SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6607 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560941 | TGCAGGAACAGAGGC[A/G]TCTTCCTGGGTTTGG | 26168 |
rs6608 | snp | C/T | 0.235273 | 0.249566 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561096 | GGCGCCAGGCATTGT[C/T]CAGACCTGGTCGGGG | 26168 |
rs1133249 | snp | A/C/T | 0.38821 | 0.208322 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571841 | TCTTCAAACTTTTAT[A/C/T]TATATATATATATAT | 26168 |
rs1133250 | snp | A/C | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571926 | aaataaataAATGCC[A/C]CGGTCCTGCTCTGGT | 26168 |
rs1140986 | snp | A/T | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571910 | ATATATATATATATA[A/T]AAATATATAAATGCC | 26168 |
rs1140987 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571916 | atatatatataaata[A/T]ataAATGCCACGGTC | 26168 |
rs4542712 | snp | C/T | 0.272511 | 0.248984 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566010 | GGGATGGGTTCCTAT[C/T]GTAACTATTGTAAAA | 26168 |
rs4602096 | snp | A/C | 0.485118 | 0.0849685 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570139 | CCATCATGGGTTCTC[A/C]AGTGTTCGTTCTGAT | 26168 |
rs4624241 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569245 | aaaaaattagccggg[C/T]gaggtggcacgtgtc | 26168 |
rs4968212 | snp | C/T | 0.444489 | 0.157079 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564899 | CTAGCCTCTCTCCCT[C/T]CTCCGACTCCTAGAG | 26168 |
rs4968213 | snp | C/T | 0.246765 | 0.249979 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570959 | GATGGGGCCACCTCC[C/T]CTAGCTCTGAAGTCA | 26168 |
rs6503039 | snp | A/G | 0.236724 | 0.249647 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566743 | ggccgaggcaggcag[A/G]cagacagattgaggc | 26168 |
rs7220171 | snp | C/G | 0.0337553 | 0.125452 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572113 | CCCAAACAAATCCCC[C/G]AGATGGGAGCAGAGA | 26168 |
rs7503669 | snp | C/T | 0 | 0 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560142 | TCCGAATCCAGGATG[C/T]TGGAGTTTATCTGCT | 26168 |
rs8068222 | snp | G/T | 0.396364 | 0.202676 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565371 | AATTTGTATTCCAGG[G/T]AGTAGTAGGTATTTC | 26168 |
rs9908405 | snp | A/C | 0.23846 | 0.249734 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564144 | CGTGTATACATCTCC[A/C]GAGGGTACCATTCCC | 26168 |
rs9913914 | snp | A/G | 0.236434 | 0.249632 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565192 | AGAGCTGAAGGGGAG[A/G]ACTCTGCAGGCAGGT | 26168 |
rs9972914 | snp | A/T | 0.00975586 | 0.0691575 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570744 | GATTTCCACCAGGGC[A/T]GGAAAGGTTACTTCA | 26168 |
rs10438740 | snp | A/G | 0.494815 | 0.0506538 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569566 | GCCCTCCCATTCAAA[A/G]GCCAGGAAATTTCTA | 26168 |
rs10468481 | snp | A/G | 0.395635 | 0.2032 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571674 | TCTGATGTGCAGGGG[A/G]TGGCTACAGAAAAGC | 26168 |
rs11078697 | snp | C/T | 0.115788 | 0.21092 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565912 | TATTAATTTCAAATC[C/T]GTAATCTTGGGCTCT | 26168 |
rs11552709 | snp | C/G | 0 | 0 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560822 | ACCTTCCTGGGGTTT[C/G]TGAAACTGTGATTGT | 26168 |
rs11654859 | snp | C/T | 0.267841 | 0.249363 | downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7562022 | CGGTGGCGCTGGTGG[C/T]GGCGGTGGCGGAGGT | 26168 |
rs11656383 | snp | C/G | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563417 | AGCGGCCCCGCCCTT[C/G]CCGCCCCACTCATCG | 26168 |
rs11658232 | snp | A/G | 0 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570232 | CTTGCCCACAATCTA[A/G]GCCTTGGGTCTTCTG | 26168 |
rs11658330 | snp | A/G | 0.00865784 | 0.0652224 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570493 | CCGCCGCTGCCCTAA[A/G]GTTTGAGGGGGTAGG | 26168 |
rs11870250 | snp | G/T | 0.067446 | 0.170804 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568465 | gctgggcgtggtggc[G/T]tgcgcctgtagtccc | 26168 |
rs12452635 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571912 | ATATATATATATAAA[A/T]ATATATAAATGCCAC | 26168 |
rs12452997 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569358 | ccactgcactccagt[C/G]tgggcaacagagcaa | 26168 |
rs12939472 | snp | C/T | 0.400682 | 0.199487 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569415 | ATTTGTTTTTTCCTC[C/T]GCAGGTTGGATGTGG | 26168 |
rs12941164 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571878 | atatatatatatata[A/T]atatatatatatata | 26168 |
rs12941193 | snp | A/T | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571918 | ATATATAAAAATATA[A/T]AAATGCCACGGTCCT | 26168 |
rs12942617 | snp | C/G | 0.0338808 | 0.12567 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565698 | CTCCATGGCAAGCTG[C/G]CTCCCATCTTCTCCC | 26168 |
rs28625968 | snp | C/T | 0.372189 | 0.218105 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571221 | AAGTAAGAACACTAG[C/T]TTTAGAGTCAGGCTG | 26168 |
rs28655557 | snp | A/G | 0.234982 | 0.249549 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567937 | GGAACAGAGCACAGT[A/G]GTCCAGGTGAGAAAC | 26168 |
rs34012149 | in-del | -/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562898 | CACAGACCCTGAAGG[-/G]CCCCTTGTGGACCGC | 26168 |
rs34349099 | in-del | -/A/AA | 0 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566684 | AAAAAAAAAAAAAAA[-/A/AA]GCCTGGTTTGTTGAC | 26168 |
rs34362644 | in-del | -/C | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560771 | GTGTCATAATTCCCC[-/C]GGGCAAGGGCGAAAC | 26168 |
rs34391610 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560179 | CAGGTAACCCCAGCC[-/C]ACACTCTGAGCTTCA | 26168 |
rs34434164 | in-del | -/G | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572184 | ATCCGAGAGGGAAGC[-/G]TGGGGAACTGGACAC | 26168 |
rs34467278 | snp | A/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569345 | AGGCAAGATCACGCC[A/T]CTGCACTCCAGTCTG | 26168 |
rs34476700 | in-del | -/G | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560092 | GCAACCAGCTCTTAG[-/G]CGTGGGAGAGGCCTA | 26168 |
rs34655408 | in-del | -/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566599 | GAACCCGGGAGGCGG[-/G]AGGTTGCAGCGAGTC | 26168 |
rs34758149 | in-del | -/C | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572333 | TGATTCCTTCATCCC[-/C]TGGCACACGTCCAGG | 26168 |
rs34995901 | snp | A/G | 1.66543e-05 | 0.00288563 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564804 | CGGCTTTCTCCCCAG[A/G]CCTCTCTGCCTCTTC | 26168 |
rs35320998 | in-del | -/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564610 | ATGCCCATTCCATTT[-/T]CCCCTGCCCTATAGG | 26168 |
rs35424738 | in-del | -/C | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561033 | TTGCTTCTGTTCCCC[-/C]ATGGAGCTCCGAATT | 26168 |
rs35596387 | snp | A/G | 0.074116 | 0.177665 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564960 | GAATTCGTCCAAGAT[A/G]CCTGGTGGAAAGGGA | 26168 |
rs35746763 | in-del | -/G | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571622 | AAATGTTTCAATTTC[-/G]TGTATTTTTTTTTCT | 26168 |
rs35994480 | in-del | -/A | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565852 | CTCTTTCATTTTACA[-/A]CAGAGAGGGTCTCTG | 26168 |
rs55738870 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563921 | AAGAGTGCCGGCTCC[A/G]GAAGAGCTGCGAAAT | 26168 |
rs56136712 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562706 | CCACGGTTATCATGT[A/C]CCTGAGGAAAGAAAC | 26168 |
rs56327661 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571846 | AAACTTTTATATATA[C/T]ATATATATATATATA | 26168 |
rs58131929 | in-del | -/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571918 | ATATATAAAAATATA[-/T]AAATGCCACGGTCCT | 26168 |
rs58682397 | in-del | -/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571916 | ATATATATAAAAATA[-/T]ATAAATGCCACGGTC | 26168 |
rs58805209 | in-del | -/A | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571843 | TTCAAACTTTTATAT[-/A]TATATATATATATAT | 26168 |
rs58840546 | in-del | -/ACA | | | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560330 | ATCCTGTTTTCTTCA[-/ACA]TCTCCCTTCCCTGCC | 26168 |
rs60236248 | snp | C/T | 0.00165016 | 0.0286768 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564403 | TTTCTTTCTTCCTGT[C/T]TATGAGTAGGAACTC | 26168 |
rs60385651 | in-del | -/ATATAAAT | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571915 | TATATATATAAAAAT[-/ATATAAAT]GCCACGGTCCTGCTC | 26168 |
rs60828368 | in-del | -/AAAAAAA/AAAAAAAAAAAAA | 0 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569398 | CAAAAAAAAAAAAAA[-/AAAAAAA/AAAAAAAAAAAAA]GATTTGTTTTTTCCT | 26168 |
rs61729121 | snp | C/G | 0.21875 | 0.248039 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564816 | AGGCCTGGGGAGAAA[C/G]CCGGCCAGCACAGCC | 26168 |
rs61760045 | snp | C/T | 0.00014843 | 0.00861354 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560448 | TATAAGAAGTATGCC[C/T]TCCCACCCGGACCGG | 26168 |
rs62059807 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561799 | CACGCGCGGCCGGGC[A/G]GCGGATGTGCGCAGG | 26168 |
rs62059821 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566274 | TGAACCCGTGAGGCG[A/G]AGGTTGCGGTGAGTC | 26168 |
rs62059822 | snp | A/G | 0.132409 | 0.220618 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567242 | AACGTGAGGCTGGGC[A/G]CAGTGGCTCACGCCT | 26168 |
rs66817720 | in-del | -/A/AA | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566669 | GCCCTGCCTCAAATA[-/A/AA]AAAAAAAAAAAAAAG | 26168 |
rs72154130 | in-del | -/CAA | 0.159664 | 0.233108 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560328 | CCATCCTGTTTTCTT[-/CAA]CATCTCCCTTCCCTG | 26168 |
rs72479718 | snp | C/T | 0.176861 | 0.239062 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566528 | AAAGTTAGCTGGGCA[C/T]AGTGGCGGGTACCTG | 26168 |
rs72827565 | snp | A/G | 0.132409 | 0.220618 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566290 | AGGTTGCGGTGAGTC[A/G]AGATCCACGCCATTG | 26168 |
rs74875436 | snp | C/T | 0.0704125 | 0.17392 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560902 | GAGACAGCCAAGAGC[C/T]GAGTATATAAAGGAG | 26168 |
rs76586164 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566970 | TAAACTCCGTACCAA[A/G]GGGTTATGATGGGGT | 26168 |
rs76849317 | snp | C/T | 0.0333238 | 0.124705 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563957 | CATTAAGCCCCACTT[C/T]GAGCAGAAAGTAAGC | 26168 |
rs77529322 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570037 | TAAATGGAGGAGCTG[C/T]ATTTGAATTCTGGCA | 26168 |
rs78153201 | snp | A/C | 0.000146883 | 0.00856855 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570477 | CGCAGCGTACCCTAA[A/C]CCGCCGCTGCCCTAA | 26168 |
rs78370612 | snp | C/T | 0.5 | 0 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561615 | TACCCCGGCTCCATT[C/T]CCCCCACTGCCTCGC | 26168 |
rs78439383 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568616 | AAAACCCGAGAGGAG[G/T]AGTTTGGAGACATTC | 26168 |
rs78496193 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560573 | TAGGAGGGAGGTTGG[A/T]AACCTAAACAGAGGC | 26168 |
rs79377982 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565202 | GGGAGGACTCTGCAG[A/G]CAGGTGCCAAATCCT | 26168 |
rs80239205 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567230 | TCAACACAGAGTAAC[A/G]TGAGGCTGGGCGCAG | 26168 |
rs111451688 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560295 | AGCGCTCCTGAGGCC[C/T]CCCAGAACTGAGCCA | 26168 |
rs111727030 | snp | C/G | | | splice-acceptor-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570355 | GGCACTATCTCTTTA[C/G]GTGGACATCTTCAAT | 26168 |
rs112246784 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560277 | CTTCTTTCTTCCCTC[A/G]TTAGCGCTCCTGAGG | 26168 |
rs113468868 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567127 | ATTAAACGTCTCTTG[C/T]GTGTGTAGGCACTAA | 26168 |
rs113967036 | snp | C/T | 0.5 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569113 | TTTTTTTGCCGGGCG[C/T]GGTGGCTCACGCCTG | 26168 |
rs114692970 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562646 | TAGAGAACTGTCTCC[C/T]ATTCCAGTCCAGTTT | 26168 |
rs116784454 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567090 | GCCCTTTCCCTGACC[A/G]TGTTCATTCAGTCTT | 26168 |
rs138292852 | snp | C/T | 0.0189856 | 0.0955633 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561301 | CGTCCTTCTCTCCAT[C/T]TATCGGACCCCAGTT | 26168 |
rs139198089 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566795 | GGCAACATAGTGAGA[C/G]CCTGTCTCTACCAAA | 26168 |
rs139268356 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567292 | GAGGCCAACACGGGC[A/G]GATCACCTGAGGTCA | 26168 |
rs139278317 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569483 | TTTTGGCCTATGTAA[C/T]GGGAAAAGTGGGAGA | 26168 |
rs139298099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568377 | CTGAGGCAGATGGAT[C/T]GCAAGGTCAAGAGAT | 26168 |
rs139336280 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571724 | CAGGGGAGTGTGGCC[C/G]TGTGGCCTGGGTGGA | 26168 |
rs139689726 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570824 | GGTAGAAGGCAGAAA[G/T]TGAAGTCCTACCCCT | 26168 |
rs139748549 | snp | C/T | 1.65007e-05 | 0.00287229 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560456 | GTATGCCCTCCCACC[C/T]GGACCGGGCCTACAA | 26168 |
rs139860832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564055 | GTCTTGAGCGCAGAT[C/G]AGAAAGGGAGATGTG | 26168 |
rs140764161 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568649 | GATAGCTGAAGGCAT[A/G]GAGGCTCCCACAGGA | 26168 |
rs140832981 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562590 | GCATCTGCACTTGAG[A/T]TGACCGCAGCCTTCC | 26168 |
rs140868033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564093 | AAAATCCTGTCCACA[C/G]GAAATCCCTTGTCGG | 26168 |
rs141602266 | snp | A/T | 3.30071e-05 | 0.00406232 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560459 | TGCCCTCCCACCCGG[A/T]CCGGGCCTACAACAG | 26168 |
rs141869920 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570305 | AGAACCTTCATGGCA[A/G]AAGGCAAGACTTCTG | 26168 |
rs141894545 | snp | C/T | 5.60596e-05 | 0.00529402 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570874 | GCCTGCTTTCTTTCT[C/T]TTCTCTAGAATGTGG | 26168 |
rs141982352 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566197 | AAATACAAAATTAGC[C/T]GGGCATGGTGGTGCA | 26168 |
rs142726310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564056 | TCTTGAGCGCAGATG[A/G]GAAAGGGAGATGTGG | 26168 |
rs143150364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567118 | CTTTCAAAGATTAAA[C/T]GTCTCTTGTGTGTGT | 26168 |
rs143187716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569773 | ACCTTGTGCAAGTCA[C/T]GACTTTCCAAGCTGC | 26168 |
rs143835142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566082 | CATGGTAGCTCATGC[C/T]TGTAATCCCAGCACT | 26168 |
rs144063411 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568386 | ATGGATCGCAAGGTC[A/G]AGAGATTGAGACCAG | 26168 |
rs144110275 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572133 | GGGAGCAGAGAGCAG[A/G]AAGGAGGGAAAGTAG | 26168 |
rs144210919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567740 | GCAGAGTGAGCAAAG[A/G]GAGATGGATACAAAA | 26168 |
rs144678797 | snp | A/G | 0.0149374 | 0.085121 | utr-variant-5-prime, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563067 | CTTTTGTTTTTCAGG[A/G]TACTGGAAGATGAAA | 26168 |
rs145250389 | snp | G/T | 1.65075e-05 | 0.00287289 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560467 | CACCCGGACCGGGCC[G/T]ACAACAGCTGCTATA | 26168 |
rs145251151 | snp | A/G | 0.000346172 | 0.0131517 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560018 | ACCTGAGAGTGCCAA[A/G]AAGTCCTGACCGACA | 26168 |
rs145345809 | snp | C/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560425 | AGGCAGGAGACTCTA[C/T]TCCGATGTATAAGAA | 26168 |
rs145439493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569091 | GTATAGTAGGAAAGA[A/T]GATTTGTTTTTTTGC | 26168 |
rs146268752 | snp | A/G/T | 0.00289077 | 0.0379096 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571342 | GTCCTGACACGGGGG[A/G/T]TTTCTCATGGCTTGC | 26168 |
rs146712887 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564232 | AGAATATTTCCCTTT[C/T]GGAGAACTCCAGCCA | 26168 |
rs146739753 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568326 | AAAGGGGCCGGGTGC[A/G]GCGGCTCACGCCTGT | 26168 |
rs146782424 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566581 | TGAGGCGGGAGAATC[A/G]CTTGAACCCGGGAGG | 26168 |
rs146903936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569255 | CCGGGCGAGGTGGCA[C/T]GTGTCTGTAGTCCAA | 26168 |
rs147080850 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569903 | TATTATGGATAGTCA[C/G]TAGTTTAATCCTCAT | 26168 |
rs147443869 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560434 | ACTCTATTCCGATGT[A/G]TAAGAAGTATGCCCT | 26168 |
rs147458538 | snp | C/T | 0.00577271 | 0.0534138 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563556 | GGGCCGGCGGCGGGG[C/T]CTCGCACACCCCAAG | 26168 |
rs147479100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567124 | AAGATTAAACGTCTC[G/T]TGTGTGTGTAGGCAC | 26168 |
rs148172875 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566196 | AAAATACAAAATTAG[C/T]CGGGCATGGTGGTGC | 26168 |
rs148497612 | snp | A/G | 3.29576e-05 | 0.00405928 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560074 | TGTGACAGAGGTGAT[A/G]TGGCAACCAGCTCTT | 26168 |
rs148692440 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567769 | AATTCGGTCAGAGAG[C/T]AGATCATGTAAGACA | 26168 |
rs149029733 | snp | C/T | 5.05531e-05 | 0.00502733 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565530 | GGCTTATAAGCGGCA[C/T]GTGCTGACCATGGAT | 26168 |
rs149219551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569114 | TTTTTTGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 26168 |
rs149568232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567627 | AATGATGAGCAGCCA[C/G]CCATGCGCAGACCTG | 26168 |
rs149609747 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561565 | CTTCTTTCTGATCAA[A/G]CCCTGCTTAAAGTTA | 26168 |
rs149722604 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564129 | CAGTATAAGAACCCC[C/T]GTGTATACATCTCCA | 26168 |
rs149819305 | in-del | -/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561454 | TGCCCCGGCGTGGCA[-/G]GGCCATTCCAAGCCC | 26168 |
rs150615265 | snp | C/G | 3.75926e-05 | 0.00433531 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570500 | TGCCCTAAGGTTTGA[C/G]GGGGTAGGAGAGAGA | 26168 |
rs150976338 | snp | A/G | 6.59011e-05 | 0.00573988 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560782 | TCCCCGGGCAAGGGC[A/G]AAACTTAACCTCTCT | 26168 |
rs151004177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564090 | ACAAAAATCCTGTCC[A/G]CACGAAATCCCTTGT | 26168 |
rs180684211 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567467 | GAGGTTGCAGTGAGC[C/T]GAGACCCCGCCATTG | 26168 |
rs181252161 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571239 | TAGAGTCAGGCTGTT[C/T]TTGAACCCCAGGCTG | 26168 |
rs181281446 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566498 | CTGGCTCAACTAAAA[A/G]TATAAAAATACAAAA | 26168 |
rs181397385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570143 | CATGGGTTCTCCAGT[A/G]TTCGTTCTGATGTCT | 26168 |
rs181995448 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571685 | GGGGGTGGCTACAGA[A/G]AAGCCCCTTTCTTCC | 26168 |
rs182090249 | snp | A/C | 1.68738e-05 | 0.00290458 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565525 | CGAGTGGCTTATAAG[A/C]GGCACGTGCTGACCA | 26168 |
rs182489607 | snp | A/G | 0.00270541 | 0.0366795 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560312 | CCAGAACTGAGCCAG[A/G]CCATCCTGTTTTCTT | 26168 |
rs182724101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568503 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 26168 |
rs182858977 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572324 | ATATCGCTGTTGATT[C/G]CTTCATCCCTGGCAC | 26168 |
rs183815427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567880 | TTCTGTTTTAAACTC[C/T]TGTTTCAATGACAGA | 26168 |
rs183855978 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562418 | GACCGGACTGGTGCC[C/G]GGTTGCATTCTGGTC | 26168 |
rs183950986 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561439 | CTTTCACGCGCTCCA[C/T]TGCCCCGGCGTGGCA | 26168 |
rs184001430 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570587 | TGGGTCTTTGAGGGG[C/T]GACCTGGGCATGGTG | 26168 |
rs184087917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562836 | AGATCTCTGAGGCCT[G/T]CTGCTTAGCCATTTT | 26168 |
rs184476887 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565962 | CTTTCTGCCAGTATT[C/T]AGTGTTTTTCGCTAT | 26168 |
rs184619204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569932 | ATATCAAATGGATGA[A/G]GTGTAGGTACTACTA | 26168 |
rs185203350 | snp | C/T | 0.000760833 | 0.0194894 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560991 | CCCTTTTCATTCCCA[C/T]CCCCTAGACTTTGAT | 26168 |
rs185581116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564233 | GAATATTTCCCTTTC[A/G]GAGAACTCCAGCCAA | 26168 |
rs185945464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567608 | CTCTCATAGCTGAGA[C/T]GTGAATGATGAGCAG | 26168 |
rs186229805 | snp | C/G | 0.000783457 | 0.0197766 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571495 | GTGAGCCTCGTACCC[C/G]AGACCCCAAGCCCAT | 26168 |
rs186315907 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572072 | TTTCCATCCCTGGCT[C/G]AGGCACTGCCAACAC | 26168 |
rs186869362 | snp | A/G/T | 0.000142233 | 0.00843206 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563198 | CACCTCCCAAACCCC[A/G/T]ACTCAAGTCAGGTGG | 26168 |
rs187007176 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568768 | GTGTTTCCATGAGTT[C/T]TGTGAGCTGCTCTAG | 26168 |
rs187497309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562737 | TGCCCTTGTTGGGCC[C/T]TCAAAGGACAGCCCT | 26168 |
rs187566077 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569379 | AACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 26168 |
rs187616708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568320 | AACCGGAAAGGGGCC[A/G]GGTGCGGCGGCTCAC | 26168 |
rs188873899 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566132 | GGATCACCTGAGGTC[A/G]GGAGTTCAAGACCAG | 26168 |
rs188893726 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561663 | ACGGGGATCTCCCGC[C/T]CTCCTGGCTCTCCTG | 26168 |
rs189002157 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570057 | GAATTCTGGCAGGCT[C/T]CAGAATCCTGGGCCT | 26168 |
rs189608582 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561257 | CCAGGTGCCCTCTGC[C/T]TCTTCACCCCACAAG | 26168 |
rs189756364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567449 | CCATGAACCTGGGAG[A/G]CAGAGGTTGCAGTGA | 26168 |
rs190035448 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571236 | CTTTAGAGTCAGGCT[A/G]TTTTTGAACCCCAGG | 26168 |
rs190437417 | snp | A/G | 0.000401923 | 0.0141704 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565023 | CACTGATGAGGTAGT[A/G]GAGAAGCTGGAGGAC | 26168 |
rs190534611 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568361 | CCGGCACTTTGGGAG[C/G]CTGAGGCAGATGGAT | 26168 |
rs190662522 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572234 | CAACCAGGATTCATG[A/G]TAGTACCCCAAAGCC | 26168 |
rs190706037 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571640 | TATTTTTTTTTCTTT[A/G]AGAGAATACTTGTTG | 26168 |
rs191896620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562766 | CTGGTGGTATTAAAA[C/T]AAAGACGTAGAACCT | 26168 |
rs192322066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568885 | GGACTGGCATCAGAA[C/T]TGGGGGCAGCCTTGT | 26168 |
rs192483306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567690 | AACCATGGCTGAGGA[A/G]CAGAGGGCTTGTGGG | 26168 |
rs192910332 | snp | G/T | 0.0693013 | 0.172766 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561989 | GAAGGAGGAGGGGGG[G/T]AGGAGTGGCGGCGGC | 26168 |
rs193285936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569553 | TTCTGGTTTCCCTGC[C/T]CTCCCATTCAAAGGC | 26168 |
rs199590994 | snp | A/G | 0.00038031 | 0.0137844 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560493 | CTATAGCGCAGGTGA[A/G]AGCCGTGTGGGCAGC | 26168 |
rs199612456 | snp | A/G | 1.68255e-05 | 0.00290043 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565536 | TAAGCGGCACGTGCT[A/G]ACCATGGATGACTTG | 26168 |
rs199654409 | snp | C/T | 0.000798403 | 0.0199641 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563485 | GCCTTCCGGATGCTG[C/T]TCTACTCAAAAAGCA | 26168 |
rs199737748 | snp | A/G | 4.98062e-05 | 0.00499005 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570438 | CTGTTGATGTGAGGC[A/G]ACGCACCATCACCTA | 26168 |
rs199816482 | snp | A/G | 5.11574e-05 | 0.00505728 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564625 | TCCCCTGCCCTATAG[A/G]CCTCCTTTCATGTAC | 26168 |
rs199872463 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566966 | TATGATAAACTCCGT[-/A]CCAAAGGGTTATGAT | 26168 |
rs200192817 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569210 | CTAACACAGTGAAAC[C/G]CTGTCTCTACTAAAA | 26168 |
rs200518047 | snp | A/G | 0.00299544 | 0.0385843 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565590 | GCTCAATGACCAGGT[A/G]AGAAAGGGTAGAGAA | 26168 |
rs200594104 | snp | C/T | 1.66377e-05 | 0.00288419 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560316 | AACTGAGCCAGGCCA[C/T]CCTGTTTTCTTCAAC | 26168 |
rs200612677 | snp | A/G | 0.000519553 | 0.0161092 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570740 | ACTGGATTTCCACCA[A/G]GGCTGGAAAGGTTAC | 26168 |
rs200617514 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560974 | CCCCGTTCCTCACTT[C/T]TCCCTTTTCATTCCC | 26168 |
rs200728441 | snp | C/G | 0.000217637 | 0.0104293 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564642 | CTCCTTTCATGTACT[C/G]TGCCCAACGGTTTTG | 26168 |
rs200751356 | in-del | -/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566671 | CCCTGCCTCAAATAA[-/T]AAAAAAAAAAAAAGC | 26168 |
rs200761830 | snp | A/G | 0.000263887 | 0.0114836 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563546 | GGCGCCACCGGGGCC[A/G]GCGGCGGGGCCTCGC | 26168 |
rs201011600 | snp | C/T | 1.65056e-05 | 0.00287272 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560461 | CCCTCCCACCCGGAC[C/T]GGGCCTACAACAGCT | 26168 |
rs201051628 | in-del | -/AAAAAG | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566040 | ACAAGATTTAAAAAA[-/AAAAAG]AAAAAGAAAAAGGCC | 26168 |
rs201323747 | snp | C/G/T | 0.000282643 | 0.0118847 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563746 | CCCCCCATGGAGGAA[C/G/T]ATGGACTCAGGTGGA | 26168 |
rs201331151 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571914 | ATATATATATAAAAA[A/T]ATATAAATGCCACGG | 26168 |
rs201401849 | snp | C/T | 0.000615594 | 0.0175333 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564993 | TCAAACGTATGGCAG[C/T]CTCATACCCCTCAGC | 26168 |
rs201454907 | snp | C/T | 0.00399197 | 0.0444977 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563731 | CCAGTGCCCTCTGGG[C/T]CCCCCATGGAGGAAG | 26168 |
rs201556634 | snp | A/G | 1.64784e-05 | 0.00287035 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560857 | TAAAAAGTGGCTCCC[A/G]GCTTGGAAGACCAGG | 26168 |
rs201692314 | snp | C/G | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563331 | AGAGGAGGAGGAGGA[C/G]GATGAAGATGAAGAG | 26168 |
rs201753954 | snp | A/G | 0.000166154 | 0.00911315 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564781 | AGGGCTCAGATTTGG[A/G]CATGGCAGAAGAGGC | 26168 |
rs201836244 | snp | C/T | 0.00199792 | 0.0315431 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561030 | TATCTTGCTTCTGTT[C/T]CCCATGGAGCTCCGA | 26168 |
rs201847654 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571835 | GCCAGATCTTCAAAC[A/T]TTTATATATATATAT | 26168 |
rs201851379 | in-del | -/TATAAATG | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571916 | ATATATATAAAAATA[-/TATAAATG]CCACGGTCCTGCTCT | 26168 |
rs367551194 | snp | A/G | 2.43876e-05 | 0.00349187 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563089 | AAGATGAAAGAGACT[A/G]TACAAGGGACCGGGT | 26168 |
rs367587411 | snp | A/C/G | 3.30613e-05 | 0.00406568 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560485 | AACAGCTGCTATAGC[A/C/G]CAGGTGAGAGCCGTG | 26168 |
rs367680093 | snp | A/G | 1.70528e-05 | 0.00291995 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570463 | CACCTATTTTGACTC[A/G]CAGCGTACCCTAAAC | 26168 |
rs367745262 | snp | A/G | 0.000168008 | 0.00916383 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571517 | CAAGCCCATAAATGG[A/G]AAGGGAGACATGGGA | 26168 |
rs367758562 | snp | A/G | 5.00847e-05 | 0.00500398 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564819 | CCTGGGGAGAAAGCC[A/G]GCCAGCACAGCCCCC | 26168 |
rs368009218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560672 | GGCAGGGGGAAACAG[G/T]GCATCTGGATGGCTG | 26168 |
rs368082044 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565426 | TTGTGTGACTCCACC[C/T]TTGGCCTACTCAGGA | 26168 |
rs368149065 | snp | C/T | 0.000133621 | 0.00817266 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564951 | CCTCCTCTCTCCCTT[C/T]CCACCAGGCATCTTG | 26168 |
rs368336956 | snp | A/G/T | 8.40858e-05 | 0.00648357 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564858 | GAGCATGTGACCTGC[A/G/T]TACAGAGTAAGGAGC | 26168 |
rs368530023 | snp | C/G | 8.2689e-05 | 0.00642944 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567046 | TGTAATGCCTTGCCT[C/G]TAAAGAATGAGAGTC | 26168 |
rs368699561 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566427 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCCGAG | 26168 |
rs368753423 | snp | A/G | 7.84529e-05 | 0.00626261 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563235 | TGGGCCAGATCCTGG[A/G]TCAGGGACCACAGTG | 26168 |
rs368860535 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569399 | CAAAAAAAAAAAAAA[A/G]ATTTGTTTTTTCCTC | 26168 |
rs368896401 | snp | A/G | 0.000165986 | 0.00910855 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570803 | TAGGGTGTTGGTGGG[A/G]ACAGTGGTAGAAGGC | 26168 |
rs368905283 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562370 | ATAGGGGCTTCTTAA[A/G]GCCCGTGTGCGCCGA | 26168 |
rs369203752 | snp | C/T | 3.35926e-05 | 0.00409819 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565623 | AGGCCTGAGAGGGGA[C/T]TCAGGGAGCAGGGTG | 26168 |
rs369283093 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566543 | TAGTGGCGGGTACCT[A/G]TAGTCCCAGCTACTC | 26168 |
rs369366358 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560005 | AGAACCAAAAAGCAC[A/C]TGAGAGTGCCAAGAA | 26168 |
rs369488631 | snp | A/C/G | 0.00216555 | 0.0328419 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563311 | GCAAGTGAAGAGGAG[A/C/G]AAGAAGAGGAGGAGG | 26168 |
rs369516848 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560673 | GCAGGGGGAAACAGG[A/G]CATCTGGATGGCTGT | 26168 |
rs369603019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567334 | CTAGCCTGGCCAACA[C/T]TGAGAAACCCCATCT | 26168 |
rs369701977 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570477 | GCAGCGTACCCTAAA[-/C]CCGCCGCTGCCCTAA | 26168 |
rs369738340 | snp | A/G | 0.000305816 | 0.0123618 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565500 | AGGCAATGCCATGGT[A/G]AGGGGCTTCCGAGTG | 26168 |
rs369914492 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561638 | TGCCTCGCCTCAGCC[C/T]GGTCCTCGTACGGGG | 26168 |
rs369974141 | snp | C/T | 6.19496e-05 | 0.00556515 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570532 | GGGCAAAATGTGGGG[C/T]GGTGCAGTGGCAAGG | 26168 |
rs370046843 | snp | A/C | 0.000313012 | 0.0125063 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560800 | ACTTAACCTCTCTCC[A/C]CATGGAACCTTCCTG | 26168 |
rs370253907 | snp | A/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568619 | ACCCGAGAGGAGGAG[A/T]TTGGAGACATTCTAG | 26168 |
rs370338627 | snp | C/T | 3.55701e-05 | 0.00421708 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563180 | AGCGTCTTCGTTGGC[C/T]CCCACCTCCCAAACC | 26168 |
rs370339345 | snp | C/T | 0.000150191 | 0.00866448 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564818 | GCCTGGGGAGAAAGC[C/T]GGCCAGCACAGCCCC | 26168 |
rs370535025 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560443 | CGATGTATAAGAAGT[A/G]TGCCCTCCCACCCGG | 26168 |
rs370808987 | snp | C/T | 4.98153e-05 | 0.00499051 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564737 | CAATGTGTGCAGCAT[C/T]GGGGACCATGTGGCC | 26168 |
rs370999140 | snp | C/G | 0.000174691 | 0.00934425 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570846 | CCTACCCCTGGGAGT[C/G]TCCATGTGAAGGGCC | 26168 |
rs371006607 | snp | A/C/G/T | 6.59235e-05 | 0.00574094 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560034 | AAGTCCTGACCGACA[A/C/G/T]ACTCTCACCTCCAGA | 26168 |
rs371091205 | snp | C/T | 0.0112252 | 0.0740716 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566962 | CTTCTATGATAAACT[C/T]CGTACCAAAGGGTTA | 26168 |
rs371139304 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566874 | AGGGGAGACTTAGTG[A/G]GAGAGTCTGAGGTCT | 26168 |
rs371422772 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566454 | CGAGGTCAGGAGTTC[C/G]AGACCAGCCTGGCCA | 26168 |
rs371439964 | snp | C/T | 1.65449e-05 | 0.00287614 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560499 | CGCAGGTGAGAGCCG[C/T]GTGGGCAGCCGAAAG | 26168 |
rs371542629 | snp | C/T | 0.000163987 | 0.00905353 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571353 | GGGGGTTTCTCATGG[C/T]TTGCTTTGTTAACAC | 26168 |
rs371581414 | snp | C/G | 1.66308e-05 | 0.00288359 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570350 | CCTGTGGCACTATCT[C/G]TTTAGGTGGACATCT | 26168 |
rs371797427 | snp | A/G | 0.000161987 | 0.00899817 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570468 | ATTTTGACTCGCAGC[A/G]TACCCTAAACCGCCG | 26168 |
rs371856271 | snp | C/T | 8.72943e-05 | 0.00660602 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563246 | CTGGGTCAGGGACCA[C/T]AGTGCCAGCCAGACG | 26168 |
rs372033281 | snp | A/G/T | 0.000148298 | 0.00860986 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560057 | CCTCCAGATGACTCC[A/G/T]ATGTGACAGAGGTGA | 26168 |
rs372272961 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565665 | CTGCATGGGGGAGCC[C/G]TGTACCCATGCCGCA | 26168 |
rs372515834 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565974 | ATTTAGTGTTTTTCG[C/G]TATGGCCAGCCCCAA | 26168 |
rs372606476 | snp | A/G | 0.000437904 | 0.0147905 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570820 | CAGTGGTAGAAGGCA[A/G]AAATTGAAGTCCTAC | 26168 |
rs372689966 | snp | A/T | 5.9423e-05 | 0.0054505 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564603 | AGTCTCTCATGCCCA[A/T]TCCATTTCCCCTGCC | 26168 |
rs372839508 | snp | A/G | 0.000165986 | 0.00910854 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570790 | TGAGGGAGGGGTATA[A/G]GGTGTTGGTGGGGAC | 26168 |
rs372855565 | snp | A/G | 0.000271153 | 0.0116406 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570533 | GGCAAAATGTGGGGC[A/G]GTGCAGTGGCAAGGC | 26168 |
rs372876754 | snp | C/T | 1.65968e-05 | 0.00288065 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565674 | GGAGCCCTGTACCCA[C/T]GCCGCACCCTCCATG | 26168 |
rs372917746 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560908 | GCCAAGAGCTGAGTA[C/T]ATAAAGGAGAGGGAA | 26168 |
rs372925134 | snp | A/C | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572065 | GTTCAGCTTTCCATC[A/C]CTGGCTCAGGCACTG | 26168 |
rs373266782 | snp | C/T | 1.65097e-05 | 0.00287308 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560161 | AGTTTATCTGCTGTA[C/T]AGCCAGGTAACCCCA | 26168 |
rs373268390 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562778 | AAATAAAGACGTAGA[A/G]CCTGGCAGTGCTATT | 26168 |
rs373336096 | snp | C/G | 3.32088e-05 | 0.00407471 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564752 | CGGGGACCATGTGGC[C/G]CAGGAGCTTTTTCAG | 26168 |
rs373583241 | snp | G/T | 0.000477763 | 0.0154484 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560850 | TGTGTTATAAAAAGT[G/T]GCTCCCAGCTTGGAA | 26168 |
rs373688972 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560910 | CAAGAGCTGAGTATA[C/T]AAAGGAGAGGGAATG | 26168 |
rs373794419 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570608 | GGGCATGGTGTCTGC[C/T]AGCACTGTACCCACC | 26168 |
rs374229965 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561079 | ATGAGGGGCGGGGGA[C/T]GGGCGCCAGGCATTG | 26168 |
rs374255124 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565796 | AGGTCAGTACCCAGA[A/G]GAACTTCTGCAGTTT | 26168 |
rs374521694 | snp | A/G | 0.000163987 | 0.00905353 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564664 | ACGGTTTTGGGGGAC[A/G]ATCTGGGCCAGAAGG | 26168 |
rs374548390 | snp | A/G | 3.35132e-05 | 0.00409334 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564838 | AGCACAGCCCCCTGC[A/G]AGAGGAGCATGTGAC | 26168 |
rs375097225 | snp | A/G | 0.00029264 | 0.0120927 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563350 | GAAGATGAAGAGGAG[A/G]AAGTGGCAGCTTGGA | 26168 |
rs375237137 | snp | A/G | 5.08341e-05 | 0.00504128 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571326 | GAAATGTGTAGCACA[A/G]GTCCTGACACGGGGG | 26168 |
rs375279225 | snp | A/C | 0.000161987 | 0.00899817 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570450 | GGCGACGCACCATCA[A/C]CTATTTTGACTCGCA | 26168 |
rs375353717 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561073 | GTGTAGATGAGGGGC[A/G]GGGGACGGGCGCCAG | 26168 |
rs375409681 | snp | C/T | 0.000249159 | 0.0111587 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563568 | GGGCCTCGCACACCC[C/T]AAGAACCATCTTTCA | 26168 |
rs375438989 | snp | A/C | 1.98801e-05 | 0.00315272 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570696 | CATATTGCCAAGTAT[A/C]TACAGGCAGAGGCGG | 26168 |
rs375482684 | snp | A/G | 0.000161987 | 0.00899818 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563214 | ACTCAAGTCAGGTGG[A/G]GGGTTTGGGCCAGAT | 26168 |
rs375549203 | snp | A/G/T | 7.52323e-05 | 0.00613281 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570870 | AAGGGCCTGCTTTCT[A/G/T]TCTCTTCTCTAGAAT | 26168 |
rs375586651 | snp | A/G | 0.000159987 | 0.00894248 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565687 | CATGCCGCACCCTCC[A/G]TGGCAAGCTGCCTCC | 26168 |
rs375784139 | snp | A/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566669 | AGGCCCTGCCTCAAA[A/T]AAAAAAAAAAAAAAA | 26168 |
rs375995657 | snp | C/T | 1.64887e-05 | 0.00287125 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560002 | GAAAGAACCAAAAAG[C/T]ACCTGAGAGTGCCAA | 26168 |
rs376071368 | snp | C/T | 3.34851e-05 | 0.00409163 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564943 | CCTCACCCCCTCCTC[C/T]CTCCCTTTCCACCAG | 26168 |
rs376292631 | snp | C/T | 1.65433e-05 | 0.002876 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560985 | ACTTTTCCCTTTTCA[C/T]TCCCACCCCCTAGAC | 26168 |
rs376321367 | snp | A/C/G/T | 0.000267708 | 0.0115668 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564833 | CGGCCAGCACAGCCC[A/C/G/T]CTGCGAGAGGAGCAT | 26168 |
rs376425137 | snp | A/G | 3.3325e-05 | 0.00408184 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564961 | CCCTTTCCACCAGGC[A/G]TCTTGGACGAATTCC | 26168 |
rs376454625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568325 | GAAAGGGGCCGGGTG[C/T]GGCGGCTCACGCCTG | 26168 |
rs376504824 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562287 | GCCCCCTCCCCTCCC[C/T]CCAGCCCTGCCTTGG | 26168 |
rs376549053 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562789 | TAGAACCTGGCAGTG[C/T]TATTGGGTTTGGCCT | 26168 |
rs376710300 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560724 | TCTCTCTTTTCTCAG[C/G]TGTCTTCCATTTACA | 26168 |
rs377041451 | snp | C/T | 0.000232146 | 0.0107712 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565709 | GCTGCCTCCCATCTT[C/T]TCCCCAGGTGATGAA | 26168 |
rs377137966 | snp | A/G | 1.67933e-05 | 0.00289765 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565592 | TCAATGACCAGGTGA[A/G]AAAGGGTAGAGAAAC | 26168 |
rs377210008 | snp | C/T | 3.55145e-05 | 0.00421379 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570479 | CAGCGTACCCTAAAC[C/T]GCCGCTGCCCTAAGG | 26168 |
rs377313690 | snp | A/G | 1.66607e-05 | 0.00288619 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565006 | AGCCTCATACCCCTC[A/G]GCACTGATGAGGTAG | 26168 |
rs377614020 | snp | A/C | 0.000161987 | 0.00899817 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564719 | TGCCAGCATCCTCAT[A/C]AGCAATGTGTGCAGC | 26168 |
rs377760309 | snp | C/T | 0.000159987 | 0.00894248 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561035 | TGCTTCTGTTCCCCA[C/T]GGAGCTCCGAATTCT | 26168 |
rs397962859 | in-del | -/AA | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571907 | ATATATATATATATA[-/AA]TAAAAATATATAAAT | 26168 |
rs398030265 | in-del | -/A | 0 | 0 | frameshift-variant, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566970 | TAAACTCCGTACCAA[-/A]GGGTTATGATGGGGT | 26168 |
rs527268388 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566231 | CTATAATCCCAGTTA[C/T]TCGGGAGGCTGAGGG | 26168 |
rs527314722 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568408 | TGAGACCAGCCTGGC[C/T]GACCTGGCGAAACCC | 26168 |
rs527605163 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561172 | GAGGGAAGCACCCGC[C/T]GGTTGGCCGAAGTCC | 26168 |
rs527718041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560543 | ACCGGGGGTAGCAGT[A/G]CAGGGAGCTACCGCT | 26168 |
rs527718837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568078 | GGTCTCCTGACCAGG[C/T]TCCTGGCATTCAACT | 26168 |
rs527778837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567515 | CAAGAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA | 26168 |
rs528211649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566383 | AACTTCGGCTGGGTG[C/T]GGTGACTCATTCCTG | 26168 |
rs528390325 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571752 | GGAGCAGTCATCCTC[C/T]CCCTTCCCCGTGCAG | 26168 |
rs528530288 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561476 | TCCAAGCCCTTCCGG[G/T]CTGGAACTGGTGTCG | 26168 |
rs529065606 | snp | A/G | 0.00143301 | 0.0267292 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560412 | AGAAGGCCAAGGAAG[A/G]CAGGAGACTCTATTC | 26168 |
rs529220640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565972 | GTATTTAGTGTTTTT[C/T]GCTATGGCCAGCCCC | 26168 |
rs529738612 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562773 | TATTAAAATAAAGAC[A/C/G]TAGAACCTGGCAGTG | 26168 |
rs529759097 | snp | A/G | 2.14434e-05 | 0.00327433 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570791 | GAGGGAGGGGTATAG[A/G]GTGTTGGTGGGGACA | 26168 |
rs529978041 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565991 | ATGGCCAGCCCCAAG[A/G]ATTGGGATGGGTTCC | 26168 |
rs530334556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568805 | AATCAAATTCAAGGA[G/T]GGGGTCATGGGAACG | 26168 |
rs530349520 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562356 | GCCCAGAGGCCCGCA[C/T]AGGGGCTTCTTAAGG | 26168 |
rs530415536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569319 | GAACCCAGGAGGTGG[A/T]GCTTGCAGTGAGGCA | 26168 |
rs530653131 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572360 | CAGGCAGTGTCGAAT[C/T]CATCTCTGCTACAGG | 26168 |
rs531169811 | snp | A/G | 2.06793e-05 | 0.00321547 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563802 | CTCGGGTAAGGTGGG[A/G]AAGGGGTGTGGGGTT | 26168 |
rs531182939 | snp | C/T | 0.000388039 | 0.0139237 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563090 | AGATGAAAGAGACTA[C/T]ACAAGGGACCGGGTC | 26168 |
rs531394744 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568730 | TACTCTTTGTACTAC[C/T]CTTTGTTAATAAACT | 26168 |
rs531648860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568677 | GGATGGTCTCCAGGC[C/T]TCTTCCCGGTACCTT | 26168 |
rs531771307 | snp | A/C | 0.00279162 | 0.0372561 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561786 | GTGGCGGGGCCGCCA[A/C]GCGCGGCCGGGCGGC | 26168 |
rs532038151 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570726 | GTAAAGAAAGACCGA[C/T]TGGATTTCCACCAGG | 26168 |
rs532180084 | snp | C/T | 9.31923e-05 | 0.0068255 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563099 | AGACTATACAAGGGA[C/T]CGGGTCCTGGGGGCC | 26168 |
rs532223537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570012 | TAGGTTGCCCACTGT[C/T]ATAAGCCAGTAAATG | 26168 |
rs532328637 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562197 | CCGTCGCCGGAGAGA[G/T]GAGCCGGGAAGCTTG | 26168 |
rs532431374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562296 | CCTCCCCCCAGCCCT[A/G]CCTTGGCCTCTCCCA | 26168 |
rs532493834 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561836 | CTCGCGTAGCGCTCT[A/G]GGCTGGCCAGTCCCG | 26168 |
rs532643166 | in-del | -/GGCGGCGCGGCGGGGTGCTC | 0.00517822 | 0.0506191 | downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7562077 | TGAAGCAGAGCCAGA[-/GGCGGCGCGGCGGGGTGCTC]GGCGGCGCGGCACGC | 26168 |
rs532776955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568735 | TTTGTACTACCCTTT[A/G]TTAATAAACTGGTAA | 26168 |
rs533403167 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566793 | TGGGCAACATAGTGA[A/G]ACCCTGTCTCTACCA | 26168 |
rs533643083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567807 | TAGGCTGAGGAGGGG[A/G]GATTTTATTGCGTGT | 26168 |
rs533827575 | snp | A/G | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563305 | GCCTCAGCAAGTGAA[A/G]AGGAGGAAGAAGAGG | 26168 |
rs533874412 | snp | C/T | 0.0154538 | 0.0865337 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561690 | CCTGTGGCGCGCCCC[C/T]CGCCGGATCAAGGTA | 26168 |
rs534308232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566803 | AGTGAGACCCTGTCT[C/T]TACCAAAAAAAAAAG | 26168 |
rs534677081 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571055 | AGGAAGTAATCTGTT[A/T]TAGAACACCAAAACA | 26168 |
rs535098130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570299 | CTCTCTAGAACCTTC[A/C]TGGCAAAAGGCAAGA | 26168 |
rs535249555 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560589 | AACCTAAACAGAGGC[A/G]GGTCTGAGGAGTGAA | 26168 |
rs535935719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564307 | CATTGAGCCTTTACA[A/G]TATGCTGGGTACTAT | 26168 |
rs535949508 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571989 | TGGTCTTCCTTAAGG[A/G]GCTTCAAATTAGTGG | 26168 |
rs536133868 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569605 | CAGGATGATTGGCTC[C/T]GGCATTCCTTAATTT | 26168 |
rs536540204 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561894 | ACCGCGCGCTTGGTG[C/G]CCGCGCCGGCGCTCT | 26168 |
rs536961619 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570203 | CCGAAGAACCGAAAC[A/G/T]TGCAGATCCTGAGCT | 26168 |
rs536970411 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561614 | ATACCCCGGCTCCAT[C/T]TCCCCCACTGCCTCG | 26168 |
rs537010046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569734 | TGAGTTTGAGTCCCA[C/T]TTCTGCCATTTCTTT | 26168 |
rs537867881 | snp | C/T | 0.00716266 | 0.059414 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561966 | TGGGCCCGGGGCTCG[C/T]GGGAGGGGAAGGAGG | 26168 |
rs537927221 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561668 | GATCTCCCGCCCTCC[C/T]GGCTCTCCTGTGGCG | 26168 |
rs537929050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568951 | AGGTAGATAGTGTTG[A/G]AATTGAATTGGGGGA | 26168 |
rs537941212 | snp | G/T | 0 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568457 | GAAAATTAGCTGGGC[G/T]TGGTGGCGTGCGCCT | 26168 |
rs538352009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560591 | CCTAAACAGAGGCGG[A/G]TCTGAGGAGTGAAGT | 26168 |
rs538735883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562552 | CCCGTTTATCAGCCT[C/T]TGCCCCCTGAACCAT | 26168 |
rs538883986 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561511 | AGCCTCGGGTGTATC[C/G]TACGCCCTGGTGTTG | 26168 |
rs538963220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568336 | GGTGCGGCGGCTCAC[A/G]CCTGTACTCCCGGCA | 26168 |
rs539328805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567725 | ACCTGTGTAGTTGGC[C/G]CAGAGTGAGCAAAGG | 26168 |
rs539951192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565154 | TTTTCTTCCATAGGG[A/C]TGTAGTTGGGGAGGA | 26168 |
rs540047152 | snp | C/T | 0.00795532 | 0.062565 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561941 | ACTAATCGTGCGCCA[C/T]CGCTGCCGGTGGGCC | 26168 |
rs540638617 | snp | A/G | 1.69258e-05 | 0.00290905 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571527 | AATGGGAAGGGAGAC[A/G]TGGGAGTCCCTTCCC | 26168 |
rs540927366 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572137 | GCAGAGAGCAGGAAG[A/G]AGGGAAAGTAGATAA | 26168 |
rs541148612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562901 | AGACCCTGAAGGGCC[C/T]CTTGTGGACCGCGTT | 26168 |
rs541210161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569785 | TCACGACTTTCCAAG[C/G]TGCAATTTCCTCATC | 26168 |
rs541573996 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571644 | TTTTTTTCTTTGAGA[A/G]AATACTTGTTGATTT | 26168 |
rs541730447 | in-del | -/AAAAAA | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566034 | TGTAAAACAAGATTT[-/AAAAAA]AAAAAGAAAAAGAAA | 26168 |
rs541960966 | snp | A/G | 1.79367e-05 | 0.00299467 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563686 | CTGCTAGGTGCTCTC[A/G]TGGCTGAGGATGGGG | 26168 |
rs542189200 | snp | G/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568236 | TGGGAGGGGAATGGG[G/T]CCAAAGGTTAAGGCA | 26168 |
rs542413889 | snp | C/T | 0.000679545 | 0.0184204 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570377 | ATCTTCAATAAGGAG[C/T]TACTGCTAATCCCCA | 26168 |
rs542516583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569141 | CTGTAATCCCAGCCC[G/T]TTGGGAGGCTGAGGC | 26168 |
rs542548615 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7562089 | AGAGGCGGCGCGGCG[A/G]GGTGCTCGGCGGCGC | 26168 |
rs542590739 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561216 | CTGCTAGGGAAAACC[C/G]CTGGTTCTCCATGCC | 26168 |
rs542911940 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561756 | GAGAAGACAGAGCGC[A/G]GCGCAAAAGGGAAAG | 26168 |
rs543323855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562782 | AAAGACGTAGAACCT[A/G]GCAGTGCTATTGGGT | 26168 |
rs543387051 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-5-prime, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562162 | TGCGCCTAAAGACAG[C/T]AGGAGTGGCGGGGCC | 26168 |
rs543558750 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568708 | TCCCTGTGCATCTTT[C/T]CATCTGTACTCTTTG | 26168 |
rs544087725 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567919 | GGGGCAAGAATGGAA[A/G]CAGGAACAGAGCACA | 26168 |
rs544384896 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567897 | GTTTCAATGACAGAT[G/T]GAAAGGGGGGCAAGA | 26168 |
rs544419637 | snp | A/G | 1.66067e-05 | 0.00288151 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564738 | AATGTGTGCAGCATC[A/G]GGGACCATGTGGCCC | 26168 |
rs544505690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567325 | AGTTCGAGACTAGCC[C/T]GGCCAACATTGAGAA | 26168 |
rs544506126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566164 | CTGACCAATATGGAG[A/G]AATCCCGTCTCTACT | 26168 |
rs545010273 | in-del | -/TTTC | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562960 | TGCGTTTTTTCCTCT[-/TTTC]TTTATTTGCATCTGA | 26168 |
rs545196019 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561709 | CGGATCAAGGTACTG[A/G]GGATGCCGCTAGGGT | 26168 |
rs545332418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568010 | GTAGGATAAATTTTA[C/T]GAGTAAAACCAGTAG | 26168 |
rs545634793 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572457 | AGAGCCCGGAAGCCT[C/T]TGGAGGCTGAGACCT | 26168 |
rs545933306 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569112 | GTTTTTTTGCCGGGC[A/G]CGGTGGCTCACGCCT | 26168 |
rs546219459 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570551 | GCAGTGGCAAGGCAT[G/T]GCAGGAAGAAGGGTG | 26168 |
rs546618207 | snp | C/T | 6.65845e-05 | 0.00576956 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564969 | ACCAGGCATCTTGGA[C/T]GAATTCCTTCAAACG | 26168 |
rs546638379 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571821 | TAGGATCACTGCCTG[C/T]CAGATCTTCAAACTT | 26168 |
rs546850834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565936 | GGGCTCTGGATTTAT[C/T]AGTTGTTTTCCTTTC | 26168 |
rs547155744 | snp | C/T | 4.61979e-05 | 0.00480592 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563130 | TGAGCCTCCTGGACC[C/T]GGCATACCCCCAGCT | 26168 |
rs547529506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562300 | CCCCCAGCCCTGCCT[C/T]GGCCTCTCCCATTCC | 26168 |
rs547553690 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561856 | GGCCAGTCCCGTGGC[A/G]CCGGCGTCCTCGGGT | 26168 |
rs547856805 | snp | A/G | 6.6548e-05 | 0.00576798 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564791 | TTTGGGCATGGCAGA[A/G]GAGGCAGAGAGGCCT | 26168 |
rs548029043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564094 | AAATCCTGTCCACAC[A/G]AAATCCCTTGTCGGC | 26168 |
rs548111420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568337 | GTGCGGCGGCTCACG[C/G]CTGTACTCCCGGCAC | 26168 |
rs548176995 | in-del | -/TCC | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562954 | GAGTTTTGCGTTTTT[-/TCC]TCTTTTCTTTATTTG | 26168 |
rs548575573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562391 | TGTGCGCCGAGCCAT[C/T]CAAGCTCGTGGGACC | 26168 |
rs548949948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568824 | GTCATGGGAACGCTG[A/C]TCTAACCAGTTGGTG | 26168 |
rs549073349 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561277 | CACCCCACAAGAAGC[C/T]TTATCCTACGTCCTT | 26168 |
rs549187813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568168 | GGCTAGCCCCTCTAG[A/G]TGGCTTCATGATTAG | 26168 |
rs549495226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567552 | ACAGTAATGTCATAG[C/T]GTGGGAAGTGGGTAC | 26168 |
rs549751432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569935 | TCAAATGGATGAGGT[A/G]TAGGTACTACTATTT | 26168 |
rs549755749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562456 | ATGAAGTAGGAGGGG[A/G]CTGGGCCGGCCTGGC | 26168 |
rs549847827 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561788 | GGCGGGGCCGCCACG[A/C]GCGGCCGGGCGGCGG | 26168 |
rs549909171 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561391 | ATGACGGTGCCTTCG[C/G]AGTCAAATTACTCTT | 26168 |
rs549984480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567659 | GAATAGCAAGTACAC[A/G]AGACCCATAGTGAAA | 26168 |
rs550878365 | snp | A/G | 2.81464e-05 | 0.00375132 | utr-variant-5-prime, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563072 | GTTTTTCAGGGTACT[A/G]GAAGATGAAAGAGAC | 26168 |
rs550895624 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568745 | CCTTTGTTAATAAAC[C/T]GGTAAATGTGTTTCC | 26168 |
rs550943565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566687 | AAAAAAAAAAAAAGC[C/T]TGGTTTGTTGACTCA | 26168 |
rs550955985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566007 | ATTGGGATGGGTTCC[A/T]ATTGTAACTATTGTA | 26168 |
rs551323483 | snp | C/T | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570954 | CAGATGATGGGGCCA[C/T]CTCCCCTAGCTCTGA | 26168 |
rs551740333 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565875 | GGTCTCTGTTTCAGG[A/G]AGAGAGGTGGTAGTG | 26168 |
rs551743227 | snp | A/C/T | 3.31111e-05 | 0.00406874 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560505 | TGAGAGCCGTGTGGG[A/C/T]AGCCGAAAGCAGGAC | 26168 |
rs551912464 | snp | A/G | 1.68635e-05 | 0.0029037 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564917 | CCGACTCCTAGAGGA[A/G]AGTCTGGAGGCCTCA | 26168 |
rs551973799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564130 | AGTATAAGAACCCCC[G/T]TGTATACATCTCCAG | 26168 |
rs552125070 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568409 | GAGACCAGCCTGGCC[A/G]ACCTGGCGAAACCCT | 26168 |
rs552952418 | snp | A/G | 0.000265582 | 0.0115204 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563091 | GATGAAAGAGACTAT[A/G]CAAGGGACCGGGTCC | 26168 |
rs553179823 | in-del | -/AC | 0.00283113 | 0.0375173 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560031 | AAGAAGTCCTGACCG[-/AC]ACACTCTCACCTCCA | 26168 |
rs553355568 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571103 | CTTCTGGACTTCTCC[A/G]TCCCACATTGGGACT | 26168 |
rs553640295 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7562002 | GGGAGGAGTGGCGGC[A/G]GCGGCGGTGGCGCTG | 26168 |
rs554024813 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561531 | CCCTGGTGTTGGTGT[C/T]GCCTCACTCCTCTGA | 26168 |
rs554062105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568513 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 26168 |
rs554085771 | snp | C/T | 4.94376e-05 | 0.00497156 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560869 | CCCAGCTTGGAAGAC[C/T]AGGGTGGGTACATAC | 26168 |
rs554478639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569676 | TTGCAGTAGAGGGAA[A/G]GGTGGTGACGTACAG | 26168 |
rs554541733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569156 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACCAGG | 26168 |
rs555225114 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561738 | GTCAGGCCCGCGAGC[A/G]CGGAGAAGACAGAGC | 26168 |
rs555414569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568391 | TCGCAAGGTCAAGAG[A/G]TTGAGACCAGCCTGG | 26168 |
rs555476650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567819 | GGGGGATTTTATTGC[A/G]TGTATACTGAGAAGC | 26168 |
rs555633518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566838 | AACCCAGAATTTGTT[C/T]TTACTGTCAGTGGAC | 26168 |
rs555941775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566113 | CTGGGAGACCAGGGC[A/G]GGTGGATCACCTGAG | 26168 |
rs556051534 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566011 | GGATGGGTTCCTATT[A/G]TAACTATTGTAAAAC | 26168 |
rs556216825 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561971 | CCGGGGCTCGCGGGA[C/G]GGGAAGGAGGAGGGG | 26168 |
rs556299484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560657 | GGTGGAGCTGGAGAA[A/G]GCAGGGGGAAACAGG | 26168 |
rs556326532 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561674 | CCGCCCTCCTGGCTC[C/T]CCTGTGGCGCGCCCC | 26168 |
rs556326843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569021 | TTGGTGGAGAGAAAG[C/T]CCCACAAACACTTCT | 26168 |
rs556372869 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571769 | CCTTCCCCGTGCAGG[C/G]AGCAGGAAATCAGTG | 26168 |
rs556387735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568461 | ATTAGCTGGGCGTGG[G/T]GGCGTGCGCCTGTAG | 26168 |
rs556473035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567054 | CTTGCCTCTAAAGAA[A/T]GAGAGTCTTGTTTTC | 26168 |
rs556802728 | in-del | -/A | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567519 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 26168 |
rs557398778 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564336 | ATGCTGGGTGTTTGG[C/T]ATATAGTGGTGACAA | 26168 |
rs557414246 | snp | A/G | 0.000114755 | 0.00757391 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565115 | GGGCTGGGGCCTTGG[A/G]GATGTGGAGAGAATA | 26168 |
rs557518141 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572047 | GTCTCTTGAGACTAA[A/T]GGGTTCAGCTTTCCA | 26168 |
rs558199926 | snp | A/G | 1.65655e-05 | 0.00287793 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571440 | TGCCCAAACTTCGTC[A/G]GCAGATCTACAAGGA | 26168 |
rs558327568 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566033 | TTGTAAAACAAGATT[A/T]AAAAAAAAAAAGAAA | 26168 |
rs558337679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565171 | GTAGTTGGGGAGGAG[A/G]AAGCTAGAGCTGAAG | 26168 |
rs558350287 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572126 | CCGAGATGGGAGCAG[A/G]GAGCAGGAAGGAGGG | 26168 |
rs558455006 | snp | C/G | 0.000127722 | 0.00799029 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563532 | CTGGAAGCTTTGGGG[C/G]CGCCACCGGGGCCGG | 26168 |
rs558698984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569769 | CATGACCTTGTGCAA[A/G]TCACGACTTTCCAAG | 26168 |
rs558904610 | snp | C/T | 0 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570263 | TTCTTTCACTTGGTT[C/T]CCTTACCTGTGTCTC | 26168 |
rs558923930 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571528 | ATGGGAAGGGAGACA[C/T]GGGAGTCCCTTCCCA | 26168 |
rs558987809 | snp | C/T | 2.02797e-05 | 0.00318425 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570755 | GGGCTGGAAAGGTTA[C/T]TTCAAAATGGTGAGT | 26168 |
rs559681208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562314 | TTGGCCTCTCCCATT[C/T]CTGGGCCTCGCTCCC | 26168 |
rs559692309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569261 | GAGGTGGCACGTGTC[C/T]GTAGTCCAAGCTACT | 26168 |
rs559823902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562984 | TTGCATCTGAATCCA[A/G]AGGAGGCATGGCCAG | 26168 |
rs559896124 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569828 | TGTTGAGAACTTCCC[A/G]GTAGGATTGTTATGA | 26168 |
rs560277062 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568060 | ACTGAGAGATACATA[C/T]TTGGTCTCCTGACCA | 26168 |
rs560403061 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561733 | CTAGGGTCAGGCCCG[C/T]GAGCGCGGAGAAGAC | 26168 |
rs560472570 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561109 | GTCCAGACCTGGTCG[A/G]GGCCCACTGGAAGCA | 26168 |
rs560540353 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567497 | GCACTCCAGCCTGGG[A/C]AACAAGAGCAAAACT | 26168 |
rs561066458 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561466 | GGCAGGCCATTCCAA[A/G]CCCTTCCGGGCTGGA | 26168 |
rs561124426 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561758 | GAAGACAGAGCGCGG[C/T]GCAAAAGGGAAAGTG | 26168 |
rs561270305 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562109 | CTCGGCGGCGCGGCA[C/G]GCGGCCCAGAAGCGT | 26168 |
rs563012894 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572350 | GGCACACGTCCAGGC[A/C]GTGTCGAATCCATCT | 26168 |
rs563739392 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563088 | GAAGATGAAAGAGAC[G/T]ATACAAGGGACCGGG | 26168 |
rs563937723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569911 | ATAGTCACTAGTTTA[A/G]TCCTCATATCAAATG | 26168 |
rs564295889 | snp | A/T | 1.66067e-05 | 0.00288151 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565780 | GTAGGCCCAACCAGA[A/T]AGGTCAGTACCCAGA | 26168 |
rs564521221 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569885 | TGTGTCTTGTTCTAA[C/G]TGTATTATGGATAGT | 26168 |
rs564687265 | snp | C/T | 0.00029074 | 0.0120534 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564422 | GAGTAGGAACTCTCT[C/T]TCCATCCCTGTAGAA | 26168 |
rs564735937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569968 | ACTCTCTGACAGATA[A/G]GGAAACTGAGGTATA | 26168 |
rs564799611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564030 | AGATGCCCTAAGTAG[A/G]TATCCCGTGGTCTTG | 26168 |
rs564955270 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562171 | AGACAGCAGGAGTGG[C/T]GGGGCCGCCGCCGTC | 26168 |
rs565069275 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561833 | AGCCTCGCGTAGCGC[C/T]CTGGGCTGGCCAGTC | 26168 |
rs565088402 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561312 | CCATCTATCGGACCC[C/T]AGTTTCCATCACTAT | 26168 |
rs565130137 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568731 | ACTCTTTGTACTACC[C/G]TTTGTTAATAAACTG | 26168 |
rs565409102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569244 | CAAAAAATTAGCCGG[A/G]CGAGGTGGCACGTGT | 26168 |
rs565741900 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563196 | CCCACCTCCCAAACC[C/G]CGACTCAAGTCAGGT | 26168 |
rs565783890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569572 | CCATTCAAAGGCCAG[C/G]AAATTTCTACAGCTA | 26168 |
rs566263759 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561893 | GACCGCGCGCTTGGT[A/G]GCCGCGCCGGCGCTC | 26168 |
rs566815047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566797 | CAACATAGTGAGACC[C/T]TGTCTCTACCAAAAA | 26168 |
rs566860716 | snp | C/T | 1.6593e-05 | 0.00288031 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560520 | CAGCCGAAAGCAGGA[C/T]GTCTCTGACCGGGGG | 26168 |
rs567029813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566040 | ACAAGATTTAAAAAA[A/G]AAAAGAAAAAGAAAA | 26168 |
rs567253568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569380 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 26168 |
rs567566655 | snp | A/C | 8.58553e-05 | 0.00655136 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566894 | GTCTGAGGTCTTTTA[A/C]TTCCATTGAGCTTTT | 26168 |
rs567661255 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561281 | CCACAAGAAGCCTTA[C/T]CCTACGTCCTTCTCT | 26168 |
rs568519809 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571179 | ACCTCCAACTCAGTG[G/T]ATTTTCTCCATCTAA | 26168 |
rs569153049 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569242 | TACAAAAAATTAGCC[A/G]GGCGAGGTGGCACGT | 26168 |
rs569495247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564110 | AAATCCCTTGTCGGC[C/T]TCTCAGTATAAGAAC | 26168 |
rs569520715 | snp | A/G | 0.000508466 | 0.0159366 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563377 | TGGAGGCTGCCCCCA[A/G]GATGGAGTCAGCTGG | 26168 |
rs569557730 | snp | G/T | 3.7805e-05 | 0.00434754 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570867 | GTGAAGGGCCTGCTT[G/T]CTTTCTCTTCTCTAG | 26168 |
rs569583887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570192 | CCTCCCTTACCCCGA[A/G]GAACCGAAACATGCA | 26168 |
rs570300930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562406 | CCAAGCTCGTGGGAC[C/T]GGACTGGTGCCGGGT | 26168 |
rs570627179 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571742 | TGGCCTGGGTGGAGC[A/G]GTCATCCTCCCCCTT | 26168 |
rs570811816 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571029 | ATTTGGCTCATAGTC[A/G]GTTGTGGAGCAGGAA | 26168 |
rs571254000 | snp | C/G | 2.36678e-05 | 0.00343996 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563095 | AAAGAGACTATACAA[C/G]GGACCGGGTCCTGGG | 26168 |
rs571266074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562537 | CCTTCAAAGTTCTTC[C/T]CCGTTTATCAGCCTC | 26168 |
rs571287090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569509 | GGAGAGGAACAGGTT[A/G]GGGGAGGAAAATGAA | 26168 |
rs571416770 | in-del | -/AAAA | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571910 | ATATATATATATATA[-/AAAA]TATATAAATGCCACG | 26168 |
rs572236512 | in-del | -/GGCGGT | 0.00520953 | 0.0507703 | downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7562022 | GGTGGCGCTGGTGGC[-/GGCGGT]GGCGGTGGCGGAGGT | 26168 |
rs572265073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569119 | TGCCGGGCGCGGTGG[C/T]TCACGCCTGTAATCC | 26168 |
rs572272839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568518 | CGCTTGAACCCGGGA[A/G]GCAGAGGTTGCAGTG | 26168 |
rs572948150 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560556 | GTGCAGGGAGCTACC[G/T]CTAGGAGGGAGGTTG | 26168 |
rs573104233 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566843 | AGAATTTGTTTTTAC[C/T]GTCAGTGGACTGAGG | 26168 |
rs573267191 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571906 | ATATATATATATATA[A/T]ATAAAAATATATAAA | 26168 |
rs573408260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565186 | GAAGCTAGAGCTGAA[A/G]GGGAGGACTCTGCAG | 26168 |
rs573444752 | snp | A/G | 0.000195695 | 0.00988985 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564520 | ATTCTGCTTCAGTGT[A/G]TCCTTCTTGCGGTCT | 26168 |
rs573529063 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561957 | CGCTGCCGGTGGGCC[C/T]GGGGCTCGCGGGAGG | 26168 |
rs573612286 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560929 | GGAGAGGGAATGTGC[A/G]GGAACAGAGGCGTCT | 26168 |
rs574125518 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572301 | AGGGGAATCCTCCCA[C/T]CCCTACGATATCGCT | 26168 |
rs574246723 | in-del | -/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561073 | GTGTAGATGAGGGGC[-/G]GGGGACGGGCGCCAG | 26168 |
rs574294709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565243 | TGGGAGAGTCTTTAC[C/T]TGGGACCCTGAAATG | 26168 |
rs574683581 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568214 | AGCCTCACCCCCACC[A/G]ACTTCCTGGGAGGGG | 26168 |
rs574723588 | snp | C/T | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572099 | ACACCTTGTCTTCAC[C/T]CAAACAAATCCCCGA | 26168 |
rs574785736 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564293 | CATATTCTAGTATTC[A/G]TTGAGCCTTTACAAT | 26168 |
rs574834128 | snp | A/G | 0.000812708 | 0.0201418 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563673 | ACCCCGGCTGGGTCT[A/G]CTAGGTGCTCTCATG | 26168 |
rs575003570 | snp | C/T | 1.67511e-05 | 0.00289401 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570318 | CAAAAGGCAAGACTT[C/T]TGTTTGTTGTACCTG | 26168 |
rs575584420 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561167 | CGCTCGAGGGAAGCA[C/T]CCGCCGGTTGGCCGA | 26168 |
rs575703202 | snp | A/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566670 | GGCCCTGCCTCAAAT[A/T]AAAAAAAAAAAAAAG | 26168 |
rs575774949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565153 | CTTTTCTTCCATAGG[G/T]CTGTAGTTGGGGAGG | 26168 |
rs575865550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564345 | GTTTGGCATATAGTG[A/G]TGACAAATATCCCGA | 26168 |
rs575886700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564372 | CCGAAGTTTTCATTT[C/T]TAAATGCTAATCCTT | 26168 |
rs576008493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569685 | AGGGAAGGGTGGTGA[C/T]GTACAGTGAAAAACA | 26168 |
rs576008562 | snp | G/T | 0.00398564 | 0.0444627 | utr-variant-5-prime, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562161 | CTGCGCCTAAAGACA[G/T]CAGGAGTGGCGGGGC | 26168 |
rs576070995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569162 | AGGCTGAGGCGGGCG[C/G]ATCACCAGGTCAGGA | 26168 |
rs576865610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562859 | GCCATTTTCCCTTGT[C/T]TCTGGACTGGGGAGA | 26168 |
rs577216566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570288 | TGTCTCTGTTCCTCT[C/G]TAGAACCTTCATGGC | 26168 |
rs577236091 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567789 | CATGTAAGACATGTA[C/T]GGTAGGCTGAGGAGG | 26168 |
rs577777709 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561984 | GAGGGGAAGGAGGAG[A/G]GGGGGAGGAGTGGCG | 26168 |
rs578201296 | snp | A/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560935 | GGAATGTGCAGGAAC[A/T]GAGGCGTCTTCCTGG | 26168 |
rs745507130 | snp | C/T | 5.01425e-05 | 0.00500687 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564825 | GAGAAAGCCGGCCAG[C/T]ACAGCCCCCTGCGAG | 26168 |
rs745513428 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560727 | CTCTTTTCTCAGGTG[C/T]CTTCCATTTACACCA | 26168 |
rs745912022 | snp | C/T | | | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563526 | ATTCCACTGGAAGCT[C/T]TGGGGGCGCCACCGG | 26168 |
rs746007767 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561119 | GGTCGGGGCCCACTG[G/T]AAGCATCCAGAACAG | 26168 |
rs746055302 | snp | A/G | 1.65677e-05 | 0.00287812 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571402 | GGCCCTGTCTCAGCC[A/G]TTCAGCTTCACCCAG | 26168 |
rs746105754 | snp | C/T | 1.67382e-05 | 0.00289289 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564944 | CTCACCCCCTCCTCT[C/T]TCCCTTTCCACCAGG | 26168 |
rs746129862 | snp | A/G | 1.67953e-05 | 0.00289782 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571516 | CCAAGCCCATAAATG[A/G]GAAGGGAGACATGGG | 26168 |
rs746136213 | in-del | -/TT | 1.64741e-05 | 0.00286998 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560715 | AATCTACTTTCTCTC[-/TT]TTCTCAGGTGTCTTC | 26168 |
rs746153822 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568382 | GCAGATGGATCGCAA[A/G]GTCAAGAGATTGAGA | 26168 |
rs746197627 | snp | C/G | 1.65693e-05 | 0.00287826 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560209 | ACAGAGGGCCTCTTT[C/G]GCCCCCTACTGAGGG | 26168 |
rs746225335 | snp | G/T | 3.29772e-05 | 0.00406048 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560391 | CATGGGTCAGGTGGT[G/T]TCTCGAGAAGGCCAA | 26168 |
rs746357619 | snp | G/T | 1.662e-05 | 0.00288266 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565787 | CAACCAGATAGGTCA[G/T]TACCCAGAGGAACTT | 26168 |
rs746430711 | snp | A/G | 2.25864e-05 | 0.00336046 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563807 | GTAAGGTGGGAAAGG[A/G]GTGTGGGGTTGCGGG | 26168 |
rs746453694 | snp | A/C/T | 0.00017979 | 0.00947987 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563819 | AGGGGTGTGGGGTTG[A/C/T]GGGGGAGGGGTTAGG | 26168 |
rs746467630 | snp | C/T | 1.66924e-05 | 0.00288893 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570336 | TTTGTTGTACCTGAC[C/T]TGTGGCACTATCTCT | 26168 |
rs746495206 | snp | G/T | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570988 | CAGTTGGGTTAAAGG[G/T]TCGGGAGGCTGTTAT | 26168 |
rs746583082 | snp | G/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569867 | TGCGTGTTTACTTTG[G/T]GCTGTGTCTTGTTCT | 26168 |
rs746729763 | snp | C/T | 3.30622e-05 | 0.00406571 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560961 | CCTGGGTTTGGCTCC[C/T]CGTTCCTCACTTTTC | 26168 |
rs746767872 | snp | C/T | 3.3712e-05 | 0.00410547 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564908 | CTCCCTTCTCCGACT[C/T]CTAGAGGAGAGTCTG | 26168 |
rs746904318 | snp | C/T | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563600 | CCCAGCAAGGGGGTG[C/T]GACGCCACAGGTGCC | 26168 |
rs746919585 | in-del | -/GAA | 5.94666e-05 | 0.0054525 | cds-indel, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563311 | GCAAGTGAAGAGGAG[-/GAA]GAAGAGGAGGAGGAG | 26168 |
rs746939766 | snp | A/G | 1.77369e-05 | 0.00297795 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570930 | TGGTGCTTTTGTGTT[A/G]CAGGTAAGCAGATGA | 26168 |
rs747188777 | snp | C/T | 1.83994e-05 | 0.00303305 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565062 | GCAGGAGTTTTCCAC[C/T]CCTTCCAGGTGAGGC | 26168 |
rs747299629 | snp | A/G | 7.35308e-05 | 0.006063 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565415 | TGCATCATCTTTTGT[A/G]TGACTCCACCCTTGG | 26168 |
rs747507967 | snp | C/T | 3.99856e-05 | 0.00447115 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564498 | GGAGTGGGATTGACA[C/T]TGGTGGATTCTGCTT | 26168 |
rs747562050 | snp | C/T | 1.69769e-05 | 0.00291345 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564627 | CCCTGCCCTATAGGC[C/T]TCCTTTCATGTACTC | 26168 |
rs747598194 | in-del | -/GAGGAT | 9.44242e-05 | 0.00687046 | cds-indel, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563328 | GAAGAGGAGGAGGAG[-/GAGGAT]GAGGATGAAGATGAA | 26168 |
rs747796501 | snp | A/G | 1.89306e-05 | 0.00307652 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570503 | CCTAAGGTTTGAGGG[A/G]GTAGGAGAGAGATGG | 26168 |
rs747825878 | snp | G/T | 1.6623e-05 | 0.00288292 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570352 | TGTGGCACTATCTCT[G/T]TAGGTGGACATCTTC | 26168 |
rs747873124 | snp | C/T | 0.000182415 | 0.00954852 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564530 | AGTGTATCCTTCTTG[C/T]GGTCTTATTTGCATG | 26168 |
rs748064341 | snp | C/T | 3.35728e-05 | 0.00409698 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564936 | CTGGAGGCCTCACCC[C/T]CTCCTCTCTCCCTTT | 26168 |
rs748075703 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566233 | ATAATCCCAGTTACT[C/T]GGGAGGCTGAGGGAG | 26168 |
rs748169284 | snp | A/C | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572416 | GTGGAGACCGGGAGC[A/C]GAAGTAAAGGGAAGT | 26168 |
rs748194575 | snp | A/G | 2.09672e-05 | 0.00323777 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570779 | GGTGAGTTTCCTGAG[A/G]GAGGGGTATAGGGTG | 26168 |
rs748217221 | snp | A/G/T | 4.94412e-05 | 0.00497178 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560094 | AACCAGCTCTTAGGC[A/G/T]TGGGAGAGGCCTACA | 26168 |
rs748375757 | snp | A/G | 0.000131692 | 0.00811347 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563549 | GCCACCGGGGCCGGC[A/G]GCGGGGCCTCGCACA | 26168 |
rs748429172 | snp | A/C | 2.03126e-05 | 0.00318683 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563659 | CGGGGGCCACCTCCA[A/C]CCCGGCTGGGTCTGC | 26168 |
rs748467838 | snp | A/G | 5.26117e-05 | 0.00512865 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565444 | GGCCTACTCAGGAAG[A/G]GCCTGGTGTTGCAGC | 26168 |
rs748702252 | snp | G/T | 3.29478e-05 | 0.00405867 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560720 | ACTTTCTCTCTTTTC[G/T]CAGGTGTCTTCCATT | 26168 |
rs748705800 | snp | A/C/G | 4.94216e-05 | 0.00497079 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560705 | CTTCACTGCGAATCT[A/C/G]CTTTCTCTCTTTTCT | 26168 |
rs748859608 | in-del | -/G | 2.11307e-05 | 0.00325037 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570781 | GAGTTTCCTGAGGGA[-/G]GGGGTATAGGGTGTT | 26168 |
rs748871336 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565328 | TCAGAAGGACCCATC[A/G]TGAGCCAGAAAAAAG | 26168 |
rs748933967 | snp | A/G | 7.86921e-05 | 0.00627215 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570724 | CGGTAAAGAAAGACC[A/G]ACTGGATTTCCACCA | 26168 |
rs748958749 | snp | G/T | 1.67506e-05 | 0.00289396 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564641 | CCTCCTTTCATGTAC[G/T]CTGCCCAACGGTTTT | 26168 |
rs748991157 | snp | C/G | 1.66211e-05 | 0.00288275 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564696 | GAGCGCAGCTTGGCA[C/G]CCCCTGATGCCAGCA | 26168 |
rs749010031 | snp | A/G | 1.65625e-05 | 0.00287766 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560510 | GCCGTGTGGGCAGCC[A/G]AAAGCAGGACGTCTC | 26168 |
rs749023620 | snp | A/G | 9.62733e-05 | 0.00693739 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570511 | TTGAGGGGGTAGGAG[A/G]GAGATGGGCAAAATG | 26168 |
rs749142196 | snp | A/C | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566471 | GACCAGCCTGGCCAA[A/C]ATGGTGAAACCCTGG | 26168 |
rs749222086 | snp | A/T | 0.000460971 | 0.0151748 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563232 | GTTTGGGCCAGATCC[A/T]GGGTCAGGGACCACA | 26168 |
rs749297883 | snp | C/T | 1.66103e-05 | 0.00288182 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571375 | TGTTAACACCCAGTA[C/T]TGCAAGCATCTGGCC | 26168 |
rs749307910 | snp | C/G | 1.67492e-05 | 0.00289384 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564836 | CCAGCACAGCCCCCT[C/G]CGAGAGGAGCATGTG | 26168 |
rs749517697 | snp | G/T | 9.48002e-05 | 0.00688412 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563788 | CCTCTGGACCCTGAC[G/T]CGGGTAAGGTGGGAA | 26168 |
rs749519316 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560103 | TTAGGCGTGGGAGAG[A/G]CCTACAGGCCCAAGG | 26168 |
rs749544365 | snp | C/T | 3.61376e-05 | 0.00425059 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570955 | AGATGATGGGGCCAC[C/T]TCCCCTAGCTCTGAA | 26168 |
rs749555993 | snp | A/G | 1.6604e-05 | 0.00288127 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565777 | AAGGTAGGCCCAACC[A/G]GATAGGTCAGTACCC | 26168 |
rs749570737 | snp | C/G | 1.65592e-05 | 0.00287738 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560202 | GAGCTTCACAGAGGG[C/G]CTCTTTGGCCCCCTA | 26168 |
rs749741493 | snp | A/C | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571198 | TTCTCCATCTAAAAC[A/C]TTCTATCAAGTAAGA | 26168 |
rs749810546 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568950 | CAGGTAGATAGTGTT[A/G]GAATTGAATTGGGGG | 26168 |
rs749832169 | snp | A/G | 3.3601e-05 | 0.00409871 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565629 | GAGAGGGGATTCAGG[A/G]AGCAGGGTGTCTGGG | 26168 |
rs749861991 | snp | C/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572294 | TCCAGCCAGGGGAAT[C/T]CTCCCATCCCTACGA | 26168 |
rs749908818 | snp | C/G | 3.80467e-05 | 0.00436141 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563052 | TTTTGATACCCTGAT[C/G]TTTTGTTTTTCAGGG | 26168 |
rs749915108 | snp | C/T | 3.32757e-05 | 0.00407881 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564990 | CCTTCAAACGTATGG[C/T]AGCCTCATACCCCTC | 26168 |
rs749930241 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562644 | GTTAGAGAACTGTCT[C/G]CCATTCCAGTCCAGT | 26168 |
rs749964025 | snp | A/G | 2.81409e-05 | 0.00375095 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563162 | ACTCAAGTCCCAGGC[A/G]GGAGCGTCTTCGTTG | 26168 |
rs750041387 | snp | G/T | 1.68439e-05 | 0.00290201 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571341 | GGTCCTGACACGGGG[G/T]GTTTCTCATGGCTTG | 26168 |
rs750109740 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571843 | TTCAAACTTTTATAT[A/T]TATATATATATATAT | 26168 |
rs750142510 | snp | A/G | 1.66529e-05 | 0.00288551 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571489 | CACTGTGTGAGCCTC[A/G]TACCCCAGACCCCAA | 26168 |
rs750200262 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570656 | GAAACTTAGGGCATC[A/G]CTTTCTTTTCCCCCA | 26168 |
rs750206267 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560327 | GCCATCCTGTTTTCT[G/T]CAACATCTCCCTTCC | 26168 |
rs750247179 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560704 | CTTCACTGCGAATCT[-/A]ACTTTCTCTCTTTTC | 26168 |
rs750432440 | snp | A/G | 1.77322e-05 | 0.00297755 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563750 | CCATGGAGGAAGATG[A/G]ACTCAGGTGGACTCC | 26168 |
rs750435092 | snp | G/T | 1.66103e-05 | 0.00288182 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560535 | CGTCTCTGACCGGGG[G/T]TAGCAGTGCAGGGAG | 26168 |
rs750590087 | in-del | -/G | 1.68553e-05 | 0.00290299 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564926 | AGAGGAGAGTCTGGA[-/G]GCCTCACCCCCTCCT | 26168 |
rs750666585 | snp | G/T | 1.66832e-05 | 0.00288814 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564652 | GTACTCTGCCCAACG[G/T]TTTTGGGGGACAATC | 26168 |
rs750741423 | snp | A/C | 1.65463e-05 | 0.00287626 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570470 | TTTGACTCGCAGCGT[A/C]CCCTAAACCGCCGCT | 26168 |
rs751040881 | snp | A/G | 9.57625e-05 | 0.00691897 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563319 | AGAGGAGGAAGAAGA[A/G]GAGGAGGAGGAGGAT | 26168 |
rs751212662 | snp | A/C/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571837 | CAGATCTTCAAACTT[A/C/T]TATATATATATATAT | 26168 |
rs751224547 | snp | A/G | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563287 | CCCCGACCCTCTTTT[A/G]ATGCCTCAGCAAGTG | 26168 |
rs751233670 | in-del | -/GAA | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570556 | GGCAAGGCATTGCAG[-/GAA]GAAGGGTGGGCTTTG | 26168 |
rs751273966 | snp | A/G | 2.78843e-05 | 0.00373381 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565113 | AAGGGCTGGGGCCTT[A/G]GGGATGTGGAGAGAA | 26168 |
rs751317153 | snp | A/G | 1.6641e-05 | 0.00288448 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564997 | ACGTATGGCAGCCTC[A/G]TACCCCTCAGCACTG | 26168 |
rs751414413 | in-del | -/TT | 1.85159e-05 | 0.00304264 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565409 | CCCAGCTGCATCATC[-/TT]TTGTGTGACTCCACC | 26168 |
rs751539243 | snp | A/G | 1.67804e-05 | 0.00289653 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571352 | GGGGGGTTTCTCATG[A/G]CTTGCTTTGTTAACA | 26168 |
rs751546337 | snp | C/G | 1.67908e-05 | 0.00289743 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565557 | GGATGACTTGGGGAC[C/G]TTGTATGGACAGAAC | 26168 |
rs751574572 | snp | C/T | 1.65499e-05 | 0.00287657 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560340 | CTTCAACATCTCCCT[C/T]CCCTGCCAGGTCCTG | 26168 |
rs751591772 | snp | C/T | 2.20885e-05 | 0.00332321 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563651 | ACTCCCCCCGGGGGC[C/T]ACCTCCACCCCGGCT | 26168 |
rs751696272 | snp | C/T | 1.65831e-05 | 0.00287945 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565712 | GCCTCCCATCTTCTC[C/T]CCAGGTGATGAACAT | 26168 |
rs751752448 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568985 | CCAGCTGTGTCCACC[A/G]CAAAATTGCTTGCTT | 26168 |
rs751845866 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560805 | ACCTCTCTCCACATG[A/G]AACCTTCCTGGGGTT | 26168 |
rs751880666 | snp | A/G | 1.66435e-05 | 0.0028847 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564671 | TGGGGGACAATCTGG[A/G]CCAGAAGGGGAGCGC | 26168 |
rs751932163 | snp | A/C | 1.64754e-05 | 0.00287009 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560674 | CAGGGGGAAACAGGG[A/C]ATCTGGATGGCTGTG | 26168 |
rs752056372 | snp | C/T | 2.13199e-05 | 0.00326489 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570673 | TTTCTTTTCCCCCAT[C/T]CACATAGCATATTGC | 26168 |
rs752103724 | snp | A/G | 1.79599e-05 | 0.00299661 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570483 | GTACCCTAAACCGCC[A/G]CTGCCCTAAGGTTTG | 26168 |
rs752108187 | snp | A/G | 1.76805e-05 | 0.0029732 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564616 | CATTCCATTTCCCCT[A/G]CCCTATAGGCCTCCT | 26168 |
rs752193515 | snp | A/G | 1.95861e-05 | 0.00312933 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570715 | AGGCAGAGGCGGTAA[A/G]GAAAGACCGACTGGA | 26168 |
rs752384426 | in-del | -/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567869 | GAGAAGTGCCTTCTG[-/T]TTTTAAACTCCTGTT | 26168 |
rs752439192 | snp | C/T | 3.7477e-05 | 0.00432864 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565396 | TATTTCTGTGTGCCC[C/T]AGCTGCATCATCTTT | 26168 |
rs752455114 | snp | C/T | 0.000205825 | 0.0101425 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563614 | GCGACGCCACAGGTG[C/T]CATCCCCCTGTTGTC | 26168 |
rs752615276 | snp | C/T | 3.34163e-05 | 0.00408742 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571502 | TCGTACCCCAGACCC[C/T]AAGCCCATAAATGGG | 26168 |
rs752726420 | snp | C/T | 1.65244e-05 | 0.00287436 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560175 | ATAGCCAGGTAACCC[C/T]AGCCACACTCTGAGC | 26168 |
rs752775192 | snp | A/G | 1.82154e-05 | 0.00301784 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567032 | TTCACATCCACTTGT[A/G]TAATGCCTTGCCTCT | 26168 |
rs752783417 | snp | A/G | 7.16897e-05 | 0.00598663 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563767 | CTCAGGTGGACTCCA[A/G]AGTCTCCTCTGGACC | 26168 |
rs752820914 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570300 | TCTCTAGAACCTTCA[C/T]GGCAAAAGGCAAGAC | 26168 |
rs753018189 | snp | C/T | 3.31609e-05 | 0.00407177 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565727 | CCCAGGTGATGAACA[C/T]GTATGGAGACCTGGT | 26168 |
rs753020067 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560832 | GGTTTGTGAAACTGT[A/G]ATTGTGTTATAAAAA | 26168 |
rs753077158 | snp | A/T | 1.65575e-05 | 0.00287724 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561057 | CCGAATTCTTGCGTG[A/T]GTGTAGATGAGGGGC | 26168 |
rs753150802 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562837 | GATCTCTGAGGCCTG[C/T]TGCTTAGCCATTTTC | 26168 |
rs753194648 | snp | G/T | 4.99122e-05 | 0.00499536 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564795 | GGCATGGCAGAAGAG[G/T]CAGAGAGGCCTGGGG | 26168 |
rs753204341 | in-del | -/GCAGGTGAGAGCCGTGTGG | 1.65295e-05 | 0.0028748 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560484 | AACAGCTGCTATAGC[-/GCAGGTGAGAGCCGTGTGG]GCAGGTGAGAGCCGT | 26168 |
rs753219905 | in-del | -/A | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566342 | GCGGAATTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 26168 |
rs753244096 | snp | C/G | 1.66222e-05 | 0.00288285 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564693 | GGGGAGCGCAGCTTG[C/G]CACCCCCTGATGCCA | 26168 |
rs753406397 | snp | A/G | 1.68752e-05 | 0.00290471 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564883 | AGGAGCCCTTAAGCA[A/G]CTAGCCTCTCTCCCT | 26168 |
rs753447114 | in-del | -/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571835 | GCCAGATCTTCAAAC[-/T]TTTATATATATATAT | 26168 |
rs753484843 | snp | C/T | 3.31472e-05 | 0.00407093 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560213 | AGGGCCTCTTTGGCC[C/T]CCTACTGAGGGTTCC | 26168 |
rs753552064 | snp | C/G | 1.64912e-05 | 0.00287147 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560138 | GGTGTCCGAATCCAG[C/G]ATGCTGGAGTTTATC | 26168 |
rs753586901 | snp | C/G | 3.13376e-05 | 0.00395826 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563637 | CTGTTGTCGTTTTGA[C/G]TCCCCCCGGGGGCCA | 26168 |
rs753603311 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569479 | AGGTTTTTGGCCTAT[A/G]TAACGGGAAAAGTGG | 26168 |
rs753640093 | snp | A/G | 1.76468e-05 | 0.00297037 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563743 | GGGCCCCCCATGGAG[A/G]AAGATGGACTCAGGT | 26168 |
rs753640456 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560056 | ACCTCCAGATGACTC[C/T]GATGTGACAGAGGTG | 26168 |
rs753711185 | snp | G/T | 1.8561e-05 | 0.00304633 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565404 | TGTGCCCCAGCTGCA[G/T]CATCTTTTGTGTGAC | 26168 |
rs753731015 | snp | A/G | 1.94128e-05 | 0.00311545 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570515 | GGGGGTAGGAGAGAG[A/G]TGGGCAAAATGTGGG | 26168 |
rs753826051 | snp | A/G | 0.000126651 | 0.00795673 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564588 | TGCTTTCCCCAGGCC[A/G]GTCTCTCATGCCCAT | 26168 |
rs753919463 | snp | A/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572336 | ATTCCTTCATCCCTG[A/G]CACACGTCCAGGCAG | 26168 |
rs753933198 | snp | C/G | 1.65002e-05 | 0.00287225 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560376 | AGACGTGACTTTCAC[C/G]ATGGGTCAGGTGGTG | 26168 |
rs753982637 | snp | A/C | 1.65295e-05 | 0.0028748 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560484 | CAACAGCTGCTATAG[A/C]GCAGGTGAGAGCCGT | 26168 |
rs754034203 | in-del | -/AGC | 1.66103e-05 | 0.00288182 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560537 | TCTCTGACCGGGGGT[-/AGC]AGTGCAGGGAGCTAC | 26168 |
rs754054056 | snp | C/T | 3.39184e-05 | 0.00411802 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570460 | CATCACCTATTTTGA[C/T]TCGCAGCGTACCCTA | 26168 |
rs754406060 | in-del | -/TG | 5.54247e-05 | 0.00526396 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564557 | CATGCATGAGTCAAC[-/TG]TGTGCATCCCATTGT | 26168 |
rs754506042 | snp | C/G | 1.87499e-05 | 0.0030618 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570498 | GCTGCCCTAAGGTTT[C/G]AGGGGGTAGGAGAGA | 26168 |
rs754555373 | in-del | -/A | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562623 | GCCCCCCGTTCATCC[-/A]AGGGTGTTAGAGAAC | 26168 |
rs754609939 | snp | G/T | 9.50074e-05 | 0.00689164 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563334 | GGAGGAGGAGGAGGA[G/T]GAAGATGAAGAGGAG | 26168 |
rs754629422 | snp | C/T | 3.99529e-05 | 0.00446932 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563188 | CGTTGGCCCCCACCT[C/T]CCAAACCCCGACTCA | 26168 |
rs754781096 | in-del | -/A | 1.68091e-05 | 0.00289901 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565607 | AAAGGGTAGAGAAAC[-/A]AGGCCTGAGAGGGGA | 26168 |
rs754868754 | snp | C/T | 1.6649e-05 | 0.00288518 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565002 | TGGCAGCCTCATACC[C/T]CTCAGCACTGATGAG | 26168 |
rs754869420 | snp | G/T | 0.000168447 | 0.00917578 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571356 | GGTTTCTCATGGCTT[G/T]CTTTGTTAACACCCA | 26168 |
rs754944826 | snp | C/T | 0.000214846 | 0.0103623 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560352 | CCTTCCCTGCCAGGT[C/T]CTGTTTCAAGACGTG | 26168 |
rs755151609 | snp | C/T | 2.14108e-05 | 0.00327184 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563653 | TCCCCCCGGGGGCCA[C/T]CTCCACCCCGGCTGG | 26168 |
rs755177643 | snp | A/G | 1.65822e-05 | 0.00287938 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565722 | TTCTCCCCAGGTGAT[A/G]AACATGTATGGAGAC | 26168 |
rs755183307 | snp | G/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568993 | GTCCACCGCAAAATT[G/T]CTTGCTTGGTTGTTG | 26168 |
rs755266941 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560685 | AGGGCATCTGGATGG[C/T]TGTGCTTCACTGCGA | 26168 |
rs755446404 | snp | A/G | 1.72436e-05 | 0.00293624 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564621 | CATTTCCCCTGCCCT[A/G]TAGGCCTCCTTTCAT | 26168 |
rs755464849 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560360 | GCCAGGTCCTGTTTC[A/G]AGACGTGACTTTCAC | 26168 |
rs755497618 | snp | C/G | 6.65126e-05 | 0.00576644 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564681 | TCTGGGCCAGAAGGG[C/G]AGCGCAGCTTGGCAC | 26168 |
rs755497715 | snp | A/G | 1.65499e-05 | 0.00287657 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560503 | GGTGAGAGCCGTGTG[A/G]GCAGCCGAAAGCAGG | 26168 |
rs755639081 | snp | C/G/T | 0.000398827 | 0.0141159 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564694 | GGGAGCGCAGCTTGG[C/G/T]ACCCCCTGATGCCAG | 26168 |
rs755741945 | snp | C/T | 1.92922e-05 | 0.00310575 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570851 | CCCTGGGAGTCTCCA[C/T]GTGAAGGGCCTGCTT | 26168 |
rs755757574 | snp | C/G | 1.64814e-05 | 0.00287061 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560038 | CCTGACCGACACACT[C/G]TCACCTCCAGATGAC | 26168 |
rs755832124 | snp | A/G | 1.96392e-05 | 0.00313356 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570720 | GAGGCGGTAAAGAAA[A/G]ACCGACTGGATTTCC | 26168 |
rs755973705 | snp | G/T | 0.000100195 | 0.00707726 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563363 | AGGAAGTGGCAGCTT[G/T]GAGGCTGCCCCCAAG | 26168 |
rs755985349 | in-del | -/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565369 | AGAATTTGTATTCCA[-/G]GGAGTAGTAGGTATT | 26168 |
rs756004440 | snp | C/T | 8.33535e-05 | 0.00645521 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565011 | CATACCCCTCAGCAC[C/T]GATGAGGTAGTAGAG | 26168 |
rs756055944 | snp | C/T | 1.86024e-05 | 0.00304973 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565402 | TGTGTGCCCCAGCTG[C/T]ATCATCTTTTGTGTG | 26168 |
rs756285578 | snp | A/G | 1.65263e-05 | 0.00287452 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560177 | AGCCAGGTAACCCCA[A/G]CCACACTCTGAGCTT | 26168 |
rs756330347 | snp | A/G | 7.52474e-05 | 0.00613335 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564359 | GGTGACAAATATCCC[A/G]AAGTTTTCATTTCTA | 26168 |
rs756364837 | snp | C/T | 1.65872e-05 | 0.00287981 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565756 | GTCATGGACACAGTC[C/T]CTGAAAAGGTAGGCC | 26168 |
rs756418126 | snp | C/T | 1.82344e-05 | 0.00301941 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563777 | CTCCAAAGTCTCCTC[C/T]GGACCCTGACTCGGG | 26168 |
rs756504701 | snp | C/T | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572070 | GCTTTCCATCCCTGG[C/T]TCAGGCACTGCCAAC | 26168 |
rs756604229 | snp | A/G | 1.68315e-05 | 0.00290094 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565626 | CCTGAGAGGGGATTC[A/G]GGGAGCAGGGTGTCT | 26168 |
rs756668264 | snp | C/T | 1.64776e-05 | 0.00287028 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560842 | ACTGTGATTGTGTTA[C/T]AAAAAGTGGCTCCCA | 26168 |
rs756730883 | in-del | -/AC | 1.65412e-05 | 0.00287582 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560493 | TATAGCGCAGGTGAG[-/AC]AGCCGTGTGGGCAGC | 26168 |
rs756786591 | snp | C/T | 4.9436e-05 | 0.00497148 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560854 | TTATAAAAAGTGGCT[C/T]CCAGCTTGGAAGACC | 26168 |
rs756885230 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560147 | ATCCAGGATGCTGGA[C/G]TTTATCTGCTGTATA | 26168 |
rs756890181 | snp | C/T | 1.69017e-05 | 0.00290699 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564888 | CCCTTAAGCAACTAG[C/T]CTCTCTCCCTTCTCC | 26168 |
rs756921576 | snp | G/T | | | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563415 | CCAGCGGCCCCGCCC[G/T]TCCCGCCCCACTCAT | 26168 |
rs756957282 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560276 | CCTTCTTTCTTCCCT[C/T]GTTAGCGCTCCTGAG | 26168 |
rs757158968 | snp | G/T | 9.55019e-05 | 0.00690955 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563441 | CTCATCGAAAAACCT[G/T]CTCACAGCGCCGCCG | 26168 |
rs757163710 | snp | A/G | 1.97128e-05 | 0.00313943 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570729 | AAGAAAGACCGACTG[A/G]ATTTCCACCAGGGCT | 26168 |
rs757204070 | snp | C/G | 2.99003e-05 | 0.00386643 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563639 | GTTGTCGTTTTGACT[C/G]CCCCCGGGGGCCACC | 26168 |
rs757218145 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570591 | TCTTTGAGGGGCGAC[C/T]TGGGCATGGTGTCTG | 26168 |
rs757376459 | in-del | -/TA | 1.66219e-05 | 0.00288283 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560539 | CTGACCGGGGGTAGC[-/TA]AGTGCAGGGAGCTAC | 26168 |
rs757392644 | snp | A/G | 0.000160655 | 0.00896113 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564405 | TCTTTCTTCCTGTCT[A/G]TGAGTAGGAACTCTC | 26168 |
rs757407161 | snp | C/T | 1.67565e-05 | 0.00289447 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571510 | CAGACCCCAAGCCCA[C/T]AAATGGGAAGGGAGA | 26168 |
rs757526373 | snp | C/G | 0.000455991 | 0.0150926 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564591 | TTTCCCCAGGCCAGT[C/G]TCTCATGCCCATTCC | 26168 |
rs757580298 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560379 | CGTGACTTTCACCAT[A/G]GGTCAGGTGGTGTCT | 26168 |
rs757683945 | snp | C/T | | | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564650 | ATGTACTCTGCCCAA[C/T]GGTTTTGGGGGACAA | 26168 |
rs757701948 | snp | C/G | 3.84904e-05 | 0.00438677 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563790 | TCTGGACCCTGACTC[C/G]GGTAAGGTGGGAAAG | 26168 |
rs757757365 | snp | C/G | 0.000283074 | 0.0118936 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563046 | CTTAGATTTTGATAC[C/G]CTGATCTTTTGTTTT | 26168 |
rs757913619 | snp | C/T | 3.34499e-05 | 0.00408948 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563176 | CGGGAGCGTCTTCGT[C/T]GGCCCCCACCTCCCA | 26168 |
rs758035302 | snp | C/T | 1.68835e-05 | 0.00290542 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564903 | CCTCTCTCCCTTCTC[C/T]GACTCCTAGAGGAGA | 26168 |
rs758057913 | snp | C/G/T | 1.87725e-05 | 0.00306364 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570872 | GGGCCTGCTTTCTTT[C/G/T]TCTTCTCTAGAATGT | 26168 |
rs758082009 | in-del | -/T | 1.65375e-05 | 0.0028755 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560972 | CTCCCCGTTCCTCAC[-/T]TTTCCCTTTTCATTC | 26168 |
rs758182033 | snp | A/G | 1.67119e-05 | 0.00289062 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564826 | AGAAAGCCGGCCAGC[A/G]CAGCCCCCTGCGAGA | 26168 |
rs758245167 | snp | C/G | 3.54604e-05 | 0.00421057 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563754 | GGAGGAAGATGGACT[C/G]AGGTGGACTCCAAAG | 26168 |
rs758298274 | snp | A/G | 3.3024e-05 | 0.00406336 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560163 | TTTATCTGCTGTATA[A/G]CCAGGTAACCCCAGC | 26168 |
rs758522053 | snp | A/G | 1.65411e-05 | 0.00287581 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560495 | ATAGCGCAGGTGAGA[A/G]CCGTGTGGGCAGCCG | 26168 |
rs758559072 | snp | A/T | 1.85057e-05 | 0.00304179 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565407 | GCCCCAGCTGCATCA[A/T]CTTTTGTGTGACTCC | 26168 |
rs758674170 | snp | A/G | 1.66081e-05 | 0.00288163 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560537 | TCTCTGACCGGGGGT[A/G]GCAGTGCAGGGAGCT | 26168 |
rs758690181 | in-del | -/GGCT | 2.37482e-05 | 0.0034458 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565100 | CCTCCTTGAAAGAAG[-/GGCT]GGCTGGGGCCTTGGG | 26168 |
rs758726661 | snp | A/T | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564852 | CGAGAGGAGCATGTG[A/T]CCTGCGTACAGAGTA | 26168 |
rs758866986 | snp | A/T | 1.67433e-05 | 0.00289333 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570323 | GGCAAGACTTCTGTT[A/T]GTTGTACCTGACCTG | 26168 |
rs758953550 | snp | C/T | 0.000141453 | 0.00840871 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564429 | AACTCTCTCTCCATC[C/T]CTGTAGAATCTCTTG | 26168 |
rs759021091 | snp | G/T | 6.92689e-05 | 0.00588469 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563604 | GCAAGGGGGTGCGAC[G/T]CCACAGGTGCCATCC | 26168 |
rs759156130 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565593 | CAATGACCAGGTGAG[A/G]AAGGGTAGAGAAACA | 26168 |
rs759208364 | snp | A/G | 8.4702e-05 | 0.00650721 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565511 | TGGTGAGGGGCTTCC[A/G]AGTGGCTTATAAGCG | 26168 |
rs759350354 | snp | C/G | 3.31884e-05 | 0.00407346 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560525 | GAAAGCAGGACGTCT[C/G]TGACCGGGGGTAGCA | 26168 |
rs759437265 | snp | A/G | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571226 | AGAACACTAGCTTTA[A/G]AGTCAGGCTGTTTTT | 26168 |
rs759526142 | snp | C/T | 3.95671e-05 | 0.0044477 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564570 | ACTGTGTGCATCCCA[C/T]TGTGCTTTCCCCAGG | 26168 |
rs759531206 | in-del | -/AAATATAT | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571910 | TATATATATATATAA[-/AAATATAT]AAATATATAAATGCC | 26168 |
rs759581000 | snp | C/G | 6.69064e-05 | 0.00578349 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564644 | CCTTTCATGTACTCT[C/G]CCCAACGGTTTTGGG | 26168 |
rs759581195 | snp | A/G | 1.65059e-05 | 0.00287275 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560462 | CCTCCCACCCGGACC[A/G]GGCCTACAACAGCTG | 26168 |
rs759733918 | snp | C/G | 3.29538e-05 | 0.00405904 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560808 | TCTCTCCACATGGAA[C/G]CTTCCTGGGGTTTGT | 26168 |
rs759742745 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570190 | TTCCTCCCTTACCCC[A/G]AAGAACCGAAACATG | 26168 |
rs759751225 | in-del | -/GCTGTATA | 1.65004e-05 | 0.00287227 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560155 | TGCTGGAGTTTATCT[-/GCTGTATA]GCCAGGTAACCCCAG | 26168 |
rs759785077 | snp | C/G | 1.65537e-05 | 0.0028769 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561042 | GTTCCCCATGGAGCT[C/G]CGAATTCTTGCGTGT | 26168 |
rs759886801 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571540 | ACATGGGAGTCCCTT[A/C]CCAAGAAACTCCAGT | 26168 |
rs759922903 | snp | G/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562971 | CTCTTTTCTTTATTT[G/T]CATCTGAATCCAGAG | 26168 |
rs759950189 | snp | A/G | 5.30059e-05 | 0.00514783 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563704 | GCTGAGGATGGGGTG[A/G]GAGGGTCTCCACCAG | 26168 |
rs759960769 | snp | A/G | 1.66288e-05 | 0.00288343 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564785 | CTCAGATTTGGGCAT[A/G]GCAGAAGAGGCAGAG | 26168 |
rs759972767 | snp | A/G | 1.95208e-05 | 0.0031241 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570841 | GAAGTCCTACCCCTG[A/G]GAGTCTCCATGTGAA | 26168 |
rs760005317 | snp | A/G | 1.64855e-05 | 0.00287097 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560121 | TACAGGCCCAAGGAT[A/G]TGGTGTCCGAATCCA | 26168 |
rs760177721 | snp | A/G | 8.24409e-05 | 0.00641979 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560130 | AAGGATATGGTGTCC[A/G]AATCCAGGATGCTGG | 26168 |
rs760294143 | snp | C/T | 3.31934e-05 | 0.00407377 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565681 | TGTACCCATGCCGCA[C/T]CCTCCATGGCAAGCT | 26168 |
rs760613996 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560072 | GATGTGACAGAGGTG[A/G]TGTGGCAACCAGCTC | 26168 |
rs760644242 | snp | A/G | 1.66045e-05 | 0.00288132 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564747 | AGCATCGGGGACCAT[A/G]TGGCCCAGGAGCTTT | 26168 |
rs760673178 | snp | A/C/G | 3.3231e-05 | 0.0040761 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560531 | AGGACGTCTCTGACC[A/C/G]GGGGTAGCAGTGCAG | 26168 |
rs760730352 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560772 | GTGTCATAATTCCCC[A/G]GGCAAGGGCGAAACT | 26168 |
rs760731865 | snp | C/T | 1.66286e-05 | 0.0028834 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570444 | ATGTGAGGCGACGCA[C/T]CATCACCTATTTTGA | 26168 |
rs760786721 | snp | G/T | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570376 | CATCTTCAATAAGGA[G/T]CTACTGCTAATCCCC | 26168 |
rs760885328 | snp | C/T | 4.28568e-05 | 0.00462889 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563031 | TGCGGTGGGGTGATG[C/T]TTAGATTTTGATACC | 26168 |
rs760941593 | snp | C/T | 2.29077e-05 | 0.00338427 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563119 | TCCTGGGGGCCTGAG[C/T]CTCCTGGACCCGGCA | 26168 |
rs760963743 | snp | A/G | 1.8627e-05 | 0.00305175 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567042 | CTTGTGTAATGCCTT[A/G]CCTCTAAAGAATGAG | 26168 |
rs761030262 | snp | C/T | 5.00714e-05 | 0.00500332 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564955 | CTCTCTCCCTTTCCA[C/T]CAGGCATCTTGGACG | 26168 |
rs761032659 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564351 | CATATAGTGGTGACA[A/G]ATATCCCGAAGTTTT | 26168 |
rs761112323 | snp | A/C | 1.68587e-05 | 0.00290329 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564875 | ACAGAGTAAGGAGCC[A/C]TTAAGCAACTAGCCT | 26168 |
rs761256181 | in-del | -/T | 0.000146671 | 0.00856235 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564420 | TGAGTAGGAACTCTC[-/T]TCTCCATCCCTGTAG | 26168 |
rs761262730 | snp | C/T | 3.29837e-05 | 0.00406088 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560446 | TGTATAAGAAGTATG[C/T]CCTCCCACCCGGACC | 26168 |
rs761284610 | snp | A/G | 1.6566e-05 | 0.00287797 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571441 | GCCCAAACTTCGTCG[A/G]CAGATCTACAAGGAG | 26168 |
rs761449966 | snp | C/T | 9.46074e-05 | 0.00687712 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566961 | TCTTCTATGATAAAC[C/T]CCGTACCAAAGGGTT | 26168 |
rs761484838 | snp | C/T | 1.66194e-05 | 0.00288261 | upstream-variant-2KB, stop-lost, splice-donor-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571481 | TGCAAACTCACTGTG[C/T]GAGCCTCGTACCCCA | 26168 |
rs761567038 | snp | C/T | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571336 | GCACAGGTCCTGACA[C/T]GGGGGGTTTCTCATG | 26168 |
rs761681888 | snp | A/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572375 | CCATCTCTGCTACAG[A/G]GGAAAACAAATAACA | 26168 |
rs761727872 | snp | A/C/G | 5.00666e-05 | 0.00500312 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564651 | TGTACTCTGCCCAAC[A/C/G]GTTTTGGGGGACAAT | 26168 |
rs761762329 | in-del | -/CCCATTGTG | 4.48521e-05 | 0.0047354 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564566 | GTCAACTGTGTGCAT[-/CCCATTGTG]CTTTCCCCAGGCCAG | 26168 |
rs761804775 | snp | C/T | 3.30923e-05 | 0.00406756 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560993 | CTTTTCATTCCCACC[C/T]CCTAGACTTTGATTT | 26168 |
rs761835689 | snp | C/T | 1.65866e-05 | 0.00287976 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565703 | TGGCAAGCTGCCTCC[C/T]ATCTTCTCCCCAGGT | 26168 |
rs761966987 | snp | A/G | 4.72579e-05 | 0.00486073 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570636 | ACCATACTGTGTTCA[A/G]TTGAGAAACTTAGGG | 26168 |
rs762098363 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567119 | TTTCAAAGATTAAAC[A/G]TCTCTTGTGTGTGTA | 26168 |
rs762208446 | snp | A/G | 9.39982e-05 | 0.00685494 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563276 | GCCTCCCTGTCCCCC[A/G]ACCCTCTTTTGATGC | 26168 |
rs762250870 | snp | C/T | | | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565749 | AGACCTGGTCATGGA[C/T]ACAGTCCCTGAAAAG | 26168 |
rs762253310 | snp | C/T | 2.62436e-05 | 0.00362231 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563155 | CCAGCTTACTCAAGT[C/T]CCAGGCGGGAGCGTC | 26168 |
rs762315525 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567419 | GCTATTCCTGGAGGC[A/G]GAGGCAGGAGAATCC | 26168 |
rs762443721 | snp | A/T | 4.55104e-05 | 0.00477002 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565095 | GAAAGCCCTCCTTGA[A/T]AGAAGGGCTGGGGCC | 26168 |
rs762458799 | snp | A/G | 2.59919e-05 | 0.0036049 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565108 | GAAAGAAGGGCTGGG[A/G]CCTTGGGGATGTGGA | 26168 |
rs762482230 | snp | C/T | 1.66704e-05 | 0.00288703 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571492 | TGTGTGAGCCTCGTA[C/T]CCCAGACCCCAAGCC | 26168 |
rs762588004 | snp | A/C | 0.000131839 | 0.00811802 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564547 | GTCTTATTTGCATGC[A/C]TGAGTCAACTGTGTG | 26168 |
rs762613205 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564245 | TTCGGAGAACTCCAG[C/T]CAAACAGTTTCAGGC | 26168 |
rs762687551 | in-del | -/GGCCACCTCCACCCCGGC | 2.33174e-05 | 0.0034144 | cds-indel, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563647 | TTGACTCCCCCCGGG[-/GGCCACCTCCACCCCGGC]GGCCACCTCCACCCC | 26168 |
rs762750590 | snp | C/T | 1.6557e-05 | 0.00287719 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560333 | CTGTTTTCTTCAACA[C/T]CTCCCTTCCCTGCCA | 26168 |
rs762868995 | in-del | -/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570090 | GTTCTTAGCTGCTAA[-/G]TGCTTCTCCCTTTAA | 26168 |
rs762962707 | snp | C/T | 5.68101e-05 | 0.00532934 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566980 | ACCAAAGGGTTATGA[C/T]GGGGTGAAAAGGTGG | 26168 |
rs762978263 | snp | G/T | 0.000152917 | 0.00874271 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563837 | GGGAGGGGTTAGGGA[G/T]GGTTAAGAGCCTGGA | 26168 |
rs763005416 | snp | A/G | 1.6585e-05 | 0.00287962 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570433 | CATCTCTGTTGATGT[A/G]AGGCGACGCACCATC | 26168 |
rs763070837 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566330 | CTGGGCAACAAGAGC[A/G]GAATTCTGTCTCAAA | 26168 |
rs763137535 | snp | C/T | 1.66827e-05 | 0.00288809 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564653 | TACTCTGCCCAACGG[C/T]TTTGGGGGACAATCT | 26168 |
rs763192671 | snp | G/T | 1.66037e-05 | 0.00288125 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564758 | CCATGTGGCCCAGGA[G/T]CTTTTTCAGGGCTCA | 26168 |
rs763300314 | in-del | -/T | 0.000289645 | 0.0120307 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564362 | ACAAATATCCCGAAG[-/T]TTTTCATTTCTAAAT | 26168 |
rs763354297 | snp | A/T | 1.64855e-05 | 0.00287097 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560022 | GAGAGTGCCAAGAAG[A/T]CCTGACCGACACACT | 26168 |
rs763377473 | snp | A/G | 2.32404e-05 | 0.00340876 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570650 | AATTGAGAAACTTAG[A/G]GCATCACTTTCTTTT | 26168 |
rs763546172 | snp | C/T | 3.33918e-05 | 0.00408592 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564817 | GGCCTGGGGAGAAAG[C/T]CGGCCAGCACAGCCC | 26168 |
rs763577432 | snp | G/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570101 | CTAAGTGCTTCTCCC[G/T]TTAAAGTGTGAAAAG | 26168 |
rs763587179 | snp | G/T | 1.71396e-05 | 0.00292737 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563581 | CCCAAGAACCATCTT[G/T]CACCCCAGCAAGGGG | 26168 |
rs763671347 | snp | C/T | 1.92888e-05 | 0.00310549 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570853 | CTGGGAGTCTCCATG[C/T]GAAGGGCCTGCTTTC | 26168 |
rs763684720 | snp | C/T | 1.76244e-05 | 0.00296848 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563735 | TGCCCTCTGGGCCCC[C/T]CATGGAGGAAGATGG | 26168 |
rs763726289 | snp | C/G/T | 3.38675e-05 | 0.00411495 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571327 | AAATGTGTAGCACAG[C/G/T]TCCTGACACGGGGGG | 26168 |
rs763738167 | snp | C/T | 1.6489e-05 | 0.00287128 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560134 | ATATGGTGTCCGAAT[C/T]CAGGATGCTGGAGTT | 26168 |
rs763756059 | snp | C/T | 1.64803e-05 | 0.00287052 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560040 | TGACCGACACACTCT[C/T]ACCTCCAGATGACTC | 26168 |
rs763770512 | snp | A/C/G/T | 3.29605e-05 | 0.00405948 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560093 | CAACCAGCTCTTAGG[A/C/G/T]GTGGGAGAGGCCTAC | 26168 |
rs763858852 | snp | G/T | 1.68408e-05 | 0.00290175 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565531 | GCTTATAAGCGGCAC[G/T]TGCTGACCATGGATG | 26168 |
rs763920120 | snp | C/T | 3.75439e-05 | 0.0043325 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563629 | CCATCCCCCTGTTGT[C/T]GTTTTGACTCCCCCC | 26168 |
rs764154908 | snp | C/T | 8.20782e-05 | 0.00640565 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567043 | TTGTGTAATGCCTTG[C/T]CTCTAAAGAATGAGA | 26168 |
rs764217881 | snp | A/G | 1.67399e-05 | 0.00289304 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570453 | GACGCACCATCACCT[A/G]TTTTGACTCGCAGCG | 26168 |
rs764234006 | in-del | -/G | 3.30983e-05 | 0.00406793 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560502 | AGGTGAGAGCCGTGT[-/G]GGCAGCCGAAAGCAG | 26168 |
rs764258130 | snp | C/T | 6.92929e-05 | 0.00588571 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564389 | AAATGCTAATCCTTT[C/T]TCTTTCTTCCTGTCT | 26168 |
rs764313308 | snp | C/G | 2.60896e-05 | 0.00361166 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564587 | GTGCTTTCCCCAGGC[C/G]AGTCTCTCATGCCCA | 26168 |
rs764357515 | snp | C/T | 3.33717e-05 | 0.0040847 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564956 | TCTCTCCCTTTCCAC[C/T]AGGCATCTTGGACGA | 26168 |
rs764418774 | snp | C/G | 2.28663e-05 | 0.00338122 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563120 | CCTGGGGGCCTGAGC[C/G]TCCTGGACCCGGCAT | 26168 |
rs764482062 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565650 | GGTGTCTGGGGCCCT[C/T]TGCATGGGGGAGCCC | 26168 |
rs764518172 | snp | A/C/T | 8.15062e-05 | 0.0063833 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563045 | GCTTAGATTTTGATA[A/C/T]CCTGATCTTTTGTTT | 26168 |
rs764584147 | snp | C/G/T | 6.64535e-05 | 0.00576395 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560308 | CCTCCCAGAACTGAG[C/G/T]CAGGCCATCCTGTTT | 26168 |
rs764608104 | snp | A/G | 1.68618e-05 | 0.00290356 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564878 | GAGTAAGGAGCCCTT[A/G]AGCAACTAGCCTCTC | 26168 |
rs764642434 | in-del | -/CTT | 3.47874e-05 | 0.00417043 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564523 | CTGCTTCAGTGTATC[-/CTT]CTTGCGGTCTTATTT | 26168 |
rs764643728 | snp | C/T | 1.66468e-05 | 0.00288498 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571488 | TCACTGTGTGAGCCT[C/T]GTACCCCAGACCCCA | 26168 |
rs764723601 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564575 | GTGCATCCCATTGTG[C/T]TTTCCCCAGGCCAGT | 26168 |
rs764776352 | in-del | -/G | 1.69229e-05 | 0.00290881 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571336 | CACAGGTCCTGACAC[-/G]GGGGGGTTTCTCATG | 26168 |
rs764822619 | snp | C/T | 1.68937e-05 | 0.0029063 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564893 | AAGCAACTAGCCTCT[C/T]TCCCTTCTCCGACTC | 26168 |
rs764880816 | snp | A/G | 1.68536e-05 | 0.00290285 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571340 | AGGTCCTGACACGGG[A/G]GGTTTCTCATGGCTT | 26168 |
rs765065942 | snp | C/T | 1.65094e-05 | 0.00287305 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560159 | GGAGTTTATCTGCTG[C/T]ATAGCCAGGTAACCC | 26168 |
rs765095475 | in-del | -/A | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570087 | GGGTTCTTAGCTGCT[-/A]AAGTGCTTCTCCCTT | 26168 |
rs765126667 | snp | A/G | 6.24005e-05 | 0.00558537 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563821 | GGGTGTGGGGTTGCG[A/G]GGGAGGGGTTAGGGA | 26168 |
rs765148222 | snp | C/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572389 | GGGGAAAACAAATAA[C/G]ATTTGAGTCCAGTGG | 26168 |
rs765217996 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561447 | CGCTCCATTGCCCCG[A/G]CGTGGCAGGCCATTC | 26168 |
rs765244242 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567342 | GCCAACATTGAGAAA[C/T]CCCATCTCTATTAAA | 26168 |
rs765315810 | snp | A/C/G | 4.00098e-05 | 0.00447254 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564602 | CAGTCTCTCATGCCC[A/C/G]TTCCATTTCCCCTGC | 26168 |
rs765384066 | in-del | -/AGA | 1.66319e-05 | 0.00288369 | cds-indel, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564788 | AGATTTGGGCATGGC[-/AGA]AGAGGCAGAGAGGCC | 26168 |
rs765389289 | snp | C/T | 4.7191e-05 | 0.00485729 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570637 | CCATACTGTGTTCAA[C/T]TGAGAAACTTAGGGC | 26168 |
rs765624852 | snp | C/T | 1.72009e-05 | 0.0029326 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570467 | TATTTTGACTCGCAG[C/T]GTACCCTAAACCGCC | 26168 |
rs765658171 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565828 | AAGCAGCTTTTTAAG[C/T]TCCTTTCATCTCTTT | 26168 |
rs765702717 | snp | C/G | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563251 | TCAGGGACCACAGTG[C/G]CAGCCAGACGCCTCC | 26168 |
rs765786938 | snp | C/G | 2.65192e-05 | 0.00364128 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563156 | CAGCTTACTCAAGTC[C/G]CAGGCGGGAGCGTCT | 26168 |
rs765803844 | snp | C/T | 2.66393e-05 | 0.00364951 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565110 | AAGAAGGGCTGGGGC[C/T]TTGGGGATGTGGAGA | 26168 |
rs765832983 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564328 | TGGGTACTATGCTGG[A/G]TGTTTGGCATATAGT | 26168 |
rs765842091 | snp | C/T | 9.40955e-05 | 0.00685849 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563285 | TCCCCCGACCCTCTT[C/T]TGATGCCTCAGCAAG | 26168 |
rs765980491 | snp | C/G | 3.39046e-05 | 0.00411718 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563177 | GGGAGCGTCTTCGTT[C/G]GCCCCCACCTCCCAA | 26168 |
rs766000267 | snp | A/C | 1.66418e-05 | 0.00288455 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564996 | AACGTATGGCAGCCT[A/C]ATACCCCTCAGCACT | 26168 |
rs766085938 | snp | C/T | 1.65551e-05 | 0.00287702 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560334 | TGTTTTCTTCAACAT[C/T]TCCCTTCCCTGCCAG | 26168 |
rs766157919 | snp | A/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567462 | AGGCAGAGGTTGCAG[A/T]GAGCCGAGACCCCGC | 26168 |
rs766228256 | snp | C/G/T | 3.33451e-05 | 0.0040831 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571494 | TGTGAGCCTCGTACC[C/G/T]CAGACCCCAAGCCCA | 26168 |
rs766274583 | snp | A/C | 6.28082e-05 | 0.00560358 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564550 | TTATTTGCATGCATG[A/C]GTCAACTGTGTGCAT | 26168 |
rs766362454 | snp | G/T | 0.000160604 | 0.0089597 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563839 | GAGGGGTTAGGGAGG[G/T]TTAAGAGCCTGGAGC | 26168 |
rs766462351 | snp | A/C | 0.000182711 | 0.00955625 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560540 | CTGACCGGGGGTAGC[A/C]GTGCAGGGAGCTACC | 26168 |
rs766514357 | snp | A/G | 3.35756e-05 | 0.00409716 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565554 | CATGGATGACTTGGG[A/G]ACCTTGTATGGACAG | 26168 |
rs766524020 | in-del | -/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561080 | TGAGGGGCGGGGGAC[-/G]GGCGCCAGGCATTGT | 26168 |
rs766538023 | snp | C/T | 1.66032e-05 | 0.0028812 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564763 | TGGCCCAGGAGCTTT[C/T]TCAGGGCTCAGATTT | 26168 |
rs766626776 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560802 | TTAACCTCTCTCCAC[A/C]TGGAACCTTCCTGGG | 26168 |
rs766686493 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568777 | TGAGTTCTGTGAGCT[C/G]CTCTAGCAAATTAAT | 26168 |
rs766717783 | snp | C/T | 4.47407e-05 | 0.00472952 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570663 | AGGGCATCACTTTCT[C/T]TTCCCCCATCCACAT | 26168 |
rs766768640 | snp | A/G | 1.66696e-05 | 0.00288696 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564657 | CTGCCCAACGGTTTT[A/G]GGGGACAATCTGGGC | 26168 |
rs766770744 | snp | C/T | 1.96126e-05 | 0.00313144 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570835 | GAAATTGAAGTCCTA[C/T]CCCTGGGAGTCTCCA | 26168 |
rs766935775 | snp | G/T | 0.000112177 | 0.00748838 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563611 | GGTGCGACGCCACAG[G/T]TGCCATCCCCCTGTT | 26168 |
rs766968531 | snp | A/G | 1.97814e-05 | 0.00314489 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570698 | TATTGCCAAGTATCT[A/G]CAGGCAGAGGCGGTA | 26168 |
rs767000067 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560029 | CCAAGAAGTCCTGAC[C/T]GACACACTCTCACCT | 26168 |
rs767097739 | snp | A/G | 1.68684e-05 | 0.00290412 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565524 | CCGAGTGGCTTATAA[A/G]CGGCACGTGCTGACC | 26168 |
rs767141898 | snp | A/T | 9.50164e-05 | 0.00689196 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563339 | AGGAGGAGGATGAAG[A/T]TGAAGAGGAGGAAGT | 26168 |
rs767330765 | snp | A/G | 6.0794e-05 | 0.00551301 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565119 | TGGGGCCTTGGGGAT[A/G]TGGAGAGAATACTGC | 26168 |
rs767508697 | snp | C/T | 1.66946e-05 | 0.00288912 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571500 | CCTCGTACCCCAGAC[C/T]CCAAGCCCATAAATG | 26168 |
rs767563130 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569107 | GATTTGTTTTTTTGC[C/T]GGGCGCGGTGGCTCA | 26168 |
rs767568787 | snp | A/C/T | 3.32332e-05 | 0.00407624 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560530 | CAGGACGTCTCTGAC[A/C/T]GGGGGTAGCAGTGCA | 26168 |
rs767678383 | snp | C/G | 1.65542e-05 | 0.00287695 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561043 | TTCCCCATGGAGCTC[C/G]GAATTCTTGCGTGTG | 26168 |
rs767693200 | snp | A/G | 1.65809e-05 | 0.00287926 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565726 | CCCCAGGTGATGAAC[A/G]TGTATGGAGACCTGG | 26168 |
rs767736252 | snp | G/T | 1.73851e-05 | 0.00294826 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567013 | CAAAAACGTGAGTTT[G/T]GAATTCACATCCACT | 26168 |
rs767911829 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560809 | CTCTCCACATGGAAC[C/T]TTCCTGGGGTTTGTG | 26168 |
rs767985513 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562772 | GTATTAAAATAAAGA[C/T]GTAGAACCTGGCAGT | 26168 |
rs768000840 | snp | A/G | 1.94301e-05 | 0.00311684 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570844 | GTCCTACCCCTGGGA[A/G]TCTCCATGTGAAGGG | 26168 |
rs768031680 | snp | C/T | 1.6486e-05 | 0.00287102 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560125 | GGCCCAAGGATATGG[C/T]GTCCGAATCCAGGAT | 26168 |
rs768148311 | snp | C/T | 8.5306e-05 | 0.00653037 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566900 | GGTCTTTTAATTCCA[C/T]TGAGCTTTTTTGTGT | 26168 |
rs768210395 | snp | A/G | 0.000107602 | 0.00733413 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564501 | GTGGGATTGACATTG[A/G]TGGATTCTGCTTCAG | 26168 |
rs768231434 | snp | A/G | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570991 | TTGGGTTAAAGGGTC[A/G]GGAGGCTGTTATGCA | 26168 |
rs768289408 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561577 | CAAGCCCTGCTTAAA[A/G]TTAAATAAAATAGAA | 26168 |
rs768362619 | snp | A/C | 1.66449e-05 | 0.00288482 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570346 | CTGACCTGTGGCACT[A/C]TCTCTTTAGGTGGAC | 26168 |
rs768400136 | snp | A/C | 2.74933e-05 | 0.00370755 | utr-variant-5-prime, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563074 | TTTTCAGGGTACTGG[A/C]AGATGAAAGAGACTA | 26168 |
rs768648307 | in-del | -/GAG | | | cds-indel, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563317 | GAAGAGGAGGAAGAA[-/GAG]GAGGAGGAGGAGGAT | 26168 |
rs768650821 | snp | A/C | 8.48932e-05 | 0.00651455 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563622 | ACAGGTGCCATCCCC[A/C]TGTTGTCGTTTTGAC | 26168 |
rs768771858 | snp | A/G | 0.000128708 | 0.00802107 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563534 | GGAAGCTTTGGGGGC[A/G]CCACCGGGGCCGGCG | 26168 |
rs768879623 | snp | C/T | 9.26484e-05 | 0.00680556 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563265 | GCCAGCCAGACGCCT[C/T]CCTGTCCCCCGACCC | 26168 |
rs768962617 | snp | C/T | 1.80804e-05 | 0.00300664 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565425 | TTTGTGTGACTCCAC[C/T]CTTGGCCTACTCAGG | 26168 |
rs769120364 | snp | C/G | 1.64825e-05 | 0.00287071 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560418 | CCAAGGAAGGCAGGA[C/G]ACTCTATTCCGATGT | 26168 |
rs769135834 | in-del | -/TA | 1.66551e-05 | 0.00288571 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570345 | CCTGACCTGTGGCAC[-/TA]TCTCTTTAGGTGGAC | 26168 |
rs769179002 | in-del | -/G | 1.69229e-05 | 0.00290881 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571337 | CACAGGTCCTGACAC[-/G]GGGGGTTTCTCATGG | 26168 |
rs769195740 | snp | C/T | 1.90601e-05 | 0.00308702 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565068 | GTTTTCCACCCCTTC[C/T]AGGTGAGGCTTGAAA | 26168 |
rs769224372 | snp | A/G | 4.97063e-05 | 0.00498505 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571456 | GCAGATCTACAAGGA[A/G]CTGTGTCACTGCAAA | 26168 |
rs769240766 | in-del | -/AA | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572383 | GCTACAGGGGAAAAC[-/AA]ATAACATTTGAGTCC | 26168 |
rs769289317 | snp | A/G | 3.38375e-05 | 0.0041131 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564531 | GTGTATCCTTCTTGC[A/G]GTCTTATTTGCATGC | 26168 |
rs769350128 | in-del | -/GAT | 9.45805e-05 | 0.00687614 | cds-indel, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563332 | GAGGAGGAGGAGGAG[-/GAT]GAAGATGAAGAGGAG | 26168 |
rs769437987 | snp | C/G/T | 5.69882e-05 | 0.00533768 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570504 | CTAAGGTTTGAGGGG[C/G/T]TAGGAGAGAGATGGG | 26168 |
rs769492800 | snp | C/T | 1.69289e-05 | 0.00290933 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564629 | CTGCCCTATAGGCCT[C/T]CTTTCATGTACTCTG | 26168 |
rs769578933 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565103 | TCCTTGAAAGAAGGG[C/G]TGGGGCCTTGGGGAT | 26168 |
rs769862994 | snp | A/G | 4.24403e-05 | 0.00460634 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570785 | TTTCCTGAGGGAGGG[A/G]TATAGGGTGTTGGTG | 26168 |
rs769912044 | snp | A/G | 1.77884e-05 | 0.00298226 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570945 | GCAGGTAAGCAGATG[A/G]TGGGGCCACCTCCCC | 26168 |
rs770109514 | snp | G/T | 1.87282e-05 | 0.00306002 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563669 | CTCCACCCCGGCTGG[G/T]TCTGCTAGGTGCTCT | 26168 |
rs770161757 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566282 | TGAGGCGGAGGTTGC[A/G]GTGAGTCGAGATCCA | 26168 |
rs770348256 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568521 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 26168 |
rs770377561 | snp | A/G | 2.40851e-05 | 0.00347015 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565102 | CTCCTTGAAAGAAGG[A/G]CTGGGGCCTTGGGGA | 26168 |
rs770430582 | snp | A/G | 1.72018e-05 | 0.00293268 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565467 | GTTGCAGCTGATCCA[A/G]TCTTACCAGCGGATG | 26168 |
rs770450277 | snp | A/G | 1.65732e-05 | 0.00287859 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560517 | GGGCAGCCGAAAGCA[A/G]GACGTCTCTGACCGG | 26168 |
rs770514066 | snp | A/G | 1.69818e-05 | 0.00291387 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565503 | CAATGCCATGGTGAG[A/G]GGCTTCCGAGTGGCT | 26168 |
rs770634550 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560721 | CTTTCTCTCTTTTCT[C/T]AGGTGTCTTCCATTT | 26168 |
rs770669994 | snp | C/G | 1.66194e-05 | 0.00288261 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564699 | CGCAGCTTGGCACCC[C/G]CTGATGCCAGCATCC | 26168 |
rs770769909 | in-del | -/CTTT | 3.80923e-05 | 0.00436403 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570864 | CATGTGAAGGGCCTG[-/CTTT]CTTTCTCTTCTCTAG | 26168 |
rs770909869 | snp | A/G | 1.65872e-05 | 0.00287981 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571383 | CCCAGTACTGCAAGC[A/G]TCTGGCCCTGTCTCA | 26168 |
rs770966992 | snp | A/C | 1.65474e-05 | 0.00287636 | utr-variant-3-prime, upstream-variant-2KB, stop-lost, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561005 | ACCCCCTAGACTTTG[A/C]TTTTACGGATATCTT | 26168 |
rs771048564 | snp | C/G | 1.67511e-05 | 0.00289401 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564942 | GCCTCACCCCCTCCT[C/G]TCTCCCTTTCCACCA | 26168 |
rs771093507 | snp | C/T | 1.80465e-05 | 0.00300382 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570957 | ATGATGGGGCCACCT[C/T]CCCTAGCTCTGAAGT | 26168 |
rs771252147 | snp | A/C | 1.65655e-05 | 0.00287793 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560205 | CTTCACAGAGGGCCT[A/C]TTTGGCCCCCTACTG | 26168 |
rs771292206 | snp | C/T | 1.66054e-05 | 0.00288139 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565670 | TGGGGGAGCCCTGTA[C/T]CCATGCCGCACCCTC | 26168 |
rs771349259 | snp | A/G | 1.77839e-05 | 0.00298189 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563695 | GCTCTCATGGCTGAG[A/G]ATGGGGTGAGAGGGT | 26168 |
rs771421264 | snp | C/G | 0.000386138 | 0.0138896 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563593 | CTTTCACCCCAGCAA[C/G]GGGGTGCGACGCCAC | 26168 |
rs771481324 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560110 | TGGGAGAGGCCTACA[A/G]GCCCAAGGATATGGT | 26168 |
rs771563419 | snp | C/T | 3.32044e-05 | 0.00407444 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565677 | GCCCTGTACCCATGC[C/T]GCACCCTCCATGGCA | 26168 |
rs771614740 | snp | C/T | 1.66974e-05 | 0.00288936 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565806 | CCAGAGGAACTTCTG[C/T]AGTTTTAAGCAGCTT | 26168 |
rs771664660 | snp | C/T | 0.000123434 | 0.00785504 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563712 | TGGGGTGAGAGGGTC[C/T]CCACCAGTGCCCTCT | 26168 |
rs771816593 | snp | G/T | 1.64784e-05 | 0.00287035 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560872 | AGCTTGGAAGACCAG[G/T]GTGGGTACATACTGG | 26168 |
rs771993709 | snp | A/C/G | 4.19096e-05 | 0.00457749 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570778 | TGGTGAGTTTCCTGA[A/C/G]GGAGGGGTATAGGGT | 26168 |
rs772047424 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560743 | CTTCCATTTACACCA[A/G]GGGGATATTCTGAGT | 26168 |
rs772090151 | snp | C/T | 3.34387e-05 | 0.00408879 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564645 | CTTTCATGTACTCTG[C/T]CCAACGGTTTTGGGG | 26168 |
rs772142304 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569827 | ATGTTGAGAACTTCC[C/T]GGTAGGATTGTTATG | 26168 |
rs772185329 | snp | C/G | 1.73957e-05 | 0.00294916 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565048 | GAGGACATTTTCCAG[C/G]AGGAGTTTTCCACCC | 26168 |
rs772309908 | snp | A/C | 1.96477e-05 | 0.00313424 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570969 | CCTCCCCTAGCTCTG[A/C]AGTCAGTTGGGTTAA | 26168 |
rs772327518 | snp | C/G/T | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563551 | CACCGGGGCCGGCGG[C/G/T]GGGGCCTCGCACACC | 26168 |
rs772422002 | snp | A/G | 2.50881e-05 | 0.00354167 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563808 | TAAGGTGGGAAAGGG[A/G]TGTGGGGTTGCGGGG | 26168 |
rs772468629 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560204 | GCTTCACAGAGGGCC[C/T]CTTTGGCCCCCTACT | 26168 |
rs772522893 | snp | A/G | 4.96915e-05 | 0.0049843 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571431 | AGCAGGACATGCCCA[A/G]ACTTCGTCGGCAGAT | 26168 |
rs772551289 | snp | A/C | 0.000131872 | 0.00811902 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560404 | GTGTCTCGAGAAGGC[A/C]AAGGAAGGCAGGAGA | 26168 |
rs772576737 | snp | C/T | 3.31203e-05 | 0.00406928 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560508 | GAGCCGTGTGGGCAG[C/T]CGAAAGCAGGACGTC | 26168 |
rs772613487 | snp | A/G | 2.57795e-05 | 0.00359014 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565105 | CTTGAAAGAAGGGCT[A/G]GGGCCTTGGGGATGT | 26168 |
rs772697573 | in-del | -/CGC | 0.000120041 | 0.00774635 | cds-indel, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563448 | AAAACCTGCTCACAG[-/CGC]CGCCGCCGCCGAGCC | 26168 |
rs772850946 | snp | A/G | 0.000166834 | 0.00913175 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563826 | TGGGGTTGCGGGGGA[A/G]GGGTTAGGGAGGGTT | 26168 |
rs772897059 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564207 | GAGTACATCATCTTA[C/G]AGTTGTGAAAGAATA | 26168 |
rs772985765 | snp | C/T | 1.64977e-05 | 0.00287203 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560454 | AAGTATGCCCTCCCA[C/T]CCGGACCGGGCCTAC | 26168 |
rs773043672 | in-del | -/GTACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGC | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566537 | TGGGCATAGTGGCGG[lengthTooLong]GGGAGAATCGCTTGA | 26168 |
rs773081681 | snp | C/T | 1.67307e-05 | 0.00289224 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564538 | CTTCTTGCGGTCTTA[C/T]TTGCATGCATGAGTC | 26168 |
rs773111345 | snp | C/T | 1.65633e-05 | 0.00287774 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570409 | CCACCTGGAGGTGCA[C/T]TGGTCCCTCATCTCT | 26168 |
rs773309586 | snp | A/T | 1.66045e-05 | 0.00288132 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564754 | GGGACCATGTGGCCC[A/T]GGAGCTTTTTCAGGG | 26168 |
rs773341015 | snp | G/T | 3.37024e-05 | 0.00410488 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566978 | GTACCAAAGGGTTAT[G/T]ATGGGGTGAAAAGGT | 26168 |
rs773362469 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560786 | CGGGCAAGGGCGAAA[C/G]TTAACCTCTCTCCAC | 26168 |
rs773504137 | snp | A/G | 6.59261e-05 | 0.00574097 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560098 | AGCTCTTAGGCGTGG[A/G]AGAGGCCTACAGGCC | 26168 |
rs773573277 | snp | C/G | 2.33353e-05 | 0.00341572 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570649 | CAATTGAGAAACTTA[C/G]GGCATCACTTTCTTT | 26168 |
rs773593630 | in-del | -/TT | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567124 | AAGATTAAACGTCTC[-/TT]GTGTGTGTAGGCACT | 26168 |
rs773693076 | snp | C/T | 1.69691e-05 | 0.00291278 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565506 | TGCCATGGTGAGGGG[C/T]TTCCGAGTGGCTTAT | 26168 |
rs773749900 | snp | A/G | 9.05756e-05 | 0.00672901 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563596 | TCACCCCAGCAAGGG[A/G]GTGCGACGCCACAGG | 26168 |
rs773836518 | snp | C/G | 1.70959e-05 | 0.00292364 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565484 | CTTACCAGCGGATGC[C/G]AGGCAATGCCATGGT | 26168 |
rs773841133 | snp | C/T | 1.67964e-05 | 0.00289792 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565548 | GCTGACCATGGATGA[C/T]TTGGGGACCTTGTAT | 26168 |
rs773904707 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570090 | GTTCTTAGCTGCTAA[A/G]TGCTTCTCCCTTTAA | 26168 |
rs773921251 | snp | C/T | 9.43352e-05 | 0.00686722 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563297 | CTTTTGATGCCTCAG[C/T]AAGTGAAGAGGAGGA | 26168 |
rs773922560 | snp | C/T | 1.66037e-05 | 0.00288125 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565672 | GGGGAGCCCTGTACC[C/T]ATGCCGCACCCTCCA | 26168 |
rs774258764 | snp | C/T | 1.6736e-05 | 0.0028927 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564643 | TCCTTTCATGTACTC[C/T]GCCCAACGGTTTTGG | 26168 |
rs774384497 | snp | A/G | 1.6552e-05 | 0.00287676 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561027 | GGATATCTTGCTTCT[A/G]TTCCCCATGGAGCTC | 26168 |
rs774437380 | snp | A/T | 2.38257e-05 | 0.00345142 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563093 | TGAAAGAGACTATAC[A/T]AGGGACCGGGTCCTG | 26168 |
rs774485442 | snp | A/G | 4.01357e-05 | 0.00447953 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570526 | AGAGATGGGCAAAAT[A/G]TGGGGCGGTGCAGTG | 26168 |
rs774489731 | snp | A/G | 5.76087e-05 | 0.00536666 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564554 | TTGCATGCATGAGTC[A/G]ACTGTGTGCATCCCA | 26168 |
rs774552935 | snp | A/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569593 | TCTACAGCTAGGCAG[A/G]ATGATTGGCTCCGGC | 26168 |
rs774580848 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570146 | GGGTTCTCCAGTGTT[C/T]GTTCTGATGTCTCCT | 26168 |
rs774583020 | snp | C/T | 1.80497e-05 | 0.00300409 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570958 | TGATGGGGCCACCTC[C/T]CCTAGCTCTGAAGTC | 26168 |
rs774614689 | snp | A/G | 1.67863e-05 | 0.00289704 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564851 | GCGAGAGGAGCATGT[A/G]ACCTGCGTACAGAGT | 26168 |
rs774738058 | snp | C/T | 3.91742e-05 | 0.00442556 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570837 | AATTGAAGTCCTACC[C/T]CTGGGAGTCTCCATG | 26168 |
rs774762296 | snp | A/G | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571316 | CATCTCATATGAAAT[A/G]TGTAGCACAGGTCCT | 26168 |
rs774834947 | snp | A/G | 0.000214283 | 0.0103487 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560119 | CCTACAGGCCCAAGG[A/G]TATGGTGTCCGAATC | 26168 |
rs774887788 | snp | A/G | 1.64871e-05 | 0.00287111 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560126 | GCCCAAGGATATGGT[A/G]TCCGAATCCAGGATG | 26168 |
rs774954022 | snp | A/T | 0.000435597 | 0.0147516 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566882 | CTTAGTGGGAGAGTC[A/T]GAGGTCTTTTAATTC | 26168 |
rs774954147 | snp | C/G | 7.04387e-05 | 0.00593417 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563726 | CTCCACCAGTGCCCT[C/G]TGGGCCCCCCATGGA | 26168 |
rs774991275 | snp | A/G | 8.88518e-05 | 0.00666468 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563696 | CTCTCATGGCTGAGG[A/G]TGGGGTGAGAGGGTC | 26168 |
rs774999161 | snp | A/G | 5.63301e-05 | 0.00530678 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563818 | AAGGGGTGTGGGGTT[A/G]CGGGGGAGGGGTTAG | 26168 |
rs775177059 | snp | A/G | 1.66131e-05 | 0.00288206 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565678 | CCCTGTACCCATGCC[A/G]CACCCTCCATGGCAA | 26168 |
rs775352322 | snp | A/G | 1.66056e-05 | 0.00288141 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564740 | TGTGTGCAGCATCGG[A/G]GACCATGTGGCCCAG | 26168 |
rs775399824 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560753 | CACCAAGGGGATATT[C/T]TGAGTGTCATAATTC | 26168 |
rs775409281 | snp | G/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564330 | GGTACTATGCTGGGT[G/T]TTTGGCATATAGTGG | 26168 |
rs775415845 | snp | A/C/T | 3.2962e-05 | 0.00405954 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560036 | GTCCTGACCGACACA[A/C/T]TCTCACCTCCAGATG | 26168 |
rs775503370 | in-del | -/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569559 | TTCCCTGCCCTCCCA[-/T]TTCAAAGGCCAGGAA | 26168 |
rs775610064 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561320 | CGGACCCCAGTTTCC[A/G]TCACTATCTCCAGAG | 26168 |
rs775621360 | snp | C/T | 1.71302e-05 | 0.00292657 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563244 | TCCTGGGTCAGGGAC[C/T]ACAGTGCCAGCCAGA | 26168 |
rs775714380 | snp | C/T | 3.32281e-05 | 0.0040759 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570440 | GTTGATGTGAGGCGA[C/T]GCACCATCACCTATT | 26168 |
rs775728169 | snp | C/T | 1.67019e-05 | 0.00288975 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564952 | CTCCTCTCTCCCTTT[C/T]CACCAGGCATCTTGG | 26168 |
rs775760057 | snp | A/G | 0.000160685 | 0.00896196 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563103 | TATACAAGGGACCGG[A/G]TCCTGGGGGCCTGAG | 26168 |
rs775771147 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571748 | GGGTGGAGCAGTCAT[C/T]CTCCCCCTTCCCCGT | 26168 |
rs775886964 | snp | C/T | 1.68213e-05 | 0.00290006 | stop-gained, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564861 | CATGTGACCTGCGTA[C/T]AGAGTAAGGAGCCCT | 26168 |
rs775980192 | in-del | -/CCC | 1.80383e-05 | 0.00300314 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570957 | ATGATGGGGCCACCT[-/CCC]CTAGCTCTGAAGTCA | 26168 |
rs775995631 | snp | A/G | 1.658e-05 | 0.00287919 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560217 | CCTCTTTGGCCCCCT[A/G]CTGAGGGTTCCTGAC | 26168 |
rs776033385 | in-del | -/CT | 5.34631e-05 | 0.00516998 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564415 | GTCTATGAGTAGGAA[-/CT]CTCTCTCTCCATCCC | 26168 |
rs776093028 | snp | A/G | 1.66112e-05 | 0.00288189 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560311 | CCCAGAACTGAGCCA[A/G]GCCATCCTGTTTTCT | 26168 |
rs776112197 | snp | C/T | 4.02666e-05 | 0.00448683 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570976 | TAGCTCTGAAGTCAG[C/T]TGGGTTAAAGGGTCG | 26168 |
rs776150190 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560445 | ATGTATAAGAAGTAT[A/G]CCCTCCCACCCGGAC | 26168 |
rs776274567 | snp | G/T | 0.000347222 | 0.0131716 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563841 | GGGGTTAGGGAGGGT[G/T]AAGAGCCTGGAGCAC | 26168 |
rs776289126 | snp | A/G/T | 1.65803e-05 | 0.00287922 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571467 | AGGAGCTGTGTCACT[A/G/T]CAAACTCACTGTGTG | 26168 |
rs776329218 | snp | A/C/G | 0.000182624 | 0.00955428 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563820 | GGGGTGTGGGGTTGC[A/C/G]GGGGAGGGGTTAGGG | 26168 |
rs776501718 | snp | C/T | 7.55487e-05 | 0.00614562 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566941 | GGTGCATTTCTTCAA[C/T]AGTTTCTTCTATGAT | 26168 |
rs776729674 | snp | C/G | 2.36712e-05 | 0.00344021 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570631 | TACCCACCATACTGT[C/G]TTCAATTGAGAAACT | 26168 |
rs776789208 | snp | A/G | 5.00973e-05 | 0.00500461 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564649 | CATGTACTCTGCCCA[A/G]CGGTTTTGGGGGACA | 26168 |
rs776880259 | snp | C/T | 1.81345e-05 | 0.00301113 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563271 | CAGACGCCTCCCTGT[C/T]CCCCGACCCTCTTTT | 26168 |
rs777107965 | snp | C/T | 4.07822e-05 | 0.00451547 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565077 | CCCTTCCAGGTGAGG[C/T]TTGAAAGCCCTCCTT | 26168 |
rs777233980 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571830 | TGCCTGCCAGATCTT[A/C]AAACTTTTATATATA | 26168 |
rs777251721 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564200 | AGTAGTGGAGTACAT[C/T]ATCTTACAGTTGTGA | 26168 |
rs777356735 | snp | A/G | 1.6817e-05 | 0.0028997 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564635 | TATAGGCCTCCTTTC[A/G]TGTACTCTGCCCAAC | 26168 |
rs777375512 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560709 | ACTGCGAATCTACTT[C/T]CTCTCTTTTCTCAGG | 26168 |
rs777389768 | in-del | -/T | 2.09325e-05 | 0.00323509 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570677 | TTTCCCCCATCCACA[-/T]TAGCATATTGCCAAG | 26168 |
rs777533494 | snp | A/G | 0.000101776 | 0.00713286 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563376 | TTGGAGGCTGCCCCC[A/G]AGATGGAGTCAGCTG | 26168 |
rs777617410 | snp | A/T | 1.8571e-05 | 0.00304715 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565403 | GTGTGCCCCAGCTGC[A/T]TCATCTTTTGTGTGA | 26168 |
rs777633328 | snp | A/C | 0.000196456 | 0.00990906 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570722 | GGCGGTAAAGAAAGA[A/C]CGACTGGATTTCCAC | 26168 |
rs777723390 | snp | A/G | 1.90297e-05 | 0.00308455 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570506 | AAGGTTTGAGGGGGT[A/G]GGAGAGAGATGGGCA | 26168 |
rs777758195 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569465 | GGAGGATGATGCCTA[C/G]GTTTTTGGCCTATGT | 26168 |
rs777801347 | snp | A/G | 3.30732e-05 | 0.00406638 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570950 | TAAGCAGATGATGGG[A/G]CCACCTCCCCTAGCT | 26168 |
rs777854212 | snp | A/C | 0.000149757 | 0.00865193 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571367 | GCTTGCTTTGTTAAC[A/C]CCCAGTACTGCAAGC | 26168 |
rs777968016 | snp | A/G | 1.6808e-05 | 0.00289892 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565627 | CTGAGAGGGGATTCA[A/G]GGAGCAGGGTGTCTG | 26168 |
rs777986960 | snp | C/T | 1.65468e-05 | 0.00287631 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560195 | ACACTCTGAGCTTCA[C/T]AGAGGGCCTCTTTGG | 26168 |
rs778040779 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560355 | TCCCTGCCAGGTCCT[A/G]TTTCAAGACGTGACT | 26168 |
rs778075922 | snp | C/T | 1.88258e-05 | 0.00306799 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563787 | TCCTCTGGACCCTGA[C/T]TCGGGTAAGGTGGGA | 26168 |
rs778088769 | snp | A/G | 1.64784e-05 | 0.00287035 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560843 | CTGTGATTGTGTTAT[A/G]AAAAGTGGCTCCCAG | 26168 |
rs778222193 | snp | C/T | 1.65976e-05 | 0.00288072 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565771 | CCTGAAAAGGTAGGC[C/T]CAACCAGATAGGTCA | 26168 |
rs778388988 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567818 | GGGGGGATTTTATTG[C/T]GTGTATACTGAGAAG | 26168 |
rs778476837 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565862 | TTTACACAGAGAGGG[C/T]CTCTGTTTCAGGGAG | 26168 |
rs778595770 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569585 | AGGAAATTTCTACAG[C/T]TAGGCAGGATGATTG | 26168 |
rs778604872 | snp | A/G | 7.86411e-05 | 0.00627012 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563049 | AGATTTTGATACCCT[A/G]ATCTTTTGTTTTTCA | 26168 |
rs778646074 | snp | C/T | 1.6708e-05 | 0.00289028 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564821 | TGGGGAGAAAGCCGG[C/T]CAGCACAGCCCCCTG | 26168 |
rs778684960 | in-del | -/TTTGT | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569094 | TAGTAGGAAAGAAGA[-/TTTGT]TTTTTTGCCGGGCGC | 26168 |
rs778704570 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570619 | CTGCCAGCACTGTAC[C/T]CACCATACTGTGTTC | 26168 |
rs778802602 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561113 | AGACCTGGTCGGGGC[C/T]CACTGGAAGCATCCA | 26168 |