SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs908225 | snp | C/T | 0.469346 | 0.119947 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291999 | TCCTTTCACTTCTAA[C/T]CAAAGCTGTGGCCGG | 54472 |
rs2271599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298116 | TTGCAGAAACAGACT[C/T]GTGCTAACCAAGTTC | 54472 |
rs2292635 | snp | C/T | 0.0973687 | 0.197999 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289915 | GTGCACGCTCTGTCC[C/T]TGGAAATCCCACCTG | 54472 |
rs3168046 | snp | C/T | 0.481627 | 0.0940692 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275419 | AATGAAGGTGTCAGG[C/T]GGGACTGGAACGTTC | 54472 |
rs3750920 | snp | C/T | 0.480178 | 0.0975602 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288726 | CTGCCTCAGGGACTC[C/T]GGGATGGTGATGTGG | 54472 |
rs3793962 | snp | C/G | 0.174288 | 0.23826 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278274 | CTCCTCCTGCAGCAG[C/G]AGCTGCAGCAGTGCA | 54472 |
rs3793963 | snp | C/T | 0.176861 | 0.239062 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280678 | TGGGGAGGCGCCGGA[C/T]GCCCCACTTTCCAGG | 54472 |
rs3793964 | snp | C/T | 0.469839 | 0.119042 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280752 | CAGGAGGAGGGAAAG[C/T]GAGGAGGGCCCCAGA | 54472 |
rs3793965 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281477 | TGGGCTCAGACACCA[C/T]GGGAGGCTCTCGGGG | 54472 |
rs3793966 | snp | C/T | 0.495855 | 0.045338 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281718 | ACAGGCCCGAAGCCA[C/T]GCAGCCAGCACCGCG | 54472 |
rs3793967 | snp | C/G | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285002 | CTGGGGTGCTGACCA[C/G]GCCTCTCCACTCCAG | 54472 |
rs3793968 | snp | C/T | 0.126219 | 0.217206 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294063 | TTTCTATGAAAGCCG[C/T]GTGGCTCACAGTGTG | 54472 |
rs3793969 | snp | A/T | 0.487995 | 0.0765403 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297654 | CCGTACTGCGAGAAC[A/T]AGCAGAGCACCCCGG | 54472 |
rs3793970 | snp | C/T | 0.485118 | 0.0849685 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297667 | ACAAGCAGAGCACCC[C/T]GGCTTCACCTCCGGA | 54472 |
rs3817288 | snp | A/C/G/T | 0.00557542 | 0.0525036 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285909 | GGGGCTTAGAGCGCC[A/C/G/T]GGGTGGGGACGTCAT | 54472 |
rs3829223 | snp | C/T | 0.495999 | 0.0445491 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279176 | AACCTGCTCTGCTGA[C/T]AATGAGGGGATGTGG | 54472 |
rs3838783 | in-del | -/G | 0.47767 | 0.103278 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283477 | CGCATGCCTGGGCAT[-/G]GGGGCTGGGGGCTCC | 54472 |
rs4963034 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293207 | AGCCACCTGCGGACA[C/T]GGGGGAGAAGCCGGG | 54472 |
rs4963060 | snp | A/G | 0.299411 | 0.245069 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299830 | CCGTCAAAACGCCCC[A/G]TCCACCAGCCAGGCA | 54472 |
rs4963061 | snp | A/G | 0.333722 | 0.235565 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303350 | CCAGAGAGGGACGGC[A/G]TGTGACGTGGCAGGC | 54472 |
rs4963062 | snp | A/G | 0.332568 | 0.235971 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305411 | CCACGGGCTCTTCAC[A/G]ACACTCAGGGGAGAG | 54472 |
rs5743851 | snp | C/T | 0.0588605 | 0.161139 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310590 | GTACGCTTGTTTATA[C/T]GTAAGATAAAAGCCA | 54472 |
rs5743852 | snp | C/T | 0.0228947 | 0.104514 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310141 | GGGCTCTTCTGGCAG[C/T]GCCTCCATCCCCGTT | 54472 |
rs5743853 | snp | A/G | 0.0215028 | 0.101435 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310128 | AGNGCCTCCATCCCC[A/G]TTCCGTTCACCCGGC | 54472 |
rs5743854 | snp | C/G | 0.385741 | 0.209939 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310024 | TGAGGGAAAGATCGC[C/G]CTGCAGGGGATGTCG | 54472 |
rs5743855 | in-del | -/T/TCCCG/TCCCGGCACCCTTATGGCCCCACAGGTGGAGGC/TCCCGGCACCCTTATGGCCCCACAGGTGGAGGCGG | 0.143457 | 0.22616 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308834 | CCCAGGTGGAGGCGG[lengthTooLong]GGGCCTGCACTCTAG | 54472 |
rs5743856 | snp | A/G | 0.093417 | 0.194889 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308608 | CTGGCAGTTTCTTCT[A/G]TAGCATTAATATTGC | 54472 |
rs5743857 | snp | C/T | 0.0984431 | 0.198823 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308340 | TTACACGTCACATGG[C/T]GAAAGCAGCAAGAGA | 54472 |
rs5743858 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308097 | CAGGCTGTCGTGAGC[A/G]GTACAGTTTTTATCA | 54472 |
rs5743859 | snp | C/T | 0.144296 | 0.226554 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308045 | TGGGTGGAAAAAGTC[C/T]TTTTTCACGATGCTC | 54472 |
rs5743860 | snp | C/G | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308012 | AGGTCCCTGCCCTCG[C/G]GCAGCCCAGTACTGG | 54472 |
rs5743861 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307953 | CACCCTTAACACTGT[A/G]TCCACAAGTCCTGGT | 54472 |
rs5743862 | snp | C/T | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307792 | TGTGGAGCCTACGGG[C/T]CGGCAGAGGTCCTGG | 54472 |
rs5743863 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307682 | AGTGCTCCTTTCTGC[C/T]TAACAGGAGACTCAG | 54472 |
rs5743864 | snp | C/T | 0.332337 | 0.236052 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307641 | GAACCAGCACCCTGC[C/T]GTTGTGTCCTCCTGG | 54472 |
rs5743865 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307373 | GGAGATGTTCTCACA[C/T]GCAGGGCCTGTGCTG | 54472 |
rs5743866 | snp | A/C/G | 0.00597534 | 0.0543715 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307266 | TATTTCAGGGGCACC[A/C/G]CCGTTGACCGGTAAA | 54472 |
rs5743867 | snp | C/T | 0.333722 | 0.235565 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307121 | ACCAACTGTGGCGTT[C/T]AGGATGGCCATGATG | 54472 |
rs5743868 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306926 | TGTTGGGGTGAGGAC[A/G]TGACATCTCTCGGAG | 54472 |
rs5743869 | snp | G/T | 0.0865458 | 0.189163 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306522 | ACACCTGTGGTGCCA[G/T]AGAGGCAGGAGGTTA | 54472 |
rs5743870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306346 | AAGGAGCAGAGGGGC[C/T]GCTAATGGGGTCCTG | 54472 |
rs5743871 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306129 | CGTTTCAAAAAGGCC[A/G]GTATTTTGGAAAGAT | 54472 |
rs5743872 | snp | C/G/T | 0.0494526 | 0.149365 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306002 | CCCTGCGAGGGGTAC[C/G/T]GTGTGGACCCCTGTG | 54472 |
rs5743873 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305980 | ACCCCTGTGAGGAGT[A/G]TCATGGGGGCCCCTG | 54472 |
rs5743874 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305954 | CCCTGCGAGGGGTAC[C/T]GTGCGGGCCCCCGCG | 54472 |
rs5743875 | snp | A/G/T | 0.0215028 | 0.101435 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305939 | CGTGCGGGCCCCCGC[A/G/T]AGGAGTATCGAGGAG | 54472 |
rs5743876 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305919 | GTATCGAGGAGTACC[A/G]TGTGGACCCCTGCCT | 54472 |
rs5743877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305735 | AGTCCAGCTGGAGGC[A/G]GCCTGGCCCCTCCCT | 54472 |
rs5743878 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305698 | CTGAGAGGCCTGTTC[C/G]TGTCCAGGTCCCCTC | 54472 |
rs5743879 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305596 | CTTTATCACTTCTTC[A/G]GTGTTTATTAACTGG | 54472 |
rs5743880 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305547 | GCTTTCCCCATCAAC[C/T]GGTGTCGGCTGGCTG | 54472 |
rs5743881 | snp | C/T | 0.131723 | 0.220251 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305516 | TCCTGAAACACAATT[C/T]GTGAAAGAAAGGCAA | 54472 |
rs5743882 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305475 | TTTCCCTCATCTTCC[C/T]GTACCTCAAGGAGAG | 54472 |
rs5743883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305317 | CTGCTCCTGGGAGGG[C/T]GTCCGTTCCTGCNGA | 54472 |
rs5743884 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305304 | GGCGTCCGTTCCTGC[C/T]GACTGCACCTGAGCC | 54472 |
rs5743885 | snp | C/T | 0.334412 | 0.235318 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305068 | TACTGGCATGGCCAC[C/T]CCAGCTGTCTTTTAG | 54472 |
rs5743886 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TOLLIP | GRCh38.p7 | 11:1304984 | TTTTGTTTAAGACAC[A/G]TGCACCATCGATAGC | 54472 |
rs5743887 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1304909 | TTTTGATGGGAATGC[A/G]CTAGTTTCATCTTTC | 54472 |
rs5743888 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | TOLLIP | GRCh38.p7 | 11:1304815 | TTTTATTTGTCCTAC[A/G]TTTTCTTATTTTTTT | 54472 |
rs5743889 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | TOLLIP | GRCh38.p7 | 11:1304802 | ACNTTTTCTTATTTT[G/T]TTTCTCTCATTGCCT | 54472 |
rs5743890 | snp | A/G | 0.0912534 | 0.193131 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304599 | AATAAATAAAGAAGA[A/G]GTTAATCATTGTCTG | 54472 |
rs5743891 | snp | A/G | 0.101301 | 0.200969 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304158 | GCTGCTGAGCAGCCC[A/G]GGAGTGGATGTCCCT | 54472 |
rs5743892 | snp | A/C | 0.0955749 | 0.196603 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304103 | GCCCTCTGTTTGCTG[A/C]CTTCTGAATACGCTG | 54472 |
rs5743893 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303810 | ggtctcaagtgatcc[A/G]cccacctcagcctcc | 54472 |
rs5743894 | snp | A/G | 0.138207 | 0.223612 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303542 | GCCCTGTTTCTTTGC[A/G]CAGCGCCTCCTGCCG | 54472 |
rs5743895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303292 | TGACTGGCTTTTGTT[C/T]CATCTGAATGAGAAG | 54472 |
rs5743896 | snp | C/G | 0.0588605 | 0.161139 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303195 | TTCCTGGCAGAGACC[C/G]CATTTAAAGTCGCTT | 54472 |
rs5743897 | snp | A/C | 0.127599 | 0.217986 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302839 | GGGCTGCTGAGCGGC[A/C]GTGGGAGGAGGATGT | 54472 |
rs5743898 | snp | C/T | 0.0952156 | 0.196321 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302514 | CAGCAGCTGAGTGGG[C/T]ATGGGGAATTGCAGT | 54472 |
rs5743899 | snp | A/G | 0.44858 | 0.151875 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302334 | TCTCTGAAACCCTGC[A/G]CACTGAGGGGTCAGT | 54472 |
rs5743900 | snp | C/G | 0.127944 | 0.218179 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302054 | CAAGGCAGGGCCAGC[C/G]CCTCAGACACAGCAG | 54472 |
rs5743901 | snp | C/T | 0.332568 | 0.235971 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301982 | CTGGACCAACTGTGC[C/T]GTTCTATGTGAGTCC | 54472 |
rs5743902 | snp | A/G | 0.484561 | 0.0864924 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301981 | TGGACCAACTGTGCT[A/G]TTCTATGTGAGTCCT | 54472 |
rs5743903 | snp | C/T | 0.0352966 | 0.128072 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301806 | CCTTTAGCCACGAGC[C/T]CAGCCCAGGTCTTCC | 54472 |
rs5743904 | snp | A/G | 0.334871 | 0.235153 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301568 | GAGGAAACTTCTGGG[A/G]TTTGGCGGCCGTGTG | 54472 |
rs5743905 | snp | C/G | 0.0912534 | 0.193131 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301483 | GGGTTTTCTGGGTGT[C/G]CCAGCACATGGATAC | 54472 |
rs5743906 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301458 | GGATACGGAGTTCTC[A/G]GAAGCCCGCGACACA | 54472 |
rs5743907 | snp | C/T | 0.334871 | 0.235153 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301391 | GGGTGGGCAGGCGCC[C/T]GCGGATGCCGTTTGT | 54472 |
rs5743908 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301355 | atcctcagtgctggt[C/G]tgagactctggcttg | 54472 |
rs5743909 | snp | A/C | 0.333491 | 0.235646 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300805 | GGCCAGCCGTGCTTC[A/C]GGGGCGACTGTGGTG | 54472 |
rs5743910 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300763 | GGTGATGTCTCCTGG[A/C]AGGCGTGAGGCCAGG | 54472 |
rs5743911 | snp | A/G | 0.495745 | 0.0459295 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300719 | AGGACTCCACGTCCT[A/G]GGCTGAGCTGGGCTC | 54472 |
rs5743912 | snp | A/G | 0.0681886 | 0.171594 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300639 | CTCTCAGTCGGAAAC[A/G]TATTCCTAACAGGTG | 54472 |
rs5743913 | snp | A/C | 0.0490535 | 0.14873 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300456 | ATTAAGACTTTATTT[A/C]TGTGCCAAAACTAAA | 54472 |
rs5743914 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300379 | GACCTCTTTTCTTTC[A/G]TGTGGAAAGGTANGC | 54472 |
rs5743915 | snp | C/T | 0.489083 | 0.0730708 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300366 | TCGTGTGGAAAGGTA[C/T]GCTGCAGTGGTTTAG | 54472 |
rs5743916 | snp | G/T | 0.0228947 | 0.104514 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300145 | CTCTGTGGGATGAGA[G/T]CCCTACCCTGTCCTT | 54472 |
rs5743917 | snp | C/T | 0.0861826 | 0.188849 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300109 | TTTAAAAGTAATTCA[C/T]GAATGTTTTTAAAAA | 54472 |
rs5743918 | snp | A/G | 0.0785177 | 0.181917 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300108 | TTAAAAGTAATTCAC[A/G]AATGTTTTTAAAAAG | 54472 |
rs5743919 | snp | A/G | 0.107694 | 0.205546 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299900 | AGTCTCCATGTGTTC[A/G]CGGCAGGGACCGCCG | 54472 |
rs5743920 | snp | C/T | 0.127599 | 0.217986 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299868 | CTCCTGGTGAGGCCG[C/T]GTGGCGATGCGCTGG | 54472 |
rs5743921 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299719 | TGTTGGCCTTCACAC[A/G]GGCATTTAGACTTGT | 54472 |
rs5743922 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299442 | TCACTGAAACGATAG[A/G]GTTTACTTCAGCACC | 54472 |
rs5743923 | snp | C/G | 0.127599 | 0.217986 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299264 | CAGTATTTGTACGGG[C/G]AGGACTGAAGCCTGG | 54472 |
rs5743924 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299043 | GCTGGGGGCATGACT[A/G]TTGGCTCCAGGTTTT | 54472 |
rs5743925 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298599 | AAATGACACTTGATC[A/C]TTAGGCCTTTGGATA | 54472 |
rs5743926 | snp | A/G | 0.021333 | 0.101051 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298511 | AGTGCAGAGCAAGGA[A/G]ATGGAGCGCTGGACG | 54472 |
rs5743927 | snp | C/G | 0.0228947 | 0.104514 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298286 | CTGTCTGTCCCCTAC[C/G]TGTGCCCAGGAGGGC | 54472 |
rs5743928 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298263 | AGGAGGGCACGAGCC[A/G]CCTGTCTGTCTGCCA | 54472 |
rs5743929 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298128 | TGTTAGTCCTGAGAA[C/G]TTGGTTAGCACGAGT | 54472 |
rs5743930 | snp | A/G | 0.0341408 | 0.126114 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297818 | GTTGAGCTGTACAGC[A/G]CCTCGAGAGAGGCTG | 54472 |
rs5743931 | snp | A/G | 0.137187 | 0.223099 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297665 | CGGAGGTGAAGCCGG[A/G]GTGCTCTGCTTGTTC | 54472 |
rs5743932 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296450 | GCCGCTGCAGGTGTG[C/T]GGGTGGTTTCGGGAT | 54472 |
rs5743933 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296109 | GGGCACACATGGTGC[A/G]AGGGAGACCCTTTAA | 54472 |
rs5743934 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295327 | GGCAGCTGGAGGAGG[C/T]GCGGCCGGCACCCCC | 54472 |
rs5743935 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295228 | CCACAGAGCAGCCCT[C/T]GGTCAGCCTCGGGGC | 54472 |
rs5743936 | snp | C/T | 0.387074 | 0.209071 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295201 | GGGCCGGCCCGTGGT[C/T]GCTTAGTGGTCTTTC | 54472 |
rs5743937 | snp | C/T | 0.441432 | 0.160792 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295157 | AATCGGCAGATTGAA[C/T]GCCGATTTTGATCAC | 54472 |
rs5743938 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293797 | TCACCCGTCCTCAGC[C/T]GCCACCTCCTGGCAG | 54472 |
rs5743939 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293519 | CTCTTGGCTTCTGGG[C/T]GGCCACACAGGTGGT | 54472 |
rs5743940 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293243 | CTCCGTGTGCCCAAG[A/G]TGGAGCTCTCGGGCC | 54472 |
rs5743941 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293189 | TCCGCAGGTGGCTGC[C/T]CCACACTCTGGAAGC | 54472 |
rs5743942 | snp | C/T | 0.475348 | 0.108251 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292798 | CGCCGTCTGCTGCGC[C/T]GTGTGTCTGCCGCGC | 54472 |
rs5743943 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292698 | TCTCTTGCCCGTTGT[C/G]GGGGAGGCAGCGGTG | 54472 |
rs5743944 | snp | A/G | 0.252421 | 0.249988 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292679 | GAGGCAGCGGTGCCC[A/G]TGTGTCCCCACGGTG | 54472 |
rs5743945 | snp | A/G | 0.0210502 | 0.100409 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292588 | GATGCTTCCATAAAC[A/G]TNGAGGAGGTCACTT | 54472 |
rs5743946 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292586 | TGCTTCCATAAACNT[C/T]GAGGAGGTCACTTCA | 54472 |
rs5743947 | snp | A/G | 0.182296 | 0.240658 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292434 | ATGTGAGCAGGCATC[A/G]GTGACAGGCACGGGC | 54472 |
rs5743948 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292407 | GGGCATGCTGGCAGG[A/G]GAGTCCCATGTGCCA | 54472 |
rs5743949 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292398 | GGCAGGGGAGTCCCA[C/T]GTGCCACCCAGAAAG | 54472 |
rs5743950 | snp | A/C/T | 0.00319098 | 0.0398384 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290892 | GGAGGAAAGCAGCCA[A/C/T]GTGGNGTCTGAATTA | 54472 |
rs5743951 | snp | C/T | 0.0912534 | 0.193131 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290887 | AAAGCAGCCACGTGG[C/T]GTCTGAATTATGTGC | 54472 |
rs5743952 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290684 | ATGGTGGGTGAGTGG[C/T]GGCCTCAGCTGTGTC | 54472 |
rs5743953 | snp | C/T | 0.00826041 | 0.0637336 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290202 | ACGTGCCAGCTATTA[C/T]GGAGGCTGCACGTGG | 54472 |
rs5743954 | snp | A/G | 0.0121054 | 0.0768516 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290180 | TGCACGTGGCTGAGC[A/G]TGGCTGCCGTGGGGA | 54472 |
rs5743955 | snp | A/C | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289967 | CAGCGTGCACGTGTC[A/C]CCTCCGCTGGGCGCA | 54472 |
rs5743956 | snp | A/G | 0.0364509 | 0.129988 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289888 | GCACGTGTCCCCTCC[A/G]CTGGGCACTGATCTG | 54472 |
rs5743957 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289798 | GGCACTCGTCTGGCC[A/G]CTCACCAGCAGGTGG | 54472 |
rs5743958 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289627 | TTTCCAGGGACAGAG[C/T]GTGCATGTGTCCGCC | 54472 |
rs5743959 | snp | C/T | 0.182296 | 0.240658 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289603 | GTCCGCCCCGCTGGG[C/T]GCACAGGGTCCGGCC | 54472 |
rs5743960 | snp | C/T | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289588 | CGCACAGGGTCCGGC[C/T]GCTCACCAGCAGGTG | 54472 |
rs5743961 | snp | A/G | 0.0919752 | 0.193722 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289484 | AGGGTCCTGAGTCCC[A/G]TCCGTGGCTGCACCT | 54472 |
rs5743962 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289392 | TGGTCCTGGCACCTC[G/T]CACCTGTGGCATTGT | 54472 |
rs5743963 | snp | A/G | 0.18325 | 0.240924 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289351 | ACTGGGTGGGGGCCG[A/G]GGAGCAGTGTGGGGC | 54472 |
rs5743964 | snp | C/T | 0.0912534 | 0.193131 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289312 | CAGCAGACGGCCAGC[C/T]CTCCCTGCCTGGGCC | 54472 |
rs5743965 | snp | C/T | 0.0898077 | 0.191933 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289309 | CAGACGGCCAGCCCT[C/T]CCTGCCTGGGCCCTG | 54472 |
rs5743966 | snp | C/T | 0.0908922 | 0.192833 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289039 | GCAGCCCAGGGCCCT[C/T]GCTTTCCCCAGCCCC | 54472 |
rs5743967 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288934 | CGATCGTGAAGCCTG[C/T]GCTGCCCGAGGGGTC | 54472 |
rs5743968 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288914 | CCCGAGGGGTCTCAT[C/T]GATGGGGTGTTGGTG | 54472 |
rs5743969 | snp | C/T | 0.00318214 | 0.0397611 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288781 | CTCCCTCTTGTCTCC[C/T]GCAGAGAGCCTTCTC | 54472 |
rs5743970 | snp | A/G | 0.109108 | 0.206518 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288553 | GGGCTATGCCGCCCC[A/G]CAGACACCCTTGTCT | 54472 |
rs5743971 | snp | C/T | 0.0210502 | 0.100409 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288545 | CCGCCCCNCAGACAC[C/T]CTTGTCTCTTTCCTG | 54472 |
rs5743972 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288325 | GGCCCCTGTGTCCTC[A/G]GAGGACCCCCACAGC | 54472 |
rs5743973 | snp | A/C | 0.111576 | 0.20818 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288217 | CCAGGCTCCTCCCCA[A/C]AGGGCAGGCATTGGC | 54472 |
rs5743974 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288201 | AGGGCAGGCATTGGC[C/T]GTGGTGTGGCAGGGC | 54472 |
rs5743975 | snp | C/T | 0.0215028 | 0.101435 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288109 | TGGCTGTGGGGCCAG[C/T]ACGTCAGCGCCCTGG | 54472 |
rs5743976 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286258 | GGAGCAGGGCCCAGC[A/G]TCCCCTGTGCACTCA | 54472 |
rs5743977 | snp | C/T | 0.000368019 | 0.01356 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286105 | CCCCGGGACCATCTC[C/T]GCTGTGTTTCAGCTG | 54472 |
rs5743978 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285892 | GGTGGGGACGTCATC[C/T]ATTCTAGAATCCTGT | 54472 |
rs5743979 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285656 | CCCTGTCAGGTGACA[C/T]GTGCTCTGCACTGTG | 54472 |
rs5743980 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285591 | GCGTGCCCTGCGCTG[C/T]GCCGTTGTGTCTGAA | 54472 |
rs5743981 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285571 | TTGTGTCTGAACCTC[A/C]CGCTCCTGTTGGGTG | 54472 |
rs5743982 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285401 | CTGCTGGTGCAAGAC[C/T]GGCCCCCACCATGGA | 54472 |
rs5743983 | snp | A/G | 0.084364 | 0.187256 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285280 | GAGGTGGCCTCTCTC[A/G]TTCTGGGGAGCTGGT | 54472 |
rs5743984 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285054 | GAGCTGCTGGCAGGC[A/G]AGAGTGCTGTGAGGC | 54472 |
rs5743985 | in-del | -/GAG | 0.0966517 | 0.197444 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284877 | GACGATGGGAAGGAG[-/GAG]ACGGCACTGGGAGAC | 54472 |
rs5743986 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284656 | GTCTTAGAAAACCAC[C/T]AGCCTGGGGGTGGGT | 54472 |
rs5743987 | snp | A/G | 0.147656 | 0.228091 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284616 | CATGCCTCTAATCCC[A/G]GCACCTTGGGAGGCC | 54472 |
rs5743988 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284509 | ACAAACAAATTAGCC[A/G]GGCGCGGTGGTGGGC | 54472 |
rs5743989 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284409 | gtgagccgagattgc[A/G]ccactgcactccagc | 54472 |
rs5743990 | snp | A/G | 0.0210502 | 0.100409 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284071 | CCCAGAGTGGCTCCT[A/G]GAGGTTCTGATTTGT | 54472 |
rs5743992 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283444 | TCCAATAAGCAGGGG[C/T]GTCCCTGGCACAGTA | 54472 |
rs5743993 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283110 | TGGTGTGACTTGCTC[A/G]TCCCTCACGGCGGGC | 54472 |
rs5743994 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282865 | ATCCATGTGCCATGT[C/T]GGTGTGCTGCACCCA | 54472 |
rs5743995 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282730 | gtgcaggtttgttac[A/G]tatgtatccgtgtgc | 54472 |
rs5743996 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281508 | GGGCTCACTGTGCAC[A/T]TTAGGTGGGCTCAGG | 54472 |
rs5743997 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281067 | AGGAAACATCTAGGC[A/G]TGAAGCATCTGGAGA | 54472 |
rs5743998 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281047 | GCATCTGGAGACCGC[A/G]TGGCCTCATGAAGCA | 54472 |
rs5743999 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280753 | CTCTGGGGCCCTCCT[C/T]ACTTTCCCTCCTCCT | 54472 |
rs5744000 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280557 | TTCCCTCGTGCACCT[C/G]CATTTCACACGGGCC | 54472 |
rs5744001 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280477 | GTCCCTCCCGTCATC[C/T]TGGCCTGCGTCTCTG | 54472 |
rs5744002 | snp | A/G | 0.497445 | 0.0356514 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280458 | CCTGCGTCTCTGTGG[A/G]CACAACCCCCACTGG | 54472 |
rs5744003 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279564 | CCGCCCATCACTCCT[C/T]CCAGGGCCGCTACAG | 54472 |
rs5744004 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279556 | CACTCCTNCCAGGGC[C/T]GCTACAGGTGGGCTC | 54472 |
rs5744005 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279463 | CAGGCCCCAGAGCTC[C/T]TGGTCTGTCCTCCTG | 54472 |
rs5744006 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279286 | CCCCTCAGCCCACAC[C/T]GTGGAAGCACCCACC | 54472 |
rs5744007 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278764 | CACCTGGCCATGGTT[C/T]GGTTCGTTTTCCGTC | 54472 |
rs5744008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278651 | GGGTGTGGAGGAAAG[A/G]TGGGCCTGGCCCTGA | 54472 |
rs5744009 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278527 | GAGTCCTGGCCTTTG[C/G]AGCAGGTGCAGGAGG | 54472 |
rs5744010 | snp | C/T | 0.0210502 | 0.100409 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278499 | AGGCTTGGTGGCAAG[C/T]CCTGTCTGCTCCGTT | 54472 |
rs5744011 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278453 | CTTGTTGCTGGTGTT[A/G]GTTCAGGCCAGGATT | 54472 |
rs5744012 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278161 | CCTGTGCTCAGGGCT[G/T]CTCGTGGTTTTAGGG | 54472 |
rs5744013 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277735 | AAAGCATCTTCTAGA[A/G]TGCCTGATAAAGGAA | 54472 |
rs5744014 | snp | C/G | 0.0905309 | 0.192535 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277309 | CTTCAGCAGGAGCTA[C/G]TGTGGCACTTCTGGA | 54472 |
rs5744015 | snp | G/T | 0.0789902 | 0.182367 | missense, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277200 | GCCCTGCCCCCGGCC[G/T]CCGTGAACGCCCAGC | 54472 |
rs5744016 | snp | C/T | 0.0013547 | 0.0259907 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277135 | GGACATGTTCCCCAA[C/T]ATGGACCAGGAGGTG | 54472 |
rs5744017 | snp | C/T | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276986 | GACACGCCGACCCGG[C/T]GCTCCCCAAGGAATG | 54472 |
rs5744018 | snp | G/T | 0.0144158 | 0.0836666 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276845 | GCGGTCCAGGACGGG[G/T]CGGGGGCTCCCCTCC | 54472 |
rs5744019 | snp | G/T | 0.000284374 | 0.0119208 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276744 | CTGGAAAATGCTCTT[G/T]CTGTAGAGAGCAGCT | 54472 |
rs5744020 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276343 | CTGATTGCCAGCCAG[C/T]GGGCNTCTGAAGCCG | 54472 |
rs5744021 | snp | A/G | 0.0210502 | 0.100409 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276338 | TGCCAGCCAGNGGGC[A/G]TCTGAAGCCGGGTCC | 54472 |
rs5744022 | snp | C/T | 0.0210502 | 0.100409 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276127 | TTGGGAGCTGCTGTG[C/T]CCAGNANGTGGGTTC | 54472 |
rs5744023 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276122 | AGCTGCTGTGCCCAG[A/G]ACGTGGGTTCAGCGT | 54472 |
rs5744024 | snp | C/T | 0.0970103 | 0.197722 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276120 | CTGCTGTGCCCAGGA[C/T]GTGGGTTCAGCGTGG | 54472 |
rs5744025 | snp | A/G | 0.0142736 | 0.0832652 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276105 | CGTGGGTTCAGCGTG[A/G]GCGAGGAAAGCCTGG | 54472 |
rs5744026 | snp | C/T | 0.021333 | 0.101051 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276089 | GCGAGGAAAGCCTGG[C/T]GAGCGTGGCCCTGTA | 54472 |
rs5744027 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276058 | AAAGCTTTCTGAGGC[A/G]GGAGGCNCTCACTTA | 54472 |
rs5744028 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276051 | TCTGAGGCGGGAGGC[A/G]CTCACTTACCTCTGA | 54472 |
rs5744029 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275941 | AGAAGCTTCTCACAA[A/G]TGATGCACTTTAAAT | 54472 |
rs5744030 | snp | C/T | 0.0225045 | 0.103662 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275521 | TATTTGTTCAGCAGA[C/T]GCCGACCACTCAGAC | 54472 |
rs5744031 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275388 | TAGATGGTATGTTCC[A/G]TGATATTAACAACTC | 54472 |
rs5744032 | snp | A/C | 0.093777 | 0.195178 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275133 | CACACAGTGGGGGCC[A/C]GCCTCGCTGGAGGGA | 54472 |
rs5744033 | snp | C/G | 0.134802 | 0.221877 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275033 | TTTTAATAGACAAAT[C/G]ACATTTTGCAAGGCC | 54472 |
rs5744034 | snp | C/T | 0.134802 | 0.221877 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275007 | AGGCCTTTAATTAAA[C/T]AAGATTCTTCTTTCC | 54472 |
rs5744035 | snp | A/C | 0.0201999 | 0.0984476 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274832 | TGGATGAGGTCGTCA[A/C]ACTCAGAAGGACAGG | 54472 |
rs5744036 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274596 | AGAAGACAGGTCGCC[A/G]GAGGCTCCCCCTCCT | 54472 |
rs5744037 | snp | A/G | 0.0916144 | 0.193427 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274366 | GGGAAGGTTTACCAT[A/G]TTTGTTCCCGAGTAT | 54472 |
rs5744038 | snp | A/G | 0.153332 | 0.230554 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274206 | GAGGAGGGAAGTCCC[A/G]GGTGCTCCTCCCTCA | 54472 |
rs5744039 | snp | A/C | 0.0337553 | 0.125452 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274104 | CTTTTCATTTCCAGG[A/C]CATTTCCATCTGGGA | 54472 |
rs6578971 | snp | A/T | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287394 | GCAGCTCCCTGCTGC[A/T]GCCTCCCCGCCGCAG | 54472 |
rs7105761 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287465 | ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC | 54472 |
rs7105782 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287535 | AGCCTCCCCGCCGCA[C/G]CCTCACCGCCGCAGC | 54472 |
rs7107064 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305419 | TCTTCACAACACTCA[A/G]GGGAGAGAAAGCCCA | 54472 |
rs7108920 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287479 | AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC | 54472 |
rs7108928 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287493 | ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs7481348 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294235 | CCTTTCCCTGCATTT[C/T]TACGAAAGCCCGCGT | 54472 |
rs10839956 | snp | C/T | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279685 | TCACGTTCTTCACGC[C/T]GTGTGAATCTGCTGT | 54472 |
rs10840239 | snp | A/G | 0.461481 | 0.133325 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294352 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs10909565 | snp | A/G | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294631 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs11041743 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280987 | CTGCTGTTGCCAGCC[C/T]GGCGGAGAGTCTCTG | 54472 |
rs11042045 | snp | C/T | 0.123798 | 0.215808 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287015 | CGAAACTGTCAGCTG[C/T]GGATAAGTCACTGCA | 54472 |
rs11042249 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292478 | CTTCTGCCACACTCA[A/G]CGTCATCCTCTCATT | 54472 |
rs11042368 | snp | A/G | 0.277778 | 0.248452 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294537 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs11042394 | snp | C/G | 0.277778 | 0.248452 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294903 | TTCTACGAAAGCCCG[C/G]GTGGCTCACAGTGTG | 54472 |
rs11042484 | snp | A/G | 0.127254 | 0.217792 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297082 | GGGGCCCCGGTCAGC[A/G]CCAGTGCCCTGGGCA | 54472 |
rs11042542 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299007 | caggggacagtcatc[A/G]aaaaaccaggacagc | 54472 |
rs11042781 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303935 | cagctactcgggagt[C/T]tgaggcaggaaaatc | 54472 |
rs11042783 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303950 | ctgaggcaggaaaat[C/T]gcttgaacctgggag | 54472 |
rs11043006 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308848 | GCCCGCCTCCACCTG[G/T]GGGGCCATCAGGGTG | 54472 |
rs11607136 | snp | A/G | 0 | 0 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274292 | TCCCAGTCTGTTGAC[A/G]AGTGAACTCTGATTC | 54472 |
rs11608022 | snp | A/C | 0.24449 | 0.249939 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287820 | CCCCGCCGCAGCCTC[A/C]CCGCCGCACCCTCCC | 54472 |
rs12278738 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286199 | CGCCAGCCCAGAATC[A/G]CCCTCCCCATGCCAG | 54472 |
rs12279847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299006 | gcaggggacagtcat[C/T]gaaaaaccaggacag | 54472 |
rs12280761 | snp | C/T | 0.324855 | 0.23853 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291965 | TCTGTTTTCTATTCT[C/T]GTCCACATACAAGTT | 54472 |
rs12290986 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303822 | gggcggatcacttga[A/G]accaggagttcgaga | 54472 |
rs12294518 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292185 | TGCTGCACACCCACA[C/T]ATCTGCTAGATCAGC | 54472 |
rs12365946 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292253 | CAACTGCCCTATTTT[C/T]TGGAGAGTATGTAGC | 54472 |
rs12421317 | snp | A/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306627 | GGGTAAAGGCCCACT[A/G]TGGGTTAATTCAGAG | 54472 |
rs12785349 | snp | C/T | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294786 | CGGTGTGTCTCCTTT[C/T]CCTGCATTTCTACGA | 54472 |
rs12788138 | snp | C/T | 0 | 0 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309750 | CCTCTCGCCCGGCGC[C/T]TGCGCACCTGCTCTC | 54472 |
rs12789854 | snp | A/G | 0.492337 | 0.0614248 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294960 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs12793865 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294572 | ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG | 54472 |
rs12793909 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294619 | ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG | 54472 |
rs12793917 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294638 | TGGCTCACGGTGTGT[C/T]TCCTTTCCCTGCATT | 54472 |
rs12795602 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281073 | GATGCTTCACGCCTA[A/G]ATGTTTCCTTAAAAT | 54472 |
rs12796761 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308915 | CGGGGCCCGCCTCCA[C/T]CTAGGGTGCCATCAG | 54472 |
rs12800885 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308904 | CCATCAGGGTGCGGG[A/G]CCCGCCTCCATCTAG | 54472 |
rs12800914 | snp | C/T | 0.291493 | 0.246533 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291707 | CCGCCCCGTCCTCGC[C/T]GACCCCCCTCTGAGG | 54472 |
rs12800917 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308957 | CGCCTCCACCTGGGG[G/T]GCCATCAGGGAGCAG | 54472 |
rs12805480 | snp | A/C | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308857 | CACCTGGGGGGCCAT[A/C]AGGGTGCGGGACCCG | 54472 |
rs12805687 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308950 | CGGGACCCGCCTCCA[C/T]CTGGGGGGCCATCAG | 54472 |
rs12808025 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308939 | CCATCAGGGTGCGGG[A/G]CCCGCCTCCACCTGG | 54472 |
rs28470184 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296837 | GTGGAGGCCTGGTTG[A/C]TGGTGGAGTGGGGTG | 54472 |
rs28513839 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296841 | AGGCCTGGTTGCTGG[A/T]GGAGTGGGGTGGAGG | 54472 |
rs34259532 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276869 | GACCGCCAGGAACCG[-/A]AAAACCCACATGCAC | 54472 |
rs34437291 | in-del | -/AG | 0.0839998 | 0.186933 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285668 | CACGTGTCACCTGAC[-/AG]GGGCGTGAGGTTCTC | 54472 |
rs34500638 | in-del | -/A | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299819 | GTCACCTGTGCCGTC[-/A]AAAACGCCCCATCCA | 54472 |
rs34569007 | in-del | -/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301675 | ACAAAGCCAGCCCAC[-/G]GGAGGCCCCAACACA | 54472 |
rs34589655 | in-del | -/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288287 | GGCTGCTCAGCTGGA[-/C]CCTAAGGGCAGAGCT | 54472 |
rs34703157 | in-del | -/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290112 | AATGAAACACCAGGT[-/G]GGGGAGCCACGCCTC | 54472 |
rs34787245 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289602 | CGGCCGGACCCTGTG[C/T]GCCCAGCGGGGCGGA | 54472 |
rs34793197 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304762 | ACAACTGAATTTTTT[-/A]AAAACTCCATTTAAT | 54472 |
rs35045124 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276388 | CCGTGCCAGGCCCCC[-/T]TTCCTCACTCCAGGT | 54472 |
rs35194940 | in-del | -/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299243 | AGCAAGAGAGGAGAC[-/G]GGAGACCAGGCTTCA | 54472 |
rs35279068 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285519 | CCTAACAGTGACACA[C/T]GACAACAGACGCAAC | 54472 |
rs35290340 | in-del | -/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292645 | CACATGCTGTTCTGG[-/T]TGCAGGAGACACTGT | 54472 |
rs35307059 | in-del | -/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273945 | GTGCCAGGGTGGCTC[-/G]GGGGTCTCTAGAGTG | 54472 |
rs35365323 | snp | C/T | 0.0363512 | 0.129824 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277097 | TCCTTGTTCCCTCGC[C/T]GGGCTTCCAGCACGG | 54472 |
rs35395733 | snp | A/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294622 | TCTACGAAAGCCCGC[A/G]TGGCTCACAGTGTGT | 54472 |
rs35446898 | in-del | -/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294899 | GCATTTCTACGAAAG[-/C]CCGCGTGGCTCACAG | 54472 |
rs35483730 | in-del | -/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293453 | CCTTGGCATCCCACT[-/G]GGGGCCCCAGGAGAC | 54472 |
rs35534043 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275249 | CACGCGTGTGGCAGT[-/C]CTCACTGCACCCCAG | 54472 |
rs35599839 | in-del | -/A | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283160 | ACCTGCGCTGGGTGG[-/A]ATCTGCGGTGGTGGC | 54472 |
rs35650910 | in-del | -/C | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299825 | TGTGCCGTCAAAACG[-/C]CCCCATCCACCAGCC | 54472 |
rs35743811 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287164 | GAAACTGTCAACTGC[A/G]GATAAGTCACTGCAC | 54472 |
rs35791007 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287822 | CCGCCGCACCCTCCC[C/T]GCCGCACCCTCCCTG | 54472 |
rs41307082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277478 | GGGCCCTCTGTGACG[C/T]CTCCTTCACTAACTC | 54472 |
rs41310328 | snp | C/T | 0.0182019 | 0.0936463 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275127 | TTGCTCTCCCTCCAG[C/T]GAGGCTGGCCCCCAC | 54472 |
rs41314515 | snp | C/T | 0.0166325 | 0.0896639 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276907 | CAGGTGTGGACGGGG[C/T]GGCACAGAAGTCCAC | 54472 |
rs41317292 | snp | C/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276035 | CGCAGCGCCCAGGCA[C/G]TCAGAGGTAAGTGAG | 54472 |
rs41317294 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275679 | ACAGTATATTTGACA[A/G]AAACCACCCCCAATC | 54472 |
rs55646946 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294171 | GCATGGCTCAGTGTG[C/T]CTCCTTTCCCTGCAT | 54472 |
rs55647350 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275605 | AGGCGCCTGCTGCCA[A/G]CATGTCCCTCCCCCA | 54472 |
rs55660304 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308968 | GGGGGGCCATCAGGG[A/T]GCAGGGCCCGCATCC | 54472 |
rs55686144 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291546 | CCCCGAAGGCACGGC[A/C/T]ACCCCATCCTCACTG | 54472 |
rs55686260 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287437 | ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC | 54472 |
rs55764960 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291742 | GGCCGCCCCGTCCTC[A/G]CCGACCCACCTCTGA | 54472 |
rs55793034 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294933 | GTCTCCTTTCCCTGC[A/G]TTTCTACGAAAGCCC | 54472 |
rs55809655 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308871 | TCAGGGTGCGGGACC[-/C]GCCTCCACCTGGGGG | 54472 |
rs55837816 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309004 | GGGGACCATTAGGGT[G/T]CAGGGCCCGCCTCCA | 54472 |
rs55883441 | snp | G/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308922 | CGCCTCCATCTAGGG[G/T]GCCATCAGGGTGCGG | 54472 |
rs56000022 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308974 | CCATCAGGGAGCAGG[A/G]CCCGCATCCATCTAG | 54472 |
rs56038704 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287451 | AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs56128747 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291545 | CCCCCGAAGGCACGG[C/G]CACCCCATCCTCACT | 54472 |
rs56156644 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292012 | AATCAAAGCTGTGGC[C/T]GGTCCTTTTAGGTCA | 54472 |
rs56178536 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308980 | GGGAGCAGGGCCCGC[A/C]TCCATCTAGGGGACC | 54472 |
rs56199234 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283818 | AGCCACAGAGCGCCC[A/G]GCCCAGAAGTTGGAG | 54472 |
rs56241462 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308864 | GGGCCATCAGGGTGC[-/C]GGGACCCGCCTCCAC | 54472 |
rs56362227 | snp | A/C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291335 | CTCCTGCAGCCAACC[A/C/T]GGCTCACCCCCAGGA | 54472 |
rs56376537 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294277 | TGTCTCCTTTCCCTG[C/T]ATTTCTACGAAAGCC | 54472 |
rs56397575 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291755 | TCACCGACCCACCTC[C/T]GAGGGCACGGCCGCC | 54472 |
rs56733424 | snp | A/G | 0.277778 | 0.248452 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295007 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs56933202 | in-del | -/TT | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299532 | TCCTAAAATTTATTT[-/TT]GCCATATGATGATGG | 54472 |
rs57461270 | snp | A/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294305 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs57827674 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282597 | AACCTGCACGTTGTG[C/T]ACATGTACCCTAAAA | 54472 |
rs58677632 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283418 | CAGTGTCAGCTTCAT[A/C]TAGATGGCCGTACTG | 54472 |
rs60020941 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308918 | GGCCCGCCTCCATCT[A/G]GGGTGCCATCAGGGT | 54472 |
rs60404204 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292089 | GGCCACAGCGTACTC[C/T]GGAATGCTATGGAGT | 54472 |
rs61869685 | snp | C/T | 0.471673 | 0.115589 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287388 | AGAAAAGCAGCTCCC[C/T]GCTGCTGCCTCCCCG | 54472 |
rs71025719 | in-del | -/CCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCCGCA | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287800 | ACCCTCCCCGCCGCA[lengthTooLong]GCCTCCCCGCCGCAC | 54472 |
rs71025722 | in-del | -/TGGGGCCATAAGGGTGCCGGGACCGCCTCCACCTG | 0 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308847 | GCCCGCCTCCACCTG[lengthTooLong]GGGGGCCATCAGGGT | 54472 |
rs71454080 | snp | C/T | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287696 | CCGCCGCACCCTCCC[C/T]GCCGCACCCTCCCCG | 54472 |
rs71454081 | snp | C/G | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287815 | AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC | 54472 |
rs71454082 | snp | C/G | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287871 | ACCCTCTCTGCTGCA[C/G]CCTCCCTGCTGCACC | 54472 |
rs71454083 | snp | A/G | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294678 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs71454084 | snp | C/T | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294833 | CAGTGTGTCTCCTTT[C/T]CCTGCATTTCTACGA | 54472 |
rs71454085 | snp | A/G | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294866 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs71454087 | snp | A/G | 0.277778 | 0.248452 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294913 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs71472142 | multinucleotide-polymorphism | CA/TG | 0 | 0 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301981 | AGGACTCACATAGAA[CA/TG]GCACAGTTGGTCCAG | 54472 |
rs72846381 | snp | A/G | 0.0268816 | 0.112775 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285998 | AGGGAGGGAGCACAC[A/G]CACCTGTGATGGGCA | 54472 |
rs72846383 | snp | C/T | 0.135143 | 0.222054 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291288 | GTCCTGCCTGGAATG[C/T]AGACGGCCTCCCTGT | 54472 |
rs72846392 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306441 | CAGGGTCTCCCGAGC[C/G]AGAGTCCTGCCCCCG | 54472 |
rs73397883 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287999 | GGTTGATGATACAGA[C/T]GAGACGGCAGGAGCT | 54472 |
rs73397894 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297340 | ACCCCGAGAGGGTCT[A/G]GCTCCTCACCTGTGT | 54472 |
rs73399804 | snp | A/G | 0.0980852 | 0.198549 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310652 | GGAACACCCTGCTCT[A/G]TGGAGTAGCCATTCT | 54472 |
rs74046285 | snp | C/T | 0.0345262 | 0.126772 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300104 | GAAACTTTTTAAAAA[C/T]ATTCGTGAATTACTT | 54472 |
rs74046287 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310856 | TGGTCAGTTCTCAGT[C/T]CTCGTCCTCCGGGAA | 54472 |
rs74503040 | snp | A/G | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294725 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs74577337 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298010 | CTGGCCACACAGGAC[A/G/T]TGCTTCCCTGCCAAC | 54472 |
rs74692168 | snp | C/T | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287867 | CCGCACCCTCTCTGC[C/T]GCAGCCTCCCTGCTG | 54472 |
rs74860345 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309041 | GGACCATTAGGGTGC[A/G]GGGCCCTCCTCCATT | 54472 |
rs74929271 | snp | C/G | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287423 | AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs75239657 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283307 | AAGATGGGGACCCCT[A/C]CAGGCCAAGGGAGGC | 54472 |
rs75406859 | snp | A/C | 4.97475e-05 | 0.00498711 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277055 | TATGGCTCCTCCCCC[A/C]TCTGCAGCAGGGAGT | 54472 |
rs75621936 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286242 | CTCGCTACACGAGCC[C/T]TGAGTGCACAGGGGA | 54472 |
rs75980902 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294340 | ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG | 54472 |
rs76167907 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274511 | TAATCAGAAGCGCAC[A/G]TTCTGAGACCACTCC | 54472 |
rs76729597 | snp | G/T | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280227 | TTCCACGTGCGAGGG[G/T]AAGCATGCCTGGGCC | 54472 |
rs77124907 | snp | A/G | 0.0383715 | 0.133092 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311132 | AAGCTATTAACCACA[A/G]GTTCCTGCTTTGGGG | 54472 |
rs77169890 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309015 | GGGTTCAGGGCCCGC[A/C]TCCACCTGGGGGACC | 54472 |
rs77240435 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309039 | GGGGACCATTAGGGT[G/T]CGGGGCCCTCCTCCA | 54472 |
rs77443790 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310097 | AGATGGGGCGCGGTT[C/T]CTCCACGGGGCGGCT | 54472 |
rs77825895 | snp | C/T | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303677 | AGGGACAGGAAACAC[C/T]TGCACAGCAGGCCTA | 54472 |
rs78406765 | snp | A/C | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299726 | TAAATGCCCGTGTGA[A/C]GGCCAACAATTCCAC | 54472 |
rs78468814 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310786 | ATCAGGACCCTTTTC[C/T]GGTAACACAACCACT | 54472 |
rs78488441 | snp | C/T | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278677 | CACCCACACCTGCCT[C/T]TTGTCCTGGCCACTG | 54472 |
rs78736015 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309023 | GGCCCGCCTCCACCT[A/G]GGGGACCATTAGGGT | 54472 |
rs78992644 | snp | A/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306104 | ATGCAGACTATATTG[A/G]AAAAAGGTTATCTTT | 54472 |
rs79145389 | snp | A/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294343 | TCTACGAAAGCCCGC[A/G]TGGCTCACGGTGTGT | 54472 |
rs79364943 | snp | A/C | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298573 | CTCATTACTGGGAGA[A/C]AATAAAATTATATCC | 54472 |
rs79892483 | snp | A/G | 0 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294584 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs79983698 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309048 | TAGGGTGCGGGGCCC[G/T]CCTCCATTCGGGAGT | 54472 |
rs80293662 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285788 | AAAAAAAAAAAAAAA[A/C]CAATTCTATTTTCTA | 54472 |
rs80326424 | snp | C/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307017 | CCCACCGGGCCGTCA[C/G]CACACAGCTCAGCTG | 54472 |
rs111163740 | snp | A/C | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296809 | GTGGAGGCCTGGTTG[A/C]TGGAGGAGTGGGGTG | 54472 |
rs111277153 | snp | A/C | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286709 | TAGTTCAAAACTGTC[A/C]ACTGTGGATAAGTCA | 54472 |
rs111352533 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286885 | ATAAGTCACTGCACT[A/G]CTGTCTCCTGAGTTC | 54472 |
rs111521887 | snp | C/G | 0.134802 | 0.221877 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291476 | GAGGGAACGGCCAAC[C/G]TGTCCACACCAACCC | 54472 |
rs111539110 | snp | A/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288883 | CGTCTTATCTGTGGA[A/G]CAGGGCTCCCACCTG | 54472 |
rs111550675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297074 | CGTCTGCAGGGGCCC[C/T]GGTCAGCGCCAGTGC | 54472 |
rs111555946 | snp | A/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296738 | TGCTGGAGGAGTGGG[A/G]TGGAGGCCTGGTTGC | 54472 |
rs111561835 | snp | A/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293576 | TGGCCCAGTGAGGAG[A/G]CAGGAATGTTTCCCA | 54472 |
rs111590044 | snp | C/T | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287890 | CCCTGCTGCACCCTC[C/T]CTGCTGCACCCTCTC | 54472 |
rs111658007 | snp | C/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279967 | TCCAGCTCAGAGACT[C/G]TTCCGGAACTCCCAA | 54472 |
rs111777511 | snp | A/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294258 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs111831428 | snp | A/G | 0.000730922 | 0.0191031 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288595 | AACATACCCCAATGC[A/G]CCCCACCCCGCCCAG | 54472 |
rs111866843 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289305 | AAGGCAGGGCCCAGG[A/C]AGGGAGGGCTGGCCG | 54472 |
rs111971432 | snp | C/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279198 | GGGATGTGGCGCCGA[C/G]TGGCCCTCAAGTGAA | 54472 |
rs111986008 | snp | C/T | 0.0100364 | 0.0701248 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277074 | GCAGCAGGGAGTTGA[C/T]GGCGGCATCCTTGTT | 54472 |
rs111992209 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297999 | CCGGGGGACACCTGG[A/C]CACACAGGACGTGCT | 54472 |
rs112045310 | snp | C/T | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295405 | GAGCCAGGCCCTACA[C/T]AGAGCAGACGCCCAC | 54472 |
rs112070965 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289736 | TGTGCGGCAAGACCC[C/T]GTGCGCCCAGCGGGG | 54472 |
rs112084278 | in-del | -/CAA | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285789 | AAAAAAAAAAAAAAA[-/CAA]TTCTATTTTCTAGAT | 54472 |
rs112321894 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279853 | CCGCCGGTGGGCAGG[G/T]GAGCATCAGCCCTGC | 54472 |
rs112434701 | snp | A/G | 0 | 0 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298715 | GAAGCAGCTCCCTGC[A/G]GATGGAGCTCATCAG | 54472 |
rs112445940 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296608 | TGCTGGTGGAGTGGG[G/T]TGGAGGCCTGGTTGC | 54472 |
rs112719982 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287804 | CTCCCTGCCGCAGCC[C/T]CCCCGCCGCAGCCTC | 54472 |
rs112732933 | snp | C/G | 0 | 0 | splice-donor-variant, intron-variant | TOLLIP | GRCh38.p7 | 11:1288623 | CAGGCGTGCAGCTCA[C/G]CGCGTAGGACATGAC | 54472 |
rs112740638 | snp | C/T | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276155 | CAAGCTGTCAGCAGT[C/T]GGCTGGCAGTGCCAC | 54472 |
rs112842927 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277689 | CGGAATGTCACGCCC[A/G]CTGATCCAAACACTG | 54472 |
rs112901594 | in-del | -/T | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284356 | GGGCTGGTGGTTTTC[-/T]TTTTTTTTTTGAGAT | 54472 |
rs112929704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291380 | CCCCGGGAGCCATCC[C/T]GGCCCTCCCACCCAC | 54472 |
rs113133696 | snp | C/T | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294948 | ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG | 54472 |
rs113314204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279842 | GTAAGTCCCGGCCGC[C/T]GGTGGGCAGGGGAGC | 54472 |
rs113471882 | in-del | -/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304158 | GGGACATCCACTCCC[-/G]GGGCTGCTCAGCAGC | 54472 |
rs113544269 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310639 | CCTCGTGCTTTTGGG[A/G]ACACCCTGCTCTATG | 54472 |
rs113644457 | snp | C/T | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287904 | CCCTGCTGCACCCTC[C/T]CTGCTGCACCCTCTC | 54472 |
rs113726728 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294403 | GCATGGCTCAGTGTG[C/T]CTCCTTTCCCTGCAT | 54472 |
rs113732307 | snp | A/G/T | 0 | 0 | splice-acceptor-variant, intron-variant | TOLLIP | GRCh38.p7 | 11:1286094 | GCAGCTGGAAGCAGC[A/G/T]GAAACACAGCGGAGA | 54472 |
rs113801730 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292848 | CCAGCTAGGAGGACC[A/G]GGTATGCGGGCTGCA | 54472 |
rs113859207 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297648 | GAGAAGCCGTACTGC[A/G]AGAACAAGCAGAGCA | 54472 |
rs113959389 | snp | A/G | 0 | 0 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302335 | CTGACCCCTCAGTGC[A/G]CAGGGTTTCAGAGAC | 54472 |
rs113978854 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294744 | TGTCTCCTTTCCCTG[C/T]ATTTCTACGAAAGCC | 54472 |
rs113979255 | snp | A/G | 0.229429 | 0.249152 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295054 | GCCTGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs114044218 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277684 | CTACACGGAATGTCA[C/T]GCCCGCTGATCCAAA | 54472 |
rs114503583 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274543 | GCCTGGCACCCTGCA[A/G]GGTAGCGCCCAGGGA | 54472 |
rs114959412 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311384 | CGTGCCACCCCCTGG[C/T]GGCGGGGCCCCCCAC | 54472 |
rs115040064 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303707 | AACCAGGGGCCTGTC[A/G]GGCAGGTCAAGGGAC | 54472 |
rs115050982 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299797 | GAGCACAGGATGCCT[A/G]AGGCTGCGTCACCTG | 54472 |
rs115437483 | snp | A/C/T | 0.0119091 | 0.0762411 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300573 | TTCCTGTTGGTGACA[A/C/T]GTCTCCAACGGAGAG | 54472 |
rs115849875 | snp | C/T | 0.169061 | 0.236535 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287876 | CTCTGCTGCAGCCTC[C/T]CTGCTGCACCCTCCC | 54472 |
rs116033108 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282546 | TGAGTCAATGGGTCC[A/G]GCACACCAACATGGC | 54472 |
rs116283238 | snp | C/T | 0.111606 | 0.2082 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287881 | CTGCAGCCTCCCTGC[C/T]GCACCCTCCCTGCTG | 54472 |
rs116593151 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285587 | GAGGTTCAGACACAA[C/T]GGCGCAGCGCAGGGC | 54472 |
rs116701390 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299825 | CTGTGCCGTCAAAAC[A/G]CCCCGTCCACCAGCC | 54472 |
rs116844349 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278487 | TGCAGGGGTGTAAAC[A/G]GAGCAGACAGGGCTT | 54472 |
rs116938768 | snp | C/T | 0.0185938 | 0.0946107 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310012 | CAGTGACAGGCCCGA[C/T]ATCCCCTGCAGGGCG | 54472 |
rs116939577 | snp | A/G | 0.0198696 | 0.0976729 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288639 | CGCGTAGGACATGAC[A/G]AGGTTGATCATGCCC | 54472 |
rs116941008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293970 | CGGTGTAGCTGTGCT[C/T]ACCACACCATGAAGC | 54472 |
rs117392832 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305953 | TCGCGGGGGCCCGCA[C/T]GGTACCCCTCGCAGG | 54472 |
rs117431642 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307357 | ACACCTCAGCACTTG[C/T]CAGCACAGGCCCTGC | 54472 |
rs117500947 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291384 | GGGAGCCATCCCGGC[C/T]CTCCCACCCACATGG | 54472 |
rs117572864 | snp | C/T | 0.0479149 | 0.147179 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303706 | TAACCAGGGGCCTGT[C/T]GGGCAGGTCAAGGGA | 54472 |
rs117595658 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292013 | ATCAAAGCTGTGGCC[A/G]GTCCTTTTAGGTCAA | 54472 |
rs117663261 | snp | A/G | 0.0228947 | 0.104514 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310983 | ACATCTTTGGGTCTC[A/G]GTTACCAGTCTCTCC | 54472 |
rs117792684 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283840 | AAGTTGGAGGAGACG[A/G]GGAGGATCCTCCTCA | 54472 |
rs117924096 | snp | C/T | 0.0228947 | 0.104514 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311086 | CAAGTTGTAGCTTAA[C/T]ATCCAGCCAATCCAC | 54472 |
rs118054222 | snp | C/G | 0.0240643 | 0.107019 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309921 | GAGTGGCGACAGGGC[C/G]TAGCCACCTGGCGGG | 54472 |
rs118085196 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287905 | CCTGCTGCACCCTCT[A/C]TGCTGCACCCTCTCT | 54472 |
rs137867760 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278926 | TTGGCCATCACCTGT[C/T]CCTGCCCATACAGCT | 54472 |
rs137869091 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295736 | TCCAGCTGGACCTGC[C/T]GCTGCTGCTGTGTGG | 54472 |
rs137973784 | snp | A/C/T | 0.000855554 | 0.0206651 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276784 | AGAAGGAGAGACGCA[A/C/T]GTCCCAGGGACAGGA | 54472 |
rs138201374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301785 | TCAGAGCTGGGACCC[A/G]CAGCAGGAAGACCTG | 54472 |
rs138382715 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287839 | CCGCACCCTCCCCGC[C/T]GCAGCCTCCCTGCCG | 54472 |
rs138633100 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276923 | GGCACAGAAGTCCAC[A/G]GGAGGGGGCGACACG | 54472 |
rs138639196 | snp | A/G | 0.000297637 | 0.0121955 | synonymous-codon, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277219 | CGGGGGCAGGGCCAC[A/G]GGCACCATGCCGGGG | 54472 |
rs138674686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280674 | AGGCTGGGGAGGCGC[C/T]GGACGCCCCACTTTC | 54472 |
rs138690831 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302146 | CACACCCAGGTCAGA[A/G]CTCAGTCTGGCCCAG | 54472 |
rs138709550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279086 | GATGGGGAAGGGACA[G/T]GAGGAGGGGAACTGC | 54472 |
rs138869815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280991 | TGTTGCCAGCCTGGC[A/G]GAGAGTCTCTGTCCA | 54472 |
rs138899584 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291027 | GTAGACCATGAGATT[C/T]GACTTCAGGCCAGGT | 54472 |
rs139059803 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295851 | GGGCACAAAGCAGCC[C/T]GACAGCAGCTGCCCC | 54472 |
rs139087935 | snp | A/G | 8.26685e-05 | 0.00642864 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277078 | CAGGGAGTTGATGGC[A/G]GCATCCTTGTTCCCT | 54472 |
rs139117968 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292748 | ACCGTGGGGACACAC[A/G]GGCACCGCTGCTTTC | 54472 |
rs139128352 | snp | C/T | 0.000188849 | 0.0097154 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288624 | AGGCGTGCAGCTCAC[C/T]GCGTAGGACATGACG | 54472 |
rs139149465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292836 | TGCAGGGAGTGACCA[A/G]CTAGGAGGACCGGGT | 54472 |
rs139390926 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310217 | GCAGGAGCCCCGCTC[C/T]TCTCCTGCTCGCTCC | 54472 |
rs139507547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303757 | AACAGAGGTTAGGGC[C/T]GGGTGCAGTGGCTCA | 54472 |
rs139544999 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276002 | CCTAAAATCTGTCCT[A/G]TAGGCCAAGATGCTA | 54472 |
rs139605906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309234 | CTCCCCAAAGCTCTG[C/T]CCCGGCACGGCGGTG | 54472 |
rs139741446 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279763 | CAGGAAAACCAAAAC[C/T]TGTCCCTTTTCCATT | 54472 |
rs139750280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281815 | CGACACACATGCTCT[A/G]GCCAAGATGCACTTT | 54472 |
rs139784409 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279543 | CCGGGGCAGCCCAGA[C/G]CCCACCTGTAGCGGC | 54472 |
rs139965382 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298530 | TTGCTCTGCACTCTT[C/T]AGGTGTCCGTTAAAG | 54472 |
rs139967607 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277596 | GATCCCTTCAGAACT[C/G]GTGAATTTGCACTGC | 54472 |
rs140032126 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286659 | CAAAACTGTCAACTG[C/T]GGATAAGTCACTGCA | 54472 |
rs140337138 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306474 | CCCTGGGGAGCATCT[C/G]TTTCTGCTGGAAAGC | 54472 |
rs140374060 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278492 | GGGTGTAAACGGAGC[A/G]GACAGGGCTTGCCAC | 54472 |
rs140439497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277422 | TGGAAAGGCAAACCC[C/T]CAAACAGCAACCCCA | 54472 |
rs140442022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301291 | CGATGGGCTAAATAC[A/G]TTCTGTGGAATTAAA | 54472 |
rs140514207 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277908 | AAAACTCAAACAAGT[C/G]GGGCAGCAGGTGCGG | 54472 |
rs140626415 | snp | C/G | 0.0166325 | 0.0896639 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310946 | CACCATGTGCTCTCA[C/G]TTTCCTCTTATCCCA | 54472 |
rs140857999 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311387 | GCCACCCCCTGGCGG[C/T]GGGGCCCCCCACCGT | 54472 |
rs140876532 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287834 | CCCCGCCGCACCCTC[C/T]CCGCCGCAGCCTCCC | 54472 |
rs140929037 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304681 | GCAGAAGCTGATAAG[C/T]GCATGTTACCATTTC | 54472 |
rs140976602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306162 | AGGGAAGCACTGCAC[A/G]GGGCTGAAGCATCCC | 54472 |
rs141097873 | snp | C/T | 0.00104498 | 0.0228342 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290259 | GATAGAAAGAGTCCA[C/T]GCCTGGGGGCACCGT | 54472 |
rs141149652 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275581 | GCCTTTAGGACCCAC[A/G]GCTGAAGAAGGCGCC | 54472 |
rs141188303 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280725 | CACCAAGCAGAAGGA[A/G]GTGGAAAGCAACAGG | 54472 |
rs141565986 | snp | A/G | 0.00113638 | 0.0238097 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290311 | GCGGGGATTCTTGGC[A/G]CCATTGTGTGCCGTG | 54472 |
rs141603148 | in-del | -/C | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290173 | GGTGTGTCCCCACGG[-/C]CAGCCACGCTCAGCC | 54472 |
rs141700822 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285169 | CCCCCAACACCACCA[A/C/T]GCATCCCTAGCGCCC | 54472 |
rs141798689 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302703 | CCACGCCAGTCTCCT[A/G]GCACTGGCATGTTCA | 54472 |
rs141833183 | snp | A/G | 0.000105448 | 0.00726037 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295675 | GTTCAGTCGGCCCAC[A/G]GTGCCCACTGCGCCT | 54472 |
rs142066785 | snp | C/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274119 | GCCTGGAAATGAAAA[C/G]GCACCACAGAACCAC | 54472 |
rs142260383 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276630 | GTGAGGGATTGTGTG[C/T]GCCTTAAATCAACAG | 54472 |
rs142300746 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280628 | AGCACAGAATGAGCT[C/G]ATGCACACCCTGGTG | 54472 |
rs142306287 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282376 | CCTAATGTTAAATGA[C/T]GAGTCAATGGGTGCA | 54472 |
rs142573629 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294192 | TTCCCTGCATTTCTA[C/T]GAAAGCCGTGTGGCT | 54472 |
rs142610147 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300606 | CCGCTGCTTCCTTGG[G/T]CCACACTTTCTGCCC | 54472 |
rs142637486 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274638 | CCCGCCTGAGGCTCC[A/G]AGATGGCACAGTCAG | 54472 |
rs142658126 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295572 | GAAATGCAGTATAAA[C/T]GCCGAAATCCGAAAT | 54472 |
rs142714391 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289844 | CATGCATGCTCTGTC[A/C]CTGGAAATCCCACCT | 54472 |
rs142729339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308039 | ACCTTGGAGCATCGT[G/T]AAAAAGGACTTTTTC | 54472 |
rs142776865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305285 | GGTGAGTGCGTTCCC[C/T]GCTGGCTCAGGTGCA | 54472 |
rs142911670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300393 | ACGAAAGAAAAGAGG[A/T]CTCCAACATTCACTT | 54472 |
rs142920490 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277536 | TTGATCTTTCAAATC[G/T]CACCCGAGTCTGTTT | 54472 |
rs142927331 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293458 | GGCATCCCACTGGGG[-/C]CCCAGGAGACAACAA | 54472 |
rs142928640 | snp | A/G | 0.00072164 | 0.0189815 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288755 | GGGTCCAGGCAATGC[A/G]GTCGTCCATGGAGAA | 54472 |
rs143013859 | snp | C/T | 0.00180058 | 0.0299508 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286138 | AAGGAGGAACATCCA[C/T]CCATCAGAACCTCGG | 54472 |
rs143078447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281887 | CATGCTTGCCTAGTC[A/G]GCCCGAGACGCCCTG | 54472 |
rs143124042 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278406 | GTTCCTTTCTACACT[C/T]GGAGGATCCTAAAGG | 54472 |
rs143125868 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292780 | CCACAATGGGCAAGA[C/G]ATGCGCGGCAGACAC | 54472 |
rs143130045 | snp | C/T | 1.67351e-05 | 0.00289263 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290388 | CCATGCGGGTCATGC[C/T]GTAATTCTTGGCCAA | 54472 |
rs143144151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293785 | GGTCACCAGGCCCTG[A/C]CAGGAGGTGGCGGCT | 54472 |
rs143210443 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290497 | CTCCCTGAACCCTTC[C/T]ACGAGGCCTTTTCCT | 54472 |
rs143406220 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278997 | GCCTGTCCCTGCCCA[C/T]ACGTCTCCCCACAGC | 54472 |
rs143476615 | snp | A/G | 0.00190964 | 0.0308411 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277287 | TTTGGTAAAAACGTC[A/G]GAAAGTTCCAGAAGT | 54472 |
rs143558857 | in-del | -/A | 0.0640965 | 0.167152 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309727 | GCTCCAGGGTAGGGC[-/A]GGCGCAGCCTCTCGC | 54472 |
rs143573396 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280495 | TGACGGGAGGGACTG[C/T]GCCGGTGAGGACGTG | 54472 |
rs143854023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307382 | CCCTGCGTGTGAGAA[C/T]ATCTCCTGCCGCTCC | 54472 |
rs143888433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288496 | CCTCTGTCCTCAGAA[C/T]GTGAGCCCTGCTGTT | 54472 |
rs144024538 | snp | C/T | 3.37171e-05 | 0.00410578 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288638 | CCGCGTAGGACATGA[C/T]GAGGTTGATCATGCC | 54472 |
rs144146461 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274951 | TACAGTAAGCCACTT[C/G]TACAGTAAGCCTTCA | 54472 |
rs144191022 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279555 | AGAGCCCACCTGTAG[C/T]GGCCCTGGGAGGAGT | 54472 |
rs144249750 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278002 | GCTACGCAGGCCCCT[C/T]GCCCCATGTCTGATG | 54472 |
rs144319382 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279128 | TGACGGTGGCTGTGA[C/T]GCTGCGACGTCACGG | 54472 |
rs144425237 | snp | A/G | 0.000687107 | 0.0185225 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277182 | CCTCCTCGCTACAGC[A/G]GGGCTGGGCGTTCAC | 54472 |
rs144473473 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287310 | ATCGTCACTCACGGC[C/T]GGGACATGATTTAAA | 54472 |
rs144679601 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287836 | CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCTG | 54472 |
rs144692249 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286763 | AAAACTGTCCACTGC[A/G]GATAAGTCATTGCAC | 54472 |
rs144799396 | snp | C/T | 0.00271739 | 0.0367602 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309562 | GGCGACCTCCTGCGC[C/T]CCCGCCGGAGCCTGC | 54472 |
rs144901649 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287829 | AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs144956879 | snp | C/T | 0.000184804 | 0.00961082 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290272 | CACGCCTGGGGGCAC[C/T]GTGCAGTGGATGACC | 54472 |
rs145057686 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306311 | GAAGCTCCCTCTACC[C/T]AAGGACAAAAGAACC | 54472 |
rs145151092 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310351 | GGCTGCATCCCCAGG[A/G]GTCGGGCGTTTACGG | 54472 |
rs145251117 | snp | A/G | 0.000116857 | 0.00764295 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290344 | CGTCTCGTACACCGC[A/G]TAGCCCAGGCGCAGT | 54472 |
rs145409553 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277047 | AGAGGCTCTATGGCT[C/T]CTCCCCCATCTGCAG | 54472 |
rs145433418 | snp | C/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274359 | TTAAAAAATACTCGG[C/G]AACAAACATGGTAAA | 54472 |
rs145435385 | snp | A/G | | | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311040 | GCCTGTTTTGATGGG[A/G]TGTAGAGAAAAAGAA | 54472 |
rs145435743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284051 | GGCTCTGGGCTGTCC[C/T]AGTTACAAATCAGAA | 54472 |
rs145462738 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287056 | CTCTGAGTTCAAAAC[C/T]GTCAGCTGCGGATAA | 54472 |
rs145505029 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307166 | AAGTCACATGTACTC[C/T]AAGCAACACCTGAGA | 54472 |
rs145542060 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280420 | CGGGCATTCATGTCC[C/T]GGTCTGGTTGGCTCC | 54472 |
rs145578982 | snp | C/T | 0.000417079 | 0.0144349 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295686 | CCACGGTGCCCACTG[C/T]GCCTCCGTACTGCAG | 54472 |
rs145616541 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276214 | TGCCTCTATCACCTC[C/T]CACCCCAGCCTCGCA | 54472 |
rs145694209 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277707 | GATCCAAACACTGCA[C/T]GGTCTGAGCCTCTTC | 54472 |
rs145715290 | snp | C/T | 0.000142035 | 0.008426 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276762 | GAGCATTTTCCAGAA[C/T]GGCATGAGAAGGAGA | 54472 |
rs145749182 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280632 | CAGAATGAGCTCATG[C/T]ACACCCTGGTGCTGC | 54472 |
rs145801768 | in-del | -/TGGGGCCATAAGGGTGCCGGGACCGCCTCCACCTG | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308813 | ACAGCCATCATCTAT[lengthTooLong]GGGACCAACTAGAGT | 54472 |
rs145957069 | snp | C/T | 0.00306418 | 0.0390244 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295774 | GCGGAGGAAGTCCTG[C/T]GGGAGCTCACCGATG | 54472 |
rs146009358 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298324 | ATGCCCTCCTGGCCA[C/T]ACGTGGGGGACAGAC | 54472 |
rs146052031 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282061 | CACTCTACAGTACTG[C/T]TAGGATAATTAAAAA | 54472 |
rs146156644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286277 | GGGCCCTGCTCCCAC[C/T]CCTGCACCACCTCCT | 54472 |
rs146173649 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298996 | TGCTGGGACAGCAGG[A/G]GACAGTCATCGAAAA | 54472 |
rs146176131 | snp | C/T | 0.000140252 | 0.00837297 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286056 | TTGGCATCAGGACCA[C/T]GGGCTGGGGTGGCAT | 54472 |
rs146203970 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283430 | CATCTAGATGGCCGT[A/C]CTGTGCCAGGGACGC | 54472 |
rs146305309 | snp | C/T | 0.00525193 | 0.0509743 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295747 | CTGCCGCTGCTGCTG[C/T]GTGGGCGTGATGCGG | 54472 |
rs146354036 | snp | C/T | 4.96085e-05 | 0.00498014 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277077 | GCAGGGAGTTGATGG[C/T]GGCATCCTTGTTCCC | 54472 |
rs146373282 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281769 | CACAGGCTTCTCCAC[C/T]ATGTGAGTCATAAAC | 54472 |
rs146395933 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279438 | ATGTGTCAAGGCTGC[C/G]TGGGGACTTCAGGAG | 54472 |
rs146558058 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279743 | CTGACAAACACAAGG[A/G]TACCCAGGAAAACCA | 54472 |
rs146576090 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278102 | CACCCCTGAAGGCAC[C/T]GTGTGGCCGGACTTA | 54472 |
rs146674626 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293958 | AGGAAGGGGTGACGG[C/T]GTAGCTGTGCTCACC | 54472 |
rs146695170 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290886 | TGCACATAATTCAGA[C/T]GCCACGTGGCTGCTT | 54472 |
rs146905441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301055 | GTCGAACGAAGTTCA[A/G]TTAAAAACTAAAATG | 54472 |
rs146941932 | in-del | -/CCC | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290525 | CTAACACATAGACTA[-/CCC]CAGCCACTCAGAGTC | 54472 |
rs147049561 | snp | C/T | 0.000116966 | 0.00764652 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290323 | GGCGCCATTGTGTGC[C/T]GTGGGCGTCTCGTAC | 54472 |
rs147065932 | snp | A/G | 0.000750932 | 0.0193624 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277174 | TTTCAGGTCCTCCTC[A/G]CTACAGCGGGGCTGG | 54472 |
rs147151682 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279040 | GGAACGGAGGCACCG[C/G/T]GCTCCCACTCTCTCC | 54472 |
rs147169583 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277341 | AAGAAAACAACGCAT[C/T]CCACCGGCCTCCCTG | 54472 |
rs147184845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287065 | CAAAACTGTCAGCTG[C/T]GGATAAGTCACTGCA | 54472 |
rs147274796 | snp | A/C/G | 0.00106201 | 0.0230194 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288613 | CCACCCCGCCCAGGC[A/C/G]TGCAGCTCACCGCGT | 54472 |
rs147375873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308519 | CAGCAATGCAAGAAG[A/G]CCCTAACAGTGAGCC | 54472 |
rs147639903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280562 | GTGTGAAATGGAGGT[A/G]CACGAGGGAACAGAT | 54472 |
rs147728317 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300582 | GTGACACGTCTCCAA[C/T]GGAGAGAGCCGCTGC | 54472 |
rs147866259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301199 | AATATCCTTAGTGAA[C/T]TGAAGCTTTTGCTTG | 54472 |
rs147873040 | snp | C/T | 0.000501655 | 0.0158296 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290303 | TTATTCCAGCGGGGA[C/T]TCTTGGCGCCATTGT | 54472 |
rs147955595 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TOLLIP | GRCh38.p7 | 11:1304898 | TCTCTTAACTAGAAA[A/G]ATGAAACTAGCGCAT | 54472 |
rs148001930 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284972 | TTTCTGCATCTGTGC[A/G]GGATGCTGGCAGGAC | 54472 |
rs148038404 | snp | A/G | 0.00993419 | 0.0697739 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311117 | AGCACAAGACCCAAG[A/G]AGCTATTAACCACAA | 54472 |
rs148070720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302917 | CCTTCCGGGGCCTTC[C/T]TCAGACAGGGCTTTC | 54472 |
rs148251270 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278407 | TTCCTTTCTACACTT[A/G]GAGGATCCTAAAGGC | 54472 |
rs148253939 | snp | C/T | 0.0010734 | 0.0231419 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295659 | CCTGTACCACCGTGA[C/T]GTTCAGTCGGCCCAC | 54472 |
rs148370374 | snp | C/T | 0.202651 | 0.245475 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287850 | CCGCCGCAGCCTCCC[C/T]GCCGCACCCTCTCTG | 54472 |
rs148472983 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289669 | GGTGAGCGGCCAGAC[A/G]AGTGCCCAGTGGACA | 54472 |
rs148529381 | snp | A/C/G | 0.00914312 | 0.0669923 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286985 | AAGTCACTGCACCGC[A/C/G]GTTGTCTCTGAGTTC | 54472 |
rs148650184 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299984 | AAGGAGGCCTCTGTC[A/G]ACACCAACTCTGGAG | 54472 |
rs148701571 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275157 | CTGTGTGGGTCCCTC[A/G]GGCCCCCACACGGGC | 54472 |
rs148718519 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282104 | CTCCTAAAAGCAGTG[C/T]TCTCCTAATGGGAAC | 54472 |
rs148775939 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279153 | TCACGGCCTGGGGTG[C/T]CCCGAGAAACCTGCT | 54472 |
rs148849410 | in-del | -/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285772 | TTCTGCCAACAATTA[-/G]AAAAAAAAAAAAAAA | 54472 |
rs148880016 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280429 | ATGTCCTGGTCTGGT[G/T]GGCTCCACAGAAACC | 54472 |
rs149013801 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1304926 | CATTCCCATCAAAAG[A/C]CTTAGTCTTCTTAGA | 54472 |
rs149141495 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310607 | ATAAACAAGCGTACC[A/C]AGGTGGACGCCTTCC | 54472 |
rs149174945 | snp | C/T | 5.00856e-05 | 0.00500403 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290360 | TAGCCCAGGCGCAGT[C/T]GGCAGTAGGGGTCCA | 54472 |
rs149230501 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276536 | ACCCAAGCCCTGGGC[A/T]GGGGCCAGGCTCACA | 54472 |
rs149279819 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279113 | CTGCTGCAAAATCGA[C/T]GACGGTGGCTGTGAC | 54472 |
rs149336361 | snp | C/T | 0.000198946 | 0.00997162 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286023 | TGGGCACATAGCCAA[C/T]GCCCTGCTGGTACAC | 54472 |
rs149350458 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286727 | TGTGGATAAGTCACT[A/G]CACTGCTGTCTCCTG | 54472 |
rs149364877 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296462 | CCCGCACACCTGCAG[C/T]GGCCGAAGGGGCCTG | 54472 |
rs149401232 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281339 | TGACCTCAGCGCCCC[A/G]GCTTCTGAGTTGCTT | 54472 |
rs149526211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293058 | GGCAGTGGGTGGGTG[C/T]GGGGGGCTCCAGGCC | 54472 |
rs149545648 | snp | C/T | 0.00875628 | 0.0656872 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307310 | ATGATGGAAACAGCC[C/T]AGGAGGCACTGGGCA | 54472 |
rs149598328 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301890 | CTAGGGATATGGGCG[C/G]AAGTCAGTCTCAAAG | 54472 |
rs149804862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280116 | GTGATAGTTTGTCTC[A/G]GAAACTTTTAAGCAT | 54472 |
rs149855698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277665 | CTCTGCATCTGGGGA[C/T]GGACTACACGGAATG | 54472 |
rs149893655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299779 | ATGCTCACTCGGGCA[C/T]GTGAGCACAGGATGC | 54472 |
rs150068184 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310309 | CCAGCTCGAACAGCG[A/C]TGGGTAAACTGAGGC | 54472 |
rs150240433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291010 | AAGGAGCCACATCAC[A/G]TGTAGACCATGAGAT | 54472 |
rs150377920 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278751 | GCCTTTCGGCAATGA[C/G/T]GGAAAACGAACCGAA | 54472 |
rs150415585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301448 | AGATCGCACATGTGT[C/T]GCGGGCTTCCGAGAA | 54472 |
rs150466681 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295168 | CGGCGTTCAATCTGC[C/T]GATTTTGGCTTTCAC | 54472 |
rs150516908 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303446 | CCATGGTGAGGTGCT[A/G]GGGCACCCCTGCTCC | 54472 |
rs150577484 | snp | C/T | 0.00179301 | 0.029888 | synonymous-codon, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277204 | GGCGTTCACGGCGGC[C/T]GGGGGCAGGGCCACG | 54472 |
rs150584968 | in-del | -/CCACCCTGT | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291582 | CCTCTGAGGGCACGG[-/CCACCCTGT]CCTCACTGAACCCTC | 54472 |
rs150673853 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277542 | TTTCAAATCTCACCC[A/G]AGTCTGTTTTATAAC | 54472 |
rs150726502 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275775 | GACTAAAATGTAAGC[A/G]CTAACTTCCTCCTTC | 54472 |
rs150764394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292787 | GGGCAAGAGATGCGC[A/G]GCAGACACACAGCGC | 54472 |
rs151017610 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283801 | GCACCCCCCAAAAAG[A/C]CAGCCACAGAGCGCC | 54472 |
rs151039898 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305354 | AGAGCCAGCGGAGAC[C/G]GGTAAGTGCCACTGG | 54472 |
rs151101451 | snp | A/G | 0.000201643 | 0.010039 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288759 | CCAGGCAATGCGGTC[A/G]TCCATGGAGAAGGCT | 54472 |
rs151185390 | in-del | -/CA | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1277856 | CCAGAATGACAACCC[-/CA]CACACACATACAAAC | 54472 |
rs151256822 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276670 | AATTACATCACATCA[A/C]AAAATGCCATGAATG | 54472 |
rs151272471 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282517 | GTTTAGGAGAAATAC[C/T]TAATGTTAAATGATG | 54472 |
rs180703833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278901 | CCCCGGCTGGCAGGC[A/G]GGCAGGAACTTGGCC | 54472 |
rs180764195 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304536 | GGCACAGCAGCACCC[A/G]CGCCAGGACGGGGCG | 54472 |
rs180879083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307928 | GAAGAATTATCTCCT[C/T]GGGAGAAACACCAGG | 54472 |
rs181257871 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276017 | GTAGGCCAAGATGCT[A/G]CACGCAGCGCCCAGG | 54472 |
rs181280088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279372 | TGAGCCGGCCCATCC[C/T]GGTTACCAAGCACGG | 54472 |
rs181336373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287990 | AAATCCTCTGGTTGA[C/T]GATACAGACGAGACG | 54472 |
rs181411651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305161 | AGTGAAAAGATGTGA[C/T]TTCCAGGCAAGCACA | 54472 |
rs181414598 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287549 | AGCCTCACCGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs181416898 | snp | C/G/T | 0.0103426 | 0.0713021 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276119 | CCCACGCTGAACCCA[C/G/T]GTCCTGGGCACAGCA | 54472 |
rs181419904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284434 | GCTCACTGCAAGCTC[C/T]ACCTCCTGGGTTCAC | 54472 |
rs181565656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280113 | CATGTGATAGTTTGT[C/T]TCGGAAACTTTTAAG | 54472 |
rs181568209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293458 | GGCATCCCACTGGGG[C/T]CCCAGGAGACAACAA | 54472 |
rs181571320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288529 | ATGGGCTCAGTGCCT[C/T]CAGGAAAGAGACAAG | 54472 |
rs181706951 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308451 | CAGCCTGCAGAACCG[G/T]GAGCCAATTAAATCT | 54472 |
rs182004927 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287794 | CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG | 54472 |
rs182032389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306552 | TAACAGAAAGAGGAC[A/G]TGATAAATACTGTGT | 54472 |
rs182088877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304087 | GGAGGCAGGCCAGAA[A/G]CAGCGTATTCAGAAG | 54472 |
rs182108346 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274546 | TGGCACCCTGCAGGG[C/T]AGCGCCCAGGGAGCA | 54472 |
rs182118263 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305590 | ACAATCCCAGTTAAT[A/C]AACACCGAAGAAGTG | 54472 |
rs182130262 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287738 | CTGCCGCAGCCTCCC[C/T]GCCGCAGCCTCCCCG | 54472 |
rs182272730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285105 | GCAGCCCCTGAGCAC[A/G]AGCAGCCGGGGCCTC | 54472 |
rs182300044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285620 | GCGTCACCCAATGGG[C/T]GTGAGGTTCGGACAC | 54472 |
rs182308113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298884 | CCCTGACCAGTCAGT[C/T]GTCCTCAAACCGTCA | 54472 |
rs182394425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287306 | ACACATCGTCACTCA[C/T]GGCCGGGACATGATT | 54472 |
rs182446518 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293950 | ACGCCGCGAGGAAGG[G/T]GTGACGGTGTAGCTG | 54472 |
rs182516011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297975 | GATTCACAGCCCAGA[A/G]CTCTCTCCCCGGGGG | 54472 |
rs182606533 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310417 | ACCCGGAACTTAGGT[C/T]CCGATGTCCGGGTAT | 54472 |
rs182611353 | snp | C/T | 0.000142643 | 0.00844401 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276717 | CACCACCTCCAACAC[C/T]CTGGCAGAAGCAGCT | 54472 |
rs182713922 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280927 | CCAGTGGCACCCGCG[C/G]TGGTCTCTCACGCAC | 54472 |
rs182822698 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281907 | GAGACGCCCTGAGCA[C/T]GCAGCCGCCAGCCTC | 54472 |
rs182958165 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299869 | CAGCGCATCGCCACG[C/T]GGCCTCACCAGGAGC | 54472 |
rs183058617 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282761 | GTTGTGCACATGTAC[C/T]CTAAAACTTAAAGTA | 54472 |
rs183090346 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295551 | AAGTTCTGTTTGCCC[A/G]CTTAGGAAATGCAGT | 54472 |
rs183400443 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276432 | GCCTTCAGGCCGGAG[C/T]CTGTCACAAGGCTGG | 54472 |
rs183430958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289318 | GGCAGGGAGGGCTGG[C/T]CGTCTGCTGGCCTGG | 54472 |
rs183432839 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274176 | GAAGAGCAGACCCAC[A/G]CCCACTGCCACTGTT | 54472 |
rs183485200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305316 | GTCAGCAGGAACGGA[C/T]GCCCTCCCAGGAGCA | 54472 |
rs183602541 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311075 | AGCCCCTTCCTCAAG[C/T]TGTAGCTTAACATCC | 54472 |
rs183669349 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286683 | CACTGCACCGCTGTC[A/G]TCTCTAAGTTTAGTT | 54472 |
rs183679660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301837 | GACAGAGGAAGCTAA[A/T]GAAACAGAGAGAAAT | 54472 |
rs183721096 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287801 | ACCCTCCCTGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs183732213 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275802 | CTTCTGCATCTTCCA[A/C]AGAAGACCCACTTGT | 54472 |
rs183751330 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306828 | CATCCTCGGCCCCTG[A/G]GGCTCCCTCCTCTCC | 54472 |
rs183814747 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283893 | CTGCCTACGGGGCTT[C/T]GACTTCCAGCCTCAG | 54472 |
rs183821506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297422 | TGAGTAAACAGAAGG[A/G]ACCCGGACGATCCAG | 54472 |
rs184060576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286487 | CTGCTGTCAACTCTG[A/G]GTTCAAAACTGTCCA | 54472 |
rs184245356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301021 | AGTCTCAGCGCTAAC[A/G]CCAGGTTAGCATAAC | 54472 |
rs184264076 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296813 | AGGCCTGGTTGATGG[A/T]GGAGTGGGGTGGAGG | 54472 |
rs184375012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283629 | TCAAAGTTTGTCTAG[A/C]CTTTCCTAAAATAAA | 54472 |
rs184409585 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279349 | GGGCAGAGGCCATGT[A/G]CCTGGCCTGAGCCGG | 54472 |
rs184441602 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291580 | CCCCTCTGAGGGCAC[A/G]GCCACCCTGTCCTCA | 54472 |
rs184460247 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277544 | TCAAATCTCACCCGA[C/G]TCTGTTTTATAACTA | 54472 |
rs184568508 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292687 | GGACACACGGGCACC[A/G]CTGCCTCCCCCACAA | 54472 |
rs184604196 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275404 | GGAACATACCATCTA[A/G]AACGTTCCAGTCCCG | 54472 |
rs184973113 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287764 | CCCCGCCGCACCCTC[C/T]CCGCCGCAGCCTCCC | 54472 |
rs185068029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305969 | GGTACCCCTCGCAGG[G/T]GCCCCCATGATACTC | 54472 |
rs185077564 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275156 | ACTGTGTGGGTCCCT[C/T]GGGCCCCCACACGGG | 54472 |
rs185092938 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277841 | AGCTGCAGCCGATGC[A/C]CAGAATGACAACCCC | 54472 |
rs185100415 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303773 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAAA | 54472 |
rs185101481 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291847 | GGGCACGGCCGCCCC[A/G]TCCTCACCGACCCCC | 54472 |
rs185231686 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306222 | GAAGATCTAAACACG[A/G]TATGATTCTCTCAGA | 54472 |
rs185233508 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287163 | CGAAACTGTCAACTG[C/T]GGATAAGTCACTGCA | 54472 |
rs185334616 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287780 | CCGCCGCAGCCTCCC[C/T]GCCGCACCCTCCCTG | 54472 |
rs185370957 | snp | C/T | 0.147991 | 0.228242 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287391 | AAAGCAGCTCCCTGC[C/T]GCTGCCTCCCCGCCG | 54472 |
rs185389355 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287470 | CCCCGCCGCAGCCTC[A/C]CCGCCGCACCCTCCC | 54472 |
rs185423253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304753 | TTGAGATAAAACAAC[C/T]GAATTTTTTAAAACT | 54472 |
rs185500124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304279 | CGCCCACCTGGAGTT[C/T]CACACACACAAAAAT | 54472 |
rs185537236 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285635 | CGTGAGGTTCGGACA[C/T]GACGGCACAGTGCAG | 54472 |
rs185541383 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298933 | GAAAGCCTGAGAGAC[A/G]GTCCCAGATTGGAGA | 54472 |
rs185803648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279773 | AAAACTTGTCCCTTT[C/T]CCATTCAGGAAAAAT | 54472 |
rs185839057 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293233 | CCGGGAGGGTGGCCC[A/G]AGAGCTCCACCTTGG | 54472 |
rs185912389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298459 | GCACTGTGGGTCCCT[C/T]GCTGCTCTGGATCCT | 54472 |
rs185939754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297750 | GAGGAGGGTGCAGAG[C/G]TGCCTGAGCGGAGTG | 54472 |
rs185979803 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288832 | GGGGCCACCCTGCCC[C/T]TGCAGCCGCACCATC | 54472 |
rs186053820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285362 | GGCTGCGGTCTCCCC[A/G]CCTGCTAAAGACGGC | 54472 |
rs186077489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280973 | AATTGAGCAGTTGGC[A/T]GCTGTTGCCAGCCTG | 54472 |
rs186107355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293769 | AGGTGGAGTGCCCTG[A/C]GGTCACCAGGCCCTG | 54472 |
rs186191440 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294004 | TGAAAGCAAGTCTTA[G/T]TTGTGAGGTCCACGG | 54472 |
rs186194176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288107 | AGCCAGGGCGCTGAC[A/G]TGCTGGCCCCACAGC | 54472 |
rs186292000 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276023 | CAAGATGCTACACGC[A/G]GCGCCCAGGCAGTCA | 54472 |
rs186348700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308013 | CAGTACTGGGCTGCG[C/T]GAGGGCAGGGACCTT | 54472 |
rs186644202 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276561 | CTCACAGCAAAGCGC[A/G]TTAGGGCAAGGGCGT | 54472 |
rs186650388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289424 | ACTGAGCAGCAGCCT[C/T]GCCACATCCCCTCTG | 54472 |
rs186749964 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275094 | GAGATGGCGGCAAGC[A/G]TGGTCATCGGCAAAG | 54472 |
rs186752636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305206 | GTACAGACTCACAAC[C/T]CGGCCTAAAAAATCC | 54472 |
rs186781358 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287745 | AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC | 54472 |
rs186856671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284584 | TTGATCTCCTGACCT[C/T]ACGATCTGCCCGCCT | 54472 |
rs186894039 | snp | C/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302055 | TGCTGTGTCTGAGGG[C/G]CTGGCCCTGCCTTGA | 54472 |
rs186925025 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287680 | CCCCGCCGCACCCTC[C/T]CCGCCGCAGCCTCCC | 54472 |
rs187220728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280190 | ATGTGCTGCTCAGCT[A/G]CAAACTCCCTATTCG | 54472 |
rs187500542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282262 | ATCCCGCCTGAGGGG[A/G]CTCCCTCTGGCCAAA | 54472 |
rs187505701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295397 | TGGTGGAAGAGCCAG[A/G]CCCTACACAGAGCAG | 54472 |
rs187565737 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274414 | TCTATTTTTATATGG[A/G]TCATTTATTAAATTA | 54472 |
rs187604555 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287710 | CCGCCGCAGCCTCCC[C/T]GCTGCACCCTCTCTG | 54472 |
rs187626472 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291634 | CCGCCCTGTTCTCAC[C/T]GCACCCCTCTGAGGG | 54472 |
rs187637433 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277564 | TTTTATAACTAGCAG[C/G]CTGGGGGTGGTGTTT | 54472 |
rs187659344 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311385 | GTGCCACCCCCTGGC[A/G]GCGGGGCCCCCCACC | 54472 |
rs187771180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286627 | GGATAAGTCACTGCA[C/G]TGCTGTCTCCTGAGT | 54472 |
rs187834909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290588 | GGCCAGGAGCAAGAA[A/G]AGTGAGCCACAGATG | 54472 |
rs187993992 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275270 | TGCACCCCAGCAACG[C/T]GAAGGCAGAAACCGG | 54472 |
rs188125954 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310442 | GGGTATCTTAAGAAC[A/T]AGAAGCATTCTTAGT | 54472 |
rs188284387 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287766 | CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG | 54472 |
rs188438557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286982 | GATAAGTCACTGCAC[C/T]GCGGTTGTCTCTGAG | 54472 |
rs188442912 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287808 | CTGCCGCAGCCTCCC[C/T]GCCGCAGCCTCCCCG | 54472 |
rs188472459 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306914 | CTCCCATTCCTCCTC[A/C/T]GAGAGATGTCACGTC | 54472 |
rs188487646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286422 | GGGAACCACACTGCA[C/T]TGCTGTGGTGTCTGA | 54472 |
rs188587492 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284254 | CTCTGAACGCCTCAA[A/G]GCTGCTTCTGCGTTT | 54472 |
rs188591370 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297612 | GACTGGGACACGTCA[C/T]GAGTGACCTTTGCCC | 54472 |
rs188665751 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296388 | CTCTGTCCACCACTG[A/C/T]CACTTCTGAGGGGAA | 54472 |
rs188794338 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301057 | CGAACGAAGTTCAAT[G/T]AAAAACTAAAATGCT | 54472 |
rs188801479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300348 | CTCACTGACGCCAGA[A/G]CTCTAAACCACTGCA | 54472 |
rs188908264 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283098 | CAGCCAGGCAGAGCC[C/T]GCCGTGAGGGACGAG | 54472 |
rs189127265 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293395 | GGATGCAGAAGTCAC[C/T]GGGATGTGTGGGCAG | 54472 |
rs189304692 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283817 | CAGCCACAGAGCGCC[C/T]GGCCCAGAAGTTGGA | 54472 |
rs189347303 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287792 | CCCCGCCGCACCCTC[C/T]CTGCCGCAGCCTCCC | 54472 |
rs189368477 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275462 | GAAATCTACACAGGC[A/G]TAAGACCAGGCCATC | 54472 |
rs189487745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292797 | TGCGCGGCAGACACA[C/T]AGCGCAGCAGACGGC | 54472 |
rs189500855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304373 | TCTAGATGAACCTGA[A/G]GCTAAAGGAAAGTGA | 54472 |
rs189527480 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310308 | TCCAGCTCGAACAGC[A/G]CTGGGTAAACTGAGG | 54472 |
rs189608452 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275992 | CCAGGTGTCACCTAA[A/C]ATCTGTCCTGTAGGC | 54472 |
rs189626375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297075 | GTCTGCAGGGGCCCC[A/G]GTCAGCGCCAGTGCC | 54472 |
rs189733280 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279362 | GTGCCTGGCCTGAGC[C/T]GGCCCATCCTGGTTA | 54472 |
rs190156264 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287472 | CCGCCGCAGCCTCCC[C/T]GCCGCACCCTCCCCG | 54472 |
rs190156697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287246 | CGTCATGATGGTTCT[C/G]TGTTTGTATGAAAGC | 54472 |
rs190188684 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305115 | AAGGCAAGAGGCCTT[C/T]ATCTTCCAAGAGGCC | 54472 |
rs190190620 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281468 | GGTGGCAGCTGGGCT[C/T]AGACACCACGGGAGG | 54472 |
rs190291294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297814 | CAGGCAGCCTCTCTC[A/G]AGGCGCTGTACAGCT | 54472 |
rs190296422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285749 | CTGAAAATTTCAACT[C/T]ACCTCATTTCTGCCA | 54472 |
rs190334482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299459 | TATCGTTTCAGTGAC[A/G]ACACTCGGTCCTTCA | 54472 |
rs190386031 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278870 | GACCCCTGGGATCCC[C/T]GTGGCTTTTTGGGCG | 54472 |
rs190393396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303879 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 54472 |
rs190559648 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284829 | CAGGCAGTTTTGTCC[A/G]AGAATGTCCTGAACA | 54472 |
rs190607240 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289889 | AGATCAGTGCCCAGC[A/G]GAGGGGACACGTGCA | 54472 |
rs190647016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292090 | GCCACAGCGTACTCC[A/G]GAATGCTATGGAGTG | 54472 |
rs190839632 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289052 | GCGAGGGCCCTGGGC[C/T]GCTGTCCTCCTTCAG | 54472 |
rs190853042 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276585 | AGGGCGTGAGTTTTC[A/G]TCTGGGAAGTTCTAA | 54472 |
rs190956035 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274459 | AAAAATATATTTTAC[A/T]ATCAAAGAAAAATCT | 54472 |
rs190967838 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305480 | CTTGAGGTACGGGAA[A/G]ATGAGGGAAAAGCAT | 54472 |
rs190984476 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287713 | CCGCAGCCTCCCCGC[C/T]GCACCCTCTCTGCCG | 54472 |
rs191108119 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294120 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs191128433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286676 | GATAAGTCACTGCAC[C/T]GCTGTCATCTCTAAG | 54472 |
rs191135690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301319 | AAATCACAAAATGTC[A/G]ACGATTCTCATTCAA | 54472 |
rs191256399 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308363 | ACGTGTAAGCTCCCA[C/T]TTGGCCTTCCGCCAT | 54472 |
rs191484187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288448 | GTGGGCAGGGCAGCC[C/T]CTCTCTGCCACCAAA | 54472 |
rs191639026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283838 | AGAAGTTGGAGGAGA[C/T]GGGGAGGATCCTCCT | 54472 |
rs191648050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305269 | GGACTCGTGAGGAGG[C/T]GGTGAGTGCGTTCCC | 54472 |
rs191673686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297117 | TTTTCAGGAAATACC[A/G]AGTGGAACCTGGAAC | 54472 |
rs191769402 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287694 | CCCCGCCGCAGCCTC[C/T]CCGCCGCAGCCTCCC | 54472 |
rs191787005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303174 | TATAAAAGCTGACTA[C/T]AGAACAAGCGACTTT | 54472 |
rs191810125 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286984 | TAAGTCACTGCACCG[C/T]GGTTGTCTCTGAGTT | 54472 |
rs191959620 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282294 | CTGGAATAATTTGAG[G/T]GAAAAAATAACATTC | 54472 |
rs191964470 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295550 | GAAGTTCTGTTTGCC[C/T]GCTTAGGAAATGCAG | 54472 |
rs192017024 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280531 | AGCAGAGAAAAGAGA[A/G]AAGCACTCCAGGCCC | 54472 |
rs192063872 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274074 | TCTCAGAACGGGGTC[A/G]TGTTCCACGCTCACT | 54472 |
rs192193034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292289 | AGTCTGAGACCAGCA[C/T]GATTTTCCAAAGCTT | 54472 |
rs192349109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293936 | CAAGGGTCTGAGACA[C/T]GCCGCGAGGAAGGGG | 54472 |
rs192485607 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291670 | CCGCCCCGTCCTCGC[C/T]GACCCCCCGCTGAGG | 54472 |
rs192497372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277702 | CCGCTGATCCAAACA[C/T]TGCACGGTCTGAGCC | 54472 |
rs192682468 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275128 | TGCTCTCCCTCCAGC[A/G]AGGCTGGCCCCCACT | 54472 |
rs192753547 | snp | G/T | 0.0017025 | 0.0291264 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277021 | GAGCGGGGGCAAAAC[G/T]GCATCGAGGCAGAGG | 54472 |
rs192761656 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310982 | CACATCTTTGGGTCT[C/T]GGTTACCAGTCTCTC | 54472 |
rs192817057 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287773 | ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC | 54472 |
rs192898159 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287752 | CCGCCGCAGCCTCCC[C/T]GCCGCACCCTCCCCG | 54472 |
rs192952885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290899 | GACGCCACGTGGCTG[C/T]TTTCCTCCCTCGTGA | 54472 |
rs193029043 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306220 | CTGAAGATCTAAACA[C/T]GGTATGATTCTCTCA | 54472 |
rs193030847 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275283 | CGCGAAGGCAGAAAC[C/T]GGTGCTGGTGGCCAC | 54472 |
rs193085344 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300710 | GCCCCGGAAGAGCCC[A/C]GCTCAGCCCAGGACG | 54472 |
rs193120829 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283216 | CCTGCCAGCAGCCCC[C/G]GGGAAACTCAGCCCT | 54472 |
rs193236650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286468 | CTTCACATAAGTCAC[G/T]GCACTGCTGTCAACT | 54472 |
rs193282571 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296449 | CATCCCGAAACCACC[C/G/T]GCACACCTGCAGCGG | 54472 |
rs199524160 | snp | A/G | 0.00699995 | 0.058745 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276994 | GGGGAGCGCCGGGTC[A/G]GCGTGTCCAAAGAGC | 54472 |
rs199578390 | snp | C/T | 6.70758e-05 | 0.0057908 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277181 | TCCTCCTCGCTACAG[C/T]GGGGCTGGGCGTTCA | 54472 |
rs199603176 | snp | C/T | 0.000521232 | 0.0161352 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276996 | GGAGCGCCGGGTCGG[C/T]GTGTCCAAAGAGCGG | 54472 |
rs199606088 | snp | C/T | 0.000522647 | 0.016157 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288764 | CAATGCGGTCGTCCA[C/T]GGAGAAGGCTCTCTG | 54472 |
rs199788465 | in-del | -/AC | 0.0437281 | 0.141251 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304305 | AAAATAGCTGTCAGG[-/AC]ACAGAGAAAAGGCAT | 54472 |
rs199855632 | snp | C/T | 0.00100197 | 0.0223602 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295599 | AAATCCCACCCCCAC[C/T]GAGCGCACCAGCCCC | 54472 |
rs199861074 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295663 | TACCACCGTGATGTT[C/G]AGTCGGCCCACGGTG | 54472 |
rs199896670 | snp | C/G | 8.35582e-05 | 0.00646314 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288747 | GGTGATGTGGGTCCA[C/G]GCAATGCGGTCGTCC | 54472 |
rs199981907 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286578 | GTCACTGCACCGCTG[C/T]CGTCTCTGAGTTTAG | 54472 |
rs200039884 | snp | C/T | 6.98934e-05 | 0.00591116 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286132 | GGGGTCAAGGAGGAA[C/T]ATCCACCCATCAGAA | 54472 |
rs200215863 | in-del | -/ACAT | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282909 | ACCTGCACGTTGTGC[-/ACAT]GTACCCTAAAACTTA | 54472 |
rs200240822 | snp | C/T | 0.00114172 | 0.0238654 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288758 | TCCAGGCAATGCGGT[C/T]GTCCATGGAGAAGGC | 54472 |
rs200356789 | in-del | -/ACCCA | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297052 | TGGAGTGGGGTGGAG[-/ACCCA]GCCGTCTGCAGGGGC | 54472 |
rs200578328 | snp | A/C/G/T | 0.00108878 | 0.02331 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277010 | GCGTGTCCAAAGAGC[A/C/G/T]GGGGCAAAACGGCAT | 54472 |
rs200790260 | in-del | -/ATAA | 0.0558544 | 0.157504 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282630 | TAAAATATAATTAAG[-/ATAA]ATAAATAAATAAAAT | 54472 |
rs200810723 | snp | A/G | 0.000165303 | 0.00908978 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288818 | CAGGCATCAGGGAAG[A/G]GGCCACCCTGCCCCT | 54472 |
rs200881444 | snp | A/G | 0.00548886 | 0.052099 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286024 | GGGCACATAGCCAAC[A/G]CCCTGCTGGTACACT | 54472 |
rs200928462 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287973 | TTCAGTAACAGCCTG[-/A]AAAATCCTCTGGTTG | 54472 |
rs200993320 | snp | C/T | 1.67503e-05 | 0.00289393 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288752 | TGTGGGTCCAGGCAA[C/T]GCGGTCGTCCATGGA | 54472 |
rs201099751 | snp | C/T | 0.000138663 | 0.00832539 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290447 | AAAAGGAGGTGCCAA[C/T]CATCAGGAGAGGGTG | 54472 |
rs201137588 | snp | A/G | 0.00199806 | 0.0315442 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288720 | CTTGCCCTGCCTCAG[A/G]GACTCCGGGATGGTG | 54472 |
rs201166699 | snp | C/T | 0.000433377 | 0.014714 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288699 | GCTGTACCACTTGTC[C/T]TCCACCTTGCCCTGC | 54472 |
rs201193280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281408 | GTCCTCGTGAGGGCT[C/T]AGCCAGCATTCAGCC | 54472 |
rs201304072 | snp | A/G | 1.66946e-05 | 0.00288912 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290339 | GTGGGCGTCTCGTAC[A/G]CCGCGTAGCCCAGGC | 54472 |
rs201394513 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308942 | TCAGGGTGCGGGACC[-/C]GCCTCCACCTGGGGG | 54472 |
rs201435614 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309659 | CCCGGCACCGCCCCA[A/C]TGCGCAGGCGCCGCG | 54472 |
rs201436284 | snp | G/T | 3.31219e-05 | 0.00406938 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277155 | GGAACATGTCCTGGA[G/T]GGCTTTCAGGTCCTC | 54472 |
rs201791881 | in-del | -/TG | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274525 | GTTCTGAGACCACTC[-/TG]CTGCCTGGCACCCTG | 54472 |
rs201951123 | snp | A/G | 0.000188319 | 0.00970176 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288625 | GGCGTGCAGCTCACC[A/G]CGTAGGACATGACGA | 54472 |
rs202103427 | snp | A/G | 7.41826e-05 | 0.00608981 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295600 | AATCCCACCCCCACC[A/G]AGCGCACCAGCCCCA | 54472 |
rs202211815 | in-del | -/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294552 | GGTGTGTCTCCTTTC[-/C]CTGCATTTCTACGAA | 54472 |
rs202220655 | snp | A/C | 0.004072 | 0.0449379 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295730 | TGGGCGTCCAGCTGG[A/C]CCTGCCGCTGCTGCT | 54472 |
rs202232442 | snp | A/C | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290151 | CCAGGAACGTGGCTG[A/C]GTTGGCAGGTGTGTC | 54472 |
rs202235332 | in-del | -/A | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291750 | CGTCCTCACCGACCC[-/A]CCTCTGAGGGCACGG | 54472 |
rs207471622 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307324 | CCAGGAGGCACTGGG[C/T]AAGAGGAGATTCTAA | 54472 |
rs367713230 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292935 | TCAGGAGTGACTAGG[A/G]TGAGGAAAACATGGG | 54472 |
rs367871552 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295031 | CCTTTCCCTGCATTT[C/G]TACGAAAGCCTGCGT | 54472 |
rs368059844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302704 | CACGCCAGTCTCCTG[A/G]CACTGGCATGTTCAA | 54472 |
rs368114023 | snp | C/T | 0.00135821 | 0.0260242 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288594 | CAACATACCCCAATG[C/T]GCCCCACCCCGCCCA | 54472 |
rs368124186 | snp | A/G | 6.60928e-05 | 0.00574822 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277116 | CTTCCAGCACGGAGC[A/G]GATCACCTCCTGGTC | 54472 |
rs368137609 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276077 | TCAGAAAGCTTTTAC[A/G]GGGCCACGCTCGCCA | 54472 |
rs368338912 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299557 | ATGATGGAGGAACTA[C/T]TTCAATGGTCACATA | 54472 |
rs368379685 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294940 | TTCCCTGCATTTCTA[C/T]GAAAGCCCGCGTGGC | 54472 |
rs368399346 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275568 | CAAAGGATCAAAGGC[C/T]TTTAGGACCCACAGC | 54472 |
rs368436119 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276926 | ACAGAAGTCCACGGG[A/G]GGGGGCGACACGGGT | 54472 |
rs368492722 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289664 | CTGCTGGTGAGCGGC[A/C]AGACGAGTGCCCAGT | 54472 |
rs368531852 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299641 | ATTACTCCCGATACA[C/T]AATGGATATTTTTCT | 54472 |
rs368620685 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297899 | TAAGCACCTGTTCCT[C/G]TTGGCACACAGGAAA | 54472 |
rs368636975 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284503 | ACAGGCGCCCACCAC[C/G]GCGCCCGGCTAATTT | 54472 |
rs368698979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301277 | ACTGACATCATTAGC[A/G]ATGGGCTAAATACGT | 54472 |
rs368699497 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278224 | ACAGAGCACAGGCAG[C/T]GTGCGCGGGGCTCGG | 54472 |
rs368708390 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309123 | TCTGGAGACCATTGG[C/G]GAGCGGGGCCTGCCT | 54472 |
rs368713777 | snp | A/G | 1.78159e-05 | 0.00298457 | missense, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277233 | CGGGCACCATGCCGG[A/G]GCTACAGACAGCGGG | 54472 |
rs368821055 | snp | A/G | 0.000190283 | 0.00975221 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295693 | GCCCACTGCGCCTCC[A/G]TACTGCAGCTGCTGG | 54472 |
rs368841341 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281968 | CTGGCAGTGGCTGCC[A/G]GGAGGATGGGCTGTG | 54472 |
rs368907142 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280405 | TTCATACTTTGTGGA[C/T]GGGCATTCATGTCCT | 54472 |
rs368973742 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275878 | CCGGCGGCAAGACAC[C/T]TGAACCACAAACACC | 54472 |
rs369071402 | snp | A/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273878 | TGGGCAGCAGAGAGG[A/G]GGCAGACACCCCACC | 54472 |
rs369086687 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297209 | TGCCATGCACACCAG[A/C]AACCCGTACCTGCCT | 54472 |
rs369144854 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306369 | TGCTCCTTCACGGCC[A/C]ATGGGATCTTGCCGT | 54472 |
rs369149324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295805 | TACACCTGCGGGGCC[A/G]GGGACCAGAGAGGCC | 54472 |
rs369154559 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288130 | CCCACAGCCAGGCCT[C/T]GACTTCCTGACCCTG | 54472 |
rs369270898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287275 | GCGTCTGTTAAAGAC[A/G]TGTCATGAGACATTT | 54472 |
rs369325002 | snp | A/G | 2.05662e-05 | 0.00320666 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295720 | CTGGGCCGCCTGGGC[A/G]TCCAGCTGGACCTGC | 54472 |
rs369336963 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309662 | GGCACCGCCCCACTG[A/C]GCAGGCGCCGCGCCA | 54472 |
rs369389832 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284371 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 54472 |
rs369509985 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282073 | CTGCTAGGATAATTA[A/C]AAAATACTTCAAAGG | 54472 |
rs369566335 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292874 | CTGCAGGATCTGGAG[G/T]AAGAGCTGCAGGAAG | 54472 |
rs369619314 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308989 | GCCCGCATCCATCTA[A/G]GGGACCATTAGGGTT | 54472 |
rs369629471 | snp | C/T | 6.42915e-05 | 0.00566936 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277286 | GTTTGGTAAAAACGT[C/T]GGAAAGTTCCAGAAG | 54472 |
rs369695317 | snp | C/T | 0.000388651 | 0.0139347 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288604 | CAATGCGCCCCACCC[C/T]GCCCAGGCGTGCAGC | 54472 |
rs369750923 | snp | A/C | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303138 | GGAAGAGTACAGGAC[A/C]GAATGAGAATAAGCA | 54472 |
rs369758521 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291992 | AGTTCCCTCCTTTCA[C/T]TTCTAATCAAAGCTG | 54472 |
rs369761966 | snp | A/G | 9.9553e-05 | 0.00705454 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290181 | CCCCACGGCAGCCAC[A/G]CTCAGCCACGTGCAG | 54472 |
rs369764814 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282787 | AAGTATAATTAAAAT[A/G]AATAAATAAATAAAT | 54472 |
rs369775019 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296628 | GGCCTGGTTGCTGGT[A/G]GAGGCCTGGTTGCTG | 54472 |
rs369775514 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289962 | CCCTGTGCGCCCAGC[A/G]GAGGGGACACGTGCA | 54472 |
rs369800147 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311020 | AACCGGCAGCCTGGC[C/T]GCTTGCCTGTTTTGA | 54472 |
rs369808375 | in-del | -/AG | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273875 | GGTTGGGCAGCAGAG[-/AG]GGGGCAGACACCCCA | 54472 |
rs369809819 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291375 | AGAGACCCCGGGAGC[C/T]ATCCCGGCCCTCCCA | 54472 |
rs369829607 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300380 | CGTACCTTTCCACAC[A/G]AAAGAAAAGAGGTCT | 54472 |
rs369963945 | snp | A/G | 0.000367273 | 0.0135463 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290335 | TGCCGTGGGCGTCTC[A/G]TACACCGCGTAGCCC | 54472 |
rs369992898 | snp | A/G | 0.000187436 | 0.00967898 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286123 | GATGGTCCCGGGGTC[A/G]AGGAGGAACATCCAC | 54472 |
rs369996833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297391 | GCACAAGCCAGTCAG[C/T]GCTCCACAACCAATG | 54472 |
rs369999254 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310595 | TTTATCTTACATATA[A/G]ACAAGCGTACCCAGG | 54472 |
rs370002766 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280667 | GCGGGCCAGGCTGGG[C/G]AGGCGCCGGACGCCC | 54472 |
rs370008179 | snp | A/G | 3.34891e-05 | 0.00409187 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277012 | GTGTCCAAAGAGCGG[A/G]GGCAAAACGGCATCG | 54472 |
rs370056014 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301810 | GACCTGGGCTGGGCT[C/T]GTGGCTAAAGGGACA | 54472 |
rs370107634 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294772 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTTC | 54472 |
rs370160205 | snp | A/G | 1.75099e-05 | 0.00295883 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290456 | TGCCAACCATCAGGA[A/G]AGGGTGGGTTCTCTA | 54472 |
rs370173941 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283696 | AATTAGGGATAGGAA[C/G]CAGAAAGAGGTAAGC | 54472 |
rs370184466 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291500 | CCAACCCCCCTCTGA[A/G]AGTACTGCCACCCTG | 54472 |
rs370193997 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274868 | GACACAGGCGGGGGC[A/G]GGGGAGGGTGGGGGT | 54472 |
rs370240528 | snp | A/G | 0.000316664 | 0.012579 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288727 | TGCCTCAGGGACTCC[A/G]GGATGGTGATGTGGG | 54472 |
rs370301597 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285825 | CAAACAAAATTCAAA[C/T]GTAAGCCTTGGCTTC | 54472 |
rs370310047 | snp | A/G | 8.69573e-05 | 0.00659326 | synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277212 | CGGCGGCCGGGGGCA[A/G]GGCCACGGGCACCAT | 54472 |
rs370421950 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281315 | TTTATTTTTGTGAAG[C/G]AGATGGTCTGACCTC | 54472 |
rs370518757 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308349 | GCTTTCGCCATGTGA[C/T]GTGTAAGCTCCCACT | 54472 |
rs370543921 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291679 | CCTCGCTGACCCCCC[G/T]CTGAGGGCACGGCCG | 54472 |
rs370559443 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274605 | AGCCTCCGGCGACCT[C/G]TCTTCTATCTCCGGA | 54472 |
rs370562981 | snp | C/G | | | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298059 | AGCCCATGCCAGCAG[C/G]CTCTATGACTAGCTC | 54472 |
rs370600804 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297169 | CTTAGGCAAAGTGCA[C/T]GTGCTGAGGCCGCCA | 54472 |
rs370752589 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300634 | CCCGACACCTGTTAG[A/G]AATACGTTTCCGACT | 54472 |
rs370840264 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308011 | TCCAGTACTGGGCTG[C/T]GCGAGGGCAGGGACC | 54472 |
rs370999509 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297706 | CATAGGCCAGGGCCC[A/G]GAGGGACCCCCTGCC | 54472 |
rs371085953 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300285 | CCTCCCCCATGTGCC[A/G]CTCTCAGAGGATCAC | 54472 |
rs371102731 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289654 | GAAATCCCACCTGCT[A/G]GTGAGCGGCCAGACG | 54472 |
rs371392619 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308869 | CATCAGGGTGCGGGA[-/C]CCGCCTCCACCTGGG | 54472 |
rs371574523 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299923 | TGGAGACTCGGGGGA[C/T]GGAGGCGGAGGCGGA | 54472 |
rs371584235 | snp | A/G | 0.000172597 | 0.0092881 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295786 | CTGCGGGAGCTCACC[A/G]ATGTACACCTGCGGG | 54472 |
rs371661227 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295042 | ATTTCTACGAAAGCC[C/T]GCGTGGCTCACAGTG | 54472 |
rs371762554 | snp | A/C | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289988 | GTGCACGCTGTATCC[A/C]TGGGTCATGCTTGTC | 54472 |
rs371815197 | snp | A/G | 5.55993e-05 | 0.00527225 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295604 | CCACCCCCACCGAGC[A/G]CACCAGCCCCAGGCA | 54472 |
rs371832813 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280369 | CCATCCCAGCAGCGG[C/T]GTCCACCTGCGTGTT | 54472 |
rs371924457 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289887 | CCAGATCAGTGCCCA[A/G]CGGAGGGGACACGTG | 54472 |
rs371926120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299720 | CAAGTCTAAATGCCC[A/G]TGTGAAGGCCAACAA | 54472 |
rs371931657 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309212 | AGGCCCCCTCCCCCG[C/G]GGCTGCCTCCCCAAA | 54472 |
rs372005060 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293696 | AGGGGGGCCAGAGGC[A/G]TGGGCAACGCCAGGG | 54472 |
rs372125723 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288868 | CCCGCCTCGAGTCCC[C/T]GTCTTATCTGTGGAA | 54472 |
rs372163559 | snp | C/T | 0.000183641 | 0.00958054 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290340 | TGGGCGTCTCGTACA[C/T]CGCGTAGCCCAGGCG | 54472 |
rs372240396 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306145 | GGCCTTTTTGAAACG[A/T]GAGGGAAGCACTGCA | 54472 |
rs372244606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305854 | TCTCTGACGGCACCG[C/T]GGTGGCTGCAGCGGA | 54472 |
rs372252798 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291080 | GAGGTCCTCGGGGTG[A/G]GAGTGAACGTGTGTT | 54472 |
rs372311105 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306597 | AAAGCAGGGCTCCTC[C/T]AGGTGCTAGTAACTG | 54472 |
rs372408377 | snp | A/G | 0.000162237 | 0.00900511 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288573 | CGGCATAGCCCCGAC[A/G]TGCTCCAACATACCC | 54472 |
rs372408628 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304022 | GCCTGGGCTACAGAG[C/T]GAGCCTCCATGTAAA | 54472 |
rs372447607 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278050 | ATGCAATCTATCGAG[C/T]AGGAGACGCACGGCG | 54472 |
rs372485985 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300338 | CCATTCCTCCCTCAC[C/T]GACGCCAGAGCTCTA | 54472 |
rs372540291 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302061 | GTCTGAGGGGCTGGC[C/T]CTGCCTTGAAGGCCC | 54472 |
rs372608430 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296312 | GAAGAACGCAGGAAG[G/T]AAATCGATTCCAAAC | 54472 |
rs372617757 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291713 | CGTCCTCGCTGACCC[A/C]CCTCTGAGGGCACGG | 54472 |
rs372802328 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303411 | GGCAGCCTCTGCGTG[C/T]CACTGTGTGCCTGAG | 54472 |
rs372869759 | snp | C/T | 0.00163836 | 0.0285744 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290182 | CCCACGGCAGCCACG[C/T]TCAGCCACGTGCAGC | 54472 |
rs372933935 | snp | C/T | 5.12886e-05 | 0.00506376 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288626 | GCGTGCAGCTCACCG[C/T]GTAGGACATGACGAG | 54472 |
rs372939460 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302982 | TTAATTATACAAAAC[A/G]CAACAGGCGCTTCAA | 54472 |
rs372968261 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310197 | CCTCCCCGCCGCGCC[C/G]CTCCGCAGGAGCCCC | 54472 |
rs373098181 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309827 | TGCGCATGCCCAGTC[A/T]TGACGGTTGTCGGCG | 54472 |
rs373099776 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291565 | CCATCCTCACTGACG[C/T]CCCTCTGAGGGCACG | 54472 |
rs373185297 | in-del | -/CCT | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284882 | CCAGTGCCGTCTCCT[-/CCT]TCCCATCGTCAGGGC | 54472 |
rs373191090 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303184 | GACTACAGAACAAGC[A/G]ACTTTAAATGGGGTC | 54472 |
rs373201520 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283362 | CGGCCTGGATGCTGC[A/G]GACTCAGACGGGCTC | 54472 |
rs373210412 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294490 | GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs373267419 | snp | A/G | 7.05293e-05 | 0.00593799 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288605 | AATGCGCCCCACCCC[A/G]CCCAGGCGTGCAGCT | 54472 |
rs373319858 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285999 | GGGAGGGAGCACACG[C/T]ACCTGTGATGGGCAC | 54472 |
rs373439059 | snp | C/G | 0.00139195 | 0.0263446 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295818 | CCGGGGACCAGAGAG[C/G]CCAGTGAGTCAGGGT | 54472 |
rs373469888 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285392 | CTGGGCCCATCCATG[G/T]TGGGGGCCGGTCTTG | 54472 |
rs373516730 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293025 | CCTACTCTGGCCACG[C/G]TGCAGGGGCTGAGCG | 54472 |
rs373521011 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278467 | CAACACCAGCAACAA[-/G]GACCTGCAGGGGTGT | 54472 |
rs373551427 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300870 | CACTTCCATGACTGG[A/C]CCCCTGCGGAGCCTT | 54472 |
rs373569115 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297214 | TGCACACCAGAAACC[C/T]GTACCTGCCTGTGCC | 54472 |
rs373630245 | snp | A/C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279407 | GTCCATCAAGCCCTC[A/C/T]GGGAACGGTGAGCGT | 54472 |
rs373631889 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298209 | CATGCACAGCTCTGA[A/G]GACATGGCAGGAAAA | 54472 |
rs373719023 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287261 | GTGTTTGTATGAAAG[C/T]GTCTGTTAAAGACGT | 54472 |
rs373785313 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299901 | GGCGGTCCCTGCCGC[A/G]AACACATGGAGACTC | 54472 |
rs373918504 | in-del | -/CTCTT | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297539 | GCGTGTGCTCAACCG[-/CTCTT]CTCTAAAAAGCAAAA | 54472 |
rs374029431 | snp | A/G | 1.67697e-05 | 0.00289561 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290281 | GGGCACCGTGCAGTG[A/G]ATGACCTTATTCCAG | 54472 |
rs374135029 | in-del | -/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294476 | GCATTTCTACGAAAG[-/C]CCGCGTGGCTCACAG | 54472 |
rs374147650 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289764 | GGGCGGACACATGCA[C/T]GCTCTGTCCCTGGAA | 54472 |
rs374198955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302626 | CCAGCCTCGGCCTCA[C/T]GCTCCACACCAGCCT | 54472 |
rs374243365 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275980 | TGACTGTCATAACCA[A/G]GTGTCACCTAAAATC | 54472 |
rs374335160 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275975 | ATTTCTGACTGTCAT[A/T]ACCAGGTGTCACCTA | 54472 |
rs374522426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293604 | CCACCACTGGAGCTG[C/T]GCCACAGAAGGCTGG | 54472 |
rs374555515 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308924 | CCTCCATCTAGGGTG[C/T]CATCAGGGTGCGGGA | 54472 |
rs374558966 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291716 | CCTCGCTGACCCCCC[G/T]CTGAGGGCACGGCCG | 54472 |
rs374561701 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308882 | GACCCGCCTCCACCT[-/G]GGGGGGCCATCAGGG | 54472 |
rs374624012 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306319 | CTCTACCCAAGGACA[A/G]AAGAACCCTCCCAGG | 54472 |
rs374648737 | snp | C/T | 7.10581e-05 | 0.0059602 | missense, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277230 | CCACGGGCACCATGC[C/T]GGGGCTACAGACAGC | 54472 |
rs374889536 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276299 | CGCAGCAGGAGAGAC[A/G]GACGGCAGCCTCCGG | 54472 |
rs374900667 | snp | A/G | 6.77679e-05 | 0.0058206 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277192 | ACAGCGGGGCTGGGC[A/G]TTCACGGCGGCCGGG | 54472 |
rs374967831 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306341 | CCTCCCAGGACCCCA[C/T]TAGCGGCCCCTCTGC | 54472 |
rs375034388 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300001 | CACCAACTCTGGAGG[A/G]GCATTCAGGAATGGA | 54472 |
rs375043112 | snp | G/T | 0.000132183 | 0.0081286 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277117 | TTCCAGCACGGAGCG[G/T]ATCACCTCCTGGTCC | 54472 |
rs375082016 | snp | C/T | 0.000155988 | 0.00883004 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295798 | ACCGATGTACACCTG[C/T]GGGGCCGGGGACCAG | 54472 |
rs375094188 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309280 | CAGCGTGGGCGCGTC[C/G]GTCCGGCCCGCCCCG | 54472 |
rs375157686 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280002 | TGTTGCTGCTTCTCA[C/T]TCCACAGAGCGTTAT | 54472 |
rs375247428 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305208 | ACAGACTCACAACCC[A/G]GCCTAAAAAATCCAG | 54472 |
rs375251753 | snp | G/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290737 | CTCCTCAGAAGTGGC[G/T]GAGGAGGGAAAGAGG | 54472 |
rs375254926 | snp | G/T | | | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311155 | CTTTGGGGGCCTAGG[G/T]ACTTCCCCGGGCCCC | 54472 |
rs375335756 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304574 | TCTCCGCGTGGATCC[A/G]GAGGTGGCACAGACA | 54472 |
rs375337623 | snp | C/T | 1.67217e-05 | 0.00289147 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290385 | GGTCCATGCGGGTCA[C/T]GCCGTAATTCTTGGC | 54472 |
rs375415946 | snp | A/G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281561 | GGGTCTCTGGGCAGC[A/G/T]ATCAGCAGGCGACAG | 54472 |
rs375446535 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303302 | AGATGAAACAAAAGC[C/T]AGTCAAGCAGCAGGC | 54472 |
rs375452637 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276584 | AAGGGCGTGAGTTTT[C/T]GTCTGGGAAGTTCTA | 54472 |
rs375469267 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278562 | GCAAGGAAGGCCACC[A/G]CTTCCCGGCTCCTTC | 54472 |
rs375477714 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298256 | GCACACATGGCAGAC[A/G]GACAGGCGGCTCGTG | 54472 |
rs375482671 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299563 | GAGGAACTATTTCAA[C/T]GGTCACATAAAAATA | 54472 |
rs375495025 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291621 | TCTGAGGGCACCGCC[A/G]CCCTGTTCTCACCGC | 54472 |
rs375639703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296020 | CTCACTCAGGAGATC[C/T]CCAAATGCAGGTTTC | 54472 |
rs375659736 | snp | C/T | 5.37658e-05 | 0.0051846 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288587 | CGTGCTCCAACATAC[C/T]CCAATGCGCCCCACC | 54472 |
rs375663195 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293462 | TCCCACTGGGGCCCC[A/G]GGAGACAACAAGGGG | 54472 |
rs375809794 | snp | C/T | 0.000368002 | 0.0135597 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286104 | GCAGCTGAAACACAG[C/T]GGAGATGGTCCCGGG | 54472 |
rs375835141 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286835 | TCACTGCACTGCTGT[C/T]GTCTCTGAGTTTAGT | 54472 |
rs375844613 | snp | C/T | 0.000100219 | 0.00707809 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290329 | ATTGTGTGCCGTGGG[C/T]GTCTCGTACACCGCG | 54472 |
rs375916147 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291945 | ATCTCTGGACTGCCA[A/G]GTCCTCTGTTTTCTA | 54472 |
rs375938675 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282508 | TAGGAAATTGTTTAG[G/T]AGAAATACCTAATGT | 54472 |
rs376080090 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280924 | GGCCCAGTGGCACCC[A/G]CGCTGGTCTCTCACG | 54472 |
rs376099623 | snp | C/G | 1.72859e-05 | 0.00293984 | synonymous-codon, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277207 | GTTCACGGCGGCCGG[C/G]GGCAGGGCCACGGGC | 54472 |
rs376105942 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289148 | GCCACCTGTCAAGCC[C/T]CAGAGCAGCCGGGGT | 54472 |
rs376184285 | snp | C/T | 0.000112159 | 0.00748779 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276843 | TGGGAGGGGAGCCCC[C/T]GCCCCGTCCTGGACC | 54472 |
rs376190069 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288611 | CCCCACCCCGCCCAG[A/G]CGTGCAGCTCACCGC | 54472 |
rs376336431 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274590 | GAGGAGAGGAGGGGG[A/G]GCCTCCGGCGACCTG | 54472 |
rs376349045 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285930 | TCTAAGCCCCGTTCC[A/C]TCCTCCCGCACCTGC | 54472 |
rs376358531 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275883 | GGCAAGACACTTGAA[A/C]CACAAACACCAGACA | 54472 |
rs376369997 | snp | A/C | 0.000316381 | 0.0125734 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286143 | GGAACATCCACCCAT[A/C]AGAACCTCGGGAATC | 54472 |
rs376389813 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281172 | AATTTGGTAATCAAA[A/G]TAATACTTTGTTTAA | 54472 |
rs376389910 | snp | A/G | 6.18028e-05 | 0.00555856 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285974 | GTTTCTACCAGGGGA[A/G]AGGCACCCAGGGAGG | 54472 |
rs376459543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285194 | GCGCCCTGCCCGCAA[C/T]TTGGCCACTTCCATG | 54472 |
rs376532852 | in-del | -/C | 0.498632 | 0.0261223 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308863 | GGGGCCATCAGGGTG[-/C]CGGGACCCGCCTCCA | 54472 |
rs376539979 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291638 | CCTGTTCTCACCGCA[C/T]CCCTCTGAGGGCACG | 54472 |
rs376669117 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286762 | CAAAACTGTCCACTG[C/T]GGATAAGTCATTGCA | 54472 |
rs376895247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297357 | CTCCTCACCTGTGTC[C/T]CCATCTAAGGCCTGG | 54472 |
rs376897582 | snp | C/T | 0.000116786 | 0.00764065 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277026 | GGGGCAAAACGGCAT[C/T]GAGGCAGAGGCTCTA | 54472 |
rs376960196 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283813 | AAGACAGCCACAGAG[C/T]GCCCGGCCCAGAAGT | 54472 |
rs377122220 | snp | A/G | 3.33806e-05 | 0.00408524 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288678 | GTCCCCCTGCCTCCC[A/G]CTCAGGCTGTACCAC | 54472 |
rs377188815 | snp | C/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289491 | GCCACGGACGGGACT[C/G]AGGACCCTCAAGGGT | 54472 |
rs377302132 | in-del | -/TT | 0.00318978 | 0.0398085 | intron-variant | TOLLIP | GRCh38.p7 | 11:1304887 | CCATCTAGGCATCTC[-/TT]AACTAGAAAGATGAA | 54472 |
rs377336238 | in-del | -/A | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300131 | ACTTTTAAAATAAAA[-/A]GGACAGGGTAGGGCT | 54472 |
rs377406606 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307679 | GCTCTGAGTCTCCTG[C/T]TAGGCAGAAAGGAGC | 54472 |
rs377407901 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291518 | TACTGCCACCCTGTC[C/T]TCACCACCCACCCCC | 54472 |
rs377495722 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279116 | CTGCAAAATCGATGA[C/T]GGTGGCTGTGACGCT | 54472 |
rs377585391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298413 | TGGTCACAGGGACGT[A/G]TGGGCGTGGGGTCCA | 54472 |
rs377618446 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288258 | GGCCCAGGGCTGTAT[C/T]TCAGACCCTGGAGGG | 54472 |
rs377619944 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283303 | GAGCAAGATGGGGAC[C/G]CCTCCAGGCCAAGGG | 54472 |
rs377636075 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300594 | CAACGGAGAGAGCCG[C/T]TGCTTCCTTGGGCCA | 54472 |
rs377664757 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297608 | TTTTGACTGGGACAC[A/G]TCACGAGTGACCTTT | 54472 |
rs377668664 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280968 | CGGGAAATTGAGCAG[G/T]TGGCTGCTGTTGCCA | 54472 |
rs377687186 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287843 | ACCCTCCCCGCCGCA[C/G]CCTCCCTGCCGCACC | 54472 |
rs377719713 | snp | A/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273949 | CCAGGGTGGCTCGGG[A/G]TCTCTAGAGTGCTGC | 54472 |
rs377736201 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288171 | CCCCCAGGCTTCCCC[A/G]ACATCTCCAGAGATG | 54472 |
rs386749663 | multinucleotide-polymorphism | CA/TG | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301390 | CACAAACGGCATCCG[CA/TG]GGCGCCTGCCCACCC | 54472 |
rs397803441 | in-del | -/G | 0.5 | 0 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283481 | TGCCTGGGCATGGGG[-/G]CTGGGGGCTCCGGTG | 54472 |
rs527242058 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294379 | TTCCCTGCATTTCTA[C/T]GAAAGCCCGCATGGC | 54472 |
rs527243866 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299857 | GGCACATCCACCCAG[A/C]GCATCGCCACGCGGC | 54472 |
rs527282843 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298539 | ACTCTTTAGGTGTCC[A/G]TTAAAGACAGTGGGA | 54472 |
rs527320923 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275241 | CCACATGTGCACGCG[C/T]GTGGCAGTCTCACTG | 54472 |