SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs146634748 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183787 | CCTTATGAGAATCTA[A/T]TGCCTGATGATCTGT | 79931 |
rs146675594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207227 | TTCAGAAGTACAGAA[A/G]AAAAGCCTCAAGATC | 79931 |
rs146755173 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212152 | ATAAAGTATTCAAGG[A/C]AGACAGAACAAAAGG | 79931 |
rs146755335 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161433 | TGCTTTACATAAATT[A/G]GTTACCAATATAATT | 79931 |
rs146792866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189673 | AGAGAATTTTGAAAG[C/T]AACATTTTCCTCGGA | 79931 |
rs146834511 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144697 | ATGAGTCACCGCACC[C/T]GGCCTGTTTTTGCTT | 79931 |
rs146872443 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141092 | AACCTAAAGGGTAGC[A/G]GGATTTGTCTGGGTA | 79931 |
rs146916264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174420 | TAAAATAATAATAAT[A/G]ATAAACAAAATAAAA | 79931 |
rs146950480 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173303 | GGCTTGACCTTTGAC[A/G]TTGTATCCAAACAAA | 79931 |
rs146983894 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190310 | GAGACAGGTTTAGCC[C/T]GCTAATCATTGTATT | 79931 |
rs147055226 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149445 | ATTTTCTGAAAAAGT[A/C]CAGAGTTGGGATTAA | 79931 |
rs147091334 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216205 | TCATAACCTACCATG[A/T]CTTTTGCCCTCTGGA | 79931 |
rs147091377 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170395 | ACACACAATGACCAC[A/C/G]GGGATACACAAAGTT | 79931 |
rs147126819 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213722 | ACAGAGTAAGACTCC[A/G]TCTCAAAAAAAAAAA | 79931 |
rs147145626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186428 | ATTGTCACTGTCACT[A/G]TAATGAATATGCCTC | 79931 |
rs147214662 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138439 | TGCATTTCTGCATTC[A/G]CACATTTTCTTTGTC | 79931 |
rs147214728 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190761 | AACCTTAACCGAAGT[A/G]TTGAGCTCAATACTC | 79931 |
rs147231005 | snp | C/T | 0.000198969 | 0.0099722 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142704 | GGGAATAAATGTATG[C/T]GTGAAAATTAGATCA | 79931 |
rs147246834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165543 | TAATCTCTGTGTCCA[C/T]GCACCCAGGCACTGA | 79931 |
rs147321197 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170824 | CGGTAAGAGATATCT[G/T]TTTTTTTTAAAGAAG | 79931 |
rs147353465 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143455 | ATAAGGGATGGTCAA[A/G]TATCCCCTTCTGAAT | 79931 |
rs147427674 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228936 | GTTTAAGCCATCCCT[A/G]CAGACTGGAATCTTC | 79931 |
rs147532240 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158237 | TCCATTTTTACTCAC[A/G]TTTTCACTGTTACCA | 79931 |
rs147551126 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121182742 | TTTTGGATGAGGAGA[C/T]GCATTTCTCTCAATC | 79931 |
rs147568126 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132980 | AAAGTAAGTCATATA[C/T]ATGACTTAGGTTAGG | 79931 |
rs147587106 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179367 | ACAGTCATATTTAAG[G/T]GTTGTTGTAGGTAGA | 79931 |
rs147664616 | in-del | -/AAT | 0.304688 | 0.243945 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163044 | GATTTTTCTTTAATA[-/AAT]AAAAATTACTGAAAA | 79931 |
rs147688582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154011 | AAACAACACACACAC[A/G]CACACACACACCCCT | 79931 |
rs147761529 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218937 | AGCCATGGTGGCTCA[C/T]GCCTGTAATCCTAGA | 79931 |
rs147791779 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133990 | TTGGATATCTAACCT[A/C]CAGAGCTATGAAAAA | 79931 |
rs147808941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139403 | CTCCAAGGCCAGCAC[C/T]TCTGTATTTAACGCT | 79931 |
rs147865997 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200018 | TTGTCCTGGGAACTG[A/C]ATCCCCTCAAAAACC | 79931 |
rs147885528 | snp | C/T | 0.000311543 | 0.0124769 | missense | TNIP3 | GRCh38.p7 | 4:121141826 | CTTACTGGGTGCTCC[C/T]GTTGCTTCTGCACAG | 79931 |
rs147902366 | snp | A/G | 0.00135211 | 0.0259659 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121164099 | TGCGGCAATCATTCT[A/G]GATGTGCCCTGTACA | 79931 |
rs147902437 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197387 | ACAAAAATTAGCTGG[G/T]CGTGGTGGCGGGTGC | 79931 |
rs147939637 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213599 | GGGCGTGGTGGCGGG[C/G]GCCTGTAGTCCCAGC | 79931 |
rs147990845 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198311 | TCATTGTAAAGAATT[A/G]CATTTAGAGAAGAAA | 79931 |
rs147997718 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196552 | AAAACCAAAGAATTT[-/G]TCACATTTTTTTTAA | 79931 |
rs148060126 | snp | C/T | 0.000115518 | 0.00759906 | missense | TNIP3 | GRCh38.p7 | 4:121150180 | TCCTCAAACAGTCCT[C/T]GGAAAATGAACACTT | 79931 |
rs148073810 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141679 | TGTACATTGACCACT[A/C]CAACTTTGCAAGTTA | 79931 |
rs148079161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176271 | CTGAGCTGACAGGCT[A/C]CTCACTGCCTGAGAA | 79931 |
rs148129635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134900 | CCCGAAGTCCCTGCC[C/G]AGGTGATTCTGGGCC | 79931 |
rs148147431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203387 | AAAAACAAACATCAT[A/G]TGTTCTCACTCACAA | 79931 |
rs148270543 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194370 | ACCTAAAAGATAAGA[C/T]CTGATTTGATCTTAA | 79931 |
rs148273153 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223721 | CACCTTTCTTAGCTT[A/C]CCTATCCATTAGCAC | 79931 |
rs148289444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214152 | GTCCTGTTGGCTCTC[A/G]CCTCTTGTCTTTATT | 79931 |
rs148305530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171239 | ATCTGGAGAATCAAA[C/T]CTTTGAATTTCAAGA | 79931 |
rs148323676 | snp | C/T | 0.000650406 | 0.0180217 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227338 | TACAACCAACCCTGG[C/T]AAGTAAGCGAAATGA | 79931 |
rs148323872 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145899 | GGAGACTAGCTTGAA[C/T]CTGGGAGGTGGAGGT | 79931 |
rs148395515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144296 | TAATTATAAACTAAA[C/T]GAAACTATTAAACAT | 79931 |
rs148431999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191575 | ATCCTGTGTCAACTA[C/T]AGTTGTCCTTTAACT | 79931 |
rs148446605 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217657 | CGCTGGAGATATTAC[A/G]CAATTCTGCAAATAT | 79931 |
rs148447317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138131 | ATACTTTGAGGTGGG[C/T]GTTGTGGGCAACCCT | 79931 |
rs148468467 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206140 | TACAATTCAAGATGA[C/G]ATTTGGGTAGAGACA | 79931 |
rs148522148 | in-del | -/G | 0.100231 | 0.200173 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210238 | ATAATTTATAATAAA[-/G]AAAGGAAAAATTACT | 79931 |
rs148608042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215645 | CCAGAAATTAGGTTA[A/C]AGCACTTCTTCGTGT | 79931 |
rs148636054 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147810 | CTATAGCTAGATTTT[A/T]ATCTATTAAAACTAA | 79931 |
rs148675951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168208 | TACCATTTTTTCTTT[C/T]TTTTTTCTTTTTTTT | 79931 |
rs148834674 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212226 | TCAAAATATGGAAAT[A/C]TGTGTTTATCCCATG | 79931 |
rs148903658 | in-del | -/ATAG/ATAGATAG | 0.480539 | 0.0967035 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203216 | TAAAGAAAATGTGAT[-/ATAG/ATAGATAG]ATAGATAGATAGATA | 79931 |
rs148909018 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197700 | AACATAAACAAAAAA[A/C]TGGGAATTACCCAAG | 79931 |
rs148925662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189685 | AAGTAACATTTTCCT[C/T]GGACAAGAAGGAACA | 79931 |
rs148976858 | snp | C/T | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183773 | CTAGGCTGCCTGCTC[C/T]TTATGAGAATCTAAT | 79931 |
rs148992279 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170387 | AGTCCAGAACACACA[A/G]TGACCACGGGGATAC | 79931 |
rs148992869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134396 | GACATAATTGTTCTA[C/T]AAACATGGAAGTCAT | 79931 |
rs149048556 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207801 | AGAATTTAGTTTATA[A/G]TTTAACTTTGAAACA | 79931 |
rs149170449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194126 | TCGATGTTCATTTTC[C/T]GATTTTGATGGTTAT | 79931 |
rs149185259 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219910 | CATAATACCTTCCTG[A/G]AAACTGTTTCATTTC | 79931 |
rs149244331 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191118 | TGTTATTTTAGTATG[C/G]CATGCTATCATTAAG | 79931 |
rs149296115 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186063 | GCACACGTCCCTCAG[A/G]ACCACAACCAAAGAG | 79931 |
rs149303414 | in-del | -/T | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143485 | TGATACCTTTCCAAG[-/T]CCCACTTATCAGAAT | 79931 |
rs149349296 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217190 | TTGAGATTGAAGAAT[C/T]TGAAGAATTGTGTAT | 79931 |
rs149419836 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175543 | ACTAAGGCAGAGAGA[A/G]TCCTCTTCTACCTAC | 79931 |
rs149435449 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158202 | AGAGCAAATATGCTT[C/T]AGATGGAAGAGGAGG | 79931 |
rs149452584 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146906 | ATCTCTTTACAAGAT[G/T]GTTTAAGAATGACTT | 79931 |
rs149489923 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163312 | TAATCAAATACAAAG[A/G]TTTGGGGGACCTTTT | 79931 |
rs149509737 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223414 | ACAAAAACAATTCAA[A/G]CTTTAATGCTGGATT | 79931 |
rs149630754 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213888 | AGTGGGACTGCTTTC[A/G]TAATAACAATATACT | 79931 |
rs149649048 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199419 | ATTACTATGTTTCTA[C/G]CCCAGAAATACTCCT | 79931 |
rs149733873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178436 | GAAGAAGTCTCTTCA[C/T]CTCAGTCGCAAGAGC | 79931 |
rs149769195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148548 | GGCTAGCACCAACAG[A/T]TACTTTAGGGGTTGA | 79931 |
rs149790323 | snp | C/T | 0.029116 | 0.117091 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209692 | GCTCCATTAAACAAA[C/T]ACAGAAGATTCAAGA | 79931 |
rs149807109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167499 | ACAGAACACAACTGG[A/G]CAAGCCTAGTTATGA | 79931 |
rs149826216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225618 | GATCTTAACAAGAAA[A/G]CAGTGTTTAGAAAAA | 79931 |
rs149892623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139670 | TCAATAAGACACTGA[G/T]AAATGCTGCTTTTAG | 79931 |
rs149904030 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191931 | AAGGTGGTGATAAGG[A/G]CATAATTTTTATGAG | 79931 |
rs149945036 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132752 | CATAAAGTTCCAGGA[C/T]GGCAAAAAAAAAAAA | 79931 |
rs149985420 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194019 | CTAAATGTAATGTAA[A/G]ATCCTGGATTGGAGC | 79931 |
rs150019142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205979 | AAGAAGGAGAAGTGC[C/T]GAGTAAAGGGGGAAG | 79931 |
rs150033782 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188079 | TGGAGGCAATATTAT[C/T]AGGCAAAGAGTTTGA | 79931 |
rs150034833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151980 | GGTAATTGTTTTCAC[C/T]TTGGTTAAACATCTG | 79931 |
rs150105485 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213392 | TTCTTGCATGGTTAT[A/G]ATTATAATTTTCTGA | 79931 |
rs150121635 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170310 | ACATTTTTATTGAAT[C/G]AGTCCGTTTATGTAT | 79931 |
rs150142243 | snp | A/G | 0.02016 | 0.0983543 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228387 | AAGCAGATGGACAAC[A/G]ATGAGCCCCTTCTAC | 79931 |
rs150144797 | snp | C/G | 3.30017e-05 | 0.00406199 | missense | TNIP3 | GRCh38.p7 | 4:121150158 | TGGCAGAATTCCACT[C/G]GAGACTTCCTCAAAC | 79931 |
rs150173780 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160988 | GAATAAGAAAGAAGG[C/T]GTTTGCTTTCAAAAT | 79931 |
rs150209338 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194704 | CCCCTAAACCTTGAG[A/T]GTCTTCATCTTTGCT | 79931 |
rs150266415 | snp | C/T | 0.0341408 | 0.126114 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216956 | CAGCTTTTTCTCCAA[C/T]AGGAGTTTATGATTA | 79931 |
rs150298195 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195366 | GCCTTGACATCAGAC[A/G]GCATCACATAGATTA | 79931 |
rs150335879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207565 | ACACTGACTTAAGAT[A/C]TTAGTTAATAAAAAC | 79931 |
rs150342130 | in-del | -/CCTT | 0.095934 | 0.196885 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218537 | CTTCCTCCCTCCCTC[-/CCTT]CCTTCCTTCCTTCTT | 79931 |
rs150348094 | snp | A/G | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154876 | GCACACTAGAATTAG[A/G]ATTGAAGGAATCTTT | 79931 |
rs150384512 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201952 | TGCTCGTGGATGGGT[A/G]GAATCAATATTGTGA | 79931 |
rs150473378 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180838 | CTATTCTGTCTCCCT[A/G]CCTTCCAATAGTCAT | 79931 |
rs150509907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150818 | TGTTAGCTCTGTTGC[A/G]TTGCTCTTCTGCCCT | 79931 |
rs150599754 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177932 | TGCCAGTGGTCTATT[A/G]GGATAAAGAATGGAG | 79931 |
rs150652556 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209142 | GGCAGGTTTGTTAAG[C/G]GCGAGGACGCTGTGT | 79931 |
rs150667512 | snp | C/G/T | 0.00915317 | 0.0671402 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157385 | TAGCTCCCACCGTCC[C/G/T]GAACACAGATCGGGA | 79931 |
rs150674203 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157217 | GAATCTTTCCGCGGC[A/G]TCCAGTTTCGTCTTC | 79931 |
rs150703265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204815 | GCAATAATTTTCATT[G/T]CTATCAGCTATGTGT | 79931 |
rs150739520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187543 | AGCCATTGTTAATAA[A/G]GAAGGACCATGGAGG | 79931 |
rs150791735 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182227 | TGAAACGAGTGGAAG[G/T]TCAAAGTCAAACAAC | 79931 |
rs150808528 | snp | A/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131975 | TCTTGTGATGCAGGC[A/G]CACAATTTCTCATCA | 79931 |
rs150861894 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171607 | TTACCACTTTCACCA[A/T]CTGCCCCAGAAGAGA | 79931 |
rs150883245 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199301 | AAAATACTGATAATA[G/T]CTACAGCACACTAAG | 79931 |
rs150919074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212899 | GAGATCATTTTAGTT[C/T]TCACTTAGCACATAC | 79931 |
rs150954110 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144451 | CTGTTGCCCAGACTG[G/T]AATGCAGTGGCCCAA | 79931 |
rs150970817 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206835 | TCAGCCTCCCAAAGT[G/T]CTAGGATTACAGGTG | 79931 |
rs150987498 | snp | G/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159940 | ACTGAATCCAGAGTG[G/T]CAGTTACTAGGTAAC | 79931 |
rs151040464 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197325 | CTGACGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 79931 |
rs151081505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216541 | TGAGGCTCAGATGTA[C/T]GTCAAGGGAAGTTAA | 79931 |
rs151110537 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148317 | TATGGAGAAAGTCAG[C/T]AGTAGAGGCACTGCA | 79931 |
rs151133080 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173264 | TTATGGGAATTAAGC[C/G]TTTTTGAGGGATAGA | 79931 |
rs151200245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200775 | CTCAGAGAGCTTTTT[C/G]TTCCTTTTTATCCAG | 79931 |
rs151254138 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153167 | TCATAAAATTTTAAA[A/G]TGTAAAATTTCGTGT | 79931 |
rs151323385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220779 | CTGTGAGCATTCAGC[A/G]TGCCTTAAGTGCCAG | 79931 |
rs180702227 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146922 | GTTTAAGAATGACTT[C/T]ATCCCAGGTGCTGAC | 79931 |
rs180726158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162991 | GTTTCCCCATAAACA[A/G]TTTTCTCTGGAAGAA | 79931 |
rs180727869 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138492 | AGGTGCATCAAATTA[A/T]AGTTATGTATGTAAC | 79931 |
rs180733308 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156071 | GGAAAAGGAAATGAC[C/T]GCTACATGGCAGAAA | 79931 |
rs180739761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197734 | TCTGAAGCAATTTGG[A/G]GGCAAATTTAGAAAT | 79931 |
rs180747177 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179449 | ATCCTTCTTCTAATG[C/T]TTTGTTCTAAATGTG | 79931 |
rs180755089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214410 | ATAATTTTCATCATT[A/G]TTAAATAGAACTAAA | 79931 |
rs180762019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206666 | ATCCTCCCACCTCAG[C/T]CTCCTGAGTAACTGA | 79931 |
rs180771330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188861 | CATCATGTTTTTAAC[A/T]TTTTGTAAATTATAC | 79931 |
rs180775714 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226009 | TGTCATTAAAATTGG[A/G]AAATTGTATAATGGC | 79931 |
rs180777252 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172612 | GTCTCATACAATATT[C/T]TGCCGTTTATCTGAA | 79931 |
rs180968108 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142549 | TTCTATGAGTGTTAG[A/G]GTTGAAAGGCCTTGG | 79931 |
rs180985228 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151489 | GAGAAAAAAAGAGCT[G/T]TTTTCATCCTTCAGG | 79931 |
rs180992694 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168342 | CTCCCAAGTAGCAGG[G/T]ATTACAGGCATGCAC | 79931 |
rs180997146 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131244 | TTGTGAGAATATACA[C/T]ATATACACACACATA | 79931 |
rs181006594 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160207 | TTACAGGCTGGGCAC[A/G]GTGGCTAACTCCTGT | 79931 |
rs181007377 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228902 | AGAAATTAATCAGTC[A/G]ACAGCAAGGAGGTTA | 79931 |
rs181014745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185229 | TTTTTCTTCCAGACA[C/T]GTTTGCATCGTCAAA | 79931 |
rs181023211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174623 | GCTAAGTCGGTTTTA[A/G]TGACAAACGTTTATT | 79931 |
rs181028997 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211404 | ATATCCCAAGCCAAA[G/T]CCTACAAGGGATGAA | 79931 |
rs181037006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193699 | AAATGTAAAAGAATA[A/T]TGCTACATTGGGGAA | 79931 |
rs181056734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221357 | AAAAAGAAAAAGGAA[C/T]TCACTTAGCCTAGAA | 79931 |
rs181177557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167683 | TACATGATCAAAGTG[G/T]TTTTTTAATTGGTTT | 79931 |
rs181185524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142994 | CAGTTTTTTGAGGCC[A/C]TTACAATTCTGTTTT | 79931 |
rs181192498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184520 | TGGGTAGAGAAATGC[G/T]GAGCTGAGAGATGGA | 79931 |
rs181192681 | snp | A/G | 1.65151e-05 | 0.00287355 | missense | TNIP3 | GRCh38.p7 | 4:121150197 | GAAAATGAACACTTG[A/G]TATTCAAGGCATCCT | 79931 |
rs181209071 | snp | A/C | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201954 | CTCGTGGATGGGTAG[A/C]ATCAATATTGTGAAA | 79931 |
rs181218646 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219930 | TGTTTCATTTCACTA[A/T]CTTTACTAAATTAAC | 79931 |
rs181290848 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160552 | TTTTCACTACTTCCT[C/T]TGTCAAGAAGAGTAA | 79931 |
rs181290894 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194530 | CTAAGATGATTTAGT[A/T]TTTGTTTTGTTTTTC | 79931 |
rs181370609 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175759 | ACCACTTCTGTCCTG[C/T]GTAGAAATTTCTGCC | 79931 |
rs181400165 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212077 | CTCCCAAACACTTTC[C/T]GGCATACAGTAATAG | 79931 |
rs181452564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212699 | AACAATATGAATGGA[C/T]GGAAGATACATTTTC | 79931 |
rs181530194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151127 | ATTACTTCCAAATAT[A/T]GTGACAGAACACTTC | 79931 |
rs181563803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184871 | TTGGACCTATCTTCA[C/G]GTTTTTTCCACAAAC | 79931 |
rs181567762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220878 | GAAAAAGAGCAATAC[A/G]TTCAGTCAAGAGTGG | 79931 |
rs181649699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168153 | ACAAAAGCCTAGAGA[C/T]TTCTCAGTTTAATAA | 79931 |
rs181651436 | snp | G/T | 0.000233653 | 0.0108061 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147219 | AGCTTCCTTTTCACT[G/T]AAGCCATTTAAATGA | 79931 |
rs181654715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180678 | AGGAGAATGGTACAT[A/G]TTTTGAGCTGGTGAG | 79931 |
rs181660542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163668 | CATTCAATTAGCAGT[A/T]GTCTCTGTTGCTGAA | 79931 |
rs181662316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214603 | CTTCCTTTCTTTTTC[C/T]CTTCCTTCTTTCTTT | 79931 |
rs181665414 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198209 | CATTTTTAGGACTTT[A/T]CAAACCAAAATGCTA | 79931 |
rs181670536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202675 | AATCTTCACAATCTA[C/T]ACATGAAACACAAGA | 79931 |
rs181838842 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171052 | AACTCTTGACCTCAG[G/T]TGATCTGCCCATCTC | 79931 |
rs181842077 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136004 | TTGGTGGTGCCCTAA[A/C]CATGATCAGCCCTCT | 79931 |
rs181921953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137428 | TAGTAGAAAGCAAAG[A/T]AAAAAGAGAGTCCTA | 79931 |
rs181925857 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188370 | TTTCCCAGACTAACA[C/T]TGGGAAATAACGGTC | 79931 |
rs181932081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171755 | TTTGTTTTTGAGATG[C/G]AGTCTCACACTGTCA | 79931 |
rs181938056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206226 | TTAGGAGATTCTTAC[C/T]TGGGATGTCTTTTAG | 79931 |
rs182105357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154463 | GCTGGGACCCACACT[A/G]CAGCCTAGATTTTGT | 79931 |
rs182128083 | snp | A/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164181 | AACAGGGGAAAAGTC[A/T]CTTAAGGTATATTTT | 79931 |
rs182140189 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210188 | GTGCCCTGAGCCCAT[A/G]GATGAAAAGGTATTT | 79931 |
rs182150651 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228006 | TTTCTTACTTAGAGG[A/G]GAAATTATATTTAGA | 79931 |
rs182155038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198293 | AAAAGTAGCACATGA[C/T]CTTCATTGTAAAGAA | 79931 |
rs182157497 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225552 | CAACTCCAAACAGAT[A/G]GGAGTACAACTATGA | 79931 |
rs182162461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164983 | AGTACAGATAAAAGC[A/G]TGGAAATGGCAGATA | 79931 |
rs182172848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148010 | CCAGAAGCACTGAAG[C/G]GAAACTACATCCAGC | 79931 |
rs182186779 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181885 | GAATCTGTCTCTACA[C/T]GATTTTTATAGTTTT | 79931 |
rs182407167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181564 | TCATGACATGAATGA[A/G]AGAAAGAGGTACAGG | 79931 |
rs182435699 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216047 | AAGGATTAAGCAAAT[A/C]AGGAGAAAAGATACA | 79931 |
rs182491782 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217687 | TGTTGAAGAGGAAAC[A/C]AAGTGATAACCATCT | 79931 |
rs182495314 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158878 | AGACAATATTTTTTT[C/G]CATCAAGTTCTGATT | 79931 |
rs182500169 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218528 | TTTTCCTTCCTTCCT[C/T]CCTCCCTCCCTTCCT | 79931 |
rs182509681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191791 | TATCTTAAAATTATT[A/C]TCTCAACTCAAACCA | 79931 |
rs182699455 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186207 | AAAGAAAAAGAGAAC[C/T]ATATGGTGGTGACCA | 79931 |
rs182703732 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161504 | AAGTCAGAGATTAAA[A/G]TTTTATGAATTTGGA | 79931 |
rs182715087 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203507 | ATAAAAGACTATACA[C/T]TGGGTAGTGTACACT | 79931 |
rs182726653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177788 | GTTTTGTTTTAAATA[C/T]AGGGTTTCTTTCTGC | 79931 |
rs182729108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177960 | GAGACTCCTGGGGGC[C/T]GTTCTAGGAGAATTT | 79931 |
rs182730449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222304 | TTGGGAATATTCCTG[C/T]ATTGTGGATTTCTAC | 79931 |
rs182735113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143866 | AGGCACATCACATCC[A/T]TCATGCTTAGGAATA | 79931 |
rs182738490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173722 | AAACCTCTGCCTCCC[A/G]AGTTCAAGCAATTCT | 79931 |
rs182751260 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139934 | CTTAATTCAGCCTTC[A/G]ATATAGACAAGAAAC | 79931 |
rs182754840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198811 | AAAATCATGGAATAC[A/G]TTATGAGAACAAGCT | 79931 |
rs182771017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213235 | AAACTGATGGCATTC[G/T]ATCCTGTTTAATATT | 79931 |
rs182778250 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176478 | TGAGAAAACCATTAA[A/G]GAAAATTTTGAGGCT | 79931 |
rs182786469 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143686 | GTTTCTGCTAGCCTC[C/T]TGTCACAACATTTGT | 79931 |
rs182792458 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160908 | ATATTACCAGACTTA[C/T]GACTTTGTCGTTTTT | 79931 |
rs182810357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194794 | TGTTGGAATCCTCAG[A/G]TTATAGAAACTTGCT | 79931 |
rs182994710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139334 | TAGATATTGAATGTC[A/G]AACAAATTGCATTGA | 79931 |
rs183001313 | snp | C/T | 6.67401e-05 | 0.00577629 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161098 | TCCTCAGCATTAATC[C/T]ATGGCACCTGTGGCT | 79931 |
rs183021249 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132403 | CTCATTTCAAGGAAA[C/T]TGGAAGTTGTATTTG | 79931 |
rs183029182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195785 | CAAGCCTGACTATAG[C/T]TGGCATTTCAGAAAT | 79931 |
rs183045150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169118 | TTCCACTGCTCAGAA[C/T]CTTTCAGTGGCTTCC | 79931 |
rs183057582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196565 | TTGTCACATTTTTTT[A/T]AATGGAATTACAAAT | 79931 |
rs183069754 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204892 | GGTATATTTGCCAAC[C/T]AAAGAATTCCATTGT | 79931 |
rs183080377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223079 | CAAAGTGCTGGGATT[A/C]CAGGCGCAAGCCACC | 79931 |
rs183189516 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182518 | ACAGGAAGTGGCTGT[A/G]TGAGAGAAGTTTTAT | 79931 |
rs183197372 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165382 | CACCTCAGATGTCTC[C/T]TCTCTGGGCCCTCCA | 79931 |
rs183204188 | snp | A/G/T | 0.00914647 | 0.0670416 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199621 | CTCCCACATTCCTCT[A/G/T]TTCTTCAATGGAATT | 79931 |
rs183241137 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139729 | CTAGACACCTAGGCC[C/T]TTGGCTCCTCTGGCT | 79931 |
rs183268238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173409 | GAGAAATTCAGTCTT[C/T]AAAAACTGTAGTAGT | 79931 |
rs183275780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190466 | AAAAAGTCCTGTGCA[A/C]GTTGGTCCCCTGTCT | 79931 |
rs183281371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157893 | TAACATTTACAGATC[C/T]GGATTGCCCCAGCAG | 79931 |
rs183283513 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151752 | GATCTACTTTTCATG[C/T]TATTTGGGATCCTAG | 79931 |
rs183316521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152261 | AGTAACTTTTGTTTA[A/T]CACATTGGTAAGAAG | 79931 |
rs183325836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209432 | CTAACTTCTGGTAGT[A/G]TCAACACCAAATTGA | 79931 |
rs183335775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213428 | TAATCCATTTTTTTT[A/T]AAAAAAGACATTCTT | 79931 |
rs183346741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187128 | TTTTTTCTTGAGATC[A/G]CTTAATAATTGCATC | 79931 |
rs183348325 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227286 | TATATGTCTTTTTAA[C/T]ATGAGAACTTTATGC | 79931 |
rs183550543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133339 | GATGTGCTAAACTAA[C/T]ATTTTGGTAACAGAA | 79931 |
rs183578314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149676 | GAGGCTGAGGCAGGA[G/T]AATCACTTGAACTTG | 79931 |
rs183580496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183623 | CCCCATGGCTCACAT[C/T]ACTCCCTGAGCTCCA | 79931 |
rs183582989 | snp | A/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166615 | ATTAACAAAGGGAAA[A/T]GTGGTAAAGGAACAA | 79931 |
rs183585995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169353 | TTGTCAGGTAATGGT[A/G]TAAGTGACATCTGTT | 79931 |
rs183591674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148856 | TGCTCAGGGCAAAAC[C/G]AGTCAGTAAATCATA | 79931 |
rs183592068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201358 | GGGTCCAGAGTGGAA[C/T]ATCTTGTTACTAGGC | 79931 |
rs183598685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204557 | TTAACTGAGACTTGT[C/T]TCAGATTTTCAGGGT | 79931 |
rs183614993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172947 | TGGTTTAAAATACTT[C/T]ATTTGCTTCAATCTG | 79931 |
rs183626580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208045 | TTTTCTCTTGCGGCC[A/G]CCATGATTCTGAGGC | 79931 |
rs183761553 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135134 | GTGCCACCATGTCCT[A/G]TCACAGACTGGTTTT | 79931 |
rs183764124 | snp | A/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229024 | CAAATTCACAATGTG[A/T]TTGCTATTATTAGAA | 79931 |
rs183772849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169782 | TAGGAGAATCGGGGA[A/G]TGGGGTGTCACAGAT | 79931 |
rs183796133 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187403 | ATAGTAAGCTTGAGC[A/G]TCAGTGAGGCTAAGC | 79931 |
rs183797777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153331 | TTCTTGGCTGTTCTA[A/T]TATCTACAAGGTTTA | 79931 |
rs183812937 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184676 | CTTTGCTTGGTTTCC[A/G]TTATCTATAATCAAA | 79931 |
rs183823652 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156915 | CTTCCTTCTTATTCT[A/G]GAGAAGTGACCCTTG | 79931 |
rs183826254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202170 | AACTACACTATAAGG[C/T]CATAGTGACCTGACA | 79931 |
rs183839874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227193 | TATTACATTTACAAC[A/G]AGTTCTATCTTATTT | 79931 |
rs183846296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220253 | GCTGGGACTCATGAA[G/T]AATAATACATTAATA | 79931 |
rs184059744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205652 | GGTAGTGAGGGATGT[A/G]GAAAGAAAAGGTGGG | 79931 |
rs184068432 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147883 | CTAAAGGTTTATCAA[C/T]TTTATTGTTCTAAGT | 79931 |
rs184069219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223930 | TGCTAAATCTAACCA[C/T]GGGAGGCTACACAAT | 79931 |
rs184076228 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179828 | TGGCCAGGGTGGGGG[A/T]GGGATGACAAGCAGA | 79931 |
rs184092626 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197820 | TCTTGTTAATAAGGA[A/G]AGCCGTATAAGAAAG | 79931 |
rs184301356 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219168 | TCACACCATTGCTCT[A/C]CAGCCTGGGCAACAA | 79931 |
rs184437681 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145251 | CATCAAACCATCTAT[C/T]ACATCTCTGTGAATT | 79931 |
rs184448027 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162063 | ATCTGTAATCTGTTT[C/T]AGGCTTAATAGTTAC | 79931 |
rs184462787 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154837 | TTTAAACTTAATGTT[C/T]CATTTGAGCAATATT | 79931 |
rs184465944 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178507 | CCACATTGAGCACAC[C/T]TGGCACAGTGAGTGG | 79931 |
rs184474217 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136437 | CCTTGCTAAATTTTA[A/T]TAACTGTGTGATTTA | 79931 |
rs184474410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213600 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 79931 |
rs184481919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196969 | ACTCAAAGAACCATG[A/G]GTAGAATAAGAATTC | 79931 |
rs184533094 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145797 | TGTGCAGAGACAACT[A/T]AAAAGAAATTAGAGT | 79931 |
rs184569851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210660 | TCTAAGGCCTCTTTT[C/T]AAGGCTTGCAGTGTG | 79931 |
rs184569879 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150817 | CTGTTAGCTCTGTTG[C/T]GTTGCTCTTCTGCCC | 79931 |
rs184683645 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167809 | TGTGACAATCAGAAT[A/C]TTTAGCACTCAGTTC | 79931 |
rs184685580 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192227 | GCCAATCTCAATCGA[C/G]GCCTGAACTGTCTGT | 79931 |
rs184706916 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159221 | GCACTCCATCCTGGG[C/T]GACAGAGTGAGACTC | 79931 |
rs184717233 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228287 | CAGCTAGCATACTGG[C/T]GATATGCTGGAGGAG | 79931 |
rs184719508 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140898 | TAAATCCTCACATTC[C/T]TTCAGCCACCCAAAG | 79931 |
rs184831496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170184 | AGCAGTTGTTAATTC[A/G]ATGTACCTTTCTCCT | 79931 |
rs184838735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135696 | GAGCCACCACTCCTG[A/G]CCTTAAACTAGTGAT | 79931 |
rs184953255 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153882 | CAACCATGTGCTAGC[A/G]CATTCCTATGTTCCA | 79931 |
rs184969315 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159759 | ACTATCTGCTAATTA[G/T]AAGGCAGAAGAAGTG | 79931 |
rs184971730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187819 | CGTCTCTTCCTGAAG[A/G]TAGGGTCTCTAACAA | 79931 |
rs184983324 | snp | A/C/T | 3.88169e-05 | 0.00440533 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141778 | AATTTCTACCAAAAC[A/C/T]GTATACTAAGCACTT | 79931 |
rs184990706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214500 | ACAAAGTCCTCAGAA[A/T]TCTCCATGTAGAAGG | 79931 |
rs185000065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211070 | AGGAACTTACATGGT[A/T]AGAACAATGAAAATA | 79931 |
rs185002987 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174391 | GCCTGAGTGACAGAG[C/T]GAGACCCTGTCTCTA | 79931 |
rs185011032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193177 | ACAAAAAGATTGGGA[C/T]ACGCTATCAGAGATG | 79931 |
rs185021965 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228562 | TTTTCTGTACTGTAT[A/C]TTAGTTTCTGTATTT | 79931 |
rs185126277 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188190 | TGGACAGAAATCTCC[C/T]TCCTTCCTGCCCTTC | 79931 |
rs185134675 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225121 | ATCCTATATCCTTTC[G/T]TCTTGCAGAATTCAT | 79931 |
rs185219245 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171053 | ACTCTTGACCTCAGG[A/T]GATCTGCCCATCTCG | 79931 |
rs185257950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205779 | GAAATAATAAAGTTG[C/T]CCTTTATTGAGACAG | 79931 |
rs185270251 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151659 | GGGCCAAATGGATTA[C/T]GGCAATGGAATATGC | 79931 |
rs185273975 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143226 | TACTATCTCAATTTT[A/G]TAGATGAGAACACTA | 79931 |
rs185275971 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168468 | CCTCCCAAAGTGCTG[C/G]GATTACAGGCATAAG | 79931 |
rs185292726 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185690 | AAATGTATGTAAATA[A/T]ACTCAAACTCATAGG | 79931 |
rs185295393 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176211 | ATTTAAATAACTTCA[C/T]CCATGTTGCCAGTAA | 79931 |
rs185309120 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203248 | ATAGATAGATAGATA[G/T]ATAGATAGATAGAAA | 79931 |
rs185312132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160680 | TGCTTTTTAACTCCC[A/G]TGTGTTTGGATGCCC | 79931 |
rs185355136 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173910 | TGCTGGGATTACAGG[C/T]GTGAGCCATTGCACC | 79931 |
rs185367098 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179124 | CAGAAAGAGTAAACA[A/G]CATGTGAAATGATAG | 79931 |
rs185398558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214062 | TACGTAGGACCGAAA[A/G]CACTTCAATGAGAAA | 79931 |
rs185501403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162471 | AGAGTGACACTGAAA[C/T]CCAAGTGTCAAGTAT | 79931 |
rs185567948 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163426 | AGCAAGGGCTGCTTA[C/T]GGAACAGTTATTCCC | 79931 |
rs185570717 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203858 | ATTCTTCCATATTTT[C/T]CTCTGTGTTTATACA | 79931 |
rs185590669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222462 | TCTTTGGGCATATTA[A/T]TTAAATACTCTGAGC | 79931 |
rs185616266 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200281 | CGACAGAGATGCTAC[A/C]AAATTACAAATTCCC | 79931 |
rs185620410 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165852 | AGATCTGACTTTAGG[A/G/T]TACAGAAGCAGCGAT | 79931 |
rs185718993 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149139 | CACAGGTAGTTTAAC[A/C]AATGCAGTATCTCCA | 79931 |
rs185759725 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, splice-donor-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183071 | TGAATCGAACACTCA[A/C]GGTGAGCCAGGTTCT | 79931 |
rs185763949 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218610 | TTCCTCCTTCTCCCC[A/G]TCCCTCTTCTTCTCC | 79931 |
rs185824137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226916 | GTCCCCTGCAGAGGA[A/G]CACACTAAATGGATG | 79931 |
rs185833144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180843 | CTGTCTCCCTACCTT[C/T]CAATAGTCATTTCAT | 79931 |
rs185851463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198213 | TTTAGGACTTTTCAA[A/G]CCAAAATGCTAAAGC | 79931 |
rs185859692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157417 | ACTCGCGTTTCAAAG[A/G]GAGCTTGGCCTTGCA | 79931 |
rs185865739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214911 | AGTCTTTCCGTTGAG[A/G]TAGGTAAAATCATAT | 79931 |
rs185866596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172980 | CTTCATAACAGCCCC[A/G]TAAGAAGAGGCAGCT | 79931 |
rs185920683 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160273 | CACTTGAGGATAGGA[A/G]TTCTAGACCAGGCTG | 79931 |
rs185924946 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193737 | AGGTACCACTTTAAT[C/T]AAATGATCAAGGTTA | 79931 |
rs186014354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142794 | AAAGACAAAACAAAG[G/T]CATTTGTTAATCAAG | 79931 |
rs186055914 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174955 | TACTTGAGAAAGAAG[G/T]CTTATTGATGCATTA | 79931 |
rs186070730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211838 | GGACAGATTTAAAAT[C/T]CATTCAGCTGGCTGC | 79931 |
rs186206484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212263 | GTTTGCATGGAAGAG[A/G]CTTTTCTGAAATGTG | 79931 |
rs186287730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155165 | AGATGGGGTTTCACT[A/G]TGTTGGCCAGGCTGG | 79931 |
rs186293929 | snp | A/G | 0.000186411 | 0.00965249 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137916 | TATGTATACTTGATG[A/G]GAATAGAAGTGGGAT | 79931 |
rs186296558 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188493 | CAAAGGTCTCCAGTA[C/T]AGAAGTCTCCAAAAA | 79931 |
rs186305039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171785 | ACCCAGGCTGGAGTG[C/T]AGTGATGCGATCTTG | 79931 |
rs186307960 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206324 | TAAACACTTTGCATG[C/T]GTTATCTCATTTAAT | 79931 |
rs186323822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225699 | AGGTCTAAGGTTTTA[A/T]CCTCAGCAGGAAGTA | 79931 |
rs186342163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194557 | TTTCTAAAAGGATGT[A/G]GAGGAAGAGCATTTG | 79931 |
rs186376846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176757 | CATGTGTCAATTTAC[A/G]GTAGTTTGCAAGAAG | 79931 |
rs186393554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160917 | GACTTATGACTTTGT[C/T]GTTTTTCATTCGTCA | 79931 |
rs186396784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213059 | ATCTGGAAGAGAGTA[C/T]GCTACTCACATGGAG | 79931 |
rs186406119 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194965 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGTC | 79931 |
rs186450478 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138866 | CATCATCTCTCCCTA[A/C]CCCCTCTTAAATCCA | 79931 |
rs186481130 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206794 | AGGCTGCTCTGAAAC[C/T]CCTGGACTCAAGGGA | 79931 |
rs186484852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172794 | ATATAAATTGCCTGA[A/G]AAAACACTGAAGTGA | 79931 |
rs186569056 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121132908 | TTCTAATTATGCCTG[A/G]GGAGGAATGTTCTAT | 79931 |
rs186641229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135170 | TGAGCATTGTAAATT[A/G]TACTTTGGTTTTCCA | 79931 |
rs186652488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156542 | TTCTCATTTTTAATA[C/T]AGCAAAAATAATATT | 79931 |
rs186657697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169856 | GGAACTCTGAAACAA[C/T]GCTTCTATGCGATAT | 79931 |
rs186666845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187639 | TAAAGAAAACAACTA[C/T]AGGTCCCTCCAACTG | 79931 |
rs186668432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153826 | ACAATTTCTGTTGCT[G/T]TTATCATGAAATATC | 79931 |
rs186681734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204974 | TTCATTATTCATTTG[C/T]TTTTCTCTTCCGTAA | 79931 |
rs186692010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223084 | TGCTGGGATTCCAGG[C/T]GCAAGCCACCGCGCC | 79931 |
rs186694577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189275 | CATTTTCTGCTTTGA[C/T]CTTATGTCATAAACC | 79931 |
rs186699365 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163788 | ATAGTATTCTTTTAA[G/T]ATTTTTATAGAACAA | 79931 |
rs186749532 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189752 | ATTTAAATAGATATC[A/G]AAGAATTGTATTTGC | 79931 |
rs186776972 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227209 | AGTTCTATCTTATTT[A/C]TCACCGGGAACACAT | 79931 |
rs186934732 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147317 | ACTGTTTTGGAGCAA[A/G]TCATCCATCCCTAAC | 79931 |
rs186976267 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208336 | TAAAACCCAGGAAGA[A/G]ATATTTTACAGACCC | 79931 |
rs187021931 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147900 | TTATTGTTCTAAGTC[A/G]ACAGCAATAGAACAA | 79931 |
rs187036048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161679 | GTAGACCCAGTAAAC[A/G]TCAGAGGAACGACAA | 79931 |
rs187044541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181674 | AACACAGAGGTATCC[A/C]AAATGCTAAGAGATG | 79931 |
rs187052439 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144611 | TTCGCCATTTTGGCC[A/G]GGCTGGTCTCAAACT | 79931 |
rs187054386 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | TNIP3 | GRCh38.p7 | 4:121216597 | CCACCTGTTAAATGC[A/G]TTTTTCATCAAAAGC | 79931 |
rs187060133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178091 | AGCTGGAGCTCTGCT[C/G]TAGTCTTCAAATAAC | 79931 |
rs187071974 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196746 | AATCTTCTGTATAAA[A/G]GTTTTTATAATAATT | 79931 |
rs187216505 | snp | A/C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164840 | TAAGTCTGTCTTTTC[A/C/T]ATAAATCAAGTCCAG | 79931 |
rs187234613 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198608 | TTCTGTTAAAAACAA[A/C]AACTATAGCATTATT | 79931 |
rs187262739 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148030 | CTACATCCAGCCACA[A/T]TGACATTTTGATGAT | 79931 |
rs187279204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165154 | TCATTAACCTGCCTA[C/T]GAGATATTCACATAT | 79931 |
rs187294046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181895 | CTACATGATTTTTAT[A/G]GTTTTCTGTGTTTAT | 79931 |
rs187299326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168243 | ACAGAGTCTCGCTCT[A/G]TCACCCAGGCTGGAG | 79931 |
rs187305788 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217933 | TAAGAATTATAATGC[C/G]ATCATTTTACAGTAG | 79931 |
rs187311136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199378 | CACTTAAAAGAAGTC[A/G]GACATGAGGTCTATA | 79931 |
rs187314571 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202745 | AAGAAAAAACAGATA[A/T]CCCCATCAAAAAGTG | 79931 |
rs187323592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143763 | AAGACAACTTATTTA[A/G]TATGTATTGTTGATT | 79931 |
rs187335964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139366 | TAAATAGTAAACCCA[C/T]AGGCCTGAATCATCA | 79931 |
rs187528287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200143 | GTTCCTTTACTGCCC[C/T]CACATGGGCACAGAC | 79931 |
rs187543610 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218532 | CCTTCCTTCCTCCCT[C/T]CCTCCCTTCCTTCCT | 79931 |
rs187571002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151318 | TAACTTACTCCACTG[C/T]ATTACTATATAATAT | 79931 |
rs187577102 | snp | A/C | 0.000353092 | 0.0132824 | missense | TNIP3 | GRCh38.p7 | 4:121161184 | TTGTTCAAGAGAATT[A/C]ATCAAGTTCTTTCTT | 79931 |
rs187582099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185163 | TCCTCAAATGATCTC[A/G]TTTCCTTGCTATCTT | 79931 |
rs187588699 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220930 | AAGCTGACATAAATT[A/G]GTGACAAGTGGTGGT | 79931 |
rs187598781 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173519 | TTTGAGTTTTTTTTT[A/T]AAAATTATTTTCTCT | 79931 |
rs187599582 | snp | C/G/T | 0.00358938 | 0.0422398 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196025 | CATGGAGCCAGGCAC[C/G/T]GCATTAAACACCACA | 79931 |
rs187603743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149286 | GCATCAGTGAATTGC[G/T]AAGTGGTGCCATCCA | 79931 |
rs187619363 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157977 | CACCTTCTAAATTCA[A/G]TACTTCTGGGTAACA | 79931 |
rs187632407 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209478 | GTTGGCATGGAGAGT[C/T]GTGGGAAAAAAACTA | 79931 |
rs187636871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190755 | GGGTAGAACCTTAAC[C/T]GAAGTGTTGAGCTCA | 79931 |
rs187647049 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227681 | AGTCTCTATGTTGTA[A/G]TGGAAACACAAGAAA | 79931 |
rs187814193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152132 | GCTGACATATTACAA[A/T]TTTTTTCTGAGTGAA | 79931 |
rs187853443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177790 | TTTGTTTTAAATATA[A/G]GGTTTCTTTCTGCAG | 79931 |
rs187855082 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134771 | GGAAGCCCTTCACTG[A/G]TGTCCCCATCTTATA | 79931 |
rs187863125 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143876 | CATCCTTCATGCTTA[G/T]GAATACTAGAGAGCA | 79931 |
rs187876393 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213454 | TTCTTCAGCCAGGCA[C/T]GGTGGCTCACGCCTG | 79931 |
rs187885157 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213286 | TGAATGAATTTAATG[A/C]CAGGTAAAAGGGTCA | 79931 |
rs187894645 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152536 | AATTGTCTACCAAAC[A/G]TATTATATACTAGCT | 79931 |
rs188075290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213685 | TGAGTCGAGATCGTG[C/T]CACTGCACTTCAGCC | 79931 |
rs188109132 | snp | C/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132439 | ATAATAACTGGCTCC[C/T]CCAATTTGATCAGGA | 79931 |
rs188112711 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173863 | CTCAAACTCCTGACC[A/G]CAAGTGATCCACCTG | 79931 |
rs188116823 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140121 | TGGGCGGATCATGAG[C/G]TCAGGAGTTTGAGAC | 79931 |
rs188130054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169245 | TAGTCCATTCTGCGC[C/T]ATGCCCTGGCCACAC | 79931 |
rs188148813 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210229 | TAATGAATTATAATT[A/C/T]ATAATAAAGAAAGGA | 79931 |
rs188349801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171794 | GGAGTGCAGTGATGC[A/G]ATCTTGGCTCACCGC | 79931 |
rs188351743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206355 | CCTCTCCTTAACACA[A/G]TTAGGAAGGAGCTGT | 79931 |
rs188369552 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225956 | TCAATTTCCCATGTT[G/T]AAAAATTATTATTTC | 79931 |
rs188390496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158945 | TTATAACTGGTTCGT[A/G]TATGAAAAACTACTG | 79931 |
rs188392028 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165435 | CCTAAGTCAATGCCT[C/T]TCTTTCCTTCTGATC | 79931 |
rs188419796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191911 | AATCTTTGGAAATTA[C/T]GACAAAGGTGGTGAT | 79931 |
rs188433010 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228026 | TTATATTTAGAGTCT[C/T]TATGTGGCTTCACTG | 79931 |
rs188460738 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224310 | AGAGGTTGCAGTGAG[C/T]AGAGATTGTGCTACT | 79931 |
rs188462494 | snp | A/G | 0.000429277 | 0.0146442 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121147163 | TTTGAAGTCTTCTTC[A/G]TATATTTGCACCTAA | 79931 |
rs188466783 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180412 | CTCAGAAAAAAAAAA[A/T]TATAGATGTCAGAGG | 79931 |
rs188469768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163461 | CATAATTTCCTATAA[C/T]TATTCCCTATAAAGT | 79931 |
rs188473692 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214544 | ATATGGAGAGGTGGC[C/T]GGGTGAGGATTGCCC | 79931 |
rs188483934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198015 | ATATTGAGTAACTAT[A/G]AAAATGTTCATCATG | 79931 |
rs188639198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148922 | TTTGTTCTATGACAC[C/T]CTGTCTCCCATTGCT | 79931 |
rs188660555 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121182698 | GAACATAGATTTCTG[C/T]GAGTTGGCATGGCCT | 79931 |
rs188673390 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183324 | AAATCCCTAAGCAGC[A/T]ACTTGCCACCACATG | 79931 |
rs188677154 | snp | C/G | 0.0944967 | 0.195752 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218767 | ATTCCCCTCCCTCAG[C/G]ATCCTGAGTAGCTGG | 79931 |
rs188711224 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184389 | GCCATGTTTCCATTG[A/T]TATGACTTGAACTTG | 79931 |
rs188711634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149909 | GAAACTCAGTTCCCT[A/G]TGTTCTAAATGGTGG | 79931 |
rs188717643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167015 | ACAATGGGATAGTAA[C/T]AGTATCCTTCTCCTA | 79931 |
rs188724592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201482 | GTTTTCTAAGAAGAC[A/G]TAAATATGGTTCTAC | 79931 |
rs188738916 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219817 | GCATGAAAACTTAAG[A/G]TAGAAAGGACTAGAA | 79931 |
rs188889719 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139759 | TTATGAAAAAGCTAG[A/G]AGAGGAAATGAGATC | 79931 |
rs188923490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169567 | CTCGAGCCCAAAGTA[A/G]TGCCATTTTAGTGCC | 79931 |
rs188937364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204770 | ATTAAAACTTTTAAT[A/C]GTGCTTCTTGGTTAT | 79931 |
rs188945934 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200388 | GACTTTATTTAGACA[A/C]AATGTCTCAAAACTG | 79931 |
rs188950047 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121166027 | TTAACTTTGTATTTG[C/T]ATAGGGATGTGGTAA | 79931 |
rs188979326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212030 | CTAAGTTGATTCTTG[A/G]GAAAATTCTAATTTG | 79931 |
rs189007957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220645 | TATATACATTTTATT[C/T]AAATATATAATGGCA | 79931 |
rs189075854 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159265 | GAAAAGAAAAAAAAG[A/G]AAAGAAAAGAAAAGA | 79931 |
rs189091008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141154 | CCTGGATAAATTTCT[A/G]TCTATGTAGGCAAAA | 79931 |
rs189099669 | snp | G/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192426 | CGCAAGCCACTTTTT[G/T]TCAGATCCTTTGCAT | 79931 |
rs189112318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174344 | CAAAATGTTGAGGTT[A/G]TAGTGAGCCATGATT | 79931 |
rs189200831 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187202 | AAACAAACAAACAAA[A/C]AAAACACCCTACCAA | 79931 |
rs189210622 | snp | C/G/T | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197590 | CACATTTGAAGTATT[C/G/T]AAATTTTTTAGATAA | 79931 |
rs189212279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222964 | GCGCCCACCACCACG[C/T]CCGCCTAATTTTTAG | 79931 |
rs189215191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162633 | TATCTTGAGGTCATC[A/G]GCAAAGTAGGGGCAC | 79931 |
rs189382949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211184 | TCTTGGAAAGAGGGG[A/T]GATGTGTGATTTAAA | 79931 |
rs189386898 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174606 | AAAAATTGCAAACAT[G/T]TGCTAAGTCGGTTTT | 79931 |
rs189391073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193432 | AGTAGGAATTACTAA[C/T]CTATACTGATGCAAA | 79931 |
rs189394833 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228658 | AATCAAAACAGAGCT[G/T]AGGAAGTAAACAGTC | 79931 |
rs189464100 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146824 | TTTATTAAAAAAAAC[A/T]TTGGAATGCAATTTC | 79931 |
rs189471147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153913 | CATATGGGTTGGCTC[C/T]TGGAAAAGTCAACAG | 79931 |
rs189481414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188098 | CAAAGAGTTTGAGGT[A/G]AGAGTAACAGAAATT | 79931 |
rs189505501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179361 | TAAAAGACAGTCATA[A/T]TTAAGTGTTGTTGTA | 79931 |
rs189515587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214074 | AAAGCACTTCAATGA[A/G]AAAGGAGTCAGTTCA | 79931 |
rs189613332 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154846 | AATGTTCCATTTGAG[C/T]AATATTCTTTGGATG | 79931 |
rs189616126 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178735 | GTAGGGGAATTATAG[A/G]GATAAATCGATGTAT | 79931 |
rs189619425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171372 | AGGGGTGGATAGATG[A/G]ATGAATAGATGGTGA | 79931 |
rs189624699 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137099 | GTAATCATTAGCTTG[C/T]GTAATATTGGTCCAG | 79931 |
rs189653015 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185975 | AGTTACTGTTCCCTC[C/T]TCATTTGGACAGAGT | 79931 |
rs189664056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168801 | AATGCCTTTTAATAA[C/G]TTTTTCAAAATGAGG | 79931 |
rs189667964 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203448 | ATGAGAATGATACAA[G/T]GGACTTTGGGGACTC | 79931 |
rs189683508 | snp | C/G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222232 | TTTCCATAGAATGTT[C/G/T]CTTCATTCTGCAGAA | 79931 |
rs189727312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170482 | AGAGCTGGCCTGTTT[A/C]CGTGTATTTTCTTTT | 79931 |
rs189738187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135789 | CAGATTAAAAGGACC[A/G]TTTTAATTAAATGAA | 79931 |
rs189745265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142937 | GATTCTTAAAATTTC[C/T]AGTTGCAGTTTGAAA | 79931 |
rs189748997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205668 | GAAAGAAAAGGTGGG[A/G]TTCTGGGCATAATTT | 79931 |
rs189881042 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155472 | ACCTTTCATTACAGA[A/T]CATTATTTAGAGCAC | 79931 |
rs189920915 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147950 | TAAAAATTTTGTATA[C/G]ATCTACATGCAGATA | 79931 |
rs190015527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168073 | CTTACATCCTGCATC[C/T]AATCTATCTGAACAT | 79931 |
rs190032053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160502 | AAGAAGGAATTACAA[A/G]ATTGACAATATACAG | 79931 |
rs190037332 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193864 | ACCTGAATCTAATTA[C/T]AAGGAAACATTAGCC | 79931 |
rs190042504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202516 | AAACCTTTCTAGACA[C/T]TGGCTTAGGTAAAGA | 79931 |
rs190044730 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228318 | ACATTGTCTCAGAGT[A/T]TGATTGTTTGCTCTA | 79931 |
rs190051945 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225263 | ACTTAGATTAATCAA[A/G]AGATTCATTTGTTTG | 79931 |
rs190171801 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148426 | AATCATTATTATAAA[C/T]TTTATGTGTAAAAGT | 79931 |
rs190182842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165238 | CCACATTTGGCCCTC[C/G]CATTTCTCCTGAATA | 79931 |
rs190201043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121182447 | AGTCACAGCTGCCTG[A/G]ACACTTTAAAGTGGA | 79931 |
rs190215342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199606 | TGAATTGATCTTTAT[C/T]TCCCACATTCCTCTA | 79931 |
rs190229655 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218423 | TAGAATTTTACATTT[C/G]TTATTATTCTATCCA | 79931 |
rs190273546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160189 | AATGAATTAGAAAAG[A/G]AATTACAGGCTGGGC | 79931 |
rs190280515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210904 | TGTTGTGTTCTAAAA[C/T]AAAGTATGATGTAGC | 79931 |
rs190282853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151054 | ATGTTTGGTAATATC[A/G]TATGAAAGACATTGC | 79931 |
rs190301175 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184699 | TAATCAAAAATCCCT[A/G]TATATGCACCTTGAC | 79931 |
rs190304455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173400 | GTCAGAAAAGAGAAA[G/T]TCAGTCTTTAAAAAC | 79931 |
rs190308146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198215 | TAGGACTTTTCAAAC[C/T]AAAATGCTAAAGCAA | 79931 |
rs190317504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189837 | GGCTCTGTTGTTGCC[C/T]TCAATCTGCATTCTT | 79931 |
rs190319321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157439 | GGCCTTGCACCAAAA[C/T]AGCCTTCTTTTCTCC | 79931 |
rs190327674 | snp | A/G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215664 | ACTTCTTCGTGTATT[A/G/T]CTATCCCACTCTCTG | 79931 |
rs190328720 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221242 | AATATCTTTAATATT[C/T]AGTCTAAATCACTCT | 79931 |
rs190423658 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151711 | GGAATAGACTACTTT[G/T]GTAGATCTTGTTATT | 79931 |
rs190511418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142280 | AGGGAAAACTAAAAT[A/C]CAGAAAGGAAATTAG | 79931 |
rs190516601 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145729 | TAAAATTGCTTTAAA[A/G]AACAAATATTTTTTG | 79931 |
rs190537108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143373 | AGACACATTTAGAGA[A/G]AGCTGGCTTTTCCTT | 79931 |
rs190551129 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176217 | ATAACTTCACCCATG[A/T]TGCCAGTAATGAGCG | 79931 |
rs190561914 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194560 | CTAAAAGGATGTGGA[C/G]GAAGAGCATTTGTGT | 79931 |
rs190568362 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160869 | GTGTGGAGGAAACAT[C/T]TAAGTTTTGAGAAAA | 79931 |
rs190578580 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212614 | TTCATCAGTGCTGCT[C/G]CTTGTTTAGTGAAAA | 79931 |
rs190579705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206066 | ATGGGGGTAACTACT[C/T]CCATGATTCAATTAC | 79931 |
rs190631056 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213336 | CATCTCATTCTTCTG[A/T]GATGAGCTCTACTTC | 79931 |
rs190771748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162117 | GCTATTTGTGAACCA[C/T]TAAGAAATATTTTCA | 79931 |
rs190815868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188320 | AACTTAAAAAAAAAA[A/C]CTCTCCCCTAAGTTA | 79931 |
rs190826367 | snp | C/T | 0.00806665 | 0.0629941 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138035 | AAAGAAAACAGAAAA[C/T]GTTAAATCAATAAAA | 79931 |
rs190837963 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164970 | AGCACTACTGGGTAG[G/T]ACAGATAAAAGCGTG | 79931 |
rs190852061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195240 | GAGTAACCCCCATAC[A/G]CCTTCAAAATCAACT | 79931 |
rs190856637 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198611 | TGTTAAAAACAAAAA[A/C]TATAGCATTATTTTG | 79931 |
rs190864442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213234 | AAAACTGATGGCATT[C/T]GATCCTGTTTAATAT | 79931 |
rs190939061 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151346 | TATGGTCATAAAGGT[A/G]GGAAAAGAAAAGCAA | 79931 |
rs190944231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168263 | CCAGGCTGGAGTGCA[C/G]TGGCACAATCTCGCC | 79931 |
rs191073553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139720 | ACCCCTACTCTAGAC[A/T]CCTAGGCCCTTGGCT | 79931 |
rs191089845 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156791 | TCCTAGGCTGAAATG[C/T]CCTAGAGAGTTAGCA | 79931 |
rs191113598 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181800 | AAAAAAGAAACAAAT[A/T]TATGGATGCAAATTA | 79931 |
rs191115301 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169945 | ATACATTAGAAGGCA[A/C]ATTGGCTTTTGTTGA | 79931 |
rs191122137 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216849 | ACTGACATGTTTGTA[A/G]TTTAATTAACCCCAG | 79931 |
rs191124716 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189406 | GTTCAAACATCAGGA[A/G]TCTGGGTGACCCAGA | 79931 |
rs191125312 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187647 | ACAACTATAGGTCCC[A/T]CCAACTGAAATGTAG | 79931 |
rs191136286 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227064 | AATAAAGCAAATAGG[A/G]TAACATTCACTTAGT | 79931 |
rs191139926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205527 | TGGAAAGATCACTCT[C/T]GTTGGTGGGTTTAGA | 79931 |
rs191155256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223274 | TAAAGGACAGCCTGA[A/G]CCAATTTATCAGATA | 79931 |
rs191246746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144079 | AAGTATTGATTTGGG[G/T]ATGACAAATGCATTT | 79931 |
rs191324279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139094 | AGGAAAAAAAGTTTA[A/T]TACAAGTTTTCTAAT | 79931 |
rs191360151 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173695 | GCGCAATGGTGAGAA[C/T]TTGGCTCACTGAAAC | 79931 |
rs191365891 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149404 | CTAGAGGCTAGCAAC[A/T]ACAGAATCACCACTC | 79931 |
rs191368841 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172807 | GAGAAAACACTGAAG[G/T]GACTGAAATTTTCTG | 79931 |
rs191380978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209587 | TAGAAGGAACAGTGA[G/T]CCCAGAGGAAATAAT | 79931 |
rs191382553 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207072 | AAAAAAACAGTCATG[A/G]AAGATCATATTAGTG | 79931 |
rs191389208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191521 | AAAATGAAGTAGAGT[A/T]TATAAGTTATGTCTG | 79931 |
rs191394963 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227717 | ATACCTCTTCAGGCA[A/G]TCAGGAGTACTACAG | 79931 |
rs191401670 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166236 | TCTTCTGTTATGCAG[A/C]TAAACAACAAACAGA | 79931 |
rs191414299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208409 | GATTCATCTGGTCTT[G/T]TGGCCCCCACCCAGG | 79931 |
rs191627068 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132251 | ACACACACACACACA[C/T]ATATGCACTTTAAAT | 79931 |
rs191636074 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132559 | CAGAAACAAGCCTCA[C/G]TATAAACAAAGAAGA | 79931 |
rs191675483 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227214 | TATCTTATTTCTCAC[C/T]GGGAACACATAAAAC | 79931 |
rs191679780 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204157 | GAAAGAAAAATAAAT[A/C]TTAGGGCCCAAAATC | 79931 |
rs191685497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169249 | CCATTCTGCGCCATG[C/T]CCTGGCCACACCGTT | 79931 |
rs191909376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185198 | ATCTCACCTTCTACT[C/G]TCTTCCTTCATGCTC | 79931 |
rs191922190 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161050 | GTGACCTGATAACAA[A/T]AATAAAAGGCACAAG | 79931 |
rs191937799 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152137 | CATATTACAAATTTT[G/T]TCTGAGTGAATGGGT | 79931 |
rs191976353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186600 | GAAAACAATGTAATG[C/T]TGTGAGGCTGACAGT | 79931 |
rs191980978 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222884 | GATCTTGGCTCACTG[C/T]AAGCTCCGCCTCCCA | 79931 |
rs191990298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159561 | CAAAGCCTAGGCTCC[A/G]TTAACTGATCACGAT | 79931 |
rs192004390 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141396 | TGGAAAATGTCAAAA[A/T]CTATTTTGCACATAT | 79931 |
rs192005927 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192796 | TGTTAAAACTTTTTT[A/T]AAAAATATGTAATGC | 79931 |
rs192021183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174368 | CATGATTGCACCACC[A/G]TACTCCAGCCTGAGT | 79931 |
rs192023759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210950 | AACAAAAAAGAGAAA[C/T]CATCAAATGGTTTGG | 79931 |
rs192043770 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228469 | AACATTATCTTTTTC[A/G]TTACAAAATGCTGTA | 79931 |
rs192123981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181060 | TCTTAGAGAGAGAGA[C/T]ATAAATTTCAGTGAA | 79931 |
rs192125939 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147660 | GTTTAATTATTGTTA[C/T]TGTTTTCAACTGACT | 79931 |
rs192179497 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153846 | CATGAAATATCTAGT[C/T]GAGAGAGGCATATCT | 79931 |
rs192217591 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177278 | ATATCATTCTCACTT[A/C]GGCAATTATTTTTCC | 79931 |
rs192229335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143772 | TATTTAATATGTATT[A/G]TTGATTAACTCTGAA | 79931 |
rs192236446 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202842 | GCTCAATTCACTAAT[A/T]ATAAGGAAAATGCAA | 79931 |
rs192237879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145153 | ACTTGGACAACAAAT[A/G]ATATGTTATTCAACT | 79931 |
rs192243389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161700 | GGAACGACAAAATCA[C/T]CGAGAAAAAGACAAA | 79931 |
rs192267184 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178487 | GGAGTTCTCGAAGAC[A/G]TATTCCACATTGAGC | 79931 |
rs192273302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213497 | TTTGGAAGTCCGAGG[C/T]GGGTGGATCATGAGG | 79931 |
rs192282060 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196760 | AGGTTTTTATAATAA[C/T]TGTTATAATAATACA | 79931 |
rs192409630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139761 | ATGAAAAAGCTAGAA[A/G]AGGAAATGAGATCAC | 79931 |
rs192423638 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134841 | TCACAGTGTGAGCGA[C/T]GTTTCCTCCAGAACA | 79931 |
rs192453455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200580 | TGGTGCTTTTAGTAA[C/T]CACCAACAAACTGCT | 79931 |
rs192457009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152844 | ACTTATGGGTCCCTA[A/G]CAGTACTGTAGGCCT | 79931 |
rs192460467 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187226 | CTACCAAACTTTTAA[A/T]CACCAATAGAACAGA | 79931 |
rs192467712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169588 | TTTTAGTGCCTGTGC[A/G]TGTTCATGTGGGACT | 79931 |
rs192489549 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163907 | AGATATTTTTTTCTA[C/T]GTTACATAATTTTGG | 79931 |
rs192518342 | snp | A/G | 0.00195069 | 0.0311695 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121161211 | TCTTGTTGATGGTTC[A/G]GCACACTTAGAAAAA | 79931 |
rs192523003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135628 | GGGCTTGAACTCCTA[A/G]GCTCAAGCAATCTGC | 79931 |
rs192528403 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213781 | ATTACCACAGGAAAG[C/T]ATCTGCTTTAGAAAA | 79931 |
rs192549314 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196513 | TAGAAATCATAACAA[G/T]TAAATGTGAAATTCC | 79931 |
rs192668118 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158980 | GGTCCGGTGGCTCAC[G/T]CCTGTAATCCCACCA | 79931 |
rs192691789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191975 | TTAAGTTATTTAGAT[A/G]CCATATATTTAAGAG | 79931 |
rs192701909 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228101 | GAAAACAGTCTGCAT[A/G]ATCATTAGTAGTGGC | 79931 |
rs192764435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158805 | TCTGCCCATTTGGAA[G/T]TTTGGTCAAAAAGAA | 79931 |
rs192775263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183416 | GCTTCCCAGAGGGAG[C/T]TGCTCATAGTCACAT | 79931 |
rs192780596 | snp | A/C | 0.0944967 | 0.195752 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218768 | TTCCCCTCCCTCAGG[A/C]TCCTGAGTAGCTGGG | 79931 |
rs192808503 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149091 | GGTCGGCCCCTCAGC[G/T]AAGTGAATTTCAGCA | 79931 |
rs192828392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183024 | ATACGGACAAGTTTA[A/G]GAATTTTCAGTCTGA | 79931 |
rs192834170 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218536 | CCTTCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 79931 |
rs192894082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173872 | CTGACCACAAGTGAT[A/C]CACCTGCCTCGGCCT | 79931 |
rs192896160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140151 | CCAGCCTGGGCAATA[C/T]GGTGAAACCCCATCT | 79931 |
rs192910003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210265 | TACTATTACATAGAG[A/G]TAAAATAAGTCCTTG | 79931 |
rs192976663 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205772 | GAAACTGGAAATAAT[A/G]AAGTTGCCCTTTATT | 79931 |
rs193031854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165743 | ACGCTTGAGTGAAAG[A/G]GAGTGACGCTGCTTT | 79931 |
rs193032100 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200144 | TTCCTTTACTGCCCC[C/T]ACATGGGCACAGACA | 79931 |
rs193091251 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223048 | CTGACCTCGTGATCC[G/T]CCCGCCTCGGCCTCC | 79931 |
rs193093962 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162303 | ATGGTATTTTAAGTA[A/G]GCAGAGATGTTCTCG | 79931 |
rs193187889 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188129 | AATGAAATTCAGTAA[A/G]TATCTGTTGGGTCTT | 79931 |
rs193190259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224821 | TGAACTATCTTCCTA[C/G]AAGATTTTTGAACAC | 79931 |
rs193242097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145736 | GCTTTAAAAAACAAA[C/T]ATTTTTTGTTCTAAA | 79931 |
rs193247910 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179041 | GGGTGAAAAGGTTTC[A/C]AAACCAGAAAGGTTT | 79931 |
rs193249216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204849 | AATTCTTATTTTCCT[A/G]CAACTGAAGTCAGTC | 79931 |
rs199499297 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198357 | TGGATTTGATATATA[C/T]AGCATAAACTTTCTG | 79931 |
rs199613420 | snp | A/G | 8.28301e-05 | 0.00643492 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164150 | TTTTCCTGGAGTCTT[A/G]GAAAGCAGAAAGAAA | 79931 |
rs199658505 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132364 | GAGATTTTCAGGGAG[A/G]CGTGCATCATCCATC | 79931 |
rs199675898 | in-del | -/AGGCT | 0.0103295 | 0.0711199 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163840 | ACCCACAGAACTGGA[-/AGGCT]GAAAGGAATTTAAGC | 79931 |
rs199678662 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222190 | GAAATATTAGTGAAT[-/A]TTCTTCCCCTGCGAA | 79931 |
rs199679774 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174432 | AATAATAAACAAAAT[-/A]AAAAAAATAAGAAAG | 79931 |
rs199703771 | snp | A/G | 0.000399281 | 0.0141238 | stop-gained | TNIP3 | GRCh38.p7 | 4:121147132 | GATTAAGTCTCTCTC[A/G]ATCCGATCGTTCCTT | 79931 |
rs199827210 | in-del | -/ATC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181284 | CCATGAAATTTCTTT[-/ATC]CTGAGGTTAGACAAG | 79931 |
rs199880242 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219220 | AAACAAACAAACAAA[-/C]AAACAAAAAACCCAT | 79931 |
rs199914154 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146027 | TATACTCTTTTTTTT[-/A]TACCAAGAGTAATCA | 79931 |
rs199963627 | in-del | -/C | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131842 | TTTCACCATGCTGGC[-/C]AGGCTGGTCTAGAAC | 79931 |
rs200038122 | in-del | -/G | 0.0267931 | 0.1126 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145989 | CTCATAAAAAAAAAA[-/G]AGAGAGAGAGAGAAT | 79931 |
rs200069310 | snp | A/G | 0.000402165 | 0.0141747 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150251 | GTACACTGTTGATCT[A/G]AGATTTACCACATGG | 79931 |
rs200081710 | snp | C/T | 0.00199808 | 0.0315444 | missense | TNIP3 | GRCh38.p7 | 4:121154648 | TCTTCTTTCAATTCA[C/T]GTAATTCTTCATTTA | 79931 |
rs200143655 | snp | A/T | 0.00199796 | 0.0315434 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157053 | CCGCCCCTTTGCTTT[A/T]ATTTGGATCCTCCGG | 79931 |
rs200264364 | in-del | -/GTAG | 0.0189856 | 0.0955633 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185563 | GTCTCTTAGCACACA[-/GTAG]GACATCAATAAGGAT | 79931 |
rs200287547 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197510 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 79931 |
rs200434182 | snp | A/G | 0.000399281 | 0.0141238 | stop-gained | TNIP3 | GRCh38.p7 | 4:121157174 | CCTTTCTCTGCCTCT[A/G]ATGCGGATCCTTCTC | 79931 |
rs200435163 | snp | C/T | 1.82161e-05 | 0.0030179 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141801 | AAGCACTTTTTCAAA[C/T]GCACTCTTACTTACT | 79931 |
rs200491379 | snp | C/G | 0.00199795 | 0.0315434 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158676 | AATACCGAATAGAGA[C/G]AGGTATTTACCTTTC | 79931 |
rs200519963 | snp | A/C/T | 5.38154e-05 | 0.00518703 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158637 | TCACACAATTGGCCC[A/C/T]ACCAGGATAATGGCT | 79931 |
rs200593787 | snp | A/G/T | 0.000122669 | 0.00783077 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141956 | CTACCAGTGGGAGAG[A/G/T]CTGAGGAGTTGCAGT | 79931 |
rs200634466 | in-del | -/AAAACCTTTCTAGACATTGGC | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202479 | GAAGATAACATTGGA[-/AAAACCTTTCTAGACATTGGC]AAAACCTTTCTAGAC | 79931 |
rs200675874 | snp | A/G/T | 3.30695e-05 | 0.00406618 | missense, stop-gained | TNIP3 | GRCh38.p7 | 4:121150108 | AGCTTCTCACCTGCT[A/G/T]CTTCAGAACTTCCAT | 79931 |
rs200710043 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212980 | TCTTCCTTTTACGAG[-/A]AAAAAAAAATGGAGC | 79931 |
rs200765017 | snp | C/T | 0.00299555 | 0.038585 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150050 | ATGCCCAAAGAAGCA[C/T]GAAAAATGGGCAGTA | 79931 |
rs200819850 | in-del | -/AG | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164619 | GCTCGGTTTCCCTAA[-/AG]GCGAGATTTTCTGGC | 79931 |
rs200857550 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150385 | TTTCTCATATATGTA[-/T]TTTTTTTTTTCAGAA | 79931 |
rs200862512 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143616 | CCATAAAGTCACCAC[A/G]GACACTGAATTAGTG | 79931 |
rs200927901 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226948 | TGGCTCTGCTCATTG[A/C]TTAATCAAGATTGTT | 79931 |
rs200989681 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121150199 | AAATGAACACTTGAT[A/G]TTCAAGGCATCCTGA | 79931 |
rs201081098 | in-del | -/GAT | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165641 | ATGATTTACAAAATC[-/GAT]GAACTTTTTGCTAGT | 79931 |
rs201084297 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223618 | GAAACTAGAAAAGGT[A/T]AAAATGCCTCATTAT | 79931 |
rs201205536 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222141 | GATTTTTGCAATGTT[A/G]CTATATTGCTCTTGA | 79931 |
rs201236693 | snp | C/G/T | 3.37963e-05 | 0.0041106 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157079 | TCCGGGCTCGAGGAC[C/G/T]CGGGCCCCGCCCACC | 79931 |
rs201282199 | in-del | -/ATAG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203217 | TAAAGAAAATGTGAT[-/ATAG]ATAGATAGATAGATA | 79931 |
rs201288851 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220591 | TGTACTGAAACAATG[-/T]TTTTTTTTTAACCTT | 79931 |
rs201290610 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200517 | CCCTGGCAGTCTCTG[G/T]ATTCATAGAGACCCC | 79931 |
rs201350525 | snp | C/T | 0.000988468 | 0.0222094 | missense | TNIP3 | GRCh38.p7 | 4:121157186 | TCTGATGCGGATCCT[C/T]CTCCCGCGTGCTGAG | 79931 |
rs201417442 | snp | A/G | 3.35329e-05 | 0.00409455 | missense | TNIP3 | GRCh38.p7 | 4:121141853 | ACAGCTCCAGGGCCT[A/G]TTGGTACCCATGGAT | 79931 |
rs201421689 | in-del | -/T | 0.302686 | 0.244385 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224369 | CTCTGTCTCAAAAAA[-/T]AAAAAGAAAAAAGAA | 79931 |
rs201452925 | snp | C/T | 1.66244e-05 | 0.00288304 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147211 | TTACTGTAAGCTTCC[C/T]TTTCACTTAAGCCAT | 79931 |
rs201500497 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153799 | TCCAATCACCTACTC[G/T]TGTTTCAGAAGACAA | 79931 |
rs201578398 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197226 | TACATGAATGCTCTC[-/T]TTTAAGAACACCTAA | 79931 |
rs201728866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195621 | TATTTGTATTAAAAT[C/T]GTTTGGAATAAAATT | 79931 |
rs201786289 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225433 | CATTTTTTCTTCTTG[-/T]TTTTTTCTTTAAGAC | 79931 |
rs201805651 | in-del | -/T/TTTTTTTTA/TTTTTTTTT | 0.0198121 | 0.0978669 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187944 | GTTTTCTTTCTTTCC[-/T/TTTTTTTTA/TTTTTTTTT]TTTTTTTTAACCATC | 79931 |
rs201850714 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161325 | CTCCTGTTGCGATTT[-/A]AAAAAATACCTGATT | 79931 |
rs201926939 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215938 | AGGCTTTAAAAAAAA[C/T]TTTGAAAGATTGATA | 79931 |
rs201930715 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219353 | CTCCTTTTCCTCTTT[C/T]TTAAGGAATTCCTAT | 79931 |
rs201976915 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152420 | AGCTTAAAGTATAGA[A/T]GTGGGATGAAGTCTT | 79931 |
rs201990839 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223723 | CCTTTCTTAGCTTCC[C/T]TATCCATTAGCACAG | 79931 |
rs202024938 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156762 | GAATAAAAGCAAAAG[-/A]AAAAAAAAATTTCTC | 79931 |
rs202028280 | in-del | -/TATATATATA/TATATATATATATATATATATG | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131180 | TTCTTGTTATATGTA[lengthTooLong]TATATATATATATGT | 79931 |
rs202032237 | snp | C/T | 0.000270184 | 0.0116198 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157080 | CCGGGCTCGAGGACC[C/T]GGGCCCCGCCCACCT | 79931 |
rs202046111 | in-del | -/TC | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121218641 | CTCTCCCTCTCTCTG[-/TC]TCTCTTTCTTTTGAG | 79931 |
rs202104406 | snp | A/C/T | 0.000214812 | 0.0103616 | utr-variant-3-prime, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121132634 | TAGTGTGTACTTCTA[A/C/T]GGATGGACTTTCTTT | 79931 |
rs202198999 | in-del | -/AGT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185562 | AGTCTCTTAGCACAC[-/AGT]AGGACATCAATAAGG | 79931 |
rs202211582 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155267 | AATTATCAGACAAAT[A/G]GGTCTGCAGGATAAG | 79931 |
rs207465020 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180836 | ATCTATTCTGTCTCC[C/T]TACCTTCCAATAGTC | 79931 |
rs367587722 | in-del | -/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176719 | CAGATTTTTTTTTTT[-/T]CCTACAGTGTGGTTA | 79931 |
rs367619040 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149353 | TATAATAAGTACAAA[C/G]TATTTTCTTTGAAAC | 79931 |
rs367697160 | snp | C/T | 4.95037e-05 | 0.00497488 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157220 | TCTTTCCGCGGCGTC[C/T]AGTTTCGTCTTCAGC | 79931 |
rs367746253 | snp | C/G | 1.65094e-05 | 0.00287305 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147042 | ATTATTTTGTTTTGA[C/G]TTGTACCTGGGAATT | 79931 |
rs367752906 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216057 | CAAATCAGGAGAAAA[G/T]ATACAGCAACTCCTT | 79931 |
rs367756968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191653 | AGTTCCAAGTTGTGA[C/T]ATTCTCTAGGAATAT | 79931 |
rs367764399 | snp | A/G | 0.0001241 | 0.00787621 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161119 | ACCTGTGGCTTTAGC[A/G]AATATTTCTAAGTTA | 79931 |
rs367770891 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226260 | GAGAGAGAGAGCGAC[A/G]GAGGCACAAAGAAAG | 79931 |
rs367798708 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177753 | TCTATCAATATCTCA[G/T]CAAAAATGTGAAGGT | 79931 |
rs367800291 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211165 | TGATTCTCTAGTTCA[A/G]TTGTCTTGGAAAGAG | 79931 |
rs367821881 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164889 | TTGAAGTGAAATCTT[C/T]TCATGGAGAATCATT | 79931 |
rs367856157 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151575 | GTGTTAAGCTCTAGG[A/G]AGTGTCAGAATAGTT | 79931 |
rs367865335 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189077 | CACATAACCACAGTC[C/T]TAGAAATAACTTGAA | 79931 |
rs367932360 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162215 | CAAGCACCTTTTTTC[A/T]TCAGAAATTATTTAT | 79931 |
rs367991503 | in-del | -/TG/TGTG | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165659 | AACTTTTTGCTAGTT[-/TG/TGTG]TGTGTGTGTGTGTGT | 79931 |
rs368053363 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219713 | TAAAAAATTACCAAC[C/G]AATTCTTATACTATT | 79931 |
rs368064546 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227881 | TGTGTTTCATCTTCC[C/T]ATTTCTTTCCCTGAG | 79931 |
rs368073389 | snp | C/T | 8.28274e-05 | 0.00643481 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132588 | GAGGGTCCTCAGCCA[C/T]GCTCCCTCGTTGCCT | 79931 |
rs368105461 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222536 | TCAAGGAAAAGTCCA[C/T]AATGATTAAACAAGA | 79931 |
rs368120073 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201695 | TAGCTATGATTTGGG[C/T]AATTACTTAGCTCAT | 79931 |
rs368124000 | snp | A/C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183135 | CCTATTAAAGTAGTC[A/C/G]CTGTCCCAGGCATTA | 79931 |
rs368128904 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155636 | GTAAACATCAACAGG[C/T]TCTGGATTCAGACAA | 79931 |
rs368376766 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174207 | AACACCGTATCTATA[G/T]ATTTAGACACTATTT | 79931 |
rs368418486 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158630 | AGACTCTTCACACAA[C/T]TGGCCCCACCAGGAT | 79931 |
rs368447863 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216143 | AAAAACCATCCACCA[A/C]GGCTTGTCAATGGAA | 79931 |
rs368477094 | snp | C/T | | | missense | TNIP3 | GRCh38.p7 | 4:121157240 | TCGTCTTCAGCTCTG[C/T]TACCTGAGGAGGTCG | 79931 |
rs368479369 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197458 | GCTTGAGCTTGGTGG[C/T]GGAGTAGAGATTGCA | 79931 |
rs368531656 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170854 | GGAATCTTGCTCTGT[C/T]GCTCAAGCTGGAGTG | 79931 |
rs368649198 | in-del | -/GTCGTCCTTTCTCTGCCT | | | cds-indel | TNIP3 | GRCh38.p7 | 4:121157154 | GTCCTCTCTCTGCCT[-/GTCGTCCTTTCTCTGCCT]CTGATGCGGATCCTT | 79931 |
rs368734449 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196817 | AATTATGATAGATTT[G/T]CTTCTATTTTCTTTC | 79931 |
rs368764910 | in-del | -/ACACAC | | | cds-indel | TNIP3 | GRCh38.p7 | 4:121132214 | TTTTTACCCCAGGAA[-/ACACAC]ACACACACACACACA | 79931 |
rs368773393 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137572 | CAGCTGTCCAGATTG[C/T]GTATTGTACTTCAGC | 79931 |
rs368878570 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223848 | TCAAATTTTCAGCAA[C/T]AGAAGCAATATCAGA | 79931 |
rs368897138 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162056 | TTCCTACATCTGTAA[G/T]CTGTTTCAGGCTTAA | 79931 |
rs368922601 | snp | C/G | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166506 | GAAATCACTTTCAGA[C/G]AAACAGAGGTGTCAT | 79931 |
rs368987300 | in-del | -/A | 0.111576 | 0.20818 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195174 | CAAACAAAACAAAAC[-/A]AAAAAAAAACTTCTT | 79931 |
rs369013447 | snp | C/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227945 | AACCTTTAAAGTAAT[C/T]TAGAAATAAGCTGGT | 79931 |
rs369038584 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224500 | TCAGACTAATTATAC[C/T]TTAATGTTCATGTTG | 79931 |
rs369054229 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150246 | GATAAGTACACTGTT[G/T]ATCTAAGATTTACCA | 79931 |
rs369067572 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222407 | TTAGAGTCAAAAGAT[A/G]TGTATTCAAATCTGT | 79931 |
rs369085480 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162375 | GACCACATTTAAAAA[C/G]AGACAGTCTTCTGTG | 79931 |
rs369103789 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132557 | GGCAGAAACAAGCCT[C/T]AGTATAAACAAAGAA | 79931 |
rs369199327 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228594 | CAAAAATTTTAAAAA[A/G]TAATCTATTATATGA | 79931 |
rs369213906 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153802 | AATCACCTACTCTTG[C/T]TTCAGAAGACAATTT | 79931 |
rs369270083 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199680 | AGCCTGAGAAGAATG[G/T]CCTGGAGAAGAGAAA | 79931 |
rs369281083 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169947 | ACATTAGAAGGCAAA[C/T]TGGCTTTTGTTGACG | 79931 |
rs369281109 | snp | A/T | 0.000163359 | 0.00903619 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216525 | AAAAATATGAAGGAC[A/T]TGAGGCTCAGATGTA | 79931 |
rs369282930 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131207 | ATGTATATACATATA[A/T]ATGTATAATTTGAGA | 79931 |
rs369287106 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165777 | GCAAAATCCAAAAAT[A/G]CAGGTAGGAATCAAA | 79931 |
rs369319590 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184642 | TTATAATGAATTCTC[C/T]CATTATTTTTAAAGC | 79931 |
rs369328109 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157734 | GAGTGACAGGTCCTC[A/G]GAGTGGCCACAGTCC | 79931 |
rs369351656 | snp | C/T | 1.65012e-05 | 0.00287234 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138732 | TATGGACTTCAAATA[C/T]AGTGGCATGTCAAAA | 79931 |
rs369438272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193159 | TTCTGCTTTATCAGC[C/T]ATACAAAAAGATTGG | 79931 |
rs369489224 | snp | A/C | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217575 | CTGGAGGAGTTGGAC[A/C]ACCAACTAGTAGAGC | 79931 |
rs369502455 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217915 | ACACTGTGGAGAACA[C/T]GCTAAGAATTATAAT | 79931 |
rs369603027 | snp | A/G | 0.000115383 | 0.00759462 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138687 | ACTGATAGTCTGGCT[A/G]TGTGGAACAATACAA | 79931 |
rs369616906 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191363 | CACTCAGGTGGGTTT[A/G]TTGATAAACACCTGG | 79931 |
rs369637189 | snp | A/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132374 | GGGAGTCGTGCATCA[A/T]CCATCTGCCAAGTCT | 79931 |
rs369638748 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143396 | TTTTCCTTGACTGTT[C/G]ATTCACATCATTGTC | 79931 |
rs369711177 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164159 | AGTCTTGGAAAGCAG[A/G]AAGAAAAACAGGGGA | 79931 |
rs369724023 | in-del | -/GTGTGT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181625 | AAGTTAATAAGACAG[-/GTGTGT]GTGTGTGTGTGTGTG | 79931 |
rs369750127 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197365 | AACACCTTCTCTGCT[-/A]AAAAATACAAAAATT | 79931 |
rs369808479 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204071 | ATTCCTTCAGTTCAT[A/T]CATATTGCTCTAATT | 79931 |
rs369812638 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187005 | AAATTTCGATTTGAC[C/T]TAGATTTATTTCACA | 79931 |
rs369819273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159621 | AACACATGATTTATA[A/G]TAAATACTCAACAAA | 79931 |
rs369833066 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140894 | TCATTAAATCCTCAC[A/G]TTCCTTCAGCCACCC | 79931 |
rs369895096 | in-del | -/CCT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182244 | CAAAGTCAAACAACT[-/CCT]TTAATCAATGAAACC | 79931 |
rs370002088 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152307 | CATTGTAAAATAGAA[A/G]AACAATAATATCTTA | 79931 |
rs370015961 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194497 | TGGGGTTTACGAAAT[C/T]AGTGCAAACCAAAGC | 79931 |
rs370062164 | snp | G/T | 1.64863e-05 | 0.00287104 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154510 | AATGTTTTATGCAGG[G/T]ACTTCTCATTTTAAT | 79931 |
rs370087414 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144149 | ATGAGGATAGACTGT[A/C]CATGTCTCTTTTACT | 79931 |
rs370097974 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225235 | TGTGACTGTCATCCA[A/C]GGTTTTTTACATACT | 79931 |
rs370114030 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162015 | GAGTCATATAAGTAA[C/T]ACAATTTATTGGATG | 79931 |
rs370169630 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214311 | ACATTTTAGATTACT[A/G]TTAAAGAACCTAACC | 79931 |
rs370185192 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187190 | GACCTGAGGGTAAAA[C/G]AAACAAACAAAAAAA | 79931 |
rs370244494 | snp | A/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132250 | CACACACACACACAC[A/G]CATATGCACTTTAAA | 79931 |
rs370272164 | snp | A/G | 8.38286e-05 | 0.00647358 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121141891 | GTGGAAAACCAAGCC[A/G]CAGTTACAGGGTGGG | 79931 |
rs370425095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140812 | CAGAACTAGCAACCC[A/G]CAATAACATGAAAAG | 79931 |
rs370464126 | snp | A/C | 0.000164834 | 0.00907689 | missense | TNIP3 | GRCh38.p7 | 4:121157138 | GGTCGCGCTGCCTGT[A/C]GTCCTCTCTCTGCCT | 79931 |
rs370511356 | in-del | -/TGGCTGTAATCCCAGCTACTCAGG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195040 | TGGCATGGTGGCAGG[-/TGGCTGTAATCCCAGCTACTCAGG]AGGCTGAGGCAGGAG | 79931 |
rs370595103 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208453 | CAAGAGGGCAGCTTC[A/C]AATCTGTATGATTTC | 79931 |
rs370640136 | snp | A/T | 1.6507e-05 | 0.00287284 | missense | TNIP3 | GRCh38.p7 | 4:121142747 | TAATTGCTTTTCTAG[A/T]TTTTCTTTCTCCATC | 79931 |
rs370644897 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197199 | CTTTACTGTTAAAGA[C/T]TTTGGATGTTCTTAC | 79931 |
rs370695895 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155676 | CCTCTTAATTTTGTA[C/T]AATAGATAGCAAACA | 79931 |
rs370698211 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193305 | AAATTGATGAGCCTG[C/G]AATTTCTTTTCGTGC | 79931 |
rs370701814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195705 | TATTTGTAGTAATGC[A/G]GCTATACAAAGGCTA | 79931 |
rs370714717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207221 | GAATTGTTCAGAAGT[A/G]CAGAAAAAAAGCCTC | 79931 |
rs370761159 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202024 | ATTCAAATCAAAATA[C/G]TACCATCATTTTTCA | 79931 |
rs370764800 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175900 | CTGTTTTCCTGGGTT[A/G]TCTGGTGGTGTACTT | 79931 |
rs370767123 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148475 | ACCTTATATGCGAGT[C/T]CCGAAGATGTCAAGT | 79931 |
rs370810670 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137375 | ACTCCATTATTGTTG[A/G]AACTCAAGAACTTCA | 79931 |
rs370815841 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153916 | ATGGGTTGGCTCTTG[A/G]AAAAGTCAACAGTAT | 79931 |
rs370822659 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170306 | CAATACATTTTTATT[G/T]AATGAGTCCGTTTAT | 79931 |
rs370836625 | in-del | -/CAAACAAA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219220 | AAACAAACAAACAAA[-/CAAACAAA]AAACCCATAGAAGTA | 79931 |
rs370867882 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209125 | TGATGTGCTGGGAAG[A/T]TGGCAGGTTTGTTAA | 79931 |
rs370953247 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189765 | TCGAAGAATTGTATT[G/T]GCATGTCTGAAATGA | 79931 |
rs370994342 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168868 | CATTTTTAAGAGCGT[A/G]TCCAGCAGTGACTGA | 79931 |
rs371037097 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226134 | GAGAGAGAGACAGAA[A/G]AACAGGCACAGTGAG | 79931 |
rs371051855 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176902 | CCCAGCCACTGGGAG[A/T]TCCTCCCTTAACTTG | 79931 |
rs371063306 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150395 | TATGTATTTTTTTTT[-/T]CAGAATCTCTGTCTT | 79931 |
rs371079077 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143172 | TTTTTACATGCAATA[A/G]CTCACTGAATTCTCC | 79931 |
rs371152966 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142652 | GTAGCAGAGCTTGAA[C/G]ATGTCTTTAATTGGG | 79931 |
rs371235980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133521 | TAACATTAAATAAAT[A/C]CACTAATGATACCTC | 79931 |
rs371261688 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224180 | CCAGCCTGGCCAATG[G/T]GGCGAAACCCCATCT | 79931 |
rs371309869 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194383 | ATCTGATTTGATCTT[-/A]AAAATTATCTTTTGC | 79931 |
rs371354640 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215650 | AATTAGGTTAAAGCA[C/T]TTCTTCGTGTATTTC | 79931 |
rs371396623 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227816 | TTTAGAATTAGTATA[A/G]CTTACTGTAAGGACC | 79931 |
rs371407019 | snp | A/G | 5.05029e-05 | 0.00502483 | missense | TNIP3 | GRCh38.p7 | 4:121141902 | AGCCGCAGTTACAGG[A/G]TGGGCAATACATCTG | 79931 |
rs371438770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212801 | TCTGCCTTTCCAGAA[C/T]AGTTTAATTTAGAGT | 79931 |
rs371452970 | in-del | -/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183511 | CTTTATACCAGGGGT[-/C]CCCCAACCCCCACTG | 79931 |
rs371454095 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202783 | GACATGAATAGATAA[C/T]TCCCAAAAGAAGATA | 79931 |
rs371461904 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180424 | AAATTATAGATGTCA[A/G]AGGAGTAAGATATTT | 79931 |
rs371489388 | in-del | -/T/TT | 0.369142 | 0.219784 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168521 | TTTTCTTTTCTTTGC[-/T/TT]TTTTTTTTTTTTTTT | 79931 |
rs371666769 | snp | A/G | 0.000231012 | 0.0107449 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121164087 | CGTAGAACTTTCTGC[A/G]GCAATCATTCTAGAT | 79931 |
rs371689001 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138613 | AATGCTCAATACAGC[C/T]GTGGTCTCACCATTT | 79931 |
rs371692869 | snp | A/T | 1.64806e-05 | 0.00287054 | missense | TNIP3 | GRCh38.p7 | 4:121147107 | ATTTGCTGTAGCTCC[A/T]CTTTCTCTTGATTAA | 79931 |
rs371738409 | snp | C/T | 4.98832e-05 | 0.00499391 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150223 | ATCCTGAAGAGCCTA[C/T]GTAATAAGATAAGTA | 79931 |
rs371745145 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206939 | TTCATGGGAGTTGTA[C/T]ATGAATTCAAATATC | 79931 |
rs371833377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192183 | ACAAAAAAGAGATGC[C/G]GAGCCAAGTCTGACC | 79931 |
rs371837705 | in-del | -/TATATATATA | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131178 | ATTTCTTGTTATATG[-/TATATATATA]TATATATATATATAT | 79931 |
rs371886366 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210307 | ATTTTTTAATAGCCT[A/G]AAGTTGAATCAGGTT | 79931 |
rs371895993 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156804 | TGCCCTAGAGAGTTA[A/G]CAAATTTATGGATCC | 79931 |
rs371927642 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222318 | GTATTGTGGATTTCT[A/G]CTGATAAATTTCATC | 79931 |
rs372045170 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142832 | AAATCATTAATTCCC[-/A]AAGCCACTCTTGACC | 79931 |
rs372116883 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193336 | CAGAAATTAGGCAGG[A/T]TTCAAAAAATTGATC | 79931 |
rs372131887 | in-del | -/A/AA | 0.0225045 | 0.103662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132755 | AAGTTCCAGGATGGC[-/A/AA]AAAAAAAAAAAAAAG | 79931 |
rs372153483 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216000 | TTTTCATAAGGAACT[C/T]AGTAAACTTCTCACC | 79931 |
rs372163333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190393 | TATTAAGTATTTGAC[A/T]AGAGAGTAAATTGAC | 79931 |
rs372175748 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163429 | AAGGGCTGCTTACGG[A/T]ACAGTTATTCCCTAT | 79931 |
rs372201938 | snp | A/G | 5.00822e-05 | 0.00500386 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150065 | TGAAAAATGGGCAGT[A/G]TGTTCTCCACAGGAT | 79931 |
rs372245218 | snp | C/G | 0.000181937 | 0.009536 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157248 | AGCTCTGCTACCTGA[C/G]GAGGTCGTTCAAAGA | 79931 |
rs372247780 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174398 | TGACAGAGCGAGACC[C/G]TGTCTCTAAAATAAT | 79931 |
rs372267751 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185355 | AATGTCACTTTATGG[C/T]GAAAGCCTCTGCTGA | 79931 |
rs372304672 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138597 | GATGTAAACATGAAA[A/G]AATGCTCAATACAGC | 79931 |
rs372360302 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227731 | AATCAGGAGTACTAC[A/G]GGAAATCTACCTGCC | 79931 |
rs372394674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205412 | CAGAAAGGTAAAAGA[C/G]AGCCAGTTCAAGGAG | 79931 |
rs372406684 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153179 | AAAATGTAAAATTTC[A/G]TGTAGAATTATTAAA | 79931 |
rs372520153 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216155 | CCAAGGCTTGTCAAT[A/G]GAAATTTACAAATAC | 79931 |
rs372561983 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216773 | GGAGAAATTGTCCAG[A/G]AGCAAGTAAAAGAAA | 79931 |
rs372588208 | in-del | -/T | 0.361263 | 0.223876 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176708 | AAAAGGAAAGCCAGA[-/T]TTTTTTTTTTTCCTA | 79931 |
rs372662175 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215880 | ATTAGGTGCCACATT[-/A]AAAAAAAAAAAAAAA | 79931 |
rs372712921 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152549 | ACATATTATATACTA[G/T]CTAATTAAATTCATC | 79931 |
rs372738899 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161855 | TCAGTTATTTTTTTC[A/G]GGAGTGAGAGTATTC | 79931 |
rs372899499 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175681 | TAAATAGAAAGCATC[C/T]TACTCAAAAGTGTGT | 79931 |
rs372943805 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176015 | CCTTTAAAAATCCTC[G/T]TAATGAATGGAAGGA | 79931 |
rs372955007 | in-del | -/GTT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221495 | CAAATGCTCAATGTT[-/GTT]AAGAATATGATAATG | 79931 |
rs373003177 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216570 | AACTATGTCAGTCAC[C/T]AAAGGAGAAAACCAC | 79931 |
rs373011696 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213708 | CTTCAGCCTGGGCGA[C/T]AGAGTAAGACTCCGT | 79931 |
rs373065745 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208385 | TGGAGCCACCCAGAT[C/T]AATAAACTGATTCAT | 79931 |
rs373119831 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225342 | TGTTTCAAAACAATG[A/G]AGATATTTAATCTTG | 79931 |
rs373130897 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222955 | GGACTACAGGCGCCC[A/G]CCACCACGCCCGCCT | 79931 |
rs373179519 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224861 | TAAAGAGTTTGGGGG[A/G]AAATGACAACATATT | 79931 |
rs373227119 | snp | C/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228747 | AGGTCCTCTAAAGCA[C/T]TTTGAATATGTCTTT | 79931 |
rs373352011 | snp | C/T | 3.85654e-05 | 0.00439104 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141782 | TCTACCAAAACAGTA[C/T]ACTAAGCACTTTTTC | 79931 |
rs373375679 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213832 | AACTGGTATTACAAG[A/G]GTACTTCAAAAAAAG | 79931 |
rs373400940 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150902 | CGAGTGGAGAGAGTG[-/C]CCTGCTTTCTTGACA | 79931 |
rs373417233 | snp | A/G/T | 0.000148871 | 0.00862641 | missense, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121158711 | ATATAACTCTTTCAT[A/G/T]CTTCTAAATTGCTGA | 79931 |
rs373451600 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229090 | TGTCTTAAGCCACAT[A/G]TCTTTTCATTTGACA | 79931 |
rs373460882 | snp | C/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132247 | ACACACACACACACA[C/T]ACACATATGCACTTT | 79931 |
rs373472329 | snp | A/C/G | 3.40845e-05 | 0.00412811 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141920 | GGCAATACATCTGAG[A/C/G]AGAACAAAACTGTGG | 79931 |
rs373510175 | in-del | -/GAAAA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159283 | GAAAAGAAAAGAAAA[-/GAAAA]ACCAGTAAGTCTCAG | 79931 |
rs373604791 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176719 | CCAGATTTTTTTTTT[-/T]CCTACAGTGTGGTTA | 79931 |
rs373662708 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218269 | GCAAAGGGAAATCTC[C/T]AGATTTAATATTGTA | 79931 |
rs373711484 | snp | C/T | 0.106633 | 0.204807 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218788 | GAGTAGCTGGGACTC[C/T]TGGGCTCAAGCAATT | 79931 |
rs373717271 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200688 | ATCCTGGAGTTACTG[C/T]CAGTAATCAGGCACC | 79931 |
rs373757511 | in-del | -/TAGG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185564 | TCTCTTAGCACACAG[-/TAGG]ACATCAATAAGGATT | 79931 |
rs373758786 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181588 | GTACAGGAGTATCCA[C/T]AGCATATTAAGTGAA | 79931 |
rs373772231 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150534 | GACTTTCTCCAGATT[A/C]TCTGCTTCAGTCAAA | 79931 |
rs373796886 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203216 | ATAAAGAAAATGTGA[G/T]ATAGATAGATAGATA | 79931 |
rs373963948 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207751 | CTCCAAGCTGACCTT[A/T]TTCACTCCTGGATGT | 79931 |
rs373999692 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132774 | AAAAAAAAAAAGTTA[C/T]GTTATATTCATAAGC | 79931 |
rs374031515 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188423 | GCCAGAGAGGACACA[A/G]GAAGAGATCAATGAT | 79931 |
rs374033583 | snp | A/G | 6.60546e-05 | 0.00574656 | missense | TNIP3 | GRCh38.p7 | 4:121154600 | TCCTTTTCCTTGTTC[A/G]CAAGAGTATTTTTTC | 79931 |
rs374280012 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137415 | CTGGCTATATTTGTA[A/G]TAGAAAGCAAAGAAA | 79931 |
rs374312985 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177093 | TTTCAAGCATTATTG[G/T]AACCATATTTGTTTA | 79931 |
rs374317418 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142397 | TTTTCAAAAGAGGCA[G/T]TATTTGATTTAGTTT | 79931 |
rs374352324 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155701 | CAAACATTTTGTGAA[A/G]TAAATTGGATTCTTA | 79931 |
rs374453366 | snp | G/T | 3.29582e-05 | 0.00405931 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154522 | AGGGACTTCTCATTT[G/T]AATCTCCCATGCTTG | 79931 |
rs374463382 | in-del | -/TTTG | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217053 | GTACTTCCGACAGAA[-/TTTG]TTTCTCATTTTTTAA | 79931 |
rs374471330 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216034 | CTTCAGGTGAGCTAA[A/G]GATTAAGCAAATCAG | 79931 |
rs374478188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190780 | AGCTCAATACTCCCC[A/G]AACAAACTCTCAGAG | 79931 |
rs374540186 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194679 | AGTAAAAAACACAAA[A/G]TAAACAAAACCCCTA | 79931 |
rs374546600 | snp | C/G | 0.000679455 | 0.0184192 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147021 | TATACATACATGCTG[C/G]CAAAGATTATTTTGT | 79931 |
rs374559857 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140169 | TGAAACCCCATCTCC[A/G]CTAAAATTACAAAAA | 79931 |
rs374565771 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141410 | ATCTATTTTGCACAT[A/G]TGTAGCAATATCCAT | 79931 |
rs374704899 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212884 | TATGATATCATAAAA[G/T]AGATCATTTTAGTTT | 79931 |
rs374793173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163557 | CAAGGTCTGATGCTA[A/C]TAAATTAAAAACTTA | 79931 |
rs374794699 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137767 | CAAATTTCAAGAATG[A/G]CCTGAAATTAGACTA | 79931 |
rs374808802 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215138 | TAAACACTATTGTTA[C/G]AGTAGCCTATTGGAA | 79931 |
rs374816602 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162137 | AAATATTTTCAAAAC[A/G/T]TGTTGTTGGTCTTTG | 79931 |
rs374857418 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224323 | AGCAGAGATTGTGCT[A/G]CTGCACTTTAGCCTG | 79931 |
rs374889567 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195328 | GAATTTTTAAAATTA[C/T]TCTTTAAACAACAGT | 79931 |
rs374918535 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159668 | TTTGAAAATTTAGAT[C/T]TTCAAGAAATTATAG | 79931 |
rs374958148 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136456 | CTGTGTGATTTAGGC[A/G]TGTTACTTAAATTCT | 79931 |
rs374992325 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149265 | TGGGGAGGAGAATGC[C/T]CTTGTGCATCAGTGA | 79931 |
rs375047341 | snp | A/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228470 | ACATTATCTTTTTCA[A/T]TACAAAATGCTGTAA | 79931 |
rs375052788 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181029 | TTTCCTCAATGAGGT[C/T]GTAGGAAAATCAGTA | 79931 |
rs375075448 | snp | C/T | 0.00036321 | 0.0134712 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138574 | ACATCCCCAAAAGAT[C/T]CCATTAAGATGTAAA | 79931 |
rs375131075 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207129 | TCTTTGTTTTGTTTT[A/G]TTTTGCTTGCTGTTT | 79931 |
rs375144287 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189860 | GCATTCTTGGCTAGC[A/T]CCCTGTTTATTTCCT | 79931 |
rs375160657 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213583 | TACAAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 79931 |
rs375167841 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159586 | CACGATTTTCTTGCA[A/C]TAATGTGTTTTAAAA | 79931 |
rs375202073 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193541 | TATCCCATTAGAAAA[A/T]CATTATTTGACAGCC | 79931 |
rs375268665 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192104 | TCTATATTGGAATTT[C/T]CTTTCAAGACATGAT | 79931 |
rs375269222 | snp | A/G | 0.000153988 | 0.00877328 | missense | TNIP3 | GRCh38.p7 | 4:121150128 | AGAACTTCCATTTCT[A/G]TTCTCATCTCCTCAT | 79931 |
rs375289902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226655 | AAATATCAGCACTGC[A/G]CCTGTAAGCATCTAG | 79931 |
rs375384831 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168787 | GCTTCTCAAAAAAAA[-/A]TGCCTTTTAATAACT | 79931 |
rs375395968 | in-del | -/AT | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163181 | GGAAAAATAGAAAAC[-/AT]AGTGACTAGGAATGG | 79931 |
rs375441832 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226256 | GAGAGAGAGAGAGAG[A/C]GACAGAGGCACAAAG | 79931 |
rs375479960 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164034 | GCTAGATGTGATCAA[C/T]TCATCTCCTAGAAAT | 79931 |
rs375515205 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199388 | AAGTCGGACATGAGG[C/T]CTATAAGAAAACAAT | 79931 |
rs375527240 | in-del | -/TAACA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137694 | TTACACTCCATAACA[-/TAACA]GACTCCTTGTATTAA | 79931 |
rs375536387 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199422 | ACTATGTTTCTAGCC[-/C]AGAAATACTCCTTTC | 79931 |
rs375653381 | in-del | -/GCTT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226947 | CTGGCTCTGCTCATT[-/GCTT]AATCAAGATTGTTCA | 79931 |
rs375684681 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185375 | GCCTCTGCTGACTAA[C/G]CTATCTGAACTAGAT | 79931 |
rs375703190 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211949 | TCCATGGAAGTAAAA[A/G]CTGAGTGATTTCCAG | 79931 |
rs375767086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204744 | AGATTGTTGGGTCCA[A/G]GGGTATGGACATTAA | 79931 |
rs375785946 | snp | C/T | 3.55492e-05 | 0.00421585 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141965 | GGAGAGACTGAGGAG[C/T]TGCAGTGACATTGCT | 79931 |
rs375813451 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186025 | AGCTGGGGCCCTGCG[C/T]CCTCTCACGTGAGCC | 79931 |
rs375851035 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224778 | TTTAATATCTATAAT[G/T]GTTTTGCCTTTCGTA | 79931 |
rs375855250 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201331 | CAATGGCTGGCTTCT[C/T]ACAAAGCAGCAGGGT | 79931 |
rs375869431 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143994 | ACAAAAAGAACACTA[A/G]GAATGTGTATATGTC | 79931 |
rs375869703 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147561 | TGGATGTATCTCATA[A/C]ATAATAGTAATATTT | 79931 |
rs375871796 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184472 | CCAGTGGGATTCTCC[C/T]CTGTGTCTGGAGTGA | 79931 |
rs376018219 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185358 | GTCACTTTATGGCGA[A/G]AGCCTCTGCTGACTA | 79931 |
rs376035997 | in-del | -/CTTC | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218550 | TCCCTTCCTTCCTTC[-/CTTC]TTTCCTTCCTTGCTT | 79931 |
rs376064167 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136151 | AGTTCATAACATATT[A/T]ATTACACACTTAATC | 79931 |
rs376103935 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134491 | AAACAAAAGCTGTAA[C/T]TCATTAATATCTGTG | 79931 |
rs376150616 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165171 | AGATATTCACATATA[C/T]ATAGGATAAAGCCTA | 79931 |
rs376167355 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170293 | GTACAGAGTATTACA[A/C]TACATTTTTATTGAA | 79931 |
rs376172189 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141181 | AAAATAAAAAGTAGA[A/G]GAGGGTAGGTGGAAT | 79931 |
rs376189789 | snp | A/C/G | 0.000103547 | 0.00719472 | missense | TNIP3 | GRCh38.p7 | 4:121141827 | TTACTGGGTGCTCCC[A/C/G]TTGCTTCTGCACAGC | 79931 |
rs376261908 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220986 | CATATCCTCCCCAAA[A/G]GTATTAAAATTCTGT | 79931 |
rs376315244 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222960 | ACAGGCGCCCACCAC[C/T]ACGCCCGCCTAATTT | 79931 |
rs376358497 | in-del | -/GTTTT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171743 | GTTTTGTTTTGTTTT[-/GTTTT]TGAGATGGAGTCTCA | 79931 |
rs376408049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154182 | ACTCCATAGTGATCA[C/T]TTTAAAGAGCAGTTT | 79931 |
rs376514651 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203386 | GAAAAACAAACATCA[C/T]ATGTTCTCACTCACA | 79931 |
rs376538087 | snp | C/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132249 | ACACACACACACACA[C/T]ACATATGCACTTTAA | 79931 |
rs376627206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140794 | AGGGGGAGGGAGAGC[A/G]GACAGAACTAGCAAC | 79931 |
rs376628645 | snp | C/T | 8.24776e-05 | 0.00642122 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138600 | GTAAACATGAAAGAA[C/T]GCTCAATACAGCTGT | 79931 |
rs376657285 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180186 | CGGGTGGATCAAGAG[A/G]TCAGGAGATCGAGAC | 79931 |
rs376698742 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182183 | CTTGAATTTTATTTG[C/T]TTATATAAAGCACCA | 79931 |
rs376740368 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210849 | CATTGGGGTTTAGGA[G/T]TTCAACATACGAATT | 79931 |
rs376761839 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198981 | ACATCTTTGAAAAGG[G/T]TATAGATCCTCTTTG | 79931 |
rs376773298 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142862 | CTACTCAAGTGTCAG[G/T]CATTGACAGCAGTAA | 79931 |
rs376867877 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208040 | CCTCATTTTCTCTTG[C/T]GGCCGCCATGATTCT | 79931 |
rs376926512 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187282 | TGTGGGTACATAGTT[A/G]TTCCCACCTTGGGAT | 79931 |
rs376942286 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144994 | AAATTCTCATATTTC[A/T]AAGTACCCTAAGCAT | 79931 |
rs377048465 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165931 | AAAAAGAAAACTCTA[C/T]TGTAAGAATATTTTT | 79931 |
rs377067371 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149935 | GGTGGGACTGAACTA[A/G]CTGATCTGTATTCTT | 79931 |
rs377075361 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200885 | CTGGAAAATCACTTA[A/T]CATGGGTAGAAATAA | 79931 |
rs377100894 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205127 | CAATGTAAGTGGAAT[C/T]AGGGTTATGAGGTGT | 79931 |
rs377143494 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156133 | CACTGTGACAAAGAC[A/T]TCCTCAGCAAGATAG | 79931 |
rs377222963 | snp | C/G | 1.65042e-05 | 0.0028726 | missense | TNIP3 | GRCh38.p7 | 4:121157126 | GGTCCCGGGTCAGGT[C/G]GCGCTGCCTGTCGTC | 79931 |
rs377244850 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220275 | ACATTAATACCATAT[G/T]AATTTAATGTCACTG | 79931 |
rs377297729 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206050 | AAATCTTGAGAACAG[C/T]ATGGGGGTAACTACT | 79931 |
rs377305267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154038 | CCCTGCATGCACACA[C/T]GCACACTTTTCCTCT | 79931 |
rs377334381 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175817 | GGGAAATATTTTCTC[-/T]CCTTTAATTTTTATG | 79931 |
rs377359733 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186793 | ATAAAGAAAAGAAAA[C/G]CACAAAAAATGTTCA | 79931 |
rs377433002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214158 | TTGGCTCTCGCCTCT[C/T]GTCTTTATTCTTCTT | 79931 |
rs377437318 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208355 | TTTTACAGACCCTGA[A/C]CTCAATGTGTCGGCT | 79931 |
rs377465736 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141536 | GAAAATGTCCTTTGG[A/G]TAGAATGAAGTATGC | 79931 |
rs377473763 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163860 | GAAAGGAATTTAAGC[C/T]CCGTGGGTTAAAAGC | 79931 |
rs377491370 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174118 | TCTGCATCATTCCTG[A/C]CAAGGGGTTGTCCAG | 79931 |
rs377571045 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213716 | TGGGCGACAGAGTAA[A/G]ACTCCGTCTCAAAAA | 79931 |
rs377668029 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131180 | TTTCTTGTTATATGT[A/G]TATATATATATATGT | 79931 |
rs377696800 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155074 | TTCAAGCAATTCTCC[C/T]GCCTCAGCCTCCCTA | 79931 |
rs377696915 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218232 | TTGAACTCTGGTAGT[A/G]AACACCCCAAAAATG | 79931 |
rs377698129 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194890 | GACTTCTTCTCAGCA[A/G]GGTAGAGTGGCTCAC | 79931 |
rs377698537 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168866 | AACATTTTTAAGAGC[A/G]TGTCCAGCAGTGACT | 79931 |
rs377727698 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121132822 | TGAGAAATCAAGAAG[C/T]GGGAGATGGAGGGTT | 79931 |
rs377764405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186054 | CCTGGTTCAGCACAC[A/G]TCCCTCAGGACCACA | 79931 |
rs377765158 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160117 | CACAATATTCTTCAA[A/G]TATCAAAGAAGAGTA | 79931 |
rs386401319 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168781 | ACCACAGCTTCTCAA[-/A]AAAAAATGCCTTTTA | 79931 |
rs386401320 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168786 | AGCTTCTCAAAAAAA[-/A]ATGCCTTTTAATAAC | 79931 |
rs386401321 | in-del | -/GAT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176535 | ATGATGATGATGATG[-/GAT]ATGATGATGATGATG | 79931 |
rs386401322 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176713 | GAAAGCCAGATTTTT[-/T]TTTTTTCCTACAGTG | 79931 |
rs386679069 | multinucleotide-polymorphism | AG/TA | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131485 | AATTAATCAAATCCA[AG/TA]GGAAGGAAAAACACA | 79931 |
rs386679070 | multinucleotide-polymorphism | ACA/GCG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185887 | AGGTACTGACTTTTC[ACA/GCG]GAAATAATCACATGC | 79931 |
rs386679071 | in-del | AT/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194387 | TGATTTGATCTTAAA[AT/C]TATCTTTTGCTCAAT | 79931 |
rs386679072 | multinucleotide-polymorphism | ATT/TTC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222191 | GAAATATTAGTGAAT[ATT/TTC]TTCCCCTGCGAAGAG | 79931 |
rs397750606 | in-del | -/AA | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160488 | CTCAAAAAAAAAAAA[-/AA]GAAGGAATTACAAAA | 79931 |
rs397755240 | in-del | -/A | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132769 | CAAAAAAAAAAAAAA[-/A]GTTATGTTATATTCA | 79931 |
rs397773338 | in-del | -/A | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223622 | CTAGAAAAGGTAAAA[-/A]TGCCTCATTATCACA | 79931 |
rs397879946 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161853 | TTTCAGTTATTTTTT[-/T]CAGGAGTGAGAGTAT | 79931 |
rs397995179 | in-del | -/GT | 0 | 0 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165692 | TGTGTGTGTGTGTGT[-/GT]TTACTTTCTTCTGGT | 79931 |
rs527282348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191225 | GAATAGGAAACATTG[A/G]CTCCTAATCAACTTT | 79931 |
rs527322664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144558 | AGGCGCGTGCCACCA[C/T]GCCCAGCTAATTTTT | 79931 |
rs527404462 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158489 | TTCTTTAGCTATTGC[A/T]CAAGACAACTCACTG | 79931 |
rs527450895 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197907 | AGTGTTTTGCGCTAT[C/G]GAAAGAAAAGTTTCT | 79931 |
rs527453066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210427 | GATATTAATAGCTGC[C/T]TAAGCCAAACTCCTT | 79931 |
rs527467952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171078 | ATCTCGGTCTCCCAA[A/G]GTGCTGAGATCACAG | 79931 |
rs527469946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163862 | AAGGAATTTAAGCCC[C/T]GTGGGTTAAAAGCAA | 79931 |
rs527555319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177629 | GGGAATCTACCTTAT[C/T]GTTCTTAGGCTAACT | 79931 |
rs527565153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223151 | AGGTGAAACTAGTAA[C/T]GGATCGCTTTCATAT | 79931 |
rs527568938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215811 | CAAGCAGCTTGAGTA[C/T]AGGGTCTGAATCTGA | 79931 |
rs527631857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216338 | CTCTTAATACACTAT[C/T]ATTGCCACAAAGCAG | 79931 |
rs527639660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189596 | GTGTCTTAATTACTT[C/G]AGTAATTGGAAATAT | 79931 |
rs527640395 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205196 | ATCAAAGGTGGGACT[G/T]ATTGAAAGGTGACAA | 79931 |
rs527646463 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189209 | CTTTCTTCCTCCACA[C/G]ACTCGCCTACCTCAA | 79931 |
rs527734292 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159192 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 79931 |
rs527735393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166913 | GAATTAGATTATCTG[A/G]ACTCACAGCTTGGCT | 79931 |
rs527804483 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216726 | TGGGTGTAAACACAG[A/G]CTCAGTGAGTTAAGG | 79931 |
rs527826181 | snp | C/T | 0.0944967 | 0.195752 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218771 | CCCTCCCTCAGGATC[C/T]TGAGTAGCTGGGACT | 79931 |
rs527836663 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135771 | GCAATTCAGTTACAC[C/T]AACAGATTAAAAGGA | 79931 |
rs527853541 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217159 | CATAGTATGTCATGG[A/G]ACTTACAGTAGAATC | 79931 |
rs527864495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185566 | TCTTAGCACACAGTA[A/G]GACATCAATAAGGAT | 79931 |
rs527928647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172026 | GCATGAGCCACCACA[C/T]CTGGCCCCTATTCCC | 79931 |
rs527945641 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184859 | ATAACAATGAGTTTG[G/T]ACCTATCTTCAGGTT | 79931 |
rs527946574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192180 | CATACAAAAAAGAGA[C/T]GCCGAGCCAAGTCTG | 79931 |
rs528005555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139214 | GCTGTTGTGAAGAAC[C/T]GATCCAGCAGAACCT | 79931 |
rs528011443 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167429 | AAGGGTAGATAGGAT[C/T]TTGACAGAGAGTGAA | 79931 |
rs528039851 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134466 | ATGTTCTTTGTAAAA[A/T]CACGTTTCTAAACAA | 79931 |
rs528045262 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176894 | AACTTGTCCCCAGCC[A/C]CTGGGAGTTCCTCCC | 79931 |
rs528049675 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227613 | GATACAAATACAACC[C/T]ACAGATAAAAGATTC | 79931 |
rs528063941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219678 | CTCACATAGGTTTTA[C/T]AGACCTTGAAAATGT | 79931 |
rs528128338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173817 | TGTAATTTTAGTAGA[G/T]GTGGAGCTTCACCAT | 79931 |
rs528152112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147578 | TAATAGTAATATTTG[A/G]GTGGAACACCTCTTG | 79931 |
rs528152167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140453 | CCTGGACTGCCTTGC[A/C]TTTTTTAATTGACAT | 79931 |
rs528161204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186845 | GAAGTTTAGTCACAC[C/T]TCAAATAAATGAGAA | 79931 |
rs528202560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226969 | CAAGATTGTTCAACC[C/T]TGTAATATCCCAAGA | 79931 |
rs528226864 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204295 | CCTCATTTGGAGAGG[C/T]TAATCAGAAAGTCAA | 79931 |
rs528288690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193175 | ATACAAAAAGATTGG[A/G]ACACGCTATCAGAGA | 79931 |
rs528300821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186253 | GGTCACACCTATGGA[A/G]AGAGTGGGCGTCAGT | 79931 |
rs528323399 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171979 | CTCAAATGATCCACC[G/T]GCCTCAGCCTCCCAA | 79931 |
rs528388248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153381 | AGGGAAATTAACTAG[A/G]CAATGTAAGAAAACT | 79931 |
rs528415323 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199106 | TGTGACATGGCAGGT[A/C]CAGCTGAAAGCACTG | 79931 |
rs528429519 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155350 | CTGAAAGTCTTAAAA[A/C]GAAAAAACTCTCATT | 79931 |
rs528465033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149886 | TTGGGTAAGCATTTA[A/G]TCTGTCTGAAACTCA | 79931 |
rs528467719 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195178 | CAAAACAAAACAAAA[A/C]AAAAACTTCTTAATT | 79931 |
rs528571080 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121172175 | AATTTCTCCACACCA[C/T]CATGGTACACGGCTG | 79931 |
rs528572309 | snp | A/T | 1.65449e-05 | 0.00287614 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121154605 | TTCCTTGTTCGCAAG[A/T]GTATTTTTTCCCTTT | 79931 |
rs528577505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155119 | AGGTGCCTGCCACCA[C/T]GCCCGGCTAATTTTT | 79931 |
rs528588821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194480 | GACCAATAAATCTTT[C/T]TTGGGGTTTACGAAA | 79931 |
rs528607337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200793 | CCTTTTTATCCAGCA[C/G]ATTTCTGGAACCCCA | 79931 |
rs528686545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161359 | GCAGTAATAATCCTC[A/G]TACCCTAAGTCCTTC | 79931 |
rs528699283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200363 | AAACTTTATAGTAGG[G/T]CCCTCAGTAGACTTT | 79931 |
rs528712222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207985 | AAATACGTCTCCTGA[A/G]ATCTGATGGTTTTAT | 79931 |
rs528727178 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202819 | ATGACCAGCAAACAT[A/G]AAACAATGCTCAATT | 79931 |
rs528774345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168622 | AACTCCTGGGGTCAA[C/G]CAATCCAGCTGCCTC | 79931 |
rs528779914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213358 | CTCTACTTCAGATTA[A/G]AATGAATCATAGTCA | 79931 |
rs528830501 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202090 | AACCAAAAAAAGAGC[C/T]CACACAGCCAAAGTA | 79931 |
rs528896603 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202836 | AACAATGCTCAATTC[A/C]CTAATTATAAGGAAA | 79931 |
rs528935321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169930 | TTTAGGGCACATCAG[A/G]TACATTAGAAGGCAA | 79931 |
rs528942179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214663 | ATATGCTTCTGCTAC[A/C]AAAGGAGGATGGGTA | 79931 |
rs528997291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170427 | TAGGCTTTGCCTCCA[A/G]ACCAGAAATGATCAG | 79931 |
rs529012245 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162998 | CATAAACAATTTTCT[C/G]TGGAAGAAAATTATA | 79931 |
rs529030490 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121182719 | GGCATGGCCTCTGGG[A/G]TGAACCGTTTTGGAT | 79931 |
rs529039471 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135517 | ATCCTCCTACCTTAG[C/T]CTCCCAAGTAGCTGG | 79931 |
rs529110765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149924 | ATGTTCTAAATGGTG[A/G]GACTGAACTAGCTGA | 79931 |
rs529114824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175720 | TCAACAAGAATGGAG[C/T]CTCAGTTTATATTCC | 79931 |
rs529140008 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173173 | CACCTAAAAATTGTA[A/G]CAGGAGACATCATTT | 79931 |
rs529175845 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136348 | TAAAGTGAGAGAGGT[A/G]CAGTAAGAGGGGCAC | 79931 |
rs529200006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221281 | AAAATAGCCAGTTTG[C/T]ATGTTCAAGAAGTTT | 79931 |
rs529218685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136033 | CTTCTCTGCTGCTGG[C/T]CAGCCATAGTTAGTT | 79931 |
rs529224589 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140111 | GAGGCCAAGGTGGGC[A/G]GATCATGAGGTCAGG | 79931 |
rs529236278 | snp | A/T | 0.000489197 | 0.015632 | missense | TNIP3 | GRCh38.p7 | 4:121216422 | GTTATTACCTTTCAG[A/T]ATCTTCAGATTGATT | 79931 |
rs529252955 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177694 | CCTGTCATTGGCTCA[C/T]GCTTGTGTTAACCAA | 79931 |
rs529313165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171242 | TGGAGAATCAAACCT[C/T]TGAATTTCAAGAGCT | 79931 |
rs529427470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144078 | CAAGTATTGATTTGG[A/G]GATGACAAATGCATT | 79931 |
rs529433005 | in-del | -/CAA | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159630 | TTTATAATAAATACT[-/CAA]CAAATAGGTAATATC | 79931 |
rs529497826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190073 | ACCACATCCTCCTAC[A/G]GGCATCCTGCTGACA | 79931 |
rs529511903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190923 | ACCCTAGTAGAGAAA[A/G]AGGACAAAACCAAGA | 79931 |
rs529543334 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199881 | CACATGGCTTAGGAG[C/T]GAAGGCTGGGATACA | 79931 |
rs529577280 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213595 | AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 79931 |
rs529584124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150008 | GCAAAAACCTTTGAC[A/T]TATTTCTAGCAGCAA | 79931 |
rs529594139 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183768 | GGGATCTAGGCTGCC[C/T]GCTCCTTATGAGAAT | 79931 |
rs529597531 | snp | C/T | 0.000133089 | 0.00815641 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157106 | CACCTCCTCCCGCTG[C/T]AGCCGGTCCCGGGTC | 79931 |
rs529618311 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226049 | CATTGAGAGAATTGT[A/C]CTGGAAGCCAATGAT | 79931 |
rs529667318 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174782 | TCTCCCCACAAGTAC[A/T]AAATAAAGTAAAAAG | 79931 |
rs529730701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159025 | GGCAGGTGGGATCAC[G/T]TGAGGTCAAGAGTTG | 79931 |
rs529822942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198121 | GTTCTTTCTTAAGGA[A/C]CTTGGCTAGGAGAAG | 79931 |
rs529850368 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150334 | CATTTCATGTTTAAC[A/G]CTGCTTACATAACCA | 79931 |
rs529862573 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147757 | AAGTAAAAACATTCC[C/T]CTAAGATTCTGATTT | 79931 |
rs529865674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204465 | ACAATCAAACGGTGC[A/G]CTGACCACCTTGGGC | 79931 |
rs529893044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164806 | TATATTGGCAGAAAG[A/G]TTAAACTTGTCTCAA | 79931 |
rs529951010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171833 | CCTCCTGGGTTCAAG[C/T]GATCCTCCTGCCTCA | 79931 |
rs529952043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165259 | CTCCTGAATATCTCC[C/T]CCTACTCTCCAACTC | 79931 |
rs529971794 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201788 | GCTATGTATCAGTAC[A/G]TGAGGATCACATTTT | 79931 |
rs529992179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210626 | GTTTGTGAGCAAGGT[A/G]CCAGCAGGTAGGTTT | 79931 |
rs530040092 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172607 | TGTTTGTCTCATACA[A/G]TATTCTGCCGTTTAT | 79931 |
rs530061112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199784 | GGAAACCAAGGAAGC[C/T]TAATCTTTTCAAGTG | 79931 |
rs530109101 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142140 | TTTCCCCATTTTGAA[G/T]AAATTAGACACACTT | 79931 |
rs530154120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167867 | CCCTGGACTCGAGAC[A/T]CCTGTATTAATTGCT | 79931 |
rs530163764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153499 | AAAAGAAAAAAAGGG[A/G]AAAGATAGATTTTGC | 79931 |
rs530172843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213198 | ATCTGAAATCCACCA[C/T]ATCATTACCAGAAGG | 79931 |
rs530216615 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189865 | CTTGGCTAGCTCCCT[G/T]TTTATTTCCTCCCTG | 79931 |
rs530234797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159807 | CTTTTTGTTGGGGAA[G/T]TTTGTAGTTTTCTGC | 79931 |
rs530277693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218798 | GACTCCTGGGCTCAA[A/G]CAATTCTCCTCCCTC | 79931 |
rs530290628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133293 | ATATGCTGAATGTTT[A/T]GTACTTGTTGTCCTC | 79931 |
rs530293805 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186195 | AGAAGTGGCAGCAAA[C/G]AAAAAGAGAACCATA | 79931 |
rs530295970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179189 | GGTAGCTAGAACACA[A/G]GGTGCACTTTGGGAA | 79931 |
rs530316645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225311 | GCTAGAATATTTTCC[C/G]CCCATATGATGTCTT | 79931 |
rs530330464 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218335 | TGGAAACAGACAAGA[C/T]GGAAATGGTCTCAAA | 79931 |
rs530361866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173364 | AGAGATTAATTTGCA[C/T]TTCCAAAATAGAAAT | 79931 |
rs530367021 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143946 | ACCAACAAATAGCAC[-/A]AAAAATGCAGGAAAC | 79931 |
rs530515159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134573 | CAAGTCTCAAATGAC[C/T]TGAAAACATTCGAAA | 79931 |
rs530528069 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158970 | CTACTGGCTGGGTCC[A/G]GTGGCTCACGCCTGT | 79931 |
rs530555958 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135093 | GTCGAGGGTCCCAGG[A/C]AGGAGGCCAGGGCTT | 79931 |
rs530577518 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206072 | GTAACTACTCCCATG[A/T]TTCAATTACCTCCCA | 79931 |
rs530587194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181122 | AGGAAGGTAATAAGG[A/T]TGTAGAAGAGGTTTT | 79931 |
rs530607580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194278 | CTGAGGAAAAAAATA[C/T]TTTTGTGCACGTCTT | 79931 |
rs530620506 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207266 | ACAATGATCAATGAC[A/G]TATTTTAACTCAAAG | 79931 |
rs530621115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187748 | TTTTTGACCAAAGTC[C/T]ATGGATGGGATTCAA | 79931 |
rs530660255 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180473 | AAATAGTGTCAAATG[C/T]AAATAAAAAGACAAG | 79931 |
rs530688664 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141341 | AGAACAACTTAAGTG[G/T]GTCACTTTTTCTTGG | 79931 |
rs530734325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180777 | TGGTTTTCAAACTCA[A/G]CTCGGTCCTCACTAC | 79931 |
rs530809697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189412 | ACATCAGGAATCTGG[G/T]TGACCCAGAATGAGA | 79931 |
rs530853960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147630 | GAAAAGTGACTAAAC[A/T]AAAAACAAAAACAGG | 79931 |
rs530870631 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193831 | TCACATCTGTAATAT[G/T]CTTGCCAAGATTATA | 79931 |
rs530872717 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121130991 | TACAGAGCTTCAGGT[A/G]TATCCAGATACTGGA | 79931 |
rs530895329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156052 | TCCTGGCTAGAGTGT[A/C]ATTGGAAAAGGAAAT | 79931 |
rs530958350 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171678 | AAAGAGTACTGCCTG[A/G]ATGTTTCTCAGTTCT | 79931 |
rs530958507 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229174 | CTGATCCAAGCAAGA[A/G]GTTATTTCCATCAAA | 79931 |
rs531055533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155209 | ACCTCGTGATCTGCC[C/T]GTCTCAGCCTCCCAA | 79931 |
rs531067547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169184 | TGGCAAGGTCCTGCA[A/C]AATCTAGCCCAGGCC | 79931 |
rs531070563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188660 | ATAATCCAAAATGTT[A/G]TGGTTTACTGCCTTG | 79931 |
rs531071574 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215881 | TTAGGTGCCACATTA[-/A]AAAAAAAAAAAAAAG | 79931 |
rs531089172 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204594 | CTTAATCATTTCTCT[A/G]TGATGGAATAGCAAG | 79931 |
rs531110000 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205929 | ATCATGGCGGAAGGC[A/G]AAGGGGAAGAAAGGC | 79931 |
rs531127977 | in-del | -/A | 0.284733 | 0.247575 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197532 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 79931 |
rs531168704 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203477 | TCAGGGGAAAGAATG[C/G]GACAGGGGTGAGGGA | 79931 |
rs531174485 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209677 | ATTTGTACCTCTGAA[G/T]CTCCATTAAACAAAT | 79931 |
rs531281393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208085 | CTTGCAGAACTGTAA[A/G]TCCAATTAAACTTCT | 79931 |
rs531293102 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158770 | GAAATCATTAAAATT[C/T]GGTGAATCAACAAAG | 79931 |
rs531311273 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154309 | TACTGTCTCTGTAAT[C/T]CCTCCTCATTTCTCT | 79931 |
rs531350651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202872 | AGTCAAAACCAAAAT[A/G]TAATACCACCTTACT | 79931 |
rs531355335 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222780 | AAAATCATGAAAATG[C/T]GGAGCTGAGGGTGTT | 79931 |
rs531385813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176497 | AATTTTGAGGCTCAA[A/G]CTCATCCTACTAGCA | 79931 |
rs531435644 | in-del | -/A | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217027 | AATGAAAAAAAAGAG[-/A]AAAAAAAACTGTACT | 79931 |
rs531439698 | snp | A/C/G | 3.29648e-05 | 0.00405974 | missense | TNIP3 | GRCh38.p7 | 4:121157180 | TCTGCCTCTGATGCG[A/C/G]ATCCTTCTCCCGCGT | 79931 |
rs531473406 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175833 | CCTTTAATTTTTATG[A/G]GTTTTAATTATTTTG | 79931 |
rs531475486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210239 | TAATTTATAATAAAG[A/G]AAGGAAAAATTACTA | 79931 |
rs531503121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137019 | CTCATACACTGACTA[C/T]AACATTTCATTATTG | 79931 |
rs531652935 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146507 | TATGTTCAATTACAC[C/T]TAATTTTAGTATGCT | 79931 |
rs531654276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165326 | TCCTGAAATGAGTGA[A/G]ATGGTTCTACGCCCC | 79931 |
rs531664701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137662 | GCAAAACTACATGTG[C/G]TGTCCCTGACTCCCT | 79931 |
rs531717939 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217051 | CTGTACTTCCGACAG[A/C]ATTTGTTTCTCATTT | 79931 |
rs531724501 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131633 | TTTTTTGGTGGTGTG[G/T]AGTGGGTGGGTAGGG | 79931 |
rs531764477 | snp | C/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164279 | GCAATAGGTTTTCAT[C/T]AAAAATGAACAGAAG | 79931 |
rs531771572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138566 | TTGAGTAAACATCCC[C/G]AAAAGATCCCATTAA | 79931 |
rs531779540 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186188 | AAAGAGGAGAAGTGG[C/T]AGCAAAGAAAAAGAG | 79931 |
rs531815725 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223430 | CTTTAATGCTGGATT[A/C]GTTCTCATTATTTCC | 79931 |
rs531844066 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161279 | ATAAACAGAAGTACT[C/G]TTCCTCAGAAACCCC | 79931 |
rs531908403 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188454 | TTTCAGGTGTTTGGA[G/T]CCCTCATATTTTTGT | 79931 |
rs531932952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191554 | ACATTCACCTCATGT[A/T]ACCACATCCTGTGTC | 79931 |
rs531933300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139333 | CTAGATATTGAATGT[C/T]GAACAAATTGCATTG | 79931 |
rs531943953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184744 | TGTTTCTTTCAGGCT[A/G]TGAAATATCTGTACA | 79931 |
rs531963876 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202289 | ACTGATCTTTGACAA[C/T]GCAAACAAAAACATA | 79931 |
rs531992648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179875 | TTGAATTCACTTCAG[A/G]AAAGACTGAGTGGAA | 79931 |
rs532012741 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151534 | GCAACAAAAGTAGTT[C/T]AATAATTTATGTTTT | 79931 |
rs532058686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153328 | GCATTCTTGGCTGTT[C/T]TAATATCTACAAGGT | 79931 |
rs532058719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146445 | TACATTTTCCTTCAT[C/T]AACATCACTATTTAC | 79931 |
rs532148369 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153325 | ACAGCATTCTTGGCT[A/G]TTCTAATATCTACAA | 79931 |
rs532226323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192503 | CAGTTGTTATTATGT[A/G]TAGGGTAATTCTACC | 79931 |
rs532251709 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199340 | TATCCTATAAAGCTA[A/G]TTGTTACTTAGACAG | 79931 |
rs532265018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158603 | CAAAGCTCTTTGTAG[C/G]TGAAATGAATGAGAC | 79931 |
rs532265486 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174624 | CTAAGTCGGTTTTAA[G/T]GACAAACGTTTATTT | 79931 |
rs532300094 | in-del | -/ATTATGATGATGATG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176512 | GCTCATCCTACTAGC[-/ATTATGATGATGATG]ATGATGATGATGATG | 79931 |
rs532307678 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150758 | ATGCCTCCAACAAGA[A/G]AGAGGGACATCCACA | 79931 |
rs532332077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193877 | TACAAGGAAACATTA[A/G]CCAAAAGAAAATTGA | 79931 |
rs532432134 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204659 | ACAATCAATGCACAA[C/T]AGAAATACCTGTCTA | 79931 |
rs532443085 | snp | C/T | 3.29533e-05 | 0.00405901 | missense | TNIP3 | GRCh38.p7 | 4:121154561 | GATACCTTATTGAGG[C/T]GTTTTATTTCACATT | 79931 |
rs532446958 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181120 | AGAGGAAGGTAATAA[A/G]GATGTAGAAGAGGTT | 79931 |
rs532494612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205164 | GGGAGATGGGAATTG[C/T]AATTTTAAATGGAGT | 79931 |
rs532510710 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144392 | AAATGTTTTCTAAAG[A/C]GTTTTTTTGTTTTTT | 79931 |
rs532513998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199882 | ACATGGCTTAGGAGC[A/G]AAGGCTGGGATACAG | 79931 |
rs532518918 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121161190 | AAGAGAATTCATCAA[A/G]TTCTTTCTTGTTGAT | 79931 |
rs532542809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207097 | TTAGTGAAAATATAG[C/T]ATGTGTGATCTGGGG | 79931 |
rs532550673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173753 | CCTGTCTCAGCTTCC[C/T]GAGCAGCTGGGGTTA | 79931 |
rs532580930 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167081 | TGGTTTTAAAGATAG[G/T]ACCATCAATCAAATT | 79931 |
rs532592566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147698 | GACTGAAGGTTAGCA[A/G]ACTGGTATATAAAGC | 79931 |
rs532621182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206436 | TTAAAAATAATCTGT[A/G]AATTATTCATTATGC | 79931 |
rs532640656 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195290 | CAGATGGGATTATAG[A/C]AGGAAGAAATGTGCA | 79931 |
rs532640991 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168293 | CTCACTGCAACCTCC[G/T]CCTCGTGGGTTCAAG | 79931 |
rs532709037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213238 | CTGATGGCATTCGAT[C/T]CTGTTTAATATTAGG | 79931 |
rs532724430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214605 | TCCTTTCTTTTTCCC[C/T]TCCTTCTTTCTTTCT | 79931 |
rs532728054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134292 | CAGAAGTGACTGGCA[A/T]GCAATGCAATCAGAA | 79931 |
rs532787399 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160535 | TGCTAAAATTGTTAT[A/T]CTTTTCACTACTTCC | 79931 |
rs532790894 | in-del | -/A | 0.477853 | 0.102875 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136858 | GTAAGACTGTCTCCG[-/A]AAAAAAAAAAAAAAA | 79931 |
rs532808070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208781 | TTGGAATTTCTTAAG[C/T]GATAAGAATGACTGT | 79931 |
rs532831128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133408 | GAAAAATTATGTTGC[C/T]GAGGACTGTGGTCAC | 79931 |
rs532846526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221093 | CCTTTTGCAGTTTCC[A/G]AAGCTTGAGATATTT | 79931 |
rs532847709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218916 | TTAAAAACCACAGAA[A/G]TGGCCAGCCATGGTG | 79931 |
rs532860123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219522 | AAAATAACCCAACTT[G/T]GAAGGATAAACTTAC | 79931 |
rs532883694 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174694 | AAAAAAGGAATAATT[C/G]ATCTTTTTTTTGCTA | 79931 |
rs532896650 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208196 | CTTCTACCTGGGGAC[A/C]AGACTGCCTCTATAG | 79931 |
rs532904480 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121218862 | CTACTTTCCCTAGCT[A/T]TAGCCACATAAAATT | 79931 |
rs532926644 | snp | G/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131538 | GTCTGAAATATTTCT[G/T]TAAGTATATATGGAC | 79931 |
rs532959819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201149 | GAGTAGGGGGCAGGA[A/G]AGAAAGTTTTGAGGT | 79931 |
rs532990568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162253 | TATTTTCTATCTTTT[C/T]TCTGTTTGTTTATGT | 79931 |
rs532992045 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204370 | TCCCTACCCACTTCA[A/T]GTTGTCCTGCCTTTT | 79931 |
rs533033875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175073 | ACATTTGCTAAACAA[C/G]TCTTATGAACATGTT | 79931 |
rs533129553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137909 | TTTTGATTATGTATA[C/T]TTGATGAGAATAGAA | 79931 |
rs533173468 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174432 | AATAATAAACAAAAT[A/T]AAAAAAATAAGAAAG | 79931 |
rs533243216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148095 | ACAGTTAAACTGATG[C/T]TCTGTAAACAATTAC | 79931 |
rs533265438 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227837 | TGTAAGGACCACATA[G/T]GTCACACACTCATTT | 79931 |
rs533268344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143974 | AACATGGCACTAAAT[A/G]GATCACAAAAAGAAC | 79931 |
rs533273405 | snp | C/T | 3.39184e-05 | 0.00411802 | missense | TNIP3 | GRCh38.p7 | 4:121141912 | ACAGGGTGGGCAATA[C/T]ATCTGAGGAGAACAA | 79931 |
rs533458632 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145113 | ATGCCAGAATGATTT[G/T]ACCTAAATATTCCTC | 79931 |
rs533460176 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229307 | AAAAAACAAACACCC[A/G]TGGCAGGGTGCGGTG | 79931 |
rs533460948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156170 | CTGGACTGGCATTGT[C/T]TGCGCGAATTTCAGA | 79931 |
rs533473083 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208069 | CTGAGGCCTTTCCAG[C/G]CTTGCAGAACTGTAA | 79931 |
rs533484640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137109 | GCTTGTGTAATATTG[G/T]TCCAGCAAGAATCTA | 79931 |
rs533497891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189914 | TCACTATACTGATGC[C/T]ACAAACTAGATCCAA | 79931 |
rs533502714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182855 | TAAAAATTATTCAGG[C/T]GTAGAGTGAGTTTAT | 79931 |
rs533523679 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210455 | CTTCACACAGCCTCT[A/G]AAATCATTATAGATC | 79931 |
rs533585819 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196392 | CTGTAACAAGTATAG[G/T]TTTTTTTTAAGTTAG | 79931 |
rs533672317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190416 | AAATTGACAAGAATA[A/T]CTAGATCTGAATTGG | 79931 |
rs533726428 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215313 | TTTAAGAAATACTGA[C/G]TTGAGAACTTGATCA | 79931 |
rs533739781 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190897 | TGGGATCTTCTACCC[A/G]GGGAGCCAGGACCCT | 79931 |
rs533828615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209014 | CTGGACATTGGGATG[C/T]AAATACTCTTAAAAA | 79931 |
rs533837442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143843 | CTCTAACACACTTTT[C/T]CTCTATAAGGCACAT | 79931 |
rs533838790 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193293 | CATATGGATGTGAAA[C/T]TGATGAGCCTGGAAT | 79931 |
rs534003314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149846 | CAAAGGTTAATTGGC[A/G]TGCCCCTCTTTTAAT | 79931 |
rs534044761 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151224 | CAAATAGAAAAGGTT[C/G]ATTTTCAGAGATCTA | 79931 |
rs534052224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186019 | CCTCAGAGCTGGGGC[C/T]CTGCGTCCTCTCACG | 79931 |
rs534072362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197373 | TCTCTGCTAAAAATA[C/T]AAAAATTAGCTGGGC | 79931 |
rs534147962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197720 | AATTACCCAAGAATT[C/T]TGAAGCAATTTGGGG | 79931 |
rs534199113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191907 | TTCAAATCTTTGGAA[A/G]TTATGACAAAGGTGG | 79931 |
rs534220842 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215974 | TGGAAAGCGCCTAAG[A/T]AAGGGATTTTTTTTC | 79931 |
rs534234302 | in-del | -/TATTTTT | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150383 | ATTTTCTCATATATG[-/TATTTTT]TATTTTTTTTTTCAG | 79931 |
rs534248322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151956 | GGTGGCACGAGCTGA[A/G]TAGCCTTAGGTAATT | 79931 |
rs534296453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166376 | TAAGAATTAATTGGG[A/T]CTTTTCTGTTACATA | 79931 |
rs534342901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204688 | TAGATATATTCTTAC[A/C]TACTAGTATTTTATT | 79931 |
rs534356628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167264 | GTGGCTGTGTGTATG[C/T]CAATATATATATATT | 79931 |
rs534368435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171552 | ACCAAGAATAACCAA[C/T]AAAACAAATTAGTAG | 79931 |
rs534416291 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173295 | TATGAGGTGGCTTGA[C/T]CTTTGACGTTGTATC | 79931 |
rs534433140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164910 | GAGAATCATTTTCAC[A/T]TTAATTATTTGACTG | 79931 |
rs534434358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133543 | TGATACCTCTCCCTA[A/G]GTATCTTAAATATTT | 79931 |
rs534441128 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149104 | GCTAAGTGAATTTCA[G/T]CAGATTGATTAAATT | 79931 |
rs534470210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178079 | GTTCCTGACACCAGC[G/T]GGAGCTCTGCTCTAG | 79931 |
rs534471295 | snp | G/T | 0.000247209 | 0.011115 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121138635 | TCACCATTTGCCTTG[G/T]GTTGTACATCTGGCG | 79931 |
rs534477946 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132209 | AGAAATTTTTACCCC[A/C]GGAAACACACACACA | 79931 |
rs534505591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223572 | AGATTTAAATTCCAC[C/T]ACATTTATTTAGACC | 79931 |
rs534546648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139849 | TGACGTGAGCCTCAG[C/T]TTTATATTCCAGGAG | 79931 |
rs534605081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146457 | CATTAACATCACTAT[C/T]TACCCATCGTGGCAA | 79931 |
rs534714097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181254 | ATGAGGGTACCAGAG[C/G]GAATTGATATTGTCA | 79931 |
rs534719255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212409 | TAAGATTGAGAGACT[C/G]CTTTCTTAGTGTGGA | 79931 |
rs534720887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218962 | CCTAGAACTTTGGGA[A/G]GCCGAGGCAGGTGGA | 79931 |
rs534736289 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227907 | CTGAGAGAGCTAGCA[A/C]CCAGGTTAACATTTA | 79931 |
rs534817797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187295 | TTGTTCCCACCTTGG[G/T]ATCTGTTCCAAGAAT | 79931 |
rs534842268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193447 | CCTATACTGATGCAA[A/G]TGTTAAAATAAACAT | 79931 |
rs534863368 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199775 | GATAAGAAAGGAAAC[C/T]AAGGAAGCCTAATCT | 79931 |
rs534901792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194036 | TCCTGGATTGGAGCC[C/T]TTTTTATGCAAAGGA | 79931 |
rs534942232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185255 | TCAAACTTTATGGAA[C/T]ATGCCAAGCAGTTCC | 79931 |
rs534946417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192731 | GGGTGTAGAGAATTT[A/G]TAGTGTACATGTGAG | 79931 |
rs534977116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142019 | TCTTAAGGTTCCACT[C/T]AATCTGGCATAATTA | 79931 |
rs535031718 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212398 | ATATAAATAAATAAG[A/C]TTGAGAGACTGCTTT | 79931 |
rs535059088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195437 | TTATAAAACCCAAGT[A/G]TTATGGACCTTGTTT | 79931 |
rs535152566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149111 | GAATTTCAGCAGATT[A/G]ATTAAATTTAGACAC | 79931 |
rs535153102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208317 | AGGGATAACATCACT[A/G]TTGTAAAACCCAGGA | 79931 |
rs535206739 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155376 | TCATTGTGAGAAAAC[A/T]ATACTAAATATCTCA | 79931 |
rs535236548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201254 | TATTTAGTGCTTGGA[A/G]GGACCACAGGAGGGC | 79931 |
rs535247321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214416 | TTCATCATTGTTAAA[C/T]AGAACTAAACAGTAA | 79931 |
rs535270179 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147279 | ATTATTGTAAAGAAC[C/T]CTCCCAACTAGTGTT | 79931 |
rs535287628 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185929 | TGTTAAAATTGTTTC[A/G]ACTTCAGTGGCAAGC | 79931 |
rs535303930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205932 | ATGGCGGAAGGCGAA[A/G]GGGAAGAAAGGCACC | 79931 |
rs535349405 | in-del | -/TTG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197173 | TAAGAGTTAAGAAAC[-/TTG]TTGTTTAGCTTTACT | 79931 |
rs535351059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213498 | TTGGAAGTCCGAGGC[A/G]GGTGGATCATGAGGT | 79931 |
rs535359274 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226654 | GAAATATCAGCACTG[A/C]GCCTGTAAGCATCTA | 79931 |
rs535362417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214024 | CTTTGAAAGGAAACC[C/T]GGTGTGGCAACCATA | 79931 |
rs535418752 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208703 | GGGCTGTTAAAAGTG[C/G]GTGTGATATAATAAA | 79931 |
rs535458469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188993 | TATGGTTACATGGTA[A/C]GGTTGCCTCATTAGT | 79931 |
rs535481016 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186996 | ATGTTTCATAAATTT[C/T]GATTTGACCTAGATT | 79931 |
rs535495501 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162285 | TCAGCATTTTAGGGT[C/T]TGATGGTATTTTAAG | 79931 |
rs535557675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135579 | ATTTTTGTATTTTTT[G/T]GTAGAGACAGGGTTT | 79931 |
rs535577278 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205198 | CAAAGGTGGGACTTA[C/T]TGAAAGGTGACAATT | 79931 |
rs535615598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137317 | AATTGCATATATTAT[A/G]CAACACACATTCCGG | 79931 |
rs535625372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168877 | GAGCGTGTCCAGCAG[C/T]GACTGATCTCTGACT | 79931 |
rs535733483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142973 | GATAGTTTTAAATTG[C/T]TATTCCAGTTTTTTG | 79931 |
rs535734017 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212661 | TAGCTCTTCAAACTA[G/T]AAGGTTCTCTTCTAC | 79931 |
rs535745368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135387 | ATGAAGTTACTTCTT[C/T]TTCTTTTTTTTTATT | 79931 |
rs535758605 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229365 | GGAGGCCAAGGCAGG[C/T]GTATTGCCTGAGCTC | 79931 |
rs535812923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209829 | AAATATTTATTGAAG[A/T]TTGCTGCAGGCCAAG | 79931 |
rs535820633 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170748 | ATATTGAAGTATTAA[C/G]TGATGATCCCCCAAA | 79931 |
rs535834964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185007 | TCTTGAGGCAGCTTT[C/T]GGACCTATTCTGAAC | 79931 |
rs535835311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178181 | CATATTTGAGTTTAG[A/G]TCCAGAATCTAAATC | 79931 |
rs535895975 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216746 | GTGAGTTAAGGAAGA[A/C]TCTCATGACAGGGAG | 79931 |
rs535930551 | in-del | -/TAA | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198839 | GCTGTTCTTTCAAAG[-/TAA]TGATGGCCTGAGCTG | 79931 |
rs535933902 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222867 | CTAGAGTGCAGTGGC[G/T]CGATCTTGGCTCACT | 79931 |
rs535943264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215240 | CTCTTTTAATGAAAA[C/T]GTTCTCATAGAGAAT | 79931 |
rs535954331 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209056 | CTGGGTTCTGTATGG[A/G]TATAAATACTCTTGA | 79931 |
rs535966677 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194158 | TTGTGGTATATCCTT[G/T]TTTAAGGATACGCAT | 79931 |
rs535976979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184495 | TGGAGTGAGCTGAGA[A/C]TGAATCATATGGGTA | 79931 |
rs536048211 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182949 | TTATGTTTTCATTAG[C/T]CCATGCCATGAGAGC | 79931 |
rs536102278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144295 | CTAATTATAAACTAA[A/G]TGAAACTATTAAACA | 79931 |
rs536112258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157374 | AGGAGAGGTTCTAGC[A/T]CCCACCGTCCCGAAC | 79931 |
rs536132287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149707 | GGAGGCGGAAGTTGC[A/G]GTGAGCGGAGGTTGT | 79931 |
rs536155422 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170475 | CGTTTAAAGAGCTGG[A/C]CTGTTTCCGTGTATT | 79931 |
rs536163654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150426 | TTTTCCATGATGATG[C/G]TTATGTTAGTCAATC | 79931 |
rs536211441 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121130916 | GAATTATGTTCCAGG[C/G]TTGCAAAGGGCTGAA | 79931 |
rs536215688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139301 | TTTTCTCCTAGGTTT[A/G]CACCAGTTAAGAACA | 79931 |
rs536271333 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224375 | CTCAAAAAATAAAAA[A/G]AAAAAAGAAAAAAGA | 79931 |
rs536328666 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144631 | GGTCTCAAACTCCTG[A/T]TCTCAGGTGATCTGC | 79931 |
rs536332339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205255 | TGGGCCATGTGGCTT[A/G]TTGGGGAAAGAGCAT | 79931 |
rs536373874 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165221 | GAGAGTGATTGAGTG[C/T]CCCACATTTGGCCCT | 79931 |
rs536376868 | snp | A/T | 1.64844e-05 | 0.00287087 | intron-variant, splice-acceptor-variant | TNIP3 | GRCh38.p7 | 4:121138686 | CACTGATAGTCTGGC[A/T]GTGTGGAACAATACA | 79931 |
rs536407056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197315 | GGTGGATCACCTGAC[A/G]TCAGGAGTTCGAGAC | 79931 |
rs536534806 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143440 | ATGTCCCACATTCCC[A/G]TAAGGGATGGTCAAA | 79931 |
rs536537105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202982 | CACTGCTGTTGGGAA[A/T]GAAAACTACTACAAC | 79931 |
rs536549987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211439 | CAACTCACTGAGGAT[A/G]TTACATTTAAATTTT | 79931 |
rs536630150 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157962 | AGGAACATTATCCTG[C/T]ACCTTCTAAATTCAA | 79931 |
rs536632173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160275 | CTTGAGGATAGGAGT[C/T]CTAGACCAGGCTGGC | 79931 |
rs536686125 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179513 | ATGCAAAGGCATTTG[A/G]TTTCAATGATGTGTG | 79931 |
rs536697569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146494 | GAGTCTACTTTAATA[C/T]GTTCAATTACACTTA | 79931 |
rs536716043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216257 | TCAGATAGATAGGCC[A/G]TACTGTTACCCGTCA | 79931 |
rs536739861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219785 | GGTGTCCAAATGTAA[C/T]TCACATACAATCAAA | 79931 |
rs536750419 | snp | A/T | 0.00756359 | 0.0610294 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213427 | ATAATCCATTTTTTT[A/T]AAAAAAAGACATTCT | 79931 |
rs536751312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152962 | ACAAATAAAGTCATA[A/T]AAGTTAGACATTATA | 79931 |
rs536779630 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137244 | CATTCCAGAGCAATA[C/T]AAAATGGAAAATTAT | 79931 |
rs536941713 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217225 | TAAAAGCCAATTCCT[G/T]CAGGCAATTAACACA | 79931 |
rs536968146 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132955 | GCTGGCATTTTGGCT[C/T]GGGCATGTGAAAGTA | 79931 |
rs537016408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206808 | CTCCTGGACTCAAGG[C/G]ATCCACTTGCCTCAG | 79931 |
rs537042333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174672 | AGCTATCTTCCTCAC[A/T]GGAAAAAAAAAAGGA | 79931 |
rs537056760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175432 | ACTTTTCACTTCAAG[C/T]CTTGGTTGCTTCCCC | 79931 |
rs537091039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226978 | TCAACCCTGTAATAT[A/C]CCAAGAGGGAAAGCA | 79931 |
rs537093505 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138330 | AGCTTTGTTGTTGTT[A/C]TAATACAGCTCTGCT | 79931 |
rs537119283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167371 | AGTGCTCATTATCAC[C/G]TTTAATAGCTATGGA | 79931 |
rs537140375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212960 | CCATAAACATTCCTA[C/T]ACTTCTCTTCCTTTT | 79931 |
rs537152998 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140734 | AATTTAATGTTATTG[A/G]TAAAGACTGAAAAGT | 79931 |
rs537212693 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121145091 | TCTGGTAAGAAAGCA[A/G]CTCAGAATGCCAGAA | 79931 |
rs537240179 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180153 | CGCCTGTAATCCCAA[A/C]ACTTTGGGAGGCCGA | 79931 |
rs537259597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173520 | TTGAGTTTTTTTTTA[A/T]AAATTATTTTCTCTG | 79931 |
rs537280606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219066 | TTAGCTGGGTGTGGT[A/G]GTGTGCACCTGTAAT | 79931 |
rs537290074 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148304 | CAGTTAAAATATTTA[G/T]GGAGAAAGTCAGCAG | 79931 |
rs537317031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154235 | GTTGACCAAGAGATA[C/T]GTTATTGTTCGCAAA | 79931 |
rs537334672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139904 | CTGTAATGTTACCAA[C/G]ACTATAGCATGTGAC | 79931 |
rs537379160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186333 | GGAACTGAAAGCACA[A/C]AGGAGGGGTGGAGCT | 79931 |
rs537400692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136175 | CTTAATCTTACATAG[C/T]ACCGTGCCTTTTACT | 79931 |
rs537470381 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221579 | CAAATAAGATTCCTA[A/C/T]ACCCAACAGGTACTT | 79931 |
rs537485599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143770 | CTTATTTAATATGTA[C/T]TGTTGATTAACTCTG | 79931 |
rs537529774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202234 | TAGACCAAGGGAACA[A/G]AATAGAGAACCCAGC | 79931 |
rs537562491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135591 | TTTTGTAGAGACAGG[C/G]TTTCACCATGTTGCC | 79931 |
rs537629712 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208531 | CATCAAATTATCCTT[A/G]GCCCTGATCCCTGAA | 79931 |
rs537740778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214477 | GAGAATGGGACTCAG[A/G]AGCTCACACAAAGTC | 79931 |
rs537754381 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173363 | TAGAGATTAATTTGC[A/T]TTTCCAAAATAGAAA | 79931 |
rs537757251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208360 | CAGACCCTGAACTCA[A/G]TGTGTCGGCTGGAGC | 79931 |
rs537798505 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183976 | TGAAACCATCCTACC[C/T]CCTGCCCCAGTCCAT | 79931 |
rs537840210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157405 | ACAGATCGGGATACT[C/T]GCGTTTCAAAGGGAG | 79931 |
rs537924481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163937 | GTTAAAAATATAGAG[A/C]AAATCTTAGCTAAAG | 79931 |
rs537927673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195493 | ACCATTTTTTCACAG[A/G]TGAAATGTCAAAAAC | 79931 |
rs537946534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209883 | GTATATTTCTTACTG[G/T]AAAAAACTAGTTGGT | 79931 |
rs537998256 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165518 | ATTACATATTTCCAT[C/G]TTCTTGTGTTAATCT | 79931 |
rs538015637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208895 | CTTCAGGGTGGGGCC[A/G]CCAGAAAGATCAAAT | 79931 |
rs538088321 | snp | C/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132113 | TTAGGATCACTGAGG[C/T]CAACAATATGTAGTC | 79931 |
rs538144525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222352 | GCACCCCAAATTACA[A/C]ATTCGCTTTTTCAAA | 79931 |
rs538165584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222916 | GTTCACGCTATTCTC[C/T]TGCCTCAGCCTCCCG | 79931 |
rs538211940 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203901 | GTATATATACAATAT[A/G]TGTGTGTATATATAT | 79931 |
rs538225698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211708 | GCCACAGAAATGGAA[C/T]GTACTGCCATGGAGG | 79931 |
rs538247015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179255 | GGAAAAATATGTACG[A/G]ACTTGGCTTTCTATC | 79931 |
rs538247054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121172256 | TCAACCTTAGAGTGG[A/T]GTGGAAGCAGAGCCA | 79931 |
rs538259199 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173167 | ATAACACACCTAAAA[A/T]TTGTAGCAGGAGACA | 79931 |
rs538342118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210721 | GAGAGAGACAGCAAG[A/C]TCTCTGGTGTCTCTT | 79931 |
rs538348805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203130 | ATACTTGTAGAAGCA[G/T]GTTTATAGCAGCACA | 79931 |
rs538355504 | in-del | -/TA | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191996 | TATTTAAGAGCTGTC[-/TA]AAAATTTTATAATAG | 79931 |
rs538383732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178856 | TGGAACACTTTATAC[C/T]CCATCCTCAAGAAAT | 79931 |
rs538489650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145370 | TCACTTTAGATATCA[C/T]TAAGATTGTCCTTTA | 79931 |
rs538500786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138777 | TGTGGCTTTTATTAA[A/G]CAGGCAACACAAAAG | 79931 |
rs538512309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151086 | TCTATTTTGAAGACC[A/T]TTGGTTCATGATAAG | 79931 |
rs538514503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144145 | GATGATGAGGATAGA[C/T]TGTACATGTCTCTTT | 79931 |
rs538543211 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148324 | AAAGTCAGCAGTAGA[-/G]GCACTGCAAAACTAC | 79931 |
rs538549603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144698 | TGAGTCACCGCACCC[A/G]GCCTGTTTTTGCTTT | 79931 |
rs538551979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138055 | AATCAATAAAAAATA[A/G]GATTTAAAAAAGTAC | 79931 |
rs538568177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183535 | CCCACTGCCAGTCTG[G/T]CCTGTTAGGGCCACA | 79931 |
rs538575438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176326 | GGTGTCCAAAGGTTT[C/T]CCAGTGAAAGCTAAA | 79931 |
rs538680149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226766 | GGGAAGTTTATTTTG[C/T]AATCTCGTTTGGGAA | 79931 |
rs538729370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199400 | AGGTCTATAAGAAAA[C/T]AATATTACTATGTTT | 79931 |
rs538734049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224603 | TCTTATTGTTTTCAC[A/C]CATATTTAGGCAGGT | 79931 |
rs538790925 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142377 | GCTCAAGAAGGCATG[A/T]TATTTTTTCAAAAGA | 79931 |
rs538825982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205846 | CCTGAGACTGGGTAA[C/T]TTACAAAGGAAAGAG | 79931 |
rs539044898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180233 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 79931 |
rs539049027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161574 | GGTAAGTTTCATGGA[C/T]ATATTTTAGGTATTT | 79931 |
rs539092895 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136523 | AACAAAACCTATTTC[A/C]TAGCTTTGTTGTGAA | 79931 |
rs539101442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153524 | TTTTGCCCCGCATTT[A/G]TATGTCTGAGCATGG | 79931 |
rs539104056 | in-del | -/TTCC | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218514 | TTCCAATAGTTTATT[-/TTCC]TTCCTTCCTTCCTCC | 79931 |
rs539106880 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151861 | AACAAACACCTATAA[C/T]CTATTCTAGAATATT | 79931 |
rs539120534 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140373 | GAAAGAAAATGTAGG[C/T]CATTCTACATGGCTT | 79931 |
rs539280299 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212987 | TTTTACGAGAAAAAA[A/T]AATGGAGCTTTAAGG | 79931 |
rs539334043 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141404 | GTCAAAATCTATTTT[G/T]CACATATGTAGCAAT | 79931 |
rs539342088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227228 | CCGGGAACACATAAA[A/T]CCTTATCTTAATTGT | 79931 |
rs539356558 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219906 | AACACATAATACCTT[A/C]CTGGAAACTGTTTCA | 79931 |
rs539372066 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209918 | CATTTTTCTAGTAAT[A/G]TATAGAGTTTTGCTG | 79931 |
rs539395294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200533 | ATTCATAGAGACCCC[A/C]GAGCACACATACCCT | 79931 |
rs539456848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194618 | TAGCCCAAGGATTCT[A/G]GAAAATGAAATGAAA | 79931 |
rs539458715 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170183 | AAGCAGTTGTTAATT[A/C]GATGTACCTTTCTCC | 79931 |
rs539521396 | in-del | -/GAT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176553 | GATGATGATGATGAT[-/GAT]AGTGTTGTGTTGGTT | 79931 |
rs539583636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200118 | GCAACACTGTGACCA[C/T]GTTCACTGGGTTCCT | 79931 |
rs539590511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213465 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 79931 |
rs539635885 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188830 | CTTGGACATGGGTTC[A/C]TTTTGTTTGCATGAC | 79931 |
rs539641493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173911 | GCTGGGATTACAGGC[A/G]TGAGCCATTGCACCT | 79931 |
rs539648578 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182238 | GAAGTTCAAAGTCAA[A/C]CAACTCCTTTAATCA | 79931 |
rs539682213 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228545 | TCTTTACTGTATTTT[C/T]TTTTTCTGTACTGTA | 79931 |
rs539710031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148367 | TGGTCTTCCCACAGG[C/G]TTTATGAAAAAAGAG | 79931 |
rs539746534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148939 | TGTCTCCCATTGCTA[A/T]TATGTTACTGACAAT | 79931 |
rs539778665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173577 | ATAGCAATGCAGATC[A/C]CTCTGTTTTTCTCTT | 79931 |
rs539814112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214894 | TATTCTGCTGCATGT[A/C]GAGTCTTTCCGTTGA | 79931 |
rs539819210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176053 | GTCATAAATTAACCA[A/T]GGGATCAAATTAACT | 79931 |
rs539878865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215449 | GTCTCTCACTCAAGA[C/G]AGAGTATCAACTGAG | 79931 |
rs539902547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222035 | TTGTCCCTGAATGTC[A/G]ATCACCAGCTCTAAA | 79931 |
rs539937100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221749 | AGAACTACCCAACAG[A/G]GCTGTAACTATTTTT | 79931 |
rs539949256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214506 | TCCTCAGAATTCTCC[A/G]TGTAGAAGGAAATGG | 79931 |
rs539979713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175691 | GCATCCTACTCAAAA[G/T]TGTGTCTTATTTATC | 79931 |
rs539994588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189182 | AAAATAAGAATTTAG[A/G]ATGTTAGTGTTCTTT | 79931 |
rs539995804 | snp | C/T | 3.32375e-05 | 0.00407647 | missense | TNIP3 | GRCh38.p7 | 4:121154609 | TTGTTCGCAAGAGTA[C/T]TTTTTCCCTTTAAAA | 79931 |
rs540111858 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195040 | TGGCATGGTGGCAGG[A/T]GGCTGTAATCCCAGC | 79931 |
rs540150913 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228063 | TATCATTAGGAATTA[C/T]GTGAATTTTTCTTGC | 79931 |
rs540156662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152071 | ATAAATTGAATAGAG[C/T]ACACATAATTGTGTG | 79931 |
rs540173957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188541 | ATATGTTGTTGAATG[C/T]CATTGTTTAATGAGC | 79931 |
rs540174219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195556 | AACAATCGAATTCAG[A/G]TGGGAATTAACAAGG | 79931 |
rs540213469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183927 | TACAATATAATAATA[A/G]TACCAATACAGTGCA | 79931 |
rs540235768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170397 | ACACAATGACCACGG[C/G]GATACACAAAGTTAT | 79931 |
rs540247475 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218385 | AACATTGTATTTCCT[C/G/T]CCTAAATTGCCTTTT | 79931 |
rs540278257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138431 | GAGGTTCATGCATTT[C/T]TGCATTCGCACATTT | 79931 |
rs540280115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144788 | TTACAGGCAGGTATA[C/T]TAAAAGAGGTTAAGG | 79931 |
rs540286327 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177651 | AGGCTAACTTCATTC[A/G]GTGTGAAAACAAGAG | 79931 |
rs540307741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185344 | GTGCTGGCTTAAATG[C/T]CACTTTATGGCGAAA | 79931 |
rs540308904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223163 | TAACGGATCGCTTTC[A/G]TATCCATTACAGGTG | 79931 |
rs540326254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137499 | CTCACATTTCATATT[C/T]CTTTTCTATGATGCT | 79931 |
rs540338963 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144414 | TTGTTTTTTTCTTTT[C/T]TTTTTGAGACAGAAT | 79931 |
rs540348750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183049 | GTCTGAGAACAATGG[C/T]AAGAATTGAATCGAA | 79931 |
rs540370745 | in-del | -/AAT | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145150 | TCCACTTGGACAACA[-/AAT]AATATGTTATTCAAC | 79931 |
rs540373588 | in-del | -/TATT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158266 | CACCATTTGTTTCTC[-/TATT]TGTGGAAAATAGGTC | 79931 |
rs540460043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143065 | TTGCTTACTGAATGA[C/T]ATTGGAATTGTCAAC | 79931 |
rs540469615 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217039 | AGAGAAAAAAAACTG[C/T]ACTTCCGACAGAATT | 79931 |
rs540504700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149991 | TTCTACTTAAAATAA[A/G]TGCAAAAACCTTTGA | 79931 |
rs540507176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148590 | AGCTTTAAGACTGTG[A/C]ATATTACCCTTATTC | 79931 |
rs540564263 | snp | A/G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140722 | TCTTGAAAAAAAAAT[A/G/T]TAATGTTATTGGTAA | 79931 |
rs540569922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209333 | GCATGTTGGTCAGAA[A/G]TATGGGTGGTCACTG | 79931 |
rs540571510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202770 | AAAGTGGGCTAACGA[C/T]ATGAATAGATAATTC | 79931 |
rs540697056 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150689 | ATTTCTCAGAAGCTG[G/T]TGCTGCTGGTCCCAG | 79931 |
rs540708578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196968 | TACTCAAAGAACCAT[A/G]GGTAGAATAAGAATT | 79931 |
rs540735562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158509 | ACAACTCACTGACAC[C/T]GTTCATTAATTTTCA | 79931 |
rs540831984 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165206 | TCCTAAAATTCAAAA[A/G]AGAGTGATTGAGTGT | 79931 |
rs540857757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157521 | GATAAAAGACTTAGA[C/T]CCCACCCAGGGGAAT | 79931 |
rs540867829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213579 | AAAATACAAAAAAAT[C/T]AGCCGGGCGTGGTGG | 79931 |
rs540870334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172459 | AAAACCCGTAAGAGA[C/T]AGACTACATCAGTGC | 79931 |
rs540899619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225390 | AATTGATTTTTTACT[C/T]ATGCTCTGTGCAATT | 79931 |
rs540933084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210036 | GCGTGATTTGAACTC[A/G]GGGAGTCTGACTCAA | 79931 |
rs540936456 | snp | G/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228086 | TTTCTTGCCATACCA[G/T]AAAACAGTCTGCATA | 79931 |
rs540986264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198012 | TAAATATTGAGTAAC[C/T]ATGAAAATGTTCATC | 79931 |
rs541000526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158979 | GGGTCCGGTGGCTCA[C/T]GCCTGTAATCCCACC | 79931 |
rs541010636 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163161 | GTGGGGGAGGATAGG[A/T]GGGAGGAAAAATAGA | 79931 |
rs541052883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213105 | TATTGTTTAATTTTC[C/T]TAATGTCCACCAATG | 79931 |
rs541056041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152170 | GCAAGCATTCAGCTT[G/T]TACATAGAGGGTAGG | 79931 |
rs541060535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173657 | TCTTTGAGATGGAAT[C/T]TGGCTCTGTTGCCCA | 79931 |
rs541087821 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166230 | TTTGCCTCTTCTGTT[A/G]TGCAGATAAACAACA | 79931 |
rs541119656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226823 | AGTAACTTTATATTC[A/G]GAAATACATTCTTTT | 79931 |
rs541121408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204962 | TATTTCAGTATGTTC[A/G]TTATTCATTTGCTTT | 79931 |
rs541142695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212665 | TCTTCAAACTATAAG[G/T]TTCTCTTCTACTTAA | 79931 |
rs541147062 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169350 | CCTTTGTCAGGTAAT[A/G]GTGTAAGTGACATCT | 79931 |
rs541179211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219271 | GGCTGAGCATCCTCT[A/G]AAGCTAAAAGCAAAC | 79931 |
rs541179653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186136 | ACAGTGAGACTGAGC[A/G]TGGTGACTACAGCTT | 79931 |
rs541179746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143854 | TTTTTCTCTATAAGG[C/G]ACATCACATCCTTCA | 79931 |
rs541209930 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139154 | TGGGGATTTGGCATT[A/G]ACAGAAGTTCAGGAT | 79931 |
rs541253605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211096 | AAATAACTGGACTTG[C/G]AAAGCAGAAATGTCC | 79931 |
rs541272913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223979 | AAACATCAATACAAA[G/T]AACTATGCTGTCTCA | 79931 |
rs541289609 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222062 | TAAAATGAGAACAGA[C/T]TGTACATTATAGTAG | 79931 |
rs541290857 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200026 | GGAACTGCATCCCCT[C/T]AAAAACCACGGTCAG | 79931 |
rs541313400 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162297 | GGTTTGATGGTATTT[G/T]AAGTAAGCAGAGATG | 79931 |
rs541336020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153208 | AATTATATAATCACC[A/G]GAATGATGAAAAATT | 79931 |
rs541347271 | snp | A/C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194808 | GATTATAGAAACTTG[A/C/G]TTTTGGAAATATGAG | 79931 |
rs541370698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146827 | ATTAAAAAAAACTTT[A/G]GAATGCAATTTCTTG | 79931 |
rs541473742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142270 | AATTGTAGCCAGGGA[A/C]AACTAAAATCCAGAA | 79931 |
rs541485944 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222142 | ATTTTTGCAATGTTG[C/G]TATATTGCTCTTGAT | 79931 |
rs541499390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180378 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 79931 |
rs541499565 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228170 | GGGAATAAAATGTTT[C/G]CTGATGAAGTGCCTA | 79931 |
rs541499636 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159346 | CAGTAACTTTTAACT[A/T]TTTTTAGTTATTTGG | 79931 |
rs541501157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133143 | GAAAAATCTGGAATA[C/T]TTTGATTGAGTACTA | 79931 |
rs541530311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148011 | CAGAAGCACTGAAGG[A/G]AAACTACATCCAGCC | 79931 |
rs541533492 | snp | C/T | 1.7688e-05 | 0.00297383 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141813 | AAATGCACTCTTACT[C/T]ACTGGGTGCTCCCGT | 79931 |
rs541546267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194266 | ATTTCCAAATGGCTG[A/T]GGAAAAAAATATTTT | 79931 |
rs541561307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134149 | TTGATCTTCTATATT[A/G]TAAAGAAGTAATTTC | 79931 |
rs541572738 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171320 | GCAATTTATTTTGAA[A/T]TGCCTCAAAAAGTTA | 79931 |
rs541600954 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144294 | GCTAATTATAAACTA[A/C]ATGAAACTATTAAAC | 79931 |
rs541632949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200171 | GACATGCTAAGGGAG[C/T]TTCCTCTTGCCTTGG | 79931 |
rs541648187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225730 | TTTAGTTGGCCAAAA[A/T]CTTAGTAAGCACCTT | 79931 |
rs541692926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154367 | AAAATTCTCTAAAGC[C/T]TCCTTAGCCAAGTAT | 79931 |
rs541734374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207008 | ACTCCAAAGGGCAAA[C/T]AGCTAAGGCAAAAAA | 79931 |
rs541757902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139637 | GACCACTGAAAGTAG[C/T]CCAGAAAGTTCAATT | 79931 |
rs541790115 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227622 | ACAACCTACAGATAA[A/C/G]AGATTCACAACCTAT | 79931 |
rs541798954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188343 | CTAAGTTATATATTA[C/T]TGTGAACTGTTTTTC | 79931 |
rs541816318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155990 | AAGAGAAAATTATTC[C/T]AATAAGATAATGGTC | 79931 |
rs541851593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220308 | AATACATAGGTGAAC[A/G]TCATTGCTAGGCTCT | 79931 |
rs541862231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181538 | TAAATGCAGAAAGCA[C/T]ACAACACTGTTCATG | 79931 |
rs541889536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149382 | ACTGCTCTTATTGTG[C/T]GAAGGCCTAGAGGCT | 79931 |
rs541944521 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174263 | AAAATTAAGAGACTA[A/G]GCATGGTGGCTGACA | 79931 |
rs541967297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201722 | TCATTCATTTGTATA[C/T]TAATTAATACACACA | 79931 |
rs541971404 | snp | A/G | 6.60153e-05 | 0.00574485 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121150181 | CCTCAAACAGTCCTC[A/G]GAAAATGAACACTTG | 79931 |
rs541980411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193775 | CTGTAATGAGAAAAA[G/T]CCAAACTATGATCAT | 79931 |
rs541993112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187653 | ATAGGTCCCTCCAAC[C/T]GAAATGTAGCTGATT | 79931 |
rs541995255 | in-del | -/AGAGAG | 0.0150606 | 0.0854603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226239 | AGGTACACATAGGAA[-/AGAGAG]AGAGAGAGAGAGAGA | 79931 |
rs542004637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153955 | TTTTCCTGAACTAGT[G/T]AGCGACCCATTCCTC | 79931 |
rs542023885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161065 | AAATAAAAGGCACAA[G/T]GATAATACATTATTT | 79931 |
rs542041558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147580 | ATAGTAATATTTGAG[C/T]GGAACACCTCTTGAG | 79931 |
rs542098124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134981 | AGTGTTGTGTGTAGA[C/G]TGGTGAGGGGTGTAT | 79931 |
rs542111821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168292 | CCTCACTGCAACCTC[C/T]GCCTCGTGGGTTCAA | 79931 |
rs542111923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160513 | ACAAAATTGACAATA[C/T]ACAGAGTGCTAAAAT | 79931 |
rs542158277 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152201 | CCCTGGATTCCATGC[G/T]GTGATGGATGGTGTG | 79931 |
rs542180807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202579 | CAAAAACAAGATAGA[C/T]GGGATTTAATTAAAC | 79931 |
rs542291317 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191562 | CTCATGTAACCACAT[C/T]CTGTGTCAACTATAG | 79931 |
rs542324944 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163781 | CACCAATATAGTATT[A/C/G]TTTTAAGATTTTTAT | 79931 |
rs542382487 | snp | C/G | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166515 | TTCAGAGAAACAGAG[C/G]TGTCATTCCATGTTT | 79931 |
rs542392724 | snp | C/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229116 | TGACAATCACATCAA[C/T]TTAAGTGTGGAGGGA | 79931 |
rs542400291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175563 | CTTCTACCTACTGCT[C/T]ACATCTTCCAAAAGA | 79931 |
rs542414690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169687 | AGAGATTAAATGGGA[C/T]CTAAAGATCAGAAAC | 79931 |
rs542468871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214538 | TTGTGAATATGGAGA[A/G]GTGGCCGGGTGAGGA | 79931 |
rs542478552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176476 | TATGAGAAAACCATT[A/G]AAGAAAATTTTGAGG | 79931 |
rs542525064 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221858 | TTTTATAGCAGTAAA[G/T]TTTTTTGCCACCACA | 79931 |
rs542529568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143217 | GATACTTAATACTAT[C/T]TCAATTTTATAGATG | 79931 |
rs542561309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189822 | TTTCTTATAAACCTG[C/G]GCTCTGTTGTTGCCC | 79931 |
rs542603430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170941 | CTGCCTTCGCCTCCC[A/G]AGTAGCTGGGATTAC | 79931 |
rs542636482 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142490 | TGGGTCTAAGGAGCA[C/G]TAAGACTTGTGCTAC | 79931 |
rs542651492 | snp | A/G | 1.65086e-05 | 0.00287298 | missense | TNIP3 | GRCh38.p7 | 4:121164124 | TGTACAAAATGTGCC[A/G]TGGAAGCTGTTTTTC | 79931 |
rs542653825 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224947 | TCAGCATACACTGTG[C/T]CCGAGAGTCATCTGG | 79931 |
rs542658119 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131566 | GACACAGCATAGCCA[C/T]ATAGCCATCATCATC | 79931 |
rs542659748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139471 | GCAGGTCTGTCTTTC[C/T]GCTCTGAATGCTCAC | 79931 |
rs542662553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223030 | CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT | 79931 |
rs542693390 | snp | C/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164231 | AAAATTTAAAAAACA[C/T]ACATCACCGTTAACT | 79931 |
rs542702035 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195536 | TTGTTTATTATAACA[C/T]GTCAAACAATCGAAT | 79931 |
rs542723875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216151 | TCCACCAAGGCTTGT[A/C]AATGGAAATTTACAA | 79931 |
rs542742034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177302 | TTTTTCCTTTGCCTA[A/C]AAGATTTTAAATGAC | 79931 |
rs542841155 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196431 | TCGACGAATATAATA[G/T]TTGGCTCTAAAGAGC | 79931 |
rs542845182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150768 | CAAGAGAGAGGGACA[G/T]CCACAGAAATGAAAG | 79931 |
rs542888348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137620 | AGTACCATGATGAGC[C/T]CCTCAGACTTGTAAA | 79931 |
rs542896648 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199389 | AGTCGGACATGAGGT[C/G]TATAAGAAAACAATA | 79931 |
rs542905057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210860 | AGGAGTTCAACATAC[A/G]AATTTAGGGGGACAC | 79931 |
rs542910676 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228970 | TCTAACTAATGTCTT[C/T]CTTTCCTGAAAGTAC | 79931 |
rs542923703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204069 | CTATTCCTTCAGTTC[A/T]TACATATTGCTCTAA | 79931 |
rs542959567 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197045 | TCTTAATGAACTTAA[A/C]AAATACAATGTGTTA | 79931 |
rs542993530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171757 | TGTTTTTGAGATGGA[A/G]TCTCACACTGTCACC | 79931 |
rs543000663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178447 | TTCACCTCAGTCGCA[A/G]GAGCAATAGTGTTTG | 79931 |
rs543004994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185361 | ACTTTATGGCGAAAG[C/T]CTCTGCTGACTAACC | 79931 |
rs543007235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153293 | CATGAAGAGTGCACA[C/T]GGACATGAGCAAAAC | 79931 |
rs543077605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145008 | CTAAGTACCCTAAGC[A/G]TCTTTCACTTTACCA | 79931 |
rs543083218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159612 | TAAAAGATTAACACA[C/T]GATTTATAATAAATA | 79931 |
rs543178902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197389 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGTGCCT | 79931 |
rs543221854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159072 | ACATGGTGACATCCC[A/G]TCTCTACTAAAAATA | 79931 |
rs543282292 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212476 | TGTGACTTTGATGTT[G/T]ATTAGTTTGAAGACA | 79931 |
rs543300108 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157562 | GTCATTCTATTCTCA[A/T]CTCTCCAGGTGAGCC | 79931 |
rs543317479 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203583 | ATTACTCATATAACC[A/C]AACACCACCTGTTCC | 79931 |
rs543368165 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218676 | ATGTCTCACTATATT[A/T]CCCAAGCTAGAGTTC | 79931 |
rs543417416 | in-del | -/AA | 0.0142736 | 0.0832652 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180401 | GAGACTCCGCCTCAG[-/AA]AAAAAAAAAATTATA | 79931 |
rs543448151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168450 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 79931 |
rs543506858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220073 | ATAAAGTAATAGGCT[A/G]AAAACCATACATATG | 79931 |
rs543515007 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222633 | AGATAGTAAGCTCCA[A/G]ATAAATGTGAGAGAA | 79931 |
rs543542687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174196 | CAATATATTTCAACA[A/C]CGTATCTATAGATTT | 79931 |
rs543551935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198703 | TCTAGTGAAGGCCAA[A/C]TCAACTGATCAAGAA | 79931 |
rs543572925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180480 | GTCAAATGCAAATAA[A/G]AAGACAAGTGAAAAG | 79931 |
rs543652851 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193182 | AAGATTGGGACACGC[C/T]ATCAGAGATGAGAAG | 79931 |
rs543675005 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139726 | ACTCTAGACACCTAG[A/G]CCCTTGGCTCCTCTG | 79931 |
rs543725982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147379 | ACTTCTAAAAGACAG[C/T]TTACTGACAATAGAT | 79931 |
rs543740304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193531 | TAGAGAACATTATCC[C/T]ATTAGAAAATCATTA | 79931 |
rs543806074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186683 | AGATGCTCAGTGATC[A/G]ATACTATTGTTATTA | 79931 |
rs543836455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221953 | AGGACTGAATCTAAA[A/C]AAGTTCCTGAACCAG | 79931 |
rs543860518 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228288 | AGCTAGCATACTGGC[A/G]ATATGCTGGAGGAGA | 79931 |
rs543898584 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224235 | GAATGTGGTGGTGGG[C/T]GCCTGTAATCCCAAC | 79931 |
rs543923921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221070 | TTTACTGTTAGCAAT[A/T]CTCATGGCCTTTTGC | 79931 |
rs543936299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194891 | ACTTCTTCTCAGCAG[A/G]GTAGAGTGGCTCACG | 79931 |
rs543941346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142391 | GTTATTTTTTCAAAA[A/G]AGGCAGTATTTGATT | 79931 |
rs543957352 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149459 | TCCAGAGTTGGGATT[A/T]ATAGTGTTCTTAAAA | 79931 |
rs543976201 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213094 | AAAGACAAAAGTATT[C/G]TTTAATTTTCTTAAT | 79931 |
rs543978129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135920 | TAAGCTATGAAATAC[A/G]TCAACTGTGGAAGCT | 79931 |
rs544060136 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140227 | TAGTCCCAGCCAGTC[A/G/T]GGAGGCTGAGGCAGG | 79931 |
rs544095875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207587 | AATAAAAACAATAAG[C/G]CTGCAGATTTGGGGC | 79931 |
rs544095931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200295 | CAAAATTACAAATTC[C/T]CTTTTGCATAATCCA | 79931 |
rs544105181 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171782 | GTCACCCAGGCTGGA[A/G]TGCAGTGATGCGATC | 79931 |
rs544107572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200699 | ACTGCCAGTAATCAG[A/G]CACCTTGGCTACCTT | 79931 |
rs544188629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, stop-gained | TNIP3 | GRCh38.p7 | 4:121182495 | TCTGCTGAAGAATTT[A/C]TTTAGTAACAGGAAG | 79931 |
rs544233879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189862 | ATTCTTGGCTAGCTC[C/T]CTGTTTATTTCCTCC | 79931 |
rs544250284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175615 | CTGTAACTCTTTCTT[C/T]TGTGGAACATGGGAC | 79931 |
rs544266237 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185123 | GCAGGATCATTTGGA[A/G]ATAAAACTCATCACG | 79931 |
rs544298433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143010 | TTACAATTCTGTTTT[A/C]GGTAGATCTATTTAG | 79931 |
rs544338761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189160 | GGGGCTAAGTGATAG[C/T]AAAGCCAAAATAAGA | 79931 |
rs544365450 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153244 | TTTCTAACTTGAAAC[A/T]ATTTTCTGTGAACTA | 79931 |
rs544412582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148032 | ACATCCAGCCACATT[A/G]ACATTTTGATGATTT | 79931 |
rs544466203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161821 | TTACTGGCATAATGA[A/T]AATTTACCACCTTTC | 79931 |
rs544501720 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161320 | CCAACTCTCCTGTTG[A/C]GATTTAAAAAATACC | 79931 |
rs544515522 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134655 | TCTCCAAAGCATTCT[A/G]AAATAACCACAGACA | 79931 |
rs544571595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204209 | AAGCTGGAAACTGCT[C/T]AGGGCAAACCTGCTT | 79931 |
rs544574055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214597 | TTCTCCCTTCCTTTC[C/T]TTTTCCCTTCCTTCT | 79931 |
rs544584277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208571 | AGACAGATTTGAGTA[A/C]GAATAAAACTGGTCT | 79931 |
rs544587415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196925 | ATCAGTCATTAAAAA[A/C]ATGTAAGAAATAAAA | 79931 |
rs544683991 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169274 | ACCGTTGCCCCTTGA[A/G]CTTGTTCTCTCTTGC | 79931 |
rs544698047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202670 | GAGAAAATCTTCACA[A/C]TCTACACATGAAACA | 79931 |
rs544715499 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155031 | GCAATGGTGTGATCT[C/T]AGCTCACTGCAACCT | 79931 |
rs544759393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196379 | AATAAGTTTTTTCCT[G/T]TAACAAGTATAGGTT | 79931 |
rs544761226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209151 | GTTAAGGGCGAGGAC[A/G]CTGTGTGACAGCATC | 79931 |
rs544784946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201947 | GCCCATGCTCGTGGA[A/T]GGGTAGAATCAATAT | 79931 |
rs544804519 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224450 | CCGATACAGAATCCA[C/T]ACTTTGGCTTTTACC | 79931 |
rs544907965 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183722 | TGAGGGGTCTAGGTT[C/G]TGAGAACATTATTGT | 79931 |
rs544943905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137687 | CTCCCTATTTACACT[A/C]CATAACAGACTCCTT | 79931 |
rs544989410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165023 | GCATAAGTGAACTGC[A/G]ATGGAACAGAAGACC | 79931 |
rs545061229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225053 | AAAACTGAGAAAGGG[A/G]TCATTTGCCTTCAAA | 79931 |
rs545063876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179526 | TGGTTTCAATGATGT[A/G]TGCAAAGAGATCTAC | 79931 |
rs545101843 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131210 | TATATACATATAAAT[G/T]TATAATTTGAGATCA | 79931 |
rs545110603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133092 | ATGGAAAATATCCTA[C/T]AGAAAGACTTGTTGG | 79931 |
rs545120619 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216899 | GGAGTGCCTACTGAC[C/T]CCAGGACACCAGCAG | 79931 |
rs545122021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225659 | GTAAAGTGTTAAAGA[A/G]CAATTTTTAAAAGTT | 79931 |
rs545172277 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140021 | GCTGAGATTTTTTTC[A/G]TCTGACTACTGCTTG | 79931 |
rs545222860 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171981 | CAAATGATCCACCTG[C/T]CTCAGCCTCCCAAAG | 79931 |
rs545240738 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167393 | AGCTATGGAAAGAGT[C/T]AGAGTTTCTGCTGGG | 79931 |
rs545275200 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197440 | GGCTGAGGCAGGGGA[A/C]TCGCTTGAGCTTGGT | 79931 |
rs545294970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138340 | TTGTTATAATACAGC[C/T]CTGCTTACAGTTTTC | 79931 |
rs545297211 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222854 | TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGCGCG | 79931 |
rs545332576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183868 | GCTCAGGGCTCCCAT[C/T]GATTCTACATTATGG | 79931 |
rs545348529 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205843 | ATACCTGAGACTGGG[A/T]AATTTACAAAGGAAA | 79931 |
rs545350312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158911 | GCTGGGATGATTAAA[C/T]TGAACACACTCTCAC | 79931 |
rs545382013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147481 | AAATGAAACCCTTAC[A/G]TATGTGGAAAAGCAA | 79931 |
rs545415310 | snp | A/C | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121216664 | CAGACCTGAGAAGAC[A/C]GACCACAAGCCTGCC | 79931 |
rs545420905 | snp | A/G | 0.000404776 | 0.0142206 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145989 | TCTCATAAAAAAAAA[A/G]AGAGAGAGAGAGAAT | 79931 |
rs545447002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139564 | AATTATCTCCTAAAA[A/G]TAACTTGAGGAAAAT | 79931 |
rs545486671 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167442 | ATTTTGACAGAGAGT[A/G]AAAGCTGAGCTATAA | 79931 |
rs545516758 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156588 | CCAAGAATGTTAAAT[C/G]AGATAATGAGGACGA | 79931 |
rs545530879 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153895 | GCGCATTCCTATGTT[C/T]CACATATGGGTTGGC | 79931 |
rs545597309 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190748 | TGAATAAGGGTAGAA[C/T]CTTAACCGAAGTGTT | 79931 |
rs545599878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185520 | CAGGAAAGAGGAAAG[A/G]CCTTTGTCTGTGTTT | 79931 |
rs545645488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206094 | TACCTCCCACTGGGT[C/T]CCTCCCACAACACCT | 79931 |
rs545692113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160404 | GAATCACTTGAACCC[C/T]GGAGGCAGAGGCTGC | 79931 |
rs545718213 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209429 | GTACTAACTTCTGGT[A/G]GTGTCAACACCAAAT | 79931 |
rs545781520 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179556 | CTTTTAAGTTTTAAC[C/T]ACTTTTAGGTTTTCA | 79931 |
rs545894890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199639 | CTTCAATGGAATTAA[C/G]AATAGTGTGTGCACC | 79931 |
rs545914941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155049 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 79931 |
rs545977839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174288 | CTGACACCTATAATC[C/T]GACCACTTTGGGAGG | 79931 |
rs545987271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198992 | AAGGGTATAGATCCT[C/T]TTTGATGGCCAGAGT | 79931 |
rs546016749 | in-del | -/AA | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145979 | AAAACACCATCTCAT[-/AA]AAAAAAAAAAAGAGA | 79931 |
rs546058186 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187890 | TTAGTTACTTTCACA[C/T]GTGACTACTTTTTTT | 79931 |
rs546075628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212582 | TATGATGTTTTGCCT[A/G]TCATTAAAAATACTT | 79931 |
rs546081782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205607 | TCTTGAAATTATGCA[C/G]GCTAGGGATGCTAGT | 79931 |
rs546082886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166700 | AAATTAGTCCAAGAG[A/G]AGAGTACTATATTTC | 79931 |
rs546140408 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227586 | CAAGAGACTATTAAT[A/G]TTCACCTCTCAGATA | 79931 |
rs546205865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181039 | GAGGTCGTAGGAAAA[C/T]CAGTATCTTAGAGAG | 79931 |
rs546268921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207103 | AAAATATAGTATGTG[G/T]GATCTGGGGTTCTTT | 79931 |
rs546283562 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200887 | GGAAAATCACTTATC[A/G]TGGGTAGAAATAAAC | 79931 |
rs546315542 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201166 | GAAAGTTTTGAGGTA[A/T]GAGGAAAGTCCAGAA | 79931 |
rs546339510 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172018 | GATTACAGGCATGAG[C/T]CACCACACCTGGCCC | 79931 |
rs546365567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220512 | TGTATTTGCCCTCAC[A/C]ATCATCCAATTCAAA | 79931 |
rs546403327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208245 | AGAATTAGAAATTAT[A/G]GTTTAGGAGTCATGC | 79931 |
rs546454337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220874 | GGATGAAAAAGAGCA[A/G]TACGTTCAGTCAAGA | 79931 |
rs546455957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213695 | TCGTGCCACTGCACT[C/T]CAGCCTGGGCGACAG | 79931 |
rs546501327 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149772 | CTCTGTCTCAAAAAC[-/A]AAAACAAAAACCATG | 79931 |
rs546541939 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220209 | GAGACCTACAGGTAG[G/T]CAGTCAGTTAATCAA | 79931 |
rs546608763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170676 | AAAGGCAGAACTGTT[G/T]TCTTTAATAATACTT | 79931 |
rs546620366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181164 | GGAGGACCAAGAAGT[C/T]GAATGAACAGAATTG | 79931 |
rs546621672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162966 | CAATGAGACAGTGTG[C/G]TTTTTGTTTGTTTCC | 79931 |
rs546664035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144003 | ACACTAGGAATGTGT[A/G]TATGTCAGGAAACAA | 79931 |
rs546730413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181805 | AGAAACAAATTTATG[A/G]ATGCAAATTAGTTAT | 79931 |
rs546732338 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131695 | GCTGGAGTGCAGTGG[C/T]GATCTCAACTTACAG | 79931 |
rs546741383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222197 | TTAGTGAATTTCTTC[A/C]CCTGCGAAGAGGACC | 79931 |
rs546746932 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210292 | CTTGTTTTCTGGAAC[A/G]TTTTTTAATAGCCTG | 79931 |
rs546750576 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228330 | AGTTTGATTGTTTGC[C/T]CTACTTTAACTCTCA | 79931 |
rs546752971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137150 | ATAAATGACCTTATG[G/T]TATTACTAAATTCTG | 79931 |
rs546757120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182911 | TATGATACTTCTCTA[C/T]GATCTCCCAAACTCT | 79931 |
rs546820044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136000 | TTTTTTGGTGGTGCC[C/T]TAACCATGATCAGCC | 79931 |
rs546827092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143661 | GCTCCTAGGAGAAAT[G/T]TTGGGTTAAGTTTCT | 79931 |
rs546833591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168845 | CTTCCTGATTTTATT[C/T]ATAGGAACATTTTTA | 79931 |
rs546847789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148993 | CTTTATGTATCCTGT[A/G]TTTATCATTATTGCC | 79931 |
rs546854065 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215168 | AATCCTTGGCTCAAA[A/G]TTCTTAATGGTACCC | 79931 |
rs546878011 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229310 | AAACAAACACCCGTG[A/G]CAGGGTGCGGTGGCT | 79931 |
rs546948725 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222738 | ATTATACATGTTATT[A/C]GTTATTAATTGTTGG | 79931 |
rs546962008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184454 | CAATTGATCCCAGTT[C/T]GGCCAGTGGGATTCT | 79931 |
rs546962053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191645 | ACAGGTACAGTTCCA[A/G]GTTGTGACATTCTCT | 79931 |
rs546978555 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220682 | TAAAATTGTCATAAA[C/T]AGCGTGGGGGAATAA | 79931 |
rs547015433 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222996 | ATTTTTAGTAGAGAT[A/G]GGGTTTCACCGTGTT | 79931 |
rs547057031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215855 | AGTAACAAACACAAT[A/T]TCTTGCATGTATTAG | 79931 |
rs547074056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151607 | AATTTTTTTTTTTCA[A/G]TTGGTGAATAGTAGT | 79931 |
rs547093468 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189925 | ATGCCACAAACTAGA[C/T]CCAAACCTCTTGTGG | 79931 |
rs547099940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191231 | GAAACATTGGCTCCT[A/G]ATCAACTTTATGAAC | 79931 |
rs547179937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164604 | GTTGACTTTTTGACA[C/G]CTCGGTTTCCCTAAA | 79931 |
rs547181252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189507 | TACTGTAACTATGCT[C/T]CTGGTGATTTTGTGA | 79931 |
rs547243861 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208209 | ACCAGACTGCCTCTA[C/T]AGGACTAATAAATTA | 79931 |
rs547258418 | snp | A/G | 0.000198689 | 0.00996518 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157262 | AGGAGGTCGTTCAAA[A/G]ACAGCTGCAGATACC | 79931 |
rs547261892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201962 | TGGGTAGAATCAATA[C/T]TGTGAAAATGACCAT | 79931 |
rs547282132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180785 | AAACTCAACTCGGTC[C/T]TCACTACTACTCTGC | 79931 |
rs547282730 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173208 | ATGATGGAAAAGCAT[C/T]GCAGGAGCCTAAGTC | 79931 |
rs547301735 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212444 | GAAGAAACTTAGTCT[A/G]TTGTCCAGAAACCCA | 79931 |
rs547311257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195395 | TAAAATGGAATTATA[C/T]CACAGCATTACCTTT | 79931 |
rs547317878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163889 | GCAATGTACTGGTTA[C/T]TTAGATATTTTTTTC | 79931 |
rs547319342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195809 | CAGAAATAAACTGAC[C/G]AGGGCTGATAGCATT | 79931 |
rs547348894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196261 | TTTTGTGTCTAAAAC[C/T]AATACTGTGATAAAA | 79931 |
rs547354617 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167182 | GACATTGTGTGGGTT[-/C]CAAAGGAAAACAAAA | 79931 |
rs547395951 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193542 | ATCCCATTAGAAAAT[A/C]ATTATTTGACAGCCG | 79931 |
rs547397188 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202969 | GGGAACACTTTTACA[C/G/T]TGCTGTTGGGAATGA | 79931 |
rs547410814 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144598 | GTAGAGACAGGGTTT[C/T]GCCATTTTGGCCAGG | 79931 |
rs547426830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151008 | ATTATCATCTTTAGT[C/T]ATTAGCTCATGATGG | 79931 |
rs547449420 | snp | A/C | 6.59228e-05 | 0.00574083 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121138645 | CCTTGTGTTGTACAT[A/C]TGGCGGAAGCTGGTC | 79931 |
rs547515941 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215442 | CTATTTAGTCTCTCA[C/T]TCAAGAGAGAGTATC | 79931 |
rs547560925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149925 | TGTTCTAAATGGTGG[C/G]ACTGAACTAGCTGAT | 79931 |
rs547564165 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217160 | ATAGTATGTCATGGG[A/T]CTTACAGTAGAATCT | 79931 |
rs547574083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157858 | AGCAGCTTAAGCATT[C/G]TCTCTGGGATCATCA | 79931 |
rs547586915 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189760 | AGATATCGAAGAATT[A/G]TATTTGCATGTCTGA | 79931 |
rs547619680 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172329 | TGAGGGTTTGAGGAG[A/G]CCTCAGAGTCAAATT | 79931 |
rs547624703 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218168 | AAATTTTTACATTAC[A/G]GATACAACATCATAA | 79931 |
rs547626657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211424 | CAAGGGATGAAAACT[C/T]AACTCACTGAGGATA | 79931 |
rs547629289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179166 | TCATGGTTTGTTAAA[A/G]GCTTATGGGTAGCTA | 79931 |
rs547662751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216343 | AATACACTATCATTG[C/T]CACAAAGCAGAAGTG | 79931 |
rs547664602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209697 | ATTAAACAAATACAG[A/G]AGATTCAAGATCTTC | 79931 |
rs547727605 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210540 | TAGTCTTCTTGAGTT[C/G]CCATAAGGAAACAGC | 79931 |
rs547745898 | in-del | -/T | 0.0737376 | 0.17729 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221759 | ACAGAGCTGTAACTA[-/T]TTTTTTTTTCCACTT | 79931 |
rs547789270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152889 | TGGTGCCTAATGGAG[G/T]AGTTGGCACAAAAAT | 79931 |
rs547805836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198246 | AAGGAATAAGCTACA[G/T]AGAAAATGCACAAAT | 79931 |
rs547806167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159207 | GAGATTGTGCCACTG[C/T]ACTCCATCCTGGGCG | 79931 |
rs547817804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159781 | GAAGAAGTGCTATGA[C/T]ATGTGGTTGGCTTTT | 79931 |
rs547850884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133554 | CCTAGGTATCTTAAA[C/T]ATTTTAAAATTAACT | 79931 |
rs547855350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219682 | CATAGGTTTTACAGA[C/T]CTTGAAAATGTTATA | 79931 |
rs547870257 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162819 | TGATTCATACTAAAG[C/T]TCAATATATTCCCAT | 79931 |
rs547886945 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216820 | CATAGAGCATGAACG[A/G]TTAAAGTTGTCAGAC | 79931 |
rs547892489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205212 | ATTGAAAGGTGACAA[C/T]TGAGCAAGGAGTGAA | 79931 |
rs547941615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121166152 | TGATGCACATACATT[G/T]TTAGGTGTGATGGCT | 79931 |
rs547942110 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175075 | ATTTGCTAAACAACT[C/G]TTATGAACATGTTAT | 79931 |
rs548015698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140508 | GTGAATTCCTTCCTT[C/T]TTTCCATAAAGAAAT | 79931 |
rs548025131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180705 | TGAGAGGTGATGGAG[A/G]GATTAGAGATACAGG | 79931 |
rs548037739 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224365 | AAGACTCTGTCTCAA[A/T]AAATAAAAAGAAAAA | 79931 |
rs548075692 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131824 | TTTATAGTAGAGATG[C/G]GGTTTCACCATGCTG | 79931 |
rs548080428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139239 | GAACCTATCCTCTAA[A/G]TTGCTCATATAGTTT | 79931 |
rs548105413 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218338 | AAACAGACAAGATGG[A/G]AATGGTCTCAAAGAC | 79931 |
rs548112020 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184486 | CTCTGTGTCTGGAGT[C/G]AGCTGAGAATGAATC | 79931 |
rs548115314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178609 | TTCAGCAGTCAATAA[C/T]TTCATGACACCAGGA | 79931 |
rs548141707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153444 | AATATAATCTCAATT[A/G]TTTATAGTTCCTTTA | 79931 |
rs548148397 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181255 | TGAGGGTACCAGAGG[G/T]AATTGATATTGTCAC | 79931 |
rs548152968 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188633 | CTTGTAGAATCCTAT[A/C]TGGTAGAGAAGATAA | 79931 |
rs548233671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155129 | CACCACGCCCGGCTA[A/C]TTTTTTATATTTTTT | 79931 |
rs548234886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218966 | GAACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 79931 |
rs548249714 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213361 | TACTTCAGATTAAAA[G/T]GAATCATAGTCATTT | 79931 |
rs548250644 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180129 | TGTCGGGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 79931 |
rs548288910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187876 | GCCCTGACACAACTT[C/T]AGTTACTTTCACATG | 79931 |
rs548348844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148271 | TAATGATTGCGGGTG[A/C]CTGATTAGAAACGTG | 79931 |
rs548366716 | in-del | -/TGT | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221491 | GAGGCAAATGCTCAA[-/TGT]TGTTAAGAATATGAT | 79931 |
rs548368423 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161385 | CCTTCATCATGGCTG[A/G]TGGATGAGTCAGCTT | 79931 |
rs548388293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194484 | AATAAATCTTTCTTG[A/G]GGTTTACGAAATTAG | 79931 |
rs548555294 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227910 | AGAGAGCTAGCACCC[A/G]GGTTAACATTTAAAC | 79931 |
rs548557644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148625 | CGTCGGTTTATTTTT[C/G]AGCTATGTATTTTAC | 79931 |
rs548596828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142587 | TAAGCACTGTCTATC[C/T]GTTGATGGTGTAGTC | 79931 |
rs548597509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142026 | GTTCCACTTAATCTG[A/G]CATAATTATAACTCA | 79931 |
rs548607439 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228443 | GGGAAATGTGAGACA[A/G]AGGGGGCCTCAACAT | 79931 |
rs548636190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135471 | GGCGTGATCTCACCT[C/T]ACCGCAACCTTGGCC | 79931 |
rs548674038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195183 | CAAAACAAAAAAAAA[A/C]CTTCTTAATTAAGTC | 79931 |
rs548678822 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147683 | AACTGACTTACTGTT[C/G]ACTGAAGGTTAGCAG | 79931 |
rs548715662 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206497 | CTGGCTTTTAAAATA[A/T]AAATGTATTTAAAGG | 79931 |
rs548791856 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135590 | TTTTTGTAGAGACAG[A/G]GTTTCACCATGTTGC | 79931 |
rs548825775 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202615 | AGCTTCTGCACAGCA[A/G]AAGAAATAATCAGCA | 79931 |
rs548847676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182022 | CATGCTCTCAAACTA[C/G]TCACATTCTCACATT | 79931 |
rs548854217 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213763 | AGACATTCTTCTTAC[A/G]ATATTACCACAGGAA | 79931 |
rs548858600 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206727 | TCACCATGCTCAGCT[A/C]ATTTTTTCTTTTTTT | 79931 |
rs548883537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199958 | TATGCCCAGAAGAAA[A/G]GGTGCTTTTTTCTCA | 79931 |
rs548884215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214427 | TAAATAGAACTAAAC[A/G]GTAAATTGCATTGCT | 79931 |
rs548895965 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168640 | ATCCAGCTGCCTCAG[C/T]CTCTTGAGTAGCTAC | 79931 |
rs548921169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207194 | AAGAGGAAGGAAGCC[C/T]GAATATTCAGAGAAT | 79931 |
rs549017290 | snp | C/T | 0.000214191 | 0.0103465 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157169 | GTCGTCCTTTCTCTG[C/T]CTCTGATGCGGATCC | 79931 |
rs549032244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138495 | TGCATCAAATTAAAG[G/T]TATGTATGTAACACA | 79931 |
rs549051656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175342 | TGAGACCTCAAGTTC[C/T]TTTTCTTCTCTTTGT | 79931 |
rs549070413 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190775 | TGTTGAGCTCAATAC[C/T]CCCCGAACAAACTCT | 79931 |
rs549133608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163074 | AAATCTAGATACCAA[A/G]TCTGCAAGAGGCTCT | 79931 |
rs549139506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222144 | TTTTGCAATGTTGCT[A/G]TATTGCTCTTGATGC | 79931 |
rs549151317 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217012 | GGAAGTGGTAATGGA[A/C]AATGAAAAAAAAGAG | 79931 |
rs549165734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215892 | CATTAAAAAAAAAAA[A/G]AAAGAAATAACTGAA | 79931 |
rs549191002 | in-del | -/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216961 | TTTCTCCAACAGGAG[-/T]TTTATGATTATTTCT | 79931 |
rs549193682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138033 | AGAAAGAAAACAGAA[A/G]ATGTTAAATCAATAA | 79931 |
rs549225771 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219140 | AGGAGGCGGAGGTTG[C/G]AGTGAGCCGAGATCA | 79931 |
rs549227821 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189937 | AGATCCAAACCTCTT[G/T]TGGCTGTGCCCAGGA | 79931 |
rs549280147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191032 | CACAGGAAGAACATA[A/G]CTTAATAGCATTTTG | 79931 |
rs549280325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140226 | GTAGTCCCAGCCAGT[C/T]GGGAGGCTGAGGCAG | 79931 |
rs549285069 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156745 | ATAAAAATAATAAAT[-/A]ACGAATAAAAGCAAA | 79931 |
rs549302116 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202508 | CATTGGCAAAACCTT[G/T]CTAGACATTGGCTTA | 79931 |
rs549307360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136984 | CTACATTTTTCCTAG[C/G]TAGACAAAAATCAGT | 79931 |
rs549339690 | snp | A/T | 0.000798403 | 0.0199641 | missense | TNIP3 | GRCh38.p7 | 4:121216426 | TTACCTTTCAGAATC[A/T]TCAGATTGATTGGTG | 79931 |
rs549341297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144446 | CCACTCTGTTGCCCA[A/G]ACTGGAATGCAGTGG | 79931 |
rs549359257 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196510 | TAATAGAAATCATAA[C/G]AATTAAATGTGAAAT | 79931 |
rs549362206 | in-del | -/TATT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221758 | CAACAGAGCTGTAAC[-/TATT]TTTTTTTCCACTTCA | 79931 |
rs549365700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143751 | TGTTTCTGATTAAAG[A/G]CAACTTATTTAATAT | 79931 |
rs549393646 | in-del | -/TGAGGTATT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198879 | ATATACATATAGCTC[-/TGAGGTATT]TAAAATTTTTAAATA | 79931 |
rs549419952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152316 | ATAGAAGAACAATAA[G/T]ATCTTACATTAGGTA | 79931 |
rs549443362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210627 | TTTGTGAGCAAGGTG[C/T]CAGCAGGTAGGTTTC | 79931 |
rs549480287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184291 | AATGGCCTAATCAAA[C/T]GCCTGTATGGCAGAG | 79931 |
rs549501253 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181467 | TTCATCTGTAACTCC[-/A]AAAATAAAGACAACC | 79931 |
rs549502276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146402 | ATGGTGCAGTTTGTT[C/T]TATTTTTTAAGGCAA | 79931 |
rs549561144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158594 | GGCTATCCACAAAGC[C/T]CTTTGTAGCTGAAAT | 79931 |
rs549568285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183477 | CAGAGCTTCCTACTC[A/G]AATCAAATTTTTATT | 79931 |
rs549648280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196468 | TCTGGAATTGGTATA[A/G]GAAGCAATTTTGTGT | 79931 |
rs549658754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190121 | TTGGGACTGCTCTGC[A/T]TGGGTGAAACAATCT | 79931 |
rs549660900 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159662 | CACCATTTTGAAAAT[G/T]TAGATTTTCAAGAAA | 79931 |
rs549669137 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174438 | AAACAAAATAAAAAA[A/T]ATAAGAAAGAACATG | 79931 |
rs549679476 | snp | G/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132272 | CACTTTAAATCAACA[G/T]ACAATATCCCTGCAG | 79931 |
rs549742892 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136288 | TTATTATCTATGTTA[C/G]AGTCCCCTTCTCATT | 79931 |
rs549796369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199841 | TAGGTACCTGAGGAC[A/G]GTTGTGTAGGTTGCT | 79931 |
rs549840047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165263 | TGAATATCTCCCCCT[A/G]CTCTCCAACTCTCCC | 79931 |
rs549849141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225346 | TCAAAACAATGGAGA[C/T]ATTTAATCTTGGTCA | 79931 |
rs549879288 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186884 | CCTACTTGGGCTTTA[C/T]AACATTCTTAGGAAA | 79931 |
rs549902528 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154387 | TAGCCAAGTATGACT[-/G]AAAGCTGCAGCTAGG | 79931 |
rs549954710 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142223 | CTCAATGAAGAAAAT[C/T]TATTCATTGAGTCAT | 79931 |
rs550008272 | snp | A/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132515 | CATGACCAGGCACAA[A/G]TAACAGGGTAGATGA | 79931 |
rs550062280 | snp | A/G | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166527 | GAGGTGTCATTCCAT[A/G]TTTCCAAGGCTGTTG | 79931 |
rs550069001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173389 | AGAAATTAGTGGTCA[A/G]AAAAGAGAAATTCAG | 79931 |
rs550071332 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147781 | CTGATTTAAATTACT[A/T]CTTATATTGGAACCT | 79931 |
rs550075600 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159255 | TCATGGAAAGAAAAG[-/A]AAAAAAAAGAAAAGA | 79931 |
rs550109008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179862 | AGCAGGAAATATATT[G/T]AATTCACTTCAGGAA | 79931 |
rs550138998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212720 | ATACATTTTCAGGGA[A/T]GTCTGTCTTTATGAA | 79931 |
rs550177257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153517 | AGATAGATTTTGCCC[C/T]GCATTTGTATGTCTG | 79931 |
rs550214257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154022 | ACACACACACACACA[A/C]CCCTGCATGCACACA | 79931 |
rs550219410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220454 | AAAGCAATCTGAAAA[C/G]AGAATGCTTTTAGGT | 79931 |
rs550219832 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165356 | CTGAGCTCTGTGCAT[C/G]CTGTTCTTGCCACCT | 79931 |
rs550229322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135128 | CTCCCTGTGCCACCA[A/T]GTCCTGTCACAGACT | 79931 |
rs550263221 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121192611 | ATTTAATGATGCCTC[C/T]AGAGGGCACTCTGCA | 79931 |
rs550269646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168762 | TGGCTTTGAATGATC[C/T]TCCCACCACAGCTTC | 79931 |
rs550332350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159877 | ACTGAGAAGACAGTC[A/G]TAATGACTAAAAAGT | 79931 |
rs550373507 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154379 | AGCCTCCTTAGCCAA[A/G]TATGACTGAAAGCTG | 79931 |
rs550392705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134585 | GACTTGAAAACATTC[A/G]AAACCCTTCATTTAA | 79931 |
rs550406721 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218351 | GGAAATGGTCTCAAA[G/T]ACATTAATTAGTTTA | 79931 |
rs550424494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213813 | TTAAAATATTAAAAT[A/G]AGGAACTGGTATTAC | 79931 |
rs550435326 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144144 | TGATGATGAGGATAG[A/C]CTGTACATGTCTCTT | 79931 |
rs550575487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175840 | TTTTTATGAGTTTTA[A/G]TTATTTTGTGTTAGG | 79931 |
rs550596394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193865 | CCTGAATCTAATTAC[A/G]AGGAAACATTAGCCA | 79931 |
rs550610460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187146 | TAATAATTGCATCCA[A/G]CAGTGTTGTGCTCTT | 79931 |
rs550624124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207330 | AGCAGAAACTTCTAA[A/T]TTAAAAAGAGCAACT | 79931 |
rs550662816 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180484 | AATGCAAATAAAAAG[A/G]CAAGTGAAAAGTAAA | 79931 |
rs550681150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173883 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 79931 |
rs550681189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181135 | GGATGTAGAAGAGGT[A/T]TTTACCATGTAAAGG | 79931 |
rs550703047 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155739 | TGAGATTTTAACCCA[A/G]TAAAATAAATATTGC | 79931 |
rs550742085 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174397 | GTGACAGAGCGAGAC[C/G]CTGTCTCTAAAATAA | 79931 |
rs550748535 | snp | C/T | 1.65149e-05 | 0.00287353 | missense | TNIP3 | GRCh38.p7 | 4:121142731 | ATCAACATACCTGTT[C/T]TAATTGCTTTTCTAG | 79931 |
rs550782218 | snp | C/T | 0.000267706 | 0.0115664 | missense | TNIP3 | GRCh38.p7 | 4:121141860 | CAGGGCCTGTTGGTA[C/T]CCATGGATCTTGCAG | 79931 |
rs550900448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154735 | AGTCAAATGAGATGA[C/T]ATTGTAGGAATTCTG | 79931 |
rs550905293 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121182745 | TGGATGAGGAGACGC[A/G]TTTCTCTCAATCAGA | 79931 |
rs550928879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197126 | CAGTGCAATATAAAA[G/T]TTGTACTCATAAATT | 79931 |
rs550969212 | in-del | -/CAGGTGGCTGTAATCCCAGCTACT | 0.0248432 | 0.108648 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195036 | AGCCTGGCATGGTGG[-/CAGGTGGCTGTAATCCCAGCTACT]CAGGAGGCTGAGGCA | 79931 |
rs550977253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137053 | ATTCTATTTAGTTTC[C/T]GAATGTCATCACAAT | 79931 |
rs551043882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222189 | GTGAAATATTAGTGA[A/T]TTTCTTCCCCTGCGA | 79931 |
rs551053480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202895 | ACCTTACTCCTGCAA[C/G]AATGGCCATAATCAA | 79931 |
rs551068737 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228495 | CTGTAAATATCAATC[A/C]TGGTTGGTAAAGCTG | 79931 |
rs551074438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195740 | ACAAATTCCTAAAAC[G/T]GGGTAAGTTAGATTA | 79931 |
rs551088275 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178744 | TTATAGGGATAAATC[A/G]ATGTATATTCAGTGT | 79931 |
rs551089715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157662 | GACATGGCCTTTAAT[C/T]TATCAGTAATTTGCA | 79931 |
rs551095407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189434 | AGAATGAGAAGTGTT[C/G]TGTAAAAGATGCTAA | 79931 |
rs551149753 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204647 | CTTGATGTCACTACA[A/G]TCAATGCACAATAGA | 79931 |
rs551226483 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177804 | AGGGTTTCTTTCTGC[A/G]GAATGCTATTGTGTA | 79931 |
rs551289065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170163 | CAACTCTAGCACTTA[C/T]TGTAAAGCAGTTGTT | 79931 |
rs551292718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162145 | TCAAAACATGTTGTT[G/T]GTCTTTGCCAGAAAT | 79931 |
rs551301934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201044 | AGTAGGAGTTGAAGG[C/T]CAAGGGGAACTTTGG | 79931 |
rs551305257 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190324 | CTGCTAATCATTGTA[-/T]TTTTCAGAGCCTCAC | 79931 |
rs551309793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176589 | CACTTTATATTTACA[A/G]GGTGCACTTTCTCTC | 79931 |
rs551347460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214715 | CAACATCACATCATA[A/T]ATTTTTTGCTTCTGT | 79931 |
rs551410518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144175 | TTACTATATTGTGAG[A/T]TATTTACTAGCAAGA | 79931 |
rs551586260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209599 | TGAGCCCAGAGGAAA[C/T]AATTAGGCTCCAGAT | 79931 |
rs551596390 | in-del | -/CAG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195339 | TTATTCTTTAAACAA[-/CAG]CAGTGGTATGAGCCT | 79931 |
rs551601462 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140473 | TTAATTGACATGGAC[C/T]GTTTGATGAGCTATA | 79931 |
rs551608983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216526 | AAAATATGAAGGACA[C/T]GAGGCTCAGATGTAC | 79931 |
rs551609088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224306 | AGGCAGAGGTTGCAG[C/T]GAGCAGAGATTGTGC | 79931 |
rs551611967 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200116 | TTGCAACACTGTGAC[A/C]ACGTTCACTGGGTTC | 79931 |
rs551656224 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176365 | ACACAACAATGCAAC[-/T]TTTTTTTTTTCTAGC | 79931 |
rs551659423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222511 | AAAGTAAGGATAACA[C/T]TTCCCTTCTTCAAGG | 79931 |
rs551713713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139135 | AGAAATTTAAGCTAT[C/T]AAATGGGGATTTGGC | 79931 |
rs551740001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165336 | AGTGAGATGGTTCTA[C/T]GCCCCTGAGCTCTGT | 79931 |
rs551754053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158631 | GACTCTTCACACAAT[C/T]GGCCCCACCAGGATA | 79931 |
rs551768258 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173417 | CAGTCTTTAAAAACT[A/G]TAGTAGTCAGAAGAG | 79931 |
rs551806956 | snp | A/T | 1.66696e-05 | 0.00288696 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146999 | GAATTTTTTTAAATG[A/T]AAAAAATATACATAC | 79931 |
rs551821782 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211567 | TTAGTGCATTTACAC[A/G]AATTCCTGTCAGAGT | 79931 |
rs551822291 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177912 | GAGGACAATTGAGGA[A/G]GATATGCCAGTGGTC | 79931 |
rs551838425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179966 | CATATATTTTGTAGT[A/T]TAATGAGCCCAGGAC | 79931 |
rs551864293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173201 | TTTACCAATGATGGA[A/G]AAGCATCGCAGGAGC | 79931 |
rs551875007 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140320 | GCCTGGATGACAGAG[C/T]GAGATGCCTTCTCAA | 79931 |
rs551875178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211320 | AAGAGGAATAAAAAG[G/T]TATTCAAAACAAATC | 79931 |
rs551933389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171967 | TGAACTTCTGACCTC[A/G]AATGATCCACCTGCC | 79931 |
rs551953435 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152767 | CATAATATATGAAAA[C/T]GTGTTTTCAACCCCA | 79931 |
rs551990084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146447 | CATTTTCCTTCATTA[A/G]CATCACTATTTACCC | 79931 |
rs552017212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171429 | ATGGCAGAATTTTGA[C/T]GGTGGGTATATGTGT | 79931 |
rs552030091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186228 | GTGGTGACCAGACGT[G/T]GGGGGGTTTGGTCAC | 79931 |
rs552031365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150796 | AAGCCCATGCAGATT[C/T]ATTATCTGTTAGCTC | 79931 |
rs552032570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191138 | CTATCATTAAGGTTA[C/T]TTTTATTTATTTGAA | 79931 |
rs552056218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144546 | AGCTGTGATTACAGG[C/T]GCGTGCCACCATGCC | 79931 |
rs552070085 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153628 | AACTTGTCCCACACA[C/G]AGATCTACTACAGGA | 79931 |
rs552187182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226368 | ATTCTGATATAAAAA[A/C]TACACTAAAAAAGTT | 79931 |
rs552196732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174770 | GTTATGCCTCACTCT[C/G]CCCACAAGTACAAAA | 79931 |
rs552240657 | in-del | -/A | 0.251296 | 0.249997 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229593 | TGAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 79931 |
rs552241259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199887 | GCTTAGGAGCGAAGG[C/T]TGGGATACAGCCCAT | 79931 |
rs552257854 | snp | A/C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202320 | AAGTGGGGAAAGGAC[A/C/T]CCCTATTCAACAAAT | 79931 |
rs552266682 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225420 | TTCATTAGAAAAGCA[G/T]TTTTTCTTCTTGTTT | 79931 |
rs552282941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193096 | TGATTCAGAATGTTT[C/T]GTATCATCTCTAACA | 79931 |
rs552301587 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207245 | AGCCTCAAGATCAGT[-/A]AAAAAACAATGATCA | 79931 |
rs552343437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168033 | CAGATCAAAAATCTT[A/G]GAGTCATCCTTGACT | 79931 |
rs552475139 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210922 | AGTATGATGTAGCAC[A/C]GCAAAAAATGAAAAC | 79931 |
rs552476795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173762 | GCTTCCCGAGCAGCT[A/G]GGGTTACAGGTGTGT | 79931 |
rs552498730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160781 | TTTCAAGGTGTGTCA[A/C]GTTGCAAGGCATAAA | 79931 |
rs552509771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187254 | AGATCCTATATAACC[C/T]TTGCATTAGTTCTGT | 79931 |
rs552523165 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206451 | AAATTATTCATTATG[C/G/T]TCACATGAATTTTAT | 79931 |
rs552541016 | snp | A/G | 4.94303e-05 | 0.00497119 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121154578 | TTTTATTTCACATTC[A/G]TAATGTTCCTTTTCC | 79931 |
rs552568791 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190559 | CCTATTCTGGGAAAA[-/G]GGGCTGACAAAGGCT | 79931 |
rs552602034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147703 | AAGGTTAGCAGACTG[A/G]TATATAAAGCTATGA | 79931 |
rs552639985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148134 | TTTTAAATGGGAGGA[A/G]CCCATCTGATTAGAA | 79931 |
rs552686755 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170159 | GCATCAACTCTAGCA[C/T]TTATTGTAAAGCAGT | 79931 |
rs552719645 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157645 | TACACCAGAGAAAAA[C/T]AGACATGGCCTTTAA | 79931 |
rs552726499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213484 | GTAATCCCAGCACTT[C/T]GGAAGTCCGAGGCGG | 79931 |
rs552728127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159990 | ATCATTATTTAGTAT[C/G]AAACTGTATAATATT | 79931 |
rs552785665 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158138 | AATTGTCTTTTATGT[A/G]TTAAAGGAGGTTTTC | 79931 |
rs552798335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212827 | AGAGTCAGGTAAGAA[A/G]GGGGTTAAAAATAAA | 79931 |
rs552812175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213008 | AGCTTTAAGGGACTT[C/T]TAATAGCCAGCAGCT | 79931 |
rs552837736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154299 | GAAATGTTCTTACTG[C/T]CTCTGTAATTCCTCC | 79931 |
rs552847409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205874 | GAGGTTTAATTGACT[C/G]ACAGTTCTGCATGGC | 79931 |
rs552866464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219668 | TCAAAGTTTACTCAC[A/G]TAGGTTTTACAGACC | 79931 |
rs552904729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162665 | GTAAGACTGGATTTT[A/G]GAATGGTGGTTCCCA | 79931 |
rs552908974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160992 | AAGAAAGAAGGCGTT[C/T]GCTTTCAAAATAGTG | 79931 |
rs552916402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154833 | AGACTTTAAACTTAA[G/T]GTTCCATTTGAGCAA | 79931 |
rs552966068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163317 | AAATACAAAGGTTTG[A/G]GGGACCTTTTCAATT | 79931 |
rs553040212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194690 | CAAAATAAACAAAAC[C/T]CCTAAACCTTGAGTG | 79931 |
rs553061464 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161596 | TAGGTATTTTTATAG[C/T]AAACATTTCATAAAA | 79931 |
rs553099161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155833 | AACTAATATTTCCCA[A/G]TATGATTATTAAATT | 79931 |
rs553120748 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182237 | GGAAGTTCAAAGTCA[A/C]ACAACTCCTTTAATC | 79931 |
rs553140139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201618 | TGTTCTCCCAGGCTT[A/G]TGTCATGATGGGAAG | 79931 |
rs553184049 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210023 | ACTTACCTAAGAAGC[A/G]TGATTTGAACTCAGG | 79931 |
rs553283445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173596 | TGTTTTTCTCTTGTA[C/T]TTTGCTCATGTGTTG | 79931 |
rs553307891 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186261 | CTATGGAGAGAGTGG[A/G]CGTCAGTGTTGACCG | 79931 |
rs553331391 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203191 | CAAATGCCCATCAAT[C/G]AATGAGTGGATAAAG | 79931 |
rs553344984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173960 | TGTATTAAATACTTA[C/T]TGATTATTGTCTGTG | 79931 |
rs553347190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167659 | CTAAAGACCTTTGGG[A/C]AAAGGAATTACATGA | 79931 |
rs553372024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209037 | CTTAAAAAATTTATG[C/T]CTACTGGGTTCTGTA | 79931 |
rs553399961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181439 | TATTTGACCTCATAA[A/C]CATTAGTACACATTC | 79931 |
rs553401383 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217571 | ATGACTGGAGGAGTT[A/G]GACCACCAACTAGTA | 79931 |
rs553482362 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166312 | AATAACTCTTCTGAA[A/G]AGCCACAAGTTTGGT | 79931 |
rs553494112 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223615 | ACAGAAACTAGAAAA[A/G]GTAAAAATGCCTCAT | 79931 |
rs553498561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182289 | ACAAAAATACAAAAC[A/G]AAACAAAAACAACTA | 79931 |
rs553521055 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228546 | CTTTACTGTATTTTC[C/T]TTTTCTGTACTGTAT | 79931 |
rs553568253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136349 | AAAGTGAGAGAGGTA[C/T]AGTAAGAGGGGCACT | 79931 |
rs553595943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220877 | TGAAAAAGAGCAATA[C/G]GTTCAGTCAAGAGTG | 79931 |
rs553612878 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135739 | AATACCACAAAATTA[A/T]TTTATGAGAATTCTG | 79931 |
rs553699366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188179 | TTAAACTTACATGGA[C/T]AGAAATCTCCTTCCT | 79931 |
rs553700415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177228 | TATAACTTGGTTATA[C/T]ATAACTTTCATTTAA | 79931 |
rs553730657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144842 | TTAGAGTAATAAGAA[A/G]CATTTTAGAGATCAT | 79931 |
rs553797361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138207 | AGGGAACACAGTTCC[A/G]AGCCTTTGGTTTCCT | 79931 |
rs553841898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183639 | ACTCCCTGAGCTCCA[A/C]CTCCTGTCAAACCAG | 79931 |
rs553851150 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133897 | GGAATACCTGGAGCT[A/T]CTAGATGCTGAAAGA | 79931 |
rs553860712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137573 | AGCTGTCCAGATTGC[A/G]TATTGTACTTCAGCA | 79931 |
rs553899345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145691 | AAAGTTGTTTTACTT[C/G]CTGTTTTACTGGCAG | 79931 |
rs553926514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210817 | CCTCCTAAGGGCCCT[A/T]TCTCCAAATGCAGTC | 79931 |
rs553961543 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216061 | TCAGGAGAAAAGATA[C/T]AGCAACTCCTTCAAC | 79931 |
rs554012138 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216685 | CAAGCCTGCCTTCTG[C/T]CTAGTTTCAATGAAA | 79931 |
rs554077129 | snp | C/G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220436 | GCAAAAATTTTAAGA[C/G/T]ATAAAGCAATCTGAA | 79931 |
rs554100431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167320 | CCAGGAAATGAATGA[G/T]AGAGACAATAAAGCC | 79931 |
rs554102253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159574 | CCATTAACTGATCAC[A/G]ATTTTCTTGCAATAA | 79931 |
rs554102907 | in-del | -/CTGCCTGTCGTCCTCTCT | 0.000115953 | 0.00761333 | cds-indel | TNIP3 | GRCh38.p7 | 4:121157129 | CCGGGTCAGGTCGCG[-/CTGCCTGTCGTCCTCTCT]CTGCCTGTCGTCCTC | 79931 |
rs554119905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143108 | GGCTTCCACAATAAA[C/T]GTTAGAAGTTATATA | 79931 |
rs554214179 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171598 | AACCTGTCCTTACCA[A/C]TTTCACCATCTGCCC | 79931 |
rs554284843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151256 | GAATAATTTGCTTCT[C/G]TATTTCTTTAGTAAC | 79931 |
rs554290480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166389 | GGTCTTTTCTGTTAC[A/G]TATGCTCTGTTCACT | 79931 |
rs554292344 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208782 | TGGAATTTCTTAAGC[A/G]ATAAGAATGACTGTC | 79931 |
rs554327974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191422 | TGCACAGAAAAATTA[C/T]GTATTTTATTGTTAG | 79931 |
rs554339587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139890 | AGAAGGTAAATATCC[C/T]GTAATGTTACCAACA | 79931 |
rs554359690 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203437 | AACTCAAATGCATGA[A/G]AATGATACAATGGAC | 79931 |
rs554376374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132848 | GGGTTATTATTTTAA[A/G]CATTGACATATGCTT | 79931 |
rs554379657 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151239 | CATTTTCAGAGATCT[A/G]AGAATAATTTGCTTC | 79931 |
rs554391163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204045 | TTGCATTTATGAAAA[A/T]ATCTCTGACTATTCC | 79931 |
rs554400904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139442 | GAGCAATCTCAGCTT[C/T]ACCTGCCCACAAAGC | 79931 |
rs554476834 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191219 | TTTAGAGAATAGGAA[A/C]CATTGGCTCCTAATC | 79931 |
rs554489708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170908 | GCAATCTCTGCCTCC[C/T]GGGTTCAAGAAATTC | 79931 |
rs554554304 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153216 | AATCACCGGAATGAT[A/G]AAAAATTGTATTTTT | 79931 |
rs554587745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205463 | CTTTGCATTTTACTC[C/T]GAGTGAATGGGGGTT | 79931 |
rs554588606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213561 | GAAACACCATCTCTA[C/T]TAAAAATACAAAAAA | 79931 |
rs554600675 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155858 | TAAATTTAAGAAATC[C/T]GCTTTAGGTAATTCA | 79931 |
rs554637742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187333 | ACTGATTGAGAGTTA[G/T]GGCTCCAATGATCTC | 79931 |
rs554640659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174159 | ATACTTCAGGTGAAA[G/T]AGAACTACCTTCTTC | 79931 |
rs554648984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219961 | ATTAAATGTTAACCA[A/G]GTTCAATACATTTAG | 79931 |
rs554655994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180921 | AGTCTCTGTAGATGT[C/G]TTTACCTCATACTTC | 79931 |
rs554673862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212422 | CTGCTTTCTTAGTGT[A/G]GAAAGAGAAGAAACT | 79931 |
rs554686097 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217522 | GTTACCACCATGGTA[A/G]CCAGTTACTAGATGA | 79931 |
rs554719871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172556 | TACAAAATATCCAGT[C/G]AAATTTGAATTTCAG | 79931 |
rs554736867 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227300 | ATATGAGAACTTTAT[A/G/T]CATTTTAAAAAAGAA | 79931 |
rs554742387 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217492 | CGGCTTGTGACAGCT[A/G]TTTGAAAATCATCTG | 79931 |
rs554774912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186538 | GTGGGACCTAGTGTA[A/T]GTCCTTTAGCTTCTA | 79931 |
rs554845456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147282 | ATTGTAAAGAACCCT[C/T]CCAACTAGTGTTCAG | 79931 |
rs554853705 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171526 | GTCTGAATCAAGGCA[C/T]AAAAACTTATACCAA | 79931 |
rs554899108 | in-del | -/TTTA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146732 | TAAAAACCACTTCAC[-/TTTA]TTTGAGTACTAGGTA | 79931 |
rs554981903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193461 | AATGTTAAAATAAAC[A/G]TAAGTGGGGGTAAGA | 79931 |
rs554993686 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134806 | ACTCTGCTCTAGCCC[C/T]CCTCCAGCCACACCC | 79931 |
rs555006206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153795 | CAAGTCCAATCACCT[A/G]CTCTTGTTTCAGAAG | 79931 |
rs555054793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134181 | CAACACAGTTTCACA[A/T]CCCTACATTTTATGC | 79931 |
rs555054938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141521 | AATACACTTTATACA[G/T]AAAATGTCCTTTGGG | 79931 |
rs555154430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226881 | GATTCTATAGCACCA[A/T]GAAGAACACGGTGAA | 79931 |
rs555191814 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200234 | TGAGAATGCTGAACA[A/C]TGGGTTCACCGAGAC | 79931 |
rs555216499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140821 | CAACCCGCAATAACA[G/T]GAAAAGACTCAATTC | 79931 |
rs555253289 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197242 | TTTAAGAACACCTAA[A/G]TCCTGCCGGGCACAG | 79931 |
rs555306723 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163061 | TAAAAATTACTGAAA[A/G]TCTAGATACCAAATC | 79931 |
rs555307079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156928 | CTAGAGAAGTGACCC[G/T]TGTTCATGGCTCTTG | 79931 |
rs555318820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200650 | TGTTGCAAACACTTA[A/C]TGCCAAAGCTATTGG | 79931 |
rs555321801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149179 | GCTGCCAATAGATAC[A/G]TGCGGAAGTTGTAGA | 79931 |
rs555336375 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184098 | TGATTAAAAACAACT[C/T]ACAAGGAAAAATGCA | 79931 |
rs555360652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142982 | AAATTGCTATTCCAG[G/T]TTTTTGAGGCCATTA | 79931 |
rs555368803 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180885 | TTCCCTTAAGCCTTG[A/G]GTCTCACCTCTTACC | 79931 |
rs555420674 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212770 | ACTTACCGCAACTGT[A/G]TAAATGATTCTTTCT | 79931 |
rs555427776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192823 | ATGCTTCACAAATTT[A/G]CATTGCATCCTTTCA | 79931 |
rs555435088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189051 | AAAATAATTACATTC[A/G]ATAGGAAAAACACAT | 79931 |
rs555460510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195459 | ACCTTGTTTATTTAT[C/T]TCTGATTATAGAGAG | 79931 |
rs555489885 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195478 | GATTATAGAGAGTGG[A/G]CCATTTTTTCACAGG | 79931 |
rs555506950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196259 | GCTTTTGTGTCTAAA[A/G]CTAATACTGTGATAA | 79931 |
rs555533046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137326 | TATTATGCAACACAC[A/G]TTCCGGTTAATGGTA | 79931 |
rs555534026 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161067 | ATAAAAGGCACAAGG[A/G]TAATACATTATTTTA | 79931 |
rs555547497 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197412 | GGGTGCCTGTAGTCC[C/T]AGCTACTTGGGAGGC | 79931 |
rs555593703 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186276 | GCGTCAGTGTTGACC[A/G]CTGTGGGAGGGATAC | 79931 |
rs555596330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136441 | GCTAAATTTTATTAA[C/G]TGTGTGATTTAGGCG | 79931 |
rs555610922 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229435 | ATCTCTACTAAAATA[C/T]AAAAAAATTAGCCAG | 79931 |
rs555655359 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184617 | AGATTCTGTGAAACA[C/T]TCCATGTCATTATAA | 79931 |
rs555656300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169719 | TCAACTTTTTGGCTT[C/T]CAACTAGTAAATCAC | 79931 |
rs555664596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214545 | TATGGAGAGGTGGCC[A/G]GGTGAGGATTGCCCC | 79931 |
rs555679113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168893 | GACTGATCTCTGACT[C/G]TGTGTCAAACCTAGT | 79931 |
rs555713413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178746 | ATAGGGATAAATCGA[G/T]GTATATTCAGTGTTA | 79931 |
rs555746633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161087 | ACATTATTTTATCCT[C/T]AGCATTAATCCATGG | 79931 |
rs555765626 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154939 | TTTTGTGACCCCAGG[-/A]AAAAAAAAAATCAAA | 79931 |
rs555817686 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177407 | CATGTTCATCAATAG[G/T]GGTTTTCTGTTTCCT | 79931 |
rs555823284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161387 | TTCATCATGGCTGGT[A/G]GATGAGTCAGCTTCA | 79931 |
rs555828592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203012 | CCACTATGGAAAACA[A/G]TGTGAATATTCCTTA | 79931 |
rs555913118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222229 | AGTTTTCCATAGAAT[A/G]TTCCTTCATTCTGCA | 79931 |
rs555916420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209839 | TGAAGTTTGCTGCAG[A/G]CCAAGAACTATTCTA | 79931 |
rs555933058 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217284 | GCTGAGAACCCATCA[G/T]AAAATTTAGGAGTTA | 79931 |
rs556015082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159099 | AATACAAAACTTAGC[C/T]GGACGTGGTGGCATG | 79931 |
rs556096574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223040 | TCGATCTCCTGACCT[A/C]GTGATCCGCCCGCCT | 79931 |
rs556097688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171674 | GCAAAAAGAGTACTG[C/T]CTGGATGTTTCTCAG | 79931 |
rs556106550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182965 | CCATGCCATGAGAGC[A/C]CTTTGAAAGAGCATT | 79931 |
rs556107792 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216830 | GAACGGTTAAAGTTG[C/T]CAGACTGACATGTTT | 79931 |
rs556119017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191261 | CAAGGCTGAGCCCCT[A/G]TATTTAGGTGAAGAA | 79931 |
rs556171172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210889 | ACAATTCAGTCCCAC[A/T]GTTGTGTTCTAAAAC | 79931 |
rs556177822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224546 | TTTGATATTTTTATT[A/G]CTTTTAAACAAGTGA | 79931 |
rs556217626 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221047 | TAATGCTCTTTAAAA[A/G]TTTTTGGTTTACTGT | 79931 |
rs556225068 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131912 | AGTGCTGGGATTATA[A/G]GCATGAGCCACTGCA | 79931 |
rs556250212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186033 | CCCTGCGTCCTCTCA[C/T]GTGAGCCTGGTTCAG | 79931 |
rs556262185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146616 | TGGGAACCACTGAAC[A/C]AAATCCTCAGTCTCA | 79931 |
rs556295247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139909 | ATGTTACCAACACTA[C/T]AGCATGTGACTTAAT | 79931 |
rs556354303 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137288 | TTCTGTTATTATACC[A/G]TAATAGATTTTAAAA | 79931 |
rs556369154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205256 | GGGCCATGTGGCTTA[C/T]TGGGGAAAGAGCATT | 79931 |
rs556385095 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192855 | GTAGGCCGTGCTAAT[C/T]GCCTCTGTATTCTTC | 79931 |
rs556406043 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138324 | TTGCAGAGCTTTGTT[G/T]TTGTTATAATACAGC | 79931 |
rs556415225 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196901 | TTTATTTTTTCTGAT[G/T]AGTGTTTTATCAGTC | 79931 |
rs556459717 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217856 | TCCAAGCATATGCGA[A/G]ATTACACATGGAGTC | 79931 |
rs556484182 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191480 | GAACATTTAAATGAT[A/G]TATTTTACAGTTGTG | 79931 |
rs556536761 | in-del | -/TTAA | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132726 | TTCTCTTCTTCTGGC[-/TTAA]TTAAGGCTGACATAA | 79931 |
rs556538477 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154240 | CCAAGAGATACGTTA[G/T]TGTTCGCAAACACCC | 79931 |
rs556545359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165886 | CTGAACTGACACTTT[A/G]TCAACACTAAAATCT | 79931 |
rs556613518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191988 | ATACCATATATTTAA[A/G]AGCTGTCTAAAAATT | 79931 |
rs556623591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185401 | TAGATTTCTGAGCCC[C/T]ATCACTATTGTCCCT | 79931 |
rs556725358 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133938 | TCTCCTCCCCAGAGG[A/G]TTTGGAAGGAGCTTG | 79931 |
rs556788548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132979 | GAAAGTAAGTCATAT[A/G]TATGACTTAGGTTAG | 79931 |
rs556820049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159328 | GTCAGCTGAACAGTT[C/T]ATCAGTAACTTTTAA | 79931 |
rs556878965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160971 | GTATGAAACATACAG[A/G]TGAATAAGAAAGAAG | 79931 |
rs556888991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175443 | CAAGTCTTGGTTGCT[G/T]CCCCCACCAAGCCTC | 79931 |
rs556923269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212977 | CTTCTCTTCCTTTTA[C/T]GAGAAAAAAAAATGG | 79931 |
rs557011587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181381 | TATGTGAGGGCTTCG[A/C]GTTGGGATGAGAAGA | 79931 |
rs557065464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214103 | CAGGAGTGATAGAGG[G/T]AAAGATGACTCAGGT | 79931 |
rs557066301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168138 | GAGGAGCACATTGCC[A/G]CAAAAGCCTAGAGAC | 79931 |
rs557070758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174679 | TTCCTCACTGGAAAA[A/T]AAAAAGGAATAATTG | 79931 |
rs557095370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181014 | AGGAGAATGAGCAAA[C/T]TTCCTCAATGAGGTC | 79931 |
rs557104841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212482 | TTTGATGTTTATTAG[C/T]TTGAAGACATGTAAT | 79931 |
rs557109791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206815 | ACTCAAGGGATCCAC[C/T]TGCCTCAGCCTCCCA | 79931 |
rs557114836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207743 | CTTCTAACCTCCAAG[A/C]TGACCTTATTCACTC | 79931 |
rs557193026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218716 | TCACAGGCACCATTA[C/T]AGTGCACTATAGTTC | 79931 |
rs557200850 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186371 | TTGTAGCACAGTAAG[A/G]ACTTGCACTCACTGT | 79931 |
rs557269635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179453 | TTCTTCTAATGTTTT[C/G]TTCTAAATGTGACAG | 79931 |
rs557285176 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137788 | AATTAGACTACATAG[C/T]TCATCTTCAGCATTT | 79931 |
rs557286561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134839 | CCTCACAGTGTGAGC[C/G]ACGTTTCCTCCAGAA | 79931 |
rs557320288 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229518 | AATTGCTTGAACCTG[A/G]GAGGTGGAGGTTGCA | 79931 |
rs557332739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180166 | AACACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 79931 |
rs557348563 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153012 | AATTCCAAGGAAAAA[C/T]TAAACCGGGAAATAC | 79931 |
rs557374148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214479 | GAATGGGACTCAGGA[A/G]CTCACACAAAGTCCT | 79931 |
rs557376651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149658 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 79931 |
rs557377704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221630 | TGGAAGAAATTGGAG[A/G]AGAGGAAAATTACAC | 79931 |
rs557497489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188090 | TTATTAGGCAAAGAG[A/T]TTGAGGTGAGAGTAA | 79931 |
rs557524700 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191373 | GGTTTATTGATAAAC[A/T]CCTGGAAGAGAACAA | 79931 |
rs557529347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143022 | TTTAGGTAGATCTAT[C/T]TAGATACAGATATAG | 79931 |
rs557545059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142082 | AGGACCAATACAAAC[A/G]AGGCTCACAGGTCAA | 79931 |
rs557555570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189163 | GCTAAGTGATAGCAA[A/G]GCCAAAATAAGAATT | 79931 |
rs557559028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202361 | TAATTGGCTAGCCAC[A/G]TGTAGAAGAATGAAA | 79931 |
rs557585448 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213127 | CCACCAATGCTTTAC[A/G]TAAAGGACGTTTGAA | 79931 |
rs557587246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227371 | GTAAAGGCACAAGAC[A/G]TTATGTTACTCACCA | 79931 |
rs557645273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201409 | TTTAAAATTAGTTTT[C/T]AAGCATTATATTGTA | 79931 |
rs557656942 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202958 | TGTGGTGAAAAGGGA[A/G]CACTTTTACACTGCT | 79931 |
rs557794776 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213363 | CTTCAGATTAAAATG[A/C]ATCATAGTCATTTTT | 79931 |
rs557800328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181510 | AGTGAGTTTTTAGAC[A/C]CGAAAAAGTGACTAA | 79931 |
rs557835124 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157597 | CTGGTCTGGAAAGGG[C/T]AATGAGGGGCAGCAG | 79931 |
rs557848776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149792 | CAAAAACCATGTCTA[C/T]GTGAAACTCCCTAGC | 79931 |
rs557933115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210742 | GGTGTCTCTTTTTAT[A/G]AGGGCACTAATCCTA | 79931 |
rs557984251 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203918 | GTGTGTATATATATA[A/T]ACTAATACACAAAAT | 79931 |
rs557998503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164885 | TCATTTGAAGTGAAA[A/T]CTTCTCATGGAGAAT | 79931 |
rs558025151 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140468 | CTTTTTTAATTGACA[G/T]GGACTGTTTGATGAG | 79931 |
rs558036973 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138206 | AAGGGAACACAGTTC[C/T]GAGCCTTTGGTTTCC | 79931 |
rs558049884 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163543 | TACCAATGTATATTC[A/G]AGGTCTGATGCTACT | 79931 |
rs558059294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162487 | CCAAGTGTCAAGTAT[A/G]TTGGGGCCCGTAATT | 79931 |
rs558084994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165747 | TTGAGTGAAAGGGAG[C/T]GACGCTGCTTTAAGG | 79931 |
rs558088446 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165804 | CAAATTGTTCATTCA[C/G]GGTTCTGAAAGTAAA | 79931 |
rs558120435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138059 | AATAAAAAATAAGAT[G/T]TAAAAAAGTACTCTT | 79931 |
rs558142536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215402 | TTTATAAACAGAAAT[A/G]TTGGCCTGTAGAATA | 79931 |
rs558146447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166339 | TGGTTTCAGAAAAAT[A/G]AGACTTTCAATATGC | 79931 |
rs558203387 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171106 | CAGGCGTGAGCCACC[A/G]TGCCTTGCCAGTAAG | 79931 |
rs558209026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197361 | GGTGAAACACCTTCT[C/T]TGCTAAAAATACAAA | 79931 |
rs558232452 | in-del | -/T/TT | 0.00874735 | 0.0655527 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146019 | ATACAATATATACTC[-/T/TT]TTTTTTTTTACCAAG | 79931 |
rs558235609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203238 | AGATAGATAGATAGA[C/T]AGATAGATAGATAGA | 79931 |
rs558306358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212336 | CTTGTCTCAAATCTC[C/T]GTGAATTTATCCATC | 79931 |
rs558330280 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145395 | CCTTTAGGTTCAAGG[A/C]AGAATTATACCATAC | 79931 |
rs558335495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170809 | AATTCTTTCTTTGCT[C/T]GGTAAGAGATATCTT | 79931 |
rs558342899 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132089 | ATATACACCTCTTCA[A/C]TTCTACGTTTAGGAT | 79931 |
rs558349297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178874 | ATCCTCAAGAAATCC[A/T]TGAGTCTCTCATAAT | 79931 |
rs558379052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210001 | TTTTAAGGTTTTAGA[G/T]TAAATGACTTACCTA | 79931 |
rs558390091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144779 | ATCTATATTTTACAG[A/G]CAGGTATACTAAAAG | 79931 |
rs558501088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211723 | TGTACTGCCATGGAG[G/T]GTCTGTATATTGAAT | 79931 |
rs558505999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139388 | GAATCATCAAGATAT[C/T]TCCAAGGCCAGCACC | 79931 |
rs558526143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177142 | AGCATCCTGTCCCTT[A/T]CTTTTATATTTGAAG | 79931 |
rs558529723 | in-del | -/ATG | 0.202959 | 0.245534 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176514 | CATCCTACTAGCATT[-/ATG]ATGATGATGATGATG | 79931 |
rs558531981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219177 | TGCTCTCCAGCCTGG[A/G]CAACAAGAATGAAAC | 79931 |
rs558540627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158922 | TAAATTGAACACACT[C/T]TCACTGTTTATAACT | 79931 |
rs558563711 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218460 | AAAAATATTAACCAG[A/T]GACAATCAGAAAAGT | 79931 |
rs558616373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193397 | GTAATAATAAGAATA[C/T]ATTAGAATTCATCAA | 79931 |
rs558646284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180268 | AGCCAGATGTGGTGG[C/T]GGGCGCCTGTAGTCC | 79931 |
rs558648673 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217329 | ACGAAGCCAGTTTGT[C/T]TGAGTTTCAAGCATT | 79931 |
rs558668441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226773 | TTATTTTGCAATCTC[A/G]TTTGGGAAATTTGAC | 79931 |
rs558714625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138848 | CTTACCCCCCATCAC[C/T]GCCATCATCTCTCCC | 79931 |
rs558717318 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134132 | ATCATAATATTTAGG[A/C]TTTGATCTTCTATAT | 79931 |
rs558749371 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131225 | GTATAATTTGAGATC[A/G]TATTTGTGAGAATAT | 79931 |
rs558754191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192977 | ATAATAGACTTACAT[C/T]CAATAACTTTCCTCG | 79931 |
rs558762446 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169320 | CCCTAGATCTCCACA[C/T]GGTACATCCCCTCAC | 79931 |
rs558775409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223883 | ATTCTTTCAAAAAAA[C/T]ATACATTATTACTAT | 79931 |
rs558837997 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198350 | AAACATATGGATTTG[A/T]TATATATAGCATAAA | 79931 |
rs558869058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153099 | TGACATTTGTATAAA[A/G]ATCTGATTTTACTCA | 79931 |
rs558910971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227254 | ATTGTTAATATTACT[A/G]AGTTCCTGATCAGTT | 79931 |
rs558992378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140797 | GGGAGGGAGAGCAGA[C/G]AGAACTAGCAACCCG | 79931 |
rs558999380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186092 | AGGGACGGGCCCTCA[C/T]GAGGATAGTGGTTTT | 79931 |
rs559016005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159464 | AGGTTCTTTTCCCAA[A/C]CTTTTTCGTATTTTT | 79931 |
rs559041006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226950 | GCTCTGCTCATTGCT[G/T]AATCAAGATTGTTCA | 79931 |
rs559055764 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140076 | CGCAGTGGCTCATGC[A/C]TGTAATCTCAGCACT | 79931 |
rs559066099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147497 | TATGTGGAAAAGCAA[A/G]GCATGATTGTTAAAA | 79931 |
rs559094457 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213419 | TGAATGCATAATCCA[-/T]TTTTTTTTAAAAAAA | 79931 |
rs559099784 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205733 | GAAAAAGCTCAAGGA[C/T]GCCTCCAAGTTCTTT | 79931 |
rs559106149 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134417 | TGGAAGTCATTTTGC[A/G]TCTCGTTCTGATAAC | 79931 |
rs559117866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180607 | CTATGTTGTGTAAGA[A/G]TGAGTTCAAACATTA | 79931 |
rs559128884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153574 | AAAGTATATTGTTTA[C/T]GAAGTTTATCCTCAT | 79931 |
rs559130001 | snp | C/T | 1.65217e-05 | 0.00287412 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147037 | CAAAGATTATTTTGT[C/T]TTGACTTGTACCTGG | 79931 |
rs559143069 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197033 | CTTGACTCAAAGTCT[C/T]AATGAACTTAAAAAA | 79931 |
rs559199367 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200296 | AAAATTACAAATTCC[C/T]TTTTGCATAATCCAC | 79931 |
rs559261341 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219371 | AAGGAATTCCTATAC[C/T]GCTAAAGAAGCAGCT | 79931 |
rs559313670 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176843 | CCAAAGAAATTTCTC[A/C/G]AGGCTTTTTACCTTG | 79931 |
rs559318855 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227598 | AATATTCACCTCTCA[A/G]ATACAAATACAACCT | 79931 |
rs559335913 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179429 | TTTACCCCAACAAGT[A/G]TTACATCCTTCTTCT | 79931 |
rs559366095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195093 | GAATTGCTTGAACCC[C/T]GGAAGCAGAGGTTGC | 79931 |
rs559404276 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161314 | ATTTGGCCAACTCTC[C/T]TGTTGCGATTTAAAA | 79931 |
rs559431491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159712 | CAATATTTAGATGCA[C/T]TTTAGGCTACAAATA | 79931 |
rs559486867 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173941 | TGACCAATGTATGCA[C/T]TCTTGTATTAAATAC | 79931 |
rs559490223 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168585 | GAGTGCAGTGGTACA[A/G]TCATAGCTCATTGTA | 79931 |
rs559516586 | in-del | -/GGAA | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173241 | AGGAATATGATTCAG[-/GGAA]GGAAGTTTTATGGGA | 79931 |
rs559560622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200362 | AAAACTTTATAGTAG[G/T]GCCCTCAGTAGACTT | 79931 |
rs559635212 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144691 | ACAGGCATGAGTCAC[C/T]GCACCCGGCCTGTTT | 79931 |
rs559659066 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175021 | GGAGACATCCACATC[C/G]TGTCACAAAGTTAAA | 79931 |
rs559665996 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166893 | GACTAAAAGATCTAG[C/G]TCTAGAATTAGATTA | 79931 |
rs559667773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155070 | CAGGTTCAAGCAATT[C/G]TCCTGCCTCAGCCTC | 79931 |
rs559682142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200785 | TTTTTGTTCCTTTTT[A/T]TCCAGCAGATTTCTG | 79931 |
rs559702410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148610 | TACCCTTATTCTCTT[C/T]GTCGGTTTATTTTTC | 79931 |
rs559705435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207120 | ATCTGGGGTTCTTTG[C/T]TTTGTTTTGTTTTGC | 79931 |
rs559711825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215519 | ACAAACTGTTAGTTG[A/C]TCCAGACACAAATAC | 79931 |
rs559722387 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209384 | AGTGTGGGCAGTCTT[G/T]TGGGACTGAGGCCTT | 79931 |
rs559769454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207843 | AACCTGATATGGTTT[C/G]GCTGTGTCCTCACCC | 79931 |
rs559770995 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147252 | TTATTTTAAATGACT[A/G]CTGCCTACTCCATTA | 79931 |
rs559780618 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151430 | AGAATACACAAATAC[C/T]GTCTAGCCTGATATG | 79931 |
rs559847247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214628 | TTCTTTCTTGTCTAC[A/G]CGGTGAAATTTTGCC | 79931 |
rs559952361 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161695 | TCAGAGGAACGACAA[A/C]ATCATCGAGAAAAAG | 79931 |
rs559989394 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229579 | CCTGGGCAACAGAGT[A/G]AGACTCTGTCTCCAA | 79931 |
rs559998562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176375 | TGCAACTTTTTTTTT[G/T]CTAGCAGAAAAAAAT | 79931 |
rs560005141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174340 | AGCCCAAAATGTTGA[A/G]GTTATAGTGAGCCAT | 79931 |
rs560084206 | in-del | -/ACAA | 0.00755907 | 0.0610114 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219198 | GAATGAAACTCCATT[-/ACAA]ACAAACAAACAAACA | 79931 |
rs560162730 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170398 | CACAATGACCACGGG[A/G/T]ATACACAAAGTTATA | 79931 |
rs560187424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134983 | TGTTGTGTGTAGAGT[C/G]GTGAGGGGTGTATGG | 79931 |
rs560188364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175699 | CTCAAAAGTGTGTCT[C/T]ATTTATCAACAAGAA | 79931 |
rs560212813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181807 | AAACAAATTTATGGA[C/T]GCAAATTAGTTATAA | 79931 |
rs560221540 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228337 | TTGTTTGCTCTACTT[C/T]AACTCTCATCACAAC | 79931 |
rs560226040 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138426 | GAATTGAGGTTCATG[C/G]ATTTCTGCATTCGCA | 79931 |
rs560231944 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149307 | GTGCCATCCATACAC[A/G]GGACTAGCTGAGAAA | 79931 |
rs560293220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224008 | CAATTCCTCAAATGA[A/G]AATAAATGGAAGACT | 79931 |
rs560312653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222086 | ATAGTAGCTAAGAGT[A/G]CTCCTAATACTTAAG | 79931 |
rs560411054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121136642 | TTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCA | 79931 |
rs560448447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157534 | GACCCCACCCAGGGG[A/T]ATCTGTAGGTTTGTC | 79931 |
rs560453262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210802 | ACTTAACCTTAATTA[C/T]CTCCTAAGGGCCCTA | 79931 |
rs560492334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216354 | ATTGCCACAAAGCAG[A/G]AGTGCTCTAATTAGA | 79931 |
rs560502288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184644 | ATAATGAATTCTCTC[A/G]TTATTTTTAAAGCTA | 79931 |
rs560526899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150691 | TTCTCAGAAGCTGGT[A/G]CTGCTGGTCCCAGGT | 79931 |
rs560553897 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225852 | TGAGATAAATGGGAA[C/T]TTTGCCTGTCTCTTC | 79931 |
rs560570620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177690 | ACTCCCTGTCATTGG[C/T]TCACGCTTGTGTTAA | 79931 |
rs560607031 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184173 | TATTTTTTTGCCTGA[C/T]TCATCATATCTCACC | 79931 |
rs560632541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165838 | TTATAACTCACATAA[G/T]ATCTGACTTTAGGGT | 79931 |
rs560634407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158554 | ATACTACACTTAGCA[C/T]CCTTCCCGTCATTTT | 79931 |
rs560678789 | in-del | -/TTA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139786 | GATCACCTCTGTTTT[-/TTA]TCTTCTCGTTTATTT | 79931 |
rs560687174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152187 | ACATAGAGGGTAGGC[C/T]CTGGATTCCATGCTG | 79931 |
rs560702458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150002 | ATAAATGCAAAAACC[C/T]TTGACATATTTCTAG | 79931 |
rs560714552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183571 | GGAAGCGAGAGGCAG[A/G]CAAGTGAGCAAAGCT | 79931 |
rs560718605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196420 | TAGAAAATAAATCGA[C/T]GAATATAATATTTGG | 79931 |
rs560728325 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201313 | TGCAAGATGGCGTGT[A/G]GTCAATGGCTGGCTT | 79931 |
rs560733425 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160423 | GGCAGAGGCTGCAGT[A/G]AGCTGAGATCGTGCC | 79931 |
rs560750118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163689 | TGTTGCTGAACAAAA[C/T]CTATGGTACCAATTG | 79931 |
rs560808230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202830 | ACATGAAACAATGCT[A/C]AATTCACTAATTATA | 79931 |
rs560869609 | snp | C/G | 0.000133089 | 0.00815641 | missense | TNIP3 | GRCh38.p7 | 4:121157105 | CCACCTCCTCCCGCT[C/G]CAGCCGGTCCCGGGT | 79931 |
rs560892370 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228558 | TTCTTTTTCTGTACT[A/G]TATCTTAGTTTCTGT | 79931 |
rs560899332 | in-del | -/TA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172463 | CCGTAAGAGATAGAC[-/TA]TACATCAGTGCCAAT | 79931 |
rs560927189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205678 | GTGGGATTCTGGGCA[C/T]AATTTGAATTTAGCC | 79931 |
rs560931927 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150550 | TCTGCTTCAGTCAAA[C/T]GTATACCCTTTCAAT | 79931 |
rs561008525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197504 | GCCACTGCACTCCAG[A/C]CTGGGTGACAGAGCG | 79931 |
rs561045311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211121 | ATGTCCCTGACATAG[A/G]AATATTTCCTAGATG | 79931 |
rs561067672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151636 | GTAAAGAGAATCTAG[G/T]GTGGGGTGGGCCAAA | 79931 |
rs561069190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211814 | CCTTAGAGTTACCAC[A/G]CACAGAAAGGACAGA | 79931 |
rs561132288 | in-del | -/TA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198035 | TGTTCATCATGTTTT[-/TA]AAAATAGATCCTAGA | 79931 |
rs561147004 | snp | A/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167662 | AAGACCTTTGGGCAA[A/T]GGAATTACATGATCA | 79931 |
rs561204670 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141978 | AGTTGCAGTGACATT[G/T]CTTTATACAAAAGGT | 79931 |
rs561217284 | in-del | -/A | 0.00120192 | 0.024485 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213427 | TAATCCATTTTTTTT[-/A]AAAAAAAGACATTCT | 79931 |
rs561240279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159787 | GTGCTATGATATGTG[C/G]TTGGCTTTTTGTTGG | 79931 |
rs561266625 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186174 | TTCAGCCACTGCAGA[A/T]AGAGGAGAAGTGGCA | 79931 |
rs561283440 | in-del | -/GAAATATGAGTGAGT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194814 | AGAAACTTGCTTTTG[-/GAAATATGAGTGAGT]GCTAATATCCATGAA | 79931 |
rs561294752 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196069 | TAAGTCTTCAGAAGG[C/T]CTTTTTAAGGTGGAA | 79931 |
rs561318147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225781 | TTCTCTACCTTGGCC[C/T]CCGACCTGGACAAGG | 79931 |
rs561329221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135078 | AGGTGGGGAGAGAAG[G/T]TCGAGGGTCCCAGGC | 79931 |
rs561342956 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228246 | TATTCATTTGTCAGA[C/T]AGGCATGGTAAGATT | 79931 |
rs561365556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135788 | ACAGATTAAAAGGAC[C/T]GTTTTAATTAAATGA | 79931 |
rs561378693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121166985 | AAGGTCTCTAAGGCT[C/T]AATTTCCATTTTATA | 79931 |
rs561403785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219364 | CTTTTTTAAGGAATT[C/T]CTATACTGCTAAAGA | 79931 |
rs561445080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173684 | CCCAGGCTGGAGCGC[A/G]ATGGTGAGAACTTGG | 79931 |
rs561447394 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132564 | ACAAGCCTCAGTATA[A/C]ACAAAGAAGAGGGTC | 79931 |
rs561447520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140192 | TACAAAAATTAGCCA[C/T]GTGTGGTGGTGTGTG | 79931 |
rs561483789 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133250 | TGCCAAGAAACAAAG[A/G]GTTATCCTTATCCCT | 79931 |
rs561485694 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213867 | ACCCCAGGATCATAC[A/G]TGTTGAGTGGGACTG | 79931 |
rs561546565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141322 | TGGGAAGACACAGCC[A/G]TGGAGAACAACTTAA | 79931 |
rs561581726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169616 | ACTCACACATACAAA[C/T]TGCCTTCCTTACCCC | 79931 |
rs561587249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193049 | ATATATATGTAGAAC[C/T]ACCCTATACATAATA | 79931 |
rs561644170 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218412 | TTTTCCTAGGCTAGA[A/G]TTTTACATTTGTTAT | 79931 |
rs561648682 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180410 | GCCTCAGAAAAAAAA[A/T]ATTATAGATGTCAGA | 79931 |
rs561696814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147599 | ACACCTCTTGAGAGG[C/T]ACTCCAAATATTTGA | 79931 |
rs561704664 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221650 | GAAAATTACACACCA[C/T]TCTCATTTACAGTAA | 79931 |
rs561732551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221022 | AAAATCAATGAGAAC[A/C]AATAAAACATAATGC | 79931 |
rs561742778 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155664 | CAATATCTCCTACCT[C/G]TTAATTTTGTATAAT | 79931 |
rs561758053 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187654 | TAGGTCCCTCCAACT[C/G]AAATGTAGCTGATTT | 79931 |
rs561769862 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188987 | GGTTTTTATGGTTAC[A/T]TGGTACGGTTGCCTC | 79931 |
rs561788689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181089 | AAGTCCCAAAAGGAG[A/G]CATAACCTGTAGCTA | 79931 |
rs561808590 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207054 | CGAAAATGTTTTCAT[C/T]GGAAAAAAACAGTCA | 79931 |
rs561833631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162730 | CTAAACATAGAGCAT[C/T]CTGAACAATGGATCA | 79931 |
rs561852396 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193781 | TGAGAAAAATCCAAA[C/G]TATGATCATATGACA | 79931 |
rs561874278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171838 | TGGGTTCAAGCGATC[C/T]TCCTGCCTCAGCCTC | 79931 |
rs561920101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162125 | TGAACCATTAAGAAA[C/T]ATTTTCAAAACATGT | 79931 |
rs561949056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194274 | ATGGCTGAGGAAAAA[A/G]ATATTTTTGTGCACG | 79931 |
rs561952680 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134513 | ATATCTGTGGACTTC[A/G]ATGTATTAAAAACAT | 79931 |
rs562033904 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200245 | AACAATGGGTTCACC[C/G]AGACAACTGCAGAAG | 79931 |
rs562065889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148731 | AAATTTTTAGATCTA[G/T]TCACAGGCTACTTCA | 79931 |
rs562089145 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229069 | AAGTGTGTTGAAAGA[C/G]GATCTTGTCTTAAGC | 79931 |
rs562117931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201748 | ACACATATTCATTTA[C/T]TCAACAGTTATATAT | 79931 |
rs562170125 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150288 | TTCTTTTATAATTGT[A/T]ACAATCATCTCAAAT | 79931 |
rs562213325 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156601 | ATGAGATAATGAGGA[C/T]GAAGGCTTTAAAAAA | 79931 |
rs562309120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200898 | TATCATGGGTAGAAA[C/T]AAACCCGGAGGGAAG | 79931 |
rs562310999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208448 | CAGCACAAGAGGGCA[C/G]CTTCAAATCTGTATG | 79931 |
rs562330157 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139791 | CCTCTGTTTTTTATC[A/T]TCTCGTTTATTTTTA | 79931 |
rs562403598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174987 | ATTCCAAAACCCAGC[C/T]TGGGTTGAGATGTCC | 79931 |
rs562417571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169174 | CTCTTTATAGTGGCA[A/C]GGTCCTGCACAATCT | 79931 |
rs562482425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170952 | TCCCGAGTAGCTGGG[A/G]TTACAGGTACCTGCC | 79931 |
rs562580179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170484 | AGCTGGCCTGTTTCC[A/G]TGTATTTTCTTTTTA | 79931 |
rs562677050 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222159 | ATATTGCTCTTGATG[C/T]ATCTTAGAGGCTTAG | 79931 |
rs562678793 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143899 | AGAGAGCATGACAGC[A/G]TATACGTGTGGGCCA | 79931 |
rs562702425 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222476 | ATTTAAATACTCTGA[G/T]CCCCACTGTCCTTAC | 79931 |
rs562714523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215605 | CTTTCCTTCTATTTT[C/T]CCATCTTTCTCCTGT | 79931 |
rs562809316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137015 | AAGTCTCATACACTG[A/C]CTACAACATTTCATT | 79931 |
rs562878645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139525 | GACACAGAGAATATA[C/G]ATTTTTTTGTTGTTC | 79931 |
rs562901572 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217046 | AAAAACTGTACTTCC[A/G]ACAGAATTTGTTTCT | 79931 |
rs562912157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211297 | AGCAAATGATATAAA[A/G]TACTAAAAAGAGGAA | 79931 |
rs562945748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147432 | TGACATGCCCAAGTT[C/T]CCAGACATAAATTAT | 79931 |
rs562963549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184725 | TTGACTTTCATATTT[A/G]TATTGTTTCTTTCAG | 79931 |
rs562970881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191553 | TACATTCACCTCATG[C/T]AACCACATCCTGTGT | 79931 |
rs563039671 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188225 | ACAAGAATAAATCAA[C/T]ATAGAAATTAAATAG | 79931 |
rs563056426 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197397 | GCTGGGCGTGGTGGC[A/G]GGTGCCTGTAGTCCC | 79931 |
rs563087208 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204665 | AATGCACAATAGAAA[A/T]ACCTGTCTAGATATA | 79931 |
rs563099961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138550 | TACGAATGAATGTAT[A/G]TTGAGTAAACATCCC | 79931 |
rs563106900 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184337 | TGCTCAATCCACCAC[C/G]CTTGTTGAGAGTAGC | 79931 |
rs563163631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186211 | AAAAAGAGAACCATA[G/T]GGTGGTGACCAGACG | 79931 |
rs563202505 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174580 | AAAAAATCTCCCAAT[A/C]TGCTAGCCTAAAAAA | 79931 |
rs563274037 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172451 | CAATGAAAAAACCCG[-/T]TAAGAGATAGACTAC | 79931 |
rs563281199 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229273 | CCAGCCTGGGCAACA[C/T]AGTGAGACTCTGCCT | 79931 |
rs563319622 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199845 | TACCTGAGGACGGTT[G/T]TGTAGGTTGCTGTGT | 79931 |
rs563322595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193536 | AACATTATCCCATTA[G/T]AAAATCATTATTTGA | 79931 |
rs563347091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192487 | TGAAACAAATCATGA[C/T]CAGTTGTTATTATGT | 79931 |
rs563357209 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193202 | GAGATGAGAAGAGAC[A/G]TTATGTTGTCATATG | 79931 |
rs563379668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200316 | GCATAATCCACTAAG[A/T]AGAGGAATATTTACA | 79931 |
rs563413316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172740 | GGTACCATTATGTGT[A/C]GGGACAGGGGATAAT | 79931 |
rs563417596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174232 | CTATTTTTAAATACC[A/C]AAAGTTATAATTATA | 79931 |
rs563447588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166540 | ATGTTTCCAAGGCTG[C/T]TGTGAAGAGTCTTCA | 79931 |
rs563472693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165902 | TCAACACTAAAATCT[G/T]CTCATCAGAAAAGAA | 79931 |
rs563515841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198145 | GGAGAAGTTTCATTC[C/T]TGTTTTTTTTTTTTT | 79931 |
rs563577544 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165279 | CTCTCCAACTCTCCC[C/G]TGTGCTCCAACCATC | 79931 |
rs563594590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206385 | TTATTCCCTGATCCT[C/T]GGTTAAGTTAAATTT | 79931 |
rs563608886 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168013 | TAATAACACCTTTTA[A/T]TCTCCAGATCAAAAA | 79931 |
rs563631783 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146430 | CAAAATTATGTTAGC[C/T]ACATTTTCCTTCATT | 79931 |
rs563632694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179870 | ATATATTGAATTCAC[G/T]TCAGGAAAGACTGAG | 79931 |
rs563671905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160660 | ACAAACTTTATTTAT[C/G]ATAATGCTTTTTAAC | 79931 |
rs563696757 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171549 | TATACCAAGAATAAC[C/G]AATAAAACAAATTAG | 79931 |
rs563705182 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171807 | GCGATCTTGGCTCAC[C/T]GCAACCTCTGCCTCC | 79931 |
rs563727838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221970 | AGTTCCTGAACCAGG[A/T]GTCAGGAGACTAAGA | 79931 |
rs563864366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221075 | TGTTAGCAATTCTCA[C/T]GGCCTTTTGCAGTTT | 79931 |
rs563864685 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228811 | TTACCCTGTTAGTTT[C/T]TTTCAATGTGAGAAA | 79931 |
rs563870293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219460 | CATCAGTGAAGATCA[C/T]AAGCTGTTTGATTGT | 79931 |
rs563883981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134258 | ATAACTCTGTACCCT[A/G]TGAAAAATTTGGAAT | 79931 |
rs563884385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220125 | ATATAAAAGTACTTA[C/T]ATTAATTTTTTAGAA | 79931 |
rs563889028 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227779 | AGATCAGCTTAATAG[A/G]GCCACAACACATAAA | 79931 |
rs563923638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136500 | TCCTCATGTGTTAAA[A/T]AGTGCAAAACAAAAC | 79931 |
rs563975403 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146942 | CAGGTGCTGACCTTT[-/A]AAAAAAAATTCAATG | 79931 |
rs563992149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200702 | GCCAGTAATCAGGCA[C/T]CTTGGCTACCTTTTT | 79931 |
rs564001898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186696 | TCGATACTATTGTTA[C/T]TATTCTGAGGGTGTG | 79931 |
rs564026329 | in-del | -/A | 0.164546 | 0.234942 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194850 | ATCCATGAACAATAG[-/A]AAAAAAAAAGTACAC | 79931 |
rs564034766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218897 | AGAACCAAAAGATTT[A/T]CAATTAAAAACCACA | 79931 |
rs564049095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140995 | AGGAAGCCAAGAGAA[A/T]CATGTTCTCTGTAAG | 79931 |
rs564051692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194995 | CAACATGGCAAAACC[C/T]TATCTCTACTAAAAT | 79931 |
rs564060310 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159222 | CACTCCATCCTGGGC[A/G]ACAGAGTGAGACTCC | 79931 |
rs564125265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143924 | GGGCCATTCTAAACC[A/G]TGAAATCACCAACAA | 79931 |
rs564136389 | snp | C/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131438 | TTTTCATTTTAATTG[C/G]CTTGAGAAGTCAGAA | 79931 |
rs564141232 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166272 | TATTAGCTCAAGAGA[A/G]CCATATGGTTATTTA | 79931 |
rs564163893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144406 | GCGTTTTTTTGTTTT[C/T]TTCTTTTCTTTTTGA | 79931 |
rs564176986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175070 | AACACATTTGCTAAA[C/G]AACTCTTATGAACAT | 79931 |
rs564201078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181799 | GAAAAAAGAAACAAA[C/T]TTATGGATGCAAATT | 79931 |
rs564260063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148565 | ACTTTAGGGGTTGAG[A/G]GTTTGACAGAGCTTT | 79931 |
rs564332406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188447 | CAATGATTTTCAGGT[A/G]TTTGGAGCCCTCATA | 79931 |
rs564419879 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148068 | GTTGAGAACTGACAT[C/T]CATTTCCAGAGACAG | 79931 |
rs564421859 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154986 | TTTTTTTTTAAAGAC[A/G]AATTCTCACACTGTC | 79931 |
rs564475954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163571 | ACTAAATTAAAAACT[G/T]AAATGAATAGAAGTT | 79931 |
rs564523195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196388 | TTTCCTGTAACAAGT[A/G]TAGGTTTTTTTTAAG | 79931 |
rs564529668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137830 | CAAATCTTTGGAAAT[C/T]AACAAGTTAGAGTCC | 79931 |
rs564534437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157034 | TTTTCTACAGGAAAT[C/G]CCCCCGCCCCTTTGC | 79931 |
rs564546791 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210331 | TCAGGTTTAGTAATG[A/G]TATCTTGAATAACAG | 79931 |
rs564587492 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197459 | CTTGAGCTTGGTGGC[A/G]GAGTAGAGATTGCAG | 79931 |
rs564601934 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143813 | AGAGTACTATAACAT[A/G]TCTTAATGAAGCTTC | 79931 |
rs564681275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158420 | ATACTCTGTGAGCCA[C/T]GATAAATGTGCACAA | 79931 |
rs564690124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208012 | TTATCAGGGGTTTCC[A/G]CTTTTGCATCTTCCT | 79931 |
rs564712438 | snp | A/G | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204229 | CAAACCTGCTTCCCA[A/G]TCTATTCAAAGTCAC | 79931 |
rs564717834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195768 | TTACTTGGCAGCAAT[A/G]GCAAGCCTGACTATA | 79931 |
rs564792842 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211032 | TAATTGAAAACCCTG[A/T]TCTGGTAATATAAAG | 79931 |
rs564867775 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201347 | ACAAAGCAGCAGGGT[C/G]CAGAGTGGAACATCT | 79931 |
rs564871616 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165150 | AACTTCATTAACCTG[A/C]CTACGAGATATTCAC | 79931 |
rs564881503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151535 | CAACAAAAGTAGTTT[A/C]ATAATTTATGTTTTT | 79931 |
rs564960034 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159582 | GATCACGATTTTCTT[-/C]GCAATAATGTGTTTT | 79931 |
rs564994671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138397 | CTCTGAGACTGAAAA[A/G]GGAACAGAAGCCAGA | 79931 |
rs565064263 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216337 | ACTCTTAATACACTA[A/T]CATTGCCACAAAGCA | 79931 |
rs565073793 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222865 | GGCTAGAGTGCAGTG[A/G]CGCGATCTTGGCTCA | 79931 |
rs565121168 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216717 | GTAAACCACTGGGTG[C/T]AAACACAGGCTCAGT | 79931 |
rs565126151 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167402 | AAGAGTCAGAGTTTC[C/T]GCTGGGCCTTGAAGG | 79931 |
rs565154633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225089 | TTTATTAACTATACT[C/G]CTTAAGACTACATTA | 79931 |
rs565161121 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189308 | TATTTTCAGGAAAGA[C/T]CCTGGAGAACAAAGC | 79931 |
rs565189042 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164377 | TCTTCCAAATAGGGA[-/T]TTCCCAGGATGTCTC | 79931 |
rs565190592 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132504 | CCAAAGGAAAACATG[A/G]CCAGGCACAAATAAC | 79931 |
rs565197378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191613 | ATGTTTCTCTCAAAT[C/T]GCTACCTGAATTTTA | 79931 |
rs565199416 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197865 | AGTGAGCAATGGAAT[A/G]TCATGGTATAGATTC | 79931 |
rs565321396 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148611 | ACCCTTATTCTCTTC[A/G]TCGGTTTATTTTTCA | 79931 |
rs565349608 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205987 | GAAGTGCCGAGTAAA[-/G]GGGGAAGTCCCCTTG | 79931 |
rs565357698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139594 | TTTTTCTAACATGAG[C/T]CAACAGAGAGCATTT | 79931 |
rs565368404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173472 | TAGTGGTTAGAAAAG[A/G]GAAATTCAGCCTTTT | 79931 |
rs565373870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185538 | TTTGTCTGTGTTTAT[C/T]CACTGCTCAGTCTCT | 79931 |
rs565383122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179564 | TTTTAACCACTTTTA[A/G]GTTTTCAGTACATTA | 79931 |
rs565458194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139190 | AGCAGGGCAAATCTT[C/T]CCCTTTTTGCTGTTG | 79931 |
rs565483756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140381 | ATGTAGGCCATTCTA[C/T]ATGGCTTGGAGTCCT | 79931 |
rs565502446 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173682 | TGCCCAGGCTGGAGC[A/G]CAATGGTGAGAACTT | 79931 |
rs565534907 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191774 | ATATGACAAAACACT[A/G]CTATCTTAAAATTAT | 79931 |
rs565547496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139795 | TGTTTTTTATCTTCT[C/T]GTTTATTTTTAGATG | 79931 |
rs565594378 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184832 | CTTCATGGTGCAAAA[A/G]GTTGCATATGCATAA | 79931 |
rs565619497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225439 | TTCTTCTTGTTTTTT[C/T]CTTTAAGACTTGTGG | 79931 |
rs565624316 | snp | C/G | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145080 | AATGAATACATTCTG[C/G]TAAGAAAGCAACTCA | 79931 |
rs565641692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150606 | AGGCAGCAAATATGC[C/T]CATCCCTTGGTACTG | 79931 |
rs565668223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145535 | CTGACAAGACTAAAA[A/G]TTCTGTAATGGCAAG | 79931 |
rs565697661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212883 | CTATGATATCATAAA[A/G]GAGATCATTTTAGTT | 79931 |
rs565719240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194457 | TATGTAGCAGGAACT[A/G]AGATGCAGACCAATA | 79931 |
rs565758645 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194009 | TTTATGAAAACTAAA[C/T]GTAATGTAAGATCCT | 79931 |
rs565786437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180090 | GGAGGGGTGGTGAGG[A/G]TGTCCAGGAATTAAT | 79931 |
rs565830610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151939 | AATCAATTTTGCCCA[C/T]GGGTGGCACGAGCTG | 79931 |
rs565866748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192594 | TTGGAAAAATTGCAT[G/T]GATTTAATGATGCCT | 79931 |
rs565894488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227272 | TTCCTGATCAGTTAT[A/G]TATGTCTTTTTAATA | 79931 |
rs565944374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134787 | TGTCCCCATCTTATA[A/G]AGGACTCTGCTCTAG | 79931 |
rs565945445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159186 | AGGTGGAGGTTGCAG[C/T]GAGCCGAGATTGTGC | 79931 |
rs565946823 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200000 | GCACTACACAAGCTA[A/C/G]CATTGTCCTGGGAAC | 79931 |
rs566029219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167238 | ATGTACACACACATA[C/T]ATATGTGTGTGTGGC | 79931 |
rs566041393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168051 | GTCATCCTTGACTCT[C/T]CTTTCTCTTACATCC | 79931 |
rs566046214 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141425 | ATGTAGCAATATCCA[C/T]AGTAGTTCAATATAA | 79931 |
rs566158139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154101 | TAGGCTTGCACTTGA[A/G]AGAGCTATCATCTCA | 79931 |
rs566209716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147713 | GACTGGTATATAAAG[C/T]TATGAAAACAAATGA | 79931 |
rs566234049 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160790 | GTGTCAAGTTGCAAG[A/C/G]CATAAAGGGTAAAGG | 79931 |
rs566252605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160028 | TGAGAGTTACTCTGT[C/T]GGCATTTTAGGGATT | 79931 |
rs566257673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206575 | CTTTTCTTTTTTGAG[G/T]TCTCCCTCTGTCACA | 79931 |
rs566261987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208316 | TAGGGATAACATCAC[C/T]ATTGTAAAACCCAGG | 79931 |
rs566265594 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199726 | ACAAATTCACAATGC[A/C]CAGAATAGAGGCATC | 79931 |
rs566271365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199930 | CAGCCAAGACACCTC[A/G]TGTGGGGCTGCATAT | 79931 |
rs566325176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213995 | AAAAGTATTCCTTCC[A/G]CTCCTTTATTTTCCT | 79931 |
rs566351756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201981 | GAAAATGACCATACT[G/T]CCAAAAGCAATCTAC | 79931 |
rs566404026 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144519 | TGATTCTCCTGCCTC[A/G]GCCTCCAAAATAGCT | 79931 |
rs566405858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213357 | GCTCTACTTCAGATT[A/T]AAATGAATCATAGTC | 79931 |
rs566416419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155362 | AAAAGAAAAAACTCT[C/T]ATTGTGAGAAAACAA | 79931 |
rs566457409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201204 | TAATCAAATGTTCCA[C/T]GAAAGGGGACAACTG | 79931 |
rs566482375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195409 | ATCACAGCATTACCT[C/T]TGGCTAGAAAAGTTA | 79931 |
rs566531466 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208272 | ATGCAGCCAGAGACA[C/T]CAAGATTCGAAATCT | 79931 |
rs566532600 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131805 | AGCCTGGCTAATTTT[C/T]GTATTTATAGTAGAG | 79931 |
rs566544157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221214 | TATAAAACCTTGGTT[A/T]TGTTTTTCTAATAAT | 79931 |
rs566554320 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186226 | TGGTGGTGACCAGAC[A/G]TGGGGGGGTTTGGTC | 79931 |
rs566554466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207440 | AATGATTTATAATAG[A/T]TAAATGTTAATGGAT | 79931 |
rs566586153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175146 | TTGTCATGAGTTTAC[A/G]TATTTCTTAACCCAC | 79931 |
rs566648420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170196 | TTCGATGTACCTTTC[C/T]CCTCTGAGATGCTAT | 79931 |
rs566665449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137927 | GATGAGAATAGAAGT[A/G]GGATTTTGATTATAG | 79931 |
rs566703959 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207501 | AATCTTACTTTCTGT[A/C]TTATTTCATAATTTC | 79931 |
rs566728862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137226 | GAAAATATCTTTAAT[A/G]GTCATTCCAGAGCAA | 79931 |
rs566788161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170709 | TACATTTTCATGGTG[C/T]TTTCTAAGATCTTAT | 79931 |
rs566798332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135349 | ATTTAATCACTCATT[A/G]TCTGCCATACCTTTT | 79931 |
rs566866913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215872 | CTTGCATGTATTAGG[C/T]GCCACATTAAAAAAA | 79931 |
rs566876363 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210499 | AATAAAATCCTTATT[A/G]AGTACCAGTAGCATA | 79931 |
rs566879392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209754 | TAAATATCAATTATA[C/T]TATTTTATTGATGTT | 79931 |
rs566886964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222858 | TCACCCAGGCTAGAG[C/T]GCAGTGGCGCGATCT | 79931 |
rs566904968 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193962 | AGTTAAGCCAAGACT[A/G]AGAAACTGACCCAGA | 79931 |
rs566927612 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196290 | AAATCCATTTTAAAC[C/T]TGTGTTTGTAAATTG | 79931 |
rs566946289 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180897 | TTGGGTCTCACCTCT[C/T]ACCCTCTCAGTCTCT | 79931 |
rs566950523 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152424 | TAAAGTATAGATGTG[A/G]GATGAAGTCTTTTCT | 79931 |
rs567005413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215178 | TCAAAATTCTTAATG[A/G]TACCCCTTGTCAAGT | 79931 |
rs567052774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189543 | CAAGTGACTCATAAA[C/T]TACTCTGTGTATGTG | 79931 |
rs567076479 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159602 | TAATGTGTTTTAAAA[C/G]ATTAACACATGATTT | 79931 |
rs567092095 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180812 | CTGCAACTCATTTTC[A/G]TTTTACTTATCTATT | 79931 |
rs567168799 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168815 | ACTTTTTCAAAATGA[A/G]GACTTTAATATTTGC | 79931 |
rs567221376 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211129 | GACATAGAAATATTT[C/G]CTAGATGTGAAACTG | 79931 |
rs567222019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163894 | GTACTGGTTACTTAG[A/T]TATTTTTTTCTATGT | 79931 |
rs567234794 | snp | C/G/T | 0.00128484 | 0.0253146 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121138677 | AGAGCATACCACTGA[C/G/T]AGTCTGGCTGTGTGG | 79931 |
rs567248535 | snp | C/T | 4.96652e-05 | 0.00498298 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132596 | TCAGCCACGCTCCCT[C/T]GTTGCCTGTTGTCTC | 79931 |
rs567259823 | in-del | -/AAG | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181950 | AAGAACTTCTTTAGA[-/AAG]AAGAACTAATGTTAT | 79931 |
rs567282308 | snp | A/G | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178112 | TTCAAATAACTCTGA[A/G]GTGAGGGAGGGAAAA | 79931 |
rs567303981 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136692 | AGACACCATCTGAAC[-/A]AAAAATAAAAATAAA | 79931 |
rs567345136 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139958 | AAGAAACATGAAATA[C/T]TATTTTTAAATTAAC | 79931 |
rs567368543 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147722 | ATAAAGCTATGAAAA[A/C]AAATGAAAGGTAAGG | 79931 |
rs567390123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205214 | TGAAAGGTGACAATT[A/G]AGCAAGGAGTGAAGG | 79931 |
rs567390993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197299 | TTGGGAAGCTGAAGC[A/G]GGTGGATCACCTGAC | 79931 |
rs567407683 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150401 | TTTTTTTTTTCAGAA[A/T]CTCTGTCTTTTTTCC | 79931 |
rs567436131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196832 | GCTTCTATTTTCTTT[C/T]GATTTATATACGTAT | 79931 |
rs567436292 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121145684 | TAAAATTAAAGTTGT[C/T]TTACTTGCTGTTTTA | 79931 |
rs567522834 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204764 | ATGGACATTAAAACT[G/T]TTAATAGTGCTTCTT | 79931 |
rs567528644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212101 | GTAATAGCCTTACAA[A/G]TGATTTCTACATTGA | 79931 |
rs567531812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198288 | GGCTGAAAAGTAGCA[C/T]ATGACCTTCATTGTA | 79931 |
rs567537296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210601 | TTCTCACAGTTCTGA[A/G]GGCTGGGAAGTTTGT | 79931 |
rs567596282 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192797 | GTTAAAACTTTTTTT[A/T]AAAATATGTAATGCT | 79931 |
rs567733347 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141156 | TGGATAAATTTCTAT[-/C]TATGTAGGCAAAATA | 79931 |
rs567762622 | snp | A/G/T | 3.3727e-05 | 0.0041064 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158678 | TACCGAATAGAGAGA[A/G/T]GTATTTACCTTTCTT | 79931 |
rs567870618 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184341 | CAATCCACCACCCTT[A/G]TTGAGAGTAGCTCAC | 79931 |
rs567878168 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140517 | TTCCTTCTTTCCATA[A/G]AGAAATATTTGACTG | 79931 |
rs567894405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165478 | CCTCTAATCAGCTAA[A/G]GAGAGCACTTCATCA | 79931 |
rs567915678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133579 | TTAACTCCTTTTCAA[C/T]TTGTACAGTGCTCTT | 79931 |
rs567947928 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215256 | GTTCTCATAGAGAAT[A/C]TGAGAATATGACTCC | 79931 |
rs568011811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168083 | GCATCCAATCTATCT[A/G]AACATTTTGTAGGCT | 79931 |
rs568102712 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151639 | AAGAGAATCTAGGGT[C/G]GGGTGGGCCAAATGG | 79931 |
rs568119349 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177747 | TCCCTTTCTATCAAT[A/G]TCTCAGCAAAAATGT | 79931 |
rs568124220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226604 | ACAGCAGGGAGTTTG[C/T]GGTTAAGCCAGAAAG | 79931 |
rs568126342 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134196 | TCCCTACATTTTATG[A/C]CTTTCTAGATACATT | 79931 |
rs568142403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182046 | TCACATTAGATTTTT[A/T]TTTTTAGTAAGAATC | 79931 |
rs568149242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173871 | CCTGACCACAAGTGA[G/T]CCACCTGCCTCGGCC | 79931 |
rs568183700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219736 | ATACTATTGTTTACA[G/T]TTATGTTGCTCAAGT | 79931 |
rs568185341 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219027 | CAAAATGGAGAAATG[C/G]TGTCTCTACTAAAAA | 79931 |
rs568196790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212956 | CACTCCATAAACATT[C/T]CTACACTTCTCTTCC | 79931 |
rs568229214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181258 | GGGTACCAGAGGGAA[C/T]TGATATTGTCACCAT | 79931 |
rs568252749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146466 | CACTATTTACCCATC[A/G]TGGCAACTTCCTGAG | 79931 |
rs568264348 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154701 | TTAAGACCAAGAAAA[G/T]AAAATAAAAGTCAGT | 79931 |
rs568268939 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227029 | TACATTTAGTTATTA[A/T]TTATAGGATTTTTAG | 79931 |
rs568298842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193192 | CACGCTATCAGAGAT[A/G]AGAAGAGACATTATG | 79931 |
rs568321542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149905 | GTCTGAAACTCAGTT[C/T]CCTATGTTCTAAATG | 79931 |
rs568325784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220686 | ATTGTCATAAATAGC[A/G]TGGGGGAATAAACAA | 79931 |
rs568328090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142644 | GGTCACCTGTAGCAG[A/G]GCTTGAACATGTCTT | 79931 |
rs568333800 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153496 | TGGAAAAGAAAAAAA[A/G]GGAAAAGATAGATTT | 79931 |
rs568423786 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228447 | AATGTGAGACAAAGG[A/G]GGCCTCAACATTATC | 79931 |
rs568452460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154226 | GCTTTTGCGGTTGAC[A/C]AAGAGATACGTTATT | 79931 |
rs568463970 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161702 | AACGACAAAATCATC[A/G]AGAAAAAGACAAACA | 79931 |
rs568466063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221412 | TGACTATAAAACTAA[A/C]CTAAATTTACAAGCA | 79931 |
rs568466610 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136148 | GTTAGTTCATAACAT[A/G]TTTATTACACACTTA | 79931 |
rs568530098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148283 | GTGCCTGATTAGAAA[C/T]GTGCACAGTTAAAAT | 79931 |
rs568534556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147887 | AGGTTTATCAATTTT[A/G]TTGTTCTAAGTCGAC | 79931 |
rs568538320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194106 | GGATTAGATGTAGTA[A/G]TGTATCGATGTTCAT | 79931 |
rs568568123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142072 | CAATAGACTCAGGAC[A/C]AATACAAACGAGGCT | 79931 |
rs568577888 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202181 | AAGGCCATAGTGACC[C/T]GACAAAGCAGCATGG | 79931 |
rs568618215 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227929 | TAACATTTAAACAGT[C/T]AACCTTTAAAGTAAT | 79931 |
rs568618672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200408 | TCTCAAAACTGTACC[C/T]AGTTAGAACTTGTCA | 79931 |
rs568679636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194492 | TTTCTTGGGGTTTAC[A/G]AAATTAGTGCAAACC | 79931 |
rs568712957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208894 | GCTTCAGGGTGGGGC[C/T]GCCAGAAAGATCAAA | 79931 |
rs568771389 | in-del | -/CTT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215650 | AATTAGGTTAAAGCA[-/CTT]CTTCGTGTATTTCTA | 79931 |
rs568809942 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149758 | GTGACAATGGGAGAC[A/T]CTGTCTCAAAAACAA | 79931 |
rs568810140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196016 | GGCAGGATTCATGGA[A/G]CCAGGCACTGCATTA | 79931 |
rs568896516 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211456 | TACATTTAAATTTTC[A/C]ATTTACGTGAAGGAA | 79931 |
rs568971424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155484 | AGATCATTATTTAGA[A/G]CACTCTATTGTTGTG | 79931 |
rs569010068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156470 | TTTAGAATCTGGAGG[A/T]TGGGTTCAAGTCCTT | 79931 |
rs569038660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162396 | GTCTTCTGTGGGTCA[A/G]TAAATTCTGAATGAT | 79931 |
rs569055650 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208879 | TGGAATCCATGGAGA[A/G]CTTCAGGGTGGGGCC | 79931 |
rs569061284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222886 | TCTTGGCTCACTGCA[A/C]GCTCCGCCTCCCAGG | 79931 |
rs569088472 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165393 | TCTCCTCTCTGGGCC[C/G]TCCATCCAACCTTAT | 79931 |
rs569115879 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182092 | TAATTGGGAGGATTA[C/T]AGAGTTTAAGAGTTC | 79931 |
rs569135983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169492 | TTGTTGATTGCCTCC[C/T]GACACTAGCTTGTAA | 79931 |
rs569180577 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217037 | AAAGAGAAAAAAAAC[C/T]GTACTTCCGACAGAA | 79931 |
rs569245976 | in-del | -/CATAA | 0.0107246 | 0.0724382 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137687 | TCCCTATTTACACTC[-/CATAA]CATAACAGACTCCTT | 79931 |
rs569258120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137331 | TGCAACACACATTCC[A/G]GTTAATGGTATGCCT | 79931 |
rs569283220 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156560 | CAAAAATAATATTTT[G/T]CTCACAGGTGGGCCA | 79931 |
rs569295137 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199067 | AACCAACCAAACAAA[C/T]AAAGGGACTTGAGAA | 79931 |
rs569340307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179249 | ACTACAGGAAAAATA[A/T]GTACGAACTTGGCTT | 79931 |
rs569359083 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209850 | GCAGGCCAAGAACTA[G/T]TCTACGTACTTCTTA | 79931 |
rs569394856 | snp | A/G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179254 | AGGAAAAATATGTAC[A/G/T]AACTTGGCTTTCTAT | 79931 |
rs569401557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190146 | CAATCTCATTCACAA[A/G]ACAGAGTGACAGATT | 79931 |
rs569405479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159888 | AGTCATAATGACTAA[A/G]AAGTAGCAAAACTTT | 79931 |
rs569428414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178848 | TACCTTCATGGAACA[C/T]TTTATACCCCATCCT | 79931 |
rs569486920 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151796 | GAGTCATAAATGAAA[C/G]ATGAGTCTAATAGAT | 79931 |
rs569499142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144083 | ATTGATTTGGGGATG[A/T]CAAATGCATTTTAGT | 79931 |
rs569526567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182979 | CACTTTGAAAGAGCA[C/T]TAGAGTTTAATTTTC | 79931 |
rs569583711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183504 | TATTTTTCCTTTATA[C/T]CAGGGGTCCCCAACC | 79931 |
rs569586734 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217302 | AATTTAGGAGTTAGG[C/G]CCATGGGAAACACGA | 79931 |
rs569592187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158020 | AAGGAAAAATGCTGC[C/T]ATATTACAATACTCA | 79931 |
rs569650273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151065 | TATCATATGAAAGAC[A/T]TTGCCTCTATTTTGA | 79931 |
rs569654554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158600 | CCACAAAGCTCTTTG[C/T]AGCTGAAATGAATGA | 79931 |
rs569692652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132732 | TTCTTCTGGCTTAAG[A/G]CTGACATAAAGTTCC | 79931 |
rs569699568 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226223 | AAAAGAGACAGAGGC[A/C]GAGGTACACATAGGA | 79931 |
rs569746834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185794 | AGCTGGTATTGCCCT[A/C]ATGGCTGCCTTGTTC | 79931 |
rs569760412 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145337 | ATTTTAAAGAAAAAA[A/T]TTCATAGCTTTAATC | 79931 |
rs569790886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191743 | TTAACTATGTATTTA[A/C]GTAAAGATTATTATC | 79931 |
rs569804849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224560 | TGCTTTTAAACAAGT[C/G]ACAGAACACTCTCTA | 79931 |
rs569810277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191292 | AAACTTGGCACTTGA[G/T]CTAACATTTGTATCA | 79931 |
rs569851399 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164444 | AGCCTTGCTATAGTA[C/T]GTAAATCGTCATTCT | 79931 |
rs569872686 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146660 | TTTAGAAATACGTAT[-/G]TTTTTGGCAGACAGG | 79931 |
rs569885362 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226645 | CAGATTCAAGAAATA[A/G/T]CAGCACTGCGCCTGT | 79931 |
rs569914249 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205295 | AGGTAGCCAGTGCAA[A/C]ATCTCTAAGGCTAGA | 79931 |
rs569928333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205781 | AATAATAAAGTTGCC[C/T]TTTATTGAGACAGTG | 79931 |
rs569936909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193317 | CTGGAATTTCTTTTC[A/G]TGCCAGAAATTAGGC | 79931 |
rs569957659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140764 | TAAGCAAACAGGTAA[A/T]GAAAAAAAAGGAAAA | 79931 |
rs570007115 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140300 | GATCGCACCACTGCA[C/T]TACAGCCTGGATGAC | 79931 |
rs570007941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173147 | ATCTGTGTGGGTAGA[C/T]GTAAATAACACACCT | 79931 |
rs570023211 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174697 | AAGGAATAATTGATC[-/T]TTTTTTTTGCTACTT | 79931 |
rs570025388 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142372 | TCAGTGCTCAAGAAG[A/G]CATGTTATTTTTTCA | 79931 |
rs570038343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154030 | ACACACACCCCTGCA[C/T]GCACACACGCACACT | 79931 |
rs570072479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193874 | AATTACAAGGAAACA[G/T]TAGCCAAAAGAAAAT | 79931 |
rs570117061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159434 | TGATTGTCTGTAAGA[C/T]TTCTTAATGCATGGA | 79931 |
rs570118076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168071 | CTCTTACATCCTGCA[C/T]CCAATCTATCTGAAC | 79931 |
rs570196881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153520 | TAGATTTTGCCCCGC[A/G]TTTGTATGTCTGAGC | 79931 |
rs570197512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167079 | TTTGGTTTTAAAGAT[A/G]GGACCATCAATCAAA | 79931 |
rs570213573 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167690 | TCAAAGTGGTTTTTT[-/A]ATTGGTTTTAGTTCA | 79931 |
rs570244142 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223301 | GATATCTTTGCATAC[C/T]AGGATTTTGTTCTGA | 79931 |
rs570256951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166265 | GATTTTCTATTAGCT[C/T]AAGAGAGCCATATGG | 79931 |
rs570263839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219875 | AATGTGTTTCTTTCT[A/G]GGTCATACAATTTAC | 79931 |
rs570327676 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220457 | GCAATCTGAAAACAG[A/T]ATGCTTTTAGGTTTT | 79931 |
rs570363941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208162 | AACTAATATACAACC[C/G]TTTCCCAAAATAAAC | 79931 |
rs570426182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207358 | ACTAACAAGTCCCAG[A/G]AAAATCAAGAAAATT | 79931 |
rs570443131 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215556 | TTCCTACCACCACGT[C/G]TTTGTACACATTCTG | 79931 |
rs570459267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160987 | TGAATAAGAAAGAAG[G/T]CGTTTGCTTTCAAAA | 79931 |
rs570472977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200502 | TGGCAGCTGTGGGGT[A/C]CCTGGCAGTCTCTGG | 79931 |
rs570508505 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184556 | TCCTGACAATTTTCT[C/G]GTTTAGAATCAGCCC | 79931 |
rs570514177 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155976 | ATTTAGCATAATTTA[A/G]GAGAAAATTATTCCA | 79931 |
rs570516627 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132035 | GCTTCCAATTAACCA[C/T]CTTATTCAGATTGAA | 79931 |
rs570533425 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168774 | ATCCTCCCACCACAG[C/T]TTCTCAAAAAAAATG | 79931 |
rs570545244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176036 | AATGGAAGGAGAAAT[A/G]TGTCATAAATTAACC | 79931 |
rs570612334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134636 | AGGGTTGATTTTCAA[C/T]GTGTCTCCAAAGCAT | 79931 |
rs570679442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187167 | TTGTGCTCTTAATAC[A/T]ATACTATGACCTGAG | 79931 |
rs570683242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148923 | TTGTTCTATGACACC[A/C]TGTCTCCCATTGCTA | 79931 |
rs570706637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133989 | TTTGGATATCTAACC[A/T]CCAGAGCTATGAAAA | 79931 |
rs570712509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180197 | AGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 79931 |
rs570805250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154739 | AAATGAGATGATATT[G/T]TAGGAATTCTGATAT | 79931 |
rs570817111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189458 | ATGCTAATCAAGCAG[A/C]AATTTTCAGGTTTTA | 79931 |
rs570875345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214854 | AGATCAATGCTTATT[A/G]TAGACCCACAGTCTT | 79931 |
rs570878361 | snp | C/T | 0.000164867 | 0.00907779 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182839 | ATTATACAAAGGTAA[C/T]TAAAAATTATTCAGG | 79931 |
rs570905563 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228499 | AAATATCAATCCTGG[C/T]TGGTAAAGCTGTAAC | 79931 |
rs570968932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136307 | CCCCTTCTCATTTTT[A/G]TATCTATACTTTCAG | 79931 |
rs570982283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196665 | AATACCAAAGATAAC[C/T]ATAAATATTTAGCAA | 79931 |
rs570999819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221739 | ACCAAAAGAAAGAAC[C/T]ACCCAACAGAGCTGT | 79931 |
rs571032078 | snp | C/T | 1.65094e-05 | 0.00287305 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121142738 | TACCTGTTTTAATTG[C/T]TTTTCTAGTTTTTCT | 79931 |
rs571036061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162148 | AAACATGTTGTTGGT[C/T]TTTGCCAGAAATGTG | 79931 |
rs571042837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195293 | ATGGGATTATAGAAG[A/G]AAGAAATGTGCATAT | 79931 |
rs571073689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188802 | CCTCATTAATTAATA[C/T]ATTGAATAAAACCTT | 79931 |
rs571106388 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204738 | AACGTTAGATTGTTG[A/G]GTCCAAGGGTATGGA | 79931 |
rs571121960 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217415 | AGATTCATTTCAGCT[A/G]TTGGCAAGCTGGCTG | 79931 |
rs571134076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201075 | TGGCTGCAATAACCA[C/T]GATTAATTTATGAAT | 79931 |
rs571204190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170176 | TATTGTAAAGCAGTT[A/G]TTAATTCGATGTACC | 79931 |
rs571214422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170526 | GGCAAATATTTTACT[C/T]CATCCTATTTTGGTT | 79931 |
rs571229935 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138090 | AGTTGTGAGTACTTC[A/G]TAAGTGACTTTTAGT | 79931 |
rs571231695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150888 | CATTAACTCACTACC[A/G]AGTGGAGAGAGTGCC | 79931 |
rs571272428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144548 | CTGTGATTACAGGCG[C/T]GTGCCACCATGCCCA | 79931 |
rs571278724 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168451 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 79931 |
rs571294346 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160546 | TTATACTTTTCACTA[C/G]TTCCTCTGTCAAGAA | 79931 |
rs571344386 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209675 | ATATTTGTACCTCTG[A/T]AGCTCCATTAAACAA | 79931 |
rs571362558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202900 | ACTCCTGCAAGAATG[A/G]CCATAATCAAAAAAA | 79931 |
rs571376719 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156661 | ACCTCATATATAAAT[A/C]TCTCTGTAAGCTTGA | 79931 |
rs571496095 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139629 | GGCTGCCAGACCACT[A/G]AAAGTAGCCCAGAAA | 79931 |
rs571523448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163247 | CTGGAGATTAATCAA[C/T]ATTTTGTTATAGTTC | 79931 |
rs571548206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204672 | AATAGAAATACCTGT[C/G]TAGATATATTCTTAC | 79931 |
rs571555504 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193280 | CTTCTGTGATCTTCA[C/T]ATGGATGTGAAATTG | 79931 |
rs571588598 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148133 | ATTTTAAATGGGAGG[A/G]GCCCATCTGATTAGA | 79931 |
rs571603349 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185971 | CAGCAGTTACTGTTC[C/T]CTCTTCATTTGGACA | 79931 |
rs571678757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211350 | CCTCAATGTAACCTG[C/T]CTACTCTCTAAACTC | 79931 |
rs571708813 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202914 | GGCCATAATCAAAAA[A/T]ATCAAGAAATAATAG | 79931 |
rs571741603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166354 | GAGACTTTCAATATG[C/T]CATCCCTAAGAATTA | 79931 |
rs571765579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171978 | CCTCAAATGATCCAC[A/C]TGCCTCAGCCTCCCA | 79931 |
rs571769077 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175243 | GCTGAAGTCATGCAA[C/G]TCTGGAAGAAGACAA | 79931 |
rs571769944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172451 | CCAATGAAAAAACCC[A/G]TAAGAGATAGACTAC | 79931 |
rs571828019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210762 | CACTAATCCTATTGT[A/G]CCAGAGCCCCACCCT | 79931 |
rs571831340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165750 | AGTGAAAGGGAGTGA[C/T]GCTGCTTTAAGGCAA | 79931 |
rs571831723 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131715 | TCAACTTACAGCAAC[C/G]TCTGCCTCCCTGGGC | 79931 |
rs571855108 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146428 | GGCAAAATTATGTTA[A/G]CTACATTTTCCTTCA | 79931 |
rs571897359 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160206 | ATTACAGGCTGGGCA[C/T]GGTGGCTAACTCCTG | 79931 |
rs571955246 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212698 | AAACAATATGAATGG[A/T]CGGAAGATACATTTT | 79931 |
rs571959565 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171772 | GTCTCACACTGTCAC[C/G]CAGGCTGGAGTGCAG | 79931 |
rs572002615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144780 | TCTATATTTTACAGG[C/T]AGGTATACTAAAAGA | 79931 |
rs572068066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219253 | AAGTAAGAGTATCCA[A/G]CTGGCTGAGCATCCT | 79931 |
rs572091491 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135745 | ACAAAATTATTTTAT[A/G]AGAATTCTGAGCAAT | 79931 |
rs572110689 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131288 | GTATACAGAGGATCA[C/T]GAAGAGGATCTCAAG | 79931 |
rs572202510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211745 | ATATTGAATTATCAA[C/T]TCAGAGATGTTTTCA | 79931 |
rs572209150 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132181 | GGGAGCAATGTTAAA[C/T]GTTTACAACTGCAGA | 79931 |
rs572257428 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169262 | TGCCCTGGCCACACC[A/G]TTGCCCCTTGAACTT | 79931 |
rs572279011 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138849 | TTACCCCCCATCACT[A/G]CCATCATCTCTCCCT | 79931 |
rs572300627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192991 | TCCAATAACTTTCCT[C/T]GTATATGCTCTGTAG | 79931 |
rs572315295 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143826 | TGTCTTAATGAAGCT[-/TC]TCTCTAACACACTTT | 79931 |
rs572372326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134144 | AGGCTTTGATCTTCT[A/G]TATTGTAAAGAAGTA | 79931 |
rs572390051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180302 | CTACTCGGGAGGCTG[A/G]GGCAGGAGAATGGCA | 79931 |
rs572430875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225720 | GCAGGAAGTATTTAG[C/T]TGGCCAAAAACTTAG | 79931 |
rs572451068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173647 | TGCACTTTTTTCTTT[A/G]AGATGGAATCTGGCT | 79931 |
rs572477589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133109 | GAAAGACTTGTTGGT[C/G]TATCATGAAGACCAA | 79931 |
rs572563663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147264 | ACTGCTGCCTACTCC[A/G]TTATTGTAAAGAACC | 79931 |
rs572603041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140805 | GAGCAGACAGAACTA[A/G]CAACCCGCAATAACA | 79931 |
rs572614873 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139049 | AAATACTCTTTTTGA[A/G]ACCCTCACACTAGAG | 79931 |
rs572696331 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159504 | TACACTGATTATAAT[G/T]AAATATTTTTTCCAG | 79931 |
rs572731164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198366 | TATATATAGCATAAA[A/C]TTTCTGGTGCAAAGA | 79931 |
rs572856367 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194698 | ACAAAACCCCTAAAC[A/C]TTGAGTGTCTTCATC | 79931 |
rs572938597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163366 | CAGTTGCTAATGAAG[C/G]CATCTGATTTGCAGT | 79931 |
rs572941672 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194243 | CTTTAAACTTTCAGT[A/C/G]GTAACTTATTTCCAA | 79931 |
rs572963287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169685 | CAAGAGATTAAATGG[G/T]ATCTAAAGATCAGAA | 79931 |
rs572974704 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152778 | AAAATGTGTTTTCAA[-/C]CCCAAAGTTTATTTT | 79931 |
rs572983695 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201225 | GGGACAACTGAGTGG[C/T]CATACTGATGCTTTA | 79931 |
rs572986842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206982 | TAAAATAGAAATAAG[C/T]TCAAATATAGACTCC | 79931 |
rs573025683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162675 | ATTTTAGAATGGTGG[C/T]TCCCACCACAAGAGC | 79931 |
rs573070483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136436 | CCCTTGCTAAATTTT[A/G]TTAACTGTGTGATTT | 79931 |
rs573111755 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161034 | CTTAAAGATAAATAC[G/T]GTGACCTGATAACAA | 79931 |
rs573122760 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176041 | AAGGAGAAATATGTC[A/G]TAAATTAACCATGGG | 79931 |
rs573167234 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210096 | TTTAAATGGTGTCAC[C/T]GAGATAGTGGATGCT | 79931 |
rs573182978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201639 | TGATGGGAAGAGCCC[C/T]GGACCTGGAATCAGA | 79931 |
rs573195355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195584 | AGGGTCATGACAATG[G/T]GGAGACCAGGAAATT | 79931 |
rs573215884 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218354 | AATGGTCTCAAAGAC[A/G]TTAATTAGTTTACTG | 79931 |
rs573227888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155922 | TTTATTTAAATAGAA[C/T]GAACATATACACTTA | 79931 |
rs573261547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216081 | ACTCCTTCAACTTAC[C/T]GGTGGAATACAGTTG | 79931 |
rs573281174 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201087 | CCATGATTAATTTAT[G/T]AATGGACTCTAAGCT | 79931 |
rs573314921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221832 | CTATTTCCTTCTAAG[A/G]AGTCTTTTTGTTTTA | 79931 |
rs573317756 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174260 | ATAAAAATTAAGAGA[C/T]TAGGCATGGTGGCTG | 79931 |
rs573341165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121182432 | TCCTCACCTTCTTGT[A/G]GTCACAGCTGCCTGG | 79931 |
rs573356144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183694 | GCGCAAATCCTATTG[C/T]GAACTGCACATGTGA | 79931 |
rs573406274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175498 | CCCACCCCATTGACC[A/C]AAATTGGAGCAGCCA | 79931 |
rs573435804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214153 | TCCTGTTGGCTCTCG[C/T]CTCTTGTCTTTATTC | 79931 |
rs573469213 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228116 | AATCATTAGTAGTGG[C/T]AAACCTCTCCAAACT | 79931 |
rs573495385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174950 | AGGCTTACTTGAGAA[A/G]GAAGGCTTATTGATG | 79931 |
rs573541210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190589 | TTAACAGTTGAGTTG[C/T]GTAACAGGGGACACA | 79931 |
rs573562293 | snp | C/G | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166479 | TTTGTTTCATGAGAA[C/G]TATCACTAGCTGAAA | 79931 |
rs573584013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170940 | CCTGCCTTCGCCTCC[C/T]GAGTAGCTGGGATTA | 79931 |
rs573599147 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140842 | GACTCAATTCTTAGC[A/G]GTGTGCTGTGTCATA | 79931 |
rs573602495 | in-del | -/TAA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163046 | TTTTTCTTTAATAAA[-/TAA]AAATTACTGAAAATC | 79931 |
rs573604538 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216725 | CTGGGTGTAAACACA[G/T]GCTCAGTGAGTTAAG | 79931 |
rs573769763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137600 | AGCAGGCTCCATTCA[C/T]ATAGAGTACCATGAT | 79931 |
rs573821923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196175 | ACCACTGCATTTACT[C/T]AGGAATAAATGATCC | 79931 |
rs573840612 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134001 | ACCTCCAGAGCTATG[-/A]AAAAAAAAGTTTTTC | 79931 |
rs573854697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149354 | ATAATAAGTACAAAG[C/T]ATTTTCTTTGAAACT | 79931 |
rs573865138 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216144 | AAAACCATCCACCAA[-/G]GCTTGTCAATGGAAA | 79931 |
rs573868215 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199782 | AAGGAAACCAAGGAA[A/G]CCTAATCTTTTCAAG | 79931 |
rs573929452 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145695 | TTGTTTTACTTGCTG[G/T]TTTACTGGCAGCAAA | 79931 |
rs573931395 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171333 | AAATGCCTCAAAAAG[C/T]TACATGAGTTGATGG | 79931 |
rs573973204 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199070 | CAACCAAACAAACAA[A/C]GGGACTTGAGAAAAC | 79931 |
rs574015340 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142153 | AAGAAATTAGACACA[A/C]TTGAAAAGTATATAG | 79931 |
rs574046079 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197753 | AAATTTAGAAATCCT[C/T]CTCAAAATACATTAG | 79931 |
rs574057137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153265 | CTGTGAACTACAAAT[A/G]TGGATACACAAACAT | 79931 |
rs574125272 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205523 | AGTTTGGAAAGATCA[C/T]TCTCGTTGGTGGGTT | 79931 |
rs574150255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191492 | GATGTATTTTACAGT[C/T]GTGTCTATGTTGCAA | 79931 |
rs574181715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144044 | CTGCTCATATGTAAG[A/G]ATGTATCACAAAGCA | 79931 |
rs574187075 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208878 | GTGGAATCCATGGAG[A/G]GCTTCAGGGTGGGGC | 79931 |
rs574248373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158291 | AAATAGGTCATGCTA[C/T]CTAATTAAAGAATTA | 79931 |
rs574257133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132868 | GACATATGCTTACCA[C/T]TTTGTGAAATAAGTT | 79931 |
rs574264024 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171599 | ACCTGTCCTTACCAC[C/T]TTCACCATCTGCCCC | 79931 |
rs574267162 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203526 | GTAGTGTACACTTTC[C/T]GGGTGATAGTGCACC | 79931 |
rs574269678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162007 | TCATCTCAGAGTCAT[A/G]TAAGTAATACAATTT | 79931 |
rs574299791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205393 | GGATTGTAGCAGATT[A/G]AACCAGAAAGGTAAA | 79931 |
rs574301666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176342 | CCAGTGAAAGCTAAA[C/T]AGATCCTCACACAAC | 79931 |
rs574302863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203326 | ATTCGCAGCAGCCTG[A/G]ATAGAATTAGAGACC | 79931 |
rs574351466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193052 | TATATGTAGAACTAC[C/G]CTATACATAATAACA | 79931 |
rs574387838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164979 | GGGTAGTACAGATAA[A/C]AGCGTGGAAATGGCA | 79931 |
rs574410010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157535 | ACCCCACCCAGGGGA[A/G]TCTGTAGGTTTGTCA | 79931 |
rs574418815 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132277 | TAAATCAACATACAA[C/T]ATCCCTGCAGCAAAC | 79931 |
rs574474886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205980 | AGAAGGAGAAGTGCC[C/G]AGTAAAGGGGGAAGT | 79931 |
rs574505071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207040 | TGTGATCAGGTAGAC[A/G]AAAATGTTTTCATTG | 79931 |
rs574548013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180927 | TGTAGATGTCTTTAC[C/T]TCATACTTCACAAAG | 79931 |
rs574722855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225519 | ATGAAATAAATATTT[A/G]AAAGATCCAAACTGT | 79931 |
rs574729454 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187341 | AGAGTTATGGCTCCA[A/G/T]TGATCTCTGCTCTGG | 79931 |
rs574735962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179071 | TGAATTGGGATAAAA[A/G]AGGCAGTTCATCAAA | 79931 |
rs574798586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179402 | AAAATAAAATATTTA[A/C]CCCAATAGGTATTTA | 79931 |
rs574814930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219381 | TATACTGCTAAAGAA[A/G]CAGCTGTTGCTTTCT | 79931 |
rs574889443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174185 | TCTTCCTGAGGCAAT[A/G]TATTTCAACACCGTA | 79931 |
rs574895801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197281 | GCCTATAATCCCAGC[A/G]TTTTGGGAAGCTGAA | 79931 |
rs574903282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136455 | ACTGTGTGATTTAGG[A/C]GTGTTACTTAAATTC | 79931 |
rs574915812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219968 | GTTAACCAGGTTCAA[C/T]ACATTTAGGATAAAA | 79931 |
rs574949951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140833 | ACATGAAAAGACTCA[A/G]TTCTTAGCGGTGTGC | 79931 |
rs574951716 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149442 | ACCATTTTCTGAAAA[A/G]GTCCAGAGTTGGGAT | 79931 |
rs575050842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226890 | GCACCATGAAGAACA[C/T]GGTGAAAAATGTCCC | 79931 |
rs575083465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200681 | TTTAATGATCCTGGA[C/G]TTACTGCCAGTAATC | 79931 |
rs575096476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134188 | GTTTCACATCCCTAC[A/G]TTTTATGCCTTTCTA | 79931 |
rs575187312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200250 | TGGGTTCACCGAGAC[A/T]ACTGCAGAAGAGTTT | 79931 |
rs575195398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149917 | GTTCCCTATGTTCTA[A/G]ATGGTGGGACTGAAC | 79931 |
rs575215681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195482 | ATAGAGAGTGGACCA[C/T]TTTTTCACAGGTGAA | 79931 |
rs575262997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188381 | AACATTGGGAAATAA[C/T]GGTCTGCCCTGTAAT | 79931 |
rs575279925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149210 | GAGTGCATCCTTACT[C/G]TTGCTGTCCACTTGG | 79931 |
rs575294608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148516 | TAAGCAGTGCTTTTG[A/G]TTTTTGAAGAAATCC | 79931 |
rs575335135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142305 | AATTAGGAATTAGGA[C/T]AAATAATATTCATTA | 79931 |
rs575353227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121182491 | TTCTTCTGCTGAAGA[A/G]TTTCTTTAGTAACAG | 79931 |
rs575353997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156958 | GGGGACTTGCGTAAC[C/T]CATGCACCCTTGCAC | 79931 |
rs575438202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168914 | CAAACCTAGTTCCAC[C/T]ACTTGCTAGTTATGT | 79931 |
rs575471613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154887 | TTAGGATTGAAGGAA[C/T]CTTTCTTTTATCAGA | 79931 |
rs575489542 | in-del | -/AAAG | 0.00295038 | 0.0382947 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161230 | CACTTAGAAAAAAAA[-/AAAG]AGAGAAGATTGAAAC | 79931 |
rs575551446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196920 | GTTTTATCAGTCATT[A/T]AAAAAATGTAAGAAA | 79931 |
rs575600132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161088 | CATTATTTTATCCTC[A/G]GCATTAATCCATGGC | 79931 |
rs575612513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161805 | TTAGATTAATAATAA[A/G]TTACTGGCATAATGA | 79931 |
rs575632584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154392 | AAGTATGACTGAAAG[C/T]TGCAGCTAGGAGTGA | 79931 |
rs575639623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163474 | AATTATTCCCTATAA[A/G]GTAGAATTTCTGTTC | 79931 |
rs575656064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204129 | AATTATGAATGGACC[A/C]AATTTACTTTGTGAA | 79931 |
rs575687241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178228 | CATGAGAAAATTGTT[C/T]AGCTGCATTGAACTC | 79931 |
rs575700713 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215292 | CACAGGATCTCAGAA[C/G]CCTAGTTTAAGAAAT | 79931 |
rs575708466 | snp | C/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203100 | CAGAGGAAAGGAAGT[C/T]ATCATATGAAAAAGA | 79931 |
rs575780664 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169162 | GTGAAAGCAGAACTC[-/T]TTATAGTGGCAAGGT | 79931 |
rs575799488 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193524 | ATAAGTGTAGAGAAC[A/G]TTATCCCATTAGAAA | 79931 |
rs575817722 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213994 | CAAAAGTATTCCTTC[C/T]GCTCCTTTATTTTCC | 79931 |
rs575824682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162756 | GATCAGAATTTCTAG[A/G]AGAGCAGCCAGGGCA | 79931 |
rs575873188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177531 | ATATCTCAGGCTCTT[C/T]CACTAAATAATATCT | 79931 |
rs575932126 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214554 | GTGGCCGGGTGAGGA[C/T]TGCCCCTACCTCTTA | 79931 |
rs575964806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175602 | ATCTCCCAGTTTTCT[C/G]TAACTCTTTCTTTTG | 79931 |
rs575983967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165022 | TGCATAAGTGAACTG[A/C]GATGGAACAGAAGAC | 79931 |
rs575991098 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156611 | GAGGACGAAGGCTTT[A/T]AAAAATGTCATAAAT | 79931 |
rs575996031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225644 | AAAAAGAGCTAAAGA[A/G]TAAAGTGTTAAAGAG | 79931 |
rs576002565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211661 | AATACCTTCTATTAT[A/T]TTAACTGGCTTTGAA | 79931 |
rs576041746 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171018 | TTGGGGTTTCATCAT[G/T]TTGGCTAGGCTGGTC | 79931 |
rs576086440 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159182 | CAGGAGGTGGAGGTT[G/T]CAGTGAGCCGAGATT | 79931 |
rs576095697 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141299 | TCAACTCTGCATTTC[A/C]TTTTGTCTGGGAAGA | 79931 |
rs576132290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138337 | TTGTTGTTATAATAC[A/G]GCTCTGCTTACAGTT | 79931 |
rs576133290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224990 | TATCTATATTTATTC[A/G]CATCAAAAGGAAACA | 79931 |
rs576137091 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223728 | CTTAGCTTCCCTATC[C/T]ATTAGCACAGTAGGT | 79931 |
rs576203532 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191696 | TTTTGAGTCATGTCT[A/G]ATAATTTTCCCTAGT | 79931 |
rs576205374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191614 | TGTTTCTCTCAAATC[A/G]CTACCTGAATTTTAG | 79931 |
rs576229417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197829 | TAAGGAGAGCCGTAT[A/G]AGAAAGTCAAAGTCC | 79931 |
rs576339250 | snp | C/T | 0.000511538 | 0.0159846 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138573 | AACATCCCCAAAAGA[C/T]CCCATTAAGATGTAA | 79931 |
rs576363859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197416 | GCCTGTAGTCCCAGC[C/T]ACTTGGGAGGCTGAG | 79931 |
rs576386923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154245 | AGATACGTTATTGTT[C/T]GCAAACACCCACTTG | 79931 |
rs576488263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179116 | AGGATTTCCAGAAAG[A/C]GTAAACAGCATGTGA | 79931 |
rs576492648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139542 | TTTTTTTGTTGTTCT[A/G]TAATTCAATTATCTC | 79931 |
rs576522786 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183061 | TGGCAAGAATTGAAT[C/G/T]GAACACTCACGGTGA | 79931 |
rs576549140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153888 | TGTGCTAGCGCATTC[C/T]TATGTTCCACATATG | 79931 |
rs576551761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179519 | AGGCATTTGGTTTCA[A/G]TGATGTGTGCAAAGA | 79931 |
rs576570671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192005 | GCTGTCTAAAAATTT[C/T]ATAATAGAAATGCAT | 79931 |
rs576628906 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182041 | CATTCTCACATTAGA[-/T]TTTTTTTTTTAGTAA | 79931 |
rs576666284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165608 | TGCTACATGAATAAA[C/T]GAATGAATATCTATA | 79931 |
rs576802286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158357 | CATATCTCACCTCAC[A/G]TATAACTTTGTGTAT | 79931 |
rs576847638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200712 | AGGCACCTTGGCTAC[C/T]TTTTTTTCAACAGAT | 79931 |
rs576866130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160401 | CAAGAATCACTTGAA[A/C]CCTGGAGGCAGAGGC | 79931 |
rs576886573 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168516 | TTTCTTTTTTCTTTT[A/C]TTTGCTTTTTTTTTT | 79931 |
rs576905501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200036 | CCCCTCAAAAACCAC[A/G]GTCAGAGGCAGAGCC | 79931 |
rs576922197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212978 | TTCTCTTCCTTTTAC[A/G]AGAAAAAAAAATGGA | 79931 |
rs576926478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194148 | GATGGTTATCTTGTG[A/G]TATATCCTTGTTTAA | 79931 |
rs576931324 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209412 | CTTAACATGTGGGGT[C/T]TGTACTAACTTCTGG | 79931 |
rs576943896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169072 | TAACACAGTGGCCAC[C/T]GTGAGACTTTTAAAA | 79931 |
rs577104329 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212559 | TATGAAAAAAATTAT[G/T]ATTGGTCTATGATGT | 79931 |
rs577114891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147939 | AGGGAAGAAATTAAA[A/G]ATTTTGTATAGATCT | 79931 |
rs577126588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207750 | CCTCCAAGCTGACCT[C/T]ATTCACTCCTGGATG | 79931 |
rs577127079 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200817 | AACCCCAGCTCAGCT[A/G]GCCATTTCAAGTCCT | 79931 |
rs577185540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222358 | CAAATTACAAATTCG[C/T]TTTTTCAAACGTGTA | 79931 |
rs577190107 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208367 | TGAACTCAATGTGTC[A/G]GCTGGAGCCACCCAG | 79931 |
rs577226319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173540 | TATTTTCTCTGGAAG[A/G]AAATTAGCTGCTGAT | 79931 |
rs577258710 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224527 | GTTGTTCATGGTTAT[A/G]TTTTTTGATATTTTT | 79931 |
rs577309363 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214132 | GTGCTCACTATTCTC[A/T]TCCTGTCCTGTTGGC | 79931 |
rs577335547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142095 | ACGAGGCTCACAGGT[A/C]AAGTTTTACCTAAGG | 79931 |
rs577337438 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186034 | CCTGCGTCCTCTCAC[A/G]TGAGCCTGGTTCAGC | 79931 |
rs577350334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181030 | TTCCTCAATGAGGTC[A/G]TAGGAAAATCAGTAT | 79931 |
rs577362196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222004 | TGTCTGTCACCAGGG[C/T]TATCACTACATTTGC | 79931 |
rs577410432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181425 | GAAGAAAGAGGCCTT[A/G]TTTGACCTCATAACC | 79931 |
rs577439717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187565 | CCATGGAGGGCTATG[C/T]TATTTCCAAAGAATT | 79931 |
rs577463242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141033 | GTAGGAAAATCCCAG[C/T]TAAAAATCTTAGATT | 79931 |
rs577481176 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228051 | TCACTGGCACTATAT[C/T]ATTAGGAATTATGTG | 79931 |
rs577482855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220140 | TATTAATTTTTTAGA[A/G]ATGACATTATACCAT | 79931 |
rs577489569 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152002 | AAACATCTGGCTTCA[A/G]GAGCCTGATAAAAAC | 79931 |
rs577500393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141771 | TGCACATAATTTCTA[C/T]CAAAACAGTATACTA | 79931 |
rs577511019 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221516 | AATATGATAATGATA[C/T]TCAAAAAAAGGATAT | 79931 |
rs577531290 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187690 | GTCAGATGTTCAGAG[A/G]GGCTTGGGAGATAAG | 79931 |
rs577537728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137444 | AAAAAGAGAGTCCTA[C/T]AGTGTTTTGATAAAT | 79931 |
rs577547957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183047 | CAGTCTGAGAACAAT[A/G]GCAAGAATTGAATCG | 79931 |
rs577548326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194997 | ACATGGCAAAACCCT[A/C]TCTCTACTAAAATTA | 79931 |
rs577548635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201422 | TTTAAGCATTATATT[G/T]TATGTCTCAAAATAA | 79931 |
rs577570981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151164 | TGGTGTGGCCTCAGA[A/G]ACCATAAAATGACTA | 79931 |
rs577571196 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144409 | TTTTTTTGTTTTTTT[C/T]TTTTCTTTTTGAGAC | 79931 |
rs577615526 | snp | C/T | 0.000812942 | 0.0201447 | utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227424 | TCAGATCTAGGTAAG[C/T]GTATTACAAGGTCTA | 79931 |
rs577638639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189717 | TTCTAAAGTTTTACC[C/T]AAGGCTATGTAATTT | 79931 |
rs577639080 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133077 | ATTATTGCCAAAGCT[A/G]TGGAAAATATCCTAT | 79931 |
rs577641614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182532 | TGTGAGAGAAGTTTT[A/G]TACTGCTTCAGTTTA | 79931 |
rs577649937 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228893 | AGAACAAGGAGAAAT[G/T]AATCAGTCAACAGCA | 79931 |
rs577656816 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213548 | TGGCTAACACAGTGA[A/G]ACACCATCTCTACTA | 79931 |
rs577660587 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149714 | GAAGTTGCGGTGAGC[A/G]GAGGTTGTACCACTG | 79931 |
rs577668856 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229601 | TGTCTCCAAAAAAAA[A/C]AAAAAAAACAAATCA | 79931 |
rs577696220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121136620 | GAGCCAGAGGCAGGA[A/G]GATCACTTGAGGCCA | 79931 |
rs577731495 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150637 | ACTCCCAGAGATGAT[C/G]AATCAGTAGGCTGGA | 79931 |
rs577757091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176344 | AGTGAAAGCTAAACA[A/G]ATCCTCACACAACAA | 79931 |
rs577760967 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169048 | CTTCCACTCCCCCCT[-/C]CCCATTATTAACACA | 79931 |
rs577775257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189181 | CAAAATAAGAATTTA[C/G]GATGTTAGTGTTCTT | 79931 |
rs577804584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143061 | TCCATTGCTTACTGA[A/G]TGACATTGGAATTGT | 79931 |
rs577806776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149824 | CCAGTGCTAATAGAA[A/C]CTCACCCAAAGGTTA | 79931 |
rs577867792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149232 | TCCACTTGGCAATAG[C/T]GCGTGAGGTTAGGTG | 79931 |
rs577896675 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140657 | AGGTTAATTCACTCC[C/T]ACAGTAAATTTCTCT | 79931 |
rs577897780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215426 | TAGAATAAATTCTCA[G/T]CTATTTAGTCTCTCA | 79931 |
rs577976616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183917 | CATTATATATTACAA[A/T]ATAATAATAATACCA | 79931 |
rs577994287 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169376 | CATCTGTTTATTGAG[A/T]CTTTACTTGGCCTCC | 79931 |
rs578007344 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228298 | CTGGCGATATGCTGG[A/C]GGAGACATTGTCTCA | 79931 |
rs578033236 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165865 | GGGTACAGAAGCAGC[A/G]ATTTCCTGAACTGAC | 79931 |
rs578055236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158211 | ATGCTTTAGATGGAA[G/T]AGGAGGTTGCTCCAT | 79931 |
rs578067768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197369 | ACCTTCTCTGCTAAA[A/C]ATACAAAAATTAGCT | 79931 |
rs578073405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203925 | TATATATATACTAAT[A/C]CACAAAATATTTTTC | 79931 |
rs578075484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191375 | TTTATTGATAAACAC[C/T]TGGAAGAGAACAAAG | 79931 |
rs578125003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203289 | AATACTATTCAGCCA[C/T]AAAAAGAAACAAAAT | 79931 |
rs578134339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164016 | ACTAGAAATGCCATC[A/G]ATGCTAGATGTGATC | 79931 |
rs578150567 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166551 | GCTGTTGTGAAGAGT[A/C]TTCATTTCTGAAGTC | 79931 |
rs578154432 | snp | C/T | 8.54664e-05 | 0.00653651 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157049 | CCCCCCGCCCCTTTG[C/T]TTTTATTTGGATCCT | 79931 |
rs578164713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177178 | TGACTGCAGATTCAT[A/G]TATTATTTTCATAAT | 79931 |
rs578197849 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188666 | CAAAATGTTATGGTT[C/T]ACTGCCTTGAATGGC | 79931 |
rs578227007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209268 | TCTGTGAGTCCTTCT[C/G]ATGAATTACCAAACC | 79931 |
rs578255396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170810 | ATTCTTTCTTTGCTC[A/G]GTAAGAGATATCTTT | 79931 |
rs745314712 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214905 | ATGTCGAGTCTTTCC[A/G]TTGAGGTAGGTAAAA | 79931 |
rs745343018 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188593 | TTTACTAGTTGATTA[C/G]AACCTAAATAAATAG | 79931 |
rs745380224 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138690 | GATAGTCTGGCTGTG[C/T]GGAACAATACAACAT | 79931 |
rs745392194 | snp | C/G | 1.64833e-05 | 0.00287078 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121138634 | CTCACCATTTGCCTT[C/G]TGTTGTACATCTGGC | 79931 |
rs745395630 | snp | A/C/T | 0.000119618 | 0.00773283 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157054 | CGCCCCTTTGCTTTT[A/C/T]TTTGGATCCTCCGGG | 79931 |
rs745427073 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180139 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAACA | 79931 |
rs745439787 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163545 | CCAATGTATATTCAA[G/T]GTCTGATGCTACTAA | 79931 |
rs745440474 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155292 | GATAAGCAAGTCCTT[A/G]TATACTGTCACTAGG | 79931 |
rs745444546 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221637 | AATTGGAGGAGAGGA[A/G]AATTACACACCACTC | 79931 |
rs745486414 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136214 | TCTAAATGTCAAATG[A/T]GTAGCATGCTGTGAG | 79931 |
rs745494391 | snp | A/G | 6.78725e-05 | 0.00582509 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161252 | GAAGATTGAAACAAA[A/G]CTGTTTACAAAATAA | 79931 |
rs745705958 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134343 | CAGAAAGGAAGAAAC[A/G]AACAACATGTTTTTC | 79931 |
rs745723821 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157073 | GGATCCTCCGGGCTC[G/T]AGGACCCGGGCCCCG | 79931 |
rs745762357 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211848 | AAAATTCATTCAGCT[C/G]GCTGCAGGTTGTCTG | 79931 |
rs745774741 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158499 | ATTGCTCAAGACAAC[C/T]CACTGACACCGTTCA | 79931 |
rs745829948 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172440 | GAGGATACAGGCCAA[C/T]GAAAAAACCCGTAAG | 79931 |
rs745846933 | snp | C/T | 1.77068e-05 | 0.00297541 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121154641 | TTTATTCTCTTCTTT[C/T]AATTCATGTAATTCT | 79931 |
rs745852166 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199029 | GTTGTAAACAATTAA[C/G]AGGAAGTTTAGTGAA | 79931 |
rs745899621 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159226 | CCATCCTGGGCGACA[C/G]AGTGAGACTCCATCT | 79931 |
rs745917542 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144547 | GCTGTGATTACAGGC[A/G]CGTGCCACCATGCCC | 79931 |
rs745930057 | snp | C/T | 1.65976e-05 | 0.00288072 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142698 | GTACATGGGAATAAA[C/T]GTATGCGTGAAAATT | 79931 |
rs745930639 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185864 | ACAATTGAGTATCCA[C/T]TATTGCAAGGTACTG | 79931 |
rs745955591 | snp | G/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217092 | TTATTAAGTTTCACT[G/T]AAGTTTGGTGCAACT | 79931 |
rs745963969 | snp | A/G | 1.65231e-05 | 0.00287424 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157234 | CCAGTTTCGTCTTCA[A/G]CTCTGCTACCTGAGG | 79931 |
rs745983002 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175589 | AAAGACAATCTGCAT[C/G]TCCCAGTTTTCTGTA | 79931 |
rs746018873 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218250 | CACCCCAAAAATGGC[A/G]TGTGCAAAGGGAAAT | 79931 |
rs746026156 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204464 | TACAATCAAACGGTG[C/T]GCTGACCACCTTGGG | 79931 |
rs746076030 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133747 | AGAATTTCCCTAAAT[A/G]TACAGTGAAGGTGGG | 79931 |
rs746115344 | snp | A/T | 1.65482e-05 | 0.00287643 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142786 | TTTTATCTAAAGACA[A/T]AACAAAGGCATTTGT | 79931 |
rs746118435 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165641 | ATGATTTACAAAATC[A/G]ATGAACTTTTTGCTA | 79931 |
rs746130881 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160589 | TCTAACATTCATTAA[-/G]CTCAGAAAAATAAAA | 79931 |
rs746150114 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152391 | ATCACTTTATATCTA[C/T]ACTTTTAAGGGACAG | 79931 |
rs746173136 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165853 | GATCTGACTTTAGGG[C/T]ACAGAAGCAGCGATT | 79931 |
rs746191560 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201243 | TACTGATGCTTTATT[C/T]AGTGCTTGGAAGGAC | 79931 |
rs746209112 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193060 | GAACTACCCTATACA[C/T]AATAACAACAGATCA | 79931 |
rs746215051 | snp | A/T | 1.65247e-05 | 0.00287438 | utr-variant-3-prime, stop-lost | TNIP3 | GRCh38.p7 | 4:121132632 | GTTAGTGTGTACTTC[A/T]ACGGATGGACTTTCT | 79931 |
rs746235839 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223747 | AGCACAGTAGGTATA[A/T]GCATAATTGTAATAC | 79931 |
rs746287520 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182213 | ATAGACAAATACCCT[A/G]AAACGAGTGGAAGTT | 79931 |
rs746304233 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225875 | GTCTCTTCTACACTG[C/T]GCCACAGGTCTCTTT | 79931 |
rs746342243 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203385 | GGAAAAACAAACATC[A/G]TATGTTCTCACTCAC | 79931 |
rs746388637 | snp | A/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183041 | AATTTTCAGTCTGAG[A/T]ACAATGGCAAGAATT | 79931 |
rs746392269 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213641 | CTGAGGCAGGAGAAT[C/G]GCATGAACCCTGGAG | 79931 |
rs746394341 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227222 | TTCTCACCGGGAACA[C/T]ATAAAACCTTATCTT | 79931 |
rs746412061 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171031 | ATGTTGGCTAGGCTG[G/T]TCTCAAACTCTTGAC | 79931 |
rs746466806 | snp | C/G/T | 5.02663e-05 | 0.00501309 | missense | TNIP3 | GRCh38.p7 | 4:121141890 | GGTGGAAAACCAAGC[C/G/T]GCAGTTACAGGGTGG | 79931 |
rs746488464 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159988 | ATATCATTATTTAGT[A/G]TGAAACTGTATAATA | 79931 |
rs746493432 | snp | C/G/T | 8.25095e-05 | 0.00642252 | missense | TNIP3 | GRCh38.p7 | 4:121164086 | CCGTAGAACTTTCTG[C/G/T]GGCAATCATTCTAGA | 79931 |
rs746547589 | snp | G/T | 1.68035e-05 | 0.00289853 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121141849 | CTGCACAGCTCCAGG[G/T]CCTGTTGGTACCCAT | 79931 |
rs746583567 | snp | C/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131653 | GGTGGGTAGGGGGCA[C/T]TGAGTCTTGCTCACT | 79931 |
rs746583913 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201420 | TTTTTAAGCATTATA[G/T]TGTATGTCTCAAAAT | 79931 |
rs746592069 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173179 | AAAATTGTAGCAGGA[A/G]ACATCATTTACCAAT | 79931 |
rs746609648 | in-del | -/CCTC | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218525 | TTATTTTCCTTCCTT[-/CCTC]CCTCCCTCCCTTCCT | 79931 |
rs746619880 | snp | A/G | 3.33957e-05 | 0.00408616 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164174 | AAAGAAAAACAGGGG[A/G]AAAGTCTCTTAAGGT | 79931 |
rs746641549 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147843 | CACATTACACTTTCA[A/T]CACTAACAGCCCAAC | 79931 |
rs746675945 | in-del | -/A | 1.74183e-05 | 0.00295107 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142826 | CAAGTTAAAATCATT[-/A]ATTCCCAAGCCACTC | 79931 |
rs746720689 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220320 | AACATCATTGCTAGG[C/T]TCTGTTTTCTAAGGA | 79931 |
rs746730725 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149948 | TAGCTGATCTGTATT[A/C]TTTCTATCAAGCTTG | 79931 |
rs746782978 | snp | C/T | 9.73473e-05 | 0.00697597 | missense | TNIP3 | GRCh38.p7 | 4:121154666 | AATTCTTCATTTAGG[C/T]GTTCCTTTTCCTTCT | 79931 |
rs746804766 | snp | C/T | 1.70504e-05 | 0.00291975 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157062 | TGCTTTTATTTGGAT[C/T]CTCCGGGCTCGAGGA | 79931 |
rs746871578 | snp | A/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167842 | CAGGGGCACTAGGAA[A/T]GGACCATATCCCTGG | 79931 |
rs746941585 | in-del | -/ACAA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219199 | GAATGAAACTCCATT[-/ACAA]ACAAACAAACAAACA | 79931 |
rs746980220 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196349 | CTAGTGATAATGGTA[A/G]AGGTAGGTCTTTTTA | 79931 |
rs746990743 | snp | A/G | 1.64874e-05 | 0.00287113 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138702 | GTGTGGAACAATACA[A/G]CATTATTATAGCAAT | 79931 |
rs747052684 | snp | A/C/T | 4.94591e-05 | 0.00497268 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121147058 | TTGTACCTGGGAATT[A/C/T]AGCCTGTTCAACTGG | 79931 |
rs747073005 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156982 | CTTGCACATCGGTCG[C/T]TGCTCAGTAGTGAGT | 79931 |
rs747074383 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198958 | TTTAACATGTAAACC[-/T]TTAAAAGACATCTTT | 79931 |
rs747122132 | snp | A/C | 1.672e-05 | 0.00289132 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142811 | ATTTGTTAATCAAGA[A/C]AAGTTAAAATCATTA | 79931 |
rs747164029 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216148 | CCATCCACCAAGGCT[A/T]GTCAATGGAAATTTA | 79931 |
rs747173249 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191541 | AGTTATGTCTGATAC[A/T]TTCACCTCATGTAAC | 79931 |
rs747175427 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226614 | GTTTGCGGTTAAGCC[-/A]GAAAGCAAATGTTAT | 79931 |
rs747211054 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201595 | TCATGCAATACATGT[C/G]TGCATGTTGTTCTCC | 79931 |
rs747220636 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174322 | AGACTGGGGAATCGT[G/T]TGAGCCCAAAATGTT | 79931 |
rs747464716 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191606 | TATCAAAATGTTTCT[C/G]TCAAATCGCTACCTG | 79931 |
rs747467022 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164821 | GTTAAACTTGTCTCA[A/C]GTTTAAGTCTGTCTT | 79931 |
rs747546979 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180646 | AGAAGATGGGGTCTC[G/T]TATATGTTTGAAGTG | 79931 |
rs747579142 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158208 | AATATGCTTTAGATG[C/G]AAGAGGAGGTTGCTC | 79931 |
rs747600424 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181767 | AGGCCTATACAATTC[C/T]GGGATTTCCTTTAAA | 79931 |
rs747610811 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212151 | CATAAAGTATTCAAG[A/G]CAGACAGAACAAAAG | 79931 |
rs747644165 | snp | A/G | 3.31752e-05 | 0.00407265 | missense | TNIP3 | GRCh38.p7 | 4:121150216 | TCAAGGCATCCTGAA[A/G]AGCCTACGTAATAAG | 79931 |
rs747674794 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140623 | TCCAATCCCCCAACC[C/T]GTAGAAGCCAACTCC | 79931 |
rs747679211 | snp | A/G | 0.000164136 | 0.00905766 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216542 | GAGGCTCAGATGTAC[A/G]TCAAGGGAAGTTAAC | 79931 |
rs747685207 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225656 | AGAGTAAAGTGTTAA[A/T]GAGCAATTTTTAAAA | 79931 |
rs747724255 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221789 | TCATATTTCTGAGAA[A/C]GGTGTCAAATCAGGG | 79931 |
rs747724429 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170895 | ATCTCAGCTCACTGC[A/G]ATCTCTGCCTCCCGG | 79931 |
rs747727353 | in-del | -/A | 2.40428e-05 | 0.00346711 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154702 | TAAGACCAAGAAAAG[-/A]AAATAAAAGTCAGTA | 79931 |
rs747818113 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159627 | TGATTTATAATAAAT[A/C]CTCAACAAATAGGTA | 79931 |
rs747839721 | snp | C/T | 1.64781e-05 | 0.00287033 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154532 | CATTTTAATCTCCCA[C/T]GCTTGACCTGACTGA | 79931 |
rs747847379 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212416 | GAGAGACTGCTTTCT[C/T]AGTGTGGAAAGAGAA | 79931 |
rs747857916 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160819 | GGTCATAAGGCACAA[A/G]CGATAAAGGCATAAA | 79931 |
rs747892737 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154882 | TAGAATTAGGATTGA[A/T]GGAATCTTTCTTTTA | 79931 |
rs747913012 | snp | C/T | 4.94792e-05 | 0.00497365 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138724 | TATAGCAATATGGAC[C/T]TCAAATATAGTGGCA | 79931 |
rs747934075 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176690 | TCAAAAAAAGGGAAA[G/T]AAGAAAAGGAAAGCC | 79931 |
rs747934221 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201236 | GTGGCCATACTGATG[C/T]TTTATTTAGTGCTTG | 79931 |
rs747967410 | snp | C/T | 1.67225e-05 | 0.00289154 | missense | TNIP3 | GRCh38.p7 | 4:121141877 | CATGGATCTTGCAGG[C/T]GGAAAACCAAGCCGC | 79931 |
rs747992211 | snp | A/G | 1.66427e-05 | 0.00288462 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157123 | GCCGGTCCCGGGTCA[A/G]GTCGCGCTGCCTGTC | 79931 |
rs748015032 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220004 | TCATCAGGTACTAAA[A/C]CATCATGAAAATTAC | 79931 |
rs748091985 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135088 | AGAAGGTCGAGGGTC[C/T]CAGGCAGGAGGCCAG | 79931 |
rs748117202 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148831 | AACAAAAATCTTTGT[-/A]CTTAGTACTTGCTCA | 79931 |
rs748141220 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178244 | AGCTGCATTGAACTC[C/T]AGTTTCCCCATCTGT | 79931 |
rs748144945 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135873 | TATGACAAGAGTGAT[A/G]TCAGAGTTCTGCCAA | 79931 |
rs748178681 | in-del | -/CACACCA | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229545 | GCAGTGAGCTGAGAT[-/CACACCA]CACACCACTACACTC | 79931 |
rs748192648 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167636 | ACCTTATAGGCCATA[C/T]GGAGTTACTAAAGAC | 79931 |
rs748252106 | snp | A/T | 1.65869e-05 | 0.00287979 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147196 | AATATTAGCTTGCTG[A/T]TACTGTAAGCTTCCT | 79931 |
rs748270793 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194851 | TCCATGAACAATAGA[-/A]AAAAAAAAGTACACA | 79931 |
rs748275006 | snp | A/G | 1.69089e-05 | 0.0029076 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157076 | TCCTCCGGGCTCGAG[A/G]ACCCGGGCCCCGCCC | 79931 |
rs748287549 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205696 | TTTGAATTTAGCCAG[C/T]AGGAGGGAAAAGGGA | 79931 |
rs748324058 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184080 | CATAATGGAGAAATT[A/C]TCTGATTAAAAACAA | 79931 |
rs748341384 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227370 | AGTAAAGGCACAAGA[C/T]ATTATGTTACTCACC | 79931 |
rs748353301 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180379 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 79931 |
rs748433079 | snp | G/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228575 | ATCTTAGTTTCTGTA[G/T]TTTCAAAAATTTTAA | 79931 |
rs748450852 | snp | A/C | 5.96214e-05 | 0.00545959 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161239 | AAAAAAAAAGAGAGA[A/C]GATTGAAACAAAGCT | 79931 |
rs748459654 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160889 | TTTTGAGAAAATTAG[A/G]ATTATATTACCAGAC | 79931 |
rs748464809 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143422 | TTGTCATTCCTACAC[C/T]CCATGTCCCACATTC | 79931 |
rs748495121 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184666 | TTAAAGCTAGCTTTG[A/C]TTGGTTTCCGTTATC | 79931 |
rs748513826 | snp | A/G | 1.65468e-05 | 0.00287631 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158765 | GAGCTGAAATCATTA[A/G]AATTTGGTGAATCAA | 79931 |
rs748545821 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215967 | TAGAATGTGGAAAGC[A/G]CCTAAGTAAGGGATT | 79931 |
rs748547292 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216823 | AGAGCATGAACGGTT[A/G]AAGTTGTCAGACTGA | 79931 |
rs748592514 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162565 | GGGTTAGAACAGACT[A/G]ACTATTAAGCATCTT | 79931 |
rs748630534 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219804 | CATACAATCAAATGC[A/C]TGAAAACTTAAGGTA | 79931 |
rs748631785 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202743 | GCAAGAAAAAACAGA[G/T]AACCCCATCAAAAAG | 79931 |
rs748687541 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189861 | CATTCTTGGCTAGCT[C/T]CCTGTTTATTTCCTC | 79931 |
rs748697847 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121147069 | AATTCAGCCTGTTCA[A/G]CTGGGATTGGGAAGT | 79931 |
rs748707737 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134828 | GCCACACCCTTCCTC[A/G]CAGTGTGAGCGACGT | 79931 |
rs748730766 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153691 | GGCACATACTTAATA[C/T]TTTGAGGATCTTTAA | 79931 |
rs748739441 | snp | A/G | 0.000191369 | 0.00977998 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137860 | CCAGGTGTGTGTCAT[A/G]TGAGACTTTAAACAT | 79931 |
rs748828182 | snp | A/C | 1.67419e-05 | 0.00289321 | missense | TNIP3 | GRCh38.p7 | 4:121154617 | AAGAGTATTTTTTCC[A/C]TTTAAAAGTTTATTC | 79931 |
rs748829049 | in-del | -/TTCC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146436 | TATGTTAGCTACATT[-/TTCC]TTCATTAACATCACT | 79931 |
rs748836571 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180597 | ATGAGCTTGGCTATG[C/T]TGTGTAAGAGTGAGT | 79931 |
rs748961601 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181340 | TCCATGAAGGAATAA[A/G]TTTCTAGTTGGGAGT | 79931 |
rs748967335 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139457 | TACCTGCCCACAAAG[C/T]AGGTCTGTCTTTCTG | 79931 |
rs748970224 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170694 | TTTAATAATACTTTC[C/T]ACATTTTCATGGTGC | 79931 |
rs749016385 | snp | A/C | 1.64947e-05 | 0.00287177 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138604 | ACATGAAAGAATGCT[A/C]AATACAGCTGTGGTC | 79931 |
rs749038042 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191585 | AACTATAGTTGTCCT[C/T]TAACTTATCAAAATG | 79931 |
rs749063486 | snp | A/G | 0.000166625 | 0.00912605 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182646 | GCTGAAGGGTACATC[A/G]AGATAAGGAGAAAAA | 79931 |
rs749064624 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199215 | AACCTGGGACACACT[C/T]ATGGAAATGGTGGCG | 79931 |
rs749153635 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200147 | CTTTACTGCCCCCAC[A/T]TGGGCACAGACATGC | 79931 |
rs749163708 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214553 | GGTGGCCGGGTGAGG[A/G]TTGCCCCTACCTCTT | 79931 |
rs749210444 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146387 | ATTTTACAAATAAAA[A/C]TGGTGCAGTTTGTTT | 79931 |
rs749252932 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175746 | ATTCCCCCCTTGCAC[C/T]ACTTCTGTCCTGTGT | 79931 |
rs749254003 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186828 | GTTCAAAATATTCTC[A/C]AGAAGTTTAGTCACA | 79931 |
rs749269731 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193256 | GCAATAATTCATATT[C/T]ATTCTCTTCTTCTGT | 79931 |
rs749310185 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209402 | GGACTGAGGCCTTAA[C/T]ATGTGGGGTCTGTAC | 79931 |
rs749325867 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219698 | CTTGAAAATGTTATA[C/T]AAAAAATTACCAACG | 79931 |
rs749329589 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176580 | TTGGTTTAGCACTTT[A/G]TATTTACAGGGTGCA | 79931 |
rs749368410 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | TNIP3 | GRCh38.p7 | 4:121157135 | TCAGGTCGCGCTGCC[C/T]GTCGTCCTCTCTCTG | 79931 |
rs749385489 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205574 | CATATGTAAAGGTAC[A/T]GAGACAGTTTAAGAA | 79931 |
rs749393268 | snp | G/T | 1.65449e-05 | 0.00287614 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132600 | CCACGCTCCCTCGTT[G/T]CCTGTTGTCTCTCTC | 79931 |
rs749414564 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206931 | ATTTTGAATTCATGG[A/G]AGTTGTACATGAATT | 79931 |
rs749432796 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149690 | AGAATCACTTGAACT[C/T]GGGAGGCGGAAGTTG | 79931 |
rs749436238 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165990 | CTCCATAGTTTTATA[C/T]AGTGTAAGGTTCTCT | 79931 |
rs749521063 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226076 | TGATAATTAAATATA[C/T]ACTTGGAGAGACAGT | 79931 |
rs749572046 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141115 | TCTGGGTAAATCCAA[A/C]ATGCAGAAAATGCAT | 79931 |
rs749619071 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222067 | TGAGAACAGATTGTA[C/T]ATTATAGTAGCTAAG | 79931 |
rs749649294 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195939 | ATTTACACTCACGTT[A/G]CTGATGCTTGTAGAA | 79931 |
rs749655213 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183120 | CAATGTGCACAGCAA[C/T]CTATTAAAGTAGTCA | 79931 |
rs749658706 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227299 | AATATGAGAACTTTA[G/T]GCATTTTAAAAAAGA | 79931 |
rs749661453 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214038 | TGGTGTGGCAACCAT[-/G]AATATCAATACGTAG | 79931 |
rs749665649 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138404 | ACTGAAAAAGGAACA[C/G]AAGCCAGAATTGAGG | 79931 |
rs749672835 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142004 | AAGGTTTGGTTTCAA[C/T]CTTAAGGTTCCACTT | 79931 |
rs749730470 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214660 | AGCATATGCTTCTGC[C/T]ACCAAAGGAGGATGG | 79931 |
rs749775265 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198069 | AGAACTAGAGGATGC[A/G]GATAATAGATGTGTT | 79931 |
rs749819553 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201525 | ATGATTTTTGCCTTA[A/G]GCAAACTTAGAGCTA | 79931 |
rs749878499 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181429 | AAAGAGGCCTTATTT[G/T]ACCTCATAACCATTA | 79931 |
rs749886227 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208387 | GAGCCACCCAGATCA[A/C]TAAACTGATTCATCT | 79931 |
rs749886341 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173894 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 79931 |
rs749904043 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216576 | GTCAGTCACCAAAGG[A/C]GAAAACCACCTGTTA | 79931 |
rs749913069 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185378 | TCTGCTGACTAACCT[A/G]TCTGAACTAGATTTC | 79931 |
rs749934905 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121145048 | TTTTCACTGACTTAA[C/T]GCATCCTCAGTGATA | 79931 |
rs749983937 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133292 | AATATGCTGAATGTT[C/T]TGTACTTGTTGTCCT | 79931 |
rs750031102 | in-del | -/GTGT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181630 | ATAAGACAGGTGTGT[-/GTGT]GTGTGTGTGTGTGTG | 79931 |
rs750051565 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191287 | AAGAAAAACTTGGCA[A/C]TTGATCTAACATTTG | 79931 |
rs750124816 | snp | C/G | 1.67008e-05 | 0.00288965 | missense | TNIP3 | GRCh38.p7 | 4:121157152 | TCGTCCTCTCTCTGC[C/G]TGTCGTCCTTTCTCT | 79931 |
rs750126978 | snp | C/G | 5.11941e-05 | 0.00505909 | missense | TNIP3 | GRCh38.p7 | 4:121141834 | GTGCTCCCGTTGCTT[C/G]TGCACAGCTCCAGGG | 79931 |
rs750179625 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149659 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 79931 |
rs750188457 | in-del | -/G | 1.68207e-05 | 0.00290001 | frameshift-variant | TNIP3 | GRCh38.p7 | 4:121141900 | CAAGCCGCAGTTACA[-/G]GGTGGGCAATACATC | 79931 |
rs750252746 | snp | G/T | 1.65048e-05 | 0.00287265 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147044 | TATTTTGTTTTGACT[G/T]GTACCTGGGAATTCA | 79931 |
rs750259749 | snp | C/G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194034 | GATCCTGGATTGGAG[C/G/T]CTTTTTTATGCAAAG | 79931 |
rs750304558 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182595 | CGGTAAATGACTTGG[A/G]GACTGTCTCCACAAA | 79931 |
rs750359661 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213037 | CTGTTTGGCTGCTCA[A/G]TGTTGCATCTGGAAG | 79931 |
rs750401987 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197363 | TGAAACACCTTCTCT[A/G]CTAAAAATACAAAAA | 79931 |
rs750412508 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214243 | CCCTCATCCTTCCTT[C/G]TGCACTTCCGGGTAT | 79931 |
rs750428875 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171440 | TTGATGGTGGGTATA[C/T]GTGTATACCATACAA | 79931 |
rs750463485 | snp | A/G | 1.64811e-05 | 0.00287059 | intron-variant, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121138664 | CGGAAGCTGGTCAAG[A/G]GCATACCACTGATAG | 79931 |
rs750542311 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160494 | AAAAAAAAAAGAAGG[A/T]ATTACAAAATTGACA | 79931 |
rs750572025 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186682 | CAGATGCTCAGTGAT[C/T]GATACTATTGTTATT | 79931 |
rs750587037 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201054 | GAAGGTCAAGGGGAA[A/C]TTTGGTGGCTGCAAT | 79931 |
rs750649800 | snp | C/G | 1.6492e-05 | 0.00287154 | missense | TNIP3 | GRCh38.p7 | 4:121147145 | TCGATCCGATCGTTC[C/G]TTTTTGAAGTCTTCT | 79931 |
rs750723769 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220726 | TGGGTAAACGTACCA[C/G]TTAACTTTTAGAGTC | 79931 |
rs750726645 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148232 | ATTTAAACCCTTTAG[A/T]GTTTCATGCGGCACT | 79931 |
rs750778197 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169943 | AGATACATTAGAAGG[C/T]AAATTGGCTTTTGTT | 79931 |
rs750810279 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154515 | TTTATGCAGGGACTT[C/T]TCATTTTAATCTCCC | 79931 |
rs750833233 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168493 | CATAAGCCAACATGC[C/T]CAGCCTTTTTCTTTT | 79931 |
rs750843511 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178981 | AAGATAAAGATGTAG[C/G]ACAAAGCAGGGAGGG | 79931 |
rs750907138 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148242 | TTTAGTGTTTCATGC[A/G]GCACTTGGTGATGTA | 79931 |
rs750911243 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168407 | GGTTTCACCATATTG[G/T]CCAGGCTGTTCTCGA | 79931 |
rs750928339 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209202 | TTCTTTTCATCTGGC[-/T]GTTCCTGAGTTGTAT | 79931 |
rs750990679 | snp | A/G | 5.00705e-05 | 0.00500327 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132683 | GAAAACAGTAGGAAA[A/G]TGTTTTAGATTAAAA | 79931 |
rs751000423 | snp | C/G | 3.45358e-05 | 0.00415532 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141936 | AGAACAAAACTGTGG[C/G]GTCACTACCAGTGGG | 79931 |
rs751013714 | snp | A/G/T | 3.30073e-05 | 0.00406236 | missense | TNIP3 | GRCh38.p7 | 4:121154597 | TGTTCCTTTTCCTTG[A/G/T]TCGCAAGAGTATTTT | 79931 |
rs751068526 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196638 | ATTAACAATTGCTTA[C/G]TAATATACATTAATA | 79931 |
rs751126120 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215718 | CCAAGAACAGTTTAT[C/G]TGTGCCTCTTTTATG | 79931 |
rs751129187 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140168 | GTGAAACCCCATCTC[C/T]GCTAAAATTACAAAA | 79931 |
rs751166462 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184354 | TTGTTGAGAGTAGCT[A/C]ACAGGAGTAGGCTCT | 79931 |
rs751172312 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202318 | TAAAGTGGGGAAAGG[A/C]CTCCCTATTCAACAA | 79931 |
rs751181443 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221384 | AGAAACAGGAACAGT[A/G]AAGCAGATCACGTGA | 79931 |
rs751216115 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216522 | TAAAAAAATATGAAG[C/G]ACATGAGGCTCAGAT | 79931 |
rs751234844 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136359 | AGGTACAGTAAGAGG[A/G]GCACTGTACTATATA | 79931 |
rs751275237 | snp | C/T | 3.30322e-05 | 0.00406387 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121142729 | AGATCAACATACCTG[C/T]TTTAATTGCTTTTCT | 79931 |
rs751293248 | snp | A/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131746 | TCAAGTGATCCTCCC[A/G]CCTCAAGCCTCCTGA | 79931 |
rs751311902 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163266 | TTGTTATAGTTCATA[C/T]GTCTCAGGTTTCTAT | 79931 |
rs751327106 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174971 | CTTATTGATGCATTA[A/G]ATTCCAAAACCCAGC | 79931 |
rs751345896 | snp | C/T | 1.65007e-05 | 0.00287229 | missense | TNIP3 | GRCh38.p7 | 4:121150143 | GTTCTCATCTCCTCA[C/T]GGCAGAATTCCACTC | 79931 |
rs751369229 | snp | C/T | 0.000134044 | 0.00818559 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164182 | ACAGGGGAAAAGTCT[C/T]TTAAGGTATATTTTA | 79931 |
rs751470365 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121192118 | TCCTTTCAAGACATG[A/T]TTACAAGTCTTGATT | 79931 |
rs751488979 | snp | C/G | 1.6569e-05 | 0.00287824 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157115 | CCGCTGCAGCCGGTC[C/G]CGGGTCAGGTCGCGC | 79931 |
rs751497260 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139109 | ATACAAGTTTTCTAA[C/T]GGTTTAAGGAAGAAA | 79931 |
rs751569428 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211634 | CCCTGAAAACTAGAA[A/T]TTTACTAATGCAATA | 79931 |
rs751624746 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218107 | AATAAAATAAAATTA[A/G]ATACTGATATATTTT | 79931 |
rs751631531 | snp | C/T | 3.30251e-05 | 0.00406343 | missense | TNIP3 | GRCh38.p7 | 4:121164067 | GTTCTTACCTCTTTA[C/T]GCTCCGTAGAACTTT | 79931 |
rs751636203 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225296 | TTGTGCTTTGCAACC[A/G]CTAGAATATTTTCCC | 79931 |
rs751649715 | snp | A/C | 4.86369e-05 | 0.00493114 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161220 | TGGTTCAGCACACTT[A/C]GAAAAAAAAAAAGAG | 79931 |
rs751726054 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212907 | TTTAGTTTTCACTTA[A/G]CACATACATAGTACA | 79931 |
rs751743267 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170376 | TTTCAGAACACAGTC[C/T]AGAACACACAATGAC | 79931 |
rs751790767 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199849 | TGAGGACGGTTGTGT[A/G]GGTTGCTGTGTAACA | 79931 |
rs751805029 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170210 | CTCCTCTGAGATGCT[A/C]TAAGCTTCTTGAAGA | 79931 |
rs751822344 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160382 | TACTTGGGAGGCTGA[A/G]GCACAAGAATCACTT | 79931 |
rs751861005 | snp | C/T | 3.306e-05 | 0.00406558 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121147172 | TTCTTCGTATATTTG[C/T]ACCTAAGAAATATTA | 79931 |
rs751876876 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186473 | AACCCTCTGAAAGAA[A/G]CATTGTGATGCAGTA | 79931 |
rs751902415 | snp | A/G | 1.65048e-05 | 0.00287265 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138585 | AGATCCCATTAAGAT[A/G]TAAACATGAAAGAAT | 79931 |
rs751927714 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133672 | CAATGAGATAATCCA[C/T]GGCAGAATGGAAATC | 79931 |
rs751934273 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144206 | CCAGTTTTCGTTTTC[-/T]TCACAGCATATAGCA | 79931 |
rs751937237 | snp | G/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218041 | CTCCTAGTCATGATC[G/T]TCCATTGTTGTTCAT | 79931 |
rs751937765 | in-del | -/GGAA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156834 | CGTTTTCTTCTTCCT[-/GGAA]GGGACTGGGGAATGA | 79931 |
rs752079246 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177092 | TTTTCAAGCATTATT[G/T]GAACCATATTTGTTT | 79931 |
rs752112797 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206210 | CAAATTTAGACTAGT[C/T]TTAGGAGATTCTTAC | 79931 |
rs752145331 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208827 | CTATACAGTCCTCTG[A/G]ACTACACCTAAGTTA | 79931 |
rs752204733 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208011 | TTTATCAGGGGTTTC[C/T]GCTTTTGCATCTTCC | 79931 |
rs752207984 | snp | A/C | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166815 | CTTCTTTGTTTCCTG[A/C]ATCTATTTGCATGAA | 79931 |
rs752273813 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182948 | ATTATGTTTTCATTA[A/G]TCCATGCCATGAGAG | 79931 |
rs752274893 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183562 | CACACAGCAGGAAGC[A/G]AGAGGCAGGCAAGTG | 79931 |
rs752326043 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224885 | ACATATTCTCTAATA[C/T]TGAAAAAAAATGACA | 79931 |
rs752512205 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215553 | ACTTTCCTACCACCA[C/T]GTCTTTGTACACATT | 79931 |
rs752514571 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206301 | CTTAATCAAAATGAA[-/C]CTTTTGCTAAACACT | 79931 |
rs752541481 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177271 | AATCTTAATATCATT[A/C]TCACTTAGGCAATTA | 79931 |
rs752543479 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173636 | TCATTCATGTATGCA[C/T]TTTTTTCTTTGAGAT | 79931 |
rs752596949 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163067 | TTACTGAAAATCTAG[A/T]TACCAAATCTGCAAG | 79931 |
rs752605546 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202060 | CTAGAAAAAACAATC[C/T]TAAAATTCATATGGA | 79931 |
rs752669294 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149902 | TCTGTCTGAAACTCA[G/T]TTCCCTATGTTCTAA | 79931 |
rs752676065 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148585 | GACAGAGCTTTAAGA[C/T]TGTGCATATTACCCT | 79931 |
rs752691363 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203171 | GCAAAAATATGAAAC[A/C]AGCCCAAATGCCCAT | 79931 |
rs752693455 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189299 | ATAAACCATTATTTT[C/T]AGGAAAGACCCTGGA | 79931 |
rs752709207 | snp | A/G | 1.6498e-05 | 0.00287206 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121150171 | CTCGAGACTTCCTCA[A/G]ACAGTCCTCGGAAAA | 79931 |
rs752724351 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137144 | TGATATATAAATGAC[C/T]TTATGGTATTACTAA | 79931 |
rs752734288 | snp | A/G | 8.94943e-05 | 0.00668873 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158638 | CACACAATTGGCCCC[A/G]CCAGGATAATGGCTT | 79931 |
rs752742923 | snp | A/T | 1.65258e-05 | 0.00287448 | synonymous-codon, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164138 | CATGGAAGCTGTTTT[A/T]CCTGGAGTCTTGGAA | 79931 |
rs752781462 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190722 | AGTCAGGCCAATACT[C/T]GAAATAAATATGAAT | 79931 |
rs752875968 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148849 | TAGTACTTGCTCAGG[A/G]CAAAACCAGTCAGTA | 79931 |
rs752884865 | snp | C/T | 1.6591e-05 | 0.00288015 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132666 | CTGAGGATAAACCTA[C/T]GGAAAACAGTAGGAA | 79931 |
rs752892275 | in-del | -/TGGG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198086 | TAATAGATGTGTTTC[-/TGGG]TGGGTGAGTATAAAT | 79931 |
rs752937416 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169554 | TCACTCTGTGTTTCT[C/T]GAGCCCAAAGTAGTG | 79931 |
rs752973030 | snp | A/T | 1.65545e-05 | 0.00287697 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132591 | GGTCCTCAGCCACGC[A/T]CCCTCGTTGCCTGTT | 79931 |
rs752974964 | snp | C/G | 1.65002e-05 | 0.00287225 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154480 | AGCCTAGATTTTGTT[C/G]CGACTGTCAGTAAGA | 79931 |
rs752984712 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173754 | CTGTCTCAGCTTCCC[A/G]AGCAGCTGGGGTTAC | 79931 |
rs753003397 | in-del | -/AAT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163043 | GATTTTTCTTTAATA[-/AAT]AATAAAAATTACTGA | 79931 |
rs753189690 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121145391 | TTGTCCTTTAGGTTC[A/C]AGGCAGAATTATACC | 79931 |
rs753225258 | snp | C/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227778 | TAGATCAGCTTAATA[C/G]GGCCACAACACATAA | 79931 |
rs753235151 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175395 | TCTTCTAATTAACAT[C/T]TATAATTTCCACACA | 79931 |
rs753291162 | snp | C/T | 1.65086e-05 | 0.00287298 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121164072 | TACCTCTTTATGCTC[C/T]GTAGAACTTTCTGCG | 79931 |
rs753354214 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205993 | CCGAGTAAAGGGGGA[A/G]GTCCCCTTGTAAAAT | 79931 |
rs753361273 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176232 | TTGCCAGTAATGAGC[A/G]TCAAATGCCATAAGG | 79931 |
rs753368851 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205138 | GAATCAGGGTTATGA[G/T]GTGTTAGCTGGGGAG | 79931 |
rs753378110 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134714 | TGACTGGAAGTCTGT[G/T]CACCATGGTACTCAG | 79931 |
rs753416459 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165525 | ATTTCCATGTTCTTG[C/T]GTTAATCTCTGTGTC | 79931 |
rs753429611 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153696 | ATACTTAATACTTTG[A/C]GGATCTTTAAATAAC | 79931 |
rs753440868 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143212 | TATGTGATACTTAAT[A/G]CTATCTCAATTTTAT | 79931 |
rs753458119 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225576 | ACTATGAGTAATAGG[C/T]GTTCCTCTAATAATT | 79931 |
rs753484729 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140366 | AAAAAAAGAAAGAAA[A/G]TGTAGGCCATTCTAC | 79931 |
rs753484953 | snp | A/G | 1.65985e-05 | 0.00288079 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154728 | CAGTACAAGTCAAAT[A/G]AGATGATATTGTAGG | 79931 |
rs753502619 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194112 | GATGTAGTAGTGTAT[C/T]GATGTTCATTTTCCG | 79931 |
rs753512819 | in-del | -/GA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157997 | TCTGGGTAACAAAAT[-/GA]GGAAGAAAGGAAAAA | 79931 |
rs753512929 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179505 | TATATATGATGCAAA[C/G]GCATTTGGTTTCAAT | 79931 |
rs753578223 | snp | A/G | 0.000111434 | 0.00746356 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154691 | CCTTCTGAAGTTAAG[A/G]CCAAGAAAAGAAAAT | 79931 |
rs753620963 | snp | A/G | 1.65277e-05 | 0.00287464 | missense | TNIP3 | GRCh38.p7 | 4:121142775 | ATCTGACAAGCTTTT[A/G]TCTAAAGACAAAACA | 79931 |
rs753632843 | snp | G/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216911 | GACCCCAGGACACCA[G/T]CAGCTTTCTTCTAGG | 79931 |
rs753680599 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135794 | TAAAAGGACCGTTTT[A/G]ATTAAATGAACCCCA | 79931 |
rs753681872 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181059 | ATCTTAGAGAGAGAG[A/C]CATAAATTTCAGTGA | 79931 |
rs753688840 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172957 | TACTTTATTTGCTTC[A/G]ATCTGAACTTCATAA | 79931 |
rs753699820 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141574 | AAATGTTATATGTTG[C/T]TCAAGGAATTATTCC | 79931 |
rs753734873 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196232 | CAAGGTCTACAATAC[-/T]TTCTTTTTATAGCTT | 79931 |
rs753827848 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133820 | AGGAAAATTTGGACA[C/T]AGATGGAAGATGGTC | 79931 |
rs753828737 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215281 | GACTCCAGACACACA[A/G]GATCTCAGAACCCTA | 79931 |
rs753832759 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201143 | CTGGATGAGTAGGGG[A/G]CAGGAAAGAAAGTTT | 79931 |
rs753849612 | snp | A/G | 1.6628e-05 | 0.00288335 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132674 | AAACCTATGGAAAAC[A/G]GTAGGAAAATGTTTT | 79931 |
rs753875737 | snp | C/T | 1.65507e-05 | 0.00287664 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147028 | ACATGCTGGCAAAGA[C/T]TATTTTGTTTTGACT | 79931 |
rs753885623 | snp | A/C | 1.64936e-05 | 0.00287168 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154496 | CGACTGTCAGTAAGA[A/C]TGTTTTATGCAGGGA | 79931 |
rs753910968 | in-del | -/A | 0.00194932 | 0.0311586 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161222 | GTTCAGCACACTTAG[-/A]AAAAAAAAAAGAGAG | 79931 |
rs753932314 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177748 | CCCTTTCTATCAATA[A/T]CTCAGCAAAAATGTG | 79931 |
rs754004293 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220788 | TTCAGCGTGCCTTAA[A/G]TGCCAGTCTGTGTGT | 79931 |
rs754024694 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211749 | TGAATTATCAACTCA[A/G]AGATGTTTTCAGCAT | 79931 |
rs754092146 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222137 | CTAGGATTTTTGCAA[C/T]GTTGCTATATTGCTC | 79931 |
rs754099683 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149426 | TCACCACTCAGCTGC[C/T]ACCATTTTCTGAAAA | 79931 |
rs754113455 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180108 | TCCAGGAATTAATAT[C/T]ATAGATGTCGGGCTG | 79931 |
rs754218524 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156296 | TCTTACTATACCTAA[A/C]ATAACGAGGGGCCAT | 79931 |
rs754227449 | snp | A/G | 1.65776e-05 | 0.00287898 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164151 | TTTCCTGGAGTCTTG[A/G]AAAGCAGAAAGAAAA | 79931 |
rs754232188 | snp | C/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228389 | GCAGATGGACAACGA[C/T]GAGCCCCTTCTACAC | 79931 |
rs754255323 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214043 | GTGGCAACCATAATA[C/T]CAATACGTAGGACCG | 79931 |
rs754284792 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186535 | ACAGTGGGACCTAGT[A/G]TAAGTCCTTTAGCTT | 79931 |
rs754301302 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143136 | ATATGCACTTAATCC[A/G]TGTCAGAAACTTATC | 79931 |
rs754342122 | snp | G/T | 0.000163199 | 0.00903176 | missense | TNIP3 | GRCh38.p7 | 4:121216421 | TGTTATTACCTTTCA[G/T]AATCTTCAGATTGAT | 79931 |
rs754389011 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168526 | CTTTTCTTTGCTTTT[C/T]TTTTTTTTTTAAGAG | 79931 |
rs754393565 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136567 | CTTTAAAAACAGGCC[A/G]GGTGTAGTGGCTCAC | 79931 |
rs754410428 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184588 | TTCTAAGGCCTGACT[A/G]CCTTCCAACTTTCAG | 79931 |
rs754497091 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206156 | ATTTGGGTAGAGACA[C/T]AGCCAAACAATATCA | 79931 |
rs754512508 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219427 | AAGATGTCCTCTGTT[C/G]TTGGATGCATTTCAG | 79931 |
rs754516039 | snp | C/T | 3.4822e-05 | 0.0041725 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141945 | CTGTGGGGTCACTAC[C/T]AGTGGGAGAGACTGA | 79931 |
rs754522908 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152112 | AACAGTATGTTAATT[A/G]CAAGGCTGACATATT | 79931 |
rs754575883 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153732 | TGAACACCAGTTAAC[C/T]ACAATCATGGGCATG | 79931 |
rs754585217 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158949 | ACTGGTTCGTATATG[-/A]AAAAACTACTGGCTG | 79931 |
rs754585230 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181454 | CCATTAGTACACATT[A/C]ATCTGTAACTCCAAA | 79931 |
rs754606730 | snp | C/T | 0.000163199 | 0.00903176 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216517 | TAAAATAAAAAAATA[C/T]GAAGGACATGAGGCT | 79931 |
rs754625443 | in-del | -/TG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140272 | CCAGGAGGTACAGGT[-/TG]CAGTGAGCCAAGATC | 79931 |
rs754639985 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225581 | GAGTAATAGGTGTTC[C/G]TCTAATAATTCATCA | 79931 |
rs754657355 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226962 | GCTTAATCAAGATTG[C/T]TCAACCCTGTAATAT | 79931 |
rs754663217 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141618 | TTCAGTTAATTTATT[C/T]GTATCTATGTGTCCT | 79931 |
rs754673094 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221490 | TGAGGCAAATGCTCA[A/T]TGTTGTTAAGAATAT | 79931 |
rs754676874 | in-del | -/TGTT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162256 | TTTCTATCTTTTCTC[-/TGTT]TGTTTATGTTTCAGC | 79931 |
rs754691823 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176756 | ACATGTGTCAATTTA[C/T]GGTAGTTTGCAAGAA | 79931 |
rs754700334 | snp | A/G | 1.67332e-05 | 0.00289246 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164178 | AAAAACAGGGGAAAA[A/G]TCTCTTAAGGTATAT | 79931 |
rs754781987 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160772 | AACCTTGAGTTTCAA[A/G]GTGTGTCAAGTTGCA | 79931 |
rs754783316 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199725 | CACAAATTCACAATG[A/C]CCAGAATAGAGGCAT | 79931 |
rs754813328 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174980 | GCATTAGATTCCAAA[A/G]CCCAGCTTGGGTTGA | 79931 |
rs754819999 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173044 | ATGGCAAATGACTTG[C/T]TCACAATTATGATGT | 79931 |
rs754835463 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200232 | CCTGAGAATGCTGAA[C/G]AATGGGTTCACCGAG | 79931 |
rs754928280 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201158 | GCAGGAAAGAAAGTT[C/T]TGAGGTATGAGGAAA | 79931 |
rs754969937 | snp | A/G/T | 3.32786e-05 | 0.00407902 | missense | TNIP3 | GRCh38.p7 | 4:121157119 | TGCAGCCGGTCCCGG[A/G/T]TCAGGTCGCGCTGCC | 79931 |
rs754974159 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161635 | GGTAGCTGTGCCCAT[G/T]AACATGTATGTGAGT | 79931 |
rs754992100 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187892 | AGTTACTTTCACATG[A/T]GACTACTTTTTTTGG | 79931 |
rs754999975 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147366 | GAATACTGCTTGAAC[G/T]TCTAAAAGACAGTTT | 79931 |
rs755007766 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189110 | ATCATTTAATTGACC[C/T]CCTGCATTAACATAA | 79931 |
rs755023443 | snp | C/T | 1.65373e-05 | 0.00287548 | missense | TNIP3 | GRCh38.p7 | 4:121147174 | CTTCGTATATTTGCA[C/T]CTAAGAAATATTAGC | 79931 |
rs755058110 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220832 | TGGACAGCAGGATTC[A/G]TTCCTGCTGTGATTT | 79931 |
rs755111543 | snp | A/C/T | 3.3022e-05 | 0.00406326 | synonymous-codon, missense | TNIP3 | GRCh38.p7 | 4:121164069 | TCTTACCTCTTTATG[A/C/T]TCCGTAGAACTTTCT | 79931 |
rs755143389 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133305 | TTTTGTACTTGTTGT[C/T]CTCATTTGGTATACC | 79931 |
rs755168464 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146754 | GAGTACTAGGTAGTT[C/T]AACTCTCATTCTACC | 79931 |
rs755195745 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196003 | TAGTCACAGTGATGG[C/T]AGGATTCATGGAGCC | 79931 |
rs755197441 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168611 | TTGTAACCTCCAACT[C/T]CTGGGGTCAAGCAAT | 79931 |
rs755229108 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136720 | AAAAATTAGCTGGGC[A/T]TGGTGGTTCATGCCT | 79931 |
rs755270519 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210066 | AGAAACCACACTCTT[A/T]ACCATAATACTGATT | 79931 |
rs755326148 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156304 | TACCTAAAATAACGA[A/G]GGGCCATTAGAGTTT | 79931 |
rs755367602 | snp | A/G | 2.53277e-05 | 0.00355854 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154707 | CCAAGAAAAGAAAAT[A/G]AAAGTCAGTACAAGT | 79931 |
rs755403164 | snp | C/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228393 | ATGGACAACGATGAG[C/T]CCCTTCTACACTTCC | 79931 |
rs755403824 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148710 | ACTTCACCATCAAAT[A/G]CTATAAAATTTTTAG | 79931 |
rs755407820 | snp | A/C | 5.07395e-05 | 0.00503659 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161227 | GCACACTTAGAAAAA[A/C]AAAAAGAGAGAAGAT | 79931 |
rs755408994 | in-del | -/TAAAAAG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224369 | CTCTGTCTCAAAAAA[-/TAAAAAG]AAAAAAGAAAAAAGA | 79931 |
rs755413350 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143200 | TCCCAATCCCTCTAT[A/G]TGATACTTAATACTA | 79931 |
rs755465124 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136857 | GTAAGACTGTCTCCG[-/A]AAAAAAAAAAAAAAA | 79931 |
rs755554964 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174008 | AGTACTAGAATATGA[A/G]GATGAGCAAAAGGCA | 79931 |
rs755585399 | snp | C/T | | | intron-variant, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121182481 | TGCCAGCAAATTCTT[C/T]TGCTGAAGAATTTCT | 79931 |
rs755603125 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223474 | TGAAAGATGGTTTTA[A/G]ATAATAACACACAAT | 79931 |
rs755631172 | snp | A/G | 0.000163948 | 0.00905246 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216549 | AGATGTACGTCAAGG[A/G]AAGTTAACTATGTCA | 79931 |
rs755724191 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205090 | TTTAACAGGTAATAG[A/G]TGTCATAGAAGAAAT | 79931 |
rs755725902 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191338 | GCACCATTGTTCTAC[A/G]GTGGAAATACACTCA | 79931 |
rs755750835 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177686 | CTTCACTCCCTGTCA[A/T]TGGCTCACGCTTGTG | 79931 |
rs755811195 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153421 | GTATCAAAAATGGGA[A/G]GATTTTAAATATAAT | 79931 |
rs755849276 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139416 | ACCTCTGTATTTAAC[A/G]CTTAGGAATGGAGCA | 79931 |
rs755852144 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180562 | TGATAGCAGAGGGAA[A/G]GTTTTGGATGCTGTG | 79931 |
rs755889442 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224143 | CAAGGCAGGAAGATC[A/C]CCTGAGGTCAGGAGT | 79931 |
rs755911996 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194867 | AAAAAAAAGTACACA[C/T]ACACACAGACTTCTT | 79931 |
rs755942781 | snp | A/G | 1.77862e-05 | 0.00298207 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158650 | CCCACCAGGATAATG[A/G]CTTTAAAGAAAATAC | 79931 |
rs755943749 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154904 | TTTCTTTTATCAGAA[C/T]TTACTGAAGTATCTT | 79931 |
rs755958522 | snp | C/G | 1.651e-05 | 0.0028731 | missense | TNIP3 | GRCh38.p7 | 4:121142758 | CTAGTTTTTCTTTCT[C/G]CATCTGACAAGCTTT | 79931 |
rs755989886 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174063 | CTGAATATAAAATCT[-/C]AACATTAGAGGGGAC | 79931 |
rs756082799 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180983 | TGCTGCCCTTTGCCT[-/G]GGAAGTGTGAAGTGC | 79931 |
rs756117393 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216818 | TACATAGAGCATGAA[C/T]GGTTAAAGTTGTCAG | 79931 |
rs756221624 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174050 | TGTTTTCTGTTTTCT[A/G]AATATAAAATCTCAA | 79931 |
rs756224950 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187765 | TGGATGGGATTCAAT[C/G]AAATTAAATACAGAA | 79931 |
rs756227751 | snp | C/T | | | utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227394 | ACTCACCATGTTCTA[C/T]CCTGAAAGTCCTTCT | 79931 |
rs756246087 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146175 | GGTTCTGCAAAACAA[A/T]TTTTTCCATGTAAAA | 79931 |
rs756255796 | snp | C/T | 1.64993e-05 | 0.00287218 | missense | TNIP3 | GRCh38.p7 | 4:121150173 | CGAGACTTCCTCAAA[C/T]AGTCCTCGGAAAATG | 79931 |
rs756267697 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151403 | GCTGGGAATTTCCTA[A/G]TAGAATGTCTTAGAA | 79931 |
rs756269605 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219547 | ACTTACTTTTGGAAG[C/T]TAACCAAGTTTTATG | 79931 |
rs756288802 | snp | A/G | 1.65919e-05 | 0.00288022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132667 | TGAGGATAAACCTAT[A/G]GAAAACAGTAGGAAA | 79931 |
rs756290069 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209324 | GAATTTGTAGCATGT[G/T]GGTCAGAAGTATGGG | 79931 |
rs756308632 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134823 | CTCCAGCCACACCCT[A/T]CCTCACAGTGTGAGC | 79931 |
rs756430908 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135756 | TTATGAGAATTCTGA[A/G]CAATTCAGTTACACC | 79931 |
rs756466388 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167179 | CTTGACATTGTGTGG[A/G]TTCCAAAGGAAAACA | 79931 |
rs756473416 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206707 | GCTGGGACTACAGGT[A/G]CATGTCACCATGCTC | 79931 |
rs756517685 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168437 | AACTTCTGACCTTGT[A/G]ATCCACCCGCCTCGG | 79931 |
rs756556703 | snp | C/T | 1.65927e-05 | 0.00288029 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147200 | TTAGCTTGCTGTTAC[C/T]GTAAGCTTCCTTTTC | 79931 |
rs756586272 | snp | A/G | 0.000132328 | 0.00813304 | missense, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164143 | AAGCTGTTTTTCCTG[A/G]AGTCTTGGAAAGCAG | 79931 |
rs756589315 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227257 | GTTAATATTACTGAG[C/T]TCCTGATCAGTTATA | 79931 |
rs756608879 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156274 | AGAGTCTTTACACTT[C/T]GTTTTTTCTTACTAT | 79931 |
rs756631580 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187879 | CTGACACAACTTTAG[-/T]TACTTTCACATGTGA | 79931 |
rs756688411 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173193 | AGACATCATTTACCA[A/G]TGATGGAAAAGCATC | 79931 |
rs756760886 | snp | A/T | 0.000153895 | 0.00877062 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157045 | AAATCCCCCCGCCCC[A/T]TTGCTTTTATTTGGA | 79931 |
rs756772487 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215800 | CTTCTAAACTTCAAG[C/G]AGCTTGAGTATAGGG | 79931 |
rs756778071 | snp | A/T | 8.4064e-05 | 0.00648266 | missense | TNIP3 | GRCh38.p7 | 4:121154618 | AGAGTATTTTTTCCC[A/T]TTAAAAGTTTATTCT | 79931 |
rs756796109 | in-del | -/ATG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176517 | CCTACTAGCATTATG[-/ATG]ATGATGATGATGATG | 79931 |
rs756824895 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184532 | TGCGGAGCTGAGAGA[C/T]GGAGAGAGTCCTGAC | 79931 |
rs756850339 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162276 | GTTTATGTTTCAGCA[C/T]TTTAGGGTTTGATGG | 79931 |
rs756883661 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173782 | TACAGGTGTGTGTCA[C/T]CATGCCCAGCTAATT | 79931 |
rs756898825 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179789 | CTAGTGATTCATTCA[C/G]CAGCATAGAAAATGT | 79931 |
rs756945138 | snp | A/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131782 | TGGGTTTATAGGTGT[A/G]TGCCACGAGCCTGGC | 79931 |
rs756979617 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189751 | AATTTAAATAGATAT[C/T]GAAGAATTGTATTTG | 79931 |
rs756988704 | snp | A/G | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164206 | TATTTTAGGGTGAGA[A/G]CAAGTATACAAAATT | 79931 |
rs756988816 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208003 | CTGATGGTTTTATCA[A/G]GGGTTTCCGCTTTTG | 79931 |
rs756993098 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191157 | TATTTATTTGAAATT[A/C]TATTTTCATGAAGAA | 79931 |
rs756999510 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133930 | CAAGGAAGTCTCCTC[C/T]CCAGAGGATTTGGAA | 79931 |
rs757005327 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222455 | CTATATGTCTTTGGG[C/T]ATATTATTTAAATAC | 79931 |
rs757081862 | in-del | -/TTGC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226944 | TGCTGGCTCTGCTCA[-/TTGC]TTGCTTAATCAAGAT | 79931 |
rs757131391 | snp | A/G | 3.32088e-05 | 0.00407471 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121161189 | CAAGAGAATTCATCA[A/G]GTTCTTTCTTGTTGA | 79931 |
rs757169956 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223931 | GCTAAATCTAACCAC[A/G]GGAGGCTACACAATG | 79931 |
rs757177374 | in-del | -/TCT | 1.71852e-05 | 0.00293127 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132715 | TTAACATTTCATTTC[-/TCT]TCTTCTGGCTTAAGG | 79931 |
rs757185918 | snp | C/T | 1.65307e-05 | 0.0028749 | splice-acceptor-variant | TNIP3 | GRCh38.p7 | 4:121142777 | CTGACAAGCTTTTAT[C/T]TAAAGACAAAACAAA | 79931 |
rs757205825 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139218 | TTGTGAAGAACCGAT[C/T]CAGCAGAACCTATCC | 79931 |
rs757258036 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211797 | GCAAAAAGAGAGCAA[A/C]TCCTTAGAGTTACCA | 79931 |
rs757271822 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169725 | TTTTGGCTTCCAACT[A/G]GTAAATCACCTCTCT | 79931 |
rs757271840 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180874 | ATCTTCCCCAATTCC[C/T]TTAAGCCTTGGGTCT | 79931 |
rs757302323 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193515 | TGCCTACTGATAAGT[A/G]TAGAGAACATTATCC | 79931 |
rs757313710 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198655 | TTATAGTGAATTTAC[C/G]CTCAAGTTCCTTAAT | 79931 |
rs757365719 | snp | C/T | 3.42836e-05 | 0.00414012 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158670 | AAAGAAAATACCGAA[C/T]AGAGAGAGGTATTTA | 79931 |
rs757399787 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185856 | ATTAAACAACAATTG[A/G]GTATCCATTATTGCA | 79931 |
rs757425853 | snp | A/C | 1.66466e-05 | 0.00288496 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132677 | CCTATGGAAAACAGT[A/C]GGAAAATGTTTTAGA | 79931 |
rs757434191 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199946 | TGTGGGGCTGCATAT[G/T]CCCAGAAGAAAGGGT | 79931 |
rs757449954 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121145880 | TACTTGGGAGGCTGA[C/G]GCAGGAGACTAGCTT | 79931 |
rs757503924 | in-del | -/CTTTG | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168516 | TTTCTTTTTTCTTTT[-/CTTTG]CTTTTTTTTTTTTTT | 79931 |
rs757522645 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211805 | AGAGCAACTCCTTAG[A/C]GTTACCACACACAGA | 79931 |
rs757528839 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186569 | TGAACCTTTTTGGCC[A/T]GTTTTGTAAATGGAG | 79931 |
rs757561704 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133687 | CGGCAGAATGGAAAT[A/C]TGAACAAAAACAAAG | 79931 |
rs757586748 | snp | C/G/T | 3.30192e-05 | 0.00406309 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157226 | CGCGGCGTCCAGTTT[C/G/T]GTCTTCAGCTCTGCT | 79931 |
rs757600062 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168333 | TGCCTCAGCCTCCCA[A/G]GTAGCAGGGATTACA | 79931 |
rs757607956 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176327 | GTGTCCAAAGGTTTC[C/T]CAGTGAAAGCTAAAC | 79931 |
rs757631275 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190606 | TAACAGGGGACACAC[C/T]TGTCTGCTATAAGCC | 79931 |
rs757648250 | snp | G/T | 1.65323e-05 | 0.00287505 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132610 | TCGTTGCCTGTTGTC[G/T]CTCTCTGTTAGTGTG | 79931 |
rs757688372 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134792 | CCATCTTATAGAGGA[C/T]TCTGCTCTAGCCCTC | 79931 |
rs757705207 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205387 | GAAGGGGGATTGTAG[A/C]AGATTAAACCAGAAA | 79931 |
rs757705728 | snp | A/C | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166825 | TCCTGAATCTATTTG[A/C]ATGAATTTTTAAGTG | 79931 |
rs757709262 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219503 | TTACACAATCCATAG[A/T]TCCAAAATAACCCAA | 79931 |
rs757722735 | snp | A/G | 3.29717e-05 | 0.00406015 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154509 | GAATGTTTTATGCAG[A/G]GACTTCTCATTTTAA | 79931 |
rs757736250 | snp | A/G | 4.95135e-05 | 0.00497537 | missense | TNIP3 | GRCh38.p7 | 4:121150185 | AAACAGTCCTCGGAA[A/G]ATGAACACTTGATAT | 79931 |
rs757743871 | snp | A/C | 1.66286e-05 | 0.0028834 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164163 | TTGGAAAGCAGAAAG[A/C]AAAACAGGGGAAAAG | 79931 |
rs757763235 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143232 | CTCAATTTTATAGAT[A/G]AGAACACTAAGACAT | 79931 |
rs757768498 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226141 | AGACAGAAAAACAGG[A/C]ACAGTGAGAGATCAA | 79931 |
rs757780069 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200851 | TTCAGGCTCTGTTAA[A/G]AGAACAAACAAAACT | 79931 |
rs757787662 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204052 | TATGAAAAAATCTCT[C/G]ACTATTCCTTCAGTT | 79931 |
rs757795235 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206339 | CGTTATCTCATTTAA[C/T]CCTCTCCTTAACACA | 79931 |
rs757815078 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225715 | CCTCAGCAGGAAGTA[C/T]TTAGTTGGCCAAAAA | 79931 |
rs757818351 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182977 | AGCACTTTGAAAGAG[A/C]ATTAGAGTTTAATTT | 79931 |
rs757842278 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153881 | TCAACCATGTGCTAG[C/T]GCATTCCTATGTTCC | 79931 |
rs757856867 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182090 | TTTAATTGGGAGGAT[A/T]ACAGAGTTTAAGAGT | 79931 |
rs757874536 | snp | C/T | 1.7e-05 | 0.00291543 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121141837 | CTCCCGTTGCTTCTG[C/T]ACAGCTCCAGGGCCT | 79931 |
rs757905062 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227119 | TTTTATCTGATGTGC[A/G]CAAAGGGGCTAACTA | 79931 |
rs757918750 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195418 | TTACCTTTGGCTAGA[A/G]AAGTTATAAAACCCA | 79931 |
rs757960167 | snp | C/G | 3.32127e-05 | 0.00407495 | missense | TNIP3 | GRCh38.p7 | 4:121157110 | TCCTCCCGCTGCAGC[C/G]GGTCCCGGGTCAGGT | 79931 |
rs757962376 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138695 | TCTGGCTGTGTGGAA[C/T]AATACAACATTATTA | 79931 |
rs757999169 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172008 | AAAGTTCTGGGATTA[C/T]AGGCATGAGCCACCA | 79931 |
rs758000417 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219293 | AAAGCAAACACATGT[C/T]TTTGTTTCCATCTTT | 79931 |
rs758011607 | in-del | -/GTGAT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211183 | GTCTTGGAAAGAGGG[-/GTGAT]GTGTGATTTAAATAA | 79931 |
rs758020233 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141678 | GTGTACATTGACCAC[G/T]CCAACTTTGCAAGTT | 79931 |
rs758054289 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173104 | GCTCATTTAGTCTTC[C/T]TGGTTTACTTCCCCC | 79931 |
rs758110548 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202235 | AGACCAAGGGAACAG[A/C]ATAGAGAACCCAGCA | 79931 |
rs758119891 | in-del | -/A | 0.000325362 | 0.0127505 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227348 | CCTGGTAAGTAAGCG[-/A]AATGAAAGTAAAGGC | 79931 |
rs758236005 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163107 | TTGTAACTGCACGAG[A/T]ACTAGTTTTTGAAAT | 79931 |
rs758240149 | in-del | -/G | 3.43802e-05 | 0.00414595 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141932 | GAGGAGAACAAAACT[-/G]TGGGGTCACTACCAG | 79931 |
rs758260672 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136186 | ATAGTACCGTGCCTT[C/T]TACTTGTGATATTCT | 79931 |
rs758298685 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135948 | GCTAGTAAAGGAGGC[A/G]TAGGAATCCCAAACA | 79931 |
rs758399236 | in-del | -/TGGGCTCAAGCAATTCCCCTCCCTCAGGATCCTGAGTAGCTGGGACTCC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121218740 | ATAGTTCTGAACTCT[lengthTooLong]TGGGCTCAAGCAATT | 79931 |
rs758424078 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222371 | CGCTTTTTCAAACGT[A/G]TATTGGAAGGATGAT | 79931 |
rs758444834 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137308 | AGATTTTAAAATTGC[A/T]TATATTATGCAACAC | 79931 |
rs758458598 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169584 | GCCATTTTAGTGCCT[A/G]TGCGTGTTCATGTGG | 79931 |
rs758489234 | snp | A/G | 9.89495e-05 | 0.00703313 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121147052 | TTTGACTTGTACCTG[A/G]GAATTCAGCCTGTTC | 79931 |
rs758526185 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214252 | TTCCTTCTGCACTTC[C/T]GGGTATATACACCCT | 79931 |
rs758576364 | snp | C/T | 8.80359e-05 | 0.00663402 | missense | TNIP3 | GRCh38.p7 | 4:121161198 | TCATCAAGTTCTTTC[C/T]TGTTGATGGTTCAGC | 79931 |
rs758580712 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157872 | TCTCTCTGGGATCAT[A/C]ATCTTTAACATTTAC | 79931 |
rs758603601 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193051 | ATATATGTAGAACTA[A/C]CCTATACATAATAAC | 79931 |
rs758662315 | snp | C/T | 1.67122e-05 | 0.00289064 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132688 | CAGTAGGAAAATGTT[C/T]TAGATTAAAAATTAA | 79931 |
rs758705686 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144364 | ACCTCTGAGCCATGA[C/T]TTGACTTGAGCTAAA | 79931 |
rs758737202 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146096 | AGGTTGCCTGAATTA[C/T]TTTCATAAAATTATT | 79931 |
rs758774301 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159143 | AGCTACTGGGGAGGC[C/T]GAGGCAGGAGAATCA | 79931 |
rs758801761 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121145643 | ATATAATTTATCATA[C/T]AAAAATAAATTATTA | 79931 |
rs758806764 | in-del | -/TTG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191093 | TTGTTTTTGTTTTTG[-/TTG]TTGTTGTTGTTATTT | 79931 |
rs758828086 | snp | A/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132096 | CCTCTTCAATTCTAC[A/G]TTTAGGATCACTGAG | 79931 |
rs758843244 | in-del | -/ACAT | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132250 | CACACACACACACAC[-/ACAT]ATGCACTTTAAATCA | 79931 |
rs758891198 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175402 | ATTAACATTTATAAT[C/T]TCCACACAGATGCCA | 79931 |
rs758893415 | snp | C/T | 1.65045e-05 | 0.00287263 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138579 | CCCAAAAGATCCCAT[C/T]AAGATGTAAACATGA | 79931 |
rs758927553 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133648 | TTTTAGATGGAGAGA[C/G]GCTGTGGCCAATGAG | 79931 |
rs758950178 | snp | A/G | 8.3071e-05 | 0.00644427 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158797 | AAAGAATTTCTGCCC[A/G]TTTGGAAGTTTGGTC | 79931 |
rs758969010 | in-del | -/AG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205409 | AACCAGAAAGGTAAA[-/AG]AGAGCCAGTTCAAGG | 79931 |
rs758981548 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134716 | ACTGGAAGTCTGTGC[A/G]CCATGGTACTCAGCA | 79931 |
rs758983220 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164402 | TGTCTCAAATAGGCA[A/G]GCCGTGACTAAGACC | 79931 |
rs759020225 | snp | C/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228733 | ATTCCATTGTTTCAA[C/G]GTCCTCTAAAGCATT | 79931 |
rs759039870 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207955 | TGGTTTCCCCCATAC[C/T]GCTCTTGTGGTAGTA | 79931 |
rs759069002 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188543 | ATGTTGTTGAATGTC[A/C]TTGTTTAATGAGCTC | 79931 |
rs759072862 | snp | A/C | 1.66377e-05 | 0.00288419 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147004 | TTTTTAAATGAAAAA[A/C]ATATACATACATGCT | 79931 |
rs759076322 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176888 | GTCTAGAACTTGTCC[C/G]CAGCCACTGGGAGTT | 79931 |
rs759106492 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135498 | GGCCTCCTGGGCTCA[A/T]GTGATCCTCCTACCT | 79931 |
rs759129869 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195094 | AATTGCTTGAACCCC[A/G]GAAGCAGAGGTTGCA | 79931 |
rs759236681 | snp | G/T | 1.65356e-05 | 0.00287533 | missense, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121132652 | ATGGACTTTCTTTAC[G/T]GAGGATAAACCTATG | 79931 |
rs759288422 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227297 | TTAATATGAGAACTT[C/T]ATGCATTTTAAAAAA | 79931 |
rs759290736 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168030 | CTCCAGATCAAAAAT[C/T]TTGGAGTCATCCTTG | 79931 |
rs759333088 | snp | A/G/T | 0.000101805 | 0.00713399 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150271 | TTACCACATGGAATG[A/G/T]ATTCTTTTATAATTG | 79931 |
rs759349004 | snp | C/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229263 | GAATTCTAGTCCAGC[C/T]TGGGCAACATAGTGA | 79931 |
rs759367528 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143711 | ATTTGTGTCAATGGA[A/T]CAATACATAACTTTG | 79931 |
rs759385397 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227574 | TCATTCTGCTGCCAA[C/G]AGACTATTAATATTC | 79931 |
rs759431051 | in-del | -/TAAT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220478 | TTTAGGTTTTTATGA[-/TAAT]TAACTACTTTTTTTT | 79931 |
rs759436890 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216292 | TTCCTTTTCTATTCT[A/G]TATAGCTCCATTCAG | 79931 |
rs759442373 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142545 | TGCTTTCTATGAGTG[G/T]TAGGGTTGAAAGGCC | 79931 |
rs759498441 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194966 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGTCA | 79931 |
rs759505106 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173555 | GAAATTAGCTGCTGA[C/T]CATTTTATAGCAATG | 79931 |
rs759505252 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215349 | ATTTCTTGAAATTAT[C/G]TTTCACTTGAAAGGT | 79931 |
rs759557052 | snp | A/G | 0.00018596 | 0.00964082 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137960 | CAGTTTATACAGCCC[A/G]CTTCTGGGTGGCCTC | 79931 |
rs759600460 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161392 | CATGGCTGGTGGATG[A/G]GTCAGCTTCATATTA | 79931 |
rs759602781 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149479 | TGTTCTTAAAATAAA[C/T]CACGTGGCTGGGTGC | 79931 |
rs759709257 | snp | A/T | 1.64988e-05 | 0.00287213 | missense | TNIP3 | GRCh38.p7 | 4:121150155 | TCATGGCAGAATTCC[A/T]CTCGAGACTTCCTCA | 79931 |
rs759730395 | snp | C/T | | | missense | TNIP3 | GRCh38.p7 | 4:121164079 | TTATGCTCCGTAGAA[C/T]TTTCTGCGGCAATCA | 79931 |
rs759774016 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190546 | AGCCTCAGTAAATCC[A/T]ATTCTGGGAAAAGGG | 79931 |
rs759780252 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152132 | CTGACATATTACAAA[-/T]TTTTTTCTGAGTGAA | 79931 |
rs759811870 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180123 | TATAGATGTCGGGCT[C/G]GGCGCGGTGGCTCAC | 79931 |
rs759865794 | snp | A/C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191852 | AATATTTGAAAGGAC[A/C/T]TTTTTCTTTAAGACA | 79931 |
rs759876935 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224462 | CCACACTTTGGCTTT[C/T]ACCTGTAAAGCTCAA | 79931 |
rs759886904 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198517 | GGGCCAGATGCATTT[C/T]TTAGTGGTGAGCATA | 79931 |
rs759892767 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197885 | GGTATAGATTCACTA[C/T]TATTCAAGTGTTTTG | 79931 |
rs759921362 | snp | G/T | 1.64841e-05 | 0.00287085 | missense | TNIP3 | GRCh38.p7 | 4:121157139 | GTCGCGCTGCCTGTC[G/T]TCCTCTCTCTGCCTG | 79931 |
rs759924481 | snp | C/T | 0.000134172 | 0.0081895 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157089 | AGGACCCGGGCCCCG[C/T]CCACCTCCTCCCGCT | 79931 |
rs759928957 | in-del | -/CTGCCTGTCGTCCTCTCT | 0.000115953 | 0.00761333 | cds-indel | TNIP3 | GRCh38.p7 | 4:121157130 | CCGGGTCAGGTCGCG[-/CTGCCTGTCGTCCTCTCT]CTGCCTGTCGTCCTT | 79931 |
rs759948051 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211241 | AGCAGAATATTTAGA[A/G]TATGAAGTGACAGCT | 79931 |
rs760018569 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212468 | AAACCCAATGTGACT[C/T]TGATGTTTATTAGTT | 79931 |
rs760035348 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139817 | TTTTAGATGTCTCAA[A/G]TAACACATAGGATAA | 79931 |
rs760059000 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159070 | CAACATGGTGACATC[C/T]CGTCTCTACTAAAAA | 79931 |
rs760207734 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219016 | ACCAGCCTGACCAAA[A/G]TGGAGAAATGGTGTC | 79931 |
rs760268325 | snp | A/C | 1.65616e-05 | 0.00287759 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164024 | TGCCATCAATGCTAG[A/C]TGTGATCAACTCATC | 79931 |
rs760288497 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133343 | TGCTAAACTAACATT[C/T]TGGTAACAGAAAAAG | 79931 |
rs760317552 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187204 | ACAAACAAACAAAAA[A/G]AACACCCTACCAAAC | 79931 |
rs760418796 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206628 | ATCACAGCTCACTAG[-/C]CTCAGCCTTCCAGAC | 79931 |
rs760451255 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121138647 | TTGTGTTGTACATCT[A/G]GCGGAAGCTGGTCAA | 79931 |
rs760455594 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207747 | TAACCTCCAAGCTGA[A/C]CTTATTCACTCCTGG | 79931 |
rs760464288 | snp | A/G | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166434 | CTCACATTGTGCCAC[A/G]TATTTTAAGAGTCTG | 79931 |
rs760469481 | snp | A/T | 0.000559232 | 0.0167124 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138013 | TAGAAAGTATAGCAG[A/T]TTCTAGAAAGAAAAC | 79931 |
rs760469791 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204653 | GTCACTACAATCAAT[A/G]CACAATAGAAATACC | 79931 |
rs760478595 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135209 | TATCAAGGTAGGAGG[A/G]TAGATTATACTTTAA | 79931 |
rs760512934 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151045 | CATTACATTATGTTT[-/G]GTAATATCATATGAA | 79931 |
rs760521996 | in-del | -/TT/TTT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222806 | TGTTTTTTGTGCGTT[-/TT/TTT]TTTTTTTTTTTTTTT | 79931 |
rs760611462 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182631 | CTTGATGAATAAACT[A/G]CTGAAGGGTACATCG | 79931 |
rs760648592 | in-del | -/TAT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176514 | TCATCCTACTAGCAT[-/TAT]GATGATGATGATGAT | 79931 |
rs760659481 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172915 | AGAAAATTACTATTT[C/T]GTACTAAGGAGCTAT | 79931 |
rs760722956 | snp | C/T | 6.60088e-05 | 0.00574457 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154481 | GCCTAGATTTTGTTG[C/T]GACTGTCAGTAAGAA | 79931 |
rs760735824 | snp | A/G | 0.00016749 | 0.0091497 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216376 | CTAATTAGAATATTA[A/G]TATTAGAAGCATATA | 79931 |
rs760738536 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227476 | ACTCTTTGAATCAAA[C/T]AGTAACTAAGTGGTT | 79931 |
rs760784220 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184386 | ACAGCCATGTTTCCA[C/T]TGATATGACTTGAAC | 79931 |
rs760793802 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199328 | TAAGCTTCAAGATAT[A/C]CTATAAAGCTAGTTG | 79931 |
rs760826585 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215070 | GTGAATGGGAGAAAT[A/C]AATATTTCTATATTT | 79931 |
rs760886178 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201772 | TATATATCAAGAATC[C/T]GCTATGTATCAGTAC | 79931 |
rs760915937 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190171 | CAGATTAAAACAGAA[C/T]ATAGAGCTTTTGAAA | 79931 |
rs760957228 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176277 | TGACAGGCTCCTCAC[C/T]GCCTGAGAACATGCA | 79931 |
rs760968184 | in-del | -/A | 1.65729e-05 | 0.00287857 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158782 | ATTTGGTGAATCAAC[-/A]AAGAATTTCTGCCCA | 79931 |
rs760974182 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189056 | AATTACATTCAATAG[C/G]AAAAACACATAACCA | 79931 |
rs761006069 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136553 | AGATTGAAATAATGC[C/T]TTAAAAACAGGCCGG | 79931 |
rs761029912 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167573 | GTATTTTCAAAGTTT[-/A]TTTGGATGAAATCAT | 79931 |
rs761047123 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209882 | GGTATATTTCTTACT[A/G]TAAAAAACTAGTTGG | 79931 |
rs761057926 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149335 | AAACCTGGTTTCAGT[C/G]ATTATAATAAGTACA | 79931 |
rs761071685 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189443 | AGTGTTGTGTAAAAG[A/T]TGCTAATCAAGCAGC | 79931 |
rs761079455 | snp | A/G | 1.70321e-05 | 0.00291818 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141919 | GGGCAATACATCTGA[A/G]GAGAACAAAACTGTG | 79931 |
rs761092997 | snp | C/T | 3.34924e-05 | 0.00409208 | missense | TNIP3 | GRCh38.p7 | 4:121157146 | TGCCTGTCGTCCTCT[C/T]TCTGCCTGTCGTCCT | 79931 |
rs761203497 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169267 | TGGCCACACCGTTGC[C/G]CCTTGAACTTGTTCT | 79931 |
rs761214407 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138871 | TCTCTCCCTACCCCC[G/T]CTTAAATCCACTCTG | 79931 |
rs761256470 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169931 | TTAGGGCACATCAGA[C/T]ACATTAGAAGGCAAA | 79931 |
rs761296243 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211206 | TGATTTAAATAATTA[C/T]GATCCAATTTAACTA | 79931 |
rs761300566 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158787 | GTGAATCAACAAAGA[A/T]TTTCTGCCCATTTGG | 79931 |
rs761374270 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175004 | GGGTTGAGATGTCCC[G/T]AGGAGACATCCACAT | 79931 |
rs761410047 | snp | A/C | 1.6604e-05 | 0.00288127 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150091 | AGGATCATGCCACTT[A/C]CAGCTTCTCACCTGC | 79931 |
rs761482335 | snp | C/T | 1.65507e-05 | 0.00287664 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164036 | TAGATGTGATCAACT[C/T]ATCTCCTAGAAATAT | 79931 |
rs761501264 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185230 | TTTTCTTCCAGACAC[A/G]TTTGCATCGTCAAAC | 79931 |
rs761501474 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199410 | GAAAACAATATTACT[A/G]TGTTTCTAGCCCAGA | 79931 |
rs761545094 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161689 | TAAACGTCAGAGGAA[C/T]GACAAAATCATCGAG | 79931 |
rs761586007 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204816 | CAATAATTTTCATTT[A/C]TATCAGCTATGTGTA | 79931 |
rs761616912 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185798 | GGTATTGCCCTCATG[A/G]CTGCCTTGTTCTTTT | 79931 |
rs761653934 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175862 | TGTGTTAGGATCCAA[C/T]TTTAGTTCACAGACC | 79931 |
rs761779040 | snp | C/T | 0.000191957 | 0.00979498 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138058 | CAATAAAAAATAAGA[C/T]TTAAAAAAGTACTCT | 79931 |
rs761793138 | snp | C/T | | | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121182477 | AAAGTGCCAGCAAAT[C/T]CTTCTGCTGAAGAAT | 79931 |
rs761801491 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202133 | AAGAATGAATCTGGA[C/G]GCATCACAATACCCA | 79931 |
rs761816740 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154346 | TGATGAATCTTTGTA[A/G]GGACAAAAATTCTCT | 79931 |
rs761864588 | snp | A/T | 3.29544e-05 | 0.00405908 | missense | TNIP3 | GRCh38.p7 | 4:121154580 | TTATTTCACATTCGT[A/T]ATGTTCCTTTTCCTT | 79931 |
rs761922784 | in-del | -/A/AA | 0.184318 | 0.241275 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161221 | GTTCAGCACACTTAG[-/A/AA]AAAAAAAAAAAGAGA | 79931 |
rs761927698 | snp | C/T | 4.03722e-05 | 0.00449272 | missense | TNIP3 | GRCh38.p7 | 4:121154675 | TTTAGGCGTTCCTTT[C/T]CCTTCTGAAGTTAAG | 79931 |
rs761932628 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179035 | TAGAGAGGGTGAAAA[G/T]GTTTCAAAACCAGAA | 79931 |
rs761966644 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226422 | TTTGTTAACGTTGAT[C/G]CATTCCACAAATATT | 79931 |
rs761984077 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176356 | ACAGATCCTCACACA[A/G]CAATGCAACTTTTTT | 79931 |
rs761984366 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222189 | TGAAATATTAGTGAA[-/T]TTTCTTCCCCTGCGA | 79931 |
rs761991464 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214772 | CAGTATAATAACTTC[A/G]TCCTTAAATGACTCC | 79931 |
rs762049621 | in-del | -/AC | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132221 | CCAGGAAACACACAC[-/AC]ACACACACACACACA | 79931 |
rs762058512 | snp | A/C | 1.64803e-05 | 0.00287052 | intron-variant, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121138652 | TTGTACATCTGGCGG[A/C]AGCTGGTCAAGAGCA | 79931 |
rs762083622 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201645 | GAAGAGCCCTGGACC[G/T]GGAATCAGAAGAGTT | 79931 |
rs762092140 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155930 | AATAGAATGAACATA[C/T]ACACTTAGAAAATAA | 79931 |
rs762146931 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148055 | GATGATTTTTTTGGT[A/T]GAGAACTGACATTCA | 79931 |
rs762153592 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160425 | CAGAGGCTGCAGTGA[G/T]CTGAGATCGTGCCAC | 79931 |
rs762156471 | snp | C/T | 5.41981e-05 | 0.00520539 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142828 | AGTTAAAATCATTAA[C/T]TCCCAAGCCACTCTT | 79931 |
rs762166640 | snp | C/G | 1.65192e-05 | 0.00287391 | missense | TNIP3 | GRCh38.p7 | 4:121142726 | ATTAGATCAACATAC[C/G]TGTTTTAATTGCTTT | 79931 |
rs762201854 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169910 | TTGATTATATACTTT[C/T]AGTTTTTAGGGCACA | 79931 |
rs762208197 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135690 | AGGCATGAGCCACCA[C/T]TCCTGGCCTTAAACT | 79931 |
rs762208434 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161292 | CTGTTCCTCAGAAAC[C/T]CCATGCATTTGGCCA | 79931 |
rs762252742 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188821 | GAATAAAACCTTGGA[C/T]ATGGGTTCATTTTGT | 79931 |
rs762423714 | in-del | -/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166620 | CAAAGGGAAATGTGG[-/T]AAAGGAACAAGGACT | 79931 |
rs762449385 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196508 | TGTAATAGAAATCAT[A/G]ACAATTAAATGTGAA | 79931 |
rs762473623 | in-del | -/TTTTT | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168522 | TTTTCTTTTCTTTGC[-/TTTTT]TTTTTTTTTTAAGAG | 79931 |
rs762531243 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157320 | TTATTCCCAGGCTAT[A/G]AACTTTGGCAGAAAC | 79931 |
rs762534280 | snp | A/C | 3.30557e-05 | 0.00406531 | utr-variant-3-prime, missense | TNIP3 | GRCh38.p7 | 4:121132641 | TACTTCTACGGATGG[A/C]CTTTCTTTACTGAGG | 79931 |
rs762540877 | snp | A/G | 1.71293e-05 | 0.00292649 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141928 | ATCTGAGGAGAACAA[A/G]ACTGTGGGGTCACTA | 79931 |
rs762540984 | snp | A/G | 1.6566e-05 | 0.00287797 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157271 | TTCAAAGACAGCTGC[A/G]GATACCTTCTCTGAA | 79931 |
rs762541647 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209437 | TTCTGGTAGTGTCAA[C/T]ACCAAATTGAATTAT | 79931 |
rs762564234 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208505 | CACTACCCATGTCCC[A/G]ATCCCCTACTCATCA | 79931 |
rs762633610 | snp | C/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229324 | GGCAGGGTGCGGTGG[C/T]TCACGCCTGTAATCC | 79931 |
rs762720591 | snp | A/C | 1.65037e-05 | 0.00287256 | missense | TNIP3 | GRCh38.p7 | 4:121164113 | TAGATGTGCCCTGTA[A/C]AAAATGTGCCATGGA | 79931 |
rs762727975 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173637 | CATTCATGTATGCAC[C/T]TTTTTCTTTGAGATG | 79931 |
rs762730918 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217224 | TTAAAAGCCAATTCC[C/T]GCAGGCAATTAACAC | 79931 |
rs762740095 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220888 | AATACGTTCAGTCAA[-/G]AGTGGGAAAATGCCT | 79931 |
rs762753138 | snp | A/G | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166578 | AGTCACTAAAATATT[A/G]TACAGAGGAAAGAAA | 79931 |
rs762766395 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143833 | AATGAAGCTTCTCTA[A/G]CACACTTTTTCTCTA | 79931 |
rs762781382 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185035 | AACCAGACTTGCCTG[A/C]CAAGATGTCACAAGA | 79931 |
rs762783003 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174815 | TTTTTATTACATTTC[A/T]TCTAGAAGGTGGACA | 79931 |
rs762785966 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224229 | TTAGCTGAATGTGGT[C/G]GTGGGCGCCTGTAAT | 79931 |
rs762795651 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216357 | GCCACAAAGCAGAAG[C/T]GCTCTAATTAGAATA | 79931 |
rs762819132 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204726 | AATAGATTTACCAAC[A/G]TTAGATTGTTGGGTC | 79931 |
rs762878225 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203232 | ATAGATAGATAGATA[A/G]ATAGATAGATAGATA | 79931 |
rs762884922 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159071 | AACATGGTGACATCC[C/T]GTCTCTACTAAAAAT | 79931 |
rs762906082 | snp | A/G | | | missense | TNIP3 | GRCh38.p7 | 4:121164103 | GCAATCATTCTAGAT[A/G]TGCCCTGTACAAAAT | 79931 |
rs762906174 | snp | A/G | | | missense | TNIP3 | GRCh38.p7 | 4:121141859 | CCAGGGCCTGTTGGT[A/G]CCCATGGATCTTGCA | 79931 |
rs762911703 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188281 | TTATCAATAGGATAG[C/T]AGGTTTCACCAATTT | 79931 |
rs762956921 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121132847 | AGGGTTATTATTTTA[A/G]GCATTGACATATGCT | 79931 |
rs762986376 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222947 | AGTAGCTGGGACTAC[A/C]GGCGCCCACCACCAC | 79931 |
rs763007927 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138985 | GAAGTATAAACACTT[C/G]TAAAACTTACTACAG | 79931 |
rs763123634 | in-del | -/AAAA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161222 | GTTCAGCACACTTAG[-/AAAA]AAAAAAAGAGAGAAG | 79931 |
rs763125863 | snp | C/T | 3.29636e-05 | 0.00405964 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121138668 | AGCTGGTCAAGAGCA[C/T]ACCACTGATAGTCTG | 79931 |
rs763173843 | snp | C/T | 1.65293e-05 | 0.00287479 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164051 | CATCTCCTAGAAATA[C/T]GTTCTTACCTCTTTA | 79931 |
rs763210570 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140010 | TCTACTGTTATGCTG[A/G]GATTTTTTTCATCTG | 79931 |
rs763213986 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193179 | AAAAAGATTGGGACA[C/T]GCTATCAGAGATGAG | 79931 |
rs763257272 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171399 | GTGAACAAGTAGAGT[-/A]AAATGTTCATGTTCA | 79931 |
rs763268226 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182348 | ATCTTGGTAACCCAA[A/T]TTAAATGGGTTACTT | 79931 |
rs763298154 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213937 | GAAATATAAAAACTA[A/T]AAAACATCATGTTTA | 79931 |
rs763306994 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186319 | CAGGAATCCAGCTGG[A/G]AACTGAAAGCACACA | 79931 |
rs763391398 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200610 | TGTCTTTTCCTATGA[C/T]AGAACAATCTAGTTC | 79931 |
rs763422021 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148284 | TGCCTGATTAGAAAC[A/G]TGCACAGTTAAAATA | 79931 |
rs763458927 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135127 | TCTCCCTGTGCCACC[A/G]TGTCCTGTCACAGAC | 79931 |
rs763486675 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156241 | TGCCTCACGATATCA[G/T]TGATAAGATTTCCCC | 79931 |
rs763508335 | snp | A/C | 1.65154e-05 | 0.00287358 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154700 | GTTAAGACCAAGAAA[A/C]GAAAATAAAAGTCAG | 79931 |
rs763543493 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187352 | TCCAATGATCTCTGC[C/T]CTGGGCCCTACCTCT | 79931 |
rs763640662 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209523 | GAAAAAAGATGTCAC[A/G]CTGGGTATAATGGAT | 79931 |
rs763641974 | snp | C/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227746 | AGGAAATCTACCTGC[C/T]CACTTAATGGAAAAG | 79931 |
rs763730182 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142895 | CCAACAAAAATAGCC[A/G]CAAGTTGGTTTTTGC | 79931 |
rs763736712 | snp | A/G | 0.000115413 | 0.00759562 | missense | TNIP3 | GRCh38.p7 | 4:121147137 | AGTCTCTCTCGATCC[A/G]ATCGTTCCTTTTTGA | 79931 |
rs763759857 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157326 | CCAGGCTATGAACTT[C/T]GGCAGAAACGCCCCA | 79931 |
rs763790356 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182856 | AAAAATTATTCAGGC[A/G]TAGAGTGAGTTTATG | 79931 |
rs763790753 | snp | C/T | 5.57958e-05 | 0.00528155 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154716 | GAAAATAAAAGTCAG[C/T]ACAAGTCAAATGAGA | 79931 |
rs763797761 | snp | A/G | 1.65718e-05 | 0.00287848 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142705 | GGAATAAATGTATGC[A/G]TGAAAATTAGATCAA | 79931 |
rs763823619 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203250 | AGATAGATAGATAGA[C/T]AGATAGATAGAAAGA | 79931 |
rs763844294 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180858 | CCAATAGTCATTTCA[C/T]ATCTTCCCCAATTCC | 79931 |
rs763847537 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143853 | CTTTTTCTCTATAAG[A/G]CACATCACATCCTTC | 79931 |
rs763941496 | snp | C/T | 3.5483e-05 | 0.00421192 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158652 | CACCAGGATAATGGC[C/T]TTAAAGAAAATACCG | 79931 |
rs763980272 | snp | A/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131703 | GCAGTGGCGATCTCA[A/G]CTTACAGCAACCTCT | 79931 |
rs764052026 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224368 | CTCTGTCTCAAAAAA[-/T]TAAAAAGAAAAAAGA | 79931 |
rs764073317 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151343 | TAATATGGTCATAAA[G/T]GTAGGAAAAGAAAAG | 79931 |
rs764141861 | snp | A/G | 4.47317e-05 | 0.00472904 | missense | TNIP3 | GRCh38.p7 | 4:121161176 | CTTATCTTTTGTTCA[A/G]GAGAATTCATCAAGT | 79931 |
rs764153082 | snp | C/T | | | missense | TNIP3 | GRCh38.p7 | 4:121154582 | ATTTCACATTCGTAA[C/T]GTTCCTTTTCCTTGT | 79931 |
rs764154427 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191982 | ATTTAGATACCATAT[A/G]TTTAAGAGCTGTCTA | 79931 |
rs764161438 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170327 | GTCCGTTTATGTATG[A/C]ATCTATAGTACAAAA | 79931 |
rs764171220 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140214 | TGGTGTGTGCCTGTA[C/G]TCCCAGCCAGTCGGG | 79931 |
rs764193327 | snp | A/C | 1.64982e-05 | 0.00287208 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154484 | TAGATTTTGTTGCGA[A/C]TGTCAGTAAGAATGT | 79931 |
rs764235001 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | TNIP3 | GRCh38.p7 | 4:121154577 | GTTTTATTTCACATT[C/T]GTAATGTTCCTTTTC | 79931 |
rs764237958 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174066 | AATATAAAATCTCAA[A/C]ATTAGAGGGGACCAC | 79931 |
rs764269837 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212847 | TTAAAAATAAAGAGG[A/C]CAAAAGAATTGTAAG | 79931 |
rs764285660 | in-del | -/AA | 0.000223264 | 0.0105632 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161222 | GTTCAGCACACTTAG[-/AA]AAAAAAAAAGAGAGA | 79931 |
rs764287993 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159191 | GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCACTG | 79931 |
rs764298440 | snp | A/G | 0.000187459 | 0.00967958 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138023 | AGCAGATTCTAGAAA[A/G]AAAACAGAAAATGTT | 79931 |
rs764314812 | snp | A/G | 4.98095e-05 | 0.00499022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132669 | AGGATAAACCTATGG[A/G]AAACAGTAGGAAAAT | 79931 |
rs764350450 | snp | A/G | | | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121182450 | CACAGCTGCCTGGAC[A/G]CTTTAAAGTGGAAAG | 79931 |
rs764355721 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199840 | GTAGGTACCTGAGGA[C/T]GGTTGTGTAGGTTGC | 79931 |
rs764455591 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187419 | TCAGTGAGGCTAAGC[A/G]GTGAGGCTAGACACC | 79931 |
rs764473068 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171183 | AACAGCCCCTGTTTG[A/G]CCTTTGCATTTCAAA | 79931 |
rs764496095 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160299 | GGCTGGCCAAAATGG[C/T]GAAACCCCATCTCTA | 79931 |
rs764519008 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147981 | CACATATTACATTTT[G/T]AAGGCTTTATTCACC | 79931 |
rs764520371 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186332 | GGGAACTGAAAGCAC[A/G]CAGGAGGGGTGGAGC | 79931 |
rs764538785 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155750 | CCCAGTAAAATAAAT[A/G]TTGCAGAAAATAGGT | 79931 |
rs764620592 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146955 | TTAAAAAAAAATTCA[A/G]TGTCAATTAACAGAA | 79931 |
rs764638949 | snp | A/C | 0.00116599 | 0.0241171 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216384 | AATATTAGTATTAGA[A/C]GCATATAATCTCCAA | 79931 |
rs764689682 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219321 | TTTTGATTACTTCTC[C/T]TTTTTCCTCCCTCCT | 79931 |
rs764856539 | snp | G/T | 5.0358e-05 | 0.00501761 | missense | TNIP3 | GRCh38.p7 | 4:121157149 | CTGTCGTCCTCTCTC[G/T]GCCTGTCGTCCTTTC | 79931 |
rs764859312 | snp | A/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166733 | TAAGTTATTGGAGGC[A/T]TTCTTTGGCAGGTAA | 79931 |
rs764861951 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196433 | GACGAATATAATATT[G/T]GGCTCTAAAGAGCTA | 79931 |
rs764882509 | in-del | -/GGACCAT | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183828 | CATCACCCCCAGATG[-/GGACCAT]CTAGTTGCAGAAAAA | 79931 |
rs764914474 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154733 | CAAGTCAAATGAGAT[A/G]ATATTGTAGGAATTC | 79931 |
rs764925620 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227073 | AATAGGGTAACATTC[A/C]CTTAGTTAAATGTGT | 79931 |
rs765025494 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184465 | AGTTTGGCCAGTGGG[A/G]TTCTCCTCTGTGTCT | 79931 |
rs765032237 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196877 | TTAGAGATACATACT[-/G]TTTTATATTTTATTT | 79931 |
rs765040751 | snp | C/T | 1.65496e-05 | 0.00287655 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164038 | GATGTGATCAACTCA[C/T]CTCCTAGAAATATGT | 79931 |
rs765041631 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173076 | ACAAGTGGGTGGCTG[A/C]ACCCATATCAGAGCT | 79931 |
rs765086922 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220881 | AAAGAGCAATACGTT[C/T]AGTCAAGAGTGGGAA | 79931 |
rs765096685 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173576 | TATAGCAATGCAGAT[C/T]ACTCTGTTTTTCTCT | 79931 |
rs765158269 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139262 | TATAGTTTAGTCTAC[A/G]GAGACAAGATTTTTC | 79931 |
rs765207491 | snp | C/T | 3.30017e-05 | 0.00406199 | missense | TNIP3 | GRCh38.p7 | 4:121164089 | TAGAACTTTCTGCGG[C/T]AATCATTCTAGATGT | 79931 |
rs765211296 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136031 | CTCTTCTCTGCTGCT[A/G]GCCAGCCATAGTTAG | 79931 |
rs765235131 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202023 | AATTCAAATCAAAAT[A/G]CTACCATCATTTTTC | 79931 |
rs765319192 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203128 | AGATACTTGTAGAAG[A/C]ATGTTTATAGCAGCA | 79931 |
rs765321247 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189185 | ATAAGAATTTAGGAT[A/G]TTAGTGTTCTTTCTT | 79931 |
rs765347506 | in-del | -/TCTG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143252 | ACTAAGACATAAGAT[-/TCTG]TCTGAGTAACTTGTT | 79931 |
rs765354854 | snp | A/C/T | 8.77626e-05 | 0.00662382 | synonymous-codon, missense | TNIP3 | GRCh38.p7 | 4:121161196 | ATTCATCAAGTTCTT[A/C/T]CTTGTTGATGGTTCA | 79931 |
rs765404045 | snp | A/G | 1.64806e-05 | 0.00287054 | intron-variant, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121138661 | TGGCGGAAGCTGGTC[A/G]AGAGCATACCACTGA | 79931 |
rs765409176 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190625 | CTGCTATAAGCCATA[A/G]AATGTCAATGTCAGT | 79931 |
rs765447924 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169483 | TTCTTCTTTTTGTTG[A/T]TTGCCTCCCGACACT | 79931 |
rs765507612 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137047 | TTGCATATTCTATTT[A/G]GTTTCTGAATGTCAT | 79931 |
rs765563606 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157714 | GCCAAATCACTCTGA[C/T]GACAGAGTGACAGGT | 79931 |
rs765565778 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180781 | TTTCAAACTCAACTC[A/G]GTCCTCACTACTACT | 79931 |
rs765612268 | in-del | -/TGTG | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165660 | AACTTTTTGCTAGTT[-/TGTG]TGTGTGTGTGTGTGT | 79931 |
rs765618412 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212519 | AAAACTAACAAATTT[C/G]AATTGCAAATAAATT | 79931 |
rs765647849 | snp | A/G | 0.000162377 | 0.00900901 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121216459 | CATTACCAGTTTATC[A/G]TCGTGTTTCTCATTT | 79931 |
rs765649530 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228608 | AATAATCTATTATAT[A/G]ATGTAGCTTGCATAT | 79931 |
rs765707157 | snp | C/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132140 | AGTCAAATAGCTAAA[C/G]AACTAAGGCCCTGTG | 79931 |
rs765752281 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185521 | AGGAAAGAGGAAAGG[C/T]CTTTGTCTGTGTTTA | 79931 |
rs765762945 | snp | C/T | 3.3305e-05 | 0.00408061 | missense | TNIP3 | GRCh38.p7 | 4:121157164 | TGCCTGTCGTCCTTT[C/T]TCTGCCTCTGATGCG | 79931 |
rs765796698 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228151 | AAGACATTTGTACCA[A/G]TTTGGGAATAAAATG | 79931 |
rs765801919 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133436 | CACTATGTTAAAAAG[A/G]TATCTAATATGTTGA | 79931 |
rs765843383 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146771 | ACTCTCATTCTACCA[A/G]GATAAATATTATGAG | 79931 |
rs765850548 | in-del | -/ATAGATAA/ATAT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203240 | TAGATAGATAGATAG[-/ATAGATAA/ATAT]ATAGATAGATAGATA | 79931 |
rs765883190 | snp | A/G/T | 5.00132e-05 | 0.00500045 | synonymous-codon, missense | TNIP3 | GRCh38.p7 | 4:121157102 | CGCCCACCTCCTCCC[A/G/T]CTGCAGCCGGTCCCG | 79931 |
rs765897295 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205115 | AGAAATATAGAGCAA[C/T]GTAAGTGGAATCAGG | 79931 |
rs766007445 | snp | G/T | 1.65157e-05 | 0.0028736 | missense | TNIP3 | GRCh38.p7 | 4:121142728 | TAGATCAACATACCT[G/T]TTTTAATTGCTTTTC | 79931 |
rs766008297 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134584 | TGACTTGAAAACATT[C/T]GAAACCCTTCATTTA | 79931 |
rs766009783 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162343 | CTTCTTCCTATTTAG[A/G]CCTATGTTACAATTA | 79931 |
rs766057452 | snp | A/G | | | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121154596 | ATGTTCCTTTTCCTT[A/G]TTCGCAAGAGTATTT | 79931 |
rs766063191 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165411 | CATCCAACCTTATGA[C/T]GGGGAAAACCTAAGT | 79931 |
rs766066173 | snp | A/C/T | 6.63585e-05 | 0.00575982 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157283 | TGCAGATACCTTCTC[A/C/T]GAAGCTCACAAGCCC | 79931 |
rs766077090 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194081 | TTGGCAAAACCTGAA[G/T]GGAGTTTGAGGATTA | 79931 |
rs766112707 | snp | A/G | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166619 | ACAAAGGGAAATGTG[A/G]TAAAGGAACAAGGAC | 79931 |
rs766117299 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153685 | TATGCAGGCACATAC[G/T]TAATACTTTGAGGAT | 79931 |
rs766159759 | snp | A/C | 3.30557e-05 | 0.00406531 | utr-variant-3-prime, missense | TNIP3 | GRCh38.p7 | 4:121132642 | ACTTCTACGGATGGA[A/C]TTTCTTTACTGAGGA | 79931 |
rs766166938 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194944 | AAGCCAAGGTGGGCG[C/G]ATCACCTGAGGTCAG | 79931 |
rs766168756 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176417 | TTCCACAGCTACAAC[C/T]TTTGAAATTAGATAA | 79931 |
rs766171767 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171760 | TTTTGAGATGGAGTC[C/T]CACACTGTCACCCAG | 79931 |
rs766180075 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141532 | TACAGAAAATGTCCT[C/T]TGGGTAGAATGAAGT | 79931 |
rs766193857 | snp | C/T | | | missense, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121182686 | CTTACCTTCAGAGAA[C/T]ATAGATTTCTGTGAG | 79931 |
rs766195233 | snp | C/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166473 | TCAAGCTTTGTTTCA[C/T]GAGAAGTATCACTAG | 79931 |
rs766215811 | snp | A/C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139933 | ACTTAATTCAGCCTT[A/C/T]GATATAGACAAGAAA | 79931 |
rs766240593 | snp | A/G | 3.30049e-05 | 0.00406219 | missense | TNIP3 | GRCh38.p7 | 4:121150134 | TCCATTTCTGTTCTC[A/G]TCTCCTCATGGCAGA | 79931 |
rs766255090 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183263 | TGTAGAATTCTACAG[C/T]CTGCCTCAACCATTT | 79931 |
rs766283556 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202231 | ACATAGACCAAGGGA[A/G]CAGAATAGAGAACCC | 79931 |
rs766329702 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226802 | ACTGTTTAAATAAAA[C/G]AGTCCAGTAACTTTA | 79931 |
rs766340489 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227562 | TTTTTAAGAAAGTCA[C/T]TCTGCTGCCAAGAGA | 79931 |
rs766344661 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142443 | GTCAGCAACTGCATG[A/T]AATACCAATGAAATC | 79931 |
rs766402816 | in-del | -/TA | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131179 | ATTTCTTGTTATATG[-/TA]TATATATATATATGT | 79931 |
rs766402958 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201789 | CTATGTATCAGTACA[A/T]GAGGATCACATTTTC | 79931 |
rs766407506 | in-del | -/TAACC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195227 | AAAAACGTCTTTGAG[-/TAACC]TAACCCCCATACACC | 79931 |
rs766419644 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214265 | TCCGGGTATATACAC[C/T]CTAGAAGGCAACTTG | 79931 |
rs766424501 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201096 | ATTTATGAATGGACT[C/G]TAAGCTATGTAAATG | 79931 |
rs766474961 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162737 | TAGAGCATCCTGAAC[A/G]ATGGATCAGAATTTC | 79931 |
rs766489219 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189070 | GGAAAAACACATAAC[C/T]ACAGTCTTAGAAATA | 79931 |
rs766567235 | in-del | -/CAGG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172008 | AAAGTTCTGGGATTA[-/CAGG]CATGAGCCACCACAC | 79931 |
rs766578511 | snp | A/C | 1.65037e-05 | 0.00287256 | missense | TNIP3 | GRCh38.p7 | 4:121164114 | AGATGTGCCCTGTAC[A/C]AAATGTGCCATGGAA | 79931 |
rs766579228 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217976 | TCCAGAGAAAACAAA[C/T]GACTTGGCTAATTAA | 79931 |
rs766590844 | snp | C/T | 3.30546e-05 | 0.00406524 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164053 | TCTCCTAGAAATATG[C/T]TCTTACCTCTTTATG | 79931 |
rs766608562 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136777 | GGATGATTTCTTGAG[-/C]CCAGGAGTTTAAGGG | 79931 |
rs766638629 | snp | A/C | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228898 | AAGGAGAAATTAATC[A/C]GTCAACAGCAAGGAG | 79931 |
rs766672058 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148328 | TCAGCAGTAGAGGCA[C/G]TGCAAAACTACGGAG | 79931 |
rs766690160 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190303 | GAAGGCAGAGACAGG[C/T]TTAGCCTGCTAATCA | 79931 |
rs766694926 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135583 | TTGTATTTTTTTGTA[G/T]AGACAGGGTTTCACC | 79931 |
rs766702416 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222051 | ATCACCAGCTCTAAA[A/T]TGAGAACAGATTGTA | 79931 |
rs766719215 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135761 | AGAATTCTGAGCAAT[A/T]CAGTTACACCAACAG | 79931 |
rs766723156 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149422 | AGAATCACCACTCAG[A/C]TGCTACCATTTTCTG | 79931 |
rs766745866 | in-del | -/T | | | utr-variant-3-prime, frameshift-variant | TNIP3 | GRCh38.p7 | 4:121132643 | CTTCTACGGATGGAC[-/T]TTCTTTACTGAGGAT | 79931 |
rs766764890 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171649 | CCTCAGGAAAATGAA[A/C]ATGATTCAGGCAAAA | 79931 |
rs766790244 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180072 | ACCAGAGAAAAAAAG[C/T]GGGGAGGGGTGGTGA | 79931 |
rs766814347 | snp | C/T | 3.30169e-05 | 0.00406293 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121154599 | TTCCTTTTCCTTGTT[C/T]GCAAGAGTATTTTTT | 79931 |
rs766848826 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136566 | GCTTTAAAAACAGGC[C/T]GGGTGTAGTGGCTCA | 79931 |
rs766856276 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157458 | CTTCTTTTCTCCAAA[C/T]CACCCAGCTCTTCCT | 79931 |
rs766869028 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150993 | GTATTCACCAGAACG[A/G]TTATCATCTTTAGTC | 79931 |
rs766909524 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144087 | ATTTGGGGATGACAA[A/G]TGCATTTTAGTCAGT | 79931 |
rs766961721 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196785 | AATACAATTTCAACG[C/T]AGAAAATTTAAAATA | 79931 |
rs766985820 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant, stop-gained | TNIP3 | GRCh38.p7 | 4:121138670 | CTGGTCAAGAGCATA[C/T]CACTGATAGTCTGGC | 79931 |
rs767063230 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216559 | CAAGGGAAGTTAACT[A/G]TGTCAGTCACCAAAG | 79931 |
rs767081876 | in-del | -/AAG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178419 | AAGCTAAAGTTGGAA[-/AAG]AAGAAGTCTCTTCAC | 79931 |
rs767139851 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175065 | TAATGAACACATTTG[C/T]TAAACAACTCTTATG | 79931 |
rs767142449 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175916 | TCTGGTGGTGTACTT[A/T]ATTAGAAAATAGAGT | 79931 |
rs767153215 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217306 | TAGGAGTTAGGCCCA[C/T]GGGAAACACGAAGCC | 79931 |
rs767156813 | in-del | -/ACAC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154002 | AGTCCATAAAACAAC[-/ACAC]ACACACACACACACA | 79931 |
rs767168025 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164635 | GGCGAGATTTTCTGG[A/C]AATACCTTCTAAATG | 79931 |
rs767171822 | in-del | -/AC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194862 | TAGAAAAAAAAAAGT[-/AC]ACACACACACAGACT | 79931 |
rs767193107 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142516 | GCTACTGGTAACATG[C/T]TCTATAAAGCATATG | 79931 |
rs767201048 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133163 | ATTGAGTACTATTTG[A/T]TAATGAATACTACAT | 79931 |
rs767223650 | snp | C/T | 3.32231e-05 | 0.00407559 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147012 | TGAAAAAAATATACA[C/T]ACATGCTGGCAAAGA | 79931 |
rs767250624 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121192179 | GCATACAAAAAAGAG[A/T]TGCCGAGCCAAGTCT | 79931 |
rs767269498 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202571 | AAATGCAACAAAAAC[A/T]AGATAGATGGGATTT | 79931 |
rs767327443 | snp | A/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167216 | AAAATTCCCTGCTTA[A/T]GATGAAATGTACACA | 79931 |
rs767393265 | snp | C/T | 4.96545e-05 | 0.00498245 | missense, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121132658 | TTTCTTTACTGAGGA[C/T]AAACCTATGGAAAAC | 79931 |
rs767469025 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194026 | TAATGTAAGATCCTG[G/T]ATTGGAGCCTTTTTT | 79931 |
rs767516513 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214178 | TTATTCTTCTTTCCC[A/T]CTTCCCTCAGACAAA | 79931 |
rs767549424 | snp | A/G | 3.30409e-05 | 0.0040644 | missense, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164133 | TGTGCCATGGAAGCT[A/G]TTTTTCCTGGAGTCT | 79931 |
rs767550114 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225392 | TTGATTTTTTACTCA[A/T]GCTCTGTGCAATTTC | 79931 |
rs767607654 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195003 | CAAAACCCTATCTCT[A/G]CTAAAATTACAAAAA | 79931 |
rs767626717 | snp | A/G | 1.65671e-05 | 0.00287807 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132589 | AGGGTCCTCAGCCAC[A/G]CTCCCTCGTTGCCTG | 79931 |
rs767647397 | snp | G/T | 0.000973552 | 0.0220415 | missense, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182761 | TTTCTCTCAATCAGA[G/T]CCTGGATTTTTTTGT | 79931 |
rs767660886 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199949 | GGGGCTGCATATGCC[C/T]AGAAGAAAGGGTGCT | 79931 |
rs767686114 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147034 | TGGCAAAGATTATTT[C/T]GTTTTGACTTGTACC | 79931 |
rs767727915 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171366 | TAAAAGAGGGGTGGA[C/T]AGATGGATGAATAGA | 79931 |
rs767796262 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151288 | TCAACAGTGTCTATT[C/T]GGTGATATTAGTGGT | 79931 |
rs767812636 | snp | C/T | 1.67497e-05 | 0.00289389 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157091 | GACCCGGGCCCCGCC[C/T]ACCTCCTCCCGCTGC | 79931 |
rs767888599 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148105 | TGATGCTCTGTAAAC[A/T]ATTACCAGAGGCATT | 79931 |
rs767905544 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221797 | CTGAGAAAGGTGTCA[A/G]ATCAGGGGACTTTCA | 79931 |
rs767906448 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161379 | CTAAGTCCTTCATCA[C/T]GGCTGGTGGATGAGT | 79931 |
rs767931700 | snp | G/T | 1.75422e-05 | 0.00296155 | missense | TNIP3 | GRCh38.p7 | 4:121141817 | GCACTCTTACTTACT[G/T]GGTGCTCCCGTTGCT | 79931 |
rs767952721 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178828 | ATTCTATGTTGTGAT[G/T]TTTATACCTTCATGG | 79931 |
rs767974828 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168364 | GGCATGCACCACCAT[G/T]CCTGGCTAATTTTTT | 79931 |
rs767991330 | in-del | -/C | 1.64855e-05 | 0.00287097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154512 | TGTTTTATGCAGGGA[-/C]TTCTCATTTTAATCT | 79931 |
rs768000945 | snp | G/T | 1.68781e-05 | 0.00290495 | stop-gained | TNIP3 | GRCh38.p7 | 4:121141906 | GCAGTTACAGGGTGG[G/T]CAATACATCTGAGGA | 79931 |
rs768023509 | snp | A/C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135692 | GCATGAGCCACCACT[A/C/T]CTGGCCTTAAACTAG | 79931 |
rs768032851 | snp | G/T | 1.64833e-05 | 0.00287078 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121138683 | TACCACTGATAGTCT[G/T]GCTGTGTGGAACAAT | 79931 |
rs768079909 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185903 | CAGAAATAATCACAT[G/T]CAGTCATCACTGTTA | 79931 |
rs768093306 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139581 | AACTTGAGGAAAATT[G/T]TTCTAACATGAGCCA | 79931 |
rs768132502 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180611 | GTTGTGTAAGAGTGA[A/G]TTCAAACATTACCCA | 79931 |
rs768188862 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169243 | GTTAGTCCATTCTGC[A/G]CCATGCCCTGGCCAC | 79931 |
rs768209854 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158573 | TCCCGTCATTTTCCA[A/G]CAGTTGGCTATCCAC | 79931 |
rs768313173 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210918 | ACAAAGTATGATGTA[A/G]CACAGCAAAAAATGA | 79931 |
rs768381713 | snp | C/G | 1.70049e-05 | 0.00291585 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157067 | TTATTTGGATCCTCC[C/G]GGCTCGAGGACCCGG | 79931 |
rs768405193 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212046 | GAAAATTCTAATTTG[G/T]TATTCTTTTCAACAT | 79931 |
rs768421439 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147858 | TCACTAACAGCCCAA[C/T]AAATTTTAACTAAAG | 79931 |
rs768443851 | snp | C/T | 1.66499e-05 | 0.00288525 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150081 | TGTTCTCCACAGGAT[C/T]ATGCCACTTCCAGCT | 79931 |
rs768463767 | snp | C/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217279 | CAATTGCTGAGAACC[C/G]ATCAGAAAATTTAGG | 79931 |
rs768490390 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121138649 | GTGTTGTACATCTGG[C/T]GGAAGCTGGTCAAGA | 79931 |
rs768490864 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199329 | AAGCTTCAAGATATC[A/C]TATAAAGCTAGTTGT | 79931 |
rs768497405 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159573 | TCCATTAACTGATCA[C/T]GATTTTCTTGCAATA | 79931 |
rs768511649 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186026 | GCTGGGGCCCTGCGT[C/T]CTCTCACGTGAGCCT | 79931 |
rs768537009 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205580 | TAAAGGTACTGAGAC[A/G]GTTTAAGAAGCTCTT | 79931 |
rs768570323 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144601 | GAGACAGGGTTTCGC[C/T]ATTTTGGCCAGGCTG | 79931 |
rs768615358 | snp | G/T | 1.64879e-05 | 0.00287118 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138705 | TGGAACAATACAACA[G/T]TATTATAGCAATATG | 79931 |
rs768625348 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146533 | ATGCTTACATTTAAT[A/G]TATTCTATTTTAATA | 79931 |
rs768637876 | snp | A/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165048 | AAGACCTCATTTTGG[A/T]CTTGGAACAAAAGGA | 79931 |
rs768652129 | in-del | -/CTT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135381 | AAATGCATGAAGTTA[-/CTT]CTTCTTCTTTTTTTT | 79931 |
rs768700780 | snp | C/T | 1.65578e-05 | 0.00287726 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164031 | AATGCTAGATGTGAT[C/T]AACTCATCTCCTAGA | 79931 |
rs768741914 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134268 | ACCCTATGAAAAATT[G/T]GGAATGTACAGAAGT | 79931 |
rs768785857 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207041 | GTGATCAGGTAGACG[A/C]AAATGTTTTCATTGG | 79931 |
rs768813975 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154179 | CCAACTCCATAGTGA[A/T]CATTTTAAAGAGCAG | 79931 |
rs768877733 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194759 | TCCCTGTGGACTTCT[C/T]ATAATAAACAAATAG | 79931 |
rs768922186 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214064 | CGTAGGACCGAAAGC[A/G]CTTCAATGAGAAAGG | 79931 |
rs768922795 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141159 | ATAAATTTCTATCTA[C/T]GTAGGCAAAATAAAA | 79931 |
rs768931807 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203974 | ATATATTTTAAATTA[A/C]ATATTTAATATTAAA | 79931 |
rs768974270 | snp | A/T | 1.66654e-05 | 0.00288659 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142812 | TTTGTTAATCAAGAC[A/T]AGTTAAAATCATTAA | 79931 |
rs769000682 | snp | C/T | | | missense | TNIP3 | GRCh38.p7 | 4:121161144 | AAGTTACCTCTTTTC[C/T]TTGTTTTTCCAAACA | 79931 |
rs769045013 | snp | C/T | 1.65636e-05 | 0.00287776 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157267 | GTCGTTCAAAGACAG[C/T]TGCAGATACCTTCTC | 79931 |
rs769064700 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183123 | TGTGCACAGCAACCT[A/G]TTAAAGTAGTCACTG | 79931 |
rs769092034 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217345 | TGAGTTTCAAGCATT[C/T]CTGTTTAATTGTAAC | 79931 |
rs769119776 | snp | C/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121172211 | TGCATGGCCTTATGA[C/T]TTGTCTAAGTAGAGA | 79931 |
rs769130290 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183992 | CCTGCCCCAGTCCAT[C/T]GAAAAACTGTCTTCC | 79931 |
rs769132743 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201544 | AACTTAGAGCTAGAA[A/T]GTTTGTAAGAGTTTT | 79931 |
rs769162885 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180279 | GTGGCGGGCGCCTGT[A/G]GTCCCAGCTACTCGG | 79931 |
rs769218941 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162402 | TGTGGGTCAATAAAT[A/T]CTGAATGATTATATT | 79931 |
rs769225364 | snp | A/C | 1.65493e-05 | 0.00287652 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142711 | AATGTATGCGTGAAA[A/C]TTAGATCAACATACC | 79931 |
rs769260721 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179380 | AGTGTTGTTGTAGGT[A/T]GAAAACAAAATAAAA | 79931 |
rs769339204 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136248 | ACACAAAGATGAGAT[G/T]ATTGAGGGTTAAATG | 79931 |
rs769339848 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149157 | TGCAGTATCTCCACA[A/G]CCCTATGCTGCCAAT | 79931 |
rs769366016 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178498 | AGACATATTCCACAT[A/T]GAGCACACTTGGCAC | 79931 |
rs769366694 | snp | A/C | 1.6477e-05 | 0.00287024 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154539 | ATCTCCCATGCTTGA[A/C]CTGACTGATACCTTA | 79931 |
rs769392602 | snp | A/G | 1.65941e-05 | 0.00288041 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121150217 | CAAGGCATCCTGAAG[A/G]GCCTACGTAATAAGA | 79931 |
rs769459470 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221664 | ACTCTCATTTACAGT[A/G]ATGGCTCAAGGGAAA | 79931 |
rs769480256 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175346 | ACCTCAAGTTCTTTT[C/T]CTTCTCTTTGTAGGG | 79931 |
rs769505568 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185799 | GTATTGCCCTCATGG[A/C]TGCCTTGTTCTTTTT | 79931 |
rs769508448 | snp | A/T | 3.37098e-05 | 0.00410533 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132705 | AGATTAAAAATTAAC[A/T]TTTCATTTCTCTTCT | 79931 |
rs769532173 | snp | A/C | 1.67309e-05 | 0.00289226 | missense | TNIP3 | GRCh38.p7 | 4:121141880 | GGATCTTGCAGGTGG[A/C]AAACCAAGCCGCAGT | 79931 |
rs769550178 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210842 | GCAGTCACATTGGGG[C/T]TTAGGAGTTCAACAT | 79931 |
rs769571741 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199062 | CCTAAAACCAACCAA[A/C]CAAACAAAGGGACTT | 79931 |
rs769599302 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169754 | CTTTGATCCCCCAAA[C/T]CTGGTTTTGAACTAG | 79931 |
rs769638306 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197345 | CCAGCCTGGCCAACA[C/T]GGTGAAACACCTTCT | 79931 |
rs769650424 | snp | C/T | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229302 | CTCTAAAAAAACAAA[C/T]ACCCGTGGCAGGGTG | 79931 |
rs769675181 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184965 | TTCCCAAGTAGCAAC[A/G]GAATTGGACTAGTCT | 79931 |
rs769740970 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212625 | TGCTGCTTGTTTAGT[A/G]AAAAGAAAAATACTT | 79931 |
rs769752225 | snp | G/T | 1.68035e-05 | 0.00289853 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132701 | TTTTAGATTAAAAAT[G/T]AACATTTCATTTCTC | 79931 |
rs769763587 | snp | A/G/T | 6.7294e-05 | 0.00580027 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164188 | GAAAAGTCTCTTAAG[A/G/T]TATATTTTAGGGTGA | 79931 |
rs769797053 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204047 | GCATTTATGAAAAAA[-/T]CTCTGACTATTCCTT | 79931 |
rs769802100 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158500 | TTGCTCAAGACAACT[C/T]ACTGACACCGTTCAT | 79931 |
rs769804175 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143718 | TCAATGGATCAATAC[A/G]TAACTTTGTTTCATG | 79931 |
rs769847099 | snp | A/G | 3.31868e-05 | 0.00407336 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150093 | GATCATGCCACTTCC[A/G]GCTTCTCACCTGCTG | 79931 |
rs769857137 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144550 | GTGATTACAGGCGCG[C/T]GCCACCATGCCCAGC | 79931 |
rs769960182 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133813 | TAAGAACAGGAAAAT[C/T]TGGACACAGATGGAA | 79931 |
rs770046500 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154018 | ACACACACACACACA[C/T]ACACCCCTGCATGCA | 79931 |
rs770068401 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152719 | TACATGTTAAAATGA[C/T]ATTTTACAAATGTGT | 79931 |
rs770083783 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224535 | TGGTTATGTTTTTTG[A/T]TATTTTTATTGCTTT | 79931 |
rs770102519 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140954 | AGGGTTTTGAGTCAC[A/G]CTCGAACAAAAGTAT | 79931 |
rs770166851 | snp | A/C | 1.69075e-05 | 0.00290748 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157077 | CCTCCGGGCTCGAGG[A/C]CCCGGGCCCCGCCCA | 79931 |
rs770173735 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225941 | AGTCATATTTAACAG[A/T]CAATTTCCCATGTTT | 79931 |
rs770196304 | snp | G/T | 1.6681e-05 | 0.00288794 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146998 | TGAATTTTTTTAAAT[G/T]AAAAAAATATACATA | 79931 |
rs770248007 | snp | A/T | 6.64209e-05 | 0.00576247 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161249 | AGAGAAGATTGAAAC[A/T]AAGCTGTTTACAAAA | 79931 |
rs770300518 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159984 | ATACATATCATTATT[C/T]AGTATGAAACTGTAT | 79931 |
rs770315168 | snp | C/T | 3.29799e-05 | 0.00406065 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138609 | AAAGAATGCTCAATA[C/T]AGCTGTGGTCTCACC | 79931 |
rs770320649 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121147103 | ATTAATTTGCTGTAG[C/T]TCCTCTTTCTCTTGA | 79931 |
rs770351656 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214633 | TCTTGTCTACACGGT[G/T]AAATTTTGCCAAGCA | 79931 |
rs770358213 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201503 | ATGGTTCTACAGCAT[A/G]AGTATCATGATTTTT | 79931 |
rs770387400 | snp | G/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121172143 | TTAAGTCCAGGGAAG[G/T]TACAAGCCTTGAAGA | 79931 |
rs770443281 | in-del | -/GAC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178371 | ACGACAAAGTGAAAG[-/GAC]GACTCTGACCCTCCG | 79931 |
rs770446094 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188364 | ACTGTTTTTCCCAGA[C/T]TAACATTGGGAAATA | 79931 |
rs770488851 | snp | C/G | 1.65603e-05 | 0.00287747 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158774 | TCATTAAAATTTGGT[C/G]AATCAACAAAGAATT | 79931 |
rs770544155 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207914 | TATGGGAGCTACCCA[A/G]TGGGAGATAATATGA | 79931 |
rs770574288 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148881 | ATCATACCCAGGGAC[A/G]TCAGAAAAATAATGC | 79931 |
rs770591577 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225420 | TTCATTAGAAAAGCA[-/T]TTTTTCTTCTTGTTT | 79931 |
rs770645146 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188284 | TCAATAGGATAGTAG[A/G]TTTCACCAATTTGAC | 79931 |
rs770671546 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221355 | TAAAAAAGAAAAAGG[A/C]ATTCACTTAGCCTAG | 79931 |
rs770761131 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209093 | AGATTTGGAAAGCTT[C/T]CTGGTTGGTAACACA | 79931 |
rs770768129 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178385 | AGGACTCTGACCCTC[C/T]GGCAAACACTGGAAT | 79931 |
rs770797184 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121227132 | GCACAAAGGGGCTAA[C/T]TAACAAAAGCTGTAA | 79931 |
rs770799417 | snp | A/T | 8.33632e-05 | 0.00645559 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150233 | GCCTACGTAATAAGA[A/T]AAGTACACTGTTGAT | 79931 |
rs770805242 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196404 | TAGGTTTTTTTTAAG[A/T]TAGAAAATAAATCGA | 79931 |
rs770838697 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | TNIP3 | GRCh38.p7 | 4:121154555 | CTGACTGATACCTTA[C/T]TGAGGCGTTTTATTT | 79931 |
rs770854619 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229064 | TCCCAAAGTGTGTTG[A/G]AAGACGATCTTGTCT | 79931 |
rs770893146 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184397 | TCCATTGATATGACT[C/T]GAACTTGCCTTTTGG | 79931 |
rs770910084 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143647 | AATATTGAACCACTG[C/T]TCCTAGGAGAAATGT | 79931 |
rs770949664 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168931 | CTTGCTAGTTATGTG[A/G]CCTTGGGCAAGATGA | 79931 |
rs770982837 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184848 | GTTGCATATGCATAA[A/C]AATGAGTTTGGACCT | 79931 |
rs771098232 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161006 | TTGCTTTCAAAATAG[C/T]GCAGTCCAGTATCTT | 79931 |
rs771129071 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220434 | GAGCAAAAATTTTAA[A/G]ACATAAAGCAATCTG | 79931 |
rs771175192 | snp | C/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132437 | GTATAATAACTGGCT[C/T]CTCCAATTTGATCAG | 79931 |
rs771185122 | snp | A/G | 3.29712e-05 | 0.00406011 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157136 | CAGGTCGCGCTGCCT[A/G]TCGTCCTCTCTCTGC | 79931 |
rs771189593 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184886 | GGTTTTTTCCACAAA[C/T]CTGTGAGGAGGAAAG | 79931 |
rs771200872 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121164001 | AGTGCACAATTAACC[A/G]CTAGAAATGCCATCA | 79931 |
rs771221496 | snp | A/G | 1.66477e-05 | 0.00288506 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142675 | TAATTGGGACAATGA[A/G]AAATGCTGTACATGG | 79931 |
rs771401973 | in-del | -/TTGTTG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121191090 | TTGTTGTTTTTGTTT[-/TTGTTG]TTGTTGTTGTTATTT | 79931 |
rs771472967 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138906 | TGGCCAGAATTTCTA[C/T]CACTTTGAGGTTGTG | 79931 |
rs771473122 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152182 | CTTGTACATAGAGGG[G/T]AGGCCCTGGATTCCA | 79931 |
rs771529572 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181943 | ACTGAGTAAGAACTT[C/T]TTTAGAAAGAAGAAC | 79931 |
rs771530110 | in-del | -/CGCTGCCTGTCGTCCTCT | 1.66363e-05 | 0.00288407 | cds-indel | TNIP3 | GRCh38.p7 | 4:121157127 | TCCCGGGTCAGGTCG[-/CGCTGCCTGTCGTCCTCT]CGCTGCCTGTCGTCC | 79931 |
rs771543203 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170933 | AAATTCTCCTGCCTT[C/T]GCCTCCCGAGTAGCT | 79931 |
rs771555657 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194113 | ATGTAGTAGTGTATC[A/G]ATGTTCATTTTCCGA | 79931 |
rs771563081 | snp | C/G | 6.74798e-05 | 0.00580821 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157081 | CGGGCTCGAGGACCC[C/G]GGCCCCGCCCACCTC | 79931 |
rs771574112 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200413 | AAACTGTACCTAGTT[A/G]GAACTTGTCAGGCTC | 79931 |
rs771615511 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172331 | AGGGTTTGAGGAGGC[C/T]TCAGAGTCAAATTGA | 79931 |
rs771621962 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157700 | ACCTCCTACTAGGTG[C/T]CAAATCACTCTGATG | 79931 |
rs771645788 | snp | C/T | 0.000212743 | 0.0103115 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161258 | TGAAACAAAGCTGTT[C/T]ACAAAATAAACAGAA | 79931 |
rs771663821 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159663 | ACCATTTTGAAAATT[C/T]AGATTTTCAAGAAAT | 79931 |
rs771718773 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160821 | TCATAAGGCACAAAC[A/G]ATAAAGGCATAAAGG | 79931 |
rs771749860 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134422 | GTCATTTTGCATCTC[A/G]TTCTGATAACAGATG | 79931 |
rs771785647 | snp | C/T | 1.65031e-05 | 0.00287251 | missense | TNIP3 | GRCh38.p7 | 4:121164082 | TGCTCCGTAGAACTT[C/T]CTGCGGCAATCATTC | 79931 |
rs771800649 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121218938 | GCCATGGTGGCTCAC[A/G]CCTGTAATCCTAGAA | 79931 |
rs771887512 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147768 | TTCCTCTAAGATTCT[C/G]ATTTAAATTACTACT | 79931 |
rs771890182 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187161 | ACAGTGTTGTGCTCT[G/T]AATACAATACTATGA | 79931 |
rs771890332 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220019 | CCATCATGAAAATTA[C/T]TATCCTTGTATCCAT | 79931 |
rs771904644 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121154569 | ATTGAGGCGTTTTAT[C/T]TCACATTCGTAATGT | 79931 |
rs771917579 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167767 | ACATTAGCAAAAGTA[A/G]TATTCAAAATATTTA | 79931 |
rs771930284 | in-del | -/ACAA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219203 | GAAACTCCATTACAA[-/ACAA]ACAAACAAACAAACA | 79931 |
rs772006251 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166233 | GCCTCTTCTGTTATG[C/T]AGATAAACAACAAAC | 79931 |
rs772019173 | snp | C/T | 3.58494e-05 | 0.0042336 | missense | TNIP3 | GRCh38.p7 | 4:121154646 | TCTCTTCTTTCAATT[C/T]ATGTAATTCTTCATT | 79931 |
rs772027562 | snp | A/G | 0.000186029 | 0.00964261 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137980 | TGGGTGGCCTCACAA[A/G]ACCATAGAAACAAGC | 79931 |
rs772044373 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155506 | ATTGTTGTGATTATT[A/G]TTTTTAAAAGGTAGA | 79931 |
rs772091634 | snp | A/G | 1.65943e-05 | 0.00288043 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142699 | TACATGGGAATAAAT[A/G]TATGCGTGAAAATTA | 79931 |
rs772096656 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178324 | TGCTGGCCAAGAGTA[C/G]GTGCTCAATACACAG | 79931 |
rs772160421 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163823 | CAAGAACAAAATAAG[G/T]AACCCACAGAACTGG | 79931 |
rs772204525 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196123 | GAGGGAACTGAGACT[C/T]ACAGAGATTAAGTAA | 79931 |
rs772243362 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156712 | AGGTATTGCCATATT[A/G]TTATTATGAACACTA | 79931 |
rs772244775 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216093 | TACTGGTGGAATACA[A/G]TTGTTTCCTAGGAGA | 79931 |
rs772296548 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184127 | CATTAATTGTGTGAT[C/T]TTTTTTTCTTTCTCT | 79931 |
rs772302879 | snp | A/G | 0.000162641 | 0.00901633 | utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227425 | CAGATCTAGGTAAGC[A/G]TATTACAAGGTCTAA | 79931 |
rs772310656 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214838 | CAAATGTATATAAAA[C/T]AGATCAATGCTTATT | 79931 |
rs772313767 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143432 | TACACTCCATGTCCC[A/G]CATTCCCATAAGGGA | 79931 |
rs772317810 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165729 | TTATGTTTGGGTCTA[C/T]GCTTGAGTGAAAGGG | 79931 |
rs772358269 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223883 | ATTCTTTCAAAAAAA[-/C]ATACATTATTACTAT | 79931 |
rs772369655 | snp | A/G | 1.65488e-05 | 0.00287647 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142787 | TTTATCTAAAGACAA[A/G]ACAAAGGCATTTGTT | 79931 |
rs772396431 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201712 | ATTACTTAGCTCATT[C/T]ATTTGTATATTAATT | 79931 |
rs772412013 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149233 | CCACTTGGCAATAGC[A/G]CGTGAGGTTAGGTGA | 79931 |
rs772485462 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222432 | ATCTGTCTCTCACGT[A/T]TAACAGACTATATGT | 79931 |
rs772516550 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176213 | TTAAATAACTTCACC[C/T]ATGTTGCCAGTAATG | 79931 |
rs772519209 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189958 | GTGCCCAGGAGGACC[A/G]TGCAGGCAGAGGAGC | 79931 |
rs772536281 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162569 | TAGAACAGACTAACT[A/G]TTAAGCATCTTTGAT | 79931 |
rs772577098 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150715 | CCCAGGTGATGTTTT[C/G]AGTAACATTCTACTA | 79931 |
rs772582563 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138772 | GGCTATGTGGCTTTT[-/A]TTAAGCAGGCAACAC | 79931 |
rs772591920 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201245 | CTGATGCTTTATTTA[A/G]TGCTTGGAAGGACCA | 79931 |
rs772627176 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180228 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 79931 |
rs772641451 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150515 | AACAAAATCTGTATC[C/T]ATAGACTTTCTCCAG | 79931 |
rs772657515 | snp | C/T | 3.29679e-05 | 0.00405991 | missense | TNIP3 | GRCh38.p7 | 4:121157141 | CGCGCTGCCTGTCGT[C/T]CTCTCTCTGCCTGTC | 79931 |
rs772741685 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159858 | TTATCTATAGGGAAC[A/G]GACACTGAGAAGACA | 79931 |
rs772818392 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195191 | AAAAAAACTTCTTAA[-/T]TTAAGTCAATAAATA | 79931 |
rs772838245 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220233 | TAATCAAAATATTAG[C/T]TAAAGCTGGGACTCA | 79931 |
rs772860884 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135111 | GAGGCCAGGGCTTAG[G/T]TCTCCCTGTGCCACC | 79931 |
rs772865926 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146667 | ATACGTATGTTTTTG[G/T]CAGACAGGAGCATTC | 79931 |
rs772887588 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166278 | CTCAAGAGAGCCATA[G/T]GGTTATTTATGAATA | 79931 |
rs772916992 | in-del | -/GATAGAT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203219 | AGAAAATGTGATATA[-/GATAGAT]GATAGATAGATAGAT | 79931 |
rs772924388 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121218972 | TGGGAGGCCGAGGCA[A/G]GTGGATCACCTGAGG | 79931 |
rs772943376 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205789 | AGTTGCCCTTTATTG[A/G]GACAGTGTATTAGTC | 79931 |
rs772983633 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134453 | AAACAAGATGAAAAT[A/G]TTCTTTGTAAAATCA | 79931 |
rs772987499 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121153672 | GCATCCTATCAACTA[C/T]GCAGGCACATACTTA | 79931 |
rs772992994 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187169 | GTGCTCTTAATACAA[C/T]ACTATGACCTGAGGG | 79931 |
rs773013726 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154526 | ACTTCTCATTTTAAT[C/T]TCCCATGCTTGACCT | 79931 |
rs773022260 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136716 | AAATAAAAATTAGCT[-/G]GGCATGGTGGTTCAT | 79931 |
rs773032127 | snp | C/T | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166372 | TCCCTAAGAATTAAT[C/T]GGGTCTTTTCTGTTA | 79931 |
rs773033245 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207698 | AAACTATGACAGTGA[A/G]AGATATCTGACCTAA | 79931 |
rs773080384 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141710 | GAGGCTGAGAGAAAA[C/G]AGAGGCTCTTGCTGT | 79931 |
rs773095003 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176782 | AAGAAGTTTTTCCCT[C/T]ACAATCTTGTGAAGT | 79931 |
rs773097880 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121185801 | ATTGCCCTCATGGCT[A/G]CCTTGTTCTTTTTTA | 79931 |
rs773176275 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141451 | TATAAATTTACAACC[A/G]AACAAAAGCATCTCA | 79931 |
rs773182918 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212686 | TTCTACTTAACAAAA[C/T]AATATGAATGGACGG | 79931 |
rs773243030 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155519 | TTATTTTTAAAAGGT[A/G]GAAATCAACTAGTCC | 79931 |
rs773298448 | in-del | -/CAAACA | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132252 | ACACACACACACACA[-/CAAACA]TATGCACTTTAAATC | 79931 |
rs773302442 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173430 | CTGTAGTAGTCAGAA[A/G]AGAGAAAATTCAGCC | 79931 |
rs773303140 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142352 | AACCCATGGGATAGA[A/G]TGCTTCAGTGCTCAA | 79931 |
rs773303349 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183222 | TCAAACTGAAACATC[A/G]GCAGGGCCAAGATCA | 79931 |
rs773320842 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201717 | TTAGCTCATTCATTT[C/G]TATATTAATTAATAC | 79931 |
rs773356225 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172824 | ACTGAAATTTTCTGC[A/G]GTCAATTAGATAAAT | 79931 |
rs773369937 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138733 | ATGGACTTCAAATAT[A/G]GTGGCATGTCAAAAA | 79931 |
rs773406168 | snp | C/T | | | utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227443 | TTACAAGGTCTAATA[C/T]GGAGACCTGTCTTTA | 79931 |
rs773430109 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143412 | ATTCACATCATTGTC[A/G]TTCCTACACTCCATG | 79931 |
rs773453331 | snp | A/G | 2.39157e-05 | 0.00345793 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154697 | GAAGTTAAGACCAAG[A/G]AAAGAAAATAAAAGT | 79931 |
rs773493035 | in-del | -/AC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194863 | GAAAAAAAAAAGTAC[-/AC]ACACACACACAGACT | 79931 |
rs773496348 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214904 | CATGTCGAGTCTTTC[C/T]GTTGAGGTAGGTAAA | 79931 |
rs773528198 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189025 | TTGGCAAGTAGTGTA[A/C]ATTCTAGAGGAAAAT | 79931 |
rs773584079 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216113 | TTCCTAGGAGAAAAA[C/T]TTGTGCAATTACAGA | 79931 |
rs773587192 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202767 | CAAAAAGTGGGCTAA[C/T]GACATGAATAGATAA | 79931 |
rs773618723 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162704 | GCACATCAAAGTCAC[C/T]GTTAAGCTTGCTAAA | 79931 |
rs773621910 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220143 | TAATTTTTTAGAAAT[A/G]ACATTATACCATTTA | 79931 |
rs773662023 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138754 | ATGTCAAAAATACAA[G/T]TAGGCTATGTGGCTT | 79931 |
rs773676844 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189971 | CCGTGCAGGCAGAGG[A/G]GCCAGTTTGGAGCAG | 79931 |
rs773722736 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196958 | CTCCTTCTTTTACTC[A/G]AAGAACCATGGGTAG | 79931 |
rs773747560 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149258 | AGGTGAGTGGGGAGG[A/C]GAATGCTCTTGTGCA | 79931 |
rs773800807 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150788 | AGAAATGAAAGCCCA[C/T]GCAGATTCATTATCT | 79931 |
rs773802218 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180619 | AGAGTGAGTTCAAAC[A/G]TTACCCATAAAAGAA | 79931 |
rs773891312 | in-del | -/AA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194850 | ATCCATGAACAATAG[-/AA]AAAAAAAAGTACACA | 79931 |
rs773950679 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186076 | AGGACCACAACCAAA[A/G]AGGGACGGGCCCTCA | 79931 |
rs773954032 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211067 | TAAAGGAACTTACAT[A/G]GTTAGAACAATGAAA | 79931 |
rs774039050 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146560 | AATAAACTGGTGACC[A/G]TTATCTGGCTTCCTT | 79931 |
rs774065565 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224348 | AGCCTGGGCAACAGA[A/G]CAAGACTCTGTCTCA | 79931 |
rs774102253 | in-del | -/AA | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229436 | TCTCTACTAAAATAC[-/AA]AAAAATTAGCCAGGC | 79931 |
rs774115453 | snp | C/T | 4.96997e-05 | 0.00498472 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158778 | TAAAATTTGGTGAAT[C/T]AACAAAGAATTTCTG | 79931 |
rs774132138 | snp | A/G | 0.000186098 | 0.00964441 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137939 | AGTGGGATTTTGATT[A/G]TAGCTCAGTTTATAC | 79931 |
rs774165746 | snp | A/G | 0.000162245 | 0.00900535 | missense, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121182726 | CCTCTGGGGTGAACC[A/G]TTTTGGATGAGGAGA | 79931 |
rs774179361 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202263 | GCAATAAGGCCAAAT[A/G]TTTAGAGCCAACTGA | 79931 |
rs774220385 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144382 | GACTTGAGCTAAATG[G/T]TTTCTAAAGCGTTTT | 79931 |
rs774255136 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165870 | CAGAAGCAGCGATTT[-/C]CTGAACTGACACTTT | 79931 |
rs774265781 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165217 | AAAAGAGAGTGATTG[A/G]GTGTCCCACATTTGG | 79931 |
rs774280047 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135384 | TGCATGAAGTTACTT[-/C]TTCTTCTTTTTTTTT | 79931 |
rs774339995 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176590 | ACTTTATATTTACAG[G/T]GTGCACTTTCTCTCA | 79931 |
rs774341102 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | TNIP3 | GRCh38.p7 | 4:121154556 | TGACTGATACCTTAT[C/T]GAGGCGTTTTATTTC | 79931 |
rs774344997 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194760 | CCCTGTGGACTTCTC[A/C]TAATAAACAAATAGG | 79931 |
rs774353054 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226374 | ATATAAAAAATACAC[G/T]AAAAAAGTTGAGAAG | 79931 |
rs774360922 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134282 | TTGGAATGTACAGAA[A/G]TGACTGGCATGCAAT | 79931 |
rs774362461 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205612 | AAATTATGCAGGCTA[C/G]GGATGCTAGTGGTTT | 79931 |
rs774411351 | snp | C/T | 6.61146e-05 | 0.00574917 | utr-variant-3-prime, synonymous-codon | TNIP3 | GRCh38.p7 | 4:121132646 | CTACGGATGGACTTT[C/T]TTTACTGAGGATAAA | 79931 |
rs774522330 | snp | C/T | 1.67911e-05 | 0.00289746 | missense | TNIP3 | GRCh38.p7 | 4:121141896 | AAACCAAGCCGCAGT[C/T]ACAGGGTGGGCAATA | 79931 |
rs774608365 | snp | C/T | 1.65053e-05 | 0.0028727 | missense | TNIP3 | GRCh38.p7 | 4:121164118 | GTGCCCTGTACAAAA[C/T]GTGCCATGGAAGCTG | 79931 |
rs774623678 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197073 | TTAAATACATCAAAA[A/G]TGGGAAAAAATCAAC | 79931 |
rs774653340 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200825 | CTCAGCTGGCCATTT[C/G]AAGTCCTCTGTTCAG | 79931 |
rs774681845 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183132 | CAACCTATTAAAGTA[A/G]TCACTGTCCCAGGCA | 79931 |
rs774729572 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214736 | TTGCTTCTGTAATGC[A/C]TATAGTATCTTAGAG | 79931 |
rs774739069 | in-del | -/AG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220455 | AAGCAATCTGAAAAC[-/AG]AATGCTTTTAGGTTT | 79931 |
rs774757024 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149172 | GCCCTATGCTGCCAA[C/T]AGATACATGCGGAAG | 79931 |
rs774778859 | snp | C/G | | | missense | TNIP3 | GRCh38.p7 | 4:121161213 | TTGTTGATGGTTCAG[C/G]ACACTTAGAAAAAAA | 79931 |
rs774779366 | snp | G/T | 0.000117577 | 0.00766646 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157088 | GAGGACCCGGGCCCC[G/T]CCCACCTCCTCCCGC | 79931 |
rs774806081 | snp | A/G/T | 4.97874e-05 | 0.00498915 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147017 | AAAATATACATACAT[A/G/T]CTGGCAAAGATTATT | 79931 |
rs774806550 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172436 | CAGTGAGGATACAGG[C/T]CAATGAAAAAACCCG | 79931 |
rs774829210 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188671 | TGTTATGGTTTACTG[C/T]CTTGAATGGCAGTTT | 79931 |
rs774882466 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135629 | GGCTTGAACTCCTAG[A/G]CTCAAGCAATCTGCC | 79931 |
rs775000680 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220617 | ACCTTTTGGTACTCA[C/T]GTATCATCGGCTTAT | 79931 |
rs775077230 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179567 | TAACCACTTTTAGGT[C/T]TTCAGTACATTAGTA | 79931 |
rs775084453 | snp | A/G | 1.65633e-05 | 0.00287774 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164023 | ATGCCATCAATGCTA[A/G]ATGTGATCAACTCAT | 79931 |
rs775090542 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221694 | ATTGAGAACAAGAAA[C/G]AGATTTTTGGCTGCA | 79931 |
rs775172042 | snp | C/T | 6.54986e-05 | 0.00572233 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161106 | ATTAATCCATGGCAC[C/T]TGTGGCTTTAGCGAA | 79931 |
rs775191728 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196446 | TTTGGCTCTAAAGAG[C/T]TAAAATTCTGGAATT | 79931 |
rs775207580 | snp | C/T | 1.85427e-05 | 0.00304483 | missense | TNIP3 | GRCh38.p7 | 4:121154655 | TCAATTCATGTAATT[C/T]TTCATTTAGGCGTTC | 79931 |
rs775214636 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121216332 | CTTCTACTCTTAATA[C/T]ACTATCATTGCCACA | 79931 |
rs775369226 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183471 | TTAAACCAGAGCTTC[C/G]TACTCAAATCAAATT | 79931 |
rs775418449 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226579 | AGAAGAACAAAGTTC[-/T]CAGCATTTCACAGCA | 79931 |
rs775496224 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175737 | TCAGTTTATATTCCC[C/T]CCTTGCACCACTTCT | 79931 |
rs775506128 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144575 | CCCAGCTAATTTTTG[C/T]GCTTTTAGTAGAGAC | 79931 |
rs775511587 | in-del | -/A | 4.97104e-05 | 0.00498525 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157274 | AAGACAGCTGCAGAT[-/A]ACCTTCTCTGAAGCT | 79931 |
rs775520928 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165805 | AAATTGTTCATTCAG[A/G]GTTCTGAAAGTAAAA | 79931 |
rs775560721 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152845 | CTTATGGGTCCCTAA[C/T]AGTACTGTAGGCCTG | 79931 |
rs775596847 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121204725 | GAATAGATTTACCAA[C/T]GTTAGATTGTTGGGT | 79931 |
rs775619485 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139019 | ATCAATAAAACAAAG[C/T]AACTTAGCATCAACA | 79931 |
rs775643894 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151297 | TCTATTTGGTGATAT[G/T]AGTGGTAACTTACTC | 79931 |
rs775650378 | snp | C/G | | | missense | TNIP3 | GRCh38.p7 | 4:121157144 | GCTGCCTGTCGTCCT[C/G]TCTCTGCCTGTCGTC | 79931 |
rs775659682 | snp | C/G/T | 3.2954e-05 | 0.00405908 | missense | TNIP3 | GRCh38.p7 | 4:121154576 | CGTTTTATTTCACAT[C/G/T]CGTAATGTTCCTTTT | 79931 |
rs775677810 | in-del | -/AA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152953 | AGCTAGAAAACAAAT[-/AA]AGTCATAAAAGTTAG | 79931 |
rs775765395 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220737 | ACCACTTAACTTTTA[A/G]AGTCAGAAATAAGTG | 79931 |
rs775773594 | in-del | -/ACA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160949 | TGCACAGACACTGAG[-/ACA]ACAAGTATGAAACAT | 79931 |
rs775780066 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212596 | TGTCATTAAAAATAC[A/T]TATTCATCAGTGCTG | 79931 |
rs775817583 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154021 | CACACACACACACAC[A/C]CCCCTGCATGCACAC | 79931 |
rs775842907 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200548 | CGAGCACACATACCC[C/T]GACCAGTGGGCTCCT | 79931 |
rs775874026 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199086 | GGGACTTGAGAAAAC[C/T]CAGATGTGACATGGC | 79931 |
rs775909490 | in-del | -/AAAACTTTCAGCA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178588 | CAGTTTGAGCACCTG[-/AAAACTTTCAGCA]GTCAATAACTTCATG | 79931 |
rs775909981 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161005 | TTTGCTTTCAAAATA[C/G]TGCAGTCCAGTATCT | 79931 |
rs775937058 | snp | A/T | | | intron-variant, stop-gained | TNIP3 | GRCh38.p7 | 4:121138633 | TCTCACCATTTGCCT[A/T]GTGTTGTACATCTGG | 79931 |
rs775942362 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141091 | AAACCTAAAGGGTAG[C/T]GGGATTTGTCTGGGT | 79931 |
rs775987571 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121171067 | GTGATCTGCCCATCT[C/T]GGTCTCCCAAAGTGC | 79931 |
rs776050168 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201510 | TACAGCATGAGTATC[A/G]TGATTTTTGCCTTAG | 79931 |
rs776089550 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213412 | TAATTTTCTGAATGC[A/G]TAATCCATTTTTTTT | 79931 |
rs776148199 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147904 | TGTTCTAAGTCGACA[G/T]CAATAGAACAAAATA | 79931 |
rs776210487 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135468 | AGTGGCGTGATCTCA[C/T]CTCACCGCAACCTTG | 79931 |
rs776221715 | snp | C/G | 1.66413e-05 | 0.0028845 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150085 | CTCCACAGGATCATG[C/G]CACTTCCAGCTTCTC | 79931 |
rs776249820 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209108 | CCTGGTTGGTAACAC[A/G]TTGATGTGCTGGGAA | 79931 |
rs776269312 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121220479 | TTAGGTTTTTATGAT[A/G]ATTAACTACTTTTTT | 79931 |
rs776311690 | snp | A/C | 1.64895e-05 | 0.00287132 | missense | TNIP3 | GRCh38.p7 | 4:121147140 | CTCTCTCGATCCGAT[A/C]GTTCCTTTTTGAAGT | 79931 |
rs776335174 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121136153 | TTCATAACATATTTA[C/T]TACACACTTAATCTT | 79931 |
rs776343582 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121227569 | GAAAGTCATTCTGCT[C/G]CCAAGAGACTATTAA | 79931 |
rs776354934 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207936 | ATAATATGAATGATG[C/G]GGGTGGTTTCCCCCA | 79931 |
rs776383356 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148340 | GCACTGCAAAACTAC[A/G]GAGATGGATTTTGGT | 79931 |
rs776405626 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183747 | TATTGTGAACTGCAC[A/C]TGTGAGGGATCTAGG | 79931 |
rs776418661 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121142491 | GGGTCTAAGGAGCAC[C/T]AAGACTTGTGCTACT | 79931 |
rs776442005 | snp | G/T | 1.64893e-05 | 0.0028713 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138711 | AATACAACATTATTA[G/T]AGCAATATGGACTTC | 79931 |
rs776474400 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167969 | TAGTTTATGATTTTC[C/G]CTGCAAAACTTGCCT | 79931 |
rs776581753 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174552 | TGTTTTGTCTGAAAA[C/T]AAGCCTGACTCAAAA | 79931 |
rs776631236 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229070 | AGTGTGTTGAAAGAC[A/G]ATCTTGTCTTAAGCC | 79931 |
rs776631904 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184852 | CATATGCATAACAAT[A/G]AGTTTGGACCTATCT | 79931 |
rs776653022 | snp | A/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132526 | ACAAATAACAGGGTA[A/G]ATGATGTGCCTTTGT | 79931 |
rs776658580 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144200 | GCAAGAACCAGTTTT[C/T]GTTTTCTCACAGCAT | 79931 |
rs776688084 | snp | A/G | 6.59196e-05 | 0.00574068 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121138650 | TGTTGTACATCTGGC[A/G]GAAGCTGGTCAAGAG | 79931 |
rs776694723 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157047 | ATCCCCCCGCCCCTT[C/T]GCTTTTATTTGGATC | 79931 |
rs776702259 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190545 | CAGCCTCAGTAAATC[C/T]TATTCTGGGAAAAGG | 79931 |
rs776730625 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203998 | TATTAAAACAAATAT[A/T]GTATTATATATAACT | 79931 |
rs776756062 | snp | A/T | 1.65509e-05 | 0.00287666 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164035 | CTAGATGTGATCAAC[A/T]CATCTCCTAGAAATA | 79931 |
rs776773515 | snp | G/T | 1.97389e-05 | 0.0031415 | missense | TNIP3 | GRCh38.p7 | 4:121154668 | TTCTTCATTTAGGCG[G/T]TCCTTTTCCTTCTGA | 79931 |
rs776780840 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162765 | TTCTAGAAGAGCAGC[C/T]AGGGCACCTCTATTT | 79931 |
rs776920655 | snp | A/T | 0.000132172 | 0.00812827 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142723 | AAAATTAGATCAACA[A/T]ACCTGTTTTAATTGC | 79931 |
rs776920826 | snp | C/T | 1.65214e-05 | 0.0028741 | stop-gained | TNIP3 | GRCh38.p7 | 4:121158730 | CTAAATTGCTGATCC[C/T]ATTGCTGGTTAACTT | 79931 |
rs776924526 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151331 | TGCATTACTATATAA[-/T]ATGGTCATAAAGGTA | 79931 |
rs776950352 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155766 | TTGCAGAAAATAGGT[A/T]ACTTGACATGCAAAA | 79931 |
rs776961765 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223245 | GGCAGATGCTCACCC[A/G]CTTGAAAGGGAAGTA | 79931 |
rs777002996 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121182087 | GTTTTTAATTGGGAG[A/G]ATTACAGAGTTTAAG | 79931 |
rs777006847 | snp | A/G | 1.65647e-05 | 0.00287786 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157269 | CGTTCAAAGACAGCT[A/G]CAGATACCTTCTCTG | 79931 |
rs777029431 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137221 | AGAAAGAAAATATCT[C/T]TAATAGTCATTCCAG | 79931 |
rs777036159 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150824 | CTCTGTTGCGTTGCT[C/T]TTCTGCCCTGGCCTA | 79931 |
rs777043563 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224436 | TGAGCACTGGACTTC[C/T]GATACAGAATCCACA | 79931 |
rs777069511 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180753 | GTGATTGGTCTTATC[A/G]TACAGTGGTGGTTTT | 79931 |
rs777108482 | in-del | -/AA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193806 | ATGACAAGATGCATT[-/AA]AAAAAGTTTCACATC | 79931 |
rs777121423 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170130 | TTCTTTATGATCTCA[G/T]GGTGCTTTGTGAAGC | 79931 |
rs777122767 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211402 | TAATATCCCAAGCCA[A/C]AGCCTACAAGGGATG | 79931 |
rs777143605 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217446 | TACATAGTGTTGGAG[A/G]GTGGCTTTTTATTTT | 79931 |
rs777145528 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121192915 | GCACAATTATTTATT[C/T]CTTAATGAAGCTGGT | 79931 |
rs777158826 | snp | A/C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138916 | TTCTACCACTTTGAG[A/C/G]TTGTGACATATTTTC | 79931 |
rs777172168 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159014 | TGGGAGGCCATGGCA[A/G]GTGGGATCACTTGAG | 79931 |
rs777176224 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170950 | CCTCCCGAGTAGCTG[A/G]GATTACAGGTACCTG | 79931 |
rs777184658 | snp | A/T | 9.04413e-05 | 0.00672402 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142816 | TTAATCAAGACAAGT[A/T]AAAATCATTAATTCC | 79931 |
rs777193311 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214577 | ACCTCTTAGAAATAA[C/T]AGGTTTCTCCCTTCC | 79931 |
rs777283057 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201309 | TCTATGCAAGATGGC[A/G]TGTGGTCAATGGCTG | 79931 |
rs777294219 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213584 | ACAAAAAAATTAGCC[C/G]GGCGTGGTGGCGGGC | 79931 |
rs777299040 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172027 | CATGAGCCACCACAC[A/C]TGGCCCCTATTCCCC | 79931 |
rs777393620 | snp | C/T | 1.75835e-05 | 0.00296504 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141958 | ACCAGTGGGAGAGAC[C/T]GAGGAGTTGCAGTGA | 79931 |
rs777556332 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222395 | GGATGATTGGGTTTA[C/G]AGTCAAAAGATGTGT | 79931 |
rs777563031 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202302 | AATGCAAACAAAAAC[A/G]TAAAGTGGGGAAAGG | 79931 |
rs777567971 | snp | C/T | 1.71513e-05 | 0.00292837 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132713 | AATTAACATTTCATT[C/T]CTCTTCTTCTGGCTT | 79931 |
rs777621200 | snp | C/T | | | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121150103 | CTTCCAGCTTCTCAC[C/T]TGCTGCTTCAGAACT | 79931 |
rs777628030 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121137904 | CTAACTTTTGATTAT[A/G]TATACTTGATGAGAA | 79931 |
rs777645093 | snp | A/G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148797 | CATAACACAATTGCT[A/G/T]AATTTTTCCATGTAT | 79931 |
rs777659363 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221104 | TTCCAAAGCTTGAGA[G/T]ATTTGTTGCCAATAT | 79931 |
rs777698433 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214521 | ATGTAGAAGGAAATG[A/G]CTTGTGAATATGGAG | 79931 |
rs777700126 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135995 | AGGAATTTTTTGGTG[G/T]TGCCCTAACCATGAT | 79931 |
rs777720456 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169034 | TGCTTCTATTTTTGC[G/T]TCCACTCCCCCCTCC | 79931 |
rs777760314 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210224 | TCCTTTAATGAATTA[C/T]AATTTATAATAAAGA | 79931 |
rs777789245 | in-del | -/TAAG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190381 | GCCTCACATACTTAT[-/TAAG]TATTTGACAAGAGAG | 79931 |
rs777821546 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121206404 | TAAGTTAAATTTGAT[C/G]ATAATCAACTTGTTC | 79931 |
rs777852302 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197174 | AAGAGTTAAGAAACT[C/T]GTTGTTTAGCTTTAC | 79931 |
rs777868187 | snp | A/T | 4.95765e-05 | 0.00497853 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121142774 | CATCTGACAAGCTTT[A/T]ATCTAAAGACAAAAC | 79931 |
rs777870833 | snp | A/G | 4.96586e-05 | 0.00498265 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132597 | CAGCCACGCTCCCTC[A/G]TTGCCTGTTGTCTCT | 79931 |
rs777875053 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198777 | GTCTGGAAAATATAA[-/G]TTCAAAGACAGTGTT | 79931 |
rs777970113 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186416 | AATATGATTGACATT[G/T]TCACTGTCACTATAA | 79931 |
rs777979732 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121209355 | TGGTCACTGGACTTA[C/T]AACTGGCCTCTGAAG | 79931 |
rs778033587 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175433 | CTTTTCACTTCAAGT[C/T]TTGGTTGCTTCCCCC | 79931 |
rs778035424 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144391 | TAAATGTTTTCTAAA[A/G]CGTTTTTTTGTTTTT | 79931 |
rs778113938 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121151452 | CTGATATGAATATCA[-/T]TTTTTTTTCAGGAAG | 79931 |
rs778120584 | snp | A/C | 1.65015e-05 | 0.00287237 | missense | TNIP3 | GRCh38.p7 | 4:121157216 | GGAATCTTTCCGCGG[A/C]GTCCAGTTTCGTCTT | 79931 |
rs778150813 | snp | A/G | 1.6507e-05 | 0.00287284 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121164075 | CTCTTTATGCTCCGT[A/G]GAACTTTCTGCGGCA | 79931 |
rs778210581 | snp | G/T | 1.64953e-05 | 0.00287182 | missense | TNIP3 | GRCh38.p7 | 4:121157131 | CGGGTCAGGTCGCGC[G/T]GCCTGTCGTCCTCTC | 79931 |
rs778213233 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198068 | AAGAACTAGAGGATG[C/T]GGATAATAGATGTGT | 79931 |
rs778213287 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133665 | CTGTGGCCAATGAGA[C/T]AATCCACGGCAGAAT | 79931 |
rs778306225 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121223512 | ATGTCCTATAAGAAA[A/T]TCACTTTTGCTACTT | 79931 |
rs778329101 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218013 | ATCTAGGATTAAACA[C/T]CAAACCATCTGACTC | 79931 |
rs778330220 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225636 | GTGTTTAGAAAAAGA[A/G]CTAAAGAGTAAAGTG | 79931 |
rs778337100 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205291 | GTAAAGGTAGCCAGT[A/G]CAAAATCTCTAAGGC | 79931 |
rs778345978 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147042 | ATTATTTTGTTTTGA[-/C]TTGTACCTGGGAATT | 79931 |
rs778349266 | snp | C/G/T | 9.96784e-05 | 0.00705906 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147206 | TGCTGTTACTGTAAG[C/G/T]TTCCTTTTCACTTAA | 79931 |
rs778402002 | snp | A/C | 6.75927e-05 | 0.00581307 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161251 | AGAAGATTGAAACAA[A/C]GCTGTTTACAAAATA | 79931 |
rs778419919 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213522 | ATGAGGTCAGGAGAT[C/G]GAGACCATTCTGGCT | 79931 |
rs778440927 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224252 | CCTGTAATCCCAACT[A/G]CTTGGGAGGCTGAGA | 79931 |
rs778442883 | snp | A/G | 6.59348e-05 | 0.00574135 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138689 | TGATAGTCTGGCTGT[A/G]TGGAACAATACAACA | 79931 |
rs778445390 | snp | G/T | 1.64844e-05 | 0.00287087 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121138629 | GTGGTCTCACCATTT[G/T]CCTTGTGTTGTACAT | 79931 |
rs778461773 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179979 | GTTTAATGAGCCCAG[A/G]ACAGATCCTTGAGTA | 79931 |
rs778465528 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121139743 | CCTTGGCTCCTCTGG[C/T]TTATGAAAAAGCTAG | 79931 |
rs778524000 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170855 | GAATCTTGCTCTGTC[G/T]CTCAAGCTGGAGTGC | 79931 |
rs778645464 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214646 | GTGAAATTTTGCCAA[A/G]CATATGCTTCTGCTA | 79931 |
rs778698872 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121214508 | CTCAGAATTCTCCAT[G/T]TAGAAGGAAATGGCT | 79931 |
rs778751974 | snp | C/G | | | | | GRCh38.p7 | 4:121218965 | AGAACTTTGGGAGGC[C/G]GAGGCAGGTGGATCA | 79931 |
rs778775892 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148504 | GTGTTTTGAACATAA[C/G]CAGTGCTTTTGGTTT | 79931 |
rs778799993 | snp | C/G | 1.69628e-05 | 0.00291224 | missense | TNIP3 | GRCh38.p7 | 4:121154625 | TTTTTCCCTTTAAAA[C/G]TTTATTCTCTTCTTT | 79931 |
rs778822793 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207085 | TGGAAGATCATATTA[A/G]TGAAAATATAGTATG | 79931 |
rs778830130 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121193608 | TGCTAAGACTGGTGG[C/T]TGAAAATTTGATAAG | 79931 |
rs778838570 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219998 | ATGTCCTCATCAGGT[A/G]CTAAACCATCATGAA | 79931 |
rs778852023 | snp | A/G | 1.64909e-05 | 0.00287144 | stop-gained | TNIP3 | GRCh38.p7 | 4:121147141 | TCTCTCGATCCGATC[A/G]TTCCTTTTTGAAGTC | 79931 |
rs778870978 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121201169 | AGTTTTGAGGTATGA[A/G]GAAAGTCCAGAAAAC | 79931 |
rs778873105 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186894 | CTTTATAACATTCTT[A/G]GGAAACCTTTTAGAT | 79931 |
rs778889507 | in-del | -/A | 1.64917e-05 | 0.00287151 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138722 | ATTATAGCAATATGG[-/A]CTTCAAATATAGTGG | 79931 |
rs778892274 | snp | A/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167519 | CCTAGTTATGAAGGA[A/T]TCTGACAAATCCAGT | 79931 |
rs778944301 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121172321 | TGGTTAACTGAGGGT[C/T]TGAGGAGGCCTCAGA | 79931 |
rs778995661 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195647 | AAATTATTTGTTGTT[C/T]TTCATAATCCTCTTT | 79931 |
rs779032597 | in-del | -/AC | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132214 | TTTTTACCCCAGGAA[-/AC]ACACACACACACACA | 79931 |
rs779050482 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135081 | TGGGGAGAGAAGGTC[A/G]AGGGTCCCAGGCAGG | 79931 |
rs779061016 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170483 | GAGCTGGCCTGTTTC[C/T]GTGTATTTTCTTTTT | 79931 |
rs779082801 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179118 | GATTTCCAGAAAGAG[A/T]AAACAGCATGTGAAA | 79931 |
rs779101405 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208636 | TCTTTATTACAATTC[A/C]TCTGTCTTGATAAGT | 79931 |
rs779103930 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135792 | ATTAAAAGGACCGTT[G/T]TAATTAAATGAACCC | 79931 |
rs779110737 | in-del | -/TATGT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186980 | AATTAGTGAAATCAA[-/TATGT]TTCATAAATTTCGAT | 79931 |
rs779194138 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196039 | CTGCATTAAACACCA[A/C]ACGCTTGATTTTATT | 79931 |
rs779255035 | snp | A/G | 3.30639e-05 | 0.00406581 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142779 | GACAAGCTTTTATCT[A/G]AAGACAAAACAAAGG | 79931 |
rs779277005 | snp | A/T | 1.66738e-05 | 0.00288732 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132681 | TGGAAAACAGTAGGA[A/T]AATGTTTTAGATTAA | 79931 |
rs779281918 | snp | C/T | 1.66305e-05 | 0.00288357 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142686 | ATGAGAAATGCTGTA[C/T]ATGGGAATAAATGTA | 79931 |
rs779288107 | snp | A/G | 3.30142e-05 | 0.00406276 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121150190 | GTCCTCGGAAAATGA[A/G]CACTTGATATTCAAG | 79931 |
rs779363492 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184034 | GCCTGGTGCCAAAAA[C/T]GTTGGGGACTACTGC | 79931 |
rs779377810 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224389 | AGAAAAAAGAAAAAA[-/G]AAAAAGAAAAGTTGA | 79931 |
rs779472523 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203645 | CAACTTAGGTCATCT[A/G]ATATAATACATAAAC | 79931 |
rs779481377 | snp | C/G | 1.65315e-05 | 0.00287498 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132613 | TTGCCTGTTGTCTCT[C/G]TCTGTTAGTGTGTAC | 79931 |
rs779482028 | in-del | -/CATATA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121132974 | CATGTGAAAGTAAGT[-/CATATA]TATGACTTAGGTTAG | 79931 |
rs779487428 | snp | A/C | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132032 | ATAGCTTCCAATTAA[A/C]CATCTTATTCAGATT | 79931 |
rs779501164 | snp | A/G | 3.36225e-05 | 0.00410001 | missense | TNIP3 | GRCh38.p7 | 4:121141848 | TCTGCACAGCTCCAG[A/G]GCCTGTTGGTACCCA | 79931 |
rs779525173 | in-del | -/C | 1.72949e-05 | 0.0029406 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141939 | ACAAAACTGTGGGGT[-/C]ACTACCAGTGGGAGA | 79931 |
rs779528962 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121196148 | AAGTAATTTGCTCAC[A/G]GTGAGCTCTTAACCA | 79931 |
rs779550526 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174088 | GGGGACCACTCCATT[G/T]ATGATGGAATCTTTT | 79931 |
rs779567664 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180589 | TGTGATCAATGAGCT[C/T]GGCTATGTTGTGTAA | 79931 |
rs779572762 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226360 | TCATTAAAATTCTGA[A/T]ATAAAAAATACACTA | 79931 |
rs779581537 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160418 | CTGGAGGCAGAGGCT[A/G]CAGTGAGCTGAGATC | 79931 |
rs779584026 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219338 | TTTTCCTCCCTCCTC[A/C]TCCTTTTCCTCTTTT | 79931 |
rs779621172 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169783 | AGGAGAATCGGGGAA[A/T]GGGGTGTCACAGATT | 79931 |
rs779650626 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121192551 | TCCTGAAAAGCTTCT[A/G]TCGAGCTTTAAAACA | 79931 |
rs779734738 | snp | A/G | | | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164302 | AACAGAAGTGACTGT[A/G]GATAGGAATTACACA | 79931 |
rs779756069 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144331 | CTCTTCTAATAGACT[-/A]AAAATAATTTATAAA | 79931 |
rs779805001 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181320 | GGCTGGAAAAAGCAC[A/G]TATTTCCATGAAGGA | 79931 |
rs779819102 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134610 | ATTTAAAATCTTTAG[G/T]TTTTGAAAGAAGGGT | 79931 |
rs779820706 | snp | A/G | 3.33456e-05 | 0.0040831 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164169 | AGCAGAAAGAAAAAC[A/G]GGGGAAAAGTCTCTT | 79931 |
rs779852470 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200035 | TCCCCTCAAAAACCA[C/T]GGTCAGAGGCAGAGC | 79931 |
rs779870188 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140321 | CCTGGATGACAGAGC[A/G]AGATGCCTTCTCAAA | 79931 |
rs779876382 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197396 | AGCTGGGCGTGGTGG[C/T]GGGTGCCTGTAGTCC | 79931 |
rs779908810 | snp | A/G | 1.65023e-05 | 0.00287244 | missense | TNIP3 | GRCh38.p7 | 4:121164085 | TCCGTAGAACTTTCT[A/G]CGGCAATCATTCTAG | 79931 |
rs779946491 | snp | A/G | 1.65658e-05 | 0.00287795 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142793 | TAAAGACAAAACAAA[A/G]GCATTTGTTAATCAA | 79931 |
rs779946930 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138699 | GCTGTGTGGAACAAT[A/G]CAACATTATTATAGC | 79931 |
rs779952224 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199127 | GAAAGCACTGAGCAA[A/G]GAGAGAGAGTGGATA | 79931 |
rs779955811 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211965 | CTGAGTGATTTCCAG[C/T]CTCTAGACACACAAA | 79931 |
rs779955950 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225463 | CTTGTGGATGTACAC[A/G]TGAAAAGTGATTTCT | 79931 |
rs779979391 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121133980 | ATCTTGATTTTTGGA[C/T]ATCTAACCTCCAGAG | 79931 |
rs780015587 | snp | C/G | 1.6588e-05 | 0.00287988 | missense | TNIP3 | GRCh38.p7 | 4:121157111 | CCTCCCGCTGCAGCC[C/G]GTCCCGGGTCAGGTC | 79931 |
rs780030923 | snp | G/T | 3.41064e-05 | 0.00412941 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157059 | CTTTGCTTTTATTTG[G/T]ATCCTCCGGGCTCGA | 79931 |
rs780047732 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213327 | ACACAAAGTCATCTC[A/G]TTCTTCTGAGATGAG | 79931 |
rs780079075 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159532 | CAGCTCTTTTAAAGC[A/G]GAATTTATGCTAACA | 79931 |
rs780104290 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121138056 | ATCAATAAAAAATAA[A/G]ATTTAAAAAAGTACT | 79931 |
rs780203198 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146300 | AAATTTTTTTATGAC[A/G]AAGAATCTTGAAGCT | 79931 |
rs780205031 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149793 | AAAAACCATGTCTAC[A/G]TGAAACTCCCTAGCC | 79931 |
rs780214752 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121187805 | TGCTATGTGTTTATC[G/T]TCTCTTCCTGAAGAT | 79931 |
rs780222993 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219637 | AAGGGCAGGGTGTTC[A/G]TATTACCAGTCATAC | 79931 |
rs780241778 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165937 | AAAACTCTATTGTAA[C/G]AATATTTTTCTTCTG | 79931 |
rs780262876 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121147238 | CCATTTAAATGACTT[C/T]ATTTTAAATGACTGC | 79931 |
rs780280030 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121134946 | TGTGGTCCTCTTCCC[A/T]GCCTGAAGGCTGTCG | 79931 |
rs780317663 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168674 | TGTGTACAACCACAT[C/T]TGGCTATTTTTATCT | 79931 |
rs780325174 | snp | C/G | 1.64904e-05 | 0.00287139 | missense | TNIP3 | GRCh38.p7 | 4:121147053 | TTGACTTGTACCTGG[C/G]AATTCAGCCTGTTCA | 79931 |
rs780355271 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141961 | AGTGGGAGAGACTGA[A/G]GAGTTGCAGTGACAT | 79931 |
rs780423841 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121146483 | GGCAACTTCCTGAGT[C/T]TACTTTAATATGTTC | 79931 |
rs780426779 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180268 | GCCAGATGTGGTGGC[-/G]GGGCGCCTGTAGTCC | 79931 |
rs780442913 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224058 | TAATAATGAATGATC[A/T]CAGCTCTCTGATTTT | 79931 |
rs780530380 | snp | A/C | 8.3757e-05 | 0.00647082 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132697 | AATGTTTTAGATTAA[A/C]AATTAACATTTCATT | 79931 |
rs780546006 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121156281 | TTACACTTTGTTTTT[A/T]CTTACTATACCTAAA | 79931 |
rs780596594 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173864 | TCAAACTCCTGACCA[A/C]AAGTGATCCACCTGC | 79931 |
rs780642390 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215820 | TGAGTATAGGGTCTG[A/T]ATCTGATTCCTCTTC | 79931 |
rs780668815 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121221788 | TTCATATTTCTGAGA[A/T]AGGTGTCAAATCAGG | 79931 |
rs780672628 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143067 | GCTTACTGAATGACA[C/T]TGGAATTGTCAACCT | 79931 |
rs780677917 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183951 | CAGTGCACAATCAAT[A/G]TAATGTGCTTGAAAC | 79931 |
rs780691072 | snp | C/T | 1.67396e-05 | 0.00289301 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164180 | AAACAGGGGAAAAGT[C/T]TCTTAAGGTATATTT | 79931 |
rs780716418 | snp | C/T | 1.65045e-05 | 0.00287263 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138584 | AAGATCCCATTAAGA[C/T]GTAAACATGAAAGAA | 79931 |
rs780720203 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219779 | TTGAGAGGTGTCCAA[A/C]TGTAATTCACATACA | 79931 |
rs780739935 | in-del | -/C | 1.64789e-05 | 0.0028704 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154528 | TTCTCATTTTAATCT[-/C]CCATGCTTGACCTGA | 79931 |
rs780761241 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148940 | GTCTCCCATTGCTAA[C/T]ATGTTACTGACAATG | 79931 |
rs780781013 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162326 | TGTTCTCGTTTCCTT[A/G]GCTTCTTCCTATTTA | 79931 |
rs780822213 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203351 | GAGACCATTATTCTA[A/G]GTGAAGTAACTCAAG | 79931 |
rs780823194 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152414 | AGGGACAGCTTAAAG[C/T]ATAGATGTGGGATGA | 79931 |
rs781072674 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121198875 | TAAAATATACATATA[A/G]CTCTGAGGTATTTAA | 79931 |
rs781089363 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210759 | GGGCACTAATCCTAT[G/T]GTACCAGAGCCCCAC | 79931 |
rs781100446 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197298 | TTTGGGAAGCTGAAG[C/T]GGGTGGATCACCTGA | 79931 |
rs781103221 | in-del | -/AC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121170368 | CCCCTGCTTTTCAGA[-/AC]ACAGTCCAGAACACA | 79931 |
rs781140718 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121188066 | GAACAGGGAATTATG[A/G]AGGCAATATTATTAG | 79931 |
rs781180008 | snp | A/G | 1.74753e-05 | 0.0029559 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141952 | GTCACTACCAGTGGG[A/G]GAGACTGAGGAGTTG | 79931 |
rs781181053 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224041 | TCAATTATAATAATG[A/T]ATAATAATGAATGAT | 79931 |
rs781202603 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212407 | AATAAGATTGAGAGA[C/T]TGCTTTCTTAGTGTG | 79931 |
rs781211428 | snp | C/T | 1.65831e-05 | 0.00287945 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147194 | GAAATATTAGCTTGC[C/T]GTTACTGTAAGCTTC | 79931 |
rs781258524 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121169737 | ACTAGTAAATCACCT[C/G]TCTTTGATCCCCCAA | 79931 |
rs781317666 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121158487 | CTTTCTTTAGCTATT[G/T]CTCAAGACAACTCAC | 79931 |
rs781326626 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121148711 | CTTCACCATCAAATG[C/T]TATAAAATTTTTAGA | 79931 |
rs781343443 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121219514 | ATAGTTCCAAAATAA[A/C]CCAACTTTGAAGGAT | 79931 |
rs781365331 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186634 | ATTAGTGATGCCATA[C/T]GTACAATGCTTAGCA | 79931 |
rs781442693 | snp | C/G | 1.69126e-05 | 0.00290792 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157075 | ATCCTCCGGGCTCGA[C/G]GACCCGGGCCCCGCC | 79931 |
rs781480478 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121197550 | AAAAAAAAAAAAAAA[-/G]AACACCTAAGTTCAA | 79931 |
rs781490471 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160187 | AGAATGAATTAGAAA[-/A]GGAATTACAGGCTGG | 79931 |
rs781550663 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218119 | TTAGATACTGATATA[C/T]TTTAATACTAATATA | 79931 |
rs781552236 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200178 | TAAGGGAGCTTCCTC[-/T]TGCCTTGGTTCTCAC | 79931 |
rs781651434 | snp | C/T | 1.64844e-05 | 0.00287087 | missense | TNIP3 | GRCh38.p7 | 4:121147065 | TGGGAATTCAGCCTG[C/T]TCAACTGGGATTGGG | 79931 |
rs781671288 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121225874 | TGTCTCTTCTACACT[G/T]TGCCACAGGTCTCTT | 79931 |
rs781715758 | snp | A/G | 0.000159562 | 0.00893059 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161231 | ACTTAGAAAAAAAAA[A/G]AGAGAGAAGATTGAA | 79931 |
rs781755983 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154872 | GGATGCACACTAGAA[A/T]TAGGATTGAAGGAAT | 79931 |
rs781781025 | snp | C/G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121140781 | AAAAAAAAGGAAAAG[C/G/T]GGGAGGGAGAGCAGA | 79931 |
rs796070139 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174954 | TTACTTGAGAAAGAA[C/G]GCTTATTGATGCATT | 79931 |
rs796195691 | in-del | -/CTT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162507 | GGCCCGTAATTGGAC[-/CTT]CTTCTTTTGGGGAAG | 79931 |
rs796297608 | in-del | -/CA | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132251 | ACACACACACACACA[-/CA]TATGCACTTTAAATC | 79931 |
rs796502454 | multinucleotide-polymorphism | AG/GT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181623 | TAAGTTAATAAGACA[AG/GT]TGTGTGTGTGTGTGT | 79931 |
rs796521543 | snp | G/T | | | missense | TNIP3 | GRCh38.p7 | 4:121157145 | CTGCCTGTCGTCCTC[G/T]CTCTGCCTGTCGTCC | 79931 |
rs796530077 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168241 | AGACAGAGTCTCGCT[C/T]TGTCACCCAGGCTGG | 79931 |
rs796547548 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121143572 | TGTACTATTTACAGG[A/C]AATTCTTGCTGCTTG | 79931 |
rs796563374 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226885 | CTATAGCACCATGAA[G/T]AACACGGTGAAAAAT | 79931 |
rs796581508 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165660 | AACTTTTTGCTAGTT[-/TG]TGTGTGTGTGTGTGT | 79931 |
rs796594901 | in-del | -/AA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215881 | ATTAGGTGCCACATT[-/AA]AAAAAAAAAAAAAGA | 79931 |
rs796827811 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121215000 | GGAAAATGCTAAATT[A/G]TATACAATTGAAGGC | 79931 |
rs796872066 | in-del | C/TT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161847 | TTTCTTTTCAGTTAT[C/TT]TTTTCAGGAGTGAGA | 79931 |
rs797007483 | multinucleotide-polymorphism | CC/GA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121218767 | TTCCCCTCCCTCAGG[CC/GA]CCTGAGTAGCTGGGA | 79931 |