SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs375325 | snp | C/G | 0.487995 | 0.0765403 | intron-variant | TLE6 | GRCh38.p7 | 19:2992522 | ATGCCTGCAATCCCA[C/G]CACTTTGGGAGGCAG | 79816 |
rs401886 | snp | C/T | 0.198324 | 0.244601 | intron-variant | TLE6 | GRCh38.p7 | 19:2994839 | CCCCTGGTCTCCACC[C/T]GTCAGCTCAAGCATG | 79816 |
rs403048 | snp | A/T | 0.412917 | 0.189626 | intron-variant | TLE6 | GRCh38.p7 | 19:2994612 | TTAATTATTATTATT[A/T]TTTTTTTAGATGGAG | 79816 |
rs417120 | snp | A/T | 0.470521 | 0.117772 | intron-variant | TLE6 | GRCh38.p7 | 19:2978451 | GGAGCCGTGTTTTTT[A/T]AAAAAAATTAAGTGT | 79816 |
rs418667 | snp | A/G | 0.368733 | 0.220005 | intron-variant | TLE6 | GRCh38.p7 | 19:2992165 | ACATAGTGAAACCCC[A/G]TCTCCACTAAAAATA | 79816 |
rs418687 | snp | A/C | 0.118235 | 0.212457 | intron-variant | TLE6 | GRCh38.p7 | 19:2992184 | ccactaaaaatacaa[A/C]aatcagagctgggcg | 79816 |
rs424628 | snp | C/G | 0.153332 | 0.230554 | intron-variant | TLE6 | GRCh38.p7 | 19:2993797 | CCACCGGCGCGGTCC[C/G]CCTCCGCCCTTCCCC | 79816 |
rs428113 | snp | C/T | 0.0567344 | 0.158582 | intron-variant | TLE6 | GRCh38.p7 | 19:2991816 | AGAGTCTTGACCTGA[C/T]TGCCTCCCGATGTCC | 79816 |
rs435806 | snp | C/T | 0.445943 | 0.155262 | intron-variant | TLE6 | GRCh38.p7 | 19:2993429 | CCACTGCCCATTACC[C/T]AGATAATGAGCCTGT | 79816 |
rs439808 | snp | A/G | 0 | 0 | intron-variant | TLE6 | GRCh38.p7 | 19:2994816 | CAAGCATGAAGCATC[A/G]TCTCTTCAAAGAAAG | 79816 |
rs445657 | snp | C/G | 0.34659 | 0.230587 | intron-variant | TLE6 | GRCh38.p7 | 19:2978137 | GCAGTGCCAGGGAAG[C/G]AAGGCACCCGTTACC | 79816 |
rs471344 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | TLE6 | GRCh38.p7 | 19:2993309 | TCCTAGCTGTGCAGC[A/C]CTGGGACAAGCAACT | 79816 |
rs487909 | snp | A/G | 0.258565 | 0.249853 | intron-variant | TLE6 | GRCh38.p7 | 19:2993126 | TGAGGCGGGAGAATC[A/G]CTTAAACCCCAGGAG | 79816 |
rs488127 | snp | A/G | 0.228253 | 0.249052 | intron-variant | TLE6 | GRCh38.p7 | 19:2993187 | ATTGTACTCCAGCCC[A/G]GCAACAGAGCGAGAC | 79816 |
rs488211 | snp | G/T | 0.35445 | 0.227135 | intron-variant | TLE6 | GRCh38.p7 | 19:2977809 | CCTGGCTAACTCCTA[G/T]TCATCCTTCAAAACC | 79816 |
rs504199 | snp | G/T | 0.498706 | 0.0254007 | intron-variant | TLE6 | GRCh38.p7 | 19:2989812 | GGGTGGGAAGGGGAA[G/T]CATCCTGTGCCAGCC | 79816 |
rs522982 | snp | A/G | 0.474903 | 0.109173 | intron-variant | TLE6 | GRCh38.p7 | 19:2984462 | AAAAGAAAGCAAGGC[A/G]AGTGATCCTATCTCT | 79816 |
rs529807 | snp | C/T | 0.434687 | 0.168495 | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2982836 | TAGATGACCCTTTGC[C/T]GGTCAGTTGCTTTGG | 79816 |
rs576938 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE6 | GRCh38.p7 | 19:2980543 | gagatcaagatcagc[C/T]tggccaacatggtga | 79816 |
rs929535 | snp | C/T | 0.349013 | 0.229557 | intron-variant | TLE6 | GRCh38.p7 | 19:2977640 | TTGCCAGGCGTGTTC[C/T]AGGGGGCTGGGGGGA | 79816 |
rs2041972 | snp | C/T | 0.406296 | 0.19512 | intron-variant | TLE6 | GRCh38.p7 | 19:2988514 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGT | 79816 |
rs2052120 | snp | A/G | 0.387263 | 0.208947 | upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2976116 | CGGTGGCTGTCTGAG[A/G]GAGACTGTCCCTGGC | 79816 |
rs2277738 | snp | A/G | 0.0715223 | 0.175059 | upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2976913 | ATAAATGCATAGCCC[A/G]GGGCTGGGACCATCA | 79816 |
rs2277739 | snp | A/G | 0.429087 | 0.174436 | upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2977364 | ACGCGACCCACGTGC[A/G]TAAACGGCCTCGCTA | 79816 |
rs2638068 | snp | C/T | 0 | 0 | intron-variant | TLE6 | GRCh38.p7 | 19:2991048 | atgtgtgtgtgtata[C/T]atatatgtatgtatg | 79816 |
rs3746074 | snp | C/G | 0.00547358 | 0.0520272 | intron-variant | TLE6 | GRCh38.p7 | 19:2989361 | GCTTCTGGGAACAGG[C/G]GGTTTGAGGTTTGAG | 79816 |
rs3746075 | snp | C/G | 0.419135 | 0.184101 | intron-variant | TLE6 | GRCh38.p7 | 19:2989382 | GAGGTTTGAGTCTGG[C/G]AGAGCCCAGATCGTG | 79816 |
rs3803911 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | TLE6 | GRCh38.p7 | 19:2977892 | AGCTTTGGCGACCTT[C/G]CCTGGGCTCCCCCGT | 79816 |
rs4807380 | snp | A/G | 0.417034 | 0.18601 | intron-variant, nc-transcript-variant | TLE6 | GRCh38.p7 | 19:2980271 | AGTGAGTGGTCTAGA[A/G]GCTGCTGGCCCAAGA | 79816 |
rs4807381 | snp | C/T | 0.416218 | 0.186739 | intron-variant | TLE6 | GRCh38.p7 | 19:2981024 | ccactgcaccctagc[C/T]cgggcaacagggtga | 79816 |
rs4807382 | snp | A/C | 0.490943 | 0.0666801 | intron-variant | TLE6 | GRCh38.p7 | 19:2981050 | ggtgagattctgttt[A/C]aaaaaaaaaaaaTTG | 79816 |
rs6510730 | snp | C/T | 0.381267 | 0.212765 | synonymous-codon | TLE6 | GRCh38.p7 | 19:2989699 | CTGCCAGGCCCTGGA[C/T]GCCAACCTGGATGCC | 79816 |
rs7248101 | snp | C/T | 0.129664 | 0.219133 | intron-variant | TLE6 | GRCh38.p7 | 19:2979911 | agagtttgcagtgag[C/T]tgagattgtgccact | 79816 |
rs7248550 | snp | C/G | 0.418169 | 0.184985 | intron-variant | TLE6 | GRCh38.p7 | 19:2988750 | TGATGCTGGGAGAAC[C/G]CAGGTGGGGCAAAGA | 79816 |
rs7252931 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TLE6 | GRCh38.p7 | 19:2989839 | AGCCTCCTGTGGCCA[C/T]CTCTGCCCACCTTAC | 79816 |
rs7259899 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | TLE6 | GRCh38.p7 | 19:2980413 | TCCTGTTCGACATGG[A/G]TTTGTTGGCATTCAA | 79816 |
rs7260215 | snp | A/G | 0.0832709 | 0.186283 | upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2975764 | cattctcccgcctca[A/G]cctcctcagtagctg | 79816 |
rs8101664 | snp | A/G | 0.456332 | 0.141164 | intron-variant | TLE6 | GRCh38.p7 | 19:2979077 | ctgcctcgcctcccg[A/G]gtagctgggactaca | 79816 |
rs8105149 | snp | A/T | 0.0854556 | 0.188216 | intron-variant | TLE6 | GRCh38.p7 | 19:2979486 | tcctgacctcaggtg[A/T]tctgctcacctcggc | 79816 |
rs8108594 | snp | C/T | 0.396909 | 0.202282 | intron-variant | TLE6 | GRCh38.p7 | 19:2994336 | attagctgagccggg[C/T]gcggtggctcacgcc | 79816 |
rs8110576 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TLE6 | GRCh38.p7 | 19:2978128 | TGCGGGTGGGGTAAC[A/G]GGTGCCTTGCTTCCC | 79816 |
rs10402462 | snp | C/G | 0.0829062 | 0.185956 | intron-variant | TLE6 | GRCh38.p7 | 19:2980684 | gagggttgcagtgag[C/G]caggatcacaccatt | 79816 |
rs10405587 | snp | G/T | 0.0821764 | 0.185298 | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2983925 | GCAGGGGGTGAGGGC[G/T]CCAGAGCAAAGGAGC | 79816 |
rs10406955 | snp | C/T | 0.0178446 | 0.0927569 | synonymous-codon | TLE6 | GRCh38.p7 | 19:2993515 | GCTGCAAAGCACCAG[C/T]GGGAGCCAGCGGCAC | 79816 |
rs10407929 | snp | C/G | 0.493893 | 0.0549205 | intron-variant | TLE6 | GRCh38.p7 | 19:2981489 | GGCTCACTCTGGGGA[C/G]GGAGTCCTGAAGCCA | 79816 |
rs10409201 | snp | A/G | 0.360421 | 0.224293 | intron-variant | TLE6 | GRCh38.p7 | 19:2990467 | aaattagccaggcgc[A/G]gtggtgggtacctgt | 79816 |
rs10409231 | snp | A/G | 0.359998 | 0.2245 | intron-variant | TLE6 | GRCh38.p7 | 19:2990499 | gtcccagctactcgg[A/G]aggctgaggcaggag | 79816 |
rs10409387 | snp | C/G | 0.36021 | 0.224397 | intron-variant | TLE6 | GRCh38.p7 | 19:2990502 | ccagctactcgggag[C/G]ctgaggcaggagaat | 79816 |
rs10417362 | snp | C/T | 0.411914 | 0.190483 | intron-variant | TLE6 | GRCh38.p7 | 19:2990600 | gacagagcaagactc[C/T]gtctcaaaaaagaaa | 79816 |
rs10417907 | snp | C/G | 0.0839998 | 0.186933 | intron-variant | TLE6 | GRCh38.p7 | 19:2977632 | GACGTGAGTTGCCAG[C/G]CGTGTTCTAGGGGGC | 79816 |
rs10418234 | snp | C/T | 0.412249 | 0.190198 | intron-variant | TLE6 | GRCh38.p7 | 19:2990935 | gagaagcggagtttg[C/T]ggtgagccaagatgg | 79816 |
rs10419284 | snp | A/G | 0.445196 | 0.1562 | intron-variant | TLE6 | GRCh38.p7 | 19:2991614 | GGCAAGGGGAGGCCT[A/G]GGTGAGGCCAAGGGG | 79816 |
rs10423222 | snp | C/T | 0.404559 | 0.196498 | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2982452 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 79816 |
rs10425071 | snp | C/T | 0.273587 | 0.248885 | intron-variant | TLE6 | GRCh38.p7 | 19:2991717 | CCAACTTTGACACTC[C/T]GTGCAGGCAGAGATT | 79816 |
rs10425323 | snp | C/T | 0.0832709 | 0.186283 | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2983987 | CCTGCCCAGCCCCCA[C/T]TGCAGGGGGCCCCAG | 79816 |
rs10425696 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | TLE6 | GRCh38.p7 | 19:2978867 | TTGCGTCCCAGAGAT[A/G]ACCATTTGTAAATTT | 79816 |
rs10445608 | snp | C/T | 0.225893 | 0.248835 | intron-variant | TLE6 | GRCh38.p7 | 19:2981931 | GAACTGAGATCACAC[C/T]GTACTGCAGCCCAGG | 79816 |
rs10445609 | snp | C/G | 0.317933 | 0.240593 | intron-variant | TLE6 | GRCh38.p7 | 19:2982049 | ACAAAAATTTAAGGT[C/G]GGGGAGTAGGGGCCA | 79816 |
rs10716796 | in-del | -/T | 0.41833 | 0.184838 | intron-variant | TLE6 | GRCh38.p7 | 19:2989955 | TTGGATTTGAGAAAG[-/T]TTAGAGGTGCGGACT | 79816 |
rs11084985 | snp | C/G | 0.116488 | 0.211364 | intron-variant | TLE6 | GRCh38.p7 | 19:2993765 | GTGGGTGCCTGGGCC[C/G]TTCCTCCCCACCCGC | 79816 |
rs11084986 | snp | G/T | 0.485255 | 0.0845871 | intron-variant | TLE6 | GRCh38.p7 | 19:2994887 | AGCTCACTGCCCACT[G/T]CCCCCCCTCCAGGTG | 79816 |
rs11667371 | snp | C/T | 0.21725 | 0.247846 | upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2976726 | CTCCTGTAACCAGCC[C/T]AGCTCTGCCTGAGAG | 79816 |
rs11668186 | snp | C/T | 0.400682 | 0.199487 | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2982894 | ACCCGGCTGTGTTCC[C/T]CTGCGTGTCTGAGTG | 79816 |
rs11671039 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | TLE6 | GRCh38.p7 | 19:2988650 | CCAACACTGGGCTCA[A/G]GGCATTTGGGGAAGA | 79816 |
rs11671928 | snp | C/T | 0.417845 | 0.185278 | intron-variant | TLE6 | GRCh38.p7 | 19:2988541 | AGGTGGAGGTTGCAG[C/T]GAGTTGAGATCGCGC | 79816 |
rs11673024 | snp | C/T | 0.225597 | 0.248806 | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2982295 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGAGG | 79816 |
rs11673337 | snp | C/G/T | 0.5 | 0 | intron-variant | TLE6 | GRCh38.p7 | 19:2992813 | GGGAGGCGGGTGGGG[C/G/T]GGGGGGAGGATGAAC | 79816 |
rs11880300 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2983417 | gagggttgcaattca[A/G]ggtggtcagggaagg | 79816 |
rs11880355 | snp | A/G | 0.465758 | 0.126286 | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2983628 | agtgagaggaggagg[A/G]ggggaggGCAGGCCA | 79816 |
rs11882483 | snp | C/T | | | intron-variant | TLE6 | GRCh38.p7 | 19:2991397 | atatatatatatata[C/T]acacacacacacaca | 79816 |
rs12104274 | snp | C/T | 0 | 0 | intron-variant | TLE6 | GRCh38.p7 | 19:2978332 | AGGGAAACCCGGGCC[C/T]AATGTGGTTCTGCCC | 79816 |
rs12151279 | snp | A/G | | | intron-variant | TLE6 | GRCh38.p7 | 19:2986399 | ccagcctgggtgtca[A/G]agtgagatcttatct | 79816 |
rs12151281 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TLE6 | GRCh38.p7 | 19:2986426 | atctgcaaaaaaGTA[C/G]ATGAAggctgggggt | 79816 |
rs12185515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE6 | GRCh38.p7 | 19:2990325 | atatataaattggcc[A/G]ggcgcagtggctcac | 79816 |
rs12185516 | snp | C/T | 0.41325 | 0.18934 | intron-variant | TLE6 | GRCh38.p7 | 19:2990223 | GGGTAATGAATAAAA[C/T]GAATTTATTCTATTT | 79816 |
rs12460504 | snp | A/T | 0.264632 | 0.249571 | intron-variant | TLE6 | GRCh38.p7 | 19:2985386 | CTAGGTATGCTGTTT[A/T]GCTGCTTGAAGCCTT | 79816 |
rs12610938 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TLE6 | GRCh38.p7 | 19:2986302 | atacctgtaacccca[G/T]ctactcaggaggctg | 79816 |
rs12977724 | snp | A/G | | | intron-variant | TLE6 | GRCh38.p7 | 19:2988171 | GCGGGGTGAGGGGCA[A/G]CGGGAATTCCTTCCT | 79816 |
rs12978022 | snp | A/G | | | intron-variant | TLE6 | GRCh38.p7 | 19:2979809 | ccaggtgtgttgccg[A/G]gggcgggcgggggag | 79816 |
rs12978030 | snp | G/T | | | intron-variant | TLE6 | GRCh38.p7 | 19:2979816 | tgttgccgggggcgg[G/T]cgggggaggggggcg | 79816 |
rs12984261 | snp | A/G | 0.295599 | 0.245806 | intron-variant | TLE6 | GRCh38.p7 | 19:2994349 | ggtgcggtggctcac[A/G]cctgtaatcccagca | 79816 |
rs12985466 | snp | C/T | | | intron-variant | TLE6 | GRCh38.p7 | 19:2992855 | AAAAAGGTAGTGGTT[C/T]TAAGTCTCACTGATG | 79816 |
rs12985900 | snp | C/T | 0.301177 | 0.244706 | intron-variant | TLE6 | GRCh38.p7 | 19:2994287 | tcgagaccagcctgg[C/T]caacatagtgagacc | 79816 |
rs13345150 | snp | A/G | 0.318896 | 0.240319 | intron-variant | TLE6 | GRCh38.p7 | 19:2992113 | ggccaaggtgggtgg[A/G]tcacctgaggtcagg | 79816 |
rs13345170 | snp | C/T | 0.447421 | 0.153379 | intron-variant | TLE6 | GRCh38.p7 | 19:2986194 | cacgtgggaggatag[C/T]ttgaggccaggaatt | 79816 |
rs17681742 | snp | C/G | 0.158302 | 0.232576 | utr-variant-5-prime, nc-transcript-variant, intron-variant | TLE6 | GRCh38.p7 | 19:2977601 | GGCTGACCTCCGCAG[C/G]TTCCGCCCGGTGAGG | 79816 |
rs28562085 | snp | C/G | 0.0755793 | 0.179102 | intron-variant | TLE6 | GRCh38.p7 | 19:2993635 | GCCCCCAGCCTCCCA[C/G]AAGACCCCACCTAAT | 79816 |
rs34080630 | in-del | -/G | | | intron-variant | TLE6 | GRCh38.p7 | 19:2988955 | AAGGCCTGAGAGAGG[-/G]ACCCCAAAATCTGAA | 79816 |
rs34084198 | in-del | -/C | | | intron-variant | TLE6 | GRCh38.p7 | 19:2977891 | AGCTTTGGCGACCTT[-/C]CCCTGGGCTCCCCCG | 79816 |
rs34256455 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2982963 | TCTGCATGGGAGGGG[-/G]CGCCCGGGCTCCCAT | 79816 |
rs34382312 | snp | A/G | 0.0486741 | 0.148216 | upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2975747 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCCGCCTC | 79816 |
rs34402049 | in-del | -/CA/CACA | | | intron-variant | TLE6 | GRCh38.p7 | 19:2991426 | ACACACACACACACA[-/CA/CACA]TATATATAATATATG | 79816 |
rs34438430 | in-del | -/T | 0.302606 | 0.244402 | intron-variant | TLE6 | GRCh38.p7 | 19:2994109 | GTACTGCGGTGGGCT[-/T]GGGGGCAGGACCCGG | 79816 |
rs34441112 | in-del | -/G | | | intron-variant | TLE6 | GRCh38.p7 | 19:2991580 | GCCTCAGAGCTCGGG[-/G]TGGACTCAGGGTGGA | 79816 |
rs34551565 | snp | C/T | 0.403755 | 0.197128 | synonymous-codon | TLE6 | GRCh38.p7 | 19:2994923 | AGAGACGTCACAGCA[C/T]GTGACTGGAGACATC | 79816 |
rs34622024 | in-del | -/A | | | intron-variant | TLE6 | GRCh38.p7 | 19:2981347 | TGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 79816 |
rs34647224 | in-del | -/A | 0 | 0 | intron-variant | TLE6 | GRCh38.p7 | 19:2993942 | AAAAAAAAAAAAAAA[-/A]GGTGGGTGGGGAGGA | 79816 |
rs34655162 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TLE6 | GRCh38.p7 | 19:2983546 | TGTGTGAAGGCCCTG[-/T]AGGCAGGACGGTGCC | 79816 |
rs34723547 | in-del | -/CC | | | intron-variant | TLE6 | GRCh38.p7 | 19:2984351 | GGAGTCCCCCCCCCC[-/CC]GCGGGGCTCCGATGG | 79816 |
rs34738322 | in-del | -/TA/TATACA | 0 | 0 | intron-variant | TLE6 | GRCh38.p7 | 19:2991396 | ATATATATATATATA[-/TA/TATACA]CACACACACACACAC | 79816 |