SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs730360 | snp | C/G | 0.284209 | 0.247648 | intron-variant | NOD1 | GRCh38.p7 | 7:30470455 | TATACGCAGTGCACC[C/G]GGCCAGATTCATTCA | 10392 |
rs730361 | snp | A/G | 0.266819 | 0.249434 | intron-variant | NOD1 | GRCh38.p7 | 7:30470205 | CTACATGGAGTAGGT[A/G]CAGTTATTATCTGTA | 10392 |
rs732038 | snp | C/T | 0.283947 | 0.247685 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466304 | CAAAGCAACACATTC[C/T]GTTTCTGCTCATGTT | 10392 |
rs736781 | snp | A/G | 0.393434 | 0.20476 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464544 | CCCTTATGTTGTCCT[A/G]CCTCTCACCATGTGT | 10392 |
rs736782 | snp | C/T | 0.338976 | 0.23363 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464657 | GCCTAAAATCACCAG[C/T]AAACATGGTCCATTT | 10392 |
rs741889 | snp | A/C | 0.261056 | 0.249755 | intron-variant | NOD1 | GRCh38.p7 | 7:30426605 | TTGAAGCAGGAGAGG[A/C]ATGTGATCAGATCTG | 10392 |
rs932272 | snp | C/T | 0.492533 | 0.0606443 | intron-variant | NOD1 | GRCh38.p7 | 7:30473543 | AAAAAAATCTGATAC[C/T]GATATTGACTAACAT | 10392 |
rs963804 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30424562 | ACTTGTCCTCTTGCC[A/C]GCTCATTTGTTAATA | 10392 |
rs1076591 | snp | C/G | 0.25801 | 0.249872 | intron-variant | NOD1 | GRCh38.p7 | 7:30426606 | TTTGAAGCAGGAGAG[C/G]CATGTGATCAGATCT | 10392 |
rs1558065 | snp | A/G | 0.283684 | 0.24772 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463163 | TATGTGTGTGTATGT[A/G]TATATATGAATATAC | 10392 |
rs1558066 | snp | A/C | 0.266546 | 0.249452 | intron-variant, utr-variant-5-prime | NOD1, LOC101928268 | GRCh38.p7 | 7:30463571 | CTCTGTCCCTGAATC[A/C]TGGGGTGGCCCCAGA | 10392 |
rs1558067 | snp | C/T | 0.462582 | 0.131564 | intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463664 | CTGTCCCAGGGGACC[C/T]TGAGCGGAGATGTGC | 10392 |
rs1558068 | snp | A/T | 0.49941 | 0.0171624 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463747 | ATGTTCTCCACATGT[A/T]CCTTTCTATGTTTTA | 10392 |
rs1558069 | snp | A/T | 0.267091 | 0.249415 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463832 | AATGCAAAAAAAAAA[A/T]TTAGAGGAATAAATT | 10392 |
rs1558070 | snp | A/C | 0.266546 | 0.249452 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463870 | CTATTATCCACATGC[A/C]ATAACCACTATTCTC | 10392 |
rs2037955 | snp | G/T | 0.404035 | 0.196909 | intron-variant | NOD1 | GRCh38.p7 | 7:30472333 | ATGCAGAGAACAGTG[G/T]GTTCAAAGACCCAGA | 10392 |
rs2066973 | snp | C/T | 0.49753 | 0.0350569 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30478950 | CTCTCGCACCGGGCG[C/T]CCCTCTGCGCGCAGC | 10392 |
rs2072687 | snp | G/T | 0.403158 | 0.197592 | intron-variant | NOD1 | GRCh38.p7 | 7:30478151 | CCTTCATGGAGTCCC[G/T]CCTGCAGACGGGACA | 10392 |
rs2075816 | snp | C/T | 0.399611 | 0.200291 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30478986 | GTCCACTCGGCCCTG[C/T]GCGGTGGCCAGGGGC | 10392 |
rs2075817 | snp | C/T | 0.492087 | 0.0623997 | intron-variant | NOD1 | GRCh38.p7 | 7:30478517 | GCAGGGAGGCGGGAT[C/T]TGCGTGCGGGCGGAA | 10392 |
rs2075818 | snp | C/G | 0.410921 | 0.191363 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456766 | TGACTACTTCTCGGC[C/G]GAAGATGCGGAGATT | 10392 |
rs2075819 | snp | A/G | 0.473634 | 0.111748 | intron-variant | NOD1 | GRCh38.p7 | 7:30455006 | TTGATTTTAGAAAGG[A/G]ACAGCTGAATCCTGT | 10392 |
rs2075820 | snp | A/G | 0.401132 | 0.199146 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452621 | CCAGAGCGGGACCCC[A/G]AGGAGGTGTTTGCCT | 10392 |
rs2075821 | snp | A/G | 0.399016 | 0.200734 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451695 | GGGCAGTGGTCCGGC[A/G]CGGGAAGACCTCTTC | 10392 |
rs2075822 | snp | C/T | 0.298905 | 0.24517 | intron-variant | NOD1 | GRCh38.p7 | 7:30451144 | GCATCGGGAATGGCA[C/T]CATGGACCAGGATCC | 10392 |
rs2108355 | snp | A/T | 0.315273 | 0.241329 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30478861 | TGGGAGAGGCCGCCG[A/T]AGGGCGGGGGCGGTC | 10392 |
rs2108356 | snp | A/C | 0.31503 | 0.241394 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30478862 | GGGAGAGGCCGCCGA[A/C]GGGCGGGGGCGGTCA | 10392 |
rs2109349 | snp | C/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30426267 | CTCTCCCCCACACCT[C/G]AAAGTAGCCACAcct | 10392 |
rs2190504 | snp | C/T | 0.481932 | 0.0933148 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467764 | TGGAGTGCGATGGCG[C/T]GATCTTGGCTCACTG | 10392 |
rs2235099 | snp | C/T | 0.401796 | 0.19864 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452934 | GGAGATCTACATGGA[C/T]ACCATCATGGAGCTG | 10392 |
rs2256023 | snp | C/T | 0.486398 | 0.0813386 | intron-variant | NOD1 | GRCh38.p7 | 7:30475375 | CTTAATCTGCCAAAA[C/T]CTGGCACTAATCTGG | 10392 |
rs2284357 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NOD1 | GRCh38.p7 | 7:30434595 | TTTGAACATACATAG[A/G]ACAAAAGGCTAGAAA | 10392 |
rs2284358 | snp | A/G | 0.344592 | 0.231414 | intron-variant | NOD1 | GRCh38.p7 | 7:30449391 | GGCCCATCTCATTAA[A/G]TTCTGCCCATACCAT | 10392 |
rs2391869 | snp | A/G | 0.266819 | 0.249434 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464335 | CCGTGGGATAGCTGC[A/G]AGGGGGTGGGCAGGG | 10392 |
rs2529440 | snp | C/T | 0.462472 | 0.13174 | intron-variant | NOD1 | GRCh38.p7 | 7:30472178 | CTTCCCTCCGCACTT[C/T]AGAATAAAATCCCAA | 10392 |
rs2709798 | snp | C/T | 0 | 0 | utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30478650 | CGCTCTCCGGGCTCT[C/T]CTCTAGCTCTCAGCG | 10392 |
rs2709799 | snp | C/G | 0.461481 | 0.133325 | intron-variant | NOD1 | GRCh38.p7 | 7:30475287 | CCTTGGCCTTCTGTT[C/G]TGTCATTGCCACCAT | 10392 |
rs2709800 | snp | G/T | 0.483491 | 0.0893421 | intron-variant | NOD1 | GRCh38.p7 | 7:30473155 | GAGTGAGGTGTGGCT[G/T]CTTTAGCATTCCTGA | 10392 |
rs2709801 | snp | C/T | 0.467439 | 0.123371 | intron-variant | NOD1 | GRCh38.p7 | 7:30473122 | ATGAGGTAGTAATTG[C/T]TTTTCTGGCTTTCTG | 10392 |
rs2709802 | snp | C/T | 0.488057 | 0.0763479 | intron-variant | NOD1 | GRCh38.p7 | 7:30473079 | GCTCTGCTGGCCCCC[C/T]ACCCTGGTGTGGAAG | 10392 |
rs2709803 | snp | C/T | 0.405776 | 0.195535 | intron-variant | NOD1 | GRCh38.p7 | 7:30470918 | CTCCAGCTTCCAGAT[C/T]GGCCACTTCTGTGGC | 10392 |
rs2736726 | snp | A/G | 0.491263 | 0.0655142 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479414 | ACTTCTTCAGTGTGA[A/G]TAAGTGACAACTTTC | 10392 |
rs2893375 | snp | A/C | 0.284209 | 0.247648 | intron-variant | NOD1 | GRCh38.p7 | 7:30471237 | TAAGAGGTTGAGAAG[A/C]TGATAGAGCCATAAC | 10392 |
rs2906765 | snp | A/G | 0.0271762 | 0.113356 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480240 | tccagctccggtcac[A/G]gactcaggaaaacag | 10392 |
rs2906766 | snp | C/T | 0.484421 | 0.0868729 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459959 | ACTTGTCTTCCCAGA[C/T]GTTTTCTGTAATCGC | 10392 |
rs2906773 | snp | C/T | 0.49928 | 0.018956 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467028 | ACTGGGTTGGTATCC[C/T]TAAAAGCCAAGCCGA | 10392 |
rs2907748 | snp | C/T | 0.31503 | 0.241394 | intron-variant | NOD1 | GRCh38.p7 | 7:30433407 | TCCTATTTCTTAGCC[C/T]AGCTACCTGTAGAGG | 10392 |
rs2907749 | snp | A/G | 0.42066 | 0.182689 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446125 | GTACCACATACATCC[A/G]TCCCCTTCTACTCAC | 10392 |
rs2952802 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | NOD1 | GRCh38.p7 | 7:30471935 | GGCAGGATTTGGAAC[A/C]AGGCCTGCCAGCCCA | 10392 |
rs2952803 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | NOD1 | GRCh38.p7 | 7:30470029 | GGACACAAAGTTGCA[C/T]GCCCTCTGAGAGAGG | 10392 |
rs2970498 | snp | C/T | 0.38934 | 0.207568 | intron-variant | NOD1 | GRCh38.p7 | 7:30438440 | AGTTGTGAGGATTCA[C/T]TGAGTTAACAGAAGC | 10392 |
rs2970499 | snp | C/T | 0.314787 | 0.241459 | intron-variant | NOD1 | GRCh38.p7 | 7:30438805 | TAGTATAGATACATA[C/T]AGTCTCACCCCTACT | 10392 |
rs2970500 | snp | C/G | 0.314787 | 0.241459 | intron-variant | NOD1 | GRCh38.p7 | 7:30438869 | GGAGAGAAAGTGAGA[C/G]AGCTTAACTGAGCTT | 10392 |
rs2970501 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NOD1 | GRCh38.p7 | 7:30456377 | CAACAAGCAGCCCTC[C/T]AGCCTTCAGAGGCAC | 10392 |
rs2970502 | snp | C/T | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459963 | GTCTTCCCAGACGTT[C/T]TCTGTAATCGCCGCC | 10392 |
rs2970503 | snp | A/G | 0.167809 | 0.236103 | intron-variant | NOD1 | GRCh38.p7 | 7:30473593 | GCCTAAGCAATGGAT[A/G]AGGTTTAATGTTATC | 10392 |
rs2975632 | snp | C/T | 0.375797 | 0.216044 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459835 | GGATGAAGGAAGCTG[C/T]GCAACACCCCTTCCC | 10392 |
rs2975633 | snp | A/T | 0.483199 | 0.0901004 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458226 | CTGTGGGATTTTTTT[A/T]AAAAATTATTATTTT | 10392 |
rs2975634 | snp | A/G | 0.0151181 | 0.0856193 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452077 | TGCAGCGGAACACAC[A/G]CAGCCCAGTGGAGAC | 10392 |
rs3020207 | snp | A/G | 0.496649 | 0.0407971 | intron-variant | NOD1 | GRCh38.p7 | 7:30457092 | GTGGGAGGTGGGGTG[A/G]GCTCTTTCTGTAGCT | 10392 |
rs3020208 | snp | C/T | 0.0151217 | 0.0856283 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452526 | CTTGGACCTGAGCCG[C/T]GTGCCTGACAGCTCC | 10392 |
rs3020209 | snp | G/T | 0 | 0 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451605 | CAAACAGAAACTCCT[G/T]CGGCATCTGGTGCCC | 10392 |
rs3075407 | in-del | -/AAA | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463403 | tcccaagacaaaaac[-/AAA]AATGATGAGCAACAG | 10392 |
rs3735433 | snp | A/G | 0.266546 | 0.249452 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30465988 | AGGAGGGAGGGTCAG[A/G]ACAGGAGCAGAGGCA | 10392 |
rs3757503 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458806 | GATGTTGCAGTGAGC[C/T]GAGATTGTGCCACTG | 10392 |
rs3823773 | snp | A/G | 0.155325 | 0.23138 | intron-variant, missense | NOD1, LOC101928268 | GRCh38.p7 | 7:30460345 | CTTTACCAAGCAAAG[A/G]AAGGAAAGGATTGCC | 10392 |
rs3832514 | in-del | -/GGACATTAT | 0.0138799 | 0.0821421 | intron-variant, cds-indel | NOD1, LOC101928268 | GRCh38.p7 | 7:30460093 | TTCAGCCAGGGCTCT[-/GGACATTAT]AAAGCAGCCTCCTTG | 10392 |
rs3857732 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30439486 | CACTTA[C/T] | 10392 |
rs4272257 | snp | C/T | 0.266546 | 0.249452 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464233 | CCCGGCCATGCCTGC[C/T]TGAACTGCTAAAGCA | 10392 |
rs4363092 | snp | A/G | 0.267091 | 0.249415 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464322 | CCATCAGCGTGACCC[A/G]TGGGATAGCTGCAAG | 10392 |
rs4409301 | snp | A/G | 0.266546 | 0.249452 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464176 | ATTCCACGTGCCAAA[A/G]GGAGGCTCAAAGATA | 10392 |
rs4720002 | snp | A/G | 0.397813 | 0.201621 | intron-variant, utr-variant-3-prime | NOD1 | GRCh38.p7 | 7:30437954 | CTTCGGAGAGCTGTC[A/G]GCCCAGGAGCCTGAG | 10392 |
rs4720003 | snp | C/T | 0.284471 | 0.247612 | intron-variant, downstream-variant-500B | NOD1, LOC101928268 | GRCh38.p7 | 7:30469376 | CTCCCGGAATCACCT[C/T]TCTCTCTCCCGGCTT | 10392 |
rs4720004 | snp | C/T | 0.259397 | 0.249823 | intron-variant | NOD1 | GRCh38.p7 | 7:30472603 | GGGAGAACCCCCGAT[C/T]TGATGGTGTTTACAG | 10392 |
rs4722985 | snp | C/T | 0.393619 | 0.204631 | intron-variant | NOD1 | GRCh38.p7 | 7:30432475 | gtggagaaattggaa[C/T]ccacatacattgctg | 10392 |
rs4722986 | snp | A/G | 0.283947 | 0.247685 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464907 | CATTTACTAATTTCT[A/G]TTATCTCAATCCTTG | 10392 |
rs4722987 | snp | A/C | 0.283947 | 0.247685 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30465084 | GTGAATGTGTGGAAG[A/C]AGAAATGAGCAGAGA | 10392 |
rs4722988 | snp | A/G | 0.277867 | 0.248442 | intron-variant | NOD1 | GRCh38.p7 | 7:30472414 | CATTCCTTGAGAGGC[A/G]TCCCCAGACTCTCCT | 10392 |
rs5743321 | snp | A/G | 0.0271762 | 0.113356 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480462 | agcccagagaaaaga[A/G]gntagagacccggag | 10392 |
rs5743322 | snp | G/T | 0.0592355 | 0.161582 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480460 | CCCAGAGAAAAGAAG[G/T]TAGAGACCCGGAGAA | 10392 |
rs5743323 | in-del | -/G | 0.0271762 | 0.113356 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480438 | cccggagaagggggG[-/G]TGGTGAGCAGCCCTG | 10392 |
rs5743324 | snp | C/T | 0.0162398 | 0.0886349 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480248 | AGGGACGACTGTTTT[C/T]CTGAGTCCGTGACCG | 10392 |
rs5743326 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480036 | GGACCCGAGGTCATA[G/T]GTGGATCTCCTCACA | 10392 |
rs5743327 | snp | A/G | 0 | 0 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479985 | gactggtctcctgaa[A/G]gagtcctcctgtccc | 10392 |
rs5743328 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479669 | CAAGGTAATGTCATC[A/G]GTTAAGGCAGGAACC | 10392 |
rs5743329 | snp | G/T | 0.0158469 | 0.0875917 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479595 | atctggatgtataca[G/T]gcaggcttgggctca | 10392 |
rs5743330 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479560 | cctgacaCAAGTTGG[C/T]ACATTTGATCCTATC | 10392 |
rs5743332 | snp | C/T | 0 | 0 | utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30478639 | CTCTTCTCTAGCTCT[C/T]AGCGGCTGCGAAGTC | 10392 |
rs5743333 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NOD1 | GRCh38.p7 | 7:30478593 | CAAGTAAGTCCCAGC[A/G]ACTGGGGGATTCGCG | 10392 |
rs5743334 | snp | C/G | 0.0998734 | 0.199905 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459495 | TTTAAAATTATTAGA[C/G]TTTTCAAAACTCAAT | 10392 |
rs5743335 | snp | A/T | 0.0295035 | 0.117819 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459213 | AATTGGAAATTGAAG[A/T]TTTAAACAATGTTGT | 10392 |
rs5743336 | snp | C/T | 0.116838 | 0.211584 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459190 | AATGTTGTTTTAAAA[C/T]ATTCTAACTTCAAAG | 10392 |
rs5743337 | in-del | -/G | 0.4262 | 0.177351 | intron-variant | NOD1 | GRCh38.p7 | 7:30456693 | CAGGGACGGGCATGG[-/G]CATTGTGTGGACCCC | 10392 |
rs5743338 | snp | C/T | 0.00388348 | 0.0438937 | intron-variant | NOD1 | GRCh38.p7 | 7:30456509 | AGCAAACCCTGACAT[C/T]TCAGTTCTCATTGCT | 10392 |
rs5743339 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | NOD1 | GRCh38.p7 | 7:30454952 | TGCGATTGAACTGCC[C/T]ACACCTCGATGGTCT | 10392 |
rs5743340 | snp | G/T | 0.0244346 | 0.107797 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452982 | CTCCAAGTTCGTGCT[G/T]TGCTATGCCCAGAAG | 10392 |
rs5743341 | snp | C/T | 0.00151431 | 0.0274747 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452574 | CCACGTGGCCCTCTT[C/T]ACCTTCGATGGCCTG | 10392 |
rs5743342 | snp | A/G | 0.00818281 | 0.0634385 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452303 | GAGCGGGCCCTGCAG[A/G]ACCGCCTGCTGAGCC | 10392 |
rs5743343 | snp | C/T | 0.000613146 | 0.0174985 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452082 | CCTGGTGCAGCGGAA[C/T]ACACGCAGCCCAGTG | 10392 |
rs5743344 | snp | C/T | 0.00038105 | 0.0137978 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451756 | CCCCTGCGGGGGCAG[C/T]GACCACGTCCTGCTA | 10392 |
rs5743345 | snp | C/T | 0.000922115 | 0.0214524 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451604 | AAACAGAAACTCCTG[C/T]GGCATCTGGTGCCCG | 10392 |
rs5743346 | snp | A/G | 0.000118069 | 0.00768248 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451589 | CGGCATCTGGTGCCC[A/G]CGGCAGCCCTGAGGA | 10392 |
rs5743347 | snp | A/G | 0.00283054 | 0.0375134 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451507 | TGAAGAGCCTGCCCC[A/G]CGTTCAGGTCGAAAG | 10392 |
rs5743348 | snp | A/G | 0.000334653 | 0.0129312 | intron-variant | NOD1 | GRCh38.p7 | 7:30451175 | ACAGGTGGGCCGGGC[A/G]GGCCAGGCTCGGAGG | 10392 |
rs5743349 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | NOD1 | GRCh38.p7 | 7:30448607 | TGTGAGGAGCCAGGG[G/T]CTGTGCTGCAGCCTC | 10392 |
rs5743350 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30448492 | TTCTCCAGGGGCGTC[C/T]ATACCTGAGAAAACT | 10392 |
rs5743351 | snp | C/T | 0.00302885 | 0.0387976 | intron-variant | NOD1 | GRCh38.p7 | 7:30448416 | CATAATGAGTGCCTG[C/T]CCTGACTCGTAATTT | 10392 |
rs5743352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30448163 | CTGGCCCAGGAGTTG[A/G]GAGTCCTGGGTTCTC | 10392 |
rs5743353 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30448137 | TTCTCTTTGTGGCTC[A/G]GCCAGTCATGAAGTC | 10392 |
rs5743354 | snp | A/G | 0.000313736 | 0.0125208 | intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30447077 | ATCAGGAGCCAGAAA[A/G]TCTCATGGCTGTGCT | 10392 |
rs5743355 | snp | C/T | 0.000118318 | 0.00769058 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446950 | TAAGTGGGGTAGGCA[C/T]CAGGTTCCTTAGTAT | 10392 |
rs5743356 | snp | G/T | 0.0718919 | 0.175435 | intron-variant | NOD1 | GRCh38.p7 | 7:30446383 | AGGGCTTCAGTTCCC[G/T]CCCTGACAGGAGGCC | 10392 |
rs5743357 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOD1 | GRCh38.p7 | 7:30446355 | GCCCAGGCCATGGCT[C/T]TTGTGGATCCCAGAA | 10392 |
rs5743358 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446001 | GTGGAGAGCTTTCAC[C/T]ATGCTGCGAAACTga | 10392 |
rs5743359 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437365 | AAGTTCTGGGATACA[C/T]GTAGAAGATGTGCAG | 10392 |
rs5743360 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30436199 | TCTGCATCCTGCCCC[A/G]AGTGAGCCTGGGCTG | 10392 |
rs5743361 | snp | C/T | 0.0527655 | 0.153618 | intron-variant | NOD1 | GRCh38.p7 | 7:30436117 | TTGAATGTAGATGTG[C/T]CTTTAATAATTCACC | 10392 |
rs5743362 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NOD1 | GRCh38.p7 | 7:30435863 | TCATTCGAACCTCCC[A/G]CCTTGGCCTTCCGAG | 10392 |
rs5743363 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NOD1 | GRCh38.p7 | 7:30433382 | ATAGGAGCCCAGGTA[C/T]AGGATTTGCATTAAA | 10392 |
rs5743364 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | NOD1 | GRCh38.p7 | 7:30433381 | TAGGAGCCCAGGTAC[A/G]GGATTTGCATTAAAA | 10392 |
rs5743365 | snp | G/T | 0.0120236 | 0.0765979 | intron-variant | NOD1 | GRCh38.p7 | 7:30433243 | AGCTCCCGCTCCTGT[G/T]AACTCTAAAACAATG | 10392 |
rs5743366 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOD1 | GRCh38.p7 | 7:30429130 | catattctgtgctct[C/T]ctgcccTGGGCCCCC | 10392 |
rs5743367 | snp | C/T | 0.29278 | 0.246313 | intron-variant | NOD1 | GRCh38.p7 | 7:30428762 | TAATTGCCTGGGTGA[C/T]GTGGGACTGGGTGGA | 10392 |
rs5743368 | snp | A/G | 0.360632 | 0.224189 | intron-variant, utr-variant-3-prime | NOD1 | GRCh38.p7 | 7:30428600 | CTTTAGAACTTGTTT[A/G]GAACTTGTCATAAAA | 10392 |
rs5743369 | snp | A/G | 0.363985 | 0.222503 | intron-variant, utr-variant-3-prime | NOD1 | GRCh38.p7 | 7:30428568 | CGATCAGTTTGGTGA[A/G]TTGCAACCAACAATA | 10392 |
rs5743370 | snp | G/T | 0.0532157 | 0.154195 | intron-variant | NOD1 | GRCh38.p7 | 7:30425808 | TACATGTGTATTGTG[G/T]GATACACGAGTGTGT | 10392 |
rs5743371 | snp | A/G | 0.112954 | 0.209089 | intron-variant | NOD1 | GRCh38.p7 | 7:30425758 | AAGGAGTGTGCGAGG[A/G]TCCTTAACATTTTAC | 10392 |
rs5743372 | snp | C/T | 0.206947 | 0.246265 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425419 | AAAGAATGTGTCTTG[C/T]GAGCTGTTGTAGTTA | 10392 |
rs5743373 | snp | A/G | 0.210605 | 0.246877 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425345 | TTTTTATCTGAAGCT[A/G]GAGGAATAAAGCTGT | 10392 |
rs5743374 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425256 | GAGCGAGTTGGTCAC[C/T]GCTCTTTTCATTGAA | 10392 |
rs5743375 | snp | A/C | 0.0252325 | 0.109451 | downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30424384 | GAAGGCCAGGGGTGT[A/C]ACCAGTTTGATCCTT | 10392 |
rs5743376 | snp | C/T | 0.0252325 | 0.109451 | downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30424366 | CAGTTTGATCCTTCA[C/T]AGGCCTCTCTGCCTA | 10392 |
rs5743377 | snp | A/G | 0.0349115 | 0.127424 | downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30424334 | CAAGGGACAGGAAGC[A/G]GCTGTGGCAGCCTCT | 10392 |
rs5743378 | snp | C/T | 0.00405678 | 0.0448546 | downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30424306 | TCTGAGGTCTCTCCA[C/T]CTGGCCTCTGAATCT | 10392 |
rs6462208 | snp | C/G | 0.473359 | 0.112298 | intron-variant | NOD1 | GRCh38.p7 | 7:30456434 | TCTTATGCTTATGTT[C/G]TTTTTCCCTCCTAAT | 10392 |
rs6947097 | snp | A/G | 0.000263626 | 0.011478 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456758 | GCACACACAATCTCC[A/G]CATCTTCGGCCGAGA | 10392 |
rs6948524 | snp | C/T | 0.283947 | 0.247685 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30465556 | CTGATGGGGCCAGAT[C/T]GAGAACAGAAACCTC | 10392 |
rs6949758 | snp | C/G | 0.487933 | 0.0767327 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462063 | TTAATTGGCTTTTCA[C/G]ATCAGTTTCATCGGC | 10392 |
rs6958462 | snp | A/G | 0.00519477 | 0.0506991 | intron-variant | NOD1 | GRCh38.p7 | 7:30438789 | AGTCTCACCCCTACT[A/G]TAGTATAGATACATA | 10392 |
rs6958571 | snp | A/C | 0.372123 | 0.218238 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446094 | CAAGGCCCGCCCCCC[A/C]CACACACAGCAGGTT | 10392 |
rs6959175 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466829 | CCTGTCTACCTCAGA[C/G]TCAGCAGTAATCTAT | 10392 |
rs6959470 | snp | C/T | 0.131723 | 0.220251 | intron-variant | NOD1 | GRCh38.p7 | 7:30430274 | GAGAATGCACCCCAT[C/T]GTTCTGGGTAGCAGT | 10392 |
rs6960411 | snp | A/T | 0 | 0 | utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456926 | TGCTCTTCCATAGTT[A/T]AAGTAGCAAGCGGCT | 10392 |
rs6960726 | snp | C/T | 0.0130921 | 0.0798413 | utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30457009 | TCAGGATTCAGGCCG[C/T]GCCCTCCAGGGCCCC | 10392 |
rs6963954 | snp | A/G | 0.15698 | 0.23205 | intron-variant | NOD1 | GRCh38.p7 | 7:30474825 | CCATTTCAGCCCTGC[A/G]TGTCTGGTATACTTT | 10392 |
rs6968200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453432 | CCTCCACCAACACTG[C/T]ttttttgttgttaga | 10392 |
rs6971352 | snp | C/T | 0.135484 | 0.22223 | intron-variant | NOD1 | GRCh38.p7 | 7:30449949 | tgtaaccccaacatt[C/T]tggaaggccgaggcg | 10392 |
rs7457115 | snp | A/G | 0 | 0 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467642 | TTTTGTGAAAGTATC[A/G]CAATAAATCTGATGG | 10392 |
rs7781700 | snp | C/T | 0.084364 | 0.187256 | intron-variant | NOD1 | GRCh38.p7 | 7:30457916 | CAGCAAAGTCTGTTA[C/T]ACACAAGCACCCTGG | 10392 |
rs7782405 | snp | A/C | 0 | 0 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437493 | TCTTCTATTAGGAGC[A/C]CGAATCACCCTTCCC | 10392 |
rs7788199 | snp | A/G | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462786 | aaaccctgtctccac[A/G]aaaaatacaaaaatt | 10392 |
rs7789045 | snp | A/T | 0.461481 | 0.133325 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454406 | GTGGTCTCTTCCAGC[A/T]GACTTGAAGCTCCCT | 10392 |
rs7790806 | snp | C/G | 0.23031 | 0.249223 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30478922 | CCGGGTCTGGCGCGG[C/G]GGGGCGAGAGAAGCT | 10392 |
rs7792535 | snp | C/T | 0.494692 | 0.0512434 | intron-variant | NOD1 | GRCh38.p7 | 7:30439366 | catctcactagggag[C/T]gccagacagtgggcg | 10392 |
rs7792821 | snp | C/G | 0.0898077 | 0.191933 | intron-variant | NOD1 | GRCh38.p7 | 7:30439570 | agaaacggcgcacca[C/G]gagactatatcccac | 10392 |
rs7793010 | snp | C/T | 0.300421 | 0.244863 | intron-variant | NOD1 | GRCh38.p7 | 7:30430537 | GGAAGACGAGGGCCC[C/T]ATGCTGTCATGAATG | 10392 |
rs7794325 | snp | C/G | 0.157972 | 0.232445 | intron-variant | NOD1 | GRCh38.p7 | 7:30427312 | CTCATCAAGGGACTT[C/G]AGACTTCCAAGTTAT | 10392 |
rs7799575 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458578 | AATGCCAGACCCCAC[A/C]CAATAGCTTTCTTTT | 10392 |
rs9942688 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461987 | tcgtgatccacccac[C/T]tcggcctcccaaagt | 10392 |
rs10224448 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30475458 | GAAAAGGACGCTTCA[A/G/T]TAAAACAAATTCTAA | 10392 |
rs10245465 | snp | A/G | 0.101301 | 0.200969 | intron-variant | NOD1 | GRCh38.p7 | 7:30438768 | TGAAAAAGGAAGGAT[A/G]CATATAGTCTCACCC | 10392 |
rs10250345 | snp | C/T | 0 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30457079 | TCAGCAAAGCAAAAG[C/T]TACAGAAAGAGCTCA | 10392 |
rs10258522 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458921 | tttgtatttttagta[A/G]agacagggtttcacc | 10392 |
rs10264580 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30455605 | Ctttttttttttttt[C/T]ttttttgagacagag | 10392 |
rs10267377 | snp | C/G | 0.439363 | 0.163222 | intron-variant | NOD1 | GRCh38.p7 | 7:30431253 | CTGCAGGCTAAAAAG[C/G]AAAGAAAAAACAATA | 10392 |
rs10951267 | snp | A/C | 0.482234 | 0.0925596 | intron-variant | NOD1 | GRCh38.p7 | 7:30457278 | GCAACATAGTGAGAC[A/C]CCCATCTCTACAAAA | 10392 |
rs11313806 | in-del | -/A | 0.371785 | 0.218331 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462965 | AAAAAAAAAAAAAAA[-/A]GATTTCATGCATATG | 10392 |
rs11382352 | in-del | -/T | 0 | 0 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30465658 | GCTCTTTTTTTTTTT[-/T]CATGTTTATATTTCA | 10392 |
rs11430536 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458756 | TTTTTTTTTTTTTTT[-/T]GACAGAGTCCCACTG | 10392 |
rs11532695 | snp | C/G | 0.138665 | 0.224207 | intron-variant | NOD1 | GRCh38.p7 | 7:30427793 | ATTAAAGCAACTGTA[C/G]GTCTTTACTACCCGC | 10392 |
rs11536450 | snp | C/G | 0.358515 | 0.225221 | intron-variant | NOD1 | GRCh38.p7 | 7:30427948 | TGGCCTGAGGGCAAA[C/G]ACCCATGCAAACAGT | 10392 |
rs11761519 | snp | C/T | 0.040671 | 0.13668 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466560 | aatgactcaggaggc[C/T]gaggcaggaggatca | 10392 |
rs11773041 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NOD1 | GRCh38.p7 | 7:30474475 | ttccacagacagcgg[C/T]gagtaggggcacagg | 10392 |
rs12538405 | snp | C/T | 0 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30476821 | AAGCCCGCTAAGGCC[C/T]TGAGCGGGGCAGCAG | 10392 |
rs12667786 | snp | A/T | 0 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30471257 | AGAGCCATAACCCCT[A/T]AAGCATCTGCCCCAG | 10392 |
rs12669082 | snp | G/T | 0.266546 | 0.249452 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466617 | GGCTACAGTGAGCTA[G/T]GATCACACCACTGTA | 10392 |
rs13226678 | snp | G/T | 0.00508903 | 0.0501858 | intron-variant | NOD1 | GRCh38.p7 | 7:30478409 | CGATTCCGCTGACTG[G/T]GAAGTTCATCCCTCT | 10392 |
rs13239522 | snp | C/T | 0 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30478441 | AACTTTCGCTACATG[C/T]TTCAAACTCGCGGGT | 10392 |
rs13239623 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30478529 | GCAAATCCCGCCTCC[C/T]TGCGCCTCCTCACTC | 10392 |
rs13239788 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30478478 | GCTTGGTTCCACCCA[A/G]AGCTCCTCCAGAGCC | 10392 |
rs17159043 | snp | C/T | 0.247053 | 0.249983 | intron-variant | NOD1 | GRCh38.p7 | 7:30429654 | TTGATATTTTTTAAA[C/T]TTTCTGTTTGTTTTT | 10392 |
rs17159048 | snp | G/T | 0.107341 | 0.205301 | intron-variant | NOD1 | GRCh38.p7 | 7:30430779 | CAGGGGGAAGGGAGC[G/T]CTTGTCACTGTTACT | 10392 |
rs17159124 | snp | C/T | 0.284471 | 0.247612 | intron-variant, missense | NOD1, LOC101928268 | GRCh38.p7 | 7:30469168 | TTAAGGAACTTAACC[C/T]GGAAAACAAGCCCGG | 10392 |
rs17770244 | snp | A/G | 0.11228 | 0.208646 | intron-variant | NOD1 | GRCh38.p7 | 7:30476196 | TTTGAACAAATATTG[A/G]ATCCTTTTCTTTGAA | 10392 |
rs28404101 | snp | A/G | 0.282632 | 0.247861 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461802 | GGAGTGCAGTGGCAC[A/G]ATCTTGGCCCACTGC | 10392 |
rs28611502 | snp | A/T | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461586 | GTTTGGATCAACCAC[A/T]TTTCCAGTGCTCAAG | 10392 |
rs34135234 | in-del | -/C | | | intron-variant | NOD1 | GRCh38.p7 | 7:30435181 | CTCAGGAGGCCACAT[-/C]CCACTTAGTAAGTGC | 10392 |
rs34218055 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467344 | ACTTTTATTCGTAAT[G/T]TTTTTTTTTTTATAA | 10392 |
rs34260660 | in-del | -/A | 0.5 | 0 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462948 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10392 |
rs34329586 | snp | C/T | 0.375 | 0.216506 | intron-variant | NOD1 | GRCh38.p7 | 7:30440091 | AAAGGACATCTACAC[C/T]GAAAACCCATCTGTA | 10392 |
rs34332214 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453196 | TCAGATGCAGGACCT[-/G]GGGGAGCGTCACAGA | 10392 |
rs34477533 | in-del | -/A | | | intron-variant | NOD1 | GRCh38.p7 | 7:30432209 | AAACCTGTATCTAGT[-/A]AAAGGTCTAGCACCC | 10392 |
rs34521303 | in-del | -/G | | | downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30424219 | GAAGGCATGAACTTT[-/G]GCCCACTTGGCCTGT | 10392 |
rs34626585 | in-del | -/TT | | | intron-variant | NOD1 | GRCh38.p7 | 7:30455591 | GGACTTCTCTACCTC[-/TT]TTTTTTTTTTTTTTC | 10392 |
rs34655613 | snp | C/T | 0.25912 | 0.249834 | intron-variant | NOD1 | GRCh38.p7 | 7:30474738 | TCCATGGCCTAGGGA[C/T]TGGGGACCCCTGAAG | 10392 |
rs34750559 | in-del | -/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30448426 | CAGGGCAGGCACTCA[-/T]TTATGAAGGACCATT | 10392 |
rs34851310 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451962 | CTCCTGCAGCCCGGA[-/G]GCCTGCACCTCCTCC | 10392 |
rs34895025 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458988 | TGATCTGCCCACCTC[-/G]GGCCTCCCAAAGTGC | 10392 |
rs34905452 | in-del | -/C | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428353 | GCATGAGCCACCATG[-/C]CCTAGCCAACAGTGT | 10392 |
rs34927032 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30424892 | CTAGAGGAGGGTAGC[C/T]TAGCAGAGGAGAAGC | 10392 |
rs34952551 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30427582 | GAACAAGCCAGGGAC[C/T]TAAGTGAAGACACTC | 10392 |
rs34981047 | in-del | -/C | | | intron-variant | NOD1 | GRCh38.p7 | 7:30472594 | CATGGTGAGGGAGAA[-/C]CCCCCGATTTGATGG | 10392 |
rs35116223 | in-del | -/G | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437184 | ACAATGAGAACACAT[-/G]GGACACATGGAGGGG | 10392 |
rs35370487 | in-del | -/G | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466905 | ACCTTCTTTATTTGT[-/G]CCTTGGGTTACATCA | 10392 |
rs35530986 | in-del | -/T | 0.466721 | 0.124627 | intron-variant | NOD1 | GRCh38.p7 | 7:30477701 | TTTTTTTTTTTTTTT[-/T]AGTAGAGACGGTTTC | 10392 |
rs35669955 | in-del | -/A | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30445783 | AAAAAAAAAAAAAAA[-/A]GGAAATCCTGTCCCA | 10392 |
rs35695062 | in-del | -/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30426603 | GCAGATCTGATCACA[-/T]TGCCTCTCCTGCTTC | 10392 |
rs35700973 | multinucleotide-polymorphism | AA/TC | | | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30478861 | TGGGAGAGGCCGCCG[AA/TC]GGGCGGGGGCGGTCA | 10392 |
rs35729036 | in-del | -/A | 0.467439 | 0.123371 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463707 | TGAGATGCTAAGATT[-/A]AAAAAAAAAAAACAT | 10392 |
rs35759727 | in-del | -/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30471193 | GGAGAGTACCCAGGG[-/T]ATTTATGTGTGGTGA | 10392 |
rs35853814 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451912 | CCGGGGCCCAGCTCC[-/G]GCAAAGCCCGCAGGA | 10392 |
rs35863198 | in-del | -/A | | | intron-variant | NOD1 | GRCh38.p7 | 7:30434202 | TTCTCACTGGTGAAC[-/A]GTTAACAGTAGAGAT | 10392 |
rs36035508 | in-del | -/A | | | intron-variant | NOD1 | GRCh38.p7 | 7:30434218 | TTAACAGTAGAGATC[-/A]GTATAGAGTGGTTGT | 10392 |
rs36039194 | in-del | -/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30475070 | GTGTTACAAGAAGCA[-/G]GGGGAAGTTCTTACT | 10392 |
rs36072587 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30476789 | GAGGGGATTTGCAGC[C/T]TAAGATTTCAGACTT | 10392 |
rs41405946 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30478694 | ACGCCGGGGCCGGGA[C/T]GCGCCGTGGCCCGGG | 10392 |
rs41524946 | snp | C/G | 0.266819 | 0.249434 | intron-variant | NOD1 | GRCh38.p7 | 7:30471638 | GGGATTTCTGGGCAA[C/G]AGCTAGGCGGAGCAG | 10392 |
rs55634181 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463719 | ATTAAAAAAAAAAAA[-/A]CATTTTATAAAGATG | 10392 |
rs55689059 | snp | A/G | 0.267636 | 0.249377 | intron-variant | NOD1 | GRCh38.p7 | 7:30471854 | CTGATGAAGGATGCC[A/G]GGTGCCTAGGAGGCC | 10392 |
rs55720335 | in-del | -/T | 0.5 | 0 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467345 | AATGTTTTTTTTTTT[-/T]ATAAGAAGGCTATAC | 10392 |
rs55740347 | snp | G/T | 0.264084 | 0.249603 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462456 | TTGCTGTTTTTTCTT[G/T]TTAAACAAGGGACTT | 10392 |
rs55785709 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30474993 | CTGCCAAAAAAGCCT[A/G]GCTTTCCCCCAGTTC | 10392 |
rs55808235 | snp | A/T | 0.00144095 | 0.0268029 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452327 | CCCGCTCGGGGAACA[A/T]CCTCCTGGCATAGGC | 10392 |
rs55813184 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459255 | TCTGCAAAATCAAAG[A/G]AAGACTTAAAAAAAT | 10392 |
rs55816947 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459143 | ATTTAAATTAGCAGT[G/T]AATAATACCTTTTTA | 10392 |
rs55841603 | snp | C/T | 0.266819 | 0.249434 | intron-variant | NOD1 | GRCh38.p7 | 7:30472021 | CTAGACACTCCAGAA[C/T]TGTTTCACACACTAA | 10392 |
rs55875433 | in-del | -/AAA | | | intron-variant | NOD1 | GRCh38.p7 | 7:30445300 | AAAAAAAAAAAAAAA[-/AAA]GAATTGAAGGCAGTC | 10392 |
rs55892134 | in-del | -/A | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428384 | TTTTTTAAAAAAAAA[-/A]CCTTTTGTCTACAAC | 10392 |
rs55901916 | snp | C/T | 0.33303 | 0.235809 | intron-variant | NOD1 | GRCh38.p7 | 7:30439386 | GACAGTGGGCGCAGG[C/T]CAGTGTGTGCGCGCA | 10392 |
rs55911117 | snp | A/C | 8.23635e-05 | 0.00641677 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30429416 | TGTAACGCATCTGCC[A/C]GCTGGGCAGTCCCCT | 10392 |
rs55924701 | snp | C/T | 2.45558e-05 | 0.0035039 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30437645 | TCATCCCCAACTTGA[C/T]TGCCCCACATCCTGA | 10392 |
rs55947865 | snp | C/T | 4.94466e-05 | 0.00497201 | missense, utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452918 | CATTGCTGAAGCCAA[C/T]CAGCTCCATGATGGT | 10392 |
rs55951189 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459081 | ACTTTAGGATCCTTA[A/G]CTTTAGAAAATCGGT | 10392 |
rs55981427 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOD1 | GRCh38.p7 | 7:30457136 | TCTCTACCTAGAGCA[A/G]GAAGGAACCATGCTT | 10392 |
rs55983406 | in-del | -/G | 0.0111196 | 0.0737302 | intron-variant, utr-variant-3-prime | NOD1 | GRCh38.p7 | 7:30437789 | AGTCCCTGGATCTGT[-/G]GCCTGGACACTAATT | 10392 |
rs55996014 | in-del | -/C | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446087 | GAACAGCAAGGCCCG[-/C]CCCCCCACACACACA | 10392 |
rs56027100 | snp | C/T | 0.144632 | 0.226711 | intron-variant | NOD1 | GRCh38.p7 | 7:30425880 | CATATTAGCATGGAT[C/T]CTCTCCAGCTGCCAT | 10392 |
rs56027389 | snp | A/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30457498 | AAAAAAATCATAATT[A/T]AATTGTTTGCACTTG | 10392 |
rs56044411 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | NOD1 | GRCh38.p7 | 7:30454969 | GCAGTTCAATCGCAG[A/C]CACCTGGGCTGCACT | 10392 |
rs56055493 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461831 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 10392 |
rs56112216 | snp | C/T | | | intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30450971 | TCTTCTTTTTCCAGA[C/T]GAGGGCGTGGAGGCT | 10392 |
rs56168419 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NOD1 | GRCh38.p7 | 7:30431524 | GATTTTTGACAAGGG[C/T]GTCAAGGCCATTCAA | 10392 |
rs56237929 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458939 | ACAGGGTTTCACCAC[A/G]TTGGCCAAGCTGGTC | 10392 |
rs56242717 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464032 | GCCCTCTTTGGAGCT[A/G]CAGAAGCTGGCTTCT | 10392 |
rs56271862 | snp | A/G | 0.0596104 | 0.162024 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454692 | GGCTGGAGTGTAGGG[A/G]CACAATCATAGCTCG | 10392 |
rs56294822 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454253 | GGTGCTGGTATGTTA[C/T]CAACAGCTGTCTCAA | 10392 |
rs56321585 | snp | G/T | 0.330482 | 0.236691 | intron-variant | NOD1 | GRCh38.p7 | 7:30439392 | GGGCGCAGGCCAGTG[G/T]GTGCGCGCACCGTGC | 10392 |
rs56770811 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | NOD1 | GRCh38.p7 | 7:30439279 | GAATAGGAACAGCTC[C/T]GGTCTACAGCTCCCA | 10392 |
rs57287806 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30477929 | CCGAAATGTTTCCTA[A/G]AATGCAGAGCTAATG | 10392 |
rs57367064 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452901 | CAGGCTGCCCAGGCT[C/T]TCATTGCTGAAGCCA | 10392 |
rs57429651 | in-del | -/AA | 0.0142736 | 0.0832652 | intron-variant, frameshift-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30460405 | TCCTCTCTTCCAGGC[-/AA]AGAGAGGACGGAGAT | 10392 |
rs57461794 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, utr-variant-5-prime | NOD1, LOC101928268 | GRCh38.p7 | 7:30460248 | ACCAAAACCATACCA[C/T]GGGAGACTGGAGATC | 10392 |
rs57588576 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | NOD1 | GRCh38.p7 | 7:30447491 | TTTCAGCCATCTCAC[C/T]GCTCAATGCCAATTC | 10392 |
rs57858917 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463270 | ACTTCCATGAAATTG[A/G]TTTTCTTTTAAGGAA | 10392 |
rs58258693 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NOD1 | GRCh38.p7 | 7:30431351 | ACCCAGAATGGTCTA[A/C]ACAATCTTGAGAAAG | 10392 |
rs58364687 | in-del | -/AG | 0.125528 | 0.21681 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458360 | AAACTCATGCATTTC[-/AG]AGAGAGAGAGTAAAA | 10392 |
rs58432605 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NOD1 | GRCh38.p7 | 7:30449056 | TACTCAACTGTGTAG[C/T]GTGAAGCAGCCAGTA | 10392 |
rs58516727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30447743 | AACCTCAAAGGCTCT[A/G]AATGCCCAAAGTTTC | 10392 |
rs58870973 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | NOD1 | GRCh38.p7 | 7:30477846 | CCTTAAAGCAGAAAG[A/G]CCAGAAGTCATCAAG | 10392 |
rs59063034 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NOD1 | GRCh38.p7 | 7:30431617 | AGAATGAGGTTAACC[C/T]TCACTTTACACTATA | 10392 |
rs59097524 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | NOD1 | GRCh38.p7 | 7:30438900 | AAATGTTAACAAGAA[G/T]CATTTTCTGAGAAGA | 10392 |
rs59696387 | in-del | -/ATAA | | | intron-variant | NOD1 | GRCh38.p7 | 7:30431235 | AATGGGATCAAATAA[-/ATAA]TTCTGCAGGCTAAAA | 10392 |
rs59749412 | snp | A/G | 0.406986 | 0.194565 | intron-variant | NOD1 | GRCh38.p7 | 7:30431495 | GAAATAAACCCATAC[A/G]TTTATGGTCAATTGA | 10392 |
rs60595955 | in-del | -/A | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462949 | TGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 10392 |
rs60914327 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459864 | CCCTCCTTTCCCGAC[A/C]TTTGCCCGCCTACCA | 10392 |
rs60977440 | snp | C/T | 0.0832709 | 0.186283 | utr-variant-5-prime, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30478750 | AGGGAGGGGCAGGAC[C/T]GGGGCGGCTGCCTCG | 10392 |
rs61245928 | in-del | -/AGCTT | | | intron-variant | NOD1 | GRCh38.p7 | 7:30477881 | TGGGTTTACTAGCTT[-/AGCTT]CCCCAGACTTAATTT | 10392 |
rs61354174 | snp | A/C | 0.0479149 | 0.147179 | intron-variant | NOD1 | GRCh38.p7 | 7:30439507 | GACGGACGCACCTGG[A/C]AAATCGGGTCACTCC | 10392 |
rs61698133 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30445450 | TGCAATGGAGTATTA[C/T]TCAGCCTTAAAAAAG | 10392 |
rs61757653 | snp | C/T | 0.000527053 | 0.0162249 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456902 | ATTATTTCCATCTCA[C/T]TGTGGCCCTGCTCTT | 10392 |
rs62447418 | snp | C/T | 0.5 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30432205 | TTGCAAAACCTGTAT[C/T]TAGTAAAGGTCTAGC | 10392 |
rs62447419 | snp | A/T | 0.5 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30433824 | TTTAAAAAAAAAAAT[A/T]CCTTGAAGGGCAGTT | 10392 |
rs62447420 | snp | C/T | 0.266273 | 0.24947 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461008 | GGAAAAAGGAGACCA[C/T]AGAGCAGCTCTGTTG | 10392 |
rs62447421 | snp | A/C | 0.266546 | 0.249452 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461074 | AACTTTCTAATAGCC[A/C]CACTAATAAAAGTAA | 10392 |
rs62447422 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463708 | GAGATGCTAAGATTA[A/T]AAAAAAAAAAACATT | 10392 |
rs62636578 | snp | A/G | 0.00279055 | 0.037249 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452586 | GGTGAAGAGGGCCAC[A/G]TGGGGGAAGCGCAGC | 10392 |
rs62636579 | snp | G/T | 6.61376e-05 | 0.00575017 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451665 | GTTGGTGAACTGGAA[G/T]TGATCCTTGTTCTTG | 10392 |
rs66765076 | in-del | -/TAGCT | 0.434253 | 0.168969 | intron-variant | NOD1 | GRCh38.p7 | 7:30477875 | AGGCCATGGGTTTAC[-/TAGCT]TAGCTTCCCCAGACT | 10392 |
rs70983304 | in-del | -/A | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454823 | TTAAAAGAAAAAAAA[-/A]TACAACCTTGAATTT | 10392 |
rs71530511 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30426779 | CAGCTTCTGGCAGTT[C/T]TTCCAGGACACCACA | 10392 |
rs71530515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454144 | AGCACTGACACTCTG[C/T]CGGCTGGCCTTGTTT | 10392 |
rs71557462 | in-del | -/G | 0.5 | 0 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479701 | GAAATTCCTTCTCCT[-/G]GCTCAGAAGCTCCCC | 10392 |
rs71557463 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479705 | TCCTTCTCCTGGCTC[-/A]AGAAGCTCCCCCACT | 10392 |
rs72470547 | snp | C/T | 0.344318 | 0.231526 | missense, utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452845 | ACACCACCGGCATCC[C/T]CAATGAGCAGGGTGA | 10392 |
rs72478563 | snp | A/G | 0.212736 | 0.247207 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30445987 | CCATGCTGCGAAACT[A/G]ACCGTGCCCATTAAG | 10392 |
rs72551105 | snp | G/T | 0.251297 | 0.249997 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452308 | GTTCCCCGAGCGGGC[G/T]GCAGGACCGCCTGCT | 10392 |
rs72551107 | snp | C/T | 0.280039 | 0.248189 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452371 | GGAAGAAGGTGCTTC[C/T]CCGGGGCTTCTCCCC | 10392 |
rs72551108 | snp | C/T | 0.280105 | 0.248181 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452847 | CCACACCACCGGCAT[C/T]CAATGAGCAGGGTGA | 10392 |
rs72551109 | snp | A/G | 0.273537 | 0.24889 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30453015 | TATACCCAGCAGCTG[A/G]CACCATCTGGGCCGT | 10392 |
rs72551110 | snp | C/T | 0.251226 | 0.249997 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452800 | CCTGGGTGATGCTGG[C/T]GGGCAAGTCCATGCT | 10392 |
rs72551112 | snp | C/T | 0.228509 | 0.249075 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452931 | GATCTACATGGACAC[C/T]ATCATGGAGCTGGTT | 10392 |
rs73083609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30473229 | AGACCTCAGGGAAGA[C/T]TGCCAGAACTCAAGA | 10392 |
rs73309227 | snp | C/T | 0.197703 | 0.244469 | intron-variant | NOD1 | GRCh38.p7 | 7:30430654 | TTGAAGAAATAAACG[C/T]ATCTGTCTGTGCCTC | 10392 |
rs73309229 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NOD1 | GRCh38.p7 | 7:30434342 | TCCATGTGATTTCAC[A/T]CTCCATGGGGCACCT | 10392 |
rs73309234 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NOD1 | GRCh38.p7 | 7:30445480 | GAAGGAAATCCTGGC[A/G]GGGCACGGTGGCTCA | 10392 |
rs73309250 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462148 | AGGAAGAAAATACAC[A/G]CTGGACCTACTGGTT | 10392 |
rs73687865 | snp | A/T | 0.261884 | 0.249717 | intron-variant | NOD1 | GRCh38.p7 | 7:30427024 | TTTTCTTTAATGTGC[A/T]TCTCCCTTTCTAGAC | 10392 |
rs73687866 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | NOD1 | GRCh38.p7 | 7:30427770 | TGCAGATTTTGAAAC[C/T]TGACAGAATTAAAGC | 10392 |
rs73687868 | snp | A/G | 0.097727 | 0.198275 | intron-variant | NOD1 | GRCh38.p7 | 7:30430807 | ACTGCCCAAGCACAC[A/G]GGACCACTGGTGGCT | 10392 |
rs73687871 | snp | C/T | 0.0402882 | 0.136092 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454032 | TTTCTTTTTTTTTCA[C/T]GGGGGAAGGAAACAA | 10392 |
rs73687872 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NOD1 | GRCh38.p7 | 7:30456296 | GGGAAGATTCTTCAC[C/T]GTGGACCCACCGTGG | 10392 |
rs73687874 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463349 | GTATCTGCACTAAAA[C/T]GAACACTAAATAGAG | 10392 |
rs73687875 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NOD1 | GRCh38.p7 | 7:30472443 | CTAATTCTAGTTCTG[C/T]TCTGATCTCCTGTCT | 10392 |
rs73687876 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | NOD1 | GRCh38.p7 | 7:30476370 | AGTGACCATCCATGA[C/T]GCACAGAGCACGTAC | 10392 |
rs73687877 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | NOD1 | GRCh38.p7 | 7:30476975 | CAGAGCACCTGCCAG[C/T]GCCACCACCTTCCAG | 10392 |
rs74599965 | snp | A/T | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466774 | CAGATACTATAACTA[A/T]TTATGGAATTAAGAT | 10392 |
rs74674289 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NOD1 | GRCh38.p7 | 7:30432798 | GACAAAAGGTCACAT[A/G]TTGCTTGATTCCATT | 10392 |
rs74758916 | snp | G/T | 0.300169 | 0.244914 | intron-variant | NOD1 | GRCh38.p7 | 7:30430707 | GAATAACTATAAGAG[G/T]GCCCCCCATCCACTG | 10392 |
rs74839208 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462201 | TCACTGCTGCATACA[A/G]TTTTGCAGCTTTGCA | 10392 |
rs74933831 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467145 | GCAGAAAGAAATATA[C/G]AGTATAATAACATTT | 10392 |
rs75087944 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30477198 | AAAAATAAAACCTAC[C/T]CTTCTTACAATATTT | 10392 |
rs75275800 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466216 | GTTCATCAAACAGTT[A/C]AGGTTCTTCTCCTAG | 10392 |
rs75292461 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30465951 | CCAGGTCATATGGAA[A/C/T]CTGGCCCAGTGCCAT | 10392 |
rs75300954 | snp | C/T | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463792 | AAGTATAAAACAATA[C/T]CTGCTCACTGTAGAA | 10392 |
rs75403793 | in-del | -/A | 0.284209 | 0.247648 | intron-variant | NOD1 | GRCh38.p7 | 7:30471569 | CTCTCAAGTGCACAC[-/A]AATGATGAATTCAGA | 10392 |
rs75437212 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NOD1 | GRCh38.p7 | 7:30438418 | TAATTAGAGCATTCC[A/G]TCATGGAGTTGTGAG | 10392 |
rs75550093 | snp | A/T | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466775 | AGATACTATAACTAT[A/T]TATGGAATTAAGATT | 10392 |
rs75891379 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | NOD1 | GRCh38.p7 | 7:30431753 | TCATTTCTTAGATAA[A/G]ACACTGAAAGCACAA | 10392 |
rs75934729 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOD1 | GRCh38.p7 | 7:30473436 | CCCCACATCTGTCTG[A/G]GTGAAGGCATGTTTT | 10392 |
rs76102059 | snp | A/C | 0.5 | 0 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461521 | GTTTACATTCTTTTT[A/C]TTCATACTATGGCTT | 10392 |
rs76406513 | snp | A/T | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466776 | GATACTATAACTATT[A/T]ATGGAATTAAGATTT | 10392 |
rs76422331 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NOD1 | GRCh38.p7 | 7:30430732 | CCACTGGGTGTGTGA[A/G]ATTTCAAGAGGAGGG | 10392 |
rs76450990 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NOD1 | GRCh38.p7 | 7:30476272 | TCACACATACACTAG[A/G]AAAACACTTGATCTT | 10392 |
rs76465324 | snp | A/C | | | intron-variant | NOD1 | GRCh38.p7 | 7:30434001 | CAAATTTAGATCAGA[A/C]ACAACTGATGAAATA | 10392 |
rs76508391 | snp | G/T | 0.141934 | 0.225437 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428233 | ATAGCACCATGTCGG[G/T]CTAATTTTTGTAGTG | 10392 |
rs76563927 | snp | C/T | 0.109108 | 0.206518 | intron-variant | NOD1 | GRCh38.p7 | 7:30426835 | ACATGCTGTTCCCTA[C/T]GCAGAATACTCACCT | 10392 |
rs76568682 | snp | G/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30448618 | ACAGCCCCTGGCTCC[G/T]CACACGACCGTGAAG | 10392 |
rs76636129 | snp | A/C | | | intron-variant | NOD1 | GRCh38.p7 | 7:30432749 | TGAATTATCATTTAG[A/C]CATAAAAAGGAATGA | 10392 |
rs76666490 | snp | A/G | 0.000875259 | 0.0209013 | intron-variant | NOD1 | GRCh38.p7 | 7:30436107 | ACACACTTGGGGTGA[A/G]TTATTAAAGACACAT | 10392 |
rs76812027 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | NOD1 | GRCh38.p7 | 7:30437826 | ACTGGTCTCTGAGTG[G/T]GCTGCTCTGGATTTC | 10392 |
rs76814914 | snp | G/T | 0.0267878 | 0.112589 | intron-variant, utr-variant-5-prime | NOD1, LOC101928268 | GRCh38.p7 | 7:30460211 | ACTGAACTCTGCCTT[G/T]GTAAACAGAATCTAA | 10392 |
rs76985555 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425304 | AGGTGTTGGAATGAG[C/G]TGAGGCTGGCCTCCT | 10392 |
rs77007401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30456149 | CTTCTGAGTCCCAGC[A/G]GGGTCATGTCATAAA | 10392 |
rs77396593 | snp | A/C | 0.0479149 | 0.147179 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463875 | ATCCACATGCAATAA[A/C]CACTATTCTCATTTT | 10392 |
rs77496953 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD1 | GRCh38.p7 | 7:30475367 | ATTAAAATCTTAATC[C/T]GCCAAAATCTGGCAC | 10392 |
rs77601900 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30424616 | CTCATGGAGCAGCCA[C/T]CACAAGCCCACCATG | 10392 |
rs77664104 | snp | C/G | 0.0854556 | 0.188216 | intron-variant | NOD1 | GRCh38.p7 | 7:30477567 | TTGCCCAGGCTGGAG[C/G]GCAACAGGGCGATCT | 10392 |
rs77774622 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428074 | TATGATGGTGTTTTT[C/T]TTTTTTTCTTTTTTG | 10392 |
rs77923370 | snp | A/T | 0.5 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30433822 | CATTTAAAAAAAAAA[A/T]TTCCTTGAAGGGCAG | 10392 |
rs77963521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30426999 | TAATTAAATAATTAC[A/G]CAAATGATTTTTTCT | 10392 |
rs78020741 | snp | A/C | 0.5 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30427130 | TTATTCAAGGAATAA[A/C]TGAAGACACAGCACT | 10392 |
rs78188315 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466848 | GCAGTAATCTATATA[A/G]GGAGATACTGCTTTA | 10392 |
rs78206797 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459226 | AATCTTCAATTTCCA[A/G]TTTATTTCTGGAATC | 10392 |
rs78217120 | snp | G/T | 0.5 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30434940 | AACCTGTAAGGAATG[G/T]TTTTTTTTTTTGTAG | 10392 |
rs78930943 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30439138 | GTTGGTGGGAACATA[A/C/G]AATGGTGCTGCTGCC | 10392 |
rs78983713 | snp | A/C | 0.0520825 | 0.152737 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461164 | TTCAGTATGTCATCC[A/C]TACAAAATTTATTTA | 10392 |
rs79068688 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | NOD1 | GRCh38.p7 | 7:30427586 | AAGCCAGGGACCTAA[C/G]TGAAGACACTCCCAA | 10392 |
rs79100492 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NOD1 | GRCh38.p7 | 7:30434222 | ACAGTAGAGATCGTA[C/T]AGAGTGGTTGTGAGG | 10392 |
rs79357452 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD1 | GRCh38.p7 | 7:30476643 | GCCATTTAAAAGATA[C/T]ATATGTGGCAACAGA | 10392 |
rs79486294 | snp | A/G | 0.136166 | 0.22258 | intron-variant | NOD1 | GRCh38.p7 | 7:30449305 | GCATGGCCAGCCCAA[A/G]ACAGCACAGGCTGCT | 10392 |
rs79507500 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | NOD1 | GRCh38.p7 | 7:30476350 | AGCACTGCTGTTAGG[A/G]TCAAAGTGACCATCC | 10392 |
rs79519442 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30468572 | CCACCACCATCCTGG[A/G]CAATAGGAATAGATA | 10392 |
rs79682524 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | NOD1 | GRCh38.p7 | 7:30476015 | AAGAAAATGGGACTT[C/T]TGAAAACTTGCAAAA | 10392 |
rs79719900 | snp | G/T | 0.0923359 | 0.194016 | intron-variant | NOD1 | GRCh38.p7 | 7:30472329 | CACCTCTGGGTCTTT[G/T]AACCCACTGTTCTCT | 10392 |
rs79897281 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NOD1 | GRCh38.p7 | 7:30439037 | AAAACCACAATGAGA[C/G]AGGACCTCACACTCA | 10392 |
rs79934170 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NOD1 | GRCh38.p7 | 7:30471808 | GAGCCAGGAAGGACT[A/G]GACTCCACCCTAGTC | 10392 |
rs79995024 | snp | C/T | 0.046775 | 0.145601 | intron-variant | NOD1 | GRCh38.p7 | 7:30438559 | TTCGTGTGGCCCACT[C/T]ACAACACAATGGCAG | 10392 |
rs80006517 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467370 | TATAAGAAGGCTATA[C/T]ACTTGCATGATTGAA | 10392 |
rs80178202 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | NOD1 | GRCh38.p7 | 7:30478034 | AATGTGATATTCAGG[A/C]GACCTTGCCAAGCAT | 10392 |
rs80318409 | snp | G/T | 0.5 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30434939 | TAACCTGTAAGGAAT[G/T]TTTTTTTTTTTTGTA | 10392 |
rs80345642 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NOD1 | GRCh38.p7 | 7:30472172 | CCAAAGCTTCCCTCC[A/G]CACTTCAGAATAAAA | 10392 |
rs111284102 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NOD1 | GRCh38.p7 | 7:30450201 | TCCATTTGGGGGAGA[A/G]AAAAAAAAGATGGAC | 10392 |
rs111365938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30471229 | AGTGGCATTAAGAGG[C/T]TGAGAAGATGATAGA | 10392 |
rs111368419 | snp | A/G/T | 0.00036388 | 0.0134838 | intron-variant | NOD1 | GRCh38.p7 | 7:30456702 | CACAATGCCATGCCC[A/G/T]TCCCTGTCCCCGGGG | 10392 |
rs111422499 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30445674 | TGAGGCGAGAGAATC[A/G]CTTGAACCCAGAAGG | 10392 |
rs111502384 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | NOD1 | GRCh38.p7 | 7:30476331 | TCTGATGTCTAATCT[A/C]AACAGCACTGCTGTT | 10392 |
rs111615297 | snp | G/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30457441 | GGGTGACAGAGCAAG[G/T]CCCTGTCTCTAAAAA | 10392 |
rs111649141 | snp | C/T | 0 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30435575 | ACTTAACTGAAAGGC[C/T]TAGAGCCTTTCCAAT | 10392 |
rs111802784 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | NOD1 | GRCh38.p7 | 7:30475237 | GAAAATATCTACCAA[A/G]TGACTACATTCTCCC | 10392 |
rs111803060 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462039 | CACCGTGCCTGGCCA[A/G]GAATGATCTTAATTG | 10392 |
rs111943432 | snp | A/G | 0 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30457814 | CCTGTGGTAGCCAGA[A/G]GCAAGGAACCTGCGG | 10392 |
rs111965844 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30445989 | ATGGGCACGGTTTCA[A/G]TTTCGCAGCATGGTG | 10392 |
rs112005959 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | NOD1 | GRCh38.p7 | 7:30450051 | ACAAAAAACTTAGCC[A/G]GACATGGTGGCGTGT | 10392 |
rs112015937 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462333 | TGGAAAGTCCTTTGA[C/T]ACAATATGTGTCAAC | 10392 |
rs112021450 | snp | A/G | 0 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30450809 | CTTCTCTGTGCCTCT[A/G]CTTCCTTATCTGCCA | 10392 |
rs112048593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30474556 | TTCTCATAAGGAATG[C/T]GCAGCCTAGATCCCT | 10392 |
rs112059001 | snp | C/G | 0.0611083 | 0.163768 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466465 | TAGCTCTTGCCAACT[C/G]GCAAAGGACATAAGA | 10392 |
rs112070346 | snp | G/T | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425316 | GAGGTGAGGCTGGCC[G/T]CCTCTGTTTGCTCAC | 10392 |
rs112230451 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | NOD1 | GRCh38.p7 | 7:30475594 | TTAGAGGACCAAGGT[A/G]AGATCCCTTCAGAGT | 10392 |
rs112319733 | snp | A/G | 0.0414363 | 0.137845 | intron-variant, utr-variant-5-prime | NOD1, LOC101928268 | GRCh38.p7 | 7:30460156 | GCTCAATTCAGCAAG[A/G]ACTTAACAAGGTATG | 10392 |
rs112365211 | snp | A/C/T | 0 | 0 | intron-variant, downstream-variant-500B | NOD1, LOC101928268 | GRCh38.p7 | 7:30469365 | GAAGTCAGTCCCTCC[A/C/T]GGAATCACCTCTCTC | 10392 |
rs112422785 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | NOD1 | GRCh38.p7 | 7:30437924 | GCACAGTTAGAGACC[A/G]AGCCTCACCACGAGC | 10392 |
rs112494029 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NOD1 | GRCh38.p7 | 7:30431379 | AAGAAGAACAAAGTA[C/G]AACTCACACCTCCTG | 10392 |
rs112535816 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462394 | CCCCTTCTAGAAACC[C/T]GCCTTTTGAAAAGAA | 10392 |
rs112558641 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | NOD1 | GRCh38.p7 | 7:30474539 | GATCATCAGGCATTA[A/G]ATTCTCATAAGGAAT | 10392 |
rs112732239 | snp | C/T | 0.077417 | 0.180873 | intron-variant | NOD1 | GRCh38.p7 | 7:30431983 | GGTGGCTGATGCCTG[C/T]AATCCCAACTACTCA | 10392 |
rs112888319 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30460811 | GGGTTAGTTTCCAGG[A/G]TAAGGGAATCCCAGG | 10392 |
rs112946300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30426455 | CTCTATGTCTTTGGC[C/T]GGCCATCTTGGTCTG | 10392 |
rs112956080 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30465265 | ATTTAGAGAGATGCT[C/G]AGTCCCAAAAACCCA | 10392 |
rs113056110 | snp | A/C | 0.0520825 | 0.152737 | intron-variant | NOD1 | GRCh38.p7 | 7:30431961 | AAATACAAAATGAGA[A/C]AGGCATGGTGGCTGA | 10392 |
rs113069315 | snp | G/T | 0.5 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30455044 | CCTGGGCCTGCTTCC[G/T]GAGGTGGCACTCAGG | 10392 |
rs113094808 | in-del | -/AATC | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | NOD1, LOC101928268 | GRCh38.p7 | 7:30460121 | CCTGGCTGAAGATTT[-/AATC]AATCAGGTGTGCAGA | 10392 |
rs113155974 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOD1 | GRCh38.p7 | 7:30436246 | AGTAGTGCCCAGGCG[C/T]TGCTGCCCCAGAGCC | 10392 |
rs113286694 | snp | C/T | 0.0887219 | 0.191022 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458421 | TCATAGATCTTTTAA[C/T]ACTATCCACATCATT | 10392 |
rs113318035 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446132 | ATACATCCATCCCCT[C/T]CTACTCACCCAACCT | 10392 |
rs113394441 | snp | A/G | 0.095934 | 0.196885 | intron-variant | NOD1 | GRCh38.p7 | 7:30429927 | TCGGGAGACTGAGGT[A/G]GGAGAATTGCTTGAA | 10392 |
rs113419138 | snp | A/G | 0 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30448640 | ACCGTGAAGGACACA[A/G]GGAGGACGTGTGAGG | 10392 |
rs113433397 | in-del | -/A | 0.283947 | 0.247685 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30465105 | TGAGCAGAGAGAGAC[-/A]GGGGGGTGCCGTGGC | 10392 |
rs113467478 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | NOD1 | GRCh38.p7 | 7:30456157 | TCCCAGCGGGGTCAT[C/G]TCATAAATGAGTTGT | 10392 |
rs113482484 | snp | C/T | 0.5 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30456617 | AAATGCAGCCCTGCC[C/T]GCTGGACTAAACTCC | 10392 |
rs113536888 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NOD1 | GRCh38.p7 | 7:30447704 | GTGTGGGGCTGGCCC[A/G]CAATCCCTTCTCTCA | 10392 |
rs113537730 | snp | C/T | 0.5 | 0 | intron-variant | NOD1 | GRCh38.p7 | 7:30436395 | GGCCTGGCAAGCTGT[C/T]CTTCTAAAGGCTGGC | 10392 |
rs113584763 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30424098 | GCCCCTGGCAGCTCG[A/G]TGCTTCTTGCCATGG | 10392 |
rs113720086 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30444824 | CACGTATGTTTATTG[C/T]GGCACTATTCACAAT | 10392 |
rs113767753 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425441 | ACATTCTTTTTCTGC[A/C]GAATTGTAGCGGGTA | 10392 |
rs113800129 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30447918 | CATAGCATGCACTCA[A/G]AATCCCCATTCGGGT | 10392 |
rs113823284 | in-del | -/A/AA | 0 | 0 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428376 | AACAGTGTTTTTTTT[-/A/AA]AAAAAAAAACCTTTT | 10392 |
rs113912845 | in-del | -/AGAG | 0.283947 | 0.247685 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30465371 | AACCCCCATGAACAT[-/AGAG]AGCCTCAGTGTGCCC | 10392 |
rs114032818 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NOD1 | GRCh38.p7 | 7:30457302 | TACAAAAATAAAAAA[A/G]ATTAGCCAGGCATGG | 10392 |
rs114221072 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NOD1 | GRCh38.p7 | 7:30473645 | GGAGGAGTGAGCTGC[C/T]ACTTTCACTTCCTAA | 10392 |
rs114320478 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459838 | AAGGGGTGTTGCACA[A/G]CTTCCTTCATCCCTC | 10392 |
rs114467355 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD1 | GRCh38.p7 | 7:30455517 | ATAAAACCACTCAGC[C/T]CTAAGAAACCAGGAG | 10392 |
rs114971396 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | NOD1 | GRCh38.p7 | 7:30473667 | ACTTCCTAAGTAAGC[G/T]GCTCTTTGGAAGCAG | 10392 |
rs114983751 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30436378 | GGGCAGGAGGCTGGC[A/G]AGGCCTGGCAAGCTG | 10392 |
rs114988327 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NOD1 | GRCh38.p7 | 7:30438607 | TCACACCAAGCAAAC[G/T]ACCTGCTTACACCAT | 10392 |
rs114998900 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462342 | CTTTGACACAATATG[C/T]GTCAACAGACTCTGA | 10392 |
rs115002719 | snp | A/G | 0.000330087 | 0.0128427 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30436016 | AGTATTTCTAGAGAC[A/G]TGTTCTGCTGCAGGG | 10392 |
rs115298888 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479910 | CAGCTTTATTGCTCA[C/T]GCAAAGCCTTTTGGT | 10392 |
rs115309399 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NOD1 | GRCh38.p7 | 7:30430685 | AGTTGTGTCATCTGT[A/G]AACTGAGAATAACTA | 10392 |
rs115461097 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NOD1 | GRCh38.p7 | 7:30456338 | TCCTGACCCTGAGTC[A/G]GTTCCCCTCCGAGTC | 10392 |
rs115516733 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464590 | CTGGGATCTCTAGAG[A/G]CAGCAGTGTTCAAAT | 10392 |
rs115520310 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NOD1 | GRCh38.p7 | 7:30435132 | AAATAAAACATTAAG[G/T]GGCCATAAAAAAGGG | 10392 |
rs115528632 | snp | A/C | 0.0138799 | 0.0821421 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479029 | GCCCAGAGGTGACAC[A/C]CTTGGGAATTTGTGG | 10392 |
rs115688376 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOD1 | GRCh38.p7 | 7:30477012 | GATGCACATCATCTC[A/G]CTGAACTATGCTAGC | 10392 |
rs115709043 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NOD1 | GRCh38.p7 | 7:30472566 | GACTGATGTTTATGT[A/C]CCTCCAAAGTTCACA | 10392 |
rs115734944 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466417 | AGATGGGGGCAGCTG[C/T]ATCAGCTCAGGCCCA | 10392 |
rs116027648 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | NOD1 | GRCh38.p7 | 7:30434047 | TCGAGATGTTGTGCA[C/G]CTTGTAGGGAGAATG | 10392 |
rs116052197 | snp | C/G | 0.0755793 | 0.179102 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479069 | GCCAGGTCCCTCCTC[C/G]TAAAAGTGCCTACCC | 10392 |
rs116245616 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30468675 | ACCTCAGAGGTGATA[A/T]AACCCAGATTGCAAA | 10392 |
rs116391059 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30465116 | AGACAGGGGGGTGCC[A/G]TGGCTCTCAAGGGCT | 10392 |
rs116473965 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467523 | CCTAGAGAGAAAATG[C/G]TTGGTCTTCATTAAA | 10392 |
rs116487385 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOD1 | GRCh38.p7 | 7:30455894 | GGCGTGAGCCACGGT[A/G]CCCAGCCTTCTCCTT | 10392 |
rs116547908 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | NOD1 | GRCh38.p7 | 7:30433811 | AACAGAAAGAACATT[A/T]AAAAAAAAAAATTCC | 10392 |
rs116632896 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480626 | ACCGTTTGACCCCAA[C/T]ACAGACTCAACAATG | 10392 |
rs116880608 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30468738 | CATAACTGGCACACA[C/T]ATACCCATGAATGGG | 10392 |
rs116885673 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458662 | GAAGGGCAAGAGATC[C/T]TCACCAAAAAAATTT | 10392 |
rs117074688 | snp | C/T | 0.000313193 | 0.0125099 | intron-variant | NOD1 | GRCh38.p7 | 7:30429487 | TAACTTGTATAAAAT[C/T]CATAATACTGGATCA | 10392 |
rs117139630 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NOD1 | GRCh38.p7 | 7:30473081 | TCCACACCAGGGTAG[A/G]GGGCCAGCAGAGCAC | 10392 |
rs117202509 | snp | C/T | 0.0287284 | 0.116357 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480707 | CTAGATAATTATTGT[C/T]GTAAAATGGGCAAAT | 10392 |
rs117334941 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NOD1 | GRCh38.p7 | 7:30449702 | GCTTGTAACTCACCA[A/T]CATTTGGGGTTTTCG | 10392 |
rs117418821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30436300 | CTGGACGGGAAATGG[A/G]TCATCAGCACAGCCT | 10392 |
rs117748553 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD1 | GRCh38.p7 | 7:30434967 | GTAGATAGAGGGTCT[C/T]GCTATATTGCCCAGG | 10392 |
rs117755164 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NOD1 | GRCh38.p7 | 7:30427424 | CCAAGCAGAGCTGCT[C/T]CCTGAACGTGGCTCC | 10392 |
rs117759498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30470249 | CATGCAGTGAGTTAA[C/T]ACACGTACATACGGT | 10392 |
rs117838683 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NOD1 | GRCh38.p7 | 7:30450421 | ATCCCTACTGCTTTT[C/T]AGAAATGCATGAGTC | 10392 |
rs117840324 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461159 | AATATTTCAGTATGT[C/T]ATCCATACAAAATTT | 10392 |
rs117894145 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30447797 | GTGGAGCTACTTATA[A/G]TCTTTCTTACCACAC | 10392 |
rs118106664 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30468132 | AGCAAAAGTCAACAA[C/T]ACTGGCTTTCAAGTG | 10392 |
rs137914894 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NOD1 | GRCh38.p7 | 7:30433232 | TACTTGGCAGACATT[A/G]TTTTAGAGTTCACAG | 10392 |
rs137947410 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | NOD1 | GRCh38.p7 | 7:30437935 | GACCGAGCCTCACCA[C/T]GAGCTTCGGAGAGCT | 10392 |
rs137991606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30476837 | TGAGCGGGGCAGCAG[A/G]GCAGGAGAAGGAATG | 10392 |
rs138046644 | snp | C/T | 0.000182048 | 0.00953892 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451651 | CCGCACAGGAAGAGG[C/T]TGGTGAACTGGAAGT | 10392 |
rs138144462 | in-del | -/AAATC | 0.040671 | 0.13668 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479515 | AGAAAGTATGTTCTT[-/AAATC]AAAAGTGAAAGTGCA | 10392 |
rs138167133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464554 | AGAGGCAGGACAACA[C/T]AAGGGTGAAATCTGT | 10392 |
rs138213714 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOD1 | GRCh38.p7 | 7:30470865 | TTTCCTGGAACTCCA[C/T]TCTGCGAGAGGGCTG | 10392 |
rs138268329 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455160 | GTGTTGACCACGACT[C/T]TGCTCTGAGTGAGCA | 10392 |
rs138287783 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458110 | TTGTCTGGGTAGGAA[A/C]AGGGACCCAGGCTAT | 10392 |
rs138330261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30426352 | GTAACCTGGGGGTCA[A/G]CCTGGACACCTTCCT | 10392 |
rs138445854 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30447674 | CAACTGCTCCAGCTT[A/G/T]CAGAGCCACCAGTTG | 10392 |
rs138474104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30427852 | CAACTGTGCTCTGCA[A/G]ACTGTTCTGTAGTCT | 10392 |
rs138567623 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30447965 | TGGATGAGGGATTAT[A/G]GACCCAAAATAGTCC | 10392 |
rs138669564 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425507 | AAGCTGGCTTGCATC[A/G]TGGAGGCAGTGGACT | 10392 |
rs138824111 | snp | A/G/T | 0.000329815 | 0.0128374 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455208 | ATCTCCAGCAGCCAA[A/G/T]GCCTGAGGTCCACGT | 10392 |
rs138873582 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NOD1 | GRCh38.p7 | 7:30471588 | GATGAATTCAGATTT[G/T]CAAAGGTGAACAGAG | 10392 |
rs138886212 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463314 | TTTTTCCAGACAAAA[A/C]CTGAGACTTTGTTGC | 10392 |
rs138887430 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30475780 | TTCAAGCCAGGAAGT[A/C]TTGCCTGAATGAACT | 10392 |
rs138903958 | snp | C/G | 0.00106771 | 0.0230807 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452487 | GGCCAGCAAGACCAG[C/G]GGGTGGGCAGGCTCC | 10392 |
rs138921755 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453572 | CACAGGCATATGCCA[C/G]CAAGCCCAACTAATT | 10392 |
rs139061346 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467482 | TTTTGAGGAACTATG[A/C]CTTTCAACTCAAAGG | 10392 |
rs139167105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30460671 | CCACCACCAAAAGCC[A/G]TCTCCTGAGGCAAAG | 10392 |
rs139263345 | snp | A/G | 0.000467204 | 0.0152769 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451912 | CCGGGGCCCAGCTCC[A/G]GCAAAGCCCGCAGGA | 10392 |
rs139280951 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD1 | GRCh38.p7 | 7:30449380 | TCTTTTAGCTGGGCC[C/T]ATCTCATTAAATTCT | 10392 |
rs139288894 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | NOD1 | GRCh38.p7 | 7:30448410 | GCAAAAAAATTACGA[A/G]TCAGGGCAGGCACTC | 10392 |
rs139576372 | snp | C/T | 3.30006e-05 | 0.00406192 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452749 | ACCCCTGCGTCTAGC[C/T]GGCCCGTGGCCCAGA | 10392 |
rs139597925 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NOD1 | GRCh38.p7 | 7:30455469 | CAACATATTGGAGCC[C/T]GAAAATCTGTGAAAT | 10392 |
rs139798493 | snp | A/G | | | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452606 | GGAAGCGCAGCAGGA[A/G]GGCAAACACCTCCTC | 10392 |
rs139805377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30473140 | ATTACTACCTCATTA[A/T]CAGGAATGCTAAAGA | 10392 |
rs139814809 | snp | C/T | 8.24273e-05 | 0.00641926 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452789 | GCCGCTGTAGCAGCA[C/T]GGACTTGCCCACCCC | 10392 |
rs139857641 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480614 | TTCTTCTGCAATACC[A/G]TTTGACCCCAATACA | 10392 |
rs140001461 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NOD1 | GRCh38.p7 | 7:30433769 | ACTTGTGCCAGTGGA[C/T]GAAAGAATCATTAGG | 10392 |
rs140015596 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30448357 | CACCTTTACCCCACC[A/G]TCAGTGATCTGGTTT | 10392 |
rs140016165 | snp | A/G | 0.029116 | 0.117091 | intron-variant | NOD1 | GRCh38.p7 | 7:30450181 | CCTGGGCAACAGAGC[A/G]GGACTCCATTTGGGG | 10392 |
rs140048521 | snp | A/G | 0.00241653 | 0.034676 | intron-variant | NOD1 | GRCh38.p7 | 7:30455349 | GGCACGGGCTGGCAT[A/G]AGGGGCATCCTCCTA | 10392 |
rs140069127 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NOD1 | GRCh38.p7 | 7:30430097 | GGACAGGAAGTCTGA[C/T]GTCTCCTTCCAGGTA | 10392 |
rs140103385 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452031 | GGCCACCTGCCCCAG[C/T]GAGCACAGAGTGTCC | 10392 |
rs140134594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30434424 | AGATGCGGCTAAACC[A/G]TCTATGATGCACAGG | 10392 |
rs140167031 | snp | A/G | 0.00072861 | 0.0190729 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451568 | CCCACAGGGCCTTGC[A/G]CTTTCTCCTCAGGGC | 10392 |
rs140176390 | snp | A/G | 0.000281791 | 0.0118666 | missense, upstream-variant-2KB, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452983 | TTCTGGGCATAGCAC[A/G]GCACGAACTTGGAGT | 10392 |
rs140327847 | snp | C/T | 8.23621e-05 | 0.00641672 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30429406 | AGTGTTGCTCTGTAA[C/T]GCATCTGCCAGCTGG | 10392 |
rs140378666 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446018 | TGAAAGCTCTCCACT[A/G]TCTCTCCCCGACAGC | 10392 |
rs140433781 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOD1 | GRCh38.p7 | 7:30436507 | TAGGAAGAACAGCAG[C/T]AGAGCCGTGGACATA | 10392 |
rs140489168 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466813 | AAATATAACACCATT[C/T]CCTGTCTACCTCAGA | 10392 |
rs140520918 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425687 | ACTTTGGCCTCCTCT[C/G]GTTTTATCAGGTTTC | 10392 |
rs140585377 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | NOD1 | GRCh38.p7 | 7:30457799 | AGCAGCATGAAGTCT[A/C]CTGTGGTAGCCAGAG | 10392 |
rs140586458 | in-del | -/TATAT | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463465 | GGGTACTAACCGAAC[-/TATAT]TATATTAATATCTCG | 10392 |
rs140653927 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | NOD1, LOC101928268 | GRCh38.p7 | 7:30469296 | AACTCCATTGACACT[C/G]ACTGACTTTAAGTAT | 10392 |
rs140668030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30474431 | CCAACCTTTTTGGCA[C/T]GAGGAACTGGTTTCA | 10392 |
rs140768949 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | NOD1 | GRCh38.p7 | 7:30435020 | AAGCGATCCTCCCAC[C/T]TCAGCCTTCCAAAGT | 10392 |
rs140817833 | snp | A/G | 0.00173647 | 0.0294146 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30446976 | ACTTACTTAAGATGC[A/G]TGAGGCCTTTGCATT | 10392 |
rs140903538 | snp | C/G/T | 3.39756e-05 | 0.00412151 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451531 | CTCTTCAGGTAGCCC[C/G/T]GCAGGCTGGAAAACA | 10392 |
rs140936324 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30470262 | AATACACGTACATAC[A/G]GTATTTAGAACAGCA | 10392 |
rs141036352 | in-del | -/C | 0.0146672 | 0.084371 | intron-variant | NOD1 | GRCh38.p7 | 7:30478585 | CTGCCCCGCGCGAAT[-/C]CCCCAGTCGCTGGGA | 10392 |
rs141149625 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30439082 | GTCAAAAAGAGAAAA[C/T]AGCAAGTGTTGGCAA | 10392 |
rs141207330 | snp | C/T | 2.02039e-05 | 0.00317829 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30437623 | CTCTGCGAAGGCTTT[C/T]GCTCCTTCATCCCCA | 10392 |
rs141260616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOD1 | GRCh38.p7 | 7:30475897 | TTGCCCTCAACGAGT[A/G]TTTGATGCGCTAAAG | 10392 |
rs141276078 | in-del | -/A | | | intron-variant | NOD1 | GRCh38.p7 | 7:30477680 | CCACCACGCCCGGTT[-/A]ATTTTTTTTTTTTTT | 10392 |
rs141294868 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466754 | AAAGTCACTACAACC[-/T]TTTTCAGATACTATA | 10392 |
rs141355375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463049 | AGATGGGAGTGGGGG[A/T]GAAATTGACTGCAAA | 10392 |
rs141381573 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, synonymous-codon | NOD1, LOC101928268 | GRCh38.p7 | 7:30460305 | CCAGAAACACCAGAC[A/T]GCCAGAGATCTGCTG | 10392 |
rs141400284 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467994 | GGAGTGAGCCACCGC[A/T]CCCGGCCTATATTTT | 10392 |
rs141422065 | snp | A/C/T | 0.000798403 | 0.0199641 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452221 | AAGTGCTGGAAGCAC[A/C/T]GGAAGATGATCCAGC | 10392 |
rs141434596 | snp | A/G | 1.65332e-05 | 0.00287512 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455162 | GTTGACCACGACTTT[A/G]CTCTGAGTGAGCAGG | 10392 |
rs141523653 | snp | G/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30478926 | GTCTGGCGCGGGGGG[G/T]CGAGAGAAGCTGCGC | 10392 |
rs141539697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30475436 | TACAGTGCTCTATAA[C/T]TTAGAGGAAAAGGAC | 10392 |
rs141577782 | snp | A/C/T | 0.000307953 | 0.0124049 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451755 | ATAGCAGGACGTGGT[A/C/T]GCTGCCCCCGCAGGG | 10392 |
rs141739378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30432448 | TGGACAATAATAAGT[A/G]TTGGTGAGGATGTGG | 10392 |
rs141740843 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NOD1 | GRCh38.p7 | 7:30427042 | TCCCTTTCTAGACAG[C/T]GAACCCATGAAGCCA | 10392 |
rs141792583 | in-del | -/TAAG | 0.039522 | 0.134904 | intron-variant | NOD1 | GRCh38.p7 | 7:30436550 | ATTTGGCCAGCAGCC[-/TAAG]TAAGCGGGGGCTGGG | 10392 |
rs141909606 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454538 | GAACTAATCAGTTAA[C/T]TGATGGGGTCTTCCA | 10392 |
rs141934741 | snp | C/T | 0.000560206 | 0.0167269 | missense, utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452852 | GCTCATTGAGGATGC[C/T]GGTGGTGTGGTCCAG | 10392 |
rs141947912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30455414 | TCTGAGTTCTTAGTA[C/T]AGCCGGTAGCTATGC | 10392 |
rs141967697 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NOD1 | GRCh38.p7 | 7:30457321 | AGCCAGGCATGGTGG[C/T]GCACCTGTAGTCCCA | 10392 |
rs142008336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463873 | TTATCCACATGCAAT[A/G]ACCACTATTCTCATT | 10392 |
rs142043110 | snp | A/G | 0.000248573 | 0.0111456 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452652 | GTAGCAGTAGTGCTT[A/G]AAGAGCAGGTCCTGC | 10392 |
rs142132816 | in-del | -/G | 0.0535932 | 0.154675 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30424633 | CAAGCCCACCATGGT[-/G]GGGGGGTGTCCAACA | 10392 |
rs142285400 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NOD1 | GRCh38.p7 | 7:30435936 | GCACTCAAGCCTGGA[C/T]GACAAAGCAAGACCC | 10392 |
rs142331140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30426529 | ACAGGTCATTTCCAC[A/G]TACTCTGGCCTTCTC | 10392 |
rs142373482 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NOD1 | GRCh38.p7 | 7:30431060 | CCAGGAAGGAGAGCA[A/C]CTAATGCCCCTAAAA | 10392 |
rs142414986 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | NOD1 | GRCh38.p7 | 7:30429903 | GTGTGCACCTGTACT[C/G]CCAGCTACTCGGGAG | 10392 |
rs142419533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30438470 | CAAAGCACTTAGAAC[C/T]GTGTGTGGCTCACAC | 10392 |
rs142522603 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NOD1 | GRCh38.p7 | 7:30472390 | TCCCAAGTCCTAGTT[C/G]AAAAGGCTCATTCCT | 10392 |
rs142705650 | in-del | -/AAC | 0.00478085 | 0.0486577 | utr-variant-5-prime, cds-indel, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459197 | GTTAGAATATTTTAA[-/AAC]AACATTGTTTAAATC | 10392 |
rs142802342 | snp | C/T | 8.37304e-05 | 0.00646979 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451958 | CTCTCTCCTGCAGCC[C/T]GGAGGCCTGCACCTC | 10392 |
rs142953877 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458128 | GGACCCAGGCTATTT[C/T]ATTTGGGCATTAAAA | 10392 |
rs143051444 | snp | C/T | 9.92162e-05 | 0.0070426 | synonymous-codon, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30436000 | CTCGAGCTATTACCA[C/T]AGTATTTCTAGAGAC | 10392 |
rs143071756 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NOD1 | GRCh38.p7 | 7:30438694 | TATGTATTTACTATA[C/T]AATTGAATGGCATCA | 10392 |
rs143093519 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30463707 | TGAGATGCTAAGATT[-/AA]AAAAAAAAAAACATT | 10392 |
rs143176690 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30431724 | GGAGTTCTTTGTGAT[A/C]TTGGATTAGGCAATC | 10392 |
rs143280655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30475241 | ATATCTACCAAATGA[C/G]TACATTCTCCCAATT | 10392 |
rs143422355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30447748 | CAAAGGCTCTGAATG[C/T]CCAAAGTTTCTCACA | 10392 |
rs143500064 | snp | A/G | 0.00021486 | 0.0103626 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451694 | TGAAGAGGTCTTCCC[A/G]CGCCGGACCACTGCC | 10392 |
rs143649035 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30465949 | ACCCAGGTCATATGG[A/G]ACCTGGCCCAGTGCC | 10392 |
rs143683154 | snp | C/G | 0.000307953 | 0.0124049 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452037 | CTGCCCCAGCGAGCA[C/G]AGAGTGTCCCGGCCG | 10392 |
rs143737061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30469791 | GGCCCTGGACTTGTC[C/T]GGATCAATCAAAACT | 10392 |
rs143756774 | snp | C/G | 0.000251078 | 0.0112016 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452547 | CAGGTCCAAGTCCGA[C/G]TGCAGCTCGTCCAGG | 10392 |
rs143765347 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | NOD1 | GRCh38.p7 | 7:30470909 | GAGGAAAGTGCCACA[G/T]AAGTGGCCGATCTGG | 10392 |
rs143815211 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30468349 | TTGATTTCTCAGCAG[C/G]AAATGGATGATGTCA | 10392 |
rs143843310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462999 | CTGAAAATCTGATCT[A/G]GAAATCAGATCAATG | 10392 |
rs143956406 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30448345 | CTCTTCGCTTAGCAC[C/T]TTTACCCCACCGTCA | 10392 |
rs143983658 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30429426 | CTGCCAGCTGGGCAG[A/T]CCCCTTAGCTGTGAT | 10392 |
rs144061661 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30447978 | ATGGACCCAAAATAG[C/T]CCAGACTAATATGTA | 10392 |
rs144105242 | snp | A/G | 0.000247674 | 0.0111254 | intron-variant | NOD1 | GRCh38.p7 | 7:30446274 | TATGCAGGGGCTCCA[A/G]TGTGGGTCACCCTCC | 10392 |
rs144216271 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462010 | CCCAAAGTGCTGGGA[G/T]TACAGGTGTGAGCCA | 10392 |
rs144218747 | in-del | -/AG | 0.0154538 | 0.0865337 | intron-variant | NOD1 | GRCh38.p7 | 7:30477068 | TACAGGTGGGAAAAC[-/AG]GGGCTTGGAGAGGTC | 10392 |
rs144396294 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOD1 | GRCh38.p7 | 7:30429516 | CAAATTTGACCCCTT[C/T]GTAAGGGAGTTGCAA | 10392 |
rs144500688 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NOD1 | GRCh38.p7 | 7:30472120 | CTTTTTCTTGTATAT[C/T]ATGAATGACAGGAAA | 10392 |
rs144535612 | snp | C/T | 0.00130194 | 0.0254809 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452776 | CAGAGGCTCTGCAGC[C/T]GCTGTAGCAGCATGG | 10392 |
rs144616515 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464955 | AGGGGTCATTGTTAC[C/T]GCCAATTTACACATG | 10392 |
rs144669423 | snp | C/T | 3.30267e-05 | 0.00406353 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455261 | CAAGTAGAGGAAGAA[C/T]TCGGACACCTCCTCG | 10392 |
rs144684378 | snp | C/T | 0.00169828 | 0.0290905 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451303 | AGGTCTAGGGCCAGC[C/T]GCTTGGGGAAGTGAT | 10392 |
rs144770950 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454211 | AACAACATATTGGAT[G/T]CTTTAAAAGGCAGGA | 10392 |
rs144818812 | in-del | -/AAAC | 0.393987 | 0.204372 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463399 | ATGATCCCAAGACAA[-/AAAC]AAAAATGATGAGCAA | 10392 |
rs144829168 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30434396 | ATCCTCACCACTGGG[A/C]GGTACAGGGCAGAGA | 10392 |
rs145004682 | snp | C/G | 0.00133466 | 0.0258006 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452055 | AGTGTCCCGGCCGGC[C/G]TGGAGGGTCTCCACT | 10392 |
rs145077265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458289 | CTTGCGTGTGTAAAA[C/T]GATCTTGGAAGTGGA | 10392 |
rs145084498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463193 | CATATAGATACATAC[A/G]ACTTGTCAAAAGTCA | 10392 |
rs145096270 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOD1 | GRCh38.p7 | 7:30431449 | GGCATAGGAGAGACA[C/T]ATAAATCAATGGACC | 10392 |
rs145135608 | snp | A/G | 0.000247719 | 0.0111265 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455178 | CTCTGAGTGAGCAGG[A/G]AAGGGGAGAAGCCGA | 10392 |
rs145259739 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NOD1 | GRCh38.p7 | 7:30474719 | GGCCACCGACTGGTA[A/T]TGGTCCATGGCCTAG | 10392 |
rs145275692 | snp | A/G/T | 6.59283e-05 | 0.00574106 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452822 | CATCACCCAGGATGA[A/G/T]GATGGTCTCACCCTG | 10392 |
rs145386746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30432979 | GTGGTGATGGTTGCA[A/C]TAAAAACCTCTGAAT | 10392 |
rs145478088 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462637 | GATACTACACTGAGT[G/T]AGAGAAGCCAGACTC | 10392 |
rs145479087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30430566 | TGAAGAGGACTCCCT[C/T]GTGAGAGGCAGTATT | 10392 |
rs145496291 | in-del | -/GT | | | intron-variant | NOD1 | GRCh38.p7 | 7:30476694 | AAGAACAGCTTTTGA[-/GT]GTGTGTGTGTCAAAA | 10392 |
rs145546882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30434542 | TGATTACAATATTTT[C/T]AGAGCCACTGCTTGA | 10392 |
rs145549183 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30455882 | GCTGGGATTACAGGC[G/T]TGAGCCACGGTGCCC | 10392 |
rs145580985 | snp | G/T | 9.88338e-05 | 0.00702902 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30429420 | ACGCATCTGCCAGCT[G/T]GGCAGTCCCCTTAGC | 10392 |
rs145716336 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NOD1 | GRCh38.p7 | 7:30457557 | GAGATAGCCAACTCT[C/T]TTTTATTTTTAAATC | 10392 |
rs145762663 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30424950 | ATCGTCATTCTTAGA[C/T]CAGCTAAGAGCTGAG | 10392 |
rs145823866 | snp | A/G | 0.000303654 | 0.0123181 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452401 | CGCAGGAACTGGCGC[A/G]GGACCTCGATGCCTG | 10392 |
rs145930052 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD1 | GRCh38.p7 | 7:30472471 | TCTCATGACATGCTG[C/T]TGTTTTCACTTAAAG | 10392 |
rs146033843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30455460 | TGTGACAGTCAACAT[A/G]TTGGAGCCCGAAAAT | 10392 |
rs146054159 | snp | A/C | 0.000234443 | 0.0108243 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451993 | TGGGTGAAGACAAAG[A/C]GGCTCTTCTCCATGC | 10392 |
rs146074604 | snp | C/G/T | 0.000149412 | 0.00864207 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452615 | GCAGGAAGGCAAACA[C/G/T]CTCCTCGGGGTCCCG | 10392 |
rs146084871 | snp | A/T | 0.000214403 | 0.0103516 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455217 | AGCCAAGGCCTGAGG[A/T]CCACGTAGGCATCTG | 10392 |
rs146205545 | snp | A/G | 0.00121831 | 0.0246509 | stop-gained, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30429402 | TGCCAGTGTTGCTCT[A/G]TAACGCATCTGCCAG | 10392 |
rs146294357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459871 | TTCCCGACCTTTGCC[A/C]GCCTACCACGAGGGG | 10392 |
rs146393799 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479055 | TGTGGTGCCATCGTG[C/T]CAGGTCCCTCCTCGT | 10392 |
rs146419415 | in-del | -/C | | | intron-variant | NOD1 | GRCh38.p7 | 7:30476927 | ATTAACGGGCACAAA[-/C]CTGCCACTCCAGTGT | 10392 |
rs146485628 | snp | A/G | 6.75733e-05 | 0.00581223 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451514 | CCTGAACGCGGGGCA[A/G]GCTCTTCAGGTAGCC | 10392 |
rs146496218 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446655 | GGGCAAGGGCCCAAG[A/C]TCTTCCTTGCAACCC | 10392 |
rs146516117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30450558 | ACAGGAAAACAACCA[C/T]GAGTCAGCATTTTAA | 10392 |
rs146567985 | snp | A/G | 6.65757e-05 | 0.00576918 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451448 | TCTCGTAGATGCAGC[A/G]CAGCATCCAGATGAA | 10392 |
rs146753148 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30437125 | AAACTAACACAGGAA[C/T]AAAAAACCAAACACT | 10392 |
rs146756818 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30445960 | GGGGAGGGGGACCGG[A/G]GAGTTATTGCTTAAT | 10392 |
rs146858663 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30468807 | TGAATATGATTCATT[G/T]TGGTGAATTTAATCC | 10392 |
rs146878262 | snp | C/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30474194 | TAGGAGAAGGAAAGA[C/G]CAGCCCTGGAACCAA | 10392 |
rs146938026 | snp | A/G | 0.000132249 | 0.00813062 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452222 | AGTGCTGGAAGCACC[A/G]GAAGATGATCCAGCA | 10392 |
rs147023071 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30426818 | TGCCCCAGACCCTTT[A/G]CACATGCTGTTCCCT | 10392 |
rs147040646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30426302 | GGGTCCCCTGGCTTA[A/G]TGAATGGACCACTCT | 10392 |
rs147183464 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466255 | TAGGATTACACTTCC[C/T]TACCCCTTTGAAGTT | 10392 |
rs147210272 | snp | A/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456921 | GGCCCTGCTCTTCCA[A/T]AGTTAAAGTAGCAAG | 10392 |
rs147212919 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NOD1 | GRCh38.p7 | 7:30471379 | CCTGGCCTGCAACAC[A/T]TCTGGCACTGCAACC | 10392 |
rs147294540 | snp | C/T | 0.000280008 | 0.011829 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30448356 | GCACCTTTACCCCAC[C/T]GTCAGTGATCTGGTT | 10392 |
rs147319394 | snp | C/G/T | 0.000362352 | 0.0134558 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30448335 | ATTTGGTCAGCTCTT[C/G/T]GCTTAGCACCTTTAC | 10392 |
rs147561327 | snp | C/T | 0.00020001 | 0.00999825 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452299 | AGCTGGCTCAGCAGG[C/T]GGTCCTGCAGGGCCC | 10392 |
rs147563269 | snp | C/G/T | 0.000263685 | 0.0114794 | synonymous-codon, missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452835 | GAAGATGGTCTCACC[C/G/T]TGCTCATTGAGGATG | 10392 |
rs147585489 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | NOD1 | GRCh38.p7 | 7:30457199 | TGACTGTAATCCCAG[C/T]GCTTTGGGAGGCTGA | 10392 |
rs147696736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30434990 | TGCCCAGGCTAGTCT[C/T]GAACTCTTGGCCTCA | 10392 |
rs147773352 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30445273 | TAATAAAAAAAAAAA[A/G]AATCTAAAAAAAAAA | 10392 |
rs148102010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30470048 | AACTTTGTGTCCTAA[A/G]TTGATTATTTTCCTT | 10392 |
rs148117301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454472 | GTCTCCCTGACATCC[A/G]GCACAGTGTAGGGTC | 10392 |
rs148120693 | snp | C/T | 4.96438e-05 | 0.00498191 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455275 | ACTCGGACACCTCCT[C/T]GCCCTTGCTCTGTAC | 10392 |
rs148201212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30438795 | ACCCCTACTATAGTA[C/T]AGATACATATAGTCT | 10392 |
rs148253610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30432233 | AGCACCCAGAATATA[C/T]AGAGAACCCCTATAA | 10392 |
rs148340769 | snp | A/G | 0.000115814 | 0.0076088 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451726 | TGCAGGCACTGGAAC[A/G]GGAGGAAGGGAGGAT | 10392 |
rs148416984 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NOD1 | GRCh38.p7 | 7:30472210 | TCCTTACCCAGCCCA[A/G]GAGGCCCTACTTGGC | 10392 |
rs148429594 | in-del | -/G | 0.0240643 | 0.107019 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461724 | GAAATACTGATGCCA[-/G]GAATGATCTTTGTTG | 10392 |
rs148452030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30456635 | TGGACTAAACTCCCA[C/T]GCTCTTCACTCAGAT | 10392 |
rs148518184 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30445330 | GTCCTTGAAGAGACA[A/T]TTGTATGCCCATGTG | 10392 |
rs148695249 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | NOD1, LOC101928268 | GRCh38.p7 | 7:30460102 | TGCTTTATAATGTCC[A/G]GAGCCCTGGCTGAAG | 10392 |
rs148784278 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30429703 | TACATGAACTGATGT[C/G]TGTGTTTGCATTTTT | 10392 |
rs148818092 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462812 | AAATTAGCAGGGCAT[C/T]GTGGTGCACACCTGT | 10392 |
rs148947449 | snp | C/G | 0.00118548 | 0.0243173 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425677 | ATCTTCATAGACTTT[C/G]GCCTCCTCTGGTTTT | 10392 |
rs149096738 | snp | A/G | 0.00308181 | 0.0391332 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451359 | GTCGGCCGAGCAGGC[A/G]TTGCAGTAGGTCAGC | 10392 |
rs149105079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30431586 | CTGCCGGGACAGCTG[A/G]ATATCCACGTGCAAG | 10392 |
rs149106716 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30433111 | CATAAATGCTTTAAC[A/G]TCTGGTTGACTTTCA | 10392 |
rs149155268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30475087 | GGGAAGTTCTTACTC[A/G]TTAGACTTTTAATCT | 10392 |
rs149404136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453824 | GCCAATCCCTGGGCC[A/G]TAGGCAACTACTGAT | 10392 |
rs149440424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30434203 | TTCTCACTGGTGAAC[A/G]TTAACAGTAGAGATC | 10392 |
rs149493411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30476853 | GCAGGAGAAGGAATG[C/G]AGCGTTGAAGGGAAC | 10392 |
rs149559447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464938 | CAACAACCCTAGGTG[A/C]CAGGGGTCATTGTTA | 10392 |
rs149725417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30455853 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 10392 |
rs149728096 | snp | A/G | 0.000329951 | 0.01284 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452750 | CCCCTGCGTCTAGCC[A/G]GCCCGTGGCCCAGAG | 10392 |
rs149860788 | in-del | -/AAAT | 0.398714 | 0.200958 | intron-variant | NOD1 | GRCh38.p7 | 7:30431229 | TTAGGGAATGGGATC[-/AAAT]AAATAATTCTGCAGG | 10392 |
rs149867784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467564 | GTTCATTAAGACCAA[A/G]CAAACTCAGATGAGA | 10392 |
rs149988811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30449843 | AAGGAAAGCTTCACC[C/T]GGGGACAGCAGGAAG | 10392 |
rs149999039 | snp | C/T | 0.000247091 | 0.0111123 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425695 | CTCCTCTGGTTTTAT[C/T]AGGTTTCCATTTAGG | 10392 |
rs150126546 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30447329 | ATAGTCCCCTTGCAG[G/T]GTGGTTATGAGGATC | 10392 |
rs150155842 | snp | A/G | 0.000390224 | 0.0139628 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451548 | CAGGCTGGAAAACAG[A/G]TGTGCCCACAGGGCC | 10392 |
rs150178516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30436752 | GTCCTCTGTCTTGAT[A/G]GGGGTGGTGGTTGGC | 10392 |
rs150185257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30470378 | GATGACAAGGGAGGG[C/T]GACCATCTGGTGAGT | 10392 |
rs150342925 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NOD1 | GRCh38.p7 | 7:30476293 | ACTTGATCTTTATGC[A/C]TATATTACTTACTGT | 10392 |
rs150425761 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464341 | GATAGCTGCAAGGGG[A/G]TGGGCAGGGGCAGAG | 10392 |
rs150469478 | snp | A/C/G | 0.00011622 | 0.00762223 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452988 | GGCATAGCACAGCAC[A/C/G]AACTTGGAGTCACGG | 10392 |
rs150478678 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30458015 | AAGAGGGAGAGCCGG[A/C]ACAGAGTTCCTGGGA | 10392 |
rs150501772 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30433435 | AGGAGCCCACCCTCC[A/C]TCCCCACCTTTGCTG | 10392 |
rs150550452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30427367 | TAAGTGTCAGTACAG[C/T]TAACAAGTCCAAGGA | 10392 |
rs150744113 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467476 | GCCTTGTTTTGAGGA[A/T]CTATGACTTTCAACT | 10392 |
rs150782149 | snp | A/C/T | 0.000774127 | 0.0196592 | missense, stop-gained, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456765 | CAATCTCCGCATCTT[A/C/T]GGCCGAGAAGTAGTC | 10392 |
rs150793011 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, synonymous-codon | NOD1, LOC101928268 | GRCh38.p7 | 7:30460395 | GACGGTCTGGTCCTC[C/T]CTTCCAGGCAAAGAG | 10392 |
rs150842987 | snp | A/C/G | 4.95212e-05 | 0.00497579 | missense, synonymous-codon, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452742 | GAATTTGACCCCTGC[A/C/G]TCTAGCCGGCCCGTG | 10392 |
rs150853162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30449297 | TGTACATGGCATGGC[C/T]AGCCCAAGACAGCAC | 10392 |
rs150897372 | snp | C/T | 1.66638e-05 | 0.00288645 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451895 | AGGACTGCTGGTCAC[C/T]CCCGGGGCCCAGCTC | 10392 |
rs151114173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463030 | GTTTCCTGAGGCAGG[A/G]GGCAGATGGGAGTGG | 10392 |
rs151154717 | in-del | -/A | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428374 | CAACAGTGTTTTTTT[-/A]TTAAAAAAAAACCTT | 10392 |
rs151170709 | snp | A/G | 0.00090018 | 0.0211962 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451465 | AGCATCCAGATGAAC[A/G]TGGGCATGGCCTGCA | 10392 |
rs151212814 | snp | C/T | 1.65732e-05 | 0.00287859 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452086 | GGGCTGCGTGTGTTC[C/T]GCTGCACCAGGCTGC | 10392 |
rs151331508 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD1 | GRCh38.p7 | 7:30457761 | GAGACGGTCTCAGCA[C/T]AAAATAGCCTGAGAA | 10392 |
rs180712416 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30448336 | TTTGGTCAGCTCTTC[A/G]CTTAGCACCTTTACC | 10392 |
rs180713994 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479940 | TGGTCTCTTCACACG[A/G]ACACGTGTGACATTT | 10392 |
rs180727128 | snp | C/T | | | intron-variant, synonymous-codon | NOD1, LOC101928268 | GRCh38.p7 | 7:30469049 | CACGGAGAACACATA[C/T]GCTTGGTCAGCTCAA | 10392 |
rs180732652 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30424599 | GTAGTATCACCCCCA[C/T]CCTCATGGAGCAGCC | 10392 |
rs180739410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30456289 | TGGAGCGGGGAAGAT[A/T]CTTCACTGTGGACCC | 10392 |
rs180757043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30431786 | AACCAAAGAAAAAAA[C/T]AGATAAATTGGACTT | 10392 |
rs180886582 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD1 | GRCh38.p7 | 7:30427461 | AGCTCAACCACAACC[C/T]TGTGGCCTGGTGTGG | 10392 |
rs181256675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461416 | CTCCTGGCCTCAAGT[C/G]ATCCTCCCACCTCAG | 10392 |
rs181282889 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456845 | ACCAGAAGTTCCCGA[C/T]TGCTTTTCAGTAATT | 10392 |
rs181291548 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30434318 | TTCTAGGTGTTGACA[C/T]TACTACTATCCATGT | 10392 |
rs181333255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30438229 | CTTGGTGGACAGGTG[C/T]GGCGATAAAGCTGTA | 10392 |
rs181370185 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30474819 | TTTCTTCCATTTCAG[C/T]CCTGCATGTCTGGTA | 10392 |
rs181415709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30448060 | CCCCAATAACCAGTT[A/G]TAAGCCTACTTGCCT | 10392 |
rs181418504 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461026 | AGCAGCTCTGTTGAA[C/T]TGAAATATGACACAG | 10392 |
rs181423080 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NOD1 | GRCh38.p7 | 7:30437851 | GATTTCAAATTCAAG[G/T]GGTGATGCAAGATCG | 10392 |
rs181491723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30476856 | GGAGAAGGAATGGAG[C/T]GTTGAAGGGAACATT | 10392 |
rs181508540 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30428996 | GGGAAGAATGAGCTC[C/T]AAACTCCTGGCCAAC | 10392 |
rs181519141 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467274 | GTGAGAAGACACACG[G/T]TGTGAGAATGAAAAT | 10392 |
rs181542739 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30424128 | GGCCTACCTGGATCC[A/G]CCACTCAGCAGTGAA | 10392 |
rs181635189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453270 | GCTTGACCTCAGATT[G/T]GCCAGAAAGAAGGTG | 10392 |
rs182001588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30475391 | CTGGCACTAATCTGG[C/T]GCTCACTTTGAAATT | 10392 |
rs182020500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428432 | TTTTATGTTGTGAAC[A/C]AACACTTATGCAAAC | 10392 |
rs182043150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30472775 | GGCAACCAGGTCTCA[C/T]ACTTCCAGCCTGCAG | 10392 |
rs182057381 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30449358 | TTCTTAGCAATAGAT[G/T]CCCCCATCTTTTAGC | 10392 |
rs182059143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30426872 | ACTAGCTCCTATTCA[C/T]CCTTCATGGCTTAGT | 10392 |
rs182097260 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NOD1 | GRCh38.p7 | 7:30456388 | CCTCCAGCCTTCAGA[C/G]GCACTGAATGAACAT | 10392 |
rs182270670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437366 | TGCACATCTTCTACA[A/T]GTATCCCAGAACTTA | 10392 |
rs182385317 | snp | C/G/T | 0.00279242 | 0.0372774 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480590 | GACCTAAAACCTAAA[C/G/T]GCCTTATTTTCTTCT | 10392 |
rs182392851 | snp | A/G/T | 0.00319098 | 0.0398384 | intron-variant | NOD1 | GRCh38.p7 | 7:30434164 | GACCTCGGGCAACAG[A/G/T]CTTAAGTTCTTTGGG | 10392 |
rs182393191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30434687 | TTTAGGAGGTACTTT[C/G]ATGTCCTCCTTTAGT | 10392 |
rs182489613 | snp | A/G | 0.00119832 | 0.0244484 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453991 | ACAGAGAAGTCTTTC[A/G]AAAGAATGATTCCTC | 10392 |
rs182490563 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NOD1 | GRCh38.p7 | 7:30477461 | GGCTTTGAGGGAGAA[C/T]AAACTCGACCCTTTG | 10392 |
rs182504764 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30429746 | GCATAATCAAAATAT[C/T]TGGGGCCGGGTGCAG | 10392 |
rs182636521 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30457558 | AGATAGCCAACTCTT[C/T]TTTATTTTTAAATCA | 10392 |
rs182739984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459665 | TGGGGCCTGTTTTCT[C/T]TCGGAAGCATTTGAG | 10392 |
rs182865688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462678 | TTAGGGCTGGGTGCA[A/G]TGGCTCACGCTTGTA | 10392 |
rs182878621 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | NOD1 | GRCh38.p7 | 7:30445235 | CCTGCACAATGTGCA[C/T]ATGTACCCTAAAACT | 10392 |
rs182916294 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464135 | TCACCTGCCACTCTG[A/C]TGCTTTAAAGCTCTG | 10392 |
rs183096030 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30449176 | TAACAAGTAAAAGGC[G/T]GAACAATTAAAAGCT | 10392 |
rs183337137 | snp | C/T | | | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479119 | AAAGCCTGGACATGA[C/T]AGGGAAACTCTTGTT | 10392 |
rs183339992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30470180 | GTGCTTCTGTTTTCT[A/T]CTCTGTAAGTACAGA | 10392 |
rs183344284 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30448683 | GACATCCACCCTTTG[C/T]GTGTGACCTATGTGT | 10392 |
rs183351780 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30472268 | TACCCTCCTGGGCTT[A/G]GGCCTTACCACACCA | 10392 |
rs183356308 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425262 | GAAAAGAGCGGTGAC[C/G]AACTCGCTCCCGTTG | 10392 |
rs183374991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30425924 | GGGTCTCACTAAGGT[C/T]ACCTGTAGCCTCCAT | 10392 |
rs183812271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459052 | ATTTTCCATGGCAGT[C/G]AATTCTATGACCCAC | 10392 |
rs183950032 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30475072 | TGTTACAAGAAGCAG[A/G]GGAAGTTCTTACTCA | 10392 |
rs183967695 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454521 | AGCAAAAAATACTTA[C/T]TGAACTAATCAGTTA | 10392 |
rs183994041 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30438811 | AGATACATATAGTCT[A/C]ACCCCTACTATATTT | 10392 |
rs184016727 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30435518 | CTGTACCTGTTTATG[A/C]TTGTAGAAGTGGCTA | 10392 |
rs184086590 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479881 | TCGGCCCACCTGCAC[A/C]CAGGTGAAATAAACA | 10392 |
rs184087971 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30455781 | TAATTTTTGTGTTTT[C/G/T]ATTAGAGACGGGTTT | 10392 |
rs184095913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30431576 | ACACGTGGTGCTGCC[A/G]GGACAGCTGGATATC | 10392 |
rs184148760 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30430201 | ATGCTGCCATGAAAT[A/G]GTTCTCATGAATAGT | 10392 |
rs184151619 | snp | C/T | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461793 | ACCCAGGCGGGAGTG[C/T]AGTGGCACAATCTTG | 10392 |
rs184247737 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30436377 | TGGGCAGGAGGCTGG[C/T]GAGGCCTGGCAAGCT | 10392 |
rs184492260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467063 | TGATGAAAAAGAACA[C/T]GGTGGAGCTGCATGT | 10392 |
rs184498088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30447577 | ACAGCCACACAGAGC[C/T]CTGGAGCCGAGTGTG | 10392 |
rs184543309 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30436898 | CAAAGGATTATAAAT[C/T]ATTCTGCTATAAAGA | 10392 |
rs184624912 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437383 | TATCCCAGAACTTAA[A/C]GTTAAAAAAAGAGAA | 10392 |
rs184640242 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30473740 | ACATCTGACTGTTAA[C/T]GGCAGGAGATGGGCA | 10392 |
rs184644917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30450835 | TGCCAAAATAGAGAC[A/C]ATAACAGTACCTAAG | 10392 |
rs184674042 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459953 | ACAGCAACTTGTCTT[C/G]CCAGATGTTTTCTGT | 10392 |
rs184761377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466177 | CCCCTTCCTTGAAAA[C/T]CAACACAGTGGTAGA | 10392 |
rs184762319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446788 | TACCAATAACGGGAG[A/G]CCCTTCCAGAATCCA | 10392 |
rs184829338 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30451154 | CCATGATGCCATTCC[A/C/T]GATGCCCTCCGAGCC | 10392 |
rs184933009 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30474473 | TTTTCCACAGACAGC[A/G]GCGAGTAGGGGCACA | 10392 |
rs184949085 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30427371 | TGTCAGTACAGTTAA[C/T]AAGTCCAAGGAGAAG | 10392 |
rs184981904 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOD1 | GRCh38.p7 | 7:30430985 | CTGCTGTTTTCTAGT[C/T]ACCACTTAGGCTTTT | 10392 |
rs185087463 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30455060 | GAGGTGGCACTCAGG[A/G]CTGGCCCAGCCATTA | 10392 |
rs185354336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30457520 | TTGCACTTGAGGGTT[A/G]CATCTCTAGGGTAGG | 10392 |
rs185356003 | snp | G/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30434334 | TACTACTATCCATGT[G/T]ATTTCACTCTCCATG | 10392 |
rs185366799 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479628 | CCTGAAGCAACTGAG[A/G]AATCACAAAGGTAGT | 10392 |
rs185465265 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, synonymous-codon | NOD1, LOC101928268 | GRCh38.p7 | 7:30460467 | TCTGCTCTCCTGGGT[A/G]GAGCTTTCCCAGGCC | 10392 |
rs185493283 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461216 | TCTCACTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 10392 |
rs185495967 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30427563 | CATGCTCTGGAGGCT[C/G]CCAGAACAAGCCAGG | 10392 |
rs185496870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30427114 | ATGCTCAAGCGTTTC[A/G]TTATTCAAGGAATAA | 10392 |
rs185513471 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30438160 | AACCCCATCAGCAAC[A/G]TTCCTGTCACATAAA | 10392 |
rs185593717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30456334 | TCATTCCTGACCCTG[A/C]GTCGGTTCCCCTCCG | 10392 |
rs185713735 | snp | A/G | | | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479945 | TCTTCACACGGACAC[A/G]TGTGACATTTGGTGC | 10392 |
rs185741933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30431935 | AAATGGTGAAACCCC[A/G]TCTCTATTAAAAATA | 10392 |
rs186036115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30434202 | TTTCTCACTGGTGAA[C/T]GTTAACAGTAGAGAT | 10392 |
rs186114803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30438471 | AAAGCACTTAGAACC[A/G]TGTGTGGCTCACACA | 10392 |
rs186233694 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30470787 | CTCTGAGGGGCCAGT[A/G]AATAAAAATATCTTA | 10392 |
rs186240107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461599 | ACATTTCCAGTGCTC[A/G]AGAGCCACATGCGGC | 10392 |
rs186247638 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467423 | TTAGGGCATCTCAGG[A/C]CATCTTGAGGCAGGC | 10392 |
rs186332074 | snp | G/T | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462044 | TGCCTGGCCAGGAAT[G/T]ATCTTAATTGGCTTT | 10392 |
rs186334163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30438847 | AAGTTGTACAAAGAG[A/G]GAGAAGGGAGAGAAA | 10392 |
rs186338277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30476111 | TTGCCTAAAAAAAAT[C/T]CCCCCAATAATAAGA | 10392 |
rs186364741 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453878 | TTTCTGGACATTTCA[C/T]ATAAACAGAATCATA | 10392 |
rs186449616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense | NOD1, LOC101928268 | GRCh38.p7 | 7:30469203 | GTGGGCCTCTGCCAT[A/G]CCAGAACACTATAGG | 10392 |
rs186461402 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425151 | GGGAAAGTGCTGAGA[A/G]GGAAGAAAATATTTC | 10392 |
rs186567012 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NOD1 | GRCh38.p7 | 7:30477106 | CTTGCCCAAAGTCAC[A/G]GCATAGAAGTGACAG | 10392 |
rs186574013 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30429154 | GAATATGGAATCAGG[C/T]ATTCTGGGCTGAATT | 10392 |
rs186633857 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30473318 | GTGGTGTACTTAGAA[C/T]AGACCACTGCACCTT | 10392 |
rs186636992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30450141 | GGAGGTTGCAGTGAG[C/T]TGAGATCACGCCACT | 10392 |
rs186650351 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30426938 | ACCTCATCTAAATCA[A/G]GTTCCCTCTTGGCCT | 10392 |
rs186770936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30477961 | GACATCAACCTCTGT[C/T]ATTTCCTATGTTTTT | 10392 |
rs186775369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30429813 | GAGGTGGGTGGATCA[C/T]GAGCTCAGGAGATCG | 10392 |
rs186927372 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30448895 | GCCAACAGCTTCCCC[C/T]CATCCAGAAACACAT | 10392 |
rs186937894 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480748 | GCCTGATGTCCAGGC[A/G]TTCTTTTACACATTG | 10392 |
rs187015983 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459751 | AGGCTGAGAGAAAAC[C/T]GGAAAGAAGTCACTT | 10392 |
rs187035831 | snp | G/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30436719 | GGGACATGCAGGGAT[G/T]GCTGAGGGGCTGGAA | 10392 |
rs187090537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30428618 | ACAAGTTCTAAAGCA[A/G]AGTTTAAAAAACACT | 10392 |
rs187127087 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425412 | TTTACTGTAACTACA[A/G]CAGCTCGCAAGACAC | 10392 |
rs187129747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30456493 | GGGAACCAATACACA[C/T]AGCAATGAGAACTGA | 10392 |
rs187270048 | snp | A/G | 0.000147642 | 0.00859066 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453084 | AGCAGGGTGAGGAGA[A/G]AGGCAGAAACAGCAT | 10392 |
rs187507400 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30431403 | CCTCCTGATTTCAAA[A/G]TGTACTACACAAAGC | 10392 |
rs187510346 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462775 | CCAACATTGTGAAAC[C/G/T]CTGTCTCCACGAAAA | 10392 |
rs187513532 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30445665 | TCGTGTGGCTGAGGC[A/G]AGAGAATCGCTTGAA | 10392 |
rs187627570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30435795 | AAAACCCCATCTCTA[C/T]AAAAAATTTTAAAAT | 10392 |
rs187701517 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446609 | CAAGCCTGGCGCACT[A/G]TCACCCCCTGCGCAG | 10392 |
rs187843300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30472389 | ATCCCAAGTCCTAGT[G/T]GAAAAGGCTCATTCC | 10392 |
rs187862154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30426651 | TCCATCACTTTTAGG[A/G]TAAAGACCAAAATGC | 10392 |
rs187975996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464626 | CTCATGAGCAAATTA[A/G]AGGGAAGTTCCTGCT | 10392 |
rs188126061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30449180 | AAGTAAAAGGCTGAA[A/C]AATTAAAAGCTTGAT | 10392 |
rs188232307 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOD1 | GRCh38.p7 | 7:30475077 | CAAGAAGCAGGGGAA[A/G]TTCTTACTCATTAGA | 10392 |
rs188246155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428155 | CCTGGCTCACTGCAG[A/C]CTTGATCTCCCATGC | 10392 |
rs188352239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461263 | GCTCACTGCAGCCTC[C/T]GCCTCCCAGGTTCAA | 10392 |
rs188358829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30455703 | ACCTCCCAGGTTCAA[A/G]GAATTCTCTTTCCTC | 10392 |
rs188363690 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479939 | GTGGTCTCTTCACAC[A/G]GACACGTGTGACATT | 10392 |
rs188382705 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30456123 | GCTTCCCCCAGAAAC[C/G/T]GTCCTGGTCTCTTCT | 10392 |
rs188384694 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NOD1 | GRCh38.p7 | 7:30431755 | ATTTCTTAGATAAGA[C/T]ACTGAAAGCACAAGC | 10392 |
rs188489450 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30450903 | TGTAATGCACTTCAC[A/C]CATTCTCAACTAACA | 10392 |
rs188513061 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NOD1 | GRCh38.p7 | 7:30427442 | TGAACGTGGCTCCCC[A/G]GCCAGCTCAACCACA | 10392 |
rs188616627 | snp | C/T | | | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479256 | CTATCCTTAAATTTG[C/T]TCTTGGCAGTGTACA | 10392 |
rs188643063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30430400 | ATAAATGCATCAAGA[A/G]GCTGTAGTGTCTCCG | 10392 |
rs188754310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30473980 | AACAAAAACCCTAAA[C/G]TCTTAGACCAGTGTG | 10392 |
rs188778821 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458227 | AAATAATAATTTTTT[A/T]AAAAAATCCCACAGA | 10392 |
rs188894875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467251 | TGTAAATGCAAAGAA[A/G]ACCACCTGTGAGAAG | 10392 |
rs188906017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454658 | CTTTTTTAGAGACAG[A/G]GTCTCACTCTGTCAC | 10392 |
rs189021977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30460862 | TCCTCACAGAAACCA[A/G]TGCCCAAGTCCCCTC | 10392 |
rs189024160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437517 | CCTTCCCCAGCAAAC[C/T]TAGAGCAGCTGGGAG | 10392 |
rs189064161 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30434692 | GAGGTACTTTCATGT[C/T]CTCCTTTAGTGTCTT | 10392 |
rs189140997 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459966 | TTCCCAGATGTTTTC[C/T]GTAATCGCCGCCACA | 10392 |
rs189157338 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466381 | TTTTTTTTTTTTGCT[C/T]CTGGCACTATGATTA | 10392 |
rs189173990 | snp | C/T | 6.62833e-05 | 0.0057565 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30446975 | CACTTACTTAAGATG[C/T]GTGAGGCCTTTGCAT | 10392 |
rs189249798 | snp | G/T | 0.00107076 | 0.0231135 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30448278 | AGGTAGTTGGCCCAG[G/T]GTTCTGGAGAAAGAC | 10392 |
rs189381625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30438178 | CCTGTCACATAAAGA[A/G]GACGTTACCCAACCA | 10392 |
rs189396407 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOD1 | GRCh38.p7 | 7:30474652 | GAGGCAGAGTTCAGG[C/T]GGTAATGCTTGCTCA | 10392 |
rs189431244 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30436934 | GCACATGTATGTTTA[C/T]TGTAGCACTATTTAC | 10392 |
rs189528015 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30468120 | AAAATAGTACAGAGC[A/C]AAAGTCAACAATACT | 10392 |
rs189545028 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30424449 | CCCTTCCCCACTGTG[A/G]AGTGAATCAGGATGG | 10392 |
rs189610105 | snp | G/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479060 | TGCCATCGTGCCAGG[G/T]CCCTCCTCGTAAAAG | 10392 |
rs189625297 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454386 | ATTTTTGAGATTGCT[A/G]ACTGGTGGTCTCTTC | 10392 |
rs189629860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30429955 | GAACTGGGAGGTGGA[A/G]GTTGCAGTGAGCCAA | 10392 |
rs189763501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30457542 | TAGGGTAGGTGACCA[A/G]AGATAGCCAACTCTT | 10392 |
rs189779757 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30434612 | CAAAAGGCTAGAAAG[C/G]AAAGGTTATTTTGGA | 10392 |
rs190187437 | snp | A/G/T | 0.00199529 | 0.0315338 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30480305 | TGCCTGATTATTCAC[A/G/T]TACATTTCATTGGTG | 10392 |
rs190198174 | snp | A/C | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30448025 | TTATTAAATATATCC[A/C]CTTATATTCTCGTTG | 10392 |
rs190207595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30432264 | CTCAGCATTAGAAGA[C/T]AAACCCAATTTTAAA | 10392 |
rs190296253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453979 | CTAACGGAACCAACA[A/G]AGAAGTCTTTCGAAA | 10392 |
rs190303969 | snp | A/G | 0.0032906 | 0.0404286 | intron-variant | NOD1 | GRCh38.p7 | 7:30429471 | GCCTGAAAGAAGAAC[A/G]TAACTTGTATAAAAT | 10392 |
rs190349371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30427163 | TCCCTAGGACCTTGA[C/T]TCAGGCCCCACCCTC | 10392 |
rs190432600 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30456551 | CACAGAAGTAAAATA[C/T]CTGACTGTGCAACCT | 10392 |
rs190447132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30434277 | AGTGTAGAATAACAC[A/G]TGGCATGCAGTCAGC | 10392 |
rs190450567 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NOD1 | GRCh38.p7 | 7:30456357 | CCCCTCCGAGTCTCA[C/G]CCAGCAACAAGCAGC | 10392 |
rs190691602 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30439107 | TGGCAAGGATGTGGA[C/G]AAACTAGAATGAACT | 10392 |
rs190701810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461689 | AGACATCAGAGTTCC[C/T]GCCTGCTGCCCTTCC | 10392 |
rs190839337 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOD1 | GRCh38.p7 | 7:30448521 | AATGGCCACAGCAAT[C/T]AGCCAAATAGCCCCT | 10392 |
rs190967263 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NOD1 | GRCh38.p7 | 7:30438547 | CAACAGAACAAGTTC[C/G]TGTGGCCCACTCACA | 10392 |
rs191066049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30472499 | AAGCACTTTCCACAA[A/G]TTACAATTATGTATT | 10392 |
rs191218057 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NOD1, LOC101928268 | GRCh38.p7 | 7:30469366 | AAGTCAGTCCCTCCC[A/C/G]GAATCACCTCTCTCT | 10392 |
rs191443007 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459828 | GAAAGCTGGGAAGGG[G/T]TGTTGCACAGCTTCC | 10392 |
rs191489078 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NOD1 | GRCh38.p7 | 7:30471771 | CCTCCACTCTTCGGG[G/T]TCTTTTGTTCCTGTT | 10392 |
rs191649596 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453128 | CTCAAAGAGGAGAGG[A/C]GAGTGCATAAACAAA | 10392 |
rs191759868 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30448896 | CCAACAGCTTCCCCC[A/C/T]ATCCAGAAACACATG | 10392 |
rs191896669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30455762 | ACCCACCACCATGCC[C/T]GACTAATTTTTGTGT | 10392 |
rs191897689 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479856 | CCTTTGCTGACTCTT[C/T]TTTTCGTACTCGGCC | 10392 |
rs191912020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30431571 | GTTCAACACGTGGTG[C/T]TGCCGGGACAGCTGG | 10392 |
rs191929759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30476234 | TAAGACTTTGATAGT[A/C]TTGTGTAAGCAAATA | 10392 |
rs191958863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30428852 | GTGGCATGGCGCTCA[A/G]TGTCACAGTAAAGCA | 10392 |
rs192096653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467041 | CCCTAAAAGCCAAGC[C/T]GACCAGTGATGAAAA | 10392 |
rs192112133 | snp | G/T | | | intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30447269 | ACAAGTCACGTTACC[G/T]CTCTGTGCCTCAGTT | 10392 |
rs192117699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30435050 | TACTGGGATTACAGA[A/T]GTGAGTCACTGCTCC | 10392 |
rs192210483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464783 | CAGCCTTTCTGTGCC[A/G]TGATTGCCTCAAGGT | 10392 |
rs192365891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30449288 | TAGTGTGTATGTACA[C/T]GGCATGGCCAGCCCA | 10392 |
rs192492880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458805 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACAT | 10392 |
rs192621414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446677 | TTGCAACCCGACAGG[A/G]AACTCCCTTGGGGCA | 10392 |
rs192655308 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD1 | GRCh38.p7 | 7:30473323 | GTACTTAGAACAGAC[C/T]ACTGCACCTTTGATG | 10392 |
rs192658510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30450828 | CCTTATCTGCCAAAA[C/T]AGAGACAATAACAGT | 10392 |
rs192674538 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOD1 | GRCh38.p7 | 7:30427014 | GCAAATGATTTTTTC[C/T]TTAATGTGCTTCTCC | 10392 |
rs192723863 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30436735 | GCTGAGGGGCTGGAA[A/G]TGTCCTCTGTCTTGA | 10392 |
rs192789245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30445667 | GTGTGGCTGAGGCGA[A/G]AGAATCGCTTGAACC | 10392 |
rs192839461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30474165 | ATTAAAAACCTTATC[G/T]GAAGTCACACAACTA | 10392 |
rs192850246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30427282 | CACCTCTAATTTCTG[C/T]TCTTAAAGACAGAAC | 10392 |
rs192916471 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454760 | GCCTCAGCCTCCTGA[A/G]TAGCTGGAACTACAG | 10392 |
rs192995694 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463477 | AACTATATTATATTA[A/G]TATCTCGTGAGGTCA | 10392 |
rs193048431 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOD1 | GRCh38.p7 | 7:30451114 | ATTCCAAGGGCCATG[C/G]TCATGAGTCCTGGGG | 10392 |
rs193157949 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479462 | CACTGATGCTTGTGA[G/T]TATTAAAATTCCCAT | 10392 |
rs193163312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30430599 | AGAGCGGGTGCAGCT[C/T]CTCTTAAACCCTCCC | 10392 |
rs193286235 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30460012 | CATCAAAGGCAGAAA[C/T]CGAAGGAAAGTCTCC | 10392 |
rs199475893 | snp | A/G | 0.00159617 | 0.0282053 | NOD1 | 7 | allele_origin=G(germline)/A(germline) | 7:30479406 | ATGCTACAGAAAGTT[A/G]TCACTTACTCACACT | 10392 |
rs199475894 | snp | C/T | | | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30478919 | CGCCCGGGTCTGGCG[C/T]GGGGGGGCGAGAGAA | 10392 |
rs199475895 | snp | C/G | 0.0138799 | 0.0821421 | NOD1 | 7 | allele_origin=G(germline)/C(germline) | 7:30478839 | CGCCCAAGAGCCTGC[C/G]GGCTGCTGGGAGAGG | 10392 |
rs199475896 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459924 | GTTTTTATGGGAATC[A/G]CAGGCTTGGAAGAGA | 10392 |
rs199475897 | snp | A/T | 0.000297142 | 0.0121854 | NOD1 | 7 | allele_origin=T(germline)/A(germline) | 7:30455259 | AGGAGGTGTCCGAGT[A/T]CTTCCTCTACTTGCT | 10392 |
rs199475898 | snp | C/T | 4.94809e-05 | 0.00497373 | NOD1 | 7 | allele_origin=T(germline)/C(germline) | 7:30455228 | CCAGCAACTCGCAGA[C/T]GCCTACGTGGACCTC | 10392 |
rs199475899 | snp | A/G | | | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455138 | GGTCAACACTGACCC[A/G]GGTAGGAGTCAGCCC | 10392 |
rs199475900 | snp | C/T | 1.67399e-05 | 0.00289304 | NOD1 | 7 | allele_origin=T(germline)/C(germline) | 7:30452048 | ACCCTCCACGCCGGC[C/T]GGGACACTCTGTGCT | 10392 |
rs199475901 | snp | A/C/T | 0.000100493 | 0.00708784 | NOD1 | 7 | allele_origin=T(germline)/C(germline) | 7:30451994 | GGCATGGAGAAGAGC[A/C/T]TCTTTGTCTTCACCC | 10392 |
rs199475902 | snp | C/T | 0.00173971 | 0.029442 | NOD1 | 7 | allele_origin=T(germline)/C(germline) | 7:30451959 | GGAGGTGCAGGCCTC[C/T]GGGCTGCAGGAGAGA | 10392 |
rs199475903 | snp | A/C/G | 9.89919e-05 | 0.00703464 | NOD1 | 7 | allele_origin=G(germline)/A(germline) | 7:30451337 | TCGGCCGACTGCAGC[A/C/G]CCCTCTCCTTCGTCC | 10392 |
rs199475904 | snp | A/C/T | 0.00318978 | 0.0398085 | NOD1 | 7 | allele_origin=T(germline)/A(germline) | 7:30447926 | GGGGCAAGACCCGAA[A/C/T]GGGGATTCTGAGTGC | 10392 |
rs199475905 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30433104 | CAACCAGACGTTAAA[C/G]CATTTATGGTAACTC | 10392 |
rs199476261 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459703 | GAAAGTCTCAATTCT[A/G]TGCTACTGTGTCTTT | 10392 |
rs199476262 | snp | C/G | 0.00279162 | 0.0372561 | NOD1 | 7 | allele_origin=G(germline)/C(germline) | 7:30457127 | TCCTTCCTGCTCTAG[C/G]TAGAGAAACCCCACA | 10392 |
rs199476263 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451925 | ATGCAGCTGGGCTTC[-/C]TGCGGGCTTTGCCGG | 10392 |
rs199476264 | snp | C/T | 0.000257798 | 0.0113505 | NOD1 | 7 | allele_origin=T(germline)/C(germline) | 7:30451180 | GAGCAACAGGTGGGC[C/T]GGGCGGGCCAGGCTC | 10392 |
rs199476265 | snp | C/T | 4.9445e-05 | 0.00497193 | NOD1 | 7 | allele_origin=T(germline)/C(germline) | 7:30448408 | GTGCCTGCCCTGACT[C/T]GTAATTTTTTTGCTG | 10392 |
rs199476266 | snp | C/T | 3.2969e-05 | 0.00405998 | NOD1 | 7 | allele_origin=T(germline)/C(germline) | 7:30448267 | GAACACTGGGCCAAC[C/T]ACCTAGTAATAATAC | 10392 |
rs199476267 | snp | A/G | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30448208 | GGTCCCTGGATGATC[A/G]GCACGGATGGCCCAG | 10392 |
rs199476268 | snp | A/G | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30448186 | ATGGCCCAGGGCTGG[A/G]AAGAGCGCTGGCCCA | 10392 |
rs199476269 | snp | C/T | 0.000399281 | 0.0141238 | NOD1 | 7 | allele_origin=T(germline)/C(germline) | 7:30448180 | CAGGGCTGGGAAGAG[C/T]GCTGGCCCAGGAGTT | 10392 |
rs199476270 | snp | A/T | 0.000798403 | 0.0199641 | NOD1 | 7 | allele_origin=T(germline)/A(germline) | 7:30448078 | AAACTGGGATCCCAG[A/T]ATAGGCAAGTAGGCT | 10392 |
rs199476271 | snp | C/G | | | intron-variant, utr-variant-3-prime | NOD1 | GRCh38.p7 | 7:30437772 | CAGATCCAGGGACTG[C/G]GCACAAACATCTGCC | 10392 |
rs199476272 | snp | A/G | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437492 | GGAAGGGTGATTCGT[A/G]CTCCTAATAGAAGAG | 10392 |
rs199476273 | snp | A/C | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437404 | GCCATCTAGTAAAGC[A/C]CATTCTTCTCTTTTT | 10392 |
rs199476274 | snp | C/G | 0.00159617 | 0.0282053 | NOD1 | 7 | allele_origin=G(germline)/C(germline) | 7:30437229 | CCTCCCCTTGCCCCC[C/G]ACCCCCAACAGGCCC | 10392 |
rs199476275 | snp | A/T | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437179 | CCATGTGTCCATGTG[A/T]TCTCATTGTTCAACT | 10392 |
rs199527440 | snp | A/G | 0.000662076 | 0.0181824 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451830 | CCTGTCGTCCAGCAC[A/G]AGGAAGAAGGCTGTA | 10392 |
rs199572588 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30446199 | GATACTTCCCTCCTT[C/T]ACTTGTTATTTTGTT | 10392 |
rs199608475 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451541 | AGCCCCGCAGGCTGG[A/G]AAACAGGTGTGCCCA | 10392 |
rs199646876 | snp | A/G | 0.00199799 | 0.0315437 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452827 | CCCAGGATGAAGATG[A/G]TCTCACCCTGCTCAT | 10392 |
rs199680419 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30436947 | TATTGTAGCACTATT[C/T]ACAATAGCAAAGACT | 10392 |
rs199701790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30473581 | TGATATTAACCAGCC[C/T]AAGCAATGGATGAGG | 10392 |
rs199705081 | snp | A/C | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463402 | ATCCCAAGACAAAAA[A/C]AAAAATGATGAGCAA | 10392 |
rs199741743 | snp | A/G | 0.000911577 | 0.0213297 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451230 | CCTGAGAACAGTGAG[A/G]CGGCTGAAGCAGGGC | 10392 |
rs199809330 | snp | A/G | 5.98641e-05 | 0.00547069 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437661 | TGCCCCACATCCTGA[A/G]GGAGGAGACAAGATA | 10392 |
rs199809506 | in-del | -/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30433809 | AGAACAGAAAGAACA[-/T]TTAAAAAAAAAAATT | 10392 |
rs199878802 | snp | C/G | 0.000164984 | 0.00908101 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451339 | ACGAAGGAGAGGGCG[C/G]TGCAGTCGGCCGAGC | 10392 |
rs199946896 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30444092 | ATCCCTTCCTTACAC[C/T]TTATACAAAAATCAA | 10392 |
rs199974975 | snp | A/T | 0.309894 | 0.242719 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428375 | CAACAGTGTTTTTTT[A/T]AAAAAAAAACCTTTT | 10392 |
rs200031703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30464581 | CTGTGGTGTCTGGGA[C/T]CTCTAGAGACAGCAG | 10392 |
rs200089743 | snp | C/T | 5.00329e-05 | 0.0050014 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451909 | CCCCCGGGGCCCAGC[C/T]CCGGCAAAGCCCGCA | 10392 |
rs200106268 | snp | C/G | 0.00013392 | 0.00818182 | intron-variant | NOD1 | GRCh38.p7 | 7:30455114 | GCACTGGTGCCTGCG[C/G]TCTTGCTGGGGCTGA | 10392 |
rs200202129 | snp | G/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30434952 | ATGTTTTTTTTTTTT[G/T]TAGATAGAGGGTCTC | 10392 |
rs200206565 | in-del | -/CC | 0.0388198 | 0.134156 | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30424592 | GATCTAGTAGTATCA[-/CC]CCCCCACCCTCATGG | 10392 |
rs200278714 | snp | C/T | 0.000131486 | 0.00810715 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30437613 | TCCGCAGAGCCTCTG[C/T]GAAGGCTTTTGCTCC | 10392 |
rs200374602 | snp | A/G | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467210 | CACAAAGCACTCCAC[A/G]TTCTCTATAGGCATA | 10392 |
rs200499912 | snp | A/G | 0.000253775 | 0.0112616 | intron-variant | NOD1 | GRCh38.p7 | 7:30455354 | GGGCTGGCATGAGGG[A/G]CATCCTCCTACCATA | 10392 |
rs200548793 | snp | C/T | 0.00199802 | 0.0315439 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451814 | GCTCCTGAGTGCCCA[C/T]CCTGTCGTCCAGCAC | 10392 |
rs200551087 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425026 | AATTAAAAGCCCGTG[A/G]TGCATCCTTTCCTTG | 10392 |
rs200583987 | snp | A/G | 0.000135017 | 0.00821523 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452387 | GAAGCACCTTCTTCC[A/G]CAGGAACTGGCGCGG | 10392 |
rs200594250 | snp | C/T | 8.42694e-05 | 0.00649058 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451505 | AGCTTTCGACCTGAA[C/T]GCGGGGCAGGCTCTT | 10392 |
rs200610248 | snp | A/C/G/T | 6.70024e-05 | 0.00578772 | stop-gained, missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452545 | CTCAGGTCCAAGTCC[A/C/G/T]AGTGCAGCTCGTCCA | 10392 |
rs200644123 | snp | C/T | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30466713 | TGTCTGAGCCCACTA[C/T]ATTAAAGGATCCCTC | 10392 |
rs200731251 | snp | A/G | 4.95905e-05 | 0.00497923 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451674 | CTGGAAGTGATCCTT[A/G]TTCTTGAAGAGGTCT | 10392 |
rs200796003 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30440103 | CACTGAAAACCCATC[C/T]GTACATCACCATCAT | 10392 |
rs200801586 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | NOD1 | GRCh38.p7 | 7:30457481 | TTAGATGCATTAAAG[-/A]AAAAAAAATCATAAT | 10392 |
rs200916106 | snp | A/G | 0.000413733 | 0.0143769 | intron-variant | NOD1 | GRCh38.p7 | 7:30433186 | TGGGTCAGCCTAAGG[A/G]AAAAAAAGGAAGTAT | 10392 |
rs200931843 | snp | A/G | 0.000371026 | 0.0136153 | intron-variant | NOD1 | GRCh38.p7 | 7:30455104 | GGCCCTGCTTGCACT[A/G]GTGCCTGCGGTCTTG | 10392 |
rs200936372 | snp | G/T | 0.00199805 | 0.0315441 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452825 | CACCCAGGATGAAGA[G/T]GGTCTCACCCTGCTC | 10392 |
rs200943217 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30465105 | TGAGCAGAGAGAGAC[C/T]GGGGGGTGCCGTGGC | 10392 |
rs200974567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOD1 | GRCh38.p7 | 7:30457649 | TGGAAAGGTGTTTAT[C/T]TTACATAATAAGGTT | 10392 |
rs201002349 | snp | A/G | 0.000285794 | 0.0119505 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455308 | GGTCCAGAATTTTGC[A/G]GACCTGGAGGTGACA | 10392 |
rs201045483 | snp | G/T | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462424 | ATCAGGGGTTCTGAT[G/T]GGTTTTTTTTTTTTT | 10392 |
rs201049502 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30435433 | AGCTTGCATGGCCAG[C/T]GTTCTAGTTCTCCTG | 10392 |
rs201065911 | snp | G/T | 5.08195e-05 | 0.00504055 | intron-variant | NOD1 | GRCh38.p7 | 7:30455090 | ACCAAACCCCCCAGG[G/T]CCCTGCTTGCACTGG | 10392 |
rs201102944 | snp | A/G | 0.000315015 | 0.0125463 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451263 | CAGCTCCCGCACGCC[A/G]TAGTCGTTGAGATTG | 10392 |
rs201122509 | snp | A/C | | | intron-variant | NOD1 | GRCh38.p7 | 7:30444107 | CTTATACAAAAATCA[A/C]TTCAAGATGGATTAA | 10392 |
rs201129988 | snp | A/C | 0.00199802 | 0.0315439 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451713 | CGGACCACTGCCCTG[A/C]AGGCACTGGAACGGG | 10392 |
rs201159934 | snp | A/C | 5.00363e-05 | 0.00500156 | utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456959 | TTTTCCCAAATTCAT[A/C]TTCAGCTGCGTGTGT | 10392 |
rs201190628 | in-del | -/A | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428373 | CCAACAGTGTTTTTT[-/A]TTAAAAAAAAACCTT | 10392 |
rs201194913 | snp | A/G | 4.98641e-05 | 0.00499295 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451437 | CTGGCTCTGTGTCTC[A/G]TAGATGCAGCGCAGC | 10392 |
rs201279601 | snp | A/G/T | 0.000399281 | 0.0141238 | missense, synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452348 | TGGCATAGGCGCGCA[A/G/T]GTGGCTGGGGGAGAA | 10392 |
rs201312055 | snp | A/C | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467170 | ACATTTATATGGCTT[A/C]CCCACATCCCCTGCC | 10392 |
rs201355211 | snp | A/T | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428374 | CCAACAGTGTTTTTT[A/T]TAAAAAAAAACCTTT | 10392 |
rs201359060 | snp | A/C/T | 1.67534e-05 | 0.0028942 | missense, stop-gained, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452318 | CCTGCAGGGCCCGCT[A/C/T]GGGGAACATCCTCCT | 10392 |
rs201384207 | in-del | -/AGAG | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30465373 | CCCCCATGAACATAG[-/AGAG]CCTCAGTGTGCCCCT | 10392 |
rs201438430 | snp | A/G | 0.00010101 | 0.00710597 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452528 | AGCTGTCAGGCACGC[A/G]GCTCAGGTCCAAGTC | 10392 |
rs201468134 | snp | A/G | 0.000107193 | 0.00732017 | intron-variant | NOD1 | GRCh38.p7 | 7:30455351 | CACGGGCTGGCATGA[A/G]GGGCATCCTCCTACC | 10392 |
rs201516813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446116 | CAGCAGGTTGTACCA[C/G]ATACATCCATCCCCT | 10392 |
rs201553599 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | NOD1 | GRCh38.p7 | 7:30474749 | GGGATTGGGGACCCC[-/T]GAAGTAAGGAATAAA | 10392 |
rs201602747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453861 | TGTCTATAGATTTAC[C/G]TTTTCTGGACATTTC | 10392 |
rs201632880 | snp | C/G | 0.00199799 | 0.0315437 | synonymous-codon, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452826 | ACCCAGGATGAAGAT[C/G]GTCTCACCCTGCTCA | 10392 |
rs201638077 | snp | A/G | 0.000149399 | 0.00864159 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451260 | CTGCAGCTCCCGCAC[A/G]CCGTAGTCGTTGAGA | 10392 |
rs201645853 | snp | A/C | | | intron-variant | NOD1 | GRCh38.p7 | 7:30442074 | CGAGAACAAAGACAC[A/C]ACATACCAGAATCTC | 10392 |
rs201703014 | snp | A/G | 0.00199793 | 0.0315432 | synonymous-codon, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452715 | GAACATGCGGCAGCG[A/G]AAGTGGAAGAAGAAT | 10392 |
rs201910425 | snp | A/C/T | 6.64071e-05 | 0.00576194 | missense, upstream-variant-2KB, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452987 | GGGCATAGCACAGCA[A/C/T]GAACTTGGAGTCACG | 10392 |
rs201912703 | snp | A/G | 0.0099618 | 0.0698689 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30455276 | CTCGGACACCTCCTC[A/G]CCCTTGCTCTGTACC | 10392 |
rs201914077 | snp | A/G | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30445709 | GGTTGCAGTGAGCCG[A/G]GATCATGCCACTGCA | 10392 |
rs201927568 | snp | C/T | 4.95176e-05 | 0.00497558 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451358 | AGTCGGCCGAGCAGG[C/T]GTTGCAGTAGGTCAG | 10392 |
rs201979222 | in-del | -/A | 5.75622e-05 | 0.00536449 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446094 | CAAGGCCCGCCCCCC[-/A]CACACACAGCAGGTT | 10392 |
rs202009071 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30445303 | AAAAAAAAAAAAAAA[C/T]AATTGAAGGCAGTCC | 10392 |
rs202110779 | snp | A/C/T | 0.000428248 | 0.0146269 | missense, stop-gained, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30425667 | TCCGCTTCTCATCTT[A/C/T]ATAGACTTTGGCCTC | 10392 |
rs202192753 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30447065 | ACTTCAAGAGAAAGC[A/C]CAGCCATGAGACTTT | 10392 |
rs202193106 | snp | C/T | 0.00199795 | 0.0315434 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452089 | CTGCGTGTGTTCCGC[C/T]GCACCAGGCTGCTGG | 10392 |
rs202207550 | in-del | -/G | 0.0107246 | 0.0724382 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30467353 | GTAATGTTTTTTTTT[-/G]TTATAAGAAGGCTAT | 10392 |
rs267601478 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30459237 | TCCAATTTATTTCTG[A/G]AATCTGCAAAATCAA | 10392 |
rs367549841 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | NOD1 | GRCh38.p7 | 7:30476582 | TGCGTGTGTGTGCAC[A/C]TACACTAATTCTGAG | 10392 |
rs367583429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30431874 | CTTTGGGAGGCTGAG[A/G]CAGGTGGATCACCTG | 10392 |
rs367621477 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30477811 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCCTGGCT | 10392 |
rs367716316 | snp | C/T | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30445813 | ATGCTTCCATGTGGA[C/T]GAATCTTGAGGACAT | 10392 |
rs367958946 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30439549 | TGCGCTTTTCAGACC[A/G]GCTTAAGAAACGGCG | 10392 |
rs367960585 | snp | C/T | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462823 | GCATCGTGGTGCACA[C/T]CTGTAATCCCAGCTA | 10392 |
rs367963834 | snp | A/C/G | 3.29957e-05 | 0.00406162 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452755 | GCGTCTAGCCGGCCC[A/C/G]TGGCCCAGAGGCTCT | 10392 |
rs367964640 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30429559 | ATAAGAGACAAGTTG[A/G]TCAGGGGAAGAACTG | 10392 |
rs367979352 | snp | C/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30473780 | AGGTAGAATAAGCAG[C/G]GGTGGGGGTACTCAC | 10392 |
rs367988047 | snp | A/C | | | intron-variant | NOD1 | GRCh38.p7 | 7:30438813 | ATACATATAGTCTCA[A/C]CCCTACTATATTTTT | 10392 |
rs368009740 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30459075 | TGACCCACTTTAGGA[A/T]CCTTAGCTTTAGAAA | 10392 |
rs368141509 | snp | A/G | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446621 | ACTGTCACCCCCTGC[A/G]CAGGGCACACCTACA | 10392 |
rs368288458 | snp | A/G | 0.000100078 | 0.00707313 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452300 | GCTGGCTCAGCAGGC[A/G]GTCCTGCAGGGCCCG | 10392 |
rs368541610 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456751 | GGGGCAGGCACACAC[A/G]ATCTCCGCATCTTCG | 10392 |
rs368548218 | snp | C/T | 4.96192e-05 | 0.00498067 | missense, intron-variant, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452707 | AAGCAGCTGAACATG[C/T]GGCAGCGAAAGTGGA | 10392 |
rs368598716 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30432414 | TTCACATCCACTAGT[A/G]TAACTAGATTTTAAA | 10392 |
rs368748622 | snp | C/G | 8.26221e-05 | 0.00642684 | intron-variant | NOD1 | GRCh38.p7 | 7:30425755 | CAGGTAAAATGTTAA[C/G]GATCCTCGCACACTC | 10392 |
rs368755214 | snp | A/G | 0.000612547 | 0.01749 | utr-variant-5-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456938 | GTTAAAGTAGCAAGC[A/G]GCTACTTTTCCCAAA | 10392 |
rs368764424 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOD1, LOC101928268 | GRCh38.p7 | 7:30458379 | AGAGAGTAAAAAAAA[-/A]GGTTTTTTTGTAGTT | 10392 |
rs368792793 | snp | A/G | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428339 | GTGCTGGTATTACAG[A/G]CATGAGCCACCATGC | 10392 |
rs368798078 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453089 | GGTGAGGAGAGAGGC[A/G]GAAACAGCATCAAAC | 10392 |
rs368807489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30461225 | CTCTGTCGCCCAGGC[G/T]GGAGTGCGGTGGCGC | 10392 |
rs368843529 | snp | A/G | 1.66774e-05 | 0.00288763 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452301 | CTGGCTCAGCAGGCG[A/G]TCCTGCAGGGCCCGC | 10392 |
rs368859245 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30424976 | CTGAGGGCATTCTCT[A/C]TCTTTGCCAGCAGAC | 10392 |
rs368866677 | in-del | -/GCTG | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30462443 | TTTTTTTTTTTTTTT[-/GCTG]TTTTTTCTTTTTAAA | 10392 |
rs368915657 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | NOD1 | GRCh38.p7 | 7:30433183 | TTTTGGGTCAGCCTA[A/T]GGAAAAAAAAGGAAG | 10392 |
rs368948087 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452426 | TGCCTGTGCGGGCTG[A/T]GAGCAGCTTGCTAGC | 10392 |
rs368955529 | snp | G/T | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30437234 | TGTTGGGGGTGGGGG[G/T]CAAGGGGAGGGCAAG | 10392 |
rs368963336 | snp | C/G | | | upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30479058 | GGTGCCATCGTGCCA[C/G]GTCCCTCCTCGTAAA | 10392 |
rs368996452 | snp | C/T | | | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451252 | AAGCAGGGCTGCAGC[C/T]CCCGCACGCCGTAGT | 10392 |
rs368998358 | snp | C/T | 0.000264817 | 0.0115038 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451749 | GGGAGGATAGCAGGA[C/T]GTGGTCGCTGCCCCC | 10392 |
rs369003942 | snp | C/T | 5.06103e-05 | 0.00503017 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452386 | AGAAGCACCTTCTTC[C/T]GCAGGAACTGGCGCG | 10392 |
rs369011792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30439440 | GAGGCATTGCCTCAC[C/T]TGGGAAGCGCAAGGG | 10392 |
rs369031059 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30453518 | TCAAACTCCCAGGCT[C/G]AAGCAATCCTCCCAC | 10392 |
rs369137547 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOD1 | GRCh38.p7 | 7:30454583 | AGGACTGGCACTCAA[C/T]GGTGACAGAATACTT | 10392 |
rs369263969 | snp | A/C | 8.2789e-05 | 0.00643332 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451791 | CCACTCCTGGAAGAA[A/C]CTGAGCAGCTCCTGA | 10392 |
rs369269480 | snp | A/G | 3.29549e-05 | 0.00405911 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30448287 | GCCCAGTGTTCTGGA[A/G]AAAGACATACCCCAA | 10392 |
rs369272376 | snp | C/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30441109 | CTCCTGAAGGAAGCG[C/G]TAAACATGGAAAGGA | 10392 |
rs369298055 | snp | C/T | 1.64795e-05 | 0.00287045 | intron-variant | NOD1 | GRCh38.p7 | 7:30429324 | CACAGTCAGTGGTGG[C/T]GAGTAAACAGTCACT | 10392 |
rs369305188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30438039 | CCTGGAGGGAAGGCC[A/G]TGTGCAGGTGCTGGG | 10392 |
rs369456248 | snp | A/C | | | intron-variant | NOD1, LOC101928268 | GRCh38.p7 | 7:30463165 | TGTGTGTGTATGTAT[A/C]TATATGAATATACAT | 10392 |
rs369523004 | snp | A/C | 0.000171089 | 0.00924745 | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30446926 | ACAGAAGGGGGTGAT[A/C]AAGAGAATATACTAA | 10392 |
rs369566061 | snp | C/T | 1.68508e-05 | 0.0029026 | missense, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30452527 | GAGCTGTCAGGCACG[C/T]GGCTCAGGTCCAAGT | 10392 |
rs369604574 | in-del | -/GTTTT | | | intron-variant, downstream-variant-500B | NOD1 | GRCh38.p7 | 7:30428539 | ATTTTGTTCTGTTCT[-/GTTTT]CTTTTTAAATATTGT | 10392 |
rs369628919 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30436942 | ATGTTTATTGTAGCA[C/T]TATTTACAATAGCAA | 10392 |
rs369644741 | snp | C/T | | | intron-variant | NOD1 | GRCh38.p7 | 7:30478075 | CCTTACTTTGTGGAG[C/T]ATGAAACCCAAGGGA | 10392 |
rs369646651 | snp | C/G | | | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30451839 | CAGCACGAGGAAGAA[C/G]GCTGTAAAGAAGGCC | 10392 |
rs369740466 | snp | C/T | 9.88712e-05 | 0.00703035 | synonymous-codon, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30456913 | CTCACTGTGGCCCTG[C/T]TCTTCCATAGTTAAA | 10392 |
rs369848302 | snp | A/G | | | intron-variant | NOD1 | GRCh38.p7 | 7:30435642 | TGCAGCCCCTGGGAT[A/G]ATTCCTGGGACCTAA | 10392 |
rs369855053 | snp | A/C | 3.29973e-05 | 0.00406172 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | NOD1 | GRCh38.p7 | 7:30446995 | GGCCTTTGCATTCAT[A/C]CAGGATTTTGGTGAC | 10392 |
rs369869601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOD1 | GRCh38.p7 | 7:30455790 | TGTTTTTATTAGAGA[C/T]GGGTTTTCCCCATGT | 10392 |