| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs1482833 | snp | G/T | 0.494526 | 0.0520307 | intron-variant | TAB3 | GRCh38.p7 | X:30840710 | CTGTGATGATTGTGA[G/T]GCCCGCCCAGTCTTG | 257397 |
| rs1905204 | snp | G/T | 0.263364 | 0.249643 | | | GRCh38.p7 | X:30836408 | TTTCCCTGTGTAACA[G/T]CAAGCATCTATCTAC | 257397 |
| rs2306530 | snp | A/T | 0.0650211 | 0.168175 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830511 | CAAAATCCATTTGGA[A/T]ATCTTGAGCTCAGCT | 257397 |
| rs2867974 | snp | A/G | 0.495377 | 0.0478567 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845524 | aactgtgctgttgaa[A/G]cacaaaggcaaccat | 257397 |
| rs3816757 | snp | C/G | 0.318088 | 0.24055 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830839 | ATACATGCACACAAA[C/G]AAAATGTTTTAAAAT | 257397 |
| rs3923111 | snp | C/T | 0.459 | 0.137183 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890728 | CAGTTGCTACCTCTG[C/T]GATACATTAAGAGTT | 257397 |
| rs4287088 | snp | C/T | 0.129174 | 0.218863 | intron-variant | TAB3 | GRCh38.p7 | X:30886467 | CAGACCACAGATTGC[C/T]CATCAAGATGCCAAG | 257397 |
| rs4456018 | snp | G/T | 0.493482 | 0.0567128 | intron-variant | TAB3 | GRCh38.p7 | X:30864805 | TGTGTGTGTGTGTGT[G/T]TTTTTTTTAAAGTTG | 257397 |
| rs4456019 | snp | G/T | 0.488958 | 0.0734796 | intron-variant | TAB3 | GRCh38.p7 | X:30864807 | TGTGTGTGTGTGTTT[G/T]TTTTTTAAAGTTGAG | 257397 |
| rs4501741 | snp | C/G | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30866728 | ataaatgaggggtgg[C/G]gggagcctcccatgc | 257397 |
| rs4578123 | snp | A/T | 0.0152462 | 0.0859689 | intron-variant | TAB3 | GRCh38.p7 | X:30879071 | aaataattcctaaaa[A/T]ggtatataaaatata | 257397 |
| rs4607776 | snp | C/T | 0.267357 | 0.249397 | intron-variant | TAB3 | GRCh38.p7 | X:30861793 | CAACTTAAAAAGAAA[C/T]AGGTGAAATTAATTG | 257397 |
| rs5005670 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30868184 | TTACAGGTGTGAGCC[A/C]CCACACCTGGCCTAT | 257397 |
| rs5901957 | in-del | -/A | 0.495066 | 0.0494232 | intron-variant | TAB3 | GRCh38.p7 | X:30852459 | GAATACACAAAGAAT[-/A]AATTCATCAAATTTT | 257397 |
| rs5901958 | in-del | -/TATAGCT | 0.259706 | 0.249812 | intron-variant | TAB3 | GRCh38.p7 | X:30868310 | AAAGCtatatatata[-/TATAGCT]tatatatatatatat | 257397 |
| rs5926966 | snp | G/T | 0.483665 | 0.0888858 | intron-variant | TAB3 | GRCh38.p7 | X:30861068 | AAATTTAGGTAAAGG[G/T]TATGCGGTGTTCTTT | 257397 |
| rs5926967 | snp | A/C | 0.272031 | 0.249027 | intron-variant | TAB3 | GRCh38.p7 | X:30868619 | GAGAGAGAGAGAGAG[A/C]GCGTGGGGGGGAGAG | 257397 |
| rs5927627 | snp | C/T | 0.392917 | 0.205122 | intron-variant | TAB3 | GRCh38.p7 | X:30840446 | CTCAAAACCTTGAAA[C/T]TTCCTGAGTAACGGC | 257397 |
| rs5927628 | snp | C/T | 0.145864 | 0.227279 | intron-variant | TAB3 | GRCh38.p7 | X:30841407 | gtgacagagagagtc[C/T]ccatctcaaaaaaaa | 257397 |
| rs5927629 | snp | A/G | 2.28022e-05 | 0.00337647 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854485 | GTGAGTGTTGATTCC[A/G]TGGAGATGGTTGATT | 257397 |
| rs5927631 | snp | C/T | 0.348932 | 0.229592 | intron-variant | TAB3 | GRCh38.p7 | X:30858727 | GGATTATATAAAACA[C/T]AACAAGGGGACAGTG | 257397 |
| rs5927632 | snp | G/T | 0.497719 | 0.0336977 | intron-variant | TAB3 | GRCh38.p7 | X:30863285 | ACTCTCAAACTTAAT[G/T]TTTTGATAACTATAT | 257397 |
| rs5927633 | snp | A/G | 0.270239 | 0.249179 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30871740 | CAACTAAGATAATTC[A/G]TCCAGTTTGACACAA | 257397 |
| rs5927634 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30878516 | caaaaaaaaaaaaaa[A/G]aaagaaagaaagaaa | 257397 |
| rs5927635 | snp | A/G | 0.301759 | 0.244583 | intron-variant | TAB3 | GRCh38.p7 | X:30887097 | GCTGGAGAAGGCAGG[A/G]ATGTGTATGTGTACC | 257397 |
| rs5927636 | snp | C/T | 0.00317376 | 0.039709 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889945 | CAGATGGCCTCACAG[C/T]TGGCAGCCACAGTCC | 257397 |
| rs5971518 | snp | A/G | 0.152078 | 0.230025 | intron-variant | TAB3 | GRCh38.p7 | X:30856563 | GAAGTAATCCATAAA[A/G]GTTTCCCAATTATTG | 257397 |
| rs5971519 | snp | A/T | 0.266995 | 0.249422 | intron-variant | TAB3 | GRCh38.p7 | X:30858527 | TCTGAGTCTCTATTT[A/T]TAATTAACCACACCT | 257397 |
| rs5971523 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | TAB3 | GRCh38.p7 | X:30868657 | gagagagaATTGTAA[C/T]CTTATTCACTTATTT | 257397 |
| rs5971524 | snp | A/G | 0.10695 | 0.205029 | intron-variant | TAB3 | GRCh38.p7 | X:30869352 | ggtgtgagccactgc[A/G]cccagccTTTTGTTT | 257397 |
| rs5971525 | snp | C/T | 0.10648 | 0.2047 | intron-variant | TAB3 | GRCh38.p7 | X:30871559 | GCCTAAATCTAAACA[C/T]ATGAAATCACTTGGA | 257397 |
| rs5971526 | snp | C/T | 0.133269 | 0.221074 | intron-variant | TAB3 | GRCh38.p7 | X:30882901 | aattctgtacaatct[C/T]tgcaacttcattgta | 257397 |
| rs5972240 | snp | A/G | 0.491052 | 0.0662862 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831059 | TTTGCATAAACTGTA[A/G]CATTTCATACTATGA | 257397 |
| rs5972242 | snp | C/T | 0.382885 | 0.211758 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843563 | GTTATATTTTGAGAC[C/T]ACTAAGCAACCTCAA | 257397 |
| rs5972245 | snp | C/G | 0.0974994 | 0.1981 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846399 | TCCCCAAATCTGATC[C/G]ATGACCATGGGACAG | 257397 |
| rs5972246 | snp | A/T | 0.265909 | 0.249493 | intron-variant | TAB3 | GRCh38.p7 | X:30848755 | AAGTTGTCTGTAAGA[A/T]AACAGGATGTTTGTA | 257397 |
| rs5972247 | snp | A/G | 0.155165 | 0.231314 | intron-variant | TAB3 | GRCh38.p7 | X:30853486 | GATTCAAATTCTTTC[A/G]TTTGATGAACTTTAG | 257397 |
| rs5972248 | snp | A/G | 0.16521 | 0.235182 | intron-variant | TAB3 | GRCh38.p7 | X:30853650 | AAACAAAGTCTATAC[A/G]TGACTCTGAAGCACT | 257397 |
| rs5972249 | snp | A/G | 0.151194 | 0.229646 | intron-variant | TAB3 | GRCh38.p7 | X:30856065 | CAATAAAATTCCTCA[A/G]GAGTTAAAACAATAA | 257397 |
| rs5972251 | snp | G/T | 0.187793 | 0.242137 | intron-variant | TAB3 | GRCh38.p7 | X:30864803 | TGTGTGTGTGTGTGT[G/T]TTTTTTTTTTAAAGT | 257397 |
| rs5972252 | snp | C/G | 0.307389 | 0.243324 | intron-variant | TAB3 | GRCh38.p7 | X:30873441 | gaggcaggagaatgg[C/G]gtgaacccgggaggc | 257397 |
| rs5972253 | snp | A/C | 0.12963 | 0.219114 | intron-variant | TAB3 | GRCh38.p7 | X:30874375 | GTTAAATTATTGGGG[A/C]GTGAAATTATGTCTT | 257397 |
| rs5972255 | snp | C/T | 0.409166 | 0.192785 | intron-variant | TAB3 | GRCh38.p7 | X:30878203 | GCAAATATTAAGACA[C/T]CTCTTGGCTGGGTGT | 257397 |
| rs5972256 | snp | A/G | 0.302092 | 0.244513 | intron-variant | TAB3 | GRCh38.p7 | X:30882241 | CAAATGTTCTAAATT[A/G]CTGAAATTATACTAA | 257397 |
| rs5972257 | snp | C/T | 0.208779 | 0.246578 | intron-variant | TAB3 | GRCh38.p7 | X:30883338 | tcttatgcactcact[C/T]atgggtcagatgcta | 257397 |
| rs5972258 | snp | C/T | 0.390699 | 0.206649 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890623 | Gtgaatcactcaggg[C/T]gatagcaggaaacaa | 257397 |
| rs6628557 | snp | C/T | 0.492348 | 0.0613792 | intron-variant | TAB3 | GRCh38.p7 | X:30871249 | TTCAGTTATTTAACA[C/T]GGATTTGAGAATAAG | 257397 |
| rs6631190 | snp | A/C | 0.496779 | 0.040003 | intron-variant | TAB3 | GRCh38.p7 | X:30832166 | AAGCTAAATTCATTC[A/C]GTATAAAAGACTTTT | 257397 |
| rs6631192 | snp | A/G | 0.490403 | 0.0686035 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844042 | GCTGGTTTTCATCAA[A/G]TCATGCACTGATTTG | 257397 |
| rs6631194 | snp | C/T | 0.489036 | 0.0732235 | intron-variant | TAB3 | GRCh38.p7 | X:30853799 | CCTGCCTTAGCCTCC[C/T]GAGTAGCTGGGATTG | 257397 |
| rs6631199 | snp | A/C | 0.0455357 | 0.143855 | intron-variant | TAB3 | GRCh38.p7 | X:30871333 | GTTATTTCTTGGGGG[A/C]AGATCTTTCAATCTC | 257397 |
| rs6631200 | snp | A/G | 0.352982 | 0.227804 | intron-variant | TAB3 | GRCh38.p7 | X:30873452 | ATGGCGTGAACCCGG[A/G]AGGCGGAGCTTGCAG | 257397 |
| rs6653845 | snp | A/G | 0.127347 | 0.217844 | intron-variant | TAB3 | GRCh38.p7 | X:30853800 | ctgccttagcctccc[A/G]agtagctgggattgc | 257397 |
| rs6653846 | snp | A/G | 0.127347 | 0.217844 | intron-variant | TAB3 | GRCh38.p7 | X:30853957 | tgggattacaggcgt[A/G]agccaccgcacccgg | 257397 |
| rs7051732 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | TAB3 | GRCh38.p7 | X:30850539 | aacatggtgaaaccc[C/T]gtctctactaaagat | 257397 |
| rs7051846 | snp | G/T | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30869636 | CTGGAAATCTAATTT[G/T]CTCTGGTCAAGGTGT | 257397 |
| rs7057279 | snp | C/G | 0.31229 | 0.242116 | intron-variant | TAB3 | GRCh38.p7 | X:30886709 | AACCTGACTAAGTGA[C/G]TTGGTGGAGGATGAC | 257397 |
| rs7063630 | snp | A/T | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30832064 | CATATGTTTTATATT[A/T]ATGGTTCATAAATAG | 257397 |
| rs7471382 | snp | G/T | 0.0245906 | 0.108123 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890432 | accatgcccggctga[G/T]tagttttggtagaga | 257397 |
| rs7884942 | snp | A/G | 0.16867 | 0.236401 | intron-variant | TAB3 | GRCh38.p7 | X:30839741 | AATGAAAAAACAAAA[A/G]AGAAATACGGGAAGC | 257397 |
| rs7886894 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | TAB3 | GRCh38.p7 | X:30855975 | ttattaatatttaaa[C/T]tgataaaaaacataa | 257397 |
| rs11095190 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835770 | TGTTtctctgtctct[C/T]tctctctctttcctt | 257397 |
| rs11095191 | snp | A/G | 0.386951 | 0.209151 | intron-variant | TAB3 | GRCh38.p7 | X:30888813 | GTCCGGCGAGGAAGG[A/G]CATCGTCCCCTCCGT | 257397 |
| rs11286233 | in-del | -/T | 0.432311 | 0.171064 | intron-variant | TAB3 | GRCh38.p7 | X:30886336 | ATTATCATTTGTTGA[-/T]TTTTTTTTTTGCCCT | 257397 |
| rs11316848 | in-del | -/A | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833853 | AAAAAAAAAAAAAAA[-/A]TTAATTTCATCTTTG | 257397 |
| rs12009228 | snp | A/T | 0.0525796 | 0.153379 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844992 | acacctagctaattt[A/T]taaaaaattatttgt | 257397 |
| rs12009876 | snp | C/T | 0.0131573 | 0.0800346 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829331 | TCCACTTCAGCATAT[C/T]ACTATGAATACTGGT | 257397 |
| rs12013226 | snp | A/G | 0.0525796 | 0.153379 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844889 | tgcagcggtgtgatc[A/G]cggctcactgcagcc | 257397 |
| rs12389825 | snp | A/G | 0.0068637 | 0.0581785 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829029 | TTGTGCACAATTAAA[A/G]ATTAACATGTACAAA | 257397 |
| rs12395424 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30862648 | ATTAGCTACCATTTA[C/G]TGGTAGCTAATAATA | 257397 |
| rs12396128 | snp | C/T | 0.10601 | 0.20437 | intron-variant | TAB3 | GRCh38.p7 | X:30881082 | gtctacaactacata[C/T]gatataaatacatct | 257397 |
| rs12560120 | snp | C/T | 0.320952 | 0.23972 | intron-variant | TAB3 | GRCh38.p7 | X:30847859 | AAAAGGCAGAATAGC[C/T]ACAATTCCACAGAAT | 257397 |
| rs12835913 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30852266 | TATCAATCAATACTG[G/T]TATCTCAGTTTCTAC | 257397 |
| rs12840578 | snp | C/T | 0.491679 | 0.0639643 | intron-variant | TAB3 | GRCh38.p7 | X:30836954 | AATGCAAGCCTTATT[C/T]AATGCCCAGCCAAGG | 257397 |
| rs12848009 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30874951 | TATGTGTAGGGATGA[G/T]AAAGGACTAGTGACA | 257397 |
| rs12848019 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30874961 | GATGAGAAAGGACTA[G/T]TGACACAGCAAGCTT | 257397 |
| rs12848235 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30875030 | TGGTACCATGTTCTA[G/T]AAATGGGGTGGGAGG | 257397 |
| rs12848273 | snp | G/T | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30875058 | AGGCGGTGAGGATGA[G/T]ATATGAAGGAGTAAT | 257397 |
| rs16989194 | snp | A/G | 0.123219 | 0.215468 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828786 | CCTCAGCAGCCAGGC[A/G]TCATCCGATTTATAT | 257397 |
| rs16989199 | snp | C/T | 0.406665 | 0.194823 | intron-variant | TAB3 | GRCh38.p7 | X:30851379 | GCTTATGCCAGGGAA[C/T]TGTAGTTACTGTCTC | 257397 |
| rs16989201 | snp | G/T | 0.138243 | 0.22363 | intron-variant | TAB3 | GRCh38.p7 | X:30852362 | TCATATTGATCTAAC[G/T]CATCTGAATTAATGT | 257397 |
| rs17283005 | snp | A/G | 0.0389457 | 0.134 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845419 | CACCCATGATGACCT[A/G]CAGCAGAGGTTGGCA | 257397 |
| rs28393463 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30869624 | CCTTGAAAATAACTG[A/G]AAATCTAATTTGCTC | 257397 |
| rs28421636 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30886033 | AAGCAGGGAGGGAAG[G/T]AGGATGTTAGAGTTG | 257397 |
| rs28425632 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30833089 | CATTCTCCTGCCTCA[A/G]CCTCCTGTGTAGCTG | 257397 |
| rs28524893 | snp | A/G | 0.338568 | 0.233786 | intron-variant | TAB3 | GRCh38.p7 | X:30860152 | CCGTGTGTCCGTATC[A/G]ATGAAGATAGCTAAA | 257397 |
| rs34085528 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30841415 | GAGAGTCTCCATCTC[-/A]AAAAAAAAAAAGAAA | 257397 |
| rs34119075 | snp | A/G | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30865634 | GAAACTTGAAGTTCA[A/G]AGAGGGCAAATAAAT | 257397 |
| rs34424836 | in-del | -/C | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843981 | TCATTTCCAGATCTA[-/C]TTTTTTTTTTCCCAA | 257397 |
| rs34426148 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831401 | TCAAAGTTTCACTTT[-/C]CAACCTGGCGCAGAC | 257397 |
| rs34468328 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848453 | TTGAACTGGGGAGGT[-/G]GGAGGTTGCAGTGAG | 257397 |
| rs34515057 | in-del | -/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30836064 | CTGCAAGTGCTTAAT[-/G]GGAAAACAAACTTGA | 257397 |
| rs34578092 | in-del | -/C | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830912 | CCCTTAATTAATTTG[-/C]CCCCCCCCCCCCAAA | 257397 |
| rs34915842 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30871944 | TTTCAGTGAATGAAA[-/A]CTTATGTTTAATTGA | 257397 |
| rs35391741 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30858938 | AGCATTAGAAAAACA[-/G]GGGAGTGGATTATCT | 257397 |
| rs35735429 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30887756 | GGTATCTATAACTGA[-/G]GGGGAAGACTCCATC | 257397 |
| rs35770876 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30883405 | TCAAGAACCCCATAA[-/G]GGGAGGCACTACTTT | 257397 |
| rs35873601 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848099 | ATGGAAGAACCTGTC[-/G]GGGAAAGTCAAGCAC | 257397 |
| rs36004559 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30865056 | CACCTGAAATGTGTT[-/G]CTGCAGAAAGGTTTA | 257397 |
| rs36041431 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30881922 | CTCAATACACACTAC[-/A]AGTCAACTGAAACAT | 257397 |
| rs36102455 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30866452 | GATGATTCTAAAACT[-/G]GGGGCAGGGAATATA | 257397 |
| rs36118419 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883862 | AAAATGGTGCTGCTT[-/A]AAAAAAAGTCTTACC | 257397 |
| rs36142402 | in-del | -/TA | | | intron-variant | TAB3 | GRCh38.p7 | X:30868299 | TGTTTAGTGAAAAGC[-/TA]TATATATATATATAT | 257397 |
| rs41305215 | snp | A/C | 0.017851 | 0.0927731 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828812 | TATATCCTACCACTT[A/C]CATGCCAATTGTCTG | 257397 |
| rs41309569 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845190 | TACTCTTAAAACACT[A/G]TAGAAAGTCTTAGCT | 257397 |
| rs55835208 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30882763 | ACAGCAAAAGGACAT[C/T]AGTGAGATTCTGGTA | 257397 |
| rs56260124 | in-del | -/TATATATA | | | intron-variant | TAB3 | GRCh38.p7 | X:30839937 | ATATATATATATATA[-/TATATATA]ATATATATTAAAAAA | 257397 |
| rs56291833 | in-del | -/TT | | | intron-variant | TAB3 | GRCh38.p7 | X:30876689 | TTCTGTATTTTTTTT[-/TT]GTAGAGATGGGGTTT | 257397 |
| rs56806483 | in-del | -/TACT | | | intron-variant | TAB3 | GRCh38.p7 | X:30839969 | AAAAAAACACACACT[-/TACT]AATATTTACTGTTTT | 257397 |
| rs57124332 | in-del | -/G/GTG | | | intron-variant | TAB3 | GRCh38.p7 | X:30864804 | TGTGTGTGTGTGTGT[-/G/GTG]TTTTTTTTTAAAGTT | 257397 |
| rs57251085 | in-del | -/AAAGAAA | | | intron-variant | TAB3 | GRCh38.p7 | X:30878519 | AAAAAAAAAAAAAAA[-/AAAGAAA]GAAAGAAAGAAAGAT | 257397 |
| rs57429165 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30852113 | ATAGGTTGGATCATC[C/G]CTTGTGAAGTCACAA | 257397 |
| rs57473665 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30864805 | GTGTGTGTGTGTGTT[-/G]TTTTTTTTAAAGTTG | 257397 |
| rs57662529 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30868315 | TATATATATATATAG[A/C]TTATATATATATATA | 257397 |
| rs58440336 | in-del | -/AAA | | | intron-variant | TAB3 | GRCh38.p7 | X:30866891 | AAAAAAAAAAAAAAA[-/AAA]GATTACAGTGAAGAA | 257397 |
| rs58473340 | in-del | -/AAA | 0.277129 | 0.248524 | intron-variant | TAB3 | GRCh38.p7 | X:30859685 | AGTCATTTTCTATTT[-/AAA]AAAAAAAAAAAAGTA | 257397 |
| rs58544319 | snp | A/G | 0.0271702 | 0.113344 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884502 | ATATTTTTAACCTCT[A/G]CACTCGCTGTGTAAT | 257397 |
| rs58960284 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | TAB3 | GRCh38.p7 | X:30880182 | TGGAAAATGACAAGA[C/T]GATATTAAAATCAAA | 257397 |
| rs59045957 | snp | G/T | 0.0251071 | 0.109193 | intron-variant | TAB3 | GRCh38.p7 | X:30857439 | GAAATAAAGTATTCT[G/T]TTTTTTTTTATAGAC | 257397 |
| rs59248674 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30887378 | GAAAAGAAAAAAAAA[-/A]CCTTGAGATTATCTG | 257397 |
| rs59375984 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884457 | TAGTTAGTGTCAGAT[C/T]TGAACATCTGGGCAT | 257397 |
| rs59723525 | in-del | -/TATATATATA | | | intron-variant | TAB3 | GRCh38.p7 | X:30839935 | ATATATATATATATA[-/TATATATATA]ATATATATTAAAAAA | 257397 |
| rs60278034 | in-del | -/TAACAAAATATTT | | | intron-variant | TAB3 | GRCh38.p7 | X:30887208 | ATAAACAAAATATTT[-/TAACAAAATATTT]GTTCTTTGAAGTATC | 257397 |
| rs60395132 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30868314 | CTATATATATATATA[G/T]CTTATATATATATAT | 257397 |
| rs60445066 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30835952 | GGTTTATCTTTTTTC[C/T]TTTTGTATTTGAGTG | 257397 |
| rs60948223 | in-del | -/GAA | | | intron-variant | TAB3 | GRCh38.p7 | X:30878518 | AAAAAAAAAAAAAAA[-/GAA]AGAAAGAAAGAAAGA | 257397 |
| rs61050544 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30831737 | TACTGGAAATGCATA[A/G]TTGAACAGAAAGTTG | 257397 |
| rs61169809 | snp | C/T | | | intron-variant, stop-gained, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836727 | GTGCGTCTGTAGTCC[C/T]AGCTACTCAGGTGGC | 257397 |
| rs61265853 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | TAB3 | GRCh38.p7 | X:30850922 | AAAATGTATATGATT[A/G]AAGAAAATTACTATG | 257397 |
| rs61276087 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30887378 | TGAAAAGAAAAAAAA[-/A]CCTTGAGATTATCTG | 257397 |
| rs61644834 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30873543 | AAAAAAAAAAAAAAA[-/A]GTTACATCAAGTGTG | 257397 |
| rs61659003 | in-del | -/T | 0.301425 | 0.244654 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890270 | CAAAGAGGAAATTCC[-/T]TTTTTTTTTTTTGAG | 257397 |
| rs61662320 | snp | G/T | 0.0110639 | 0.0735497 | intron-variant | TAB3 | GRCh38.p7 | X:30853502 | TTTGATGAACTTTAG[G/T]CCATTCTCCATGAAT | 257397 |
| rs62590398 | snp | C/T | 0.466372 | 0.125232 | intron-variant | TAB3 | GRCh38.p7 | X:30876136 | TTCACACACTGAATG[C/T]GATGTGGCCTTGAGT | 257397 |
| rs62590400 | snp | C/G | 0.0307697 | 0.120159 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885286 | ATGATCAATATGCTA[C/G]GTTTCCAAGCCCGCT | 257397 |
| rs63202161 | in-del | -/T | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890654 | ACCACCCCAATTATT[-/T]CAACCAAGAGAATTT | 257397 |
| rs66818218 | in-del | -/A | 0.362865 | 0.223073 | intron-variant | TAB3 | GRCh38.p7 | X:30850849 | CTTCCAATGAAAAAC[-/A]AAAAAAAACCAATAT | 257397 |
| rs67040429 | in-del | -/TA | | | intron-variant | TAB3 | GRCh38.p7 | X:30868349 | AGCTTTTATATATAT[-/TA]AGCTTATATATATAT | 257397 |
| rs71953930 | in-del | -/TC | 0.10648 | 0.2047 | intron-variant | TAB3 | GRCh38.p7 | X:30853517 | TCCATTCTCCATGAA[-/TC]TCTTTTTTCCTACTC | 257397 |
| rs71961280 | in-del | -/GGA | 0.00896606 | 0.0663524 | intron-variant | TAB3 | GRCh38.p7 | X:30885888 | GTGGAGAAGGGACTT[-/GGA]GGAGTTTTGGTGCCT | 257397 |
| rs73208293 | snp | C/T | 0.114895 | 0.210349 | intron-variant | TAB3 | GRCh38.p7 | X:30865114 | TCTAGTGTGTCTCAA[C/T]GGCATACTATTGATG | 257397 |
| rs73454153 | snp | A/G | 0.137341 | 0.223177 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834770 | AGACTACAGGTGCAT[A/G]CCACTACCACGCCCA | 257397 |
| rs73454154 | snp | C/T | 0.0271702 | 0.113344 | intron-variant | TAB3 | GRCh38.p7 | X:30837859 | ATGATGTGAGGTAGG[C/T]AGAGATCAGACTGTG | 257397 |
| rs73454162 | snp | C/G | 0.0271702 | 0.113344 | intron-variant | TAB3 | GRCh38.p7 | X:30849361 | ACAACCTCCCTCCCC[C/G]ACATAGCTGGTCACA | 257397 |
| rs73454171 | snp | A/G | 0.0312828 | 0.12109 | intron-variant | TAB3 | GRCh38.p7 | X:30858780 | GAAAGTGGTAGGCCA[A/G]CTTCTCTGTTTGTTG | 257397 |
| rs73454174 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30869385 | TTTTTGCCATCCCAC[A/G]TTTATGTTAACCCCC | 257397 |
| rs73454179 | snp | C/G | 0.186955 | 0.24192 | intron-variant | TAB3 | GRCh38.p7 | X:30873856 | AACAGTAGGCTATTA[C/G]TAGTTAAGTTCTGGG | 257397 |
| rs73454186 | snp | C/T | 0.0271702 | 0.113344 | intron-variant | TAB3 | GRCh38.p7 | X:30882132 | AAGTTAGAGTAACAA[C/T]GGCACCTGTTACATA | 257397 |
| rs73454188 | snp | C/T | 0.133269 | 0.221074 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884980 | ACTGCAAGATCTGTC[C/T]GCTTTAATGACAATA | 257397 |
| rs73454190 | snp | C/G | 0.0251071 | 0.109193 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889915 | ATTAATCAAGAGCTT[C/G]TTGCTGTGTGCTTGC | 257397 |
| rs73454192 | snp | C/T | 0.133269 | 0.221074 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889922 | AAGAGCTTCTTGCTG[C/T]GTGCTTGCAGATGGC | 257397 |
| rs73617005 | snp | C/G | 0.00738971 | 0.0603345 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845541 | ACAAAGGCAACCATA[C/G]GCAATATGTAAACAA | 257397 |
| rs73617006 | snp | C/T | 0.0282 | 0.115346 | intron-variant | TAB3 | GRCh38.p7 | X:30864716 | TTCCTGAAACAGTTA[C/T]ATCAGAGGTTGCAAA | 257397 |
| rs73617007 | snp | C/T | 0.321902 | 0.239437 | intron-variant | TAB3 | GRCh38.p7 | X:30870070 | CTTGTTACCTTCTTC[C/T]AAATAGATGGAAGCT | 257397 |
| rs73617008 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30872323 | GTAAGCACCACACCC[A/G]CACTGCAAGCCCACA | 257397 |
| rs74406581 | snp | C/T | 0.275949 | 0.24865 | intron-variant | TAB3 | GRCh38.p7 | X:30863419 | GTTTGGATGTTTGTC[C/T]CCTCCAAATCTCATG | 257397 |
| rs74426369 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | TAB3 | GRCh38.p7 | X:30864585 | TTCCCCACACTCTAG[A/G]AAATGATGTCGACAT | 257397 |
| rs75647627 | snp | A/T | 0.5 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30859682 | CACAGTCATTTTCTA[A/T]TTAAAAAAAAAAAAA | 257397 |
| rs76020043 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30842192 | CATTTTTATGTAACA[A/C]CTATCCAAAAATGAT | 257397 |
| rs76047811 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835377 | ATAAGGTAAAGTTCT[C/G]TTTCTTAGATTTGCA | 257397 |
| rs76887656 | snp | C/T | 0 | 0 | intron-variant, missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836799 | AATGAGCTATGATCA[C/T]GCCACTGCACTCCAG | 257397 |
| rs77069353 | snp | G/T | 0.5 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30886901 | GTTCCTGCTGTTTCA[G/T]CAACACCTCAGATAC | 257397 |
| rs77283332 | snp | A/T | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30868340 | TATATATATAAGCTT[A/T]TATATATATAGCTTA | 257397 |
| rs77390803 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30842193 | ATTTTTATGTAACAA[C/T]TATCCAAAAATGATT | 257397 |
| rs77657831 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30841536 | TAAATAAAAAAAAAA[A/C]CACTCTGTAATGAGC | 257397 |
| rs77821721 | snp | A/G | 0 | 0 | intron-variant, missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836800 | ATGAGCTATGATCAT[A/G]CCACTGCACTCCAGC | 257397 |
| rs77823519 | snp | A/C | 0.00738971 | 0.0603345 | intron-variant | TAB3 | GRCh38.p7 | X:30841619 | GTATTATTTAGATAG[A/C]ATTTATACATTCTTT | 257397 |
| rs77868699 | in-del | -/AAAAA | | | intron-variant | TAB3 | GRCh38.p7 | X:30866887 | AAAAAAAAAAAAAAA[-/AAAAA]GATTACAGTGAAGAA | 257397 |
| rs77897645 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30864809 | TGTGTGTGTGTTTTT[G/T]TTTTAAAGTTGAGCT | 257397 |
| rs78983192 | snp | A/C | 0.5 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30860338 | TAGGGGAAAATCTGG[A/C]TGAAGAGTAGGAAAT | 257397 |
| rs79033006 | snp | C/T | 0.5 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30838998 | TATGCTTTTTTTTTT[C/T]CTCTCTTACTGCATG | 257397 |
| rs79125112 | snp | C/T | 4.71659e-05 | 0.004856 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852922 | CTCCATCCTTGCTCG[C/T]TGATGTAACAGCAAG | 257397 |
| rs111271719 | snp | A/G | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884539 | ACTTGGTAAACTCTT[A/G]AAATGAACACAGCGT | 257397 |
| rs111397909 | snp | A/G | 0.126432 | 0.217327 | intron-variant | TAB3 | GRCh38.p7 | X:30888371 | AAATAATTTAAATAA[A/G]TTACATTTCAGTAGA | 257397 |
| rs111578099 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30862441 | CAAGGGCAATACCAT[C/T]GTCTTTTTTATGAGC | 257397 |
| rs111589218 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30874919 | TGAGACATGTCTAAA[A/G]AGAGAGAAAGGGACT | 257397 |
| rs111759031 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30889136 | CTGCTGCTCTCTGGC[C/G]GCCGCCGCCGCCGCC | 257397 |
| rs112084797 | in-del | -/T | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30868063 | ACCATACCTGGCTAA[-/T]TTTTTTTATTTTTCA | 257397 |
| rs112450160 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30871462 | CTAATAGCAAATGAA[C/T]TGTCCAAAGAACTTG | 257397 |
| rs112861312 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30870449 | GATACAGAAGACCCA[C/T]GTCCTCGTAGTGAGA | 257397 |
| rs113012379 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844102 | TCCCCCCGTCACCAC[C/T]GAAAAAGGTTTAGAT | 257397 |
| rs113150307 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30853623 | TTATTAGGCCTACAT[C/T]TTCATGTTTTAAAAC | 257397 |
| rs113307967 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875582 | AGGAAAGTATTCTCT[C/T]CCATGAGAGGAAAAA | 257397 |
| rs113329798 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30864602 | AATGATGTCGACATC[G/T]AGTGCTTTGTTTCCA | 257397 |
| rs113359712 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834212 | CAACTGCAAGAGTGA[A/G]CAGGCTCACAAGATC | 257397 |
| rs113369086 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30836154 | TATAGAATTTAATCA[A/G]GTTCTACTGTTTCTA | 257397 |
| rs113607106 | snp | C/T | 0.1121 | 0.208527 | intron-variant | TAB3 | GRCh38.p7 | X:30868282 | CTGTTTTCTGTTTAG[C/T]TCTGTTTAGTGAAAA | 257397 |
| rs113663623 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30868581 | CTTATATATATATAT[A/G]TATATAGAGAGAGAG | 257397 |
| rs113777005 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30875958 | AAGCACCTCCCTATC[C/T]GAAGGCAAGGAATAG | 257397 |
| rs113910772 | snp | C/T | 0.5 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30859198 | AATGTCTAAAGACAT[C/T]TTCAGTTGTCACAAC | 257397 |
| rs113911527 | snp | C/G | 0.0535814 | 0.15466 | intron-variant | TAB3 | GRCh38.p7 | X:30848511 | TGAGCAACAGAGTGA[C/G]ACTCTGTCTCAGAAA | 257397 |
| rs137921689 | in-del | -/ACA/CA/CACA/CACCACACACACACA/CCACACACACA | 0.00581518 | 0.0536683 | intron-variant | TAB3 | GRCh38.p7 | X:30859360 | ACACACACACACACA[lengthTooLong]AGAAAACATACCTGG | 257397 |
| rs137929593 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30880053 | ACCTAAATAAATGGC[A/G]TAGTGTATCATGTTC | 257397 |
| rs138198057 | snp | C/T | 0.0194105 | 0.0965841 | intron-variant | TAB3 | GRCh38.p7 | X:30853735 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 257397 |
| rs138249025 | snp | A/G | 0.00528398 | 0.051128 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891119 | TGTGGTCAGAAAGGG[A/G]GTCATTCACTCCTAT | 257397 |
| rs138250338 | in-del | -/A | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830454 | CACAAAATTGGAAGG[-/A]AAAAAAAAAGGCCCT | 257397 |
| rs138280257 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30875085 | TAATCTCCCAATTGT[A/C]TCAATCTTCAGGACA | 257397 |
| rs138335494 | snp | C/G | 9.1219e-05 | 0.00675287 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855198 | GATGGCTGTTGAGGT[C/G]GTTGTGAAGGAGGAG | 257397 |
| rs138358033 | snp | A/G | 0.125056 | 0.216539 | intron-variant | TAB3 | GRCh38.p7 | X:30857902 | TTTTTTGCCTCATTC[A/G]TTTCAAAAGTGTTCA | 257397 |
| rs138433290 | snp | C/G | 0.00528398 | 0.051128 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835766 | GGTTTGTTTCTCTGT[C/G]TCTTTCTCTCTCTTT | 257397 |
| rs138528610 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30847950 | ACACATTAATGTCAC[C/T]TAGTTTTAGCCCATA | 257397 |
| rs138678884 | snp | A/G | 0.0307697 | 0.120159 | intron-variant | TAB3 | GRCh38.p7 | X:30867378 | GTGCAGGGTATATGG[A/G]GACTCCCTGTACCAT | 257397 |
| rs138681542 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30848897 | CTCAAAGCTGTGGGA[C/T]AGTCCAAAAATGTAA | 257397 |
| rs138692777 | snp | A/C | 0.0445249 | 0.142408 | intron-variant | TAB3 | GRCh38.p7 | X:30858602 | AGGTAGAGTTTGAAC[A/C]TGAGTACTGACTGTG | 257397 |
| rs138718384 | snp | A/G | 2.64019e-05 | 0.00363322 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854995 | AACCAGGAGACCCAT[A/G]GAGATTGCTTGGAAT | 257397 |
| rs138904648 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | TAB3 | GRCh38.p7 | X:30872797 | TGTCACCACTTGAAC[C/T]CTCTGATGAATCTTC | 257397 |
| rs138970303 | snp | C/G | 0.0105399 | 0.0718252 | intron-variant | TAB3 | GRCh38.p7 | X:30841702 | AAAATAAGGCATTCT[C/G]CACTGTTCTATGTGT | 257397 |
| rs138973042 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | TAB3 | GRCh38.p7 | X:30886036 | CAGGGAGGGAAGTAG[C/G]ATGTTAGAGTTGGAC | 257397 |
| rs138985507 | snp | G/T | 0.0147244 | 0.0845304 | intron-variant | TAB3 | GRCh38.p7 | X:30851222 | AGTCACTAAATTAGT[G/T]AATATGCCAATTTCT | 257397 |
| rs139272751 | snp | G/T | 0.00896606 | 0.0663524 | intron-variant | TAB3 | GRCh38.p7 | X:30882120 | GGCATGTGTGAAAAG[G/T]TAGAGTAACAATGGC | 257397 |
| rs139553292 | snp | C/T | 0.0115877 | 0.0752302 | intron-variant | TAB3 | GRCh38.p7 | X:30868807 | CATACAAGTTTCTAA[C/T]TGATCTCCTGAGTCA | 257397 |
| rs139699892 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | TAB3 | GRCh38.p7 | X:30887929 | GGGCTGTCCCTACGG[C/T]TGTAAAGATTCATAT | 257397 |
| rs139972526 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30833308 | CCTCTTTTGTCTTTA[C/T]CTTTTAAAAGAACAA | 257397 |
| rs140007310 | snp | C/T | 2.82279e-05 | 0.00375674 | missense, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831437 | TGAATTCAGGTGTAC[C/T]GTGGCATCTCGCACT | 257397 |
| rs140121568 | snp | A/T | 0.0358881 | 0.129059 | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834350 | GCAGTGGTTCTTACA[A/T]CTTTTTTCCATCTTC | 257397 |
| rs140161833 | in-del | -/A | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842888 | TAACCTCTAGTGGAA[-/A]TTTCTTCAGATAAAT | 257397 |
| rs140216460 | snp | A/T | 0.0026455 | 0.0362733 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889977 | CCTGTTTCCCACATC[A/T]CCATCTAACTTTCTC | 257397 |
| rs140250377 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30860132 | AACCTGTAGAAAAGA[A/G]GGAGCCGTGTGTCCG | 257397 |
| rs140290769 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884981 | CTGCAAGATCTGTCC[C/G]CTTTAATGACAATAT | 257397 |
| rs140534111 | snp | G/T | 0.016289 | 0.0887646 | intron-variant | TAB3 | GRCh38.p7 | X:30847820 | CCATTAAATAAGCAG[G/T]TATCAAAGTTTAAAA | 257397 |
| rs140662477 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | TAB3 | GRCh38.p7 | X:30887148 | TCAAACCCCTATAGA[C/T]AGTTGCCATGTAATA | 257397 |
| rs140736203 | snp | C/T | 0.00528398 | 0.051128 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884225 | AAGGCGTATCATCTT[C/T]GAAAGTAGCTAAAGT | 257397 |
| rs140769916 | snp | A/G | 0.0353775 | 0.128208 | intron-variant | TAB3 | GRCh38.p7 | X:30841022 | AGTCACTGAGGTGTA[A/G]AGTTAGCATTGATCA | 257397 |
| rs140845779 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | TAB3 | GRCh38.p7 | X:30878370 | CCAGGTGTGGTGGCA[C/T]GTGCCTGTAGCCCCA | 257397 |
| rs140872082 | snp | A/G | 0.00016909 | 0.00919329 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854843 | CTGAGAAGGCTGATA[A/G]TTCTGTTGGTGTGGA | 257397 |
| rs140915660 | snp | A/G | 0.017851 | 0.0927731 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835010 | ATTCAGGAAATGATT[A/G]GGGAGCACGTGGTTG | 257397 |
| rs141293756 | snp | A/C/G | 0.00011405 | 0.00755072 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854239 | CTGGTGCTGCAGAGC[A/C/G]CTCTTCTTGGTCCAC | 257397 |
| rs141303169 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | TAB3 | GRCh38.p7 | X:30858013 | AAACTGCTGAGCTTC[A/G]TACATTTTAATGTGA | 257397 |
| rs141303942 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant, utr-variant-5-prime | TAB3 | GRCh38.p7 | X:30883588 | GTCTCCACTACTTAC[C/T]CTCGGCCTCTACCAG | 257397 |
| rs141348848 | in-del | -/A | 0.498438 | 0.0279033 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842660 | AAAAATAAAAAAAAA[-/A]TTAGCTGGGCATGGT | 257397 |
| rs141445915 | snp | G/T | 0.0323082 | 0.122924 | intron-variant | TAB3 | GRCh38.p7 | X:30879553 | AAAATCCAGTATCTA[G/T]TCATGATGTAAGCTC | 257397 |
| rs141569817 | snp | A/G | 4.74952e-05 | 0.00487292 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855457 | TAATATGTAAAAGGC[A/G]ATTTCTATTCATCCT | 257397 |
| rs141707503 | snp | C/G | 0.018891 | 0.0953342 | intron-variant | TAB3 | GRCh38.p7 | X:30858604 | GTAGAGTTTGAACAT[C/G]AGTACTGACTGTGTG | 257397 |
| rs141782925 | snp | C/T | 0.0292288 | 0.117303 | intron-variant | TAB3 | GRCh38.p7 | X:30851839 | CAGACAAGATTTACA[C/T]GTGCAGAGCTTTTTA | 257397 |
| rs141790277 | snp | C/G | 0.0121112 | 0.0768695 | intron-variant | TAB3 | GRCh38.p7 | X:30866966 | ACAGTGATAAGTCAC[C/G]TTGATAGTATGGACT | 257397 |
| rs141854102 | snp | A/G | 0.0079437 | 0.06252 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854351 | TGGTGATGGAGTACA[A/G]GAAGGTCCAGTTGGC | 257397 |
| rs141860001 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30886940 | AACCTGTTAAGGTCT[C/T]TCATTCCCTTGCCCC | 257397 |
| rs142143364 | snp | A/G | 0.0261392 | 0.111294 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833889 | AGAAAATTTTAAATT[A/G]TATATGTGGCTTGCA | 257397 |
| rs142193731 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830572 | GTGCTACTGGCAAAG[C/T]GCAGTTTTACGAGAA | 257397 |
| rs142229981 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833983 | GGTATGGTTTTACTT[A/G]TAATTCTACATGGAT | 257397 |
| rs142268253 | snp | G/T | 0.00738971 | 0.0603345 | intron-variant | TAB3 | GRCh38.p7 | X:30881359 | GTAAGAGGTTTTTTG[G/T]TTTTTTTTTAAGTGT | 257397 |
| rs142391267 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30862639 | ATCACTATAATTAGC[C/T]ACCATTTACTGGTAG | 257397 |
| rs142510904 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | TAB3 | GRCh38.p7 | X:30857237 | AATACTTTGAGTGAC[A/G]GAAAGATGTATTAAT | 257397 |
| rs142542306 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30850145 | TTGAGAGCCTACTCA[C/T]GGTCTCAACCACCAC | 257397 |
| rs142648955 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852507 | TCATTTCTATTTTGA[C/T]AGCAATTTACAAATA | 257397 |
| rs142650336 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840936 | TAAAGTTTGTCTGGC[A/G]ATACTTCTTTAGTAG | 257397 |
| rs142690348 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30867664 | AGACAGGATGCTAGA[C/T]CACACTTTCAGGGCA | 257397 |
| rs142722114 | snp | A/G | 0.0323082 | 0.122924 | intron-variant | TAB3 | GRCh38.p7 | X:30872919 | GAAAATATATTATGA[A/G]CCTAATTAAGCATAT | 257397 |
| rs142880484 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30878152 | AAAGGTTGACAAAAC[G/T]TCTAGGAGAATGAGA | 257397 |
| rs142924416 | snp | C/T | 4.55986e-05 | 0.00477464 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855234 | GCACTTCTGTTCTGT[C/T]CGTTCATAAAAAATG | 257397 |
| rs142938832 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | TAB3 | GRCh38.p7 | X:30875511 | CAAGGGCAGATATAT[A/G]TTATACCTACATATA | 257397 |
| rs142986201 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30869902 | TGTTTCACACACAGT[A/G]ATGGCAAATACTCAT | 257397 |
| rs143001205 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30880759 | TGAAAGCACAAACCT[A/G]TTACCTGGAAGATTT | 257397 |
| rs143096712 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30880096 | ATGATAAAGATGTCA[A/G]TTCTTCCCAAATTGC | 257397 |
| rs143129845 | snp | A/C | 0.0323082 | 0.122924 | intron-variant | TAB3 | GRCh38.p7 | X:30887169 | CCATGTAATAATGTA[A/C]TTTGAAATACTATTC | 257397 |
| rs143370025 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant | TAB3 | GRCh38.p7 | X:30853283 | CTTGAAACAATCTGA[A/G]TAGACTTTTTAAAAA | 257397 |
| rs143475818 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30847051 | AAAATTACAACAGTA[C/T]GGTGTTTACCAGAAT | 257397 |
| rs143517830 | snp | A/G | 0.0323082 | 0.122924 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830109 | TTATATCTCTTATCC[A/G]CACCCTGAAGTTCTA | 257397 |
| rs143546430 | snp | A/G | 0.0183711 | 0.0940641 | intron-variant | TAB3 | GRCh38.p7 | X:30866551 | TGATGAGGGCATGTC[A/G]AAATGACACAGGAGC | 257397 |
| rs143652667 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30857642 | GTTGGAATTGTCAGC[A/G]TATCTATAGTGACAA | 257397 |
| rs143822093 | snp | A/C | 0.0068637 | 0.0581785 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843893 | TAAACGATTACAGTT[A/C]ACTGTAGCCATACTT | 257397 |
| rs143834843 | snp | A/G | 0.0323082 | 0.122924 | intron-variant | TAB3 | GRCh38.p7 | X:30886609 | AGGCCCCCAAACAAT[A/G]TACTTCTTAAAAGAT | 257397 |
| rs143861401 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30877286 | CAGGCTCAGACAAAT[A/G]AAAACAGAGTTCATC | 257397 |
| rs143879115 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | TAB3 | GRCh38.p7 | X:30860129 | ATAAACCTGTAGAAA[A/G]GAGGGAGCCGTGTGT | 257397 |
| rs144267193 | snp | A/C | 0.134629 | 0.221787 | intron-variant | TAB3 | GRCh38.p7 | X:30856671 | AGTACATTTTATATA[A/C]AAATGAAAGGAAATA | 257397 |
| rs144404233 | snp | C/G | 0.0100156 | 0.0700533 | intron-variant | TAB3 | GRCh38.p7 | X:30879002 | ATGTCAGGAAGGAAA[C/G]AAGGGTATAAACACC | 257397 |
| rs144408952 | snp | A/C | 0.00581083 | 0.0535878 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836424 | CAAGCATCTATCTAC[A/C]TAATTGAGCTACGCA | 257397 |
| rs144632945 | snp | C/T | 0.0665023 | 0.16979 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835635 | ACTGTATTGTTTAAC[C/T]ACAAAGTCCAATCTA | 257397 |
| rs144688799 | snp | A/T | 0.016289 | 0.0887646 | intron-variant | TAB3 | GRCh38.p7 | X:30841051 | CTTTCGGCAAGAAAC[A/T]GCATATGATGCTGCC | 257397 |
| rs144718785 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | TAB3 | GRCh38.p7 | X:30849395 | GTGCACTGCAGTATC[A/G]TTAGGCAAGCAACTT | 257397 |
| rs144789541 | snp | A/G | 0.133723 | 0.221313 | intron-variant | TAB3 | GRCh38.p7 | X:30869117 | CCAGGCTGGAGTGCA[A/G]TGGCACGATCTCAGC | 257397 |
| rs144849666 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30840158 | TGTGTTCTCTTTTTT[-/T]ACAGATCAGTCTACC | 257397 |
| rs144884244 | snp | A/C | 2.44511e-05 | 0.00349642 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831545 | TCTCGAGGTTGTGTC[A/C]GAGGACTTTGTGTGG | 257397 |
| rs145014290 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | TAB3 | GRCh38.p7 | X:30872084 | TGAGATTTTAGCTTC[A/G]GAGAAAGCTAGCAAG | 257397 |
| rs145265402 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30833559 | AAATTTGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 257397 |
| rs145305101 | snp | C/T | 0.0271702 | 0.113344 | intron-variant, utr-variant-5-prime | TAB3 | GRCh38.p7 | X:30883632 | CTTCCCAAGGCTTGA[C/T]GGTCCTTGCTAGGAC | 257397 |
| rs145385355 | snp | A/G | 0.0100156 | 0.0700533 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890233 | AGGAGTGACAGATAT[A/G]GGGGGAGGATATAAA | 257397 |
| rs145473152 | snp | C/T | 0.0220041 | 0.102557 | intron-variant | TAB3 | GRCh38.p7 | X:30838247 | GGACTATAGGTGAGG[C/T]TGCAATGAGCTATTT | 257397 |
| rs145535995 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | TAB3 | GRCh38.p7 | X:30846918 | ATACAAGATACTACC[A/G]TTTTAATCATAGAGC | 257397 |
| rs145554772 | snp | A/G | 0.0625469 | 0.165413 | intron-variant | TAB3 | GRCh38.p7 | X:30851948 | ATTCTCTCATTACCC[A/G]TGAACATATACAGCA | 257397 |
| rs145856658 | snp | A/G | 0.0251071 | 0.109193 | intron-variant | TAB3 | GRCh38.p7 | X:30857309 | CCTTGCTTGAAAATC[A/G]TATTGAGCAAGGAAG | 257397 |
| rs146038809 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30850209 | TCCATTTTACACTAG[A/G]CTTGGCAATGGAAAC | 257397 |
| rs146104271 | snp | C/G | 0.0266548 | 0.112325 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30867188 | AAGGAGACATAACAA[C/G]CAACTGTGATGGGGT | 257397 |
| rs146114527 | snp | C/T | 0.000260247 | 0.0114042 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855378 | CTATGTACCAGTGTT[C/T]GACCACCATTAAGTT | 257397 |
| rs146126438 | snp | C/T | 0.0328205 | 0.123827 | intron-variant | TAB3 | GRCh38.p7 | X:30880992 | ACAAACTGAGATCTA[C/T]GTACATATCCCTCAA | 257397 |
| rs146167521 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30876115 | GGGTGAATCGCAATG[A/T]ATCAGTTCACACACT | 257397 |
| rs146302537 | snp | C/T | 0.0261392 | 0.111294 | intron-variant | TAB3 | GRCh38.p7 | X:30877499 | ATTTACCTACCTTGT[C/T]ACATACATATTGTTG | 257397 |
| rs146319957 | snp | C/T | 0.00670615 | 0.0575161 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855128 | GTATGAAGGAGGTGG[C/T]GGTGGTGGTGAAGGC | 257397 |
| rs146362092 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830833 | AATCACATTTTAAAA[C/T]ATTTTGTTTGTGTGC | 257397 |
| rs146424598 | snp | C/T | 0.0302564 | 0.119217 | intron-variant | TAB3 | GRCh38.p7 | X:30841021 | TTGATCAATGCTAAC[C/T]ATACACCTCAGTGAC | 257397 |
| rs146523065 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884628 | AACCATCTTGCCTTT[-/T]ATTAGGAGTATTTCC | 257397 |
| rs146547887 | snp | A/T | 0.00633741 | 0.0559334 | intron-variant | TAB3 | GRCh38.p7 | X:30864257 | TAAAGACATAAACCC[A/T]ATGATCATCACACAG | 257397 |
| rs146997033 | snp | A/G | 0.0635374 | 0.166528 | intron-variant | TAB3 | GRCh38.p7 | X:30879697 | AAAAAAGACAATAGC[A/G]CCACTATTACTACTT | 257397 |
| rs147101613 | snp | C/T | 0.00449972 | 0.0472188 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30842988 | AGATGGCTTGGGTGG[C/T]ACAACTGGGCCAGGT | 257397 |
| rs147263445 | snp | G/T | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30838254 | AGGTGAGGCTGCAAT[G/T]AGCTATTTTTAAATT | 257397 |
| rs147280760 | snp | A/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844022 | TTACCAAAAATCACA[A/G]AAAAGCTGGTTTTCA | 257397 |
| rs147454335 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | TAB3 | GRCh38.p7 | X:30836997 | CAACACCATGTATTC[C/T]AGGTGGGAGGTTCCT | 257397 |
| rs147474281 | snp | A/G | 0.0323082 | 0.122924 | intron-variant | TAB3 | GRCh38.p7 | X:30887534 | GAACACACACTCTAG[A/G]ATCAGACCTACATGA | 257397 |
| rs147490042 | snp | C/T | 0.0261392 | 0.111294 | intron-variant | TAB3 | GRCh38.p7 | X:30833264 | ATGGCATAGTAGGCC[C/T]GGTGCGGTGGCTCAC | 257397 |
| rs147504035 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30874368 | TAGAGATGTTAAATT[A/G]TTGGGGAGTGAAATT | 257397 |
| rs147616296 | snp | C/T | 0.0261392 | 0.111294 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833691 | AAAAAATTAGCCGGG[C/T]GTGGTGGCAGGCACC | 257397 |
| rs147653098 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828625 | TAACAAAATGGCAAA[C/T]GTGCTTTCTAAAATC | 257397 |
| rs147720934 | snp | A/G | 0.0110639 | 0.0735497 | intron-variant | TAB3 | GRCh38.p7 | X:30856793 | CATCTGCTCCAATTC[A/G]ACGCACATTTACAGA | 257397 |
| rs147799245 | snp | A/G | 4.59807e-05 | 0.00479461 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852864 | CTTCAGACTTCAACC[A/G]CTCTAGCTCCTCTTT | 257397 |
| rs148023412 | snp | A/T | 0.0152462 | 0.0859689 | intron-variant | TAB3 | GRCh38.p7 | X:30866605 | CAAAGCTGGAAAAAT[A/T]TGAACACCAAAATAA | 257397 |
| rs148370384 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836544 | GAGTTAAATGAGTCA[C/T]AGAAAAGAGTCTTTC | 257397 |
| rs148412357 | snp | A/T | 0.0317957 | 0.122012 | intron-variant | TAB3 | GRCh38.p7 | X:30855639 | CAGGCTTTGCCAGAG[A/T]GTTATGCAAATACTA | 257397 |
| rs148459223 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30849421 | AACTTTCTAATCAAT[C/T]TTGTATATACTGCCT | 257397 |
| rs148479473 | snp | A/G | 0.0445249 | 0.142408 | intron-variant | TAB3 | GRCh38.p7 | X:30840754 | CAGCAGCGTGAAAAC[A/G]GACTAATACACCACA | 257397 |
| rs148501440 | snp | C/T | 0.0147244 | 0.0845304 | intron-variant | TAB3 | GRCh38.p7 | X:30877635 | TAATCACAAAAAGAA[C/T]AAAAATGAATAAGTG | 257397 |
| rs148743009 | snp | C/G | 0.00633741 | 0.0559334 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844039 | AAAGCTGGTTTTCAT[C/G]AAGTCATGCACTGAT | 257397 |
| rs148779121 | snp | A/G | 9.49544e-05 | 0.00688971 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855431 | GCTACTAGGAGAATG[A/G]ATACCCAGGTTAATA | 257397 |
| rs148815498 | snp | C/G/T | 0.022522 | 0.1037 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829914 | CTAAGACGATATCCT[C/G/T]AGGTAAAATCCTTTA | 257397 |
| rs148847394 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30846989 | ACTGTAAGAATCAAC[C/T]TGTTAAACGAGTCAT | 257397 |
| rs148935751 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | TAB3 | GRCh38.p7 | X:30857513 | ACATAAGGTAGTCAT[A/G]GATACTTTAACATCT | 257397 |
| rs149023983 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30880080 | GTTCATGAATTAGAA[A/C]ATGATAAAGATGTCA | 257397 |
| rs149043136 | snp | C/T | 0.000281717 | 0.011865 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834105 | GTACTTTGGAGGTCA[C/T]GCTAATTCTTCGGGC | 257397 |
| rs149077162 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30872268 | GTCTGATGTAGTCTC[C/T]GGTAAAGTAGAGGAA | 257397 |
| rs149292536 | in-del | -/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890233 | GGAGTGACAGATATG[-/G]GGGGGAGGATATAAA | 257397 |
| rs149351132 | snp | A/T | 0.00141535 | 0.0265645 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855068 | AGGGAGGTTCTGGGA[A/T]ACTGTAACAGTAATT | 257397 |
| rs149414277 | snp | C/T | 0.0333324 | 0.12472 | intron-variant | TAB3 | GRCh38.p7 | X:30869000 | GCACTGACATAAATG[C/T]TGTTTCTACCATGTG | 257397 |
| rs149432846 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | TAB3 | GRCh38.p7 | X:30842077 | CTTAAATGACTGCAC[A/G]TGTAAATTCAATTAA | 257397 |
| rs149468489 | snp | C/T | 0.0131573 | 0.0800346 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859664 | GTAATGATCTTCTAG[C/T]ACCACAGTCATTTTC | 257397 |
| rs149767695 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | TAB3 | GRCh38.p7 | X:30833261 | GGTGTGAGCCACCGC[A/G]CCCGGCCTACTATGC | 257397 |
| rs149856446 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | TAB3 | GRCh38.p7 | X:30857262 | ATTAATTGAAGAAAA[C/T]CATTACAACTCAAAG | 257397 |
| rs149858533 | snp | C/T | 0.000186724 | 0.0096606 | missense, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831461 | TCGCACTGCTCACAG[C/T]GATTTAGTGCTGGGT | 257397 |
| rs149910140 | snp | A/G | 0.0414859 | 0.13792 | intron-variant | TAB3 | GRCh38.p7 | X:30851318 | TTGACCTAGCATTCA[A/G]GGTCAAAGCCCCAGT | 257397 |
| rs150051149 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30863836 | AAACACAAAGTTTTA[C/G]AGTAAAGTATTATGC | 257397 |
| rs150176434 | snp | A/G | 0.0027759 | 0.0371517 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854949 | GTTTGTCTTCCTGAT[A/G]AACTCTGAGATGTCT | 257397 |
| rs150243660 | snp | C/T | 0.0317957 | 0.122012 | intron-variant | TAB3 | GRCh38.p7 | X:30841682 | CTCTCTGGTAATTTT[C/T]TTCAAAAATAAGGCA | 257397 |
| rs150296533 | snp | A/G | 0.0220041 | 0.102557 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834583 | AGTAAGGCTATTACA[A/G]TGATGAAATGTGATG | 257397 |
| rs150393516 | in-del | -/AAG/GAA | 0.498286 | 0.0292213 | intron-variant | TAB3 | GRCh38.p7 | X:30878516 | AAAAAAAAAAAAAAA[-/AAG/GAA]AAAGAAAGAAAGAAA | 257397 |
| rs150417486 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30871752 | TTCATCCAGTTTGAC[A/G]CAACACAATCCACGG | 257397 |
| rs150528508 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30874544 | TGTCAAGTACCTACA[A/G]ATAAACAAGGGTATT | 257397 |
| rs150685307 | snp | C/G | 0.0328205 | 0.123827 | intron-variant | TAB3 | GRCh38.p7 | X:30831630 | TAGATTAACCTTTTT[C/G]CAAGTATAATCCAAA | 257397 |
| rs150720700 | snp | C/T | 0.0317957 | 0.122012 | intron-variant | TAB3 | GRCh38.p7 | X:30851191 | CTAATATTGACTATA[C/T]ACGATATTACAAAAA | 257397 |
| rs150896197 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | TAB3 | GRCh38.p7 | X:30881488 | AAAAAGCAATATACT[A/G]ATTACCAAAAATATA | 257397 |
| rs150917850 | snp | A/C | 0.000189982 | 0.00974449 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859566 | AGAACCTGAATATCA[A/C]GCTGTGGGCTGCTTT | 257397 |
| rs151005631 | snp | C/T | 0.0220041 | 0.102557 | intron-variant, utr-variant-5-prime | TAB3 | GRCh38.p7 | X:30883718 | AGTACTTGATGTACT[C/T]AGTGCATGTTCCTGC | 257397 |
| rs151218748 | snp | A/G | 0.0018473 | 0.0303354 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834172 | ATAAAAATAAACAAC[A/G]CCAGAAAGAAGTGAT | 257397 |
| rs151300607 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30847069 | TGTTTACCAGAATTC[C/T]CTCATTCCTTCTTCT | 257397 |
| rs180679552 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30846766 | TACGGCCTTAGTCCA[C/T]AAGAGGGCATGTTTA | 257397 |
| rs180839293 | snp | A/G | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885003 | TGACAATATTAGGCT[A/G]AGATGGACTAACTTA | 257397 |
| rs180843738 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30856824 | TGAGGAAAAAGATGC[A/C]TGGGAAGTTACATGG | 257397 |
| rs180851247 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30874922 | GACATGTCTAAAAAG[A/G]GAGAAAGGGACTGTA | 257397 |
| rs180873418 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30839203 | AAAGTTTTTGTCTGT[A/C]AGGAATGGCTGTTGA | 257397 |
| rs180889796 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30870571 | CTGAGGAAAGCTTCA[A/G]GGAAGAGATGACATT | 257397 |
| rs180890128 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30867100 | ATCCCAATTGAGTGA[C/T]AGTCTACAAAATACC | 257397 |
| rs180891224 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30842463 | TTAACTATGTAATAT[A/G]GTGTTTCAGCTTCTG | 257397 |
| rs180897364 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30862303 | CAGAACACTTCATGG[C/G]TATTTAATCAAACCT | 257397 |
| rs180904332 | snp | A/C | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889870 | CAAAGCCTCAGCTGC[A/C]CCTTCTTCATCCTGT | 257397 |
| rs180913833 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30850998 | AGTACCCAACTACTA[C/T]GGGTGGATTCCCATA | 257397 |
| rs180928650 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30879826 | AGAAGACTGAATACA[C/T]AGTAAAAGATCAAAT | 257397 |
| rs180948039 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30831653 | AATCCAAACTGAAAA[C/G]AAAAATACCACAAAA | 257397 |
| rs181276430 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30867866 | CATCCTGAGCCTCCA[C/T]TCTATTTAGAAAAGA | 257397 |
| rs181281739 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885479 | CCCATAACTGGAAGT[C/T]TGAGCTTCCCTAGGA | 257397 |
| rs181284289 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30847189 | TTATAAAGCTAGTAA[C/T]TGGTAGAGCCAGGAT | 257397 |
| rs181306361 | snp | A/C | 0.000529661 | 0.016265 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30826969 | AAAGTGTTGGGATTA[A/C]AAGCATAAGCCACCG | 257397 |
| rs181417506 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30836959 | AAGCCTTATTCAATG[A/C]CCAGCCAAGGAGGAT | 257397 |
| rs181629818 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | TAB3 | GRCh38.p7 | X:30874575 | TGACATTCACAGGCC[C/T]AACGTAAAATAATTG | 257397 |
| rs181647960 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30856587 | ATTATTGTGACCTTC[C/T]CTGTAGTTCATAAAT | 257397 |
| rs181655574 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838310 | ACACTTTTAATTACA[C/T]CATGTCTGGCTAATT | 257397 |
| rs181697648 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890093 | TGTTGTTCAGTTTCC[C/T]ATGTGCCAGCTACTG | 257397 |
| rs181720593 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30851678 | TGAGGGAGTGGCTGC[A/T]GACATGCTGACTGCA | 257397 |
| rs181746802 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30868584 | ATATATATATATATA[G/T]ATAGAGAGAGAGAGA | 257397 |
| rs181834565 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30871930 | TTTTACTACATGAAA[C/T]TTCAGTGAATGAAAC | 257397 |
| rs181838557 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891296 | GACTTTTCCTTATTA[C/T]GTGGCAAAAGTGGAC | 257397 |
| rs181851032 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30871298 | GAAGTTGGAAGATTC[A/G]TATATCCCACACACA | 257397 |
| rs181935461 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30886425 | TTAACGCTTTCTTGG[A/G]AGTATAACTATATTT | 257397 |
| rs182001343 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30851959 | ACCCGTGAACATATA[C/T]AGCACTTACCACACT | 257397 |
| rs182016738 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30847610 | TTAAATACTAGGGTG[A/G]TTTTAACTATAACAT | 257397 |
| rs182018940 | snp | A/G | 0.0266548 | 0.112325 | intron-variant | TAB3 | GRCh38.p7 | X:30833205 | CGATCTCCTGACCTC[A/G]TGATCCGCCTGCCTC | 257397 |
| rs182239740 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30878989 | GCTTTAAATATGTAT[A/G]TCAGGAAGGAAACAA | 257397 |
| rs182244235 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | TAB3 | GRCh38.p7 | X:30841872 | GGAGTACAGTGGCGC[A/G]ATCTCGGCTCACTGC | 257397 |
| rs182254590 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant | TAB3 | GRCh38.p7 | X:30848274 | CACTCCTGTAATCCC[A/G]GCACTTTGGGGGGCC | 257397 |
| rs182265264 | snp | G/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828626 | AACAAAATGGCAAAC[G/T]TGCTTTCTAAAATCC | 257397 |
| rs182302208 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30864989 | CCGTAGCTGATTCCA[A/G]ACACTGCAGCCTGGC | 257397 |
| rs182314622 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30872764 | AGTAAAAGGTTGGGC[G/T]TCACAAAGGGATCAA | 257397 |
| rs182316446 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844464 | TATGCTTTAAGAAGC[C/T]GCATATGTATTTCTT | 257397 |
| rs182501501 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30861330 | GAAAAATATATAGAC[A/T]AGCCTTTTAGATGAC | 257397 |
| rs182501586 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858563 | TAGGTTTAGGTTATG[A/T]CCTGAGCTGCTCACA | 257397 |
| rs182521664 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30887163 | TAGTTGCCATGTAAT[A/C]ATGTAATTTGAAATA | 257397 |
| rs182552510 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30869869 | GAAAAGAAAAAGAAA[A/T]AACAGAAAATATCGA | 257397 |
| rs182561661 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30887672 | TTAGCATAGGGTAGC[C/T]GTGAGGATCTCCAGT | 257397 |
| rs182569889 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848859 | TGTTCTTTGGTGGCT[G/T]GGACTCAGTTATGCC | 257397 |
| rs182603079 | snp | C/G | 0.00317376 | 0.039709 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833713 | GCAGGCACCTGTAGT[C/G]CCAGCTACACAGGAG | 257397 |
| rs182767812 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30876967 | GGAAAAGAGACAGAA[G/T]GGGGCAGAGGCAATA | 257397 |
| rs182770620 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840243 | TTTTTCTGTTTTCTA[G/T]CTCATTGACTTTCCT | 257397 |
| rs182849338 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30881106 | TACATCTCAAATTCA[C/T]GATGTTGCATAAAAG | 257397 |
| rs182861759 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843760 | CTGTCTGTCTTCAAA[C/T]GTTCATTCCCTGGTC | 257397 |
| rs182865922 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30862551 | GATCTTGAGAGCGGC[C/T]AGCTCTCACCTAGCT | 257397 |
| rs182870305 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30875402 | AAAAAAGTTTGTAAA[G/T]CACAATGTTCATTGA | 257397 |
| rs182883105 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | TAB3 | GRCh38.p7 | X:30852190 | ACTCATATATATTAA[C/T]CAACATGTTAAAACT | 257397 |
| rs182890623 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875902 | GAGAAAATGACAGTC[C/T]TTGCCACTTCTAAGA | 257397 |
| rs182902769 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30858441 | CTGTAACACAAAAAC[C/T]ATAAGCCCAAAGCTC | 257397 |
| rs182912592 | snp | A/T | 0.0121112 | 0.0768695 | intron-variant | TAB3 | GRCh38.p7 | X:30839824 | AAATATTTGGTGGAA[A/T]TTACCCACCAGTGAA | 257397 |
| rs183037496 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30882744 | TGCAACATGGTATCC[C/T]GGAACAGCAAAAGGA | 257397 |
| rs183115477 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30839362 | CAACTTGGTCATAAT[A/G]TATTATCTTTTTTTA | 257397 |
| rs183164870 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30857300 | TTATTTTTACCTTGC[C/T]TGAAAATCGTATTGA | 257397 |
| rs183165030 | snp | C/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829899 | CGTCTATGGATATTC[C/G]TAAGACGATATCCTC | 257397 |
| rs183366190 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30852617 | TTTTGATGAGAACTA[C/T]TAAAGGCAAAAGTCC | 257397 |
| rs183480636 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30827833 | TTGGGGATGCAAATA[A/G]TACAGGAAAAAAAGT | 257397 |
| rs183549628 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889554 | GGAAATGGGCAGTAC[C/G]AGTTACCGAAGAAGT | 257397 |
| rs183563114 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30850441 | TCGGGGGCCAGGTGC[A/G]GTGGCTCATGCCTGG | 257397 |
| rs183565914 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30870547 | AAGGTAGAACAAAGA[A/G]AAGGAGAGCTGAGGA | 257397 |
| rs183575383 | snp | A/G | 0.0026455 | 0.0362733 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831353 | GCTGGGTGGATGAAT[A/G]GAGTCCCGAGGTTTC | 257397 |
| rs183609450 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30873193 | GTGACCCTTGAACAG[C/T]ACAGGTTTGAATTAT | 257397 |
| rs183613487 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833940 | ACAGCCTTAGAAACT[C/T]GGTAATGTTTTTAAA | 257397 |
| rs183738142 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30882216 | AGGATTTTCTAAAAG[C/T]GCATATAAACAAATG | 257397 |
| rs183752390 | snp | C/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843985 | TTCCAGATCTACTTT[C/T]TTTTTTCCCAACAAG | 257397 |
| rs183759600 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885082 | ATCTAAAAAGCCTAT[C/T]AGTTTATCTCCCACA | 257397 |
| rs183772428 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30867411 | TCTCAATTTTTCTGT[A/G]AAACTAAAACTGTTT | 257397 |
| rs183812816 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889890 | CTTCATCCTGTTATG[A/G]GTTCACATTATTAAT | 257397 |
| rs183826251 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870887 | AATCTGCGAAACCCT[G/T]AACTCAACCCAAATA | 257397 |
| rs183934245 | snp | C/G | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30863513 | GAGCCCTTGTAAATG[C/G]TTAAGCACCATCCTA | 257397 |
| rs184038958 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840955 | CTTCTTTAGTAGACA[C/T]TCAGGCAAAATCGAG | 257397 |
| rs184452194 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30865809 | TGCTTTTAAAACAGA[A/G]GAGTTTTTGTACTAC | 257397 |
| rs184458032 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30883536 | ACAGCCTTTTAAGGA[A/G]CCAAGCCAGAAAAAA | 257397 |
| rs184459237 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30837864 | GTGAGGTAGGTAGAG[A/T]TCAGACTGTGTGTTT | 257397 |
| rs184460674 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845073 | CAAGTGATCCTCTCA[C/T]CTTGGCCTCCCAAAC | 257397 |
| rs184530959 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30873919 | TAGCTCACGCCTGTA[A/G]TCCTAGTACTTTGGG | 257397 |
| rs184543072 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836436 | TACATAATTGAGCTA[C/T]GCATTGAGCATTCAA | 257397 |
| rs184578620 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30853261 | GAAAACTAAATTCTC[C/T]GGTTATCTTGAAACA | 257397 |
| rs184587823 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30878025 | AAAGAAAAAGGATCA[C/T]TAGAGTTAAAAAGAG | 257397 |
| rs184593079 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851124 | CCTTTCCATTAAAGA[C/T]AACTTTGTTATTTTC | 257397 |
| rs184594521 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835416 | CTGTCGAGTCACATA[C/T]CTTATCTCACTAACT | 257397 |
| rs184679657 | snp | A/C/G | 7.86139e-05 | 0.00626912 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854998 | CAGGAGACCCATAGA[A/C/G]ATTGCTTGGAATTTG | 257397 |
| rs184699828 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30878473 | CCACTGCACACTCCA[A/G]CCTGGGCAACAGGGC | 257397 |
| rs184706913 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | TAB3 | GRCh38.p7 | X:30841560 | AATGAGCTTAATATA[C/T]GTAGAAAACTATTCA | 257397 |
| rs184713053 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30859936 | ATTTAAAAAAAAAAA[A/C]CAAAAAACAAAAACC | 257397 |
| rs184734184 | snp | C/G | 2.67695e-05 | 0.00365842 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859558 | GATCATGGAGAACCT[C/G]AATATCAAGCTGTGG | 257397 |
| rs184741999 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30831904 | AAATGTTTTATAGCA[A/T]GTTAAATTCTGTCGC | 257397 |
| rs185076665 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30856127 | CCTAAATTTATCCTT[C/G]AATAACTTCAACTGT | 257397 |
| rs185175302 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830068 | TATTAAGTTTCCAGC[A/G]ATGCACCCTAGTGAG | 257397 |
| rs185196221 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30874138 | GATCATGCCACTGCA[C/T]TCTAGCCTGGGGGAC | 257397 |
| rs185236138 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30846847 | ATCAAAATGGCCACA[C/T]ATAAACAAAATCTGC | 257397 |
| rs185271679 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30880224 | AGGGCCAAGAATAGC[A/G]AAGATGCTTTCGAAG | 257397 |
| rs185288937 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30862414 | CAACCTTAATTACAA[A/G]CCTTTAAAATACAAG | 257397 |
| rs185293665 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30849817 | TTGATTAATTTCCTA[C/T]ATAAGTATAATCTTA | 257397 |
| rs185302546 | snp | C/G/T | 0.00362318 | 0.0424083 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843071 | AGAAAGTAAATTCAT[C/G/T]AGGCATTTAAGAACT | 257397 |
| rs185363094 | snp | A/T | 0.016289 | 0.0887646 | intron-variant | TAB3 | GRCh38.p7 | X:30870272 | TTAAAAGATTTTTTT[A/T]AAAAATGAATAATCA | 257397 |
| rs185392239 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884164 | TGCATTAAAAAATTG[C/T]TACCAGGTAAACAAA | 257397 |
| rs185421160 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846299 | CACAGTAAATGACAA[A/G]AAGAGGATAAATGCA | 257397 |
| rs185465992 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30888764 | TGGGGGCTTAAAGCC[A/G]GTCCACAGAGGCTCA | 257397 |
| rs185529314 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866452 | GGATGATTCTAAAAC[G/T]GGGGCAGGGAATATA | 257397 |
| rs185547062 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30868196 | GCCACCACACCTGGC[A/C]TATATGATTTTTAAT | 257397 |
| rs185557275 | snp | A/G | 0.0152462 | 0.0859689 | intron-variant | TAB3 | GRCh38.p7 | X:30839682 | GGCAGGAGGTATATG[A/G]AAAATCTCCGCAACT | 257397 |
| rs185558870 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885492 | GTCTGAGCTTCCCTA[A/G]GACCACAGACCTCGG | 257397 |
| rs185989969 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30862628 | CCATTATTTTTATCA[C/T]TATAATTAGCTACCA | 257397 |
| rs185993578 | snp | G/T | 0.01368 | 0.0815649 | intron-variant | TAB3 | GRCh38.p7 | X:30841939 | TTAGCCACCTGAGTA[G/T]CTGGGATTACAGGCG | 257397 |
| rs185997019 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30881309 | GAGTTGTTCACTACC[A/G]TACTTTCTGTGTACT | 257397 |
| rs186001264 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843882 | TCTGCTTGTTCTAAA[C/T]GATTACAGTTAACTG | 257397 |
| rs186098228 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875024 | AGCTGGTGGTACCAT[A/G]TTCTAGAAATGGGGT | 257397 |
| rs186102422 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30839263 | TGAAACGATCACATG[C/G]TTTTCCTCCCTTTGT | 257397 |
| rs186224126 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30856873 | ACTAGTTAACAGAAA[A/C]GCCAATTCTAGATTC | 257397 |
| rs186292605 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30874588 | CCTAACGTAAAATAA[C/T]TGTTCAAGGCTATCA | 257397 |
| rs186300201 | snp | A/C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30856621 | CACACAGATATGTAC[A/C/G]TGCATAGATATTACT | 257397 |
| rs186311094 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838328 | TGTCTGGCTAATTTT[A/C/T]AAATTTTTTTTTGTA | 257397 |
| rs186488930 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30872656 | TTTCAGCTAATAATA[C/G]CAGAAGTGACCAAAT | 257397 |
| rs186494950 | snp | A/C | 0.00105904 | 0.0229869 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891320 | AGTGGACTAATACGG[A/C]AGCTCTGTTCCACAA | 257397 |
| rs186499347 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30852022 | TCCCACTGGTAGGTA[C/T]GTACTAAGCATCTAG | 257397 |
| rs186511056 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833570 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 257397 |
| rs186609131 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875614 | TTTTAGTTGATATTA[C/T]GCATCCTAATTTCAA | 257397 |
| rs186653373 | snp | A/T | 0.0317957 | 0.122012 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827149 | ATGACAAAGATTTTT[A/T]AAAAAAGAAAACTAT | 257397 |
| rs186654275 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30847306 | TGAAAACTTCAGAAA[C/G]AAATGAATTCCATTT | 257397 |
| rs186909354 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30887263 | AAGTAACTGAAAATA[C/T]CTGAATTTCAGATAG | 257397 |
| rs186914167 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30848350 | CCAACATGGCAAAAC[C/T]GTCTCTATTTAAAAT | 257397 |
| rs186923747 | snp | A/G | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30869533 | CTATAAATCTTGAGA[A/G]CAAGAATCAAACATG | 257397 |
| rs186941631 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832119 | TCCTCAGAATAGTGA[A/G]AAGAGGAAGATTCTA | 257397 |
| rs186998695 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30847841 | AAGTTTAAAATAAGT[G/T]ATAAAAGGCAGAATA | 257397 |
| rs187119255 | snp | C/T | 0.016289 | 0.0887646 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890305 | AGTCTCACTCTGTTG[C/T]CTAGGCTGGAGTGCA | 257397 |
| rs187126023 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851802 | AAAAAGTAGAGGTTA[A/C]GTTGAGCCTTGAAGA | 257397 |
| rs187128058 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30882783 | AGATTCTGGTAAAAT[C/T]GAGTAAAATCTACAG | 257397 |
| rs187136938 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844700 | CTATAGAGTGACTAG[C/G]CTTCTGAAAATGACT | 257397 |
| rs187142259 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30865518 | CATATTTACTGAGCC[A/G]TATCTGAGTATCAAG | 257397 |
| rs187174826 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30886553 | CTGAGGAACACAAGA[C/T]TCCTTTTTCTGTTTC | 257397 |
| rs187195806 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30887926 | CGGGGGCTGTCCCTA[C/T]GGTTGTAAAGATTCA | 257397 |
| rs187199230 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30868586 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 257397 |
| rs187204109 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828079 | TATTAAAATAATTCA[A/G]TTTTTAACTATAAAG | 257397 |
| rs187304605 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30861731 | AGGCAGCATTGTCCA[G/T]TAAAAAATATGTGAG | 257397 |
| rs187429002 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883723 | TTGATGTACTCAGTG[C/T]ATGTTCCTGCTGAGA | 257397 |
| rs187487287 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834272 | TTACCCTACCTATTA[C/T]TTCATGTTACCTTTA | 257397 |
| rs187575759 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30879373 | GGCCAATCCCACTCA[C/T]GAACAAAGATCTAAA | 257397 |
| rs187688055 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30877162 | CTTAATTTTCAACAA[A/C]AAAAATGGCAGCTAA | 257397 |
| rs187692929 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | TAB3 | GRCh38.p7 | X:30840459 | AATTTCCTGAGTAAC[A/G]GCAGTGTCTTTGTTA | 257397 |
| rs187739304 | snp | C/T | 0.00158814 | 0.0281345 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830412 | TGGCACAAAGTTTTA[C/T]CTGTGCTGTAAACAT | 257397 |
| rs187744557 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30876454 | TTCAAGGAGATGAAA[C/G]CCAAACTTAAAAATC | 257397 |
| rs187750315 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30839842 | ACCCACCAGTGAATC[C/T]ATCTGGATCTGGAGT | 257397 |
| rs187757041 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858464 | CAAAGCTCTAGACTA[A/G]TAAAGGGCTTGCAAA | 257397 |
| rs187783653 | snp | C/T | 0.0183711 | 0.0940641 | intron-variant | TAB3 | GRCh38.p7 | X:30873506 | CTCCCGCCTGGGCGA[C/T]AGAACGAGACTCCGT | 257397 |
| rs187794882 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852321 | CTCTGCCTTAAAATA[G/T]TCTACAGTTAACACT | 257397 |
| rs187802663 | snp | A/C | 0.0121112 | 0.0768695 | intron-variant | TAB3 | GRCh38.p7 | X:30853398 | ACTTTTTAGCTAATC[A/C]AATAATTCCACTTCT | 257397 |
| rs187814685 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835590 | AAGGTTGGGGAAGCT[A/G]TCTAAGCCCACTGAA | 257397 |
| rs187967279 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | TAB3 | GRCh38.p7 | X:30859075 | CAAAAACTTCAAAAA[A/G]TGAAACATAAGGAGA | 257397 |
| rs188025460 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869948 | CAGGTATGTGCGTAT[A/G]TACTAGATCACGATT | 257397 |
| rs188027452 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30870553 | GAACAAAGAGAAGGA[A/G]AGCTGAGGAAAGCTT | 257397 |
| rs188037668 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889824 | TAACCCTTTGCTTGT[C/T]CTTATGGGTTTTGTC | 257397 |
| rs188044747 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30850644 | TTGAACCTGGGAGGC[A/G]GAGGTTGCCGTGAGC | 257397 |
| rs188051573 | snp | C/T | 0.00317376 | 0.039709 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829905 | TGGATATTCCTAAGA[C/T]GATATCCTCAGGTAA | 257397 |
| rs188070175 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833818 | CCTGGCCTAAAGAGC[A/G]AGACTCCGTCTCAAA | 257397 |
| rs188258261 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30872946 | ATATAGATCTAATTT[C/T]CGGTCCATATGAAGT | 257397 |
| rs188323738 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30849140 | TGATTTACTGCCTTA[C/T]ATTTTCTCTCTCACA | 257397 |
| rs188479949 | snp | A/G | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885321 | AAAGCCTAAATGTCC[A/G]AAAGGTTACAGAAGT | 257397 |
| rs188490109 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30847170 | TTATATAATTTTCTT[A/G]AAGTTATAAAGCTAG | 257397 |
| rs188494194 | snp | C/T | 0.0026455 | 0.0362733 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30867549 | TCAGTAGTCTAGAAA[C/T]CTGAGAAAACGAAAA | 257397 |
| rs188501681 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30873252 | CAATAAAATAAAAAG[A/T]TACGGCCGGGCGCGG | 257397 |
| rs188694855 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30878241 | CATGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 257397 |
| rs188709022 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30859771 | AGTAGTGGTGGCATC[C/T]CCTCTAAGGAGGCTT | 257397 |
| rs188730518 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30889003 | GAGTCCCCGGGACGC[C/T]GCAGTTGCGCACACG | 257397 |
| rs188740721 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30849973 | GGGCATTGTGTAAAC[C/T]GCTTCACATATATTA | 257397 |
| rs188829892 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30863536 | CCATCCTAGGTGAGT[C/T]CTTGTTCCATTCACT | 257397 |
| rs188936732 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30874503 | CATTTGTGTACATTT[A/T]GAAATGTTCAAATAA | 257397 |
| rs188952580 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30856548 | TTATCCACTACTTTT[A/G]AAGTAATCCATAAAA | 257397 |
| rs188971714 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30838143 | CAGCCTGTCACCCAG[G/T]CTGGAGTATAGTGCT | 257397 |
| rs189025344 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30879541 | AAAACATTTGATAAA[A/C]TCCAGTATCTATTCA | 257397 |
| rs189058888 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30842026 | GTTGGCCAGGCTAGT[C/G]TCGAACTCCTGGCCT | 257397 |
| rs189094042 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30882323 | CTCCAATTCATTTCA[A/G]TTAGCTTCTATATCC | 257397 |
| rs189130035 | snp | C/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844141 | TAGCTTAAAAGTTTA[C/G]ATTGGAAACTCAGTA | 257397 |
| rs189326493 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30861822 | TGTAACATTTAACCC[A/C]TGTCAAAAGTATTGT | 257397 |
| rs189414386 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30878624 | CTTGATCAATGGACA[G/T]ATATAGAATGCTGTG | 257397 |
| rs189426746 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30861219 | ATTTACAGAGCCCAA[C/T]TACTCAAGTATCTGT | 257397 |
| rs189478406 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30856796 | CTGCTCCAATTCAAC[A/G]CACATTTACAGATGA | 257397 |
| rs189579614 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30871193 | CACTAACAAAATTAT[A/G]CCCTTATTTGTTCAT | 257397 |
| rs189587718 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30831918 | ATGTTAAATTCTGTC[A/G]CCTCTGTAAGTTTTC | 257397 |
| rs189643004 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30874822 | GAGTGACTGGAGAAG[A/C]AACAAAGGAAGCCCT | 257397 |
| rs189691474 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30872730 | ATGCACCAGTAATCA[A/G]TGGATGCTAACAGCA | 257397 |
| rs189709367 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852026 | ACTGGTAGGTATGTA[C/G]TAAGCATCTAGCATA | 257397 |
| rs189721867 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833708 | TGGTGGCAGGCACCT[A/G]TAGTCCCAGCTACAC | 257397 |
| rs189804172 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30873939 | AGTACTTTGGGAAGG[A/C]AAGGCGGGAGGATCC | 257397 |
| rs189810114 | snp | C/T | 0 | 0 | intron-variant, missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836721 | GGTGGTGTGCGTCTG[C/T]AGTCCCAGCTACTCA | 257397 |
| rs189867906 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851550 | TTATGAAAATCTGAT[A/G]AAAGCTATAGACCCA | 257397 |
| rs189937893 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30869795 | AGTGTTTTTCAAATG[G/T]TGGGTTTTGATTTAT | 257397 |
| rs189945139 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30887285 | TTCAGATAGGTCACT[A/G]CCAGCTATCAGGAAT | 257397 |
| rs190034036 | snp | A/G | 0.00738971 | 0.0603345 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889897 | CTGTTATGGGTTCAC[A/G]TTATTAATCAAGAGC | 257397 |
| rs190090157 | snp | C/G/T | 0.00211696 | 0.0324653 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845397 | ATTGTATTTCTTACA[C/G/T]AAACCACACCCATGA | 257397 |
| rs190131831 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866194 | GGCCTCCAGAAACGA[C/T]AGATTCATATTTAAT | 257397 |
| rs190147530 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848701 | GTCAAAAGTAGTTTT[C/T]GTGCAGGAGGAATTT | 257397 |
| rs190169945 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829873 | GGGTTGGGGGAGAAA[C/T]CTGATGGGAGCGTCT | 257397 |
| rs190283773 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30880446 | TTAGCTATCCATATA[A/G]GAAAAGACGGTATTA | 257397 |
| rs190294132 | snp | G/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843750 | AAATTTTCACCTGTC[G/T]GTCTTCAAATGTTCA | 257397 |
| rs190298173 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30862440 | ACAAGGGCAATACCA[C/T]TGTCTTTTTTATGAG | 257397 |
| rs190331802 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30875671 | TGAGTCATTCCAGAC[A/G]TAGCTGAAATTTAAA | 257397 |
| rs190348311 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30858096 | TTATTAATCCCAAAG[C/G]AAGAAAAAAGTGAAA | 257397 |
| rs190357990 | snp | C/T | 0.0183711 | 0.0940641 | intron-variant | TAB3 | GRCh38.p7 | X:30839749 | AACAAAAAAGAAATA[C/T]GGGAAGCGTTCCCTC | 257397 |
| rs190406715 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866554 | TGAGGGCATGTCGAA[A/G]TGACACAGGAGCCAA | 257397 |
| rs190586330 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841858 | CTGTCGCCTAGGCTG[C/G]AGTACAGTGGCGCGA | 257397 |
| rs190639086 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884583 | CATTTTTCAAACGAA[A/G]GAGTGGTTTGGAAAC | 257397 |
| rs190669061 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846471 | TGTCTCTTAAATCTA[C/T]AAAACCAAAGTTATT | 257397 |
| rs190803538 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30881751 | ACAAATGAAGAAACC[A/G]AGGTCTTTTGAAGTT | 257397 |
| rs190957207 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30851865 | TTTTAGAAGGGCATT[C/T]CAGCAGGAGGATTAA | 257397 |
| rs190982099 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30832121 | CTCAGAATAGTGAAA[A/G]GAGGAAGATTCTACA | 257397 |
| rs191092477 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30873602 | TTTCTGCCTCTGCCA[C/T]GCCTGAGACAGCAAG | 257397 |
| rs191093776 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30856878 | TTAACAGAAAAGCCA[A/G]TTCTAGATTCTTATT | 257397 |
| rs191105100 | snp | A/G | 9.12222e-05 | 0.00675298 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854465 | TGGCGTGGTGGCTGT[A/G]TACAGTGAGTGTTGA | 257397 |
| rs191207993 | snp | A/C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30847895 | AGGAACAAAAAAAGT[A/C/T]GTTTAGAAATATTTA | 257397 |
| rs191217999 | snp | C/T | 0.00211696 | 0.0324653 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828376 | ACACTTCCCATTTCT[C/T]CCAGGGAAATAAACA | 257397 |
| rs191346508 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875287 | CGACAGACGAGTTAC[A/T]TAACCTCTTAGGCCC | 257397 |
| rs191350703 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30839283 | CCTCCCTTTGTTTAA[C/T]ATGGTAAATTACACT | 257397 |
| rs191354415 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30872947 | TATAGATCTAATTTC[C/T]GGTCCATATGAAGTA | 257397 |
| rs191359320 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833916 | TGCATTATATTTCTA[C/T]TGGACAGCACAGCCT | 257397 |
| rs191419510 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885516 | ACCTCGGCTTCCACT[A/T]TGAAGGAGGGCAAAA | 257397 |
| rs191454109 | snp | C/G | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30847473 | TACTTCCCATGTCAT[C/G]CTTAATTTCTTTATT | 257397 |
| rs191607921 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30852469 | AGAATAAATTCATCA[A/C]ATTTTTGGTCAGGGT | 257397 |
| rs191716263 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827314 | CAAATCTAACATTAC[A/G]TGTTCTAATAAAGGA | 257397 |
| rs191881062 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30863265 | ATTTCACAGTAATAT[A/G]TAACACTCTCAAACT | 257397 |
| rs191897310 | snp | A/G/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30883311 | CTGAATAATTAAAAA[A/G/T]TACATAACACTTCTT | 257397 |
| rs191900125 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891162 | ATACTGGGGCCCATC[A/G]TGCTGAAACATTTGT | 257397 |
| rs191907243 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844948 | TGCCTTAGCCTCCCA[C/T]GTAGCTGGGATCACA | 257397 |
| rs191911801 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30865605 | AATATTATCATCCAC[A/G]TTTTACAAATAAGGA | 257397 |
| rs191957316 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841549 | AAACACTCTGTAATG[A/C]GCTTAATATACGTAG | 257397 |
| rs191960042 | snp | A/T | 0.108827 | 0.206325 | intron-variant | TAB3 | GRCh38.p7 | X:30859925 | AGGTCTCACCTATTT[A/T]AAAAAAAAAAACAAA | 257397 |
| rs191967259 | snp | C/T | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30838353 | TTTGTAGATGAGGTC[C/T]ATGTTGCCCAGGCTA | 257397 |
| rs192149937 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30882678 | TTCACTAAAGAACTG[A/G]AGGGCTCCATGATAT | 257397 |
| rs192150291 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30878340 | TACTAAAAATACAAA[A/C]ATTACAAAAATTAGC | 257397 |
| rs192178068 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844275 | CTCATTGTCCAATGC[A/G]GACAAAAAACACAGC | 257397 |
| rs192192180 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853218 | ACCAGGCATACTGAA[C/T]AATTACTTCCCTTCT | 257397 |
| rs192199565 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843883 | CTGCTTGTTCTAAAC[A/G]ATTACAGTTAACTGT | 257397 |
| rs192219993 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30871505 | GCAGTAGTAGTAGTA[C/G]TAGTACTAGTAGTAG | 257397 |
| rs192398588 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30859238 | GCTATTGTTATTTAC[G/T]GGGTAGAGGCCTCGG | 257397 |
| rs192408088 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834968 | CTTGAAAAATCAGAA[C/G]CAACTCGATATAATA | 257397 |
| rs192474147 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30887064 | GAAAAACAGGGTCAG[C/T]TGTCAAGTACTCCAC | 257397 |
| rs192532378 | snp | C/G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835696 | GAGACATTCTAAGCC[C/G/T]GCTGAAGAGCACGTA | 257397 |
| rs192552777 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30863710 | GGTGCCATGCTTATG[A/C]AGCCTGTAGAATCCT | 257397 |
| rs192645795 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30850249 | ACACTTAAATGTCTT[A/C]TCTCTCAGATGTTAG | 257397 |
| rs192651620 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30870471 | GTAGTGAGAGAAACA[C/G]TGGCAGTTATAATAG | 257397 |
| rs192653113 | snp | C/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830527 | TCCAAATGGATTTTG[C/G]AATGGACTTGCATTT | 257397 |
| rs192658470 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30876537 | TTGAGACCGGGTCTC[A/G]CTCTGTCACCCAGGC | 257397 |
| rs192747139 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30877627 | TGCTAGGGTAATCAC[A/C]AAAAGAATAAAAATG | 257397 |
| rs192765135 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30840922 | TTGAATCAATGAACT[A/G]AAGTTTGTCTGGCGA | 257397 |
| rs192771998 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30873965 | GATCCCTTGATCCCA[A/G]GAGTTCAAGACTGGC | 257397 |
| rs192805447 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888285 | AAAATGACTGCCTGA[C/T]TGACAAACGTCACTG | 257397 |
| rs192819875 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30849790 | GGGAAATCTGACTAA[A/G]TGATTTATTTCTTGA | 257397 |
| rs192936766 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30866290 | TATAAATATGCATAA[A/G]TATATAGACTATATA | 257397 |
| rs193020254 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | TAB3 | GRCh38.p7 | X:30869975 | GATTAAAATGTATTT[C/T]TTACTGTGGGTTTGA | 257397 |
| rs193025570 | snp | A/C | 0.00211696 | 0.0324653 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830037 | CAACAATGGCAGAGA[A/C]CTTAATGAAATGTGC | 257397 |
| rs193143136 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840073 | ACTGCATAAAGATGT[A/C]CATCACTTTCCCTTA | 257397 |
| rs193173160 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883804 | CAGATATGTTGGGCT[G/T]GCTTGGGAATCTGAA | 257397 |
| rs193175836 | snp | A/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846170 | GTTTATTTTAAAACT[A/G]AGAAATCTGATACTC | 257397 |
| rs193286189 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889427 | CACAAAGATGGCGCC[G/T]CCGGGTACTGCCCAG | 257397 |
| rs193295993 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858529 | TGAGTCTCTATTTTT[A/C]ATTAACCACACCTGT | 257397 |
| rs199729385 | in-del | -/TG | 0.00791544 | 0.0624105 | intron-variant | TAB3 | GRCh38.p7 | X:30846976 | CATGGTAAGGGAAAC[-/TG]TAAGAATCAACCTGT | 257397 |
| rs199733634 | in-del | -/AAG | | | intron-variant | TAB3 | GRCh38.p7 | X:30859698 | TTAAAAAAAAAAAAA[-/AAG]TATGGTTAAGTCTAG | 257397 |
| rs199786384 | in-del | -/C | 0.0455357 | 0.143855 | intron-variant | TAB3 | GRCh38.p7 | X:30858655 | GTAGAAGTACTGCTG[-/C]CCCAAAGTTAAGCAA | 257397 |
| rs199836754 | in-del | -/GCT | 0.145864 | 0.227279 | intron-variant | TAB3 | GRCh38.p7 | X:30833101 | TCAGCCTCCTGTGTA[-/GCT]GGGACTACAGGCGCC | 257397 |
| rs199883292 | in-del | -/T | 0.181059 | 0.240306 | intron-variant | TAB3 | GRCh38.p7 | X:30883484 | TGAAGATAAGCACTC[-/T]TGAGTGGACAGTCCA | 257397 |
| rs199919281 | snp | G/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830317 | TTGGCCAACTGTAAT[G/T]CCCCTCACACTGGTT | 257397 |
| rs199941884 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30850849 | CTTCCAATGAAAAAC[A/C]AAAAAAAACCAATAT | 257397 |
| rs200022374 | in-del | -/TCT | 0.0168099 | 0.0901243 | intron-variant | TAB3 | GRCh38.p7 | X:30839399 | ACTATAAGTCAATGA[-/TCT]GATAGAAAACAGAAT | 257397 |
| rs200072408 | in-del | -/AAAA | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30873123 | AACAAACCAACTATC[-/AAAA]AACGAATTTTTTTTA | 257397 |
| rs200110044 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835249 | GAGCCCACAGTACAA[A/C]TCATCTTTGGAAATC | 257397 |
| rs200135860 | in-del | -/TTC | 0.00738971 | 0.0603345 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843610 | TCAGCAGTTTATGTA[-/TTC]TTATTTTCAAGAAAA | 257397 |
| rs200299443 | in-del | -/CG | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830920 | TAATTTGCCCCCCCC[-/CG]CCCCAAATATTCTAG | 257397 |
| rs200339063 | snp | G/T | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834585 | TAAGGCTATTACAAT[G/T]ATGAAATGTGATGAA | 257397 |
| rs200342812 | in-del | -/ATAA | 0.0256233 | 0.11025 | intron-variant | TAB3 | GRCh38.p7 | X:30863002 | TTTTAAAAAATGGTT[-/ATAA]ATACTTTCCTTTGAA | 257397 |
| rs200391183 | snp | A/T | 0.000159903 | 0.00894013 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854498 | CCATGGAGATGGTTG[A/T]TTACTGATGGGTGAA | 257397 |
| rs200395635 | snp | C/T | 0.000529661 | 0.016265 | missense, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846578 | GGAGGTCAACTTCTT[C/T]CAGTGTACAGTCAAC | 257397 |
| rs200396766 | snp | C/T | 4.89428e-05 | 0.00494662 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831538 | GTCTTCATCTCGAGG[C/T]TGTGTCCGAGGACTT | 257397 |
| rs200406434 | snp | A/G | 2.64673e-05 | 0.00363771 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859502 | CTGTAACATGCACTG[A/G]GACACCACGCCCTCT | 257397 |
| rs200434716 | in-del | -/TGCTGTTTT | 0.0157677 | 0.0873799 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844362 | TTATCCACTTGAATA[-/TGCTGTTTT]AAGATAATTTTCTGA | 257397 |
| rs200490956 | in-del | -/TAAT | | | intron-variant | TAB3 | GRCh38.p7 | X:30870507 | GTTGAGTTCTATAAT[-/TAAT]AAGTAGTCAGAAAAA | 257397 |
| rs200702269 | in-del | -/AGAAATCAC | 0.00791544 | 0.0624105 | intron-variant | TAB3 | GRCh38.p7 | X:30871095 | AAAGATAAACTATGT[-/AGAAATCAC]GGCTGATATTGTTAT | 257397 |
| rs200706267 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30859921 | TAAAGGTCTCACCTA[-/T]TTTAAAAAAAAAAAA | 257397 |
| rs200740617 | in-del | -/T | 0.0525796 | 0.153379 | intron-variant | TAB3 | GRCh38.p7 | X:30850326 | GGGTTCATTATACTA[-/T]TTTTATGTATCTTTG | 257397 |
| rs200752279 | in-del | -/G | 0.335239 | 0.23502 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885599 | GGAAAGAAGGATGGA[-/G]GCGGGGGATGGCAGC | 257397 |
| rs200799431 | in-del | -/A | 0.0115877 | 0.0752302 | intron-variant | TAB3 | GRCh38.p7 | X:30887369 | GACGCATCTGAAAAG[-/A]AAAAAAAAACCTTGA | 257397 |
| rs200834080 | in-del | -/T | 0.0105399 | 0.0718252 | intron-variant | TAB3 | GRCh38.p7 | X:30888961 | CCCCGCAGTTCCCGC[-/T]TGTCAGCCGCAGTCC | 257397 |
| rs200840089 | in-del | -/GCT | | | intron-variant | TAB3 | GRCh38.p7 | X:30868515 | ATATATATATATATA[-/GCT]TATATATATATATAT | 257397 |
| rs201000757 | in-del | -/T | 0.0168099 | 0.0901243 | intron-variant | TAB3 | GRCh38.p7 | X:30839401 | TATAAGTCAATGAGA[-/T]TAGAAAACAGAATTA | 257397 |
| rs201037374 | in-del | -/TCCTGTG | 0.144971 | 0.226868 | intron-variant | TAB3 | GRCh38.p7 | X:30833092 | TCTCCTGCCTCAGCC[-/TCCTGTG]TAGCTGGGACTACAG | 257397 |
| rs201049952 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30864801 | GTGTGTGTGTGTGTG[-/T]TGTTTTTTTTTTAAA | 257397 |
| rs201079856 | in-del | -/TATATATATATAGCT | | | intron-variant | TAB3 | GRCh38.p7 | X:30868302 | TTTAGTGAAAAGCTA[-/TATATATATATAGCT]TATATATATATATAT | 257397 |
| rs201285240 | snp | G/T | 4.89087e-05 | 0.00494489 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831541 | TTCATCTCGAGGTTG[G/T]GTCCGAGGACTTTGT | 257397 |
| rs201334462 | in-del | -/AATAAAAAT | 0.00528398 | 0.051128 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842831 | ACCCTGTCTCAAAAA[-/AATAAAAAT]AATAAAAATATGGTA | 257397 |
| rs201346527 | in-del | -/CT | 0.0121112 | 0.0768695 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843939 | TGTATGGTACTAATA[-/CT]GATAGTTTAAATATA | 257397 |
| rs201358626 | in-del | -/TATATATA | | | intron-variant | TAB3 | GRCh38.p7 | X:30839915 | TATACATATATATAT[-/TATATATA]TATATATATATATAT | 257397 |
| rs201609627 | snp | C/T | 0.148089 | 0.228285 | intron-variant | TAB3 | GRCh38.p7 | X:30850785 | ATCTGGGGCTTTTTT[C/T]TTTTTTTTTTTTTTA | 257397 |
| rs201655531 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30873975 | TCCCAGGAGTTCAAG[A/C]CTGGCCTGGGCAACA | 257397 |
| rs201728663 | snp | A/C/T | 0.00106975 | 0.0231047 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854918 | TGGTGAGGACTGCCA[A/C/T]GGCGTACTCTGAGGA | 257397 |
| rs201835842 | in-del | -/A | 0.00581083 | 0.0535878 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844011 | CAAGTTTTCCTTACC[-/A]AAAAATCACAAAAAA | 257397 |
| rs202013109 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833688 | CACAAAAAATTAGCC[A/G]GGCGTGGTGGCAGGC | 257397 |
| rs202027373 | in-del | -/TA | | | intron-variant | TAB3 | GRCh38.p7 | X:30863001 | TTTTTAAAAAATGGT[-/TA]TAAATACTTTCCTTT | 257397 |
| rs202074143 | snp | A/G | 0.00108813 | 0.0232998 | intron-variant | TAB3 | GRCh38.p7 | X:30831580 | AGTTCGATGCTCTGA[A/G]GGAGGTTAGGATTAA | 257397 |
| rs202151512 | snp | C/T | 2.67351e-05 | 0.00365607 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859499 | TACCTGTAACATGCA[C/T]TGAGACACCACGCCC | 257397 |
| rs202189770 | in-del | -/T | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842659 | CATCTCTACAAAAAA[-/T]TAAAAAAAAATTAGC | 257397 |
| rs202194789 | in-del | -/TA | 0.0220041 | 0.102557 | intron-variant | TAB3 | GRCh38.p7 | X:30868422 | TATATATATATAGCT[-/TA]TATATATATATAGCT | 257397 |
| rs202218229 | snp | A/C/G | 2.47509e-05 | 0.0035178 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842948 | TTCTATCGTATTTGT[A/C/G]ACATTTTTCATACTC | 257397 |
| rs207478217 | snp | C/G | | | intron-variant, missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836725 | GTGTGCGTCTGTAGT[C/G]CCAGCTACTCAGGTG | 257397 |
| rs367663654 | snp | C/T | 4.97816e-05 | 0.00498882 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831569 | TGTGTGGAGCCAGTT[C/T]GATGCTCTGAGGGAG | 257397 |
| rs367680513 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30840391 | ATCGCATGGGAAAGA[A/G]TTTTGCCTTGCCCAA | 257397 |
| rs367688080 | snp | A/G | 0.0220041 | 0.102557 | intron-variant | TAB3 | GRCh38.p7 | X:30869364 | TGCGCCCAGCCTTTT[A/G]TTTGTTTTTTGCCAT | 257397 |
| rs367732976 | snp | A/G | 6.8483e-05 | 0.00585122 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855276 | GGAGTAGCAGCAACA[A/G]CAGCTGGAGCTGAGT | 257397 |
| rs367779638 | snp | A/T | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842670 | AAAAATAAAAAAAAA[A/T]TAGCTGGGCATGGTG | 257397 |
| rs367789627 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30841526 | TAAATAAAAAAAAAA[-/A]CACTCTGTAATGAGC | 257397 |
| rs367840374 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30874399 | ATGTCTTGGCTATGC[C/G]TTAATTCTTGGAAAA | 257397 |
| rs367909665 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30866813 | CCTCCCACCTCTTAA[A/G]TGTGGAATGCACATG | 257397 |
| rs367994043 | snp | A/G/T | 3.07962e-05 | 0.00392392 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831411 | CACTTTCAACCTGGC[A/G/T]CAGACTTTTCTGAAT | 257397 |
| rs368010119 | snp | G/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885005 | ACAATATTAGGCTGA[G/T]ATGGACTAACTTAAA | 257397 |
| rs368089077 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30855956 | TAAGTATAAGTAATA[C/T]CCATTATTAATATTT | 257397 |
| rs368248486 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30831985 | GTATAATACTATCCA[C/T]ACTATATTAAACATC | 257397 |
| rs368317516 | snp | A/C | 0.000113989 | 0.0075486 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854583 | ATCTTCTTCATGGAA[A/C]CTTTGGATAAACTAG | 257397 |
| rs368413168 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843437 | AACTGTGAGAAAGAA[C/T]ACTTAAATAATGAAA | 257397 |
| rs368500180 | snp | C/T | 2.38709e-05 | 0.00345469 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834127 | TCTTCGGGCTTTTCT[C/T]TCAATTGTGCAGGGG | 257397 |
| rs368509679 | in-del | -/AATA | | | intron-variant | TAB3 | GRCh38.p7 | X:30863005 | TAAAAAATGGTTATA[-/AATA]CTTTCCTTTGAAGAA | 257397 |
| rs368568488 | snp | A/G | 2.28344e-05 | 0.00337886 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854291 | CGTTGCTCGGCCTAC[A/G]GTAATTTTAAAAACT | 257397 |
| rs368714323 | snp | A/C | 0.000529661 | 0.016265 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30826943 | AAGCCTTCCTCCCAC[A/C]TCGACCTCCCAAAGT | 257397 |
| rs368855165 | snp | A/C | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889463 | TCTCGCGAGGCTTCC[A/C]CCACAGGAACAGGAG | 257397 |
| rs368939145 | snp | A/G | 4.59865e-05 | 0.00479491 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842937 | TTGACATTTATTTCT[A/G]TCGTATTTGTGACAT | 257397 |
| rs368979392 | in-del | -/TTT | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834616 | AATGACAGGATTTTT[-/TTT]GTTTTGTTTTTGTTT | 257397 |
| rs368982906 | snp | A/T | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890902 | TTTGAGTGGGGCTCA[A/T]GACGTTGTCTCTGCA | 257397 |
| rs369089245 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835335 | GTAAACAAAAGCAGA[A/G]TGAATGTCTCCTTAA | 257397 |
| rs369163682 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30873791 | ACAGTAATATATGTA[A/T]CATACAAAATATGTG | 257397 |
| rs369252239 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884967 | CTCTTTCAACAAAAC[C/T]GCAAGATCTGTCCGC | 257397 |
| rs369358528 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30862774 | CTGCCTGCTCCAAAG[C/T]CTGTGTTCTTTCCAC | 257397 |
| rs369421706 | snp | C/G | 9.35366e-05 | 0.0068381 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859593 | CTTTGCGCCATGCCA[C/G]AGCAAATGGTGGCCA | 257397 |
| rs369498124 | in-del | -/TA | 0.367813 | 0.220499 | intron-variant | TAB3 | GRCh38.p7 | X:30868340 | ATATATATAAGCTTT[-/TA]TATATATATAGCTTA | 257397 |
| rs369633697 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858628 | CTGTGTGTGAGGAAG[A/G]CCAGTGAGCATGGTA | 257397 |
| rs369645813 | snp | A/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828040 | CGGTAACATGGACTC[A/T]TTCAAGGTCTAACAA | 257397 |
| rs369706987 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30869279 | TGGCCAGGCTGGTCT[C/T]AAACTCCTGACCTCA | 257397 |
| rs369890880 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30873308 | TTTGGGAGGCCGAGG[C/G]GGGCGGATCACGAGG | 257397 |
| rs369947964 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30878599 | ACAGAGATACGATAC[A/G]ATTACCAAACTTGAT | 257397 |
| rs369949404 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30870456 | AAGACCCATGTCCTC[A/G]TAGTGAGAGAAACAC | 257397 |
| rs369983275 | snp | C/T | 2.41362e-05 | 0.00347384 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855499 | GACTATGGTATTCCA[C/T]ATATAAGTATTTGCT | 257397 |
| rs370073249 | snp | C/T | 4.80267e-05 | 0.00490011 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854159 | AGAACTAGAACTTCT[C/T]TGATATTTATGGCTT | 257397 |
| rs370355984 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30840394 | GCATGGGAAAGAATT[C/T]TGCCTTGCCCAAACA | 257397 |
| rs370702875 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | TAB3 | GRCh38.p7 | X:30837053 | CATCTTTTTTTTTTT[-/TTTTTTTTTTTTT]GGAGACAGCATCTTG | 257397 |
| rs370782356 | snp | C/T | 7.66577e-05 | 0.00619056 | intron-variant | TAB3 | GRCh38.p7 | X:30852977 | TTGCAGAGAACAACA[C/T]TGAACAAGCGACTGG | 257397 |
| rs370810517 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30839865 | TCTGGAGTTTTCTTT[G/T]TGGGGGAAAATTTTG | 257397 |
| rs370859916 | snp | G/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885583 | GAAGGCAAGACCAAC[G/T]GGGAAAGAAGGATGG | 257397 |
| rs370989999 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30865675 | TACACAGTCAACCAG[C/T]AGCAAAGCTAGGATA | 257397 |
| rs371008423 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30838194 | CCTCAACCTCCTGGG[A/C]TCCAGCAATCCTACC | 257397 |
| rs371082636 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30875202 | GCAAGAGTTACCTGG[C/G]CATTATAGCTGAAAC | 257397 |
| rs371156237 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30874982 | CAGCAAGCTTTCTAA[C/T]AGGGCAGAGAGGTTG | 257397 |
| rs371296444 | snp | A/G | 4.75313e-05 | 0.00487477 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855473 | ATTTCTATTCATCCT[A/G]TTGTCATCTGGACTA | 257397 |
| rs371431555 | snp | C/T | 0.000189982 | 0.00974449 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854453 | AGAACTTGAAGGTGG[C/T]GTGGTGGCTGTGTAC | 257397 |
| rs371570536 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830209 | GTTATGTTAAATTTT[A/G]AAAGTTGTTTCAAAG | 257397 |
| rs371585325 | snp | A/G | 0.000439024 | 0.0148094 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842919 | GTGAAATCCCAAATT[A/G]TTTTGACATTTATTT | 257397 |
| rs371665379 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30869443 | TTTCATAAATGCCTA[C/T]AAAAGTCACTGTGTG | 257397 |
| rs371775792 | snp | C/T | 5.21805e-05 | 0.00510759 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854903 | AGGCACTGGGCCCTG[C/T]GGTGAGGACTGCCAC | 257397 |
| rs371819023 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30888947 | GCAAACCTCCGGCAG[C/G]CCCGCAGTTCCCGCT | 257397 |
| rs371891712 | snp | C/G | 0.000189982 | 0.00974449 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834129 | TTCGGGCTTTTCTCT[C/G]AATTGTGCAGGGGTC | 257397 |
| rs371936578 | snp | A/G | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833788 | GTGAGCCGGGATAGC[A/G]CCACTGCACTCCAGC | 257397 |
| rs372131584 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30868569 | ATATATATATAGCTT[A/T]TATATATATATATAT | 257397 |
| rs372254351 | snp | A/C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30878616 | TTACCAAACTTGATC[A/C/G]ATGGACATATATAGA | 257397 |
| rs372423618 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30833265 | TGAGCCACCGCACCC[A/G]GCCTACTATGCCATT | 257397 |
| rs372612783 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30846817 | TTTAAAGGAATAGTC[A/G]GGTAAAATGGGGACA | 257397 |
| rs372678326 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30857768 | CCAGAATAGATTCTA[A/G]TGTCACATTTGACTG | 257397 |
| rs372813228 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30873341 | AGGAGATCGAGACCA[A/C]GGTGAAACCCCGTCT | 257397 |
| rs372820259 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828123 | TTCCAGGATACATCA[C/T]TGATATTTTTAGAGG | 257397 |
| rs372926441 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30863251 | AATAATCATTTAGTA[G/T]TTCACAGTAATATAT | 257397 |
| rs372934980 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30879374 | GCCAATCCCACTCAC[A/G]AACAAAGATCTAAAA | 257397 |
| rs372988854 | snp | C/T | | | intron-variant, utr-variant-5-prime | TAB3 | GRCh38.p7 | X:30883685 | GCCATATCTGCAAGA[C/T]TGTGTTCATAATCTT | 257397 |
| rs373068267 | snp | A/C/G | 5.31491e-05 | 0.00515478 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843087 | AGGCATTTAAGAACT[A/C/G]TTTTTTCCTGTTATT | 257397 |
| rs373101666 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829170 | ACCAAAGGATTGAAA[C/T]CATGCATCTACTGTA | 257397 |
| rs373280759 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30869280 | GGCCAGGCTGGTCTT[A/G]AACTCCTGACCTCAG | 257397 |
| rs373300291 | snp | G/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834423 | TTCACTGTTTTCTAC[G/T]TTTTAATGGATTAGG | 257397 |
| rs373355139 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30873795 | TAATATATGTAACAT[A/G]CAAAATATGTGTTAA | 257397 |
| rs373393073 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885050 | ATGTGCCTAAATTTA[A/G]AAATTCTTCATTGAC | 257397 |
| rs373743461 | snp | A/T | 0.000441902 | 0.0148578 | intron-variant | TAB3 | GRCh38.p7 | X:30854064 | ATATATTTGAATGGG[A/T]GACTGCTGCCTCACC | 257397 |
| rs373755553 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30878164 | AACTTCTAGGAGAAT[A/G]AGACATGCATTAGTA | 257397 |
| rs373779065 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30853699 | TGTTTGTTTTGGACA[C/T]AGTCTCCCTCTGTTG | 257397 |
| rs373809703 | snp | A/C | 9.58023e-05 | 0.0069204 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859596 | TGCGCCATGCCAGAG[A/C]AAATGGTGGCCAAGT | 257397 |
| rs373923149 | snp | C/T | 0.000318573 | 0.0126169 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842939 | GACATTTATTTCTAT[C/T]GTATTTGTGACATTT | 257397 |
| rs374056104 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848224 | ACAGTTGCTCGTAAC[A/G]AAAACATACTTTCAT | 257397 |
| rs374056782 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30840235 | TTGTTAACTTTTTCT[A/G]TTTTCTATCTCATTG | 257397 |
| rs374166334 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30838797 | AAATGAAATTCTCTT[A/G]AATTTTATTTTCCAA | 257397 |
| rs374194573 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30886246 | ATGAGGCAATTTCCT[A/G]GTGTTTTATCTTTAT | 257397 |
| rs374389096 | snp | C/G/T | 4.56817e-05 | 0.00477903 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854506 | ATGGTTGATTACTGA[C/G/T]GGGTGAAGGACTCCT | 257397 |
| rs374426886 | snp | A/C | 0.00051716 | 0.0160721 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834092 | TGGATGTCTGCCTGT[A/C]CTTTGGAGGTCACGC | 257397 |
| rs374429012 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30888299 | ATTGACAAACGTCAC[C/T]GAAGAAACACATCGA | 257397 |
| rs374526541 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30864211 | GTGGAGCTGTGTAGG[C/T]GGTAACCCTAGATCA | 257397 |
| rs374829888 | snp | C/G | 9.72526e-05 | 0.00697258 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842924 | ATCCCAAATTATTTT[C/G]ACATTTATTTCTATC | 257397 |
| rs374854539 | snp | A/G | 4.62743e-05 | 0.00480989 | missense, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846571 | GATTGAAGGAGGTCA[A/G]CTTCTTTCAGTGTAC | 257397 |
| rs374855378 | snp | C/T | 2.73703e-05 | 0.00369924 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854977 | TCTGTCTAATATAAA[C/T]AGAACCAGGAGACCC | 257397 |
| rs374857694 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884791 | ACACGCTAACACTTT[A/G]TTTTAAAATCTTGAA | 257397 |
| rs374867058 | snp | C/T | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833817 | GCCTGGCCTAAAGAG[C/T]GAGACTCCGTCTCAA | 257397 |
| rs374893623 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30865775 | GTCATAACTCTTAAC[A/C]ACAGTTTAAAGCAAA | 257397 |
| rs374974237 | snp | A/G | 0.000219995 | 0.0104857 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831546 | CTCGAGGTTGTGTCC[A/G]AGGACTTTGTGTGGA | 257397 |
| rs374990188 | snp | C/T | 8.47422e-05 | 0.00650876 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834171 | CATAAAAATAAACAA[C/T]GCCAGAAAGAAGTGA | 257397 |
| rs375209019 | snp | A/C | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889401 | TCCGTCGGGCGCCGT[A/C]GCTCGCCAGGCACAA | 257397 |
| rs375215277 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | TAB3 | GRCh38.p7 | X:30842399 | CATTATTTTATGAGA[A/G]TTATCTTTTAGGGTT | 257397 |
| rs375254935 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831344 | AATGAAAAGGCTGGG[G/T]GGATGAATAGAGTCC | 257397 |
| rs375264569 | multinucleotide-polymorphism | GTG/TTT | | | intron-variant | TAB3 | GRCh38.p7 | X:30864805 | TGTGTGTGTGTGTGT[GTG/TTT]TTTTTTAAAGTTGAG | 257397 |
| rs375527262 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30869262 | ATGGGGTTTCACCAT[G/T]TTGGCCAGGCTGGTC | 257397 |
| rs375563798 | snp | A/G | 0.000382094 | 0.0138167 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854162 | ACTAGAACTTCTCTG[A/G]TATTTATGGCTTCCC | 257397 |
| rs375602091 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30875081 | GGAGTAATCTCCCAA[C/T]TGTCTCAATCTTCAG | 257397 |
| rs375736651 | snp | A/T | 4.24304e-05 | 0.0046058 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843070 | AAGAAAGTAAATTCA[A/T]CAGGCATTTAAGAAC | 257397 |
| rs375792200 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835130 | TTCTATAAATTTATA[C/G]TTTATTAGTAAGCAA | 257397 |
| rs375980559 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30855703 | CCACAAAAAACTTCA[C/T]GGTCATCTATCCTGA | 257397 |
| rs376094771 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30873772 | CTTACTTTATTGTAA[A/G]AATACAGTAATATAT | 257397 |
| rs376097862 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30873438 | GCTGAGGCAGGAGAA[C/T]GGCGTGAACCCGGGA | 257397 |
| rs376119288 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30883328 | ACATAACACTTCTTA[C/T]GCACTCACTCATGGG | 257397 |
| rs376480142 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30873753 | AACATTTTCTTTTCT[C/G]TAGCTTACTTTATTG | 257397 |
| rs376629540 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858159 | CACTGAGCTGAATTT[C/G]AAGTTCTATTTCTTC | 257397 |
| rs376704878 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30875108 | TCAGGACATGAGTCA[A/T]GGGGTCAGGATATTA | 257397 |
| rs376786880 | snp | C/T | 2.38299e-05 | 0.00345173 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855480 | TTCATCCTATTGTCA[C/T]CTGGACTATGGTATT | 257397 |
| rs376829023 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30878772 | CTCTAAGGAAAATGT[A/G]TTAAAGCCAGAAACA | 257397 |
| rs376927653 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884614 | AAAAAAAAAAAAAAA[-/A]CCATCTTGCCTTTTA | 257397 |
| rs376965295 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30865437 | CAAAACACAGTATGT[A/G]TATGAGTATAAAGCT | 257397 |
| rs377153694 | snp | C/T | 0.000189982 | 0.00974449 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859548 | CGTTGTCGAAGATCA[C/T]GGAGAACCTGAATAT | 257397 |
| rs377172274 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30847300 | AGCACATGAAAACTT[C/G]AGAAACAAATGAATT | 257397 |
| rs377353427 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30881167 | AAGTACAAAAGTAGG[C/T]AAAATTAATCTGTGG | 257397 |
| rs377402609 | snp | A/T | 3.17733e-05 | 0.00398568 | intron-variant | TAB3 | GRCh38.p7 | X:30854082 | CTGCTGCCTCACCAC[A/T]GAAATTAAATTTCAT | 257397 |
| rs377496888 | snp | A/C | 0.000169644 | 0.00920832 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859606 | CAGAGCAAATGGTGG[A/C]CAAGTTTCTCTTAGG | 257397 |
| rs377508172 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885245 | ATCATCTATTTGAAA[C/T]TCAGACTTTGCCTTT | 257397 |
| rs377634051 | snp | C/T | 2.51699e-05 | 0.00354744 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846532 | TTACTTATGGTTTAC[C/T]AAATAATCAAGTCTA | 257397 |
| rs386419292 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885600 | GAAAGAAGGATGGAG[-/G]CGGGGGATGGCAGCT | 257397 |
| rs386824577 | in-del | A/CCTGTGTAGCT | | | intron-variant | TAB3 | GRCh38.p7 | X:30833093 | CTCCTGCCTCAGCCT[A/CCTGTGTAGCT]GGGACTACAGGCGCC | 257397 |
| rs386824578 | multinucleotide-polymorphism | AG/GA | | | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30867493 | ATCAACCCTGGCACA[AG/GA]AATTTTATTCACATC | 257397 |
| rs397960032 | in-del | -/CCC | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830924 | TTGCCCCCCCCCCCC[-/CCC]AAATATTCTAGGTGC | 257397 |
| rs528319323 | snp | A/T | 0.0115877 | 0.0752302 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885035 | ATTTTATTTCAAAAC[A/T]TGTGCCTAAATTTAG | 257397 |
| rs529000646 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30840162 | TTCTCTTTTTTTACA[A/G]ATCAGTCTACCTTGA | 257397 |
| rs530717864 | snp | C/G | 0.00633741 | 0.0559334 | intron-variant | TAB3 | GRCh38.p7 | X:30847281 | TGAAGGAGGCAGTTA[C/G]TCTAGCACATGAAAA | 257397 |
| rs530779669 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30872804 | ACTTGAACCCTCTGA[C/T]GAATCTTCACAACAC | 257397 |
| rs531114215 | snp | A/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844433 | AGTGCTATTTGATGT[A/G]TTAATTGAATCTTTT | 257397 |
| rs531173930 | in-del | -/CAC | 0.0105399 | 0.0718252 | intron-variant | TAB3 | GRCh38.p7 | X:30833428 | TAAGTGTAAAATATA[-/CAC]CACATTTCAAAGACT | 257397 |
| rs531838161 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30888556 | AACTCTAATCTGTTG[C/T]TGGACCTCAGAGGAC | 257397 |
| rs532463785 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30846856 | GCCACATATAAACAA[A/C]ATCTGCATATAAAGT | 257397 |
| rs532803607 | snp | A/G | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842521 | ATTACCTCTGACAGT[A/G]ATTCTAAGAGTTACT | 257397 |
| rs532917953 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30865040 | ACCTGCTGGGTTTGT[A/G]ACACCTGAAATGTGT | 257397 |
| rs533672841 | snp | C/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828862 | AGATCCTTTTGAAAA[C/G]GCATCTTGAAAGTTG | 257397 |
| rs535079306 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30849148 | TGCCTTATATTTTCT[C/T]TCTCACACAAATACA | 257397 |
| rs538686989 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30850868 | AAAAACCAATATTTT[A/C]TTTAGCAGGGATTAT | 257397 |
| rs538944171 | in-del | -/AA | | | intron-variant | TAB3 | GRCh38.p7 | X:30866870 | AGGAAAGGGGTGTTT[-/AA]AAAAAAAAAAAAAAA | 257397 |
| rs539273775 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30838706 | AAATATCTTTTGACA[A/G]TGTTTTATAGTTTTC | 257397 |
| rs539360695 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832049 | AAGCTCTACAATATG[C/G]ATATGTTTTATATTA | 257397 |
| rs540470499 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30878320 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 257397 |
| rs540690548 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30864337 | TGCATGTCAGCTTTG[A/T]GAGGATTCTTTTCTT | 257397 |
| rs542303137 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30870044 | ATACAAGGAAAAATA[C/T]TACTACTTTCCTTGT | 257397 |
| rs542807171 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30861806 | AATAGGTGAAATTAA[C/T]TGTAACATTTAACCC | 257397 |
| rs542846046 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant, missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836664 | CCCGGGCAACATGGC[A/G]AAACCCTGTCTCCAC | 257397 |
| rs543237868 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30856154 | CTGTCTGAACCATTA[C/T]GTAAGATTTAAGCAA | 257397 |
| rs544721172 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30868588 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 257397 |
| rs545649037 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30833009 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 257397 |
| rs546276124 | snp | C/G | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885218 | TTTCTGGAGCACAAG[C/G]TGATTTTTAAAATCA | 257397 |
| rs546564215 | snp | A/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846195 | ATACTCTGATTTGGG[A/T]TCCCTTTTTACAGAT | 257397 |
| rs547051903 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888654 | AAACCTCCTCTCCAA[C/T]AATTCTTACTATACT | 257397 |
| rs547093788 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30840847 | AACTTGGTCCTGTTT[C/T]CAGGGTAAAAACTTT | 257397 |
| rs548052703 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828657 | CAGTTTACAAAATAG[C/T]GAAATAATGTAAAAT | 257397 |
| rs548109087 | in-del | -/AAA | | | intron-variant | TAB3 | GRCh38.p7 | X:30878501 | GCAAGACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 257397 |
| rs549248316 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30847416 | CACTGAAATGTGAAG[A/G]GAGTCCTAATCTTCT | 257397 |
| rs549307567 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30874450 | ACTAGTATGGTAAAA[C/T]GTATGTAACTGTAGC | 257397 |
| rs549343700 | snp | C/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830519 | TCAAGATTTCCAAAT[C/G]GATTTTGGAATGGAC | 257397 |
| rs549350958 | in-del | -/A | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833830 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 257397 |
| rs550287704 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30862472 | TAGAAGAAAAGGCAA[A/G]AAGAATCAAAACACG | 257397 |
| rs552064262 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828944 | ACACAGTTAAACATA[C/T]CAGATTTATCAGTGT | 257397 |
| rs552125532 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835030 | ATTTCCTGAATTCCA[A/G]TTACCTATGTGTGCA | 257397 |
| rs552784000 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30881783 | GGTGATTTCTTCAAG[A/G]TCATAAGAAGCTCTG | 257397 |
| rs553207536 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30849686 | TCAGATATAGCCAGT[C/G]AGCGCCTGAGCAATT | 257397 |
| rs553358898 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830958 | TTCCTGTTGTCCTCT[G/T]TAGTAGGAAGCAATG | 257397 |
| rs554197397 | snp | A/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884355 | CCTCTGGCTCATTTA[A/T]TCCTTGTATGAGGTA | 257397 |
| rs554693169 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30862516 | CAGGTGTCAAAAGCA[C/T]AGGCTCCATATACTT | 257397 |
| rs557280228 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30850166 | CAACCACCACGTACT[A/G]TCCCTCTGCTGTGTA | 257397 |
| rs557615543 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30851679 | GAGGGAGTGGCTGCA[C/G]ACATGCTGACTGCAA | 257397 |
| rs559204162 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30864801 | AGTGTGTGTGTGTGT[A/G]TGTTTTTTTTTTAAA | 257397 |
| rs559258331 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30841545 | AAAAAAACACTCTGT[A/C]ATGAGCTTAATATAC | 257397 |
| rs559462841 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30842053 | GCCTCATGTGATCCA[C/T]CCGTCTGGCTTAAAT | 257397 |
| rs561438088 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836821 | GCACTCCAGCCTGGG[C/T]GACAGAGCGGGACCC | 257397 |
| rs562521098 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30879608 | ACTTCCTTAATCTGA[C/T]GATAGCTAGAAAAAA | 257397 |
| rs562668814 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30886785 | GCTGTTCCACTTCAA[C/T]TCTATTCAGATGTGG | 257397 |
| rs563027383 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30858222 | AATAAAGGGCTAAGT[A/G]AAATAAAACAAGGTC | 257397 |
| rs563597979 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30871156 | TACCAATGGTTCAAA[A/G]CAAGAATTATGGTTA | 257397 |
| rs563850510 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30833125 | ACAGGCGCCTGCCAC[C/T]GCACCCGGCTAATTT | 257397 |
| rs563860913 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835055 | TGTGCAGAAGCCCAG[C/T]AGACACTTTGCAACA | 257397 |
| rs565557995 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30838608 | GTATCTATATATCAA[A/C]CTTGTAAGAACAGGT | 257397 |
| rs566745664 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30873954 | CAAGGCGGGAGGATC[C/T]CTTGATCCCAGGAGT | 257397 |
| rs567436981 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30874897 | TCTCTTTTAGAACTG[A/G]AAAAATTGAGACATG | 257397 |
| rs567475937 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30847654 | TTAAATATCTGCTAC[C/T]ATAGGAAGACAGAAC | 257397 |
| rs567603300 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30836911 | CTAGATGAAGCTTGA[C/T]ATTAATGGGACCACA | 257397 |
| rs569886798 | snp | C/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846460 | CGGATAAAAACTGTC[C/T]CTTAAATCTACAAAA | 257397 |
| rs571590127 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30850445 | GGGCCAGGTGCGGTG[G/T]CTCATGCCTGGAATC | 257397 |
| rs571686601 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890255 | GGATATAAAATACAT[C/G]AAAGAGGAAATTCCT | 257397 |
| rs573062410 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30864888 | TCTCTGAAAAATCAC[A/G]TGATCTAGCAACTGC | 257397 |
| rs573110841 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30862773 | CCTGCCTGCTCCAAA[A/G]TCTGTGTTCTTTCCA | 257397 |
| rs573703635 | snp | A/G | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833763 | GTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 257397 |
| rs574705967 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30876395 | TCAGAAGGACTCCAA[A/G]TATTGGAATTATCAG | 257397 |
| rs575773437 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835135 | TAAATTTATAGTTTA[G/T]TAGTAAGCAACCCTT | 257397 |
| rs575887535 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30853831 | AGGCATGCGCCACCA[C/T]ACCCAGCTAAGTTTT | 257397 |
| rs576267488 | snp | C/G/T | 0.00105904 | 0.0229869 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833630 | AGGTCAGGAGATCGA[C/G/T]ACCATCCTGGCTAAC | 257397 |
| rs577446938 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30867679 | CCACACTTTCAGGGC[A/G]GGTTGGCTCTTTCCC | 257397 |
| rs577506816 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30875610 | AAAATTTTAGTTGAT[A/T]TTATGCATCCTAATT | 257397 |
| rs577859514 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30849708 | TGAGCAATTCTGACT[C/T]CCAAGCCTATGTGGG | 257397 |
| rs577968372 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30833003 | TGAGACGGAGTCTTG[C/T]TCTGTTGCCCAGGCT | 257397 |
| rs745347439 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30836044 | TTTCAAATACAATAT[A/G]AGAATCTGCAAGTGC | 257397 |
| rs745351943 | snp | C/T | 2.4003e-05 | 0.00346423 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855489 | TTGTCATCTGGACTA[C/T]GGTATTCCATATATA | 257397 |
| rs745361909 | in-del | -/AATAC | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30836034 | GCCGATTTAGTTTCA[-/AATAC]AATATGAGAATCTGC | 257397 |
| rs745415281 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30838136 | TTGGAGACAGCCTGT[C/T]ACCCAGGCTGGAGTA | 257397 |
| rs745421723 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30868477 | TATAGCTTATATATA[C/T]AGCTTATATATATAT | 257397 |
| rs745466157 | snp | A/G | 3.31724e-05 | 0.00407248 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859604 | GCCAGAGCAAATGGT[A/G]GCCAAGTTTCTCTTA | 257397 |
| rs745481424 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841025 | TCAATGCTAACTATA[C/T]ACCTCAGTGACTTTC | 257397 |
| rs745512091 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30859308 | GACTCCCACAACAGA[G/T]AATTATCCAGGCTAG | 257397 |
| rs745544669 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30882923 | TTCATTGTAAGTCTA[A/C]AATTATTCCAAAATA | 257397 |
| rs745549004 | snp | A/G | 2.41025e-05 | 0.00347141 | intron-variant | TAB3 | GRCh38.p7 | X:30846676 | CAAAATAGCAATTGT[A/G]GGAAAGTCATTATCA | 257397 |
| rs745570180 | in-del | -/GGGAGTCTT | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889799 | ACTTTTTGCGTCCCC[-/GGGAGTCTT]CTAACCCTTTGCTTG | 257397 |
| rs745577621 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30886831 | CAGGCTCTGCAGCAC[A/G]TAAGAAATGCAACAG | 257397 |
| rs745584689 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827490 | AATCTTTGACTTTCC[A/G]AATATGTACTGTTTG | 257397 |
| rs745596173 | in-del | -/AACAAAATATTTT | 0.0271702 | 0.113344 | intron-variant | TAB3 | GRCh38.p7 | X:30887196 | TTCAGGACTAGAATA[-/AACAAAATATTTT]AACAAAATATTTGTT | 257397 |
| rs745618892 | in-del | -/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890980 | TTCTCCTGTCCCTCT[-/G]GGAGCTTCCAATCTC | 257397 |
| rs745664618 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30874226 | GATTTTTGACTCTGC[A/C]GGCAGTCAGCACTCC | 257397 |
| rs745712113 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30851940 | ATGTATAAATTCTCT[A/C]ATTACCCGTGAACAT | 257397 |
| rs745745618 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30886517 | CTAAAGCTACATAAT[A/G]CACACACATACTGAT | 257397 |
| rs745806670 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844110 | TCACCACCGAAAAAG[G/T]TTTAGATTCCTTCCC | 257397 |
| rs745832148 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30867916 | ATGAAGCATGCATAT[A/C]ATTTTTTTTTTTTTT | 257397 |
| rs745834206 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30876430 | GGATTTTAAATTATG[C/T]TTGCTATGTTCAAGG | 257397 |
| rs745849719 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30853912 | ACTCCTGACCTCAGG[G/T]GATCCACCTGCCTCA | 257397 |
| rs745879925 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30879058 | AAGAAAAAGAGCAAA[A/C]TAATTCCTAAAAAGG | 257397 |
| rs745919960 | in-del | -/TTT | 2.59761e-05 | 0.0036038 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846527 | CACTATTACTTATGG[-/TTT]ACCAAATAATCAAGT | 257397 |
| rs745963325 | snp | A/T | 2.27998e-05 | 0.0033763 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855108 | CTATACCGAGGTATG[A/T]GCATGTATGAAGGAG | 257397 |
| rs745970591 | snp | C/T | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842780 | GCAATGAGCCATGAT[C/T]ACACCACTGCACTCT | 257397 |
| rs745978682 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30861298 | TAGATTTGGATAAAA[C/T]ACTATTCATATTCAA | 257397 |
| rs746004285 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889671 | CTAGTGGCGCGGGGC[A/G]GGGTAATGAAACCCA | 257397 |
| rs746029224 | snp | A/C/T | 0.00105918 | 0.022993 | intron-variant | TAB3 | GRCh38.p7 | X:30878142 | TATATAAAGCAAAGG[A/C/T]TGACAAAACTTCTAG | 257397 |
| rs746048579 | snp | C/G | 2.51203e-05 | 0.00354394 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834046 | CTGGACACACAAGTA[C/G]AAACCATCTGCAGCT | 257397 |
| rs746050787 | snp | A/G | 9.12024e-05 | 0.00675225 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855236 | ACTTCTGTTCTGTTC[A/G]TTCATAAAAAATGGA | 257397 |
| rs746064328 | in-del | -/TAGT | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30838894 | ACTTATTAGTTCTAA[-/TAGT]TAGTTGTTTTCCAGT | 257397 |
| rs746133469 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838006 | GGTATAAACCTGGGC[C/T]CCCTATTCTGTTCCA | 257397 |
| rs746135288 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890820 | ATTTAGACGTTTAGA[A/G]GAATTGCCTTGTGGA | 257397 |
| rs746186077 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30850088 | ACTTATCCAAGGATA[C/T]ATGAGTGACAAATAG | 257397 |
| rs746202022 | snp | A/T | 0.0338441 | 0.125605 | intron-variant | TAB3 | GRCh38.p7 | X:30841526 | TTGCAACTTATAAAT[A/T]AAAAAAAAAACACTC | 257397 |
| rs746206557 | in-del | -/ATTGCT | 0.0121112 | 0.0768695 | intron-variant | TAB3 | GRCh38.p7 | X:30864514 | ATGTCTCCCAACAGA[-/ATTGCT]CCTCCCAATCAGAGA | 257397 |
| rs746233414 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30878371 | CAGGTGTGGTGGCAC[A/G]TGCCTGTAGCCCCAG | 257397 |
| rs746234212 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30873580 | TCTCCTTCCACCTCC[C/T]CCCCTTTTTCTGCCT | 257397 |
| rs746330597 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30832932 | GAGGAATAAAGCCTT[C/T]GGTTGGAGGAAAAAT | 257397 |
| rs746364938 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888750 | CTCAAACACCTTCCT[A/G]GGGGCTTAAAGCCGG | 257397 |
| rs746393528 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30865312 | TGAGGTGAGTGAGCA[C/T]TTCCCAGGTTTGAAG | 257397 |
| rs746434979 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30833032 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 257397 |
| rs746482494 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30851841 | GACAAGATTTACACG[C/T]GCAGAGCTTTTTAGA | 257397 |
| rs746520323 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30867706 | TCCCAAGTATCCTTA[C/T]AAACTGAATCTTCTT | 257397 |
| rs746541627 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834244 | TTCAAGCAACCCACA[C/G]AGCTGAGTGCATTTA | 257397 |
| rs746558840 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875427 | CATTGATTAGGTTGT[C/T]TGAGGGTTCTCATAT | 257397 |
| rs746599206 | snp | G/T | | | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854416 | ATGGAGGTTTTGGTT[G/T]ACTAGATATCCCTCT | 257397 |
| rs746612903 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848579 | GATAGTAGAACCACT[C/T]GATCTTACTAAGGGT | 257397 |
| rs746618313 | snp | C/T | 2.32829e-05 | 0.00341188 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852904 | CAGTTGCTTTGCTAA[C/T]CTCTCCATCCTTGCT | 257397 |
| rs746672248 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30857437 | GTGAAATAAAGTATT[C/T]TTTTTTTTTTTATAG | 257397 |
| rs746722414 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834829 | GAGACAGGGTCTCTC[A/G]CTATGTTGCCCAGGC | 257397 |
| rs746800428 | snp | A/G | 0.00370173 | 0.0428621 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830455 | ACAAAATTGGAAGGA[A/G]AAAAAAAAGGCCCTA | 257397 |
| rs746804879 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30861741 | GTCCAGTAAAAAATA[C/T]GTGAGTCATATGTAT | 257397 |
| rs746812975 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851095 | AGGCAGAAATTTGAT[A/T]TATATTAACATCACC | 257397 |
| rs746814436 | snp | C/T | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890601 | GACAGGCATAGGATT[C/T]AGTCCAGTGAATCAC | 257397 |
| rs746837141 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30870188 | TGTGTGATTTCTCTC[A/C]AGTGCAGCCTAGATG | 257397 |
| rs746856162 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870688 | CAGTAGTTCCCAACC[-/A]GGGGTGACTTTTCCC | 257397 |
| rs746858282 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30860408 | TGCAAAGGGGAAAAA[C/T]TTAATTATACAGTGG | 257397 |
| rs746878484 | snp | C/T | 2.73913e-05 | 0.00370066 | missense, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831447 | TGTACCGTGGCATCT[C/T]GCACTGCTCACAGCG | 257397 |
| rs746881054 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843105 | TTTCCTGTTATTTGA[-/T]TTTTTTTTTAAAGAA | 257397 |
| rs746944527 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30874879 | CTGGAAAGCAAAGAC[A/G]CATCTCTTTTAGAAC | 257397 |
| rs746950718 | in-del | -/AAG | | | intron-variant | TAB3 | GRCh38.p7 | X:30841492 | ATATTAAACAATAAA[-/AAG]AAGAACAGATACTAT | 257397 |
| rs746967488 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30886415 | TATATTTTATTTAAC[A/G]CTTTCTTGGGAGTAT | 257397 |
| rs746968206 | snp | G/T | 3.29625e-05 | 0.00405958 | intron-variant | TAB3 | GRCh38.p7 | X:30831600 | GTTAGGATTAAGGGG[G/T]AGGGGGAAGGTAAAT | 257397 |
| rs746989671 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830984 | CAATGGGAAGAAGCA[C/T]GGGGAGCCTTGGTTT | 257397 |
| rs747044778 | snp | A/C | 4.67388e-05 | 0.00483396 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842935 | TTTTGACATTTATTT[A/C]TATCGTATTTGTGAC | 257397 |
| rs747093536 | snp | A/G | 2.42736e-05 | 0.00348371 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855508 | ATTCCATATATAAGT[A/G]TTTGCTACTCTCCTG | 257397 |
| rs747097048 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30857697 | AAAATTTAAAAAACC[A/G]CAAAACCAAGATATT | 257397 |
| rs747139238 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30864258 | AAAGACATAAACCCT[A/G]TGATCATCACACAGT | 257397 |
| rs747148144 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30887542 | ACTCTAGAATCAGAC[C/G]TACATGAGTTTGAGT | 257397 |
| rs747188105 | snp | A/G | 7.11288e-05 | 0.00596317 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843100 | CTCTTTTTTCCTGTT[A/G]TTTGATTTTTTTTTA | 257397 |
| rs747211747 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30846734 | TGTTAATTGTAATGA[C/T]TGGGTATTACCAAGA | 257397 |
| rs747252218 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30877895 | AAAACATAAGAATAC[A/T]GAAAGGTTAAAAGTA | 257397 |
| rs747259524 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30841031 | CTAACTATACACCTC[A/G]GTGACTTTCGGCAAG | 257397 |
| rs747291163 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30858936 | TTTAGCATTAGAAAA[A/T]CAGGGAGTGGATTAT | 257397 |
| rs747302764 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889618 | CCCGGAACGGCCCCT[A/G]AAGTAGGACCTAGTT | 257397 |
| rs747314807 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30866541 | AATCCCATGATGATG[A/G]GGGCATGTCGAAATG | 257397 |
| rs747321418 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30871848 | CAAACTGTGAAAGCT[C/T]TAAATACAACAGTAT | 257397 |
| rs747342121 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30849189 | CAGATATACCTATCT[C/T]ATTTCACATACAGAT | 257397 |
| rs747398340 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30881885 | TTCCACCTACCAAGA[C/G]AGTTTGTTTACTGGC | 257397 |
| rs747448391 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30841470 | ATCAGATGAAACATC[A/G]ATGGTAATATTAAAC | 257397 |
| rs747452248 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829548 | AAGAACGTTGTTTTG[A/G]GGACCATGCTTTTAA | 257397 |
| rs747479152 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832123 | CAGAATAGTGAAAAG[A/G]GGAAGATTCTACAGT | 257397 |
| rs747573424 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840967 | ACATTCAGGCAAAAT[C/G]GAGTTTAAAGACTGA | 257397 |
| rs747627779 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851695 | ACATGCTGACTGCAA[G/T]AGGCCTGACATATGC | 257397 |
| rs747627895 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30842395 | TCCTCATTATTTTAT[A/G]AGAATTATCTTTTAG | 257397 |
| rs747632817 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30869820 | ATTTATTAATGTATT[A/G]TATAACAAATGTACT | 257397 |
| rs747636232 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30874746 | ACAAGGCAGATAAGC[G/T]TTTTGCCCTTCTTAA | 257397 |
| rs747665367 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30871455 | GAGGTTTCTAATAGC[A/T]AATGAATTGTCCAAA | 257397 |
| rs747677579 | snp | C/T | 0.0446399 | 0.142574 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854175 | TGATATTTATGGCTT[C/T]CCTTTTCTCCCCCAG | 257397 |
| rs747688071 | in-del | -/A | 0.492672 | 0.0600846 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833831 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 257397 |
| rs747758746 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885473 | TTCCCTCCCATAACT[-/G]GAAGTCTGAGCTTCC | 257397 |
| rs747826758 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866687 | CCATACTGAGATAAA[G/T]AAATGACTGAATAAA | 257397 |
| rs747856384 | snp | C/T | 0.000529661 | 0.016265 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30842981 | CTTTTTTAGATGGCT[C/T]GGGTGGTACAACTGG | 257397 |
| rs747859384 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30851662 | AGTAGAAACTTCTCT[A/C]TGAGGGAGTGGCTGC | 257397 |
| rs747884438 | snp | C/G | 2.70702e-05 | 0.00367891 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834005 | TACATGGATTAACAT[C/G]TGTCTTTGGACATTC | 257397 |
| rs747912260 | in-del | -/ACTTTTAT | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30837802 | AAGCTTTATAGTTTA[-/ACTTTTAT]ACTTAGGTGTATGAG | 257397 |
| rs747959260 | in-del | -/AA/ACAT | 0.0168099 | 0.0901243 | intron-variant | TAB3 | GRCh38.p7 | X:30859385 | CACACACACACACAC[-/AA/ACAT]ACACACAAGAAAACA | 257397 |
| rs747970472 | in-del | -/TTTTCCTGTTA | 5.61577e-05 | 0.00529865 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843090 | CATTTAAGAACTCTT[-/TTTTCCTGTTA]TTTGATTTTTTTTTA | 257397 |
| rs747978473 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30878969 | ACTTGAAAATGAAAT[A/G]TATAGCTTTAAATAT | 257397 |
| rs747988247 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30887512 | ACTTACGCAGAGTAT[A/G]GTGAAAGAACACACA | 257397 |
| rs748012744 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30869146 | GCTTACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 257397 |
| rs748017072 | snp | C/T | 0.00158814 | 0.0281345 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830300 | AGTGTGCAACTTTGT[C/T]GTTGGCCAACTGTAA | 257397 |
| rs748028579 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30842135 | CAATTAAACATTTGC[C/T]ACATAAAAATAAGAA | 257397 |
| rs748034928 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30840405 | AATTTTGCCTTGCCC[-/A]AACAGAGGTCTGGCT | 257397 |
| rs748099449 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30888617 | TTTTCTCCTTACTCA[A/G]CACCTACCAACAGTC | 257397 |
| rs748133996 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30886638 | ATGAAGCAGCAAACC[C/G]CAAATTTCAAAACTT | 257397 |
| rs748147784 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829421 | TTAAAACCAAGTGGG[A/G]TTGACCATCACTAAA | 257397 |
| rs748160789 | in-del | -/TT | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30863107 | TAATAGTAGACTGAC[-/TT]TTCACAACAAATAGG | 257397 |
| rs748185725 | in-del | -/AAGG/AGA | | | intron-variant | TAB3 | GRCh38.p7 | X:30878517 | AAAAAAAAAAAAAAA[-/AAGG/AGA]AAGAAAGAAAGAAAG | 257397 |
| rs748205942 | snp | C/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829326 | TTGCCTCCACTTCAG[C/G]ATATCACTATGAATA | 257397 |
| rs748214616 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831289 | TCGTGAGCACAACGA[C/T]GACCACAAAGCCATT | 257397 |
| rs748273925 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30871763 | TGACACAACACAATC[A/C]ACGGTCAAAAACTTG | 257397 |
| rs748373314 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30855763 | TACAAACATTTAGCT[C/T]ACATTACTAGTACTA | 257397 |
| rs748402945 | in-del | -/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30864159 | GACACCCTTGAAACA[-/C]CCCCCACTAAAGTCC | 257397 |
| rs748437881 | snp | C/T | 2.28172e-05 | 0.00337759 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854646 | CTTCCCTGTTTCTGA[C/T]AGCTAGGAGGTCCTT | 257397 |
| rs748453561 | in-del | -/A | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30880587 | TCTTATGAGAATACC[-/A]TGAAATAGAAAAAGC | 257397 |
| rs748472483 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30877885 | AGCCCCATCTAAAAC[A/G]TAAGAATACAGAAAG | 257397 |
| rs748477999 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30862124 | ATGGCCTAGCACAGG[C/T]TAGCTGTTCAATAAA | 257397 |
| rs748516529 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890495 | AACTCCTGACCTCAG[A/G]TGATCTGCCCGCCTC | 257397 |
| rs748526039 | snp | C/T | 2.35846e-05 | 0.00343391 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855374 | TGAGCTATGTACCAG[C/T]GTTCGACCACCATTA | 257397 |
| rs748533034 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30864046 | GCTATTTTTTATACA[A/G]TAAGTGCTGAATGAT | 257397 |
| rs748558698 | snp | A/G | 0.0157677 | 0.0873799 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30867494 | TCAACCCTGGCACAG[A/G]AATTTTATTCACATC | 257397 |
| rs748559354 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30849075 | CTAACATTTCTATCT[C/G]AAAACTCTGAAAGTA | 257397 |
| rs748612177 | snp | C/T | 9.96947e-05 | 0.00705956 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855534 | TCCTGGGAAAGGGCT[C/T]GGCAACAGGCTTCAA | 257397 |
| rs748646194 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30840014 | AGTTTGGGTAGATTA[C/T]ATTGTTCAGGAAATC | 257397 |
| rs748649350 | snp | A/G | 8.59993e-05 | 0.00655685 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845970 | AAGTATGCAGCAGCT[A/G]TGGACATCAGTCAGT | 257397 |
| rs748686560 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30881659 | ATCTTGTAGGTTTTT[A/G]TTAAACAAGAGGGTT | 257397 |
| rs748705683 | in-del | -/CT | 0.0121112 | 0.0768695 | intron-variant | TAB3 | GRCh38.p7 | X:30848513 | AGCAACAGAGTGAGA[-/CT]CTGTCTCAGAAACAA | 257397 |
| rs748726252 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884377 | TATGAGGTAGGTACC[A/C]CATTATCCCTTCAAA | 257397 |
| rs748735194 | snp | G/T | 4.56908e-05 | 0.00477947 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854510 | TTGATTACTGATGGG[G/T]GAAGGACTCCTATTA | 257397 |
| rs748797082 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30840888 | CCCTTAGACAGGGCA[A/G]TTGCTCTAAGACAGC | 257397 |
| rs748797746 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30888527 | TAGTAAACTACAGAA[C/T]TCCAACTGGGAATAA | 257397 |
| rs748805247 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30850278 | AGCACCCACATGAAC[C/T]ACCAATTTCTCAATC | 257397 |
| rs748850738 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829103 | ACCTATCCAATAGAC[C/T]GTTTTCTCTCTTTTC | 257397 |
| rs748961949 | snp | A/G | 2.63978e-05 | 0.00363293 | intron-variant | TAB3 | GRCh38.p7 | X:30855578 | CTAGGGGAGAAAAAT[A/G]GTAAAAGTAACATTG | 257397 |
| rs748974277 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30877771 | ACTTAACCCCAAAAT[G/T]TCAATAATTATATTA | 257397 |
| rs749026344 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848653 | TAAACTGAGGGGGGA[A/G]AAAAAGCAGTTTCTG | 257397 |
| rs749053196 | in-del | -/T | 0.0100156 | 0.0700533 | intron-variant | TAB3 | GRCh38.p7 | X:30868494 | GCTTATATATATATA[-/T]AGCTTATATATATAT | 257397 |
| rs749055292 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845230 | AAGAAAAGTTAAGTG[G/T]GGGGGATGGGGGGCA | 257397 |
| rs749082719 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30875850 | CAGCTATATAAAACA[A/C]AGCTTAAACAGAACT | 257397 |
| rs749114173 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30827615 | CATGGTATTTACAAG[A/G]TTTAATAAGTTTTTG | 257397 |
| rs749123127 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30855663 | AATACTACTGTCACA[A/G]AATAAATAGAGAGCA | 257397 |
| rs749154617 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30837270 | GACAGGCTGGTCTCA[A/G]ACTCCAGACCTCAAG | 257397 |
| rs749170068 | in-del | -/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30876664 | GCATGCACCAGCATG[-/C]CCAGCTAATTTCTGT | 257397 |
| rs749213636 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30869028 | GTGTAATACTTTTTT[C/G]TACTTTCTGATACAA | 257397 |
| rs749292573 | snp | A/G | 4.56892e-05 | 0.00477939 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854315 | AAAAACTGTAGTTGG[A/G]TTTGGTATCACTCGA | 257397 |
| rs749293275 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30863622 | TTTTGCCATATTACA[G/T]GCCTGCTCTTGCTTC | 257397 |
| rs749299469 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848443 | ACGAGAATTGCTTGA[A/C]CTGGGGAGGTGGAGG | 257397 |
| rs749345327 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30846728 | GTTTCATGTTAATTG[C/T]AATGATTGGGTATTA | 257397 |
| rs749454349 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831157 | GAAGAGCTCTTGACT[A/T]CTGTGTGTACATTCT | 257397 |
| rs749458479 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30827803 | AGCCATGCAGAATCT[A/G]CTTGTATTAAATATT | 257397 |
| rs749533539 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830547 | GACTTGCATTTGGCA[C/T]ACATTCACTGTGCTA | 257397 |
| rs749540202 | in-del | -/ATAG | 2.44051e-05 | 0.00349313 | intron-variant | TAB3 | GRCh38.p7 | X:30852949 | CAAGGCTACAGCATT[-/ATAG]ATAATGTCATTGCAG | 257397 |
| rs749542466 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30861892 | ATTTTTCAAATGATA[G/T]CTTTGAAATCCAGTG | 257397 |
| rs749555141 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30871720 | TTTTTCAACTGGTGA[A/T]AATTCAACTAAGATA | 257397 |
| rs749562610 | snp | A/G | 2.28131e-05 | 0.00337728 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855078 | TGGGATACTGTAACA[A/G]TAATTGGATTTGTAC | 257397 |