SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs527327416 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281019 | CCACTCTGCAGCTCC[A/G]TGGAAGAGAACATGC | 54472 |
rs527341485 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297329 | CACTTCAAAGGACCC[C/T]GAGAGGGTCTAGCTC | 54472 |
rs527433983 | in-del | -/TGAT | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291127 | CCGTGGCAAGTAAGA[-/TGAT]TGATTGTTCAGCAAA | 54472 |
rs527575690 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283731 | CAATGTTATCTGTCA[C/T]CTGAATGCTCTTTCA | 54472 |
rs527724006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287082 | GATAAGTCACTGCAC[C/T]GCTGCCGTCTCTGAG | 54472 |
rs527725597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288798 | GAGACAAGAGGGAGA[A/G]GCCCCAGGCATCAGG | 54472 |
rs527762138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292847 | ACCAGCTAGGAGGAC[C/T]GGGTATGCGGGCTGC | 54472 |
rs527767561 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275837 | ATTCTCTTTCTGTCC[A/G]TTATCAGTGGGTTTA | 54472 |
rs527806118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298415 | GTCACAGGGACGTGT[A/G]GGCGTGGGGTCCAGA | 54472 |
rs527839476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303356 | AGGGACGGCATGTGA[C/T]GTGGCAGGCCCTGGG | 54472 |
rs527978970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308576 | TCATCTCTGAGTCAG[G/T]CTACACCAGCTCTCC | 54472 |
rs528015510 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308053 | TGAAAAAGGACTTTT[C/T]CCACCCACGGCATGT | 54472 |
rs528066905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279030 | GGCAACATGAGGAAC[C/G]GAGGCACCGTGCTCC | 54472 |
rs528119342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278742 | TGCTCATCAGCCTTT[C/T]GGCAATGACGGAAAA | 54472 |
rs528141153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288230 | CTGTGGGGAGGAGCC[C/T]GGTGTCCTGCAGGGC | 54472 |
rs528158121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283330 | AGGGAGGCAAGGCCA[C/T]GGAGGGCCAGTGACC | 54472 |
rs528311908 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291858 | CCCCGTCCTCACCGA[A/C]CCCCGAGGGCACGGC | 54472 |
rs528348842 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291534 | TCACCACCCACCCCC[C/T]GAAGGCACGGCCACC | 54472 |
rs528358784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297149 | CTCGGTGTGTCGGAC[A/G]TGAGCTTAGGCAAAG | 54472 |
rs528596551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306863 | CCAGACCCCACACCT[C/G]TCTTTCCGTGCCCTG | 54472 |
rs528630262 | snp | C/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301822 | GCTCGTGGCTAAAGG[C/G]ACAGAGGAAGCTAAT | 54472 |
rs528633900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306261 | GGGCTGGCTAGCTTC[A/G]CACGTCCTCTCCACA | 54472 |
rs528682166 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287654 | CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG | 54472 |
rs528763394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286677 | ATAAGTCACTGCACC[A/G]CTGTCATCTCTAAGT | 54472 |
rs528800054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290772 | GGTCCCGGGACAGAG[C/G]TGAGAGCCAGAGCAT | 54472 |
rs528800382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286368 | AGAGAGGATGGTGAC[A/C]GGAGGGACATCCCAG | 54472 |
rs528847501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308646 | TCAGGAGAGAATTCA[C/G]AGCAGGAAAGGTTCT | 54472 |
rs528881976 | snp | C/T | 1.65274e-05 | 0.00287462 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277094 | GCATCCTTGTTCCCT[C/T]GCTGGGCTTCCAGCA | 54472 |
rs528885733 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279384 | TCCTGGTTACCAAGC[A/G]CGGATGTGTCCATCA | 54472 |
rs528886698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308119 | GACAGCCTGCCCCAG[C/T]CCAGCCTCAGTGAGT | 54472 |
rs528919839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284311 | GAAGCATTCTTTCCT[C/T]GGTGACGGGGTGCAG | 54472 |
rs528927870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279092 | GAAGGGACAGGAGGA[A/G]GGGAACTGCTGCAAA | 54472 |
rs528933100 | in-del | -/GAGCACAGGCAGCGTGCGCGGGGCTCAGCGACCAGTGAGGCACA | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278168 | ACCACGAGCAGCCCT[lengthTooLong]GAGCACAGGCAGCGT | 54472 |
rs529162735 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292480 | TCTGCCACACTCAGC[A/G]TCATCCTCTCATTCC | 54472 |
rs529175681 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287963 | CAGCACCATTTTTCA[A/G]TAACAGCCTGAAAAT | 54472 |
rs529210168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291883 | CACGGCTGTCCCGTC[C/T]ACGCCAACCCTCGCC | 54472 |
rs529256302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297180 | TGCACGTGCTGAGGC[C/T]GCCAGAACGCCTCTG | 54472 |
rs529385139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306288 | CACACCTACCCACCC[A/G]GGCCCCTGAAGCTCC | 54472 |
rs529417041 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276182 | CCACCACACCCTCTC[A/G]GAATCATGCACAGTG | 54472 |
rs529435647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301627 | GTCAATATCACCCCC[A/G]CATTGAGAACAAGCG | 54472 |
rs529451752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306915 | TCCCATTCCTCCTCC[A/G]AGAGATGTCACGTCC | 54472 |
rs529454471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278486 | CTGCAGGGGTGTAAA[C/T]GGAGCAGACAGGGCT | 54472 |
rs529481463 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273894 | GGCAGACACCCCACC[A/G]TGTCCATGGACGCTC | 54472 |
rs529517240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278169 | CCACGAGCAGCCCTG[A/G]GCACAGGCAGCGTGC | 54472 |
rs529614822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281935 | CTCTCCAAGGTCTCC[A/G]CAGACTTCGCCCTTC | 54472 |
rs529676526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284247 | CCTCTAACTCTGAAC[C/G]CCTCAAGGCTGCTTC | 54472 |
rs529695310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291381 | CCCGGGAGCCATCCC[A/G]GCCCTCCCACCCACA | 54472 |
rs529754243 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286728 | GTGGATAAGTCACTG[A/C]ACTGCTGTCTCCTGA | 54472 |
rs529800311 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301004 | GCAAGCAAGGCTCAA[A/C]GAGTCTCAGCGCTAA | 54472 |
rs529801614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295414 | CCTACACAGAGCAGA[C/T]GCCCACCTACACCCA | 54472 |
rs529927774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300741 | TGGAGTCCTGAACAC[A/G]TGCAGTCCTGGCCTC | 54472 |
rs529964330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305866 | CCGCGGTGGCTGCAG[C/T]GGAGTCTCCCGCAAA | 54472 |
rs530063250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281233 | GGCCATGATCATGGC[A/G]TAAAAGCTTTAATAA | 54472 |
rs530098365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280857 | CAGTGGCTGCAGCCC[A/G]AGTGCCCCTCTGTGC | 54472 |
rs530100385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286257 | CTGAGTGCACAGGGG[A/G]CGCTGGGCCCTGCTC | 54472 |
rs530137315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285910 | TGACGTCCCCACCCC[A/G]GCGCTCTAAGCCCCG | 54472 |
rs530304635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289555 | CACCCAGTAGGCAGC[C/T]GCACTCTCTGGAAAT | 54472 |
rs530406623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294219 | GGCTCACAGTGTGTC[A/T]CCTTTCCCTGCATTT | 54472 |
rs530540178 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291404 | CACCCACATGGAGCC[C/T]GCCAGTTCCTCCTTC | 54472 |
rs530571441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282568 | CAACATGGCACACGG[A/G]TACATATGTAACAAA | 54472 |
rs530574150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296371 | CCTATGTCTCCTCGA[A/C]CCTCTGTCCACCACT | 54472 |
rs530613035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287125 | AGCTGTGGATAAGTC[A/G]CTGCACCGCTGTCTT | 54472 |
rs530707621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295913 | TCCTTATCAAGTCCT[A/G]GACTGTGCTCAGCCT | 54472 |
rs530887663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281801 | CTTGAAACTGTGGGC[A/G]ACACACATGCTCTGG | 54472 |
rs530899999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306182 | TGAAGCATCCCTTAG[A/T]GGCTATTCAGGGAAC | 54472 |
rs530923286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281333 | ATGGTCTGACCTCAG[C/T]GCCCCGGCTTCTGAG | 54472 |
rs531183465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286290 | ACCCCTGCACCACCT[C/T]CTCAAATCCAGGAGG | 54472 |
rs531211166 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304144 | GGAAAGCCGGAGGAA[C/G]GGACATCCACTCCCG | 54472 |
rs531257194 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288028 | CTCTGCGTCTTGGAG[-/C]CTCTAACTGGCCCTC | 54472 |
rs531285736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294415 | GTGTCTCCTTTCCCT[A/G]CATTTCTACGAAAGC | 54472 |
rs531405448 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300892 | CGGAGCCTTTTTAAA[C/T]CTTCTCACCGTTCCC | 54472 |
rs531426993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300138 | AAATAAAAAGGACAG[A/G]GTAGGGCTCTCATCC | 54472 |
rs531462182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299886 | GCCTCACCAGGAGCC[A/G]GCGGTCCCTGCCGCG | 54472 |
rs531493256 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294092 | TGTCTCCTTTCCCTG[A/C]ATTTCTACGAAAGCC | 54472 |
rs531502298 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311345 | CCATGCCTGGACCAA[A/T]CCCTTCCCTGTGAAA | 54472 |
rs531531954 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276844 | GGGAGGGGAGCCCCC[A/G]CCCCGTCCTGGACCG | 54472 |
rs531570554 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276482 | GCCAGGCCAGAGGCC[A/G]GCCCCACACCATCCA | 54472 |
rs531648699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279954 | GTGGGGACGACCGTC[C/T]AGCTCAGAGACTGTT | 54472 |
rs531658217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285045 | CCAGCACTGGCCTCA[C/T]AGCACTCTCGCCTGC | 54472 |
rs531742987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299008 | AGGGGACAGTCATCG[A/G]AAAACCAGGACAGCC | 54472 |
rs531781590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289463 | ACTCTGCCTCAGAAG[C/T]GCTGCAGGTGCAGCC | 54472 |
rs531827605 | snp | C/T | 3.42483e-05 | 0.00413799 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288780 | GGAGAAGGCTCTCTG[C/T]GGGAGACAAGAGGGA | 54472 |
rs531893712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292890 | AAGAGCTGCAGGAAG[C/T]GGGAGGAGAACGGCC | 54472 |
rs532022421 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304126 | CAGAGGGCCAAAAAC[G/T]AAGGAAAGCCGGAGG | 54472 |
rs532106962 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287626 | CCGCCGCAGCCTCCC[C/T]GCCGCAGCCTCCCCG | 54472 |
rs532129211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294836 | TGTGTCTCCTTTTCC[C/T]GCATTTCTACGAAAG | 54472 |
rs532131811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305807 | GAGCAGCCTGGACAC[A/G]GCACAGCGCACCCAC | 54472 |
rs532166088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300256 | ACTTCAAATTTCTTG[A/G]AATTGCTGATTCTCC | 54472 |
rs532217184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295354 | TGCCGGCGGGGGTCC[A/G]GGAGGTGTCCTTGGG | 54472 |
rs532232106 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286894 | TGCACTGCTGTCTCC[G/T]GAGTTCAAAACTGTC | 54472 |
rs532255815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300700 | CCTTGACAGAGCCCC[A/G]GAAGAGCCCAGCTCA | 54472 |
rs532269566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305399 | ATGCAGGAAAATCCA[C/T]GGGCTCTTCACAACA | 54472 |
rs532341419 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310931 | ACTCCCCATCCAGGA[C/T]ACCATGTGCTCTCAC | 54472 |
rs532419888 | snp | C/T | 0.00402713 | 0.0446917 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276858 | CGCCCCGTCCTGGAC[C/T]GCCAGGAACCGAAAA | 54472 |
rs532430580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280498 | CGGGAGGGACTGCGC[C/T]GGTGAGGACGTGGGG | 54472 |
rs532451685 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289806 | TGGTGAGCGGCCAGA[C/T]GAGTGCCCAGTGGCG | 54472 |
rs532466745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285537 | CAACAGACGCAACAG[C/T]GCAGTAGAGAGCACG | 54472 |
rs532475655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289489 | CAGCCACGGACGGGA[C/T]TCAGGACCCTCAAGG | 54472 |
rs532609674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289282 | GGGGAGAGAAAAGCC[A/G]GGAGGAAAAGGCAGG | 54472 |
rs532643530 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299780 | TGCTCACTCGGGCAC[A/G]TGAGCACAGGATGCC | 54472 |
rs532647885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293437 | GGGCTGAGGACCAGA[C/G]CCCTTGGCATCCCAC | 54472 |
rs532714018 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299057 | ACAGTCATGCCCCCA[G/T]CTCAGCGCCACAGCT | 54472 |
rs532749598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304178 | TGCTCAGCAGCCACT[C/T]CAGGAGCCAGGAGAG | 54472 |
rs532871403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279518 | TGGGCAGAGAGGACG[C/T]CATGGGAGCCCGGGG | 54472 |
rs533016231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279835 | CAGCATGGTAAGTCC[C/T]GGCCGCCGGTGGGCA | 54472 |
rs533043514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303563 | GAAACAGGGCAAGGC[C/T]GGGTGGCAGGGGCAC | 54472 |
rs533051357 | in-del | -/ATTTA | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275007 | GGAAAGAAGAATCTT[-/ATTTA]ATTAAAGGCCTTGCA | 54472 |
rs533056780 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310131 | GGGTGAACGGAACGG[A/G]GATGGAGGCGCTGCC | 54472 |
rs533092073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309045 | CATTAGGGTGCGGGG[C/T]CCTCCTCCATTCGGG | 54472 |
rs533133429 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304466 | AAACAAGCGCTGACT[C/G]GAGAGAAGTAACACA | 54472 |
rs533239567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283950 | CTTTCAGGTTGGCCA[C/T]TGGCCTCCAACTCAG | 54472 |
rs533285296 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292801 | CGGCAGACACACAGC[A/G]CAGCAGACGGCGTTA | 54472 |
rs533295828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302838 | CACATCCTCCTCCCA[C/T]GGCCGCTCAGCAGCC | 54472 |
rs533322026 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292651 | GCTGTTCTGGTGCAG[C/G]AGACACTGTGGACAC | 54472 |
rs533409851 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305762 | GACTCCATGGCCAAC[C/G]AGCACCTCCAGAAGC | 54472 |
rs533436410 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276022 | CCAAGATGCTACACG[C/T]AGCGCCCAGGCAGTC | 54472 |
rs533465020 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283238 | CTCAGCCCTACCCTG[C/G]AAGGCCACGTCAGCA | 54472 |
rs533484841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297359 | CCTCACCTGTGTCCC[C/G]ATCTAAGGCCTGGAG | 54472 |
rs533506541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288887 | TTATCTGTGGAACAG[A/G]GCTCCCACCTGCACC | 54472 |
rs533521258 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279408 | TCCATCAAGCCCTCC[A/G]GGAACGGTGAGCGTA | 54472 |
rs533526100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302239 | GCAAGAGGGCGGGAA[C/T]GCGCACCAGGGCTGA | 54472 |
rs533650906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293039 | GCTGCAGGGGCTGAG[C/T]GGGGGCAGTGGGTGG | 54472 |
rs533673944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307404 | TGCCGCTCCCACTTC[C/T]TCATCGCGGGTGTAA | 54472 |
rs533675050 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278203 | GGGCTCAGCGACCAG[C/T]GAGGCACAGAGCACA | 54472 |
rs533675688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298743 | CAGCCCCACGCAGCC[C/T]GGGGACCGCAGCCAG | 54472 |
rs533731489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293485 | ACAAGGGGAAGCAGC[A/G]AGGGGACGCAAGCAG | 54472 |
rs533977767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309318 | GTGTGGACGCCGCCG[C/T]TCCCCTCCGGCCGGC | 54472 |
rs534055772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279530 | ACGCCATGGGAGCCC[A/G]GGGCAGCCCAGAGCC | 54472 |
rs534122111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308299 | GATCTGGTCATTACA[A/G]TGTGTGGCACCTCCC | 54472 |
rs534222553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283995 | ACTTCACTAGCCCCA[C/T]GAACTGCACATCACA | 54472 |
rs534258433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302370 | GTGCCAGCCTGCACA[C/T]GCCCCAGGCCTGCAC | 54472 |
rs534263699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288516 | GCCCTGCTGTTTTAT[A/G]GGCTCAGTGCCTCCA | 54472 |
rs534292283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307448 | CGGTGCCCCTCAGAA[C/T]AGGAAGGGCCTGCCT | 54472 |
rs534302346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288061 | GATGCCCCCAGGAGC[G/T]GCAGGTGCCCTGAGA | 54472 |
rs534327214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307187 | ACACCTGAGACCCCC[A/G]TCGCTGACAACACCT | 54472 |
rs534345387 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311463 | ATTTCTCTTTCTCCT[A/C/T]GCTGCTATGTCTGCT | 54472 |
rs534388981 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278239 | CGTGCGCGGGGCTCG[C/G]CGACCAGCGAGGCAC | 54472 |
rs534448092 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291153 | GCAAACAAACTCAAC[A/G]TGGATGGCAGGTTCA | 54472 |
rs534451177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306518 | TGCTTAACCTCCTGC[A/C]TCTCTGGCACCACAG | 54472 |
rs534547188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297043 | GGTTGCTGGTGGAGT[G/T]GGGTGGAGACCCAGC | 54472 |
rs534553641 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287699 | CCGCAGCCTCCCCGC[C/T]GCAGCCTCCCCGCTG | 54472 |
rs534581752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286871 | ACTGTCCACTGCAGA[C/T]AAGTCACTGCACTGC | 54472 |
rs534589255 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274625 | CTATCTCCGGAGCCC[C/T]GCCTGAGGCTCCAAG | 54472 |
rs534619201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286568 | CTGCGGATAAGTCAC[C/T]GCACCGCTGTCGTCT | 54472 |
rs534619377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291001 | CCCAATCACAAGGAG[C/G]CACATCACATGTAGA | 54472 |
rs534628216 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274139 | CACAGAACCACCCAG[A/T]GGGGAGAGGGTGCCT | 54472 |
rs534651271 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290519 | CCTTTTCCTAACACA[C/G/T]AGACTACAGCCACTC | 54472 |
rs534653364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295979 | GTCCAGCCTGGGGCC[C/T]GGCCCCCAGCGGTAC | 54472 |
rs534716321 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277921 | GTGGGGCAGCAGGTG[C/T]GGTGTACAGTGGACC | 54472 |
rs534737348 | snp | A/T | | | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297764 | GGTGCCTGAGCGGAG[A/T]GGGCCCATGCCAGGA | 54472 |
rs534805595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301149 | ATGTATCAAATCACA[C/T]GTAGAAATAAACAAC | 54472 |
rs534930332 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300799 | GAGCCGCACCACAGT[C/T]GCCCCTGAAGCACGG | 54472 |
rs534963622 | in-del | -/CCCTCTTCCTATCACCCCCTC | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302935 | GACAGGGCTTTCCTT[-/CCCTCTTCCTATCACCCCCTC]CCCTCTTCCTATCAC | 54472 |
rs535034425 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288315 | GCTTGGAAGGGCTGT[A/G]GGGGTCCTCCGAGGA | 54472 |
rs535038230 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308689 | GCGCCTATCCTCTCA[C/T]TTGCAAATGAAGAAA | 54472 |
rs535049794 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297494 | GGGAAGCTCTCTGCA[C/G]GCTGCACCCCAACCT | 54472 |
rs535049842 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302991 | CAAAACACAACAGGC[A/G]CTTCAAAGCCAACAT | 54472 |
rs535118717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289269 | AGCAGGTAGGGACGG[A/G]GAGAGAAAAGCCGGG | 54472 |
rs535173152 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274755 | CTGGGCCCTCAGACA[A/C]CAGGGGCCTAAACCC | 54472 |
rs535185803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278762 | ATGACGGAAAACGAA[C/G]CGAACCATGGCCAGG | 54472 |
rs535312492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283455 | GGACGCCCCTGCTTA[C/T]TGGAAACGCATGCCT | 54472 |
rs535314317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278339 | AAGCACGAACCATCT[A/C]CCAGCTAGGATCACT | 54472 |
rs535349334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282784 | TTAAAGTATAATTAA[A/C]ATAAATAAATAAATA | 54472 |
rs535545314 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274238 | AATTCAATCTGGGAA[A/G]CAAAGGCCAGGCTTG | 54472 |
rs535618594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307264 | CGTTTACCGGTCAAC[A/G]GGGGTGCCCCTGAAA | 54472 |
rs535680600 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302907 | CCTTGTCTCCCCTTC[C/T]GGGGCCTTCCTCAGA | 54472 |
rs535713830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289352 | CCCCACACTGCTCCC[C/T]GGCCCCCACCCAGTC | 54472 |
rs535802386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286895 | GCACTGCTGTCTCCT[A/G]AGTTCAAAACTGTCC | 54472 |
rs535858349 | snp | A/G | 1.71422e-05 | 0.0029276 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290233 | CCCTCTCACCTCATC[A/G]AAGATCTCGAGATAG | 54472 |
rs535886968 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299268 | GCTTCAGTCCTCCCC[A/G]TACAAATACTGGTTA | 54472 |
rs535942323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291073 | GACATTTGAGGTCCT[C/T]GGGGTGGGAGTGAAC | 54472 |
rs536059960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300826 | ACGGCTGGCCACACG[C/T]AGGCGGCAGGAGACC | 54472 |
rs536156747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277372 | AGGAAGGGGCCACCT[C/T]GGGTCTCAGCAAACA | 54472 |
rs536166702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300341 | TTCCTCCCTCACTGA[C/T]GCCAGAGCTCTAAAC | 54472 |
rs536182091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293995 | TGAAGCCCCTGAAAG[C/G]AAGTCTTATTTGTGA | 54472 |
rs536187965 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305964 | CGCACGGTACCCCTC[A/G]CAGGGGCCCCCATGA | 54472 |
rs536245550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305125 | GCCTTTATCTTCCAA[A/G]AGGCCCGTGGGTCCC | 54472 |
rs536301082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281478 | GGGCTCAGACACCAC[A/G]GGAGGCTCTCGGGGC | 54472 |
rs536339764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286429 | ACACTGCACTGCTGT[A/G]GTGTCTGAGTTTGAA | 54472 |
rs536351307 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276280 | CCCACGGAGCTGGCA[C/T]GAGCGCAGCAGGAGA | 54472 |
rs536407110 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289973 | CAGCGGAGGGGACAC[A/G]TGCACGCTGTATCCC | 54472 |
rs536486864 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280284 | TCTGGAACTCACAGG[A/C]GCTGCGAACGCCGGC | 54472 |
rs536525462 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285209 | CTTGGCCACTTCCAT[A/G]GCCTGGGCCTCTGGC | 54472 |
rs536536533 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295053 | AGCCTGCGTGGCTCA[C/T]AGTGTGTCTCCTTTC | 54472 |
rs536675686 | snp | C/G | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311540 | CACTGGTAACACTTT[C/G]ACTCCTTAACATCGG | 54472 |
rs536682689 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303324 | GCAGCAGGCCAAGGG[C/T]GGACAGAGATCCAGA | 54472 |
rs536718031 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276599 | CGTCTGGGAAGTTCT[A/G]AAAAAAACCCACAGT | 54472 |
rs536732199 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282024 | GGGCATCAGCTTCCA[A/G]TGAAGAAGGGTGCCT | 54472 |
rs536766490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286779 | GATAAGTCATTGCAC[C/T]GCTGTTGTCTCTGAG | 54472 |
rs536793400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292986 | CAGGACAGTGCCCAC[A/G]AGAAAGGCCCACGCG | 54472 |
rs536980044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295527 | GGTTTCAGGAAAAGC[A/G]GGAATCAGAAGTTCT | 54472 |
rs537016138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295141 | TACAGACGGTTTTCG[G/T]GTGATCAAAATCGGC | 54472 |
rs537022895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306400 | CTCCCCTTATCACTA[A/G]GGGGAGGCAACGGCT | 54472 |
rs537087337 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287231 | GTAAAATCACTGGAG[C/T]GTCATGATGGTTCTG | 54472 |
rs537155268 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276982 | ACAGCATTCCTTGGG[A/G]AGCGCCGGGTCGGCG | 54472 |
rs537165221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281546 | CTGCACCCTGTGCGG[G/T]GGTCTCTGGGCAGCG | 54472 |
rs537202234 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287806 | CCCTGCCGCAGCCTC[A/C]CCGCCGCAGCCTCCC | 54472 |
rs537206326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286452 | AGTTTGAAAGTGTCA[A/G]CTTCACATAAGTCAC | 54472 |
rs537292414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280925 | GCCCAGTGGCACCCG[C/T]GCTGGTCTCTCACGC | 54472 |
rs537329822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280566 | GAAATGGAGGTGCAC[A/G]AGGGAACAGATGGAA | 54472 |
rs537375892 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1304985 | CTATCGATGGTGCAC[A/G]TGTCTTAAACAAAAG | 54472 |
rs537400118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285236 | TGGCCTCCACCCTCC[A/G]TGCAGAGGGACCAGT | 54472 |
rs537404567 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290946 | TGTGCTATCGGAGTA[C/T]GTGGGGTTTTGGGGA | 54472 |
rs537518692 | snp | C/T | | | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311022 | CCGGCAGCCTGGCCG[C/T]TTGCCTGTTTTGATG | 54472 |
rs537540709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289320 | CAGGGAGGGCTGGCC[A/G]TCTGCTGGCCTGGCT | 54472 |
rs537573874 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289321 | AGGGAGGGCTGGCCG[C/T]CTGCTGGCCTGGCTG | 54472 |
rs537598920 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306715 | GCGTGTGCCAGGCAA[C/T]ACTTTACAGAGTGCT | 54472 |
rs537830689 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309712 | CTCGCGCGCACGCGC[A/G]CTCCAGGGTAGGGCA | 54472 |
rs537843250 | in-del | -/G | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311387 | CCACCCCCTGGCGGC[-/G]GGGGCCCCCCACCGT | 54472 |
rs537972138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293520 | CCACCTGTGTGGCCG[C/G]CCAGAAGCCAAGAGA | 54472 |
rs538006433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299326 | AGAGGCGGCTTGCCT[A/G]CTGCTGCAATGCCCT | 54472 |
rs538043140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298770 | CCAGCGCCATGTGGC[A/G]GGGCAGGTGCGCGTC | 54472 |
rs538048182 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284963 | AAGGTGGCCTTTCTG[C/T]ATCTGTGCAGGATGC | 54472 |
rs538050878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304408 | AAATGGAAGGCCCGA[C/G]ACACCAGAAGGGATA | 54472 |
rs538052042 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307301 | CTCGTCTACATGATG[G/T]AAACAGCCCAGGAGG | 54472 |
rs538153901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292704 | TGCCTCCCCCACAAC[A/G]GGCAAGAGACGCACG | 54472 |
rs538330034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284505 | AGGCGCCCACCACCG[C/T]GCCCGGCTAATTTGT | 54472 |
rs538330104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279261 | GGGAGCAGGCACCCC[C/T]GGGGGAAGAGGTGGG | 54472 |
rs538360226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288834 | GGCCACCCTGCCCCT[A/G]CAGCCGCACCATCGT | 54472 |
rs538365239 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284036 | TGACCCCACGACGGC[A/G]GCTCTGGGCTGTCCC | 54472 |
rs538660856 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310315 | CGAACAGCGCTGGGT[A/G]AACTGAGGCTGAACC | 54472 |
rs538679105 | snp | C/T | 3.65384e-05 | 0.00427409 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286077 | GGGGTGGCATCACCA[C/T]GGCAGCTGGAAGCAG | 54472 |
rs538717489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289954 | CGGCCAGACCCTGTG[C/T]GCCCAGCGGAGGGGA | 54472 |
rs538760220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279638 | CACCTGCACGCACGC[A/G]GACGGATGTGCAGCA | 54472 |
rs538797291 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309781 | TCCTCGAGCCCTGCA[G/T]CCCGGCGAAATGGCT | 54472 |
rs538920065 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299912 | CCGCGAACACATGGA[G/T]ACTCGGGGGACGGAG | 54472 |
rs538925553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293605 | CACCACTGGAGCTGC[A/G]CCACAGAAGGCTGGG | 54472 |
rs538927132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288856 | CACCATCGTGGGCCC[A/G]CCTCGAGTCCCCGTC | 54472 |
rs538964345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293001 | GAGAAAGGCCCACGC[A/G]GGAACGGACCTACTC | 54472 |
rs539001180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292747 | CACCGTGGGGACACA[C/T]GGGCACCGCTGCTTT | 54472 |
rs539018756 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305467 | AAGCAACTCTCTCCT[C/T]GAGGTACGGGAAGAT | 54472 |
rs539078513 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306791 | CAGGACCCTCCGGCG[A/G]CCTCCAGCTCCTGCC | 54472 |
rs539156782 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275238 | GAGCCACATGTGCAC[A/G]CGTGTGGCAGTCTCA | 54472 |
rs539193109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303060 | AACACTAGAATTTGT[A/G]TAAGGGAAGCTGGGA | 54472 |
rs539293205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279134 | TGGCTGTGACGCTGC[A/G]ACGTCACGGCCTGGG | 54472 |
rs539295107 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274861 | CACACCTGACACAGG[C/T]GGGGGCGGGGGAGGG | 54472 |
rs539299860 | snp | A/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273991 | GGCGCTTTGCTCCCT[A/G]AGCATGAGCCAGTCA | 54472 |
rs539359153 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280115 | TGTGATAGTTTGTCT[C/T]GGAAACTTTTAAGCA | 54472 |
rs539372242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283507 | CGGTGGGGCGTCAGG[G/T]GGACGAGTCCTCACA | 54472 |
rs539408853 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288000 | GTTGATGATACAGAC[A/G]AGACGGCAGGAGCTC | 54472 |
rs539495672 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292449 | CGATGCCTGCTCACA[C/T]TGGATCCTGCCTGCT | 54472 |
rs539590395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302591 | ACCAGTACCTGACCC[C/T]GCAGCCCCTGGCACT | 54472 |
rs539612443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308171 | CCCGCCAAATCTCAC[A/G]CTGAATTATGATCCC | 54472 |
rs539651688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307810 | CGTAGGCTCCACACC[C/T]GAGTCTCATAAGTGT | 54472 |
rs539739567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301728 | GTACCCTGAGCCCTA[G/T]GTTTCTCCAGTTCCT | 54472 |
rs539752870 | snp | A/C | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309006 | GGACCATTAGGGTTC[A/C]GGGCCCGCCTCCACC | 54472 |
rs539777312 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287689 | ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs539779770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307042 | CAGCTGTCCTTATGT[A/G]CTGCCATGTCTACCG | 54472 |
rs539863803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282982 | AAATTGTAAATCCAC[A/T]TTGCTGGGGAAGTCG | 54472 |
rs539957480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291673 | CCCCGTCCTCGCTGA[C/T]CCCCCGCTGAGGGCA | 54472 |
rs539976105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288254 | GCAGGGCCCAGGGCT[C/G]TATCTCAGACCCTGG | 54472 |
rs539995638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296518 | AGGTCGCTGATGAGG[C/T]CCTGAGCATGGGTCT | 54472 |
rs540054599 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297647 | AGAGAAGCCGTACTG[A/C/T]GAGAACAAGCAGAGC | 54472 |
rs540112009 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274073 | CTCTCAGAACGGGGT[C/T]GTGTTCCACGCTCAC | 54472 |
rs540132142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296159 | CCACAGCTAAAGGCA[A/G]GGCCACTGAACTGCA | 54472 |
rs540157336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301325 | CAAAATGTCGACGAT[G/T]CTCATTCAATTCTCC | 54472 |
rs540347173 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278435 | GGCAGCAGAAGCCAC[G/T]TCAATCCTGGCCTGA | 54472 |
rs540359158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292769 | CGCTGCTTTCCCCAC[A/C]ATGGGCAAGAGATGC | 54472 |
rs540448667 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291821 | CCCCGTCCTCACCGA[C/G]CCACCTCTGAGGGCA | 54472 |
rs540512514 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275044 | TGTGATTTGTCTATT[-/A]AAAAAAATAAAGCGC | 54472 |
rs540524758 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274956 | TAAGCCACTTCTACA[A/G]TAAGCCTTCAAACAG | 54472 |
rs540559420 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297154 | TGTGTCGGACGTGAG[C/T]TTAGGCAAAGTGCAC | 54472 |
rs540572789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302655 | CTCCTGACACTCCCC[A/C]AAACCCACTCCAGCC | 54472 |
rs540609006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302053 | CCTGCTGTGTCTGAG[A/G]GGCTGGCCCTGCCTT | 54472 |
rs540643272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307340 | AAGAGGAGATTCTAA[C/T]GACACCTCAGCACTT | 54472 |
rs540659337 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307427 | GGGTGTAACAGCGCT[A/G]CACGCCGGTGCCCCT | 54472 |
rs540662364 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278889 | GCTTTTTGGGCGCCC[C/T]GGCTGGCAGGCGGGC | 54472 |
rs540736958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278123 | GCCGGACTTAAGACT[C/T]GCCTCCCAGCCTGGT | 54472 |
rs540773806 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282440 | CAAACCTGCACATTG[A/C/T]GCACATGTACCCTAA | 54472 |
rs540805500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306077 | AGGTACTCACCCATG[C/T]TTTCTGATAATATGC | 54472 |
rs540916557 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287039 | CACTGCACCACTGTC[A/G]CCTCTGAGTTCAAAA | 54472 |
rs540939436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288550 | AAGAGACAAGGGTGT[C/T]TGTGGGGCGGCATAG | 54472 |
rs540943800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281633 | CCCTAAGAAGCCGGG[C/G]TCTCCTTTCCTGGCC | 54472 |
rs540963716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291365 | AGCTGGTGATAGAGA[A/C]CCCGGGAGCCATCCC | 54472 |
rs541002222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290855 | CCTCGCTCTAGGTGA[C/G]AGTGAGGACACCTGC | 54472 |
rs541014711 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297334 | CAAAGGACCCCGAGA[C/G]GGTCTAGCTCCTCAC | 54472 |
rs541021405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295761 | GTGTGGGCGTGATGC[A/G]GAGGAAGTCCTGCGG | 54472 |
rs541021807 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280393 | GCGTGTTTTGCTTTC[A/G]TACTTTGTGGACGGG | 54472 |
rs541055438 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299088 | GTGAGAGCTGTTCCC[A/G]GGGAGGGGAGCGTCG | 54472 |
rs541114439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290123 | CAGGTGGGGAGCCAC[A/G]CCTCGAAGCCAGCCA | 54472 |
rs541153238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289821 | CGAGTGCCCAGTGGC[A/G]GGGGACACATGCATG | 54472 |
rs541160022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300966 | TGTGCCACGCATGCA[C/T]CTGCACTTGGCATGT | 54472 |
rs541172310 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287582 | CCCCGCCGCACCCTC[C/T]CCGCCGCAGCCTCCC | 54472 |
rs541203929 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295169 | GGCGTTCAATCTGCC[A/G]ATTTTGGCTTTCACT | 54472 |
rs541331061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281185 | AAATAATACTTTGTT[C/T]AAAAAAATCAAAACT | 54472 |
rs541431951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291832 | CCGACCCACCTCTGA[G/T]GGCACGGCCGCCCCG | 54472 |
rs541557171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296181 | TGAACTGCAGGTCAC[C/T]TGGTCAAACGAATGA | 54472 |
rs541568331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296286 | AACAGCTGAAATTCA[A/G]AAGTATCCCAGAAGA | 54472 |
rs541588705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294175 | GGCTCAGTGTGTCTC[C/T]TTTCCCTGCATTTCT | 54472 |
rs541675241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306741 | GTGCTGCGCTGAGCC[A/G]GTAAACTCCAGGGCA | 54472 |
rs541794639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305259 | CAGAGAGAAAGGACT[C/T]GTGAGGAGGCGGTGA | 54472 |
rs541918547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286612 | AAAACTGTCCACTGC[A/G]GATAAGTCACTGCAC | 54472 |
rs541993502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290658 | GACAGCAGAAACCTA[C/T]GACGCTCACAGACAC | 54472 |
rs542130102 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297421 | GTGAGTAAACAGAAG[A/G]GACCCGGACGATCCA | 54472 |
rs542410247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293939 | GGGTCTGAGACACGC[C/T]GCGAGGAAGGGGTGA | 54472 |
rs542450808 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280617 | CAGCCACGGTGAGCA[C/T]AGAATGAGCTCATGC | 54472 |
rs542554900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289729 | CTGCTGGTGTGCGGC[A/G]AGACCCTGTGCGCCC | 54472 |
rs542613116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299646 | TCCCGATACATAATG[A/G]ATATTTTTCTAGAAT | 54472 |
rs542624885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305671 | GCAGGAATTATCAAC[A/G]ATGTGAAGAGTGAGG | 54472 |
rs542662628 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311224 | CCTTCCTCATTTTCA[C/T]GCTAAAAATCACACC | 54472 |
rs542806608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285674 | TCACCTGACAGGGGC[A/G]TGAGGTTCTCCTGCA | 54472 |
rs542906513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308600 | GCTCTCCTGCAATAT[G/T]AATGCTATAGAAGAA | 54472 |
rs542943394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285375 | CCGCCTGCTAAAGAC[A/G]GCTGGGCCCATCCAT | 54472 |
rs542981238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293668 | GTGGGCTCCAGGGTG[C/T]GGGAGAGGACCAAGG | 54472 |
rs543057589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305985 | GCCCCCATGATACTC[C/T]TCACAGGGGTCCACA | 54472 |
rs543219569 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309905 | TCCTCGGTCCTCTGT[C/T]GAGTGGCGACAGGGC | 54472 |
rs543243316 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310078 | TTCTGTTTCACAGGG[C/T]TAAAGATGGGGCGCG | 54472 |
rs543328314 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275231 | ACCCACAGAGCCACA[C/T]GTGCACGCGTGTGGC | 54472 |
rs543347600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286152 | ACCCATCAGAACCTC[A/G]GGAATCGCCCTCCCC | 54472 |
rs543404325 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301015 | TCAACGAGTCTCAGC[A/G]CTAACGCCAGGTTAG | 54472 |
rs543414100 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295345 | TCCTCCAGCTGCCGG[C/T]GGGGGTCCGGGAGGT | 54472 |
rs543436790 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286717 | AACTGTCCACTGTGG[A/G]TAAGTCACTGCACTG | 54472 |
rs543478836 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287615 | CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG | 54472 |
rs543540489 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293705 | AGAGGCGTGGGCAAC[A/G]CCAGGGCCACCTCCA | 54472 |
rs543542639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300020 | TTCAGGAATGGAACT[C/T]GAGGGAAACAGGCAG | 54472 |
rs543545566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289468 | GCCTCAGAAGCGCTG[A/C]AGGTGCAGCCACGGA | 54472 |
rs543549005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305751 | GCCTCCAGCTGGACT[C/T]CATGGCCAACCAGCA | 54472 |
rs543555900 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294034 | GCGATTCTTCTGCCT[C/G]CTGTATTTGTGCATT | 54472 |
rs543564370 | snp | C/T | 1.65504e-05 | 0.00287662 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277148 | ATGTTGGGGAACATG[C/T]CCTGGATGGCTTTCA | 54472 |
rs543601149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281137 | CCTACCACGAATTAT[C/T]TGAAATCTGTAAAGT | 54472 |
rs543695091 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276313 | CGGACGGCAGCCTCC[A/G]GCGGGCGAAGGACCC | 54472 |
rs543717836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285758 | TCAACTCACCTCATT[C/T]CTGCCAACAATTAGA | 54472 |
rs543729182 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276084 | GCTTTTACAGGGCCA[C/T]GCTCGCCAGGCTTTC | 54472 |
rs543755972 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289752 | GTGCGCCCAGCGGGG[C/T]GGACACATGCATGCT | 54472 |
rs544003519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304722 | CCTGTACTTTCCCAG[C/G]ACAGTGTGTATGTAC | 54472 |
rs544009171 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284312 | AAGCATTCTTTCCTC[A/G]GTGACGGGGTGCAGG | 54472 |
rs544140985 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310500 | CAGATGCTTGCGGAG[A/G]ACAGGCGTTATGCAA | 54472 |
rs544216435 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275324 | CTGGACACCGAAGCC[A/C]CCAGCACAGTGAGGC | 54472 |
rs544287679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302709 | CAGTCTCCTGGCACT[A/G]GCATGTTCAATAAAC | 54472 |
rs544391175 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293162 | CCAGCAGCACGAGGG[C/T]TTTGGGCCTCAGCTT | 54472 |
rs544425041 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308000 | CCTCCACCACGTCCA[A/G]TACTGGGCTGCGCGA | 54472 |
rs544434926 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288394 | GAACACAAACAACCC[C/T]TATGCTGTTTCCCCA | 54472 |
rs544574683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303239 | AGCCTTGCATCCTAA[A/G]TGCTGGGACGGTCAA | 54472 |
rs544612877 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287722 | CCCCGCTGCACCCTC[C/T]CTGCCGCAGCCTCCC | 54472 |
rs544649082 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276319 | GCAGCCTCCGGCGGG[C/T]GAAGGACCCGGCTTC | 54472 |
rs544736774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278974 | AAGAGGAATGGGGCT[C/T]GGCCATCGCCTGTCC | 54472 |
rs544774343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283715 | AAAGAGGTAAGCCAA[G/T]CAATGTTATCTGTCA | 54472 |
rs544798767 | snp | A/C/G | 0.00037371 | 0.0136653 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283594 | GTTCCAAAATTTACA[A/C/G]TGTCTATCAAAAGAA | 54472 |
rs544826786 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284850 | GTCCTGAACACCAGT[G/T]GACAGCCCAGAGTCT | 54472 |
rs545006977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304788 | TTAATAAATTCAAAA[A/G]GCAATGAGAGAAAAA | 54472 |
rs545019536 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294100 | TTCCCTGCATTTCTA[C/T]GAAAGCCCGCGTGGC | 54472 |
rs545064557 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280332 | CCACCGCGTGCACGT[C/T]CTCTATGGGCCTCCC | 54472 |
rs545085068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298411 | GGTGGTCACAGGGAC[G/T]TGTGGGCGTGGGGTC | 54472 |
rs545102838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285287 | CCCCAGAACGAGAGA[A/G]GCCACCTCAGCAGGA | 54472 |
rs545175836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289355 | CACACTGCTCCCCGG[A/C]CCCCACCCAGTCTCT | 54472 |
rs545181396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308541 | CAGTGAGCCAGGAGG[C/T]CACTCACGCCAGGAG | 54472 |
rs545221244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303332 | CCAAGGGCGGACAGA[A/G]ATCCAGAGAGGGACG | 54472 |
rs545221600 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285631 | TGGGCGTGAGGTTCG[A/G]ACACGACGGCACAGT | 54472 |
rs545300596 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293937 | AAGGGTCTGAGACAC[A/G]CCGCGAGGAAGGGGT | 54472 |
rs545313437 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289002 | ACCAGGATGGGCCAG[G/T]GCCAGGGCCAGGGCC | 54472 |
rs545359244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298895 | CAGTCGTCCTCAAAC[C/T]GTCAAGGTCCCAAAA | 54472 |
rs545386472 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292813 | AGCGCAGCAGACGGC[A/G]TTACCACTGCAGGGA | 54472 |
rs545394986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303847 | TCGAGAACAGCCTGG[C/T]CAACATGGTGAAACC | 54472 |
rs545395779 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283811 | AAAAGACAGCCACAG[A/G]GCGCCCGGCCCAGAA | 54472 |
rs545453130 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310512 | GAGGACAGGCGTTAT[A/G]CAAAGATTGGCAATC | 54472 |
rs545493272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290099 | CCTGTCATGCACCCA[A/G]TGAAACACCAGGTGG | 54472 |
rs545521245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291855 | CCGCCCCGTCCTCAC[C/T]GACCCCCGAGGGCAC | 54472 |
rs545596358 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287633 | AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC | 54472 |
rs545654663 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275110 | TGGTCATCGGCAAAG[A/G]GTTGCTCTCCCTCCA | 54472 |
rs545657969 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274329 | ATTCGTTACTCCTGC[A/G]TATTGTGAATTAAGT | 54472 |
rs545665092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284099 | GGGGGGCAGCCAGGG[C/T]GCATCAGGGCCCCCA | 54472 |
rs545696672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278364 | ATCACTGGAGCGCTA[C/G]AGCCCCAATCTTAGG | 54472 |
rs545697334 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278999 | CTGTCCCTGCCCACA[C/T]GTCTCCCCACAGCGT | 54472 |
rs545834378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278062 | GAGCAGGAGACGCAC[A/G]GCGGTTCAGCCACTG | 54472 |
rs545918454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297605 | CGTTTTTGACTGGGA[C/T]ACGTCACGAGTGACC | 54472 |
rs545959896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282266 | CGCCTGAGGGGGCTC[C/T]CTCTGGCCAAATCTG | 54472 |
rs546165561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306826 | TCCATCCTCGGCCCC[G/T]GGGGCTCCCTCCTCT | 54472 |
rs546168163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307282 | GGTGCCCCTGAAATA[C/T]CTGCTCGTCTACATG | 54472 |
rs546181019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302375 | AGCCTGCACATGCCC[C/G]AGGCCTGCACACTCA | 54472 |
rs546182601 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308081 | TGTTCAGAGCCACTG[C/T]TGATAAAAACTGTAC | 54472 |
rs546218474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307475 | GCCTCCCACTGCTCC[C/T]TGCCTGCTCAGCACC | 54472 |
rs546361616 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287913 | ACCCTCTCTGCTGCA[C/G]CCTCTCTGCTGTCAC | 54472 |
rs546400323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287186 | TCACTGCACCACTGT[C/T]GTCTCTGAGTTCGAA | 54472 |
rs546453429 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308422 | GAGCAGATGCCGGCA[C/T]CATGCTACCTGTACA | 54472 |
rs546466708 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290386 | GTCCATGCGGGTCAT[A/G]CCGTAATTCTTGGCC | 54472 |
rs546511315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290759 | GGAAAGAGGAGGAGG[A/T]CCCGGGACAGAGCTG | 54472 |
rs546581631 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282424 | ACGGATACATATGTA[A/G]CAAACCTGCACATTG | 54472 |
rs546783362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291879 | AGGGCACGGCTGTCC[C/T]GTCCACGCCAACCCT | 54472 |
rs546987860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296013 | TGCAGCCCTCACTCA[C/G]GAGATCCCCAAATGC | 54472 |
rs547030760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301576 | CGCCAAACCCCAGAA[G/T]TTTCCTCCCCCAAGA | 54472 |
rs547070701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301195 | AAAAAATATCCTTAG[C/T]GAACTGAAGCTTTTG | 54472 |
rs547117998 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304527 | CCCACACAAGGCACA[A/G]CAGCACCCGCGCCAG | 54472 |
rs547181725 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301280 | GACATCATTAGCGAT[A/G]GGCTAAATACGTTCT | 54472 |
rs547207914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306265 | TGGCTAGCTTCACAC[A/G]TCCTCTCCACACCTA | 54472 |
rs547215325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295396 | CTGGTGGAAGAGCCA[C/G]GCCCTACACAGAGCA | 54472 |
rs547375214 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311400 | GGCGGGGCCCCCCAC[C/T]GTTTTCCTTTCATGG | 54472 |
rs547390476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286398 | GTGTAGGTGTCGAGT[C/T]GGCCTGGGGGGAACC | 54472 |
rs547390607 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276899 | CCCAAGAACAGGTGT[A/G]GACGGGGCGGCACAG | 54472 |
rs547512759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285551 | GCGCAGTAGAGAGCA[C/T]GCATCACCCAACAGG | 54472 |
rs547516431 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294791 | TGTCTCCTTTTCCTG[C/T]ATTTCTACGAAAGCC | 54472 |
rs547546180 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294854 | ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG | 54472 |
rs547549555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289496 | GGACGGGACTCAGGA[C/T]CCTCAAGGGTCACGA | 54472 |
rs547584487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300281 | TTCTCCTCCCCCATG[C/T]GCCGCTCTCAGAGGA | 54472 |
rs547596336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289292 | AAGCCGGGAGGAAAA[C/G]GCAGGGCCCAGGCAG | 54472 |
rs547681609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303009 | TCAAAGCCAACATGC[C/T]GGGAGGTTCCCTGGC | 54472 |
rs547859926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280499 | GGGAGGGACTGCGCC[A/G]GTGAGGACGTGGGGG | 54472 |
rs547987390 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295443 | CACTACTCATCACTT[A/C/G]AGTTATGTTTGGTAG | 54472 |
rs547999376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301014 | CTCAACGAGTCTCAG[C/T]GCTAACGCCAGGTTA | 54472 |
rs548123948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300742 | GGAGTCCTGAACACA[A/T]GCAGTCCTGGCCTCA | 54472 |
rs548179239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281943 | GGTCTCCGCAGACTT[C/T]GCCCTTCAGCTGGCA | 54472 |
rs548271007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305887 | CTCCCGCAAACGTCC[C/T]GAGATCTCACTGCAG | 54472 |
rs548271786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281289 | TCCCTTCCTCACTGA[A/T]GCGGTCACACTTTAT | 54472 |
rs548307538 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280859 | GTGGCTGCAGCCCGA[A/G]TGCCCCTCTGTGCCA | 54472 |
rs548345952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285921 | CCCCGGCGCTCTAAG[C/T]CCCGTTCCCTCCTCC | 54472 |
rs548347428 | snp | G/T | 1.69069e-05 | 0.00290743 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290413 | GGCCAACTTTGCCTG[G/T]AATGAAGCCAATGTC | 54472 |
rs548372449 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287657 | CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG | 54472 |
rs548447660 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299870 | AGCGCATCGCCACGC[A/G]GCCTCACCAGGAGCC | 54472 |
rs548483815 | snp | C/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301844 | GAAGCTAATGAAACA[C/G]AGAGAAATAAATCCC | 54472 |
rs548506591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289871 | ACCTGCTGGTGAGCG[C/G]CCAGATCAGTGCCCA | 54472 |
rs548621386 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311640 | CCATTCCTTTAAATG[A/C]CATCCATATGCTGAT | 54472 |
rs548657558 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276938 | GGGAGGGGGCGACAC[A/G]GGTGCTCTTTCACGG | 54472 |
rs548686829 | snp | C/T | | | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311008 | CTCTCCTTTTAAAAC[C/T]GGCAGCCTGGCCGCT | 54472 |
rs548722050 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293493 | AAGCAGCGAGGGGAC[A/G]CAAGCAGGGAACCAC | 54472 |
rs548824756 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276431 | TGCCTTCAGGCCGGA[A/G]TCTGTCACAAGGCTG | 54472 |
rs548868512 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306449 | CCCGAGCCAGAGTCC[C/T]GCCCCCGGACCCTGG | 54472 |
rs548908160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289560 | AGTAGGCAGCCGCAC[C/T]CTCTGGAAATCCCAC | 54472 |
rs548944544 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293806 | GGTGGCGGCTGAGGA[C/T]GGGTGATGGCACTGG | 54472 |
rs549006677 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275865 | TTACATCCGAAGGCC[A/G]GCGGCAAGACACTTG | 54472 |
rs549052293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1304851 | AAAGAAAACATGTAA[A/C]AAATCTGTAAATCTG | 54472 |
rs549056052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299293 | TGGTTACGCAACCTG[C/T]TGCCCCGCCTACCAG | 54472 |
rs549066879 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276270 | TGGGAGGACACCCAC[A/G]GAGCTGGCACGAGCG | 54472 |
rs549081491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289062 | TGGGCTGCTGTCCTC[C/T]TTCAGTTCCACTTCA | 54472 |
rs549144557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298418 | ACAGGGACGTGTGGG[C/T]GTGGGGTCCAGAGGC | 54472 |
rs549183160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303387 | CGCCGGGCACAGGGC[A/G]CGCGCTGCGGCAGCC | 54472 |
rs549190415 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310212 | GCTCCGCAGGAGCCC[C/T]GCTCCTCTCCTGCTC | 54472 |
rs549191280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304288 | GGAGTTCCACACACA[C/G]AAAAATAGCTGTCAG | 54472 |
rs549294342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292697 | GCACCGCTGCCTCCC[C/T]CACAACGGGCAAGAG | 54472 |
rs549297613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279903 | CCCTGGGCTCCAGAC[A/G]TCTCGCACCACAGTG | 54472 |
rs549334236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285005 | GGGTGCTGACCAGGC[C/T]TCTCCACTCCAGCTG | 54472 |
rs549368813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284437 | CACTGCAAGCTCCAC[C/T]TCCTGGGTTCACACC | 54472 |
rs549430326 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301558 | TGGGGAGGCACACAC[A/G]GCCGCCAAACCCCAG | 54472 |
rs549471946 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306306 | CCCCTGAAGCTCCCT[C/G]TACCCAAGGACAAAA | 54472 |
rs549623004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302042 | TCACCAGCCTCCCTG[C/T]TGTGTCTGAGGGGCT | 54472 |
rs549626625 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310808 | ACAACCACTCCACTA[A/T]AAACTCTTTGTCAGT | 54472 |
rs549769561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289905 | GAGGGGACACGTGCA[C/T]GCTCTGTCCCTGGAA | 54472 |
rs549812336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294425 | TCCCTGCATTTCTAC[A/G]AAAGCCGCGTGGCTC | 54472 |
rs549850842 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305337 | CCCAGGAGCAGCCCA[C/T]CAGAGCCAGCGGAGA | 54472 |
rs549860653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285520 | CTAACAGTGACACAC[A/G]ACAACAGACGCAACA | 54472 |
rs549910405 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284265 | TCAAGGCTGCTTCTG[C/T]GTTTCTGGCTCACCT | 54472 |
rs549934423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299888 | CTCACCAGGAGCCGG[C/T]GGTCCCTGCCGCGAA | 54472 |
rs550034044 | in-del | -/CT | 0.00478085 | 0.0486577 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291582 | CTCTGAGGGCACGGC[-/CT]CACCCTGTCCTCACT | 54472 |
rs550072884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288848 | TGCAGCCGCACCATC[A/G]TGGGCCCGCCTCGAG | 54472 |
rs550077610 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276498 | GCCCCACACCATCCA[C/T]AGGAAGCTGCTCAGC | 54472 |
rs550106687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298460 | CACTGTGGGTCCCTC[A/G]CTGCTCTGGATCCTG | 54472 |
rs550113948 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276157 | AGCTGTCAGCAGTCG[G/T]CTGGCAGTGCCACCA | 54472 |
rs550152886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279971 | GCTCAGAGACTGTTC[C/T]GGAACTCCCAAGGCT | 54472 |
rs550300369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285638 | GAGGTTCGGACACGA[C/T]GGCACAGTGCAGAGC | 54472 |
rs550315342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283911 | CTTCCAGCCTCAGGA[A/G]GCTGGAGGGCCTGGG | 54472 |
rs550361423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308139 | CCTCAGTGAGTGACA[C/T]GGTTTGAATCTGTGT | 54472 |
rs550452242 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283477 | CGCATGCCTGGGCAT[G/T]GGGGCTGGGGGCTCC | 54472 |
rs550484007 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308206 | GTTGGAGGTGGGGCC[C/T]GGCAGGGTGGGTGTG | 54472 |
rs550509691 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275688 | TTGACAAAAACCACC[C/T]CCAATCGATGGCAGA | 54472 |
rs550534004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303473 | CTCCTGGGATGCTTA[A/C]ACGTGAGTGGAAGAA | 54472 |
rs550570832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308715 | AGAAACTGAGGTTTT[C/G]CACGGTGGCCACTAA | 54472 |
rs550667995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291895 | GTCCACGCCAACCCT[C/T]GCCGCACAGCTGAAC | 54472 |
rs550833164 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287682 | CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG | 54472 |
rs550844324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288336 | CCTCCGAGGACACAG[G/T]GGCCTGCAGTGGAGA | 54472 |
rs550855114 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273945 | GGTGCCAGGGTGGCT[C/T]GGGGTCTCTAGAGTG | 54472 |
rs551041650 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276108 | GGCTTTCCTCGCCCA[C/T]GCTGAACCCACGTCC | 54472 |
rs551139886 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302181 | AATGGCCCATCCACC[A/C]GATGCCCGCACACCT | 54472 |
rs551140859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303598 | CACTTCCCACAGGGC[A/G]GCAAGGCAGGCCTCA | 54472 |
rs551179565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301642 | ACATTGAGAACAAGC[A/G]TCAAGGACTCCTGAA | 54472 |
rs551279077 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280801 | CACCTTCCACCTCAG[C/T]GCCTGTCAGTCTCGT | 54472 |
rs551291767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278187 | ACAGGCAGCGTGCGC[A/G]GGGCTCAGCGACCAG | 54472 |
rs551328831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277831 | ACCTCAGCAAAGCTG[C/T]AGCCGATGCCCAGAA | 54472 |
rs551330441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282538 | TTAAATGATGAGTCA[A/G]TGGGTCCGGCACACC | 54472 |
rs551331757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299126 | GACATGGGTGAGACA[C/T]ACAGGACCTCTTCGT | 54472 |
rs551376139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279137 | CTGTGACGCTGCGAC[A/G]TCACGGCCTGGGGTG | 54472 |
rs551410231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304211 | CGGGGTCCCACCTTC[A/G]AGGCACTGAGGACAA | 54472 |
rs551414712 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283957 | GTTGGCCATTGGCCT[C/T]CAACTCAGGACAACC | 54472 |
rs551423521 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311225 | CTTCCTCATTTTCAC[A/G]CTAAAAATCACACCT | 54472 |
rs551462416 | snp | A/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290963 | TGGGGTTTTGGGGAC[A/T]GGAACTTGTCTTTCT | 54472 |
rs551505193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279519 | GGGCAGAGAGGACGC[C/T]ATGGGAGCCCGGGGC | 54472 |
rs551618843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307437 | GCGCTGCACGCCGGT[A/G]CCCCTCAGAACAGGA | 54472 |
rs551640536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284418 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAAGCTC | 54472 |
rs551670252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297372 | CCCATCTAAGGCCTG[A/G]AGCGCACAAGCCAGT | 54472 |
rs551711620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302241 | AAGAGGGCGGGAACG[C/T]GCACCAGGGCTGAGA | 54472 |
rs551787135 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281232 | GGGCCATGATCATGG[C/T]GTAAAAGCTTTAATA | 54472 |
rs551800273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292670 | CACTGTGGACACCGT[A/G]GGGACACACGGGCAC | 54472 |
rs551899938 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297740 | ACGGACAATCGAGGA[A/G]GGTGCAGAGGTGCCT | 54472 |
rs551955606 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290947 | GTGCTATCGGAGTAC[A/G]TGGGGTTTTGGGGAC | 54472 |
rs551963781 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296381 | CTCGACCCTCTGTCC[A/C]CCACTGCCACTTCTG | 54472 |
rs552013809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287126 | GCTGTGGATAAGTCA[C/G]TGCACCGCTGTCTTC | 54472 |
rs552100447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295967 | GGGGTCAAGGGTGTC[C/T]AGCCTGGGGCCTGGC | 54472 |
rs552106761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283300 | TAGGAGCAAGATGGG[A/G]ACCCCTCCAGGCCAA | 54472 |
rs552154114 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278228 | AGCACAGGCAGCGTG[A/C]GCGGGGCTCGGCGAC | 54472 |
rs552192675 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299816 | CTGCGTCACCTGTGC[C/T]GTCAAAACGCCCCGT | 54472 |
rs552233059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277685 | TACACGGAATGTCAC[A/G]CCCGCTGATCCAAAC | 54472 |
rs552271777 | snp | A/C/T | 0.000218629 | 0.0104532 | missense, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277245 | CGGGGCTACAGACAG[A/C/T]GGGCATCCCTGGAAG | 54472 |
rs552283135 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280013 | CTCACTCCACAGAGC[A/G]TTATCACAAAGAAGA | 54472 |
rs552313994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286826 | GTGGATAAGTCACTG[A/C]ACTGCTGTCGTCTCT | 54472 |
rs552488563 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284746 | AGCCCTGGCACCTGC[A/G]CGGGCGGCTTCACAT | 54472 |
rs552565803 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300796 | AAGGAGCCGCACCAC[A/T]GTCGCCCCTGAAGCA | 54472 |
rs552586603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286297 | CACCACCTCCTCAAA[A/T]CCAGGAGGTGACATG | 54472 |
rs552600543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305950 | TCCTCGCGGGGGCCC[A/G]CACGGTACCCCTCGC | 54472 |
rs552618102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307256 | TTACTATGCGTTTAC[C/T]GGTCAACGGGGGTGC | 54472 |
rs552618343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301437 | CAGCAGGTCTGAGAT[C/T]GCACATGTGTCGCGG | 54472 |
rs552686376 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297049 | TGGTGGAGTGGGGTG[G/T]AGACCCAGCCGTCTG | 54472 |
rs552760853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282130 | GGAACCAGGGCTCCT[A/G]GGAGAAACAGCTAAC | 54472 |
rs552767639 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286955 | TCTCTGAGTTCAAAA[C/T]TGTCAACTGTGGATA | 54472 |
rs552866388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277957 | TGCACTGGGGCCACC[A/G]TCCAGGGTTCCTGGC | 54472 |
rs552894464 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286878 | ACTGCAGATAAGTCA[C/T]TGCACTGCTGTCTCC | 54472 |
rs552910136 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287825 | CCGCAGCCTCCCCGC[C/T]GCACCCTCCCCGCCG | 54472 |
rs552932974 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286573 | GATAAGTCACTGCAC[C/T]GCTGTCGTCTCTGAG | 54472 |
rs552971763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290551 | GAGTCGCCTGAACAC[A/G]GCTGTGACCTGCTTC | 54472 |
rs553069556 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278252 | CGGCGACCAGCGAGG[A/C]ACAGAGCTCCTCCTG | 54472 |
rs553200168 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278225 | CAGAGCACAGGCAGC[A/G]TGCGCGGGGCTCGGC | 54472 |
rs553277901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281655 | TTCCTGGCCCACTCC[C/G]GCAGCCCCGTCTCAC | 54472 |
rs553523460 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295170 | GCGTTCAATCTGCCG[A/T]TTTTGGCTTTCACTT | 54472 |
rs553595738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300812 | GTCGCCCCTGAAGCA[C/T]GGCTGGCCACACGCA | 54472 |
rs553633772 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305955 | GCGGGGGCCCGCACG[A/G]TACCCCTCGCAGGGG | 54472 |
rs553672351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305616 | AAGTGATAAAGTTCA[A/G]AAACTACCCTCTGCC | 54472 |
rs553698556 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276767 | TTTTCCAGAACGGCA[C/T]GAGAAGGAGAGACGC | 54472 |
rs553699616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293963 | GGGGTGACGGTGTAG[C/T]TGTGCTCACCACACC | 54472 |
rs553736203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299944 | CGGAGGCGGAGGTGC[C/G]GCACGACCTGCTGCA | 54472 |
rs553779754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304546 | CACCCGCGCCAGGAC[A/G]GGGCGGCCGAGGTCT | 54472 |
rs553818470 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310319 | CAGCGCTGGGTAAAC[C/T]GAGGCTGAACCCCGC | 54472 |
rs553846050 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311138 | TTAACCACAAGTTCC[C/T]GCTTTGGGGGCCTAG | 54472 |
rs553994224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293623 | ACAGAAGGCTGGGTG[A/G]GCTCACGTGGAGGAA | 54472 |
rs554075740 | snp | A/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291289 | TCCTGCCTGGAATGC[A/T]GACGGCCTCCCTGTA | 54472 |
rs554094100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288860 | ATCGTGGGCCCGCCT[C/T]GAGTCCCCGTCTTAT | 54472 |
rs554216025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284103 | GGCAGCCAGGGCGCA[A/T]CAGGGCCCCCAGGGC | 54472 |
rs554303873 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276226 | CTCTCACCCCAGCCT[C/T]GCAAGGCCTGTTGAG | 54472 |
rs554473822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290003 | CTGGGTCATGCTTGT[C/G]ACTGGGGATGTTTCC | 54472 |
rs554555070 | snp | A/G | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311496 | TCTCTCTTTATTTCT[A/G]TCCTGGGAGATTACA | 54472 |
rs554562384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299999 | GACACCAACTCTGGA[A/G]GAGCATTCAGGAATG | 54472 |
rs554603093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305140 | GAGGCCCGTGGGTCC[C/T]CACACAGTGAAAAGA | 54472 |
rs554604897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293770 | GGTGGAGTGCCCTGC[A/G]GTCACCAGGCCCTGC | 54472 |
rs554690956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296039 | AATGCAGGTTTCTGC[C/T]GCTAAAAATGGGTTC | 54472 |
rs554695326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286437 | CTGCTGTGGTGTCTG[A/G]GTTTGAAAGTGTCAA | 54472 |
rs554735172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281052 | CATGAGGCCACGCGG[G/T]CTCCAGATGCTTCAC | 54472 |
rs554750390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280285 | CTGGAACTCACAGGC[A/G]CTGCGAACGCCGGCT | 54472 |
rs554790585 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287703 | AGCCTCCCCGCCGCA[C/G]CCTCCCCGCTGCACC | 54472 |
rs554889315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285226 | CCTGGGCCTCTGGCC[G/T]CCACCCTCCGTGCAG | 54472 |
rs554891669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289738 | TGCGGCAAGACCCTG[C/T]GCGCCCAGCGGGGCG | 54472 |
rs554926060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284703 | GCCCTCTCAGACACA[C/T]GCTCTGCTCTTTCCT | 54472 |
rs554947163 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287584 | CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG | 54472 |
rs555002842 | in-del | -/ACA | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307194 | AGACCCCCGTCGCTG[-/ACA]ACACCTTCTTAAGAG | 54472 |
rs555117751 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276284 | CGGAGCTGGCACGAG[C/T]GCAGCAGGAGAGACG | 54472 |
rs555138738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300391 | ACACGAAAGAAAAGA[C/G]GTCTCCAACATTCAC | 54472 |
rs555177063 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310418 | CCCGGAACTTAGGTC[C/T]CGATGTCCGGGTATC | 54472 |
rs555217638 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285153 | TCCCCTAACACCACC[A/T]CCCCCAACACCACCA | 54472 |
rs555343358 | snp | A/C | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274520 | GCGCACGTTCTGAGA[A/C]CACTCCTGCCTGGCA | 54472 |
rs555449722 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274974 | AGCCTTCAAACAGGA[A/G]ATAAAGCATAAAATG | 54472 |
rs555594025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298750 | ACGCAGCCCGGGGAC[C/T]GCAGCCAGCGCCATG | 54472 |
rs555620261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298264 | GGCAGACAGACAGGC[A/G]GCTCGTGCCCTCCTG | 54472 |
rs555702183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279226 | GAATCCCAACAGCAC[A/G]GCCCCAACACACTCA | 54472 |
rs555703479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280296 | AGGCGCTGCGAACGC[C/T]GGCTGCTCCCGTGCA | 54472 |
rs555717418 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299342 | CTGCTGCAATGCCCT[C/T]GTTTCTCAACTTAGA | 54472 |
rs555728598 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308316 | GTGTGGCACCTCCCC[A/C]CCCCCAACTCTCTTG | 54472 |
rs555741554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291782 | CGCCCCGTCCTCACC[A/G]ACCCACCTCTGAGGG | 54472 |
rs555805718 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284030 | GCACTTTGACCCCAC[A/G]ACGGCGGCTCTGGGC | 54472 |
rs555851304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285629 | AATGGGCGTGAGGTT[C/T]GGACACGACGGCACA | 54472 |
rs555948045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292083 | TTGGGTGGCCACAGC[A/G]TACTCCGGAATGCTA | 54472 |
rs555981510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288101 | GCTGGGAGCCAGGGC[A/G]CTGACGTGCTGGCCC | 54472 |
rs555985041 | in-del | -/TGAA | 0.00478085 | 0.0486577 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291585 | TGAGGGCACGGCCAC[-/TGAA]CCTGTCCTCACTGAA | 54472 |
rs556016353 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287409 | TGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC | 54472 |
rs556065834 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296517 | AAGGTCGCTGATGAG[A/G]CCCTGAGCATGGGTC | 54472 |
rs556124494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285245 | CCCTCCGTGCAGAGG[G/T]ACCAGTGCTCTGCCT | 54472 |
rs556143806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304481 | CGAGAGAAGTAACAC[A/C]TTCCTGCGGGAGCCC | 54472 |
rs556371533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293546 | AGAGAAGCAGGAAAC[A/G]GGGGCTGAGCTACCT | 54472 |
rs556458938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298794 | GCGCGTCCAGCTCCC[C/T]GAGATGACACACGCC | 54472 |
rs556480767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292728 | ACGCACGTCAGACAG[C/T]AGACACCGTGGGGAC | 54472 |
rs556555945 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309731 | CAGGGTAGGGCAGGC[A/G]CAGCCTCTCGCCCGG | 54472 |
rs556560821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297590 | CCCCACACTTTACCC[C/T]GTTTTTGACTGGGAC | 54472 |
rs556683286 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275475 | GCGTAAGACCAGGCC[A/G]TCTGAGACAGGGAAT | 54472 |
rs556685120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284048 | GGCGGCTCTGGGCTG[C/T]CCCAGTTACAAATCA | 54472 |
rs556726215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279263 | GAGCAGGCACCCCCG[A/G]GGGAAGAGGTGGGTG | 54472 |
rs556779345 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279569 | GCGGCCCTGGGAGGA[A/G]TGATGGGCGGCTTTG | 54472 |
rs556829531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278342 | CACGAACCATCTCCC[A/G]GCTAGGATCACTGGA | 54472 |
rs556830893 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274319 | ATTCTGACTGATTCG[G/T]TACTCCTGCGTATTG | 54472 |
rs556905095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282260 | AGATCCCGCCTGAGG[A/G]GGCTCCCTCTGGCCA | 54472 |
rs556942702 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1277477 | AGGGCCCTCTGTGAC[A/G]CCTCCTTCACTAACT | 54472 |
rs556977898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302515 | CTGCAATTCCCCATG[C/T]CCACTCAGCTGCTGG | 54472 |
rs557034755 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274831 | GCCTGTCCTTCTGAG[A/T]GTGACGACCTCATCC | 54472 |
rs557039943 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285569 | ATCACCCAACAGGAG[C/T]GTGAGGTTCAGACAC | 54472 |
rs557043840 | snp | A/G | 0.000152748 | 0.00873789 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290244 | CATCGAAGATCTCGA[A/G]ATAGAAAGAGTCCAC | 54472 |
rs557216717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291164 | CAACATGGATGGCAG[G/T]TTCAAATATAAAACC | 54472 |
rs557259141 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287731 | ACCCTCTCTGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs557395003 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298495 | TCCCGGTATTTGAAG[A/G]CGTCCAGCGCTCCAT | 54472 |
rs557438030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306870 | CCACACCTCTCTTTC[C/T]GTGCCCTGCCCTCCC | 54472 |
rs557589005 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306343 | TCCCAGGACCCCATT[A/G]GCGGCCCCTCTGCTC | 54472 |
rs557609742 | snp | C/T | 0.000111262 | 0.00745777 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295603 | CCCACCCCCACCGAG[C/T]GCACCAGCCCCAGGC | 54472 |
rs557646504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300862 | TTCCTGGCCACTTCC[A/G]TGACTGGCCCCCTGC | 54472 |
rs557877206 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283060 | GTGCCTCCCACACAG[A/G]ACATATTTTAGTTCC | 54472 |
rs557923691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303078 | AGGGAAGCTGGGAGA[C/T]GACAGTATTGAAACG | 54472 |
rs557959830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292686 | GGGACACACGGGCAC[C/T]GCTGCCTCCCCCACA | 54472 |
rs558008584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308189 | GAATTATGATCCCCA[A/G]TGTTGGAGGTGGGGC | 54472 |
rs558047767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307822 | ACCTGAGTCTCATAA[C/G]TGTCAGGAGGTTTCC | 54472 |
rs558059713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278884 | CCGTGGCTTTTTGGG[C/T]GCCCCGGCTGGCAGG | 54472 |
rs558086205 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309390 | GCCAGCCGCAGCTGA[A/G]CAGTAGCCCTGACCC | 54472 |
rs558118456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296164 | GCTAAAGGCAGGGCC[A/C]CTGAACTGCAGGTCA | 54472 |
rs558184727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288051 | TGGCCCTCCTGATGC[C/T]CCCAGGAGCTGCAGG | 54472 |
rs558310834 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288468 | CTGCCACCAAACCAC[C/G]CAGGGCCCCTGCCCT | 54472 |
rs558344097 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296674 | GGCCTGGTTGCTGGT[A/G]GAGTGGGGTGGAGGC | 54472 |
rs558370274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291698 | AGGGCACGGCCGCCC[C/T]GTCCTCGCTGACCCC | 54472 |
rs558381109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301782 | CTTTCAGAGCTGGGA[C/T]CCACAGCAGGAAGAC | 54472 |
rs558408762 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291336 | TCCTGCAGCCAACCC[A/G]GCTCACCCCCAGGAG | 54472 |
rs558432579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281571 | GCAGCGATCAGCAGG[A/C]GACAGCTGAATGAAC | 54472 |
rs558503708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290116 | GAAACACCAGGTGGG[A/G]AGCCACGCCTCGAAG | 54472 |
rs558515225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295532 | CAGGAAAAGCGGGAA[G/T]CAGAAGTTCTGTTTG | 54472 |
rs558617412 | snp | A/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298822 | GCCTCACATCTGGGT[A/T]TTCTTCCCAAAAACC | 54472 |
rs558643762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282039 | GTGAAGAAGGGTGCC[C/T]TATTCACACTCTACA | 54472 |
rs558673429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277894 | AAGAAAATGCTCACA[A/G]AACTCAAACAAGTGG | 54472 |
rs558712141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277501 | ACTAACTCATCTTCC[C/T]TCCATATAAAAATCA | 54472 |
rs558847993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280587 | ACAGATGGAAACAGC[A/G]TCAACGGGCAGCTGC | 54472 |
rs558851364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286159 | AGAACCTCGGGAATC[A/G]CCCTCCCCACAATTG | 54472 |
rs558882693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305570 | GGGAAAGCTAATCTT[C/T]ACAAACAATCCCAGT | 54472 |
rs558949290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280294 | ACAGGCGCTGCGAAC[A/G]CCGGCTGCTCCCGTG | 54472 |
rs559027121 | in-del | -/A | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280174 | CGTATTTTAAATGGC[-/A]ATGTGCTGCTCAGCT | 54472 |
rs559096159 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300093 | AGTTATTTTTAGAAA[C/G]TTTTTAAAAACATTC | 54472 |
rs559117125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300993 | ATGTAAACACTGCAA[A/G]CAAGGCTCAACGAGT | 54472 |
rs559193349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305855 | CTCTGACGGCACCGC[A/G]GTGGCTGCAGCGGAG | 54472 |
rs559331392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296191 | GTCACTTGGTCAAAC[A/G]AATGAGACAAAAGCT | 54472 |
rs559359429 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287638 | CCCCGCCGCAGCCTC[C/T]CCGCCGCACCCTCCC | 54472 |
rs559380216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290128 | GGGGAGCCACGCCTC[A/G]AAGCCAGCCAGGAAC | 54472 |
rs559470168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281216 | TAAAACTGTTCTCTT[C/T]GGGCCATGATCATGG | 54472 |
rs559515062 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289831 | GTGGCGGGGGACACA[G/T]GCATGCTCTGTCCCT | 54472 |
rs559718623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280814 | AGCGCCTGTCAGTCT[C/T]GTGGGGACCCTCAGG | 54472 |
rs559763873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300106 | AACTTTTTAAAAACA[C/T]TCGTGAATTACTTTT | 54472 |
rs559830456 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299858 | GCACATCCACCCAGC[A/G]CATCGCCACGCGGCC | 54472 |
rs559899229 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276328 | GGCGGGCGAAGGACC[C/T]GGCTTCAGATGCCCG | 54472 |
rs560039218 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280374 | CCAGCAGCGGCGTCC[A/G]CCTGCGTGTTTTGCT | 54472 |
rs560048232 | snp | G/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290416 | CAACTTTGCCTGGAA[G/T]GAAGCCAATGTCAGG | 54472 |
rs560268071 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310637 | CTCCTCGTGCTTTTG[A/G]GAACACCCTGCTCTA | 54472 |
rs560277476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279843 | TAAGTCCCGGCCGCC[A/G]GTGGGCAGGGGAGCA | 54472 |
rs560282749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293208 | GCCACCTGCGGACAC[A/G]GGGGAGAAGCCGGGA | 54472 |
rs560298483 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310151 | GAGGCGCTGCCAGAA[A/G]AGCCCGAGCTCGAGC | 54472 |
rs560313521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298914 | AAGGTCCCAAAAACA[C/T]AAGGAAAGCCTGAGA | 54472 |
rs560357534 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308553 | AGGCCACTCACGCCA[G/T]GAGCCCATCATCTCT | 54472 |
rs560376118 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285332 | ACAGGCTCCCCCCTA[C/G]CACCTCCTCTCAGGG | 54472 |
rs560409021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284941 | CTAGGGCGAGGTCCC[A/G]ACTCCCAAGGTGGCC | 54472 |
rs560473227 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297447 | ATCCAGGCACCGCTT[C/T]GAGCAGTTACGGACT | 54472 |
rs560531584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279288 | TGGGTGCTTCCACGG[C/T]GTGGGCTGAGGGGCA | 54472 |
rs560639925 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275560 | TTCTTCTTCAAAGGA[A/T]CAAAGGCCTTTAGGA | 54472 |
rs560664704 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285621 | CGTCACCCAATGGGC[A/G]TGAGGTTCGGACACG | 54472 |
rs560848172 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276791 | GAGACGCACGTCCCA[A/G]GGACAGGAGAGCGCG | 54472 |
rs560889833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279000 | TGTCCCTGCCCACAC[A/G]TCTCCCCACAGCGTG | 54472 |
rs560901278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300125 | TGAATTACTTTTAAA[A/G]TAAAAAGGACAGGGT | 54472 |
rs561142828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293678 | GGGTGCGGGAGAGGA[C/T]CAAGGGGGGCCAGAG | 54472 |
rs561181955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298431 | GGCGTGGGGTCCAGA[A/G]GCCTCTGAGGGAGCA | 54472 |
rs561184653 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310749 | CTTCCACAAGATCCA[C/T]GAATCCTCTTTTGGG | 54472 |
rs561187706 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278843 | AGGCTTGGGCGCTGT[C/G]TGTCCTGGAGGGACC | 54472 |
rs561219579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303388 | GCCGGGCACAGGGCG[C/T]GCGCTGCGGCAGCCT | 54472 |
rs561246731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285016 | AGGCCTCTCCACTCC[A/G]GCTGGGCTGGACACC | 54472 |
rs561351011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289248 | TCTGAGGGCCAGGGA[A/G]GGGAAAGCAGGTAGG | 54472 |
rs561387548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293336 | GGGTGGAGCTGAGTG[G/T]TCGGCTCAGGCTGGG | 54472 |
rs561480784 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280436 | GGTCTGGTTGGCTCC[A/G]CAGAAACCAGTGGGG | 54472 |
rs561653438 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275677 | CAACAGTATATTTGA[A/C]AAAAACCACCCCCAA | 54472 |
rs561789162 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291880 | GGGCACGGCTGTCCC[A/G]TCCACGCCAACCCTC | 54472 |
rs561932224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297170 | TTAGGCAAAGTGCAC[A/G]TGCTGAGGCCGCCAG | 54472 |
rs561937551 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306336 | AGAACCCTCCCAGGA[C/T]CCCATTAGCGGCCCC | 54472 |
rs561965756 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287759 | AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs562077799 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287661 | ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC | 54472 |
rs562123605 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274507 | AAAATAATCAGAAGC[A/G]CACGTTCTGAGACCA | 54472 |
rs562134018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307350 | TCTAACGACACCTCA[A/G]CACTTGCCAGCACAG | 54472 |
rs562145806 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279789 | CCATTCAGGAAAAAT[C/T]GCTCCGAGAAGGCCC | 54472 |
rs562252019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283118 | TGAGGGACGAGCAAG[C/T]CACACCACTAGCCCT | 54472 |
rs562288112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282474 | TTAAAGTATAATTAA[A/G]ATAAATAAATAAATA | 54472 |
rs562322023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280696 | CCCACTTTCCAGGCC[A/G]ATTCTCCTCCCACCA | 54472 |
rs562484322 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284760 | CGCGGGCGGCTTCAC[A/T]TGGAAACAGAGTCTA | 54472 |
rs562486467 | in-del | -/C | 0.0221141 | 0.102801 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294429 | GCATTTCTACGAAAG[-/C]CCGCGTGGCTCACAG | 54472 |
rs562518688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288968 | ATCAGCCTCCGTAGG[G/T]GACTTCTTCCCTCTC | 54472 |
rs562675977 | snp | A/C | | | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295680 | GTCGGCCCACGGTGC[A/C]CACTGCGCCTCCGTA | 54472 |
rs562680118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284323 | CCTCGGTGACGGGGT[A/G]CAGGTGCTACCTCTG | 54472 |
rs562779947 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303267 | CAAGCAAGGCAGAGG[C/T]GGAAAACCCCTTCTC | 54472 |
rs562857927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292649 | ATGCTGTTCTGGTGC[A/G]GGAGACACTGTGGAC | 54472 |
rs562870147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298369 | CCGGAGACAGCAGCA[C/T]GGAGAAGCCAGTCGG | 54472 |
rs562890069 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289939 | CCACCTGCTGGTGAG[C/T]GGCCAGACCCTGTGC | 54472 |
rs562942040 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283755 | TCTTTCAGCCAGATA[C/T]ACCCTGGCGCTGTAT | 54472 |
rs562959840 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291833 | CGACCCACCTCTGAG[A/G]GCACGGCCGCCCCGT | 54472 |
rs562973418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302782 | GCAAGGCAGCTCCCA[C/T]GCCAGTGTGGACGGG | 54472 |
rs563033782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278981 | ATGGGGCTCGGCCAT[C/T]GCCTGTCCCTGCCCA | 54472 |
rs563041747 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310283 | GGTCAGGCGCTCCAA[C/T]CAGAGCGACTCCAGC | 54472 |
rs563141755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296368 | CATCCTATGTCTCCT[C/T]GACCCTCTGTCCACC | 54472 |
rs563153436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287088 | TCACTGCACCGCTGC[C/T]GTCTCTGAGTTCAAA | 54472 |
rs563178913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295854 | CACAAAGCAGCCCGA[C/G]AGCAGCTGCCCCCGG | 54472 |
rs563180581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301474 | GAGAACTCCGTATCC[A/G]TGTGCTGGGACACCC | 54472 |
rs563188512 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291397 | GCCCTCCCACCCACA[A/T]GGAGCCCGCCAGTTC | 54472 |
rs563213511 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283222 | AGCAGCCCCGGGGAA[A/G]CTCAGCCCTACCCTG | 54472 |
rs563254846 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287619 | ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC | 54472 |
rs563272989 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287724 | CCGCTGCACCCTCTC[C/T]GCCGCAGCCTCCCCG | 54472 |
rs563273616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278046 | TGAGATGCAATCTAT[C/T]GAGCAGGAGACGCAC | 54472 |
rs563331851 | in-del | -/GGGGCCCGCACGGTACCCCTCGCA | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305943 | TCGATACTCCTCGCG[-/GGGGCCCGCACGGTACCCCTCGCA]GGGGCCCCCATGATA | 54472 |
rs563351183 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299672 | AGAATTTTGCTTCCA[C/T]GTACAAGATGCACAT | 54472 |
rs563445811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306177 | AGGGCTGAAGCATCC[C/T]TTAGTGGCTATTCAG | 54472 |
rs563483445 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281292 | CTTCCTCACTGATGC[C/G]GTCACACTTTATTTT | 54472 |
rs563571473 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306752 | AGCCGGTAAACTCCA[C/G]GGCAAGTCCAGTCCT | 54472 |
rs563745360 | snp | C/T | 0.000175649 | 0.00936983 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290190 | AGCCACGCTCAGCCA[C/T]GTGCAGCCTCCATAA | 54472 |
rs563799027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287870 | CACCCTCTCTGCTGC[A/G]GCCTCCCTGCTGCAC | 54472 |
rs563846965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286622 | ACTGCGGATAAGTCA[C/T]TGCACTGCTGTCTCC | 54472 |
rs563884078 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290683 | AGACACAGCTGAGGC[C/T]GCCACTCACCCACCA | 54472 |
rs563931387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295259 | GGAGGGAGGGTGCAG[A/G]CACCGGCACTGAGGC | 54472 |
rs563936435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291856 | CGCCCCGTCCTCACC[A/G]ACCCCCGAGGGCACG | 54472 |
rs563937850 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299924 | GGAGACTCGGGGGAC[A/G]GAGGCGGAGGCGGAG | 54472 |
rs564149597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278064 | GCAGGAGACGCACGG[C/T]GGTTCAGCCACTGCA | 54472 |
rs564228563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301564 | GGCACACACGGCCGC[C/T]AAACCCCAGAAGTTT | 54472 |
rs564249862 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298691 | TGTGGATAGAACACG[-/A]AAAGGGGAGAAGCAG | 54472 |
rs564289063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277688 | ACGGAATGTCACGCC[C/T]GCTGATCCAAACACT | 54472 |
rs564332740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297145 | AACCCTCGGTGTGTC[A/G]GACGTGAGCTTAGGC | 54472 |
rs564506933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281824 | TGCTCTGGCCAAGAT[A/G]CACTTTGAGATTCCA | 54472 |
rs564731895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290763 | AGAGGAGGAGGTCCC[A/G]GGACAGAGCTGAGAG | 54472 |
rs564752868 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287769 | CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG | 54472 |
rs564830181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305802 | AGTCAGAGCAGCCTG[C/G]ACACGGCACAGCGCA | 54472 |
rs564901568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295353 | CTGCCGGCGGGGGTC[C/T]GGGAGGTGTCCTTGG | 54472 |
rs564921164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300888 | CCTGCGGAGCCTTTT[C/T]AAACCTTCTCACCGT | 54472 |
rs564988956 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294073 | AGCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC | 54472 |
rs564992906 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280942 | CTGGTCTCTCACGCA[C/T]GAAGAACGCACGGGA | 54472 |
rs565072163 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280729 | AAGCAGAAGGAGGTG[A/G]AAAGCAACAGGAGGA | 54472 |
rs565076561 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276852 | AGCCCCCGCCCCGTC[C/T]TGGACCGCCAGGAAC | 54472 |
rs565090520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281169 | TCTAATTTGGTAATC[A/G]AAATAATACTTTGTT | 54472 |
rs565110837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285786 | AGAAAAAAAAAAAAA[A/C]AACAATTCTATTTTC | 54472 |
rs565136476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293742 | AGCCAGCTCTGGAGC[C/T]TGAACTGTGTGAGGT | 54472 |
rs565137947 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297086 | CCCCGGTCAGCGCCA[A/G]TGCCCTGGGCAGTTG | 54472 |
rs565186566 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290144 | AAGCCAGCCAGGAAC[A/G]TGGCTGTGTTGGCAG | 54472 |
rs565222404 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283620 | AAGAAAATTTCAAAG[C/T]TTGTCTAGCCTTTCC | 54472 |
rs565268053 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276315 | GACGGCAGCCTCCGG[C/T]GGGCGAAGGACCCGG | 54472 |
rs565303601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285529 | ACACACGACAACAGA[C/T]GCAACAGCGCAGTAG | 54472 |
rs565404526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304730 | TTCCCAGCACAGTGT[G/T]TATGTACTTGAGATA | 54472 |
rs565536966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299045 | AACCTGGAGCCAACA[A/G]TCATGCCCCCAGCTC | 54472 |
rs565573483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304161 | GACATCCACTCCCGG[G/T]CTGCTCAGCAGCCAC | 54472 |
rs565608802 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300316 | GACGCAAGCCTGTGA[A/C]TGACGACCATTCCTC | 54472 |
rs565643461 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305450 | CACACATCTACAAAG[A/G]AAAGCAACTCTCTCC | 54472 |
rs565735378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286117 | AGCGGAGATGGTCCC[A/G]GGGTCAAGGAGGAAC | 54472 |
rs565780686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305085 | TGGCCATGCCAGTAT[C/G]AGACAAAATAATCAA | 54472 |
rs565889600 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302619 | ACTCCAGCCAGCCTC[A/G]GCCTCACGCTCCACA | 54472 |
rs565950482 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295867 | GACAGCAGCTGCCCC[C/T]GGCATTCCCGCGGCC | 54472 |
rs565965293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289518 | GGGTCACGACCATTC[A/G]CACCACCAAGAACAG | 54472 |
rs565965390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285201 | GCCCGCAACTTGGCC[A/G]CTTCCATGGCCTGGG | 54472 |
rs565974282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299966 | CCTGCTGCAGGGAGC[C/T]ATAAGGAGGCCTCTG | 54472 |
rs565999518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280508 | TGCGCCGGTGAGGAC[A/G]TGGGGGCAGCAGAGA | 54472 |
rs566071757 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306927 | TCCGAGAGATGTCAC[A/G]TCCTCACCCCAACAC | 54472 |
rs566100657 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306951 | CCAACACCCAGCCCT[A/G]GTGAGGCCCATTTAC | 54472 |
rs566111071 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311401 | GCGGGGCCCCCCACC[G/T]TTTTCCTTTCATGGT | 54472 |
rs566317197 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275817 | CAGAAGACCCACTTG[C/T]GGGCATTCTCTTTCT | 54472 |
rs566353449 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275306 | GTGGCCACACCTGGG[C/T]GCCTGGACACCGAAG | 54472 |
rs566376578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299243 | GAGCAAGAGAGGAGA[C/T]GGAGACCAGGCTTCA | 54472 |
rs566423168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289267 | AAAGCAGGTAGGGAC[A/G]GGGAGAGAAAAGCCG | 54472 |
rs566471272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288310 | GCAGAGCTTGGAAGG[C/G]CTGTGGGGGTCCTCC | 54472 |
rs566493513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293031 | CTGGCCACGCTGCAG[A/G]GGCTGAGCGGGGGCA | 54472 |
rs566530726 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298607 | GGCCTAATGATCAAG[G/T]GTCATTTTTCAACAA | 54472 |
rs566542774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304264 | GTCCACCTGGAGTAC[C/T]GCCCACCTGGAGTTC | 54472 |
rs566569829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279529 | GACGCCATGGGAGCC[C/T]GGGGCAGCCCAGAGC | 54472 |
rs566606562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284427 | AATCTCGGCTCACTG[C/T]AAGCTCCACCTCCTG | 54472 |
rs566719795 | snp | C/T | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309248 | GCCCCGGCACGGCGG[C/T]GAGCTCAAGCCTCCT | 54472 |
rs566756697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308263 | GCTTGGTGCTGTCCC[A/G]GTGATAGTGAGTTCT | 54472 |
rs566840188 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307445 | CGCCGGTGCCCCTCA[A/G/T]AACAGGAAGGGCCTG | 54472 |
rs566855780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283973 | CAACTCAGGACAACC[A/G]GACAGAACTTCACTA | 54472 |
rs566888938 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287787 | AGCCTCCCCGCCGCA[C/G]CCTCCCTGCCGCAGC | 54472 |
rs566903834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288497 | CTCTGTCCTCAGAAC[A/G]TGAGCCCTGCTGTTT | 54472 |
rs566940196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288060 | TGATGCCCCCAGGAG[C/G]TGCAGGTGCCCTGAG | 54472 |
rs566945803 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293219 | ACACGGGGGAGAAGC[C/T]GGGAGGGTGGCCCGA | 54472 |
rs566968888 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304535 | AGGCACAGCAGCACC[C/T]GCGCCAGGACGGGGC | 54472 |
rs567096725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297376 | TCTAAGGCCTGGAGC[A/G]CACAAGCCAGTCAGC | 54472 |
rs567140594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289572 | CACTCTCTGGAAATC[A/C]CACCTGCTGGTGAGC | 54472 |
rs567214763 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274617 | CCTGTCTTCTATCTC[C/T]GGAGCCCCGCCTGAG | 54472 |
rs567246050 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279516 | TGTGGGCAGAGAGGA[C/T]GCCATGGGAGCCCGG | 54472 |
rs567306419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293925 | AGCTGCACAAGCAAG[A/G]GTCTGAGACACGCCG | 54472 |
rs567379820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299295 | GTTACGCAACCTGCT[A/G]CCCCGCCTACCAGGG | 54472 |
rs567389275 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281449 | AGCTTGCACTCTCCA[C/T]AGAGGTGGCAGCTGG | 54472 |
rs567401262 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290191 | GCCACGCTCAGCCAC[A/G]TGCAGCCTCCATAAT | 54472 |
rs567575112 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309595 | CGGAGACAGTTGTCA[A/C]CTCGAGGCCGCCGCC | 54472 |
rs567589021 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275915 | GCAGGTGTCTCAATG[A/G]CATGCAGATTATTTA | 54472 |
rs567629547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297427 | AAACAGAAGGGACCC[A/G]GACGATCCAGGCACC | 54472 |
rs567629608 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302949 | TTCCCTCTTCCTATC[A/C]CCCCCTCCCCTCTTC | 54472 |
rs567713421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284033 | CTTTGACCCCACGAC[C/G]GCGGCTCTGGGCTGT | 54472 |
rs567764650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302449 | CTCACTGGTGGCCAC[G/T]GCCATTGCCCTGTAA | 54472 |
rs567836682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288537 | AGTGCCTCCAGGAAA[C/G]AGACAAGGGTGTCTG | 54472 |
rs567867385 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292810 | CACAGCGCAGCAGAC[A/G]GCGTTACCACTGCAG | 54472 |
rs567928938 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275154 | CCACTGTGTGGGTCC[C/T]TCGGGCCCCCACACG | 54472 |
rs567931731 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287918 | CTCTGCTGCACCCTC[C/T]CTGCTGTCACATCTG | 54472 |
rs567933322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282762 | TTGTGCACATGTACC[C/G]TAAAACTTAAAGTAT | 54472 |
rs567953065 | snp | C/T | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311500 | TCTTTATTTCTATCC[C/T]GGGAGATTACAAGAT | 54472 |
rs567968249 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287232 | TAAAATCACTGGAGC[A/G]TCATGATGGTTCTGT | 54472 |
rs568049720 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274687 | TGCCACGGAGCTGGC[A/G]ATCGGCCTGCATCTT | 54472 |
rs568131009 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299986 | GGAGGCCTCTGTCGA[C/T]ACCAACTCTGGAGGA | 54472 |
rs568134734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307564 | CAGGAGGCAGAGGAT[A/G]TCTCCCAGACCACAC | 54472 |
rs568189883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278758 | GGCAATGACGGAAAA[C/T]GAACCGAACCATGGC | 54472 |
rs568245801 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297854 | GCTCTGGCTCAGGAG[A/G]GCGCTGAGAGGCCCC | 54472 |
rs568354113 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302889 | GAGCACTCATTCGCC[A/G]TGCCTTGTCTCCCCT | 54472 |
rs568516628 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275691 | ACAAAAACCACCCCC[A/G]ATCGATGGCAGAAAG | 54472 |
rs568530774 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290940 | CCTGCCTGTGCTATC[A/G]GAGTACGTGGGGTTT | 54472 |
rs568530858 | in-del | -/GGAGA | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274572 | GAGCATCTGCAGAGG[-/GGAGA]GGAGAGGAGGGGGAG | 54472 |
rs568537938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301620 | TCTCAGGGTCAATAT[C/T]ACCCCCACATTGAGA | 54472 |
rs568580930 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286198 | ACGCCAGCCCAGAAT[C/T]GCCCTCCCCATGCCA | 54472 |
rs568620902 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302240 | CAAGAGGGCGGGAAC[A/G]CGCACCAGGGCTGAG | 54472 |
rs568652977 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275166 | TCCCTCGGGCCCCCA[C/T]ACGGGCTGCTCAAGG | 54472 |
rs568696257 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274835 | GTCCTTCTGAGTGTG[A/C]CGACCTCATCCACAC | 54472 |
rs568701008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277347 | ACAACGCATCCCACC[A/G]GCCTCCCTGAGGAAG | 54472 |
rs568733448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278770 | AAACGAACCGAACCA[C/T]GGCCAGGTGGGGACG | 54472 |
rs568756479 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305959 | GGGCCCGCACGGTAC[C/T]CCTCGCAGGGGCCCC | 54472 |
rs568811630 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281929 | GCCAGCCTCTCCAAG[G/T]TCTCCGCAGACTTCG | 54472 |
rs568911654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303010 | CAAAGCCAACATGCC[A/G]GGAGGTTCCCTGGCT | 54472 |
rs568947820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308170 | CCCCGCCAAATCTCA[C/T]GCTGAATTATGATCC | 54472 |
rs568948928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308991 | CCGCATCCATCTAGG[A/G]GACCATTAGGGTTCA | 54472 |
rs568971046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283943 | CTCTGTTCTTTCAGG[A/T]TGGCCATTGGCCTCC | 54472 |
rs568971910 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276933 | TCCACGGGAGGGGGC[A/G]ACACGGGTGCTCTTT | 54472 |
rs569007730 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288338 | TCCGAGGACACAGGG[A/G]CCTGCAGTGGAGACC | 54472 |
rs569094905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283492 | GGGGGCTGGGGGCTC[C/T]GGTGGGGCGTCAGGT | 54472 |
rs569194504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287298 | AGACATTTACACATC[A/G]TCACTCACGGCCGGG | 54472 |
rs569253043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302234 | GGCGTGCAAGAGGGC[A/G]GGAACGCGCACCAGG | 54472 |
rs569311084 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291899 | ACGCCAACCCTCGCC[A/G]CACAGCTGAACTCTC | 54472 |
rs569374957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296492 | GGGGTAAACCATGCT[C/T]CACAGGTGAAAGGTC | 54472 |
rs569439151 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274067 | TGGGCTCTCTCAGAA[C/T]GGGGTCGTGTTCCAC | 54472 |
rs569473532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301717 | AGTGAAACTCTGTAC[C/G]CTGAGCCCTAGGTTT | 54472 |
rs569493569 | in-del | -/A | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285773 | TCTGCCAACAATTAG[-/A]AAAAAAAAAAAAAAA | 54472 |
rs569511036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307012 | ACAGACCCACCGGGC[C/T]GTCACCACACAGCTC | 54472 |
rs569589994 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295477 | CCGGGGTCAATGCCA[A/G]TATCTTTCACACAGA | 54472 |
rs569610069 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278194 | GCGTGCGCGGGGCTC[A/G]GCGACCAGTGAGGCA | 54472 |
rs569615226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295115 | CAGTGTGTTTCCTTT[C/T]CCTGCAGTCTTACAG | 54472 |
rs569625665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300761 | GTCCTGGCCTCACGC[C/G]TGCCAGGAGACATCA | 54472 |
rs569646403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277836 | AGCAAAGCTGCAGCC[A/G]ATGCCCAGAATGACA | 54472 |
rs569719219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281532 | TGAGCCCCCGAGACC[C/T]GCACCCTGTGCGGGG | 54472 |
rs569739440 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286450 | TGAGTTTGAAAGTGT[A/C/T]AACTTCACATAAGTC | 54472 |
rs569754487 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300365 | TCTAAACCACTGCAG[C/T]GTACCTTTCCACACG | 54472 |
rs569777034 | snp | A/T | 1.71997e-05 | 0.0029325 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290438 | AATGTCAGGAAAAGG[A/T]GGTGCCAACCATCAG | 54472 |
rs569852916 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276943 | GGGGCGACACGGGTG[A/C]TCTTTCACGGGAATC | 54472 |
rs569875255 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294645 | CGGTGTGTCTCCTTT[C/T]CCTGCATTTCTACGA | 54472 |
rs569891582 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280920 | CTGAGGCCCAGTGGC[A/G]CCCGCGCTGGTCTCT | 54472 |
rs569964981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285608 | AGCGCAGGGCACGCG[C/T]CACCCAATGGGCGTG | 54472 |
rs569973905 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309838 | AGTCATGACGGTTGT[C/T]GGCGCGGGCCCTAGC | 54472 |
rs570060916 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302324 | TGCCCAGCTGACTGA[-/C]CCCTCAGTGCGCAGG | 54472 |
rs570067032 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311659 | CCATATGCTGATGAT[C/T]CTAAAATCTGTATCT | 54472 |
rs570080722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305904 | AGATCTCACTGCAGA[A/C]GGCAGGGGTCCACAC | 54472 |
rs570184745 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311021 | ACCGGCAGCCTGGCC[A/G]CTTGCCTGTTTTGAT | 54472 |
rs570211643 | snp | A/C/T | 0.000153787 | 0.00876755 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276637 | ATTGTGTGTGCCTTA[A/C/T]ATCAACAGCTCTATT | 54472 |
rs570244567 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293269 | CGGAGTCCGGAGTGC[C/T]CACGGAACACCTGGG | 54472 |
rs570246245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285938 | CCGTTCCCTCCTCCC[A/G]CACCTGCCCTAGGCC | 54472 |
rs570276364 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281733 | CGCAGCCAGCACCGC[C/G]TAGCCAGGCAGAGCA | 54472 |
rs570339006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278702 | CCACTGGACACCTCA[A/C]CTCACTGGGGAAGCA | 54472 |
rs570347021 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291491 | CTGTCCACACCAACC[C/G]CCCTCTGAGAGTACT | 54472 |
rs570347057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286836 | CACTGCACTGCTGTC[A/G]TCTCTGAGTTTAGTT | 54472 |
rs570384351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290977 | CTGGAACTTGTCTTT[C/T]TTGTGTCTCCCAATC | 54472 |
rs570446266 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278233 | AGGCAGCGTGCGCGG[A/G]GCTCGGCGACCAGCG | 54472 |
rs570485000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282720 | CACCAACATGGCACA[C/T]GGATACATATGTAAC | 54472 |
rs570526988 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287685 | CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG | 54472 |
rs570575737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284740 | AAAGGCAGCCCTGGC[A/C]CCTGCGCGGGCGGCT | 54472 |
rs570640821 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288847 | CTGCAGCCGCACCAT[C/T]GTGGGCCCGCCTCGA | 54472 |
rs570654660 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306704 | GGCCCTGCCTTGCGT[A/G]TGCCAGGCAACACTT | 54472 |
rs570680916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288173 | CCCAGGCTTCCCCGA[C/T]ATCTCCAGAGATGCC | 54472 |
rs570728391 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295970 | GTCAAGGGTGTCCAG[C/G]CTGGGGCCTGGCCCC | 54472 |
rs570736241 | snp | C/T | 1.68371e-05 | 0.00290143 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276988 | TTCCTTGGGGAGCGC[C/T]GGGTCGGCGTGTCCA | 54472 |
rs570837729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300804 | GCACCACAGTCGCCC[C/T]TGAAGCACGGCTGGC | 54472 |
rs570864829 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301091 | AGCACTTCATGACTA[C/T]GCGCTGAGCAGCGCT | 54472 |
rs570882420 | snp | A/C | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302165 | AGTCTGGCCCAGGAG[A/C]AATGGCCCATCCACC | 54472 |
rs570938719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306242 | ATTCTCTCAGAACGA[C/T]GTCGGGCTGGCTAGC | 54472 |
rs571017606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280972 | AAATTGAGCAGTTGG[C/T]TGCTGTTGCCAGCCT | 54472 |
rs571048771 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281387 | TTTCACTGAGGAAAG[G/T]GGACGGTCCTCGTGA | 54472 |
rs571085690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286304 | TCCTCAAATCCAGGA[A/G]GTGACATGGCTCGGG | 54472 |
rs571251562 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291062 | AGCTGGGCAGGGACA[C/T]TTGAGGTCCTCGGGG | 54472 |
rs571289887 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276902 | AAGAACAGGTGTGGA[C/T]GGGGCGGCACAGAAG | 54472 |
rs571321116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300166 | TCCCACAGAGCTCAC[A/G]GCATTTTATCTTCTC | 54472 |
rs571329791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294789 | TGTGTCTCCTTTTCC[C/T]GCATTTCTACGAAAG | 54472 |
rs571368891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293945 | GAGACACGCCGCGAG[A/G]AAGGGGTGACGGTGT | 54472 |
rs571431741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1304942 | CTTAGTCTTCTTAGA[C/T]TTGACTTTTTAAAAA | 54472 |
rs571439262 | snp | C/G | | | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298117 | TGCAGAAACAGACTC[C/G]TGCTAACCAAGTTCT | 54472 |
rs571543481 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293401 | AGAAGTCACCGGGAT[A/G]TGTGGGCAGAGAGGG | 54472 |
rs571582902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293000 | CGAGAAAGGCCCACG[C/T]GGGAACGGACCTACT | 54472 |
rs571614847 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276516 | GAAGCTGCTCAGCTC[A/T]CCAGACCCAAGCCCT | 54472 |
rs571690639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280090 | ATAAACACAACAGCA[C/G]AGAGTTCCATGTGAT | 54472 |
rs571746842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289281 | CGGGGAGAGAAAAGC[C/T]GGGAGGAAAAGGCAG | 54472 |
rs571811563 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284550 | GAGACGGGGTTTCAC[C/T]GTGTTGGCCAGGATG | 54472 |
rs571845638 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288855 | GCACCATCGTGGGCC[C/T]GCCTCGAGTCCCCGT | 54472 |
rs571881988 | in-del | -/AGC | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311306 | GCAAAGCTACTGAGA[-/AGC]AGCACTAGACAAACC | 54472 |
rs571960619 | snp | C/G | 0.000284819 | 0.0119301 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276778 | GGCATGAGAAGGAGA[C/G]ACGCACGTCCCAGGG | 54472 |
rs572001716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280650 | ACCCTGGTGCTGCCT[A/C]TGCGGGCCAGGCTGG | 54472 |
rs572030590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305279 | GGAGGCGGTGAGTGC[A/G]TTCCCCGCTGGCTCA | 54472 |
rs572044493 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311223 | CCCTTCCTCATTTTC[A/C]CGCTAAAAATCACAC | 54472 |
rs572085828 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TOLLIP | GRCh38.p7 | 11:1291359 | CCCAGGAGCTGGTGA[C/T]AGAGACCCCGGGAGC | 54472 |
rs572176578 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285705 | CAGAGCTGGGCACAA[A/C/T]GGGGTTTCAAAGCCA | 54472 |
rs572189900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304569 | CGAGGTCTCCGCGTG[A/G]ATCCGGAGGTGGCAC | 54472 |
rs572230566 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304031 | ACAGAGCGAGCCTCC[A/C]TGTAAAAAAAAAAAA | 54472 |
rs572254549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293630 | GCTGGGTGAGCTCAC[A/G]TGGAGGAAACAGGCT | 54472 |
rs572260296 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285673 | GTCACCTGACAGGGG[C/T]GTGAGGTTCTCCTGC | 54472 |
rs572267631 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309865 | TAGCGTGGCGGCGCT[A/G]CAGTCTGGGCAGTGG | 54472 |
rs572338129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289393 | CAATGCCACAGGTGC[A/G]AGGTGCCAGGACCAC | 54472 |
rs572357492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284624 | AAGGTGCCGGGATTA[C/G]AGGCATGAGCCCCCA | 54472 |
rs572375708 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293594 | GGAATGTTTCCCACC[A/G]CTGGAGCTGCGCCAC | 54472 |
rs572394757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299465 | TTCAGTGACGACACT[C/T]GGTCCTTCAGTAAAT | 54472 |
rs572411826 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280329 | GTGCCACCGCGTGCA[C/T]GTTCTCTATGGGCCT | 54472 |
rs572432691 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291810 | GGGCACGGCCGCCCC[A/G]TCCTCACCGACCCAC | 54472 |
rs572463431 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276229 | TCACCCCAGCCTCGC[A/G]AGGCCTGTTGAGAAG | 54472 |
rs572496719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284226 | ACTTACCCAGATGCC[C/T]ACCCTCCTCTAACTC | 54472 |
rs572498569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288861 | TCGTGGGCCCGCCTC[A/G]AGTCCCCGTCTTATC | 54472 |
rs572525838 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276025 | AGATGCTACACGCAG[C/T]GCCCAGGCAGTCAGA | 54472 |
rs572568621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279686 | CACGTTCTTCACGCT[A/G]TGTGAATCTGCTGTC | 54472 |
rs572649311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282145 | GGGAGAAACAGCTAA[C/T]GCCAGGGCTAAGGCC | 54472 |
rs572654089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279300 | CGGTGTGGGCTGAGG[A/G]GCAGTGGCCTGGCTC | 54472 |
rs572819056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292754 | GGGACACACGGGCAC[C/T]GCTGCTTTCCCCACA | 54472 |
rs572858218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298248 | TCTCCTGGGCACACA[C/T]GGCAGACAGACAGGC | 54472 |
rs572878007 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287750 | CCCCGCCGCAGCCTC[C/T]CCGCCGCACCCTCCC | 54472 |
rs573038654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297640 | CCCTGTGAGAGAAGC[C/T]GTACTGCGAGAACAA | 54472 |
rs573118283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303149 | GGACAGAATGAGAAT[A/G]AGCATAGATTATAAA | 54472 |
rs573145835 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303792 | TGTAATCCCAAAACT[C/T]TGGGAGGCTGAGGTG | 54472 |
rs573151232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278885 | CGTGGCTTTTTGGGC[A/G]CCCCGGCTGGCAGGC | 54472 |
rs573158874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302629 | GCCTCGGCCTCACGC[C/T]CCACACCAGCCTCCT | 54472 |
rs573193750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307863 | TCAGAAAAAGCAGCT[A/G]TGCCCAAAACCTGGG | 54472 |
rs573290934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279764 | AGGAAAACCAAAACT[C/T]GTCCCTTTTCCATTC | 54472 |
rs573292770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285227 | CTGGGCCTCTGGCCT[C/T]CACCCTCCGTGCAGA | 54472 |
rs573329535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1284718 | CGCTCTGCTCTTTCC[C/T]CTGGAGAAAGGCAGC | 54472 |
rs573439114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296829 | GGAGTGGGGTGGAGG[C/T]CTGGTTGCTGGTGGA | 54472 |
rs573488918 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296165 | CTAAAGGCAGGGCCA[C/G]TGAACTGCAGGTCAC | 54472 |
rs573507013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287016 | GAAACTGTCAGCTGC[A/G]GATAAGTCACTGCAC | 54472 |
rs573618573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288927 | TCGATGAGACCCCTC[A/G]GGCAGCGCAGGCTTC | 54472 |
rs573654819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293059 | GCAGTGGGTGGGTGC[A/G]GGGGGCTCCAGGCCT | 54472 |
rs573932447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298764 | CCGCAGCCAGCGCCA[C/T]GTGGCGGGGCAGGTG | 54472 |
rs573967356 | in-del | -/AG | 0.00159617 | 0.0282053 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273871 | CGGGGGTTGGGCAGC[-/AG]AGAGGGGGCAGACAC | 54472 |
rs573996938 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275000 | AAATGAAGGAAAGAA[G/T]AATCTTATTTAATTA | 54472 |
rs573998177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303219 | CCAGGAACTCCACTG[C/G]AGGCAGCCTTGCATC | 54472 |
rs574050852 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307647 | GGACACAACAGCAGG[A/G]TGCTGGTTCCCTTGT | 54472 |
rs574070465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307965 | GGATACAGTGTTAAG[A/G]GTGGGGAGCCCTGGT | 54472 |
rs574095821 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279256 | ACTTGGGGAGCAGGC[A/C]CCCCCGGGGGAAGAG | 54472 |
rs574143830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297069 | CCAGCCGTCTGCAGG[A/G]GCCCCGGTCAGCGCC | 54472 |
rs574179624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288106 | GAGCCAGGGCGCTGA[C/T]GTGCTGGCCCCACAG | 54472 |
rs574182993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301833 | AAGGGACAGAGGAAG[C/T]TAATGAAACAGAGAG | 54472 |
rs574237347 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOLLIP | GRCh38.p7 | 11:1287412 | CTCCCCGCCGCAGCC[C/T]CCCCGCCGCACCCTC | 54472 |
rs574311497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283215 | CCCTGCCAGCAGCCC[C/T]GGGGAAACTCAGCCC | 54472 |
rs574347097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282141 | TCCTGGGAGAAACAG[A/C]TAACGCCAGGGCTAA | 54472 |
rs574416011 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291292 | TGCCTGGAATGCAGA[C/T]GGCCTCCCTGTACCA | 54472 |
rs574435713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296276 | TTCCACATGAAACAG[A/C]TGAAATTCAAAAGTA | 54472 |
rs574450817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299387 | ACGAGGAGGGAGTGC[C/T]ACCAGTTCATGCTTC | 54472 |
rs574489275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300883 | GGCCCCCTGCGGAGC[C/T]TTTTTAAACCTTCTC | 54472 |
rs574519293 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286579 | TCACTGCACCGCTGT[C/T]GTCTCTGAGTTTAGT | 54472 |
rs574582790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1296126 | CACCATGTGTGCCCA[C/T]GGCTTCTTTCTCCTT | 54472 |
rs574593234 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277996 | CCCACAGCTACGCAG[A/G]CCCCTCGCCCCATGT | 54472 |
rs574621415 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282997 | ATTGCTGGGGAAGTC[A/G]GATAAACTCAGGGGC | 54472 |
rs574699846 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295948 | TTCCTCATCTCTAAA[A/C]GGAGGGGTCAAGGGT | 54472 |
rs574776550 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287587 | CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG | 54472 |
rs574838985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290171 | GCAGGTGTGTCCCCA[C/T]GGCAGCCACGCTCAG | 54472 |
rs574942163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292217 | CTTACACTCCAAACT[C/G]TGCCCCTGTAAACTC | 54472 |
rs574971772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1297602 | CCCCGTTTTTGACTG[C/G]GACACGTCACGAGTG | 54472 |
rs574983645 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288335 | TCCTCCGAGGACACA[A/G]GGGCCTGCAGTGGAG | 54472 |
rs575118508 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274328 | GATTCGTTACTCCTG[C/T]GTATTGTGAATTAAG | 54472 |
rs575133767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300825 | CACGGCTGGCCACAC[A/G]CAGGCGGCAGGAGAC | 54472 |
rs575155708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278359 | CTAGGATCACTGGAG[C/T]GCTAGAGCCCCAATC | 54472 |
rs575170466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300569 | AATATTCCTGTTGGT[A/G]ACACGTCTCCAACGG | 54472 |
rs575231376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1278047 | GAGATGCAATCTATC[A/G]AGCAGGAGACGCACG | 54472 |
rs575235677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305638 | CCCTCTGCCATCCCT[A/G]ATGAAGTCACCGATT | 54472 |
rs575261081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302588 | TGGACCAGTACCTGA[C/G]CCTGCAGCCCCTGGC | 54472 |
rs575350597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301916 | CAAAGCCTCTTGGGC[A/G]AGGTCTGAGTGTCTG | 54472 |
rs575408206 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279326 | GGCTCACTCCCCTCC[C/T]TCCTGCAGGGCAGAG | 54472 |
rs575445589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283600 | AAATTTACAATGTCT[A/G]TCAAAAGAAAATTTC | 54472 |
rs575481291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306786 | GTGCCCAGGACCCTC[C/T]GGCGGCCTCCAGCTC | 54472 |
rs575547280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1282938 | ACTTAAAATATAATT[A/T]AAATAAATAAATAAA | 54472 |
rs575796355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1307263 | GCGTTTACCGGTCAA[C/T]GGGGGTGCCCCTGAA | 54472 |
rs575819559 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291235 | GCCCTCGTAAGCTGG[A/G/T]TTGGGTTCAGCCCTG | 54472 |
rs575841958 | snp | C/G | 0.000186272 | 0.0096489 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283582 | AAGTGCGGGGCTGTT[C/G]CAAAATTTACAATGT | 54472 |
rs576060320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300588 | CGTCTCCAACGGAGA[C/G]AGCCGCTGCTTCCTT | 54472 |
rs576066936 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294062 | ATTTCTATGAAAGCC[A/G]CGTGGCTCACAGTGT | 54472 |
rs576114567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293704 | CAGAGGCGTGGGCAA[C/T]GCCAGGGCCACCTCC | 54472 |
rs576121845 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277449 | CCCAGGCACAGCCAC[A/G]GGGAAGGTGGGCAGG | 54472 |
rs576222040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286150 | CCACCCATCAGAACC[C/T]CGGGAATCGCCCTCC | 54472 |
rs576261203 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290012 | GCTTGTCACTGGGGA[A/T]GTTTCCAAATGTAAG | 54472 |
rs576269041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289750 | CTGTGCGCCCAGCGG[A/G]GCGGACACATGCATG | 54472 |
rs576280891 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280289 | AACTCACAGGCGCTG[C/T]GAACGCCGGCTGCTC | 54472 |
rs576440293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293348 | GTGGTCGGCTCAGGC[A/T]GGGGCCAGCACATGG | 54472 |
rs576495566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305146 | CGTGGGTCCCCACAC[A/C]GTGAAAAGATGTGAT | 54472 |
rs576511076 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304692 | TAAGTGCATGTTACC[A/T]TTTCCAGGGGAGCCC | 54472 |
rs576514565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1306498 | GGAAAGCTGAGCGAG[C/T]GCCCTGCTTAACCTC | 54472 |
rs576578561 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276303 | GCAGGAGAGACGGAC[A/G]GCAGCCTCCGGCGGG | 54472 |
rs576734578 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290500 | CCTGAACCCTTCCAC[A/G]AGGCCTTTTCCTAAC | 54472 |
rs576773317 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287736 | CTCTGCCGCAGCCTC[C/T]CCGCCGCAGCCTCCC | 54472 |
rs576817740 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301363 | AGTCTCACACCAGCA[A/C]TGAGGATCCCACACA | 54472 |
rs576834547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279947 | AGAGCAGGTGGGGAC[A/G]ACCGTCCAGCTCAGA | 54472 |
rs576846336 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300937 | CGAGGCTGTGGAGGT[A/G]CTGTTTGTGTCTGTG | 54472 |
rs576856208 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301449 | GATCGCACATGTGTC[A/G]CGGGCTTCCGAGAAC | 54472 |
rs576871798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290122 | CCAGGTGGGGAGCCA[C/T]GCCTCGAAGCCAGCC | 54472 |
rs576943773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1294135 | AGTGTGTCTCCTTTC[C/T]CTGCATTTCTACAAA | 54472 |
rs577000072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOLLIP | GRCh38.p7 | 11:1281587 | GACAGCTGAATGAAC[A/G]AGCGGCTGAAGGGGC | 54472 |
rs577070169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286173 | CGCCCTCCCCACAAT[C/T]GCCCTCCCCACGCCA | 54472 |
rs577217625 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276316 | ACGGCAGCCTCCGGC[A/G]GGCGAAGGACCCGGC | 54472 |
rs577321334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300098 | TTTTTAGAAACTTTT[C/T]AAAAACATTCGTGAA | 54472 |
rs577459283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1305231 | AAATCCAGCGCAAAG[C/G]TTCACAGGAACCCAG | 54472 |
rs577565877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280592 | TGGAAACAGCGTCAA[C/T]GGGCAGCTGCAGCCA | 54472 |
rs577598023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1280325 | CATGGTGCCACCGCG[C/T]GCACGTTCTCTATGG | 54472 |
rs577670776 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310602 | TACATATAAACAAGC[C/G]TACCCAGGTGGACGC | 54472 |
rs577707023 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309753 | CTCGCCCGGCGCCTG[C/T]GCACCTGCTCTCTCC | 54472 |
rs577848907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299436 | AGTCCAGGTGCTGAA[A/G]TAAACCCTATCGTTT | 54472 |
rs577913129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303833 | TTGAGACCAGGAGTT[C/T]GAGAACAGCCTGGCC | 54472 |
rs577924092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298410 | GGGTGGTCACAGGGA[C/T]GTGTGGGCGTGGGGT | 54472 |
rs577926654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1292736 | CAGACAGCAGACACC[A/G]TGGGGACACACGGGC | 54472 |
rs577957541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288969 | TCAGCCTCCGTAGGG[A/G]ACTTCTTCCCTCTCT | 54472 |
rs577986037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1293198 | GTGTGGGGCAGCCAC[C/G]TGCGGACACGGGGGA | 54472 |
rs578112558 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275479 | AAGACCAGGCCATCT[A/G]AGACAGGGAATCCCA | 54472 |
rs578115666 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279613 | ATCTGCCGCGCTCAG[C/T]CCCACCAGCCACCTG | 54472 |
rs578133277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289433 | CAGCCTCGCCACATC[C/T]CCTCTGACCTTCTGA | 54472 |
rs578168030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288569 | GGGGCGGCATAGCCC[C/T]GACGTGCTCCAACAT | 54472 |
rs578176877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283789 | GTTGATGGAACTGCA[C/T]CCCCCAAAAAGACAG | 54472 |
rs578216369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOLLIP | GRCh38.p7 | 11:1279264 | AGCAGGCACCCCCGG[A/G]GGAAGAGGTGGGTGC | 54472 |
rs745316051 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297634 | CCTTTGCCCTGTGAG[A/C]GAAGCCGTACTGCGA | 54472 |
rs745333203 | in-del | -/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294244 | GCATTTCTACGAAAG[-/C]CCGCGTGGCTCACAG | 54472 |
rs745355871 | snp | A/G | 0.000187494 | 0.00968049 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283501 | GGGCTCCGGTGGGGC[A/G]TCAGGTGGACGAGTC | 54472 |
rs745365179 | snp | C/T | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274285 | TTCCTGCTCCCAGTC[C/T]GTTGACGAGTGAACT | 54472 |
rs745408327 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282321 | ATTCATAAGGGATTC[C/T]GACCCAAGGAAAAAA | 54472 |
rs745479963 | snp | C/T | 3.53369e-05 | 0.00420324 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295672 | GATGTTCAGTCGGCC[C/T]ACGGTGCCCACTGCG | 54472 |
rs745564863 | snp | A/G | 4.88424e-05 | 0.00494154 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295737 | CCAGCTGGACCTGCC[A/G]CTGCTGCTGTGTGGG | 54472 |
rs745642953 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279012 | CACGTCTCCCCACAG[C/T]GTGGCAACATGAGGA | 54472 |
rs745828096 | snp | C/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298538 | CACTCTTTAGGTGTC[C/G]GTTAAAGACAGTGGG | 54472 |
rs745831903 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287274 | AGCGTCTGTTAAAGA[C/T]GTGTCATGAGACATT | 54472 |
rs745863976 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293305 | CATGTGGCCATGGTC[C/T]GTACCTAGGGATCTG | 54472 |
rs745892746 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284318 | TCTTTCCTCGGTGAC[A/G]GGGTGCAGGTGCTAC | 54472 |
rs745957373 | snp | A/G | 0.000115895 | 0.00761144 | missense, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309491 | TGAGTGCTGACGGTG[A/G]TCGCCATGGTGCTGC | 54472 |
rs746015012 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292712 | CCACAACGGGCAAGA[A/G]ACGCACGTCAGACAG | 54472 |
rs746054511 | snp | A/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304593 | GTGGCACAGACAATG[A/T]TTAACTTCTTCTTTA | 54472 |
rs746105178 | snp | A/G | 3.32784e-05 | 0.00407898 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277032 | AAACGGCATCGAGGC[A/G]GAGGCTCTATGGCTC | 54472 |
rs746113571 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279511 | CAAAATGTGGGCAGA[A/G]AGGACGCCATGGGAG | 54472 |
rs746207071 | snp | C/T | 1.66735e-05 | 0.00288729 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288694 | CTCAGGCTGTACCAC[C/T]TGTCCTCCACCTTGC | 54472 |
rs746335376 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310227 | CGCTCCTCTCCTGCT[C/G]GCTCCGGAGAACCCC | 54472 |
rs746384403 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285198 | CCTGCCCGCAACTTG[C/G]CCACTTCCATGGCCT | 54472 |
rs746435542 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288476 | AAACCACCCAGGGCC[C/T]CTGCCCTCTGTCCTC | 54472 |
rs746448684 | snp | A/G | 8.68832e-05 | 0.00659045 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288615 | ACCCCGCCCAGGCGT[A/G]CAGCTCACCGCGTAG | 54472 |
rs746543908 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275159 | GTGTGGGTCCCTCGG[A/G]CCCCCACACGGGCTG | 54472 |
rs746556447 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298756 | CCCGGGGACCGCAGC[C/T]AGCGCCATGTGGCGG | 54472 |
rs746633236 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308057 | AAAGGACTTTTTCCA[C/T]CCACGGCATGTTCAG | 54472 |
rs746707461 | snp | C/T | 3.4845e-05 | 0.00417388 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290451 | GGAGGTGCCAACCAT[C/T]AGGAGAGGGTGGGTT | 54472 |
rs746801284 | in-del | ACCTCTGAGGGCACGGCCGCCCCGTCCTCACCGACCCA/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291787 | CGTCCTCACCGACCC[lengthTooLong]CCTCTGAGGGCACGG | 54472 |
rs746886563 | snp | A/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304727 | ACTTTCCCAGCACAG[A/T]GTGTATGTACTTGAG | 54472 |
rs746904361 | snp | A/G | 3.53033e-05 | 0.00420124 | missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277226 | AGGGCCACGGGCACC[A/G]TGCCGGGGCTACAGA | 54472 |
rs746987940 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274510 | ATAATCAGAAGCGCA[C/T]GTTCTGAGACCACTC | 54472 |
rs747030195 | snp | C/G | 0.000141453 | 0.00840871 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276868 | TGGACCGCCAGGAAC[C/G]GAAAACCCACATGCA | 54472 |
rs747137810 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285295 | CGAGAGAGGCCACCT[C/T]AGCAGGAGAACCAGG | 54472 |
rs747147065 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302790 | CTCCCACGCCAGTGT[-/G]GGACGGGCAGTGGTG | 54472 |
rs747168250 | snp | A/G | 1.79745e-05 | 0.00299782 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288813 | GGCCCCAGGCATCAG[A/G]GAAGGGGCCACCCTG | 54472 |
rs747260630 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293563 | GGGCTGAGCTACCTG[A/G]CCCAGTGAGGAGGCA | 54472 |
rs747375576 | snp | A/G | 3.98764e-05 | 0.00446504 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286092 | TGGCAGCTGGAAGCA[A/G]CTGAAACACAGCGGA | 54472 |
rs747426885 | snp | C/T | 3.49327e-05 | 0.00417913 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295760 | TGTGTGGGCGTGATG[C/T]GGAGGAAGTCCTGCG | 54472 |
rs747435406 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301687 | CCACGGAGGCCCCAA[C/T]ACAGAAGCCCAACTA | 54472 |
rs747453098 | snp | A/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302897 | ATTCGCCGTGCCTTG[A/T]CTCCCCTTCCGGGGC | 54472 |
rs747545736 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279631 | CACCAGCCACCTGCA[C/T]GCACGCGGACGGATG | 54472 |
rs747591575 | snp | C/G | 5.14681e-05 | 0.00507261 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309428 | CGCCCGCAACCGCAG[C/G]TCACCGCCCCCGCCC | 54472 |
rs747674247 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288948 | CGCAGGCTTCACGAT[C/T]GTATATCAGCCTCCG | 54472 |
rs747682221 | snp | G/T | 5.00805e-05 | 0.00500378 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290345 | GTCTCGTACACCGCG[G/T]AGCCCAGGCGCAGTC | 54472 |
rs747714909 | snp | C/T | 0.000122334 | 0.00781997 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288612 | CCCACCCCGCCCAGG[C/T]GTGCAGCTCACCGCG | 54472 |
rs747815447 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276020 | GGCCAAGATGCTACA[C/T]GCAGCGCCCAGGCAG | 54472 |
rs747839576 | snp | C/G | 1.91349e-05 | 0.00309307 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295834 | CCAGTGAGTCAGGGT[C/G]GGGGCACAAAGCAGC | 54472 |
rs747843055 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280675 | GGCTGGGGAGGCGCC[A/G]GACGCCCCACTTTCC | 54472 |
rs747921776 | snp | C/T | 6.99839e-05 | 0.00591499 | missense, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277218 | CCGGGGGCAGGGCCA[C/T]GGGCACCATGCCGGG | 54472 |
rs748072745 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293050 | TGAGCGGGGGCAGTG[G/T]GTGGGTGCGGGGGGC | 54472 |
rs748102705 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291171 | GATGGCAGGTTCAAA[C/T]ATAAAACCTAAAACT | 54472 |
rs748152746 | snp | A/C | 1.75047e-05 | 0.00295839 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288800 | GACAAGAGGGAGAGG[A/C]CCCAGGCATCAGGGA | 54472 |
rs748152949 | snp | A/G | 1.65638e-05 | 0.00287778 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277156 | GAACATGTCCTGGAT[A/G]GCTTTCAGGTCCTCC | 54472 |
rs748173658 | in-del | -/AG | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283677 | GAAAGGCATCTACAA[-/AG]AGAATTAGGGATAGG | 54472 |
rs748195691 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288821 | GCATCAGGGAAGGGG[C/T]CACCCTGCCCCTGCA | 54472 |
rs748203339 | in-del | -/CT | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299758 | TCAGGAGCCAGTCCC[-/CT]GTCAATGCTCACTCG | 54472 |
rs748223536 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1277773 | TGGCAAGTGTGTCAC[C/T]AAACTGTGTGCCGGT | 54472 |
rs748276802 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287148 | GCTGTCTTCTGAGTT[C/T]GAAACTGTCAACTGC | 54472 |
rs748279004 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276908 | AGGTGTGGACGGGGC[A/G]GCACAGAAGTCCACG | 54472 |
rs748356234 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310028 | ATCCCCTGCAGGGCG[A/T]TCTTTCCCTCAGCTG | 54472 |
rs748403718 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286298 | ACCACCTCCTCAAAT[A/C]CAGGAGGTGACATGG | 54472 |
rs748439890 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288206 | GCCACACCACGGCCA[A/T]TGCCTGCCCTGTGGG | 54472 |
rs748466457 | snp | A/G | 3.33389e-05 | 0.00408269 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288729 | CCTCAGGGACTCCGG[A/G]ATGGTGATGTGGGTC | 54472 |
rs748528354 | snp | A/G | 8.79752e-05 | 0.00663173 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295750 | CCGCTGCTGCTGTGT[A/G]GGCGTGATGCGGAGG | 54472 |
rs748563320 | snp | A/C | 0.000142501 | 0.0084398 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276725 | CCAACACCCTGGCAG[A/C]AGCAGCTGCTCTCTA | 54472 |
rs748637327 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290782 | CAGAGCTGAGAGCCA[C/G]AGCATGACATGGAGT | 54472 |
rs748791889 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281440 | TCAGTCTCCAGCTTG[C/T]ACTCTCCATAGAGGT | 54472 |
rs748842880 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290436 | CCAATGTCAGGAAAA[A/G]GAGGTGCCAACCATC | 54472 |
rs748844883 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280583 | GGGAACAGATGGAAA[C/T]AGCGTCAACGGGCAG | 54472 |
rs748967805 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289756 | GCCCAGCGGGGCGGA[C/T]ACATGCATGCTCTGT | 54472 |
rs748972033 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287226 | TGCAGGTAAAATCAC[A/T]GGAGCGTCATGATGG | 54472 |
rs748987248 | snp | G/T | 0.00163332 | 0.0285305 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309636 | GCTGACAGCCGCCGC[G/T]CCCCGCCCCCGGCAC | 54472 |
rs748996297 | snp | A/G | 0.000106125 | 0.00728363 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286057 | TGGCATCAGGACCAC[A/G]GGCTGGGGTGGCATC | 54472 |
rs749010912 | snp | C/T | 3.31879e-05 | 0.00407343 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277042 | GAGGCAGAGGCTCTA[C/T]GGCTCCTCCCCCATC | 54472 |
rs749051977 | snp | G/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291053 | CAGGTGCTCAGCTGG[G/T]CAGGGACATTTGAGG | 54472 |
rs749138695 | snp | C/T | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274202 | CTGTTGAGGGAGGAG[C/T]ACCTGGGACTTCCCT | 54472 |
rs749188185 | snp | A/G | 1.68539e-05 | 0.00290287 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290260 | ATAGAAAGAGTCCAC[A/G]CCTGGGGGCACCGTG | 54472 |
rs749210546 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295907 | CCCATGTCCTTATCA[A/G]GTCCTGGACTGTGCT | 54472 |
rs749210547 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307257 | TACTATGCGTTTACC[A/G]GTCAACGGGGGTGCC | 54472 |
rs749248053 | snp | A/G | 0.00011687 | 0.00764339 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290342 | GGCGTCTCGTACACC[A/G]CGTAGCCCAGGCGCA | 54472 |
rs749337956 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309946 | GGCGGGGGTGACCTT[C/G]GGACGTGCGACCCGC | 54472 |
rs749455035 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303115 | TGTAAGCTGAAGAGC[A/G]GTGAAAGGGAAGAGT | 54472 |
rs749635021 | snp | A/G | 0.000713012 | 0.0188679 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276712 | CGCTCCACCACCTCC[A/G]ACACCCTGGCAGAAG | 54472 |
rs749721078 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283885 | GAGTGGCCCTGCCTA[C/T]GGGGCTTCGACTTCC | 54472 |
rs749743149 | snp | C/T | 1.66668e-05 | 0.00288672 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288704 | ACCACTTGTCCTCCA[C/T]CTTGCCCTGCCTCAG | 54472 |
rs749808523 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288091 | AATGGAGATGGCTGG[C/G]AGCCAGGGCGCTGAC | 54472 |
rs749858766 | in-del | -/AG | 0.000142197 | 0.00843079 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276746 | CTGCTCTCTACAGCA[-/AG]AGCATTTTCCAGAAC | 54472 |
rs749898213 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293054 | CGGGGGCAGTGGGTG[C/G]GTGCGGGGGGCTCCA | 54472 |
rs749948104 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283463 | CTGCTTATTGGAAAC[C/G]CATGCCTGGGCATGG | 54472 |
rs750262958 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279818 | CCTGATCTCAGACCA[C/T]GCAGCATGGTAAGTC | 54472 |
rs750343352 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284596 | CCTCACGATCTGCCC[A/G]CCTTGGCCTCCCAAG | 54472 |
rs750357564 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309657 | CCCCCGGCACCGCCC[C/G]ACTGCGCAGGCGCCG | 54472 |
rs750385575 | snp | C/T | 1.79081e-05 | 0.00299228 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288589 | TGCTCCAACATACCC[C/T]AATGCGCCCCACCCC | 54472 |
rs750436133 | in-del | -/A | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1277879 | CATACAAACTACACC[-/A]AGAAAATGCTCACAA | 54472 |
rs750467931 | snp | A/C | 1.65269e-05 | 0.00287457 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277122 | GCACGGAGCGGATCA[A/C]CTCCTGGTCCATGTT | 54472 |
rs750520175 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280926 | CCCAGTGGCACCCGC[A/G]CTGGTCTCTCACGCA | 54472 |
rs750543906 | in-del | -/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299224 | TTTAACCTGAAGACA[-/G]GAAGAGCAAGAGAGG | 54472 |
rs750573151 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290127 | TGGGGAGCCACGCCT[C/T]GAAGCCAGCCAGGAA | 54472 |
rs750630501 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280142 | AGCATCCAATTCTCA[C/T]TTTGAATGGAACCAT | 54472 |
rs750664805 | snp | A/C | 1.67944e-05 | 0.00289775 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290400 | TGCCGTAATTCTTGG[A/C]CAACTTTGCCTGGAA | 54472 |
rs750685650 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289464 | CTCTGCCTCAGAAGC[A/G]CTGCAGGTGCAGCCA | 54472 |
rs750775456 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301988 | ACATAGAACAGCACA[A/G]TTGGTCCAGATGAAG | 54472 |
rs750825110 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296206 | GAATGAGACAAAAGC[C/T]GAGCCTCAGGTCTAA | 54472 |
rs750836999 | snp | C/G | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311391 | CCCCCTGGCGGCGGG[C/G]CCCCCCACCGTTTTC | 54472 |
rs750868280 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275381 | TGGGTTAGAGTTGTT[A/G]ATATCACGGAACATA | 54472 |
rs750949656 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306902 | GCCCAACCCCTACTC[C/T]CATTCCTCCTCCGAG | 54472 |
rs751009667 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308580 | CTCTGAGTCAGTCTA[C/T]ACCAGCTCTCCTGCA | 54472 |
rs751025957 | snp | A/G | 0.000147308 | 0.00858092 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276824 | GAGACCTCCCAGCAC[A/G]AGATGGGAGGGGAGC | 54472 |
rs751122359 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284745 | CAGCCCTGGCACCTG[C/T]GCGGGCGGCTTCACA | 54472 |
rs751211641 | snp | A/G | 1.68658e-05 | 0.0029039 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288765 | AATGCGGTCGTCCAT[A/G]GAGAAGGCTCTCTGC | 54472 |
rs751224628 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308314 | GTGTGTGGCACCTCC[C/G]CACCCCCAACTCTCT | 54472 |
rs751227418 | in-del | -/CGCCGGGCGACCTCCTGCGCCCC | 0.000110748 | 0.00744055 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309541 | GACCCGACAGTGACG[-/CGCCGGGCGACCTCCTGCGCCCC]CGCCGGGCGACCTCC | 54472 |
rs751232717 | snp | C/T | 0.000299895 | 0.0122416 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276648 | CTTAAATCAACAGCT[C/T]TATTCCAATTACATC | 54472 |
rs751283160 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293157 | GAGCACCAGCAGCAC[A/G]AGGGCTTTGGGCCTC | 54472 |
rs751360385 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289510 | ACCCTCAAGGGTCAC[A/G]ACCATTCGCACCACC | 54472 |
rs751365751 | snp | A/G | 0.000101999 | 0.00714067 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290242 | CTCATCGAAGATCTC[A/G]AGATAGAAAGAGTCC | 54472 |
rs751369813 | snp | A/G | 0.000132319 | 0.00813277 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286009 | ACACGCACCTGTGAT[A/G]GGCACATAGCCAACG | 54472 |
rs751384463 | snp | A/C | 2.32393e-05 | 0.00340868 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295731 | GGGCGTCCAGCTGGA[A/C]CTGCCGCTGCTGCTG | 54472 |
rs751426226 | snp | C/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301541 | AAATCCAGGAGCTGT[C/G]CTGGGGAGGCACACA | 54472 |
rs751456325 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276181 | GCCACCACACCCTCT[C/T]GGAATCATGCACAGT | 54472 |
rs751526929 | snp | A/G | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311554 | TGACTCCTTAACATC[A/G]GAGTGCCTTACCTCA | 54472 |
rs751558926 | snp | A/C | 4.70024e-05 | 0.00484758 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277304 | AAAGTTCCAGAAGTG[A/C]CACACTAGCTCCTGC | 54472 |
rs751591973 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299687 | TGTACAAGATGCACA[C/T]ACTGAGTTCAACACT | 54472 |
rs751648815 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307020 | ACCGGGCCGTCACCA[C/T]ACAGCTCAGCTGTCC | 54472 |
rs751662283 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292336 | TCTCTGCCTAGCTGC[C/T]ATGACTTATTTTTAT | 54472 |
rs751669567 | snp | A/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273929 | AACGCGTCCGTGCCC[A/G]GGTGCCAGGGTGGCT | 54472 |
rs751847765 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281040 | GAGAACATGCTTCAT[C/G]AGGCCACGCGGTCTC | 54472 |
rs752015473 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277111 | CTGGGCTTCCAGCAC[A/G]GAGCGGATCACCTCC | 54472 |
rs752083742 | snp | A/G | | | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297944 | AGGCCAGGGCCCTTC[A/G]CCTGCCTCCCAGAAG | 54472 |
rs752085961 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287031 | GGATAAGTCACTGCA[C/T]CACTGTCGCCTCTGA | 54472 |
rs752140732 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301408 | GCGCCTGCCCACCCT[C/T]CCCACCCACCTCACA | 54472 |
rs752238933 | in-del | -/GCCGCAGCCTCCCCGCCGCAGCCTCCCC | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287795 | CGCCGCACCCTCCCT[-/GCCGCAGCCTCCCCGCCGCAGCCTCCCC]GCCGCACCCTCCCCG | 54472 |
rs752257387 | snp | C/G | 0.000156262 | 0.0088378 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276629 | TGTGAGGGATTGTGT[C/G]TGCCTTAAATCAACA | 54472 |
rs752258393 | snp | C/T | | | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310863 | TTCTCAGTCCTCGTC[C/T]TCCGGGAACTACAGC | 54472 |
rs752357982 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286915 | CAAAACTGTCCACTG[C/T]GGATAAGTCACTGCA | 54472 |
rs752410068 | snp | A/C | 1.67038e-05 | 0.00288992 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288666 | GCCCTCCTTGTCGTC[A/C]CCCTGCCTCCCGCTC | 54472 |
rs752477013 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281129 | ACATGATGCCTACCA[C/T]GAATTATTTGAAATC | 54472 |
rs752481801 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307140 | GCCACAGTTGGTAGC[A/G]CTGGTTGATTAAGTC | 54472 |
rs752522549 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281967 | GCTGGCAGTGGCTGC[C/T]GGGAGGATGGGCTGT | 54472 |
rs752535779 | snp | C/G | 3.84741e-05 | 0.00438584 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295716 | GCTGCTGGGCCGCCT[C/G]GGCGTCCAGCTGGAC | 54472 |
rs752566191 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285412 | GGCCGGTCTTGCACC[A/T]GCAGCTACCACAGTC | 54472 |
rs752568534 | in-del | -/C | 1.73993e-05 | 0.00294947 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295798 | ACCGATGTACACCTG[-/C]GGGGCCGGGGACCAG | 54472 |
rs752656167 | snp | A/G | 3.3592e-05 | 0.00409815 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290273 | ACGCCTGGGGGCACC[A/G]TGCAGTGGATGACCT | 54472 |
rs752716243 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288309 | GGCAGAGCTTGGAAG[A/G]GCTGTGGGGGTCCTC | 54472 |
rs752730324 | snp | A/G | 1.80866e-05 | 0.00300715 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295649 | CCAAGGCCCACCTGT[A/G]CCACCGTGATGTTCA | 54472 |
rs752812201 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274908 | GCTAATTCTGGGGAC[C/T]GCTCGGAGGGGCTCA | 54472 |
rs752968195 | snp | C/T | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273996 | TTTGCTCCCTAAGCA[C/T]GAGCCAGTCATCACT | 54472 |
rs752973555 | snp | A/G | 6.03336e-05 | 0.0054921 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285977 | TCTACCAGGGGAGAG[A/G]CACCCAGGGAGGGAG | 54472 |
rs753002093 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307782 | CAGAGGCCGTCCAGG[A/G]CCTCTGCCGACCCGT | 54472 |
rs753157997 | snp | C/T | 1.67094e-05 | 0.0028904 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290315 | GGATTCTTGGCGCCA[C/T]TGTGTGCCGTGGGCG | 54472 |
rs753163109 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279334 | CCCCTCCTTCCTGCA[A/G]GGCAGAGGCCATGTG | 54472 |
rs753207564 | snp | A/G | 1.77896e-05 | 0.00298237 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290216 | CATAATAGCTGGCAC[A/G]TCCCTCTCACCTCAT | 54472 |
rs753216242 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278890 | CTTTTTGGGCGCCCC[A/G]GCTGGCAGGCGGGCA | 54472 |
rs753314727 | snp | C/T | 1.77719e-05 | 0.00298088 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288598 | ATACCCCAATGCGCC[C/T]CACCCCGCCCAGGCG | 54472 |
rs753434222 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302692 | GGCCTCATGCTCCAC[A/G]CCAGTCTCCTGGCAC | 54472 |
rs753477389 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278390 | TTAGGATAGGACTTT[C/T]GTTCCTTTCTACACT | 54472 |
rs753616897 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308667 | GAAAGGTTCTCTGAA[A/G]TTCCTGGCGCCTATC | 54472 |
rs753616952 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298465 | TGGGTCCCTCGCTGC[C/T]CTGGATCCTGGTTGT | 54472 |
rs753643659 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274979 | TCAAACAGGAAATAA[A/G]GCATAAAATGAAGGA | 54472 |
rs753643804 | snp | A/G | 1.70758e-05 | 0.00292192 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290426 | TGGAATGAAGCCAAT[A/G]TCAGGAAAAGGAGGT | 54472 |
rs753725179 | snp | A/G | 1.67548e-05 | 0.00289432 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288649 | ATGACGAGGTTGATC[A/G]TGCCCTCCTTGTCGT | 54472 |
rs753786197 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292219 | TACACTCCAAACTCT[G/T]CCCCTGTAAACTCCT | 54472 |
rs753786267 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282114 | CAGTGTTCTCCTAAT[A/G]GGAACCAGGGCTCCT | 54472 |
rs753798329 | in-del | -/AGAA | 1.69484e-05 | 0.002911 | frameshift-variant, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290247 | CGAAGATCTCGAGAT[-/AGAA]AGAGTCCACGCCTGG | 54472 |
rs753866833 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282274 | GGGGCTCCCTCTGGC[C/T]AAATCTGGAATAATT | 54472 |
rs753947060 | snp | A/C | 2.08901e-05 | 0.00323181 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277282 | TCAAGTTTGGTAAAA[A/C]CGTCGGAAAGTTCCA | 54472 |
rs753965639 | snp | C/G | 0.000110867 | 0.00744454 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295616 | AGCGCACCAGCCCCA[C/G]GCAGGCAGGAGGGTG | 54472 |
rs754062309 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275593 | CACAGCTGAAGAAGG[C/T]GCCTGCTGCCAGCAT | 54472 |
rs754136374 | snp | C/T | 3.4647e-05 | 0.00416201 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295692 | TGCCCACTGCGCCTC[C/T]GTACTGCAGCTGCTG | 54472 |
rs754146163 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295513 | TTCAACATCACACAG[A/G]TTTCAGGAAAAGCGG | 54472 |
rs754280676 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293247 | CGAGAGCTCCACCTT[A/G]GGCACACGGAGTCCG | 54472 |
rs754283499 | snp | G/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290023 | GGGATGTTTCCAAAT[G/T]TAAGTATGTTCAAGG | 54472 |
rs754370533 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279963 | ACCGTCCAGCTCAGA[A/G]ACTGTTCCGGAACTC | 54472 |
rs754515386 | snp | C/T | 1.67494e-05 | 0.00289386 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288650 | TGACGAGGTTGATCA[C/T]GCCCTCCTTGTCGTC | 54472 |
rs754558708 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309950 | GGGGTGACCTTCGGA[C/G]GTGCGACCCGCTCGG | 54472 |
rs754655632 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284940 | TCTAGGGCGAGGTCC[C/T]GACTCCCAAGGTGGC | 54472 |
rs754656564 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302513 | AACTGCAATTCCCCA[C/T]GCCCACTCAGCTGCT | 54472 |
rs754681451 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281048 | GCTTCATGAGGCCAC[A/G]CGGTCTCCAGATGCT | 54472 |
rs754769806 | snp | A/G | 3.42695e-05 | 0.00413927 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290431 | TGAAGCCAATGTCAG[A/G]AAAAGGAGGTGCCAA | 54472 |
rs754824984 | snp | A/T | 3.65344e-05 | 0.00427386 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295636 | GCAGGAGGGTGCCCC[A/T]AGGCCCACCTGTACC | 54472 |
rs754899704 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301382 | GGATCCCACACAAAC[A/G]GCATCCGCAGGCGCC | 54472 |
rs754949925 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300659 | CCGACTGAGAGTGCC[A/G]CTGCTTCCTTGGGCC | 54472 |
rs755015129 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287038 | TCACTGCACCACTGT[C/T]GCCTCTGAGTTCAAA | 54472 |
rs755167572 | snp | A/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273979 | CTCACATTTATGGGC[A/G]CTTTGCTCCCTAAGC | 54472 |
rs755200585 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275857 | CAGTGGGTTTACATC[C/T]GAAGGCCGGCGGCAA | 54472 |
rs755204095 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306221 | TGAAGATCTAAACAC[A/G]GTATGATTCTCTCAG | 54472 |
rs755225179 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307051 | TTATGTGCTGCCATG[A/T]CTACCGTGCTGCCCT | 54472 |
rs755327679 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291870 | CGACCCCCGAGGGCA[C/T]GGCTGTCCCGTCCAC | 54472 |
rs755406670 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302883 | CTCGCTGAGCACTCA[C/T]TCGCCGTGCCTTGTC | 54472 |
rs755412103 | in-del | -/AAC | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296325 | AGTAAATCGATTCCA[-/AAC]AACCACGAAAGACCT | 54472 |
rs755432979 | snp | A/G | 3.43601e-05 | 0.00414474 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288783 | GAAGGCTCTCTGCGG[A/G]AGACAAGAGGGAGAG | 54472 |
rs755460687 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288295 | AGCTGGACCCTAAGG[A/G]CAGAGCTTGGAAGGG | 54472 |
rs755555553 | snp | A/G | 1.93508e-05 | 0.00311047 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290193 | CACGCTCAGCCACGT[A/G]CAGCCTCCATAATAG | 54472 |
rs755566728 | snp | C/G | 3.74665e-05 | 0.00432803 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295822 | GGACCAGAGAGGCCA[C/G]TGAGTCAGGGTGGGG | 54472 |
rs755638226 | snp | A/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301445 | CTGAGATCGCACATG[A/T]GTCGCGGGCTTCCGA | 54472 |
rs755652801 | snp | A/G | 7.3373e-05 | 0.00605649 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286033 | GCCAACGCCCTGCTG[A/G]TACACTGTTGGCATC | 54472 |
rs755740101 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1277402 | ACCAGTCCCGCAAGA[C/T]ACCCTGGAAAGGCAA | 54472 |
rs755763044 | snp | A/T | 2.783e-05 | 0.00373017 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295745 | ACCTGCCGCTGCTGC[A/T]GTGTGGGCGTGATGC | 54472 |
rs755806800 | snp | C/T | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274004 | CTAAGCATGAGCCAG[C/T]CATCACTAGGGGCTC | 54472 |
rs756020760 | snp | G/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291165 | AACATGGATGGCAGG[G/T]TCAAATATAAAACCT | 54472 |
rs756046185 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1277886 | ACTACACCAAGAAAA[C/T]GCTCACAAAACTCAA | 54472 |
rs756054421 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281298 | CACTGATGCGGTCAC[A/G]CTTTATTTTTGTGAA | 54472 |
rs756335263 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297442 | GGACGATCCAGGCAC[C/T]GCTTCGAGCAGTTAC | 54472 |
rs756348964 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298344 | GGGGGACAGACAGGC[A/G]ACTCATGTCCCGGAG | 54472 |
rs756374711 | snp | C/G | 1.65296e-05 | 0.00287481 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277129 | GCGGATCACCTCCTG[C/G]TCCATGTTGGGGAAC | 54472 |
rs756485574 | snp | C/T | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311438 | TTCCTTGTGCACAAG[C/T]TAAATAAAGATTTCT | 54472 |
rs756518479 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305312 | TGCAGTCAGCAGGAA[C/T]GGACGCCCTCCCAGG | 54472 |
rs756548591 | snp | A/G | 1.70907e-05 | 0.00292319 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288779 | TGGAGAAGGCTCTCT[A/G]CGGGAGACAAGAGGG | 54472 |
rs756565157 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292613 | AGCATCTGCCCATTC[A/G]CTATGACTGCACACA | 54472 |
rs756725002 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291316 | TGTACCACTGCCACC[C/T]GCTCTCCTGCAGCCA | 54472 |
rs756740577 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292236 | CCCTGTAAACTCCTT[A/T]GCAACTGCCCTATTT | 54472 |
rs756820124 | snp | A/C/T | 0.00028401 | 0.0119132 | intron-variant, utr-variant-5-prime, synonymous-codon, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295732 | GGCGTCCAGCTGGAC[A/C/T]TGCCGCTGCTGCTGT | 54472 |
rs756843676 | snp | C/T | 0.000143709 | 0.00847549 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276690 | TGCCATGAATGGAAT[C/T]GGAAGGCGCTCCACC | 54472 |
rs756888211 | in-del | -/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288224 | CCTGCCCTGTGGGGA[-/G]GAGCCTGGTGTCCTG | 54472 |
rs756916416 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290476 | TGGGTTCTCTAGGCC[A/G]TCTGCCTCCCTGAAC | 54472 |
rs756962046 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288326 | CTGTGGGGGTCCTCC[A/G]AGGACACAGGGGCCT | 54472 |
rs757013337 | snp | A/C | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308718 | AACTGAGGTTTTGCA[A/C]GGTGGCCACTAACCG | 54472 |
rs757063402 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276092 | AGGGCCACGCTCGCC[A/G]GGCTTTCCTCGCCCA | 54472 |
rs757073865 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299411 | ATGCTTCACGAGTCA[C/T]AGGGGAGAGAGTCCA | 54472 |
rs757128876 | snp | A/C | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298503 | TTTGAAGGCGTCCAG[A/C]GCTCCATCTCCTTGC | 54472 |
rs757152762 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283431 | ATCTAGATGGCCGTA[C/T]TGTGCCAGGGACGCC | 54472 |
rs757186826 | snp | C/T | 4.15584e-05 | 0.00455823 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286016 | CCTGTGATGGGCACA[C/T]AGCCAACGCCCTGCT | 54472 |
rs757207243 | snp | C/T | 0.000171615 | 0.00926164 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283482 | GCCTGGGCATGGGGG[C/T]TGGGGGCTCCGGTGG | 54472 |
rs757221969 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280069 | AGCGACCAAGTTAGC[A/G]GGTTAATAAACACAA | 54472 |
rs757362731 | snp | A/G | 6.69804e-05 | 0.00578668 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290389 | CATGCGGGTCATGCC[A/G]TAATTCTTGGCCAAC | 54472 |
rs757362749 | snp | A/G | 1.66549e-05 | 0.00288568 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277030 | CAAAACGGCATCGAG[A/G]CAGAGGCTCTATGGC | 54472 |
rs757384582 | snp | A/C | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304545 | GCACCCGCGCCAGGA[A/C]GGGGCGGCCGAGGTC | 54472 |
rs757468926 | snp | C/T | 1.70159e-05 | 0.00291679 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290241 | CCTCATCGAAGATCT[C/T]GAGATAGAAAGAGTC | 54472 |
rs757526937 | snp | A/G | 1.66994e-05 | 0.00288953 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290330 | TTGTGTGCCGTGGGC[A/G]TCTCGTACACCGCGT | 54472 |
rs757689176 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293262 | GGGCACACGGAGTCC[A/G]GAGTGCCCACGGAAC | 54472 |
rs757740465 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305415 | GGGCTCTTCACAACA[C/G]TCAGGGGAGAGAAAG | 54472 |
rs757765746 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305942 | CTCGATACTCCTCGC[C/G]GGGGCCCGCACGGTA | 54472 |
rs757852980 | snp | C/G | 0.00148893 | 0.0272442 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283573 | TTTTCTATGAAGTGC[C/G]GGGCTGTTCCAAAAT | 54472 |
rs757867155 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308014 | AGTACTGGGCTGCGC[A/G]AGGGCAGGGACCTTG | 54472 |
rs757918277 | in-del | -/G | 8.64827e-05 | 0.00657525 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295799 | CCGATGTACACCTGC[-/G]GGGCCGGGGACCAGA | 54472 |
rs758143000 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300493 | TTTTTGTCATGCAAT[A/G]TGTGTAGTCAATCCA | 54472 |
rs758165263 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303928 | GTAATCCCAGCTACT[C/T]GGGAGTCTGAGGCAG | 54472 |
rs758206107 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297361 | TCACCTGTGTCCCCA[C/T]CTAAGGCCTGGAGCG | 54472 |
rs758303453 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275821 | AGACCCACTTGTGGG[C/G]ATTCTCTTTCTGTCC | 54472 |
rs758340141 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299466 | TCAGTGACGACACTC[A/G]GTCCTTCAGTAAATG | 54472 |
rs758378739 | snp | C/G | 1.80745e-05 | 0.00300615 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295650 | CAAGGCCCACCTGTA[C/G]CACCGTGATGTTCAG | 54472 |
rs758413376 | snp | C/T | 1.7403e-05 | 0.00294978 | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290224 | CTGGCACGTCCCTCT[C/T]ACCTCATCGAAGATC | 54472 |
rs758468865 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290831 | CATGATGACCCGGGA[A/G]AGGTGCATCCTCGCT | 54472 |
rs758611901 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305470 | CAACTCTCTCCTTGA[A/G]GTACGGGAAGATGAG | 54472 |
rs758675362 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280217 | TTCGCTGGAATTCCA[C/T]GTGCGAGGGGAAGCA | 54472 |
rs758744443 | in-del | -/CA | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294163 | AAAGCCCGCATGGCT[-/CA]CAGTGTGTCTCCTTT | 54472 |
rs758805454 | snp | A/G | 0.00012566 | 0.00792553 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285971 | GGGGTTTCTACCAGG[A/G]GAGAGGCACCCAGGG | 54472 |
rs758815028 | snp | A/G | 0.000144645 | 0.00850302 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295844 | AGGGTGGGGGCACAA[A/G]GCAGCCCGACAGCAG | 54472 |
rs758879462 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296299 | CAAAAGTATCCCAGA[A/G]GAACGCAGGAAGTAA | 54472 |
rs759199631 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306654 | AGAGGGGCTGGGGTG[A/G]GTCATGCTCAGCGAA | 54472 |
rs759207750 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295576 | TGCAGTATAAACGCC[A/G]AAATCCGAAATCCCA | 54472 |
rs759284098 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285222 | ATGGCCTGGGCCTCT[A/G]GCCTCCACCCTCCGT | 54472 |
rs759330126 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290939 | CCCTGCCTGTGCTAT[C/T]GGAGTACGTGGGGTT | 54472 |
rs759333385 | in-del | -/A | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288306 | AAGGGCAGAGCTTGG[-/A]AGGGCTGTGGGGGTC | 54472 |
rs759344430 | in-del | -/GAGA | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286352 | AACTGGGATGTGACT[-/GAGA]GAGGATGGTGACAGG | 54472 |
rs759445552 | snp | G/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307781 | TCAGAGGCCGTCCAG[G/T]ACCTCTGCCGACCCG | 54472 |
rs759488068 | snp | A/C | | | synonymous-codon, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277210 | CACGGCGGCCGGGGG[A/C]AGGGCCACGGGCACC | 54472 |
rs759496131 | snp | C/T | | | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298092 | TCTGCTCACCAGGAA[C/T]GGGTTATCTTGCAGA | 54472 |
rs759537645 | snp | C/T | 0.000334392 | 0.0129261 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274611 | CGGCGACCTGTCTTC[C/T]ATCTCCGGAGCCCCG | 54472 |
rs759599269 | in-del | -/C | 1.83374e-05 | 0.00302793 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295632 | GCAGGCAGGAGGGTG[-/C]CCCAAGGCCCACCTG | 54472 |
rs759644394 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303283 | GGAAAACCCCTTCTC[A/G]TTCAGATGAAACAAA | 54472 |
rs759716943 | snp | C/T | 6.30034e-05 | 0.00561228 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277283 | CAAGTTTGGTAAAAA[C/T]GTCGGAAAGTTCCAG | 54472 |
rs759838134 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289106 | CTCCTCCCCAGCCCT[C/T]GGGGCCCCATCCTTG | 54472 |
rs759838249 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279188 | TGACAATGAGGGGAT[A/G]TGGCGCCGACTGGCC | 54472 |
rs760134367 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302351 | CAGGGTTTCAGAGAC[C/T]GAAGTGCCAGCCTGC | 54472 |
rs760209716 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286916 | AAAACTGTCCACTGC[A/G]GATAAGTCACTGCAC | 54472 |
rs760219268 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291368 | TGGTGATAGAGACCC[C/T]GGGAGCCATCCCGGC | 54472 |
rs760286482 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287311 | TCGTCACTCACGGCC[A/G]GGACATGATTTAAAA | 54472 |
rs760460010 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283208 | GCGGGGGCCCTGCCA[A/G]CAGCCCCGGGGAAAC | 54472 |
rs760523188 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281813 | GGCGACACACATGCT[C/T]TGGCCAAGATGCACT | 54472 |
rs760671756 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299284 | TACAAATACTGGTTA[C/T]GCAACCTGCTGCCCC | 54472 |
rs760715472 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275619 | AGCATGTCCCTCCCC[C/G]ACGGCCACCACACAC | 54472 |
rs760800248 | in-del | -/A | 1.6676e-05 | 0.00288751 | frameshift-variant, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288689 | TCCCGCTCAGGCTGT[-/A]CCACTTGTCCTCCAC | 54472 |
rs760961428 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308634 | GCCAGGCAACTCTCA[C/G]GAGAGAATTCAGAGC | 54472 |
rs760985550 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274939 | GCAAGCTGCTTCTAC[A/G]GTAAGCCACTTCTAC | 54472 |
rs761083128 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279908 | GGCTCCAGACGTCTC[A/G]CACCACAGTGGAAAG | 54472 |
rs761153223 | snp | C/T | 6.65181e-05 | 0.00576668 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285954 | CACCTGCCCTAGGCC[C/T]TGGGGTTTCTACCAG | 54472 |
rs761185521 | snp | A/T | 1.96423e-05 | 0.00313381 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277267 | CCCTGGAAGCAAAGA[A/T]CAAGTTTGGTAAAAA | 54472 |
rs761343792 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278451 | TCAATCCTGGCCTGA[A/G]CCAACACCAGCAACA | 54472 |
rs761359436 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307947 | GAAACACCAGGACTT[-/G]GTGGATACAGTGTTA | 54472 |
rs761447147 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279141 | GACGCTGCGACGTCA[C/T]GGCCTGGGGTGTCCC | 54472 |
rs761498621 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288534 | CTCAGTGCCTCCAGG[A/G]AAGAGACAAGGGTGT | 54472 |
rs761541013 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285511 | TGCTCACTCCTAACA[C/G]TGACACACGACAACA | 54472 |
rs761563594 | snp | C/G | 0.000454236 | 0.0150636 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276839 | GAGATGGGAGGGGAG[C/G]CCCCGCCCCGTCCTG | 54472 |
rs761623414 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293047 | GGCTGAGCGGGGGCA[A/G]TGGGTGGGTGCGGGG | 54472 |
rs761631158 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310454 | AACAAGAAGCATTCT[C/T]AGTTGAAGTTTCGCT | 54472 |
rs761651237 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284554 | CGGGGTTTCACCGTG[G/T]TGGCCAGGATGGTCT | 54472 |
rs761775355 | snp | A/T | 1.65644e-05 | 0.00287783 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277056 | ATGGCTCCTCCCCCA[A/T]CTGCAGCAGGGAGTT | 54472 |
rs761872443 | snp | G/T | 0.000197103 | 0.00992534 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309590 | TGCGACGGAGACAGT[G/T]GTCACCTCGAGGCCG | 54472 |
rs761880996 | snp | C/T | 3.40148e-05 | 0.00412386 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288628 | GTGCAGCTCACCGCG[C/T]AGGACATGACGAGGT | 54472 |
rs761923998 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285052 | TGGCCTCACAGCACT[C/T]TCGCCTGCCAGCAGC | 54472 |
rs761984410 | in-del | -/C | 6.49203e-05 | 0.00569701 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285966 | GCCCTGGGGTTTCTA[-/C]CAGGGGAGAGGCACC | 54472 |
rs762051229 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300984 | GCACTTGGCATGTAA[A/G]CACTGCAAGCAAGGC | 54472 |
rs762102583 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300351 | ACTGACGCCAGAGCT[C/T]TAAACCACTGCAGCG | 54472 |
rs762166944 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306771 | AAGTCCAGTCCTCCT[C/G]TGCCCAGGACCCTCC | 54472 |
rs762285237 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298710 | GGGGAGAAGCAGCTC[C/T]CTGCGGATGGAGCTC | 54472 |
rs762377289 | snp | C/T | 1.704e-05 | 0.00291885 | missense, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277197 | GGGGCTGGGCGTTCA[C/T]GGCGGCCGGGGGCAG | 54472 |
rs762377396 | snp | C/T | 1.75391e-05 | 0.00296129 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295677 | TCAGTCGGCCCACGG[C/T]GCCCACTGCGCCTCC | 54472 |
rs762396044 | snp | A/C | 0.112256 | 0.20863 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288823 | ATCAGGGAAGGGGCC[A/C]CCCTGCCCCTGCAGC | 54472 |
rs762411425 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280776 | CCCCAGAGGACAGCG[C/T]GGCCGGCACCACCTT | 54472 |
rs762530134 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293079 | GCTCCAGGCCTGGAC[A/G]GGCTGAAGGTGGCGC | 54472 |
rs762560146 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305679 | TATCAACGATGTGAA[A/G]AGTGAGGGGACCTGG | 54472 |
rs762625625 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279741 | TACTGACAAACACAA[G/T]GATACCCAGGAAAAC | 54472 |
rs762684163 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305276 | TGAGGAGGCGGTGAG[C/T]GCGTTCCCCGCTGGC | 54472 |
rs762710011 | snp | A/G | 1.68465e-05 | 0.00290223 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288763 | GCAATGCGGTCGTCC[A/G]TGGAGAAGGCTCTCT | 54472 |
rs762716399 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276168 | GTCGGCTGGCAGTGC[C/T]ACCACACCCTCTCGG | 54472 |
rs762734928 | snp | A/G | 3.49999e-05 | 0.00418315 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276804 | CAGGGACAGGAGAGC[A/G]CGCTGAGACCTCCCA | 54472 |
rs762769226 | snp | A/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301170 | AATAAACAACTTATA[A/T]AAACACAATAAAAAA | 54472 |
rs762769513 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285552 | CGCAGTAGAGAGCAC[C/G]CATCACCCAACAGGA | 54472 |
rs762771209 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289204 | GCCTCCCACAGCTGA[C/T]TCTGCACTTCCCATG | 54472 |
rs762808712 | snp | A/C | 5.69622e-05 | 0.00533646 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295784 | TCCTGCGGGAGCTCA[A/C]CGATGTACACCTGCG | 54472 |
rs762819049 | snp | A/G | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311435 | GACTTCCTTGTGCAC[A/G]AGCTAAATAAAGATT | 54472 |
rs762865574 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286641 | ACTGCTGTCTCCTGA[A/G]TTCAAAACTGTCAAC | 54472 |
rs762911622 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304462 | ATCTAAACAAGCGCT[-/G]ACTCGAGAGAAGTAA | 54472 |
rs762922260 | in-del | -/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287191 | CACCACTGTCGTCTC[-/T]TGAGTTCGAAACTGT | 54472 |
rs763010921 | snp | A/G | 8.39807e-05 | 0.00647945 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276995 | GGGAGCGCCGGGTCG[A/G]CGTGTCCAAAGAGCG | 54472 |
rs763034319 | snp | C/G | 0.00155279 | 0.0278206 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309536 | CTCGCCGACCCGACA[C/G]TGACGCGCCGGGCGA | 54472 |
rs763085247 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281711 | CGTGCACACAGGCCC[A/G]AAGCCACGCAGCCAG | 54472 |
rs763213773 | snp | C/T | 6.0033e-05 | 0.0054784 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285978 | CTACCAGGGGAGAGG[C/T]ACCCAGGGAGGGAGC | 54472 |
rs763255086 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298930 | AAGGAAAGCCTGAGA[A/G]ACGGTCCCAGATTGG | 54472 |
rs763255290 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295884 | GCATTCCCGCGGCCC[C/T]GCCCCCACCCATGTC | 54472 |
rs763313968 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298419 | CAGGGACGTGTGGGC[A/G]TGGGGTCCAGAGGCC | 54472 |
rs763332463 | snp | C/T | 1.85606e-05 | 0.0030463 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295595 | TCCGAAATCCCACCC[C/T]CACCGAGCGCACCAG | 54472 |
rs763336098 | snp | A/C/T | 7.49485e-05 | 0.00612116 | intron-variant | TOLLIP | GRCh38.p7 | 11:1286140 | GGAGGAACATCCACC[A/C/T]ATCAGAACCTCGGGA | 54472 |
rs763493280 | snp | C/T | 1.67186e-05 | 0.0028912 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290383 | GGGGTCCATGCGGGT[C/T]ATGCCGTAATTCTTG | 54472 |
rs763499190 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285857 | TGGCCTGAAAGGATC[C/T]GTGTGCGGTCAGCAC | 54472 |
rs763587191 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282620 | CCCTAAAACTTAAAA[C/T]ATAATTAAGATAAAT | 54472 |
rs763623332 | snp | A/G | 0.000115263 | 0.00759066 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288828 | GGAAGGGGCCACCCT[A/G]CCCCTGCAGCCGCAC | 54472 |
rs763646527 | in-del | -/AA | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1277423 | GAAAGGCAAACCCCC[-/AA]AAACAGCAACCCCAG | 54472 |
rs763646997 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287315 | CACTCACGGCCGGGA[C/T]ATGATTTAAAATATC | 54472 |
rs763706104 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278367 | ACTGGAGCGCTAGAG[C/G]CCCAATCTTAGGATA | 54472 |
rs763715117 | snp | C/T | 0.000287646 | 0.0119892 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276805 | AGGGACAGGAGAGCG[C/T]GCTGAGACCTCCCAG | 54472 |
rs763753534 | snp | C/T | 5.72525e-05 | 0.00535004 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295785 | CCTGCGGGAGCTCAC[C/T]GATGTACACCTGCGG | 54472 |
rs763895447 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283247 | ACCCTGCAAGGCCAC[A/G]TCAGCAGCCCCACCA | 54472 |
rs763952628 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292188 | TGCACACCCACACAT[C/T]TGCTAGATCAGCTCT | 54472 |
rs763963866 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307796 | GACCTCTGCCGACCC[A/G]TAGGCTCCACACCTG | 54472 |
rs763995925 | snp | C/T | 0.000266276 | 0.0115355 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309561 | GGGCGACCTCCTGCG[C/T]CCCCGCCGGAGCCTG | 54472 |
rs764073212 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291272 | CGGCTGCCTGTAAAG[C/T]GTCCTGCCTGGAATG | 54472 |
rs764148191 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303638 | TGCCAGGGCAGGGCC[C/T]GCAGGATCTGGAGAC | 54472 |
rs764227120 | snp | A/G | 1.67052e-05 | 0.00289004 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290324 | GCGCCATTGTGTGCC[A/G]TGGGCGTCTCGTACA | 54472 |
rs764297378 | snp | G/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300140 | ATAAAAAGGACAGGG[G/T]AGGGCTCTCATCCCA | 54472 |
rs764335602 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284530 | ATTTGTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 54472 |
rs764352104 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299373 | GCAAAGCCCTTCAAA[C/T]GAGGAGGGAGTGCTA | 54472 |
rs764356549 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310352 | GCTGCATCCCCAGGA[A/G]TCGGGCGTTTACGGT | 54472 |
rs764361038 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275667 | AAATATTTATCAACA[A/G]TATATTTGACAAAAA | 54472 |
rs764384006 | snp | C/T | 5.07859e-05 | 0.00503889 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277191 | TACAGCGGGGCTGGG[C/T]GTTCACGGCGGCCGG | 54472 |
rs764463572 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305400 | TGCAGGAAAATCCAC[A/G]GGCTCTTCACAACAC | 54472 |
rs764473151 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308663 | GCAGGAAAGGTTCTC[C/T]GAAGTTCCTGGCGCC | 54472 |
rs764483427 | snp | A/T | 1.65241e-05 | 0.00287433 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277102 | GTTCCCTCGCTGGGC[A/T]TCCAGCACGGAGCGG | 54472 |
rs764545732 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292278 | TGTAGCAGGAAAGTC[A/T]GAGACCAGCATGATT | 54472 |
rs764683709 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292385 | TGAGCAAAGCCAGCT[C/T]TCTGGGTGGCACATG | 54472 |
rs764764201 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283290 | GAACATACCCTAGGA[A/G]CAAGATGGGGACCCC | 54472 |
rs764810129 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305136 | CCAAGAGGCCCGTGG[A/G]TCCCCACACAGTGAA | 54472 |
rs764896585 | in-del | -/A | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286901 | CTGTCTCCTGAGTTC[-/A]AAACTGTCCACTGCG | 54472 |
rs764910941 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310496 | GATACAGATGCTTGC[A/G]GAGGACAGGCGTTAT | 54472 |
rs764966866 | snp | C/T | 0.000284981 | 0.0119335 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276780 | CATGAGAAGGAGAGA[C/T]GCACGTCCCAGGGAC | 54472 |
rs765041844 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275770 | AAAAAGACTAAAATG[C/T]AAGCACTAACTTCCT | 54472 |
rs765073678 | in-del | -/GCT | 4.80798e-05 | 0.00490281 | intron-variant, cds-indel, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295737 | CCAGCTGGACCTGCC[-/GCT]GCTGCTGTGTGGGCG | 54472 |
rs765095016 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284579 | TGGTCTTGATCTCCT[C/G]ACCTCACGATCTGCC | 54472 |
rs765129306 | snp | A/C | 0.000220192 | 0.0104903 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274813 | TTGTGAGCTGGCAGA[A/C]AAGCCTGTCCTTCTG | 54472 |
rs765163732 | snp | C/T | 5.57295e-05 | 0.00527841 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295711 | CTGCAGCTGCTGGGC[C/T]GCCTGGGCGTCCAGC | 54472 |
rs765279626 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293053 | GCGGGGGCAGTGGGT[G/T]GGTGCGGGGGGCTCC | 54472 |
rs765348234 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280953 | CGCACGAAGAACGCA[C/T]GGGAAATTGAGCAGT | 54472 |
rs765365888 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282181 | TGCAGAGAGCCTGGG[A/G]CTTCCTGCAGTGCCA | 54472 |
rs765378076 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280104 | AGAGAGTTCCATGTG[A/T]TAGTTTGTCTCGGAA | 54472 |
rs765487474 | snp | C/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301036 | GCCAGGTTAGCATAA[C/G]TAAGTCGAACGAAGT | 54472 |
rs765534435 | snp | A/G | 4.22066e-05 | 0.00459364 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277284 | AAGTTTGGTAAAAAC[A/G]TCGGAAAGTTCCAGA | 54472 |
rs765578822 | snp | A/G | 3.33884e-05 | 0.00408572 | stop-gained, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290361 | AGCCCAGGCGCAGTC[A/G]GCAGTAGGGGTCCAT | 54472 |
rs765673572 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306853 | CTCTCCACCTCCAGA[C/T]CCCACACCTCTCTTT | 54472 |
rs765753844 | snp | C/T | 5.01786e-05 | 0.00500867 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277020 | AGAGCGGGGGCAAAA[C/T]GGCATCGAGGCAGAG | 54472 |
rs765842689 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284715 | ACACGCTCTGCTCTT[C/T]CCTCTGGAGAAAGGC | 54472 |
rs766059349 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301274 | CAAACTGACATCATT[A/G]GCGATGGGCTAAATA | 54472 |
rs766071540 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293097 | CTGAAGGTGGCGCCT[A/G]TGCTGAGGGTCAGGC | 54472 |
rs766203053 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305278 | AGGAGGCGGTGAGTG[C/T]GTTCCCCGCTGGCTC | 54472 |
rs766211794 | snp | A/G | 0.000544218 | 0.0164867 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274577 | TCTGCAGAGGGGAGA[A/G]GAGAGGAGGGGGAGC | 54472 |
rs766263496 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303992 | AGTGAGTTGAGATTG[C/T]GCCACTGCACTCCAG | 54472 |
rs766281769 | snp | C/T | 1.67615e-05 | 0.0028949 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288648 | CATGACGAGGTTGAT[C/T]ATGCCCTCCTTGTCG | 54472 |
rs766316766 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305584 | TTACAAACAATCCCA[C/G]TTAATAAACACCGAA | 54472 |
rs766331271 | snp | A/G | 3.46807e-05 | 0.00416403 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295687 | CACGGTGCCCACTGC[A/G]CCTCCGTACTGCAGC | 54472 |
rs766336771 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276178 | AGTGCCACCACACCC[G/T]CTCGGAATCATGCAC | 54472 |
rs766389620 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285596 | ACACAACGGCGCAGC[A/G]CAGGGCACGCGTCAC | 54472 |
rs766414183 | snp | A/G | 5.15681e-05 | 0.00507754 | synonymous-codon, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277201 | CTGGGCGTTCACGGC[A/G]GCCGGGGGCAGGGCC | 54472 |
rs766415165 | snp | C/T | | | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277115 | GCTTCCAGCACGGAG[C/T]GGATCACCTCCTGGT | 54472 |
rs766425453 | snp | A/G | 2.03279e-05 | 0.00318803 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277275 | GCAAAGATCAAGTTT[A/G]GTAAAAACGTCGGAA | 54472 |
rs766439766 | in-del | -/C | 0.000458857 | 0.01514 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288820 | GCATCAGGGAAGGGG[-/C]CCACCCTGCCCCTGC | 54472 |
rs766450992 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307007 | AGATCACAGACCCAC[C/T]GGGCCGTCACCACAC | 54472 |
rs766590329 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281771 | CAGGCTTCTCCACCA[A/T]GTGAGTCATAAACAC | 54472 |
rs766643365 | snp | C/G | 1.85214e-05 | 0.00304309 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295608 | CCCCACCGAGCGCAC[C/G]AGCCCCAGGCAGGCA | 54472 |
rs766815911 | snp | C/G | | | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297778 | GTGGGCCCATGCCAG[C/G]AGTCCCAGGCCAGCC | 54472 |
rs767009296 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1296063 | TGGGTTCCTGTCCTC[A/G]AAGCCTGCTCAGGTG | 54472 |
rs767035073 | snp | A/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1273919 | ACGCTCCAGCAACGC[A/G]TCCGTGCCCGGGTGC | 54472 |
rs767088985 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288570 | GGGCGGCATAGCCCC[A/G]ACGTGCTCCAACATA | 54472 |
rs767157606 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286765 | AACTGTCCACTGCGG[A/G]TAAGTCATTGCACTG | 54472 |
rs767210686 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285691 | GAGGTTCTCCTGCAC[A/G]GAGCTGGGCACAACG | 54472 |
rs767250508 | snp | A/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290944 | CCTGTGCTATCGGAG[A/T]ACGTGGGGTTTTGGG | 54472 |
rs767253596 | snp | C/T | 0.000151114 | 0.00869105 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276840 | AGATGGGAGGGGAGC[C/T]CCCGCCCCGTCCTGG | 54472 |
rs767255576 | snp | C/T | 8.37107e-05 | 0.00646903 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290297 | ATGACCTTATTCCAG[C/T]GGGGATTCTTGGCGC | 54472 |
rs767333579 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295463 | ATGTTTGGTAGAACC[C/T]GGGGTCAATGCCAAT | 54472 |
rs767388195 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302189 | ATCCACCCGATGCCC[A/G]CACACCTGTGTGATT | 54472 |
rs767399615 | snp | A/G | 1.69571e-05 | 0.00291174 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288631 | CAGCTCACCGCGTAG[A/G]ACATGACGAGGTTGA | 54472 |
rs767462016 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279682 | ACCTCACGTTCTTCA[C/T]GCTGTGTGAATCTGC | 54472 |
rs767522924 | snp | C/T | 1.67483e-05 | 0.00289377 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290393 | CGGGTCATGCCGTAA[C/T]TCTTGGCCAACTTTG | 54472 |
rs767682183 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281913 | CCCTGAGCACGCAGC[C/T]GCCAGCCTCTCCAAG | 54472 |
rs767732605 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1307708 | GCACTTGGCTGCCAC[A/G]GCAACTTGCGGGGAC | 54472 |
rs767773440 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283034 | GGGCGGGATCTTCAC[A/G]TGGTCCTGGGGTGCC | 54472 |
rs767827904 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292099 | TACTCCGGAATGCTA[C/T]GGAGTGACAGTTTTC | 54472 |
rs767968862 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299102 | CGGGGAGGGGAGCGT[C/T]GGCCAGGGGACATGG | 54472 |
rs767974020 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308406 | CCAGAGGCCTCCCCA[A/G]GAGCAGATGCCGGCA | 54472 |
rs767987464 | snp | A/G | 3.41886e-05 | 0.00413438 | synonymous-codon, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277198 | GGGCTGGGCGTTCAC[A/G]GCGGCCGGGGGCAGG | 54472 |
rs768032741 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275271 | GCACCCCAGCAACGC[A/G]AAGGCAGAAACCGGT | 54472 |
rs768071236 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288303 | CCTAAGGGCAGAGCT[A/T]GGAAGGGCTGTGGGG | 54472 |
rs768075105 | snp | C/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299809 | CCTGAGGCTGCGTCA[C/T]CTGTGCCGTCAAAAC | 54472 |
rs768289079 | snp | C/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298758 | CGGGGACCGCAGCCA[C/G]CGCCATGTGGCGGGG | 54472 |
rs768334174 | snp | A/G/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275318 | GGGCGCCTGGACACC[A/G/T]AAGCCCCCAGCACAG | 54472 |
rs768385278 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276560 | GCTCACAGCAAAGCG[C/G]GTTAGGGCAAGGGCG | 54472 |
rs768430034 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291089 | GGGGTGGGAGTGAAC[A/G]TGTGTTCAGAATAAG | 54472 |
rs768444618 | snp | C/T | 0.00413359 | 0.0452737 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277049 | AGGCTCTATGGCTCC[C/T]CCCCCATCTGCAGCA | 54472 |
rs768461739 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292809 | ACACAGCGCAGCAGA[C/T]GGCGTTACCACTGCA | 54472 |
rs768680488 | snp | C/T | 6.67757e-05 | 0.00577784 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290343 | GCGTCTCGTACACCG[C/T]GTAGCCCAGGCGCAG | 54472 |
rs768705218 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279578 | GGAGGAGTGATGGGC[A/G]GCTTTGCTGTGTCCC | 54472 |
rs768718970 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298899 | CGTCCTCAAACCGTC[A/G]AGGTCCCAAAAACAC | 54472 |
rs768744957 | snp | A/G | 2.05489e-05 | 0.00320531 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276849 | GGGAGCCCCCGCCCC[A/G]TCCTGGACCGCCAGG | 54472 |
rs768890824 | snp | A/G | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311319 | AGAAGCACTAGACAA[A/G]CCCCTCCTATCCATG | 54472 |
rs768914871 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290554 | TCGCCTGAACACGGC[C/T]GTGACCTGCTTCCCA | 54472 |
rs768971463 | snp | A/C | 1.85682e-05 | 0.00304693 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295597 | CGAAATCCCACCCCC[A/C]CCGAGCGCACCAGCC | 54472 |
rs768975507 | in-del | -/TCC | 1.66131e-05 | 0.00288206 | cds-indel, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277166 | TGGATGGCTTTCAGG[-/TCC]TCCTCGCTACAGCGG | 54472 |
rs769026579 | snp | C/T | 7.04647e-05 | 0.00593527 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295674 | TGTTCAGTCGGCCCA[C/T]GGTGCCCACTGCGCC | 54472 |
rs769056964 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300037 | AGGGAAACAGGCAGG[A/G]AAGATTCTATTTCAA | 54472 |
rs769133619 | snp | A/G | 0.000373902 | 0.0136679 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283512 | GGGCGTCAGGTGGAC[A/G]AGTCCTCACAGGCTC | 54472 |
rs769175597 | in-del | -/TAT | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284524 | CGGCTAATTTGTTTG[-/TAT]TTTTAGTAGAGACGG | 54472 |
rs769310531 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289740 | CGGCAAGACCCTGTG[C/T]GCCCAGCGGGGCGGA | 54472 |
rs769362054 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279646 | CGCACGCGGACGGAT[A/G]TGCAGCACAGGACAG | 54472 |
rs769551416 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293749 | TCTGGAGCTTGAACT[A/G]TGTGAGGTGGAGTGC | 54472 |
rs769583601 | snp | C/T | 0.000100939 | 0.00710346 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276993 | TGGGGAGCGCCGGGT[C/T]GGCGTGTCCAAAGAG | 54472 |
rs769586893 | snp | A/G | 3.37941e-05 | 0.00411046 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290254 | CTCGAGATAGAAAGA[A/G]TCCACGCCTGGGGGC | 54472 |
rs769590037 | snp | C/G/T | 0.000877463 | 0.0209281 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288820 | GGCATCAGGGAAGGG[C/G/T]CCACCCTGCCCCTGC | 54472 |
rs769789809 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306409 | TCACTAGGGGGAGGC[A/C]ACGGCTAGACCACAG | 54472 |
rs769926714 | snp | A/C/G | 0.00108651 | 0.0232873 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309512 | ATGGTGCTGCGGCGG[A/C/G]CCCCGTGGCTCGCCG | 54472 |
rs769990375 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305270 | GACTCGTGAGGAGGC[A/G]GTGAGTGCGTTCCCC | 54472 |
rs769991375 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276937 | CGGGAGGGGGCGACA[C/T]GGGTGCTCTTTCACG | 54472 |
rs769993275 | snp | A/G | 3.32629e-05 | 0.00407803 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277034 | ACGGCATCGAGGCAG[A/G]GGCTCTATGGCTCCT | 54472 |
rs770016344 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274497 | GGACCCCAGTAAAAT[A/C]ATCAGAAGCGCACGT | 54472 |
rs770025043 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301858 | AGAGAGAAATAAATC[C/T]CCCGTAGTAGGAACA | 54472 |
rs770050518 | in-del | -/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306974 | CCATTTACAAACTCT[-/C]CCAGCACCTGACGCT | 54472 |
rs770099049 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286317 | GAGGTGACATGGCTC[A/G]GGCTTACAGACCCCC | 54472 |
rs770173867 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307411 | CCCACTTCCTCATCG[A/C]GGGTGTAACAGCGCT | 54472 |
rs770286623 | snp | C/T | 1.78055e-05 | 0.00298369 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295667 | ACCGTGATGTTCAGT[C/T]GGCCCACGGTGCCCA | 54472 |
rs770420666 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291886 | GGCTGTCCCGTCCAC[A/G]CCAACCCTCGCCGCA | 54472 |
rs770422514 | snp | A/G | 0.000121094 | 0.00778024 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288618 | CCGCCCAGGCGTGCA[A/G]CTCACCGCGTAGGAC | 54472 |
rs770426227 | snp | C/T | 0.00018365 | 0.00958078 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277175 | TTCAGGTCCTCCTCG[C/T]TACAGCGGGGCTGGG | 54472 |
rs770431240 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281448 | CAGCTTGCACTCTCC[A/G]TAGAGGTGGCAGCTG | 54472 |
rs770473731 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290818 | CCTGCCCCCGGAGCA[C/T]GATGACCCGGGAGAG | 54472 |
rs770549876 | in-del | -/GAC | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300318 | CGCAAGCCTGTGACT[-/GAC]GACCATTCCTCCCTC | 54472 |
rs770563507 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295211 | TAAGCAACCACGGGC[C/T]GGCCCCGAGGCTGAC | 54472 |
rs770587684 | snp | A/G | 1.74042e-05 | 0.00294988 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290452 | GAGGTGCCAACCATC[A/G]GGAGAGGGTGGGTTC | 54472 |
rs770600258 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306488 | TCTTTCTGCTGGAAA[A/G]CTGAGCGAGCGCCCT | 54472 |
rs770718419 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278173 | GAGCAGCCCTGAGCA[A/C]AGGCAGCGTGCGCGG | 54472 |
rs770727408 | snp | A/G | 3.61135e-05 | 0.00424917 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288814 | GCCCCAGGCATCAGG[A/G]AAGGGGCCACCCTGC | 54472 |
rs770770955 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286653 | TGAGTTCAAAACTGT[A/C]AACTGTGGATAAGTC | 54472 |
rs770918842 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295207 | CCACTAAGCAACCAC[A/G]GGCCGGCCCCGAGGC | 54472 |
rs770942485 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292004 | TCACTTCTAATCAAA[A/G]CTGTGGCCGGTCCTT | 54472 |
rs770995599 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303244 | TGCATCCTAAGTGCT[A/G]GGACGGTCAAGCAAG | 54472 |
rs771092450 | snp | A/G | 3.80916e-05 | 0.00436398 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295765 | GGGCGTGATGCGGAG[A/G]AAGTCCTGCGGGAGC | 54472 |
rs771193459 | snp | G/T | 3.44382e-05 | 0.00414945 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276880 | AACCGAAAACCCACA[G/T]GCACCCAAGAACAGG | 54472 |
rs771337221 | snp | C/T | 5.18175e-05 | 0.0050898 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309430 | CCCGCAACCGCAGGT[C/T]ACCGCCCCCGCCCGA | 54472 |
rs771367841 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305029 | GTAAAATCATAGAAG[A/G]AAAAAGTACTAGGTG | 54472 |
rs771372814 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276021 | GCCAAGATGCTACAC[A/G]CAGCGCCCAGGCAGT | 54472 |
rs771413256 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308417 | CCCAGGAGCAGATGC[C/T]GGCACCATGCTACCT | 54472 |
rs771437658 | snp | C/T | 6.69411e-05 | 0.00578499 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285955 | ACCTGCCCTAGGCCC[C/T]GGGGTTTCTACCAGG | 54472 |
rs771495222 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279245 | CCAACACACTCACTT[A/G]GGGAGCAGGCACCCC | 54472 |
rs771579764 | snp | A/C | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274350 | TGAATTAAGTTAAAA[A/C]ATACTCGGGAACAAA | 54472 |
rs771607986 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282745 | TGTAACAAACCTGCA[C/T]GTTGTGCACATGTAC | 54472 |
rs771630136 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297641 | CCTGTGAGAGAAGCC[A/G]TACTGCGAGAACAAG | 54472 |
rs771667248 | snp | A/G | 1.66946e-05 | 0.00288912 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290353 | CACCGCGTAGCCCAG[A/G]CGCAGTCGGCAGTAG | 54472 |
rs771676395 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306667 | TGGGTCATGCTCAGC[A/G]AAGCAGGCTGGTGCC | 54472 |
rs771720197 | snp | C/G | 1.65436e-05 | 0.00287602 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277067 | CCCATCTGCAGCAGG[C/G]AGTTGATGGCGGCAT | 54472 |
rs771720658 | snp | A/G | 1.72133e-05 | 0.00293366 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290440 | TGTCAGGAAAAGGAG[A/G]TGCCAACCATCAGGA | 54472 |
rs771730262 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282325 | ATAAGGGATTCTGAC[C/T]CAAGGAAAAAAATAG | 54472 |
rs771882334 | snp | G/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303456 | GTGCTGGGGCACCCC[G/T]GCTCCTGGGATGCTT | 54472 |
rs772058499 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284319 | CTTTCCTCGGTGACG[A/G]GGTGCAGGTGCTACC | 54472 |
rs772085030 | in-del | -/CA | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300154 | GTAGGGCTCTCATCC[-/CA]CAGAGCTCACAGCAT | 54472 |
rs772120928 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278268 | ACAGAGCTCCTCCTG[C/T]AGCAGCAGCTGCAGC | 54472 |
rs772126719 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288839 | CCCTGCCCCTGCAGC[C/T]GCACCATCGTGGGCC | 54472 |
rs772129338 | snp | A/T | 1.66228e-05 | 0.0028829 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277166 | TGGATGGCTTTCAGG[A/T]CCTCCTCGCTACAGC | 54472 |
rs772140957 | snp | A/C | 3.50594e-05 | 0.0041867 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288802 | CAAGAGGGAGAGGCC[A/C]CAGGCATCAGGGAAG | 54472 |
rs772148346 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293484 | AACAAGGGGAAGCAG[C/T]GAGGGGACGCAAGCA | 54472 |
rs772152476 | snp | C/T | 1.66782e-05 | 0.0028877 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288737 | ACTCCGGGATGGTGA[C/T]GTGGGTCCAGGCAAT | 54472 |
rs772176226 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287307 | CACATCGTCACTCAC[A/G]GCCGGGACATGATTT | 54472 |
rs772261080 | snp | C/T | 3.10573e-05 | 0.00394052 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295753 | CTGCTGCTGTGTGGG[C/T]GTGATGCGGAGGAAG | 54472 |
rs772273048 | snp | A/C | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292714 | ACAACGGGCAAGAGA[A/C]GCACGTCAGACAGCA | 54472 |
rs772340970 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300777 | TGCCAGGAGACATCA[C/T]CCCAAGGAGCCGCAC | 54472 |
rs772343571 | in-del | -/A | 0.000194313 | 0.00985489 | intron-variant | TOLLIP | GRCh38.p7 | 11:1285968 | CCTGGGGTTTCTACC[-/A]GGGGAGAGGCACCCA | 54472 |
rs772383397 | snp | C/T | 9.24855e-05 | 0.00679957 | missense, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277251 | TACAGACAGCGGGCA[C/T]CCCTGGAAGCAAAGA | 54472 |
rs772450266 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289182 | GACTGGAAAGGACAC[A/G]GGGTCTGCCTCCCAC | 54472 |
rs772606653 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276059 | AAGTGAGCGCCTCCC[A/G]CCTCAGAAAGCTTTT | 54472 |
rs772622731 | snp | A/G | 1.7403e-05 | 0.00294978 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295682 | CGGCCCACGGTGCCC[A/G]CTGCGCCTCCGTACT | 54472 |
rs772744383 | snp | A/G | 8.34759e-05 | 0.00645995 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290355 | CCGCGTAGCCCAGGC[A/G]CAGTCGGCAGTAGGG | 54472 |
rs772816013 | snp | A/G | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311388 | CCACCCCCTGGCGGC[A/G]GGGCCCCCCACCGTT | 54472 |
rs772847038 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305597 | CAGTTAATAAACACC[G/T]AAGAAGTGATAAAGT | 54472 |
rs772890199 | snp | C/T | 1.66793e-05 | 0.0028878 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277173 | CTTTCAGGTCCTCCT[C/T]GCTACAGCGGGGCTG | 54472 |
rs772949834 | snp | A/G | 5.0229e-05 | 0.00501118 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290298 | TGACCTTATTCCAGC[A/G]GGGATTCTTGGCGCC | 54472 |
rs772971966 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276156 | AAGCTGTCAGCAGTC[A/G]GCTGGCAGTGCCACC | 54472 |
rs772987032 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295868 | ACAGCAGCTGCCCCC[A/G]GCATTCCCGCGGCCC | 54472 |
rs773056185 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289480 | CTGCAGGTGCAGCCA[C/T]GGACGGGACTCAGGA | 54472 |
rs773105923 | snp | G/T | 0.000141955 | 0.00842361 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276759 | CAAGAGCATTTTCCA[G/T]AACGGCATGAGAAGG | 54472 |
rs773107962 | in-del | -/CTT | 1.67237e-05 | 0.00289164 | cds-indel, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288657 | GTTGATCATGCCCTC[-/CTT]GTCGTCCCCCTGCCT | 54472 |
rs773108179 | snp | A/T | 1.66907e-05 | 0.00288879 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288743 | GGATGGTGATGTGGG[A/T]CCAGGCAATGCGGTC | 54472 |
rs773382907 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301943 | TCTGCTAGGAAGGGA[A/G]CCCCAGACTCGGTCA | 54472 |
rs773414168 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290845 | AGAGGTGCATCCTCG[C/T]TCTAGGTGAGAGTGA | 54472 |
rs773429643 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288294 | CAGCTGGACCCTAAG[A/G]GCAGAGCTTGGAAGG | 54472 |
rs773491764 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276991 | CTTGGGGAGCGCCGG[A/G]TCGGCGTGTCCAAAG | 54472 |
rs773537408 | snp | C/T | 1.73924e-05 | 0.00294888 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295684 | GCCCACGGTGCCCAC[C/T]GCGCCTCCGTACTGC | 54472 |
rs773540448 | in-del | -/AGG | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279085 | TGATGGGGAAGGGAC[-/AGG]AGGAGGGGAACTGCT | 54472 |
rs773710266 | snp | A/G | 1.90293e-05 | 0.00308453 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277260 | CGGGCATCCCTGGAA[A/G]CAAAGATCAAGTTTG | 54472 |
rs773801820 | snp | A/G | 3.19514e-05 | 0.00399684 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295754 | TGCTGCTGTGTGGGC[A/G]TGATGCGGAGGAAGT | 54472 |
rs773864199 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281732 | ACGCAGCCAGCACCG[C/T]GTAGCCAGGCAGAGC | 54472 |
rs773956914 | snp | C/T | 1.67863e-05 | 0.00289704 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277009 | GGCGTGTCCAAAGAG[C/T]GGGGGCAAAACGGCA | 54472 |
rs773988681 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295990 | GGCCTGGCCCCCAGC[A/G]GTACAGGTGCAGCCC | 54472 |
rs774078781 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305702 | GGACCTGGACAGGAA[C/T]AGGCCTCTCAGGGAG | 54472 |
rs774220236 | snp | A/C | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1291103 | CGTGTGTTCAGAATA[A/C]GACAGAAGACCGTGG | 54472 |
rs774377465 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281796 | AAACACTTGAAACTG[C/T]GGGCGACACACATGC | 54472 |
rs774432292 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297631 | TGACCTTTGCCCTGT[A/G]AGAGAAGCCGTACTG | 54472 |
rs774633513 | snp | A/G | 8.51752e-05 | 0.00652536 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288627 | CGTGCAGCTCACCGC[A/G]TAGGACATGACGAGG | 54472 |
rs774743394 | snp | A/C/G | 3.67089e-05 | 0.00428408 | synonymous-codon, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277246 | GGGGCTACAGACAGC[A/C/G]GGCATCCCTGGAAGC | 54472 |
rs774785537 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284317 | TTCTTTCCTCGGTGA[C/T]GGGGTGCAGGTGCTA | 54472 |
rs774847653 | snp | C/G | 1.8561e-05 | 0.00304633 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295598 | GAAATCCCACCCCCA[C/G]CGAGCGCACCAGCCC | 54472 |
rs774941253 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275500 | GGGAATCCCAGGGGC[C/T]CCTCCGTCTGAGTGG | 54472 |
rs774949064 | snp | A/G | | | intron-variant, downstream-variant-500B | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1297727 | ACCCCCTGCCCTTAC[A/G]GACAATCGAGGAGGG | 54472 |
rs775016530 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307315 | GGAAACAGCCCAGGA[A/G]GCACTGGGCAAGAGG | 54472 |
rs775065741 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274583 | GAGGGGAGAGGAGAG[A/G]AGGGGGAGCCTCCGG | 54472 |
rs775250164 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292150 | GCATGCTCAGCCTCT[A/G]GCAGCTTCCAATTCC | 54472 |
rs775397228 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285281 | CCAGCTCCCCAGAAC[A/G]AGAGAGGCCACCTCA | 54472 |
rs775506012 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279064 | TCTCTCCAGCCTTTA[C/T]CAGTCTGATGGGGAA | 54472 |
rs775579068 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283089 | CCCGGGGAACAGCCA[A/G]GCAGAGCCCGCCGTG | 54472 |
rs775607066 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275591 | CCCACAGCTGAAGAA[G/T]GCGCCTGCTGCCAGC | 54472 |
rs775632629 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288430 | AGAACATGGGCAGGA[A/G]CAGTGGGCAGGGCAG | 54472 |
rs775681599 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281590 | AGCTGAATGAACGAG[C/T]GGCTGAAGGGGCTGG | 54472 |
rs775690258 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292755 | GGACACACGGGCACC[G/T]CTGCTTTCCCCACAA | 54472 |
rs775712183 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1310294 | CCAACCAGAGCGACT[C/G]CAGCTCGAACAGCGC | 54472 |
rs775765525 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308623 | TAGAAGAAACTGCCA[A/G]GCAACTCTCAGGAGA | 54472 |
rs775788200 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303535 | ATGCTAACGGCAGGA[A/G]GCGCTGTGCAAAGAA | 54472 |
rs775795961 | snp | C/G | 5.06855e-05 | 0.0050339 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295779 | GGAAGTCCTGCGGGA[C/G]CTCACCGATGTACAC | 54472 |
rs775919908 | snp | A/G | 1.66938e-05 | 0.00288905 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290362 | GCCCAGGCGCAGTCG[A/G]CAGTAGGGGTCCATG | 54472 |
rs775972833 | snp | C/T | 6.6107e-05 | 0.00574884 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277086 | TGATGGCGGCATCCT[C/T]GTTCCCTCGCTGGGC | 54472 |
rs776090376 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284439 | CTGCAAGCTCCACCT[C/G]CTGGGTTCACACCAT | 54472 |
rs776207180 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295415 | CTACACAGAGCAGAC[A/G]CCCACCTACACCCAC | 54472 |
rs776256118 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285189 | CCCTAGCGCCCTGCC[C/T]GCAACTTGGCCACTT | 54472 |
rs776278589 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1293662 | CCTGTGGTGGGCTCC[A/G]GGGTGCGGGAGAGGA | 54472 |
rs776280277 | snp | C/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298876 | GACAAAATCCCTGAC[C/G]AGTCAGTCGTCCTCA | 54472 |
rs776399459 | snp | A/G | 0.000110195 | 0.00742195 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288816 | CCCAGGCATCAGGGA[A/G]GGGGCCACCCTGCCC | 54472 |
rs776450739 | snp | A/G | 0.000284455 | 0.0119225 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276773 | AGAACGGCATGAGAA[A/G]GAGAGACGCACGTCC | 54472 |
rs776554465 | snp | C/T | 3.35374e-05 | 0.00409482 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288754 | TGGGTCCAGGCAATG[C/T]GGTCGTCCATGGAGA | 54472 |
rs776624473 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285967 | CCCTGGGGTTTCTAC[C/G]AGGGGAGAGGCACCC | 54472 |
rs776821338 | snp | A/C | 4.18945e-05 | 0.00457662 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295770 | TGATGCGGAGGAAGT[A/C]CTGCGGGAGCTCACC | 54472 |
rs776836443 | snp | A/C | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300917 | GTTCCCACCCCATGA[A/C]GCTGCGAGGCTGTGG | 54472 |
rs776885230 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303142 | GAGTACAGGACAGAA[C/T]GAGAATAAGCATAGA | 54472 |
rs776893062 | snp | A/C | | | upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1311369 | TGTGAAACTAACCCA[A/C]GTGCCACCCCCTGGC | 54472 |
rs776907739 | snp | A/C | 0.000541272 | 0.0164421 | missense, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309471 | GCTGCCTCACCGGCC[A/C]GCGCTGAGTGCTGAC | 54472 |
rs776947983 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1279253 | CTCACTTGGGGAGCA[C/G]GCACCCCCGGGGGAA | 54472 |
rs777007400 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290080 | TCCTTGGGGAGAGCA[A/G]GACCCTGTCATGCAC | 54472 |
rs777020468 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281534 | AGCCCCCGAGACCTG[C/G]ACCCTGTGCGGGGGT | 54472 |
rs777044667 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300918 | TTCCCACCCCATGAC[A/G]CTGCGAGGCTGTGGA | 54472 |
rs777046915 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306728 | AACACTTTACAGAGT[C/G]CTGCGCTGAGCCGGT | 54472 |
rs777213812 | snp | C/T | 5.39593e-05 | 0.00519391 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295654 | GCCCACCTGTACCAC[C/T]GTGATGTTCAGTCGG | 54472 |
rs777263539 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281399 | AAGTGGACGGTCCTC[G/T]TGAGGGCTCAGCCAG | 54472 |
rs777299495 | snp | C/T | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300750 | GAACACATGCAGTCC[C/T]GGCCTCACGCCTGCC | 54472 |
rs777358348 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289753 | TGCGCCCAGCGGGGC[A/G]GACACATGCATGCTC | 54472 |
rs777435443 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306264 | CTGGCTAGCTTCACA[C/T]GTCCTCTCCACACCT | 54472 |
rs777489826 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283575 | TTCTATGAAGTGCGG[G/T]GCTGTTCCAAAATTT | 54472 |
rs777491500 | in-del | -/G | 0.000552029 | 0.0166045 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309510 | CCATGGTGCTGCGGC[-/G]GCCCCCGTGGCTCGC | 54472 |
rs777604288 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1297478 | CAGGACCCCCAAGTT[C/T]GGGAAGCTCTCTGCA | 54472 |
rs777606086 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1274397 | TTAAAGGACTTTATT[C/T]CTCTATTTTTATATG | 54472 |
rs777616624 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276623 | CCACAGTGTGAGGGA[C/T]TGTGTGTGCCTTAAA | 54472 |
rs777644883 | snp | C/T | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274175 | GGAAGAGCAGACCCA[C/T]GCCCACTGCCACTGT | 54472 |
rs777645548 | snp | A/C | 4.35701e-05 | 0.00466724 | intron-variant | TOLLIP | GRCh38.p7 | 11:1277289 | TGGTAAAAACGTCGG[A/C]AAGTTCCAGAAGTGC | 54472 |
rs777692372 | snp | G/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299559 | GATGGAGGAACTATT[G/T]CAATGGTCACATAAA | 54472 |
rs777703622 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1303038 | GCTCTGCTAAAGTCT[C/G]AAAGCAAACACTAGA | 54472 |
rs777772934 | snp | C/G | 1.71876e-05 | 0.00293147 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290232 | TCCCTCTCACCTCAT[C/G]GAAGATCTCGAGATA | 54472 |
rs777801988 | snp | A/G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1288319 | GGAAGGGCTGTGGGG[A/G/T]TCCTCCGAGGACACA | 54472 |
rs777817100 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1307214 | ACCTTCTTAAGAGAC[C/T]CTGGCAGCTCCGAGC | 54472 |
rs777860701 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278912 | AGGCGGGCAGGAACT[C/T]GGCCATCACCTGTCC | 54472 |
rs777868416 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306420 | AGGCAACGGCTAGAC[C/G]ACAGTCAGGGTCTCC | 54472 |
rs777876240 | snp | C/T | 1.75925e-05 | 0.00296579 | synonymous-codon, missense, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277222 | GGGCAGGGCCACGGG[C/T]ACCATGCCGGGGCTA | 54472 |
rs777978307 | snp | C/G | 0.000154707 | 0.00879372 | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309423 | GGCCCCGCCCGCAAC[C/G]GCAGGTCACCGCCCC | 54472 |
rs777978898 | snp | A/G | 0.000148732 | 0.00862229 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276859 | GCCCCGTCCTGGACC[A/G]CCAGGAACCGAAAAC | 54472 |
rs778002091 | snp | A/G | 1.76083e-05 | 0.00296712 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288804 | AGAGGGAGAGGCCCC[A/G]GGCATCAGGGAAGGG | 54472 |
rs778039315 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288904 | CTCCCACCTGCACCA[A/G]CACCCCATCGATGAG | 54472 |
rs778119896 | snp | A/C/G | 0.000116661 | 0.00763662 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277027 | GGGCAAAACGGCATC[A/C/G]AGGCAGAGGCTCTAT | 54472 |
rs778149966 | snp | A/C | 7.63126e-05 | 0.00617661 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1286083 | GCATCACCATGGCAG[A/C]TGGAAGCAGCTGAAA | 54472 |
rs778210720 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298365 | TGTCCCGGAGACAGC[A/G]GCATGGAGAAGCCAG | 54472 |
rs778351050 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304459 | GAAATCTAAACAAGC[A/G]CTGACTCGAGAGAAG | 54472 |
rs778378867 | in-del | -/CGCCGGA | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280671 | GCCAGGCTGGGGAGG[-/CGCCGGA]CGCCCCACTTTCCAG | 54472 |
rs778380034 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292631 | ATGACTGCACACAAC[C/T]ACATGCTGTTCTGGT | 54472 |
rs778692383 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302818 | GTGACTTTGTCCCCA[A/G]TTCCCACATCCTCCT | 54472 |
rs778792958 | snp | C/T | 1.82058e-05 | 0.00301705 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295641 | AGGGTGCCCCAAGGC[C/T]CACCTGTACCACCGT | 54472 |
rs778819526 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299416 | TCACGAGTCACAGGG[A/G]AGAGAGTCCAGGTGC | 54472 |
rs778867436 | snp | A/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274234 | CTCTAATTCAATCTG[A/G]GAAGCAAAGGCCAGG | 54472 |
rs778938620 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305441 | GAAAGCCCACACACA[A/T]CTACAAAGAAAAGCA | 54472 |
rs779024062 | snp | A/C | 1.7169e-05 | 0.00292988 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290435 | GCCAATGTCAGGAAA[A/C]GGAGGTGCCAACCAT | 54472 |
rs779063448 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1304573 | GTCTCCGCGTGGATC[C/T]GGAGGTGGCACAGAC | 54472 |
rs779088825 | snp | A/G | 6.8956e-05 | 0.00587139 | intron-variant | TOLLIP | GRCh38.p7 | 11:1288788 | CTCTCTGCGGGAGAC[A/G]AGAGGGAGAGGCCCC | 54472 |
rs779129491 | snp | A/G | | | upstream-variant-2KB, intron-variant | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1311074 | AAGCCCCTTCCTCAA[A/G]TTGTAGCTTAACATC | 54472 |
rs779176763 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285898 | TTCTAGAATGGATGA[C/T]GTCCCCACCCCGGCG | 54472 |
rs779251563 | snp | G/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278991 | GCCATCGCCTGTCCC[G/T]GCCCACACGTCTCCC | 54472 |
rs779332552 | snp | A/G | 0.000417673 | 0.0144451 | synonymous-codon, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288663 | CATGCCCTCCTTGTC[A/G]TCCCCCTGCCTCCCG | 54472 |
rs779418015 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285196 | GCCCTGCCCGCAACT[C/T]GGCCACTTCCATGGC | 54472 |
rs779418567 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287405 | CTGCTGCCTCCCCGC[C/T]GCAGCCTCCCCGCCG | 54472 |
rs779517141 | snp | C/T | | | upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1309701 | CCCTTCCGGCTCTCG[C/T]GCGCACGCGCGCTCC | 54472 |
rs779585038 | snp | A/C | 0.000153716 | 0.00876552 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276722 | CCTCCAACACCCTGG[A/C]AGAAGCAGCTGCTCT | 54472 |
rs779593872 | snp | C/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1298736 | AGCTCATCAGCCCCA[C/G]GCAGCCCGGGGACCG | 54472 |
rs779642849 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1282359 | ATTGTTTAGGAGAAA[C/T]ACCTAATGTTAAATG | 54472 |
rs779689281 | snp | A/G | 0.000132635 | 0.00814247 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295832 | GGCCAGTGAGTCAGG[A/G]TGGGGGCACAAAGCA | 54472 |
rs779750383 | snp | C/T | 1.70496e-05 | 0.00291967 | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290425 | CTGGAATGAAGCCAA[C/T]GTCAGGAAAAGGAGG | 54472 |
rs779825248 | snp | C/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299981 | CATAAGGAGGCCTCT[C/G]TCGACACCAACTCTG | 54472 |
rs779870113 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1289485 | GGTGCAGCCACGGAC[A/G]GGACTCAGGACCCTC | 54472 |
rs779882402 | snp | C/T | 0.00010019 | 0.00707709 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1290341 | GGGCGTCTCGTACAC[C/T]GCGTAGCCCAGGCGC | 54472 |
rs779907424 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1275965 | AGCTTCTCAAATTTC[C/T]GACTGTCATAACCAG | 54472 |
rs779921833 | snp | A/G | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299547 | TTGCCATATGATGAT[A/G]GAGGAACTATTTCAA | 54472 |
rs779936024 | snp | A/G | 1.66247e-05 | 0.00288307 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277035 | CGGCATCGAGGCAGA[A/G]GCTCTATGGCTCCTC | 54472 |
rs780149859 | snp | C/G | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274055 | CCACGGTCCCAGTGG[C/G]CTCTCTCAGAACGGG | 54472 |
rs780158081 | snp | C/T | 1.65299e-05 | 0.00287483 | missense, utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277131 | GGATCACCTCCTGGT[C/T]CATGTTGGGGAACAT | 54472 |
rs780248364 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306975 | CATTTACAAACTCTC[C/T]CAGCACCTGACGCTT | 54472 |
rs780256994 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1301649 | GAACAAGCGTCAAGG[A/G]CTCCTGAAGCCACAA | 54472 |
rs780257979 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305474 | TCTCTCCTTGAGGTA[C/T]GGGAAGATGAGGGAA | 54472 |
rs780309998 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300640 | ACCTGTTAGGAATAC[A/G]TTTCCGACTGAGAGT | 54472 |
rs780318280 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1277558 | AGTCTGTTTTATAAC[A/T]AGCAGGCTGGGGGTG | 54472 |
rs780483707 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1280323 | TGCATGGTGCCACCG[C/T]GTGCACGTTCTCTAT | 54472 |
rs780539691 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276785 | GAAGGAGAGACGCAC[A/G]TCCCAGGGACAGGAG | 54472 |
rs780628940 | snp | C/T | 0.000143421 | 0.00846698 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276697 | AATGGAATCGGAAGG[C/T]GCTCCACCACCTCCA | 54472 |
rs780637471 | snp | G/T | 0.000187564 | 0.00968231 | intron-variant | TOLLIP | GRCh38.p7 | 11:1283497 | CTGGGGGCTCCGGTG[G/T]GGCGTCAGGTGGACG | 54472 |
rs780661093 | snp | A/G | | | intron-variant, nc-transcript-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1300704 | GACAGAGCCCCGGAA[A/G]AGCCCAGCTCAGCCC | 54472 |
rs780732936 | snp | A/T | 8.34676e-05 | 0.00645963 | missense, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288703 | TACCACTTGTCCTCC[A/T]CCTTGCCCTGCCTCA | 54472 |
rs780776582 | in-del | -/AACCC | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1281099 | AAATTGAGGCTAAAA[-/AACCC]AACCCCCTATAACCA | 54472 |
rs780858700 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1287270 | TGAAAGCGTCTGTTA[A/G]AGACGTGTCATGAGA | 54472 |
rs780899434 | snp | A/G | 3.55107e-05 | 0.00421356 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1295669 | CGTGATGTTCAGTCG[A/G]CCCACGGTGCCCACT | 54472 |
rs781028380 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306274 | TCACACGTCCTCTCC[A/G]CACCTACCCACCCGG | 54472 |
rs781186627 | snp | A/C | 1.66504e-05 | 0.0028853 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1277031 | AAAACGGCATCGAGG[A/C]AGAGGCTCTATGGCT | 54472 |
rs781396054 | in-del | -/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1292405 | GGTGGCACATGGGAC[-/T]CCCCTGCCAGCATGC | 54472 |
rs781418715 | snp | C/T | 1.70362e-05 | 0.00291853 | utr-variant-3-prime, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1276885 | AAAACCCACATGCAC[C/T]CAAGAACAGGTGTGG | 54472 |
rs781483413 | snp | A/G | 8.61289e-05 | 0.00656179 | intron-variant | TOLLIP | GRCh38.p7 | 11:1295799 | CCGATGTACACCTGC[A/G]GGGCCGGGGACCAGA | 54472 |
rs781671896 | snp | C/T | 1.66754e-05 | 0.00288746 | stop-gained, intron-variant, nc-transcript-variant | TOLLIP | GRCh38.p7 | 11:1288690 | CCCGCTCAGGCTGTA[C/T]CACTTGTCCTCCACC | 54472 |
rs781674775 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1291871 | GACCCCCGAGGGCAC[A/G]GCTGTCCCGTCCACG | 54472 |
rs781709423 | snp | C/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1277772 | TTGGCAAGTGTGTCA[C/G]TAAACTGTGTGCCGG | 54472 |
rs781743709 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305035 | TCATAGAAGGAAAAA[A/G]TACTAGGTGAATACT | 54472 |
rs781782582 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1306838 | CCCTGGGGCTCCCTC[C/T]TCTCCACCTCCAGAC | 54472 |
rs796087440 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1290786 | GCTGAGAGCCAGAGC[A/G]TGACATGGAGTGTGA | 54472 |
rs796201078 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOLLIP | GRCh38.p7 | 11:1304622 | TATTTATTCTTTAGC[C/T]GGGCAGCCTCCGGAG | 54472 |
rs796294448 | snp | C/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308865 | GGGCCATCAGGGTGC[C/G]GGACCCGCCTCCACC | 54472 |
rs796325427 | in-del | -/GGGAGA | | | downstream-variant-500B | TOLLIP | GRCh38.p7 | 11:1274140 | CAGAACCACCCAGTG[-/GGGAGA]GGGAGAGGGTGCCTG | 54472 |
rs796345073 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1294249 | TCTACGAAAGCCCGC[A/G]TGGCTCACAGTGTGT | 54472 |
rs796400614 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308868 | CCATCAGGGTGCGGG[A/G]CCCGCCTCCACCTGG | 54472 |
rs796510139 | in-del | -/GCTCATC | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278728 | AAGCATCATCCCCAT[-/GCTCATC]AGCCTTTCGGCAATG | 54472 |
rs796521391 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278735 | ATCCCCATGCTCATC[A/T]GCCTTTCGGCAATGA | 54472 |
rs796577306 | in-del | -/T | | | intron-variant | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1299422 | TCACAGGGGAGAGAG[-/T]TCCAGGTGCTGAAGT | 54472 |
rs796611052 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1283786 | CCAGTTGATGGAACT[A/G]CACCCCCCAAAAAGA | 54472 |
rs796616842 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOLLIP, LOC105376512 | GRCh38.p7 | 11:1302910 | TGTCTCCCCTTCCGG[A/G]GCCTTCCTCAGACAG | 54472 |
rs796652025 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1286399 | TGTAGGTGTCGAGTC[A/G]GCCTGGGGGGAACCA | 54472 |
rs796714153 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1278449 | CTTCAATCCTGGCCT[A/G]AACCAACACCAGCAA | 54472 |
rs796812074 | snp | A/G | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1284933 | AGGTGGGTCTAGGGC[A/G]AGGTCCCGACTCCCA | 54472 |
rs796854154 | snp | C/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1285560 | AGAGCACGCATCACC[C/T]AACAGGAGCGTGAGG | 54472 |
rs796861560 | in-del | -/A | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1295431 | CCACCTACACCCACT[-/A]ACTCATCACTTGAGT | 54472 |
rs796978247 | snp | A/C | | | intron-variant, upstream-variant-2KB | TOLLIP, TOLLIP-AS1 | GRCh38.p7 | 11:1308869 | CATCAGGGTGCGGGA[A/C]CCGCCTCCACCTGGG | 54472 |
rs796997564 | snp | A/T | | | intron-variant | TOLLIP | GRCh38.p7 | 11:1305617 | AGTGATAAAGTTCAG[A/T]AACTACCCTCTGCCA | 54472 |