G]TCCACATGCTTTTCA | 337867 |
rs769670046 | snp | C/G | 0.00170989 | 0.0291894 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351430 | CATAGTATCTTTGAT[C/G]TCTTGCCTCTTTATC | 337867 |
rs769702853 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359984 | AGACTGAGAAGAAAG[A/G]GTGCATTTGTTTCCA | 337867 |
rs769726777 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370472 | TCATAATACTTTGAA[A/G]TTTCCCTCTGCCTGT | 337867 |
rs769744895 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235294 | AGAGGACATAAAAAA[A/G]TGAAAGGGTATTCCA | 337867 |
rs769755344 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349496 | GTAGTGGCCCTGAAC[A/G]GCTGGGTGCGCTGAT | 337867 |
rs769770992 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278155 | CAACATTATTCTGTG[G/T]ATTAATTTGGTTATT | 337867 |
rs769772454 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319018 | GTCTGCTCATTTTGT[A/T]AAAAGACATTGTCAC | 337867 |
rs769792746 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288299 | ATCAGTTGCAGTAGG[C/T]GCCATGTGGGGCAGA | 337867 |
rs769813216 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345852 | GCTTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCC | 337867 |
rs769833927 | in-del | -/TTGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373169 | TCTCTCTCTTTTTTA[-/TTGT]TTTTTTTTTTTTTTT | 337867 |
rs769834277 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251747 | GAGATTCCAGCTCTG[-/C]CTCTTACTAGTTATG | 337867 |
rs769858070 | snp | C/T | 1.65089e-05 | 0.00287301 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385311 | TGACCTCAATGTCGC[C/T]ACCAACTTCCTGCTG | 337867 |
rs769872706 | snp | A/G | 0.000171209 | 0.0092507 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385377 | ACCGGCAGCCGAGTG[A/G]CAGTGCGTGGTCCCC | 337867 |
rs769873147 | snp | G/T | 1.99842e-05 | 0.00316097 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243971 | GTTTTTATGTATTTT[G/T]TCTTTGCTACTTAGG | 337867 |
rs769889378 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253557 | CTCGCTTTGTCACCC[A/G]GGCTGGAGTGCAATG | 337867 |
rs769937957 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225846 | TAAAATTGGAACGTG[C/T]CTTGTAATTGATGAC | 337867 |
rs769942467 | in-del | -/T | 1.65164e-05 | 0.00287366 | intron-variant, frameshift-variant, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201532 | CTGTGCTGCTGGATG[-/T]TGCTGTTTTCCTGGC | 337867 |
rs769956685 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366824 | GCTCACAGTGTGCGG[C/G]TCTGCTTCCCACGCC | 337867 |
rs769963252 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318085 | GTAAGTGTGACTACC[C/T]TTTTACACCCAATTC | 337867 |
rs769968108 | in-del | -/G | 1.64814e-05 | 0.00287061 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255408 | TAGAGCAGTAGCAGA[-/G]GGGGTGGTCGTGGTC | 337867 |
rs770049613 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234099 | GCATGTTATTTCAGC[A/G]GTTTTCCTAGATTGA | 337867 |
rs770103157 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286624 | TGACCATAGTACCCC[A/G]TATGTGGCTTTTCAA | 337867 |
rs770105366 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382109 | TTCTGGGCTCTTTGA[C/T]CTGACGTGTTTGACA | 337867 |
rs770108621 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363858 | TTACCAGGCTCAATT[C/G]AGGAACATGCTGAAT | 337867 |
rs770111844 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340645 | GTGATTGCATGTGAG[A/G]TAGAGACTACATTTT | 337867 |
rs770120913 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336638 | GGCTCTTGTTCTCTT[C/G]GTCTATTTAAGTAAC | 337867 |
rs770122317 | snp | C/T | 5.00263e-05 | 0.00500106 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200765 | CTGACTGCGCATGCG[C/T]CGGGTGCGCCGTTCG | 337867 |
rs770125750 | snp | A/G | 1.65894e-05 | 0.00288 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340298 | TACATTTAAACAATC[A/G]CATTGGACGTTTTTC | 337867 |
rs770133991 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335778 | GGCTGCAGTGGAATG[A/G]GCCTCAAAGCTCTAC | 337867 |
rs770165212 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282767 | ATTTTAGATTTAGAT[C/G]ATTGTATTGTTCTAA | 337867 |
rs770184396 | snp | G/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306021 | CTGCCTCACCCTCTT[G/T]AGTAGCTGGGATTAT | 337867 |
rs770218278 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207112 | GATGCTTTCTCCTGC[A/G]GGTGCCTTAGTGGCA | 337867 |
rs770234399 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328511 | GTCAACACTTGGTAT[G/T]GTCAGTTGTTTTAGC | 337867 |
rs770240347 | in-del | -/AGAC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271130 | GTAATTGAGGGTAAA[-/AGAC]AGTAAACAAAATAAA | 337867 |
rs770262224 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217597 | GGCTTGGGGCCAGCT[G/T]TTACCCGCGCTCGCC | 337867 |
rs770283376 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375378 | TCTCGGCCATGCGTC[A/T]GCATGGGGGTGGGCA | 337867 |
rs770292622 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332753 | GCCTGCCGGAGACTG[C/T]GCCACTGCTGCCTTC | 337867 |
rs770296588 | snp | G/T | 4.95544e-05 | 0.00497742 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201536 | GCTGCTGGATGTTGC[G/T]GTTTTCCTGGCGTGT | 337867 |
rs770298281 | snp | A/G | 3.30836e-05 | 0.00406702 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356213 | ATGTACTCTGTAGAT[A/G]TCTTTGCACCTTCTG | 337867 |
rs770306193 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207809 | TTAGGATCCTGCCTT[C/T]GGAACCTGAATACCC | 337867 |
rs770322872 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294610 | AGAACGAAACAAAAC[A/G]AAACATTGGTGTTAT | 337867 |
rs770332445 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210913 | CACCATGCTGGGCCC[C/T]GCTTTTTCCCTTTGT | 337867 |
rs770364716 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346766 | ACACTGCCTGTCTCT[C/T]GTGGCACCGCAAACC | 337867 |
rs770387531 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385245 | CGCCCGGCTCATGGA[A/G]ATGGGATTTTCCAGA | 337867 |
rs770388041 | in-del | -/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299875 | TGCACAGGAAAAAAA[-/T]TTGGAGTGGTTCTTA | 337867 |
rs770414208 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263696 | GGACAAGAATGTTCA[C/T]GGTAACATTATTTAC | 337867 |
rs770424839 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371575 | GTTTGTTTAACCACT[C/G]TCTAAAATATTTGTT | 337867 |
rs770433042 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285433 | TGTCTTGCTCTGTCA[C/T]CCAGGCTGGAGTGCA | 337867 |
rs770435983 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262382 | CTGTATAGTTAACAC[C/T]TAGTAATATGAGGAA | 337867 |
rs770460685 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220787 | TACTAGTGACTTGCC[C/T]CATCTCAGTGCATAA | 337867 |
rs770474653 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315241 | TGTAACCAAATAGCC[C/T]GTTTCTGCATTTGAT | 337867 |
rs770497954 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339015 | GCTGTGTCTCCTCCT[-/C]CCCCCCCATTTTATC | 337867 |
rs770498776 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322572 | TATTCCTCAGACTTC[A/T]CCCTTCAACGCAGCC | 337867 |
rs770508923 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272633 | TTGCAGATGGCCACC[C/G]TCTTGCTGTGTCCTT | 337867 |
rs770514440 | snp | A/C | 1.64795e-05 | 0.00287045 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255344 | TTAGATAGATGATGT[A/C]AGAAATCTTGAGGCA | 337867 |
rs770525982 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360187 | GCCACCTGGGAAATA[C/T]GTTCAGGTCTTCCAT | 337867 |
rs770544158 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227739 | TGTCCACAGTTTATT[G/T]CTGTGCCTCAGGACC | 337867 |
rs770544591 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99333744 | TGAATACATAGTTTT[A/G]TGAGTGTATACTCAC | 337867 |
rs770545638 | snp | C/T | 1.74885e-05 | 0.00295701 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296118 | TTGCAGAGGGCGGAG[C/T]AAAATTGTTTGCCAT | 337867 |
rs770583844 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291532 | GGGCTAATTTAAGAT[A/C]AGTGCTTCCCCTTCT | 337867 |
rs770585282 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226413 | CAACCTCCCTCTTCA[C/T]CTACACCTCCACCCT | 337867 |
rs770586841 | snp | G/T | 1.79978e-05 | 0.00299976 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255895 | CTTGTTGGTAGGCAT[G/T]ATACTTAGAAACTGT | 337867 |
rs770595311 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268416 | CCTGGAGACCATCCT[A/G]GGCAACATAGCAAAA | 337867 |
rs770605332 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378324 | TTGAGGTCAGGAGTT[C/G]GAGACCAGCCTGGCC | 337867 |
rs770631488 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274196 | CATAATAGAGATGTG[A/G]ACTCTTCTGTATCTT | 337867 |
rs770633315 | snp | A/G | 6.64463e-05 | 0.00576357 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314069 | AAAATTCACTATTAT[A/G]GTGATTTTTTTTTAT | 337867 |
rs770642053 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298464 | ATGATGAAAGTACTA[A/C]CTGTGAAAACTGTGG | 337867 |
rs770644404 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336861 | ACCCATAATCCACCA[A/T]GCAGGTACAGACCAT | 337867 |
rs770668422 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310325 | TGACTGACAGATACC[A/G]GTGTCTCAAGAAAAA | 337867 |
rs770671900 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239414 | CATATCTATACTTAC[A/G]TGAAGGTATAATTTA | 337867 |
rs770676340 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323617 | TCAGTGCTTGTCCAA[C/T]GTACACCCCACACAC | 337867 |
rs770690318 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302801 | ATTCTATTAATAATA[C/T]GCTGCTAACCAACTG | 337867 |
rs770692106 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349950 | CGGTCTGCTAAGTAA[C/T]GGGTGTCTTCGCAGA | 337867 |
rs770714276 | snp | C/T | 1.66241e-05 | 0.00288302 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254911 | ATATTGCTTAGTGAC[C/T]GTAGACTACCAGATC | 337867 |
rs770718557 | in-del | -/TCACAGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335155 | TGAACAAATCAACAA[-/TCACAGT]TGAATACTTTGAGAC | 337867 |
rs770723559 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312160 | AACAGTAGAATTGAG[A/T]GGACAGTGCATTTTT | 337867 |
rs770790611 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236403 | TAAAAGTGGGCAAAA[G/T]ATCTGAATAGACATT | 337867 |
rs770790643 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222524 | TGAGGTTAGATCAAA[C/G]GGGTAGCCCATTGGT | 337867 |
rs770805812 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361090 | ATGTCAGAAACTTTT[A/G]CTGCTCCTCGGTTGG | 337867 |
rs770837707 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323112 | TTGCTTGTGCCCAGC[C/T]CTCTCTTCTCTCCGT | 337867 |
rs770864830 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323001 | ATGGAAACAGCATAA[C/G]CTGCTGTGGAAGCAT | 337867 |
rs770878400 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223430 | CCAGCTTTGAGTTTC[A/G]TTGATTTGTCTCTAT | 337867 |
rs770887167 | in-del | -/TTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204907 | TTTCGTTTCCTTTTT[-/TTT]TTTTTTTTTTTTTGC | 337867 |
rs770889284 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386163 | CTGGCCCTCCTGGCT[C/T]GCAGCCAGCCAGCCC | 337867 |
rs770906712 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339170 | CTAATAGACACTCCC[A/G]AGCTCGGGCTGCGCA | 337867 |
rs770907997 | snp | C/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256629 | GTAAATCCAAAAAAG[C/G]AGTATCTAAGACAAG | 337867 |
rs770918432 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267308 | TTTTTTCTCTTACTC[C/G]GTAGGGTGCCTCTTT | 337867 |
rs770919890 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312234 | GGCCAGGAGGGTCCT[A/G]TGTTTCCACAAAAAT | 337867 |
rs770922411 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293582 | GGAGTGAAGGAAAGG[C/T]AGTAAGATTTGGGCT | 337867 |
rs770923051 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292879 | AGTATGTTATATAAT[A/G]AAGTCATGTTCTGTA | 337867 |
rs770926543 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307817 | GACAGTGCTTTTTAC[C/T]TGGAAACTTGGTATC | 337867 |
rs770932117 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346841 | TCCGGATGGAGCAGA[C/T]TTGTTTTCTGTATAT | 337867 |
rs770934602 | snp | C/T | 3.35756e-05 | 0.00409716 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295830 | ACACTAGCGCAGTTA[C/T]CCTACACAAGGCATC | 337867 |
rs770936017 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232057 | TTTTGTACCATGTCT[A/G]CATGTGTATTTATAT | 337867 |
rs770950248 | in-del | -/CA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379841 | AAATCTTTTTCTTAT[-/CA]CTGTTACCCAGAGGG | 337867 |
rs770955574 | snp | G/T | 3.52454e-05 | 0.00419779 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340606 | ATTTAGAAATTCTCA[G/T]TGGCCCAAGCAAATC | 337867 |
rs770974042 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295708 | CACGCCTTTTGCATG[C/T]TCAATCCTTTTTATC | 337867 |
rs770988120 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217665 | GGGTGCCCACCCCGC[A/G]GTGCTTCTCCAGGCC | 337867 |
rs771002259 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306164 | GCCTCCCAAAGTGCT[C/G]GGATTACAGGAGTGA | 337867 |
rs771026225 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219027 | ATGAGAAAGTTACTT[G/T]ATGAGACACCAAGTC | 337867 |
rs771032526 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245308 | CAAAATTAATTTGTA[C/T]GAAGTTAAGCTTCTG | 337867 |
rs771046353 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99229091 | AGGGACGGTGCTAGG[C/T]TTTATGGTGGATGTA | 337867 |
rs771052019 | snp | C/G | 7.62398e-05 | 0.00617366 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200924 | ATGTTCACCAGCACC[C/G]GCTCCAGTGGGCTCT | 337867 |
rs771056369 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235524 | TACTGCCTGACTTCA[A/G]AATATACTACAGAGT | 337867 |
rs771056670 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348049 | GCCTTCTCCAAAGCA[G/T]GTGGCATCTCAGAGT | 337867 |
rs771058931 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335845 | CTTCACCTTCCCTCG[C/G]GACTGTGTGAGAGTT | 337867 |
rs771111132 | snp | C/T | 8.5168e-05 | 0.00652509 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201133 | TTCGGCCTGGAGGGG[C/T]GAATGGGGACAAAGC | 337867 |
rs771132347 | in-del | -/A | 1.64788e-05 | 0.00287039 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255593 | CTCCAAGAATCTGGC[-/A]GAAGTACTCTCCAAA | 337867 |
rs771182443 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288328 | GAAAGTAACGTGGCC[C/T]CTGCTCTGGAGTGGT | 337867 |
rs771184049 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213664 | TGCACCCGGTCGATT[A/G]TAACATTTTATCGTA | 337867 |
rs771212065 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255536 | CAGCACTAATAAAGG[C/T]AAGAAGCCATAAAGC | 337867 |
rs771213998 | snp | A/G | 3.31329e-05 | 0.00407005 | missense, synonymous-codon, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238534 | GTGTATGACCTTCAC[A/G]CAGTCAAGAACGACT | 337867 |
rs771214165 | in-del | -/CTTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369431 | CCGTTCTGTTTTTCA[-/CTTG]CAGCACGATACTCAA | 337867 |
rs771237434 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276878 | TACATTTTTGTAGAA[C/T]ACCACAGCCAGCCAG | 337867 |
rs771247505 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385464 | AGGGAGGTTCCACCG[C/T]ACCCCTGCCCTCAAC | 337867 |
rs771250036 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246373 | TTATTGGGGAAAATA[A/G]TGTAGTCATCAGGAA | 337867 |
rs771256422 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331405 | GGAAAAGCCTAGAGC[A/T]GGTTTCTAAGACAGT | 337867 |
rs771267046 | snp | C/G | 1.81391e-05 | 0.00301152 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99243950 | GAAGCAGAAAATTTG[C/G]AGTAAGTTTTTATGT | 337867 |
rs771280549 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325801 | AGTATTTGTCTTTCC[A/G]TGACTGGCTTGTTTC | 337867 |
rs771286084 | snp | A/T | 0.000182183 | 0.00954244 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200722 | TCCCCGGCAGGAAGG[A/T]GGGCGCTGACCCAGC | 337867 |
rs771286531 | snp | A/C/T | 1.69965e-05 | 0.00291513 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385371 | GACCGGACCGGCAGC[A/C/T]GAGTGACAGTGCGTG | 337867 |
rs771315891 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202220 | AACTTCTCAGGTTTT[C/G]AAGTGGTTTCAATAT | 337867 |
rs771322863 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318101 | TTTTACACCCAATTC[C/T]CTCTCTCTCCTGTAA | 337867 |
rs771325627 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208846 | TCAGTGGGCTCTTCA[C/G]AGACTCCCGACTTCT | 337867 |
rs771340457 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267830 | GGATATTTCAGTAAT[-/G]GTGGAGGCTAAGCTT | 337867 |
rs771341952 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198476 | GGCGGGCAAATGTCT[C/T]TAATGTCTGGTTCAA | 337867 |
rs771362169 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278712 | ATAGATATTTTAGAT[A/C]TCTTCTCTCCTTTAA | 337867 |
rs771381315 | snp | A/G | 1.66377e-05 | 0.00288419 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314238 | ACAGTATGCATTTTT[A/G]TGTTCACTTTTCTTT | 337867 |
rs771384072 | snp | A/G | 4.94303e-05 | 0.00497119 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295219 | CCCTTTACATGCAAA[A/G]AAGTAGATAAAAGGG | 337867 |
rs771385111 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239411 | TCCATATCTATACTT[-/A]ACGTGAAGGTATAAT | 337867 |
rs771400174 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336731 | GGACTTACGTTTCTT[C/T]AAAATTGCCTTGCCT | 337867 |
rs771414193 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370968 | GTCAAGTTCAGCTGA[A/G]AAGAAATATCAAAAT | 337867 |
rs771435262 | snp | G/T | 8.23798e-05 | 0.00641741 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255125 | GGAAAGCGAAACAGA[G/T]GTGGAAGGGCATAAA | 337867 |
rs771456387 | snp | A/T | 1.65449e-05 | 0.00287614 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295089 | AAGACTTGGAATGTA[A/T]CATCATCTGCGTTTC | 337867 |
rs771463552 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343867 | ACGAGTACCGTACAG[A/G]GTGCAGTTGTATTGG | 337867 |
rs771473406 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283481 | TGAACAATTTTGTAC[C/T]GTAGAGCCTTGTTTG | 337867 |
rs771473420 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220206 | ATATTAGAAAGAAAT[A/G]GTTTCTTTATAGTCA | 337867 |
rs771476092 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205981 | TGTGTATTCTGGTAG[G/T]TTGTGTCAATAAAGC | 337867 |
rs771515546 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297077 | TCCAATGTGTCAATG[C/T]ATAATTTGCTTAGCT | 337867 |
rs771520550 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251000 | GTGATCAGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 337867 |
rs771536922 | in-del | -/CAGTGAGCCAAGAATG | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262643 | GGGAGATGGAGGTTG[-/CAGTGAGCCAAGAATG]CAGTGAGCTGAGGCT | 337867 |
rs771540648 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99318052 | TCCTACATCTGGATT[G/T]TAGCCATAAGTGGAC | 337867 |
rs771548719 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265703 | GGCCCTCAGTTAACA[A/G]GCATATGGATTCGAC | 337867 |
rs771555580 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361564 | GCCTTTGCATGTTTT[C/T]GTATCTTTACTACAT | 337867 |
rs771571146 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364006 | CAATAGAGGGAATGT[C/T]ACTTTTTAATCATAC | 337867 |
rs771579815 | snp | C/T | 1.71319e-05 | 0.00292672 | intron-variant, synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201456 | GTTTTTAGACAAACA[C/T]ACACTGATGAGAGTG | 337867 |
rs771597971 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348708 | GTCATAATATGAACG[C/T]TGTCTGAAGGGATGA | 337867 |
rs771608551 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362406 | AGTTGCCAGGTCATA[C/G]ACTAGAATAGTTTCA | 337867 |
rs771611060 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304824 | CAGAAGTCACATTCA[A/G]TACAATACATTTTAT | 337867 |
rs771615863 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323711 | TATGCTACCTTTCCC[A/T]CTCCTGACCACAGGG | 337867 |
rs771620687 | in-del | -/TTC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219650 | TGTGGCCCAAGATAA[-/TTC]TTCTTTTCCAGTGTG | 337867 |
rs771665561 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371977 | TTTTTAGTTCTTCAG[A/G]ATCCACTCCCGTTTT | 337867 |
rs771666108 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99293010 | CAGTGAGAGGATGCC[C/T]ACAGCCGTGTATGAA | 337867 |
rs771668133 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216394 | ACAGGTGTGAGCCAC[C/T]GTGCCCGGCCCAGTG | 337867 |
rs771678454 | snp | G/T | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367810 | GATCAATTGGAATCG[G/T]CTTTTTCCTCCTTTA | 337867 |
rs771698443 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262170 | CACAGTGTCACAGTG[C/T]TTGTGTTCCAGTAAC | 337867 |
rs771701077 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224655 | CCATATACCCACCAC[A/C]TAGATTCTACACAAT | 337867 |
rs771706957 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340804 | CTTGTTCCACCTATA[C/T]TAGATAAGCATGACT | 337867 |
rs771716787 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263336 | GGATCTCTGCCATTC[C/G]ATGGCCAAAAGACTT | 337867 |
rs771716920 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249687 | TTCCCTTTTCTCACT[C/T]ATATACAACAGTGTA | 337867 |
rs771718157 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328955 | AGTTTCTGCTATTAC[A/G]TTTAGGTCTGTGATC | 337867 |
rs771798615 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203061 | ATTTATTTATTGAGA[-/T]TGGAGTCTCACTGTT | 337867 |
rs771815746 | snp | G/T | 1.65496e-05 | 0.00287655 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99296008 | TAGTAAGTTTCCCAC[G/T]AGCCCAATGATGAAG | 337867 |
rs771816007 | snp | A/G | 1.6517e-05 | 0.00287372 | intron-variant, stop-gained, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201528 | GCAGCTGTGCTGCTG[A/G]ATGTTGCTGTTTTCC | 337867 |
rs771822439 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345351 | TCATTTTATTGCACA[A/G]TGTAAGATGGACGGG | 337867 |
rs771846768 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312447 | TCATTCATATTACCT[G/T]CCTAGCACTTGTAGG | 337867 |
rs771895410 | in-del | -/AG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377054 | AGCACAGTCTTTTCC[-/AG]AGTCTCAGTGTCCTA | 337867 |
rs771930913 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211853 | GTCATTGGAAACTGC[A/G]TCATTGTGTCCTGGC | 337867 |
rs771936052 | snp | A/T | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351446 | TCTTGCCTCTTTATC[A/T]TCCAAACCTAAAATG | 337867 |
rs771937842 | in-del | -/AAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241266 | TGAGACCCTGTCTCA[-/AAA]AAAAAAAAAAAAAAA | 337867 |
rs771950732 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369268 | TGACCTATAATTGTC[A/G]AACTTTAACAATTTT | 337867 |
rs771953548 | snp | A/C | 1.64879e-05 | 0.00287118 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255673 | ATAAATATCAAGTCC[A/C]CTAATGCCACATTCA | 337867 |
rs771991092 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349447 | AGAAAACAGCTGGGC[C/G]CGAGGGACCACTGCC | 337867 |
rs772005424 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267118 | ATTTCCATTTCCGAT[C/G]ATGAGTGACTTCAAG | 337867 |
rs772012318 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236544 | GAATGGCTTTTATCA[A/G]AAAGACAGGAATAAC | 337867 |
rs772013140 | snp | C/T | 3.29685e-05 | 0.00405995 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340325 | TTTCTTCTAGATGTC[C/T]GGTCTGTGCTACGAC | 337867 |
rs772018668 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200823 | GATTCGTCGCTCCGC[C/G]AAGAGTGCGCCTGCG | 337867 |
rs772038734 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268700 | TGAGTCTTAAAAATC[A/G]GCTGTAGAGGCACTG | 337867 |
rs772040295 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377396 | CTGTGGATGTTAGAT[C/T]GGATCAGGTGCTCAT | 337867 |
rs772072027 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282533 | CATTTGAGTGTGTCA[A/G]AATTTCCAGTCTAAT | 337867 |
rs772073119 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270356 | GAACCACAGACTGTT[G/T]TCACTAGAATGCACA | 337867 |
rs772079575 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339272 | AAGATCTTCGCTCAA[A/G]TATCACTTTCTCTGA | 337867 |
rs772082766 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336857 | ATATACCCATAATCC[A/T]CCATGCAGGTACAGA | 337867 |
rs772091491 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365384 | ACTTCTTAAATTGGG[C/T]ATAGTTAACCCTTTA | 337867 |
rs772151061 | snp | C/G | | | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254434 | CCTTGTAGTAAGTAA[C/G]AGTAATGAGTTCAAC | 337867 |
rs772160150 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208951 | GACTCCTCAGCACCT[A/G]GGAACTTAGATCCCC | 337867 |
rs772172810 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99298856 | CAGGCAAGGGTTGCA[A/G]CTTTGGAATAGGCAA | 337867 |
rs772182986 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284939 | AAATTTCAGTGACAC[-/A]AAGCAGAGAGAATAA | 337867 |
rs772209273 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325968 | TAGGTTGTTTCCCCA[C/T]GTTGGCTATTGCAAA | 337867 |
rs772210936 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360367 | CACATGAATTAACTC[-/TT]TTGATTCTCATACTC | 337867 |
rs772217641 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278005 | CTGCTGTTCTCGATG[A/C]GCAGATTAATGTAGG | 337867 |
rs772219231 | in-del | -/CTT/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207994 | CCTCTCATCGTCTCT[-/CTT/TT]TTTTTTTTTTTTTTT | 337867 |
rs772222254 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255386 | TGGAGTCTTTATCTG[A/G]GTCTTTATAGAGCAG | 337867 |
rs772239825 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308809 | TGTGTATAAAATAAA[C/G]GTATTGAACTAAATG | 337867 |
rs772271862 | in-del | -/TGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373170 | CTCTCTCTTTTTTAT[-/TGT]TTTTTTTTTTTTTTT | 337867 |
rs772277565 | snp | C/T | 1.65386e-05 | 0.00287559 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238418 | AAGTGCTTTCCTTTT[C/T]CCCTCCAGACAAGGC | 337867 |
rs772288944 | in-del | -/TTTTTTGTG | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325271 | CCATGCCCAGCTAAT[-/TTTTTTGTG]TTTTTTGTAGAGACG | 337867 |
rs772314647 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322310 | TCTTCTTGTGGTTCT[G/T]CAGAGAGCTTTTGAG | 337867 |
rs772341102 | in-del | -/TGA | | | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386759 | GTTGCAAGGAACAGT[-/TGA]TGGTGGTGGAGATGT | 337867 |
rs772342420 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219350 | TCAGTTAAAATTGGC[C/T]ATTTTAACCATTTAA | 337867 |
rs772346481 | snp | A/G | 0.000115472 | 0.00759756 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295696 | GACAAATATGCACAC[A/G]CCTTTTGCATGTTCA | 337867 |
rs772398940 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207650 | GTAGGGAGCCTTGGG[C/T]CAGATGCAGTTAGAG | 337867 |
rs772400483 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233690 | AGTGATACCGAGATA[C/T]AAGGAGAATGAAGAC | 337867 |
rs772402107 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308079 | ACTCATGCCATTCAC[C/T]TCATAGTTGTAGTTG | 337867 |
rs772429767 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316579 | TCCAATACTTAAATC[A/G]GTATCACCCACTGGG | 337867 |
rs772435955 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323086 | TAGGTGTGAGTTCCT[C/T]TGCGCCGCCTTTGCT | 337867 |
rs772441588 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315511 | TTTATTAATTGTGGA[C/G]TAGGAGTTCAGTGTG | 337867 |
rs772443312 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373420 | GATGAGCAAATTTCA[A/G]CTTCCTCTCTTCGAT | 337867 |
rs772456977 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284440 | AGAAAAGTTGCAAGG[A/G]TAAAACAAAGAACTC | 337867 |
rs772491845 | snp | C/G | 1.65225e-05 | 0.00287419 | synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238497 | GCTCGCCCTCCTCCT[C/G]CCTCACTGCCAGAAG | 337867 |
rs772492839 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198584 | GAAAACCTGGCTTCA[C/T]CTAGATACACCCCCA | 337867 |
rs772498130 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303877 | ACTCAAGGCAGGGGT[C/T]GTGAAGGCGCCCAGG | 337867 |
rs772503811 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227820 | TTGAGAATACCAAAG[C/T]AAACCGTTCATTTAT | 337867 |
rs772507419 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272808 | TAGTGCTTCAACATA[A/T]GAATTTAGGGGTGGG | 337867 |
rs772513512 | snp | C/G | 1.64836e-05 | 0.0028708 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314226 | GGGACTGCAGGTACA[C/G]TATGCATTTTTATGT | 337867 |
rs772516180 | snp | A/G | 1.65477e-05 | 0.00287638 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367954 | AAATCCATGTTTCAG[A/G]GTTGAAGCAGTTTCG | 337867 |
rs772522594 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215570 | TTCAAGTCCCTCTGC[A/G]GTGAGGTACTCCAGG | 337867 |
rs772550177 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217610 | CTGTTACCCGCGCTC[A/G]CCCTGGCATGCAGCC | 337867 |
rs772556140 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291012 | AGGGTGGAACCTCTT[-/A]ACTAACCAAGTTTCA | 337867 |
rs772557298 | in-del | -/GTTTAGCAGTCTACT | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303236 | CAAGACTGAAAAAGG[-/GTTTAGCAGTCTACT]GTTTCCTCTTTGTGC | 337867 |
rs772611996 | in-del | -/C | 0.000111111 | 0.00745273 | utr-variant-5-prime, upstream-variant-2KB, frameshift-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200896 | CTCTGGGGCTCCGAG[-/C]CCCGGCGGGACCATG | 337867 |
rs772640552 | in-del | -/CT | | | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258335 | GTTTCCAGTGTAACG[-/CT]TGGCGTCGGAGTTGG | 337867 |
rs772654489 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290080 | TGCAGACCATGGAGC[C/G]AGACCCCAGAGTGTA | 337867 |
rs772677488 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385236 | CCTGCAGGTCGCCCG[A/G]CTCATGGAGATGGGA | 337867 |
rs772681490 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238712 | CTTTTCTAGTTATTG[A/G]TTTTTCAGCAAAACA | 337867 |
rs772712959 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288484 | AATTTATTGTATTGC[C/T]CTCTTAAACAGCTTC | 337867 |
rs772721020 | snp | A/G | 6.8018e-05 | 0.00583132 | intron-variant, synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201459 | TTTAGACAAACACAC[A/G]CTGATGAGAGTGCTT | 337867 |
rs772730651 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353855 | CCTTGATTTCGTGCA[A/G]CCCCCAAGGTTTCAG | 337867 |
rs772736453 | snp | A/T | 1.65165e-05 | 0.00287367 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201529 | CAGCTGTGCTGCTGG[A/T]TGTTGCTGTTTTCCT | 337867 |
rs772738152 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257122 | TTCTTCCCTTCTTCT[C/T]CTTCTTTCCTTCTCA | 337867 |
rs772744547 | snp | C/G | 1.64876e-05 | 0.00287116 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255683 | AGTCCACTAATGCCA[C/G]ATTCATCATATAGAT | 337867 |
rs772750118 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214460 | GTATGCAAGGAATAT[G/T]AATAGGCTGGTTTGC | 337867 |
rs772774470 | snp | A/G | 3.30814e-05 | 0.00406689 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356207 | TTCCCGATGTACTCT[A/G]TAGATGTCTTTGCAC | 337867 |
rs772779557 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302736 | GCTGTGGAGCTGTGA[C/G]CAGCATAGTCAGAGC | 337867 |
rs772848158 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225113 | TTATTAGTTCAGTAA[A/G]TATTTGCTTATATTT | 337867 |
rs772851284 | in-del | -/TCTC | 0.000181283 | 0.00951887 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318099 | CCTTTTACACCCAAT[-/TCTC]TCTCTCTCCTGTAAA | 337867 |
rs772864568 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213407 | GCTCTGTCGTCCAGC[C/T]TGGAGTGCAATGGTG | 337867 |
rs772902934 | in-del | -/CCC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347320 | TACTATCCCCGGGCG[-/CCC]CCCCCCCCCCCCAGG | 337867 |
rs772903963 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380582 | GCACTGCACTGCACC[C/T]CTCCACTGGGGAGTA | 337867 |
rs772954926 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369732 | AATTCTACAGAAGAG[A/C]AATTGGACACCACCT | 337867 |
rs772980659 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347035 | GTAATCCCAGCACTT[G/T]GGGAAGCCCAGGCGG | 337867 |
rs772983750 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342444 | GGCCCAGCATAGTCT[C/T]GGCGCTGAGTGACTG | 337867 |
rs772991358 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278177 | TTGGTTATTTAGACC[A/T]ATTTAAAAGAATCCA | 337867 |
rs773023649 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99301306 | TTCAAGGCTCCTGTA[C/T]CTTCTGCTGGGAGCC | 337867 |
rs773034513 | in-del | -/TTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211391 | CAATGGCAATATGAC[-/TTG]TTAAGTGCTAGGACA | 337867 |
rs773042777 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335596 | GAAGATGAGCGCAAC[-/AT]GTGATACCTTCTATG | 337867 |
rs773044444 | snp | A/G | 3.29576e-05 | 0.00405928 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340446 | TCAGAACCCACCAGC[A/G]AAGCCAGAATTGGGA | 337867 |
rs773052777 | in-del | -/TTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204902 | GGGAGTTTCGTTTCC[-/TTTTTTTT]TTTTTTTTTTTTTGC | 337867 |
rs773059297 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309352 | TTGACCTCATGATCT[G/T]CCTGCATTGGCCTCC | 337867 |
rs773059850 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267217 | TTGCCCATTTGTTAA[C/T]CTTTCTTGGTTGTTG | 337867 |
rs773067864 | snp | A/G | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340326 | TTCTTCTAGATGTCC[A/G]GTCTGTGCTACGACA | 337867 |
rs773090634 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321281 | AGCTTATTTTATTTA[A/G]CTAGGTACTGGTTGA | 337867 |
rs773102924 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306365 | ACTCCCCATTTTACA[A/G]GTAAAGCAGCTGAAG | 337867 |
rs773112224 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297263 | CAATAAATCCTGTGT[A/G]ATTATTTTTAAAAGA | 337867 |
rs773134509 | in-del | -/G | 1.64787e-05 | 0.00287038 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255550 | GCAAGAAGCCATAAA[-/G]CAATGCTTGGGTAAA | 337867 |
rs773143488 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322502 | TTTTACAGTTCACAC[A/G]TTTATCTTTACTTGA | 337867 |
rs773145839 | snp | G/T | 1.66651e-05 | 0.00288657 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295426 | TGTGTTGAGAGCCTT[G/T]TTGTTTACACCAGAT | 337867 |
rs773150538 | in-del | -/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304658 | GTGTTCCAGGCACTG[-/C]CCCTGGGCACTCTAT | 337867 |
rs773157019 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305376 | ACCACGCGTCCTCTA[C/T]ACAGGCCACGTCCAG | 337867 |
rs773192014 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239275 | GTCTTTTAGTTATTT[A/G]TCCGTATTACTGATT | 337867 |
rs773245543 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345935 | TTTAGTAAAGACGGG[G/T]TTTCACCATGTTGGC | 337867 |
rs773250986 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368033 | CAGCAGTCCATCTGC[C/T]ACCATGATAGAGACT | 337867 |
rs773252636 | snp | C/G | 1.6777e-05 | 0.00289624 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254902 | TCACTGTTTATATTG[C/G]TTAGTGACCGTAGAC | 337867 |
rs773270677 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99360131 | GGCACCAACTTGTAC[A/G]AGCAGTCAGCTCAGG | 337867 |
rs773281961 | in-del | -/AC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244402 | CATGTGTGTATATAC[-/AC]ACACACACACATACA | 337867 |
rs773306281 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233902 | ATGTTTTTGTAACCA[A/C]ATCTGCTGGTACCAC | 337867 |
rs773308226 | snp | C/T | 0.000273112 | 0.0116825 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200869 | GCACTTCAGCTTCCC[C/T]TCCCCCGGCGCCCTC | 337867 |
rs773314899 | snp | A/G | 3.08675e-05 | 0.00392846 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200789 | CCGTTCGTCAGCGGC[A/G]AGTGGCCTCGCGGCG | 337867 |
rs773324804 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316985 | ATGGTTCCATCCTTA[C/T]TATTATCAGAGTCAT | 337867 |
rs773338645 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348338 | CTGTGCAAAGAGAAG[A/G]AAAAAGAACCCTGAG | 337867 |
rs773347902 | snp | A/C/G | 3.30127e-05 | 0.00406269 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385309 | AATGACCTCAATGTC[A/C/G]CCACCAACTTCCTGC | 337867 |
rs773352795 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355375 | GCCACTGTCTCAGTC[C/G]TCGCTGTGTGGCCCT | 337867 |
rs773356360 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199749 | ATTGTGCAACCATCT[A/T]ATCAGGGTAATTAGC | 337867 |
rs773362812 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243339 | TTTCAAACCTAGTCA[C/T]ATTTAGCAGCAGTTG | 337867 |
rs773370310 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234172 | TGTGCTAGCCGTTTC[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 337867 |
rs773375308 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275784 | TTTGGATTTAAGATC[C/T]AGCTTTTTAAAAGCT | 337867 |
rs773388616 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306051 | TAGGTGAGTGCCACC[A/G]TGCCTGGCTAACTTT | 337867 |
rs773392323 | snp | G/T | 1.65348e-05 | 0.00287526 | missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238512 | GCCTCACTGCCAGAA[G/T]CTCTTTGTGTATGAC | 337867 |
rs773410647 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207860 | AATGGACACCAACAT[C/T]GACTCCTGAGGCTCT | 337867 |
rs773421789 | in-del | -/TCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249864 | TTGGCCGCTTGCGTG[-/TCT]TCTTTTGAAAAGTAT | 337867 |
rs773431473 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325288 | TTTTGTGTTTTTTGT[A/G]GAGACGGGGTTTCAC | 337867 |
rs773436092 | in-del | -/GT | 1.69384e-05 | 0.00291014 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201617 | GGCTTTTCTCACTGA[-/GT]GTGTGGAATTGACTT | 337867 |
rs773462379 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255393 | TTTATCTGGGTCTTT[A/G]TAGAGCAGTAGCAGA | 337867 |
rs773479420 | snp | A/C | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356402 | GTTGGAAACTTCTGT[A/C]CCCTAAGCCAAAAGG | 337867 |
rs773496055 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263876 | TGTTAAGTTGAAAAA[A/G]CCAGACATGAAGGAA | 337867 |
rs773500767 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237698 | CGTGGCCCATGCCTG[C/T]AATCCCAGCACTTTG | 337867 |
rs773507850 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282847 | TACAGCACACAAAAA[A/T]AATCTCATACCTGTC | 337867 |
rs773515717 | snp | A/G | 0.000115673 | 0.00760415 | synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238434 | CCCTCCAGACAAGGC[A/G]CCTCTGTCGAAGAGC | 337867 |
rs773517280 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314115 | GGCACCTGTGTTTGC[C/T]CTGTTTGTACCATTT | 337867 |
rs773537226 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291191 | GTAGTGAGGGTTAAA[G/T]AAGATGATGCCTGTA | 337867 |
rs773568961 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274139 | AGAAGTCTACACTGA[C/G]TTTTAACACCCTGAT | 337867 |
rs773584064 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330316 | ATACAAAAATTAGCC[A/C]GGCTTGGTGGCGGAT | 337867 |
rs773594548 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335807 | ACTTGGTGTTGCCAC[A/G]TTGCTCCCCAGAGGC | 337867 |
rs773625551 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252431 | AGACTGTAAGGGAAG[A/G]CCTTTGAACCACAGA | 337867 |
rs773659061 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346816 | ACTGCCCTTTCTCCA[C/T]CAGTGTGTCTCCGGA | 337867 |
rs773672493 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259442 | ATACTTTTGATTGTT[A/G]CAACCTGCCAGAATG | 337867 |
rs773701321 | in-del | -/T/TT/TTT | 0.619594 | 0.1775 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314262 | TTCTTTAACCAGATC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 337867 |
rs773704914 | in-del | -/AGTT | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201658 | AGACTGCGTGTTAAC[-/AGTT]AGTTAGGCACGGGTA | 337867 |
rs773711764 | snp | A/G | 1.64876e-05 | 0.00287116 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314230 | CTGCAGGTACAGTAT[A/G]CATTTTTATGTTCAC | 337867 |
rs773712081 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254990 | CACTAATGACTCGAG[C/T]CTGAAATTGTTTTGA | 337867 |
rs773716054 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335006 | AAAGTAGACTTCTCT[A/T]TGAGTATTACTAAAA | 337867 |
rs773736681 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294812 | GGGAGTTATTAAGAG[C/T]GCCTCCTTTTGGTGT | 337867 |
rs773737252 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363863 | AGGCTCAATTCAGGA[A/T]CATGCTGAATCTTTC | 337867 |
rs773750160 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99243233 | GCCTTTGAGTAGCTC[-/T]TTTTTTTTTTTTTTT | 337867 |
rs773766771 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217643 | CTGGTGTCTCAGCTG[C/T]GCTGATGGGTGCCCA | 337867 |
rs773771128 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324235 | TCAAAATATGTTCTG[C/T]CCCTCTCTACTGAAG | 337867 |
rs773773228 | snp | A/G | 1.65658e-05 | 0.00287795 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295086 | TTGAAGACTTGGAAT[A/G]TATCATCATCTGCGT | 337867 |
rs773795295 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280432 | CTTCTACCAAGAAAA[C/T]AAGGAGAACTTCAAG | 337867 |
rs773800762 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99264558 | TGGGACTGGATAGCT[C/G]TGCAGGAGCCCAGCA | 337867 |
rs773809447 | snp | A/G | 0.000369617 | 0.0135894 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351885 | TGTGTTTTGCCTGCA[A/G]GGAAAGAAGCTACTG | 337867 |
rs773814638 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205184 | TGGGATTATAGGCGT[C/G]AGCCACTGTGCCCGG | 337867 |
rs773837678 | snp | C/T | | | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255028 | TAGTAGAGAATCACA[C/T]CCAGACACGTGCTGA | 337867 |
rs773841206 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322583 | CTTCTCCCTTCAACG[C/T]AGCCCTTCACTGTAC | 337867 |
rs773870004 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207134 | TTAGTGGCACCCCTC[C/T]CTGAGTTGGGAGTCT | 337867 |
rs773872948 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214677 | TTACCCCAAGCTCTC[C/T]TCTACTTTTTTGCAG | 337867 |
rs773878235 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271474 | ATGAGGCCAGGGAGG[-/T]TAAGAGTGGTCACTG | 337867 |
rs773886281 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309505 | TATATTAGATCATTT[A/C]ATGAGCTCACAAACC | 337867 |
rs773898833 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363076 | GGTGGTGTGAAGTAA[A/G]GGCCTAGTTTTATCT | 337867 |
rs773906701 | snp | A/G/T | 3.29681e-05 | 0.00405995 | missense, synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255078 | AAAGGCTCCCCAGGG[A/G/T]TTGTAACTGTTCTCC | 337867 |
rs773920225 | snp | G/T | 3.29592e-05 | 0.00405938 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255555 | AAGCCATAAAGCAAT[G/T]CTTGGGTAAAACACT | 337867 |
rs773937537 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291601 | CTGTCTGCCCTTGCC[C/T]CTTGAAATATAAAAT | 337867 |
rs773941066 | snp | A/T | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260837 | AAGAGGGATTTTACT[A/T]ATTCCCAGAGACTGC | 337867 |
rs773963673 | snp | C/T | 6.59109e-05 | 0.0057403 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255116 | CCAGCATCAGGAAAG[C/T]GAAACAGATGTGGAA | 337867 |
rs773963892 | snp | C/T | 3.10169e-05 | 0.00393795 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201363 | CCCCCCGCCCCCACT[C/T]GCAAAGTTCAGCCTC | 337867 |
rs773973408 | snp | C/T | 0.000162853 | 0.0090222 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351520 | CTGTAGAAGGTTATA[C/T]AGCCAGCAGCTTTCA | 337867 |
rs773987634 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357302 | GTCACCCAACAGCAC[-/AT]TTCTCAGAATGAAGC | 337867 |
rs774009005 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343617 | CTTGCTGGGCTTTTA[C/T]GTTGAGTGGTCTGCT | 337867 |
rs774018277 | snp | C/T | 1.79457e-05 | 0.00299542 | intron-variant, synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201445 | CTCCAAGAAGAGTTT[C/T]TAGACAAACACACAC | 337867 |
rs774045601 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347316 | ACGTTACTATCCCCG[G/T]GCGCCCCCCCCCCCC | 337867 |
rs774046292 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379393 | TTGGCAAACTCACCA[A/G]TGAATTTCTTTGCTG | 337867 |
rs774071072 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299752 | GTTGTGTACCTTTGC[A/G]TTGTGTCATCATGTA | 337867 |
rs774089376 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235599 | AGTGGAGCAGATTAG[A/T]AGACCAAGATACAAA | 337867 |
rs774094847 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234394 | GGGGTTTCGCCATGT[C/T]GGCCAGGCTGGTCTC | 337867 |
rs774097727 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349847 | TTCGGATGACTGCGG[A/G]CAGACTGGGATAATA | 337867 |
rs774110094 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267397 | TATCATATTTTGATG[A/T]TAAGGATGAATTTCA | 337867 |
rs774125037 | snp | C/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327482 | GGTTTTTCTCTCTCT[C/G]TCTGTGTGTGTGTGT | 337867 |
rs774165033 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376956 | TGAAGCCAACACTGA[C/T]GAAGTTGCAGTATGC | 337867 |
rs774174166 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290448 | AAAACAGGCAAGGCC[A/G]GGCGCAGTGGTTTAC | 337867 |
rs774185481 | snp | C/T | 1.71605e-05 | 0.00292915 | missense, intron-variant, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99244587 | GCTATGCAGTATTTC[C/T]TTGGCATCACTGCAG | 337867 |
rs774187999 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309681 | TCTTGGCTCACTGCA[A/C]CCTCTGCCTCCTGGG | 337867 |
rs774192368 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256631 | AAATCCAAAAAAGGA[A/G]TATCTAAGACAAGTA | 337867 |
rs774218952 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99214730 | TCCTTAAGCAGATTG[-/T]CCCCCACCCCACCCT | 337867 |
rs774228340 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294928 | CTTCCGAGTTGGAGA[C/T]GGGAAAGTGCCCAAT | 337867 |
rs774234534 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200775 | ATGCGCCGGGTGCGC[A/C]GTTCGTCAGCGGCGA | 337867 |
rs774235725 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366848 | CCACGCCCACTTGTT[C/T]CTGAGGCCTTGCAAC | 337867 |
rs774243122 | in-del | -/TC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207991 | TTGCCTCTCATCGTC[-/TC]TCTTTTTTTTTTTTT | 337867 |
rs774259880 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285659 | GGCCTCCCAGAGTGT[C/T]GGGATTATAGGCATG | 337867 |
rs774264447 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339203 | ATCTGCTGCTTTCTC[C/T]GCCCAAAATGTTATT | 337867 |
rs774278507 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361343 | TCATATTTAACCCTA[C/T]GTAAAGAGCAGATTC | 337867 |
rs774283657 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234174 | GTGCTAGCCGTTTCT[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 337867 |
rs774289478 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272042 | TGTTGTTTCAGCAGA[-/C]TATAAATGGAATATT | 337867 |
rs774299675 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217873 | CGAGCTCGTGCCCAC[C/T]TTCTTGCCATCGACT | 337867 |
rs774323234 | snp | A/T | 2.36354e-05 | 0.0034376 | intron-variant | UBAC2 | GRCh38.p7 | 13:99244475 | TAGTTTATTTTTAGG[A/T]GACTCATCTCTATCA | 337867 |
rs774329900 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210734 | TGCCTGCCTTGGCCT[C/T]CTAAAGTGCTGGGAT | 337867 |
rs774332443 | snp | A/C | 1.64773e-05 | 0.00287026 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295271 | ATCAGGCATACTGTA[A/C]AGTGCAGAGAAATCT | 337867 |
rs774338816 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207163 | CTTTACCTGCTGCTG[C/T]GTTGACCTGGGGGTT | 337867 |
rs774352675 | snp | C/T | 3.29603e-05 | 0.00405944 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255570 | GCTTGGGTAAAACAC[C/T]GTGAGAGCTCCAAGA | 337867 |
rs774362976 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221267 | TGGATCTGTGTTGCA[A/G]CCTCCACAAACTGCA | 337867 |
rs774365615 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201685 | GGTACAGCAACGGAG[A/G]ACAGCTCTAATTTTG | 337867 |
rs774379721 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357390 | CAGTCCTGAAGTGCT[G/T]CTTGTTTAGTTTTTA | 337867 |
rs774394516 | snp | C/T | 1.64803e-05 | 0.00287052 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318109 | CCAATTCTCTCTCTC[C/T]CCTGTAAAAACATTA | 337867 |
rs774396380 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335903 | CTCACACCTGGAATC[C/T]CAGCACTTAGGGAGG | 337867 |
rs774400927 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378386 | ACAAAAATTAGCCAG[A/G]CATGGTGGCACATGC | 337867 |
rs774410120 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276982 | CTGCAACCTTTGGGA[A/T]GTCAAATGTTAATCA | 337867 |
rs774440060 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99229108 | TTATGGTGGATGTAG[C/T]GAAGGGTAAGGCATG | 337867 |
rs774450634 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222543 | TAGCCCATTGGTAAT[G/T]ACATAGCAGTAAGTG | 337867 |
rs774451554 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219031 | GAAAGTTACTTTATG[A/G]GACACCAAGTCACCC | 337867 |
rs774468490 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348097 | CTGTGATCATCTTTA[C/T]ACTGCCAGGGCCATT | 337867 |
rs774469999 | snp | A/G | 1.66579e-05 | 0.00288595 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295538 | GGAAGTACATATCCT[A/G]TGAAACATGCCCCAA | 337867 |
rs774483995 | snp | A/G | 1.6546e-05 | 0.00287624 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340303 | TTAAACAATCACATT[A/G]GACGTTTTTCTTCTA | 337867 |
rs774485975 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99231077 | TCTTGTGATTGCATA[C/G]AATCCAGCTGGATAT | 337867 |
rs774486782 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374755 | AAGCATGGCAGCACA[C/T]TGGGTATTGGGTTAG | 337867 |
rs774489073 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270118 | TAAACCTAAGAATGA[-/T]TTTTTAGTTCTGATT | 337867 |
rs774505822 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307984 | GTCAGAGGCTGTGTG[A/C]GTACTTGAATAACAG | 337867 |
rs774516642 | in-del | -/TA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373188 | TTTTTTTTTTTTTTT[-/TA]AACAGGTATCTTTAT | 337867 |
rs774523251 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375541 | CCGTCTTCAGGTGGG[C/T]ATCGCTTTCTGCAAG | 337867 |
rs774527819 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198536 | TCTGCTTTCAGTTTG[C/T]TGGGATACATTGCTT | 337867 |
rs774552277 | in-del | -/AC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244401 | TGCATGTGTGTATAT[-/AC]ACACACACACATACA | 337867 |
rs774554168 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265746 | TTTTCTGTAAGAAAG[A/G]TTATGCCATGTCTCA | 337867 |
rs774555038 | in-del | -/TTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382302 | TGTAGAGTCCTAGAC[-/TTT]TTAAAAGGTCAGGTA | 337867 |
rs774575965 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232085 | TATAGGTTAATGTGT[A/G]TTACTTGTTTTTTAA | 337867 |
rs774582362 | snp | C/T | 0.000331219 | 0.0128647 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295390 | GAAACAGAGAACAAA[C/T]ACAACAATAATAAGA | 337867 |
rs774597801 | in-del | -/TTCTTTTTTTTTTTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99287641 | TTCTTTTTTTTTTCT[-/TTCTTTTTTTTTTTTT]TTTTTTTTGGTAGAG | 337867 |
rs774624914 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346913 | GGGAATTAATGAGCA[A/G]ATATGAGCATAATAA | 337867 |
rs774631614 | snp | C/T | 0.000469594 | 0.0153159 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200859 | GCTGGGGCTCGCACT[C/T]CAGCTTCCCCTCCCC | 337867 |
rs774634231 | snp | A/G | 1.64806e-05 | 0.00287054 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255366 | CTTGAGGCAGGTGGC[A/G]GGAGTGGAGTCTTTA | 337867 |
rs774635906 | snp | A/T | 3.29522e-05 | 0.00405894 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255269 | AGCACCCAATCATGA[A/T]GAACAAAGGAATCAA | 337867 |
rs774636483 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252616 | TAACTCATTCCTGCC[A/G]CACATCTGGCCTTAT | 337867 |
rs774640168 | snp | C/G/T | 4.94249e-05 | 0.00497096 | missense, synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367846 | GCGACAAAACGTAAA[C/G/T]TATCAGGGCGGTCGG | 337867 |
rs774645390 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271993 | CTGTTTGATCTTTTT[A/G]TTTCCAAGGCTTTTA | 337867 |
rs774658633 | snp | A/G | 3.5727e-05 | 0.00422637 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99296140 | GTTTGCCATTTGTAT[A/G]TCCATTGGTGGTGGT | 337867 |
rs774686748 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386337 | GACTCTTGCAATGTG[C/T]AACTGTTATGTTCTG | 337867 |
rs774702686 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381816 | TGTTCCTAAGGAAAA[A/G]GAAAGTGTGAATTCT | 337867 |
rs774736489 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99325817 | TGACTGGCTTGTTTC[A/G]CTTAGCATATAGGTC | 337867 |
rs774758795 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99226596 | TAGACCTCCCCAAAG[C/T]ACCCTGTCACATCCA | 337867 |
rs774826753 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353663 | TGTACTCTGGAGCAG[C/T]ATCATGTTAAACCAG | 337867 |
rs774847906 | snp | A/G | 1.68935e-05 | 0.00290628 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255805 | AAGACAAGGGCTGCA[A/G]TTTTGTATTCATCTG | 337867 |
rs774856554 | in-del | -/CTCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280831 | TTCCTTCTTCTTTCC[-/CTCT]CTCTCTCTCTCTCTC | 337867 |
rs774858437 | snp | A/G | 1.65094e-05 | 0.00287305 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367928 | AATCAGTAATACCTG[A/G]TACTCATTCTAAATC | 337867 |
rs774859035 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323783 | TCCTTGTGGCAATTG[C/T]AACTCAGGCCCAGGA | 337867 |
rs774875177 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211680 | CTGCTGAGGAGCAGG[C/T]CTAGGATTTGAACCC | 337867 |
rs774887226 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283482 | GAACAATTTTGTACC[A/G]TAGAGCCTTGTTTGA | 337867 |
rs774904413 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302879 | GTACACTGTAAGGTG[A/G]CTTTTTCCCAGCCAA | 337867 |
rs774911815 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208144 | CTGGGATTACAGGCG[C/T]GTACCACCACGCCTG | 337867 |
rs774946573 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314107 | CATAGCCTGGCACCT[A/G]TGTTTGCTCTGTTTG | 337867 |
rs774989675 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205365 | TATGCTTCTCATTGC[C/T]GTAGGAGGGAAGAGG | 337867 |
rs775036733 | snp | C/T | 0.000733837 | 0.0191411 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200951 | CTCTGTGAGTACCGG[C/T]CTCCGCCATCCTGGC | 337867 |
rs775041766 | in-del | -/CAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227977 | GAAATGCTGGTCAGT[-/CAA]GGAGAGTGTCACCTT | 337867 |
rs775055576 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99352881 | ACTCTCTACCTCCGT[C/T]TCCACCCCTGTGTCC | 337867 |
rs775064105 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365193 | TGTTTATTTGTGCTC[A/C]TTCCTTTGTCTTTTC | 337867 |
rs775064617 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249844 | TGAGCATTTTTTCTT[C/G]TGTGTTGGCCGCTTG | 337867 |
rs775078910 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367070 | AAGCAGCATGTGATG[C/G]ATTTTTCTTCCCATG | 337867 |
rs775084549 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281495 | TAGTCAGCAAGCACA[A/C]GCCAGGCTCATCCCA | 337867 |
rs775111679 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222643 | ATGGTTTCATAGTAT[A/G]CTTTAACTTGTTGAT | 337867 |
rs775133834 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369658 | TCGTAGGTTGAGGAG[C/T]GCTTGTAATCTCAAA | 337867 |
rs775141601 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268781 | TTGACACTAATATGC[C/T]CCTAGATGCCATTTG | 337867 |
rs775150665 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373534 | CTAAGATGGATAAGG[C/T]GGAATGTCCTGCCCT | 337867 |
rs775152463 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251033 | GCTGGGATTATAGGC[A/G]TGAGCCACCAAGCCT | 337867 |
rs775154268 | snp | C/T | 3.29685e-05 | 0.00405995 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255070 | AAGGTGGTAAAGGCT[C/T]CCCAGGGATTGTAAC | 337867 |
rs775189014 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361576 | TTTTGTATCTTTACT[A/G]CATACATACTTATCA | 337867 |
rs775224144 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323236 | TGCACAAGCCTCCCA[A/G]TTAAACTTACTTTAG | 337867 |
rs775234807 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99235664 | CATACAATGGAGAAA[C/T]GACAGTCCCTTCAAA | 337867 |
rs775243080 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339328 | CCCCAGAGTAGGTTC[A/G]TGCCCCATGTCACTT | 337867 |
rs775251681 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339667 | TACAAAGGAATAGCC[-/AT]AGTCATTTTTAACTA | 337867 |
rs775281609 | in-del | -/T | 1.64855e-05 | 0.00287097 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255637 | TTGCATAATAAAACA[-/T]TTCGAAAGGGTAAAG | 337867 |
rs775292571 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255545 | TAAAGGCAAGAAGCC[A/G]TAAAGCAATGCTTGG | 337867 |
rs775297501 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334540 | CTGTAGGGTCTTGCA[A/G]GCTTCTCCTGTTTTA | 337867 |
rs775357211 | in-del | -/CTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378562 | AAACTTCAATATCCA[-/CTT]CTTCTGGCTTACTGA | 337867 |
rs775361216 | snp | A/G | | | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351450 | GCCTCTTTATCTTCC[A/G]AACCTAAAATGTTTA | 337867 |
rs775370315 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99283875 | GAGTAGCTGAAATTA[C/T]AGGCGTGTGCCACCA | 337867 |
rs775372962 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221167 | TCACTATTATAAACA[C/G]TGCTGCGATGAACAT | 337867 |
rs775383089 | snp | C/T | 0.000474909 | 0.0154022 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200970 | CGCCATCCTGGCTGC[C/T]CCCTACACGCCACCC | 337867 |
rs775386474 | snp | C/T | | | intron-variant, downstream-variant-500B | UBAC2, MIR623 | GRCh38.p7 | 13:99356486 | AAACTGCCTTCTGTT[C/T]TGCCTAGAAGAAATA | 337867 |
rs775399117 | snp | A/G | | | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254508 | TAAAGTATTGGATTT[A/G]TAATTCCATTCCTAG | 337867 |
rs775407222 | snp | A/G | 1.65154e-05 | 0.00287358 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385316 | TCAATGTCGCCACCA[A/G]CTTCCTGCTGCAGCA | 337867 |
rs775412936 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245383 | AAACATAAAACAAAG[C/T]CGGTGTATAGGTTAT | 337867 |
rs775417048 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276345 | TTCTTCTGACTGACC[C/T]GCTGTAAATTGGGGG | 337867 |
rs775445604 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255477 | TTTGCACGTGTTTTT[A/G]AGTTCTTTGGCGTAC | 337867 |
rs775497140 | snp | C/T | 3.55935e-05 | 0.00421847 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314257 | TCACTTTTCTTTAAC[C/T]AGATCTTTTTTTTTT | 337867 |
rs775497626 | snp | A/G | 1.64806e-05 | 0.00287054 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295734 | TTATCTTGTTGTAGC[A/G]TAGAGGGTGCACCAC | 337867 |
rs775514130 | snp | C/T | 1.68411e-05 | 0.00290177 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295846 | CCTACACAAGGCATC[C/T]CCGATTCTCCAGTCA | 337867 |
rs775547334 | in-del | -/AGAG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284944 | TTCAGTGACACAAGC[-/AGAG]AGAATAAAATGAGCC | 337867 |
rs775548684 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270086 | CACTGGTATAGCAAT[C/T]GTGAAACTCCTATGA | 337867 |
rs775554960 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322445 | GACTGATCTGATTCT[-/G]GCATGATTAAAATAG | 337867 |
rs775569244 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339378 | GCCAGAAATAGTTTT[A/G]TGTGTTGACTTGATT | 337867 |
rs775574788 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233757 | ATTATCAAAATTATC[A/G]TTATGTAAACCCTAG | 337867 |
rs775577349 | snp | A/C | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328953 | ATAGTTTCTGCTATT[A/C]CATTTAGGTCTGTGA | 337867 |
rs775581092 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99336862 | CCCATAATCCACCAT[A/G]CAGGTACAGACCATG | 337867 |
rs775586345 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314697 | GCTTGATTATTTCCT[A/T]GTTTGTGAAGCTGTG | 337867 |
rs775591304 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220973 | AAAAAGTATTTATAT[A/G]TTATTTTTGTATAAT | 337867 |
rs775613643 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364243 | TATTGAATTTTGTCA[A/G]ATTGTTTTCATACCT | 337867 |
rs775644887 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297148 | TTGTTATAAATAATG[G/T]TAAAGCAGAAATTTT | 337867 |
rs775660060 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365444 | TCAATATTTAAAAAT[G/T]ACATCAACCACTTTA | 337867 |
rs775669174 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274615 | ACAGGCATGAGGCAC[A/G]TGCCTGGCCTCATAA | 337867 |
rs775674167 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375880 | GCTATCATGGCTCAC[C/T]GCAACCTCGACCTCC | 337867 |
rs775698583 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208481 | AAAAGGCCACATAAG[C/G]TGATGATCTTAGGTG | 337867 |
rs775703195 | snp | C/T | 1.71849e-05 | 0.00293124 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385381 | GCAGCCGAGTGACAG[C/T]GCGTGGTCCCCACCA | 337867 |
rs775708614 | snp | A/G | 4.63833e-05 | 0.00481555 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200768 | ACTGCGCATGCGCCG[A/G]GTGCGCCGTTCGTCA | 337867 |
rs775719629 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318088 | AGTGTGACTACCCTT[C/T]TACACCCAATTCTCT | 337867 |
rs775729105 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377397 | TGTGGATGTTAGATC[A/G]GATCAGGTGCTCATG | 337867 |
rs775741578 | in-del | -/TCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99280832 | TCCTTCTTCTTTCCC[-/TCT]CTCTCTCTCTCTCTC | 337867 |
rs775754532 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215578 | CCTCTGCGGTGAGGT[A/T]CTCCAGGATGGCTGC | 337867 |
rs775767555 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238741 | CAGATAATAATGAAG[C/G]AATGGCAGTATTTCC | 337867 |
rs775777245 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346741 | CCCAGGGCTCTCTCT[C/G]CCCCTGTAGACACTG | 337867 |
rs775780614 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219379 | AAAAATGTTCACTTA[C/T]TGACTTCCAGTACAT | 337867 |
rs775830203 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285306 | CTCCTCTTCTTCCTC[C/T]CTTTGGTAGAGTATT | 337867 |
rs775832259 | snp | A/G | 6.65425e-05 | 0.00576774 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201478 | ATGAGAGTGCTTTCA[A/G]GTGGAGGGAAGTTAG | 337867 |
rs775879710 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296233 | TTACTCATTAGTTTT[A/T]AAAAAGTTTAAATAA | 337867 |
rs775880912 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227138 | AGGAGGCAGAGGTTG[C/G]AATGAGCCGAGATTG | 337867 |
rs775894070 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218120 | AATTTTTTAAACTTA[C/T]TTTGGCTTTTAAAAT | 337867 |
rs775905121 | snp | C/T | 3.30918e-05 | 0.00406753 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356222 | GTAGATGTCTTTGCA[C/T]CTTCTGTCCTCATTG | 337867 |
rs775941638 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294453 | CATCATTTATAATGT[G/T]GCAGTTCAAAGTCTA | 337867 |
rs775948922 | snp | A/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306222 | CTTTATGTAAAATAT[A/C]CATAACATATCTGTT | 337867 |
rs775955752 | snp | C/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256778 | AAATATCATTGACTC[C/T]TCAGTGTGAAACTTC | 337867 |
rs775958889 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379781 | ACACTTACACTGCTC[A/T]CCACTTTCTCCAACA | 337867 |
rs775967157 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239086 | ACTGGGTTCTTGTCT[A/G]TGAATTGGAGTGTTC | 337867 |
rs775979933 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344547 | ACTTGATTTTTAGAT[A/G]CTTTTCATAGAATCT | 337867 |
rs775990761 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315526 | GTAGGAGTTCAGTGT[A/G]GCATTGTGGAAAGTC | 337867 |
rs775996860 | snp | A/G | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367833 | CTCCTTTACGTCAGC[A/G]ACAAAACGTAAACTA | 337867 |
rs776008331 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271437 | GAGTGATGGGGGGAT[A/G]GGGTGTGGGAAGATA | 337867 |
rs776009591 | in-del | -/TATT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244811 | ATAGAATCAATTTTA[-/TATT]TATTCTTTCTTTAAA | 337867 |
rs776009605 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353899 | GTGCTGTGGTTGACA[A/G]ACGTGGTTTTGTGGA | 337867 |
rs776057364 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99300993 | AAGATATATTTATAT[A/G]AACTAAGGTATACTA | 337867 |
rs776095402 | snp | C/T | 1.65231e-05 | 0.00287424 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201544 | ATGTTGCTGTTTTCC[C/T]GGCGTGTTAGCGGTG | 337867 |
rs776099259 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341308 | CTCTGTCTTCCACTA[A/G]CATTGGATGCAAGAA | 337867 |
rs776115198 | snp | A/C | 3.29484e-05 | 0.00405871 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255234 | CCTGCCGTGAAGGAG[A/C]TTATGAATAATGACC | 337867 |
rs776118847 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382122 | GACCTGACGTGTTTG[A/T]CATTTTCATCAATAA | 337867 |
rs776130635 | snp | A/C | 1.67094e-05 | 0.0028904 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255793 | ATACAGCTATAGAAG[A/C]CAAGGGCTGCAATTT | 337867 |
rs776134200 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341420 | CAGAGTTTATATCAG[-/G]GGGGGGGAGGAAGGG | 337867 |
rs776154558 | snp | A/G | 1.74876e-05 | 0.00295694 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99296119 | TGCAGAGGGCGGAGT[A/G]AAATTGTTTGCCATT | 337867 |
rs776158820 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270514 | TGTTAGATTTTAATT[A/G]CTACTTTTTACATTT | 337867 |
rs776160463 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99224889 | TCTTGAGTTGATGAG[C/T]GAATCTTGTTGTCTA | 337867 |
rs776166360 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227914 | GGAGAGAGGAAGAGA[G/T]AGTGTGAGGTAAGAA | 337867 |
rs776180193 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99359931 | TGTGCTTCACACTTC[-/A]AAACCTGGCATGCTG | 337867 |
rs776181586 | snp | A/G | 1.66015e-05 | 0.00288105 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254912 | TATTGCTTAGTGACC[A/G]TAGACTACCAGATCG | 337867 |
rs776200097 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299898 | GGTTCTTAAAAGCCA[C/T]GCTGGGCTTAAATGC | 337867 |
rs776204301 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236774 | AGAATCACTTGAATC[C/T]GGGGGGCAGAGGTTG | 337867 |
rs776210664 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350861 | TGATGTTATCTCCTG[A/G]GAGACAGTGTGGGGA | 337867 |
rs776251286 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202072 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 337867 |
rs776282847 | in-del | -/T | 0.0030888 | 0.0391773 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318003 | TTATTTTTAGTTGCC[-/T]TTTTTTTTTCTTTTA | 337867 |
rs776288248 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237566 | AGACGGTGTTCAGTA[A/G]GTCAGGAGCGTGTCT | 337867 |
rs776290445 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223937 | TGCTCCATATGCACT[G/T]GAAAAAATGTGTAAC | 337867 |
rs776329472 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322333 | CTTTTGAGCCATCTA[C/T]ATCTCAGAACTTCTT | 337867 |
rs776345664 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258084 | TTATTAAAATGAAAT[A/G]ATTTTTGAAATGCAG | 337867 |
rs776352819 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344135 | AGTATATGTTATCTC[A/T]TTTATGCCCGGTGTA | 337867 |
rs776352875 | in-del | -/ATT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364161 | TTGGTTTTTGTTCTC[-/ATT]ATTATGCTGTGACTT | 337867 |
rs776354100 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289948 | ACCTGCTCTTCCTCC[C/T]CACCCCCAAGGAACT | 337867 |
rs776361924 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99270871 | GCTTGACACTTCCTT[-/G]TATAAAGTAGCCACT | 337867 |
rs776369756 | snp | C/G | 0.000124302 | 0.00788261 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340612 | AAATTCTCAGTGGCC[C/G]AAGCAAATCTTTCCT | 337867 |
rs776371800 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99245574 | AAACAAAAAAACAGG[C/T]CGGGCGCGGTGGCTC | 337867 |
rs776382195 | snp | A/G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269163 | GAGTGCGAGGCAGGG[A/G/T]TGTTGCAGGAAGTCC | 337867 |
rs776393119 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379813 | CTTGACTTTCTGTGC[G/T]ATAGATAAACATAAA | 337867 |
rs776393992 | snp | C/G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330591 | CAACATAGGTGGTCT[C/G/T]TGTCATCCAGAAATA | 337867 |
rs776415234 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99279687 | TTATTTCTCACAGTT[C/T]TGGAGGCTGAGAAGT | 337867 |
rs776433456 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324897 | GAAAAAATATATATA[A/T]ATGAAAATATATATC | 337867 |
rs776436108 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203554 | AAACTTGCCTTTCTC[G/T]CTCATCCATTCAATA | 337867 |
rs776437016 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99319800 | GCCAGACTCCCCCAA[C/G]TCTAGGCTCACCCAG | 337867 |
rs776460239 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347217 | AAGAACCCCCAGGGA[C/T]CAAGGAGAAAACCAG | 337867 |
rs776461577 | snp | A/G/T | 6.59341e-05 | 0.00574137 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295712 | CCTTTTGCATGTTCA[A/G/T]TCCTTTTTATCTTGT | 337867 |
rs776467721 | in-del | -/GAGCA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332351 | AATTATTTGCCTGAT[-/GAGCA]TTATTTCATGATTCC | 337867 |
rs776472823 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321001 | TGCACAGATAATTAT[A/G]ATTATAGATGATATT | 337867 |
rs776477394 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278018 | TGAGCAGATTAATGT[A/G]GGGCACAGGTCTTAC | 337867 |
rs776487636 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99265052 | TCGACCTCTTGGAGA[C/T]ATTATAATCAACCTT | 337867 |
rs776498934 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99342198 | AGCAAAAGCCTCGCT[C/G]GTCTTATGGAGCACA | 337867 |
rs776512241 | snp | C/T | 0.000614062 | 0.0175115 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200875 | CAGCTTCCCCTCCCC[C/T]GGCGCCCTCTGGGGC | 337867 |
rs776541076 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232485 | GGTATCTTAAACTTC[A/G]CCCAGTGGGCTTAAT | 337867 |
rs776554722 | snp | G/T | 3.29625e-05 | 0.00405958 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255412 | AGCAGTAGCAGAGGG[G/T]TGGTCGTGGTCAGGG | 337867 |
rs776571858 | snp | A/G | 1.65693e-05 | 0.00287826 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295618 | GCATGTAATCCTTTC[A/G]GCCTCCTGCTTTGAC | 337867 |
rs776585568 | in-del | -/AC | 5.20129e-05 | 0.00509939 | intron-variant, frameshift-variant, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201453 | AGAGTTTTTAGACAA[-/AC]ACACACTGATGAGAG | 337867 |
rs776610948 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329667 | AGGTCCACATGGCCA[A/G]CAATCGTGGCCTCCT | 337867 |
rs776625270 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204052 | GCTCTACGTTGAGTA[-/AT]ATGTGTATCATTCAC | 337867 |
rs776626598 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228008 | GAGACTTGAGACCAA[G/T]AATTTATGGTGAAAT | 337867 |
rs776630621 | snp | A/C | 1.65798e-05 | 0.00287917 | intron-variant | UBAC2 | GRCh38.p7 | 13:99385192 | ATAAGCGGCAATGTC[A/C]GCGCCCTCAGGTTTC | 337867 |
rs776649940 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99369438 | GTTTTTCACTTGCAG[C/T]ACGATACTCAATAAT | 337867 |
rs776660722 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249376 | GGACATGATTTCATT[-/C]TTTTTTATGGCTGCA | 337867 |
rs776676710 | in-del | -/TACTCCATGCATG | 1.65877e-05 | 0.00287986 | intron-variant, frameshift-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99295595 | TCTTCAAAGTTTGGA[-/TACTCCATGCATG]TAATCCTTTCAGCCT | 337867 |
rs776677891 | snp | A/C | 7.30327e-05 | 0.00604243 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200929 | CACCAGCACCGGCTC[A/C]AGTGGGCTCTGTGAG | 337867 |
rs776704349 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99222346 | GGACGTGGGAAGAAC[A/G]TTTTGGGTAGAGAGA | 337867 |
rs776732528 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303982 | CATCCGTGTCTGTCT[C/G]TCTGCCTGTTGTGTG | 337867 |
rs776732786 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210643 | CCACCACGTCCGGCT[A/C]ATTTTGTGTTTTTAG | 337867 |
rs776743314 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246544 | ACTTTGGAGATGGAT[A/G]GTAACTTAGCATTAT | 337867 |
rs776752710 | snp | A/G | 1.648e-05 | 0.0028705 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255469 | AGCACGGCTTTGCAC[A/G]TGTTTTTAAGTTCTT | 337867 |
rs776770088 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357461 | GGCCATAGGAAATTA[A/G]TCATTTCTCTGTGTC | 337867 |
rs776772126 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99370438 | CAAAATCTATAAAAG[A/G]AAGTTAAGAGTGTTG | 337867 |
rs776777158 | snp | A/G | | | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255451 | CAGACTCCCACACAC[A/G]CCAGCACGGCTTTGC | 337867 |
rs776791011 | in-del | -/TTTA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315165 | TTCTCATGAAATCTT[-/TTTA]TTCTCCATCTCTCAA | 337867 |
rs776792704 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99285551 | GCATGTGCCACCACG[C/T]CCAGCTAATTCTTAA | 337867 |
rs776799309 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355248 | GCTGGGAAGGAAAAA[A/G]TGACCCCAAATTTGG | 337867 |
rs776806085 | snp | C/G | 1.65872e-05 | 0.00287981 | missense, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99238551 | AGTCAAGAACGACTT[C/G]CAGGTAAGCTCTGCC | 337867 |
rs776809491 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99316862 | AATTGCTTAACCACT[C/T]GGTTTTACTGAAGTG | 337867 |
rs776822215 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99251563 | TGAAAGCATTCCATA[C/T]AATGCTGTCAGAAGT | 337867 |
rs776822502 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378216 | GAACAGCTGGAGCCC[C/G]CTTATCGATATTAAA | 337867 |
rs776850512 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383537 | CATAGTGTCCCAGGT[A/G]CTGGGCATCTTGCTG | 337867 |
rs776863620 | snp | C/T | 1.91665e-05 | 0.00309562 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243963 | TGCAGTAAGTTTTTA[C/T]GTATTTTGTCTTTGC | 337867 |
rs776873787 | snp | C/G | | | intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99256494 | ATTTCAGCTGCTCTA[C/G]TTCAGTGGTTCACAG | 337867 |
rs776898037 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99209294 | CCTGTCCTGTCTTCA[C/T]GGGAGGGAACCCTCA | 337867 |
rs776917685 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274683 | TTTGGGAATAGTACA[A/G]ATACTGTTATTATGA | 337867 |
rs776918692 | snp | C/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305945 | TGGTCGCCCAGGCTA[C/G]AGTGCAGTGGCGCAA | 337867 |
rs776941769 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99356123 | TTGGGACACATGTCT[A/G]TCAGACTGTACACAG | 337867 |
rs777000891 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299573 | AACGTTTCTATTCAG[A/T]ATGTTCATTTCTAGT | 337867 |
rs777013772 | snp | A/G | 3.32701e-05 | 0.00407847 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314240 | AGTATGCATTTTTAT[A/G]TTCACTTTTCTTTAA | 337867 |
rs777024776 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250072 | TAGTTTAAATGGGTC[A/C]CATTTGTCAATTTTT | 337867 |
rs777040003 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373621 | TCGGGTGCTGCTGAG[A/G]CCAAGAAAGGCCGTC | 337867 |
rs777040923 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384465 | TGCCTGTAGAGAAAA[A/G]TACAGGAAATCTCCG | 337867 |
rs777073611 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99374394 | CCATTTAGTTTGGTC[G/T]TCTGGTTTGTTGGAG | 337867 |
rs777095588 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217525 | CGGGCAGCCTTACTT[G/T]TCACCCTGTTTGGTT | 337867 |
rs777095729 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206175 | GGGTTTGCAGAGTCC[A/G]GTCAGAGGTACTCGG | 337867 |
rs777105144 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272607 | TGGTGAGGGCCTGCC[A/G]TCTTCCTGACTTGCA | 337867 |
rs777116931 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271174 | ATATATATGCCAGAT[C/G]ATGATCTGTGTTGTA | 337867 |
rs777126501 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312958 | GGTTTTTTTGTTTTG[-/T]TTTTTTATTTTTTTT | 337867 |
rs777135034 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99344602 | TTTTTTTCAGTTACT[A/C]ACTGCTGTATGTTAC | 337867 |
rs777151535 | in-del | -/GA/GCGAGT/GT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368684 | ATCGTAAACTCATGA[-/GA/GCGAGT/GT]GAGAGTGTGTGTGTG | 337867 |
rs777152648 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207934 | CATTCTTTCTTAAGT[A/G]TGCATTCAGTGTGTG | 337867 |
rs777173201 | snp | A/G | 3.29549e-05 | 0.00405911 | intron-variant | UBAC2 | GRCh38.p7 | 13:99318082 | CTTGTAAGTGTGACT[A/G]CCCTTTTACACCCAA | 337867 |
rs777192337 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99229507 | GCCCAGAATGTAGGG[A/G]GGTCTGGACAACCAG | 337867 |
rs777202672 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366468 | CGATATCTCCATCCC[A/G]AAACCAATCTTTATG | 337867 |
rs777204056 | snp | A/G | 3.30704e-05 | 0.00406622 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295091 | GACTTGGAATGTATC[A/G]TCATCTGCGTTTCTG | 337867 |
rs777207059 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338117 | GGCTGGAGTGCAGCG[G/T]CACAATCTCGACTTA | 337867 |
rs777217273 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207658 | CCTTGGGCCAGATGC[-/A]GTTAGAGAAGTTTGA | 337867 |
rs777223166 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284965 | AATAAAATGAGCCCT[A/G]TTACCCAGATTCAGT | 337867 |
rs777229237 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255127 | AAAGCGAAACAGATG[C/T]GGAAGGGCATAAAGC | 337867 |
rs777255090 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275662 | CACCCCCCAGGTTTT[A/T]TTTCTCTACACAGTT | 337867 |
rs777262331 | in-del | -/ACCAAA | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355597 | GCATTCTCATTCTCT[-/ACCAAA]ACCAAAACCAAACCA | 337867 |
rs777271321 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215652 | GTCCTAGATTTCAGG[G/T]GTTGATGAATACAGC | 337867 |
rs777285651 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99337604 | TTATTCTAGAAAACT[A/C]TCAGCTGTTTATCTC | 337867 |
rs777296990 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382632 | AACTGGATCCTGAAA[C/T]ACAGGAATGAGCAAA | 337867 |
rs777314985 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354842 | CAGTCATGTCATCCA[A/G]GAAGTTGTTGGCATA | 337867 |
rs777342346 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286276 | TATATATACAAAGCA[A/G]CATACCTGGATCTGA | 337867 |
rs777342780 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334053 | CTTGGGTCAAGTGAC[C/T]CTCCCACATCAGCCT | 337867 |
rs777343495 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99220388 | TACATGTAAAGTGCT[C/T]TTATTAGCACAGTGC | 337867 |
rs777345251 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210660 | TTTTGTGTTTTTAGT[A/G]GAGACGGGGTTTCTC | 337867 |
rs777345685 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273801 | CTCTTCCATTTTTCT[C/G]AGTTCTTTCTGGAAA | 337867 |
rs777349420 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367821 | ATCGTCTTTTTCCTC[C/G]TTTACGTCAGCGACA | 337867 |
rs777357516 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204908 | TTCGTTTCCTTTTTT[-/TT]TTTTTTTTTTTTTGC | 337867 |
rs777363722 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199273 | CCAGGGTGGTGTCAG[C/G]TGCCTGTAGTCCCAG | 337867 |
rs777364107 | snp | C/G | 1.67795e-05 | 0.00289646 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295474 | TTGTTTGGCAGTTCT[C/G]AAGAGTTTGCAGCAG | 337867 |
rs777379016 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292664 | TTTTTACTATCCTCT[C/T]GCTGAATAGTCAGTG | 337867 |
rs777382001 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240710 | CCGGTACTGTTTCTC[C/T]TTGAGCCCAGCTATG | 337867 |
rs777402873 | in-del | -/GG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247587 | ACTGGGGCTGTCTAT[-/GG]GTAAGGGGCAAGGGG | 337867 |
rs777410440 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99361065 | TTCCATGGAACTTCT[G/T]CTTAATAAAATGTCA | 337867 |
rs777415461 | snp | C/T | 3.314e-05 | 0.00407049 | intron-variant | UBAC2 | GRCh38.p7 | 13:99238384 | GTGGTTTTTTAAATC[C/T]TAGGAACAATCATTC | 337867 |
rs777430313 | snp | A/C | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367880 | TCTGAGCCAGCAGCG[A/C]CCCCTCTAGAAGTTT | 337867 |
rs777479807 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303580 | TAAGAAAGATATTCT[A/G]TGTTTGTATCTGGCA | 337867 |
rs777481240 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255333 | GTTCACAGCTTTTAG[A/G]TAGATGATGTCAGAA | 337867 |
rs777498833 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99205755 | CACCCCATTGATCGC[C/T]AGAGTTGATTCGGCT | 337867 |
rs777502393 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99364928 | TCTAGTCCATGTCTT[C/T]TGATGAACATGTGTT | 337867 |
rs777510204 | snp | C/T | 1.71631e-05 | 0.00292938 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99296103 | CATTTCCCTGAGGAG[C/T]TGCAGAGGGCGGAGT | 337867 |
rs777535718 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323089 | GTGTGAGTTCCTCTG[C/T]GCCGCCTTTGCTTGT | 337867 |
rs777542437 | snp | A/G | 1.79416e-05 | 0.00299507 | utr-variant-5-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255890 | TACAGCTTGTTGGTA[A/G]GCATGATACTTAGAA | 337867 |
rs777543682 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99334336 | ATGGGAAGACATTAC[A/G]TGGAACTGTAGTAAG | 337867 |
rs777549445 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376462 | TGGACACCTCCAGAG[G/T]GGGTCTTCATCCCCG | 337867 |
rs777569805 | in-del | -/ATTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244222 | TTTAATAAAATTATA[-/ATTT]ATTTTGCTTAGTGGT | 337867 |
rs777599485 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263116 | TTTTGCATTATAATA[A/T]TATACTTCGTTTTAG | 337867 |
rs777604960 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266685 | AATTTGACATGTTAA[-/AT]ATATATATATATGTA | 337867 |
rs777626935 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366193 | ACCTTATTCTTTTCT[C/T]TAAGGTCCTCCTGTG | 337867 |
rs777627786 | in-del | -/AAA | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299614 | AATGAATAAATAGGT[-/AAA]AAAAATTTTAATGGG | 337867 |
rs777640114 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372726 | GATAAATAGAAACTG[C/T]TTGTCAACAACAACA | 337867 |
rs777674805 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215215 | CTCAAATGCAGAAAT[G/T]TGGTTGGAAAGCTAA | 337867 |
rs777701244 | snp | C/G | | | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295362 | GTTGAATAATTGCAA[C/G]ATGGTAAGGTGTGAA | 337867 |
rs777702335 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99261939 | CAGTTACCTTCAGTC[A/G]AATATGGTCTGAAAA | 337867 |
rs777717787 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289295 | AGGATTAAGGGAGGC[A/G]GTGTGATTTGGATGT | 337867 |
rs777734678 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291407 | TGTAATCCACATGCT[G/T]TTCATTTTCTCATTC | 337867 |
rs777757697 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99250492 | GTCAGGTAATGTGAT[A/G]CCTCTGGCTTTGTTT | 337867 |
rs777773084 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343698 | TTCTAGGGTCCGCAC[A/G]TGGGTACACCCAAAC | 337867 |
rs777795815 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257729 | CCATTAAGTTATTTC[A/G]TGAAACAATGTAATT | 337867 |
rs777821209 | snp | A/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99304659 | GTGTTCCAGGCACTG[A/C]CCTGGGCACTCTATG | 337867 |
rs777857539 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99288321 | TGGGGCAGAAAGTAA[C/T]GTGGCCCCTGCTCTG | 337867 |
rs777863652 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201788 | AATATTAAAGATCTG[C/T]TGGCCGGGCGCGGTG | 337867 |
rs777876713 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99246339 | TAATTAGACTGAGAA[A/G]TTAAAGTTGAGTATT | 337867 |
rs777880406 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254966 | GAAGGTAATTACGGT[A/G]TAGCATGACACTAAT | 337867 |
rs777902757 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272029 | AGCTAACTTTCTTTG[C/T]TGTTTCAGCAGACTA | 337867 |
rs777926850 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381036 | TCAAAACCAGCACCG[C/T]GGCACATGTCGTTCA | 337867 |
rs777933832 | snp | C/G | 8.70739e-05 | 0.00659768 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200907 | CCGAGCCCGGCGGGA[C/G]CATGTTCACCAGCAC | 337867 |
rs777935684 | snp | C/G | 4.94499e-05 | 0.00497217 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255034 | AGAATCACATCCAGA[C/G]ACGTGCTGAGGTTCA | 337867 |
rs777948575 | snp | C/T | 5.21707e-05 | 0.00510712 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340594 | TAATCACTAAAAATT[C/T]AGAAATTCTCAGTGG | 337867 |
rs777955919 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213859 | GAGTCTTGCTTTGTC[A/G]CTCAGGCTGGAGTAT | 337867 |
rs778001002 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276789 | ATGTGGTTGAAAGGG[G/T]CTCATTATGAAGAAG | 337867 |
rs778004508 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99213481 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGTTGGG | 337867 |
rs778018054 | snp | A/G | | | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352216 | GAATTCACATACCAT[A/G]TAACTCACCCCCTCG | 337867 |
rs778024374 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345542 | CTACTGAGCTTTTCA[C/T]GTTAGACACCCAAGG | 337867 |
rs778037455 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99228562 | GCCTCTCAAAGTGCT[A/G]GGATTATAGGCATGA | 337867 |
rs778049222 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332190 | TGGCCAAAGAAAGCA[A/G]TCGACACCTGTGTGT | 337867 |
rs778053129 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385998 | TTAGCCACTAGGCTG[C/T]GGGTGAAATGGGATG | 337867 |
rs778075318 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324005 | GGCAAAAATCTAGCC[G/T]CCTTTCAAAATGCGA | 337867 |
rs778085265 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258650 | AGCTTCTTTGCTTTA[C/T]AAGCTATGTGACTTT | 337867 |
rs778100524 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99348961 | AAGGTGCAATCACGG[A/C]TCAAAAAGAAAAAGA | 337867 |
rs778102472 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99340679 | CCAGTGCCTTGCAAG[C/T]GGATTTTGACATTTC | 337867 |
rs778122070 | snp | C/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257993 | CACTATGGTGCTCCT[C/G]GGCACAACTGATCCT | 337867 |
rs778123834 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277651 | CTCTACAATCATTCA[C/G]ACATTTTATTAAGGC | 337867 |
rs778128954 | snp | A/G | 1.83552e-05 | 0.0030294 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200979 | GGCTGCCCCCTACAC[A/G]CCACCCTAGGCACCT | 337867 |
rs778140409 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99308584 | GGATGATGTAAACAG[A/G]ATTGAATCATTTGGT | 337867 |
rs778150585 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201885 | ACCATCCTGGCTAAC[-/A]ACGGTGAAACCCCGT | 337867 |
rs778163364 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99279486 | CTTTCTTATAGCACT[C/T]ATCACTATAGATAGT | 337867 |
rs778169058 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331331 | TTTAAGCCACTGTTG[-/T]TTGAAGTTTTCTACT | 337867 |
rs778176350 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296984 | CTTGCTTTATTCACC[A/G]AACATCTTCATGTCA | 337867 |
rs778188669 | in-del | -/TTCTT | 0.000167238 | 0.00914282 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351808 | GAGTCCTTGGTGCTC[-/TTCTT]TTAACTGCCTCCTCA | 337867 |
rs778197141 | snp | A/G | 1.8183e-05 | 0.00301515 | splice-acceptor-variant, intron-variant | UBAC2 | GRCh38.p7 | 13:99244513 | GCTGTTTTATTTTGT[A/G]GTCCTTTTTGCTGGG | 337867 |
rs778202167 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238130 | TCTATTTCTTTACAC[C/T]TGGGTAGCCATTTTC | 337867 |
rs778221044 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331214 | GAAGGCTCCTTAAAG[C/T]CGCCTTTTGTCCTTT | 337867 |
rs778248300 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238846 | AAACAATGTTTAATC[-/T]TTTTTTAATGCCCAG | 337867 |
rs778250186 | snp | A/T | 4.94531e-05 | 0.00497234 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255628 | CATTCATCTTTTGCA[A/T]AATAAAACATTCGAA | 337867 |
rs778250526 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216219 | GGGTTCTCATTCCTC[A/C]GCCTCCGAAGTAGTA | 337867 |
rs778260964 | in-del | -/AA | 0.000105513 | 0.0072626 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243993 | CTACTTAGGCTGTAG[-/AA]AAAAATTTTGTTTAA | 337867 |
rs778262306 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233036 | AAAAATATATTTTCT[A/C]GCTCTGATTACTGAA | 337867 |
rs778304682 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377017 | CATTGCCTCCACTCA[C/T]GCCAGAACAAGTGTC | 337867 |
rs778343087 | snp | A/G | 6.66644e-05 | 0.00577302 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99243901 | TGCAGTAGTCTGCTT[A/G]TTTATAATTTTAGGA | 337867 |
rs778346385 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295186 | CCGTTTCAGCATCCT[C/T]ATAACCTTTCTCTTA | 337867 |
rs778351577 | snp | C/G | 1.64966e-05 | 0.00287194 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385300 | GCTTCAAACAATGAC[C/G]TCAATGTCGCCACCA | 337867 |
rs778356507 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275288 | CTGTTGGCAGGAAGC[C/T]TCAGCTCCTCACCAC | 337867 |
rs778360457 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2, GPR18 | GRCh38.p7 | 13:99262096 | CCAGTGTCTCCACAC[C/T]GTAGACATTCCCACT | 337867 |
rs778365731 | snp | C/T | 1.69275e-05 | 0.0029092 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385364 | ACACTGGGACCGGAC[C/T]GGCAGCCGAGTGACA | 337867 |
rs778413731 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384889 | AGGGAATCAAACGAC[A/G]CTGAGTCGTGTGTCC | 337867 |
rs778416609 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317209 | TAGCACAATGCCAGC[A/G]ATGAACCTGGGCTGT | 337867 |
rs778417826 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372885 | TTTGGGAGGCTGAGG[C/T]GGACGGATCACGAGG | 337867 |
rs778449472 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99230182 | AAACAAAAGAAATAT[A/G]GCCAGGCACAGTGGC | 337867 |
rs778455727 | snp | C/T | 9.8912e-05 | 0.0070318 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99318038 | TTTTCACCTCTGGTT[C/T]CTACATCTGGATTGT | 337867 |
rs778470064 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307524 | AGCCTCGTGTACGTG[G/T]GTGCACTTTGTGTTT | 337867 |
rs778477617 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366792 | AGCAGGGCCTCTGCT[-/C]CCCCGTCTCCCAGGC | 337867 |
rs778483670 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200487 | GGGCGTCCAGTCTCG[A/G]GAGAGATTAGAAGTG | 337867 |
rs778519835 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289416 | ACTTGAAAGGCCCAT[A/G]TTGGGCAATGGAGAT | 337867 |
rs778549323 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378434 | TGGGAGGCTGAGGCA[A/G]GAGAATGGCTTGAAC | 337867 |
rs778550941 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351230 | TGGGCATCTGTTTTT[A/G]TGGCTCTCAGGAAGT | 337867 |
rs778581423 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99269987 | ACTATTTCATAAAGG[C/T]GTGTGCTGTAGTTAG | 337867 |
rs778592569 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99199423 | AACAAAACAAGACTG[A/T]GAAAATGAACTTTAC | 337867 |
rs778598512 | snp | C/T | 1.64849e-05 | 0.00287092 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295320 | TACATTCCAGGAAAT[C/T]AGAGAAACGAAGCTT | 337867 |
rs778609952 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99312167 | GAATTGAGAGGACAG[C/T]GCATTTTTTAAAATA | 337867 |
rs778613356 | snp | A/G | 1.67506e-05 | 0.00289396 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340279 | ACATTTTTTAAAATA[A/G]TACTACATTTAAACA | 337867 |
rs778614471 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367808 | ATGATCAATTGGAAT[C/T]GTCTTTTTCCTCCTT | 337867 |
rs778616059 | snp | A/G | 1.65266e-05 | 0.00287455 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201511 | AGTCGTGGCGAGGGA[A/G]CGCAGCTGTGCTGCT | 337867 |
rs778629861 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292890 | TAATAAAGTCATGTT[C/G]TGTAACAGAATATAA | 337867 |
rs778649813 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255217 | GGTTTCAGCTTAGAC[A/G]TCCTGCCGTGAAGGA | 337867 |
rs778651718 | snp | C/T | 1.65405e-05 | 0.00287576 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356196 | TGTGCTGGAGCTTCC[C/T]GATGTACTCTGTAGA | 337867 |
rs778660837 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99227664 | TGTATATCTACCTTG[-/T]TTTTGTTTGTTGTTG | 337867 |
rs778662139 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355001 | ACATCCGCCTGCCAC[C/G]GTGAACGCAGATAGG | 337867 |
rs778701139 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99240855 | TAGAGACATATGTGA[C/T]AGGTTTTGACAGTTG | 337867 |
rs778715296 | snp | C/T | | | | | GRCh38.p7 | 13:99355850 | CAGACCCACTGGACG[C/T]CCTGGTGCATGGCTG | 337867 |
rs778734777 | in-del | -/T | 0.000336222 | 0.0129614 | | | GRCh38.p7 | 13:99314073 | TCACTATTATAGTGA[-/T]TTTTTTTTTATTTGT | 337867 |
rs778738765 | snp | C/T | | | | | GRCh38.p7 | 13:99252082 | TTTCCTTTCAGAGTC[C/T]TCCTCATCTGACCAC | 337867 |
rs778739012 | snp | A/G | | | | | GRCh38.p7 | 13:99335368 | ACTTCCTTGCCTCCA[A/G]TTCATTACTGTTTTT | 337867 |
rs778754688 | snp | A/C | | | | | GRCh38.p7 | 13:99374086 | TATTTGCAACTTATG[A/C]ATTAGTGCAGCCTCC | 337867 |
rs778805282 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282400 | AATAGCTTTGGTTGA[A/G]GCTATTAGTAAAAAT | 337867 |
rs778809881 | snp | C/T | 6.76178e-05 | 0.00581415 | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201613 | AAACGGCTTTTCTCA[C/T]TGAGTGTGTGGAATT | 337867 |
rs778853089 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267755 | TATTTTATCAGTGAT[-/A]AAAAAATACCAAAAT | 337867 |
rs778865538 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99279887 | GAGCATCACACTGGG[C/G]GTTAGGATTTTAACA | 337867 |
rs778879715 | in-del | -/CA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237266 | GCGTATATATATATA[-/CA]TATATACACACACAC | 337867 |
rs778884457 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99217086 | TCTGCCTGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 337867 |
rs778885739 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206539 | AGTGTATCAGCCCAT[C/T]TGTGGCATCTCTTTC | 337867 |
rs778913464 | snp | A/T | 3.74749e-05 | 0.00432852 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99296180 | TAGAAAAAAACCAAG[A/T]AGGATCATATAAGTA | 337867 |
rs778916159 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291024 | TCTTACTAACCAAGT[G/T]TCAGTAAGTGGTGGC | 337867 |
rs778928737 | in-del | -/TACC | 6.60077e-05 | 0.00574452 | intron-variant | UBAC2 | GRCh38.p7 | 13:99367922 | GTAATTAATCAGTAA[-/TACC]TGGTACTCATTCTAA | 337867 |
rs778964878 | snp | C/T | | | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99294122 | TACTCGGATCGTATT[C/T]AGCAAGCAGCAGCTA | 337867 |
rs778981015 | snp | A/T | 1.70359e-05 | 0.0029185 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99296092 | GAGGTCACAGTCATT[A/T]CCCTGAGGAGTTGCA | 337867 |
rs779000601 | snp | C/G | 1.64855e-05 | 0.00287097 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254963 | TTCGAAGGTAATTAC[C/G]GTATAGCATGACACT | 337867 |
rs779008168 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99233557 | GAGCAGGCGTTGAGG[C/G]CCCTGGTTGAAAGGC | 337867 |
rs779057665 | snp | C/T | 0.00010665 | 0.0073016 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200898 | TCTGGGGCTCCGAGC[C/T]CGGCGGGACCATGTT | 337867 |
rs779079190 | snp | A/C | 3.55398e-05 | 0.00421528 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255871 | TTGTTCAGGGTGATC[A/C]TTTTACAGCTTGTTG | 337867 |
rs779123790 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260478 | CACTTTGACCAGCTT[A/G]TGAGATGGGGAGACT | 337867 |
rs779162043 | in-del | -/TCCT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207354 | GTAGTATTAACTGGA[-/TCCT]TCCTTCTTCTGAGCC | 337867 |
rs779181779 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322830 | GCCTTATCAGGGTTC[A/G]TAGATCATAGGACAG | 337867 |
rs779211779 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371075 | AAGGTGATATATTTC[G/T]CAGTTTGGGCACTTC | 337867 |
rs779216656 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99248258 | AATGAGGTCTTATTC[A/C]GTTGCCCAGGCCTAG | 337867 |
rs779223574 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241242 | TGCACTACAGCCTGG[A/G]CAACAGAGTGAGACC | 337867 |
rs779228126 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99266831 | CTGTACCCATCATAC[A/G]GCAAATATCTCTTCA | 337867 |
rs779247635 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298611 | GTCCAAAGCAAGTGG[A/C]AGAAAACAATAGAGA | 337867 |
rs779247999 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338865 | CACTTCTTAGCTTCA[C/G]TGATAACTAAACTCT | 337867 |
rs779249511 | in-del | -/AAAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232954 | TCAAAAAAAGAAAAG[-/AAAA]AAAAATAGCACTGTA | 337867 |
rs779259883 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99215098 | TCTGCATTACAATTA[A/C]AATCCAAACAGTTTT | 337867 |
rs779263783 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358464 | CAAAAATGGAAAACA[G/T]TGCCACTCTTCTCAG | 337867 |
rs779283249 | snp | C/T | 1.66054e-05 | 0.00288139 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295791 | AGGTCATAAAGTTCA[C/T]ACCTGCATATGTGTT | 337867 |
rs779284185 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210060 | AGGATGCTTTTAGAA[A/G]ATGTTTCTTTTCATC | 337867 |
rs779314155 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298186 | AAGACTTATTTACTC[-/A]ACATGATTTAAAAGC | 337867 |
rs779320116 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375724 | GTCCCATTTTACTTA[C/T]GTCAAAGAGGAGTTG | 337867 |
rs779332805 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99371042 | CCTCATGGGGCAGCC[G/T]TTAAGACGAGGTATT | 337867 |
rs779382672 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99234729 | CAGGGGCTTGTTTTC[A/G]GGATCTATGAGAGAG | 337867 |
rs779403697 | in-del | -/AAAAAAAAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268612 | GTGAGACTCTGTCTC[-/AAAAAAAAA]AAAAAAAAAAAAAAG | 337867 |
rs779442891 | snp | A/C | 1.64817e-05 | 0.00287064 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255456 | TCCCACACACGCCAG[A/C]ACGGCTTTGCACGTG | 337867 |
rs779464837 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239500 | CTGGTGGTGGCGCCT[A/G]GGCATTGCTGTACAT | 337867 |
rs779491818 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350323 | GATGACTGATGTCCA[C/G]GCTCTCCTGGATAGC | 337867 |
rs779504180 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267771 | AAAAAATACCAAAAT[A/G]TAGTGTGTTTGCTCA | 337867 |
rs779520622 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99356891 | GCCAGTTTGTGTGTG[A/G]TTCTGGTGGTGGGCT | 337867 |
rs779538837 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378054 | AAAATGCATGCTGCT[C/G]TAGTCCTTCAGTAAG | 337867 |
rs779543318 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358284 | ATGTCTGTAGTCATC[C/T]GAAAAGGCCCTTAAT | 337867 |
rs779546500 | in-del | -/AA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281661 | TAGAAGATACATAAC[-/AA]GAGGAAGAGGCTTTT | 337867 |
rs779559481 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99276614 | TTCACTGCAGAAGAG[A/T]TTTTATAGGGCTCCA | 337867 |
rs779579624 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375970 | ACCAAGCCCAGCTAA[-/TT]TTTTTTTTTTTTTTT | 337867 |
rs779593606 | snp | A/G | 6.58968e-05 | 0.00573969 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255228 | AGACGTCCTGCCGTG[A/G]AGGAGATTATGAATA | 337867 |
rs779604591 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264328 | AGTTTGGACCCACCA[A/G]CCTCTGGGACAGAGA | 337867 |
rs779604868 | snp | C/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305813 | CGCAGAGAGAAAACA[C/T]GCTAAAATATAAGAA | 337867 |
rs779623454 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99263385 | GAGTAGATCCAAATG[A/G]TCAGCAACATGTAAA | 337867 |
rs779640592 | snp | A/G | 8.14631e-05 | 0.00638161 | intron-variant | UBAC2 | GRCh38.p7 | 13:99243805 | ATTTTACTCTTGTTT[A/G]TTGTTCTTTTTTAAA | 337867 |
rs779652453 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201293 | CCGCGCTGAAGGAAG[A/G]GGCCGTCCCCCTTAC | 337867 |
rs779653821 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99324646 | AACCTGAGGAACTAC[A/G]GAATATTCTCCCTAT | 337867 |
rs779655808 | snp | A/C/G | 1.68238e-05 | 0.00290028 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385356 | CCAGGCCAACACTGG[A/C/G]ACCGGACCGGCAGCC | 337867 |
rs779664234 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241741 | CTTTTTTTTTTTTTC[-/A]ACTTTTTTTTTTTTT | 337867 |
rs779674325 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354843 | AGTCATGTCATCCAA[G/T]AAGTTGTTGGCATAA | 337867 |
rs779676095 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275767 | AAGCCTTTGATTATC[-/T]GTTTGGATTTAAGAT | 337867 |
rs779676583 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225594 | TTCCTCCCGCCAGTA[C/T]GTGAGCACCTCCTTC | 337867 |
rs779683865 | in-del | -/AA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318822 | GTGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 337867 |
rs779711866 | snp | A/G | 3.29544e-05 | 0.00405908 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295173 | ATACACTGACTTGCC[A/G]TTTCAGCATCCTCAT | 337867 |
rs779756224 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99331428 | AAGACAGTATGTGAG[A/T]AACGAATAATCTGTG | 337867 |
rs779777994 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282583 | AAAAGAAATAAAGAT[A/G]TTTATAACTGTTGGG | 337867 |
rs779814347 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99353115 | GTCAACAAAGCAGTC[C/T]AATCAGTTAAAGCTA | 337867 |
rs779821515 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385978 | TTTGCTCAGAGTATC[C/T]AGAGTTAGCCACTAG | 337867 |
rs779848379 | snp | A/C | 2.05857e-05 | 0.00320818 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB, splice-acceptor-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201427 | ATGTGTTTCTTCTTC[A/C]GTCTCCAAGAAGAGT | 337867 |
rs779853609 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346497 | AAGCCCTTAGGCCAG[C/T]CATGCCTCACCGGGT | 337867 |
rs779854425 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99317617 | AAAATGAGAAAGTTA[A/T]TTACATAAATATCAC | 337867 |
rs779881837 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302208 | TTATATGTGTATATT[A/G]TTAAGTGAGGAGTGT | 337867 |
rs779924393 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363637 | AGGATCTTCCTGGTC[G/T]GCCCATATTCCCTTT | 337867 |
rs779941958 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343019 | GGGCCCACCAGCTGT[A/G]GTAGTCGGTGTTAGC | 337867 |
rs779955876 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99271304 | GAGCAAAGACCTGAA[A/G]GGGTCAAGGTGTGAG | 337867 |
rs779958942 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236031 | GAAAGACCCATATTT[C/T]TTACTATACATAAAA | 337867 |
rs779971131 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350465 | GGCCAGTGATATAAT[C/T]AATTATATCTACATA | 337867 |
rs779973646 | snp | C/T | | | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352382 | AATCTACTTTCTGTC[C/T]CTGTAGACTTGCTTA | 337867 |
rs779983773 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238133 | ATTTCTTTACACTTG[A/G]GTAGCCATTTTCTGA | 337867 |
rs780008853 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272289 | TAGAGAAATTTTTAA[G/T]CATGTATAAGAAAGG | 337867 |
rs780009101 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207724 | GGACATTTGTCTCAC[C/T]GTAGAGCTGGGTGAG | 337867 |
rs780017009 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381332 | TGTGGCCTAAAGTCA[C/T]ACTTCATCACTCCAG | 337867 |
rs780043335 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299385 | GTTTCTTGACTGGGA[A/T]TTATGTTAAGTGAGG | 337867 |
rs780044078 | in-del | -/ATATATAC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237266 | TGCGTATATATATAT[-/ATATATAC]ACACACACACACACA | 337867 |
rs780059041 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311750 | AAGGATTATTTTGTG[A/G]CCCTAAATGTAGTGA | 337867 |
rs780067698 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281175 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA | 337867 |
rs780077251 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267166 | CTTGGCCATTTATAT[A/G]TATTTCTTCTTTAGA | 337867 |
rs780085075 | snp | A/G | 1.65397e-05 | 0.00287569 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356177 | GTTGGGTTGCATCCT[A/G]AGCTGTGCTGGAGCT | 337867 |
rs780090117 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99321871 | TGGCTGTCAGACCTC[A/C]GTCCTATTTTGTTAT | 337867 |
rs780094002 | in-del | -/TC | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327474 | GGTTTTTGGTTTTTC[-/TC]TCTCTCTCTCTGTGT | 337867 |
rs780105154 | snp | A/C | 1.64909e-05 | 0.00287144 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255746 | TGAAAACCCATAATG[A/C]AGTGATGTTAACAAA | 337867 |
rs780106883 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99204663 | AGAGATTTTCAAAAC[A/G]GGCCTGAAGCGCGAC | 337867 |
rs780126217 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378118 | CACTTTTTCTGCAGC[A/G]TTAGCATCATCTCCA | 337867 |
rs780143447 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99221757 | GTTCCAGCACCTGTC[A/G]GAAACATCTGTCACT | 337867 |
rs780161923 | snp | C/T | 1.72737e-05 | 0.0029388 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254885 | TTATTATTCATAACA[C/T]TTCACTGTTTATATT | 337867 |
rs780167144 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99267961 | CAAGGGCCTGGTCTG[A/G]TGGAGCACCTCTGCT | 337867 |
rs780172880 | snp | A/G | 6.58913e-05 | 0.00573945 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367793 | TCTTTTTAGGGAGGA[A/G]TGATCAATTGGAATC | 337867 |
rs780174780 | snp | C/T | 1.64917e-05 | 0.00287151 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295950 | TTGAATAGAGGGTGG[C/T]AGAGTTGATTTTTTT | 337867 |
rs780219422 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99309999 | ATCGAGTGCGATCAT[G/T]AATATATAGCAGTAG | 337867 |
rs780232065 | in-del | -/TTGTGTGTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216082 | TGTACCAACCTATAT[-/TTGTGTGTG]TGTGTGTGTGTGTGT | 337867 |
rs780235298 | snp | A/G | 1.64866e-05 | 0.00287106 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255647 | AAAACATTCGAAAGG[A/G]TAAAGTCATTATAAA | 337867 |
rs780298716 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292508 | GTTAGGTTTCTTTAT[A/G]AAGTATGGGTGACAC | 337867 |
rs780325778 | snp | G/T | 1.79506e-05 | 0.00299583 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200849 | CTGCGCGGTCGCTGG[G/T]GCTCGCACTTCAGCT | 337867 |
rs780337848 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200655 | CAGGCGGTTCTGACC[A/G]CCATCGTTTCAACCT | 337867 |
rs780343450 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99323021 | TGTGGAAGCATAAGC[A/G]TCTTTAGAGTATGTT | 337867 |
rs780344355 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99298205 | TGATTTAAAAGCTAA[C/T]AGAACTTGTACTGAA | 337867 |
rs780354881 | in-del | -/TGCAGTGAGCCAAGAA | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262640 | CCGGGAGATGGAGGT[-/TGCAGTGAGCCAAGAA]TGCAGTGAGCCAAGA | 337867 |
rs780359014 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372335 | ATGTCTGGGGAAAGA[C/G]AAGTCTAAATCTGAT | 337867 |
rs780361248 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256195 | GGAACTTTTGATGAG[A/G]TGATTCACAGCAACT | 337867 |
rs780363514 | in-del | -/TC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338046 | CTTTTTTTCTTTTTT[-/TC]TTTTTTTTTTTTTTT | 337867 |
rs780386610 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99349453 | CAGCTGGGCCCGAGG[G/T]ACCACTGCCATCAAG | 337867 |
rs780396822 | snp | G/T | 1.6489e-05 | 0.00287128 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254954 | TGCGCATGCTTCGAA[G/T]GTAATTACGGTATAG | 337867 |
rs780404266 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223158 | TCCCTTTCAAAAAAA[A/C]ATTTAGTTGTGATAA | 337867 |
rs780419013 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99286138 | CAATTGTATAAGCAC[C/T]GAATTCTGTGTACTA | 337867 |
rs780424043 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99249314 | TTCTGTTCCTGCATT[A/G]ATTTATTTAGGATAA | 337867 |
rs780432768 | snp | C/T | 1.65231e-05 | 0.00287424 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295669 | GAGTGTCTGAGCAAA[C/T]ACTAGAATCCAGACA | 337867 |
rs780444109 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99318266 | TCTGCCTCCCGGATT[C/G]GAGTGATTCTCCTGC | 337867 |
rs780451316 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241171 | CAGGAGGCTGAGCTG[A/C]GAGTATTGATTCAGT | 337867 |
rs780470541 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99378839 | TTGCTAGCATGTTGT[G/T]CAAGAAGGTACTTTT | 337867 |
rs780472407 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275424 | ATATTTTTGTGATTT[C/T]AGTTCACATTTCCTT | 337867 |
rs780511333 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244381 | CAAATATATATACAC[A/C]CATATGCATGTGTGT | 337867 |
rs780511373 | snp | A/C | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340416 | TCTTGGACACTTGAA[A/C]CCATCTTCTCTTCTT | 337867 |
rs780513949 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210279 | GTGCAATGTAGGAAA[A/G]CACTAGGAAGAAATA | 337867 |
rs780530654 | in-del | -/ACCTCTCAGTGAA | 2.80446e-05 | 0.00374453 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201392 | CCGCTTTAGAAGCTG[-/ACCTCTCAGTGAA]ACCTCTCAGTTTCAC | 337867 |
rs780550413 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99328128 | GTGTTTTACTTCTTT[C/T]ACTTGAACATGAAAA | 337867 |
rs780550866 | in-del | -/AAG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368212 | TGAAGGATCGGGGAC[-/AAG]GAGGTGGGAGGATGG | 337867 |
rs780566988 | in-del | -/TAAGATGCTTA | | | intron-variant, downstream-variant-500B | UBAC2, GPR183 | GRCh38.p7 | 13:99294077 | TATTGTAAAGAATCC[-/TAAGATGCTTA]ATTTTGTAAGTTTGC | 337867 |
rs780599760 | in-del | -/A | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305241 | TCTCTTTGGGCTTCC[-/A]AAACACCACAGCCAT | 337867 |
rs780605500 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211234 | AAACGAGTCTTTTCA[C/T]GCTCAGAAAATGATT | 337867 |
rs780622512 | in-del | -/G | 1.79197e-05 | 0.00299325 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254850 | GAAGTGAATTTTGAT[-/G]GGATTGAAATGAAAG | 337867 |
rs780628153 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99296786 | ACGACCGCAACAACC[A/G]TGACTAAAATGACAA | 337867 |
rs780633917 | snp | A/T | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257306 | AGTAATCTTGGAGGC[A/T]TAAATCTTATTTTTA | 337867 |
rs780653865 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99375277 | TCAACCAAGAGATGT[A/G]AAAGGAGGGGGGATC | 337867 |
rs780663650 | in-del | -/TTTATTTA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203031 | GTTTTATTTTATTTA[-/TTTATTTA]TTTATTTATTTATTT | 337867 |
rs780668095 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347743 | CATCATTAAGCACAG[A/G]CATGTGATAACGTCA | 337867 |
rs780677920 | snp | A/C | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299457 | AAGCAAATACACACA[A/C]ACACGCACACACACA | 337867 |
rs780715055 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373462 | TTTCCTTTAGCTGAC[A/G]GTGACCAGCTGTCTG | 337867 |
rs780718165 | snp | A/C | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99367905 | AAGTTTCTGAGGAAC[A/C]GGTAATTAATCAGTA | 337867 |
rs780722015 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99238276 | TCCCCAGGTCGATGT[C/T]TTGAAAGTGGATATT | 337867 |
rs780735302 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99253913 | GCAGAGAGGAAGTTA[C/T]AGTTGAATCATTTAT | 337867 |
rs780747416 | snp | A/G | | | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99261497 | TCTAACCCAGTTAGT[A/G]TACCTCCTTTCTGTT | 337867 |
rs780757727 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311238 | AGGCTGTAAGTGCTG[G/T]GGGGGAGGACAGTCA | 337867 |
rs780758311 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99284187 | ATTGTATTCAAACTT[C/T]GCTGCTAAAATAAGA | 337867 |
rs780778564 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99363732 | CACGTATATACACAC[C/G]CAAGAAAACCAAAAC | 337867 |
rs780790126 | snp | A/C | 1.6483e-05 | 0.00287076 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255449 | TCCAGACTCCCACAC[A/C]CGCCAGCACGGCTTT | 337867 |
rs780802441 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99208668 | ACAGGCTTCTGGTGC[A/G]TTCGGCTCCTCTCTG | 337867 |
rs780805223 | in-del | -/GGCCCCGGT | | | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200255 | GGGACCACGACAGTC[-/GGCCCCGGT]GGTGGGGATTCCGCG | 337867 |
rs780805914 | snp | G/T | 1.65773e-05 | 0.00287895 | intron-variant | UBAC2 | GRCh38.p7 | 13:99314076 | ACTATTATAGTGATT[G/T]TTTTTTATTTGTTTG | 337867 |
rs780831880 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252370 | TTGCCCTACATTTAG[C/T]AATGTTGAAGAGCAA | 337867 |
rs780835766 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332491 | CAGACTTACAGGGTC[A/C]CAGCTTCTGCTGTTG | 337867 |
rs780859002 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99314190 | GTTGTCCATCACAAA[C/T]AAGACATTGATTTAT | 337867 |
rs780903231 | snp | A/G | 1.69983e-05 | 0.00291528 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295057 | ACCAAAATACAATCC[A/G]TTTCACTTTCCATTT | 337867 |
rs780917588 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99291258 | AAGGTCTTAATCGAA[C/T]AGAAATTTGGGGGCT | 337867 |
rs780920496 | in-del | -/C | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256051 | TGGTTAACTACTGAA[-/C]ATTCACAGTAATTCT | 337867 |
rs780951689 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335612 | TGTGATACCTTCTAT[A/G]TGTATTTTTCATTCC | 337867 |
rs780958175 | snp | G/T | 1.64849e-05 | 0.00287092 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255059 | GGTTCATGAGGAAGG[G/T]GGTAAAGGCTCCCCA | 337867 |
rs780968999 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376891 | CTTTTTAGAAAATTT[C/T]TTTGAGACATTTTTA | 337867 |
rs780994707 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219884 | TCATCTATGTTGTAG[C/T]ATGTATCAGGATCCA | 337867 |
rs780995637 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225542 | TGCCACATTTTGTTT[A/G]CCCGTTTATGCATTC | 337867 |
rs780996723 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207786 | GCACTCTCCACCTTC[A/G]TTCCAGCTTAGGATC | 337867 |
rs781019222 | in-del | -/AAATA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277537 | TCTCAAAAAATAAAT[-/AAATA]AAATAAAATAAAAGG | 337867 |
rs781029659 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99273553 | ATGATTAAGGAAATG[A/C]TATCTCTTGGTAGGT | 337867 |
rs781052082 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99203611 | CACACACTGTTGATA[C/T]ACAGAGGATAAAGTA | 337867 |
rs781064699 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99305390 | ACACAGGCCACGTCC[A/G]GGGCTGCCTAACAAC | 337867 |
rs781068219 | in-del | -/TCTCAAAAGCCGAGG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99322409 | GGGATGCACCCTAAT[-/TCTCAAAAGCCGAGG]TCTCAGGACTGATCT | 337867 |
rs781073887 | snp | C/T | 9.8868e-05 | 0.00703024 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295156 | CACAGCACTAGAAAT[C/T]GATACACTGACTTGC | 337867 |
rs781096249 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99225884 | AATTATATTTGGCAG[C/T]GTTTATTTTTTAGTG | 337867 |
rs781096275 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99239278 | TTTTAGTTATTTATC[C/T]GTATTACTGATTTGT | 337867 |
rs781108564 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343221 | TGCTGACCACATGCT[C/T]ACTTTGTGGCCTACA | 337867 |
rs781122516 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99381549 | GGGCCATGGCATCAT[C/G]GTGGTGGATAGTAGG | 337867 |
rs781143267 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358680 | ACTCTGGAGCCACCC[C/T]GGCCATGGACTGTGG | 337867 |
rs781158447 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380180 | GTTGGTACTCAAAAA[A/G]TTTCAAATTCTGGAG | 337867 |
rs781173255 | snp | A/G | 1.65411e-05 | 0.00287581 | intron-variant, nc-transcript-variant | UBAC2, MIR623 | GRCh38.p7 | 13:99356158 | AGCATCCCTTGCAGG[A/G]GCTGTTGGGTTGCAT | 337867 |
rs781174167 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99272496 | TGTCTTAGTAAACTC[A/G]TGCTGTCATAGAGTG | 337867 |
rs781182706 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275937 | TGGGTTGGTCAGATT[-/C]CCCCAGATCATACTC | 337867 |
rs781225119 | snp | A/G | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302504 | CCTGGTTTGATAAGT[A/G]TTTGTCAATTATTTG | 337867 |
rs781261354 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295926 | GTATATCAGAAATCA[C/T]CAAATTTGTTGAATA | 337867 |
rs781262587 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292912 | AGAATATAACAATTA[C/T]ACAGCCCTGTCCTGT | 337867 |
rs781270916 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323645 | CACACTCACATTCAC[A/G]TTGACTCATCCATAT | 337867 |
rs781276555 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99367560 | AGAGCTTTTACACTG[C/T]CTATTACTTTCTTTT | 337867 |
rs781291697 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99211294 | GGAAGAGCTGAGATT[G/T]GACTCCGATTTGCCT | 337867 |
rs781299149 | snp | A/C | 0.000166389 | 0.00911959 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201180 | ACCCCACCTGGTATC[A/C]CCAGGTGCTCTGCCC | 337867 |
rs781302246 | snp | A/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257546 | TATTCATTTGCTGAC[A/G]TTTGAAAAAAAATGA | 337867 |
rs781302368 | in-del | -/T | | | intron-variant, downstream-variant-500B | GPR18, UBAC2 | GRCh38.p7 | 13:99254597 | TGTATGGTAGCTCGA[-/T]TTCCCCCCTACTGAC | 337867 |
rs781313554 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315148 | ACCACTTTTACAACC[A/G]TTTCTCATGAAATCT | 337867 |
rs781336778 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99268315 | CTTTATAGTCAAAAT[A/G]TGAAACATAGAAGGA | 337867 |
rs781365371 | snp | A/T | 1.64825e-05 | 0.00287071 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255537 | AGCACTAATAAAGGC[A/T]AGAAGCCATAAAGCA | 337867 |
rs781365572 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99206439 | ATGTGCCTTCTTCCA[C/T]GGAATCACGCGTCCC | 337867 |
rs781377492 | snp | C/T | 5.04876e-05 | 0.00502407 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295837 | CGCAGTTATCCTACA[C/T]AAGGCATCTCCGATT | 337867 |
rs781381681 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277888 | GGGAACTTGCTTAGT[C/G]TCGGGATCCATCTGT | 337867 |
rs781390568 | in-del | -/T/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314260 | TTTTCTTTAACCAGA[-/T/TT]TCTTTTTTTTTTTTT | 337867 |
rs781407366 | snp | C/T | 0.000181256 | 0.00951816 | synonymous-codon, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340445 | TTCAGAACCCACCAG[C/T]GAAGCCAGAATTGGG | 337867 |
rs781435251 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99379004 | AAGGTATAACAAAAT[A/G]TTTCAGTCATCATCC | 337867 |
rs781436736 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99362007 | GCAAGACCCTCATCC[C/T]CAAAAAAAGTTAAAA | 337867 |
rs781461032 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99282013 | ATGAAGGGCAGTGGC[A/G]TCATTGACCTAAGCT | 337867 |
rs781475866 | snp | A/G | 1.69367e-05 | 0.00290999 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99244550 | GGTTTTGTCAGCCTT[A/G]TTTGACTTTCTCCTC | 337867 |
rs781489648 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223302 | ATCCTTTTAATGTCT[C/G]TGGGGTCAGTAGTGA | 337867 |
rs781501815 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343367 | CTGTAAACTCCGCAC[A/G]GTGTCTTTCCCCCCA | 337867 |
rs781512756 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99358097 | AGGTGTGAGAGCACG[C/T]AGAGGAGTACAGGGT | 337867 |
rs781529703 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99212840 | TTTACTCTTCTTGAA[C/T]GAATTCACTCCATGT | 337867 |
rs781534556 | in-del | -/ATGAGCAAAT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99346905 | GAACTGTGGGAATTA[-/ATGAGCAAAT]ATGAGCAAATATGAG | 337867 |
rs781547944 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244689 | TTAAAGTGTTATTAT[A/T]ATTATGTGAAAGTCA | 337867 |
rs781548760 | in-del | -/TTA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338071 | TTTTTTTTTTTTTTT[-/TTA]TTTTGAGACAGAGTC | 337867 |
rs781557262 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320339 | TTAAAAGGAATCAGA[A/C]GTTTAAAATAAAATT | 337867 |
rs781558665 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236220 | GGATTAAATCAAACT[A/G]AAAAGCTCCAGTTGC | 337867 |
rs781568914 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99339068 | ATGTCATATCATATC[C/G]AGTGACTCTGAAATC | 337867 |
rs781568983 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99351105 | CCTGGGTTGACAGGG[A/G]CATCTATACACAATC | 337867 |
rs781572341 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99330954 | TCCGCTTGTTAAAAT[-/G]GGATATTAGAAGGTG | 337867 |
rs781573978 | in-del | -/TTC | 6.74635e-05 | 0.00580751 | intron-variant, cds-indel, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201418 | TTCACTTGGATGTGT[-/TTC]TTCTTCAGTCTCCAA | 337867 |
rs781598886 | snp | A/G | 0.00163532 | 0.028548 | utr-variant-5-prime, upstream-variant-2KB, missense | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200836 | GCCAAGAGTGCGCCT[A/G]CGCGGTCGCTGGGGC | 337867 |
rs781649181 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99231820 | GCAACACAACTACAT[A/G]CTTTACTGTCTGTGC | 337867 |
rs781659489 | snp | A/G | 1.78086e-05 | 0.00298396 | utr-variant-3-prime, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99254864 | TGGGATTGAAATGAA[A/G]GAACCTTATTATTCA | 337867 |
rs781664176 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99264437 | TTAAAAACTGCCTTA[C/T]AGCTTGTGTAAAGTG | 337867 |
rs781664348 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GPR18, UBAC2 | GRCh38.p7 | 13:99258488 | AAGTCACACTTAGCA[G/T]AAGCTCCCCTTGAAA | 337867 |
rs781694906 | in-del | -/GG | 1.64844e-05 | 0.00287087 | frameshift-variant, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255074 | GGTAAAGGCTCCCCA[-/GG]GGGATTGTAACTGTT | 337867 |
rs781698987 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99277545 | AATAAATAAATAAAA[G/T]AAAATAAAAGGCAAT | 337867 |
rs781712277 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99357143 | GTTTAGATACACAAC[C/T]ACCATTGTGTTACAG | 337867 |
rs781714059 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99201333 | TTCTTTTAGGCTTGG[A/G]GGACCGAACTAACTC | 337867 |
rs781760585 | snp | A/G | 4.98484e-05 | 0.00499216 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340295 | TACTACATTTAAACA[A/G]TCACATTGGACGTTT | 337867 |
rs781765000 | snp | A/C | 4.94246e-05 | 0.0049709 | missense, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99340397 | CTGGATGGCAAAATT[A/C]TTTTCTTGGACACTT | 337867 |
rs781773234 | snp | A/T | 1.64936e-05 | 0.00287168 | intron-variant, missense | UBAC2, GPR183 | GRCh38.p7 | 13:99295337 | GAGAAACGAAGCTTC[A/T]TAATCATATGTTGAA | 337867 |
rs796072223 | in-del | -/GTGTGTGTGTGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368725 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGT]ACACATACCCTCACT | 337867 |
rs796076154 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281207 | AAAAACAAAACAAAA[A/C]AAAACAAAAAAAAAC | 337867 |
rs796089797 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99274092 | TCCCTAAAAGGTCCA[C/G]TTTTGCTACCTTACA | 337867 |
rs796094671 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99314263 | TTCTTTAACCAGATC[-/TT]TTTTTTTTTTTTTTT | 337867 |
rs796096988 | in-del | -/AT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380127 | ACTGCAGCCCATCAC[-/AT]GAGGTCAGGTGTGGA | 337867 |
rs796100519 | in-del | -/TGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99244035 | TTTTGTTAAACTTGG[-/TGT]TGTTATTTACAGTTA | 337867 |
rs796101868 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99202437 | GGAACTACTGGTTAT[A/G]AAATTAATGGTGGAA | 337867 |
rs796103799 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99366637 | AGTTTGATTTTTTTT[-/T]CATCCCTTTCGCTGA | 337867 |
rs796131995 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210226 | AAAATGAGTACGTGT[C/T]CATCAGAGACAATTC | 337867 |
rs796133188 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99332827 | TGAGGGCCTGCAAGA[C/T]CTCCTTGGTAGAGTT | 337867 |
rs796137971 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99218507 | ACCTTTTTTTTTTTT[-/T]CCCTGGAAACTTCTT | 337867 |
rs796175256 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347328 | CCGGGCGCCCCCCCC[C/G]CCCCCCAGGAAAAAA | 337867 |
rs796175632 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99252449 | TTTGAACCACAGACC[C/T]GTTCATTTCTTTTTC | 337867 |
rs796181873 | in-del | -/TTTC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338042 | TAACTTTTTTTCTTT[-/TTTC]TTTTCTTTTTTTTTT | 337867 |
rs796187716 | in-del | -/TG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99247208 | CTGTTTTTTTTTTTT[-/TG]TTTTGTTTTGTTTTG | 337867 |
rs796194668 | in-del | -/TTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373186 | GTTTTTTTTTTTTTT[-/TTT]AAACAGGTATCTTTA | 337867 |
rs796198577 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99343339 | CCCATTGTGGTTCTC[C/T]TTTCCTGCCTTGCTG | 337867 |
rs796209225 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99380119 | GCATTTTGACTGCAG[C/T]CCATCACATGAGGTC | 337867 |
rs796225531 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR18 | GRCh38.p7 | 13:99262719 | CCCTCTCAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 337867 |
rs796251085 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377897 | CTGCATGTGGTCACA[C/T]GGGGCCAACTCCAAA | 337867 |
rs796262595 | in-del | -/CC | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347333 | CGCCCCCCCCCCCCC[-/CC]AGGAAAAAAAAGGCA | 337867 |
rs796269206 | in-del | -/TGTGTGTGTGTG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216083 | GTACCAACCTATATT[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 337867 |
rs796321384 | in-del | -/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384123 | TGAGCAGAGGAAGGG[-/G]TGGTGATACTGGGCC | 337867 |
rs796326498 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329895 | TGCTTATTGTTTCAA[A/G]CCACTGAGTCTTAGG | 337867 |
rs796327419 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297796 | TACAGGACAGAGACT[A/G]TCGGTTTAGATTAAA | 337867 |
rs796350712 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259497 | AACCATAGCAACTAT[C/T]TCTTGTGTGGATGAA | 337867 |
rs796355639 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373187 | TTTTTTTTTTTTTTT[-/TT]AAACAGGTATCTTTA | 337867 |
rs796362577 | multinucleotide-polymorphism | GC/TT | | | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385918 | ATGGTGATAACCATG[GC/TT]CTGGTTCAAGGTTCT | 337867 |
rs796384531 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99372137 | GCCACACAGTGCGCC[C/T]TGTGCTGCCTGGCCT | 337867 |
rs796420668 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311905 | GTGGGGGTAGGAACC[C/T]GCTGTGCCGTGCACC | 337867 |
rs796427954 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99281668 | TACATAACAAGAGGA[A/G]GAGGCTTTTCTTGTC | 337867 |
rs796430489 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232766 | GTCTCTACACACACA[A/C]AAAAACAAAAACAAC | 337867 |
rs796440720 | in-del | -/CCG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347332 | CGCCCCCCCCCCCCC[-/CCG]CCAGGAAAAAAAAGG | 337867 |
rs796445153 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99377211 | TGGTGCCAGCCCTCA[-/A]GGGAGCTCACCGTCT | 337867 |
rs796476053 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325179 | GCGATCTTGGTTCAC[C/T]GCAAGCTCCACCTCC | 337867 |
rs796476748 | snp | A/T | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299543 | TTACTCATATATTCT[A/T]GATTTTTAATGCTGA | 337867 |
rs796488981 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99383369 | AAATGAATTCTTTTC[A/G]ATTCTAGTTTTGTTA | 337867 |
rs796512212 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99382253 | AATTCATTTTGGTTG[A/G]CTGGAAAATGATCAG | 337867 |
rs796559769 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99311074 | TTTTACTGTTTTAAA[A/G]GAAAATTCATTTCTT | 337867 |
rs796565049 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99242367 | GGACGGGGCGGCTGT[C/G]CGGGCAGAGGGGCTC | 337867 |
rs796570730 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99320264 | TAAAATTATATGTTA[C/T]GATTATAGTCTTTTC | 337867 |
rs796646610 | snp | C/G | | | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99257472 | CTTACAAACCATCTT[C/G]AGTCTTTTTTCCCAC | 337867 |
rs796673519 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99323853 | TAGCGACCAGTTGAC[A/G]TGTGATTTTTAAATG | 337867 |
rs796682831 | in-del | -/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99207994 | GCCTCTCATCGTCTC[-/TT]TTTTTTTTTTTTTTT | 337867 |
rs796695226 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290584 | ACAAAAATTAGCTGG[A/G]TGCAGTGGTGGGCAC | 337867 |
rs796703186 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373493 | CTCTGCACCGGGGCT[A/G]AGCGCTGTGCTGAAT | 337867 |
rs796703929 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99315948 | ATTGCGGTTTTTGCC[A/T]TTAAAGTAAGGCAAA | 337867 |
rs796707568 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325269 | ACCATGCCCAGCTAA[-/T]TTTTTTTGTGTTTTT | 337867 |
rs796718004 | snp | A/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99210446 | GTAATCATAATGAGC[A/T]TGTATATGCTCCGCT | 337867 |
rs796721558 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99219209 | CTTGTGGAGGCAGGC[A/G]GAGTTTCTGGGTTGC | 337867 |
rs796726682 | in-del | -/TTGTTT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99373169 | TCTCTCTCTTTTTTA[-/TTGTTT]TTTTTTTTTTTTTTA | 337867 |
rs796737986 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99232877 | AGCCTAGGAGGTGGA[A/G]GTTGCAGTCAGCTGA | 337867 |
rs796770550 | in-del | -/CA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99237297 | ACACACACACACACA[-/CA]GTGGAATATTATTCA | 337867 |
rs796779122 | snp | C/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216834 | ACTCTTTTCTTTTTT[C/T]TTTTTTTTTTTTTGA | 337867 |
rs796798318 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99236987 | TCTTAAAAAAAAAAA[-/A]TAAAACTACCATATG | 337867 |
rs796800785 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99290754 | AAAAAAGAAAGAAAG[A/G]AAGAAAAAGAAAAGA | 337867 |
rs796804408 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99341419 | CAGAGTTTATATCAG[-/C]GGGGGGGGAGGAAGG | 337867 |
rs796806390 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99347130 | TTTAAAGAAAAAAAA[-/A]GATCTACGGATACTC | 337867 |
rs796808653 | in-del | -/TG | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99216083 | GTACCAACCTATATT[-/TG]TGTGTGTGTGTGTGT | 337867 |
rs796826936 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99335361 | CATTTCTACTTCCTT[G/T]CCTCCAATTCATTAC | 337867 |
rs796831997 | snp | G/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99310559 | TGGTATTTTGTGAAG[G/T]CTGTGTGTGTAGAAA | 337867 |
rs796834447 | in-del | -/CCTCA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99376995 | CCTCGCCTCGCCTCG[-/CCTCA]CCTCACCATTGCCTC | 337867 |
rs796842817 | in-del | -/T | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99289616 | CTCTGTGTATTGGTC[-/T]TTTTTTTTTTCATTC | 337867 |
rs796850913 | in-del | -/CA | | | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299463 | ATACACACACACACG[-/CA]CACACACACACAGAA | 337867 |
rs796877414 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99309119 | GTCCTCCCAACCTTC[-/T]TTTTTTTTTTTTGAG | 337867 |
rs796884715 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99223839 | ATTTTTTTGTGGCCA[A/G]GGAACATGCTTTATA | 337867 |
rs796905765 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99329447 | TACACATCAAGAGGT[A/G]GAGCTTATTTTTCCT | 337867 |
rs796935845 | in-del | -/AAA | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99241281 | AAAAAAAAAAAAAAA[-/AAA]GAAAAGAGTTACTAT | 337867 |
rs796949743 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99278661 | GAAGCGATCACATTA[A/C]CATGTTTGGAATAAT | 337867 |
rs796966114 | in-del | -/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99338052 | TCTTTTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT | 337867 |
rs796973877 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99384339 | ATAAGTACAAAAAAA[-/A]TGTATTCCTGTGGCA | 337867 |
rs796975721 | snp | C/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365395 | TGGGTATAGTTAACC[C/G]TTTAATTTTCAGTTT | 337867 |
rs796976422 | snp | A/C | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99275223 | TGTACTCAGGATGTC[A/C]GGGACCACAGTCATC | 337867 |
rs797010454 | snp | A/G | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99345367 | TGTAAGATGGACGGG[A/G]GAAAGGAGAAACCAC | 337867 |
rs797016884 | in-del | -/A | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99365768 | TATATGTCCATTCAG[-/A]AATAAACTTGTTATT | 337867 |