SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9111 | snp | A/G | 0.32955 | 0.237006 | intron-variant, utr-variant-5-prime | BACH2 | GRCh38.p7 | 6:90271934 | TCTTTCAGCGCGTTC[A/G]TTCACATAGCTCCCA | 60468 |
rs85706 | snp | A/C | 0.26518 | 0.249539 | intron-variant | BACH2 | GRCh38.p7 | 6:90098285 | TTTGCCCCCCCCGCA[A/C]CCCCCACCCTTCCCT | 60468 |
rs112841 | snp | A/C | 0.491732 | 0.0637633 | intron-variant | BACH2 | GRCh38.p7 | 6:90111878 | CTAATTAATCACCTG[A/C]TGTGTTCCAAGTATT | 60468 |
rs176713 | snp | A/G | 0.178465 | 0.239547 | intron-variant | BACH2 | GRCh38.p7 | 6:89961395 | GAGGCAGTTTTTCGA[A/G]TGAAACCATAAACCT | 60468 |
rs182382 | snp | C/G | 0.499929 | 0.00593782 | intron-variant, downstream-variant-500B | BACH2 | GRCh38.p7 | 6:89938040 | AAGGGTCACCCTTTG[C/G]GGAAGTTTGGGTTTA | 60468 |
rs185927 | snp | A/G | 0 | 0 | intron-variant | BACH2 | GRCh38.p7 | 6:90214693 | CCTTCAGGCCAACTA[A/G]AGTTTTCTTCTGCAG | 60468 |
rs188249 | snp | C/T | 0.00829861 | 0.0638783 | intron-variant | BACH2 | GRCh38.p7 | 6:90202200 | GGCATATACAGAGCT[C/T]TAGTTGGTAAAACAT | 60468 |
rs206910 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | BACH2 | GRCh38.p7 | 6:90233821 | GCATTCTCTCTGATC[A/G]CAGAAAATTGAAATG | 60468 |
rs206911 | snp | C/G | 0.335788 | 0.23482 | intron-variant | BACH2 | GRCh38.p7 | 6:90232001 | CTTCTCTCTCTCTCT[C/G]TCTCTCTCTCTCTCT | 60468 |
rs206912 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | BACH2 | GRCh38.p7 | 6:90230490 | AATAAGTTGTCCTAC[G/T]ACCAGTACTGTCAGC | 60468 |
rs206913 | snp | G/T | 0.406986 | 0.194565 | intron-variant | BACH2 | GRCh38.p7 | 6:90227175 | AAGATGCTGCACTTT[G/T]AAAATGTTATTCACA | 60468 |
rs206914 | snp | A/G | 0.155325 | 0.23138 | intron-variant | BACH2 | GRCh38.p7 | 6:90226519 | TCAGTATTGTgagtc[A/G]tttatgcacatctct | 60468 |
rs206915 | snp | A/G | 0.154993 | 0.231244 | intron-variant | BACH2 | GRCh38.p7 | 6:90224483 | ATAAATGAATCATTG[A/G]TTAGGAACTTCCATC | 60468 |
rs206916 | snp | A/G | 0.412917 | 0.189626 | intron-variant, utr-variant-5-prime | BACH2 | GRCh38.p7 | 6:90218009 | GAGGAAAATATTGTG[A/G]AGGATTGCTGCGAGG | 60468 |
rs206917 | snp | A/G | 0.163564 | 0.234582 | intron-variant | BACH2 | GRCh38.p7 | 6:90217617 | AAGAATAGTGAGTAG[A/G]TTATCTAAATGTACA | 60468 |
rs206918 | snp | A/G | 0.164219 | 0.234823 | intron-variant | BACH2 | GRCh38.p7 | 6:90213711 | TAGTACAAAATAGAC[A/G]AGATCTCTTCTTGTG | 60468 |
rs207252 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | BACH2 | GRCh38.p7 | 6:90079310 | CACACAAAAAGTTTT[C/T]CAATCTCTAGGGCAA | 60468 |
rs207253 | snp | A/G | 0.47709 | 0.104548 | intron-variant | BACH2 | GRCh38.p7 | 6:90098704 | TGTAAAAGAACTCCA[A/G]TACTTCTCTTTGTCT | 60468 |
rs207254 | snp | C/G | 0.499984 | 0.00279548 | intron-variant | BACH2 | GRCh38.p7 | 6:90100853 | tccaaaatggctgta[C/G]caggacaatcccacc | 60468 |
rs207255 | snp | C/T | 0.499974 | 0.00359416 | intron-variant | BACH2 | GRCh38.p7 | 6:90101895 | aaatttattcctgaa[C/T]atttaattatttttg | 60468 |
rs207256 | snp | C/T | 0.499977 | 0.00339449 | intron-variant | BACH2 | GRCh38.p7 | 6:90102140 | CATGACTTAAAACTT[C/T]ACTATAAATATAAGG | 60468 |
rs207257 | snp | C/T | 0.139903 | 0.224452 | intron-variant | BACH2 | GRCh38.p7 | 6:90104715 | ACACCACCTGAAGGG[C/T]GAGAGAATGGCCAAG | 60468 |
rs207258 | snp | C/G | 0.315273 | 0.241329 | intron-variant | BACH2 | GRCh38.p7 | 6:90104777 | TGGACATGTGGGCTG[C/G]GGTGTCCATGTGCAT | 60468 |
rs207259 | snp | A/G | 0.499974 | 0.00359416 | intron-variant | BACH2 | GRCh38.p7 | 6:90106099 | AGACAAGGACTGCTA[A/G]GAAAGGGCCTTTTCA | 60468 |
rs207260 | snp | A/C | 0.137187 | 0.223099 | intron-variant | BACH2 | GRCh38.p7 | 6:90106718 | CCACCAAGTGGGTGG[A/C]GCTGATTAAATACCT | 60468 |
rs207261 | snp | C/G | 0.49089 | 0.0668743 | intron-variant | BACH2 | GRCh38.p7 | 6:90107484 | AGCACAATTTTATTA[C/G]TGAAGAGTACATAGA | 60468 |
rs207262 | snp | C/T | 0.499989 | 0.00239614 | intron-variant | BACH2 | GRCh38.p7 | 6:90108542 | ATCACAAAGCACTTT[C/T]TGTCTAATTCTTCCC | 60468 |
rs207263 | snp | C/T | 0.499998 | 0.000998401 | intron-variant | BACH2 | GRCh38.p7 | 6:90110328 | aataaacttttttta[C/T]tttgttaatattaaa | 60468 |
rs207264 | snp | A/G | 0.488846 | 0.0738428 | intron-variant | BACH2 | GRCh38.p7 | 6:90110862 | actctggtatacggt[A/G]gaagggcttatgtgt | 60468 |
rs207265 | snp | A/T | 0.49306 | 0.0584955 | intron-variant | BACH2 | GRCh38.p7 | 6:90113327 | tctccacaaggcaca[A/T]actctaaaatagacc | 60468 |
rs207266 | snp | A/G | 0.148326 | 0.228391 | intron-variant | BACH2 | GRCh38.p7 | 6:90114777 | aaaccctatagtctc[A/G]gcccaaaagctcctt | 60468 |
rs207267 | snp | A/G | 0.49995 | 0.00499176 | intron-variant | BACH2 | GRCh38.p7 | 6:90115521 | tacaaaaatcaattc[A/G]agatggattaaacac | 60468 |
rs207268 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | BACH2 | GRCh38.p7 | 6:90116990 | GGGTTGCTCCTTCTT[C/T]CTCTGGCACAGATGA | 60468 |
rs207269 | snp | C/T | 0.499824 | 0.00938333 | intron-variant | BACH2 | GRCh38.p7 | 6:90118450 | TTGCATCTAAGTACA[C/T]TGCTAGTCTCACTGG | 60468 |
rs207270 | snp | C/T | 0.493793 | 0.055364 | intron-variant | BACH2 | GRCh38.p7 | 6:90119163 | ACTTGCAAGCTTCCA[C/T]GTGCCTATGACATTT | 60468 |
rs207271 | snp | C/T | 0.499824 | 0.00938333 | intron-variant | BACH2 | GRCh38.p7 | 6:90119512 | AGTTTACTGAGCTAT[C/T]AATTTAAACTTAAAA | 60468 |
rs207272 | snp | G/T | 0.499839 | 0.00898417 | intron-variant | BACH2 | GRCh38.p7 | 6:90120100 | TCATGCCAGCTGCTG[G/T]GGACATCAATGAACA | 60468 |
rs207273 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | BACH2 | GRCh38.p7 | 6:90120229 | TTAAATCAAACATCA[C/T]AGGAAGAGGTCCATG | 60468 |
rs207274 | snp | A/G | 0.499831 | 0.00918375 | intron-variant | BACH2 | GRCh38.p7 | 6:90120901 | ATTATGTTGGCCCAT[A/G]AAATATGAGTGTGAA | 60468 |
rs207275 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | BACH2 | GRCh38.p7 | 6:90121404 | GGTTCCTTCTTGTTG[C/T]TTTTTCTGATTTTTA | 60468 |
rs207276 | snp | C/T | 0.499801 | 0.00998203 | intron-variant | BACH2 | GRCh38.p7 | 6:90121441 | TCTAACTTTTCTTAA[C/T]GGTTATTATTTGCTT | 60468 |
rs207277 | snp | A/T | 0.499994 | 0.00179711 | intron-variant | BACH2 | GRCh38.p7 | 6:90121550 | ATTAATTAATTAATT[A/T]ATTTATTTTGAGACG | 60468 |
rs210051 | snp | C/T | 0.498059 | 0.0310896 | intron-variant | BACH2 | GRCh38.p7 | 6:89942381 | GCTTTCCAAGGTCTG[C/T]TGGCCTTCTCTGACT | 60468 |
rs210052 | snp | A/G | 0.497182 | 0.037434 | intron-variant | BACH2 | GRCh38.p7 | 6:89942066 | TTTTTCACCTGGGAG[A/G]AAGTCTATAGTTGAC | 60468 |
rs210053 | snp | A/G | 0.430285 | 0.173197 | intron-variant | BACH2 | GRCh38.p7 | 6:89965045 | ACAAAAAAATTAGCC[A/G]GGTGTGGTGGCACAC | 60468 |
rs210054 | snp | C/T | 0.307176 | 0.243374 | intron-variant | BACH2 | GRCh38.p7 | 6:89963379 | ttgagcctgggaagt[C/T]gagcctgcagtgaac | 60468 |
rs210055 | snp | A/G | 0.181659 | 0.240478 | intron-variant | BACH2 | GRCh38.p7 | 6:89962998 | atgagagttctttac[A/G]taggggttctttata | 60468 |
rs210056 | snp | A/G | 0.18134 | 0.240387 | intron-variant | BACH2 | GRCh38.p7 | 6:89962659 | ATTCAGGAGGGCTAG[A/G]AGTGTCCAAAACAAA | 60468 |
rs210057 | snp | A/T | 0.172997 | 0.237846 | intron-variant | BACH2 | GRCh38.p7 | 6:89958282 | AATGAAAAAATGAGT[A/T]TGGATggacacagtg | 60468 |
rs210058 | snp | A/T | 0.222811 | 0.248517 | intron-variant | BACH2 | GRCh38.p7 | 6:89954307 | GCATAATAATAATAA[A/T]AAAAAAAAGAAAAAC | 60468 |
rs210059 | snp | A/G | 0.299916 | 0.244966 | intron-variant | BACH2 | GRCh38.p7 | 6:89949877 | TATATCTTCCTTTAC[A/G]CTGAACGGGTGAAGG | 60468 |
rs292250 | snp | A/G | 0.499663 | 0.0129749 | intron-variant | BACH2 | GRCh38.p7 | 6:89937435 | GATAAAGGAGTGCCT[A/G]AGTCATAGCGTTCAT | 60468 |
rs292251 | snp | C/T | 0.499998 | 0.000998401 | intron-variant | BACH2 | GRCh38.p7 | 6:89936507 | CTTGTGCCTATGCCA[C/T]TTCCTCTCTGCCTTG | 60468 |
rs292252 | snp | C/G | 0.461703 | 0.132974 | intron-variant | BACH2 | GRCh38.p7 | 6:89934883 | AGGTCTCCGACACGG[C/G]AGCTGCATGTGCCGT | 60468 |
rs292253 | snp | C/T | 0.475259 | 0.108435 | intron-variant | BACH2 | GRCh38.p7 | 6:89933656 | actctctgtatagtg[C/T]gttcagttttgctgt | 60468 |
rs292254 | snp | C/T | 0.396 | 0.202938 | intron-variant | BACH2 | GRCh38.p7 | 6:89933602 | gggggatgctgacag[C/T]gggggaggctgtgtg | 60468 |
rs292255 | snp | C/T | 0.495999 | 0.0445491 | intron-variant | BACH2 | GRCh38.p7 | 6:89933562 | gtcagtgtaggttca[C/T]tgactaacacatgta | 60468 |
rs292256 | snp | C/T | 0.496483 | 0.0417852 | intron-variant | BACH2 | GRCh38.p7 | 6:89933372 | AAAGATCTGTGGTTG[C/T]TAGGGGTAAAAGGGG | 60468 |
rs292257 | snp | C/T | 0.479258 | 0.0997024 | intron-variant | BACH2 | GRCh38.p7 | 6:89933279 | CCCAAATGTATCAGG[C/T]TGCCATTTTTGAAAG | 60468 |
rs292258 | snp | A/C | 0.499104 | 0.0211472 | intron-variant | BACH2 | GRCh38.p7 | 6:89933181 | GAAAACTTCAGAGTC[A/C]ATGTTTTGGTTTCCT | 60468 |
rs370409 | snp | G/T | 0.331179 | 0.236453 | intron-variant | BACH2 | GRCh38.p7 | 6:90212021 | CTAGACTTCAGAGCC[G/T]GTTCACCTTGTATTA | 60468 |
rs373652 | snp | G/T | | | intron-variant | BACH2 | GRCh38.p7 | 6:90222814 | ctaaggacagagcag[G/T]tgactaaggatgact | 60468 |
rs388384 | snp | A/T | | | intron-variant | BACH2 | GRCh38.p7 | 6:90092293 | AGTAAAAAAAAAAAA[A/T]ATATATATATATATA | 60468 |
rs390883 | snp | C/T | | | intron-variant | BACH2 | GRCh38.p7 | 6:90198240 | caagcaagccatggg[C/T]acaAGCAAGCCATGG | 60468 |
rs404256 | snp | C/T | 0.489837 | 0.0705577 | intron-variant | BACH2 | GRCh38.p7 | 6:89948064 | AAAATGTGTTCTTGC[C/T]GTGGCCCCAAGACTT | 60468 |
rs597244 | snp | C/T | 0.136166 | 0.22258 | intron-variant | BACH2 | GRCh38.p7 | 6:90243904 | aTGAATGTCCTATGA[C/T]TGAGGTTTATTGCTC | 60468 |
rs597325 | snp | A/G | 0.423881 | 0.179625 | intron-variant | BACH2 | GRCh38.p7 | 6:90292775 | AGCCCCCAGGCCGAC[A/G]CTAGCTCTTACATAT | 60468 |
rs603498 | snp | A/G | 0.148661 | 0.22854 | intron-variant | BACH2 | GRCh38.p7 | 6:90260457 | tagaccatatgttag[A/G]ccacaaaatttaaga | 60468 |
rs604912 | snp | A/G | 0.425432 | 0.178112 | intron-variant | BACH2 | GRCh38.p7 | 6:90276601 | CAAATTCTTTTGCCT[A/G]CAGATTACGCTAAGC | 60468 |
rs606745 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | BACH2 | GRCh38.p7 | 6:90276144 | ACCACAGCAATACAT[A/G]TGTAAAACGTTTCAT | 60468 |
rs614120 | snp | C/G | 0.421842 | 0.181577 | intron-variant | BACH2 | GRCh38.p7 | 6:90286261 | AACCCACAATATCAA[C/G]ACGCTTAACATAAGT | 60468 |
rs618371 | snp | A/G | 0.32955 | 0.237006 | intron-variant | BACH2 | GRCh38.p7 | 6:90269110 | TTTTTCTCCCCTCTC[A/G]TCCTTCTGAATGAAG | 60468 |
rs619192 | snp | A/G | 0.440884 | 0.161442 | intron-variant | BACH2 | GRCh38.p7 | 6:90259230 | aaggaaagcttctct[A/G]tgtaataaaggccat | 60468 |
rs629485 | snp | C/T | 0.040671 | 0.13668 | intron-variant | BACH2 | GRCh38.p7 | 6:90293991 | TCTCCCAGGCACTGG[C/T]AATACAGAAAGTGAA | 60468 |
rs632043 | snp | A/G | 0.110167 | 0.207236 | intron-variant | BACH2 | GRCh38.p7 | 6:90287974 | CAAAAAAGTGAGCAC[A/G]GAAGGAGGATGGGGG | 60468 |
rs633833 | snp | A/G/T | 0.0459008 | 0.145722 | intron-variant | BACH2 | GRCh38.p7 | 6:90258251 | aattggactgttatc[A/G/T]tataccacatacaaa | 60468 |
rs633937 | snp | C/T | 0.110519 | 0.207473 | intron-variant | BACH2 | GRCh38.p7 | 6:90266929 | tcaatttTTTAAAAG[C/T]ACACATGGCAACGCA | 60468 |
rs639575 | snp | A/T | 0.422787 | 0.180679 | intron-variant | BACH2 | GRCh38.p7 | 6:90281412 | TTTTAAAAACAATTA[A/T]GAAGAAAGAATATCC | 60468 |
rs644940 | snp | A/G | 0.434543 | 0.168653 | intron-variant | BACH2 | GRCh38.p7 | 6:90288603 | GGGGGTTACTGCCAT[A/G]CCAACTGCCTGAGTC | 60468 |
rs654537 | snp | A/G | 0.426813 | 0.17674 | intron-variant | BACH2 | GRCh38.p7 | 6:90280331 | AAAATACAACGTTAT[A/G]TAATATTTTAATTCT | 60468 |
rs656214 | snp | C/T | 0.325799 | 0.238232 | intron-variant | BACH2 | GRCh38.p7 | 6:90281769 | atatagaatgtattg[C/T]ctgccagtcattctc | 60468 |
rs657569 | snp | G/T | 0.148996 | 0.228688 | intron-variant | BACH2 | GRCh38.p7 | 6:90246209 | TAAAGGTCAAGGGAG[G/T]GTAGTAGAGGCACAG | 60468 |
rs661713 | snp | C/T | 0.429087 | 0.174436 | intron-variant | BACH2 | GRCh38.p7 | 6:90266280 | TGGGATCTGTTTTCA[C/T]TGGCTTCAGTATCTT | 60468 |
rs662685 | snp | C/T | 0.148661 | 0.22854 | intron-variant | BACH2 | GRCh38.p7 | 6:90259617 | actcttccaaaaaaa[C/T]agaactagaaggaat | 60468 |
rs673780 | snp | C/T | 0.438806 | 0.163867 | intron-variant | BACH2 | GRCh38.p7 | 6:90250610 | GAATGCAAGCACCAT[C/T]GGGGCAGGGAGTTTA | 60468 |
rs679528 | snp | A/T | 0.148661 | 0.22854 | intron-variant | BACH2 | GRCh38.p7 | 6:90254970 | AGAACCCACTGTATT[A/T]ACAATCTTGACTTAT | 60468 |
rs680137 | snp | C/T | 0.148661 | 0.22854 | intron-variant | BACH2 | GRCh38.p7 | 6:90258062 | gggggctgggcgcag[C/T]ggctcacgcctgtaa | 60468 |
rs680672 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | BACH2 | GRCh38.p7 | 6:90257900 | taattccagctactt[A/G]ggaggctgaggcagg | 60468 |
rs732147 | snp | G/T | 0 | 0 | intron-variant | BACH2 | GRCh38.p7 | 6:90098192 | AACAGGGTTTTAAAG[G/T]CTTGGCACAGAACAC | 60468 |
rs736496 | snp | C/T | 0.121717 | 0.214577 | intron-variant | BACH2 | GRCh38.p7 | 6:90118941 | ATAAAATGGAGATAA[C/T]AGTACTTACCAAGTA | 60468 |
rs755178 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | BACH2 | GRCh38.p7 | 6:90289744 | caagcttgtccaacc[C/T]atggccagcaggcct | 60468 |
rs766153 | snp | C/T | 0.414576 | 0.188188 | intron-variant | BACH2 | GRCh38.p7 | 6:90195328 | AACTGCCTTCCCCTC[C/T]GCTCGCTCTCCTTGC | 60468 |
rs766154 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | BACH2 | GRCh38.p7 | 6:90195279 | TGTAATGTCAGAAAC[G/T]CTAATCATGTCAGAC | 60468 |
rs905670 | snp | C/T | 0.305934 | 0.243663 | intron-variant | BACH2 | GRCh38.p7 | 6:90248783 | AATCCAGCCTCCTCC[C/T]CGGAGTTGGTGGGAG | 60468 |
rs905671 | snp | A/T | 0.331179 | 0.236453 | intron-variant | BACH2 | GRCh38.p7 | 6:90274131 | GACAATATTCTGAAA[A/T]GGGCTTTTCCATGCC | 60468 |
rs927183 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | BACH2 | GRCh38.p7 | 6:90198180 | AAGCCGTTACATACA[A/G]CATTAGCAGGGTAAT | 60468 |
rs943689 | snp | A/G | 0.331179 | 0.236453 | intron-variant | BACH2 | GRCh38.p7 | 6:90274316 | TGTGTGGACTTTCTG[A/G]GTTTTGTAAAAATGA | 60468 |
rs953233 | snp | A/G | 0.274393 | 0.248807 | intron-variant | BACH2 | GRCh38.p7 | 6:90286098 | AAAATTAACTGGCTC[A/G]TGAGATTTCAGTGCA | 60468 |
rs969577 | snp | C/T | 0.284209 | 0.247648 | intron-variant | BACH2 | GRCh38.p7 | 6:90272668 | CAAATCTTAGATTCA[C/T]TTTTGCTCATTCCCT | 60468 |
rs990482 | snp | G/T | 0.489142 | 0.0728777 | intron-variant | BACH2 | GRCh38.p7 | 6:90097116 | TGCCCTCTCTTCCCA[G/T]GTCCAAGCTCATGGA | 60468 |