SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3924 | snp | A/G | 0.494468 | 0.0523031 | utr-variant-3-prime, downstream-variant-500B | TNIP1 | GRCh38.p7 | 5:151030574 | AGTTCAGGGACTGGT[A/G]TACAAGCTGGCCACC | 10318 |
rs736775 | snp | C/T | 0.498059 | 0.0310896 | downstream-variant-500B | TNIP1 | GRCh38.p7 | 5:151029787 | CTTCCACTGCCCCGG[C/T]TGCCCTACCCTCAGG | 10318 |
rs869594 | snp | C/G | 0 | 0 | intron-variant | TNIP1 | GRCh38.p7 | 5:151053480 | GGTTCATGGACACTT[C/G]CACTCTCACTGTCTC | 10318 |
rs871269 | snp | C/T | 0.494358 | 0.0528145 | intron-variant | TNIP1 | GRCh38.p7 | 5:151052827 | GGGACCCCTAACCAT[C/T]CTCTTGTTCACTGCC | 10318 |
rs888989 | snp | C/T | 0.269809 | 0.249214 | intron-variant | TNIP1 | GRCh38.p7 | 5:151051469 | AGGAGGCCCAAGTTC[C/T]TGTTGTAAGACTCCA | 10318 |
rs918498 | snp | C/T | 0.446902 | 0.154045 | intron-variant | TNIP1 | GRCh38.p7 | 5:151080227 | ACATGCACACAAATG[C/T]CTCCAACAATGTGCA | 10318 |
rs918499 | snp | A/G | 0.474091 | 0.11083 | intron-variant | TNIP1 | GRCh38.p7 | 5:151085994 | AGCCTAGAAGCCACC[A/G]TCAGACTTGGCCTCT | 10318 |
rs960709 | snp | A/G | 0.491368 | 0.0651254 | upstream-variant-2KB, intron-variant | TNIP1 | GRCh38.p7 | 5:151081488 | AGTTCCGTCCAGGGC[A/G]CTCCAGGACTCTTCT | 10318 |
rs1053457 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | TNIP1 | GRCh38.p7 | 5:151030263 | GACCTGCCCCACGCA[A/C]ACCCCTACCCCTCTG | 10318 |
rs1107239 | snp | A/T | 0.253824 | 0.249971 | intron-variant | TNIP1 | GRCh38.p7 | 5:151075045 | CTCTGCCTCCCAAAG[A/T]GCCAGTAAGGCATGA | 10318 |
rs1422673 | snp | C/T | 0.45692 | 0.1403 | intron-variant | TNIP1 | GRCh38.p7 | 5:151059427 | CCACCTGAGGGGGCC[C/T]TGCACTGGGCACTGA | 10318 |
rs1422674 | snp | G/T | 0.319856 | 0.240042 | intron-variant, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151066048 | GCATCGACTCCGTGC[G/T]AGGCACCAGTCTGGG | 10318 |
rs1559126 | snp | C/G | 0.117188 | 0.211804 | intron-variant, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151066843 | AGCCAGGACACAGAG[C/G]CAGAGGGGCAGACAG | 10318 |
rs1559127 | snp | C/T | 0.361053 | 0.22398 | intron-variant | TNIP1 | GRCh38.p7 | 5:151067192 | CAGCATAGCACAAAG[C/T]GCAGATGTTTCCACC | 10318 |
rs1862363 | snp | A/G | 0.118235 | 0.212457 | intron-variant | TNIP1 | GRCh38.p7 | 5:151068584 | GTGGCAGTATCTGGA[A/G]TTCAGAGCCCAGGAG | 10318 |
rs1862364 | snp | A/G | 0.404209 | 0.196773 | intron-variant | TNIP1 | GRCh38.p7 | 5:151068815 | CCACCACATCTTCTC[A/G]GAGTCTCTTTCCACC | 10318 |
rs2001542 | snp | A/G | 0.16846 | 0.236329 | intron-variant | TNIP1 | GRCh38.p7 | 5:151053298 | acatggtgaaacccc[A/G]tctgtactgaaaata | 10318 |
rs2017638 | snp | A/G | 0.471673 | 0.115589 | intron-variant | TNIP1 | GRCh38.p7 | 5:151086042 | GCCAGGGACTTCCCT[A/G]GGCTGTGAAAAGATG | 10318 |
rs2042234 | snp | A/G | 0.17138 | 0.237316 | intron-variant | TNIP1 | GRCh38.p7 | 5:151059570 | TAACAACAATTAAAG[A/G]AAAAAACTTAAAAGT | 10318 |
rs2080982 | snp | G/T | | | intron-variant | TNIP1 | GRCh38.p7 | 5:151042806 | TACTGGGGCTCAGCG[G/T]GGCCACTCCCCAAGG | 10318 |
rs2080983 | snp | G/T | | | intron-variant | TNIP1 | GRCh38.p7 | 5:151042808 | CTGGGGCTCAGCGTG[G/T]CCACTCCCCAAGGTT | 10318 |
rs2112635 | snp | C/T | 0.304688 | 0.243945 | intron-variant | TNIP1 | GRCh38.p7 | 5:151052592 | CCAGCTGACTTCTAC[C/T]CTTCTTTGAAGTCTT | 10318 |
rs2161359 | snp | A/G | 0.3512 | 0.228601 | intron-variant | TNIP1 | GRCh38.p7 | 5:151046973 | actacagtaataact[A/G]ctgcaggtggagatc | 10318 |
rs2161360 | snp | C/G | 0.469937 | 0.118861 | intron-variant | TNIP1 | GRCh38.p7 | 5:151085340 | GATCATTATGATCAT[C/G]AATTCTATGAGGCAG | 10318 |
rs2161361 | snp | C/T | 0.469937 | 0.118861 | intron-variant | TNIP1 | GRCh38.p7 | 5:151085344 | ATTATGATCATCAAT[C/T]CTATGAGGCAGCAGG | 10318 |
rs2233273 | snp | C/T | 0.487241 | 0.0788465 | upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087915 | TGCACAGGCTGGTCT[C/T]AAACTCCTAGGCTTA | 10318 |
rs2233274 | snp | A/G | 0.493568 | 0.0563433 | upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087914 | GCACAGGCTGGTCTC[A/G]AACTCCTAGGCTTAA | 10318 |
rs2233275 | snp | C/T | 0.0123036 | 0.0774623 | upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087851 | aataggcgtgagcca[C/T]ggtgccggccCATCA | 10318 |
rs2233276 | snp | C/T | 0.0505692 | 0.150756 | upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087840 | GCCACGGTGCCGGCC[C/T]ATCATTTTATTTTAA | 10318 |
rs2233277 | snp | A/G | 0.496746 | 0.040204 | upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087768 | AAGCAGGAGATCACT[A/G]GGGCTCAGGATGATG | 10318 |
rs2233278 | snp | C/G | 0.128632 | 0.218563 | utr-variant-5-prime, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087628 | TGGGCCCCTTCTTCA[C/G]TATGGATGGAGAAGC | 10318 |
rs2233279 | snp | A/G | 0.493613 | 0.0561475 | utr-variant-5-prime, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087609 | GGATGGAGAAGCCTC[A/G]GAGAGTAAGTGGCAA | 10318 |
rs2233280 | snp | C/G | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087420 | GGTGCCTTTTCCCAG[C/G]CCAGCTGAGGAAGCA | 10318 |
rs2233281 | snp | A/C | 0.0298908 | 0.118541 | intron-variant, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087373 | TCTCCCCAGATCCCC[A/C]CCAACCCCAACTCCC | 10318 |
rs2233282 | snp | C/T | 0.0611083 | 0.163768 | intron-variant, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087343 | CTGGAATTCACAGCA[C/T]GGGACAGCCAGTCTG | 10318 |
rs2233283 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087249 | CTCAGCTGGGCCTTG[C/T]GGGGCTGCCTGGTGG | 10318 |
rs2233284 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TNIP1 | GRCh38.p7 | 5:151064827 | TCCCTCCTGGCCCAG[C/T]GCTGGCTCCTGCCTC | 10318 |
rs2233285 | snp | A/C/G | 0.000598335 | 0.0172861 | intron-variant | TNIP1 | GRCh38.p7 | 5:151063786 | GCAGCACACTGAGCC[A/C/G]AGTAAATGCTTTTGC | 10318 |
rs2233286 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TNIP1 | GRCh38.p7 | 5:151063525 | CTTCTTATGCCAAAA[C/T]CCACATTCTCTCGTT | 10318 |
rs2233287 | snp | C/T | 0.171704 | 0.237423 | intron-variant | TNIP1 | GRCh38.p7 | 5:151060536 | CCTGCTTTGTGATCT[C/T]ATGTGAGATGATATG | 10318 |
rs2233288 | snp | C/T | | | intron-variant | TNIP1 | GRCh38.p7 | 5:151060214 | CAGATCCCTTAGGTA[C/T]CCTGGAGTCACTTGG | 10318 |
rs2233289 | snp | C/T | 0.0246314 | 0.108208 | missense | TNIP1 | GRCh38.p7 | 5:151056956 | CTTTCCCTCTCCAGG[C/T]GCTGGGCCCCCTGCC | 10318 |
rs2233290 | snp | C/G | 0.164434 | 0.234901 | missense | TNIP1 | GRCh38.p7 | 5:151056942 | GCGCTGGGCCCCCTG[C/G]CCCGTGAGGACGGCA | 10318 |
rs2233291 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | TNIP1 | GRCh38.p7 | 5:151056657 | TGGGGACTTCTGAAG[C/G]CTGTGTTGTGGGCAG | 10318 |
rs2233292 | snp | A/G | 0.00245288 | 0.0349345 | missense | TNIP1 | GRCh38.p7 | 5:151052189 | AGGGCCTGGAACAGC[A/G]GGATCAGGCTGCCGA | 10318 |
rs2233293 | snp | A/G | 0.040671 | 0.13668 | intron-variant | TNIP1 | GRCh38.p7 | 5:151052111 | GGCTGCAGGAGGAGG[A/G]GCTGGTGTGCAGCAC | 10318 |
rs2233294 | snp | G/T | 0.184521 | 0.241273 | intron-variant | TNIP1 | GRCh38.p7 | 5:151050002 | CATTAAGGAGCCCTG[G/T]AGGTTTCTTAACTCA | 10318 |
rs2233295 | snp | A/C/T | 0.0175866 | 0.0921099 | missense | TNIP1 | GRCh38.p7 | 5:151049891 | GCAACAAAGAGGGTG[A/C/T]GTCTGGGCGGCCAGG | 10318 |
rs2233296 | snp | A/G | 0 | 0 | missense | TNIP1 | GRCh38.p7 | 5:151049835 | AAGAAGGCAGTGGCT[A/G]GACAGCAGCAGGTAT | 10318 |
rs2233297 | snp | A/G | 0.109814 | 0.206997 | intron-variant | TNIP1 | GRCh38.p7 | 5:151049679 | CGTGTTTTTTTCTTT[A/G]CTTGGCCTGACCTCC | 10318 |
rs2233298 | snp | A/G | 0.000726804 | 0.0190492 | synonymous-codon | TNIP1 | GRCh38.p7 | 5:151045939 | CCAGGCTAGTGTGAC[A/G]GCAGGTAAGGTCCCA | 10318 |
rs2233299 | snp | C/T | 0.328932 | 0.237213 | synonymous-codon | TNIP1 | GRCh38.p7 | 5:151045906 | GGTGGTGGCCTTGGG[C/T]GCAGCCGAGAAGAAG | 10318 |
rs2233300 | snp | C/G | 0.000823506 | 0.020275 | intron-variant | TNIP1 | GRCh38.p7 | 5:151042879 | TAATGTGGGGTTCCT[C/G]GCCACGCCCACAGGG | 10318 |
rs2233301 | snp | G/T | 0.031825 | 0.122064 | intron-variant | TNIP1 | GRCh38.p7 | 5:151042844 | CCTGGTCTTCATCTC[G/T]CTGCCTCTTTAGCAG | 10318 |
rs2233302 | snp | C/G | 0.203396 | 0.245623 | intron-variant | TNIP1 | GRCh38.p7 | 5:151035537 | CTGGCCTGTCCTCGT[C/G]GGGAGAGGGGGCATG | 10318 |
rs2233303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP1 | GRCh38.p7 | 5:151035149 | CAGCCGGTCAGTCCT[C/T]GTGGCTGGTTAGGCC | 10318 |
rs2233304 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | TNIP1 | GRCh38.p7 | 5:151035148 | AGCCGGTCAGTCCTC[G/T]TGGCTGGTTAGGCCC | 10318 |
rs2233305 | snp | G/T | 0.301975 | 0.244538 | intron-variant | TNIP1 | GRCh38.p7 | 5:151033845 | TGAGATGGGTGTCCT[G/T]TGCAGCCTGTTGCAG | 10318 |
rs2233306 | snp | C/T | 0.000880815 | 0.0209674 | missense, intron-variant | TNIP1 | GRCh38.p7 | 5:151033729 | ACCCCTACGCCTACC[C/T]GCCCATGCCAGCCAT | 10318 |
rs2233307 | snp | C/G | 2.95714e-05 | 0.0038451 | intron-variant | TNIP1 | GRCh38.p7 | 5:151033569 | TCCAGGGCACACACA[C/G]AGGCTGCCCCAGACA | 10318 |
rs2233308 | snp | C/T | 0.0204407 | 0.0990078 | intron-variant | TNIP1 | GRCh38.p7 | 5:151033490 | TGAACTAAACAGCAC[C/T]GTGGTGGCAGGTGGG | 10318 |
rs2233309 | snp | A/G | 0.000404725 | 0.0142197 | intron-variant | TNIP1 | GRCh38.p7 | 5:151032419 | TTGTAATTTTTGGGT[A/G]TGATTATTGATTATT | 10318 |
rs2233310 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TNIP1 | GRCh38.p7 | 5:151032202 | GTTTGGGGGTGATGT[C/T]GTTAGTTTCTGCTCT | 10318 |
rs2233311 | snp | G/T | 0.231023 | 0.249279 | utr-variant-3-prime, missense, downstream-variant-500B | TNIP1 | GRCh38.p7 | 5:151030658 | AGCCAGCTGATCTCA[G/T]ATTGCCAAGAAACTA | 10318 |
rs2233312 | snp | A/G | 0.0106471 | 0.0721816 | utr-variant-3-prime, missense, downstream-variant-500B | TNIP1 | GRCh38.p7 | 5:151030649 | ATCTCAGATTGCCAA[A/G]AAACTAGAAGCCACT | 10318 |
rs2277940 | snp | C/T | 0.274393 | 0.248807 | downstream-variant-500B | TNIP1 | GRCh38.p7 | 5:151029916 | TTGACAGGGGAACAT[C/T]AGCGCATAAATGAAC | 10318 |
rs2287719 | snp | A/G | 0.00468574 | 0.0481759 | synonymous-codon | TNIP1 | GRCh38.p7 | 5:151035635 | CCACTTGCTTCTTCA[A/G]CTCTTCCTTCTCCTC | 10318 |
rs2287720 | snp | C/T | 0.478932 | 0.10045 | intron-variant | TNIP1 | GRCh38.p7 | 5:151035777 | CTCCTCAGGCCCAGA[C/T]TCCCATGCCTCCTGC | 10318 |
rs2287721 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNIP1 | GRCh38.p7 | 5:151039019 | CTAAGCTGAATGGTT[A/G]GGGGTGCCAGTGATG | 10318 |
rs2287722 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNIP1 | GRCh38.p7 | 5:151042815 | TCAGCGTGGCCACTC[C/T]CCAAGGTTCAAAGCT | 10318 |
rs2287723 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TNIP1 | GRCh38.p7 | 5:151046041 | GACCCCTCACCCAAG[G/T]GGCCCCAGCCCTCTG | 10318 |
rs2287724 | snp | A/G | 0.493386 | 0.0571263 | intron-variant | TNIP1 | GRCh38.p7 | 5:151086937 | TGGGAAGAGCAAGCT[A/G]GGCTGAGAGCAGCAG | 10318 |
rs2287725 | snp | A/G | 0.49645 | 0.0419827 | intron-variant | TNIP1 | GRCh38.p7 | 5:151086943 | GAGCAAGCTAGGCTG[A/G]GAGCAGCAGACCCTG | 10318 |
rs2303018 | snp | A/G | 0.000627197 | 0.0176976 | missense | TNIP1 | GRCh38.p7 | 5:151062177 | CACTGGGGCATGCAG[A/G]GGCTGTGGGAGATGC | 10318 |
rs2346024 | snp | C/G | 0.426201 | 0.177351 | intron-variant | TNIP1 | GRCh38.p7 | 5:151084674 | AGAACATTCCTCATT[C/G]CATTAGGAGAATGAG | 10318 |
rs3749657 | snp | G/T | 0.000240583 | 0.0109651 | intron-variant | TNIP1 | GRCh38.p7 | 5:151052129 | GAAGGGGTGAGGAGT[G/T]GGGGCTGCAGGAGGA | 10318 |
rs3763001 | snp | C/T | 0.49334 | 0.057322 | upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151088075 | gctggagtgcagtgg[C/T]gccataatggttcac | 10318 |
rs3763002 | snp | A/G | 0.496842 | 0.0396107 | upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087978 | GGCAAGTGCCACCAC[A/G]CCCAGCTAGTTTTTG | 10318 |
rs3763003 | snp | A/G | 0.493703 | 0.0557558 | upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151087969 | CACCACACCCAGCTA[A/G]TTTTTGTATTTTTTG | 10318 |
rs3763009 | snp | C/T | 0.367913 | 0.220446 | intron-variant | TNIP1 | GRCh38.p7 | 5:151032579 | AGCTTAGCCATTCTC[C/T]TTGCTAGATGACCTT | 10318 |
rs3792779 | snp | G/T | 0.493432 | 0.0569306 | intron-variant | TNIP1 | GRCh38.p7 | 5:151086824 | CTGCCCCTCTTCTTC[G/T]GGCCTTGCCTTCTTG | 10318 |
rs3792780 | snp | G/T | 0.493386 | 0.0571263 | intron-variant | TNIP1 | GRCh38.p7 | 5:151086632 | AGCGTGTATGTGTCT[G/T]TCTGTGTGGGTGTAA | 10318 |
rs3792781 | snp | C/T | 0.178144 | 0.239451 | intron-variant | TNIP1 | GRCh38.p7 | 5:151077308 | TCCCCCAAAAGTTCA[C/T]ATCTTGGAAACGTAA | 10318 |
rs3792782 | snp | A/G | 0.5 | 0 | intron-variant | TNIP1 | GRCh38.p7 | 5:151077116 | CATGACCCTTGTCAG[A/G]TGGTGGTGTCATGCA | 10318 |
rs3792783 | snp | C/T | 0.400504 | 0.199621 | intron-variant | TNIP1 | GRCh38.p7 | 5:151076171 | CCACCATGACCATTG[C/T]GGGAAGTTCTTGATG | 10318 |
rs3792784 | snp | C/T | 0.267091 | 0.249415 | intron-variant | TNIP1 | GRCh38.p7 | 5:151076111 | CTCTTCAGATTGGAA[C/T]GGATGACTGGTGAGC | 10318 |
rs3792785 | snp | A/G | 0.254664 | 0.249956 | intron-variant | TNIP1 | GRCh38.p7 | 5:151072089 | TCAGGCAAATGACTT[A/G]ACTTCTCTGAGTCTG | 10318 |
rs3792786 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | TNIP1 | GRCh38.p7 | 5:151067277 | CCCCCAATGTCTGCC[A/G]ACATTTTTGAGTACT | 10318 |
rs3792788 | snp | C/T | 0.121369 | 0.214369 | intron-variant, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151067055 | TGGGTGCCTCCCACA[C/T]GGTGTATTCATCTTG | 10318 |
rs3792789 | snp | C/T | 0.5 | 0.00019968 | intron-variant, upstream-variant-2KB | TNIP1 | GRCh38.p7 | 5:151066407 | TTGGGAGGAAGGTGC[C/T]GAGCCCCCAAACCCT | 10318 |
rs3792790 | snp | G/T | 0.459914 | 0.13578 | intron-variant | TNIP1 | GRCh38.p7 | 5:151062610 | GTGGCTGTGGGCAAG[G/T]TGATGACCTTCCCAA | 10318 |
rs3792791 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TNIP1 | GRCh38.p7 | 5:151061385 | GTGCAGGGAAAGAAG[A/G]ACCTGTTCTGAGGTT | 10318 |
rs3792792 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | TNIP1 | GRCh38.p7 | 5:151060945 | GAAGGCCAGCACAGG[A/G]CATGCTTGGTGGTGG | 10318 |
rs3792794 | snp | A/G | 0.311369 | 0.242351 | intron-variant | TNIP1 | GRCh38.p7 | 5:151055161 | TGTATTCACTGTTGC[A/G]TCCCAGTTCGTGGCA | 10318 |
rs3805430 | snp | C/G | 0.312481 | 0.242066 | intron-variant | TNIP1 | GRCh38.p7 | 5:151068129 | GGATATTTCTCCTGC[C/G]TCTCCTCTGCCCACT | 10318 |
rs3805431 | snp | C/T | 0.313082 | 0.241911 | intron-variant | TNIP1 | GRCh38.p7 | 5:151059978 | GGGAGAAAGAAGGGT[C/T]AGGAAGGCCCAGGGC | 10318 |
rs3805432 | snp | A/G | 0.067446 | 0.170804 | intron-variant | TNIP1 | GRCh38.p7 | 5:151059943 | TAAGACAGGTGATTT[A/G]CTCTTTGTGCAGACT | 10318 |
rs3805433 | snp | C/G | 0.408871 | 0.193029 | intron-variant | TNIP1 | GRCh38.p7 | 5:151055919 | GGCTTTAGCAGCGGG[C/G]AAGTGTTCAGTTATA | 10318 |
rs3805434 | snp | C/G | 0.231189 | 0.249291 | intron-variant | TNIP1 | GRCh38.p7 | 5:151040778 | CTGGATTGCCTTTCA[C/G]AGTTCCTCCCGTCAG | 10318 |
rs3815720 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | TNIP1 | GRCh38.p7 | 5:151060636 | TTGTAGAAGGGAGAT[A/G]TGGGACTAGCTGACC | 10318 |