SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs748855 | snp | A/G | 0.357877 | 0.225527 | intron-variant | NOD2 | GRCh38.p7 | 16:50717487 | ACCTGATGCCTTTAA[A/G]TTGCCCCTCTAGCTG | 64127 |
rs749910 | snp | A/G | 0.17332 | 0.23795 | intron-variant | NOD2 | GRCh38.p7 | 16:50724938 | TCATTCTTAGCCTGT[A/G]ACTTCATTCACATGG | 64127 |
rs751271 | snp | A/C | 0.495596 | 0.0467178 | intron-variant | NOD2 | GRCh38.p7 | 16:50717264 | CGTGGAACTCAGTAA[A/C]CCCAGAAAGCTGTGA | 64127 |
rs1077861 | snp | A/T | 0.44546 | 0.155869 | intron-variant | NOD2 | GRCh38.p7 | 16:50725636 | GCGGCCCAGATCTTA[A/T]TCAGAAATGCCCCTT | 64127 |
rs1078327 | snp | C/T | 0.00258314 | 0.0358454 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711322 | GCGGACCGCCTCATC[C/T]GCCTGCTCCAAGAGA | 64127 |
rs1861756 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | NOD2 | GRCh38.p7 | 16:50724927 | AAGTCACAGGCTAAG[A/G]ATGATGGAACAGGAA | 64127 |
rs1861757 | snp | A/G | 0.319376 | 0.240181 | intron-variant | NOD2 | GRCh38.p7 | 16:50718904 | acttccccttttaGG[A/G]CTTTTCCCCAATAAA | 64127 |
rs1861758 | snp | C/T | 0.365853 | 0.221536 | intron-variant | NOD2 | GRCh38.p7 | 16:50717876 | ctctcctgcacatac[C/T]ggaggactactgTGT | 64127 |
rs1861759 | snp | A/C | 0.442351 | 0.15969 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711672 | CACGACACCTTTGGC[A/C]CGCACCAGGAAGCCA | 64127 |
rs2066842 | snp | C/T | 0.300841 | 0.244784 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710713 | GTGGGCATGGCTGGA[C/T]CCCCGCAGAAGAGCC | 64127 |
rs2066843 | snp | C/T | 0.303319 | 0.244256 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711288 | GTACCTGAGGAAGCG[C/T]CATCATGAGCCCGGG | 64127 |
rs2066844 | snp | C/T | 0.0444529 | 0.142304 | NOD2 | 16 | allele_origin=T(germline)/C(germline) | 16:50712015 | GAGAAGGCCCTGCTC[C/T]GGCGCCAGGCCTGTG | 64127 |
rs2066845 | snp | C/G | 0.0200117 | 0.0980354 | NOD2 | 16 | allele_origin=G(germline)/C(germline) | 16:50722629 | CTTTTCAGATTCTGG[C/G]GCAACAGAGTGGGTG | 64127 |
rs2066846 | in-del | A/CT | 0.375 | 0.216506 | intron-variant | NOD2 | GRCh38.p7 | 16:50725356 | GAATCCCCACAACGT[A/CT]CTTTATCTGTTCTTT | 64127 |
rs2066847 | in-del | -/C | 0.0257735 | 0.110555 | frameshift-variant | NOD2 | GRCh38.p7 | 16:50729867 | AAGCCCTCCTGCAGG[-/C]CCCTTGAAAGGAATG | 64127 |
rs2066850 | snp | A/G | 0.207559 | 0.246371 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696318 | GGGCCCACGTGGGTC[A/G]CCCCTTGACCCTCTC | 64127 |
rs2067085 | snp | C/G | 0.446189 | 0.154969 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699948 | GATCTTCACACCGTC[C/G]CAGAGGGTGAGGCAC | 64127 |
rs2076752 | snp | A/G | 0.242201 | 0.249878 | utr-variant-5-prime, intron-variant | NOD2 | GRCh38.p7 | 16:50697185 | CACTGGGCTTTTGGC[A/G]TTCTGCACAAGGCCT | 64127 |
rs2076753 | snp | G/T | 0.317776 | 0.240637 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50699463 | TTCTGGAGAAGTCCC[G/T]CACTGACCTTGTTCT | 64127 |
rs2076754 | snp | C/T | 0.000248602 | 0.0111463 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711206 | CGGCCGCTGTGTCGG[C/T]GTTCCTCAGGAAGTA | 64127 |
rs2076755 | snp | A/T | 0.0950001 | 0.196151 | intron-variant | NOD2 | GRCh38.p7 | 16:50723158 | aaaaaaaaaaaagaa[A/T]aaagaaaGAGCACCG | 64127 |
rs2076756 | snp | A/G | 0.175254 | 0.238565 | intron-variant | NOD2 | GRCh38.p7 | 16:50722970 | cattttatcttaagg[A/G]ccaattccaatccat | 64127 |
rs2111234 | snp | C/T | 0.499663 | 0.0129749 | intron-variant | NOD2 | GRCh38.p7 | 16:50700122 | AAAGAAAGAGTTGTA[C/T]GTTTCCTGCCAAGAG | 64127 |
rs2111235 | snp | C/T | 0.499203 | 0.0199521 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50700058 | TTAGGGGAAATCCCA[C/T]GGACCAAGTTACCCC | 64127 |
rs2357791 | snp | A/G | 0.353371 | 0.227628 | intron-variant | NOD2 | GRCh38.p7 | 16:50730925 | AAAGCTTTGCTGGGC[A/G]TGGCAGCTCACACCT | 64127 |
rs3135499 | snp | A/C | 0.459801 | 0.135955 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732216 | CACAAAAGACCCCTT[A/C]CCACTGCTCTGATGA | 64127 |
rs3135500 | snp | A/G | 0.456332 | 0.141164 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732975 | GGTTAATATTTATAG[A/G]TCACTTTGTTTTACT | 64127 |
rs3813758 | snp | C/T | 3.30153e-05 | 0.00406283 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712189 | GCTCGGAAGGCTGCA[C/T]GTGGCCTGAATGTTG | 64127 |
rs4785224 | snp | A/G | 0.387642 | 0.208697 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696535 | TAGGAAACAGATAAT[A/G]AGTGAATATTTTTTC | 64127 |
rs4785225 | snp | C/G | 0.495174 | 0.0488838 | intron-variant | NOD2 | GRCh38.p7 | 16:50712635 | CTACAACCACCCTGG[C/G]GGGTAGGCAGGAATG | 64127 |
rs4785449 | snp | C/T | 0.496905 | 0.0392151 | intron-variant | NOD2 | GRCh38.p7 | 16:50704636 | cctcctgggtttaag[C/T]gattcttcttcctca | 64127 |
rs4990643 | snp | A/T | 0.35894 | 0.225016 | intron-variant | NOD2 | GRCh38.p7 | 16:50725358 | ATCCCCACAACGTAC[A/T]TTATCTGTTCTTTCT | 64127 |
rs5743259 | snp | G/T | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696177 | TCCTGTCTGCAAGGG[G/T]TCAGTGGGCTGAGAT | 64127 |
rs5743260 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696236 | TGGCCCCAGAGAAAC[C/T]GGGCTGGCTGTGGTC | 64127 |
rs5743261 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696659 | GAGAACAGCACTAAG[A/G]CCAGGTTCTCCTCCC | 64127 |
rs5743262 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696881 | GCCCAACGTCACTAG[C/G]TGGGGTGTGTATGGC | 64127 |
rs5743263 | snp | C/T | 0.0325976 | 0.123435 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696954 | GGGGCCCCTACTTAC[C/T]TGTGGCCTGTCCCCT | 64127 |
rs5743264 | snp | C/T | 0.029116 | 0.117091 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697111 | CCTCCGGCTTTTCCT[C/T]TGGGAATTTCCCTTG | 64127 |
rs5743265 | in-del | -/T | 0.0162398 | 0.0886349 | utr-variant-5-prime, intron-variant | NOD2 | GRCh38.p7 | 16:50697148 | GGGTTGGTAGACAGA[-/T]CCAGGCTCACCAGTC | 64127 |
rs5743267 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697469 | CGGCGGGTTTTTTTC[C/T]CCAGGACCTGGGCAG | 64127 |
rs5743268 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707728 | CTCATGTGGTTGTTC[A/G]GTTGTTTTTTTGACC | 64127 |
rs5743269 | snp | C/T | 0.00159675 | 0.0282103 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707947 | ACCAGTCCCATTGGC[C/T]CTGCCTTTGGAAGGT | 64127 |
rs5743270 | snp | A/G | 0.0520825 | 0.152737 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708151 | TAAAAGGACAAAAGC[A/G]TGTAATGTTAGCTAT | 64127 |
rs5743271 | snp | A/G | 0.00848912 | 0.0645948 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710777 | CCCCTGGCCACCTCA[A/G]TGACGATGCGGACAC | 64127 |
rs5743272 | snp | A/G | 0.00218928 | 0.0330128 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710966 | CTCTACTCTTTGAGC[A/G]CTGCTGTTGGCCTGA | 64127 |
rs5743273 | snp | C/T | 0.000527478 | 0.0162315 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711105 | CCACTGCTCCCCGAC[C/T]GACCCCACCTCTGTC | 64127 |
rs5743274 | snp | C/T | 0.0058901 | 0.0539477 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711364 | CACGGTTTGTGCCAC[C/T]TGCCTGTCTTCTCAT | 64127 |
rs5743275 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711914 | TGCAGAAGGCCGAGC[C/T]GCACAACCTTCAGAT | 64127 |
rs5743276 | snp | C/G/T | 0.000736013 | 0.0191696 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711961 | GCAGGGCTGTTGTCC[C/G/T]GGGAGCACTGGGGCC | 64127 |
rs5743277 | snp | C/G/T | 0.00654076 | 0.0568141 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712018 | AAGGCCCTGCTCCGG[C/G/T]GCCAGGCCTGTGCCC | 64127 |
rs5743278 | snp | C/G | 0.00809797 | 0.0631143 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712085 | ACTCCATCCCGCCAG[C/G]TGCACCGGGTGAGGC | 64127 |
rs5743279 | snp | A/G | 0.00590431 | 0.054012 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712280 | TGCTGCAGCACCTCC[A/G]GCGGCCCGTGGCCCT | 64127 |
rs5743280 | snp | C/T | 0.000181427 | 0.00952263 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712287 | GCACCTCCNGCGGCC[C/T]GTGGCCCTGCAGCTG | 64127 |
rs5743281 | snp | C/T | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50712618 | atgacctcatctaat[C/T]tctacaaccaccctn | 64127 |
rs5743282 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | NOD2 | GRCh38.p7 | 16:50712632 | ntctacaaccaccct[-/G]ggngggtaggcagga | 64127 |
rs5743284 | snp | C/T | 0.00594539 | 0.0541973 | intron-variant | NOD2 | GRCh38.p7 | 16:50716849 | GTGCTCACTGTCCAA[C/T]GTGCTTTGCTTCTGT | 64127 |
rs5743285 | snp | G/T | 0.0024843 | 0.0351565 | intron-variant | NOD2 | GRCh38.p7 | 16:50716880 | GTCTCCTCTCTTCTG[G/T]AACTGAACAGTCTAT | 64127 |
rs5743286 | snp | C/T | 0.00402413 | 0.0446752 | intron-variant | NOD2 | GRCh38.p7 | 16:50720166 | GGCCCTTGACTGCCA[C/T]CTTCATACTTGGTCT | 64127 |
rs5743287 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | NOD2 | GRCh38.p7 | 16:50720242 | CAGTGCCCACGAGCT[C/G]GTGACAGGAAGCCCT | 64127 |
rs5743288 | in-del | -/G | 0.00462326 | 0.0478566 | intron-variant | NOD2 | GRCh38.p7 | 16:50722741 | GCAGTTTTCTTGGGG[-/G]AGATCAGGTGAAGAG | 64127 |
rs5743289 | snp | C/T | 0.0988422 | 0.199274 | NOD2 | 16 | allele_origin=T(germline)/C(germline) | 16:50722863 | TCAAGAGAGGACACT[C/T]GAGTCTTTCTGGGTG | 64127 |
rs5743290 | snp | C/T | 0.0026695 | 0.0364366 | intron-variant | NOD2 | GRCh38.p7 | 16:50723277 | CCCTGCTCTGACATA[C/T]TTTTGTTCCATGATT | 64127 |
rs5743291 | snp | A/G | 0.114777 | 0.210273 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50723365 | ATGCTGGCAAAGAAC[A/G]TCATGCTAGAAGAAC | 64127 |
rs5743292 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | NOD2 | GRCh38.p7 | 16:50725820 | CCAATAAAGGGGAGT[A/T]ATCAAGCCAGTTATC | 64127 |
rs5743293 | in-del | -/C | 0.0210502 | 0.100409 | frameshift-variant | NOD2 | GRCh38.p7 | 16:50729870 | CCCTCCTGCAGGCCC[-/C]TTGAAAGGAATGACA | 64127 |
rs5743294 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50729970 | tgtaaaatggggtga[C/T]gggagagaggaatgg | 64127 |
rs5743295 | snp | A/G/T | 0.000181287 | 0.00951929 | missense | NOD2 | GRCh38.p7 | 16:50731752 | TCTGCTTTAGGCTCC[A/G/T]AGGGAACACTTTCTC | 64127 |
rs5743296 | snp | A/C/G | 0.000346661 | 0.0131618 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50731839 | TCCGGGAGGATGTTC[A/C/G]TCTCAGTTTGTTTGT | 64127 |
rs5743297 | snp | C/T | 0.0240643 | 0.107019 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732340 | CCTCCTGGACTCCTG[C/T]ACACGCTCCTTCCTC | 64127 |
rs5743298 | snp | G/T | 0.0215028 | 0.101435 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732559 | TATGACCACACTCCA[G/T]CTGGGATCACATGTG | 64127 |
rs5743299 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732842 | GAAAAAAAATTAGGC[C/T]GTTCCTTCAAAGCAA | 64127 |
rs5743300 | snp | A/C | 0.0599851 | 0.162463 | downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50733208 | ttgagaccaacctga[A/C]caacatggagaaacc | 64127 |
rs5816717 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50725357 | AATCCCCACAACGTA[A/C]TTTATCTGTTCTTTC | 64127 |
rs6413461 | snp | C/T | 1.65833e-05 | 0.00287948 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712107 | GGGTGAGGCCAAGAG[C/T]GTGCATGCCATGCCC | 64127 |
rs6500328 | snp | A/G | 0.440471 | 0.161928 | intron-variant | NOD2 | GRCh38.p7 | 16:50702745 | AAGCCTCACAAGGGT[A/G]TAGTGTGACTACACT | 64127 |
rs7187857 | snp | A/G | 0.494315 | 0.0530107 | intron-variant | NOD2 | GRCh38.p7 | 16:50726927 | gggtggatcacctga[A/G]gtggggagttccata | 64127 |
rs7190413 | snp | A/T | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50701628 | CAAGATTGTGTCTTG[A/T]CATCTTTAAAAGTTC | 64127 |
rs7198979 | snp | A/G | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50718369 | gcgtatagagcgtgg[A/G]tgcgctggacggggg | 64127 |
rs7203344 | snp | A/G | 0.206336 | 0.246157 | intron-variant | NOD2 | GRCh38.p7 | 16:50731465 | TTGACAGATTCTCTT[A/G]TTGCCTTAAAAAGAA | 64127 |
rs7203691 | snp | A/G | 0.368733 | 0.220005 | intron-variant | NOD2 | GRCh38.p7 | 16:50719513 | GCCCAGCGCTCTTGT[A/G]CAACAGGTAAAGCCT | 64127 |
rs7204911 | snp | C/T | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50704427 | actggattgatagtt[C/T]ggctgggtataaaat | 64127 |
rs7206340 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698511 | TATTCTGAGTCTACC[C/T]CTTGGAGTAGCAGTG | 64127 |
rs7206582 | snp | A/G | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50701805 | tcatgatggaaatca[A/G]aaaatattcagaacc | 64127 |
rs7359452 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50731080 | gaggctgggatggaa[A/G]gatcccttgaaccca | 64127 |
rs7498256 | snp | C/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710916 | ATTCAGCTGCCGGCA[C/G]CTGCAGTGCATGGCC | 64127 |
rs7500036 | snp | C/T | 0.216048 | 0.247684 | intron-variant | NOD2 | GRCh38.p7 | 16:50703587 | gatgttgcagtgagc[C/T]gagatcgcactgctt | 64127 |
rs7500826 | snp | A/G | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50704520 | caatattgcttctaa[A/G]aattccaaaaccttt | 64127 |
rs8045009 | snp | C/T | 0.365646 | 0.221644 | intron-variant | NOD2 | GRCh38.p7 | 16:50702030 | AAATCACTGAAGTCT[C/T]GAACTTCTGGGCTGA | 64127 |
rs8046608 | snp | C/T | 0.0433465 | 0.140692 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696970 | TGTGGCCTGTCCCCT[C/T]GTGAATGTGTCTCAT | 64127 |
rs8057341 | snp | A/G | 0.49934 | 0.0181589 | intron-variant | NOD2 | GRCh38.p7 | 16:50704069 | GGCAGCGGGAGTTGA[A/G]AAGAAACGATATTAG | 64127 |
rs8061316 | snp | A/G | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697807 | CTGTGCCCCAGCAGC[A/G]TTCTGAGAGATTGGA | 64127 |
rs8061636 | snp | C/G | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697984 | GACGAGTAAGACCCA[C/G]GCTCCCACGTGGCCC | 64127 |
rs8061960 | snp | C/T | 0.36021 | 0.224397 | intron-variant | NOD2 | GRCh38.p7 | 16:50727523 | taaaaattcatgctt[C/T]gggattcaacaaact | 64127 |
rs8063130 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50722918 | CAGGGTTTTGATACA[C/G]TATCTGTAAATTGAA | 64127 |
rs9921146 | snp | A/C | 0.494526 | 0.0520291 | intron-variant | NOD2 | GRCh38.p7 | 16:50726069 | TCAGGCAGAGAGTGG[A/C]AGGTCTTCTCTGCAA | 64127 |
rs9925315 | snp | A/T | 0.495445 | 0.0475058 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715463 | ttctgttgcccaggc[A/T]gggggtacagtggca | 64127 |
rs9931711 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713759 | GGGAAGGTATGGAGA[C/T]GGCTGCCTGAGCTTC | 64127 |
rs10451131 | snp | C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50710180 | ATCCCAGCCCAGAGC[C/G]CCTTCCCGTCATCTA | 64127 |
rs10521209 | snp | G/T | 0.362523 | 0.223246 | intron-variant | NOD2 | GRCh38.p7 | 16:50721798 | TTGCTCAGCCTGACC[G/T]CATTTTTCAAAGAGC | 64127 |
rs11292073 | in-del | -/A | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50723101 | AAAAAAAAAAAAAAA[-/A]GAGCACTGCATTCAA | 64127 |
rs11326665 | in-del | -/A | 0.449218 | 0.151037 | intron-variant | NOD2 | GRCh38.p7 | 16:50723086 | ATGTCTAAAAAAGCT[-/A]AAAAAAAAAAAAAAA | 64127 |
rs11423748 | in-del | -/A | 0.5 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50723154 | AAAAAAAAAAAAAAA[-/A]GAAAAAAGAAAGAGC | 64127 |
rs11642482 | snp | C/G | 0.36021 | 0.224397 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706853 | aggcacctgccacca[C/G]gcctggctaattttt | 64127 |
rs11642646 | snp | A/C | 0.363359 | 0.222822 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707275 | gtgactccaagactt[A/C]ggggcagagcacctg | 64127 |
rs11642651 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NOD2 | GRCh38.p7 | 16:50724857 | ATGTAGGCAGTGTAG[G/T]GTTTGTACAGTGGCT | 64127 |
rs11645386 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NOD2 | GRCh38.p7 | 16:50726620 | CCAGGTGTGGATATG[G/T]CAGGTTTGTCTTCCC | 64127 |
rs11645448 | snp | A/G | 0.499673 | 0.0127754 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50693164 | TGTGTGTATTGGGAA[A/G]CATGTTTGCGTGTGG | 64127 |
rs11646168 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715158 | gagccaagccgccta[A/G]gctcaaagcctttat | 64127 |
rs11647841 | snp | A/G | 0.355525 | 0.226637 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709420 | CTACCAGCCTGGGAC[A/G]CTAAACCAGCACTTC | 64127 |
rs11649521 | snp | A/G | 0.203575 | 0.245652 | intron-variant | NOD2 | GRCh38.p7 | 16:50704919 | gtgttcttccattat[A/G]ttagtcacccaagag | 64127 |
rs12918060 | snp | G/T | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50704414 | aaagttccctcatac[G/T]ggattgatagtttgg | 64127 |
rs12919099 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50723155 | aaaaaaaaaaaaaaa[A/G]aaaaaagaaaGAGCA | 64127 |
rs12920040 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50723024 | acattaaaaagaatt[C/T]taaggctgcacctgg | 64127 |
rs12920425 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50723006 | gtgggtgcccagtgc[A/C]ccacattaaaaagaa | 64127 |
rs12920558 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50723054 | ggcttaaagaagagc[A/C]ctataatcaattagt | 64127 |
rs12920721 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50723156 | aaaaaaaaaaaaaag[A/G]aaaaagaaaGAGCAC | 64127 |
rs12922299 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50704734 | tgttggccaggctgg[G/T]cttgaacttctgact | 64127 |
rs12925051 | snp | A/C | 0 | 0 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708309 | AGTTAGGGCTGGTAT[A/C]TCTTGATCTCTGAAA | 64127 |
rs12929565 | snp | A/G | 0 | 0 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708537 | ttttccaccttatag[A/G]tgtggaaactgggca | 64127 |
rs13331327 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706168 | agccagagccaaggc[C/T]cagaggcaggagcat | 64127 |
rs13332952 | snp | A/G | 0.492727 | 0.0598633 | intron-variant | NOD2 | GRCh38.p7 | 16:50718061 | ATTATAACAATCAAT[A/G]TACTATAATAACACT | 64127 |
rs13339578 | snp | A/G | 0.497803 | 0.033074 | intron-variant | NOD2 | GRCh38.p7 | 16:50705194 | attttaatttgcaag[A/G]ggtaggtttgactga | 64127 |
rs13380733 | snp | A/G | 0.233527 | 0.249457 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708770 | GGTCTATCACCCTGG[A/G]CTGTGTCCTCTGGGC | 64127 |
rs13380741 | snp | A/G | 0.233527 | 0.249457 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709027 | GGTGACAATTGGTGT[A/G]TTTATTTCTCTATAA | 64127 |
rs16948754 | snp | A/G | 0.0170251 | 0.090679 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698205 | GACCCCATGACAATC[A/G]CAGAACTGACCATGC | 64127 |
rs16948755 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50700013 | GTGCTTAGTCACCAA[A/G]ACTGATTTGTCCTCA | 64127 |
rs16948773 | snp | C/G | 0.0228947 | 0.104514 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50713280 | GGCTTTGGGCTACAC[C/G]TGGATGACCTTAATT | 64127 |
rs17221417 | snp | C/G | 0.203882 | 0.245709 | intron-variant | NOD2 | GRCh38.p7 | 16:50705671 | CAGTTCCGGAGGTCC[C/G]TCATGCTGATCATTC | 64127 |
rs17312836 | snp | A/C | 0.36021 | 0.224397 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707551 | CTTCTCTTCCAAATG[A/C]TTTACAGCCTGCAGA | 64127 |
rs17313265 | snp | C/T | 0.219349 | 0.248114 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713793 | AAAGTGGAAGAATAC[C/T]GCTTGGCCCTAACTC | 64127 |
rs34103974 | in-del | -/T | 0.467234 | 0.12373 | intron-variant | NOD2 | GRCh38.p7 | 16:50721367 | CTGTAACTTGCTTGG[-/T]TTTTTTTTTTGTTTG | 64127 |
rs34133110 | snp | C/T | 0.418343 | 0.184826 | intron-variant, missense | NOD2 | GRCh38.p7 | 16:50710008 | GTGGACCCAGGTTTT[C/T]AAACTCAGGTGTGTC | 64127 |
rs34192073 | in-del | -/A | | | intron-variant | NOD2 | GRCh38.p7 | 16:50727642 | GGCTAGAGGTCAGGT[-/A]AAATATGGCGGATGA | 64127 |
rs34231814 | snp | A/T | 0.49995 | 0.00499176 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692811 | GTTGGGAAAGCAGGG[A/T]GTGTAGTGTGTGTTT | 64127 |
rs34281847 | snp | A/C/G | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698400 | GGCAAGTGTGTGTGG[A/C/G]AAGTGTTGATGGGGG | 64127 |
rs34333043 | in-del | -/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50725092 | CCCACCTGTCGACTT[-/C]CCCCTTATGTATCAA | 64127 |
rs34409335 | in-del | -/G | | | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709470 | CTAAACTCTGACACA[-/G]GGAAATGGTTTGCTT | 64127 |
rs34430742 | snp | A/G | 0.0195694 | 0.0969626 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696496 | GTAATAAAGGAGTAA[A/G]AGGAAGGATGTTAAG | 64127 |
rs34456998 | in-del | -/G | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698004 | CACGTGGCCCAGGCA[-/G]GGGAGAGAGACACAT | 64127 |
rs34627107 | snp | A/C/G | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698374 | GCGTGGGAGGGAGGT[A/C/G]AGGGCCCTAGGGCAA | 64127 |
rs34684955 | snp | A/G | 0.00396568 | 0.0443522 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699832 | CAGAGTCACCGGCCA[A/G]CCATTGTCAGGAGGC | 64127 |
rs34810706 | snp | C/T | 0.00989172 | 0.0696277 | intron-variant | NOD2 | GRCh38.p7 | 16:50725658 | CTGGGCCGCTCTCCG[C/T]TGGGCTAACTCATGT | 64127 |
rs34829738 | in-del | -/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50730531 | ATAAGTAAAGGCTTT[-/C]CCCTGGCCTAATGTG | 64127 |
rs34912053 | in-del | -/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50714603 | TTGCTGTGAGTGCAC[-/T]GTGTGTGTGTGTGTG | 64127 |
rs34936594 | snp | C/G | 0.000232022 | 0.0107684 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699655 | CTCCTGGGCCAGCCT[C/G]TCTCCCACTTGGCCA | 64127 |
rs34939799 | snp | C/T | 0.0322114 | 0.122752 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50700057 | TGGGGTAACTTGGTC[C/T]ATGGGATTTCCCCTA | 64127 |
rs35085911 | in-del | -/A | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698400 | GCAAGTGTGTGTGGG[-/A]AAGTGTTGATGGGGG | 64127 |
rs35090774 | snp | C/T | 0.00218146 | 0.0329541 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710727 | ACCCCCGCAGAAGAG[C/T]CCAGCCACCCTGGGC | 64127 |
rs35095295 | snp | C/G/T | 1.66807e-05 | 0.00288792 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699743 | CGGCTGCCCAAGAAG[C/G/T]CCAGGCCGACAGCCA | 64127 |
rs35263569 | in-del | -/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50714604 | TGCTGTGAGTGCACT[-/G]TGTGTGTGTGTGTGT | 64127 |
rs35285618 | snp | A/G | 0.00403278 | 0.0447228 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712034 | GCCAGGCCTGTGCCC[A/G]CTGGTGTCTGGCCCG | 64127 |
rs35322998 | in-del | -/GT | | | intron-variant | NOD2 | GRCh38.p7 | 16:50714612 | TGCACTGTGTGTGTG[-/GT]TGTGTGTGTGTGTGT | 64127 |
rs35378728 | in-del | -/G | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696994 | TCTCATGTCCCCAGT[-/G]GGGGTTTTTCAGTGA | 64127 |
rs35422070 | snp | C/T | 0.0259695 | 0.110952 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711582 | ACTGGCTCTGTGGGG[C/T]CTGGGCATGTGCTGC | 64127 |
rs35617724 | in-del | -/A | | | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50700072 | CATGGGATTTCCCCT[-/A]AAAAGGTAGCCAGGC | 64127 |
rs35701609 | snp | G/T | 0.022575 | 0.103816 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50699459 | TGGCTTCTGGAGAAG[G/T]CCCKCACTGACCTTG | 64127 |
rs35832802 | in-del | -/A | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695259 | GGCCCAGAGGTGGTT[-/A]AAAAAAAAGAAAACC | 64127 |
rs35863026 | in-del | -/A | | | intron-variant | NOD2 | GRCh38.p7 | 16:50704372 | GAATGTATGAAAGTT[-/A]AAAATTTCTGAGGTC | 64127 |
rs35980453 | in-del | -/G | | | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50731951 | CTGAACTTGTTTTCT[-/G]GGGAACACCATAGGT | 64127 |
rs36034720 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50699406 | CTCGGGTTCTGCTGG[C/G]GCTGACTTGCCCTGG | 64127 |
rs41449646 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NOD2 | GRCh38.p7 | 16:50701544 | AGGTCAGTCCAATAA[C/T]GAATATGTCTTCTGT | 64127 |
rs45575333 | in-del | GCATGGGAGCGGGGTTTCA/TCAGCCAGTATGAATGTGATGAAATCAGGT | | | frameshift-variant, cds-indel, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699898 | GGGAGCGGGGTTTCG[lengthTooLong]TCAGCCAGTATGAAT | 64127 |
rs56170908 | in-del | -/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50725360 | CCCCACAACGTACTT[-/T]ATCTGTTCTTTCTTT | 64127 |
rs56250614 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | NOD2 | GRCh38.p7 | 16:50700381 | CTCCCGCCTTGGCCT[C/G]CCAAACTGTTGGGAT | 64127 |
rs56341238 | snp | A/C | 0.0858192 | 0.188533 | intron-variant | NOD2 | GRCh38.p7 | 16:50718533 | TGAAACCATAGAAGG[A/C]GAAGCTGCGGATAAG | 64127 |
rs56930767 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50721328 | GCTAAAACCCCCAAA[C/T]GCTGTCATATGATAC | 64127 |
rs57627342 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709149 | ATCTGATATGTACTG[C/G]AGAGGAAGATATCTA | 64127 |
rs57701669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50700030 | CTGATTTGTCCTCAT[A/G]AAGTCAGCCTGTGGG | 64127 |
rs58046161 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50721739 | CTCAGGTGATCCTCC[A/C]TCCTTTGCCTCCCAA | 64127 |
rs58342974 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | NOD2 | GRCh38.p7 | 16:50718671 | ATGTCTGTGTGCCTC[C/T]GTTTCCCCTTCTGTA | 64127 |
rs58586167 | snp | C/T | | | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50722625 | TGGCCTTTTCAGATT[C/T]TGGGGCAACAGAGTG | 64127 |
rs58936029 | in-del | -/GT/GTGT | | | intron-variant | NOD2 | GRCh38.p7 | 16:50714643 | TGTGTGTGTGTGTGT[-/GT/GTGT]ATGAGAGAGAGAGAG | 64127 |
rs59171756 | in-del | -/A | | | intron-variant | NOD2 | GRCh38.p7 | 16:50723140 | GTCTAAAAAGGGTAG[-/A]AAAAAAAAAAAAAAG | 64127 |
rs59368189 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NOD2 | GRCh38.p7 | 16:50694693 | TTGGTTCCATGTCTG[A/T]CTCCCGGAGCCATGC | 64127 |
rs59712090 | snp | A/G | 0.0322114 | 0.122752 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698878 | CTCTCACCCTGCTTC[A/G]AAGAGAATGAATTCC | 64127 |
rs59780176 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50722764 | GTGAAGAGGGAGGAG[C/T]TGGGGCCAGTTCTGA | 64127 |
rs60699834 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | NOD2 | GRCh38.p7 | 16:50721894 | TTTTGTTATTACAGT[A/G]TCATATCCCTGGGGC | 64127 |
rs60727336 | snp | C/T | | | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732670 | CTTTAAAAAATTAAT[C/T]TGGGCCAGAATTTCA | 64127 |
rs60799995 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | NOD2 | GRCh38.p7 | 16:50728126 | TATCGAGGTTTTTCA[C/T]CTTTCCAATTTGCTT | 64127 |
rs61030085 | in-del | -/T | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692340 | GCTAATTAGATAGTT[-/T]CAGAGCCAAGTAATC | 64127 |
rs61193331 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | NOD2 | GRCh38.p7 | 16:50710226 | TCAGTAATGATAACG[G/T]CAGTCACTGATGTCT | 64127 |
rs61199363 | snp | G/T | 0.114387 | 0.210022 | intron-variant | NOD2 | GRCh38.p7 | 16:50694695 | GGTTCCATGTCTGTC[G/T]CCCGGAGCCATGCAG | 64127 |
rs61736931 | snp | A/G | 0.21366 | 0.247345 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712337 | ACATTGGCGTGGAGC[A/G]GCTGCTGCCTTGCCT | 64127 |
rs61736932 | snp | C/T | 0.0194819 | 0.0967544 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711744 | CCAGTGCTTCTTTGC[C/T]GCGTTCTACCTGGCA | 64127 |
rs61747625 | snp | C/T | 0.00462593 | 0.0478703 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712175 | AGGAGGAGCGGCTGG[C/T]TCGGAAGGCTGCACG | 64127 |
rs61755182 | snp | C/T | 0.00517557 | 0.0506063 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707880 | TGCTTGATCTTGCCA[C/T]GGTGAAAGCGAATGG | 64127 |
rs61755272 | snp | A/G/T | 0.00059004 | 0.0171662 | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50716594 | CTCTTTAGTTTGCGC[A/G/T]ATAACAATATCTCAG | 64127 |
rs62027635 | snp | A/G | 0.203882 | 0.245709 | intron-variant | NOD2 | GRCh38.p7 | 16:50705539 | ATATCTTTAGATCTC[A/G]CCTCCTGGGTTGATC | 64127 |
rs62029861 | snp | C/T | 0.000131961 | 0.00812176 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712279 | GTGCTGCAGCACCTC[C/T]GGCGGCCCGTGGCCC | 64127 |
rs62029862 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715466 | TGTTGCCCAGGCAGG[G/T]GGTACAGTGGCACAA | 64127 |
rs62029863 | snp | G/T | 0.19459 | 0.243782 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715497 | TCTCGGCTCATGCAA[G/T]CTCTGCCTCCCGGGT | 64127 |
rs62029864 | snp | A/G | 0.173643 | 0.238054 | intron-variant | NOD2 | GRCh38.p7 | 16:50718253 | CTGACCACACTTCAG[A/G]AGGAGAATCATCTGC | 64127 |
rs62029865 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50724261 | CCTTGGCTGTTGCAG[A/G]GCTTACTAGCTCTAC | 64127 |
rs62029866 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50726515 | GGGTGGAAATGGGCT[A/G]GGAAGTTGGGGTGAA | 64127 |
rs67189633 | in-del | -/T | | | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715421 | TACTATTGTTCCCTC[-/T]TTTTTTTTTTTTGAG | 64127 |
rs67559630 | in-del | -/ACAC | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50714642 | CTCTCTCTCTCTCAT[-/ACAC]ACACACACACACACA | 64127 |
rs68101465 | in-del | -/GT | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692597 | AAGCGATGTGTGTGT[-/GT]TGGGAAGCGATGTGT | 64127 |
rs71309350 | in-del | -/G | 0.5 | 0 | utr-variant-5-prime, splice-acceptor-variant, upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699485 | CACATTTCACAACCT[-/G]GGGGAGGAGAACAAG | 64127 |
rs71715899 | in-del | -/T | 0.416545 | 0.186448 | intron-variant | NOD2 | GRCh38.p7 | 16:50704532 | CCTTTTTTTTTTTTT[-/T]CTTTTTGAGACAGTG | 64127 |
rs72227112 | in-del | -/TG | | | intron-variant | NOD2 | GRCh38.p7 | 16:50714603 | TTGCTGTGAGTGCAC[-/TG]TGTGTGTGTGTGTGT | 64127 |
rs72796346 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692158 | GATGCCAGTTATTTT[C/T]GTTATTTTTAAAAAT | 64127 |
rs72796353 | snp | A/C | 0.0240623 | 0.107015 | intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712383 | TCTGTAGTGAGTGTT[A/C]CTGGGCATTGCTGTT | 64127 |
rs72796355 | snp | C/G | 0.201418 | 0.245234 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713828 | CCCCAACTCTTGCTC[C/G]TGGCCAGCGCCTTCC | 64127 |
rs72796365 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NOD2 | GRCh38.p7 | 16:50727755 | GACCCTTTCTGTTGA[C/T]GAATGCCGGCTGCAG | 64127 |
rs72796366 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50727962 | GTCCAACCACTGAGC[G/T]AGTCATTGCCAGTTG | 64127 |
rs72796367 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NOD2 | GRCh38.p7 | 16:50728860 | TCTAATCTCTGTCTC[C/T]GTGCCCTCAAAGACC | 64127 |
rs73575744 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NOD2 | GRCh38.p7 | 16:50700224 | GCCTTGAATTCCTGC[A/G]CTCAAGTGATCTTCT | 64127 |
rs73575751 | snp | A/C/G | 0.10111 | 0.201411 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706263 | GAAACTTGGGTCCAC[A/C/G]TGGTTCTAGACAGGT | 64127 |
rs73575756 | snp | A/G | 0.0970103 | 0.197722 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713963 | TCTGGCCAGGCAAAT[A/G]GAAAACAGCCAGCAC | 64127 |
rs73575762 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | NOD2 | GRCh38.p7 | 16:50719639 | TCACCCTCGCTGTCC[C/T]GGGGAAACCACCTCC | 64127 |
rs73575767 | snp | C/G | 0.11228 | 0.208646 | intron-variant | NOD2 | GRCh38.p7 | 16:50722387 | GCCCTCTACTATTCT[C/G]TAAGTCTGTAATGTA | 64127 |
rs73575772 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | NOD2 | GRCh38.p7 | 16:50727659 | AATATGGCGGATGAG[A/G]CAAAACTTCATAGTC | 64127 |
rs73575774 | snp | A/G | 0.138886 | 0.22395 | intron-variant | NOD2 | GRCh38.p7 | 16:50730205 | GAAAAGTCAGCTCCC[A/G]CCCTCCTAGAAATTG | 64127 |
rs73575775 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | NOD2 | GRCh38.p7 | 16:50730315 | TGCACAGTGTTTCCA[A/G]TTCTCTATAATTAAA | 64127 |
rs73575776 | snp | C/T | 0.136847 | 0.222927 | intron-variant | NOD2 | GRCh38.p7 | 16:50730488 | CAAAGATTTGTCCTT[C/T]TTGTTTCCAGGGATC | 64127 |
rs74017777 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | NOD2 | GRCh38.p7 | 16:50703838 | AAGTCAGTCGGCAAT[G/T]CCATGAATGAGTCTG | 64127 |
rs74017778 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50705229 | TTTTTGTAGTATCTT[A/C]CTCTTGTTTTATGGA | 64127 |
rs74017781 | snp | A/G | 0.0283406 | 0.115616 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709025 | AAGGTGACAATTGGT[A/G]TGTTTATTTCTCTAT | 64127 |
rs74017785 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | NOD2 | GRCh38.p7 | 16:50726352 | CTAGGAAAACGCTTG[A/C]CTTTAGAGACAGACA | 64127 |
rs74017786 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | NOD2 | GRCh38.p7 | 16:50726492 | GAAAACACTTCCACT[A/T]ATTATTTGGGTGGAA | 64127 |
rs74457704 | snp | A/G | 0.029116 | 0.117091 | intron-variant | NOD2 | GRCh38.p7 | 16:50730923 | CAAAAGCTTTGCTGG[A/G]CGTGGCAGCTCACAC | 64127 |
rs74477363 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NOD2 | GRCh38.p7 | 16:50694107 | GGCCACATCCCCCAG[C/T]TGTTTGCTCTCCTAT | 64127 |
rs74561522 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706871 | CTRGCTAATTTTTTG[G/T]ATTTTTAGTAGTGAT | 64127 |
rs74600858 | snp | C/T | 0.089084 | 0.191327 | intron-variant | NOD2 | GRCh38.p7 | 16:50710163 | AGAATACAGGTCTTC[C/T]GATCCCAGCCCAGAG | 64127 |
rs75135978 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50703223 | ACTGGCTTGACTTTT[G/T]TGTAAATCATCTCTT | 64127 |
rs75279868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706156 | AGCTGAGAGGACAGC[C/T]AGAGCCAAGGCCCAG | 64127 |
rs75391704 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NOD2 | GRCh38.p7 | 16:50694502 | TTTGCCTCGCTGCAC[C/T]CTGGGATCTGAGGCT | 64127 |
rs75419932 | snp | C/G/T | 0.00597455 | 0.054357 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695161 | GAGAATGGATCATGG[C/G/T]GGGGGTGGGGTAAGG | 64127 |
rs75423837 | snp | A/G | 0.029116 | 0.117091 | intron-variant | NOD2 | GRCh38.p7 | 16:50718373 | ATAGAGCGTGGATGC[A/G]CTGGACGGGGGGCTG | 64127 |
rs75616141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50703815 | AATTTATAAGGACCT[A/C]TTCTGGGAAGTCAGT | 64127 |
rs75668898 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50694942 | GGGCTGGGTATTGCA[G/T]TGTATATAGCACAAC | 64127 |
rs75858791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50713070 | TTTGGAGAATCTGTG[A/C]CCCTGAACTCGGGGG | 64127 |
rs75873381 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50700885 | TAGATCATAGATGTT[A/C]AGAGTTGGTATATAA | 64127 |
rs75877771 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50719856 | TGTGTTTCCCTGGCC[A/G]GGGCACAGACGGCCC | 64127 |
rs75925741 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | NOD2 | GRCh38.p7 | 16:50694587 | GACACATGCCCAGTG[C/G]TGGGGAGCTTATTAC | 64127 |
rs75974290 | in-del | -/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50724796 | ACCTCCATCTATAGA[-/G]GTTTAAACAAGGAAA | 64127 |
rs76006016 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50726152 | CTGACTCAGTGGCTT[G/T]GGACTTGTGCCACAA | 64127 |
rs76043235 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707740 | TTCGGTTGTTTTTTT[G/T]ACCTTTTATTCTGGA | 64127 |
rs76078984 | snp | A/G | 0.0685596 | 0.171987 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699242 | AGACCAAGCATGGAT[A/G]TGGGAGTTAGGGGTC | 64127 |
rs76305317 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706858 | CCTGCCACCACGCCT[A/G]GCTAATTTTTTGKAT | 64127 |
rs76416629 | snp | G/T | 0.285257 | 0.247501 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692849 | AAAGTGGTGTGTGTG[G/T]GGGGTGTGTGTGTGT | 64127 |
rs76549067 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50720503 | GGATAAGAGGGGCTG[G/T]GCTAGGTCCCTCGGA | 64127 |
rs76626344 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709665 | TTCCCTTGCTAGGTC[C/T]ACCCAGATCAATCAG | 64127 |
rs76685241 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695565 | CACCATATAACTGGT[A/G]TTTAAAGCCACAAGA | 64127 |
rs76689881 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | NOD2 | GRCh38.p7 | 16:50729285 | TTTAGGCATGCAGAG[A/G]GTGGTGGGTCTTCCC | 64127 |
rs76721226 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50723734 | TGTCTGTAAAATGAG[A/G]GTAAGAATACTTCCA | 64127 |
rs76873248 | in-del | -/GTGT | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692578 | AAGTGAGGCGTGTGT[-/GTGT]TGGGAAGCGATGTGT | 64127 |
rs76959347 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50721422 | TTGTTGTTTTTTTTT[G/T]CTTCGCCATATATTA | 64127 |
rs76961626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50700045 | GAAGTCAGCCTGTGG[A/G]GTAACTTGGTCCATG | 64127 |
rs77125128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50719859 | GTTTCCCTGGCCAGG[A/G]CACAGACGGCCCTCC | 64127 |
rs77153279 | snp | A/G | 3.32386e-05 | 0.00407654 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699933 | TGAAATCAGGTTGCC[A/G]ATCTTCACACCGTCC | 64127 |
rs77238200 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715030 | GCTCAGGACCTTCAA[A/G]ATGATTTGCATGACC | 64127 |
rs77304531 | snp | A/G | | | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709381 | GGCAGTGAGGCTGTG[A/G]TGGCGGGGGACCATG | 64127 |
rs77343505 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NOD2 | GRCh38.p7 | 16:50726127 | GGAGTACTGTGGCCT[C/T]CTCCAGTGGCTGACT | 64127 |
rs77762224 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NOD2 | GRCh38.p7 | 16:50701228 | AGTTTGTTGTGTTCA[C/T]AGAGCTTTGCACACG | 64127 |
rs77766374 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | NOD2 | GRCh38.p7 | 16:50702513 | GGATGGTGCTTGTGG[C/T]ATATCCAACCAACAT | 64127 |
rs77920611 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715404 | CCTGGTGAGGCTGAT[A/G]ATACTATTGTTCCCT | 64127 |
rs77966199 | snp | G/T | 0.00132212 | 0.025677 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711180 | TGCCCGCAAGGTGGT[G/T]ACCAGCCGTCCGGCC | 64127 |
rs78012689 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707123 | TAAAAAATATGTCTG[G/T]TAGAGGATTTGAAAT | 64127 |
rs78015461 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50721382 | TTTTTTTTTTTGTTT[G/T]TTTGTTTGTTTTGTT | 64127 |
rs78145604 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50710245 | TCACTGATGTCTTTT[G/T]AGCACTTACTTTGTG | 64127 |
rs78200189 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NOD2 | GRCh38.p7 | 16:50705662 | CATTTCCTTCAGTTC[C/T]GGAGGTCCCTCATGC | 64127 |
rs78779315 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706179 | AGGCCCAGAGGCAGG[A/G]GCATACCTGGTAGTT | 64127 |
rs78803476 | snp | A/T | 3.30082e-05 | 0.00406239 | intron-variant | NOD2 | GRCh38.p7 | 16:50731726 | CCTCACTCAAACCTC[A/T]GTTCACTTGATCTGC | 64127 |
rs78821446 | snp | C/T | 0.5 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50700114 | GCTCTTGACTCTTGG[C/T]AGGAAACGTACAACT | 64127 |
rs78848722 | snp | C/G | 1.65551e-05 | 0.00287702 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711855 | CCTGCCCACGATGTG[C/G]ATCCAGGCCTCGGAG | 64127 |
rs78909275 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706444 | GGCTGTGGGGGCAGG[A/G]ACAGAAGCAGGGGGA | 64127 |
rs79112000 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50723083 | GTGATGTCTAAAAAA[A/G]CTAAAAAAAAAAAAA | 64127 |
rs79250217 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NOD2 | GRCh38.p7 | 16:50701055 | TCCACTTTATAAATC[A/G]GGAAGTTGAGACCAA | 64127 |
rs79541155 | snp | A/T | 0.0168055 | 0.0901129 | intron-variant | NOD2 | GRCh38.p7 | 16:50714647 | GTGTGTGTGTGTATG[A/T]GAGAGAGAGAGAGAT | 64127 |
rs79609469 | snp | C/T | 0.0322114 | 0.122752 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692394 | AAACCCTATTAGTAC[C/T]AAACTGAGAAATAAA | 64127 |
rs79824136 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NOD2 | GRCh38.p7 | 16:50716224 | CAGGCTGCACCTTTC[A/G]CATATATCAGCTCCT | 64127 |
rs79852086 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715432 | CCTCTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 64127 |
rs79877183 | snp | A/G | 0.093777 | 0.195178 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698222 | AGAACTGACCATGCT[A/G]AGAGATTTTCTTGGC | 64127 |
rs79897742 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50717643 | GGCTGGGTTTGTGGA[G/T]GGGAGCCGCCATTTT | 64127 |
rs79916676 | snp | C/G | 0.0228947 | 0.104514 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50713504 | ACATAACATATATAG[C/G]GAATATATATATGTA | 64127 |
rs79984321 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | NOD2 | GRCh38.p7 | 16:50731077 | TGGGAGGCTGGGATG[A/G]AAGGATCCCTTGAAC | 64127 |
rs80099838 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOD2 | GRCh38.p7 | 16:50703103 | CATACAGAAGAGTGT[A/G]TATATTTCATATGTA | 64127 |
rs80199944 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NOD2 | GRCh38.p7 | 16:50710187 | CCCAGAGCCCCTTCC[C/T]GTCATCTAGAACTCC | 64127 |
rs104895419 | snp | A/G/T | 9.96496e-05 | 0.00705796 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50699729 | TCAGAAGCTCATCGC[A/G/T]GCTGCCCAAGAAGCC | 64127 |
rs104895420 | snp | C/T | 0.00018203 | 0.00953845 | NOD2 | 16 | allele_origin=T(germline)/C(unknown) | 16:50699883 | ATGCTGGACCTGGCA[C/T]GGGAGCGGGGTTTCG | 64127 |
rs104895421 | snp | A/G/T | 0.00352286 | 0.0418218 | NOD2 | 16 | allele_origin=T(germline)/A(unknown) | 16:50699481 | CTGACCTTGTTCTCC[A/G/T]CCCCAGGTTGTGAAA | 64127 |
rs104895422 | snp | C/T | 0.000263709 | 0.0114798 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50710614 | GTGTCTGCTCAGTCT[C/T]GCTTCCTCAGTACCT | 64127 |
rs104895423 | snp | G/T | 0.00112232 | 0.0236622 | NOD2 | 16 | allele_origin=G(unknown)/T(germline) | 16:50710654 | CAGAGACGCTCTGCC[G/T]GGAGGACATATACAC | 64127 |
rs104895424 | snp | A/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710782 | GGCCACCTCAATGAC[A/G]ATGCGGACACTGTGC | 64127 |
rs104895425 | snp | C/G | 0.00319374 | 0.039833 | NOD2 | 16 | allele_origin=G(unknown)/C(germline) | 16:50710792 | ATGACGATGCGGACA[C/G]TGTGCTGGTGGTGGG | 64127 |
rs104895426 | snp | C/T | 0.000116001 | 0.00761491 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50710813 | TGGTGGTGGGTGAGG[C/T]GGGCAGTGGCAAGAG | 64127 |
rs104895427 | snp | C/T | 0.00102698 | 0.0226371 | NOD2 | 16 | allele_origin=T(germline)/C(germline) | 16:50710842 | AGCACGCTCCTGCAG[C/T]GGCTGCACTTGCTGT | 64127 |
rs104895428 | snp | C/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710953 | CTCTCTGTGCGGACT[C/G]TACTCTTTGAGCACT | 64127 |
rs104895429 | snp | A/G | 0.000115566 | 0.00760063 | NOD2 | 16 | allele_origin=G(unknown)/A(germline) | 16:50711152 | ACCTTCTGCAGGGCA[A/G]CCTGCTGAAGAATGC | 64127 |
rs104895430 | snp | A/C/G | 0.000264802 | 0.0115036 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50711192 | GGTGACCAGCCGTCC[A/C/G]GCCGCTGTGTCGGCG | 64127 |
rs104895431 | snp | C/T | 0.0016559 | 0.0287265 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50711203 | GTCCGGCCGCTGTGT[C/T]GGCGTTCCTCAGGAA | 64127 |
rs104895432 | snp | A/G | 0.000664176 | 0.0182112 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50711232 | AAGTACATCCGCACC[A/G]AGTTCAACCTCAAGG | 64127 |
rs104895433 | snp | C/T | | | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711277 | GGCATCGAGCTGTAC[C/T]TGAGGAAGCGCCATC | 64127 |
rs104895434 | snp | A/G | 3.36072e-05 | 0.00409908 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50711420 | ACTGTTGCTGCAGGA[A/G]GGGGGGTCCCCAAAG | 64127 |
rs104895435 | snp | C/G | 1.66944e-05 | 0.0028891 | NOD2 | 16 | allele_origin=G(unknown)/C(germline) | 16:50711492 | GCTGCATGCCACCCC[C/G]CCAGACTCAGCTTCC | 64127 |
rs104895436 | in-del | -/CTGGGC | | | cds-indel, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711583 | CTGGCTCTGTGGGGC[-/CTGGGC]ATGTGCTGCTACGTG | 64127 |
rs104895437 | snp | A/G | 0.000779107 | 0.0197217 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50711699 | CGTGCCAGGGAGTAC[A/G]GCGCCCCTGGAATTC | 64127 |
rs104895438 | snp | A/G/T | 0.0013525 | 0.0259711 | NOD2 | 16 | allele_origin=G(germline)/A(germline) | 16:50711745 | CAGTGCTTCTTTGCC[A/G/T]CGTTCTACCTGGCAC | 64127 |
rs104895439 | snp | C/T | 3.3006e-05 | 0.00406226 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50711746 | AGTGCTTCTTTGCCG[C/T]GTTCTACCTGGCACT | 64127 |
rs104895440 | snp | C/T | 1.68431e-05 | 0.00290194 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50712048 | CGCTGGTGTCTGGCC[C/T]GCAGCCTCCGCAAGC | 64127 |
rs104895441 | snp | A/C/T | | | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712131 | CATGCCCGGGTTCAT[A/C/T]TGGCTCATCCGGAGC | 64127 |
rs104895442 | snp | C/T | 3.3024e-05 | 0.00406336 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50712184 | GGCTGGCTCGGAAGG[C/T]TGCACGTGGCCTGAA | 64127 |
rs104895443 | snp | A/G | 0.00041213 | 0.014349 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50712243 | AGTGTGGGCCCCACT[A/G]AGTGTGCTGCCCTGG | 64127 |
rs104895444 | snp | A/G | 0.00210904 | 0.0324048 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50712288 | CACCTCCGGCGGCCC[A/G]TGGCCCTGCAGCTGG | 64127 |
rs104895445 | snp | A/G | 0.000132648 | 0.00814287 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50716651 | TGTGCTCTTCACTGC[A/G]AGCAATTGCAGAAGT | 64127 |
rs104895446 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50716902 | ACAGTCTATTCAACA[A/G]CAAATTGACTGACGG | 64127 |
rs104895447 | snp | A/G | 0.00240214 | 0.0345731 | NOD2 | 16 | allele_origin=G(unknown)/A(germline) | 16:50716931 | GGCTGTGCACACTCC[A/G]TGGCTAAGCTCCTTG | 64127 |
rs104895448 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50716963 | ATGCAGGCAGAACTT[C/T]TTGGCATTGAGGTGA | 64127 |
rs104895449 | snp | A/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50717009 | ATTCCCTGGAAACTA[A/T]TTTTTGCCCCATTCC | 64127 |
rs104895450 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50719920 | TCCTCTGTCTTCCCT[C/T]CCAGGCTGGGGAATA | 64127 |
rs104895451 | snp | C/T | 4.94173e-05 | 0.00497053 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50722646 | CAACAGAGTGGGTGA[C/T]GAGGGGGCCCAGGCC | 64127 |
rs104895452 | snp | A/C | 0.000790384 | 0.0198637 | NOD2 | 16 | allele_origin=A(unknown)/C(germline) | 16:50722660 | ACGAGGGGGCCCAGG[A/C]CCTGGCTGAAGCCTT | 64127 |
rs104895453 | snp | A/G | 0.000164715 | 0.0090736 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50722678 | TGGCTGAAGCCTTGG[A/G]TGATCACCAGAGCTT | 64127 |
rs104895454 | snp | C/T | 5.00697e-05 | 0.00500323 | NOD2 | 16 | allele_origin=T(germline)/C(unknown) | 16:50723319 | GGTGGGGAACAACAT[C/T]GGCAGTGTGGGTGCC | 64127 |
rs104895455 | snp | A/G | | | missense | NOD2 | GRCh38.p7 | 16:50725520 | CTCCAGGATGAAGGT[A/G]TATGTTCTCTCGCAG | 64127 |
rs104895456 | snp | A/G | 0.000165651 | 0.00909934 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50699827 | ACCTGCAGAGTCACC[A/G]GCCAGCCATTGTCAG | 64127 |
rs104895457 | snp | A/G | 6.62438e-05 | 0.00575478 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50725539 | GTTCTCTCGCAGAAG[A/G]ACTGAAGAAAAATTC | 64127 |
rs104895458 | snp | C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50731645 | GCTGGGCCAGAGAGT[C/G]AGCCCATCCCAGGCA | 64127 |
rs104895459 | snp | A/G | | | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50731828 | GCTTTGAAGTCTCCG[A/G]GAGGATGTTCGTCTC | 64127 |
rs104895460 | snp | C/T | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711316 | GGGGTGGCGGACCGC[C/T]TCATCCGCCTGCTCC | 64127 |
rs104895461 | snp | A/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710912 | TCCCATTCAGCTGCC[A/G]GCAGCTGCAGTGCAT | 64127 |
rs104895462 | snp | C/T | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710911 | TTCCCATTCAGCTGC[C/T]GGCAGCTGCAGTGCA | 64127 |
rs104895463 | snp | C/T | 0.00014904 | 0.00863121 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50725531 | AGGTGTATGTTCTCT[C/T]GCAGAAGGACTGAAG | 64127 |
rs104895464 | snp | A/G | 0.00311262 | 0.0393271 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50712283 | TGCAGCACCTCCGGC[A/G]GCCCGTGGCCCTGCA | 64127 |
rs104895465 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50722541 | GCTGGGACTGCAGAG[A/G]GAGGAGGACTGTTAG | 64127 |
rs104895466 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50722547 | ACTGCAGAGGGAGGA[A/G]GACTGTTAGTTCATG | 64127 |
rs104895467 | snp | A/G | 0.00243501 | 0.0348077 | NOD2 | 16 | allele_origin=G(unknown)/A(germline) | 16:50716899 | TGAACAGTCTATTCA[A/G]CAACAAATTGACTGA | 64127 |
rs104895468 | snp | A/G | 6.68148e-05 | 0.00577953 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50699751 | CAAGAAGCCCAGGCC[A/G]ACAGCCAGTCCCCCA | 64127 |
rs104895469 | snp | A/C | 0.000411872 | 0.0143446 | NOD2 | 16 | allele_origin=A(germline)/C(unknown) | 16:50710981 | ACTGCTGTTGGCCTG[A/C]TGTTGGTCAAGAAGA | 64127 |
rs104895470 | snp | A/T | 0.00011533 | 0.00759287 | NOD2 | 16 | allele_origin=T(unknown)/A(germline) | 16:50710998 | GTTGGTCAAGAAGAC[A/T]TCTTCCAGTTACTCC | 64127 |
rs104895471 | snp | C/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711559 | CCCACCCTCCTGCAC[C/G]TGGGCAGACTGGCTC | 64127 |
rs104895472 | snp | A/T | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711398 | TGGTGTCCAAATGCC[A/T]CCAGGAACTGTTGCT | 64127 |
rs104895473 | snp | C/T | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711449 | AGACCACTACAGATA[C/T]GTACCTGCTGATTCT | 64127 |
rs104895474 | snp | A/C | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711724 | GAATTCCTTCACATC[A/C]CTTTCCAGTGCTTCT | 64127 |
rs104895475 | snp | A/C/T | 3.34074e-05 | 0.00408688 | NOD2 | 16 | allele_origin=A(unknown)/C(germline) | 16:50711921 | GGCCGAGCCGCACAA[A/C/T]CTTCAGATCACAGCA | 64127 |
rs104895476 | snp | C/G/T | 8.23784e-05 | 0.00641735 | NOD2 | 16 | allele_origin=G(germline)/C(germline) | 16:50711057 | CTTTGATGGCTTTGA[C/G/T]GAGTTCAAGTTCAGG | 64127 |
rs104895477 | snp | A/G/T | 3.29533e-05 | 0.00405901 | NOD2 | 16 | allele_origin=G(germline)/A(germline) | 16:50711058 | TTTGATGGCTTTGAC[A/G/T]AGTTCAAGTTCAGGT | 64127 |
rs104895478 | snp | A/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711395 | GGATGGTGTCCAAAT[A/G]CCACCAGGAACTGTT | 64127 |
rs104895479 | snp | C/T | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711670 | CTTGGCTTCCTGGTG[C/T]GTGCCAAAGGTGTCG | 64127 |
rs104895480 | snp | G/T | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711380 | TGCCTGTCTTCTCAT[G/T]GATGGTGTCCAAATG | 64127 |
rs104895481 | snp | C/T | 0.000115366 | 0.00759405 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50711082 | TTCAGGTTCACGGAT[C/T]GTGAACGCCACTGCT | 64127 |
rs104895482 | snp | C/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711298 | AAGCGCCATCATGAG[C/G]CCGGGGTGGCGGACC | 64127 |
rs104895483 | snp | A/G | 0.000690218 | 0.0185643 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50712049 | GCTGGTGTCTGGCCC[A/G]CAGCCTCCGCAAGCA | 64127 |
rs104895484 | snp | C/T | 4.94849e-05 | 0.00497393 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50712282 | CTGCAGCACCTCCGG[C/T]GGCCCGTGGCCCTGC | 64127 |
rs104895485 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50716599 | TAGTTTGCGCGATAA[C/G]AATATCTCAGACCGA | 64127 |
rs104895486 | snp | C/G/T | 0.000216105 | 0.0103927 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50716670 | AATTGCAGAAGTTAG[C/G/T]GTAAGTCAGCCTGGG | 64127 |
rs104895487 | snp | G/T | 4.99588e-05 | 0.00499769 | NOD2 | 16 | allele_origin=G(germline)/T(unknown) | 16:50699527 | CTTTTCAGGCACAGA[G/T]GAGCCAGCTGGTCGA | 64127 |
rs104895488 | snp | A/G | | | stop-gained, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710976 | TGAGCACTGCTGTTG[A/G]CCTGATGTTGGTCAA | 64127 |
rs104895489 | snp | C/T | 3.3295e-05 | 0.00408 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50712091 | TCCCGCCAGCTGCAC[C/T]GGGTGAGGCCAAGAG | 64127 |
rs104895490 | snp | C/T | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50722626 | GGCCTTTTCAGATTC[C/T]GGGGCAACAGAGTGG | 64127 |
rs104895491 | snp | C/G/T | 6.59265e-05 | 0.00574104 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50731751 | ATCTGCTTTAGGCTC[C/G/T]GAGGGAACACTTTCT | 64127 |
rs104895492 | snp | A/G/T | 0.000267002 | 0.0115513 | NOD2 | 16 | allele_origin=G(germline)/T(unknown) | 16:50711301 | CGCCATCATGAGCCC[A/G/T]GGGTGGCGGACCGCC | 64127 |
rs104895493 | snp | A/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711059 | TTGATGGCTTTGACG[A/G]GTTCAAGTTCAGGTT | 64127 |
rs104895494 | snp | A/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711353 | CCTCAGCCCTGCACG[A/G]TTTGTGCCACCTGCC | 64127 |
rs104895495 | snp | G/T | 0.00392162 | 0.044107 | NOD2 | 16 | allele_origin=G(germline)/T(unknown) | 16:50712317 | GGACTACAACTCTGT[G/T]GGTGACATTGGCGTG | 64127 |
rs111164073 | snp | A/G | 0.0150606 | 0.0854603 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692911 | GGGGTGTATGTGTTG[A/G]GAAAGCAGGGTGTGT | 64127 |
rs111164074 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50693062 | GTGTATGTGAGTGTT[A/G]GGAAGCAAGGTATGT | 64127 |
rs111266631 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50729398 | GGATGTGAATAGGAG[C/G]CTGCTTACACCCATC | 64127 |
rs111400183 | snp | C/G | 0.000415832 | 0.0144133 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711890 | AGGACAGCAGCGTGG[C/G]AGCTTTGCTGCAGAA | 64127 |
rs111475857 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708248 | GGTGTTACTTACCAT[A/C]CAAACTCTCATTATC | 64127 |
rs111491166 | in-del | -/TG | 0.5 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50714602 | TTGCTGTGAGTGCAC[-/TG]TGTGTGTGTGTGTGT | 64127 |
rs111608429 | snp | C/T | 0.000132837 | 0.00814868 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711600 | GGGCATGTGCTGCTA[C/T]GTGTTCTCAGCCCAG | 64127 |
rs111719717 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715410 | GAGGCTGATAATACT[A/G]TTGTTCCCTCTTTTT | 64127 |
rs111816216 | snp | A/G | 0.0349115 | 0.127424 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698615 | AGTCATACATGGCTC[A/G]TGTTGAAATCCTGAC | 64127 |
rs112008121 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50721626 | GCCTCCTGAGTAGCT[G/T]GGACTACAGGCACAA | 64127 |
rs112011764 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50731875 | GGCTGTGAGTTTGGG[C/T]CCCAGAGGCTGGGTG | 64127 |
rs112082457 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | NOD2 | GRCh38.p7 | 16:50718198 | AAGTGAGGTGGATGA[C/T]GCATGCAGCACTGTG | 64127 |
rs112111999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50730859 | GTCTTCTCTCAAAAA[A/G]CACATCAAGGCTGCA | 64127 |
rs112119469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50712777 | CTCCCACCAGTCTAT[A/G]GATACACTTCAGAGG | 64127 |
rs112160974 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NOD2 | GRCh38.p7 | 16:50717076 | CACACTGGCTCCTGA[C/T]CTCCTGATTGAATGC | 64127 |
rs112423156 | snp | A/G/T | 0.5 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50721427 | GTTTTTTTTTGCTTC[A/G/T]CCATATATTATAGGA | 64127 |
rs112499122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50731599 | GGCCAAGGGTAAAAA[C/T]AGCCCTGACTTCCCT | 64127 |
rs112503057 | snp | A/C | 0.5 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50720549 | AGGACCATGCTAGGG[A/C]CTGCCAGGGAGGGGA | 64127 |
rs112512433 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NOD2 | GRCh38.p7 | 16:50721374 | TTGCTTGGTTTTTTT[G/T]TTTGTTTGTTTGTTT | 64127 |
rs112706859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50716466 | CTCCATCTATGCAGG[A/G]TTTCCTGGAAGCACA | 64127 |
rs112804988 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | NOD2 | GRCh38.p7 | 16:50728214 | ATCAGCTTTGATGAT[A/T]GCTCTCAATTGGTCA | 64127 |
rs113184087 | snp | C/G | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50717496 | CTTTAAATTGCCCCT[C/G]TAGCTGGCCGCTGGG | 64127 |
rs113315711 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698624 | TGGCTCGTGTTGAAA[C/T]CCTGACTCTGCCTGT | 64127 |
rs113372118 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50724885 | GCTACAAGAGGCCAG[A/G]AGGGGTCTCAGCTCT | 64127 |
rs113503001 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NOD2 | GRCh38.p7 | 16:50710123 | TTATCCAAAGCCACC[C/T]GGCCACTATGGCAGG | 64127 |
rs113569829 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NOD2 | GRCh38.p7 | 16:50714703 | GGGAGGGCACAGGCT[C/T]CTCTCCCACAGTGCC | 64127 |
rs113619162 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50718794 | TTATATAGTAAGCGA[A/G]TGGCTGAAAGATGAT | 64127 |
rs113656815 | snp | C/T | 0.111576 | 0.20818 | intron-variant | NOD2 | GRCh38.p7 | 16:50693726 | GCGCCGAGGGTCCCA[C/T]CCCCGGGACTTGAAC | 64127 |
rs113706344 | snp | A/G | 0.000249047 | 0.0111562 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699727 | TGTCAGAAGCTCATC[A/G]CGGCTGCCCAAGAAG | 64127 |
rs113884530 | snp | A/G | | | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732843 | AAAAAAAATTAGGCC[A/G]TTCCTTCAAAGCAAA | 64127 |
rs113924970 | snp | C/T | 0.0901694 | 0.192235 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698596 | TTAGAGACATGCATT[C/T]CGGAGTCATACATGG | 64127 |
rs113951051 | snp | G/T | 0.5 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50701686 | GAGGGGTTTGGAGAA[G/T]GTAGCCTAGATCCCT | 64127 |
rs114013302 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NOD2 | GRCh38.p7 | 16:50726453 | TGTTGCTTTCACAAG[C/T]TAGGAAGTTTCCAAA | 64127 |
rs114178645 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715765 | TAACTAGTAAGTCGC[C/T]GATCAGGATCACAAT | 64127 |
rs114196027 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | NOD2 | GRCh38.p7 | 16:50728222 | TGATGATTGCTCTCA[A/G]TTGGTCATTGTCAGC | 64127 |
rs114204986 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706995 | GAGCCACCATGCTCA[A/G]CCATATCTTGCTATT | 64127 |
rs114354193 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50702575 | AAGAAGTAGTTGTCA[C/T]TGATTGCAGGTTAGG | 64127 |
rs114368954 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | NOD2 | GRCh38.p7 | 16:50724758 | TTTAGTTTAACTATA[A/T]GTTAAGCTGCAGGTG | 64127 |
rs114555387 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NOD2 | GRCh38.p7 | 16:50717810 | CAGACCTGGCTGGCC[C/T]ATCCCTGAGAAGGGT | 64127 |
rs114664276 | snp | A/G | 0.000652539 | 0.0180511 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711962 | CAGGGCTGTTGTCCC[A/G]GGAGCACTGGGGCCT | 64127 |
rs114671178 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50705924 | CAGGGGAGAGGGACA[A/G]TAAGCCAAAGGAAGG | 64127 |
rs114754685 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50710164 | GAATACAGGTCTTCC[A/G]ATCCCAGCCCAGAGC | 64127 |
rs114870756 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708579 | TGACGAGGGAGGGGA[A/T]GATGGGTCTGATTGT | 64127 |
rs114894126 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NOD2 | GRCh38.p7 | 16:50726100 | GCAGTGGCTGGGGAG[A/G]TGATGTGATGGGGAG | 64127 |
rs114899313 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732618 | TCTTCAGTTAAGCCT[C/T]TGGAAACAGCTCGAC | 64127 |
rs114948922 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | NOD2 | GRCh38.p7 | 16:50719514 | CCCAGCGCTCTTGTG[C/G]AACAGGTAAAGCCTA | 64127 |
rs114958760 | snp | C/T | 0.0372196 | 0.131242 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707022 | TATTTTCTACATGGA[C/T]TACATGTTGAAATGG | 64127 |
rs115081170 | snp | C/T | 0.0193772 | 0.0965046 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698115 | ATAAAAAGAAGCTGA[C/T]GGCCCTCTTTGTTGT | 64127 |
rs115114567 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NOD2 | GRCh38.p7 | 16:50721837 | GTTACATAATGTATT[C/T]AACTGGTCACTTTTT | 64127 |
rs115438848 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NOD2 | GRCh38.p7 | 16:50724593 | GGCATTTTCTTTATA[C/T]GGATATAGACTGATC | 64127 |
rs115600893 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NOD2 | GRCh38.p7 | 16:50718636 | AACCCTCATTAGCTG[C/T]GTGACCTCAGGTCAG | 64127 |
rs115658760 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | NOD2 | GRCh38.p7 | 16:50702050 | TTCTGGGCTGAAGTG[A/T]TCCTCCCGCCTCAGC | 64127 |
rs115688894 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | NOD2 | GRCh38.p7 | 16:50726777 | ATTGAACTTCTGATA[C/T]ATCTTTTATAAAAAA | 64127 |
rs115702706 | snp | A/G | 0.0379877 | 0.132479 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50691589 | TAGATGGTTCTGTGC[A/G]CTGCCCAGAATGAAT | 64127 |
rs115801989 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NOD2 | GRCh38.p7 | 16:50717650 | TTTGTGGATGGGAGC[C/T]GCCATTTTAAAATGG | 64127 |
rs115809446 | snp | A/G/T | 0.0283406 | 0.115616 | intron-variant | NOD2 | GRCh38.p7 | 16:50727729 | CAGTCGGGTGTTGTC[A/G/T]TGGAGAATTGGACCC | 64127 |
rs115870097 | snp | C/G | 0.0271762 | 0.113356 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50693328 | GTTGTTCCGAGGACT[C/G]CCCGATTCCCTCCTG | 64127 |
rs116211052 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | NOD2 | GRCh38.p7 | 16:50727799 | CAGTGCATCTCATTG[A/T]CTTGCCGAGCATACT | 64127 |
rs116213743 | snp | A/G | 0.00993419 | 0.0697739 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732439 | CACCCAGGGTGGGAA[A/G]GGCTACACCTTAGCC | 64127 |
rs116283239 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707550 | ACTTCTCTTCCAAAT[A/G]ATTTACAGCCTGCAG | 64127 |
rs116382327 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698395 | CCTAGGGCAAGTGTG[C/T]GTGGGAAGTGTTGAT | 64127 |
rs116437754 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NOD2 | GRCh38.p7 | 16:50720114 | CCCAGAGGCAGCCCA[A/G]CTCCAGTGGGGAGGA | 64127 |
rs116455309 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NOD2 | GRCh38.p7 | 16:50716191 | GGTAAATTGTCCCCA[A/G]GGGTAGCCTGTCTAG | 64127 |
rs116525091 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | NOD2 | GRCh38.p7 | 16:50723969 | TAAAGTGATTTTGAG[C/T]TCCTAGGAGCACTGG | 64127 |
rs116626119 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NOD2 | GRCh38.p7 | 16:50714330 | TGTGTAAAGGCACTC[A/G]TGGCAATGCAGATTC | 64127 |
rs116765287 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713833 | ACTCTTGCTCCTGGC[C/T]AGCGCCTTCCACCAG | 64127 |
rs116779994 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50700206 | CAATCATAGCTCACT[A/G]TAGCCTTGAATTCCT | 64127 |
rs117149242 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706457 | GGAACAGAAGCAGGG[A/G]GACCAGTTTTGCAGC | 64127 |
rs117227497 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50691764 | TCTCTGGTGCCAGAG[A/G]AAAGGGGGCATCTCG | 64127 |
rs117241679 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NOD2 | GRCh38.p7 | 16:50703708 | AAAAAAAAAAAGAAA[A/G]GTTACTATTGCCTTT | 64127 |
rs117317173 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50726208 | GAACCCACCTAGTGA[C/T]CATCATGGGTTTGTC | 64127 |
rs117575447 | snp | C/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692325 | AACAATGCTATTAAA[C/G]CTAATTAGATAGTTT | 64127 |
rs117582370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50702303 | GCAAAAGCAAACATT[A/G]AAGGTTGGGACTGAG | 64127 |
rs117611225 | snp | C/T | 0.000279916 | 0.0118271 | utr-variant-5-prime, intron-variant | NOD2 | GRCh38.p7 | 16:50697230 | TGCCTGCTCCCCCAG[C/T]CTAATGGGCTTTGAT | 64127 |
rs117823701 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NOD2 | GRCh38.p7 | 16:50701126 | GCCAGTGCTGGACCA[A/G]TTGGCCAGCACTGGT | 64127 |
rs117836686 | snp | A/G | 0.000363264 | 0.0134722 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710657 | AGACGCTCTGCCTGG[A/G]GGACATATACACAGA | 64127 |
rs118191897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50730800 | GACCCTTTGGCAACT[A/C]ATTCCCATAAGCCTG | 64127 |
rs137899748 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50700470 | GGTGGCCAGGAACTC[A/C]GATTCTGGAGCCAGA | 64127 |
rs137984638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707276 | TGACTCCAAGACTTC[A/G]GGGCAGAGCACCTGG | 64127 |
rs138041175 | snp | A/C/G | 3.3157e-05 | 0.00407154 | synonymous-codon, missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699717 | TACTTGGGCCTGTCA[A/C/G]AAGCTCATCGCGGCT | 64127 |
rs138142895 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713924 | CCCAGGAGCCAGGGA[C/T]GGGTAGAGAAGGGGG | 64127 |
rs138193434 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50728039 | GTTCGCTGTTGTTGT[C/G]TAGAATAAGAGAAGA | 64127 |
rs138198313 | in-del | -/C | 0.35894 | 0.225016 | intron-variant | NOD2 | GRCh38.p7 | 16:50725357 | AATCCCCACAACGTA[-/C]TTTATCTGTTCTTTC | 64127 |
rs138313319 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732949 | TTTAAACATTATGAT[A/G]TGTGAAAACTGGTTA | 64127 |
rs138367392 | snp | C/G | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698729 | ATAGGCACTACTTCA[C/G]AGTGGCTGGGAGGGT | 64127 |
rs138401601 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695342 | TGCAAGAGAAAGGTA[C/G]AGTCAAAGATGATTC | 64127 |
rs138544617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50704060 | GCTGACTGAGGCAGC[A/G]GGAGTTGAAAAGAAA | 64127 |
rs138646630 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706980 | TGGGATTACAGGCAT[A/G]AGCCACCATGCTCAG | 64127 |
rs138660655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709714 | AAGTTTAACTTTATC[A/G]CATCTCAGAGTTCCT | 64127 |
rs138700796 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707792 | GTTGCAGTAATCAGT[A/G]AGCCTTCCCACATTG | 64127 |
rs138705580 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NOD2 | GRCh38.p7 | 16:50704295 | ATCCTGAATCCTATG[G/T]CCTCTTCTTCCCTGG | 64127 |
rs138768201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50694878 | TGGCGTAGCAGGTGG[C/T]GGGAAGTACTACGAG | 64127 |
rs138881230 | snp | A/G | 6.63372e-05 | 0.00575884 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699629 | CCTGGGAGGACTACG[A/G]GGGCTTCCACCTCCT | 64127 |
rs138889062 | snp | C/T | 0.000216373 | 0.010399 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699753 | AGAAGCCCAGGCCGA[C/T]AGCCAGTCCCCCAAG | 64127 |
rs138929689 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699163 | GCGCTCCTGATCTCA[A/G]GTGACCTTGGGAGAT | 64127 |
rs138956307 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50728325 | CTGCACTATACGTTA[G/T]TTAGCAGTTCCTGGG | 64127 |
rs138958152 | snp | C/T | 5.01551e-05 | 0.0050075 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711935 | ACCTTCAGATCACAG[C/T]AGCCTTCCTGGCAGG | 64127 |
rs139092983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50724150 | GGCAGCTTCAGATTA[C/T]GTCAGGGAGATAAAA | 64127 |
rs139097081 | snp | C/T | 3.31263e-05 | 0.00406965 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712115 | CCAAGAGCGTGCATG[C/T]CATGCCCGGGTTCAT | 64127 |
rs139104022 | snp | A/G | 8.4081e-05 | 0.00648332 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712016 | AGAAGGCCCTGCTCC[A/G]GCGCCAGGCCTGTGC | 64127 |
rs139112440 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NOD2 | GRCh38.p7 | 16:50717119 | TCATTTTAAGCAGGG[A/G]TTCTCTAATGCTGTG | 64127 |
rs139126461 | snp | A/G/T | 0.00123601 | 0.0248293 | intron-variant | NOD2 | GRCh38.p7 | 16:50719888 | CCTTTTCTGCCTGCC[A/G/T]CTGTGTTCTCTCAGC | 64127 |
rs139160786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50701613 | CCATCTGAGAAGTTA[C/G]AAGATTGTGTCTTGT | 64127 |
rs139313263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708334 | CTGAAATTTAGCAGC[C/T]CACAATGGGAAACTC | 64127 |
rs139356723 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50717901 | GGAGAGATGTTCTAA[C/G]ACCCCAGTGGATGCC | 64127 |
rs139457545 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50691691 | GTATTTACTTGAAAG[C/T]GGTATGGGGTAGTGG | 64127 |
rs139485985 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-5-prime, intron-variant | NOD2 | GRCh38.p7 | 16:50697186 | ACTGGGCTTTTGGCG[C/T]TCTGCACAAGGCCTA | 64127 |
rs139512247 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NOD2 | GRCh38.p7 | 16:50702255 | GAATTTTAATGAGCT[A/G]AGAATTCATCTTAAG | 64127 |
rs139571975 | snp | A/G | 0.000281646 | 0.0118635 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699898 | TGGGAGCGGGGTTTC[A/G]TCAGCCAGTATGAAT | 64127 |
rs139654579 | in-del | -/GT | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692853 | TGGTGTGTGTGTGGG[-/GT]GTGTGTGTGTGTGCA | 64127 |
rs139663808 | snp | G/T | 0.000150011 | 0.00865928 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711512 | ACTCAGCTTCCCAAG[G/T]TCTGGGACCCAGTCT | 64127 |
rs139711137 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706026 | TTGGGAAGGGGATAA[A/G]TGATGGCAATTGTAA | 64127 |
rs139787730 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715460 | TCGTTCTGTTGCCCA[C/G]GCAGGGGGTACAGTG | 64127 |
rs139886679 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50722697 | TCACCAGAGCTTGAG[A/G]TGGCTCAGGTAAGCT | 64127 |
rs140188515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50719036 | TAAGACATCTTGGCA[A/G]GGCTGATGAGGAGTT | 64127 |
rs140299615 | snp | C/G | 0.0329836 | 0.124112 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715598 | TTTTTTTGTATTTTT[C/G]GTAGCGACAGGGTTT | 64127 |
rs140312093 | snp | A/G | 0.000132626 | 0.0081422 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711702 | GCCAGGGAGTACGGC[A/G]CCCCTGGAATTCCTT | 64127 |
rs140318749 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50712874 | ACCAAATCAGAGGTG[A/G]CTTGTGCCCCATCAG | 64127 |
rs140414374 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NOD2 | GRCh38.p7 | 16:50700962 | AAATGACCACTGAGT[A/G]TTTTTGAAACTCTTT | 64127 |
rs140423929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50727833 | CATATGTAATGGTTT[C/T]GCAGGGATTCAGAAA | 64127 |
rs140505719 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697992 | AGACCCAGGCTCCCA[C/T]GTGGCCCAGGCAGGG | 64127 |
rs140545201 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698543 | GCAAAACACACAGCA[C/T]GGGCTTGGGGCCCCC | 64127 |
rs140573469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50703820 | ATAAGGACCTCTTCT[A/G]GGAAGTCAGTCGGCA | 64127 |
rs140643942 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732696 | TTTCAAACGGCCTCA[A/C]TAGGCTTCTGGTTGA | 64127 |
rs140716236 | snp | C/T | 0.000247205 | 0.0111149 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711088 | TTCACGGATCGTGAA[C/T]GCCACTGCTCCCCGA | 64127 |
rs140788774 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709578 | GGTGCATGGGGAGGA[C/T]GGGGAAGTGGAGGCA | 64127 |
rs140806020 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50720479 | TGGGGAAGGATAGGA[A/G]GGCACCCAGGATAAG | 64127 |
rs140828549 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NOD2 | GRCh38.p7 | 16:50714404 | GGGCCCAGGAAATCT[A/G]TATTTTTCACAGACA | 64127 |
rs140876663 | snp | C/T | 0.000148678 | 0.00862073 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712141 | TTCATCTGGCTCATC[C/T]GGAGCCTGTACGAGA | 64127 |
rs140918872 | snp | A/G | 0.000197769 | 0.00994209 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711089 | TCACGGATCGTGAAC[A/G]CCACTGCTCCCCGAC | 64127 |
rs140956945 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732098 | CCCTCCTCCATAGTA[C/T]GGGACTGGCCTCTGC | 64127 |
rs140977130 | snp | C/G | 0.000359809 | 0.013408 | missense, intron-variant | NOD2 | GRCh38.p7 | 16:50697256 | TTGATGGGGGAAGAG[C/G]GTGGTTCAGCCTCTC | 64127 |
rs141132426 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696654 | TTAGTGAGAACAGCA[C/T]TAAGGCCAGGTTCTC | 64127 |
rs141173109 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707233 | AGTCAACAGGATTTG[C/G]CAGATTACAGACGAG | 64127 |
rs141237959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50701218 | ATTTGCTTAAAGTTT[A/G]TTGTGTTCATAGAGC | 64127 |
rs141309626 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOD2 | GRCh38.p7 | 16:50703588 | ATGTTGCAGTGAGCC[A/G]AGATCGCACTGCTTG | 64127 |
rs141325216 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698760 | TCAGTGAATTCCTGC[A/G]GGAGAGCACTTAGAA | 64127 |
rs141355588 | snp | A/G | 0.000215501 | 0.0103781 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711867 | GTGCATCCAGGCCTC[A/G]GAGGGAAAGGACAGC | 64127 |
rs141370282 | snp | A/T | 0.093417 | 0.194889 | intron-variant | NOD2 | GRCh38.p7 | 16:50727177 | GAAAAATAATAATTT[A/T]AAAAAAAGAGTCCAG | 64127 |
rs141414002 | snp | A/C | 3.29468e-05 | 0.00405861 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707856 | TGCCTTTCCTGTAGG[A/C]AAGAAGGCTGCTTGA | 64127 |
rs141462423 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NOD2 | GRCh38.p7 | 16:50720996 | TTTTAGTAGAGACAG[A/G]GTTTCACCATGTTGG | 64127 |
rs141612356 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50729599 | TGGCTACTTAATTTG[A/C]TAAACTCATCTAGTG | 64127 |
rs141758527 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | NOD2 | GRCh38.p7 | 16:50705053 | ACTATTAATTCAATG[G/T]TAGAATTCCTTGACT | 64127 |
rs141773998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50713516 | TAGCGAATATATATA[A/T]GTATTATATGCAATG | 64127 |
rs141795834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709770 | CAGGTTCTGAGAATC[C/T]GGACATGGACATCTT | 64127 |
rs141833420 | snp | C/T | 0.00491349 | 0.0493214 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707852 | CTTCTGCCTTTCCTG[C/T]AGGCAAGAAGGCTGC | 64127 |
rs141926253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50723210 | AATGGAGCAGACCAG[A/G]AGAGCACCACGAATT | 64127 |
rs142077546 | snp | C/T | 8.29993e-05 | 0.00644149 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711698 | TCGTGCCAGGGAGTA[C/T]GGCGCCCCTGGAATT | 64127 |
rs142152232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50726534 | AGTTGGGGTGAAGCC[C/T]GGATGTGTCTGAGCC | 64127 |
rs142195807 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NOD2 | GRCh38.p7 | 16:50728630 | CACCAATCTAATAGA[A/C]GTTCAATAAATACTG | 64127 |
rs142204463 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692490 | CACTCTTACCTAACA[C/T]GTAACCTGTCACACT | 64127 |
rs142226455 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50723631 | TGACTGCCTCCACAT[A/G]GCATAAGTGTTAAGA | 64127 |
rs142257193 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698478 | TTCACTTCGCCTAGG[A/G]CAGGACCTTTAGAGC | 64127 |
rs142273770 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708044 | ACACACCTCGGTTAA[C/T]ATCCCATATGCTGGC | 64127 |
rs142376491 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50722630 | TTTTCAGATTCTGGG[C/G]CAACAGAGTGGGTGA | 64127 |
rs142538307 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50721367 | CTGTAACTTGCTTGG[G/T]TTTTTTTTTTGTTTG | 64127 |
rs142559533 | snp | A/G | 0.000115638 | 0.00760302 | synonymous-codon, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50720006 | CTCCTTGCAGTTCCT[A/G]GGGTAGGTTGGATTC | 64127 |
rs142904241 | snp | A/G | 0.000153988 | 0.00877328 | missense | NOD2 | GRCh38.p7 | 16:50729828 | TCCAGGTTGTCCAAT[A/G]ACTGCATCACCTACC | 64127 |
rs142961158 | in-del | -/A | 0.0356815 | 0.128715 | intron-variant | NOD2 | GRCh38.p7 | 16:50701879 | GCTAAAGCAGGACAT[-/A]GGGGGAAATTTACAA | 64127 |
rs142969988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715152 | GGTTTGGAGCCAAGC[C/T]GCCTAGGCTCAAAGC | 64127 |
rs142997491 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695909 | GTACAGGCAACAGAC[A/G]AGGGGGCCTGCTGTA | 64127 |
rs143037511 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50691592 | ATGGTTCTGTGCGCT[G/T]CCCAGAATGAATTTT | 64127 |
rs143080077 | snp | C/T | 4.94197e-05 | 0.00497066 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707939 | CAGGAATTACCAGTC[C/T]CATTGGCCCTGCCTT | 64127 |
rs143110172 | snp | A/G | 0.000398367 | 0.0141076 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711227 | TCAGGAAGTACATCC[A/G]CACCGAGTTCAACCT | 64127 |
rs143131977 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50719451 | CTCTCTCCTTCCTTT[C/T]TGGAAGGCTCAGTGG | 64127 |
rs143304873 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NOD2 | GRCh38.p7 | 16:50703638 | GCAGTGAGCCAAGAT[C/T]GCACCACTGCACTCT | 64127 |
rs143380517 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50704077 | GAGTTGAAAAGAAAC[A/G]ATATTAGTTCATGGT | 64127 |
rs143395754 | snp | C/T | 3.32154e-05 | 0.00407512 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711231 | GAAGTACATCCGCAC[C/T]GAGTTCAACCTCAAG | 64127 |
rs143411401 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50733415 | GATGTTTTCAACCCG[A/G]TAATGTATAGCTTAA | 64127 |
rs143451061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709082 | ATTTTAGTATCATTG[A/G]TGATGACTGGAAAAC | 64127 |
rs143469103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50700902 | GAGTTGGTATATAAC[A/C]GCCCCTGAGAATGTA | 64127 |
rs143557663 | snp | C/T | 0.0310518 | 0.120672 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50712903 | AGAGACTTTAACACC[C/T]CAACCAGATGGGAAT | 64127 |
rs143684688 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NOD2 | GRCh38.p7 | 16:50722500 | CCAGTGAGGCCACTC[G/T]GGGATTGAGTGGTCC | 64127 |
rs143767182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706358 | GGACGCTATTGGGAC[A/G]TTTGTACAGGAGCAA | 64127 |
rs143782684 | snp | A/G | 1.67419e-05 | 0.00289321 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711985 | TGGGGCCTGCTGGCT[A/G]AGTGCCAGACATCTG | 64127 |
rs143794185 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NOD2 | GRCh38.p7 | 16:50716784 | GCTGTTTGCATGATG[C/G]GGGGTGCAGGTGATT | 64127 |
rs143885661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50714206 | GATTAGGGATGTCCC[C/T]GTGATTACCAGGGTG | 64127 |
rs143963486 | snp | C/G | 1.65403e-05 | 0.00287574 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712125 | GCATGCCATGCCCGG[C/G]TTCATCTGGCTCATC | 64127 |
rs144083291 | snp | C/T | 0.00100434 | 0.0223866 | synonymous-codon, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50716915 | CAACAAATTGACTGA[C/T]GGCTGTGCACACTCC | 64127 |
rs144184080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50705729 | ACACTGCATGGTTTT[C/T]AACTTTCTTGTTTTG | 64127 |
rs144204109 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NOD2 | GRCh38.p7 | 16:50703563 | AGAATCGCTTGAACC[C/T]GGGAGGCAGATGTTG | 64127 |
rs144368009 | snp | A/C/T | 6.66271e-05 | 0.00577146 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699944 | TGCCGATCTTCACAC[A/C/T]GTCCCAGAGGGTGAG | 64127 |
rs144368230 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50718424 | GGAGCTGGATGGCAC[A/G]TGATCAGAATAGCAT | 64127 |
rs144388393 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695968 | AAATGAAGAAGGGGA[C/G]TGTCAAGAGAGTGCT | 64127 |
rs144417308 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698197 | TGTCCACAGACCCCA[C/T]GACAATCGCAGAACT | 64127 |
rs144439629 | snp | C/G | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710940 | CATGGCCAAACCACT[C/G]TCTGTGCGGACTCTA | 64127 |
rs144468550 | snp | A/C/G | 0.000216281 | 0.0103969 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712092 | CCCGCCAGCTGCACC[A/C/G]GGTGAGGCCAAGAGC | 64127 |
rs144512258 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | NOD2 | GRCh38.p7 | 16:50704746 | TGGTCTTGAACTTCT[G/T]ACTTTAGGTGATCTG | 64127 |
rs144582983 | in-del | -/GTGT | 0.499989 | 0.00239614 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692572 | GTTGGGAAGTGAGGC[-/GTGT]GTGTGTTGGGAAGCG | 64127 |
rs144636959 | in-del | -/G | 0.105214 | 0.203807 | intron-variant | NOD2 | GRCh38.p7 | 16:50693941 | TGCCAGTGAGTGGGT[-/G]GGGTATAAGTGAGAG | 64127 |
rs144689141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50710411 | TCCTCAAAGTGCACA[A/G]CTTGTGAATGGAGGA | 64127 |
rs144708671 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709612 | TCACAGACTCTTGTT[C/T]GAGTGCTCAGCTGGG | 64127 |
rs144717883 | in-del | -/GT | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50693037 | GGGGGGAAGCAGGGC[-/GT]GTGTGTGTGTGTATG | 64127 |
rs144738371 | snp | A/G | 3.31461e-05 | 0.00407086 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710838 | CAAGAGCACGCTCCT[A/G]CAGCGGCTGCACTTG | 64127 |
rs144798502 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOD2 | GRCh38.p7 | 16:50714710 | CACAGGCTCCTCTCC[C/T]ACAGTGCCAACCTGC | 64127 |
rs144827713 | snp | A/G | 3.31274e-05 | 0.00406972 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711196 | ACCAGCCGTCCGGCC[A/G]CTGTGTCGGCGTTCC | 64127 |
rs144887729 | snp | A/G | 0.000823316 | 0.0202726 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707881 | GCTTGATCTTGCCAC[A/G]GTGAAAGCGAATGGA | 64127 |
rs144919013 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708482 | TGCTTTATGGACAAT[A/G]TCTACCCTTTGCAAC | 64127 |
rs144991170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715904 | CCTGGGCCCCACCCC[A/G]CAGATACTTGATTGC | 64127 |
rs144993105 | snp | C/T | 8.84369e-05 | 0.00664911 | synonymous-codon, intron-variant | NOD2 | GRCh38.p7 | 16:50697303 | AGCAAGTGTCCTCCT[C/T]GGACATTCTCCGGGT | 64127 |
rs145051635 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732565 | CACACTCCAGCTGGG[A/C]TCACATGTGGACTTT | 64127 |
rs145071209 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NOD2 | GRCh38.p7 | 16:50728075 | CTTCAAAATGACGAT[A/T]TTCTTGGTTTTCACT | 64127 |
rs145186019 | in-del | -/GT | 0.107341 | 0.205301 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50693274 | TGTGTGTGTGTGTGT[-/GT]ATGTGTATGTGTTGG | 64127 |
rs145190613 | snp | C/T | 0.000283307 | 0.0118985 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711514 | TCAGCTTCCCAAGGT[C/T]TGGGACCCAGTCTTC | 64127 |
rs145206030 | snp | C/T | 0.0349115 | 0.127424 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692234 | ACATTTACATTAACA[C/T]GTTAAATGGAAAACC | 64127 |
rs145244357 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOD2 | GRCh38.p7 | 16:50730876 | ACATCAAGGCTGCAG[C/T]GAATGCAGATATCAA | 64127 |
rs145293873 | snp | C/T | 0.000345927 | 0.013147 | NOD2 | 16 | allele_origin=T(unknown)/C(germline) | 16:50711028 | CTTGACCACCCTGAC[C/T]GTGTCCTGTTAACCT | 64127 |
rs145294952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50727390 | TAATTGTGGTTTCAG[A/G]CCATGAACTTTAAAT | 64127 |
rs145522024 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708362 | CTCAAGAACCAAGTG[G/T]ATCTAGAGACTCTGG | 64127 |
rs145685412 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698597 | TAGAGACATGCATTC[C/T]GGAGTCATACATGGC | 64127 |
rs145694647 | snp | A/G | | | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710655 | AGAGACGCTCTGCCT[A/G]GAGGACATATACACA | 64127 |
rs145719554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50694969 | CAACCAGGGAAGGCT[C/T]CCCCAAGACCACGAT | 64127 |
rs145786503 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 16:50706285 | TAGACAGGTATTTTT[A/G]TCTGTTTTGGGCCCT | 64127 |
rs145787795 | snp | A/C | 0.00557542 | 0.0525036 | | | GRCh38.p7 | 16:50704098 | AGTTCATGGTGAAGA[A/C]AAGTCAAATATAGAT | 64127 |
rs145816297 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732865 | CAAAGCAAATGTCTT[C/T]CTGGATTATTCAAAA | 64127 |
rs145834617 | snp | A/G/T | 0.000116004 | 0.00761519 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711204 | TCCGGCCGCTGTGTC[A/G/T]GCGTTCCTCAGGAAG | 64127 |
rs145891076 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708606 | TTGTAAATTGTCCCC[A/G]CCTACACTTTCTCTT | 64127 |
rs145984493 | in-del | -/GT | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692540 | TTTGGCTGTGTGTGC[-/GT]GTGTGTGTGTGTGTG | 64127 |
rs146004368 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707772 | GGAAGAGAGATGCTT[A/G]TGAAGTTGCAGTAAT | 64127 |
rs146054564 | snp | A/G | 0.0012728 | 0.0251948 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699874 | GTGGAGAACATGCTG[A/G]ACCTGGCATGGGAGC | 64127 |
rs146074127 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710750 | CCCTGGGCCTGGAGG[A/G]GCTCTTCAGCACCCC | 64127 |
rs146128859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50723220 | ACCAGGAGAGCACCA[C/T]GAATTTTGCCCTCCA | 64127 |
rs146149433 | snp | C/G | 1.65825e-05 | 0.00287941 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699614 | CCTGGGAGGTCCTCT[C/G]CTGGGAGGACTACGA | 64127 |
rs146162876 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50691689 | AGGTATTTACTTGAA[A/G]GCGGTATGGGGTAGT | 64127 |
rs146276010 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50719941 | CTGGGGAATAACTAC[A/C]TCACTGCCGCGGGAG | 64127 |
rs146313066 | snp | C/T | 4.97426e-05 | 0.00498686 | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50716648 | GAATGTGCTCTTCAC[C/T]GCGAGCAATTGCAGA | 64127 |
rs146395646 | snp | C/T | 0.000166152 | 0.00911308 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699794 | GCTGGGACCCCCACT[C/T]GCTCCACCCAGCCCG | 64127 |
rs146396987 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50717030 | GCCCCATTCCTGAGT[C/G]AGTCTGATCTGGTCT | 64127 |
rs146435555 | snp | C/T | 4.94507e-05 | 0.00497221 | missense | NOD2 | GRCh38.p7 | 16:50731748 | TTGATCTGCTTTAGG[C/T]TCCGAGGGAACACTT | 64127 |
rs146458676 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712140 | GTTCATCTGGCTCAT[C/G]CGGAGCCTGTACGAG | 64127 |
rs146529290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50702218 | GGATTACAGGCATGA[A/G]CCACTGCGCCCATCT | 64127 |
rs146540577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50705949 | GGAAGGAAATTACAG[C/T]GTGTGCTAGAAGGTG | 64127 |
rs146658210 | snp | C/G/T | 0.00422069 | 0.0457484 | intron-variant | NOD2 | GRCh38.p7 | 16:50719730 | CCCGCTGCCCCTTTC[C/G/T]CTTTGCTGGGGGAAA | 64127 |
rs146684845 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715576 | GCCTGCCACCACGCC[C/T]GGCTAATTTTTTTGT | 64127 |
rs146912653 | snp | A/C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706944 | CTTAGGGGATCTACC[A/C/T]GCCTTGGCCTCCCAA | 64127 |
rs146923251 | snp | C/T | 8.2848e-05 | 0.00643561 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699687 | GCGCCTTCTGGACAC[C/T]GTCTGGAATAAGGGT | 64127 |
rs147017626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50721150 | TATGTTGCTCTAGAA[A/G]TCAACATCTTTTCCA | 64127 |
rs147154782 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NOD2 | GRCh38.p7 | 16:50700911 | TATAACAGCCCCTGA[A/G]AATGTAGTAACTCAG | 64127 |
rs147177623 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697821 | CGTTCTGAGAGATTG[C/G]AGCTTTCTCCTTTTG | 64127 |
rs147227748 | in-del | -/TATT | 0.0337553 | 0.125452 | intron-variant | NOD2 | GRCh38.p7 | 16:50721278 | ACCTCTTTCAACACA[-/TATT]TATTAGGGCACCTGT | 64127 |
rs147260064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50714329 | GTGTGTAAAGGCACT[C/T]GTGGCAATGCAGATT | 64127 |
rs147283871 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711079 | AAGTTCAGGTTCACG[A/G]ATCGTGAACGCCACT | 64127 |
rs147389278 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOD2 | GRCh38.p7 | 16:50730803 | CCTTTGGCAACTCAT[C/T]CCCATAAGCCTGTGA | 64127 |
rs147417132 | snp | C/T | 6.67078e-05 | 0.0057749 | stop-gained, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711508 | CCAGACTCAGCTTCC[C/T]AAGGTCTGGGACCCA | 64127 |
rs147609425 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692247 | CATGTTAAATGGAAA[A/G]CCGGTGTCATTTGCT | 64127 |
rs147631943 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NOD2 | GRCh38.p7 | 16:50730960 | TCCTAGCACTTTGGG[A/T]GGCTGAGGCAGGAGG | 64127 |
rs147642146 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50727762 | TCTGTTGACGAATGC[C/T]GGCTGCAGGTGTTGC | 64127 |
rs147735728 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706673 | AATATGAAAGAAAGA[A/T]TGAAACGTACCTTGC | 64127 |
rs147750423 | snp | A/C/G | 1.6477e-05 | 0.00287024 | missense | NOD2 | GRCh38.p7 | 16:50729829 | CCAGGTTGTCCAATA[A/C/G]CTGCATCACCTACCT | 64127 |
rs147818479 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NOD2 | GRCh38.p7 | 16:50726916 | GAGGCTGAGGCGGGT[A/G]GATCACCTGAAGTGG | 64127 |
rs147874812 | snp | A/G | 0.000280128 | 0.0118316 | missense | NOD2 | GRCh38.p7 | 16:50731790 | GAGGTTGACAAGCTC[A/G]GCTGCAGGGACACCA | 64127 |
rs147979215 | in-del | -/GT | 0.0368353 | 0.130617 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692718 | TGTGTGTGGGGTGTG[-/GT]GTGTGTGTGTTGGGA | 64127 |
rs147998582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709153 | GATATGTACTGGAGA[C/G]GAAGATATCTATCTT | 64127 |
rs148169898 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NOD2 | GRCh38.p7 | 16:50729165 | ACTGTAATGAGAACA[A/G]GATGGGATTCAATTA | 64127 |
rs148191280 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50733529 | CAGCTGTGCAGGAGC[A/C]TCCCCGTACCCAGCC | 64127 |
rs148377539 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696613 | ATAATGATTAACTTC[C/T]CAAGCTGGTGAGCTT | 64127 |
rs148452508 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50704809 | AGGCGTGAGCCACCA[A/C]ACCCAGCCTCCAAAA | 64127 |
rs148516118 | snp | C/T | 6.5999e-05 | 0.00574414 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710645 | ATGATGGAGCAGAGA[C/T]GCTCTGCCTGGAGGA | 64127 |
rs148526508 | snp | A/G | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710840 | AGAGCACGCTCCTGC[A/G]GCGGCTGCACTTGCT | 64127 |
rs148561632 | snp | A/G | 0.000397364 | 0.0140899 | missense | NOD2 | GRCh38.p7 | 16:50725532 | GGTGTATGTTCTCTC[A/G]CAGAAGGACTGAAGA | 64127 |
rs148567369 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOD2 | GRCh38.p7 | 16:50714950 | TTCACAAAATGACTT[C/T]GCTTTATGAACTCTG | 64127 |
rs148642485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50726425 | TGCTACCCACTCTGG[C/T]GACACTCATTTGTGT | 64127 |
rs148683734 | snp | A/G | 0.000282301 | 0.0118773 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711685 | CGTGCCAAAGGTGTC[A/G]TGCCAGGGAGTACGG | 64127 |
rs148716069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708038 | AGCAGAACACACCTC[A/G]GTTAACATCCCATAT | 64127 |
rs148753593 | snp | A/T | 0.000198505 | 0.00996057 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699878 | AGAACATGCTGGACC[A/T]GGCATGGGAGCGGGG | 64127 |
rs148811839 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708804 | AAGCAAGCCTGTGGG[C/T]GGGGTGGCTGGAAGT | 64127 |
rs148906342 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698434 | AGGCACCAGAACGCT[C/T]GGAAACAACTTAGTT | 64127 |
rs148941214 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NOD2 | GRCh38.p7 | 16:50721818 | TTTCAAAGAGCTGCA[A/G]AGTGTTACATAATGT | 64127 |
rs148968521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706312 | CCCTGAAGGTTACTA[C/T]TGGACTTGGACTCTT | 64127 |
rs149002807 | snp | G/T | 0.000936361 | 0.0216172 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711957 | CCTGGCAGGGCTGTT[G/T]TCCCGGGAGCACTGG | 64127 |
rs149071116 | snp | C/T | 9.88338e-05 | 0.00702902 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707889 | TTGCCACGGTGAAAG[C/T]GAATGGATTGGCTGC | 64127 |
rs149096966 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50716187 | TGATGGTAAATTGTC[C/T]CCAGGGGTAGCCTGT | 64127 |
rs149117350 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NOD2 | GRCh38.p7 | 16:50731042 | AAATTCAGCTGGGTG[C/T]GGTGTAGTTCCTAGC | 64127 |
rs149122717 | snp | C/T | 0.000538068 | 0.0163934 | missense, intron-variant | NOD2 | GRCh38.p7 | 16:50697314 | TCCTCGGACATTCTC[C/T]GGGTAAGAGGAGCAG | 64127 |
rs149158606 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOD2 | GRCh38.p7 | 16:50728058 | AATAAGAGAAGATGA[C/T]ACTTCAAAATGACGA | 64127 |
rs149264907 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50704332 | ACATTTTGCTAGACC[A/G]TATCCTCCAGTCAAT | 64127 |
rs149338478 | snp | C/T | 0.000348325 | 0.0131925 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710786 | ACCTCAATGACGATG[C/T]GGACACTGTGCTGGT | 64127 |
rs149340820 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50710390 | GTTAGGAAGTTTCCT[C/T]GACTGTCCTCAAAGT | 64127 |
rs149390911 | snp | C/T | 0.000481964 | 0.0155161 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699788 | ATGGCTGCTGGGACC[C/T]CCACTCGCTCCACCC | 64127 |
rs149425221 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699204 | TAATATTACCTCAAG[C/T]CTTTTTAAACGTTTT | 64127 |
rs149615228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50718355 | ATTACCAAATGGGAG[C/G]GTATAGAGCGTGGAT | 64127 |
rs149678585 | snp | C/G | 0.0130921 | 0.0798413 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50691799 | TGGGGAGGCCCCTGG[C/G]AGGAGTGAGAAGTCC | 64127 |
rs149691662 | snp | A/G | 1.6937e-05 | 0.00291002 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50723304 | GATTACCTCCAGCCT[A/G]GTGGGGAACAACATT | 64127 |
rs149796343 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706056 | AATAGAGTAGTCAGA[A/G]TTCTCACTTAGAAGG | 64127 |
rs149870902 | snp | C/T | 0.000280456 | 0.0118385 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711750 | CTTCTTTGCCGCGTT[C/T]TACCTGGCACTCAGT | 64127 |
rs149879666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50724804 | CTATAGAGGTTTAAA[C/T]AAGGAAAGGGTTTAT | 64127 |
rs149939201 | snp | A/G | 8.76309e-05 | 0.00661874 | synonymous-codon, intron-variant | NOD2 | GRCh38.p7 | 16:50697279 | AGCCTCTCACGATGA[A/G]GAGGAAAGAGCAAGT | 64127 |
rs149952929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50701796 | AAGAAGAAATCATGA[C/T]GGAAATCAGAAAATA | 64127 |
rs150039378 | in-del | -/GT | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50693226 | AGCGGTGTGTGTGTG[-/GT]GTGTGTGTGTGCGCG | 64127 |
rs150078153 | snp | C/T | 0.000214307 | 0.0103493 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711101 | AACGCCACTGCTCCC[C/T]GACCGACCCCACCTC | 64127 |
rs150143485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50720867 | TAGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 64127 |
rs150176843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713725 | GAAGGGGGAAGGGGA[A/G]GGAGACTAATTAGCT | 64127 |
rs150194835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50694212 | CCCCTGGGGAGGACC[G/T]CCTGAAGCTGCATGA | 64127 |
rs150236752 | snp | A/G | 6.64055e-05 | 0.0057618 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711880 | TCGGAGGGAAAGGAC[A/G]GCAGCGTGGCAGCTT | 64127 |
rs150247629 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699073 | GCTGGGATTACAGGC[A/G]CTCGCCACCACGCCT | 64127 |
rs150323147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707245 | TTGGCAGATTACAGA[C/T]GAGAGGCTTCAAGGG | 64127 |
rs150330370 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715763 | AATAACTAGTAAGTC[A/G]CTGATCAGGATCACA | 64127 |
rs150406622 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50727916 | TTTGGTGCGAATTTG[A/C]CTTTGGGAAGTGCTT | 64127 |
rs150482606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50704059 | AGCTGACTGAGGCAG[C/T]GGGAGTTGAAAAGAA | 64127 |
rs150515706 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50729628 | TGAATGGAAGAGAGA[C/T]GGTTACATTTCACTG | 64127 |
rs150861979 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NOD2 | GRCh38.p7 | 16:50717432 | TGCATTTCTGCTACT[C/G]CAGTGTCTCCCAGTT | 64127 |
rs150970652 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50720351 | GCCTCCCACCCCAGA[C/T]TGATGAAATGCAAAT | 64127 |
rs150996156 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699890 | ACCTGGCATGGGAGC[A/G]GGGTTTCGTCAGCCA | 64127 |
rs151031891 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | NOD2 | GRCh38.p7 | 16:50731614 | CAGCCCTGACTTCCC[G/T]GCAAGAAACACTGCA | 64127 |
rs151040672 | in-del | -/TGTG | | | intron-variant | NOD2 | GRCh38.p7 | 16:50714603 | TTGCTGTGAGTGCAC[-/TGTG]TGTGTGTGTGTGTGT | 64127 |
rs151234925 | snp | C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50693682 | GTGCTGTGCCCAGCG[C/G]CTGGGGGTGGGCTGG | 64127 |
rs151241829 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698537 | CAGTGTGCAAAACAC[A/G]CAGCACGGGCTTGGG | 64127 |
rs151315883 | snp | C/T | 0.000132868 | 0.00814963 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711237 | CATCCGCACCGAGTT[C/T]AACCTCAAGGGCTTC | 64127 |
rs180755544 | snp | C/T | 2.8458e-05 | 0.00377203 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697395 | GACATGCTCCCAGGC[C/T]TGGGGTCAGATGGGG | 64127 |
rs180983780 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NOD2 | GRCh38.p7 | 16:50714802 | ATACACAGTGCCCCT[A/G]TATAGGTTTCTTTAG | 64127 |
rs181004830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50704967 | ACTTCTCTATGTTTT[C/G]GGAAATGTTCTTGAT | 64127 |
rs181025534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50727616 | AGATTCTTGAAGAAA[A/T]GGTAGTCAGTTGGCT | 64127 |
rs181216641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709697 | ATCATCTCCCCATCT[C/T]GAAGTTTAACTTTAT | 64127 |
rs181248152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50716339 | TCATTTCCTAAGGAT[C/T]CCAGGGTTCTTTAGT | 64127 |
rs181255947 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698333 | ATGATAGCAGTGGCA[A/G]CAGTCTGTGCACGGT | 64127 |
rs181256415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50722200 | GCAGGAGATAAAGAG[A/C]TAGCTTGCAGAAGAA | 64127 |
rs181311321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50704313 | TCTTCTTCCCTGGTT[A/T]ACTACATTTTGCTAG | 64127 |
rs181339032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50701495 | GGTATTTACAGAGCA[A/G]AAGTGGTGCAGTCCT | 64127 |
rs181363812 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50733389 | ATTTTCTACTTGAAG[C/T]GGAGGAAAATGATGT | 64127 |
rs181629522 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50722156 | AGTTGAAGCTGATGG[C/T]GTGAAGGAATTAGGG | 64127 |
rs181635751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50700671 | CTTAGGATAGTGTCT[A/G]TTACCACTGGCTGCT | 64127 |
rs181947344 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692319 | AACAAAAACAATGCT[A/G]TTAAAGCTAATTAGA | 64127 |
rs181977800 | snp | C/T | 0.000115845 | 0.00760981 | intron-variant | NOD2 | GRCh38.p7 | 16:50710509 | TGTCTGGTTAGGTCC[C/T]GTCTTCACCATGGTG | 64127 |
rs182095235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715202 | TTGGCAAAGTCACTT[C/T]GCTTGTCTGTGCCTC | 64127 |
rs182333666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50730243 | CTTCACAGGTCAAGG[A/G]TATTGGATCAGACCT | 64127 |
rs182345605 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697741 | CCAAGCAGCCAGACA[C/G]ACAAGTAACCTCATT | 64127 |
rs182384245 | snp | A/G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695163 | GAATGGATCATGGGG[A/G/T]GGGTGGGGTAAGGGC | 64127 |
rs182431042 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NOD2 | GRCh38.p7 | 16:50721307 | CCTGTCTGGGCCAGG[C/T]GTTGTGCTAAAACCC | 64127 |
rs182712299 | snp | A/C | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698862 | CAGCATGAAAGAGCC[A/C]CTCTCACCCTGCTTC | 64127 |
rs183104943 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50705886 | GACAAAAATCTTTGT[C/G/T]TTGGAAATACACACA | 64127 |
rs183145280 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50702739 | TTATTTAAGCCTCAC[A/C]AGGGTATAGTGTGAC | 64127 |
rs183183447 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50724241 | AAACAGATTTTATGG[A/G]TGGACCTTGGCTGTT | 64127 |
rs183220464 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50728243 | CATTGTCAGCTTCTG[A/T]TGGCCTGCCAGTACA | 64127 |
rs183350453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50705682 | GTCCCTCATGCTGAT[C/T]ATTCCAGAGCCCTTT | 64127 |
rs183357209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50729495 | TGGGACTAATTTGCT[C/T]GAGATCAAAAAAGAA | 64127 |
rs183358340 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50712636 | TACAACCACCCTGGC[G/T]GGTAGGCAGGAATGT | 64127 |
rs183539461 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50694025 | TGCCTCCTCCTTCTC[C/T]CTTGTTGGGTGTGAG | 64127 |
rs183563307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50703608 | CGCACTGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 64127 |
rs183640762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50717968 | TGCTTTTCCCAATAC[C/G]TACACACCTGCAATA | 64127 |
rs183866622 | snp | C/T | 0.0221141 | 0.102801 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699129 | GACAGCGTTTCACCG[C/T]GTTGGCCGGGCTGGT | 64127 |
rs183940420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50701720 | GCCCAGAGAAGACAG[A/G]ATGTGAACAGAGGAA | 64127 |
rs183985819 | snp | G/T | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692741 | GTGGTGTGTGTGTGG[G/T]GTGTGTGTATGTGCA | 64127 |
rs183996226 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50714562 | AAAACTGCCAAGGCC[A/G]TAGGGGAGGGGAAGC | 64127 |
rs184004210 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697094 | TGGTTGGCCAACTCT[A/G]GCCTCCGGCTTTTCC | 64127 |
rs184101811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50722805 | ACTTTATTTCTACCC[C/T]ACAATGTTAGGCAAT | 64127 |
rs184148848 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695874 | GGAATGGGAGGGGAT[A/G]GGAGGACTTGGGGAC | 64127 |
rs184266356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50714855 | GAGTGATGGCTTTAA[A/G]AGTTTTTTGAATGTT | 64127 |
rs184374878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50725230 | TGAAATGAGACTTCC[A/G]TTAATAAGGAAGAAA | 64127 |
rs184492197 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50726360 | ACGCTTGCCTTTAGA[A/G]ACAGACAGACAGACA | 64127 |
rs184502667 | snp | A/C/T | | | synonymous-codon, missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699826 | GACCTGCAGAGTCAC[A/C/T]GGCCAGCCATTGTCA | 64127 |
rs184505299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50703919 | ATTAGGTGCTGTGTC[C/T]GGAGGAAAATGGCCA | 64127 |
rs184545855 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50731908 | ATGTGTTGGCAGCCT[C/T]TTCAAAATGAGCCCT | 64127 |
rs184551304 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708788 | GTGTCCTCTGGGCAG[C/G]AAGCAAGCCTGTGGG | 64127 |
rs184585895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50700140 | CAACTCTTTCTTTCT[C/T]CTTTTCTTTTCTTTT | 64127 |
rs184591129 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50724364 | GAGAGCATCAGTTAT[G/T]ATTACTGTTAAAAGA | 64127 |
rs184673983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50720536 | TCTTGCTCCCTGTAG[G/T]ACCATGCTAGGGCCT | 64127 |
rs185076904 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709263 | ACATAAACACAGGGC[A/G]TCCCCTTTGTGTGAC | 64127 |
rs185245868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50705302 | TCTTTGTTTGTTTGT[C/T]TGACTGTTTTTCACC | 64127 |
rs185282880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50728008 | TCATCGCACGTCACA[A/G]TCAGATCAAGAAATG | 64127 |
rs185331963 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696837 | GTCACGTGGCTTGGG[C/T]GGGCCTCCCCTTCCT | 64127 |
rs185333424 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50733503 | AGAAAAGTTTAACCC[C/T]GTGAAGTTTTCAGCT | 64127 |
rs185362389 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698654 | TCTAGCTGTGACACA[C/T]CGTACAAATCACTTA | 64127 |
rs185442358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713729 | GGGGAAGGGGAGGGA[C/G]ACTAATTAGCTGGGG | 64127 |
rs185488643 | snp | C/T | 0.00241344 | 0.0346539 | intron-variant | NOD2 | GRCh38.p7 | 16:50710030 | AGGTGTGTCTGGCTT[C/T]AGAGACTGGGCTCCT | 64127 |
rs185799967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50722157 | GTTGAAGCTGATGGC[G/T]TGAAGGAATTAGGGG | 64127 |
rs185809098 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50701028 | AGAGGCAGATGGAAC[A/G]ATCATTAACATTCCA | 64127 |
rs185966486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50701527 | TCTGATTAGTTGCAC[A/G]TACAGAAGACATATT | 64127 |
rs185988710 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697601 | CTCTTCCCCTGTCCT[C/T]GGCCACCCCACCCTC | 64127 |
rs186089527 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NOD2 | GRCh38.p7 | 16:50722391 | TCTACTATTCTCTAA[G/T]TCTGTAATGTAAAGC | 64127 |
rs186095479 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50705883 | ACAGACAAAAATCTT[A/T]GTCTTGGAAATACAC | 64127 |
rs186135087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50728289 | GCTCTTATCTCCTTC[A/G]CAAAACTTCTTGAAC | 64127 |
rs186204675 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50726751 | CCTAAACTATATCAT[A/C]CCCCACAAAAATTGA | 64127 |
rs186364089 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50704425 | ATACTGGATTGATAG[A/T]TTGGCTGGGTATAAA | 64127 |
rs186638353 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NOD2 | GRCh38.p7 | 16:50730420 | GACTAGCCTTGGGAG[G/T]CTGGGCAGCTGGGTC | 64127 |
rs186642294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708164 | GCGTGTAATGTTAGC[C/T]ATTAGCTTTCATTAT | 64127 |
rs186695824 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695313 | TTCAAAGGCCGTGTC[A/G]ATAGGGTTTGGGGTG | 64127 |
rs186719861 | snp | C/T | 0.000133136 | 0.00815783 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711267 | CTCTGAACAGGGCAT[C/T]GAGCTGTACCTGAGG | 64127 |
rs186780800 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697874 | GACGGATACAGAGTG[A/T]TCCCCCCACCCCCAG | 64127 |
rs186889410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50694575 | GAGCCCCTCTGTGAC[A/C]CATGCCCAGTGGTGG | 64127 |
rs186985425 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715326 | TAGTGATCAGTGCTA[A/G]CGATCATGATTCTAG | 64127 |
rs187041894 | snp | G/T | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692629 | TGTGTTGGGAAGTGG[G/T]GTGTGTGTATATTGG | 64127 |
rs187264529 | snp | A/G/T | 0.00031479 | 0.0125421 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699688 | CGCCTTCTGGACACC[A/G/T]TCTGGAATAAGGGTA | 64127 |
rs187308148 | snp | A/C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50720274 | TGATCCTCAGGGGGC[A/C/G]CTAGGGCTGTACTTT | 64127 |
rs187478122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50702969 | GTAATACCAGCTGTC[C/T]GTCTGACTCATGCAA | 64127 |
rs187513655 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50724262 | CTTGGCTGTTGCAGG[A/G]CTTACTAGCTCTACT | 64127 |
rs187540953 | snp | A/G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699150 | CCGGGCTGGTCTAGC[A/G/T]CTCCTGATCTCAAGT | 64127 |
rs187560298 | snp | A/C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50717346 | CCCAGCTGTGGCAGC[A/C/G]AGTTGCTGCAACACT | 64127 |
rs187656790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50703519 | TGGCATGTGCCTGTA[A/G]TCCCAGCTACTCGGG | 64127 |
rs187777065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50702057 | CTGAAGTGATCCTCC[C/T]GCCTCAGCCTTCCAA | 64127 |
rs187831680 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699078 | GATTACAGGCGCTCG[A/C]CACCACGCCTGGCTA | 64127 |
rs187929610 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50724458 | CAGCATTCAGAACTG[A/G]GAGTGCTCCACCCAG | 64127 |
rs188014793 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50723209 | AAATGGAGCAGACCA[C/G]GAGAGCACCACGAAT | 64127 |
rs188089251 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NOD2 | GRCh38.p7 | 16:50710188 | CCAGAGCCCCTTCCC[A/G]TCATCTAGAACTCCT | 64127 |
rs188090012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50729683 | GCTCATTGGGAATCT[C/T]AGACATGAGCAGGAT | 64127 |
rs188099195 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692270 | CATTTGCTCCGGAGA[A/C]CAGAAGAATGTAAAA | 64127 |
rs188131383 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50733504 | GAAAAGTTTAACCCC[A/G]TGAAGTTTTCAGCTG | 64127 |
rs188341692 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NOD2 | GRCh38.p7 | 16:50697191 | GCTTTTGGCGTTCTG[C/T]ACAAGGCCTACCCGC | 64127 |
rs188379009 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOD2 | GRCh38.p7 | 16:50714593 | AACCATGAGGTTGCT[A/G]TGAGTGCACTGTGTG | 64127 |
rs188384574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706900 | ATGGGGTTTCACCAT[G/T]TTGTCCAGGCTGGTC | 64127 |
rs188686605 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50718015 | TTAGGCACAGTAAGA[C/G]AGTAATAGCAACTCA | 64127 |
rs188746777 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50726555 | TGTCTGAGCCAGATG[C/T]CAGCTTTGCACTGAG | 64127 |
rs188892430 | snp | A/C/G | 0.00993419 | 0.0697739 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696139 | CACTTGGGAAGTTGA[A/C/G]CTTCCCTGGGCTTCC | 64127 |
rs188988267 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732285 | TCCCCATGTCTCGAC[A/T]CATCCATCCAGGCCA | 64127 |
rs188993260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50720936 | CAGCTTCTCAAGTAG[C/T]TGGGATTATAGGCAC | 64127 |
rs189020179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50721840 | ACATAATGTATTTAA[C/T]TGGTCACTTTTTGAT | 64127 |
rs189031685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50700605 | TAATAGTCAAATGGT[A/G]CCTATCCTATAAGGC | 64127 |
rs189163488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50713027 | CCGTATTGCTTAGAG[C/T]CCCAGCCAAAGATGT | 64127 |
rs189257007 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOD2 | GRCh38.p7 | 16:50704522 | ATATTGCTTCTAAGA[A/G]TTCCAAAACCTTTTT | 64127 |
rs189453919 | snp | A/G | 6.62252e-05 | 0.00575397 | missense | NOD2 | GRCh38.p7 | 16:50725503 | GCCTGGAGGAGAACC[A/G]TCTCCAGGATGAAGG | 64127 |
rs189463614 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50703748 | AAGGTTCCCAAGGCA[A/G]GGAAAGCTAAGTGGA | 64127 |
rs189768472 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50733379 | TTAAAGCACAATTTT[C/T]TACTTGAAGCGGAGG | 64127 |
rs189769053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50727106 | GATCACACCATTGCA[A/C]CCTAGACTGGACAAG | 64127 |
rs189967877 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713936 | GGACGGGTAGAGAAG[C/G/T]GGGAGAGTGGATCTG | 64127 |
rs189973750 | snp | A/G | | | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709680 | CACCCAGATCAATCA[A/G]GATCATCTCCCCATC | 64127 |
rs190017853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50716729 | GTCTCACCCCAGGTC[A/G]TGCAGCCTGGGAAGC | 64127 |
rs190026427 | snp | C/G | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698792 | GGCACTTGGTGTGTA[C/G]TTTATGCTTAATTAA | 64127 |
rs190047263 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708964 | TCATCAAGCACAGCT[A/C]GTCACTGTAAGACCA | 64127 |
rs190057349 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50704096 | TTAGTTCATGGTGAA[A/G]ACAAGTCAAATATAG | 64127 |
rs190253946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50694915 | AAAGCTGGGAAGCAG[A/G]ATGGGGTGCTGGGGC | 64127 |
rs190262090 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50722178 | GAATTAGGGGTGTTA[A/G]GAAGAAGCAGGAGAT | 64127 |
rs190268820 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50701246 | AGCTTTGCACACGGT[A/G]GGTACTCCATAAACA | 64127 |
rs190342161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715344 | ATCATGATTCTAGGT[A/G]ACTTTTACTGTGTAC | 64127 |
rs190350266 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698311 | CAGAACGCACAGCAG[A/G]TCACTGATGATAGCA | 64127 |
rs190512896 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697635 | GCTCCTCTGCTTAGA[G/T]GTGGGCACAAGGAGG | 64127 |
rs190807316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715101 | GCCATAAGAGGCCCT[G/T]AGGGAGAAGCTGCAC | 64127 |
rs190870639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50701578 | TTTCTCTTATAATTT[A/G]TTAGGGGAATTGAAT | 64127 |
rs190942390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50702301 | CAGCAAAAGCAAACA[C/T]TGAAGGTTGGGACTG | 64127 |
rs190982294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50723573 | CCTGGTATGTACATG[C/T]TAATTTTTTTATTTA | 64127 |
rs191152954 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695642 | GTCTAACCATTGAGT[G/T]CTGGGGCCCCCAGTG | 64127 |
rs191188883 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50705397 | TAGATGCTTTCTCTG[A/G]GCTCATGATACTCTT | 64127 |
rs191224013 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50728202 | AGTTGTAAGAAAATC[A/C]GCTTTGATGATTGCT | 64127 |
rs191443913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50728673 | GGCATTGCCTTAGGG[C/T]CAACTTGTAAGACAT | 64127 |
rs191709420 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50705884 | CAGACAAAAATCTTT[G/T]TCTTGGAAATACACA | 64127 |
rs191757515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50720387 | GGTGCAAGGCCCAGG[C/T]ATCAGGAGTTTTAAA | 64127 |
rs191781908 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50714516 | TTACTGTCCTTGAGC[A/G]AGTTTTACTGCTCTT | 64127 |
rs191791166 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697038 | CAGGATGCACAAGGC[G/T]TTGTGCCAGAATTGC | 64127 |
rs191797196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50724263 | TTGGCTGTTGCAGGG[A/C]TTACTAGCTCTACTC | 64127 |
rs191901394 | snp | C/T | 0.000215308 | 0.0103734 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710831 | GCAGTGGCAAGAGCA[C/T]GCTCCTGCAGCGGCT | 64127 |
rs191958826 | snp | G/T | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50693128 | AAGCATGTTTGTGTG[G/T]GGGGGGAAGCGAGGG | 64127 |
rs192014376 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699337 | TCTCAATTTTCACAT[C/G]TATATGGTGGGGAGC | 64127 |
rs192049619 | snp | C/T | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692671 | GTGTGTGTTGGGAAG[C/T]GGTGTGTGTGTTGGG | 64127 |
rs192054785 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50718708 | AGGTAATAACCCTGG[A/C]TACCTCACAGGCTGT | 64127 |
rs192123676 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699119 | TTTTAGTAGAGACAG[C/T]GTTTCACCGTGTTGG | 64127 |
rs192210471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50724707 | TTGCAGTTTGCTACA[C/T]AGGAACTCAAAGTAC | 64127 |
rs192451626 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50725998 | GCACTGATTCTCCAG[C/T]ACTTCCAGCTCACCC | 64127 |
rs192492726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50717571 | CCTCCTGTGATTTGT[A/G]AGGCAGTAAAAAAAG | 64127 |
rs192508483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708372 | AAGTGGATCTAGAGA[C/T]TCTGGTATCCCTCAG | 64127 |
rs192626903 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NOD2 | GRCh38.p7 | 16:50703531 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 64127 |
rs192663765 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707257 | AGACGAGAGGCTTCA[A/G]GGGTGACTCCAAGAC | 64127 |
rs192792151 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOD2 | GRCh38.p7 | 16:50702972 | ATACCAGCTGTCCGT[C/G]TGACTCATGCAACTG | 64127 |
rs192842874 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732809 | TAGGATGTACAGTTA[C/T]GGATTGAAAGTTTAC | 64127 |
rs192882135 | snp | A/G | 0.000104252 | 0.00721907 | intron-variant | NOD2 | GRCh38.p7 | 16:50729936 | CTGTTTTAGCTCTCC[A/G]AACCTCAGTTTTTCT | 64127 |
rs193051767 | snp | A/G | | | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709018 | ACTTCTAAAGGTGAC[A/G]ATTGGTGTGTTTATT | 64127 |
rs193068786 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713697 | TTAGTAACAGCTGGG[A/G]GAGGGTAGACTTGAA | 64127 |
rs193238729 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696819 | GGGAGGACAGAGCTC[C/T]GAGTCACGTGGCTTG | 64127 |
rs199475906 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696420 | TAGTAACTGAAGTAG[A/G]GATCAAAAGGCAATG | 64127 |
rs199475907 | snp | A/C | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696869 | GTGTCCACAGAAGCC[A/C]AACGTCACTAGCTGG | 64127 |
rs199475908 | snp | C/T | 0.00119737 | 0.0244387 | NOD2 | 16 | allele_origin=T(germline)/C(germline) | 16:50697082 | GTTCTGGAAGGCTGG[C/T]TGGCCAACTCTGGCC | 64127 |
rs199475909 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697100 | GCCAACTCTGGCCTC[C/T]GGCTTTTCCTTTGGG | 64127 |
rs199475910 | snp | C/G | | | utr-variant-5-prime, intron-variant | NOD2 | GRCh38.p7 | 16:50697153 | GGTAGACAGATCCAG[C/G]CTCACCAGTCCTGTG | 64127 |
rs199475911 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697467 | GTCGGCGGGTTTTTT[C/T]CCCCAGGACCTGGGC | 64127 |
rs199475912 | snp | C/T | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710942 | TGGCCAAACCACTCT[C/T]TGTGCGGACTCTACT | 64127 |
rs199475913 | snp | A/G | 4.95798e-05 | 0.0049787 | NOD2 | 16 | allele_origin=G(germline)/A(germline) | 16:50711170 | TGCTGAAGAATGCCC[A/G]CAAGGTGGTGACCAG | 64127 |
rs199475914 | snp | A/G/T | 0.000183651 | 0.00958114 | NOD2 | 16 | allele_origin=G(germline)/A(germline) | 16:50711915 | GCAGAAGGCCGAGCC[A/G/T]CACAACCTTCAGATC | 64127 |
rs199475915 | snp | A/G | 1.65493e-05 | 0.00287652 | NOD2 | 16 | allele_origin=G(germline)/A(germline) | 16:50712173 | GCAGGAGGAGCGGCT[A/G]GCTCGGAAGGCTGCA | 64127 |
rs199475916 | snp | C/G/T | 9.91087e-05 | 0.00703886 | NOD2 | 16 | allele_origin=G(germline)/C(germline) | 16:50712329 | TGTGGGTGACATTGG[C/G/T]GTGGAGCAGCTGCTG | 64127 |
rs199475917 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50712572 | TTTATTGACTGGCCT[A/G]TGTGCTGGGTCTGGT | 64127 |
rs199475918 | snp | A/G | 0.000798403 | 0.0199641 | NOD2 | 16 | allele_origin=G(germline)/A(germline) | 16:50712591 | GCTGGGTCTGGTGCT[A/G]TGCTTTCCGGAATGA | 64127 |
rs199475919 | snp | A/G | 1.66918e-05 | 0.00288888 | NOD2 | 16 | allele_origin=G(germline)/A(germline) | 16:50716698 | GGGCTGTGGACAATG[A/G]GCTCCAAGTGCCCTG | 64127 |
rs199475920 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50716850 | TGCTCACTGTCCAAT[A/G]TGCTTTGCTTCTGTG | 64127 |
rs199475921 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50719609 | TGAGACCAGAGGGAA[A/G]GGTGTGACCCTGAGT | 64127 |
rs199475922 | snp | A/G | 0.000798403 | 0.0199641 | NOD2 | 16 | allele_origin=G(germline)/A(germline) | 16:50722853 | CCATTGGATTTCAAG[A/G]GAGGACACTCGAGTC | 64127 |
rs199475923 | snp | A/C/G | 8.24795e-05 | 0.00642135 | NOD2 | 16 | allele_origin=G(germline)/A(germline) | 16:50731827 | TGCTTTGAAGTCTCC[A/C/G]GGAGGATGTTCGTCT | 64127 |
rs199475924 | snp | C/T | 0.000399281 | 0.0141238 | NOD2 | 16 | allele_origin=T(germline)/C(germline) | 16:50731899 | CTGGGTGACATGTGT[C/T]GGCAGCCTCTTCAAA | 64127 |
rs199475925 | snp | C/T | | | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732011 | CAGTGCCCTCCAGGA[C/T]AGACTTTTCCCAAGC | 64127 |
rs199475926 | snp | A/C/T | | | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732033 | TTCCCAAGCCTACTT[A/C/T]TGCCATTGACTTCTT | 64127 |
rs199525467 | snp | C/G | 0.000642509 | 0.0179121 | intron-variant | NOD2 | GRCh38.p7 | 16:50729802 | TTGAAGCTCACCATT[C/G]TATCTTCTTTTCCAG | 64127 |
rs199544441 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50699467 | GGAGAAGTCCCGCAC[C/G/T]GACCTTGTTCTCCTC | 64127 |
rs199552944 | snp | C/T | 3.30115e-05 | 0.00406259 | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50719993 | TCCGAGGCAACACCT[C/T]CTTGCAGTTCCTGGG | 64127 |
rs199581219 | in-del | -/AAA | | | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715723 | CCCGGCCTGTTCCCT[-/AAA]CTTTTATAGATGAAG | 64127 |
rs199770660 | snp | A/G | 1.65288e-05 | 0.00287474 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711832 | GGCAACTCACCAATG[A/G]CCAGGCTCCTGCCCA | 64127 |
rs199826939 | in-del | -/TTTG | 0.0256215 | 0.110247 | intron-variant | NOD2 | GRCh38.p7 | 16:50705289 | AAGATAGGTGGGTTC[-/TTTG]TTTGTTTGTTTGACT | 64127 |
rs199858111 | snp | C/T | 0.00026357 | 0.0114767 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711019 | CAGTTACTCCTTGAC[C/T]ACCCTGACCGTGTCC | 64127 |
rs199883290 | snp | C/G | | | missense | NOD2 | GRCh38.p7 | 16:50729867 | GAAGCCCTCCTGCAG[C/G]CCCTTGAAAGGAATG | 64127 |
rs199919884 | snp | C/T | 0.000214304 | 0.0103492 | intron-variant | NOD2 | GRCh38.p7 | 16:50719892 | TTCTGCCTGCCGCTG[C/T]GTTCTCTCAGCCTCC | 64127 |
rs199951979 | snp | A/G | | | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710865 | CTTGCTGTGGGCTGC[A/G]GGGCAAGACTTCCAG | 64127 |
rs199975570 | snp | C/T | 0.000148929 | 0.00862799 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710861 | TGCACTTGCTGTGGG[C/T]TGCAGGGCAAGACTT | 64127 |
rs200035357 | snp | A/G | 0.000218284 | 0.0104448 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712058 | TGGCCCGCAGCCTCC[A/G]CAAGCACTTCCACTC | 64127 |
rs200089552 | snp | A/G | 0.000182823 | 0.00955919 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699541 | AGGAGCCAGCTGGTC[A/G]AGCTGCTGGTCTCAG | 64127 |
rs200132892 | snp | C/T | 0.000242311 | 0.0110044 | intron-variant | NOD2 | GRCh38.p7 | 16:50729935 | CCTGTTTTAGCTCTC[C/T]GAACCTCAGTTTTTC | 64127 |
rs200160605 | snp | C/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699803 | CCCACTCGCTCCACC[C/G]AGCCCGAGACCTGCA | 64127 |
rs200268837 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692539 | TTTTGGCTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 64127 |
rs200397914 | in-del | -/A/AG | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692455 | GAAAATGAAAAAAAA[-/A/AG]GAACCTTAAATGACC | 64127 |
rs200428513 | snp | C/G/T | 8.25585e-05 | 0.00642443 | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50720000 | CAACACCTCCTTGCA[C/G/T]TTCCTGGGGTAGGTT | 64127 |
rs200434929 | snp | C/G | 0.000285701 | 0.0119486 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697363 | TTGATCCTCAGCCTT[C/G]TTTCATCCTTGGCCG | 64127 |
rs200463498 | snp | C/T | 6.62295e-05 | 0.00575416 | missense | NOD2 | GRCh38.p7 | 16:50725527 | ATGAAGGTGTATGTT[C/T]TCTCGCAGAAGGACT | 64127 |
rs200509396 | in-del | -/C | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706701 | GCTATTTCTTTCTTT[-/C]TTTTTTTTTTTTTGA | 64127 |
rs200519856 | snp | G/T | 0.000345989 | 0.0131482 | intron-variant | NOD2 | GRCh38.p7 | 16:50729807 | GCTCACCATTGTATC[G/T]TCTTTTCCAGGTTGT | 64127 |
rs200573252 | snp | A/G | 0.000231661 | 0.01076 | intron-variant | NOD2 | GRCh38.p7 | 16:50710510 | GTCTGGTTAGGTCCC[A/G]TCTTCACCATGGTGC | 64127 |
rs200613932 | snp | C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50717006 | CTTATTCCCTGGAAA[C/G]TATTTTTTGCCCCAT | 64127 |
rs200635188 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50723139 | TGTCTAAAAAGGGTA[A/G]AAAAAAAAAAAAAAA | 64127 |
rs200656015 | snp | C/T | 0.000150239 | 0.00866585 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711300 | GCGCCATCATGAGCC[C/T]GGGGTGGCGGACCGC | 64127 |
rs200744970 | snp | A/C | 1.66507e-05 | 0.00288532 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710747 | CCACCCTGGGCCTGG[A/C]GGAGCTCTTCAGCAC | 64127 |
rs200761103 | in-del | -/TGTTTCT | 0.030665 | 0.119967 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50699301 | TGTGGAACCTTGAGG[-/TGTTTCT]TGTTTCTTGCCTTCT | 64127 |
rs200863522 | snp | G/T | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692587 | CGTGTGTTGGGAAGC[G/T]ATGTGTGTGTTGGGA | 64127 |
rs201028429 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50704546 | CCTTTTTTTTTTTTT[C/T]TTTTTGAGACAGTGT | 64127 |
rs201035873 | snp | A/C | 0.000957017 | 0.0218539 | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50719998 | GGCAACACCTCCTTG[A/C]AGTTCCTGGGGTAGG | 64127 |
rs201076024 | snp | C/T | 0.000283752 | 0.0119078 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712079 | ACTTCCACTCCATCC[C/T]GCCAGCTGCACCGGG | 64127 |
rs201107567 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710978 | AGCACTGCTGTTGGC[C/T]TGATGTTGGTCAAGA | 64127 |
rs201115206 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707911 | ATTGGCTGCCTTCCT[C/T]CTACAACATGTTCAG | 64127 |
rs201146502 | snp | A/G | 0.00113885 | 0.0238354 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707991 | CAGTTAATCAGAAAG[A/G]GAAGGGCAGTCAGTG | 64127 |
rs201196641 | snp | A/G | 9.88696e-05 | 0.00703029 | intron-variant | NOD2 | GRCh38.p7 | 16:50729804 | GAAGCTCACCATTGT[A/G]TCTTCTTTTCCAGGT | 64127 |
rs201214915 | snp | C/T | 6.59174e-05 | 0.00574059 | synonymous-codon | NOD2 | GRCh38.p7 | 16:50731789 | GGAGGTTGACAAGCT[C/T]GGCTGCAGGGACACC | 64127 |
rs201247669 | in-del | -/A | 0.0372196 | 0.131242 | intron-variant | NOD2 | GRCh38.p7 | 16:50704537 | TTCCAAAACCTTTTT[-/A]TTTTTTTTCTTTTTG | 64127 |
rs201329309 | snp | A/T | 1.66338e-05 | 0.00288386 | intron-variant | NOD2 | GRCh38.p7 | 16:50716676 | AGAAGTTAGCGTAAG[A/T]CAGCCTGGGCTGTGG | 64127 |
rs201402134 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50721412 | TTTGTTTTTGTTGTT[G/T]TTTTTTTTTGCTTCG | 64127 |
rs201440399 | in-del | -/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50721412 | TTTGTTTTTGTTGTT[-/G]TTTTTTTTTGCTTCG | 64127 |
rs201573238 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707345 | TCGGTTTGGCAGGTG[C/T]ATGGGCAGGTTAGGA | 64127 |
rs201586544 | snp | C/T | 0.000365151 | 0.0135071 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699554 | TCGAGCTGCTGGTCT[C/T]AGGGTCCCTGGAAGG | 64127 |
rs201591164 | snp | A/G | 4.95872e-05 | 0.00497907 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710870 | TGTGGGCTGCAGGGC[A/G]AGACTTCCAGGAATT | 64127 |
rs201615690 | snp | A/G | 9.33402e-05 | 0.00683091 | intron-variant | NOD2 | GRCh38.p7 | 16:50697340 | AGCAGGCATTGTCCC[A/G]TCCCAGCTTGATCCT | 64127 |
rs201709367 | snp | A/C | 6.69042e-05 | 0.00578339 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711968 | TGTTGTCCCGGGAGC[A/C]CTGGGGCCTGCTGGC | 64127 |
rs201712814 | snp | A/C | 0.0167023 | 0.0898454 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711362 | TGCACGGTTTGTGCC[A/C]CCTGCCTGTCTTCTC | 64127 |
rs201759367 | snp | A/T | 0.000397463 | 0.0140916 | intron-variant | NOD2 | GRCh38.p7 | 16:50716578 | AATGTATTTATTTTG[A/T]CTCTTTAGTTTGCGC | 64127 |
rs201781416 | snp | A/G | 0.000217143 | 0.0104175 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50723317 | CTGGTGGGGAACAAC[A/G]TTGGCAGTGTGGGTG | 64127 |
rs201790577 | snp | A/G/T | 9.88963e-05 | 0.00703132 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710615 | TGTCTGCTCAGTCTC[A/G/T]CTTCCTCAGTACCTA | 64127 |
rs201806207 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50716959 | TTGCATGCAGGCAGA[A/G]CTTCTTGGCATTGAG | 64127 |
rs201831159 | snp | A/G | 1.64953e-05 | 0.00287182 | missense, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50719981 | TGGCCGAGGGGCTCC[A/G]AGGCAACACCTCCTT | 64127 |
rs201884393 | snp | A/G/T | 3.29913e-05 | 0.00406135 | missense, stop-gained, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50719971 | GCCCAAGTGCTGGCC[A/G/T]AGGGGCTCCGAGGCA | 64127 |
rs202002250 | in-del | -/A/AAAAAAAAA/AAAAAAAAAG | 0.035045 | 0.128417 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692447 | ACTGAAAGGAAAATG[-/A/AAAAAAAAA/AAAAAAAAAG]AAAAAAAAGAACCTT | 64127 |
rs202052365 | snp | C/T | 0.000149466 | 0.00864352 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699728 | GTCAGAAGCTCATCG[C/T]GGCTGCCCAAGAAGC | 64127 |
rs202059016 | snp | A/G | 0.000112759 | 0.00750777 | intron-variant | NOD2 | GRCh38.p7 | 16:50723282 | CTCTGACATACTTTT[A/G]TTCCATGATTACCTC | 64127 |
rs202111813 | snp | G/T | 0.000316601 | 0.0125778 | intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712380 | GGCTCTGTAGTGAGT[G/T]TTACTGGGCATTGCT | 64127 |
rs202137892 | snp | A/G | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692588 | GTGTGTTGGGAAGCG[A/G]TGTGTGTGTTGGGAA | 64127 |
rs202190367 | snp | A/G | 3.29755e-05 | 0.00406038 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710630 | GCTTCCTCAGTACCT[A/G]TGATGGAGCAGAGAC | 64127 |
rs202215862 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50703347 | TGTGTAAAGAAAGGT[C/T]ACTTAAATTAGGCTG | 64127 |
rs367578799 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50720074 | TGAGGATTTAGGGGC[A/G]GGTGAAACTCTTCAG | 64127 |
rs367630707 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711123 | CCCCACCTCTGTCCA[C/G]ACCCTGCTCTTCAAC | 64127 |
rs367632486 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOD2 | GRCh38.p7 | 16:50726997 | AATACAAAATTAGCC[A/G]GGCGTGGTGGCATAC | 64127 |
rs367637762 | snp | C/T | 3.3123e-05 | 0.00406945 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711857 | TGCCCACGATGTGCA[C/T]CCAGGCCTCGGAGGG | 64127 |
rs367756419 | snp | G/T | 1.65729e-05 | 0.00287857 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699713 | AGGGTACTTGGGCCT[G/T]TCAGAAGCTCATCGC | 64127 |
rs367766667 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706451 | GGGGCAGGAACAGAA[G/T]CAGGGGGACCAGTTT | 64127 |
rs367809955 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695164 | AATGGATCATGGGGG[C/G]GGTGGGGTAAGGGCA | 64127 |
rs367819045 | snp | A/G | 1.66832e-05 | 0.00288814 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711332 | TCATCCGCCTGCTCC[A/G]AGAGACCTCAGCCCT | 64127 |
rs367841016 | snp | C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50714368 | TGCCTCTAGTGATTC[C/G]CATTCAGTAGGTTTG | 64127 |
rs367883043 | snp | C/T | 8.26139e-05 | 0.00642652 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711169 | CTGCTGAAGAATGCC[C/T]GCAAGGTGGTGACCA | 64127 |
rs367883697 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50695023 | TGAGGGGTGAGCCAC[A/G]TGAGTATCTGGGGGG | 64127 |
rs367895771 | snp | C/G/T | 6.63354e-05 | 0.00575881 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699600 | GGACTGGCTGCTGTC[C/G/T]TGGGAGGTCCTCTCC | 64127 |
rs367905706 | snp | A/G | 4.94817e-05 | 0.00497377 | missense | NOD2 | GRCh38.p7 | 16:50729880 | AGGCCCTTGAAAGGA[A/G]TGACACCATCCTGGA | 64127 |
rs368178268 | snp | C/T | 0.000581831 | 0.0170463 | intron-variant | NOD2 | GRCh38.p7 | 16:50716839 | CTGGGATTTGGTGCT[C/T]ACTGTCCAATGTGCT | 64127 |
rs368217718 | snp | C/T | | | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713972 | GCAAATGGAAAACAG[C/T]CAGCACCAAACTCTA | 64127 |
rs368237819 | snp | A/C | | | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715199 | ACCTTGGCAAAGTCA[A/C]TTCGCTTGTCTGTGC | 64127 |
rs368240261 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697415 | GTCAGATGGGGAGTG[C/T]TGACTCTGTTTCTGG | 64127 |
rs368316739 | snp | A/C/G | 8.35812e-05 | 0.00646409 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711467 | ACCTGCTGATTCTGC[A/C/G]GCATTTTCTGCTGCA | 64127 |
rs368346234 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50694121 | GCTGTTTGCTCTCCT[A/G]TGCTTCTCAGGTTGA | 64127 |
rs368351360 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50701085 | AGGAAAGTAGTTTGA[A/G]TAAGCTCACAGTAGT | 64127 |
rs368391102 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant | NOD2 | GRCh38.p7 | 16:50722613 | TGTTGACTCTTTTGG[C/T]CTTTTCAGATTCTGG | 64127 |
rs368433191 | snp | A/G | | | downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50733133 | TGGGCACAGTGGCTC[A/G]CGCCTGTAATCCCAG | 64127 |
rs368474657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50726072 | GGCAGAGAGTGGAAG[C/G]TCTTCTCTGCAAGCA | 64127 |
rs368499349 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50719154 | CAGCAGCTGGGGCCC[C/T]TGGCTACCTCCAAGG | 64127 |
rs368509202 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696652 | GGTTAGTGAGAACAG[C/T]ACTAAGGCCAGGTTC | 64127 |
rs368517116 | snp | C/T | | | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715489 | TGGCACAATCTCGGC[C/T]CATGCAAGCTCTGCC | 64127 |
rs368523477 | snp | A/G | | | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709771 | AGGTTCTGAGAATCC[A/G]GACATGGACATCTTT | 64127 |
rs368528423 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706346 | CTGAGGAAATAGGGA[C/T]GCTATTGGGACGTTT | 64127 |
rs368673506 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692871 | TGTGTGTGTGTGCAC[A/G]TGTGTGTTGGGAAGC | 64127 |
rs368677255 | snp | C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50702423 | AATCCAGCTCTCTCT[C/G]AGCTCCCTTTGAGCT | 64127 |
rs368687248 | snp | A/G | 2.00138e-05 | 0.00316331 | intron-variant | NOD2 | GRCh38.p7 | 16:50723272 | TCTTTCCCTGCTCTG[A/G]CATACTTTTGTTCCA | 64127 |
rs368878082 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50703054 | CTATAACAATATTAA[C/T]TTAAACATTTTTTAA | 64127 |
rs368952727 | snp | C/T | 3.34913e-05 | 0.00409201 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712065 | CAGCCTCCGCAAGCA[C/T]TTCCACTCCATCCCG | 64127 |
rs369051907 | snp | C/T | | | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715798 | CCAGCTGAGGCACTC[C/T]AGAGCCTGAGCTGTT | 64127 |
rs369059091 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698538 | AGTGTGCAAAACACA[C/T]AGCACGGGCTTGGGG | 64127 |
rs369085294 | snp | A/G | 6.65591e-05 | 0.00576846 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711555 | CCTCCCCACCCTCCT[A/G]CACCTGGGCAGACTG | 64127 |
rs369098015 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NOD2 | GRCh38.p7 | 16:50720263 | AGGAAGCCCTCTGAT[C/T]CTCAGGGGGCGCTAG | 64127 |
rs369098290 | snp | A/C | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710609 | CCACGGTGTCTGCTC[A/C]GTCTCGCTTCCTCAG | 64127 |
rs369122423 | snp | A/G | 4.94181e-05 | 0.00497057 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707890 | TGCCACGGTGAAAGC[A/G]AATGGATTGGCTGCC | 64127 |
rs369291258 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50729496 | GGGACTAATTTGCTC[A/G]AGATCAAAAAAGAAG | 64127 |
rs369307707 | in-del | AG/T | 0.5 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50725357 | AGAAAGAACAGATAA[AG/T]TACGTTGTGGGGATT | 64127 |
rs369310865 | snp | A/G | 3.32452e-05 | 0.00407695 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711586 | GCTCTGTGGGGCCTG[A/G]GCATGTGCTGCTACG | 64127 |
rs369363319 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707399 | GTGTTTATGAAACTT[C/T]TAAGTGGAGATGGAA | 64127 |
rs369389691 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50721584 | TGTAGCCTTGAACTC[C/T]TGAGCTCAAGTGATC | 64127 |
rs369391225 | in-del | -/TCT | | | intron-variant | NOD2 | GRCh38.p7 | 16:50717533 | TGGCTTCTCTCTCCT[-/TCT]CTCTCTCTCAGATAT | 64127 |
rs369410275 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50693633 | CGTGGCCCGGAGTGG[C/G]CCTTGGAGTCGGCGC | 64127 |
rs369413188 | snp | C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50716069 | GAGTGGTGCCATTGG[C/G]GTTAAGGACTGGGCA | 64127 |
rs369454774 | snp | A/G | 1.67077e-05 | 0.00289026 | intron-variant | NOD2 | GRCh38.p7 | 16:50720046 | GGACCTGCATGGAGG[A/G]GCTTGGGACTTTTGA | 64127 |
rs369518318 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698850 | CCTGAATCCAGCCAG[C/T]ATGAAAGAGCCCCTC | 64127 |
rs369524794 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50724204 | GAAGCAGAAAGGCAC[C/T]GCAACATATGGGCAT | 64127 |
rs369575405 | in-del | -/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50727894 | CCAGTGACCATGACC[-/T]TTTTTTTTTGGTGCG | 64127 |
rs369701066 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50720652 | CCAGCAGCCTCTCTC[C/G/T]TATCCTGTCATGCCC | 64127 |
rs369719210 | snp | A/G/T | 1.66095e-05 | 0.00288175 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711669 | TCTTGGCTTCCTGGT[A/G/T]CGTGCCAAAGGTGTC | 64127 |
rs369732140 | snp | C/G/T | 9.89012e-05 | 0.00703149 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710939 | GCATGGCCAAACCAC[C/G/T]CTCTGTGCGGACTCT | 64127 |
rs369740939 | snp | A/G | 1.66302e-05 | 0.00288355 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710761 | GAGGAGCTCTTCAGC[A/G]CCCCTGGCCACCTCA | 64127 |
rs369764782 | snp | A/G | | | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707921 | TTCCTTCTACAACAT[A/G]TTCAGGAATTACCAG | 64127 |
rs369766227 | snp | A/G | 1.65847e-05 | 0.0028796 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712106 | CGGGTGAGGCCAAGA[A/G]CGTGCATGCCATGCC | 64127 |
rs369766454 | snp | A/C/G | 0.000100021 | 0.00707117 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710718 | CATGGCTGGACCCCC[A/C/G]CAGAAGAGCCCAGCC | 64127 |
rs369795120 | snp | A/T | 6.64044e-05 | 0.00576175 | intron-variant | NOD2 | GRCh38.p7 | 16:50725458 | ATAATCAATGTTGTA[A/T]CAACTGGATTTTCTC | 64127 |
rs369901813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD2 | GRCh38.p7 | 16:50704159 | TAGGAGATAACTGCC[C/G]TCAACTTGTTTGAAT | 64127 |
rs369957746 | snp | C/G | 0.000149739 | 0.00865143 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711892 | GACAGCAGCGTGGCA[C/G]CTTTGCTGCAGAAGG | 64127 |
rs369971131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50715485 | ACAGTGGCACAATCT[C/T]GGCTCATGCAAGCTC | 64127 |
rs370009097 | in-del | -/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50714964 | CGCTTTATGAACTCT[-/T]GAGACACTCTGCTCT | 64127 |
rs370148148 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50728440 | TTTTTGTCTAACATC[A/G]TTTTCATAGTCTAAA | 64127 |
rs370152851 | snp | C/T | | | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709457 | TCCTGAAAGGGGAAC[C/T]AAACTCTGACACAGG | 64127 |
rs370158939 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695319 | GGCCGTGTCGATAGG[A/G]TTTGGGGTGCAAGAG | 64127 |
rs370224479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50704718 | AGATGGGGTTTTGCT[A/G]TGTTGGCCAGGCTGG | 64127 |
rs370298984 | snp | A/G | 1.67008e-05 | 0.00288965 | intron-variant | NOD2 | GRCh38.p7 | 16:50725619 | TAATTGCTGGCCTTT[A/G]GAAGGGGCATTTCTG | 64127 |
rs370309346 | snp | G/T | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696238 | GCCCCAGAGAAACCG[G/T]GCTGGCTGTGGTCTC | 64127 |
rs370316846 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50693643 | AGTGGGCCTTGGAGT[C/G]GGCGCGCAGGCGGCT | 64127 |
rs370399990 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50718298 | AATCTTTGAGCAACA[A/G]TGAGGTCGGCAGCTG | 64127 |
rs370405233 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50718016 | TAGGCACAGTAAGAG[A/C]GTAATAGCAACTCAT | 64127 |
rs370406032 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50700684 | CTATTACCACTGGCT[A/G]CTATTTATTATTTCT | 64127 |
rs370447004 | snp | C/T | 0.000157988 | 0.00888644 | utr-variant-5-prime, intron-variant | NOD2 | GRCh38.p7 | 16:50697212 | GCCTACCCGCAGATG[C/T]CATGCCTGCTCCCCC | 64127 |
rs370488756 | snp | G/T | | | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50709585 | GGGGAGGATGGGGAA[G/T]TGGAGGCAGGATCAC | 64127 |
rs370498233 | snp | A/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50693848 | GACGGAAAGGGGGCA[A/T]CTCGAGGTTGGGGAG | 64127 |
rs370500651 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50705494 | CTACCATGAATTTCA[C/T]TGTAGATATTTTGGA | 64127 |
rs370519531 | snp | C/T | 8.31207e-05 | 0.0064462 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711885 | GGGAAAGGACAGCAG[C/T]GTGGCAGCTTTGCTG | 64127 |
rs370557520 | snp | C/T | | | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732836 | TTACAGGAAAAAAAA[C/T]TAGGCCGTTCCTTCA | 64127 |
rs370615110 | snp | C/T | 6.61737e-05 | 0.00575174 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711848 | CCAGGCTCCTGCCCA[C/T]GATGTGCATCCAGGC | 64127 |
rs370644320 | in-del | -/GT | | | upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50692921 | TGTTGGGAAAGCAGG[-/GT]GTGTGTGTGTTGGGA | 64127 |
rs370645343 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50695916 | CAACAGACAAGGGGG[C/T]CTGCTGTAAAGGGAG | 64127 |
rs370728357 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711252 | CAACCTCAAGGGCTT[C/T]TCTGAACAGGGCATC | 64127 |
rs370734707 | snp | A/C/G | 0.00013262 | 0.00814211 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699652 | CACCTCCTGGGCCAG[A/C/G]CTCTCTCCCACTTGG | 64127 |
rs370750269 | in-del | -/AG | | | intron-variant | NOD2 | GRCh38.p7 | 16:50714889 | CACAATGATTGAGAA[-/AG]AGAGAGAGAGAGCAC | 64127 |
rs370833461 | snp | C/G | | | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713674 | AGGGTTGGTGCAGGG[C/G]CCTGGGGTTAGTAAC | 64127 |
rs370856888 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50693808 | GTTTCTCCTGGGGGA[A/G]TCCCAGAATGTAGAT | 64127 |
rs370883542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50722400 | CTCTAAGTCTGTAAT[A/G]TAAAGCCACTGAAAA | 64127 |
rs371005935 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50705405 | TTCTCTGGGCTCATG[A/C]TACTCTTTGGTTTTC | 64127 |
rs371044393 | snp | C/T | 0.000117439 | 0.00766196 | utr-variant-5-prime, synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699489 | GTTCTCCTCCCCAGG[C/T]TGTGAAATGTGCTCG | 64127 |
rs371063908 | snp | C/T | 0.000371678 | 0.0136272 | intron-variant | NOD2 | GRCh38.p7 | 16:50697339 | GAGCAGGCATTGTCC[C/T]GTCCCAGCTTGATCC | 64127 |
rs371163141 | snp | C/G/T | 3.29659e-05 | 0.00405981 | missense, synonymous-codon, intron-variant, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50719965 | GCGGGAGCCCAAGTG[C/G/T]TGGCCGAGGGGCTCC | 64127 |
rs371181834 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50726450 | TTGTGTTGCTTTCAC[A/G]AGCTAGGAAGTTTCC | 64127 |
rs371193432 | snp | A/G | 3.47156e-05 | 0.00416612 | intron-variant | NOD2 | GRCh38.p7 | 16:50729937 | TGTTTTAGCTCTCCG[A/G]ACCTCAGTTTTTCTA | 64127 |
rs371220165 | snp | G/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50720086 | GGCAGGTGAAACTCT[G/T]CAGCCAGGAGGCCCC | 64127 |
rs371305304 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD2 | GRCh38.p7 | 16:50721308 | CTGTCTGGGCCAGGC[A/G]TTGTGCTAAAACCCC | 64127 |
rs371339573 | snp | A/G | 1.67091e-05 | 0.00289038 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711949 | GCAGCCTTCCTGGCA[A/G]GGCTGTTGTCCCGGG | 64127 |
rs371389581 | snp | A/G | 1.65581e-05 | 0.00287728 | missense | NOD2 | GRCh38.p7 | 16:50725515 | ACCATCTCCAGGATG[A/G]AGGTGTATGTTCTCT | 64127 |
rs371422328 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50703212 | TAGAGGTAAACACTG[A/G]CTTGACTTTTGTGTA | 64127 |
rs371487527 | snp | C/T | | | intron-variant | NOD2 | GRCh38.p7 | 16:50694861 | TGAAATAAGTAAATA[C/T]ATGGCGTAGCAGGTG | 64127 |
rs371516582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50706572 | TATGTAGATATTGGC[C/T]ACAGATGGCATTTGA | 64127 |
rs371531407 | in-del | -/AATT | | | intron-variant | NOD2 | GRCh38.p7 | 16:50705044 | CATGAAACTACTATT[-/AATT]CAATGTTAGAATTCC | 64127 |
rs371534458 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50731260 | TCTGTGGCCTATGAC[A/G]TCATCAGGTTCTGGG | 64127 |
rs371543474 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696872 | TCCACAGAAGCCCAA[C/T]GTCACTAGCTGGGGT | 64127 |
rs371707099 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NOD2 | GRCh38.p7 | 16:50703707 | AAAAAAAAAAAAGAA[A/C]GGTTACTATTGCCTT | 64127 |
rs371730003 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50718991 | AGGAAGGAAGGTTGA[C/G]ACTGGGCACCTTGGA | 64127 |
rs371916256 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697734 | CTCTCTCCCAAGCAG[C/G]CAGACACACAAGTAA | 64127 |
rs372022771 | snp | A/T | | | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732078 | CCAGGATGTACAAGG[A/T]CAGCCCCTCCTCCAT | 64127 |