SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7461 | snp | A/G | 0.331642 | 0.236293 | utr-variant-3-prime | TNIP2 | GRCh38.p7 | 4:2741706 | AAATAGGTGAATAAA[A/G]TAAGTGTGCTTTAAC | 79155 |
rs10587 | snp | C/T | 0.125528 | 0.21681 | utr-variant-3-prime | TNIP2 | GRCh38.p7 | 4:2741951 | CTGGTGTGCCAGCCC[C/T]TCCCCCAGCCTGCCT | 79155 |
rs231175 | snp | A/T | 0.284209 | 0.247648 | intron-variant | TNIP2 | GRCh38.p7 | 4:2753079 | ccctgtctctaaaaa[A/T]ataaaaataaaaata | 79155 |
rs231176 | snp | C/G | 0 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2752669 | GCCTGCAGGAGGTGA[C/G]AAACCTCTCCATTCT | 79155 |
rs231177 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750821 | TCAGCATTTGACCAA[C/T]GCAGGAAGGAGGCTC | 79155 |
rs231178 | snp | C/T | 0.359575 | 0.224707 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750045 | tggacttgagtgatc[C/T]gcctgcctcagcctc | 79155 |
rs232712 | snp | C/T | 0.300707 | 0.244804 | synonymous-codon | TNIP2 | GRCh38.p7 | 4:2742272 | CCTCAGGCATGTGGC[C/T]GAGTGCTGCCAGTGA | 79155 |
rs762856 | snp | A/G | 0.45198 | 0.147323 | intron-variant | TNIP2 | GRCh38.p7 | 4:2745171 | CAGCAAAGCTGCACC[A/G]AGTCCACCTCCGTTC | 79155 |
rs1263496 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP2 | GRCh38.p7 | 4:2754638 | agccaggatggtctc[A/G]atctcctgacctcgt | 79155 |
rs1708989 | snp | C/T | 0 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2755940 | CCCGGGGCCCGCTCG[C/T]TCACCCACCCAGGAC | 79155 |
rs1708991 | snp | C/G/T | 0.000481928 | 0.0155155 | upstream-variant-2KB, synonymous-codon | TNIP2 | GRCh38.p7 | 4:2756248 | CGCGGCAGCTGCGCG[C/G/T]GGGGCCTTCTCCCAT | 79155 |
rs1794377 | snp | C/G | 0.148661 | 0.22854 | intron-variant | TNIP2 | GRCh38.p7 | 4:2755555 | GAGGCGTCACCAGGT[C/G]CTGGTGGAGGTGAGG | 79155 |
rs2269495 | snp | C/T | 0.49115 | 0.0659296 | missense | TNIP2 | GRCh38.p7 | 4:2742360 | GGCATCCTGGCGCGG[C/T]CCAGAGAGGCCAGGG | 79155 |
rs2295498 | snp | C/G | 0.326035 | 0.238157 | intron-variant | TNIP2 | GRCh38.p7 | 4:2747342 | GAGGAGGAGCTGAGC[C/G]TGGCAGAGCTGCCTG | 79155 |
rs2341303 | snp | A/G | 0.492823 | 0.0594727 | intron-variant | TNIP2 | GRCh38.p7 | 4:2745748 | CCAGAGCCCGGATGG[A/G]AGGTCTTCAGGCCAC | 79155 |
rs3208469 | snp | C/G | 0.0846055 | 0.187491 | intron-variant | TNIP2 | GRCh38.p7 | 4:2742562 | CCTGGCTTTGTGACC[C/G]TCAGCACAGCCCACG | 79155 |
rs3733222 | snp | C/T | 0.450483 | 0.149354 | intron-variant | TNIP2 | GRCh38.p7 | 4:2744007 | ATGTAGATGTGATGG[C/T]CCTGGGTGTCCAGTA | 79155 |
rs3733223 | snp | G/T | 0.499035 | 0.0219437 | intron-variant | TNIP2 | GRCh38.p7 | 4:2743781 | CCAGGAGAAGTTTAT[G/T]TAGCTCCTCATCAAG | 79155 |
rs3733224 | snp | A/G | 0 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2743528 | TTCTCCTCCGCATGA[A/G]GGGCACGGGAGAGTC | 79155 |
rs3733225 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TNIP2 | GRCh38.p7 | 4:2743503 | AGAGTCATGGTGGAC[C/T]ATGGGACTAACCCTG | 79155 |
rs3733226 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | TNIP2 | GRCh38.p7 | 4:2743210 | CGAGGGTTGCTCAGT[C/T]CCTAGATGGCACAGC | 79155 |
rs4690055 | snp | A/G | 0.490007 | 0.0699769 | intron-variant | TNIP2 | GRCh38.p7 | 4:2746936 | TGCTGAAACTCCCAC[A/G]GTCCTTCTCTCTCCC | 79155 |
rs4690059 | snp | A/G | 0.445987 | 0.155207 | upstream-variant-2KB | TNIP2 | GRCh38.p7 | 4:2758303 | GAGGCCGAGGCAGGC[A/G]GATCACTTGAGGCCG | 79155 |
rs6600767 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | TNIP2 | GRCh38.p7 | 4:2749319 | GTGGAGTTTCTACCT[A/T]TCCCATCAAAAAAGT | 79155 |
rs6600768 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TNIP2 | GRCh38.p7 | 4:2749181 | gagtttaagaccagc[C/T]tgggctatatatagc | 79155 |
rs6851171 | snp | A/G | 0.451359 | 0.148171 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750078 | tggtggctcgtgcct[A/G]taatcccagcacttt | 79155 |
rs7659351 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | TNIP2 | GRCh38.p7 | 4:2755435 | TGGGGGATGGTGAGG[A/G]GGCACTGGGTTCTGA | 79155 |
rs7690432 | snp | C/T | 0.357024 | 0.225933 | intron-variant | TNIP2 | GRCh38.p7 | 4:2749083 | TAGAATTTggcaggg[C/T]gtggtggctcacacc | 79155 |
rs9291158 | snp | C/T | 0.270621 | 0.249148 | downstream-variant-500B | TNIP2 | GRCh38.p7 | 4:2741288 | AAGCAGGCAGAAAAA[C/T]GTGAAAAGAGAGACT | 79155 |
rs9683949 | snp | C/T | 0.48491 | 0.0855403 | intron-variant | TNIP2 | GRCh38.p7 | 4:2742753 | CCTGGCGTGGTCCAC[C/T]CCCCAGCCCCTTGGT | 79155 |
rs10011484 | snp | A/G | 0.046775 | 0.145601 | intron-variant | TNIP2 | GRCh38.p7 | 4:2754707 | ggcatgagccaccgc[A/G]tccggACCCTTGTGT | 79155 |
rs10937910 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | TNIP2 | GRCh38.p7 | 4:2746098 | TGATTCTGGACACAG[C/G]AATCTAACCTCTGCC | 79155 |
rs10937911 | snp | A/C | 0.493013 | 0.058691 | intron-variant | TNIP2 | GRCh38.p7 | 4:2746135 | AGGGTCAGGAGTCAC[A/C]GAAGCCACAACCCAA | 79155 |
rs10937912 | snp | A/T | 0.492435 | 0.0610346 | intron-variant | TNIP2 | GRCh38.p7 | 4:2749825 | TAAAATGACAATTTT[A/T]TTTTGAGATAGGGTC | 79155 |
rs10937913 | snp | A/G | 0.491936 | 0.0629843 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750698 | TTTTTTTTTTTGATA[A/G]AGACAGGGTGTGGCT | 79155 |
rs11381502 | in-del | -/C/CC | 0.470521 | 0.117772 | intron-variant | TNIP2 | GRCh38.p7 | 4:2755444 | GTGCCTCCTCACCAT[-/C/CC]CCCCCAGGACCCAGT | 79155 |
rs11414404 | in-del | -/G | 0.469839 | 0.119042 | intron-variant | TNIP2 | GRCh38.p7 | 4:2755445 | TGCCTCCTCACCATC[-/G]CCCCAGGACCCAGTG | 79155 |
rs11414405 | in-del | -/C | 0 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2755733 | CCCAGGACCTAGTGT[-/C]CCCTCAACCCCAGGA | 79155 |
rs11728346 | snp | A/C | 0.314301 | 0.241589 | intron-variant | TNIP2 | GRCh38.p7 | 4:2744580 | TTCTCCCACCCCCAC[A/C]GTGACCACTGCCCAC | 79155 |
rs11729691 | snp | A/G | 0.123105 | 0.215401 | intron-variant | TNIP2 | GRCh38.p7 | 4:2745980 | AGAGGATCTCCAGTG[A/G]GGGGGCCCCCAGCTG | 79155 |
rs11939864 | snp | A/G | 0.00947846 | 0.0681864 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750770 | cctcctcctgcctca[A/G]cAGGGGTCACCGTGC | 79155 |
rs11946511 | snp | G/T | 0 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750906 | TAGATCCTGAGGGCG[G/T]GGCTCTCTCTTGCCT | 79155 |
rs13105492 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | TNIP2 | GRCh38.p7 | 4:2747574 | TCTGGGGCGCCCCCC[C/G]ACCTCTGTGATCAGG | 79155 |
rs13111143 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | TNIP2 | GRCh38.p7 | 4:2753720 | TTCGGAGTGTCCTTC[C/T]GGGTCCTTGGTCTGT | 79155 |
rs13121085 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | TNIP2 | GRCh38.p7 | 4:2753612 | GACACCAGGGAACAC[A/G]TGTGAGCGGAACACC | 79155 |
rs13129007 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | TNIP2 | GRCh38.p7 | 4:2754881 | cgggcacgtgccacc[A/G]tgcccggctaatttt | 79155 |
rs13135456 | snp | A/C | 0.0729998 | 0.176553 | intron-variant | TNIP2 | GRCh38.p7 | 4:2744559 | GGAGGAAGCGCCCCA[A/C]CAGGCTTCTCCCACC | 79155 |
rs13137485 | snp | C/T | 0 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2742585 | AAGCCAGGTCTCAGG[C/T]TCCAGCAACCAGAGG | 79155 |
rs13138665 | snp | G/T | 0.0777841 | 0.181223 | intron-variant | TNIP2 | GRCh38.p7 | 4:2748392 | ctgtcgctcaggctc[G/T]agtgcagtggagcga | 79155 |
rs13145281 | snp | A/C | 0.499978 | 0.0033402 | intron-variant | TNIP2 | GRCh38.p7 | 4:2744558 | AGGAGGAAGCGCCCC[A/C]CCAGGCTTCTCCCAC | 79155 |
rs13146313 | snp | C/T | 0.0766824 | 0.180169 | downstream-variant-500B | TNIP2 | GRCh38.p7 | 4:2741333 | gcctacatcttgctc[C/T]gtgctggatgcttcc | 79155 |
rs16843109 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | TNIP2 | GRCh38.p7 | 4:2742677 | GCCCAGACAAGGGGG[C/T]GCTCAGTGAATGACT | 79155 |
rs16843312 | snp | C/T | 0.0177142 | 0.09243 | utr-variant-3-prime | TNIP2 | GRCh38.p7 | 4:2742243 | GAGGCCGCAAGGGCA[C/T]GGGTGAGTCTCGGTC | 79155 |
rs16843316 | snp | A/G | 0.114464 | 0.210071 | utr-variant-3-prime | TNIP2 | GRCh38.p7 | 4:2742256 | CACGGGTGAGTCTCG[A/G]TCACTGGCAGCACTC | 79155 |
rs16843328 | snp | C/G | 0.123452 | 0.215605 | intron-variant | TNIP2 | GRCh38.p7 | 4:2743246 | CCACAGGCTACTGTT[C/G]AAAGGGAACCAGAGG | 79155 |
rs16843335 | snp | G/T | 0.0068583 | 0.058156 | intron-variant | TNIP2 | GRCh38.p7 | 4:2744365 | AAACCTAAGCAGGAA[G/T]AAAAACGCCCTCATA | 79155 |
rs16843344 | snp | A/C | 0.0586789 | 0.160923 | intron-variant | TNIP2 | GRCh38.p7 | 4:2747616 | GATGCTCCCAGCACA[A/C]AGAGGTCTTCCCCAC | 79155 |
rs16843349 | snp | C/T | 0.121022 | 0.21416 | intron-variant | TNIP2 | GRCh38.p7 | 4:2748032 | CAAAAGAAGACCTGG[C/T]GTGGATGCCCCATCA | 79155 |
rs17412860 | snp | C/T | 0.492918 | 0.0590819 | intron-variant | TNIP2 | GRCh38.p7 | 4:2748111 | TACTCACTCAGAAGT[C/T]GGGCATTTGAACTAT | 79155 |
rs17831665 | snp | C/T | 0.305685 | 0.24372 | intron-variant | TNIP2 | GRCh38.p7 | 4:2742794 | TTCAGTTGGACCTAT[C/T]GGCCCCAGGAGACCT | 79155 |
rs28570362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP2 | GRCh38.p7 | 4:2742707 | TGAGGATCACACACA[C/T]GCTCCGTCATGTGCT | 79155 |
rs34228786 | in-del | -/C | | | intron-variant | TNIP2 | GRCh38.p7 | 4:2755793 | ATGCTCCCCCAACCC[-/C]TCAGGAGCCGGGGCC | 79155 |
rs34388908 | snp | A/T | 0.0766824 | 0.180169 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750096 | GCACGAGCCACCACA[A/T]CTGACCTGACAATTT | 79155 |
rs34644790 | in-del | -/A | | | intron-variant | TNIP2 | GRCh38.p7 | 4:2752735 | GGGATGAGCAATAAA[-/A]TATGTAATTGCATAA | 79155 |
rs35009805 | in-del | -/C | | | intron-variant | TNIP2 | GRCh38.p7 | 4:2755499 | GCATTCGCTTATCCC[-/C]TTCAGAACCTTGCAC | 79155 |
rs35326135 | in-del | -/G | | | intron-variant | TNIP2 | GRCh38.p7 | 4:2755125 | ATGGGTGAGGGCTGG[-/G]AAGGGACTCTAGAAC | 79155 |
rs35355125 | in-del | -/T | | | intron-variant | TNIP2 | GRCh38.p7 | 4:2750679 | GTTTTTTTTTTTTTT[-/T]GATAAAGACAGGGTG | 79155 |
rs35410287 | in-del | -/C | | | intron-variant | TNIP2 | GRCh38.p7 | 4:2754031 | AACACTAGTCATCCC[-/C]TGCACTGTGGGACTA | 79155 |
rs35955732 | snp | C/G | | | missense | TNIP2 | GRCh38.p7 | 4:2742417 | TGGGACCCAGTCCCA[C/G]GCCTCCAGCCACCAG | 79155 |
rs35971342 | in-del | -/G | | | frameshift-variant, intron-variant | TNIP2 | GRCh38.p7 | 4:2744853 | TCGGGCTCGTGGGGG[-/G]ATCTGCAGCCCCCTG | 79155 |
rs56128852 | snp | C/T | 0.455621 | 0.142197 | intron-variant | TNIP2 | GRCh38.p7 | 4:2749619 | AGGAAGCTGAAGAGG[C/T]GAGGAAGGGTCCTTC | 79155 |
rs56215402 | snp | A/G | 0.43978 | 0.162738 | intron-variant | TNIP2 | GRCh38.p7 | 4:2755185 | GACACACATGTGTGC[A/G]TACACACACACACCA | 79155 |
rs57232780 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | TNIP2 | GRCh38.p7 | 4:2742792 | TGTTCAGTTGGACCT[A/G]TCGGCCCCAGGAGAC | 79155 |
rs57796386 | snp | C/T | 0.450357 | 0.149522 | intron-variant | TNIP2 | GRCh38.p7 | 4:2748391 | TCTGTCGCTCAGGCT[C/T]GAGTGCAGTGGAGCG | 79155 |
rs57909164 | snp | C/T | 0.121369 | 0.214369 | intron-variant | TNIP2 | GRCh38.p7 | 4:2748633 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 79155 |
rs58303793 | snp | A/G | 0.134119 | 0.221521 | intron-variant | TNIP2 | GRCh38.p7 | 4:2748623 | TCAGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 79155 |
rs58852067 | snp | C/T | 0.154993 | 0.231244 | intron-variant | TNIP2 | GRCh38.p7 | 4:2754720 | GCGTCCGGACCCTTG[C/T]GTCCATTTTTAATTT | 79155 |
rs59776048 | in-del | -/TT | | | intron-variant | TNIP2 | GRCh38.p7 | 4:2748812 | TTTTTTTTTTTTTTT[-/TT]GAGGCAGGGTCTCAC | 79155 |
rs61734614 | snp | C/T | 0.0369631 | 0.130825 | synonymous-codon | TNIP2 | GRCh38.p7 | 4:2745467 | CACCTTCTGTTTTAA[C/T]AGTCGATTTTCTTCC | 79155 |
rs61791171 | snp | A/C | | | intron-variant | TNIP2 | GRCh38.p7 | 4:2755352 | ACGAACCTCAAAATA[A/C]CCCTAAGAGCCCACC | 79155 |
rs71608234 | snp | A/C | 0.5 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2753110 | AAAAAACAAACAAAC[A/C]AAACTAAATCATTAA | 79155 |
rs71644358 | in-del | -/A/ATT | 0.5 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750433 | ATTATTATTATTATT[-/A/ATT]TTATTATTTTAGAGA | 79155 |
rs71644359 | in-del | -/TTATTTTA | 0.5 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750444 | TATTTTATTATTTTA[-/TTATTTTA]GAGACAGGGTCTCGC | 79155 |
rs73080328 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP2 | GRCh38.p7 | 4:2746632 | GCTGCTGATGGGTGC[A/G]GGATGTACTGTCTGC | 79155 |
rs73189423 | snp | C/G | 0.029116 | 0.117091 | intron-variant | TNIP2 | GRCh38.p7 | 4:2747348 | GCTCTGCCAGGCTCA[C/G]CTCCTCCTCCTCATC | 79155 |
rs73791856 | snp | G/T | 0.129664 | 0.219133 | intron-variant | TNIP2 | GRCh38.p7 | 4:2749540 | CCACGTGACAACAAA[G/T]ATAGGAGTGACGTCT | 79155 |
rs73791858 | snp | C/T | 0.0271762 | 0.113356 | upstream-variant-2KB | TNIP2 | GRCh38.p7 | 4:2757732 | CAGAGCGAGTGCCCA[C/T]CCTACCTGGTTGGGC | 79155 |
rs74548850 | snp | C/G | 0.124102 | 0.215993 | upstream-variant-2KB, missense | TNIP2 | GRCh38.p7 | 4:2756073 | GCTGCTCCCGGAAGC[C/G]CGCAACCTGCTCCAG | 79155 |
rs74605152 | snp | C/T | 0.0199697 | 0.0979085 | intron-variant | TNIP2 | GRCh38.p7 | 4:2744371 | AAGCAGGAAGAAAAA[C/T]GCCCTCATACTCTAC | 79155 |
rs74794660 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | TNIP2 | GRCh38.p7 | 4:2742653 | CTTTGCTTCCTGCTG[C/T]GCCCCAGAGCCCAGA | 79155 |
rs75040025 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | TNIP2 | GRCh38.p7 | 4:2745281 | GGACAGGACATGTCC[C/T]GTACGTCGTTTTAAG | 79155 |
rs75666282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP2 | GRCh38.p7 | 4:2750206 | TGAAGCAGGCTCAAC[C/T]AGTCCATCCCACAAG | 79155 |
rs75692427 | snp | C/G/T | 0.0475728 | 0.146896 | intron-variant | TNIP2 | GRCh38.p7 | 4:2752226 | GAAAGGGGGCTGATA[C/G/T]GCCAGGACCAGGCAA | 79155 |
rs76167779 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TNIP2 | GRCh38.p7 | 4:2747181 | CTGTGCCTGCATGCA[C/G]TCAGACACACTGAGC | 79155 |
rs76280223 | snp | A/C/G | 0.0341408 | 0.126114 | upstream-variant-2KB | TNIP2 | GRCh38.p7 | 4:2757970 | GCCTCTGCCTCAACT[A/C/G]TAAAAGGTGCATGTG | 79155 |
rs77122417 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | TNIP2 | GRCh38.p7 | 4:2745797 | CTTATCCCGTCCCAC[C/T]TACCAGTTTGAGCTG | 79155 |
rs77516273 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNIP2 | GRCh38.p7 | 4:2752141 | GAAGGAAAGAAAGAA[A/G]AGAAGAGAAGAGAAA | 79155 |
rs77704885 | in-del | -/AAAA | | | intron-variant | TNIP2 | GRCh38.p7 | 4:2752114 | GTTTAAAAAAAAAAA[-/AAAA]GGAACAAGGAAGGAA | 79155 |
rs77982793 | snp | C/T | 0.0154538 | 0.0865337 | upstream-variant-2KB | TNIP2 | GRCh38.p7 | 4:2757628 | CAAGTGCTTATGGCC[C/T]GGACATTGGGCTACA | 79155 |
rs78433643 | snp | A/G | 0.5 | 0 | intron-variant | TNIP2 | GRCh38.p7 | 4:2752119 | AAAAAAAAAAAAAAG[A/G]AACAAGGAAGGAAAG | 79155 |