SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7896 | snp | C/G | 0.314544 | 0.241524 | utr-variant-3-prime | TAB2 | GRCh38.p7 | 6:149410340 | TGCAGCGAAATACCC[C/G]AAAGCTTTTCCTACT | 23118 |
rs47546 | snp | C/T | 0.49168 | 0.063958 | intron-variant | TAB2 | GRCh38.p7 | 6:149297532 | TATATGCACACtttt[C/T]tttctctttttgaga | 23118 |
rs92605 | snp | A/G | 0.349013 | 0.229557 | intron-variant | TAB2 | GRCh38.p7 | 6:149339132 | gccctttgggaggcc[A/G]agacgggcggatcat | 23118 |
rs237011 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAB2 | GRCh38.p7 | 6:149408993 | TTAAAAACCACATTT[A/G]GTATGGTAAAGTAGA | 23118 |
rs237012 | snp | A/G | 0.45692 | 0.1403 | intron-variant | TAB2 | GRCh38.p7 | 6:149408062 | CCATCCTACTTACTA[A/G]AATTTTGGTCTCAGG | 23118 |
rs237019 | snp | C/T | 0.45866 | 0.137698 | intron-variant | TAB2 | GRCh38.p7 | 6:149405928 | atattcaacacctca[C/T]atagcttatctcccc | 23118 |
rs237020 | snp | A/C | 0.230017 | 0.2492 | intron-variant | TAB2 | GRCh38.p7 | 6:149403395 | ggcctttattaagtt[A/C]CTTCtatatgtgtat | 23118 |
rs237021 | snp | A/G | 0 | 0 | intron-variant | TAB2 | GRCh38.p7 | 6:149403295 | tatatatatatatat[A/G]tgtgtgtgtgtatat | 23118 |
rs237022 | snp | A/G | 0.216649 | 0.247765 | intron-variant | TAB2 | GRCh38.p7 | 6:149403126 | ctgcctcagcctcct[A/G]agtacctgggattac | 23118 |
rs237023 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | SUMO4, TAB2 | GRCh38.p7 | 6:149400904 | ATGTCAATCAAAACA[C/T]ACCATTGGCTGTTTG | 23118 |
rs237024 | snp | A/G | 0.418007 | 0.185132 | utr-variant-3-prime, intron-variant | SUMO4, TAB2 | GRCh38.p7 | 6:149400829 | TTCATGTATAATAAA[A/G]GAATGTGGAAGGGGG | 23118 |
rs237025 | snp | C/T | 0.493933 | 0.0547435 | SUMO4, TAB2 | 6 | allele_origin=T(germline)/C(germline) | 6:149400554 | ATCTGATCTGCTTCA[C/T]TGACAATCCCCGTGG | 23118 |
rs237026 | snp | C/T | 0.417845 | 0.185278 | upstream-variant-2KB, intron-variant | SUMO4, TAB2 | GRCh38.p7 | 6:149399545 | AAATTAAACTAAATA[C/T]TCATGGGGGGGGGGA | 23118 |
rs237027 | snp | A/G | 0.230603 | 0.249246 | upstream-variant-2KB, intron-variant | SUMO4, TAB2 | GRCh38.p7 | 6:149398767 | AATGTAATTTTAAAC[A/G]ATCAAACATGGACTT | 23118 |
rs237028 | snp | A/G | 0.45574 | 0.142025 | intron-variant | TAB2 | GRCh38.p7 | 6:149397514 | AACAAGAATTTGTCA[A/G]AAATCCCAAAGCTAC | 23118 |
rs237029 | snp | C/T | 0.455621 | 0.142197 | intron-variant | TAB2 | GRCh38.p7 | 6:149396289 | gctcacacctgtaac[C/T]ccagcactttgggga | 23118 |
rs237030 | snp | C/T | 0.230603 | 0.249246 | intron-variant | TAB2 | GRCh38.p7 | 6:149396183 | taaaaatacaaaaag[C/T]tgccgggcgtggtgg | 23118 |
rs237031 | snp | A/G | 0.230603 | 0.249246 | intron-variant | TAB2 | GRCh38.p7 | 6:149396110 | gaattgcttgaaccc[A/G]ggaggcagaggttgc | 23118 |
rs237032 | snp | C/T | 0.230603 | 0.249246 | intron-variant | TAB2 | GRCh38.p7 | 6:149395036 | CAAAGGGTAAACAgg[C/T]aggcaaactatggcc | 23118 |
rs237033 | snp | A/G | 0.190833 | 0.242898 | intron-variant | TAB2 | GRCh38.p7 | 6:149393013 | ACTACAGGGAAAAAA[A/G]GGGTCAAAGTGAATT | 23118 |
rs237034 | snp | G/T | 0.656927 | 0.0594679 | intron-variant | TAB2 | GRCh38.p7 | 6:149390726 | GCATGCAACTCTCTC[G/T]TAGTTGTTGTTAAAA | 23118 |
rs237035 | snp | A/G | 0.457388 | 0.139608 | intron-variant | TAB2 | GRCh38.p7 | 6:149389712 | ATATAACTTGGATGA[A/G]TCATTATGCGACGTG | 23118 |
rs237036 | snp | A/G | 0.229723 | 0.249176 | intron-variant | TAB2 | GRCh38.p7 | 6:149387232 | agaatataagaacta[A/G]tattatataactctt | 23118 |
rs237037 | snp | A/C | 0.216349 | 0.247725 | intron-variant | TAB2 | GRCh38.p7 | 6:149386668 | aaaaggtggaaaaaa[A/C]caaaatgtctattaa | 23118 |
rs406199 | snp | G/T | 0 | 0 | intron-variant | TAB2 | GRCh38.p7 | 6:149392849 | ATTATGAAACAATGT[G/T]AGTAGATCATTAAAC | 23118 |
rs471469 | snp | A/G | 0.471578 | 0.115772 | intron-variant | TAB2 | GRCh38.p7 | 6:149219584 | ACTTCTCTGACTTTA[A/G]TTGGTCATAAGAAAT | 23118 |
rs472620 | snp | A/G | 0.342134 | 0.232404 | intron-variant | TAB2 | GRCh38.p7 | 6:149323562 | CTGAAAAGTGAAAAC[A/G]TCCCACCAGCATCCC | 23118 |
rs472810 | snp | A/C | 0.341909 | 0.232492 | intron-variant | TAB2 | GRCh38.p7 | 6:149348443 | GAAAGAAAGAAAAAA[A/C]AAAACTGTTAGCATC | 23118 |
rs473451 | snp | C/T | 0.486266 | 0.0817214 | upstream-variant-2KB, intron-variant | TAB2 | GRCh38.p7 | 6:149317062 | cgggcccccggaccc[C/T]acccgcgcggcgccg | 23118 |
rs473864 | snp | A/G | 0.19646 | 0.2442 | intron-variant | TAB2 | GRCh38.p7 | 6:149348291 | CTACTAAGGAAGCTG[A/G]GGAGGGAAGATCCTT | 23118 |
rs474369 | snp | A/T | 0.342134 | 0.232404 | intron-variant | TAB2 | GRCh38.p7 | 6:149322826 | TGTCATCATTTTGCT[A/T]GTTAATTCAAAGAAT | 23118 |
rs474587 | snp | A/G | 0.229723 | 0.249176 | intron-variant | TAB2 | GRCh38.p7 | 6:149348265 | GTGGGGTTGCGCACC[A/G]GTAGTCCCTGCTACT | 23118 |
rs474726 | snp | G/T | 0.145305 | 0.227022 | intron-variant | TAB2 | GRCh38.p7 | 6:149348218 | GGCAATATAGGGAGA[G/T]CCTACCAAAAAAATA | 23118 |
rs475342 | snp | C/T | 0.486266 | 0.0817214 | upstream-variant-2KB, intron-variant | TAB2 | GRCh38.p7 | 6:149317260 | GCGGAGAAAGGGGGT[C/T]TCAGCCCTCCCCGGG | 23118 |
rs476816 | snp | C/T | 0.185155 | 0.241444 | intron-variant | TAB2 | GRCh38.p7 | 6:149310790 | TCTACGTTACTTCAC[C/T]GTTTTTGTTAATAGA | 23118 |
rs477088 | snp | G/T | 0.497881 | 0.0324789 | intron-variant | TAB2 | GRCh38.p7 | 6:149297921 | CTGCTTAGTATTTTT[G/T]CTGATTATACTGCAG | 23118 |
rs478531 | snp | C/T | 0.279726 | 0.248226 | intron-variant | TAB2 | GRCh38.p7 | 6:149360381 | gcttacaatcatggc[C/T]gaaggcacaggggaa | 23118 |
rs478767 | snp | C/G | 0.341685 | 0.232581 | intron-variant | TAB2 | GRCh38.p7 | 6:149328964 | CTTTTTAGATAGAGA[C/G]AAACACCATGCATGA | 23118 |
rs479676 | snp | C/T | 0.495818 | 0.0455352 | intron-variant | TAB2 | GRCh38.p7 | 6:149312820 | ggaatggctgaattg[C/T]gataattaacatatc | 23118 |
rs480526 | snp | A/G | 0.345482 | 0.231048 | intron-variant | TAB2 | GRCh38.p7 | 6:149327245 | ATAGGCAAGATGGTC[A/G]TTTTTTAAAAATTTA | 23118 |
rs480670 | snp | C/T | 0.230896 | 0.249269 | intron-variant | TAB2 | GRCh38.p7 | 6:149328744 | ACACATGTGATATAC[C/T]GTGACAAATGCTGTG | 23118 |
rs481651 | snp | A/G | 0.491577 | 0.0643472 | intron-variant | TAB2 | GRCh38.p7 | 6:149295201 | TTTAGTAGAGCTGCC[A/G]GTGAAGCTATCTAGG | 23118 |
rs481769 | snp | C/T | 0.341909 | 0.232492 | intron-variant | TAB2 | GRCh38.p7 | 6:149328585 | GCACGAGCCACCGCA[C/T]CCGGCCTCTACATTC | 23118 |
rs482388 | snp | A/G | 0.49614 | 0.0437598 | intron-variant | TAB2 | GRCh38.p7 | 6:149311386 | TGATCTTCTCCTCTC[A/G]AAACTCCCAGAGTAA | 23118 |
rs483329 | snp | C/G | 0.224412 | 0.248687 | intron-variant | TAB2 | GRCh38.p7 | 6:149312466 | CTCCCGGGTTCAAGC[C/G]ATTCTCATGCCTCAG | 23118 |
rs483877 | snp | A/C | 0.23031 | 0.249223 | intron-variant | TAB2 | GRCh38.p7 | 6:149336982 | TGAAATTTAGCATTT[A/C]CTTTTAATAAGATTT | 23118 |
rs484969 | snp | C/T | 0.229723 | 0.249176 | intron-variant | TAB2 | GRCh38.p7 | 6:149343693 | CAGTTTTTGGTTTTG[C/T]TGTTACACTCCAGGA | 23118 |
rs485360 | snp | G/T | 0.496175 | 0.0435625 | intron-variant | TAB2 | GRCh38.p7 | 6:149312189 | AACTTCGGGTGCTTC[G/T]CCCCACAGTGGCATC | 23118 |
rs487525 | snp | C/T | 0.48546 | 0.0840147 | upstream-variant-2KB | TAB2 | GRCh38.p7 | 6:149216191 | GGCCCTCCCTGGAGA[C/T]AGCATCATTGGAGGG | 23118 |
rs489551 | snp | C/T | 0.487995 | 0.0765403 | intron-variant | TAB2 | GRCh38.p7 | 6:149368321 | gccactatacacttt[C/T]agtttatgaaaccca | 23118 |
rs490529 | snp | A/G | 0.341685 | 0.232581 | intron-variant | TAB2 | GRCh38.p7 | 6:149331150 | aaatgtcagtttcgg[A/G]gaaattgacattttt | 23118 |
rs491576 | snp | A/G | 0.49962 | 0.0137727 | intron-variant | TAB2 | GRCh38.p7 | 6:149302125 | TTCAAAAATATGTCC[A/G]AGATAGACTAAAGAG | 23118 |
rs492461 | snp | A/G | 0.498059 | 0.0310896 | intron-variant | TAB2 | GRCh38.p7 | 6:149308589 | ctggagtgcagtggc[A/G]caatctcaggctcac | 23118 |
rs492956 | snp | A/G | 0.341909 | 0.232492 | intron-variant | TAB2 | GRCh38.p7 | 6:149347391 | TTAATGTTTATTGTT[A/G]TTCTTTAGAAAGTAA | 23118 |
rs494228 | snp | C/T | 0.459004 | 0.137176 | intron-variant | TAB2 | GRCh38.p7 | 6:149304705 | AGCATAGGTACACCA[C/T]TATCAGGATTGCCTC | 23118 |
rs494340 | snp | A/G | 0.341909 | 0.232492 | intron-variant, upstream-variant-2KB | TAB2 | GRCh38.p7 | 6:149341813 | TACAGTTTTCACAAC[A/G]TCTATGATAATTTGA | 23118 |
rs496091 | snp | A/C | 0.492386 | 0.0612297 | intron-variant | TAB2 | GRCh38.p7 | 6:149308217 | tacatctagttattt[A/C]ttcctaggagtggaa | 23118 |
rs496124 | snp | A/T | 0.49263 | 0.0602539 | intron-variant | TAB2 | GRCh38.p7 | 6:149308203 | cacatcttcaaatgt[A/T]catctagttatttat | 23118 |
rs496157 | snp | C/G | 0.49263 | 0.0602539 | intron-variant | TAB2 | GRCh38.p7 | 6:149308190 | gcatcctttgacaca[C/G]atcttcaaatgtaca | 23118 |
rs497036 | snp | C/G | 0.499992 | 0.00199679 | intron-variant | TAB2 | GRCh38.p7 | 6:149308130 | aaatagaaaacaacc[C/G]taatacatcttacta | 23118 |
rs497388 | snp | C/T | 0.223225 | 0.248562 | intron-variant | TAB2 | GRCh38.p7 | 6:149357286 | tcgggcgtggtggtg[C/T]gcacctgtagtccca | 23118 |
rs497628 | snp | C/T | 0.480223 | 0.0974544 | intron-variant | TAB2 | GRCh38.p7 | 6:149220168 | gtattcaatctgtta[C/T]gctgtcttggttgaa | 23118 |
rs497631 | snp | C/G | 0.286825 | 0.247273 | intron-variant | TAB2 | GRCh38.p7 | 6:149220170 | attcaatctgttacg[C/G]tgtcttggttgaaat | 23118 |
rs497886 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | TAB2 | GRCh38.p7 | 6:149314548 | TGCAATCTTCTTATA[A/G]CTTTCCCTGATATCT | 23118 |
rs498416 | snp | A/G | 0.489665 | 0.0711382 | intron-variant | TAB2 | GRCh38.p7 | 6:149357421 | ACTCCGTCTCAAGGA[A/G]AAAAAAAAAACACAC | 23118 |
rs500860 | snp | A/G | 0.23031 | 0.249223 | intron-variant | TAB2 | GRCh38.p7 | 6:149367060 | ttttattcaacaaat[A/G]tgttgcatcttctgt | 23118 |
rs501651 | snp | C/T | 0.491525 | 0.0645418 | intron-variant | TAB2 | GRCh38.p7 | 6:149295461 | ttatctcttcaaata[C/T]taccttttcccatgt | 23118 |
rs501926 | snp | A/G | 0.341909 | 0.232492 | intron-variant | TAB2 | GRCh38.p7 | 6:149333812 | TAGTAAAGTTTGTAA[A/G]AAGAATGTCTTTCTC | 23118 |
rs503177 | snp | C/T | 0.192088 | 0.2432 | intron-variant | TAB2 | GRCh38.p7 | 6:149308521 | TTATTTATTTATTTA[C/T]TTATTTATTTATTTA | 23118 |
rs504762 | snp | C/T | 0.341685 | 0.232581 | intron-variant | TAB2 | GRCh38.p7 | 6:149351529 | AATGAAATGATAGTA[C/T]TGATATTTTATTTAC | 23118 |
rs504985 | snp | G/T | 0.487995 | 0.0765403 | intron-variant | TAB2 | GRCh38.p7 | 6:149337842 | GGTCATTTATATGTT[G/T]GATGATAGGGATAGG | 23118 |
rs505765 | snp | A/G | 0.23031 | 0.249223 | intron-variant | TAB2 | GRCh38.p7 | 6:149351669 | AAACTGAGGCACAGA[A/G]AAATTAAATGATTTG | 23118 |
rs506268 | snp | C/T | 0.499663 | 0.0129749 | intron-variant | TAB2 | GRCh38.p7 | 6:149364481 | CGAGTGCAGAAGACG[C/T]AGACAGAAGATAAAA | 23118 |
rs506573 | snp | C/T | 0.230603 | 0.249246 | intron-variant | TAB2 | GRCh38.p7 | 6:149334337 | GGGAGGAAAGTGACA[C/T]GATTCAGCCAGTTTT | 23118 |
rs506779 | snp | C/T | 0.229723 | 0.249176 | intron-variant | TAB2 | GRCh38.p7 | 6:149337658 | AAACTCATCTTGTAA[C/T]ACCACAGTCACTATC | 23118 |
rs508534 | snp | A/T | 0.497855 | 0.0326773 | intron-variant | TAB2 | GRCh38.p7 | 6:149299024 | GATTTGCTTAAAGAA[A/T]CTTTTCATGCTAAAT | 23118 |
rs510343 | snp | C/T | 0.256061 | 0.249927 | intron-variant | TAB2 | GRCh38.p7 | 6:149311790 | GATCTTATATTGGAA[C/T]CTAGTCTCAAAAATG | 23118 |
rs511100 | snp | A/G | 0.485255 | 0.0845871 | intron-variant | TAB2 | GRCh38.p7 | 6:149371093 | AAAAAAAAAAAAAGT[A/G]TCCGGGGCTCAGTCA | 23118 |
rs511105 | snp | A/T | 0.341909 | 0.232492 | intron-variant | TAB2 | GRCh38.p7 | 6:149327763 | CTTAGGATGATTTTA[A/T]AGGAAATGGAAAAAT | 23118 |
rs511924 | snp | A/G | 0.254664 | 0.249956 | intron-variant | TAB2 | GRCh38.p7 | 6:149311649 | AGTAATGGTACCACT[A/G]TCAATGCTAGTGTTA | 23118 |
rs514839 | snp | A/T | 0.487933 | 0.0767327 | intron-variant | TAB2 | GRCh38.p7 | 6:149327304 | TGAGCACAAATTATG[A/T]CATAGTTGCCTGGTT | 23118 |
rs515133 | snp | G/T | 0.341909 | 0.232492 | intron-variant | TAB2 | GRCh38.p7 | 6:149354136 | CTAATTGGTCCCAGC[G/T]TCTGCTATCCAAAGT | 23118 |
rs515295 | snp | A/G | 0.493523 | 0.0565391 | intron-variant | TAB2 | GRCh38.p7 | 6:149301839 | TTTATAAAGCTCTTG[A/G]GTTAGTCACTAAGCT | 23118 |
rs517207 | snp | A/G | 0.492337 | 0.0614248 | intron-variant | TAB2 | GRCh38.p7 | 6:149291987 | TGCCAACCCTTGAAA[A/G]TTTATAGTCTAGCTA | 23118 |
rs517365 | snp | C/G | | | upstream-variant-2KB, intron-variant | TAB2 | GRCh38.p7 | 6:149317601 | ccccccaccccccca[C/G]ctctcgctcgctctc | 23118 |
rs517366 | snp | C/G | | | upstream-variant-2KB, intron-variant | TAB2 | GRCh38.p7 | 6:149317600 | cccccacccccccag[C/G]tctcgctcgctctcg | 23118 |
rs518836 | snp | G/T | 0.499464 | 0.016365 | intron-variant | TAB2 | GRCh38.p7 | 6:149305083 | TTTGTTATTGTTATT[G/T]TTATTATATATTTTC | 23118 |
rs518879 | snp | C/T | 0.341685 | 0.232581 | intron-variant | TAB2 | GRCh38.p7 | 6:149338512 | AAAGAAATTGCTATT[C/T]CTGACAAAAATGGAA | 23118 |
rs520551 | snp | A/T | 0.145305 | 0.227022 | intron-variant | TAB2 | GRCh38.p7 | 6:149348137 | GTGGCTCACACCTGT[A/T]ATCCCAGCACTTTGG | 23118 |
rs520683 | snp | A/T | 0.23031 | 0.249223 | intron-variant | TAB2 | GRCh38.p7 | 6:149354755 | TTAACTGAGTATTGT[A/T]TCTTGGGGATTATTC | 23118 |
rs520852 | snp | A/G | 0.486266 | 0.0817214 | upstream-variant-2KB, intron-variant | TAB2 | GRCh38.p7 | 6:149317261 | GCCCGGGGAGGGCTG[A/G]GACCCCCTTTCTCCG | 23118 |
rs521845 | snp | G/T | 0.497473 | 0.0354532 | intron-variant | TAB2 | GRCh38.p7 | 6:149350562 | GGTTGAGAAGTGAAC[G/T]TTATGTATTTCTTCC | 23118 |
rs521989 | snp | C/G | 0.203267 | 0.245593 | upstream-variant-2KB, intron-variant | TAB2 | GRCh38.p7 | 6:149317088 | CGCCGCCGGCCGCCC[C/G]GCAAGTCCCGCCACC | 23118 |
rs522646 | snp | C/T | 0.341909 | 0.232492 | intron-variant | TAB2 | GRCh38.p7 | 6:149334462 | AGGCAAGAGGATTGC[C/T]GAAGCCAGGAGTTTG | 23118 |
rs524027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAB2 | GRCh38.p7 | 6:149357960 | cctgccttggcctcc[C/T]aaagtgccaggatta | 23118 |
rs524092 | snp | C/T | 0.230896 | 0.249269 | intron-variant | TAB2 | GRCh38.p7 | 6:149348501 | AACGTTCTGCCGTCC[C/T]ATTTGGCATCCTGGA | 23118 |
rs524161 | snp | A/C | 0.486266 | 0.0817214 | intron-variant | TAB2 | GRCh38.p7 | 6:149315099 | AAAATTCTGGTTACT[A/C]AGAACAGAGGGACAG | 23118 |
rs527010 | snp | A/G | 0.49681 | 0.0398085 | intron-variant | TAB2 | GRCh38.p7 | 6:149308854 | TAAAAAATTCTCTGT[A/G]CCTTGTGGGGTTTTT | 23118 |
rs527079 | snp | G/T | 0.47614 | 0.106587 | intron-variant | TAB2 | GRCh38.p7 | 6:149308878 | GGTTTTTCTCCCTTA[G/T]GATTTTTAATAACCG | 23118 |
rs527971 | snp | C/T | 0.341909 | 0.232492 | intron-variant | TAB2 | GRCh38.p7 | 6:149347076 | AATAATAATGAGGTA[C/T]GAATTATAAAATGCA | 23118 |