SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs896621 | snp | C/G | 0.419936 | 0.183362 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200428 | TGTGGAAAACCCCCT[C/G]AGCCTGACAAGTTCT | 79931 |
rs896623 | snp | C/T | 0.474 | 0.111014 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212944 | ACATCTGCCTGTCAC[C/T]CCATAAACATTCCTA | 79931 |
rs921551 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189820 | GCAACAACAGAGCCC[A/G]GGTTTATAAGAAACA | 79931 |
rs959268 | snp | A/C | 0.210909 | 0.246925 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153308 | TGGACATGAGCAAAA[A/C]TACAGCATTCTTGGC | 79931 |
rs998327 | snp | C/T | 0.304937 | 0.243889 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162957 | CAAAAAGCACACTGT[C/T]TCATTGTTCCACATC | 79931 |
rs1014556 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152543 | TACCAAACATATTAT[A/G]TACTAGCTAATTAAA | 79931 |
rs1031413 | snp | A/G | 0.210301 | 0.246828 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174798 | AAATGTAATAAAAAC[A/G]CTTTTTACTTTATTT | 79931 |
rs1397640 | snp | A/G | 0.498632 | 0.0261223 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177120 | CAGGATGCTTGAAAT[A/G]TATTTCTTGGATAAA | 79931 |
rs1452498 | snp | A/C | 0.382279 | 0.212137 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220493 | AGGGCAAATACAAAA[A/C]AAAAGTAGTTAATTA | 79931 |
rs1452500 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205237 | agtgaaggaggtgta[G/T]tatgggccatgtggc | 79931 |
rs1470821 | snp | A/G | 0.370162 | 0.219229 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177796 | AGCATTCTGCAGAAA[A/G]AAACCCTATATTTAA | 79931 |
rs1511093 | snp | C/T | 0.109814 | 0.206997 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133532 | ATACCTAGGGAGAGG[C/T]ATCATTAGTGGATTT | 79931 |
rs1562988 | snp | C/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152527 | TGGGTCCAGAATTGT[C/T]TACCAAACATATTAT | 79931 |
rs1597829 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208427 | gcccccacccaggaa[A/C]tgactcagcacaaga | 79931 |
rs1858291 | snp | C/T | 0.41507 | 0.187755 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134801 | TGGCTGGAGGAGGGC[C/T]AGAGCAGAGTCCTCT | 79931 |
rs1877167 | snp | A/G | 0.498611 | 0.0263212 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178380 | AGTGTTTGCCGGAGG[A/G]TCAGAGTCCTTTCAC | 79931 |
rs2044970 | snp | C/T | 0.153665 | 0.230694 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227632 | GTATTTTCACATAGG[C/T]TGTGAATCTTTTATC | 79931 |
rs2136941 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184524 | TCTCTCCATCTCTCA[A/G]CTCCGCATTTCTCTA | 79931 |
rs2136942 | snp | A/C | 0.409552 | 0.192466 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184500 | TTCTCTACCCATATG[A/C]TTCATTCTCAGCTCA | 79931 |
rs2136943 | snp | A/G | 0.420733 | 0.18262 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184485 | ATTCATTCTCAGCTC[A/G]CTCCAGACACAGAGG | 79931 |
rs2136945 | snp | G/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152880 | CCAACTCCTCCATTA[G/T]GCACCAGAAGCACAG | 79931 |
rs2198315 | snp | A/T | 0.412249 | 0.190198 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173694 | tttcagtgagccaag[A/T]tctcaccattgcgct | 79931 |
rs2198316 | snp | A/T | 0.0752113 | 0.178743 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173518 | GAGAAAATAATTTTT[A/T]AAAAAAAACTCAAAC | 79931 |
rs2198317 | snp | A/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169362 | GACTCAATAAACAGA[A/T]GTCACTTACACCATT | 79931 |
rs2218959 | snp | A/C | 0.411914 | 0.190483 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169145 | AGTTCTGCTTTCACT[A/C]TGAGTGACATGGGAA | 79931 |
rs3028475 | in-del | -/GT/GTGT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181656 | TGTGTGTGTGTGTGT[-/GT/GTGT]AAAACACAGAGGTAT | 79931 |
rs3817171 | snp | C/T | 0.304188 | 0.244057 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142580 | CCATCAACGGATAGA[C/T]AGTGCTTAGGCACCA | 79931 |
rs3899636 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207976 | tgaggtagtaaatac[G/T]tctcctgaaatctga | 79931 |
rs4455437 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215608 | TCCTTCTATTTTTCC[A/G]TCTTTCTCCTGTTTC | 79931 |
rs4513592 | snp | C/T | 0.499527 | 0.0153681 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222966 | GCCCACCACCACGCC[C/T]GCCTAATTTTTAGTA | 79931 |
rs4833203 | snp | A/G | 0.498734 | 0.0251279 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195236 | CTTTGAGTAACCCCC[A/G]TACACCTTCAAAATC | 79931 |
rs4833204 | snp | C/T | 0.499515 | 0.0155675 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224223 | CAAAAATTAGCTGAA[C/T]GTGGTGGTGGGCGCC | 79931 |
rs4833205 | snp | C/T | 0.461481 | 0.133325 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224317 | GCAGTGAGCAGAGAT[C/T]GTGCTACTGCACTTT | 79931 |
rs4833206 | snp | A/T | 0.289424 | 0.246872 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224369 | CTCTGTCTCAAAAAA[A/T]AAAAAGAAAAAAGAA | 79931 |
rs4833706 | snp | A/G | 0.473359 | 0.112298 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143905 | CATGACAGCATATAC[A/G]TGTGGGCCATTCTAA | 79931 |
rs4833708 | snp | C/T | 0.487113 | 0.0792303 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224208 | TCTCTACTAAAAGTA[C/T]AAAAATTAGCTGAAT | 79931 |
rs6534254 | snp | A/C | 0.368324 | 0.220226 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164839 | TTAAGTCTGTCTTTT[A/C]TATAAATCAAGTCCA | 79931 |
rs6534255 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208361 | agaccctgaactcaa[C/T]gtgtcggctggagcc | 79931 |
rs6534256 | snp | A/C/G | 0.0995577 | 0.199816 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208386 | ggagccacccagatc[A/C/G]ataaactgattcatc | 79931 |
rs6811411 | snp | C/T | 0.309154 | 0.242901 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197603 | tttaaattttttaGA[C/T]aaaaatGAAGAATCG | 79931 |
rs6812399 | snp | A/G | 0.37138 | 0.218556 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201026 | CTGTGTGCTGGGGAA[A/G]AGAGTAGGAGTTGAA | 79931 |
rs6812515 | snp | A/C | 0.337614 | 0.234145 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201300 | CAAGGACGTTCTATG[A/C]AAGATGGCGTGTGGT | 79931 |
rs6814480 | snp | C/T | 0.307423 | 0.243316 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175085 | CAACTCTTATGAACA[C/T]GTTATTTATGGTACC | 79931 |
rs6817294 | snp | A/T | 0.102014 | 0.201495 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170497 | CCGTGTATTTTCTTT[A/T]TATTCATTTTATAGG | 79931 |
rs6820363 | snp | C/G | 0.366266 | 0.221319 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161780 | TGAATAAAGTCACTA[C/G]GTTACTAGTTTAGAT | 79931 |
rs6820783 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154743 | GAGATGATATTGTAG[A/G]AATTCTGATATATCA | 79931 |
rs6821331 | snp | A/G | 0.366266 | 0.221319 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162273 | TTTGTTTATGTTTCA[A/G]CATTTTAGGGTTTGA | 79931 |
rs6825601 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195843 | TAGTAAGAACAAGGA[C/T]CAGCAGGGAGTGAAG | 79931 |
rs6833114 | snp | A/C | 0.318174 | 0.240525 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139453 | GCTTTACCTGCCCAC[A/C]AAGCAGGTCTGTCTT | 79931 |
rs6834599 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157025 | AACGGTAGGTTTTCT[A/G]CAGGAAATCCCCCCG | 79931 |
rs6835076 | snp | C/T | 0.289942 | 0.246789 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222193 | AATATTAGTGAATTT[C/T]TTCCCCTGCGAAGAG | 79931 |
rs6835704 | snp | C/T | 0.469346 | 0.119947 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222509 | ACAAAGTAAGGATAA[C/T]ACTTCCCTTCTTCAA | 79931 |
rs6835790 | snp | C/G | 0.304688 | 0.243945 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157361 | AGGACGTCCCCTAAG[C/G]AGAGGTTCTAGCTCC | 79931 |
rs6836120 | snp | C/T | 0.469247 | 0.120128 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222699 | AGCCTGTAGAGAAAG[C/T]GATTTTTATGGGACA | 79931 |
rs6837332 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152116 | GTATGTTAATTACAA[A/G]GCTGACATATTACAA | 79931 |
rs6837539 | snp | A/C | 0.118933 | 0.212888 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145184 | AAGGTAATGTCAGTT[A/C]TTTTTAAAATATCAT | 79931 |
rs6837596 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210270 | TTACATAGAGATAAA[A/G]TAAGTCCTTGTTTTC | 79931 |
rs6838000 | snp | A/G | 0.216048 | 0.247684 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175587 | CAAAAGACAATCTGC[A/G]TCTCCCAGTTTTCTG | 79931 |
rs6839386 | snp | A/C | 0.368529 | 0.220116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170297 | AGAGTATTACAATAC[A/C]TTTTTATTGAATGAG | 79931 |
rs6839726 | snp | C/T | 0.326035 | 0.238157 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140288 | gcagtgagccaagat[C/T]gcaccactgcactac | 79931 |
rs6840309 | snp | C/G | 0.0832709 | 0.186283 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170486 | CTGGCCTGTTTCCGT[C/G]TATTTTCTTTTTATT | 79931 |
rs6842037 | snp | A/G | 0.499515 | 0.0155675 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223095 | CAGGCGCAAGCCACC[A/G]CGCCCAGCCAGGTGT | 79931 |
rs6845343 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170795 | TGTTTTATGTAGCTA[A/G]TTCTTTCTTTGCTCG | 79931 |
rs6845524 | snp | C/T | 0.466927 | 0.124269 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225359 | GATATTTAATCTTGG[C/T]CATGTTTTCAAATAT | 79931 |
rs6846458 | snp | G/T | 0.351418 | 0.228505 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133715 | AAGATAGGTCTTTAG[G/T]TTCTTGAAGGGAAGG | 79931 |
rs6846553 | snp | C/T | 0.471483 | 0.115954 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132068 | ACTTATTTAATTTAA[C/T]GAGGTATATACACCT | 79931 |
rs6847595 | snp | A/G | 0.100231 | 0.200173 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199523 | GGAGGAGGAAGTGAC[A/G]CCTGGGAACCATTGA | 79931 |
rs6847834 | snp | A/G | 0.100231 | 0.200173 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199652 | AAGAATAGTGTGTGC[A/G]CCAAGCTTCAACAGC | 79931 |
rs6847971 | snp | A/G | 0.100944 | 0.200705 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199500 | TTATGAGCAGGGATC[A/G]ATGAATGGGAGGAGG | 79931 |
rs6848563 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159093 | actaaaaatacaaaa[C/T]ttagccggacgtggt | 79931 |
rs6851067 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204880 | CTAGGTGTTATTGGT[A/G]TATTTGCCAACCAAA | 79931 |
rs6851990 | snp | C/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226174 | CAAAAAAGAGAGAAA[C/T]AGACAAAGGGGGACA | 79931 |
rs6852366 | snp | C/G | 0.0858192 | 0.188533 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147450 | AGACATAAATTATAA[C/G]TTGAATGCAAAAAAG | 79931 |
rs6855628 | snp | C/T | 0.422158 | 0.181278 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151050 | CATTATGTTTGGTAA[C/T]ATCATATGAAAGACA | 79931 |
rs6856825 | snp | G/T | 0.303438 | 0.244222 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144402 | TAAAGCGTTTTTTTG[G/T]TTTTTTCTTTTCTTT | 79931 |
rs7356195 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167335 | TAGAGACAATAAAGC[C/T]TGTAAGAATTCAGAG | 79931 |
rs7436617 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208125 | caatctcagatatgt[C/G]tttatcagcagcatg | 79931 |
rs7661427 | snp | A/G | 0.479014 | 0.100263 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121166986 | AGGTCTCTAAGGCTC[A/G]ATTTCCATTTTATAC | 79931 |
rs7663440 | snp | G/T | 0.188082 | 0.242211 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216507 | ACATGGAATCTAAAA[G/T]AAAAAAATATGAAGG | 79931 |
rs7680038 | snp | C/G | 0.397813 | 0.201621 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210147 | GAACTTTTGCTATCA[C/G]CTTTGCTCAAAAGGG | 79931 |
rs7682759 | snp | A/T | 0.084728 | 0.187577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154266 | CACCCACTTGCTTTA[A/T]GTGGTTCTTCAAACT | 79931 |
rs7684167 | snp | A/G | 0.409212 | 0.192748 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185887 | AGGTACTGACTTTTC[A/G]CAGAAATAATCACAT | 79931 |
rs7684168 | snp | A/G | 0.388587 | 0.208071 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185889 | GTACTGACTTTTCAC[A/G]GAAATAATCACATGC | 79931 |
rs7684215 | snp | C/T | 0.100231 | 0.200173 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193048 | TATATATATGTAGAA[C/T]TACCCTATACATAAT | 79931 |
rs7684241 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193086 | GATCATGATTTGATT[C/T]AGAATGTTTCGTATC | 79931 |
rs7684464 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193225 | GTCATATGTAAGCTC[A/G]TTTTTATAAAAAATT | 79931 |
rs7684586 | snp | A/G | 0.100231 | 0.200173 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193092 | GATTTGATTCAGAAT[A/G]TTTCGTATCATCTCT | 79931 |
rs7687870 | snp | A/G | 0.215144 | 0.247558 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204345 | tcttatctacctatg[A/G]tctggaagctcccta | 79931 |
rs7693320 | snp | A/G | 0.154993 | 0.231244 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212078 | TCCCAAACACTTTCT[A/G]GCATACAGTAATAGC | 79931 |
rs9284633 | snp | A/G | 0.420255 | 0.183066 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180317 | aggcaggagaatggc[A/G]tgaactcaggaggcg | 79931 |
rs9307490 | snp | G/T | 0.409552 | 0.192466 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178400 | CGGCAAACACTGGAA[G/T]TGCAAGCTAAAGTTG | 79931 |
rs9685224 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208854 | gttatgctaatgaag[G/T]ctgtcagggtggaat | 79931 |
rs9784553 | snp | A/G | 0.10237 | 0.201756 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179102 | TGGGCAAAGAAGCAA[A/G]GATTTCCAGAAAGAG | 79931 |
rs9985644 | snp | A/G | 0.206336 | 0.246157 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218891 | TTTCTGAGAACCAAA[A/G]GATTTACAATTAAAA | 79931 |
rs9985938 | snp | C/T | 0.195214 | 0.243923 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121218659 | ctctttcttttgaga[C/T]gatgtctcactatat | 79931 |
rs9992473 | snp | G/T | 0.102014 | 0.201495 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179709 | GTGAATGGTGCCACC[G/T]GAGTGGTGCAGCATG | 79931 |
rs9992960 | snp | A/C | 0.420255 | 0.183066 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183336 | AGCTACTTGCCACCA[A/C]ATGGAAATAATATAT | 79931 |
rs9992978 | snp | A/C | 0.084364 | 0.187256 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203813 | TGCTTCCTTCAGTTC[A/C]ACTCTACTCTGATAA | 79931 |
rs9993163 | snp | C/T | 0.420255 | 0.183066 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183561 | CCACACAGCAGGAAG[C/T]GAGAGGCAGGCAAGT | 79931 |
rs9995558 | snp | A/T | 0.0836354 | 0.186609 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150477 | GATATTGGACCCTCC[A/T]CCTCCACCTAGCCAA | 79931 |