SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs140102596 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35097276 | TCTTTGGAAAAAGCA[G/T]CCAGATGCATCTGTG | 8453 |
rs140165922 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CUL2 | GRCh38.p7 | 10:35053912 | TCAATAAAGATGTAT[C/T]AAATGAATAAACAAG | 8453 |
rs140177507 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114567 | TTTGTATTTTTAGTA[G/T]AGACAGGGTTTCGCT | 8453 |
rs140182820 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35029709 | ATTGGTTAATAATAA[C/T]GTGTCGGTATTGCTA | 8453 |
rs140231917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35049256 | GAATTAGGCAAGTTA[C/T]TGATTATAACACTGA | 8453 |
rs140245456 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CUL2 | GRCh38.p7 | 10:35123043 | CTCAGGAGGCTGAGG[C/T]GGGAGGATTGCTTGA | 8453 |
rs140246869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069640 | ACTGAAGGGGTCACT[C/T]TCCAGGGAAGTAATC | 8453 |
rs140248793 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021530 | ATACATGTTTATATT[-/A]AATGTCAATTTTAAT | 8453 |
rs140270825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35048887 | GAGTCCCATACTAAA[C/T]ACCACGGCTTTGACA | 8453 |
rs140315330 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | CUL2 | GRCh38.p7 | 10:35114056 | GGGACTACAGGTGCC[C/T]GCCACCACACCTGGC | 8453 |
rs140436110 | snp | C/G | 0.00145847 | 0.0269649 | missense | CUL2 | GRCh38.p7 | 10:35033264 | CTGACTCCACAAATA[C/G]TGTTGGCATCTAAAA | 8453 |
rs140445558 | in-del | -/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009070 | GTCTCTTATTTTTTT[-/T]AAAATAAAGAAAAAT | 8453 |
rs140460398 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL2 | GRCh38.p7 | 10:35050638 | TGTGAAACCCATCCA[A/G]TGGAAACATACAGCC | 8453 |
rs140511463 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35086581 | CCTGAGCCACCGTAC[A/G]TGGCCGGAAACAGCT | 8453 |
rs140526714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046261 | ACATGCGTGACCTCA[A/C]ATAAGCCCACATTCA | 8453 |
rs140526934 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35098200 | TTTATATTTCTTTGC[A/T]GTCACTTTTAGACAG | 8453 |
rs140557038 | in-del | -/GAGCCCAGGAGTTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030812 | GCGGGAGGATCGCTT[-/GAGCCCAGGAGTTA]GAGTCCAGCCTGGGC | 8453 |
rs140595641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035811 | GTTACTGTGTCAAAG[C/T]TTAATCTTGTAGACA | 8453 |
rs140596254 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35117818 | TTCTAAAATTACACT[C/G]CATTACATGTATTTT | 8453 |
rs140636399 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CUL2 | GRCh38.p7 | 10:35055374 | GAAGGGTCCACTCAG[C/T]ATTTACAGACAAATT | 8453 |
rs140651281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35081829 | GCCCAAGATGTGACC[A/G]CACCACTACAATCTA | 8453 |
rs140660485 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35113306 | TTCGTGACCAGCCTG[A/G]CCAACATGGTGAAAT | 8453 |
rs140685173 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35027189 | TCGCTCTATCACCCA[A/G]GCTAAAGTGCAGTGG | 8453 |
rs140730307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35111703 | GACCAGCCTGGCCAA[C/T]ATGGTGAAAACTGGT | 8453 |
rs140809447 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35056414 | TTATGTGGCTGAATA[C/T]TATAAGACAGATGTA | 8453 |
rs140820266 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35076712 | TCTGTTTTACATAAA[C/T]GGTATACTATTCAGA | 8453 |
rs140838578 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35073086 | AAGGAATCCCAGGAA[C/T]AGACTCCATGGAAAA | 8453 |
rs140908828 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008547 | TATTTAAGAAAAAAA[G/T]GAATCAATTTGGAAA | 8453 |
rs140997018 | snp | C/T | 5.19206e-05 | 0.00509486 | missense, intron-variant | CUL2 | GRCh38.p7 | 10:35049707 | TCTCGGAGCAGCATT[C/T]GGATAAGGATGGCCT | 8453 |
rs141009035 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35043864 | TCAAGTTGAGGAGTT[C/G]TGAGACCAGCCTGGG | 8453 |
rs141060026 | snp | A/G | 0.000153988 | 0.00877328 | missense | CUL2 | GRCh38.p7 | 10:35011903 | TTCATGATACGAACT[A/G]TAGCAGCTTGGAGAT | 8453 |
rs141067588 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092192 | ACTCCTGAGCTCAAG[C/T]GATCTGCCCACCTCA | 8453 |
rs141130302 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35020401 | TACTAACATCCCTCC[C/T]TATTTTTAGCTGTTG | 8453 |
rs141143156 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CUL2 | GRCh38.p7 | 10:35094503 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGGGA | 8453 |
rs141171687 | snp | A/C | 0.00993419 | 0.0697739 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008133 | TCCTTTTTCCTTTTC[A/C]TAGCTCTGAGCTGTT | 8453 |
rs141177816 | snp | G/T | 0.254385 | 0.249962 | intron-variant | CUL2 | GRCh38.p7 | 10:35093583 | AGAATCACTTGAACC[G/T]GGGAGGCAGATGTTG | 8453 |
rs141211442 | snp | C/T | 0.000592613 | 0.0172033 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35028849 | CTGGGGAATTGCAAA[C/T]GTAGATGAAGGAGCC | 8453 |
rs141222936 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35089773 | TGCAGTCTGCGGAAA[C/T]AAAAGTGAAAACACT | 8453 |
rs141242692 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119585 | TTATTTATTTATTTA[-/T]TTATTTATTTATTTA | 8453 |
rs141242730 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35087310 | TGAATACAGTTTTTG[C/T]TCAAAACATTAGTAT | 8453 |
rs141283609 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35014206 | TTTTTTTACAAATGC[C/T]GCAGTAACAAAATAC | 8453 |
rs141320035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35012210 | AGGTATGCACCACAA[C/T]ATTGAGCAAATTATA | 8453 |
rs141347911 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35061897 | ACAGGTGTAAGCCAC[C/T]GCACCAGGCCAGTTC | 8453 |
rs141378448 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35084000 | ATATAAAAGAGGCCA[A/G]GCACAGTGGCTCACA | 8453 |
rs141415543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079250 | CACTGTGCTGTACTC[A/G]CCCTTCTTGTGAAGG | 8453 |
rs141498630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35024802 | CAAGAGGATCTGGCA[C/T]ACTTAGAGAACAAGT | 8453 |
rs141607566 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35062793 | AGTGAGCCATGATCG[C/T]GCCACTGCACCCTAG | 8453 |
rs141698647 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35045456 | TGGTGGCACACACCT[A/G]TGGTCCCAGCTACTC | 8453 |
rs141701847 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CUL2 | GRCh38.p7 | 10:35047490 | TGGTGCGCGTCTGTA[A/G]TCCCAGCTACTCGGG | 8453 |
rs141707528 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35021537 | TTTATATTAATGTCA[A/G]TTTTAATGTATGAAT | 8453 |
rs141735406 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CUL2 | GRCh38.p7 | 10:35046854 | GCCAAGATCGTGCCA[C/T]GGCATTCTAGCCTGG | 8453 |
rs141769428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042990 | CTGGAGGACACCTAG[C/G]TGGTGTCTGCTGCTT | 8453 |
rs141770618 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35040301 | TATCAACAAGAACTA[G/T]CCCATAAGGAAAATA | 8453 |
rs141836921 | snp | C/T | 1.66114e-05 | 0.00288192 | missense | CUL2 | GRCh38.p7 | 10:35044631 | CTTGTTTGTAATACT[C/T]TCCTGTTTCAGTCAG | 8453 |
rs141890709 | in-del | -/C | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074319 | TCTCCTCCTGGTACT[-/C]CCTACTGTGACATCA | 8453 |
rs141944375 | snp | A/G | 0.00279162 | 0.0372561 | missense | CUL2 | GRCh38.p7 | 10:35100968 | CATGGGTTTTCGTCC[A/G]TGTCCTTTGCCACCT | 8453 |
rs141945227 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35116470 | TAGATAAGCTGAAAA[G/T]ATCTATATCTATTGT | 8453 |
rs141957162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032317 | TATACAATGTAGATA[A/C]TTTTCCTTCTATTTT | 8453 |
rs142066561 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081185 | AAGCTACAATGGCAC[C/T]ACCACACTCCAGCCT | 8453 |
rs142073543 | in-del | -/AGAGC | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35045402 | CCTGGGCAATAGAGC[-/AGAGC]GAGACCTCATTCAAA | 8453 |
rs142108199 | in-del | -/TT | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35082740 | TTGGTTCAGACAGAC[-/TT]TTATCAAATAAAAGA | 8453 |
rs142121016 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CUL2 | GRCh38.p7 | 10:35022173 | AAGTACCTGAGACAT[A/G]GAAAATGTTCTTTGA | 8453 |
rs142129431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108524 | TTGTGGGAAAGACAG[A/G]GAGAAATGAAAAATT | 8453 |
rs142138525 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35112239 | AACTCTGCTTTCAGC[A/G]AAGATGGAAAGACCA | 8453 |
rs142140457 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35059120 | CTACTCCTAATAAGA[C/T]GGTATGAACATTGTT | 8453 |
rs142152605 | snp | C/T | 0.254385 | 0.249962 | intron-variant | CUL2 | GRCh38.p7 | 10:35105639 | CTTGACCCCGGGAGG[C/T]AGAGGTTGCAGTGAG | 8453 |
rs142165581 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35028947 | TCTAAATTCAAAGTA[A/G]ATATTTATTAAATAA | 8453 |
rs142170496 | snp | C/T | 0.0611083 | 0.163768 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075511 | GTCCCATCAAGTTAA[C/T]TGCAAAAATCCAAAT | 8453 |
rs142186259 | snp | A/C | 0.254664 | 0.249956 | intron-variant | CUL2 | GRCh38.p7 | 10:35018589 | ACCAACATGGAGAAA[A/C]CCCGTCTCTACTAAA | 8453 |
rs142269717 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | CUL2 | GRCh38.p7 | 10:35065863 | ACACCATCTCAAAAA[A/C]GAAAAAAAACACAAA | 8453 |
rs142283877 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35065085 | TTGGGTCTCAAATCA[C/G]TGTATAATTTTAACC | 8453 |
rs142308365 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050335 | CTCAAAAAAAAAAAA[A/C]AAACTTAATTTTTTG | 8453 |
rs142366341 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023610 | GTTGTTAAAATGAGC[C/T]CCTTACTAAAATTAC | 8453 |
rs142476156 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35010931 | CCAGGGACCAGCCCA[A/G]CTGTCTATCACATGG | 8453 |
rs142495023 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35085520 | GACACTGAGGAAGGC[A/G]GACCACAAGGTCAGG | 8453 |
rs142558045 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35082690 | TGCATTCTAATCAAA[A/G]TAATACTTGGTACTA | 8453 |
rs142567889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084329 | AATTCTCCAGAATAA[C/T]AAAGCTTAAAGCAAA | 8453 |
rs142604835 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35072929 | TCTCGTCTCCCATCA[C/T]AGGGGAAAGGGGAGG | 8453 |
rs142637339 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35119241 | ATCTTGGAGGAGGTA[A/G]GGCTCAGTTTCAGCT | 8453 |
rs142649231 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021567 | TATGTATTAAATAAA[A/G]ACCCATTTCATTTAC | 8453 |
rs142689942 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35042095 | TATGTTGTGTAATCA[C/G]CCCCATTGTCTACTT | 8453 |
rs142765484 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35056831 | CCATTCCAGTAACCT[C/T]GCCTAAAACATCAGA | 8453 |
rs142773079 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35105920 | ACAATGTACTTTACA[C/G]ATAGATAGCTAGGAA | 8453 |
rs142811993 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009108 | TGAGGGAGGAGGGGT[A/G]TGGTGGTGGTGGTGA | 8453 |
rs142857403 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35117927 | GGTGCACAGCAAAAA[C/T]GAGCAGAAAGTACAC | 8453 |
rs142857963 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092596 | TGACTTACAGGCTGA[A/G]CTACCTGCATTTTTC | 8453 |
rs142903918 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070941 | TATAATAGAAAGGAA[-/T]TTTTTTTTGTTCACC | 8453 |
rs142949763 | snp | A/G | 6.59598e-05 | 0.00574243 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071249 | TTCCAACATGACCAC[A/G]GCTTTTATTGTCGTC | 8453 |
rs142962074 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CUL2 | GRCh38.p7 | 10:35065573 | GCAGTGAGCCAAGAT[C/T]GCACCACTGCACTCC | 8453 |
rs142992837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35054200 | TTTCACAATGCAGAA[C/T]CATTAACTCTATCAT | 8453 |
rs142998594 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | CUL2 | GRCh38.p7 | 10:35117442 | ACTATGTTTCCCAGT[C/G]TGGTCTTGAACTCCT | 8453 |
rs143019671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35068676 | CATAAATGCATGCTA[A/G]AAGTTCAAATAATAA | 8453 |
rs143036133 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017141 | CTCCTGGGAGGTCCA[-/C]CAGCCACATGGAAAA | 8453 |
rs143064995 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35019231 | TCACTGATGCTGTAA[C/T]ATGCTGCCGTGGGTT | 8453 |
rs143142909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037293 | ACCATCTTTTACCTG[C/T]CGCTCTGCAGCGCCA | 8453 |
rs143146246 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35121817 | CCTGTCTCAAAAAAA[A/T]AAAAAAAAATAAAAA | 8453 |
rs143148255 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124490 | AATAACAAACAAATG[G/T]GTGGTGAAGAAGTGA | 8453 |
rs143159515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098283 | GCCCACTATTTGAGA[C/T]AGATAACTCACTATT | 8453 |
rs143159534 | in-del | -/TTTA | 0.313326 | 0.241847 | intron-variant | CUL2 | GRCh38.p7 | 10:35119561 | GGTTTTAAAATTAAT[-/TTTA]TTTATTTATTTATTT | 8453 |
rs143160816 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35035565 | ACAGTGTACTGTATT[G/T]TGTATATTATTTGTA | 8453 |
rs143237887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128212 | TCACTTAGGGGTTTC[A/C]TGCATGCTGCTCAGT | 8453 |
rs143257978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041835 | AGCCACCGTGCCCAG[A/C]CTGAAATAAGCTTTT | 8453 |
rs143277896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35096512 | CAGCTACTCTGGAGG[C/T]TGAAATGGGAGGATC | 8453 |
rs143367908 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124235 | GTAGTATCTGATGAG[A/G]AAAATAGGTCAAGTA | 8453 |
rs143376723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35010579 | GTATGAAAATAGGAA[A/C]TACAATGTGGAAAAT | 8453 |
rs143413651 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35096007 | AATCCCAGCACTTTC[A/G]GAGTCCGAGGCGGGT | 8453 |
rs143434966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023254 | CTTATCAAAGTTGGG[A/G]AGAAAAACAACTCTA | 8453 |
rs143437940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110271 | CTGGGTGGATTAAAG[A/C]ATAGAAATTTATCCA | 8453 |
rs143476139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35095581 | TATATATTTTTGAGA[C/T]AGAGTCTCCCTCCGT | 8453 |
rs143479297 | snp | A/T | 0.000153988 | 0.00877328 | missense | CUL2 | GRCh38.p7 | 10:35029597 | ACACTCATATCTGTA[A/T]ACATCCGATGTAGCT | 8453 |
rs143565298 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CUL2 | GRCh38.p7 | 10:35097421 | CTTGAGTTCAGGAGA[C/T]TGAGATTGCAGTGAA | 8453 |
rs143589800 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CUL2 | GRCh38.p7 | 10:35055827 | CTGAGTTTCCAACCA[C/T]GCCTTCCAGCTAAGG | 8453 |
rs143660953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101329 | CCAGTTGCTTTCAGC[A/G]TGGAGACAACGGGTC | 8453 |
rs143680505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35083454 | GGCAATGGGCACACA[C/T]AGAACTTAGATCTTG | 8453 |
rs143729753 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35016468 | ACTTTATTTCAGACA[C/T]TTTCTTCGGAAAGAG | 8453 |
rs143752297 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35031690 | CTCAAAGGAGGCAAA[G/T]TGGTGATACAAGGTA | 8453 |
rs143786549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35077898 | GCTGTCTGAAATCTG[C/T]TTCACAATTAAACAG | 8453 |
rs143825235 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074724 | CTCCTGAGGCTCAAG[A/T]GATCCGCCCGCCTTG | 8453 |
rs143838436 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125391 | AGAGCAAATACTTTG[C/G]AAATAAGAAATTGCC | 8453 |
rs143899262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35010621 | AATCTAATAATGATA[C/T]ATAATTAAGTGAAAC | 8453 |
rs144025429 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080857 | GCAGGAAAACATCTT[C/G]AAGTCTCAAAAAGGG | 8453 |
rs144074830 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126621 | TCGAGACCCTGAAGA[C/T]CTGACAACAGCCGTT | 8453 |
rs144191257 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35055470 | AGGCGTCGGGGCTCA[C/T]GCCTGTAATCCCAGT | 8453 |
rs144207791 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35049097 | TCTTTGAGCCAGAGC[C/T]AATCCAAGGATGTTC | 8453 |
rs144258009 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35059473 | ATTTTTTTTAGCAAT[A/G]AAGTAATTTTAAATT | 8453 |
rs144296249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35112931 | AGGCGTGGTGGCTCA[C/T]GTCTGTAATCCCAGT | 8453 |
rs144309375 | in-del | -/AAATAAAT | 0.0679481 | 0.171339 | intron-variant | CUL2 | GRCh38.p7 | 10:35086720 | GCGAACACCATCTCA[-/AAATAAAT]AAATAAATAAATAAA | 8453 |
rs144388001 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35113593 | ATCTACGAAAAATTA[C/G]CAAGAATGCAAAGAA | 8453 |
rs144406968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35012025 | CACTGAACTTGTTTT[C/T]AATTCATTTTATCAG | 8453 |
rs144457250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35084845 | TGATAGTTGGACAGG[C/T]CTGGTGGCTCACACT | 8453 |
rs144457852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109400 | AGGTGCTGGGCACAA[C/T]ATTTGTAGGGTCCTT | 8453 |
rs144479573 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35067277 | AACAATCATTTTGGA[C/G]TTACTATAACCTTTA | 8453 |
rs144608290 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35030446 | GGAGTGCAGTGGTAT[A/G]ATCATGGCTCACAGC | 8453 |
rs144629321 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35034001 | GTTAAAAAGCCAATA[A/G]TCCTGAGAACAGAGA | 8453 |
rs144630025 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35115516 | AGTGAGCTGAGATCG[C/T]GCCACTACACTCTAG | 8453 |
rs144630361 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113223 | TTCAGCGGCCAGGTG[C/T]GGTGGCTCACTTCTG | 8453 |
rs144633778 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35118055 | ACATCATAATCATCC[A/G]AAGTGCATACATTAG | 8453 |
rs144799361 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092360 | GCCACCAACCTGTCC[A/G]GGTGGTCATTGGATC | 8453 |
rs144815058 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35015471 | TGAATTAATGAGAGA[A/C]ATAAACTGTAGGCTA | 8453 |
rs144819334 | snp | A/G | 0.000798403 | 0.0199641 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35100951 | TTTTCTTTCCATGTC[A/G]CCATGGGTTTTCGTC | 8453 |
rs144863577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35085865 | GCTTTTTACAGCGAG[G/T]GAGGAAGGGCATAAG | 8453 |
rs144908150 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35043769 | GTACTGGTTTAGTGA[C/T]CAATTAAAATTTCTT | 8453 |
rs144926221 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071227 | TCCATGTTGCTCTTT[C/T]GACGTATTCCAACAT | 8453 |
rs144941198 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114591 | TTTCGCTATGTTGGC[C/T]AGGCTGGTCTCGAAC | 8453 |
rs144942239 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068412 | AAAAAGAACTACAAC[A/G]CACTATGTCTAATAA | 8453 |
rs144949337 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | CUL2 | GRCh38.p7 | 10:35114423 | GTCTTGCTCTTGTCA[A/C]CCAGGCTGGAGTGCT | 8453 |
rs145000075 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008244 | GACTTCAATCTCCTG[A/G]CCTAACTTGACAAGA | 8453 |
rs145037677 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090991 | CAAACTCTTTTTCTT[C/G]TTAGTTTTTATCTAC | 8453 |
rs145140514 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35111735 | TCTACTAAAAGTGAA[A/C]AAATTAGCTGGGCGT | 8453 |
rs145146631 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35024113 | GTGCTGGGGTTACAG[A/G]TGTGAGCCACTGCAC | 8453 |
rs145177144 | in-del | -/TGAGG | 0.20511 | 0.245937 | intron-variant | CUL2 | GRCh38.p7 | 10:35047701 | GAAAGTTGGATCTCT[-/TGAGG]TAGGAGCTCGAGACC | 8453 |
rs145243674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35097256 | TACTGAACTTCCTGC[A/G]AACCTCTTTGGAAAA | 8453 |
rs145244350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35068298 | ATGGTGGCGGGCACT[C/T]TTAATCCCAGACACT | 8453 |
rs145308183 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038425 | CAGCTACTCAGGAGT[C/T]TGAGGCAGGAGAATC | 8453 |
rs145319498 | in-del | -/TTTCT | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35041546 | GAGCTTTTCTTTTTC[-/TTTCT]TTTGTCAGACAGGAT | 8453 |
rs145366778 | snp | C/G | 0.0140354 | 0.0825875 | intron-variant | CUL2 | GRCh38.p7 | 10:35049676 | TAAGATAAATGTCAG[C/G]ACTCACTTTTTGATT | 8453 |
rs145410963 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35124217 | ATAAGGCAGTAGTCA[C/T]TGGTAGTATCTGATG | 8453 |
rs145509225 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35022513 | GAGAGATCTGTCCAG[C/T]CTCAGAGCCAGTGTT | 8453 |
rs145513036 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35087418 | ATTTTTTAACCACTA[C/T]ATCCACACATCTGGT | 8453 |
rs145520682 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35038397 | CAGGTGTGGTGATGA[A/G]CGCCTGTAATCCCAG | 8453 |
rs145595932 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35017437 | GGTAGCTTATGCCTG[C/T]AATCCCAGCACTTTG | 8453 |
rs145619962 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CUL2 | GRCh38.p7 | 10:35101703 | TCAGTTCCAAACTAA[C/T]CTTTTGTATCATTCA | 8453 |
rs145631132 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35085051 | CTTAAATGCCAGAGG[C/T]GGAGAATGCAGTCAG | 8453 |
rs145660510 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35050683 | GGCACTGCTATACAG[A/C]ATCCTGTTGCATAAA | 8453 |
rs145664387 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021628 | CTTTCATTTATTATT[A/T]TTTATTTTCATTTAT | 8453 |
rs145722929 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CUL2 | GRCh38.p7 | 10:35013126 | CGGGCGGATCACGAT[A/G]TCAGGAGATCGAGAC | 8453 |
rs145824714 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35102749 | TTAGCCGGGTGCAGT[A/G]GCAGGCGCCTGTAAT | 8453 |
rs145831270 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092536 | CACATGCACTTCTGC[A/C]TGCCAAAGTGGGATG | 8453 |
rs145837030 | in-del | -/T | 0.254105 | 0.249966 | intron-variant | CUL2 | GRCh38.p7 | 10:35092789 | CCCTAAAACTACCCC[-/T]GCTCTTGCTTAGGGA | 8453 |
rs145852897 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35069831 | TTTTAGCTAAAATAT[C/T]CTTAAAAGCACCTAT | 8453 |
rs145868556 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35077298 | GACTCCGTCTCAAAA[A/C]AAAAAACAAAAAACA | 8453 |
rs145957894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084444 | AATCTTAACCTAACA[C/T]TACTACTGTCTCAAA | 8453 |
rs145994688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042148 | TCAGAAACTTTATAA[C/T]CATTAAGTAACAACT | 8453 |
rs145998192 | in-del | -/C | 0.206336 | 0.246157 | intron-variant | CUL2 | GRCh38.p7 | 10:35117090 | GAGTATTTTTGAATT[-/C]TATCGAAGAGTTGAG | 8453 |
rs146013838 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CUL2 | GRCh38.p7 | 10:35037918 | CAGCACTTCGGGAGG[C/G]CGGGGCAAGCAGATT | 8453 |
rs146014357 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35088444 | ACTGGGAGGTTGCAG[A/T]GAGCCCAGATCGTGC | 8453 |
rs146027574 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | CUL2 | GRCh38.p7 | 10:35056493 | GAGGTTAAAGAGCTT[C/G]CCAAAGGTCAATCGG | 8453 |
rs146117281 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35021556 | TAATGTATGAATATG[C/T]ATTAAATAAAAACCC | 8453 |
rs146137705 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35016122 | ACAGCCTTATTTTAA[A/G]ACTGCAAACATCTCA | 8453 |
rs146157778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35104520 | TATTTATTTTGATTG[C/T]CTAGAACCTTGGTGT | 8453 |
rs146278820 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35084231 | GCAGTGAGCTGAGAT[C/T]GCGCCACTGCACTAC | 8453 |
rs146330095 | snp | C/G | 0.254385 | 0.249962 | intron-variant | CUL2 | GRCh38.p7 | 10:35105644 | CCCCGGGAGGCAGAG[C/G]TTGCAGTGAGCCGAG | 8453 |
rs146372843 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35112397 | GACTCCTACAATTGA[C/G]CCAGCTTACTGTCTG | 8453 |
rs146373248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35059187 | TAGCTGATAAGGTGG[C/T]GGCAGGGTTTGAGAG | 8453 |
rs146434757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35076585 | CGTGTACGACCTCAT[C/T]GCCACCTCCCATTGA | 8453 |
rs146441125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35034459 | AGCTAAGGTAACAGC[C/T]TCTAAAAAGTGCTCC | 8453 |
rs146444553 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021622 | TTCCTTCTTTCATTT[A/T]TTATTTTTTATTTTC | 8453 |
rs146459354 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CUL2 | GRCh38.p7 | 10:35030029 | TTGCCCATGCTGCAA[C/T]GCAGTGGCTATTCAT | 8453 |
rs146460678 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080878 | TCAAAAAGGGTGACA[C/T]GGTGGGGAGTAGGGA | 8453 |
rs146467338 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35082846 | ATTATTTTGGTAACT[A/C]TACACTTACATAATT | 8453 |
rs146558019 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35055503 | TTTGGGAGGCTGAGG[C/T]GGGAGGATCACTTGA | 8453 |
rs146565928 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35012119 | AGTTCAGTGACTCGC[C/T]CTCAGCTCACCGCAA | 8453 |
rs146579745 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35078728 | GGTGTTTTGTATTTT[A/C]CTTACCTTCTAAAAG | 8453 |
rs146584372 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35059480 | TTAGCAATAAAGTAA[C/T]TTTAAATTAAGTTGT | 8453 |
rs146653935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122084 | TGCCAAATGGCAAAT[A/C]AAAGACATCATAAAT | 8453 |
rs146691741 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075855 | TATGCATGATTGTCA[A/G]TAATAATTACAAAAG | 8453 |
rs146797609 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CUL2 | GRCh38.p7 | 10:35097911 | TTGCAGTGAGCCACA[A/G]TCATGCCACTGCACT | 8453 |
rs146812977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054753 | CCTTACAATACCCTT[A/C]TAGCCCAACAGCTCT | 8453 |
rs146846826 | in-del | -/AAG | 0.468047 | 0.122292 | intron-variant | CUL2 | GRCh38.p7 | 10:35049501 | AAAGAAAAAAAAAGA[-/AAG]AAGAAGAAGAAGAAG | 8453 |
rs146856364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037055 | CAATCGTTCCTTTGT[A/G]GTTAGGGCTTTTTGT | 8453 |
rs146871552 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35115927 | TAAATAAATGTTGAT[A/T]CTTTGAAGAGAGCAA | 8453 |
rs146929643 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021535 | TGTTTATATTAATGT[C/T]AATTTTAATGTATGA | 8453 |
rs146949667 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | CUL2 | GRCh38.p7 | 10:35061906 | AGCCACCGCACCAGG[C/G]CAGTTCTTACCATTT | 8453 |
rs147061473 | in-del | -/A | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009992 | CCTTTAAGATACATT[-/A]AAAAAAAAAAAAAAG | 8453 |
rs147066513 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35124715 | AAGGAGCCAAGAGGA[C/T]GAAAAAGGCTGTAGG | 8453 |
rs147082630 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35081999 | TCTTGACACCTCCTG[C/T]TTACAATCCCAAAGA | 8453 |
rs147146977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096292 | GAGCTTACAAAAGTG[C/T]GAGTCTCTTTAAAGA | 8453 |
rs147185728 | in-del | -/AT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050646 | CCATCCAGTGGAAAC[-/AT]ACAGCCATAGCTCAA | 8453 |
rs147208583 | snp | G/T | 0.268452 | 0.249318 | intron-variant | CUL2 | GRCh38.p7 | 10:35027324 | TAATTTTTTCTATTT[G/T]TAGTAGAGACGGGGT | 8453 |
rs147241096 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35026595 | GTAAAGTTTTATTGA[C/T]GATAATATCAATATG | 8453 |
rs147257983 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074737 | AGTGATCCGCCCGCC[C/T]TGGCCTCCCAAAGTG | 8453 |
rs147263895 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021621 | CTTCCTTCTTTCATT[A/T]ATTATTTTTTATTTT | 8453 |
rs147323023 | snp | A/G | 0.0456336 | 0.143994 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091796 | CGGCTAATTTTTTGT[A/G]TTTTGTAGAGACAGG | 8453 |
rs147364097 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053199 | CTGGGAAGAGAAGTG[A/T]GCTTGACAGTGCTGG | 8453 |
rs147420294 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35072586 | TGTTAGCCAGGATGG[C/T]CTTCATCTCCTGACC | 8453 |
rs147465118 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | CUL2 | GRCh38.p7 | 10:35117450 | TCCCAGTCTGGTCTT[G/T]AACTCCTGAGCTCAA | 8453 |
rs147470094 | snp | A/G | 0.00181109 | 0.0300377 | intron-variant | CUL2 | GRCh38.p7 | 10:35033149 | ACATATATAGTATAT[A/G]TGTATTTAAAACTTA | 8453 |
rs147493997 | in-del | -/ATA | 0.0119091 | 0.0762411 | intron-variant | CUL2 | GRCh38.p7 | 10:35036243 | GTGTTCAACATGTGT[-/ATA]ATAAGGATCATCTAT | 8453 |
rs147525182 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35049209 | AGCCATGGGTAGAGT[A/G]GGAAACCATTTTCCC | 8453 |
rs147622212 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35017857 | CATGTCTACACTCTG[A/T]AATGTTCCATACGTG | 8453 |
rs147641470 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | CUL2 | GRCh38.p7 | 10:35107610 | GACTTGGGCCTGGCG[C/T]GGTGGCTCATGCCTG | 8453 |
rs147647442 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35022162 | TTGGCGTTTAGAAGT[A/G]CCTGAGACATAGAAA | 8453 |
rs147679315 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CUL2 | GRCh38.p7 | 10:35021790 | TCCACTCCAGCTTAC[A/G]TGAGGTGGGGTGAGG | 8453 |
rs147710520 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082379 | AAGAAGGATGAGATG[C/T]TATCAGATGCTGGGG | 8453 |
rs147756953 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021563 | TGAATATGTATTAAA[C/T]AAAAACCCATTTCAT | 8453 |
rs147797534 | snp | A/C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109602 | ACATTTGCGTTTACA[A/C/T]GGCAAGGAGAGGCCA | 8453 |
rs147832659 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | CUL2 | GRCh38.p7 | 10:35061416 | ATCGCACCGAGACCC[C/G]ACCACTGCACTCCAG | 8453 |
rs147833336 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113852 | GCTGGGATTACAGGC[A/G]CCCACCACACCCAGC | 8453 |
rs147855716 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35067829 | GAACCACAAAAGGGC[C/T]GGACGTGGTGGCTCA | 8453 |
rs147937108 | snp | C/G/T | 3.37811e-05 | 0.0041097 | missense | CUL2 | GRCh38.p7 | 10:35016299 | GCTCTTTATAACTGA[C/G/T]AGTTTCACTGTTGTT | 8453 |
rs147963401 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35044963 | GCTCCTTATTCTATT[A/G]GTCTAATCAAAGTGT | 8453 |
rs147972341 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | CUL2 | GRCh38.p7 | 10:35111645 | GTAATACCAACACTT[C/T]GGGATGCCGAGACGG | 8453 |
rs148002055 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35047316 | TAAAAAATAATTTGG[C/T]TAAAGATTTCTGGGC | 8453 |
rs148008291 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35062568 | ATATATTTTTAAAAT[A/G]CTGATTAAGAAGCAA | 8453 |
rs148018075 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35095740 | ATTTTTTTGTATTTT[G/T]AGTAGAGACAAGGTT | 8453 |
rs148058375 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008452 | TCTCTGTAGACCTCC[A/G]CACAAGTATTTTGTC | 8453 |
rs148059038 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35041989 | GTATATTACATTATC[A/T]ATGTTTTTAAATTGT | 8453 |
rs148116694 | snp | A/T | 4.03291e-05 | 0.00449031 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35039074 | TTCATCTTTTAATCT[A/T]CCTAGAACCTATAAA | 8453 |
rs148132300 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35116144 | GGTCAGGAGTTTGAG[A/G]CTAGGCTGGCCAACA | 8453 |
rs148146132 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021662 | TTTTCTTTTTGGGCC[C/T]GCCTGGTCTTCTCAC | 8453 |
rs148149218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35031775 | TGCCAGGCTGGATTG[C/T]AGTGGACAAGATCAT | 8453 |
rs148184793 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35069153 | ATTGTAGGCGTGAGA[A/C]AACGTGCCCGGCCTG | 8453 |
rs148214640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088812 | AAGGAATTTTTCCCA[C/T]GCTATGTGCATGCAC | 8453 |
rs148266500 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083624 | ACAAAGAGGGTGGGG[A/G]CATATCGAAAGGACA | 8453 |
rs148278049 | snp | C/T | 2.87559e-05 | 0.00379172 | intron-variant | CUL2 | GRCh38.p7 | 10:35013652 | TTGTAAAGTCCAATG[C/T]TTAAATGTTTCCCCC | 8453 |
rs148320062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124407 | GACAAGAGACTCCAT[A/G]TCTACATATAAAAAT | 8453 |
rs148390673 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CUL2 | GRCh38.p7 | 10:35039357 | ACACCATTCATCCTA[C/T]TACATGGACAACATA | 8453 |
rs148406906 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35084886 | GCACTTTGGTAAGCC[A/G]AGGCAAGTGAATCAT | 8453 |
rs148443256 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35118981 | GTCCCCAGGCACAGG[A/C]TGGCCAATCCACACT | 8453 |
rs148447377 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35034255 | ATGGAATCTATAAAC[A/G]TAATAATGTAAACTA | 8453 |
rs148455667 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121826 | AAAAAAAAAAAAAAA[-/A]TAAAAATTAGTTTAG | 8453 |
rs148596710 | snp | A/G | 0.00199481 | 0.0315187 | missense | CUL2 | GRCh38.p7 | 10:35100964 | TCGCCATGGGTTTTC[A/G]TCCATGTCCTTTGCC | 8453 |
rs148599955 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081097 | TGGTAACATGCGCCC[A/G]CAGGGAGTCCCAGCT | 8453 |
rs148651675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075469 | ATTCCTGTGCCTTAA[C/T]GAGATTCCCACGCGC | 8453 |
rs148667424 | in-del | -/AAAAT | 0.0681886 | 0.171594 | intron-variant | CUL2 | GRCh38.p7 | 10:35085435 | ACACCGTCCCAAAAA[-/AAAAT]AAAAATAAAAATAAC | 8453 |
rs148701693 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CUL2 | GRCh38.p7 | 10:35027998 | CTGCCAGCTCCTATT[C/T]TCTCCCTTAATTTCA | 8453 |
rs148704047 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35113112 | GGCTTGAATCCGGGA[A/G]GTGGAGATAGCAGTG | 8453 |
rs148753017 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021546 | ATGTCAATTTTAATG[G/T]ATGAATATGTATTAA | 8453 |
rs148755305 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CUL2 | GRCh38.p7 | 10:35065853 | ACAGAGCGAGACACC[A/C]TCTCAAAAAAGAAAA | 8453 |
rs148796179 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35010653 | ATAAACTAATTAACC[C/T]AAGTACTCACACACA | 8453 |
rs148799698 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35058779 | ATGTATAAACACTAA[A/C]CCTCCTAAGAACCTC | 8453 |
rs148858353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109949 | AAGGCTGAGGCAGGA[A/G]GATTGCTTCAGGCCA | 8453 |
rs148863420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35022895 | ACTAAAAATACAAAA[A/C]TTAGCTGGGAGTGGT | 8453 |
rs148909774 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35102037 | CTGAAGTAGAGAGTT[C/T]GAGACCAGCCTGGCC | 8453 |
rs148926622 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057484 | GGTGAAACCCCGTCT[C/T]TACTAAAAAAATACA | 8453 |
rs148970814 | snp | C/G/T | 0.0174481 | 0.0920063 | intron-variant | CUL2 | GRCh38.p7 | 10:35077419 | GGAGAATCGCTTGAA[C/G/T]CTGAGAGGTGGAGGT | 8453 |
rs148984351 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092567 | GCTGTCTTGAAGAAA[A/G]GCACTTGTGTGGTTG | 8453 |
rs149025512 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021564 | GAATATGTATTAAAT[A/G]AAAACCCATTTCATT | 8453 |
rs149066880 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35068466 | AGGCACAAAAATCAA[C/G]ATAGTAGTTAGCTCC | 8453 |
rs149107302 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35013171 | CAGTGAAACCCCGTC[C/T]ATACTAAAAGTACAA | 8453 |
rs149132443 | in-del | -/GT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022077 | ACTGTAACTATGTAC[-/GT]ATGTCTGTCTTCCTA | 8453 |
rs149143059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055666 | CTAGTCAAGGCTCTA[A/G]ACTCCATGGCTTACA | 8453 |
rs149189736 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CUL2 | GRCh38.p7 | 10:35124232 | TTGGTAGTATCTGAT[A/G]AGGAAAATAGGTCAA | 8453 |
rs149195366 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087286 | GACTAACATCTTAAA[-/T]TTTTGAGCCATGTGA | 8453 |
rs149246491 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35100123 | GTACAGTCATTTAAT[A/G]TTTAATAAAATATTA | 8453 |
rs149250759 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35015449 | AATCCTAGGGATGTC[A/G]GCAAAATGAATTAAT | 8453 |
rs149296220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079870 | GAACACAAATACTGC[A/G]AAACTGCAACAGTCT | 8453 |
rs149298332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094765 | AGGGAAATAATATTC[A/G]TAAAATAGTTATTAG | 8453 |
rs149344968 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35066882 | CATGGTTACTAAGAC[-/CTT]CTTCTTCTAACACTT | 8453 |
rs149516385 | snp | G/T | 0.000449135 | 0.0149789 | missense | CUL2 | GRCh38.p7 | 10:35038977 | GTAAAAACTGTAAGT[G/T]GTCTGCTACCATTCG | 8453 |
rs149516467 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35052581 | TAGTGGTGTTCACTG[C/G]AGTGTTGTTTGTAAT | 8453 |
rs149551263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041623 | GCTCACTGCAACTTC[C/T]GCCTCTCAGGCTCAA | 8453 |
rs149593970 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114566 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCGC | 8453 |
rs149595648 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35025354 | CAGAGGAGAAAGCAC[A/G]TTCCTGTGGTCCCTA | 8453 |
rs149649855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104192 | TGGCTCACACCTGTA[A/G]TCCCAGCACTTACGG | 8453 |
rs149665948 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084732 | ATAACATTCCAAATC[A/G]CTGCTTGTTTTTCCA | 8453 |
rs149685586 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35073358 | CTCTTCCTTGTTTAC[C/T]ACATCCTATCATCAA | 8453 |
rs149775076 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | CUL2 | GRCh38.p7 | 10:35059976 | TTTAATAGTACTAAT[G/T]TAGCCAGGCACAGTG | 8453 |
rs149948299 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075321 | TTTCTTAAAAATGTT[C/T]AATAATAACATTCAG | 8453 |
rs149949353 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | CUL2 | GRCh38.p7 | 10:35107247 | CCAAAGTGCTGGGAT[C/T]ACAGGCATGAGCCAC | 8453 |
rs149983611 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017403 | GTTTTCATAAATATG[C/T]TCTATATGTGCTGGG | 8453 |
rs149984910 | snp | C/T | 0.000198013 | 0.00994824 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35011869 | AATAAGGGCATTGTG[C/T]CGAAGCACTTTTCGT | 8453 |
rs149993702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35101565 | ACTAATTCCTGCTGT[A/G]GAACCCCTGAGACCA | 8453 |
rs150034549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35049408 | AGCTCTGAAAAGCAA[C/T]AAGTCACTTCCCTCA | 8453 |
rs150036414 | snp | G/T | 3.31466e-05 | 0.0040709 | missense, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054515 | TGTTAATTTATTCTT[G/T]TTAATAAACTGGGTG | 8453 |
rs150038850 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35097052 | TGTCTCCACATGACC[C/G/T]GTCCACCTCAACCTC | 8453 |
rs150090300 | snp | A/T | 8.25226e-05 | 0.00642296 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35032489 | ATTTACAACTGACGT[A/T]AGGGCCTGAATAAAA | 8453 |
rs150100376 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35062812 | ACTGCACCCTAGCCT[A/G]GGCAACAGAGCAAGA | 8453 |
rs150134132 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008704 | TCATTATAAGTTCAG[C/T]AGATTTTTAAAACAC | 8453 |
rs150136431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35094551 | GAGTAATTTTTAAGC[A/G]TGTAAAGAAACTGAA | 8453 |
rs150187182 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35045796 | AATCTAGCTCTAAAT[A/T]GGGATTTTGTGACTC | 8453 |
rs150207973 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35116883 | AATCGCTTAAACCTG[G/T]GAGGTAGAGGTTGCA | 8453 |
rs150264249 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | CUL2 | GRCh38.p7 | 10:35076943 | TGTAGTCCCAGCTAC[G/T]CCGGAGGCTGAGGCA | 8453 |
rs150308567 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | CUL2 | GRCh38.p7 | 10:35020510 | TTACTTTTATTCTGG[A/C/T]AAACACTAGTAACTA | 8453 |
rs150362048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098914 | ACTCCAGCCTGGGCA[A/G]CAAAGCAAGACTCTG | 8453 |
rs150422388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35040643 | TCACAGACTCAGGTC[A/G]GGCAAGAAGGGGTCT | 8453 |
rs150456156 | in-del | -/TTTT | 0.206029 | 0.246103 | intron-variant | CUL2 | GRCh38.p7 | 10:35072373 | GTGAACTTAATGGGC[-/TTTT]TTTTTTTTTTGAGAC | 8453 |
rs150473531 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036148 | CTGCAAAGGTAACCA[C/T]TGCTGTGACTTCTAA | 8453 |
rs150505722 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CUL2 | GRCh38.p7 | 10:35014671 | AACCCGGTCTCTACT[A/G]AAAATTAAAAAATTA | 8453 |
rs150540671 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35047837 | TTGAACCCAGGAGGC[A/G]GAGGCTGCAGTGAGC | 8453 |
rs150559100 | in-del | -/ACAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123177 | CAAAACAAAACAAAA[-/ACAAA]CAAAGGACTTCATGC | 8453 |
rs150577768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CUL2, MIR3611 | GRCh38.p7 | 10:35079628 | AATTTCTTTCTTCAC[A/C]ATTTCTTTTCTTTCA | 8453 |
rs150623395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106203 | CTTCAGTCATGTGAG[C/G]ACATAGCAAGAGGAC | 8453 |
rs150626475 | snp | C/T | 1.65012e-05 | 0.00287234 | missense | CUL2 | GRCh38.p7 | 10:35044806 | TTATACTGTTCAACA[C/T]GAACAAAGGAGTTAA | 8453 |
rs150674583 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35101184 | AGAGTCTCATAGCCA[A/G]TTGGGCATTTAATTT | 8453 |
rs150696727 | snp | C/T | 0.000214544 | 0.010355 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054494 | GCCATACTGAAGGTC[C/T]GCTTCTGTTAATTTA | 8453 |
rs150734563 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35042993 | GAGGACACCTAGCTG[C/G]TGTCTGCTGCTTGGT | 8453 |
rs150745706 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021893 | GGGTGAGGTGGGGTG[A/G]GGTGGGGTGAGGTGG | 8453 |
rs150750984 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090756 | CTGTCAATGAGGCAA[G/T]TGCGGTTCGCTGAGC | 8453 |
rs150752281 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103509 | TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCACC | 8453 |
rs150784840 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35037793 | GGTTATAGTGAACAG[A/C]GATCGCGCCACTGCA | 8453 |
rs150787526 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126275 | CATTTCCAGTCAAAT[A/G]CTGGGATAAACTGCA | 8453 |
rs150793924 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087763 | TTGTACCTTAACCCT[-/C]CCACAGCCACTGCTC | 8453 |
rs150838413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073898 | GGCATGGGCCACTGC[A/G]CCTGACCTGTTCTCC | 8453 |
rs150888766 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35025055 | AAACTGTAATTGGGC[C/T]ATAGAAAACCTCTTT | 8453 |
rs150909367 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35011026 | GAAGACTCAATGAAT[C/G]AGCAAGTTTTAGACC | 8453 |
rs150956584 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35120108 | CTATGGTATTCAGAT[G/T]TATTTTATCATTTAA | 8453 |
rs150963156 | snp | C/T | 0.000676729 | 0.0183822 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35031581 | CTCTGTCATCCCTTT[C/T]GCTGACTTCTTCAGT | 8453 |
rs150992953 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35073044 | CTGGGAGAGGCCCTT[C/T]TGTGTTTCCAGATGA | 8453 |
rs151011584 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35055934 | ATATTCTGAGGGTAG[C/T]CAGTCCCCTTTCATC | 8453 |
rs151064747 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35093180 | CCCTGCTCACCAAAT[C/T]GTCCATAAAAACCCC | 8453 |
rs151076234 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113065 | GCCGGCATGTGTAAT[C/T]TCAGCTACTCTGGAG | 8453 |
rs151114297 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35039781 | AATCACTTCATCCCG[A/G]GAGGTGGGGGTTGTA | 8453 |
rs151150248 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35035657 | ATTTTACAGCTGCAC[A/C]GTACTCCATTATGTG | 8453 |
rs151189459 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021638 | TTATTTTTTATTTTC[A/G]TTTATTTATTTTCTT | 8453 |
rs151203848 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35028960 | TAAATATTTATTAAA[C/T]AATCTAAGCATCTAA | 8453 |
rs151224483 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35098788 | AAAACCAAAAAATTA[A/G]CTGGGCACGGTGGCA | 8453 |
rs151254883 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35066038 | CAGAATGAAAGCTCA[C/T]AGCTGCAACCAAAAG | 8453 |
rs151272870 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | CUL2 | GRCh38.p7 | 10:35085892 | TAAGGGTTGAAAAAC[G/T]GTTGGGTACTATGTT | 8453 |
rs151278001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017048 | GGAGAAGGAGAAATG[C/G]ACAGACAAAGGGCAA | 8453 |
rs151323943 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081476 | TCATATATGTATCCC[C/T]GATCTCAGGTAAATT | 8453 |
rs180730887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014561 | TTAAAGGCCAGGCAT[A/G]GTGGCTCACGTCTGT | 8453 |
rs180742720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035356 | ATTTATTAGGTAATA[C/T]ATGGATCCAAGTGCA | 8453 |
rs180748793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051611 | GCAAGACTCCGTCTC[A/G]AAACAACAACAACAA | 8453 |
rs180867295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35011251 | TGAGATGGGGTCTCC[C/T]TGTGTTGCCCAGGCT | 8453 |
rs180868195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35019593 | TAGGTTGGCAAACCC[C/T]AAGAGACTAAAAACT | 8453 |
rs180874703 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35032682 | TCTCTAATTACAAAA[G/T]ATCTATATATCCTGT | 8453 |
rs180885588 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056408 | AGCATTTTATGTGGC[C/T]GAATACTATAAGACA | 8453 |
rs180919766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35038131 | CTCCAGCCTGGGCGA[C/T]GGAGCGAGACTCCAT | 8453 |
rs180966557 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125006 | CTAACGTAAACATGA[A/G]TAGGTTTTTAAGTAT | 8453 |
rs180975334 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065939 | TCTTTTCCTAAGTCA[C/T]TTTTTAGGGAGCCAG | 8453 |
rs180975477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35108994 | GAAGTGGGTGGACCA[C/T]CTGCGCTCAGGAGTT | 8453 |
rs180988834 | snp | A/C | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090927 | ACACACTTCCATGGG[A/C]TTTGCAAATGATCAA | 8453 |
rs180991829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116936 | CACTCCAGCCTGGGC[A/G]ACAGGGTGAGATTCC | 8453 |
rs180999540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074324 | TCCTGGTACTCCCTA[C/T]TGTGACATCATAATC | 8453 |
rs181018591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082840 | TTATTCATTATTTTG[G/T]TAACTATACACTTAC | 8453 |
rs181021259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35102155 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 8453 |
rs181079158 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075400 | GACCACAGTCACACT[A/C]TTTCTACCCCCCAAG | 8453 |
rs181100595 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35101248 | GTATTAAGCCATCAA[C/T]AGACATTCACCTGAT | 8453 |
rs181105997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35082545 | TATACCCTTAATGAC[A/G]GTTAAAATGGTAAAT | 8453 |
rs181119300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065536 | AGGCAGGAGAATGGC[A/G]TGAACCCGAGAGATG | 8453 |
rs181236174 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031729 | GGACAGAATTTTTGC[C/T]GTTTTTTTTAGAGAC | 8453 |
rs181244919 | snp | C/T | 1.70551e-05 | 0.00292015 | intron-variant | CUL2 | GRCh38.p7 | 10:35010489 | CCAGTTCTTCAGCTA[C/T]TAAGTAATGACTTTT | 8453 |
rs181257891 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126109 | TTACAGGCGTGAGCC[C/G]CCGGCCGACCTTTCT | 8453 |
rs181263241 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35109638 | ACAAACATTTGCAGA[A/G]CAAGATTTCCAAACA | 8453 |
rs181266914 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35087422 | TTTAACCACTATATC[C/T]ACACATCTGGTTTAA | 8453 |
rs181271348 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35057198 | GATGTATATTCTTGA[G/T]CCAGGTATTGATTTA | 8453 |
rs181272473 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35069445 | ACTCAGGAGGCTGAG[A/C]TAGGAGGATCTCTTG | 8453 |
rs181274495 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092418 | CAGTTTTTAAGGCTA[C/T]TGATTTAGGAATATC | 8453 |
rs181289507 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047659 | GCGGTGGCTCACTCC[G/T]GTAATCCCCACACTT | 8453 |
rs181322990 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35113680 | AAACTCAGAAATAAT[A/G]GATATGATGAATCTA | 8453 |
rs181338774 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079175 | ACTAGCAGTAAGATA[C/T]AACAATTATAACAAT | 8453 |
rs181346524 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35106536 | ATGAGGTTTCACCGT[A/G]TTAGCCAGGATGGTC | 8453 |
rs181368912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35042819 | AATGGAACCCAAACA[A/G]TGTACTGTAGGACTT | 8453 |
rs181447892 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35096991 | TTTTTTGTATTTTTC[A/G]TAGAGACGGGGTTTC | 8453 |
rs181449770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35119860 | GAGATTATAGGCACA[A/G]GCCACCTTGCCCAGC | 8453 |
rs181470900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35062119 | TCTCATCCAGTTCCT[A/G]ATTAGATCAGTAGTC | 8453 |
rs181504437 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030720 | AATTAAGTTTCTTTT[G/T]GGAGGTTTAAAAAAG | 8453 |
rs181505132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024673 | TTAAAATTGGAAACT[A/C]TTGAAAATTAAGTAG | 8453 |
rs181511113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047023 | AACTAAACAGTAGGT[A/G]AGAAGAAGCATATCT | 8453 |
rs181516998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020249 | TGGTCTGTTCAAAAC[A/G]GTGTGTCAAAGAATG | 8453 |
rs181523690 | snp | G/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009185 | ACACTGCTGTTGAGA[G/T]ATATATATATATATA | 8453 |
rs181526552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064984 | ACTTCTGCACTGTTG[C/G]ACTCCTTCAGAATAT | 8453 |
rs181616511 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35024076 | CTGGGATTAAGTGAC[C/T]CACCTGTCTCAGCCT | 8453 |
rs181705981 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35113455 | GTGAGCCGATATCAC[A/G]CTACTGCACTCCAGC | 8453 |
rs181712209 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096109 | AAAAATAAGCCTGGG[C/T]TGGTGGTGTGTGCCT | 8453 |
rs181720970 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078596 | GTGAGCTACTGCACC[C/T]AGCCCGACATTTTTC | 8453 |
rs181725769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35060661 | CGAGTACAGTTTTAC[C/T]TTTCACAGAACGTTC | 8453 |
rs181732295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35070737 | TCCCTCGCTGCATTC[C/T]AGTCTCTGCTCTAAT | 8453 |
rs181840299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120839 | AGGTTGAGACTGCAG[C/T]GAGCCAAGATCATGC | 8453 |
rs181867991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120635 | TGGCTGGGCTCATGC[A/G]TGTGAAATCTCAGCA | 8453 |
rs181869505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107145 | GTGCCCGGCTAATTT[C/T]TTGTATTTTCAGTAG | 8453 |
rs181886147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023601 | ACACCACTGGTTGTT[A/C]AAATGAGCCCCTTAC | 8453 |
rs181890648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042213 | ATCTTCTGTCCTTTT[A/G]AATTTGTCTGTTCTA | 8453 |
rs181914393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014089 | CTACTTTTTGATAAA[A/G]TAAGAGTCAAGCTCA | 8453 |
rs181932796 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CUL2 | GRCh38.p7 | 10:35095807 | CTCAAGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 8453 |
rs181948199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059619 | CAATATTCCCTTTAC[A/G]TGTGGTGGTCTGGAA | 8453 |
rs182069257 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35035861 | GCCAACAGCAGAGAG[G/T]TCCTTTGCCAACAAT | 8453 |
rs182172885 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126256 | GCGGGCCCAGCATGC[A/G]GACCATTTCCAGTCA | 8453 |
rs182174466 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084992 | GGGGGTGGTGGTGGG[C/T]GCCTGTAATCCCAGT | 8453 |
rs182189996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109202 | GGTTTTTAAGAAACA[C/T]TTAAAAAATGTTTAG | 8453 |
rs182202904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35113350 | AAAATACAAAAAAAC[C/T]AGCCAGGCGTAGTGG | 8453 |
rs182205026 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074729 | GAGGCTCAAGTGATC[C/T]GCCCGCCTTGGCCTC | 8453 |
rs182221184 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35039408 | GTACAGATGATTAAA[A/T]TCAGAACAGGTGATC | 8453 |
rs182221923 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CUL2 | GRCh38.p7 | 10:35077748 | CTTGAACCCAGGAGG[C/T]GGGGGTTGCGGTGAG | 8453 |
rs182359008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015456 | GGGATGTCAGCAAAA[A/T]GAATTAATGAGAGAA | 8453 |
rs182368888 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35050253 | TTGAACCTGGGAGGT[A/G]GAGGTTGCAGTGAGC | 8453 |
rs182374471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35052412 | GAGGCTCCACTTCCT[A/G]ACACCCAGTCTATAA | 8453 |
rs182384823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35110864 | AATGACCTAATCTCC[A/G]GATATGGTTACATTC | 8453 |
rs182390585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35067679 | AACCCAGGAGGGGGA[A/G]GCTGCAGTGAGCCAA | 8453 |
rs182401950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093517 | TACAAAATTTAGCCA[A/G]GCATGGTGGTGTGTG | 8453 |
rs182439022 | snp | A/C | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125260 | GTGTATCTCACCTCC[A/C]GTATTGATCTTTGTA | 8453 |
rs182446788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35118542 | TTTCCAACATTCTCC[C/T]TTCTTTCTCTGAAGC | 8453 |
rs182458901 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092103 | GACTACAGGCGCGTG[C/T]GCCACCACACCCAGC | 8453 |
rs182495925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35057044 | CATCTAAAAATTCTG[C/T]TGTCAGGATGTTACT | 8453 |
rs182623796 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021846 | CGAGGTGAGGTGAGG[C/T]GAGGTGAGGTGAGGT | 8453 |
rs182637288 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35057668 | AAAAAAAAAAAAAAG[A/G]AAAAAAGAAAATAAA | 8453 |
rs182653933 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021119 | ATGGACCTTAGGGGT[C/T]AGAGCTTCAACAGAA | 8453 |
rs182664975 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35039740 | CATGCCTGTAATCCC[A/T]GCTCCTTGGGAGGCC | 8453 |
rs182707750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35107742 | AAAAAATTAGCCAGG[C/T]GTGGTGGCAGGCGCT | 8453 |
rs182709183 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35104917 | TATCTTAAGTAGAAA[C/G]GGAGTTTCTCCATGT | 8453 |
rs182717696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088690 | GTGAGGGTAAAAGAC[A/G]TGGATAATCTTCACA | 8453 |
rs182725433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071849 | CAGACTATTTACATT[C/G]ATTACAAGCTCTAGG | 8453 |
rs182786281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35114890 | CATCAATGAATTTGA[C/T]GACACCAATATAGAA | 8453 |
rs182788281 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35017550 | AATACAAAAATTCGC[C/T]GGGCATGATGGCATA | 8453 |
rs182791252 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35036979 | AGCTCAAGCAATCTT[C/G]CTCCCTCTTAATGGC | 8453 |
rs182797802 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35053620 | TTTTCCAAGTATGGA[A/T]CACTAGGCTTAGGAC | 8453 |
rs182908061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35040401 | TGGAAACACTCTGGA[A/G]CATAAAGCTGTGTAA | 8453 |
rs182948140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35045325 | CAGGCACCGTGGCTC[A/G]TGCCTGTAATCCCAA | 8453 |
rs182969344 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103545 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 8453 |
rs182970928 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075807 | ATTTGAAAACACTTG[C/T]AGATTTGATTTCCTC | 8453 |
rs182980260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080419 | TCATGACTTTCTGGC[C/T]TTAGAATTCCTATTT | 8453 |
rs182985611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066980 | GTTTGAAAGAGATGC[C/T]TGATAGAATATAAAC | 8453 |
rs182988685 | snp | A/G | 0.00196542 | 0.0312866 | intron-variant | CUL2 | GRCh38.p7 | 10:35063086 | ATTATTAAGGTTTTC[A/G]TATTTATTGGAGACA | 8453 |
rs182993070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35033680 | AGGTGGAGGTTGCAG[C/T]GAGCAGAGATCGCAC | 8453 |
rs183018389 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35115139 | ATCACTTGAACCCAG[A/G]AGGCAGGAGATTCTC | 8453 |
rs183065693 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35048567 | AGTATATTTTAGCAG[A/C/G]AGAAATTATATTAGA | 8453 |
rs183070648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35016475 | TTCAGACATTTTCTT[C/T]GGAAAGAGTGAACCA | 8453 |
rs183221853 | snp | A/C/T | 3.66866e-05 | 0.00428278 | intron-variant | CUL2 | GRCh38.p7 | 10:35025114 | TCATTAAGCCAGATA[A/C/T]AATTAAATGCATTTT | 8453 |
rs183228541 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | CUL2 | GRCh38.p7 | 10:35043546 | TGTAGGATGACAGCT[C/T]ACCCACTTAAACTAC | 8453 |
rs183234647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117977 | CCCATATATGCACAG[C/T]CTCCCTATCAACATC | 8453 |
rs183235072 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35062489 | TTCATTTACTAATTA[A/C]GAGATGCTGAGCAAG | 8453 |
rs183257784 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35084170 | TAGTCCCAGCTACTT[A/G]GGAGGCTGAGGCAGG | 8453 |
rs183259749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012677 | TTATTAGCCTGGAGG[A/C]AAATGGAATCTTGAC | 8453 |
rs183277211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117452 | CCAGTCTGGTCTTGA[A/T]CTCCTGAGCTCAAGC | 8453 |
rs183281596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102650 | AGCACTTTGAGAGAC[C/T]GAGGCGGGTGGATCA | 8453 |
rs183291762 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35099549 | GCAGGTGGATCACCT[A/G]AGGTCACGAGTTCAA | 8453 |
rs183297810 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35121211 | AGTTTATATTCTGGC[C/T]GGAAGATAGGCTTTA | 8453 |
rs183322712 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | CUL2 | GRCh38.p7 | 10:35121822 | CTCAAAAAAAAAAAA[A/T]AAAATAAAAATTAGT | 8453 |
rs183327568 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CUL2 | GRCh38.p7 | 10:35083112 | CAGTGAGCCAAGATC[A/G]AGCCACTGCACTCCA | 8453 |
rs183334853 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35108131 | TGCAGGCTGATCAGT[A/T]AAGAGGCTATTGCAC | 8453 |
rs183337106 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35066740 | TGAGAACAAATATCA[A/G]TTAGCCTGATATAAT | 8453 |
rs183394028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048296 | GGAAGCCGATTATAA[C/T]AACAAAAATAAGACA | 8453 |
rs183396664 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022030 | TTCTGTGATATGCCC[C/T]GGGCTGGCCTCTATC | 8453 |
rs183406708 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35040858 | TCACAATGGAGTTTG[C/T]GCTCTGTGAGAATCT | 8453 |
rs183492845 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35052882 | CCTGGGTGACACAGC[A/G]AGACTCCGTCTCAAA | 8453 |
rs183499988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026532 | TGGCTTTAAAAGGTA[C/T]ATTCCAAGCTCTAAA | 8453 |
rs183507485 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128807 | TGGGATTACAGGCAT[C/G]AGCCACCGCTCCCGG | 8453 |
rs183511859 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35112932 | GGCGTGGTGGCTCAC[A/G]TCTGTAATCCCAGTA | 8453 |
rs183646859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037134 | TCTATATTATCTTCT[A/G]GAAGTGTTATTTTTT | 8453 |
rs183724993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036263 | GGATCATCTATGTTG[C/T]TGTGCATGGCTTTAA | 8453 |
rs183800368 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35071563 | GCACCCGCCACCATG[C/T]CCAGCTAATTTTTTG | 8453 |
rs183811308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35022775 | GACAAGGCTGGGCAC[A/G]GTGGCTCATGCCTGT | 8453 |
rs183817370 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35041418 | AGCTATAAGAGGAAC[A/G]CAGCAAGGAGGCAGG | 8453 |
rs183828114 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014198 | ACCACATTTTTTTTT[A/G]CAAATGCCGCAGTAA | 8453 |
rs183841405 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35072647 | TGCAGGGATTACAGG[C/T]GTGAGCCACTGCACC | 8453 |
rs183850044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35098336 | ATTTCTCAAAATTGG[A/G]AATACAGAGTAAATC | 8453 |
rs183854096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013436 | AATGTGGGAATTTTC[A/G]GAGAGAATGCATAGT | 8453 |
rs183865062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35034211 | CCTTGACACAAAATT[C/T]GATGCTTCTATGCCC | 8453 |
rs183869852 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35053932 | GAATAAACAAGCTTG[A/T]ACAATAATACTTCTT | 8453 |
rs183916397 | snp | G/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127579 | AGAAGTAAGGACCTC[G/T]GATTTGAGTGCCCCC | 8453 |
rs183916810 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35111613 | GACATTCAGGCCAGG[C/T]GTGGTGGCTCACGCC | 8453 |
rs183927990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075915 | CCAGCAATTCCACTC[C/T]GAAGTATAAAGAGAA | 8453 |
rs183940983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111752 | AATTAGCTGGGCGTG[C/G]TGTGGCATGTGCCTG | 8453 |
rs183945996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094270 | GATGGAGTTTCGCTC[C/T]TGTTGCCCAGGCTGG | 8453 |
rs183953625 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | CUL2 | GRCh38.p7 | 10:35077314 | AAAAAACAAAAAACA[A/G]AAACAAACAAACAAA | 8453 |
rs183963825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35058389 | TCCTGATGACTAACC[C/T]GCCTCAAAAAGTCAC | 8453 |
rs183992918 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090747 | CTGGGCTTGCTGTCA[A/G]TGAGGCAATTGCGGT | 8453 |
rs183996979 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35073658 | AGCCTGGGCTGGGGT[A/G]CAATGGCGCAATCTC | 8453 |
rs184002650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011997 | AGAAAAAAGACCCAA[C/T]AAGACATTAAGTCAC | 8453 |
rs184022098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114492 | GGTTCCAGCGATTCT[A/C]CTGCCTCAGCCTCCC | 8453 |
rs184037588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079858 | TCAGGGTGACTTGAA[C/G]ACAAATACTGCAAAA | 8453 |
rs184048012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017959 | GTTTGACGACTAACA[A/C]ACACACGGCCTGCAT | 8453 |
rs184064364 | snp | G/T | 0.0123036 | 0.0774623 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126652 | ACTCTGGCTGACAAG[G/T]CATTGGATTTCTGGC | 8453 |
rs184082385 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35093844 | TTCTATTAAATCAAA[C/T]ATTTAGAGAGTTGCA | 8453 |
rs184128200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018972 | ACAAAAGGAGGTTTA[A/C]TATATTAAATTCAAT | 8453 |
rs184135426 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35038056 | TACTTGGGAGGCTGA[A/G]GCAGAATTGCTTGAA | 8453 |
rs184143089 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35055565 | GCGAGACTGTCTCTT[A/G]AGGAAATAATAATAA | 8453 |
rs184154509 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | CUL2 | GRCh38.p7 | 10:35124716 | AGGAGCCAAGAGGAC[A/G]AAAAAGGCTGTAGGT | 8453 |
rs184163819 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35108763 | TGACTGTGGTTGGGG[A/G]ATCCTGCTACCAAAC | 8453 |
rs184176101 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094515 | GCTGGGATTACAGGC[A/G]GGAGCCACTGCACCC | 8453 |
rs184195145 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35058030 | TTGAATCTGGGAGGC[A/G]GATGCTGCAGTGAGC | 8453 |
rs184204472 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35059006 | GAACTCAGAAGTGGA[A/T]CCTGAAGATGGGACT | 8453 |
rs184334871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35077357 | ACAAAAATTAGCCGG[A/G]TGTGGTGGTGGCTGC | 8453 |
rs184391352 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35116561 | CTCGTTTAACCCTCT[C/T]TGAATCCTTTCAATC | 8453 |
rs184397139 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35100981 | CCATGTCCTTTGCCA[C/T]CTGAGTTTTTCTCCC | 8453 |
rs184402988 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35018241 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 8453 |
rs184406865 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35082432 | GCCTAATGGTTGTAC[A/G]GTTTCTGTCTAGTAA | 8453 |
rs184411689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35037339 | AAGTGGCCACATATG[C/T]TTGGGTTGTTTCTAG | 8453 |
rs184421347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065310 | CTTTGGGAAGCCAAG[C/G]CGGGCAGATCACCAG | 8453 |
rs184441773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023103 | ACAGTAGATGTTAAA[C/T]GCTCTCACCACAAAT | 8453 |
rs184578023 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35041805 | GCCTCCCAAAGTGCT[C/G]CAATTACAGGTCTGA | 8453 |
rs184585382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35034928 | TTTTCCTGTGGAAAG[C/T]TAACAACTGTTCAAT | 8453 |
rs184621336 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125210 | CTTACAGCAAGGGTA[C/T]AGCAGAGGCCATGAA | 8453 |
rs184624845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109013 | CGCTCAGGAGTTGGA[A/G]AGCAGCCTGGGCAGG | 8453 |
rs184632330 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071584 | TAATTTTTTGTATTT[A/T]TTTTTAGTAGAGACG | 8453 |
rs184675186 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CUL2 | GRCh38.p7 | 10:35106368 | TCTGTAGCCCAGGCT[A/G]GAGTGCAGTGGCGCG | 8453 |
rs184696265 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35069088 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 8453 |
rs184723459 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CUL2 | GRCh38.p7 | 10:35051471 | ACAAAAAATTAGCCG[A/G]GCGAGGTGGCGGGCG | 8453 |
rs184740629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35028642 | TTAGTATCAATATTA[A/G]TAACTACAATAACTT | 8453 |
rs184750513 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046760 | AGCTGGGCATGGTGG[C/T]GCATGTCTATAATCC | 8453 |
rs184796392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081100 | TAACATGCGCCCGCA[C/G]GGAGTCCCAGCTACT | 8453 |
rs184812529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119159 | GCAGCCGAACAAATA[A/G]CATTCAAAGTTTGTT | 8453 |
rs184826586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35086500 | CCATGTTGCCCAAGC[C/T]GGTCTCAAGCTGCTG | 8453 |
rs184869021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35081998 | TTCTTGACACCTCCT[A/G]TTTACAATCCCAAAG | 8453 |
rs184874934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064031 | ACCTCCTGGTGGTTA[C/T]ACTCCAGACTGTTCC | 8453 |
rs184911866 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008294 | TCTCTGCAGGGGAAG[A/G]TGTGCGCTGCAATGA | 8453 |
rs184919383 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35118848 | TTCCAGGATAATGAT[C/G]CAGTTAAAGCATTCC | 8453 |
rs184921133 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CUL2 | GRCh38.p7 | 10:35105990 | ACAGATAAAAATTTA[A/G]AGGGTTGGAGATTAA | 8453 |
rs184922273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119978 | TAATATTTATTTCTT[A/G]TTCTTACCTTTTCAG | 8453 |
rs184923042 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35063577 | ATTCTATCAGAAGAA[A/C]TATACCATGAATAGG | 8453 |
rs184928471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046043 | TTACCTTTACATACT[A/G]GAGTCCTTCCCTGCC | 8453 |
rs184929742 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35085381 | CTTGCAGTGAGCTGA[C/G]ATCGCGCCACTGCGC | 8453 |
rs184934200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35106945 | TGTCTGCATTGCCCT[C/T]AACCTGTTTTTTTTT | 8453 |
rs184938170 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35087461 | CTTGAGAAGCCCTCG[C/T]TGGATGGCTGAATCA | 8453 |
rs184941814 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35068003 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 8453 |
rs184950447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070364 | TCTTCTTGCATCCAC[A/G]TTCAGCTTAATATTA | 8453 |
rs184983868 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35015014 | CCTATTTTGGCCAGG[C/G]ACAGTGGCTCACGCC | 8453 |
rs184994565 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35035440 | CCCACCTCCCAGCCA[A/C]CCAAGCCCCTCTCCC | 8453 |
rs185006077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051799 | AAAGCTAGAGTTTTT[A/T]ATATATTGTGGAAAT | 8453 |
rs185047450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123138 | GTGAGATCCGATCTA[C/T]AAACAAGCAAAACAT | 8453 |
rs185057498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35089319 | TAAGATTCTAAAGGG[C/T]AGGCAACAGTGTTTT | 8453 |
rs185072391 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35030752 | GCACACAGCAACTGG[G/T]TGCAGTGGTGCACAC | 8453 |
rs185081505 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35023654 | TTGATTATTGCTGAA[A/C]TAATGAGAATAACCA | 8453 |
rs185092942 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042367 | CTGTGTGGTGTTGTG[A/G]TATGTAAGTACATTG | 8453 |
rs185161838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108698 | TTTTTCAGGGTTTCT[C/G]ATGAGATTTCAGTCA | 8453 |
rs185178644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073369 | TTACTACATCCTATC[A/G]TCAACTGTGCACATG | 8453 |
rs185196379 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047122 | TGCTGACTAAATTAC[C/T]AATTTCTTCATTTCC | 8453 |
rs185265294 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35054212 | GAACCATTAACTCTA[A/T]CATTCATCCATTATA | 8453 |
rs185382012 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009280 | AATGTACAATTTTCT[G/T]TTTTAAAAAAGTATT | 8453 |
rs185493672 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074445 | CTTATCTTTTCCTTA[A/G]CTGCCCCCTCCACCC | 8453 |
rs185496646 | snp | C/T | 0.000399281 | 0.0141238 | missense | CUL2 | GRCh38.p7 | 10:35100941 | TATCACAGGGTTTTC[C/T]TTCCATGTCGCCATG | 8453 |
rs185560417 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35078007 | GTTTACAATTTTCCA[A/T]AATAAAGGAATTTAA | 8453 |
rs185564266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35042551 | CTGACTGTGGGTCAT[A/G]AGACCCTCCCCAGAG | 8453 |
rs185569005 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35017282 | GGAGAGACAAACAGG[C/T]AGACCCATTCTCTTG | 8453 |
rs185578610 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35036367 | TGAGCTGTTCCAGTT[C/T]ATGGAGCTATTACAA | 8453 |
rs185607233 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35113594 | TCTACGAAAAATTAC[C/G]AAGAATGCAAAGAAA | 8453 |
rs185614195 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091356 | CCTGCCTCCAGACCT[A/G]ATCAGTCCCTAGAGC | 8453 |
rs185619698 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35096333 | GTGATGGCCGGGTAC[A/G]GTGGCTCATGCCTGT | 8453 |
rs185625073 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35115654 | AACTCAGCACTTTGG[A/G]AGGCCAAGGCATGAG | 8453 |
rs185630277 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35078614 | CCCGACATTTTTCAT[A/G/T]TAAAGAGATTTGTTC | 8453 |
rs185638191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35060783 | AGTTTTGCATATGTG[A/T]ATGAGAAATAGGCAA | 8453 |
rs185639326 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35010524 | AATCAGTTTAAAGTG[A/C]CTCAAATGTACTGAG | 8453 |
rs185688307 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35117566 | GTAAAAGGCAACTAT[C/G/T]GAAAGCAAAAATAGC | 8453 |
rs185688575 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35102747 | AATTAGCCGGGTGCA[A/G]TGGCAGGCGCCTGTA | 8453 |
rs185701890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013914 | AGCCTCCACTCTCAT[A/C]ACTTTTATATTATAG | 8453 |
rs185703085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084054 | GGCCAAAGAGGGCGG[A/C]TCTCTTGAGGTCAGG | 8453 |
rs185709416 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CUL2 | GRCh38.p7 | 10:35039972 | AGCCTGGCCAACATG[A/G]TGAAACCCCGTCTCT | 8453 |
rs185716099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051246 | TGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 8453 |
rs185717601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057480 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAAAA | 8453 |
rs185734897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35113390 | GTAATCCCAGCTACT[C/T]GGGAGGCTGGGGCAG | 8453 |
rs185790998 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35097444 | GCAGTGAACTGTGAT[C/T]GCACCATTGCCCTCC | 8453 |
rs185805998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062151 | AAATTAAGTTGGAAA[A/T]GCTGTCTATAGCAAA | 8453 |
rs185839946 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35034693 | GAGTATTAGGGATAT[A/G]AGGGTTATTGTTTTG | 8453 |
rs185840794 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126195 | TGGGCTCAAGCGATC[C/T]TCCCACCTTGGCCTC | 8453 |
rs185858564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35110068 | TGGTCTCAGCTACTC[A/G]GGAGGCTGAGTTAGG | 8453 |
rs185864483 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35092917 | TACTCCCTTACTGCT[C/G]AGGGGTCATGTGGCC | 8453 |
rs185871520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075482 | AACGAGATTCCCACG[C/T]GCACTCAGATTGTGT | 8453 |
rs185882203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095948 | ACGTTTGGAGTGGCT[A/C]ATTAAGGAGCTATTT | 8453 |
rs185884440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024749 | AAGTAAAAATCAAAT[C/G]GTTAGGTCTCCTTAT | 8453 |
rs185913732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114435 | TCACCCAGGCTGGAG[G/T]GCTATGGCACAATCT | 8453 |
rs185926691 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079336 | ATCGGAAGGTCGGCA[C/T]TGGGCTACTTACTAC | 8453 |
rs186012790 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35020260 | AAACAGTGTGTCAAA[A/G]AATGCTGAGAAGTGG | 8453 |
rs186021232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039503 | TATTTTACGTTGGTT[C/T]CTCTTCTTGTAAATG | 8453 |
rs186022427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043199 | GACATCTGGGCTACT[A/G]CCACCACTTGCCAGT | 8453 |
rs186030903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35057078 | CTATTCAGAATTCTA[C/T]AGGAGCTTCCTTTAC | 8453 |
rs186119882 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35032706 | ATCCTGTTGCTATTC[C/T]AAGATATTCTGTAAC | 8453 |
rs186130091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047888 | CCAGCCTAGTAGACA[C/G]AGTGGGAATCCTGTC | 8453 |
rs186163212 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | CUL2 | GRCh38.p7 | 10:35102164 | AGAATCGCTTGAACC[C/G/T]GGGAGGCAGAGGTTA | 8453 |
rs186167225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082855 | GTAACTATACACTTA[A/C]ATAATTACAAAGGTA | 8453 |
rs186178430 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35066120 | AAAGGTGTTTCCTAC[A/C/G]CTTGGCTTAATTTTG | 8453 |
rs186262181 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35071696 | TACAGGCATGAACCA[C/T]CACACCCGGCCAGTT | 8453 |
rs186355399 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35024180 | ACCACTAAGAGTATC[A/C]GTAAAAAATCTCATT | 8453 |
rs186434402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107149 | CCGGCTAATTTTTTG[C/T]ATTTTCAGTAGAGAC | 8453 |
rs186439658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088340 | TGTTGAAACCCAGTC[A/T]CTACTAAAAATACAA | 8453 |
rs186515327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116850 | TAGTCCCAGCTACCC[A/G]GGAGGCTGAGGTGGG | 8453 |
rs186530761 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35047734 | CCAACCTGGCCAACA[A/T]GGTGAAAACCGGTCT | 8453 |
rs186530956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082596 | AGTGCTTAAAAACTA[A/G]ATCACAGGTACAAAG | 8453 |
rs186535504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35021545 | AATGTCAATTTTAAT[A/G]TATGAATATGTATTA | 8453 |
rs186562911 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125742 | TGTAAGTTGTTTGGC[G/T]TAAAGCCATGATTTC | 8453 |
rs186581934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066903 | CTTCTAACACTTGTG[A/G]AAAGTGTCAAGGATA | 8453 |
rs186588360 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092155 | ACATGGGGTCTCACT[A/G]TGTTGCCCAGGCTCC | 8453 |
rs186600176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121758 | GAGGCTACAGTGAAC[C/T]ATGATCGCACTACTG | 8453 |
rs186604273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35108000 | CTAATGTGGCACTTA[C/T]CTGAATTCATTGCAA | 8453 |
rs186622692 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35088702 | GACATGGATAATCTT[C/T]ACATTTATAGAACAC | 8453 |
rs186628586 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | CUL2 | GRCh38.p7 | 10:35071870 | AAGCTCTAGGAAATG[G/T]AAAGCTTCTAGTACA | 8453 |
rs186742791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017558 | AATTCGCCGGGCATG[A/G]TGGCATATGCCTGTA | 8453 |
rs186746829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35031971 | AAGAACAAGTCAAAT[A/G]TCAAATCATCACTTA | 8453 |
rs186749359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101900 | ATGAAAAACAGGATA[A/T]CTGTGTTGTAGCTGT | 8453 |
rs186750757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35037049 | CTGGATCAATCGTTC[C/T]TTTGTGGTTAGGGCT | 8453 |
rs186753395 | snp | A/C/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008376 | CCTCTCTTCCTCATG[A/C/G/T]GAGAGATGTTTCCTT | 8453 |
rs186756968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053886 | CCATTGTATCCCCAA[C/T]GCCTGGCTACTCAAT | 8453 |
rs186766527 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35065640 | AAATAAATAAATAAA[A/C]ATTTAAAAAAAGAGA | 8453 |
rs186816864 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CUL2 | GRCh38.p7 | 10:35109279 | AACAAAAAACCTGAC[C/G]GTCATTTCAACCAGG | 8453 |
rs186831361 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074736 | AAGTGATCCGCCCGC[C/T]TTGGCCTCCCAAAGT | 8453 |
rs186840123 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35118563 | TCTCTGAAGCTCTAT[G/T]AAGCTTATTTTCAAT | 8453 |
rs186857077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35105178 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 8453 |
rs186861092 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CUL2 | GRCh38.p7 | 10:35085155 | AATAACTGGCTGGGT[A/G]TGGTGGCTCACACCT | 8453 |
rs186863099 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35107683 | GTCAGGAGATGGAGA[C/T]CATCCTGGCTAACAT | 8453 |
rs186864648 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126464 | CCCAGCTACTCAGGA[A/G]GCTGAGGCCGGAGGA | 8453 |
rs186871551 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | CUL2 | GRCh38.p7 | 10:35067889 | GAGGCAGGCGGATCA[C/G]GAGGTCAGGAGATCG | 8453 |
rs186891180 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35034380 | ATAAAAAAATAGAAA[A/G]CTTACACATTATTGT | 8453 |
rs186902293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050909 | TCAAGCCAAATGATT[C/T]TCCAATTTATACTTG | 8453 |
rs186916667 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048465 | AAATTATATTAAAAA[A/T]GATATTTCACAAAAG | 8453 |
rs187027171 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35038251 | ATCAGAGAGGCCGGG[A/C]GCAGTGGCTCACGCC | 8453 |
rs187051362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35120975 | TATAATTCCCTTATG[C/T]TTTATAGAGACTTAC | 8453 |
rs187063776 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CUL2 | GRCh38.p7 | 10:35088442 | GAACTGGGAGGTTGC[A/C]GTGAGCCCAGATCGT | 8453 |
rs187107961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128071 | GCTGGTCTCGAACTC[C/T]TGACCTTCCACCCAC | 8453 |
rs187137481 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35111803 | GCTGAGGCAGGAGAA[A/T]CACTTGACTCTGGGA | 8453 |
rs187139668 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094359 | TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGAGATT | 8453 |
rs187148146 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35077334 | AAACAAACAAACAAA[A/C]AAAACAAACAAAAAT | 8453 |
rs187153109 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35058486 | GGTCCATTGTAACTC[C/G]AGATCTGTAGTCTAA | 8453 |
rs187185105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35052441 | AAAAAGTTCTGCTCA[C/T]GTACCAAGAGATACA | 8453 |
rs187189077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35013136 | ACGATGTCAGGAGAT[C/T]GAGACCACCCTGGCT | 8453 |
rs187194409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35033731 | GACAGAGTGAGACTC[C/T]GTCTCAGAAAAACAA | 8453 |
rs187217307 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35076864 | AGATCAGCTGGCTGA[C/G]ATGGTGAAACCCCAT | 8453 |
rs187222227 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35019879 | GGTTCCTGGAACAGG[A/G]TATTCATGCCAAAGT | 8453 |
rs187237831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35056754 | ATATTACCATTTACA[C/T]ATGCCTTCCAATACG | 8453 |
rs187334458 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35022071 | CACCGTACTGTAACT[A/G]TGTACGTATGTCTGT | 8453 |
rs187341058 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35040859 | CACAATGGAGTTTGC[A/G]CTCTGTGAGAATCTA | 8453 |
rs187347302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058089 | GGAAACAGCGAGACT[C/T]GGTCCCAAAAATTAG | 8453 |
rs187364550 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35114579 | GTAGAGACAGGGTTT[C/T]GCTATGTTGGCCAGG | 8453 |
rs187406039 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35015763 | TGCTGACATTAAGAA[C/G]ACTTGGAATGGAGTT | 8453 |
rs187432469 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35115024 | CGAGACCAGCCTGGC[C/T]GATATGGCAAAACCC | 8453 |
rs187441951 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35063674 | AAGGAGTGGAAAGAA[G/T]TAAGACCTGAGACTT | 8453 |
rs187443314 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35098777 | CTCTACTAAAAAAAA[A/C]CAAAAAATTAGCTGG | 8453 |
rs187446334 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080968 | CCTGTAATCCTAGTA[C/T]TTTGGGAGGCTGAGG | 8453 |
rs187454614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063353 | GGAGTTTCTGGAAAA[C/T]CAAATTACCCAGAAT | 8453 |
rs187572439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35028324 | AGGACTCTCCTCTAT[C/T]AGTTATTACCACGAA | 8453 |
rs187594154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099763 | AATAAAATAAAAAAA[C/T]AAAATAGCTTACTTA | 8453 |
rs187660766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35111279 | TTTTTTTGATTCGGG[C/T]TCTGGTTCTGTTGCC | 8453 |
rs187666148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071413 | TTGTTGTTTTTTGTT[G/T]GTTTGCTTTGAGACG | 8453 |
rs187672625 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35035984 | ATACATATACAGAAA[A/T]GTATACAAACCATAA | 8453 |
rs187677112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075832 | TTCCTCACAGCATAA[C/T]TTCTAAATATGCATG | 8453 |
rs187688313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081418 | TTGTTCAATAATCTA[A/G]TCAACGAATTTAAGA | 8453 |
rs187767252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025424 | CAACTTGTTCTAGAG[C/T]TCTCTCCACTAAACC | 8453 |
rs187775310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043690 | GTGGTTTAATTTGTA[G/T]GAACACTTTTTTCTT | 8453 |
rs187786876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013875 | GCTGCAAGCAATTCT[A/G]CTAAATTAATGACCA | 8453 |
rs187837796 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021878 | GGGTGGGGTGAGGTG[A/G]GGTGAGGTGGGGTGA | 8453 |
rs187846000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046090 | CCTCTTTGATTCTTC[C/G]TTTAATTATTTGGAT | 8453 |
rs187851260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35115316 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCGGAGG | 8453 |
rs187882574 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045503 | ATGATCCCTTGAGTC[C/T]TGAGTTTGAGACTAG | 8453 |
rs187909622 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098359 | AGTAAATCTGGGTAA[C/T]GGATTGCAAGGACTT | 8453 |
rs187919472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079985 | TCTGAGCAGGACAGT[A/G]CAAGATTTCATCACA | 8453 |
rs187927339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062828 | GGCAACAGAGCAAGA[C/T]CCTGTATTTAAAAAA | 8453 |
rs187951163 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093728 | TGAATTTCACTATAG[A/T]ATCAAAGAAGAATAT | 8453 |
rs187955732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055910 | CTCCACCTAAGTGCC[C/T]CATCCCAGATATTCT | 8453 |
rs188012131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35049896 | CAAAATTCAAATAAA[A/G]CCTGAACAAAAATTT | 8453 |
rs188012888 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35121823 | TCAAAAAAAAAAAAA[A/T]AAATAAAAATTAGTT | 8453 |
rs188111872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124799 | CTTACAGTTGGATTC[A/G]GAGAGGAAAAAGAGG | 8453 |
rs188114567 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35118058 | TCATAATCATCCAAA[C/G]TGCATACATTAGGCT | 8453 |
rs188128278 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35108804 | TACTGTTGGCAGGAG[A/C]CCTCAGTTCCATGCA | 8453 |
rs188132147 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090781 | CTGAGCTGATGGACA[C/T]AGTACCCACCCACTA | 8453 |
rs188143618 | snp | A/G/T | 0.0138799 | 0.0821421 | intron-variant | CUL2 | GRCh38.p7 | 10:35073766 | TCTGCCACCACACCC[A/G/T]GCTAATTTTTTATTT | 8453 |
rs188149472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038094 | GGCAGGGGTTGCAAT[A/G]AGCCAAGATCATGCC | 8453 |
rs188151110 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35027004 | CCCAGACTAAACTTA[C/T]TTTAAAATAAACAGG | 8453 |
rs188173203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120018 | AAAAAACGTTTGGCC[C/T]CAATTTCTTTGCACA | 8453 |
rs188176809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35107011 | GCAGAGTTTCACTCT[A/G]TCACCCAGAGTAGAG | 8453 |
rs188188825 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35087751 | AAAACGTTTTCACTT[A/G]TACCTTAACCCTCCA | 8453 |
rs188196873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070619 | AAACTCTCAATTCAC[A/G]CATGTAGGCAATCTA | 8453 |
rs188295234 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35035484 | TGTGGTTATTTAACA[A/C/T]CTTCCCAAAGATATT | 8453 |
rs188302589 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35051936 | TCTTCTTTATCATGG[A/G]TATTTTTTAAGAAAT | 8453 |
rs188309213 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35041606 | GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACTT | 8453 |
rs188318011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35033552 | CCATCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 8453 |
rs188368112 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CREM, CUL2 | GRCh38.p7 | 10:35127422 | CGAGGCCGCCGGCTC[C/G]CCGCCCCACGCCCGC | 8453 |
rs188402777 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35104212 | AGCACTTACGGATGC[C/T]GAGGAAGGTGGATTG | 8453 |
rs188423867 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067103 | AAGATTGCACTATTG[C/G]ACTCCAGCCTGGGCA | 8453 |
rs188427894 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35108723 | CAGTCAAAGTATTGG[C/T]CTGGGCTACAGCCAT | 8453 |
rs188596500 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35012308 | AAGATTAGAAAAAAA[A/T]TTACATTATTGTAAA | 8453 |
rs188601323 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35014252 | TGATGACAAGAGAAA[A/G]CTGTGCCTCCAGTAG | 8453 |
rs188603711 | snp | C/G | 3.2962e-05 | 0.00405954 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35035229 | ATGGATGTGGTTTTG[C/G]AGCTCCTGAATCATA | 8453 |
rs188656282 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111625 | AGGCGTGGTGGCTCA[C/T]GCCTGTAATACCAAC | 8453 |
rs188663916 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35040568 | GCTCCAGACAGTAGG[A/T]TCCCACAGTCCTGTC | 8453 |
rs188696802 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CUL2 | GRCh38.p7 | 10:35124234 | GGTAGTATCTGATGA[A/G]GAAAATAGGTCAAGT | 8453 |
rs188721696 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35090286 | GGAGGCGGCGGCGGC[A/G]GCGGCTGTCAGCTCG | 8453 |
rs188804734 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35018016 | TGAAATTGGGCCAGG[C/T]GTGGTGGCTCACGCC | 8453 |
rs188817373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053955 | TACTTCTTTCACAAT[A/C]AGCATAATTTTCCAT | 8453 |
rs188878175 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35042411 | GTTCCTGGTTCATAA[C/T]TCCCTTAGCCCTAGT | 8453 |
rs188931112 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021898 | AGGTGGGGTGAGGTG[A/G]GGTGAGGTGGGGCGA | 8453 |
rs188951875 | snp | A/C | 0.089084 | 0.191327 | intron-variant | CUL2 | GRCh38.p7 | 10:35057819 | AAGACATGGGCTGGA[A/C]GCAGTGGCTCACGCC | 8453 |
rs189037763 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018325 | AAAAAGATGAAATCA[A/G]CATGAGATTTGATTT | 8453 |
rs189039609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095975 | ATTTTGAGGCTGGGC[A/G]TGATGGCTTAGCCTG | 8453 |
rs189042914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35118984 | CCCAGGCACAGGCTG[A/G]CCAATCCACACTCAC | 8453 |
rs189050263 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CUL2 | GRCh38.p7 | 10:35037795 | TTATAGTGAACAGAG[A/C]TCGCGCCACTGCATT | 8453 |
rs189051178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078408 | GTGAGCAATTCTCCT[A/G]CCTCAGCCTCCCAAG | 8453 |
rs189057601 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35060471 | AATTTATCTAACATC[A/G]TTTGCATCAAACATA | 8453 |
rs189058175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054282 | TTCCTGAGGATTCTT[A/G]GGAAATCACTATAGC | 8453 |
rs189059247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106130 | CGTCATCAGGGTGGA[A/G]GTCTTCTGAATGGGA | 8453 |
rs189071728 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35023783 | AAAATCTAAAACCCT[C/G]GTCCAGCATTTTTTT | 8453 |
rs189088465 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35037168 | CTTGTACATTTAGAG[A/G]AAAAACTCAATAGTG | 8453 |
rs189101600 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116688 | ATTAGATGCTCTGGC[A/T]GGGCATGGTGGCTCA | 8453 |
rs189105689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101067 | GCCTCTATCCTAGGA[C/G]TGAGAAAAGGGAGAG | 8453 |
rs189124918 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CUL2 | GRCh38.p7 | 10:35101983 | CCTCCCAAAATGCTG[A/G]GATTACAGGTGTGAG | 8453 |
rs189145185 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35065847 | CTGGCAACAGAGCGA[C/G]ACACCATCTCAAAAA | 8453 |
rs189184545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35108199 | ACAGTGGCTCATGCC[C/T]GTAATCCCAGCACTC | 8453 |
rs189203205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073095 | CAGGAATAGACTCCA[C/T]GGAAAAGAATGAAAA | 8453 |
rs189212548 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35113261 | AGCATTTTGGGAGCC[C/T]GAGGTGGGTGGATCA | 8453 |
rs189229982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35077609 | CATTACCTGAGGTCA[C/T]GAGTTCAAGACCAGC | 8453 |
rs189298332 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35041965 | AAAGTGTGCAATTCA[A/G]TGGTTTTGGTATATT | 8453 |
rs189307425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015163 | CTGGGCATGGTGGCA[C/T]GTGCCTGTAGTCCCA | 8453 |
rs189402788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35116852 | GTCCCAGCTACCCGG[A/G]AGGCTGAGGTGGGAG | 8453 |
rs189418808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35082703 | AAATAATACTTGGTA[C/T]TATGATGACAAAATA | 8453 |
rs189447651 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077706 | CCTATAATCCCAGCT[A/G]CTCAGGAGGCTGAGG | 8453 |
rs189471053 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119650 | CAGGTTACAGTCCAG[C/T]GGTGCAAACTCCTAG | 8453 |
rs189504875 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009062 | GAAACCCCGTCTCTT[A/G]TTTTTTTTAAAATAA | 8453 |
rs189505461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095303 | CACTCCAGCCTGACA[A/G]TAGAGCAAGACTCCA | 8453 |
rs189512135 | snp | A/G | 3.96707e-05 | 0.00445351 | intron-variant | CUL2 | GRCh38.p7 | 10:35029451 | TCAACGTACTGAAAT[A/G]ATTAGTAAATGCTCA | 8453 |
rs189521746 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059424 | AGACTGGCAAAAGGA[A/T]TACAACTTGCTGAAG | 8453 |
rs189523654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011142 | CTCAAGCAATCCTCC[C/T]GCCTCAGCCTCCCAA | 8453 |
rs189527642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032591 | ATCCAAAAATTACCC[C/T]GCCACATAAAACACA | 8453 |
rs189573197 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35023356 | ATAAGGTTCTCTTTC[A/C/T]AAAGGAAGTAACTAT | 8453 |
rs189574808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116083 | CACAGCGGTTCACAC[C/G]TGTAATCCCAGCACT | 8453 |
rs189582962 | snp | C/G | 0.000798403 | 0.0199641 | missense | CUL2 | GRCh38.p7 | 10:35100944 | CACAGGGTTTTCTTT[C/G]CATGTCGCCATGGGT | 8453 |
rs189586558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082273 | CCTTGAAGATATTAC[A/G]CTAAGTCAAATACAC | 8453 |
rs189596849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35064779 | AACTCTTGGGCTCAG[A/G]CAATCCTTCTGCCTC | 8453 |
rs189607165 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35022842 | ACGAGGTCAGGCGTT[C/T]GAGACCAGCCTGGCC | 8453 |
rs189700929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086900 | AAGTGTACTACTGTT[G/T]CTGCAAAGTGGGAAC | 8453 |
rs189768140 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126235 | TGGGATTACAGGCCC[A/G]AGCCAGCGGGCCCAG | 8453 |
rs189782621 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110423 | TACAAAAATTAGCTG[A/G]GTGTGGTGGTGCACG | 8453 |
rs189784720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35093087 | GCCCCACCCAGAGGC[A/G]GGCTCAGCACTCAAG | 8453 |
rs189793111 | snp | C/T | 0.030665 | 0.119967 | intron-variant | CUL2 | GRCh38.p7 | 10:35068034 | AGAATGGCATGAACC[C/T]GGGAGGCGGAGCTTG | 8453 |
rs189797283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075726 | AAATAAAAATTTATA[C/T]TTAATTACCTGTTTC | 8453 |
rs189872339 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35024759 | CAAATGGTTAGGTCT[C/T]CTTATGATGCTATAA | 8453 |
rs189945553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106444 | CCTGCCTCAGCGTCC[C/G]GAGTAGCTGTGACTA | 8453 |
rs189969984 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034694 | AGTATTAGGGATATG[A/T]GGGTTATTGTTTTGG | 8453 |
rs190026569 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | CUL2 | GRCh38.p7 | 10:35121821 | TCTCAAAAAAAAAAA[A/T]AAAAATAAAAATTAG | 8453 |
rs190033350 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35108065 | ATGTTGGAAAAATAA[C/T]ATCTTCGCCTTTTGT | 8453 |
rs190034217 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35082480 | TGGTGGTTTTGGAAA[C/T]GGTGGTGAGGGTCAC | 8453 |
rs190055500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35073490 | TTGTGTATACTGCAA[A/G]CCAAGCACTAGTCTA | 8453 |
rs190110769 | snp | A/G | 3.35492e-05 | 0.00409554 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35010320 | GCGACATCACGCGAC[A/G]TAGCTGTATTCATCT | 8453 |
rs190120432 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113626 | AACAAAATATAATTC[A/C]TAATCAGGAGAAAAA | 8453 |
rs190128296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071704 | TGAACCATCACACCC[A/G]GCCAGTTATTTGTTT | 8453 |
rs190136994 | snp | A/G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096474 | AAATAGCAGCTGGGT[A/G/T]TGGTGGTGCATGCCT | 8453 |
rs190141306 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35078848 | TACTGATCAGCAGCA[A/C]CAATAAAAATTTGGC | 8453 |
rs190149193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35036802 | GCAGTGGCAGGATCT[C/T]GGCTCACTGCAACCA | 8453 |
rs190156069 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CUL2 | GRCh38.p7 | 10:35053069 | TGTGTGCCGTTTTAT[C/T]GCAGTTTGAAAAATA | 8453 |
rs190202037 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35113446 | GAGGTTGCAGTGAGC[C/T]GATATCACGCTACTG | 8453 |
rs190210247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35014058 | GCTATTTTCTGGTCC[C/T]ACTATTCTATATACA | 8453 |
rs190230591 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35051332 | AAAAGAAAAAAAACC[A/G]GCCAGGCGCGGTGGC | 8453 |
rs190273631 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125227 | GCAGAGGCCATGAAC[C/T]GATGGGCTTGTAAGT | 8453 |
rs190334185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017422 | ATATGTGCTGGGCAC[A/G]GTAGCTTATGCCTGT | 8453 |
rs190337947 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35026401 | TTTATAACACATTTA[C/G]AATGAATCTGGACAA | 8453 |
rs190348270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35043827 | ATCCCAGCGCTTTGG[A/G]AGGCTGAGGCAGGAG | 8453 |
rs190367917 | snp | A/G | 4.95372e-05 | 0.00497656 | missense | CUL2 | GRCh38.p7 | 10:35031582 | TCTGTCATCCCTTTC[A/G]CTGACTTCTTCAGTA | 8453 |
rs190422677 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35114766 | AGCATGGTGAGGAGA[A/G]AGAAAATATTTTTAA | 8453 |
rs190430357 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35098556 | AGAAAAAAAAAATGT[C/G]TGTTACCAAGAGCAA | 8453 |
rs190432443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120756 | CAAAAATTAGCCTGG[C/T]ATGGTGATGCACACC | 8453 |
rs190434618 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080402 | CATAAACAACATTTC[C/T]ATCATGACTTTCTGG | 8453 |
rs190445375 | snp | A/G | 0.000198863 | 0.00996956 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35063050 | ATAGGCCACACATAA[A/G]GCATAGATATCTCTA | 8453 |
rs190449957 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35020177 | AATTTAAAAAAAAAA[A/T]AAATAAATCACAAAT | 8453 |
rs190468907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35056972 | CTGACCCTCTGCCCC[A/G]ATTATGTGGAACACT | 8453 |
rs190487750 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091918 | CAGGCCTGAGCCACC[A/G]TGTCAGGCCCCCCCT | 8453 |
rs190523118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109139 | GATTGCTTGAGCCTG[A/G]AGGTTGAGGCTCCAG | 8453 |
rs190617679 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35040080 | ACTGCTTGAACCCAG[A/G]AGGAGGAGGTTGCAG | 8453 |
rs190658161 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092248 | GGAGTGAGCCACCAT[A/G]CCTGGCCTCCTCTGT | 8453 |
rs190666261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074970 | AAAAAGCTAGCGATG[A/C]TCCCCTCACATTCGC | 8453 |
rs190680191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35117696 | TGCTACATGTGAGTG[A/G]TGTATTACTGAAGGT | 8453 |
rs190708394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039264 | TTTTTATTTAAGCTA[C/T]TAGCTGTCATCTACA | 8453 |
rs190744452 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074677 | TGTTAATAGAGACAG[C/G]GTTTCACCATGTTGG | 8453 |
rs190757147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117230 | AGCTAGAAGAATTGC[A/G]GAATTCACGAAGGCT | 8453 |
rs190780933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35021075 | AGTGCTAGATTACTA[C/T]GACCTTATTTAACCT | 8453 |
rs190781498 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35083065 | AGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 8453 |
rs190787667 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35066368 | GCGGTGGCGTGATCT[C/T]GGCTCACTGCAAACT | 8453 |
rs190789313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039527 | GTAAATGGAACTGTA[C/T]GTGCATGATAGTTAA | 8453 |
rs190797718 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CUL2 | GRCh38.p7 | 10:35057121 | TGTAAACTGCCTAGC[A/G]TAGAAGCAGATGCTA | 8453 |
rs190800195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079406 | CTTAGAGTAAATGGT[C/T]TGGTGTCATTCGTCT | 8453 |
rs190853268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047778 | AAAAATTAGCAGGGC[A/G]TGGTGGTGCCCAGCT | 8453 |
rs190857343 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35021768 | ATGTGGGCTGTGATC[A/G]CGCACCTCCACTCCA | 8453 |
rs190878572 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35057597 | GGCGGAGGTTGCAGT[A/G]AGCCGAGATCGTGCC | 8453 |
rs190943435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043524 | TTTGTGACTTGTGGC[C/T]TAGGGATGTAGGATG | 8453 |
rs190975766 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35114490 | CAGGTTCCAGCGATT[C/T]TCCTGCCTCAGCCTC | 8453 |
rs190981246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35032730 | CTGTAACTCATTATC[A/G]AAATTTGAACAGATA | 8453 |
rs190986612 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047984 | TCCCTAGAATTATTA[C/T]TAGATGGAGGCTGGA | 8453 |
rs191029973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121153 | CAGGCAATTCAGGAG[C/T]TATTAGAGAAAGAGT | 8453 |
rs191037304 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35097965 | CTCTGACTCAAAAAA[A/T]TTAATTAATTAAATA | 8453 |
rs191055722 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088539 | AATGTAATGTGTCTT[A/G]TTTACCCTTGTAACC | 8453 |
rs191260541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024542 | CTGCTTTGGCTTACA[A/T]CTTCAGGCAACTCCA | 8453 |
rs191270870 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35013303 | TGAGCCGAGATCACA[C/T]CACTGCACTCCAGCC | 8453 |
rs191274904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034028 | GAGACCCCTTGAACT[C/T]GGCAAGACAATCCCT | 8453 |
rs191285118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050203 | GCATGCGCCTGTAAT[C/T]CCAGCTACTCGGGAG | 8453 |
rs191289670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062005 | CATTTTATAGATAAA[C/G]TCAAAACTCAGTCCA | 8453 |
rs191292369 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35107730 | TACTAAAAATACAAA[A/T]AATTAGCCAGGCGTG | 8453 |
rs191362862 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35067153 | TCAAAAAAAAAAAAA[A/G]AAAAAGAAATGAAGA | 8453 |
rs191400042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036108 | TCCCCTTCATGCCTC[A/C]TTCCAATCACACACT | 8453 |
rs191430884 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35071955 | TGCGAGGGAAAGAAA[C/T]GGGGACCCACTTAAC | 8453 |
rs191433676 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046522 | CTCTCTAGTTTAAGT[C/G]TGAGTTCATCCTGGT | 8453 |
rs191506086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35042649 | GACTGGGTTCCACAG[A/G]GATAGAAGCTCCTGC | 8453 |
rs191511081 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090732 | CCAAGTGATTCCTTG[C/T]TGGGCTTGCTGTCAA | 8453 |
rs191519440 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35073509 | AGCACTAGTCTAAGT[A/G]CCCTGTACAAACTCG | 8453 |
rs191520855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115056 | ATCTCTACTAAAAAT[A/C]CAAAAATTAGCTGGA | 8453 |
rs191522479 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35099262 | TGGGCATGGTGTTAC[A/G]CGCCTGTAGTCCCAG | 8453 |
rs191527099 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35107346 | GTGGTTTTGAAAGTA[A/G]GCTGAAGGTCAAGAT | 8453 |
rs191541427 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35071506 | GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 8453 |
rs191584018 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084122 | TCTCTACTAAAAATA[C/T]AAAAATTAGTCAGGT | 8453 |
rs191588367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109344 | ATTCCTTGATTGATT[A/G]CATCATTATTTCATA | 8453 |
rs191607276 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35053891 | GTATCCCCAATGCCT[A/G]GCTACTCAATAAAGA | 8453 |
rs191608810 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008411 | ATAAAATGGAGAAAG[A/G]ATGTGAAGAAAACTC | 8453 |
rs191608985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088774 | ATGCAGGAGAACATC[C/T]AAATACTCAAAAAGC | 8453 |
rs191610523 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35028345 | TTACCACGAAACTAA[G/T]AACCACTATCAATCA | 8453 |
rs191614136 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35018930 | TGGGAATACCAAGAG[A/T]AAAAATTCATAGCCC | 8453 |
rs191618737 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35037830 | CCTGGGCCACAGAGC[A/G]GGACTCCGTCTCAAA | 8453 |
rs191628469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055465 | TGGCCAGGCGTCGGG[A/G]CTCACGCCTGTAATC | 8453 |
rs191644288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015994 | AATCAAACTATAAAC[A/G]GCACATGGCACCAAC | 8453 |
rs191660041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35052863 | TCACACCACTGCACT[A/C]CAGCCTGGGTGACAC | 8453 |
rs191744196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35012494 | AAAGGGAAGAGCTGT[A/G]AAGTGGCATTTTATG | 8453 |
rs191763581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048467 | ATTATATTAAAAAAG[A/G]TATTTCACAAAAGTA | 8453 |
rs191769847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128211 | ATCACTTAGGGGTTT[C/T]CTGCATGCTGCTCAG | 8453 |
rs191773564 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35111845 | CAGTGAGCTGAGATC[A/G]CATCATTGCACTCCA | 8453 |
rs191790704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088372 | AATTAGCTGGGCGTG[C/G]TGACGTGCGCCTGTA | 8453 |
rs191823571 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126638 | TGACAACAGCCGTTA[C/T]TCTGGCTGACAAGTC | 8453 |
rs191845764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093811 | TCATATATTTCAACC[A/G]TAGAGAACCTAGCTA | 8453 |
rs191887396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066930 | GATACAGGTACTTGC[C/G]TCAATATTTTTCAAT | 8453 |
rs191901641 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35057966 | AGCCAGGTGTGGTGG[C/T]GCGTGCCAGTAATCC | 8453 |
rs191933247 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120668 | TTGAGAGGCCAAGGC[A/C]GGCAGATTGCTTGAG | 8453 |
rs192058480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35033560 | GCCAACACGGTGAAA[A/C]CCCGTCTCTACTAAA | 8453 |
rs192087507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103237 | AGCTTCAAACTCCTG[C/G]GCTCAAGGGATCCTC | 8453 |
rs192096676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058287 | TAAATGGCCATCCTC[C/T]TCCTGGACGAATAAC | 8453 |
rs192141674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111553 | GTAAGCCATTGCACC[C/G]AGCCAATAATTCTAA | 8453 |
rs192156522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075883 | AAGTGAATTATAAAA[C/T]GCAGCTACCATATGA | 8453 |
rs192199783 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041739 | ATGGGGTTTTGCCAC[A/G]TTGCCCAGGCTTGTC | 8453 |
rs192233110 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35077355 | AAACAAAAATTAGCC[A/G]GGTGTGGTGGTGGCT | 8453 |
rs192234648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104307 | AAAAATTAGCTAGAC[A/G]TGGTGTAGTGCATTT | 8453 |
rs192267541 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35111658 | TTTGGGATGCCGAGA[C/T]GGGTGGATCACTTGA | 8453 |
rs192277430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094033 | TACAATAACTATTTA[C/T]AGATAGATAGTTTCC | 8453 |
rs192280681 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022128 | GAGGGCCAAGGCTCT[G/T]TATTTTATTTCTGTC | 8453 |
rs192288893 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076983 | CGTGAACCCAGGAGG[A/C]GGAGCTTGCAATGAG | 8453 |
rs192290577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041113 | TTACATCAGCTAAGA[A/C]AGGCACTTTGATTAA | 8453 |
rs192376182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35118816 | TTGGGAAAAAGGTAT[A/G]TCTCATGTCAAAGTG | 8453 |
rs192379067 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105460 | ACTAAGTAATTGGGC[C/T]GGGTGCGGTGGCTCA | 8453 |
rs192392589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35085255 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAA | 8453 |
rs192399688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35067946 | CCCTGTCTCTACTAA[A/G]AAAATACAAAAAAAT | 8453 |
rs192470542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35050943 | AGCAAAGCACAAGAT[C/T]TCCCATTAGTCCCCA | 8453 |
rs192491552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017950 | GAAGTTGTGGTTTGA[C/T]GACTAACACACACAC | 8453 |
rs192539594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35124487 | GGAAATAACAAACAA[A/G]TGGGTGGTGAAGAAG | 8453 |
rs192585538 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063406 | AGAATGGATATTAGT[A/T]TCAATAGTATCAATG | 8453 |
rs192590002 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35100963 | GTCGCCATGGGTTTT[C/T]GTCCATGTCCTTTGC | 8453 |
rs192590956 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35022873 | AACATGGTGAAACAC[C/T]GTCTCTACTAAAAAT | 8453 |
rs192595302 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35082354 | ATGTGGGCAAATTCA[C/T]AAAGACAGAAAGAAG | 8453 |
rs192640620 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027005 | CCAGACTAAACTTAT[C/T]TTAAAATAAACAGGA | 8453 |
rs192644308 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35118425 | CTTGCTCTAATCTTC[C/G/T]GGTTCATGAGTGAAC | 8453 |
rs192650375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058807 | CTCTTTGGACAAAAC[A/T]GCCACAGATGCATCT | 8453 |
rs192656087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084675 | TTACTGAGAGAGGGT[C/T]CAGTCATACATCTCA | 8453 |
rs192804900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037087 | TCCTATTTAAAATAT[A/C]TTTCCCTGTCTCAAG | 8453 |
rs192808075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063737 | TTCCTAGCCTCTCTC[A/G]GGTGGCATTTCCTTT | 8453 |
rs192824724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108728 | AAAGTATTGGCCTGG[A/G]CTACAGCCATCTGAA | 8453 |
rs192843421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080990 | AGGCTGAGGTGGGAG[A/G]ATCACTTGAGCCTGG | 8453 |
rs192854391 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108692 | TAGTTCTTTTTCAGG[G/T]TTTCTCATGAGATTT | 8453 |
rs192864266 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35073289 | GAGTGGAGGAGGTGG[A/G]AGAACCTACTGAGTT | 8453 |
rs192876344 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35046040 | CAATTACCTTTACAT[A/C]CTAGAGTCCTTCCCT | 8453 |
rs192975692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119081 | TCCAATGCTCCTTGC[A/G]TGTTCCTTTTATCTA | 8453 |
rs192984072 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35085649 | CTCGGGAGGCTGAGG[A/C]AGAATGGTGTGAACC | 8453 |
rs193038195 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35018156 | GCAGGGCGCAGTGGC[A/G]GACACCTGTAATCCC | 8453 |
rs193045235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35054121 | CTAGCCTGTCTTTTA[A/G]GTACTTGTCCCCTGC | 8453 |
rs193054630 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35021966 | AAAACAAGTTGAGAT[C/G]TGATTTCCCCAGAAG | 8453 |
rs193066965 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35034514 | TACTATCTTATAGAT[A/G]AAGGGCAAACAGCTC | 8453 |
rs193067261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35089295 | ATGTGTCTGTCTTGA[A/C]AAGGAATGTAAGATT | 8453 |
rs193156151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35034749 | TTACAGAAGATTATT[C/T]TAATCTAAATTTGCT | 8453 |
rs193194246 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35106350 | TTTGAGAAGGAGTCT[C/T]ACTCTGTAGCCCAGG | 8453 |
rs193196210 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127527 | AGAGCCGTGCGGCTC[A/G]GGGGAGCGGTTTAAC | 8453 |
rs193197748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35069058 | ATTTTTAGTAGAGAC[A/G]AGGTTTCGCCATGTT | 8453 |
rs193232191 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35040829 | GCACATCCTAGACCC[C/T]TTGCATGCAGAGTTC | 8453 |
rs193234610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013876 | CTGCAAGCAATTCTG[A/C]TAAATTAATGACCAA | 8453 |
rs193277525 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35122169 | ACACTATCTTTGTAA[C/G]TCTCAAATCCTAAAG | 8453 |
rs199616893 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102755 | GGGTGCAGTGGCAGG[C/G]GCCTGTAATCCCGGC | 8453 |
rs199618380 | snp | A/G | 0.448832 | 0.151545 | intron-variant | CUL2 | GRCh38.p7 | 10:35025203 | AATAATTCAAACTGT[A/G]AAAAAAAAAAAAAAA | 8453 |
rs199633648 | in-del | -/A | 0.434543 | 0.168653 | intron-variant | CUL2 | GRCh38.p7 | 10:35030825 | TTGAGCCCAGGAGTT[-/A]GAGTCCAGCCTGGGC | 8453 |
rs199658136 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013069 | CTGTAGGCCAGGCGC[A/G]GTGGTTCACACCTGT | 8453 |
rs199665263 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104742 | ATCAAAGACTTTTCT[-/G]GGGGGGGGGACAGTC | 8453 |
rs199677160 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022079 | TGTAACTATGTACGT[A/T]TGTCTGTCTTCCTAC | 8453 |
rs199678326 | snp | A/T | 0.000165033 | 0.00908236 | intron-variant | CUL2 | GRCh38.p7 | 10:35032397 | TTTTCTAATACTGAC[A/T]TTTCATAAGATTACT | 8453 |
rs199703931 | snp | C/T | 0.000439194 | 0.0148123 | intron-variant | CUL2 | GRCh38.p7 | 10:35061004 | TTTTTACTTGAAAAG[C/T]AATAATCATTTTCAC | 8453 |
rs199712281 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116957 | AAAAAAAAAAAAAAA[-/A]GTTAGCCAGGGCTGA | 8453 |
rs199744148 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117090 | AGAGTATTTTTGAAT[A/G]TATCGAAGAGTTGAG | 8453 |
rs199806303 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35032465 | GCAAACAGACTTAGG[C/T]TCTCTGTAATTTACA | 8453 |
rs199816765 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105827 | AGAGGCAATGTCCTG[-/AA]AAAAAAAAAAAAAAG | 8453 |
rs199816897 | in-del | -/AAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033742 | ACTCCGTCTCAGAAA[-/AAC]AACAACAACAACAAA | 8453 |
rs199822354 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127857 | TATTAAACATACTTT[-/G]TTTTTTTTGAGACGG | 8453 |
rs199872765 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087884 | TAATGTATCTAAGAA[A/C]AAAGCCAACATGATC | 8453 |
rs199934302 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant | CUL2 | GRCh38.p7 | 10:35023351 | ACTTATAAGGTTCTC[-/T]TTTCCAAAGGAAGTA | 8453 |
rs199989127 | in-del | -/GAT | 0.0607341 | 0.163335 | intron-variant | CUL2 | GRCh38.p7 | 10:35021496 | TGATAAAACTATATA[-/GAT]GATATTTCCATAATT | 8453 |
rs200046265 | snp | A/G | 0.00397837 | 0.0444225 | intron-variant | CUL2 | GRCh38.p7 | 10:35033287 | ATCTAAAAATGAAAT[A/G]TAAGTACAAAACCAC | 8453 |
rs200104650 | snp | C/G | 0.00199796 | 0.0315435 | missense | CUL2 | GRCh38.p7 | 10:35038992 | GGTCTGCTACCATTC[C/G]TTGTTGACATTCATG | 8453 |
rs200180031 | in-del | -/TAA | 0.205417 | 0.245993 | intron-variant | CUL2 | GRCh38.p7 | 10:35021529 | AATACATGTTTATAT[-/TAA]TGTCAATTTTAATGT | 8453 |
rs200223718 | snp | C/T | 0.0002472 | 0.0111148 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060945 | ATACATAACAAGTAC[C/T]TGTTCTTCTGACTCC | 8453 |
rs200285461 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060867 | TAGATTTTAAAGGCA[A/C]ACTCACCTATATAAG | 8453 |
rs200287719 | in-del | -/TTTC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041542 | AAATGAGCTTTTCTT[-/TTTC]TTTCTTTTGTCAGAC | 8453 |
rs200339343 | snp | C/T | 4.11497e-05 | 0.00453577 | intron-variant | CUL2 | GRCh38.p7 | 10:35028778 | ATTATTAAAATTCCT[C/T]TAGTCTTCTAATATA | 8453 |
rs200343397 | in-del | -/AC | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35021442 | TGTATGTATATATAT[-/AC]ACACACACACACATA | 8453 |
rs200356394 | snp | A/C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049518 | GAAGAAGAAGAAGAA[A/C/T]AAAATAAAACAACTT | 8453 |
rs200363384 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045340 | GTGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 8453 |
rs200407938 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35027653 | AAATCATCACTAAGG[C/T]AGGATGGATTAATTT | 8453 |
rs200430726 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030823 | GCTTGAGCCCAGGAG[C/T]TAGAGTCCAGCCTGG | 8453 |
rs200442371 | in-del | -/A | 0.321292 | 0.23962 | intron-variant | CUL2 | GRCh38.p7 | 10:35105708 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAGAAA | 8453 |
rs200538637 | snp | A/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009201 | ATATATATATATATA[A/T]TATATATATATATAT | 8453 |
rs200548701 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124519 | GAATACAACCCCTGC[C/T]TTGCCTTCTTCTCTT | 8453 |
rs200566199 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085426 | AAAGCGAGACACCGT[-/C]CCCAAAAAAAAATAA | 8453 |
rs200570073 | in-del | -/TTATT/TTATTTTATTTTATTTTATTTTA | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35122622 | GTAGTAATAATATCC[lengthTooLong]TTATTTTATTTTATT | 8453 |
rs200579794 | in-del | -/TAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023755 | ATATTAGTTTTCTTA[-/TAC]GGGGAAAAAAAAAAA | 8453 |
rs200610448 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110178 | AACAAAACAAAACAA[G/T]AAATGAAATAGCCAT | 8453 |
rs200615688 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070889 | AGCAATGACATTAGA[-/T]TTTTTTTTTTACCTG | 8453 |
rs200639181 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097511 | AAAAAAAAAAAAAAA[C/T]AACTTACAGTGGTGC | 8453 |
rs200659464 | snp | A/T | 1.66194e-05 | 0.00288261 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35063057 | ACACATAAAGCATAG[A/T]TATCTCTAGTTAAAT | 8453 |
rs200683733 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021458 | ACACACACACACATA[A/C]ATACACACACACAAA | 8453 |
rs200693975 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113416 | GGCAGTAGAATTGCT[G/T]GAACCTGGGAGGTGG | 8453 |
rs200699967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35033284 | GGCATCTAAAAATGA[A/T]ATATAAGTACAAAAC | 8453 |
rs200748345 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049503 | AGAAAAAAAAAGAAA[A/G]AAGAAGAAGAAGAAG | 8453 |
rs200796040 | in-del | -/A | 0.275137 | 0.248733 | intron-variant | CUL2 | GRCh38.p7 | 10:35077818 | TCAAAAAAAAAAAAA[-/A]GAAAAGAAATAAAAA | 8453 |
rs200810888 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35105720 | TCAAAAAAAAAAAAG[-/A]AAAAAAACCCAAAAC | 8453 |
rs200836087 | in-del | -/GGAGGC | 0.445196 | 0.1562 | intron-variant | CUL2 | GRCh38.p7 | 10:35088432 | GAATTGCTTGAACTG[-/GGAGGC]GGAGGTTGCAGTGAG | 8453 |
rs200876780 | snp | C/G | 0.000754024 | 0.0194021 | intron-variant | CUL2 | GRCh38.p7 | 10:35025091 | TTAATATAATCATCA[C/G]GTAAATTTCATTAAG | 8453 |
rs200879561 | in-del | -/AAAAG | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35095334 | TCTCAAAAAAAAAAA[-/AAAAG]AAAGAAAGAAATACA | 8453 |
rs200888055 | in-del | -/AG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111254 | TCTTCTCTTATGAGA[-/AG]ATTTTTTTTTTTTTT | 8453 |
rs200890116 | in-del | -/AGTAA | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35022686 | GTTTCAGTTAGGACC[-/AGTAA]AGTAAGTTCTGGAGA | 8453 |
rs200915983 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35092893 | AGTGTAGGCATATTT[A/C]TATTAATATACTCCC | 8453 |
rs200930222 | in-del | -/GTT | 0.0678696 | 0.171256 | intron-variant | CUL2 | GRCh38.p7 | 10:35023595 | TCTTATACACCACTG[-/GTT]GTTAAAATGAGCCCC | 8453 |
rs200951580 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021519 | TTCCATAATTAATAC[A/G]TGTTTATATTAATGT | 8453 |
rs200961602 | in-del | -/A/AC/C | 0.000327579 | 0.0127938 | intron-variant | CUL2 | GRCh38.p7 | 10:35025218 | AAAAAAAAAAAAAAA[-/A/AC/C]CACACATTATTTTTA | 8453 |
rs201007750 | in-del | -/TTTATTTATTTATTTATTTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119561 | GGTTTTAAAATTAAT[-/TTTATTTATTTATTTATTTA]TTTATTTATTTATTT | 8453 |
rs201027415 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009515 | GACAACTTTTGAATG[A/G]AAAGCTCTCTCTGTG | 8453 |
rs201028974 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092406 | GCCATACATTCCCAG[C/T]TTTTAAGGCTATTGA | 8453 |
rs201084429 | snp | C/T | 0.000380502 | 0.0137879 | intron-variant | CUL2 | GRCh38.p7 | 10:35060836 | ACTGAATGCAGGCAA[C/T]GCTGCTTAGCTTGTC | 8453 |
rs201140168 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015294 | GTGGAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs201197680 | snp | C/T | 3.07017e-05 | 0.00391789 | missense | CUL2 | GRCh38.p7 | 10:35038923 | GGTGTCACTTACCAT[C/T]TTTTTTCTCTTGTCG | 8453 |
rs201206980 | in-del | -/TCCT | 0.0115144 | 0.0749975 | intron-variant | CUL2 | GRCh38.p7 | 10:35021596 | ACATATACATGTATA[-/TCCT]TCCTTCCTTCCTTCT | 8453 |
rs201233391 | in-del | -/TA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022074 | CGTACTGTAACTATG[-/TA]CGTATGTCTGTCTTC | 8453 |
rs201250299 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35072380 | TAATGGGCTTTTTTT[C/T]TTTTTTGAGACAGAG | 8453 |
rs201317468 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074658 | CGCACCCTAATTTTT[C/G]TATTGTTAATAGAGA | 8453 |
rs201321176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35023641 | TTTAGGAGACACATT[G/T]ATTATTGCTGAAATA | 8453 |
rs201325556 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020167 | ATAGAAAACAAATTT[A/T]AAAAAAAAAAAAATA | 8453 |
rs201340882 | in-del | -/AAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105827 | AGAGGCAATGTCCTG[-/AAA]AAAAAAAAAAAAAGT | 8453 |
rs201354494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080222 | AATATGTTGCCATCA[C/T]TTAATATTAAAATAA | 8453 |
rs201387968 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35053758 | CTGCCTCTTAGCCTG[-/T]TTTATTTCCTTCATT | 8453 |
rs201395769 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054269 | CACATCTTTTTCGTT[A/G]CTGAGGATTCTTAGG | 8453 |
rs201400506 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025217 | TAAAAAAAAAAAAAA[A/C]ACACACATTATTTTT | 8453 |
rs201412901 | snp | A/C | 0.0530306 | 0.153958 | intron-variant | CUL2 | GRCh38.p7 | 10:35032524 | ACGCCATAATTAACC[A/C]CCAGCCATAGGGAAA | 8453 |
rs201427131 | snp | A/C | 8.84369e-05 | 0.00664911 | intron-variant | CUL2 | GRCh38.p7 | 10:35016188 | TTGGAATATTACTAC[A/C]TACCTTTTCTGAATC | 8453 |
rs201427985 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106315 | TTTGTTTTTTTTTTT[-/T]GTGGGTTTTTTTTTG | 8453 |
rs201437691 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103322 | ATTTTTTTTTTTTTT[-/A]TTTTTTTTTTATTTT | 8453 |
rs201468701 | in-del | -/ACATACACACACAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021457 | TACACACACACACAT[-/ACATACACACACAC]AAATATGTAGTGATA | 8453 |
rs201471344 | in-del | -/AATAAT | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35055570 | ACTGTCTCTTAAGGA[-/AATAAT]AATAATAACTCCTAG | 8453 |
rs201494962 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022689 | TCAGTTAGGACCAGT[-/A]AAGTTCTGGAGATCT | 8453 |
rs201555816 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036752 | TTAATGGCTTTTTTT[G/T]AGACAGGGTCTTACT | 8453 |
rs201561949 | in-del | -/AAAC | 0.00700786 | 0.0587777 | intron-variant | CUL2 | GRCh38.p7 | 10:35025216 | GTAAAAAAAAAAAAA[-/AAAC]ACACATTATTTTTAG | 8453 |
rs201568282 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023756 | ATATTAGTTTTCTTA[-/G]GGGAAAAAAAAAAAA | 8453 |
rs201586230 | snp | C/G/T | 8.26694e-05 | 0.00642877 | missense | CUL2 | GRCh38.p7 | 10:35031600 | GACTTCTTCAGTAAG[C/G/T]TGTCACAGTACTTAG | 8453 |
rs201589712 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057809 | CTTCTTAATAAAGAC[A/G]TGGGCTGGACGCAGT | 8453 |
rs201639356 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077865 | ATTAAAAATATATAT[C/T]TACAGATGTAATGAT | 8453 |
rs201639792 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027027 | TAAACAGGATAAAAA[A/C]CAGCATTTTTCAAAC | 8453 |
rs201652391 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092459 | CGGAAGCATTAATTT[C/T]ATTAAATTTTGGCCC | 8453 |
rs201677936 | in-del | -/TTTC | 0.0225045 | 0.103662 | intron-variant | CUL2 | GRCh38.p7 | 10:35021243 | TAATCTGCAGCATGT[-/TTTC]TTTCTTTCTTTCTTT | 8453 |
rs201693666 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | CUL2 | GRCh38.p7 | 10:35041539 | CTGAAATGAGCTTTT[A/C]TTTTTCTTTCTTTTG | 8453 |
rs201725305 | in-del | -/AAAG | 0.205881 | 0.246076 | intron-variant | CUL2 | GRCh38.p7 | 10:35095335 | CTCAAAAAAAAAAAA[-/AAAG]AAAGAAAGAAATACA | 8453 |
rs201737638 | in-del | -/GAG | 0.0283406 | 0.115616 | intron-variant | CUL2 | GRCh38.p7 | 10:35088276 | GCACTCTGGGAGGCT[-/GAG]GAGGGCGGATCATGA | 8453 |
rs201737927 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077330 | AAACAAACAAACAAA[-/C]AAAAAAAACAAACAA | 8453 |
rs201741060 | snp | C/T | 0.000181295 | 0.00951918 | missense | CUL2 | GRCh38.p7 | 10:35035215 | CGAAGGCCCTCATCA[C/T]GGATGTGGTTTTGCA | 8453 |
rs201741916 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078296 | TTAAGATCAGGTGAA[-/T]TTTTTTTTTTTTTTT | 8453 |
rs201754531 | in-del | -/A/AC | 0.434253 | 0.168969 | intron-variant | CUL2 | GRCh38.p7 | 10:35092890 | AAAGTGTAGGCATAT[-/A/AC]TTCTATTAATATACT | 8453 |
rs201841516 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116045 | TAGACATTAAAGGAT[-/A]AAAAAAAATATTATG | 8453 |
rs201843090 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044169 | ACTATATTTTCCTCA[C/T]ATTTTTCCTCTCATT | 8453 |
rs201844081 | snp | A/C/T | 0.0123036 | 0.0774623 | intron-variant | CUL2 | GRCh38.p7 | 10:35105629 | AGGAGAATCACTTGA[A/C/T]CCCGGGAGGCAGAGG | 8453 |
rs201846177 | snp | A/G | 0.0130582 | 0.0797406 | intron-variant | CUL2 | GRCh38.p7 | 10:35035124 | AAGGAAAGGCTCCAC[A/G]CTGGATCTGATTAGG | 8453 |
rs201908485 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35015729 | TATGGTGGTTAAAAA[A/C]AGATGACAGTTAATT | 8453 |
rs201932448 | snp | C/T | 0.00199807 | 0.0315443 | intron-variant | CUL2 | GRCh38.p7 | 10:35035351 | TTTTCATTTATTAGG[C/T]AATATATGGATCCAA | 8453 |
rs202014147 | snp | C/T | 1.8069e-05 | 0.00300569 | intron-variant | CUL2 | GRCh38.p7 | 10:35033148 | TACATATATAGTATA[C/T]ATGTATTTAAAACTT | 8453 |
rs202046289 | snp | A/G | 8.27438e-05 | 0.00643157 | missense | CUL2 | GRCh38.p7 | 10:35010339 | CTGTATTCATCTGCC[A/G]ACGCCTGGCTGCGTT | 8453 |
rs202048847 | snp | C/G | 3.3315e-05 | 0.00408122 | intron-variant | CUL2 | GRCh38.p7 | 10:35031418 | TTTAAAAGATTACTT[C/G]CTTTCTAATGATTTA | 8453 |
rs202057047 | snp | A/G | 3.3e-05 | 0.00406189 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071262 | ACGGCTTTTATTGTC[A/G]TCAAAAGTTTGTTCC | 8453 |
rs202076466 | in-del | -/AATT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115586 | TTAACAAGGGAGATA[-/AATT]AATTAATCTAAATGT | 8453 |
rs202130531 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35110500 | TACCTGGGAGGTGGA[-/G]GTTGCAGTGAGCTAA | 8453 |
rs202133506 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35055939 | CTGAGGGTAGTCAGT[-/C]CCCTTTCATCCGAGT | 8453 |
rs202169800 | snp | A/G | 4.96454e-05 | 0.00498199 | intron-variant | CUL2 | GRCh38.p7 | 10:35071166 | AAATTTATCAATTTT[A/G]GAACATTGATCAAGC | 8453 |
rs202174023 | snp | A/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009200 | TATATATATATATAT[A/T]TTATATATATATATA | 8453 |
rs202182539 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027406 | GCCTCGGCCTCCCAA[A/G]GTGCTGGGATTACAG | 8453 |
rs202219393 | snp | A/T | 0.000200371 | 0.0100073 | intron-variant | CUL2 | GRCh38.p7 | 10:35044695 | AATAAATCAATTACA[A/T]CATATTAGAAGAAAT | 8453 |
rs202223170 | in-del | -/TTC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021260 | TCTTTCTTTCTTTCT[-/TTC]TTTTTTTTTTTTGAG | 8453 |
rs202239751 | in-del | -/CACTGTG | 0.030665 | 0.119967 | intron-variant | CUL2 | GRCh38.p7 | 10:35107171 | GTAGAGACGGGGTTT[-/CACTGTG]CACTGTGTTAGCCAG | 8453 |
rs202245860 | in-del | -/C | 0.445196 | 0.1562 | intron-variant | CUL2 | GRCh38.p7 | 10:35088429 | GGAGAATTGCTTGAA[-/C]CTGGGAGGTTGCAGT | 8453 |
rs207470790 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018436 | AATTAGTAACTCTGA[A/T]TAAGGTTTTCTGCTT | 8453 |
rs207470791 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050835 | ACAGATTCTCTGATA[C/T]ACATCTACAAGTTGA | 8453 |
rs207470792 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107104 | CTCAGCCTCCCGAGT[A/T]GCTGGGACTACATGC | 8453 |
rs367560139 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126742 | CCGCCCCACCTCCAG[G/T]CTAGTTCCTCCTCTT | 8453 |
rs367610615 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095119 | TAAGGTGGATCACTT[C/T]GAGACCAGCCTGGCC | 8453 |
rs367617457 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110027 | CAATAATTGAAAAAT[C/T]AGCTGGGTGTGGTGT | 8453 |
rs367644539 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033359 | AGACTTATTAGTAAA[A/T]TTTTCCTCAAGGAAA | 8453 |
rs367719869 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037304 | CCTGCCGCTCTGCAG[C/T]GCCACCTTGGTCTTA | 8453 |
rs367761644 | snp | A/C | 8.52115e-05 | 0.00652675 | missense | CUL2 | GRCh38.p7 | 10:35028863 | ACGTAGATGAAGGAG[A/C]CTGAGTAAGAGGCCA | 8453 |
rs367846082 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078899 | ATACAATAGAGTGGT[C/T]TAAGTTGACTTCAGA | 8453 |
rs367864303 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35020737 | TCACACTGTCTGGTT[A/G]TATCTCTTTATCAAG | 8453 |
rs367934644 | snp | C/T | 1.76908e-05 | 0.00297407 | intron-variant | CUL2 | GRCh38.p7 | 10:35031291 | TACCACATTAAAGAC[C/T]TACATTACCTTTAAT | 8453 |
rs367971568 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011452 | GTGAAACCCTGTCTC[C/T]ACGAAAAATACAAAA | 8453 |
rs368017593 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103147 | TTGACTCAAAAAAAT[A/T]TTTTTTTGTTTTTGA | 8453 |
rs368023611 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114335 | CTCCTCAAGTGCTGG[C/G]ATTACAGGTGTGAGG | 8453 |
rs368025770 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116683 | TAAATATTAGATGCT[C/T]TGGCTGGGCATGGTG | 8453 |
rs368027208 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123361 | CCTTAAGTTTCAGTC[C/T]CTCCTAGTCACTGTA | 8453 |
rs368036525 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064879 | CAAAATCTACTGGAA[G/T]GATTTGTGCCAAATC | 8453 |
rs368049158 | snp | A/C | 1.66123e-05 | 0.00288199 | intron-variant | CUL2 | GRCh38.p7 | 10:35035134 | TCCACGCTGGATCTG[A/C]TTAGGAGGAAAACAT | 8453 |
rs368069804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081242 | AAAAAAGCAGCTACC[C/T]GCTTCCAAAAATAAA | 8453 |
rs368115507 | snp | C/T | 0.00154738 | 0.0277722 | intron-variant | CUL2 | GRCh38.p7 | 10:35054406 | AAAAACATACTTATG[C/T]TTGCTAGTCACTTAA | 8453 |
rs368180586 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35117631 | GAAATATATGGCAAC[A/T]TTGGCACAATGAATA | 8453 |
rs368223375 | in-del | -/CCT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078405 | GGTGTGAGCAATTCT[-/CCT]GCCTCAGCCTCCCAA | 8453 |
rs368275077 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070333 | AATGGTTTTCTGTTG[G/T]TCTAAAGAACTTTAC | 8453 |
rs368318547 | snp | C/T | 5.26995e-05 | 0.00513293 | intron-variant | CUL2 | GRCh38.p7 | 10:35033286 | CATCTAAAAATGAAA[C/T]ATAAGTACAAAACCA | 8453 |
rs368354967 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076988 | ACCCAGGAGGCGGAG[C/T]TTGCAATGAGCCGAG | 8453 |
rs368360947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35035496 | ACATCTTCCCAAAGA[C/T]ATTTTGTGCAAATTC | 8453 |
rs368363807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35040332 | ACCAAAGAATTTGAC[C/T]AATTTCTGTCTCAAG | 8453 |
rs368423758 | snp | C/T | 4.94588e-05 | 0.00497262 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060879 | GCACACTCACCTATA[C/T]AAGCAGTCCATATAG | 8453 |
rs368435601 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35096527 | CTGAAATGGGAGGAT[C/T]ACTTGAGTCCAGGAG | 8453 |
rs368452619 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102982 | AAGTTGAACAATGCT[G/T]CCTGTCTATTATGGG | 8453 |
rs368515235 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032326 | TAGATAATTTTCCTT[A/C]TATTTTTCTGAAAAA | 8453 |
rs368518633 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038116 | GATCATGCCATTGCA[A/C]TCCAGCCTGGGCGAC | 8453 |
rs368525133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35027463 | TAGATACTTCTAATA[C/T]TATTCAGGTTTTTGG | 8453 |
rs368530802 | snp | A/T | 1.76705e-05 | 0.00297236 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35029500 | TACCTGTAGAACATA[A/T]ATTTGAAAACTAATT | 8453 |
rs368549649 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073795 | TTTTAGTAGAGACAG[C/G]GTTTTTCACCATGTT | 8453 |
rs368597756 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114826 | ATGCAAGGTCTGAAA[A/T]AAAAAATACATTGGA | 8453 |
rs368608310 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110687 | GGAGTCTGTTGCAGG[C/T]CTCTCTCCTTGGCTT | 8453 |
rs368638735 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110134 | GAGCCTGATTGTGCC[A/T]TTGCAACACAGCAAG | 8453 |
rs368716743 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055009 | CAGATAGTAAGTATG[C/G]GCAAGATTGACAGAT | 8453 |
rs368754459 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35032183 | CAGATGTAACAGAAT[C/G]TACATGAAAAGTATT | 8453 |
rs368835006 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088620 | CTGTCAACTGCCAGA[C/G]AACGCAAAAATGACT | 8453 |
rs368871909 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35068272 | ACCAAAAATACAAAA[A/G]TTAGCCAGGCATGGT | 8453 |
rs368900872 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042518 | CTCAAGGCAGGACTC[C/T]AATCTTGCCCTACCT | 8453 |
rs368917888 | snp | G/T | 6.63867e-05 | 0.00576099 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35010427 | GATTAAACCTAGCTC[G/T]TGACTGGCTAATCAC | 8453 |
rs369008160 | snp | A/C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118004 | CATCCTGCACCAGCA[A/C/T]GTTCTACTTGTTAGA | 8453 |
rs369025824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35076732 | TACTATTCAGATTGT[C/T]ATATATCTGCTTTTT | 8453 |
rs369043439 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075334 | TTTAATAATAACATT[C/T]AGGGAAAGTTTACAC | 8453 |
rs369055557 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123550 | CTTAGCATTTAGCAT[A/G]GGGCCTGGAACATAG | 8453 |
rs369064157 | in-del | -/ACA | 0.434253 | 0.168969 | intron-variant | CUL2 | GRCh38.p7 | 10:35092893 | GTGTAGGCATATTTC[-/ACA]TATTAATATACTCCC | 8453 |
rs369095828 | snp | C/T | 1.6612e-05 | 0.00288196 | intron-variant | CUL2 | GRCh38.p7 | 10:35035130 | AGGCTCCACGCTGGA[C/T]CTGATTAGGAGGAAA | 8453 |
rs369109038 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047780 | AAATTAGCAGGGCGT[A/G]GTGGTGCCCAGCTAC | 8453 |
rs369177715 | in-del | -/TTTA | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080433 | TTTAGAATTCCTATT[-/TTTA]TTTATTTATTTATTT | 8453 |
rs369237704 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35098934 | GCAAGACTCTGTCTC[G/T]AAATAAATAAATTAA | 8453 |
rs369250154 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034622 | TGATGGGAAAGACAA[-/A]CTGTTACAGTACAAA | 8453 |
rs369254229 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067484 | GCCGGTCACAGTGGC[C/T]CATACCTATAATCTC | 8453 |
rs369254411 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081540 | GGCAAGCCCATCGTG[C/T]ATGAATACTAGACAA | 8453 |
rs369258701 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074749 | GCCTTGGCCTCCCAA[A/C]GTGCTGGGATTATAG | 8453 |
rs369267033 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35034509 | ACAGATACTATCTTA[C/T]AGATGAAGGGCAAAC | 8453 |
rs369276040 | snp | C/T | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074275 | AGCATTCAGTTTGGG[C/T]TCAACTGCAACATGG | 8453 |
rs369284098 | in-del | -/TTTATTTATTTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119561 | GGTTTTAAAATTAAT[-/TTTATTTATTTA]TTTATTTATTTATTT | 8453 |
rs369347102 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110890 | CATTCTGAGGTACTA[C/G]AGGTTGAGACTTAGA | 8453 |
rs369440496 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103410 | ACTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 8453 |
rs369445470 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099127 | GCTGGGTGCATTGGC[C/T]CATGCCTTTAATCCC | 8453 |
rs369476603 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082016 | TACAATCCCAAAGAG[A/G]GCCAGTGAGTTGGAT | 8453 |
rs369482307 | in-del | -/T | 0.283421 | 0.247756 | intron-variant | CUL2 | GRCh38.p7 | 10:35106487 | ACCACGCCCGGCTAA[-/T]TTTTTTTTTTCTTTT | 8453 |
rs369507628 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035885 | CAACAATGTGTTGCC[A/G]AATGTTTTGATCTCT | 8453 |
rs369521955 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046361 | CTGTGGAGGACATAC[C/T]GGCAAAACTCTAAGT | 8453 |
rs369531712 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027588 | ATACTTTGGTGTAAA[A/G]TAAAGGTAATTCTTG | 8453 |
rs369536206 | snp | A/G | 2.48111e-05 | 0.00352207 | intron-variant | CUL2 | GRCh38.p7 | 10:35049808 | GCTGAATTACTTAGT[A/G]TATGTTTAACATTTC | 8453 |
rs369623582 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35124844 | CAGAAAGGGAGGGAA[A/G]GTTTAAGATATTTTG | 8453 |
rs369674711 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048476 | AAAAAGATATTTCAC[A/C]AAAGTACATTTAGAA | 8453 |
rs369694333 | snp | G/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074576 | ACTGCAACCTCCACC[G/T]CCCACGTTCAAGTGA | 8453 |
rs369709338 | snp | A/G | 1.65048e-05 | 0.00287265 | intron-variant | CUL2 | GRCh38.p7 | 10:35031468 | ACCAAAATACAAATG[A/G]AACTTTTCTGTTCAC | 8453 |
rs369753780 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111749 | AAAAATTAGCTGGGC[A/G]TGGTGTGGCATGTGC | 8453 |
rs369865613 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126866 | TGGATTGTGGCGCTT[C/T]ACTCCTGCTGGCGGC | 8453 |
rs369873007 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111577 | ATTCTAATTTGAACA[C/T]ATTATGTCTAAAACA | 8453 |
rs369885942 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106960 | TAACCTGTTTTTTTT[-/T]GTTGTTTTTTTGTTT | 8453 |
rs369892235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119244 | TTGGAGGAGGTAAGG[C/T]TCAGTTTCAGCTTCA | 8453 |
rs369896444 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35101969 | AAAATAAGAAACAGC[C/T]TCCCAAAATGCTGGG | 8453 |
rs369920913 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35073141 | CAAATATCCAAAAGA[A/G]GGTATGCCTTGTTGA | 8453 |
rs369928960 | snp | C/T | 0.0001812 | 0.00951667 | missense | CUL2 | GRCh38.p7 | 10:35035279 | CAGCACGGAGTAAGA[C/T]GTACATATTTGCCAT | 8453 |
rs369929438 | snp | G/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092059 | CTGGGCTCAAGCGAG[G/T]GTACCATCTCAGTTT | 8453 |
rs369951515 | in-del | -/GA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35024022 | GGATTTTTTAGTAGA[-/GA]CAGGTTTTGTCATGT | 8453 |
rs369951777 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063365 | AAATCAAATTACCCA[C/G]AATCCTACAAAATAA | 8453 |
rs370057463 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045507 | TCCCTTGAGTCCTGA[G/T]TTTGAGACTAGCCTG | 8453 |
rs370061545 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35053709 | TGATCAATTTCTTTC[A/G]GAAAGGATTACACTA | 8453 |
rs370071519 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018122 | GCTCTACTAAAAATA[A/C]AAAAAAAAAAAAAAA | 8453 |
rs370099961 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068930 | TGTAGTGCAATGGCC[C/T]GATCTTGGCTCACTG | 8453 |
rs370160074 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105584 | TGGTGGCGGGCGCCT[-/T]GTAGTCCCAGCTCCT | 8453 |
rs370171417 | snp | G/T | 1.65941e-05 | 0.00288041 | intron-variant | CUL2 | GRCh38.p7 | 10:35044760 | TATTTGTTTTTAAAG[G/T]AGGCTGTTTACCTTT | 8453 |
rs370232235 | snp | A/G | 2.4981e-05 | 0.0035341 | intron-variant | CUL2 | GRCh38.p7 | 10:35039128 | ACAAAGTTTTACTAT[A/G]AGGAAAAATCTGTAA | 8453 |
rs370244654 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102154 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 8453 |
rs370252491 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125664 | ATGAAACCGATTTTT[A/G]TTATCATCAATATTA | 8453 |
rs370272046 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078629 | ATAAAGAGATTTGTT[C/G]CTGTGAACTCACTTG | 8453 |
rs370325411 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082986 | AACATGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 8453 |
rs370338913 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35029283 | GCTGGTCTGGAACTC[C/T]TGAGCTCAAGAGATC | 8453 |
rs370350334 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116540 | CTGTGGCTTTTTTTT[-/T]GTGATCTCGTTTAAC | 8453 |
rs370401674 | snp | A/G | 5.35681e-05 | 0.00517505 | intron-variant | CUL2 | GRCh38.p7 | 10:35025123 | CAGATATAATTAAAT[A/G]CATTTTACCTGTACA | 8453 |
rs370474165 | snp | A/C | 0.000133076 | 0.008156 | intron-variant | CUL2 | GRCh38.p7 | 10:35031668 | GGTGCTTCTGTATAT[A/C]TCACGCCTCAAAGGA | 8453 |
rs370482788 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100171 | TGGCATAACACCAAC[C/G]TAAAAAAAGGTTAGC | 8453 |
rs370483516 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073431 | GCCCTACAAATGATC[C/T]GGAATCAGGCCCTCA | 8453 |
rs370484015 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35031745 | GTTTTTTTTAGAGAC[C/T]GGGTCTTGCTCTGTT | 8453 |
rs370496640 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061230 | TGTAATTCCAGCACT[C/T]TGGGAGGCCAAGGCG | 8453 |
rs370560709 | in-del | -/CTTTT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041549 | CTTTTCTTTTTCTTT[-/CTTTT]GTCAGACAGGATCTC | 8453 |
rs370570975 | snp | C/T | 0.000564625 | 0.0167927 | intron-variant | CUL2 | GRCh38.p7 | 10:35033137 | AGAGTTTTATGTACA[C/T]ATATAGTATATATGT | 8453 |
rs370586557 | snp | G/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080483 | TATTTATTTATTTTT[G/T]AGACAGGGTCTTGTT | 8453 |
rs370586798 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095107 | GATCACTTGAGGTAA[C/G]GTGGATCACTTCGAG | 8453 |
rs370653086 | snp | C/T | 0.00018134 | 0.00952036 | intron-variant | CUL2 | GRCh38.p7 | 10:35032426 | CTTTTCAGCAACCAC[C/T]AAACTTACCAGTTCA | 8453 |
rs370660635 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104554 | GAAGGAGGTGGAATT[G/T]CTGGGCTTCTTTTCC | 8453 |
rs370663199 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118424 | CCTTGCTCTAATCTT[C/T]CGGTTCATGAGTGAA | 8453 |
rs370671295 | snp | G/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35087820 | TTCTCCAATCAACAG[G/T]CTGATTCTCAATCAG | 8453 |
rs370753194 | snp | A/T | 1.97506e-05 | 0.00314243 | intron-variant | CUL2 | GRCh38.p7 | 10:35016148 | TCTCATGAAAAAGCT[A/T]TAATGCTGATGATGC | 8453 |
rs370765533 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030321 | AATTCTGTTGTTACC[A/G]GGTCAGAAAATCTGA | 8453 |
rs370804193 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35121991 | CAAAAACCAAAAGCA[C/T]GTAAACACACATACA | 8453 |
rs370890358 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35038398 | AGGTGTGGTGATGAG[A/C]GCCTGTAATCCCAGC | 8453 |
rs370910408 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040536 | AAAGCGGATCAGAAA[C/T]TTTCAATAAAAATGA | 8453 |
rs370961634 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35028484 | AAGGAAAACTGGTAA[A/G]TGATATTTTAGGTGT | 8453 |
rs371008516 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070320 | TTGTAATGAATTAAA[C/T]GGTTTTCTGTTGGTC | 8453 |
rs371044324 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077725 | AGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 8453 |
rs371044907 | snp | A/G | 0.000611555 | 0.0174758 | intron-variant | CUL2 | GRCh38.p7 | 10:35060840 | AATGCAGGCAACGCT[A/G]CTTAGCTTGTCTAGA | 8453 |
rs371051425 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095841 | GTTGAGATTACAGGC[A/G]TGAGCCACCAAGCCC | 8453 |
rs371051731 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069510 | CACACCACTGTACTC[C/T]AGCCTGGGTGACAAA | 8453 |
rs371064727 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116327 | TCCAGCCTGGGCGAC[A/G]GAGCCAGACTCCATC | 8453 |
rs371080445 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064635 | CAGCCCTCTCCACAT[C/T]TATTTACTTACTTAT | 8453 |
rs371113039 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033563 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 8453 |
rs371151353 | in-del | -/GGATC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030821 | CGCTTGAGCCCAGGA[-/GGATC]GTTAGAGTCCAGCCT | 8453 |
rs371162171 | snp | C/T | 1.95204e-05 | 0.00312407 | intron-variant | CUL2 | GRCh38.p7 | 10:35029463 | AATGATTAGTAAATG[C/T]TCATAGTAAAACACA | 8453 |
rs371238969 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089604 | TCACAGATGTTTTAT[C/T]TGCATGCACGTAATG | 8453 |
rs371286852 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35064773 | GTCTCAAACTCTTGG[A/G]CTCAGGCAATCCTTC | 8453 |
rs371363302 | snp | C/T | 1.65581e-05 | 0.00287728 | intron-variant | CUL2 | GRCh38.p7 | 10:35044767 | TTTTAAAGGAGGCTG[C/T]TTACCTTTAAGGGGA | 8453 |
rs371403705 | snp | G/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126780 | CCCCCTGACCTTCCT[G/T]CTCCCTATCCCTAGG | 8453 |
rs371440945 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009361 | ATCTAAACTGTTGGA[A/G]GAGGGTTGTAAGGGT | 8453 |
rs371503016 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037875 | AGCCTGATTAATGGC[A/C]GGGCGCGGTGACTCA | 8453 |
rs371507189 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013079 | GGCGCGGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 8453 |
rs371560518 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115424 | ATTTAGCCAGGCATG[A/C]TGGCAGGCGCCTGTA | 8453 |
rs371582562 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056265 | TCCAGACAGCAAGGA[C/T]AGCAAAAGCTAACAG | 8453 |
rs371637614 | snp | A/G | 4.97368e-05 | 0.00498657 | intron-variant | CUL2 | GRCh38.p7 | 10:35054416 | TTATGTTTGCTAGTC[A/G]CTTAAAGAATGTCCT | 8453 |
rs371645683 | in-del | -/AT | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009183 | AACACTGCTGTTGAG[-/AT]ATATATATATATATA | 8453 |
rs371652116 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059703 | TCTACTTAAGTGAAA[C/T]ACCATGTTTCTGGAA | 8453 |
rs371668656 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062604 | AGGGAGGCCAAGGCC[A/G]GAGGATCACTGGAGC | 8453 |
rs371699386 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072558 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 8453 |
rs371707923 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015200 | CAGGAGGCTGAGACA[A/G]GAGAATCATTTGAAC | 8453 |
rs371749297 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040943 | TAATGCTCACACAGT[A/G]GCTGCTCACTCCCTG | 8453 |
rs371786426 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034059 | CACATCTCAGAGAGA[A/C]GAAATACCTAATAGT | 8453 |
rs371788677 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090627 | GCCAAATCCCCCCCG[C/T]CACCCGGAAAGCAAT | 8453 |
rs371794629 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065645 | AATAAATAAAAATTT[A/T]AAAAAAGAGATTGAG | 8453 |
rs371811530 | snp | C/G | 0.0603597 | 0.1629 | intron-variant | CUL2 | GRCh38.p7 | 10:35039633 | ACTTTGGGAGGCCAA[C/G]GCAGGTGGATCATCT | 8453 |
rs371834005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011574 | AGTGAGCCAAGATCA[C/T]GCCACTGTACTCCAG | 8453 |
rs371912862 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020630 | TTCATCATTTCTCAA[A/C]GTGTCTTTCAGCAAC | 8453 |
rs371936937 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097553 | TACCCTTCAGTCAGG[-/T]GATCAAGCCCAGTAT | 8453 |
rs371939971 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044910 | TCTTGAGAATACAAA[A/T]TATCTATGGAAATAT | 8453 |
rs371964363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35090007 | GGTCAGCGCTCTGGG[A/G]AGCCGAGGTCACTTA | 8453 |
rs372007614 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120637 | GCTGGGCTCATGCGT[G/T]TGAAATCTCAGCAAT | 8453 |
rs372022621 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097698 | GGGCACAGTGGCTCA[C/T]GCCTGCAATTGACAC | 8453 |
rs372032965 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122497 | AACAAACTTGGCCAA[A/G]TCATAAAATAATAAT | 8453 |
rs372036036 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023032 | TGGGTGACAGAGCAA[A/G]ACCCCATCTCAAAGA | 8453 |
rs372054726 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CUL2 | GRCh38.p7 | 10:35032309 | CCAAACTATATACAA[C/T]GTAGATAATTTTCCT | 8453 |
rs372056649 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021193 | TGGTGACAATTTTAT[G/T]CCATTCTAACTGCAG | 8453 |
rs372225683 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35103473 | GGGACTACAGGCGCG[C/T]GCCACCATGCCTGGC | 8453 |
rs372233307 | snp | G/T | 1.65734e-05 | 0.00287862 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060966 | TTCTGACTCCAAAAC[G/T]CTCTATATAAAGAGG | 8453 |
rs372235136 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031124 | GAATCTTCATATATA[A/T]ACATATACATTTTGT | 8453 |
rs372259714 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098752 | CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC | 8453 |
rs372262806 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078218 | GTTAACATAGCCTGA[C/T]AAAATGTCCACCCCT | 8453 |
rs372270681 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098377 | ATTGCAAGGACTTAT[A/G]CATGACATGTGAAAG | 8453 |
rs372276914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35032683 | CTCTAATTACAAAAT[A/G]TCTATATATCCTGTT | 8453 |
rs372309687 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | CUL2 | GRCh38.p7 | 10:35031654 | TAAATCTTACAAAGG[G/T]TGCTTCTGTATATAT | 8453 |
rs372375073 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060909 | GTCTGCACCCTTGCT[A/G]TATTCTTCCCAGTAC | 8453 |
rs372387039 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046709 | GCAGCCTGGCCAACA[C/T]GGTGAAATCCAGTCT | 8453 |
rs372421552 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119944 | GCCAGTCTGAGGTTA[C/T]TCTTTTGGCTCCACA | 8453 |
rs372463631 | snp | A/T | 1.66504e-05 | 0.0028853 | intron-variant | CUL2 | GRCh38.p7 | 10:35031395 | CGTAGAACTACATTT[A/T]AAAATATTTTAAAAG | 8453 |
rs372480321 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103355 | TTTGAGACGGAGTTT[C/T]GCTCTGTCGCCCAGG | 8453 |
rs372495463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35087587 | CATCCCATACAACAG[A/C]CTGCTTCCCCCAACC | 8453 |
rs372498422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066088 | AAGTTACTTATTTTA[C/T]TTCATGTTCTCTATT | 8453 |
rs372509367 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | CUL2 | GRCh38.p7 | 10:35049652 | AACAACAAAATAAAA[A/T]TGACTCAGTAAGATA | 8453 |
rs372537030 | snp | C/T | 0.000767705 | 0.0195771 | intron-variant | CUL2 | GRCh38.p7 | 10:35029644 | ACCACAGGCTTGCTA[C/T]AAAAAAGTTTTAGAA | 8453 |
rs372541823 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121239 | TTATTTATTTATTTT[C/T]TTGGGATGGAGTCTC | 8453 |
rs372600803 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35077885 | GATGTAATGATATGC[-/T]GTCTGAAATCTGCTT | 8453 |
rs372712945 | in-del | -/A/AA/AAA | 0.494896 | 0.0502606 | intron-variant | CUL2 | GRCh38.p7 | 10:35018763 | GCGAAACTCCGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 8453 |
rs372799014 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045054 | GAGTTAATATTCATG[A/C]TAGTTAATGTATACA | 8453 |
rs372812629 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039686 | CATGGCCAATATGGC[A/G]AAACCCTGTCTCTAC | 8453 |
rs372814900 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022866 | CCTGGCCAACATGGT[C/G]AAACACCGTCTCTAC | 8453 |
rs372851008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074634 | TGGGGGATTACAGGC[A/G]TGAGCCATCGCACCC | 8453 |
rs372868476 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115907 | CAAAAAATATAATAA[A/G]ATAATAAATAAATGT | 8453 |
rs372873577 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126963 | GTGGGGGAGGGGAGG[A/G]CGGGGCGGGAGGACG | 8453 |
rs372895258 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043973 | CTTCGTAGGCTGAGA[C/T]AGGAGGACCACTTGA | 8453 |
rs372923177 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096342 | GGGTACAGTGGCTCA[G/T]GCCTGTAATCCCAGC | 8453 |
rs372966036 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015684 | TAATATACTAATGGC[C/T]TGTTATTCTTGTGAC | 8453 |
rs372978935 | snp | G/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075167 | ATGGATAGCAAATCT[G/T]GAAGCCAACGTGCAA | 8453 |
rs373007858 | snp | C/T | 3.32375e-05 | 0.00407647 | missense | CUL2 | GRCh38.p7 | 10:35044643 | ACTCTCCTGTTTCAG[C/T]CAGAAAGGGAGACTC | 8453 |
rs373022986 | snp | A/G | 1.9435e-05 | 0.00311723 | intron-variant | CUL2 | GRCh38.p7 | 10:35033320 | TTTAAGAGGTTCAAG[A/G]ATATCCAAACTATGA | 8453 |
rs373109952 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068798 | GGGTCAGAAGTGAAC[C/T]TTATATTCTTGGGCA | 8453 |
rs373116641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35049085 | TGCTTCTGAGAGTCT[C/T]TGAGCCAGAGCTAAT | 8453 |
rs373130077 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023809 | TTTTTCTTAAAATCA[A/G]TTATGTTTACTAAAT | 8453 |
rs373135607 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109676 | CAGCAAGTGAAAAAG[A/C]CTGAAGGATGGATGA | 8453 |
rs373152516 | in-del | -/CT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040147 | AATAAGAGCGAGGCT[-/CT]GTCTCAAAAAATAAA | 8453 |
rs373155856 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | CUL2 | GRCh38.p7 | 10:35044700 | ATCAATTACATCATA[C/T]TAGAAGAAATTAGAA | 8453 |
rs373173285 | snp | A/T | 2.60916e-05 | 0.0036118 | intron-variant | CUL2 | GRCh38.p7 | 10:35013676 | TTCCCCCTCAAAAAA[A/T]ACTTGACATTAAAAG | 8453 |
rs373183306 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061119 | ATTAACTACACGTAT[G/T]AAAAATGAAACAACT | 8453 |
rs373187305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35041960 | CATTTAAAGTGTGCA[A/G]TTCAATGGTTTTGGT | 8453 |
rs373208151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35028620 | GTATGACATTCTTCT[C/T]AGCATTTTAGTATCA | 8453 |
rs373225148 | snp | C/T | 6.6177e-05 | 0.00575188 | intron-variant | CUL2 | GRCh38.p7 | 10:35060823 | TATCCTGTCAACTAC[C/T]GAATGCAGGCAACGC | 8453 |
rs373279691 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034820 | TTGCAAGTCGTCTAT[-/T]ATTACCACTGATTAA | 8453 |
rs373325411 | snp | A/C/T | 3.99736e-05 | 0.00447048 | intron-variant | CUL2 | GRCh38.p7 | 10:35038903 | TTTAATTTCTACTCA[A/C/T]GTTTGGTGTCACTTA | 8453 |
rs373341522 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048892 | CCATACTAAATACCA[C/T]GGCTTTGACAAAGTA | 8453 |
rs373343862 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098975 | TAGGCCATCTCATTT[C/G]AGAAGATAGGAACAA | 8453 |
rs373394007 | snp | C/T | 1.7731e-05 | 0.00297744 | intron-variant | CUL2 | GRCh38.p7 | 10:35062921 | TAGTAAAGTATACAA[C/T]TATCAACATATTTAT | 8453 |
rs373408054 | snp | A/G | 3.30666e-05 | 0.00406598 | missense | CUL2 | GRCh38.p7 | 10:35010342 | TATTCATCTGCCGAC[A/G]CCTGGCTGCGTTCTA | 8453 |
rs373440324 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099725 | AGGTTGCAGCCTGGG[C/T]GACAGAGCAAGACTC | 8453 |
rs373466019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061945 | ATCTACTCCTGACCA[C/T]GTGCAGGGTTAGACA | 8453 |
rs373495312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121820 | GTCTCAAAAAAAAAA[A/T]AAAAAATAAAAATTA | 8453 |
rs373496320 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063961 | CAAGGCATTTTGGAG[A/G]TAACAGCTCATTTGT | 8453 |
rs373500651 | snp | G/T | 2.89666e-05 | 0.00380558 | missense | CUL2 | GRCh38.p7 | 10:35038925 | TGTCACTTACCATTT[G/T]TTTTCTCTTGTCGAA | 8453 |
rs373524568 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013290 | GCAGAGCTTGCAGTG[A/T]GCCGAGATCACACCA | 8453 |
rs373598813 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019240 | CTGTAATATGCTGCC[A/G]TGGGTTTGAAAGCAG | 8453 |
rs373680699 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35065902 | GTCAGATTTCAACTT[-/A]AACATTCTTTCACTA | 8453 |
rs373708101 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102165 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTAC | 8453 |
rs373715310 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058296 | ATCCTCTTCCTGGAC[A/G]AATAACTCTTACAAG | 8453 |
rs373759453 | snp | C/T | 8.60652e-05 | 0.00655936 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35025154 | CAGATAATGTAACCA[C/T]GTAAGTTTCCTTCCA | 8453 |
rs373818779 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093682 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAGAA | 8453 |
rs373843343 | snp | C/G | 1.79072e-05 | 0.0029922 | intron-variant | CUL2 | GRCh38.p7 | 10:35054560 | AAATAAATGTAATAT[C/G]AATGGATATTAAGTT | 8453 |
rs373861002 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35038273 | GCTCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 8453 |
rs373868044 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123158 | AAGCAAAACATAACA[A/C]AAAACAAAACAAAAC | 8453 |
rs373868566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35085181 | CACCTGTAATCCCAG[A/C]ACTCTGGGAGGCTGA | 8453 |
rs373908876 | snp | A/C/T | 0.000236524 | 0.0108725 | intron-variant | CUL2 | GRCh38.p7 | 10:35049813 | ATTACTTAGTATATG[A/C/T]TTAACATTTCCTCAA | 8453 |
rs373965981 | snp | C/T | 3.30792e-05 | 0.00406675 | missense | CUL2 | GRCh38.p7 | 10:35011882 | TGCCGAAGCACTTTT[C/T]GTGCTTTCATGATAC | 8453 |
rs373970968 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051569 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 8453 |
rs373997423 | snp | C/T | 0.000157006 | 0.00885881 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010293 | GATCTTCTCACACCA[C/T]GCTGGAGGAGAGCGA | 8453 |
rs373999428 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35030807 | CTGAGGCGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 8453 |
rs374039637 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028042 | GATATTTAAAAAGAA[A/C]TGTAAAAGACTGCCA | 8453 |
rs374049129 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126633 | AGACCTGACAACAGC[A/C]GTTACTCTGGCTGAC | 8453 |
rs374072002 | snp | C/T | | | synonymous-codon | CUL2 | GRCh38.p7 | 10:35100972 | GGTTTTCGTCCATGT[C/T]CTTTGCCACCTGAGT | 8453 |
rs374073947 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075016 | AATGGAATCATATTA[C/T]ACACACTGCTTGTAA | 8453 |
rs374107777 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038485 | GAGCCAAGAGCACGC[C/T]GCTGCACTCCAGCCT | 8453 |
rs374118664 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35035379 | CAAGTGCAGGAGTAC[A/G]ATATACGGATCCAAG | 8453 |
rs374136217 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35107868 | GCCTGGGCAACAGAG[C/T]GAGACTCCATCTCAA | 8453 |
rs374140737 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038525 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 8453 |
rs374247748 | snp | A/C/T | 6.67583e-05 | 0.00577714 | intron-variant | CUL2 | GRCh38.p7 | 10:35054398 | CAGTGTATAAAAACA[A/C/T]ACTTATGTTTGCTAG | 8453 |
rs374258166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35116826 | GCTGGGCGTGGTGGC[A/G]CACGCCTGTAGTCCC | 8453 |
rs374300496 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043079 | GTTGCTGTGGTGTGA[C/G]AGTAGAGGAAAAACA | 8453 |
rs374361194 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35069693 | CAAGAAATTCACTGT[C/T]GATTCTGTACAATGA | 8453 |
rs374376940 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35081714 | ACCTGGGCAACATGG[G/T]GAACCCCGCCTGTAC | 8453 |
rs374400488 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060521 | CAAATAAGAACATAT[C/T]GAGGGGACATGAGCT | 8453 |
rs374404647 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120892 | TAGAGTAAGAGATCC[C/T]GTCTCAAAAAAACAA | 8453 |
rs374417496 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036224 | TCTTTCGTGTCTGGC[C/T]TCTTGTGTTCAACAT | 8453 |
rs374482510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35071651 | CTGACCTCGTGATCC[A/G]CCCACCTTGGCCTCC | 8453 |
rs374489467 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051925 | AAATTTACCAATCTT[C/T]TTTATCATGGGTATT | 8453 |
rs374528501 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083862 | TTAAAACAAGGCTGA[A/G]ATATTTTTAAAAATT | 8453 |
rs374532708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020462 | TTAGTCAATAGAATC[A/G]TTATCTTTTAAGGTA | 8453 |
rs374581051 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108693 | AGTTCTTTTTCAGGG[C/T]TTCTCATGAGATTTC | 8453 |
rs374607746 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079816 | GGATCACTACTCCTG[C/T]ACTTTGGGGGCCCTT | 8453 |
rs374665089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35049223 | TGGGAAACCATTTTC[C/T]CATAAATTTATCTCA | 8453 |
rs374707250 | snp | A/C | 0.0640965 | 0.167152 | intron-variant | CUL2 | GRCh38.p7 | 10:35085430 | GCGAGACACCGTCCC[A/C]AAAAAAAATAAAAAT | 8453 |
rs374713992 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104101 | TGTTATTGAGATAAG[C/T]ATACACATGTGCGCA | 8453 |
rs374767352 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025361 | GAAAGCACGTTCCTG[C/T]GGTCCCTAATCAAGG | 8453 |
rs374809071 | snp | A/T | 6.59217e-05 | 0.00574078 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35032441 | CAAACTTACCAGTTC[A/T]GGTGCTTTGCAAACA | 8453 |
rs374829122 | in-del | -/AACTC | 0.00953873 | 0.0683987 | intron-variant | CUL2 | GRCh38.p7 | 10:35010686 | CCCAAGCTTCTATTT[-/AACTC]AACTCTCAGCTCTTA | 8453 |
rs374838970 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111469 | TCACTATGTTGCCCA[G/T]GCTGGTCTCAAACTC | 8453 |
rs374847737 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086389 | ACCTCCTGGGTTCAA[C/G]TAATCCTCTCACCTC | 8453 |
rs374865696 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065064 | ATGTTTTAACTCACC[A/G]TAGTTTTGGGTCTCA | 8453 |
rs374868426 | in-del | -/GTAT | 5.12352e-05 | 0.00506112 | intron-variant | CUL2 | GRCh38.p7 | 10:35062942 | ACATATTTATATCAC[-/GTAT]GTATCATTGCTTACC | 8453 |
rs374884970 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038132 | TCCAGCCTGGGCGAC[A/G]GAGCGAGACTCCATC | 8453 |
rs374889619 | snp | A/G | 1.64936e-05 | 0.00287168 | missense, intron-variant | CUL2 | GRCh38.p7 | 10:35054447 | ACCTCTCCTATTTCC[A/G]TAAGTGGTTCATTCA | 8453 |
rs374890018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35114485 | CCTCCCAGGTTCCAG[C/T]GATTCTCCTGCCTCA | 8453 |
rs374911422 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35016943 | AAAAAAAAAAAAAAA[-/C]AAAAAAAAAAGTCTT | 8453 |
rs374913312 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090772 | TGCGGTTCGCTGAGC[C/T]GATGGACACAGTACC | 8453 |
rs374960418 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35047382 | TTGGAAGGCCGAGGC[A/G]GGTGGATCACGAGGT | 8453 |
rs375005991 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068712 | ATTTGAAACAATGTG[A/G]AGGGACCTGTTTTTT | 8453 |
rs375165477 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35050685 | CACTGCTATACAGCA[C/T]CCTGTTGCATAAATA | 8453 |
rs375179176 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CUL2 | GRCh38.p7 | 10:35039874 | AAATAAAAATAAGGC[C/T]AGGCAAGGTGGCTCA | 8453 |
rs375186569 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030578 | GGTAGAGACAGGGTT[G/T]TGCCATGTTTCCCAG | 8453 |
rs375195582 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014877 | AAGTGCAAACAAGGA[A/G]TCTATGTTTACTTTG | 8453 |
rs375212848 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124039 | GGGAGACTATGTTAA[C/G]AAAGTGGCAGGCTTA | 8453 |
rs375213225 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037262 | TCCAATTGACTGAGC[A/G]ATGCGTGTTGAAAAG | 8453 |
rs375285928 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | CUL2 | GRCh38.p7 | 10:35060849 | AACGCTGCTTAGCTT[A/G]TCTAGATTTTAAAGG | 8453 |
rs375293438 | snp | A/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127682 | GCCGGAGGGCCTCGC[A/T]GCTGAGTCATTCGGT | 8453 |
rs375383181 | in-del | -/AAGGTAGGCTTGGC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089422 | GAAGGTAGGCTTGGC[-/AAGGTAGGCTTGGC]CAGGTCTAGTTCAAA | 8453 |
rs375458062 | in-del | -/T/TT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106960 | AACCTGTTTTTTTTT[-/T/TT]GTTGTTTTTTTGTTT | 8453 |
rs375546107 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35043819 | CATCTAAAATCCCAG[A/C/T]GCTTTGGGAGGCTGA | 8453 |
rs375547675 | snp | C/T | 1.85689e-05 | 0.00304698 | intron-variant | CUL2 | GRCh38.p7 | 10:35029482 | TAGTAAAACACATAT[C/T]CATACCTGTAGAACA | 8453 |
rs375549018 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012737 | AATATTTGTCTCCCC[C/G]CATCGGGAATTAAGT | 8453 |
rs375648174 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033829 | ATAGACTGTCTAGTA[C/G]CTGTCAGAAGAACCC | 8453 |
rs375660054 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062046 | GTTAAGTGAGTTGCC[A/C]GTGGTTACAACAGCT | 8453 |
rs375675942 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042687 | GTGATTTCAGACCTT[C/T]CCTTATGTGTCTCCT | 8453 |
rs375677319 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031876 | ACAGGCATGCACAAC[C/T]ACACCAGGCTTCTAA | 8453 |
rs375688497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020276 | AATGCTGAGAAGTGG[A/G]GAGGTGGAAGGGAAA | 8453 |
rs375700239 | snp | G/T | 4.03145e-05 | 0.0044895 | intron-variant | CUL2 | GRCh38.p7 | 10:35044523 | AATAAAACCAGGCCA[G/T]ATACAAAATAGATAA | 8453 |
rs375706384 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057399 | CGGTGGCTCATGTCT[A/G]TAATCCTGGCACTTT | 8453 |
rs375739277 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034998 | CTTTCTAATAATCTG[A/G]TAATTCCAAAATGAG | 8453 |
rs375832227 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090771 | TTGCGGTTCGCTGAG[C/T]TGATGGACACAGTAC | 8453 |
rs375909482 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35104975 | CTCAGATGATCCACC[A/C]GCCTGGGCCTCCCAA | 8453 |
rs375958768 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038123 | CCATTGCACTCCAGC[A/C]TGGGCGACGGAGCGA | 8453 |
rs376065425 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023021 | GCACTCCAGCCTGGG[G/T]GACAGAGCAAGACCC | 8453 |
rs376084940 | snp | A/G | 5.28947e-05 | 0.00514242 | intron-variant | CUL2 | GRCh38.p7 | 10:35016397 | ATTTTAACTTCACCT[A/G]CAATTAAAACAAAAA | 8453 |
rs376096495 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CUL2 | GRCh38.p7 | 10:35062941 | AACATATTTATATCA[C/T]GTATGTATCATTGCT | 8453 |
rs376106930 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099826 | AGTGTCAATGCCTTT[C/T]CCAATAAATAAAATA | 8453 |
rs376144838 | snp | C/T | 1.66382e-05 | 0.00288424 | intron-variant | CUL2 | GRCh38.p7 | 10:35035123 | AAAGGAAAGGCTCCA[C/T]GCTGGATCTGATTAG | 8453 |
rs376154529 | snp | C/T | 9.97821e-05 | 0.00706266 | intron-variant | CUL2 | GRCh38.p7 | 10:35044887 | AAACAAGGTATAACA[C/T]AAAATATTCTTGAGA | 8453 |
rs376242775 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048728 | TGGAATCACTCAAAC[A/G]GTCAGTGACAATTTT | 8453 |
rs376255923 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085725 | AAAAAAAAACTGATA[-/G]TGCATATGAAACATT | 8453 |
rs376283550 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121827 | AAAAAAAAAAAAAAA[-/T]AAAAATTAGTTTAGT | 8453 |
rs376285545 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037326 | TTGGTCTTACATCAA[A/G]TGGCCACATATGCTT | 8453 |
rs376301517 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041693 | ACGACTACACCACCA[C/T]GTGTGGCTAGTTTTT | 8453 |
rs376314865 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116074 | TGGGCCGGGCACAGC[A/G]GTTCACACCTGTAAT | 8453 |
rs376362980 | snp | C/T | 9.92507e-05 | 0.00704383 | intron-variant | CUL2 | GRCh38.p7 | 10:35032510 | CTGAATAAAAAAACA[C/T]GCCATAATTAACCAC | 8453 |
rs376389007 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036230 | GTGTCTGGCTTCTTG[G/T]GTTCAACATGTGTAT | 8453 |
rs376392350 | in-del | -/AAATAGCTTGTCATTCAACA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033782 | AAAAAGGAAGAAAGA[-/AAATAGCTTGTCATTCAACA]CAACAAGCTGTCATA | 8453 |
rs376398984 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018485 | TTAAAGATTTTAGGC[C/T]GGGCGCAGTGGCTCA | 8453 |
rs376459009 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118220 | TCATTTCTCTGAAGC[C/T]AGAAATCCCAAAGTT | 8453 |
rs376459163 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101095 | GAGGGAATTAGAGGA[C/G]AGGTCTTCTGGGTTG | 8453 |
rs376467046 | snp | A/C/G | 0.000171797 | 0.00926681 | intron-variant | CUL2 | GRCh38.p7 | 10:35028791 | CTTTAGTCTTCTAAT[A/C/G]TATTTCCTGCAAACT | 8453 |
rs376477780 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35037532 | TACATTGCCCTGGAT[C/T]TATGAAATTAATGTT | 8453 |
rs376524340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011575 | GTGAGCCAAGATCAC[C/G]CCACTGTACTCCAGC | 8453 |
rs376570147 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040635 | GGGCAAAGTCACAGA[C/T]TCAGGTCGGGCAAGA | 8453 |
rs376580684 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041380 | CAAACAGCTGTAAAA[A/C]CCCTGGGGGAAAGAA | 8453 |
rs376586766 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030834 | GGAGTTAGAGTCCAG[C/T]CTGGGCAACATAGTG | 8453 |
rs376654254 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060928 | TCTTCCCAGTACCTA[C/T]GATACATAACAAGTA | 8453 |
rs376800875 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065716 | AATACAAAATTAGCC[A/C]GGTGTGGTGGCACAT | 8453 |
rs376870052 | snp | C/T | 2.15631e-05 | 0.00328346 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35013723 | GTCTTTCTGCATTGA[C/T]GTAGTAATTTTAAAT | 8453 |
rs376871076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35113658 | AGAAAAATCAATCAA[C/T]AGGAACAAACTCAGA | 8453 |
rs376908075 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049388 | TAGAAAGTCTAAGAG[G/T]TTTCAGCTCTGAAAA | 8453 |
rs376916907 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059511 | GCACATTTTTTTAGA[C/T]AATGCTACTGCACAC | 8453 |
rs376926490 | snp | A/C | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091668 | TGTCACCCAGGCTGG[A/C]ATGCAGTGGCGGCAC | 8453 |
rs376958709 | snp | C/G | 1.65927e-05 | 0.00288029 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060967 | TCTGACTCCAAAACT[C/G]TCTATATAAAGAGGA | 8453 |
rs376961810 | snp | C/T | 5.04638e-05 | 0.00502289 | missense | CUL2 | GRCh38.p7 | 10:35010319 | AGCGACATCACGCGA[C/T]GTAGCTGTATTCATC | 8453 |
rs376979581 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35038213 | GCCTATAAAAGTAAT[A/G]CATGTTTTTTGTTTT | 8453 |
rs377017634 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35054602 | GAAAGCAAATGACTT[C/G]CAACTTTAGAAGAAT | 8453 |
rs377051760 | snp | G/T | 2.1728e-05 | 0.00329599 | intron-variant | CUL2 | GRCh38.p7 | 10:35029654 | TGCTATAAAAAAGTT[G/T]TAGAAAATACATGAA | 8453 |
rs377058841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35114010 | TCTCCTGGATTCACG[C/T]CATTCTCCTGCCTCA | 8453 |
rs377190044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35116064 | AAAAATATTATGGGC[C/T]GGGCACAGCGGTTCA | 8453 |
rs377220799 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35035661 | TACAGCTGCACAGTA[C/G]TCCATTATGTGGATA | 8453 |
rs377234385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35039909 | TGCAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 8453 |
rs377244893 | snp | A/G | 1.66247e-05 | 0.00288307 | missense | CUL2 | GRCh38.p7 | 10:35044652 | TTTCAGTCAGAAAGG[A/G]AGACTCAAAAATTTC | 8453 |
rs377268945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082003 | GACACCTCCTGTTTA[C/T]AATCCCAAAGAGAGC | 8453 |
rs377338651 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062792 | CAGTGAGCCATGATC[A/G]CGCCACTGCACCCTA | 8453 |
rs377350047 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116215 | AGGTGTGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 8453 |
rs377428976 | snp | C/T | 1.64936e-05 | 0.00287168 | intron-variant | CUL2 | GRCh38.p7 | 10:35071196 | CTGCCATTAAAAGGA[C/T]ACGAGAAACGGTCAT | 8453 |
rs377432508 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013389 | CTTTCCCTTATTTTA[A/C]AAATGAAAAATATGA | 8453 |
rs377436049 | snp | G/T | 0.000117066 | 0.00764978 | intron-variant | CUL2 | GRCh38.p7 | 10:35044711 | CATATTAGAAGAAAT[G/T]AGAACAAGCAGTTTA | 8453 |
rs377482297 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047259 | TTGCTTAATTCTCTA[C/T]GATAGTTCCTCAATT | 8453 |
rs377489530 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038483 | GCGAGCCAAGAGCAC[A/G]CCGCTGCACTCCAGC | 8453 |
rs377556187 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017586 | GTAAACCCAGCTACT[C/T]GGGAGGCTAAGGTAT | 8453 |
rs377574658 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113571 | TGTGAAATTCACAAC[A/C]TCTGGCATCTACGAA | 8453 |
rs377579990 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089240 | GGATCTTCCAGATAC[C/T]GTATAAGGGCAAAAG | 8453 |
rs377639676 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044029 | GCACTCTAGTCTGGG[A/C]ACCAGAGCAAGACCA | 8453 |
rs377670704 | snp | A/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080481 | TTTATTTATTTATTT[A/T]TGAGACAGGGTCTTG | 8453 |
rs377682451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099264 | GGCATGGTGTTACGC[A/G]CCTGTAGTCCCAGCT | 8453 |
rs377746353 | snp | A/T | 1.98509e-05 | 0.00315041 | intron-variant | CUL2 | GRCh38.p7 | 10:35029447 | TGTATCAACGTACTG[A/T]AATGATTAGTAAATG | 8453 |
rs386371178 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038526 | TGAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 8453 |
rs386371179 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038549 | AAAAAAAAAAAAAAA[-/AA]ATCAGATATAGCTGA | 8453 |
rs386371180 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088500 | CGAGACTCCGCCTCA[-/A]AAAAAAAAAAAAAAA | 8453 |
rs386742914 | in-del | GTA/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022077 | ACTGTAACTATGTAC[GTA/T]TGTCTGTCTTCCTAC | 8453 |
rs386742917 | multinucleotide-polymorphism | CA/TG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066981 | TTTGAAAGAGATGCC[CA/TG]ATAGAATATAAACTA | 8453 |
rs386742918 | in-del | CTGGGAGGC/TG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088431 | GAGAATTGCTTGAAC[CTGGGAGGC/TG]GGAGGTTGCAGTGAG | 8453 |
rs386742919 | in-del | ACACA/TTC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35092891 | AAAGTGTAGGCATAT[ACACA/TTC]TATTAATATACTCCC | 8453 |
rs386742920 | multinucleotide-polymorphism | ACA/CCG | | | upstream-variant-2KB, cds-indel, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126625 | GACCCTGAAGACCTG[ACA/CCG]ACAGCCGTTACTCTG | 8453 |
rs397692591 | in-del | -/T | 0.375 | 0.216506 | intron-variant | CUL2 | GRCh38.p7 | 10:35039429 | ACAGGTGATCTCTGT[-/T]ATGAATAACTATCAA | 8453 |
rs397695065 | in-del | -/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35029075 | TTGTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 8453 |
rs397713240 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128543 | TTTTTTTTTTTTTTT[-/T]GAGACGGGGTCTCGC | 8453 |
rs397723197 | in-del | -/TGCTCAT | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35118690 | TCCCTCTGTGCTCAT[-/TGCTCAT]ACTTATTCCTTGGGA | 8453 |
rs397735480 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018137 | AAAAAAAAAAAAAAA[-/A]CTAGCAGGGCGCAGT | 8453 |
rs397747358 | in-del | -/T | 0.375 | 0.216506 | intron-variant | CUL2 | GRCh38.p7 | 10:35021274 | TTTCTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 8453 |
rs397750566 | in-del | -/A | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35087887 | GTATCTAAGAACAAA[-/A]GCCAACATGATCCAG | 8453 |
rs397752489 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127865 | ATACTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 8453 |
rs397757607 | in-del | -/CT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054271 | ATCTTTTTCGTTCCT[-/CT]GAGGATTCTTAGGAA | 8453 |
rs397760128 | in-del | -/A | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35068126 | AAAAAAAAAAAAAAA[-/A]CGAACCACAAAAGGC | 8453 |
rs397797753 | in-del | -/AA | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35083168 | TCAAAAAAAAAAAAA[-/AA]GAAAGAAAAAGAAAA | 8453 |
rs397811416 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047623 | AAAAAAAAAAAAAAA[-/A]TACAGGCATAAAGGC | 8453 |
rs397816031 | in-del | -/A/T/TA | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35059466 | AATTACTTTATTGCT[-/A/T/TA]AAAAAAAATGCTGTT | 8453 |
rs397845052 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017708 | AAAAAAAAAAAAAAA[-/A]TTCTATATGCTAAAT | 8453 |
rs397845287 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061478 | AAAAAAAAAAAAAAA[-/A]TCACACTTATAATGT | 8453 |
rs397845751 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012071 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTTTCAC | 8453 |
rs397846045 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055749 | TCATACTCTTTTTTT[-/T]CCCCTTTAAAATGCC | 8453 |
rs397959134 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049632 | CTATTTTAAAACCAT[-/T]ATCAAACAACAAAAT | 8453 |
rs397975596 | in-del | -/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009514 | GACAACTTTTGAATG[-/G]AAAAGCTCTCTCTGT | 8453 |
rs398013209 | in-del | -/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35033771 | TATTTTCTTTCTTCC[-/T]TTTTTTTTTTTTTTG | 8453 |
rs398013210 | in-del | -/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35114832 | ATTCCATCCAATGTA[-/T]TTTTTTATTTCAGAC | 8453 |
rs398114247 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057813 | TAATAAAGACATGGG[-/G]CTGGACGCAGTGGCT | 8453 |
rs527262013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054327 | CTTTTAAATCTTGAC[C/G]ATTTTAAGCTAGCCA | 8453 |
rs527319487 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089473 | ACAATCTATAGCGAA[C/T]GTTAATATTTTGCAT | 8453 |
rs527336680 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028727 | TGAACCCTTAAGACT[C/G]TGAAAAAATATTAAA | 8453 |
rs527384275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35097818 | ACAAAAATTAGCCAG[G/T]CTTGGTGGTGCATGC | 8453 |
rs527384612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35090310 | CAGCTCGCGTTCCCC[C/T]GCTCACAGCGCTGCC | 8453 |
rs527402975 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059228 | AATTTCGTAAGAATT[C/T]CTACTGCAGGTAAAA | 8453 |
rs527454039 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35069175 | CCCGGCCTGTACTCT[G/T]TAATCATTATTTTTG | 8453 |
rs527504292 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35069715 | GTACAATGATGAAGA[A/C]CACATTTTAATTATT | 8453 |
rs527525364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109840 | TCACTGGAGGTTTTT[A/G]AGCATGAATAATGAT | 8453 |
rs527548759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103504 | TAATTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 8453 |
rs527588325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013409 | GAAAAATATGAAATT[A/T]TATTACTTCTCAATG | 8453 |
rs527601291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104074 | CATAGTCCATTAGCT[A/G]TACAAAAACACTGTT | 8453 |
rs527632101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062263 | GTCACAGAGACAGCT[C/T]CTATCACCATTTACC | 8453 |
rs527666415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039401 | AAAGTGGGTACAGAT[G/T]ATTAAATTCAGAACA | 8453 |
rs527687864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123608 | GCTCCTGAATGACAT[A/G]AGTAGAAGAATGACC | 8453 |
rs527779070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081664 | TTTGCGAGGCCAAGA[C/T]GGGCAGACTGCTTGA | 8453 |
rs527780898 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074785 | AGCCATTGTGCCCGG[A/C]CTTCATCTGCTTTTA | 8453 |
rs527798947 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35015792 | TTACACATATTAAAT[A/G]TGTGTACAAACAGAC | 8453 |
rs527799760 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023773 | GGAAAAAAAAAAAAT[C/T]TAAAACCCTGGTCCA | 8453 |
rs527847362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051866 | TCAACTGCTCGGTTT[C/T]TTTATTGTGTTTTGG | 8453 |
rs527889768 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35052721 | TAACACGGTGAAACC[C/T]CGCCTCTACTAAATA | 8453 |
rs527911896 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35102686 | TCAGGAGTTCAAGAC[C/T]AGCCTGGCCAAGGTG | 8453 |
rs527976429 | snp | A/G | 0.00585712 | 0.0537983 | intron-variant | CUL2 | GRCh38.p7 | 10:35095334 | TCTCAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 8453 |
rs527980466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35087680 | CCCATCCCAACTGCA[C/T]GCTCATCCAAAACAT | 8453 |
rs527983245 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35085600 | ATACAAAAAATTAGC[C/T]GGGCATGGTGGCAGG | 8453 |
rs528036214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078230 | TGACAAAATGTCCAC[C/T]CCTAAAAAACTTAAA | 8453 |
rs528088437 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127212 | AGTGGTGCGTCGGCT[C/T]CGGCCCCGAGACCCA | 8453 |
rs528105528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128070 | GGCTGGTCTCGAACT[C/T]CTGACCTTCCACCCA | 8453 |
rs528125464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35031229 | GTTACTGTACACAAT[A/G]CTGCAATGAACATCT | 8453 |
rs528147668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120945 | TAAGGCATTTTATAT[A/G]CAAGGTAATATGGAT | 8453 |
rs528155821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35022922 | TGGTAGTGTGTGCCT[A/G]TAATCCCAGCTACTC | 8453 |
rs528163345 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35031773 | GTTGCCAGGCTGGAT[G/T]GCAGTGGACAAGATC | 8453 |
rs528169681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35078750 | TTCTAAAAGTATAAT[C/T]ATCAATAATGTAAAT | 8453 |
rs528185379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072229 | TGACCTTTTAAGATT[A/T]AAAAAAAAAGATTCC | 8453 |
rs528236135 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080210 | GCACAATGACCAAAT[A/G]TGTTGCCATCATTTA | 8453 |
rs528257264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35057059 | CTGTCAGGATGTTAC[C/T]TTCCTATTCAGAATT | 8453 |
rs528271808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35049327 | AATAGGTGGTCCTCA[C/G]GAGGATTTAAACAGG | 8453 |
rs528275472 | in-del | -/A | 0.119571 | 0.21328 | intron-variant | CUL2 | GRCh38.p7 | 10:35095323 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 8453 |
rs528295344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050104 | AAGGTGGGCACATCA[C/T]GAGGTCAGGAGATCA | 8453 |
rs528305693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099368 | TGCACTCCAGCCTGG[C/T]GACAAAGTGAGACTC | 8453 |
rs528318891 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091296 | GCTTTTCCCTCCCAT[C/T]CCTTCCTTCCAAACT | 8453 |
rs528388416 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35107155 | AATTTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 8453 |
rs528443712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35063189 | TTATAATATACATAA[C/T]ACTGTTGTATATATG | 8453 |
rs528453250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119011 | TCACACACCACACTT[C/T]CAAATGTCTTGGCTG | 8453 |
rs528461972 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35029743 | CTTTGATCAAAGGTT[A/C]TTGCATATACACTTA | 8453 |
rs528480911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35021139 | CTTCAACAGAAGACT[C/T]TGTAGGGAGCACATT | 8453 |
rs528507438 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35021917 | GAGGTGGGGCGAAGT[A/G]GGGCGAGGGGGCACC | 8453 |
rs528520572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014363 | GCAAGTGGCCTTTGC[C/T]CAGGGGAAAACTGTT | 8453 |
rs528550141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35014770 | CCCAGGAGGTGGGGA[C/T]TGCAGTGAGCTGAGA | 8453 |
rs528553981 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009160 | ATGATAATAGATCGC[A/G]GTACTCTTAACACTG | 8453 |
rs528601911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098818 | AGGCGCCTGTAATCC[C/T]AGTTACTTGGGAGGC | 8453 |
rs528611894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35056104 | ATCCTATGCTTTTAT[C/T]GGTTTCTTTTTTTGT | 8453 |
rs528657660 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35041304 | ACAATGATAACTTGG[A/G]AGAGAGAGGCGCATA | 8453 |
rs528712560 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066655 | TATCTACGAAATCAT[A/G/T]CATTAGCAAACAAGG | 8453 |
rs528715745 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100139 | TTTAATAAAATATTA[C/T]ATAAAATAAAATAGT | 8453 |
rs528717292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35029240 | TTTTTGCATTTTTAG[C/T]AGAGACGGGTTTTCA | 8453 |
rs528719166 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037919 | AGCACTTCGGGAGGC[C/T]GGGGCAAGCAGATTA | 8453 |
rs528766340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114580 | TAGAGACAGGGTTTC[A/G]CTATGTTGGCCAGGC | 8453 |
rs528780841 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036457 | GGAGGTAAAGCTGGG[G/T]GGTGGTTATATGTTT | 8453 |
rs528817956 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35070830 | TGCTCCAAGCCTCCC[C/T]CACGTCCTTATCCTG | 8453 |
rs528829686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059787 | ATCTGGGTTTAAATC[C/T]TGCCTTTGTGATTCA | 8453 |
rs528867488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116015 | GCTTGAAAGATGATA[A/T]CACTACAGATCTGAT | 8453 |
rs528910087 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058008 | GAGGCTGAGGAAGGA[C/G]AATCACTTGAATCTG | 8453 |
rs528925250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011415 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 8453 |
rs528926268 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35018709 | TGGAGGTTGCTGTGA[A/G]CCGAGATCGCGCCAT | 8453 |
rs528955532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35102791 | GGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 8453 |
rs528961582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011797 | AGACTGAATCTGTAC[A/G]ATGACAATGCCCTCT | 8453 |
rs528998827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35095461 | AAATATATTTTTATA[C/T]GTATCAGAACATATA | 8453 |
rs529004351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35052810 | TGAGGCAGGAGACTA[A/G]TGTGAACCTGGGAGG | 8453 |
rs529018400 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35103387 | TGGAGCGCAGTGGCA[C/T]GATCTCGACTCACTG | 8453 |
rs529020234 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35022349 | CTTGTGCACCATCAA[C/T]CATTTGTGAAGACTC | 8453 |
rs529037924 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35034819 | ATTGCAAGTCGTCTA[-/T]TATTACCACTGATTA | 8453 |
rs529050522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032705 | TATCCTGTTGCTATT[C/G]CAAGATATTCTGTAA | 8453 |
rs529056351 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080437 | AGAATTCCTATTTTT[A/T]TTTATTTATTTATTT | 8453 |
rs529082480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038399 | GGTGTGGTGATGAGC[A/G]CCTGTAATCCCAGCT | 8453 |
rs529086304 | snp | A/G | 1.89299e-05 | 0.00307646 | intron-variant | CUL2 | GRCh38.p7 | 10:35033142 | TTTATGTACATATAT[A/G]GTATATATGTATTTA | 8453 |
rs529090046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122614 | GTGAGGCAGGTAGTA[A/G]TAATATCCTTATTTT | 8453 |
rs529119781 | snp | C/T | 2.45336e-05 | 0.00350231 | intron-variant | CUL2 | GRCh38.p7 | 10:35025241 | TATTTTTAGCTACTA[C/T]AACTTGCCTAGTTAA | 8453 |
rs529122409 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053157 | AAGTTCAGAAAAGAT[A/G]CGAACTAAATTGTTT | 8453 |
rs529149248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115371 | TCAAGACCAGCCTGG[C/G]AAACATAATGAAACC | 8453 |
rs529165874 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021904 | GGTGAGGTGGGGTGA[A/G]GTGGGGCGAAGTGGG | 8453 |
rs529177671 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095563 | ATTTTGTGTGTGTGT[A/G]TATATATATTTTTGA | 8453 |
rs529197245 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056156 | TGTACAGTATACAAA[C/G]CAAGAACCTCCTCTT | 8453 |
rs529206969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35067596 | TCTCTACCAAAAATA[C/G]AAAAATTAGCCAGGT | 8453 |
rs529290721 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35043887 | AGCCTGGGCAACACA[C/G]CAAGACCCCATCTCT | 8453 |
rs529328281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038043 | CTGCAATCCCAGCTA[C/T]TTGGGAGGCTGAGGC | 8453 |
rs529328547 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049473 | AAGAAAAGACCAGAG[C/T]TCCCCCCACCAAAAA | 8453 |
rs529345817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045085 | TTAGATGTCATTTCA[A/G]GAAATAAAAAGAAAA | 8453 |
rs529380624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35068789 | AGATATTAAGGGTCA[A/G]AAGTGAACTTTATAT | 8453 |
rs529382479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094298 | TGGAGTGCAATGGTG[C/T]GATCTTGGCTCACTG | 8453 |
rs529399551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086266 | CTTAGGGAGGCTGAG[C/G]TGGGAGAATTGTTTG | 8453 |
rs529402668 | in-del | -/TTTATTTATTTATTTATTTATTTA | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080434 | TTTAGAATTCCTATT[-/TTTATTTATTTATTTATTTATTTA]TTTATTTATTTATTT | 8453 |
rs529410320 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102242 | TCCATCTCAAAAAAC[A/T]ATAATAATAACATTA | 8453 |
rs529411674 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045821 | TGACTCTAGTACCAA[C/T]GCTCAAATCAAACCA | 8453 |
rs529426442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079693 | GCTTACAGTAGGTCT[C/T]AGCAATCTCAGTCTA | 8453 |
rs529502129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066416 | GCAATTATCCTGCCT[A/G]CCTCCTGAGTAGCTG | 8453 |
rs529504971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016692 | AGCACTGTGGGAGGC[C/T]GAGGCAGACAGATCA | 8453 |
rs529516771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057969 | CAGGTGTGGTGGCGC[A/G]TGCCAGTAATCCCAG | 8453 |
rs529522655 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009690 | TTTATGCTGAATGCA[A/G]TCCTATGCAGTCAAG | 8453 |
rs529550839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35010501 | CTATTAAGTAATGAC[A/T]TTTAACCAATCAGTT | 8453 |
rs529553634 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018161 | GCGCAGTGGCGGACA[A/C]CTGTAATCCCAGCTA | 8453 |
rs529561472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35017387 | AACATTTAATCTGAA[C/T]GTTTTCATAAATATG | 8453 |
rs529629422 | in-del | -/GTCAGT | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35089361 | AGCGATTATTATGTA[-/GTCAGT]TGTCAATCAGATCAA | 8453 |
rs529645223 | in-del | -/ATTT | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080477 | TTTATTTATTTATTT[-/ATTT]TTGAGACAGGGTCTT | 8453 |
rs529664024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050745 | TGATGACTGCTGATG[G/T]GTCTGTGATTCCTAT | 8453 |
rs529698953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048408 | ATCATATTGATTTTT[A/C]GCAAACTAACAATCA | 8453 |
rs529717116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35041318 | GGAGAGAGAGGCGCA[C/T]ATCAAGAGAAATGTA | 8453 |
rs529758901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084035 | TAATCCCAGCACCTT[A/G]GAAGGCCAAAGAGGG | 8453 |
rs529792308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35083121 | AAGATCGAGCCACTG[C/T]ACTCCAGCCTGCATG | 8453 |
rs529881212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110961 | AGTCAAGAATGGAAG[G/T]AGCAAGATCAGTTAG | 8453 |
rs529927454 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35014105 | TAAGAGTCAAGCTCA[G/T]TGCCTAGAGTTTGAC | 8453 |
rs529942691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013494 | TACAACAAAACCATA[C/T]CCTTTTCCTTAGAAA | 8453 |
rs529980380 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019442 | TTTCTTAGCACCATA[C/G]TCTTACTGAAAAGAC | 8453 |
rs529993833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082361 | CAAATTCATAAAGAC[A/G]GAAAGAAGGATGAGA | 8453 |
rs530009625 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044052 | CAAGACCACATCTCC[A/C]AAAAAAAAAAAAAAA | 8453 |
rs530064424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055292 | TGACAATACAAGTAT[A/T]TTAGGCAACAACCCA | 8453 |
rs530105583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35019735 | CATCCAAGTCACTCC[C/T]CAGTATCTGTGTCAG | 8453 |
rs530112455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124558 | TGAAGGTGAGGGGAT[A/G]GCAAGGGATGGAACA | 8453 |
rs530132009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069208 | GACTTTTTATTTTGG[A/G]GGTGAGAGAAAATTC | 8453 |
rs530145053 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35027387 | CTGACCTCATGATCC[A/G]CCCGCCTCGGCCTCC | 8453 |
rs530184147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117430 | AGACAAGGTCTCACT[A/C]TGTTTCCCAGTCTGG | 8453 |
rs530184701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35028326 | GACTCTCCTCTATTA[G/T]TTATTACCACGAAAC | 8453 |
rs530204868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35123132 | GACAGAGTGAGATCC[A/G]ATCTACAAACAAGCA | 8453 |
rs530246686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069877 | AATCTCACTAACACA[C/T]AAGTAGCAACACTTT | 8453 |
rs530254254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039482 | AATCAAGTAGATGAA[C/T]CTAATTATTTTACGT | 8453 |
rs530337468 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090464 | CAGCAAAGTCCAAGG[C/T]CGCCGCCGCTCCCCG | 8453 |
rs530342572 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087302 | GAGCCATGTGAATAC[A/T]GTTTTTGTTCAAAAC | 8453 |
rs530351300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096188 | CAGAGGCAGAGGTTT[C/T]AGTGAGTTGAGATCT | 8453 |
rs530379576 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35072830 | AAATGTTTTAACAGC[C/T]TCCCTCATGTCTCCC | 8453 |
rs530380053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039898 | TGGCTCATGCCTGCA[A/G]TCCCAGCACTTTGGG | 8453 |
rs530421383 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059499 | AAATTAAGTTGTGCA[A/C]ATTTTTTTAGACAAT | 8453 |
rs530424369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35031869 | TGGGACTACAGGCAT[A/G]CACAACCACACCAGG | 8453 |
rs530461013 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014086 | ACACTACTTTTTGAT[A/G]AAATAAGAGTCAAGC | 8453 |
rs530512884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35073344 | AACCATGCCTCCTTC[C/T]CTTCCTTGTTTACTA | 8453 |
rs530513537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128872 | AAACTTTCCCTTCCT[A/G]AGTCATAGTAGTCTT | 8453 |
rs530515648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35120974 | ATATAATTCCCTTAT[A/G]TTTTATAGAGACTTA | 8453 |
rs530528974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121678 | AATGAGGCATGGTGG[C/T]ACATGTCTGTAGTTC | 8453 |
rs530536521 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35114173 | GTGATCCGCCTGCCT[A/C]GGCCTCCCAAAGTGC | 8453 |
rs530547659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023754 | ATATATTAGTTTTCT[C/T]AGGGGAAAAAAAAAA | 8453 |
rs530551260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066499 | AAGATGGGGTTTAAC[C/T]ATGTTGGCCAGGCTG | 8453 |
rs530582358 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107838 | AGTGAGCCTAGATCG[C/T]GCCACTGCACTCCAG | 8453 |
rs530584906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35024251 | GTAAAGATCGACTTA[C/T]ATAAGTAATGCAAAA | 8453 |
rs530604730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050610 | CCCCTCAGGTTATTA[C/G]AATCCACAATTTTGT | 8453 |
rs530623676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065884 | AAAACACAAAATAAC[C/T]AGGTCAGATTTCAAC | 8453 |
rs530655944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102137 | CCCAGCTACTTGAAA[A/G]GCTGAGGCAGGAGAA | 8453 |
rs530672134 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084107 | CATGGCAAAACCCTA[C/T]CTCTACTAAAAATAT | 8453 |
rs530703917 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35077137 | TTAAAATGCAATATA[G/T]CCATACAATAAATTA | 8453 |
rs530717407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075227 | AACTGACAAACCAAT[A/C]GCAGGAAGGTATGCT | 8453 |
rs530767198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35084951 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 8453 |
rs530794379 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35113252 | TGTAATCCCAGCATT[C/T]TGGGAGCCCGAGGTG | 8453 |
rs530848381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015522 | ACAAAACATTATTTA[C/T]AGGAATTTTTTCTTA | 8453 |
rs530884653 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008578 | ACTTTTATCAATCAA[C/T]AAGTTATCAAAACAA | 8453 |
rs530901649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35056393 | TCAGACACAGCCCTA[A/G]GCATTTTATGTGGCT | 8453 |
rs530915663 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35105694 | GCCTGGGCGACAGAG[C/T]GAGACTCTGTCTCAA | 8453 |
rs531015890 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103914 | TAGATCTTGGAATTG[A/G]GGGGATCCACTTAAA | 8453 |
rs531036907 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038680 | GCATTAAGGAAATTA[A/G]CTCTTGTAATATATA | 8453 |
rs531037228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030058 | ATTGGAGCCATCATG[A/G]TGCACTACAACTTCG | 8453 |
rs531046534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35100501 | GCGTGGTGGCTCATG[C/T]CTGTAATCCCAGCAC | 8453 |
rs531081623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35119847 | CTCAACCTGTGTTGA[A/G]ATTATAGGCACAGGC | 8453 |
rs531171397 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118900 | GTCCAGATCATTTCA[C/T]AATTCCTCTACTCCA | 8453 |
rs531185570 | snp | C/T | 4.96208e-05 | 0.00498076 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35010341 | GTATTCATCTGCCGA[C/T]GCCTGGCTGCGTTCT | 8453 |
rs531192836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102863 | ACTCCAGCCTGGGCA[A/G]TAGAGTGAGACTCTG | 8453 |
rs531204513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35112581 | TAGAGACTTGGAAAA[C/T]GAGTTTCCTCAAGTC | 8453 |
rs531224672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071572 | ACCATGCCCAGCTAA[C/T]TTTTTGTATTTTTTT | 8453 |
rs531236311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014913 | TTCTGGGCAGCAAAA[A/T]TAGCATGTTTTAGAA | 8453 |
rs531264932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064048 | CTCCAGACTGTTCCA[C/T]GATAAAGCTATGCCA | 8453 |
rs531331789 | in-del | -/G | 0.006635 | 0.0572143 | intron-variant | CUL2 | GRCh38.p7 | 10:35082469 | AGTTTTGGAAATGGT[-/G]GTTTTGGAAATGGTG | 8453 |
rs531338614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053804 | TTAACATTAATTTCC[A/T]ATTTGGCATCTGCTT | 8453 |
rs531342446 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35046932 | CAAAACAAAACAAAA[A/C]CAAAAAACTGGGTTA | 8453 |
rs531396545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35096293 | AGCTTACAAAAGTGC[A/G]AGTCTCTTTAAAGAA | 8453 |
rs531398155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123502 | AAAAAAAAAAGGGAT[A/G]GATGCAAGTTTCTAC | 8453 |
rs531402321 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35025312 | AGAAGAGACATTAAA[G/T]CCCATCTGGTTTACC | 8453 |
rs531412111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116060 | AAAAAAAAATATTAT[C/G]GGCCGGGCACAGCGG | 8453 |
rs531424981 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089094 | GCAGAAGAATTGCTT[A/G]AACCCGGGAGGCGGA | 8453 |
rs531435552 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35085256 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAAAA | 8453 |
rs531459757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096766 | TGAAACTAAATTGCT[C/T]GTGTTAGGTTTTTAG | 8453 |
rs531466829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018739 | TTGCACTCCAGCCTG[C/G]GTAACAAGAGCGAAA | 8453 |
rs531503703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019400 | ATACTCTACCAGGGA[C/T]CAGGGGTACACTGAC | 8453 |
rs531621930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038459 | TGAATCTGGGAGGCG[C/G]AGGTTGCAGCGAGCC | 8453 |
rs531629643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35068453 | CCACAAAAACAACAG[A/G]CACAAAAATCAAGAT | 8453 |
rs531644143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35087200 | GGTACTACAGGCGTG[C/T]GCCACCACGCCTGGC | 8453 |
rs531659950 | snp | C/T | 8.90813e-05 | 0.00667328 | intron-variant | CUL2 | GRCh38.p7 | 10:35033150 | CATATATAGTATATA[C/T]GTATTTAAAACTTAC | 8453 |
rs531660591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35122694 | CCAGGCTGGAGTGCA[A/G]TGGCACAATCTTGGC | 8453 |
rs531667276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069119 | TAATCCGCCTGCCTC[A/G]GCCTATCAAACTGCT | 8453 |
rs531689745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080709 | TTCCACCAGCCTTGG[C/T]CTCCCAAATTACTAG | 8453 |
rs531715262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045238 | ACTCACTACAAACTA[C/T]AAAGTCTTAATCATA | 8453 |
rs531758576 | snp | C/T | | | synonymous-codon, intron-variant | CUL2 | GRCh38.p7 | 10:35049685 | TGTCAGCACTCACTT[C/T]TTGATTTCTCGGAGC | 8453 |
rs531790909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039278 | ACTAGCTGTCATCTA[C/T]ATTCCACCAGTCTTA | 8453 |
rs531799516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107662 | CCGAGGCGGGTGAAT[C/T]ACGAGGTCAGGAGAT | 8453 |
rs531834537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101453 | CTCACATCAAAACAG[C/T]TGCTTTGATTTTTAG | 8453 |
rs531846909 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35101991 | AATGCTGGGATTACA[A/G]GTGTGAGCCATTGCC | 8453 |
rs531856792 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018657 | AATCTCATCTACTCC[A/G]GAGGCTGAGGCAGGA | 8453 |
rs531857709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35074018 | ACCCGTGCTGCGGCC[A/G]GTGCTCTAGGCTGCT | 8453 |
rs531904701 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35094318 | TTGGCTCACTGCAAC[C/T]TCCGCCTCCCAGGTT | 8453 |
rs531944222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051330 | AAAAAAGAAAAAAAA[A/C]CGGCCAGGCGCGGTG | 8453 |
rs531980806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108081 | ATCTTCGCCTTTTGT[A/G]AATGGAAAATGGATT | 8453 |
rs532040176 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035946 | TGTAGTAGGTTTAAT[A/T]TTAAACGTTTCATTA | 8453 |
rs532070667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051779 | AGTTTGTCTTGTTCT[C/T]AATAAAAGCTAGAGT | 8453 |
rs532107076 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115327 | AGCACTTTGGGAGGC[A/G]GAGGCGGGCGGATAG | 8453 |
rs532122492 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35042015 | ATTGTGGTAAAAACA[C/T]AGATAATAAAATTTA | 8453 |
rs532198134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036995 | CTCCCTCTTAATGGC[C/T]TTTTAATAATCCAAA | 8453 |
rs532235089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098789 | AAACCAAAAAATTAG[C/G]TGGGCACGGTGGCAG | 8453 |
rs532243863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35112210 | CAAAAATTTGTTGAA[C/T]TCTCGTCTGCTGGAA | 8453 |
rs532254809 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35105559 | AAAAATACAAAAAAA[A/T]TTGCCGGGTGTGGTG | 8453 |
rs532258547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071612 | ACGGGGTTTCACTGT[G/T]TTAGCCAGGATGGTC | 8453 |
rs532263490 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090479 | CCGCCGCCGCTCCCC[A/G]GCGGGACAGGGGCGG | 8453 |
rs532269925 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35076545 | GCATAAAATTCTGAA[A/G]TCTCAATCTCTCTCC | 8453 |
rs532282135 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35047963 | TTAGATTAGCCCAGA[C/T]GTGAATCCCTAGAAT | 8453 |
rs532297844 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091165 | TATAGAATTACTCAT[C/T]ACCTCCTCATATATG | 8453 |
rs532323807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069889 | ACACAAGTAGCAACA[C/T]TTTTTCAACTTTTAT | 8453 |
rs532341645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048493 | AAGTACATTTAGAAA[G/T]TATAACAGTATTGTC | 8453 |
rs532395759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014708 | CATAGTGGCTTACAC[C/T]TGTGGTCCCAGCTAC | 8453 |
rs532438739 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35029046 | CATTTCATTCCAAAC[C/T]AATAGGACCTTTTTT | 8453 |
rs532443028 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35010709 | TCTCAGCTCTTAGTT[C/G]AAACACTTTCTCAAG | 8453 |
rs532458029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070701 | CAAGCACACTCTTCC[C/T]CCCAAAATCACATGG | 8453 |
rs532458075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062450 | ACATTTTAAAACTCA[A/G]CAAACCCTGAGCTGA | 8453 |
rs532462370 | in-del | -/CTCATGAAAT | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35094590 | GAACCACTGCTCTAA[-/CTCATGAAAT]TCCTTCACTCTCATC | 8453 |
rs532490569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041464 | CATTCCCCAATTAAC[C/T]AAATGGAGAGCAAAG | 8453 |
rs532530986 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126053 | CAGGCTGCTCCTGAC[C/G/T]TCAGGTGATCTGCCC | 8453 |
rs532536952 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095553 | GCAAATAATTATTTT[G/T]TGTGTGTGTGTATAT | 8453 |
rs532545307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039922 | CTTTGGGAGGCCGAG[A/G]TGGGTGGATCACATG | 8453 |
rs532586881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020319 | ATACAATTAGTGACC[G/T]CTGACAGTCAAGCAA | 8453 |
rs532602091 | snp | A/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080246 | AAAATAAGCTCCAAG[A/T]ATGCATCTAAACATT | 8453 |
rs532626282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35021027 | GATCTTGAACTCCTG[A/G]GCTCAAGTGATACTC | 8453 |
rs532658348 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066410 | GTTCAAGCAATTATC[C/T]TGCCTACCTCCTGAG | 8453 |
rs532663610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014240 | CTGTAAATGGCCTGA[C/T]GACAAGAGAAAGCTG | 8453 |
rs532669997 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063384 | CCTACAAAATAAGGT[G/T]TATATTAGAATGGAT | 8453 |
rs532739096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066605 | CGCCCCGCCAGATTT[C/G]CTGGCATTTCTAATG | 8453 |
rs532791243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035042 | AGGTTTAAAACATTT[A/G]AATAAAGACATTTCT | 8453 |
rs532823277 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125207 | CATCTTACAGCAAGG[A/G]TATAGCAGAGGCCAT | 8453 |
rs532845403 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097377 | CAGAAGTGCAAGACC[A/T]GCCTGGGGAGGCTGA | 8453 |
rs532853054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35067228 | TCCTACCTGGAAGAA[A/G]TACGTTGAGGGAAGG | 8453 |
rs532855421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076286 | GGGAAAATGGGAAAT[C/G]ACTGCCAACAGGGTG | 8453 |
rs532891738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35059583 | TGGGAAACCAAACAA[C/T]TTGTGTGACTTGTCT | 8453 |
rs532898535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102058 | CAGCCTGGCCAATAA[A/G]GTGAAACCCCATCTC | 8453 |
rs532913486 | in-del | -/GGACA | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35011006 | TTTCCTTCAATAACT[-/GGACA]GAAGACTCAATGAAT | 8453 |
rs532921852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122517 | AAAATAATAATTATA[A/G]TTTACATTTATTTAA | 8453 |
rs532931215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35115718 | GGGCAACATAGTGAC[A/G]CCCCCATCACTACAA | 8453 |
rs532933526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35114670 | ACAGGCATGAGCCAC[C/T]GCGCCTGGCCCGCAG | 8453 |
rs532939394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037671 | AACATAGTGAAACCT[C/T]GTCTCTACTAAAAAT | 8453 |
rs532950778 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114977 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA | 8453 |
rs532988113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35107698 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGCCT | 8453 |
rs533008755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35108159 | CACCTGCCTAAGTGA[A/G]AAGTGACAGTAGTTT | 8453 |
rs533033539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017936 | GCTTCCTAAAGCACG[A/G]AGTTGTGGTTTGACG | 8453 |
rs533034149 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022843 | CGAGGTCAGGCGTTC[A/G]AGACCAGCCTGGCCA | 8453 |
rs533051611 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052830 | AACCTGGGAGGCAGA[A/G]CTTGCAGTGAGCCAA | 8453 |
rs533073260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108900 | ATCTGATGTTTGCTG[A/C]ATTAATGTTTTTTAA | 8453 |
rs533076672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079531 | CCCACCAGTGTAATG[C/T]CTTTTCCAAATTAAC | 8453 |
rs533080998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080291 | TCAAATGAGCAAGCC[A/C]CTGGATGTAACTAAG | 8453 |
rs533096937 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058198 | ATGCTGATTCTATAA[A/C]GGGAAATAAAATCTC | 8453 |
rs533110140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078972 | GGCTTAGAGCAGATT[A/T]CCTTCCAAATGCATA | 8453 |
rs533122901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086177 | GCACTCCAGACTGAG[A/C]GACTCTGTCTCAAAA | 8453 |
rs533199037 | snp | C/T | 0.000399281 | 0.0141238 | missense | CUL2 | GRCh38.p7 | 10:35100851 | CCACTTACAGCCATG[C/T]GTGGCCATCACCGCA | 8453 |
rs533201417 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009439 | TCCTAAGACTCAGGG[A/G]AGGCCACAGAGCTAG | 8453 |
rs533294697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043305 | CTAGAGGCTTCAACA[A/G]AAGTCTAAGGTGCAA | 8453 |
rs533325517 | snp | A/G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104743 | ATCAAAGACTTTTCT[A/G/T]GGGGGGGGACAGTCT | 8453 |
rs533325579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050204 | CATGCGCCTGTAATC[C/T]CAGCTACTCGGGAGG | 8453 |
rs533352640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030907 | ATATTATATTCAAAA[C/T]GTCTACTATGCAAGA | 8453 |
rs533392640 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011253 | AGATGGGGTCTCCCT[A/G]TGTTGCCCAGGCTGG | 8453 |
rs533401343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35113851 | AGCTGGGATTACAGG[C/T]GCCCACCACACCCAG | 8453 |
rs533454092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093008 | ACTTTAGATTGCTTT[C/T]TGAGATATTTTTCAG | 8453 |
rs533455807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101267 | CATTCACCTGATGCC[A/G]CTGGCAATAGTGGCT | 8453 |
rs533466669 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35085637 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA | 8453 |
rs533470887 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071962 | GAAAGAAACGGGGAC[A/C]CACTTAACCAAAAGG | 8453 |
rs533511654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051170 | AATACAAAAAATTAG[C/T]GGGGCGTGGTGGCGG | 8453 |
rs533514102 | in-del | -/AG | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35024019 | TTTGGATTTTTTAGT[-/AG]AGACAGGTTTTGTCA | 8453 |
rs533516052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072128 | GGCTTTACCTTCCTG[A/G]AGCATCAGTATAAGA | 8453 |
rs533537780 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35047021 | GTAACTAAACAGTAG[G/T]TGAGAAGAAGCATAT | 8453 |
rs533566354 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070888 | AGCAATGACATTAGA[-/T]TTTTTTTTTTTACCT | 8453 |
rs533570314 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35022105 | CCTACTAGACATGAG[G/T]TTTTTTTGAGGGCCA | 8453 |
rs533575316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35124097 | CCGAGGTGGGAGGAT[C/T]GCTTTAGACTAGGTA | 8453 |
rs533600491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034682 | TCGAGAAAGATGAGT[A/G]TTAGGGATATGAGGG | 8453 |
rs533626073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106440 | TTCTCCTGCCTCAGC[A/G]TCCCGAGTAGCTGTG | 8453 |
rs533660521 | snp | A/C | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008194 | GGGCGGCCAGGTCAG[A/C]GCTCTGGGCTGTGTG | 8453 |
rs533693407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065788 | TGCTTAAACTCAGGA[A/G]GCGGAGGTTGCAGTG | 8453 |
rs533708041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057369 | AATGTTTTAAAATAA[A/G]GTCATGGCCAGGCAC | 8453 |
rs533718839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35052439 | ATAAAAAGTTCTGCT[C/T]ATGTACCAAGAGATA | 8453 |
rs533735204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011508 | CTGTATTCCCAACTA[A/C]TCGGGAGGCTGAGGC | 8453 |
rs533754733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045714 | AGAGCAAGACCCTGT[C/T]TCAAAAATTAAAAAA | 8453 |
rs533771692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012153 | CCATCTCCTGGGTTC[A/T]TGTGATTCTCATGCC | 8453 |
rs533816279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081493 | ATCTCAGGTAAATTA[C/G]AGAATTTGAATTTCT | 8453 |
rs533856450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35081995 | ACTTTCTTGACACCT[A/C]CTGTTTACAATCCCA | 8453 |
rs533891348 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025283 | CTACAAAAGCAATGA[A/C]AACCATTCATATTAG | 8453 |
rs533908901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075583 | TCCACTCTTGCAACA[A/G]TGGGGTTTTAGACAC | 8453 |
rs533922111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115137 | GAATCACTTGAACCC[A/G]GGAGGCAGGAGATTC | 8453 |
rs533935513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115578 | AGAAAATATTAACAA[A/G]GGAGATAAATTAATT | 8453 |
rs533948917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061011 | TTGAAAAGCAATAAT[A/C]ATTTTCACTGTCAAC | 8453 |
rs533956088 | in-del | -/GAGAGAAAATAT | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35114764 | TGAGCATGGTGAGGA[-/GAGAGAAAATAT]TTTTAAAGTCCCAAA | 8453 |
rs533958891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017806 | CAGCAGCATGACATC[A/G]GCACACTGAAAGCTC | 8453 |
rs533996040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108673 | TGGGAGTGGCTTAGC[C/T]GAATAGTTCTTTTTC | 8453 |
rs534035181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102966 | CCAATTATTAAAATC[A/G]AAGTTGAACAATGCT | 8453 |
rs534036917 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35089317 | TGTAAGATTCTAAAG[C/G]GTAGGCAACAGTGTT | 8453 |
rs534065678 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124774 | GATATGGGAAAGAAA[G/T]GACATCTAACTTACA | 8453 |
rs534086110 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116412 | AATAGAGAAATTCTC[C/T]GAAAGGCATAAACTA | 8453 |
rs534096312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088048 | CCTCAGAATTTCAAA[C/T]TTCACCTCAGGAAGT | 8453 |
rs534101875 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078056 | ACATTAATATTTTCA[C/T]AAATTTAGGGGAGAA | 8453 |
rs534102867 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35116723 | TGTAATCCCAGCATT[G/T]TGGGAGGCCAATGCA | 8453 |
rs534131533 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121646 | TTCCTCTTTTCCTCA[C/T]GCCTTTCTTCTCCCT | 8453 |
rs534141027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046410 | CAAGCAAACATCTAC[A/G]TATGTGTACAACAGA | 8453 |
rs534144286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066916 | TGAAAAGTGTCAAGG[A/T]TACAGGTACTTGCCT | 8453 |
rs534151552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086517 | GTCTCAAGCTGCTGG[C/G]CTCAAGTGATCCACC | 8453 |
rs534188072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122774 | TCTTAAGTAGCTGGG[A/T]TTACAGGCATGCGCC | 8453 |
rs534210198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080016 | CTACTGAGGACAGTA[C/T]AGAATTTAATTATGA | 8453 |
rs534212501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35087250 | TTTTGTAGACATGGG[G/T]TCTCACCATGTTGCC | 8453 |
rs534256932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018242 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 8453 |
rs534287546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35067747 | AGACCCTGCCACAAA[A/C]AAAAAAAAAAATTCA | 8453 |
rs534321486 | snp | A/G | 3.29663e-05 | 0.00405981 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071231 | TGTTGCTCTTTCGAC[A/G]TATTCCAACATGACC | 8453 |
rs534326203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35068671 | CTCCCCATAAATGCA[C/T]GCTAAAAGTTCAAAT | 8453 |
rs534373820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037794 | GTTATAGTGAACAGA[A/G]ATCGCGCCACTGCAT | 8453 |
rs534374418 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078544 | AACCTCAGGTGATCC[C/T]CCTGCCTCAACCTCC | 8453 |
rs534385765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106037 | GCTATAGAAAAAATG[C/T]GTTCCCCCAAAATTC | 8453 |
rs534387287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35044358 | AAAAAGCATCAATTA[C/T]GATGAAAACTGGAAG | 8453 |
rs534404855 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099030 | TAAGTCTGGAGGGAA[A/G]CTAATTCACAGAAAG | 8453 |
rs534416944 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008239 | GTGATGACTTCAATC[A/T]CCTGACCTAACTTGA | 8453 |
rs534460293 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35023595 | TCTTATACACCACTG[A/G]TTGTTAAAATGAGCC | 8453 |
rs534492484 | snp | A/G | 5.35662e-05 | 0.00517496 | intron-variant | CUL2 | GRCh38.p7 | 10:35054558 | GAAAATAAATGTAAT[A/G]TCAATGGATATTAAG | 8453 |
rs534493593 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067667 | GAGAATCACTTAAAC[C/T]CAGGAGGGGGAGGCT | 8453 |
rs534515519 | in-del | -/AAAAAAAAAAAA | 0.493247 | 0.0577133 | intron-variant | CUL2 | GRCh38.p7 | 10:35044052 | CAAGACCACATCTCC[-/AAAAAAAAAAAA]AAAAAAAAAAAACAC | 8453 |
rs534530773 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080788 | TTTTACAAAAACAAA[G/T]GAGTTGGGGAAAAAA | 8453 |
rs534537831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35083328 | ACACAAACACACATA[C/T]ACATGCAGATAAAAA | 8453 |
rs534539895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35038504 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 8453 |
rs534587750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35077112 | CAAGTGTCTATCAAC[C/T]GATAAATGGTTAAAA | 8453 |
rs534645856 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126779 | GCCCCCTGACCTTCC[C/T]TCTCCCTATCCCTAG | 8453 |
rs534646583 | in-del | -/TTCA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118475 | CATCCATTGAGTTAT[-/TTCA]TTAATATTTGTCAAC | 8453 |
rs534692536 | snp | A/G | | | synonymous-codon, intron-variant | CUL2 | GRCh38.p7 | 10:35049765 | ACATATCCAATGCTA[A/G]CTGCCGGGAAAAACG | 8453 |
rs534710257 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070786 | GCCTTCCTTGGCCAC[A/C]CATTCTAAAAGAGCA | 8453 |
rs534751157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35089877 | ACGTAAATATGTAGA[A/C]GAATACACGCACTCT | 8453 |
rs534826188 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090534 | GGACGGGCCGATCAC[C/G]GGATCCGTAAAACAA | 8453 |
rs534860847 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093127 | CCACACCCCTATGAT[G/T]CCATCCCCAACCCAT | 8453 |
rs534865015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076323 | ATGCTCTAAAGTTGA[C/T]TGTCATGATAGTTGC | 8453 |
rs534868779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35029431 | CCATTTATGAATCAT[A/T]TGTATCAACGTACTG | 8453 |
rs534873527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036520 | TATATCCCACTTAGC[A/G]GTCAGTGCCAGTTTC | 8453 |
rs534921846 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033630 | TAATCCCAGCTACAC[A/G]GGAGGCTGAGGCAGG | 8453 |
rs534928382 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070017 | GGAAAGCATAGGAAA[C/T]TGGATCTTTAAGATA | 8453 |
rs534954307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35118771 | AAAAGCCTCAATGTT[G/T]GTTTGTGCTGCTCCA | 8453 |
rs535001347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070067 | CCATCAATTACTACC[C/T]GTATGACCCTGGGCA | 8453 |
rs535016169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062567 | TATATATTTTTAAAA[C/T]GCTGATTAAGAAGCA | 8453 |
rs535024655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047867 | CTGAAATCATGTCAC[C/T]GCACTCCAGCCTAGT | 8453 |
rs535059793 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35105033 | CGTGCCCAGCCCAAA[C/G]ACTCTTAAAGATATA | 8453 |
rs535092570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051946 | CATGGGTATTTTTTA[A/G]GAAATCCTTCTCTGC | 8453 |
rs535115441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35044438 | AACTCAGAGTTAATG[A/C]TTAAATAGATTAAAT | 8453 |
rs535130749 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095925 | CTAGATACTGTACAA[A/C]AGTTTTAACGTTTGG | 8453 |
rs535150539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093982 | ATTTTTAAAATTAAT[A/C]AGTAATTTAAAAATT | 8453 |
rs535160621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086605 | AACAGCTTTTTAAAC[A/T]ACTCCACACCTGTAG | 8453 |
rs535177835 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35069518 | TGTACTCCAGCCTGG[C/G]TGACAAAGTGAGACC | 8453 |
rs535210386 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077584 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGCATTAC | 8453 |
rs535214204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35027608 | GGTAATTCTTGATAG[C/T]TATATTTAAGATTAA | 8453 |
rs535240686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110289 | AGAAATTTATCCAGG[A/C]ACAGTGGCTCATGCC | 8453 |
rs535250652 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35019973 | TATCTGGTGGTTACC[C/G]CCTTCATCAAGTGAC | 8453 |
rs535265903 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048796 | ATTGGGTATCAAAAA[C/T]TTAAAAATATTCTCT | 8453 |
rs535291016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35114354 | ACAGGTGTGAGGCAC[C/T]GCCCCCAGCTGCATT | 8453 |
rs535291610 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020015 | TCTCTAATAGTGAGA[C/T]AATCTGACATTAGAT | 8453 |
rs535303005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012898 | GAGTTAAAATAATGA[A/G]GAGCAGAAGTCCCCT | 8453 |
rs535355558 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010116 | TTTTAAGAAATGTCA[C/T]AATGACATGAGCTTG | 8453 |
rs535403719 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075450 | TCTATCAGTCTTGTT[C/T]TTCATTCCTGTGCCT | 8453 |
rs535407281 | in-del | -/A | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35014577 | GTGGCTCACGTCTGT[-/A]ATCCCACCACTTTGG | 8453 |
rs535416716 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127592 | TCGGATTTGAGTGCC[A/C]CCAGCGCCTCTGCCC | 8453 |
rs535424549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101609 | ACTGAAGAGTTACAA[A/G]TGGGATGCTAGGTCC | 8453 |
rs535467117 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35037235 | AAATTTCATTTTCTT[A/C]TGAAATGGATATCCA | 8453 |
rs535479878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128403 | TTCCCTTGAAACAAA[A/G]ATCTAGATTGAACAG | 8453 |
rs535596002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073035 | AGCCACGGACTGGGA[A/G]AGGCCCTTCTGTGTT | 8453 |
rs535611370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35121098 | GGGAGCTACTTAACG[C/T]ATTCCCCATAATGTC | 8453 |
rs535636321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106492 | GCCCGGCTAATTTTT[G/T]TTTTTCTTTTTTTTT | 8453 |
rs535653184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107254 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 8453 |
rs535707265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017568 | GCATGATGGCATATG[A/C]CTGTAAACCCAGCTA | 8453 |
rs535720265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099706 | GCTTGAACCTGAGAG[A/G]CAGAGGTTGCAGCCT | 8453 |
rs535750101 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052692 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 8453 |
rs535822202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35042969 | GTAGATGGTGTTAGA[A/G]TTGAACTGGAGGACA | 8453 |
rs535827077 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35043412 | GCTCAGGGGACAGAG[A/C]TAACTAGTAAGAAAA | 8453 |
rs535857752 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35027818 | ATAGTATTTTTGGAA[A/T]CAGAATTTTACAGAC | 8453 |
rs535862789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037704 | AAAAATTAGCCAGGT[G/T]TGGGGGCGGATGCCT | 8453 |
rs535882582 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35085674 | TGAACCCGGGAACCA[A/G]AGACACAGCCAGACT | 8453 |
rs535886661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041873 | ACATTCTTTTCCAAA[C/T]ATAATTTATTCCAAT | 8453 |
rs535893634 | snp | A/C/G | 8.24265e-05 | 0.00641929 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35035205 | GCTGGTTGCTCGAAG[A/C/G]CCCTCATCATGGATG | 8453 |
rs535894907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078578 | AGTGCTGGGATTACA[G/T]GCGTGAGCTACTGCA | 8453 |
rs535935038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079154 | CACAGTAAGAGATTA[A/G]CAAAAACTAGCAGTA | 8453 |
rs535968501 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011489 | CAAGTATGGTGGTGC[A/G]CGCCTGTATTCCCAA | 8453 |
rs536021106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103559 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGTCTC | 8453 |
rs536027717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057477 | CCAACATGGTGAAAC[A/C]CCGTCTCTACTAAAA | 8453 |
rs536031422 | snp | C/T | 0.00018547 | 0.0096281 | intron-variant | CUL2 | GRCh38.p7 | 10:35049779 | AGCTGCCGGGAAAAA[C/T]GAAAATCATCAGGGC | 8453 |
rs536044309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095828 | AGCCTCCCAAAGAGT[A/T]GAGATTACAGGCGTG | 8453 |
rs536133108 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35112555 | AAGACAGAGCTCTAT[A/G]GAGAGAGGTCTAGAG | 8453 |
rs536176163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35085052 | TTAAATGCCAGAGGC[A/G]GAGAATGCAGTCAGC | 8453 |
rs536193342 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35106314 | TTTTTGTTTTTTTTT[G/T]TGTGGGTTTTTTTTT | 8453 |
rs536235231 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35045019 | GAATCTTAACAATGA[-/T]TTTTTTTTATATCAC | 8453 |
rs536269592 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029430 | TCCATTTATGAATCA[C/T]TTGTATCAACGTACT | 8453 |
rs536320214 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35103145 | ACTTGACTCAAAAAA[A/T]TTTTTTTTTGTTTTT | 8453 |
rs536331703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35076472 | CTGCCAAAAATTTTA[C/G]AGCAATTTAACGGGG | 8453 |
rs536402256 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125457 | GTTACAGAGACAATT[A/G]TTGTGGATACATTCC | 8453 |
rs536411571 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086963 | TCCAAGGAGATCTAA[A/G]AAACAGCTAACAATG | 8453 |
rs536416605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046471 | AGGAACCTAATATAC[A/G]CCACTAGGAGAAGAG | 8453 |
rs536424613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053954 | ATACTTCTTTCACAA[C/T]CAGCATAATTTTCCA | 8453 |
rs536460223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047050 | ATCTTGATAAAATTT[C/T]CCAGGTAATAAAGAA | 8453 |
rs536464703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122835 | TAGAGATGGGGTTTT[G/T]CCATATTAGCCAGGC | 8453 |
rs536505985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088840 | CACATTGTAGAAATG[C/T]TCCCCCAACTCATAA | 8453 |
rs536589574 | snp | C/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128773 | CTCGTGATCCGCCCG[C/G]GTCGGCCTCCCAAAG | 8453 |
rs536602699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35068735 | TGTTTTTTCCTTTTC[A/C]AAGTATTTACATTGT | 8453 |
rs536612767 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35052168 | TTGCTAGCCTCCCTA[C/T]TGTTTCCCTAGGGTA | 8453 |
rs536637475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026639 | CTGATTCATCCTTAC[A/G]TTTAAAATCTGACTA | 8453 |
rs536643981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116216 | GGTGTGGTGGCAGGC[G/T]CCTGTAATCCCAGCT | 8453 |
rs536677670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019107 | AAGTAAAACATTACA[C/T]AAATTGCATTTTGTT | 8453 |
rs536721164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35099922 | ACTAGATCTCTGTGG[A/G]CAAGTGAATAAGACT | 8453 |
rs536741511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061199 | ATAAACTGAGCCGAG[C/T]GCAGTGGCTCACGCC | 8453 |
rs536771195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053292 | TTGGTATTTCTCATT[C/G]ATCTTTTTCTCTATA | 8453 |
rs536820408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036649 | CTATTCTGCAGTGCC[C/T]GTTTTTTGAGCATTT | 8453 |
rs536860299 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35033444 | AGAAATTTACAACTT[C/T]GGTGTTGAAGGCTGG | 8453 |
rs536872056 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023522 | TTAGGTGATATTGGT[A/G]ACTATTTTCAAACTA | 8453 |
rs536874013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35030629 | CTCAAACAATCTACA[C/T]GCCTTGGCCTCCCAA | 8453 |
rs536885394 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35077643 | ACCAACATGGAGAAA[A/C]CCGGTCTCTACTAAA | 8453 |
rs536895599 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020965 | TTTTATTTTATGGGT[-/T]TTTTTTTTTTTTTTT | 8453 |
rs536899748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025632 | ATTCAATTAGACACA[A/G]ATACGAAGTTTTAGG | 8453 |
rs536924603 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35071685 | AGTGCTGGGATTACA[C/G]GCATGAACCATCACA | 8453 |
rs536926538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078390 | AACCTTCACATCCCA[C/G]GTGTGAGCAATTCTC | 8453 |
rs536933654 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026089 | TCCAGCCAAGAAAAT[A/G]AGTCAATTCCTTCAG | 8453 |
rs536937142 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046384 | CTCTAAGTATACACA[C/T]CCTATGACCCCAAGC | 8453 |
rs536965816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072407 | AGAGTCTCACTCTGT[G/T]GCCCAGGCTGGAGTG | 8453 |
rs536984825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123775 | TTGGAAATGCTCATG[C/G]GCCATGTAAGTGAGA | 8453 |
rs537013703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048735 | ACTCAAACGGTCAGT[A/G]ACAATTTTTAAAAAT | 8453 |
rs537032674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023123 | TCACCACAAATAAAG[A/G]TAAGTGAGAAGCTAC | 8453 |
rs537047889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015362 | CATTTCTCAAAATTA[C/T]GAAAACATTGATTTG | 8453 |
rs537050724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35049566 | GAAGTAAAATGAGGC[C/T]CATTACAGTAAAACC | 8453 |
rs537111367 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091437 | TATTTCAGTAAAGGG[C/T]TTTTATATACGAAAT | 8453 |
rs537123655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107119 | AGCTGGGACTACATG[C/T]GCCCACCACCGTGCC | 8453 |
rs537129076 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121847 | ATTAGTTTAGTTTAA[C/T]GACTGCAATCTTATA | 8453 |
rs537152570 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009827 | TATATTTTGTGGTCA[A/G]CCTGATACTCCATCC | 8453 |
rs537169139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35050318 | ACAGTGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 8453 |
rs537236178 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126892 | GCGGCCGGCAGGGGG[C/T]GGAGTTCGAGCCTGG | 8453 |
rs537246654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119312 | AAAAGGAGGTAAATA[C/T]TAAACAAAGTTAGAA | 8453 |
rs537262976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127384 | CGCGAGTTCACCTGA[C/T]GCGGCCCCTCGCTCG | 8453 |
rs537274271 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35021279 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 8453 |
rs537313901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35031280 | TTCTAGGACAATACC[A/G]CATTAAAGACTTACA | 8453 |
rs537335568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063292 | GAGAATTATTTGAAG[A/G]CACTGTAAGGAAAAT | 8453 |
rs537337805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054974 | ACAATCAGTAGGTAA[A/G]AAAATGGAACACAGT | 8453 |
rs537365484 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35064698 | AAGCTTTATTTATTT[A/T]TATTTTTACTTGAAA | 8453 |
rs537370354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055486 | GCCTGTAATCCCAGT[C/G]CTTTGGGAGGCTGAG | 8453 |
rs537377139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120203 | ACAGAAAGGCTTAGA[C/T]ACAAATACCAAATTA | 8453 |
rs537429436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098553 | CCAAGAAAAAAAAAA[A/T]GTGTGTTACCAAGAG | 8453 |
rs537491448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098870 | ACCTAGGAGGCAGAG[G/T]TTGTAGTGAGTTGAG | 8453 |
rs537500355 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090637 | CCCCGCCACCCGGAA[A/G]GCAATGGTACAGGCC | 8453 |
rs537512744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35083535 | AAGTGATTGATTCCA[A/G]GGCTGAAGCAGGAAA | 8453 |
rs537530782 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080962 | CTCACACCTGTAATC[C/T]TAGTACTTTGGGAGG | 8453 |
rs537541379 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036582 | TTCAGTGTTCAACAA[C/G]TTCCTGCTACTTCAC | 8453 |
rs537595146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070995 | TAGTCCTTGACAGAT[A/G]CTAAGTACTCAACAA | 8453 |
rs537606439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062645 | GAGACCAGCCTAGGC[A/G]ATATAGTGAGACCCC | 8453 |
rs537621849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107839 | GTGAGCCTAGATCGC[A/G]CCACTGCACTCCAGC | 8453 |
rs537647227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35111317 | AGTGCAGTGGTACAA[C/T]TGTGGCTCACTGCAG | 8453 |
rs537649996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35017672 | CACTCAAACCTGGGC[A/G]ACAGAATGAGTATCT | 8453 |
rs537651852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104649 | ACTCAATAAATTAAT[A/G]GCAAATTAATTAAAT | 8453 |
rs537679712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013853 | CAAAATCTTTAAATA[A/C]GAGTTTGCTGCAAGC | 8453 |
rs537686758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018148 | AAAAACTAGCAGGGC[A/G]CAGTGGCGGACACCT | 8453 |
rs537713720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35105373 | GGAGCTTGCAGTGAG[C/T]CGAGATGGCGCCACT | 8453 |
rs537828467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032306 | ATGCCAAACTATATA[C/T]AATGTAGATAATTTT | 8453 |
rs537909817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024735 | CACTGCAGTATCACA[A/G]GTAAAAATCAAATGG | 8453 |
rs537943514 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053698 | AAGAAAGACACTGAT[C/G]AATTTCTTTCGGAAA | 8453 |
rs537949315 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056122 | TTTCTTTTTTTGTGC[A/G]TTCATCTTCTCTCTA | 8453 |
rs538007700 | in-del | -/AC/C | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35025214 | TGTAAAAAAAAAAAA[-/AC/C]AAAACACACATTATT | 8453 |
rs538012622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35081959 | AGTTATGGCAGATGC[A/G]TATCAATTAACCCTC | 8453 |
rs538023587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35115433 | GGCATGCTGGCAGGC[A/G]CCTGTAATCCCAGCT | 8453 |
rs538035404 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092580 | AAAGCACTTGTGTGG[C/T]TGACTTACAGGCTGA | 8453 |
rs538078065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101708 | TCCAAACTAATCTTT[G/T]GTATCATTCAATTCT | 8453 |
rs538083587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35108479 | AAAAGGAAAAAAAGA[A/G]AAAAAACACAGTTAT | 8453 |
rs538090159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102193 | TACAGTGAGCTGAGA[C/T]TGTGCCACTCCAGCC | 8453 |
rs538099346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093135 | CTATGATTCCATCCC[C/T]AACCCATCAGCAGAA | 8453 |
rs538116305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011471 | AAAAATACAAAAATT[A/G]GCCAAGTATGGTGGT | 8453 |
rs538138923 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043963 | GTCCCAGCTACTTCG[C/T]AGGCTGAGACAGGAG | 8453 |
rs538151559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094617 | CTTCACTCTCATCAT[A/G]TTCCTCTTAACTCTG | 8453 |
rs538175611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128662 | TCCTGAGTAGCTGGG[A/T]CTACAGGCGCCCGCC | 8453 |
rs538196785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037732 | CCTGTAGTCCCAGCT[A/C]CTCAGGAGGCTGAGG | 8453 |
rs538196872 | snp | C/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126436 | TAGAAGTCAGAAGAA[C/G]CACGCCTGCAGTCCC | 8453 |
rs538214730 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35038065 | GGCTGAGGCAGAATT[C/G]CTTGAACCTGGGAGG | 8453 |
rs538219193 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35076970 | GGCAGGAGAATGGCG[C/T]GAACCCAGGAGGCGG | 8453 |
rs538234770 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35117754 | GACCATTCCATGAAA[A/G]TTGTAGGCATGAAAG | 8453 |
rs538277950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35029362 | ACGCCCAGCCCAAAT[C/T]AATAGGACTTTAGAA | 8453 |
rs538278430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079913 | AGACAGCTACTAAGT[A/G]ACTAATGGCAGGAGG | 8453 |
rs538310135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111959 | GTCCAGAGATTGGGA[A/G]TGTGGTAGAAGAGGA | 8453 |
rs538314733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35021350 | CAATCTCCGCCACCC[A/G]GGTTCATGCCATTCT | 8453 |
rs538319949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35073531 | ACAAACTCGTTTAAT[C/T]CTCCCAACATTCTGA | 8453 |
rs538354897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066789 | GTTGCTGATGCACCA[A/C]ATACACCTGACTATA | 8453 |
rs538395664 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109707 | GTTAGGTGTGTTTGT[A/G]AAATAAAATGAAAGC | 8453 |
rs538420540 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35022113 | ACATGAGTTTTTTTT[A/G]AGGGCCAAGGCTCTG | 8453 |
rs538423849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047815 | GAGGCTGAGGCAGGA[A/G]AATTGCTTGAACCCA | 8453 |
rs538517550 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078026 | AAAGGAATTTAAAAA[C/T]CCTACTCCTCATAAA | 8453 |
rs538554052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086498 | CGCCATGTTGCCCAA[C/G]CTGGTCTCAAGCTGC | 8453 |
rs538598218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070546 | ACTGTCATGGAGGAA[C/T]ACAGGAAACTAGGCT | 8453 |
rs538612714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35028730 | ACCCTTAAGACTCTG[A/G]AAAAATATTAAAGGT | 8453 |
rs538700609 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35096531 | AATGGGAGGATCACT[C/T]GAGTCCAGGAGGTCA | 8453 |
rs538735953 | snp | C/T | 1.65124e-05 | 0.00287331 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071279 | CAAAAGTTTGTTCCA[C/T]GTTTCATCAAAATCT | 8453 |
rs538744026 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116768 | TCAAGAGATTGAGAC[C/T]ATCCTGGTGAAAACC | 8453 |
rs538760576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35097215 | TTGCTCACTGCCACC[A/C]CCTTGATTTAAGAAA | 8453 |
rs538786723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054629 | GAATATTTTTAAGAT[G/T]ACATATAAGCCATGG | 8453 |
rs538911580 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35082677 | ATTTTTAAATGGATG[C/T]ATTCTAATCAAAATA | 8453 |
rs538923147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35068816 | ATATTCTTGGGCAAA[A/G]TAACAGGGAAAATGA | 8453 |
rs538924402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35027471 | TCTAATATTATTCAG[A/G]TTTTTGGCCTAGGTA | 8453 |
rs538929690 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067284 | ATTTTGGACTTACTA[C/T]AACCTTTAGATGCCA | 8453 |
rs538948676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35076576 | CACCACTCCCGTGTA[C/T]GACCTCATTGCCACC | 8453 |
rs538971543 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030073 | GTGCACTACAACTTC[A/G]AACACCTGGGCTCAA | 8453 |
rs538975349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061997 | TTTATTCCCATTTTA[C/T]AGATAAAGTCAAAAC | 8453 |
rs538979554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061212 | AGCGCAGTGGCTCAC[A/G]CCTGTAATTCCAGCA | 8453 |
rs538999744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35110199 | AAATAGCCATACTGC[C/T]ATAGGAACAAGGAGG | 8453 |
rs539019685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058090 | GAAACAGCGAGACTC[A/G]GTCCCAAAAATTAGT | 8453 |
rs539069885 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35050978 | TGACAACAAGTGGTA[A/C]TGCCAGGCTTTAGTC | 8453 |
rs539072341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012741 | TTTGTCTCCCCCCAT[C/T]GGGAATTAAGTTTCT | 8453 |
rs539142187 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042864 | GTCGGTCAGTAGTCC[A/G]GAGGCCCAGACTTGT | 8453 |
rs539162767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35085975 | TACCCGGGTAACAAA[C/G]CTACGTGTGTACCTC | 8453 |
rs539163848 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35124374 | ATTGCTTAAGCCCAG[C/G]AGTTCCAGACTAGCC | 8453 |
rs539164236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047266 | ATTCTCTATGATAGT[C/T]CCTCAATTCTGTGAG | 8453 |
rs539164503 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35093977 | TTATTATTTTTAAAA[G/T]TAATCAGTAATTTAA | 8453 |
rs539203771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043570 | AAACTACTCGACCTT[C/T]CTTGGCTACATAAAC | 8453 |
rs539218371 | snp | A/C/T | 0.00398635 | 0.0444788 | intron-variant | CUL2 | GRCh38.p7 | 10:35072525 | AGGCGCCCGCCACCA[A/C/T]GCCCGGCTCATTTTT | 8453 |
rs539227786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123925 | TGTTTGAGGACAGTA[A/T]AGAAGATGATGTCCA | 8453 |
rs539241804 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35116420 | AATTCTCTGAAAGGC[A/G]TAAACTACAAAACTT | 8453 |
rs539244307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026725 | CAATTCATATGGCAC[C/T]ACAAAGACCAAAGTT | 8453 |
rs539310548 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033506 | TTCTGGGAGGCTGAG[G/T]CGGGCGGATCATGAG | 8453 |
rs539327121 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35087297 | ATTTTGAGCCATGTG[A/C]ATACAGTTTTTGTTC | 8453 |
rs539346088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065544 | GAATGGCGTGAACCC[A/G]AGAGATGGAGGTTGC | 8453 |
rs539384740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057689 | AGAAAATAAAGTCAC[A/T]ATTTAAAATATAAAC | 8453 |
rs539389641 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CUL2 | GRCh38.p7 | 10:35061573 | ACCAAAGCTCACTAG[C/T]TTACAATAGCAGAAC | 8453 |
rs539401598 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125512 | GAACAAAGGTTCAGA[C/T]TGGATTTAGATTAAG | 8453 |
rs539435129 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009114 | AGGAGGGGTGTGGTG[C/G]TGGTGGTGATGGTGT | 8453 |
rs539437051 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35016947 | AAAAAAAAAAACAAA[A/C]AAAAAAGTCTTTAAA | 8453 |
rs539452189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35042863 | AGTCGGTCAGTAGTC[C/T]GGAGGCCCAGACTTG | 8453 |
rs539452517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036713 | TACATTACCCTATAA[C/T]TGTCTTCTGATGATC | 8453 |
rs539471359 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010055 | AGCATGGTACCCAAC[C/T]GAATTTCCACTTTTC | 8453 |
rs539572834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078470 | CGGTGTAATTTTGTA[A/T]TTTTTTTTTTAGTAG | 8453 |
rs539575006 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127505 | GAGTTGGAAAATCCT[C/T]CCTGAGAGAGCCGTG | 8453 |
rs539587524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037195 | AGTGAATTGATTTTG[C/T]ATATGGTATCTTGAG | 8453 |
rs539636871 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35032031 | TACAAATTTTTAAAA[A/G]AACACCTAGGTGAGT | 8453 |
rs539640910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014430 | TTAAGAAAGCCACTG[A/G]TATCATAGAGTGGAA | 8453 |
rs539643786 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35121020 | TATCCCTTTCTAAGT[A/T]CATTTTTCCATGATT | 8453 |
rs539645784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35113636 | AATTCATAATCAGGA[A/G]AAAAATAGAAAAATC | 8453 |
rs539678158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023843 | AATAGAACATATTGA[C/T]TGACTGGTTGAGACA | 8453 |
rs539682554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35105807 | CCATGAACCTGGCTC[C/T]TGAAAGAGGCAATGT | 8453 |
rs539687766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35106606 | CAAAGTGCTGGGATT[A/G]CAGGTGTGAGCCACC | 8453 |
rs539833331 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126950 | AGGCCGTCCCGGCGT[C/G]GGGGAGGGGAGGACG | 8453 |
rs539868938 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092359 | TGCCACCAACCTGTC[C/T]GGGTGGTCATTGGAT | 8453 |
rs539868948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084259 | TACAGCTTGGGTGAC[C/G]AGTGAAACTCTGTCT | 8453 |
rs539903186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026905 | TAGTTACATATGCAT[A/T]CATGTGCCATGCTGG | 8453 |
rs539929253 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35085006 | GCGCCTGTAATCCCA[C/G]TTACTTGGGAAGCTG | 8453 |
rs539945165 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039514 | GGTTTCTCTTCTTGT[A/T]AATGGAACTGTATGT | 8453 |
rs539970812 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35068921 | TGCCCAGGCTGTAGT[G/T]CAATGGCCCGATCTT | 8453 |
rs539991453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064163 | ACCCAAATAAATTCA[C/T]ATATGTTAAAGTACT | 8453 |
rs540003491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35105400 | CACTGCACTCCAGCC[C/T]GGGCGACAGGGAGAG | 8453 |
rs540064062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35098655 | AAATAAGCAGGCGGG[A/G]CACAGTGGCTCATGC | 8453 |
rs540150616 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091633 | TGGTCCTTTTTTTTT[C/T]TGGATACAGAGTCTT | 8453 |
rs540187418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123153 | CAAACAAGCAAAACA[C/T]AACAAAAAACAAAAC | 8453 |
rs540209887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122521 | TAATAATTATAGTTT[A/C]CATTTATTTAATGCT | 8453 |
rs540235027 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35107869 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA | 8453 |
rs540240217 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35025986 | CTTTACCTTTTGTAC[C/T]TTAAAAAGGAAGTTC | 8453 |
rs540276966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018688 | GAATGGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 8453 |
rs540288065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35010844 | ATATCATTTCAATAG[C/T]GTATTTCTTCCCCCA | 8453 |
rs540307789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35068177 | TGTAATCTCAGCACT[G/T]CAGGAGTGCCAAGGC | 8453 |
rs540370644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051171 | ATACAAAAAATTAGC[A/G]GGGCGTGGTGGCGGG | 8453 |
rs540372788 | snp | C/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009560 | ACCAAGCATCCTGCT[C/T]ACACTCTGCGATGTC | 8453 |
rs540401482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094256 | TTTTTTTTTTTTGAG[A/G]TGGAGTTTCGCTCTT | 8453 |
rs540408377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043850 | GGCAGGAGGACTGCT[C/G]AAGTTGAGGAGTTCT | 8453 |
rs540448449 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35113894 | TTTTTTGTTATTTTT[A/T]AAATTATTATTATTA | 8453 |
rs540470911 | in-del | -/TTG | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35106302 | AAATAAATGTGTTTT[-/TTG]TTTTTTTTTTTGTGG | 8453 |
rs540476554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086909 | ACTGTTTCTGCAAAG[A/T]GGGAACAATATTTGC | 8453 |
rs540481055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016647 | AAACAGTCTTTAAGG[C/G]CAGGCGCAGCGGCTC | 8453 |
rs540488505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35087460 | GCTTGAGAAGCCCTC[A/G]TTGGATGGCTGAATC | 8453 |
rs540506016 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088193 | CCATCCCAAGCCAGA[A/T]GTGACACTCCAAGAG | 8453 |
rs540516860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072686 | AATGGGCTTTTAAGG[C/G]AGTTCAAAGACTCCT | 8453 |
rs540525151 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105132 | ATTTAGGTTTTAAAA[-/AA]CTAAGTAATTGGCTG | 8453 |
rs540558889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114486 | CTCCCAGGTTCCAGC[A/G]ATTCTCCTGCCTCAG | 8453 |
rs540632775 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35105489 | CACGCCAGTAATCCC[A/G/T]CACTTTGGGAGGGAG | 8453 |
rs540641320 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126279 | TCCAGTCAAATACTG[A/G]GATAAACTGCAATAA | 8453 |
rs540662982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35014073 | TACTATTCTATATAC[A/G]CTACTTTTTGATAAA | 8453 |
rs540689020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101867 | GTTTCTAATTAGAGG[A/G]AGTAGAACTAACAGA | 8453 |
rs540753293 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35051540 | ATGGCGTGAACCGGC[A/C]GGGCGGAGCCTGCAG | 8453 |
rs540776505 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066547 | TCAGGTGATCCACCC[A/G]CCTCAACCTCCCAAG | 8453 |
rs540782159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128780 | TCCGCCCGCGTCGGC[C/T]TCCCAAAGTGCTGGG | 8453 |
rs540803140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35049050 | AATTTACTGGATATA[C/T]ATTTGTGTGACTGAC | 8453 |
rs540829485 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125759 | AAAGCCATGATTTCT[A/G]AGAACCTATCGTTAA | 8453 |
rs540845214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121231 | GATAGGCTTTATTTA[C/T]TTATTTTTTTGGGAT | 8453 |
rs540852453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110906 | AGGTTGAGACTTAGA[G/T]AAGTGAATTTGGGAG | 8453 |
rs540868099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079335 | CATCGGAAGGTCGGC[A/T]TTGGGCTACTTACTA | 8453 |
rs540877987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024078 | GGGATTAAGTGACCC[A/C]CCTGTCTCAGCCTCC | 8453 |
rs540892778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117862 | CTCTTATGCTTTAAA[A/C]AACTGTCTTTGTTTT | 8453 |
rs540904786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073226 | ATTCCCGAACTATCT[A/G]TAACGGATTAGCAGC | 8453 |
rs540913404 | snp | A/C/T | 0.00438476 | 0.0466401 | intron-variant | CUL2 | GRCh38.p7 | 10:35076597 | CATTGCCACCTCCCA[A/C/T]TGAATGAGGCAATAA | 8453 |
rs540923408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020805 | ATTCTATCCAAAGCC[C/T]TAGTCATAAATCCAG | 8453 |
rs540930860 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017843 | AATAATATGGCAAAC[A/G]TGTCTACACTCTGTA | 8453 |
rs540947281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066326 | TTTTTTTTTTGAGAC[A/G]GAGTTTCGCTCTTTT | 8453 |
rs540950396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35070593 | AAATCACCAATCTGC[A/G]TTGTTACATAAAACT | 8453 |
rs540964775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111653 | AACACTTTGGGATGC[C/T]GAGACGGGTGGATCA | 8453 |
rs540974040 | snp | C/T | 3.50324e-05 | 0.00418509 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010288 | GCAATGATCTTCTCA[C/T]ACCACGCTGGAGGAG | 8453 |
rs540985859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063472 | AATATGACAAGAGGC[A/G]GACATGTCTAAGCAA | 8453 |
rs540987830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055270 | TTCTGCTAGTGTAAA[C/T]AGCTACTGACAATAC | 8453 |
rs541029203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35097878 | ACATGAGAATCACTT[A/G]AGCCCAGGAGGCAGA | 8453 |
rs541040208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047377 | GCACTTTGGAAGGCC[A/G]AGGCGGGTGGATCAC | 8453 |
rs541051941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014496 | ATGAAATAATTCTCA[A/G]TAATAATCTAAGACA | 8453 |
rs541071202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35089130 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 8453 |
rs541076990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35040366 | AAACAACAACATATA[C/T]ACAGACAAATGCACC | 8453 |
rs541090905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35090353 | CGAGGCCGCCTCCCC[A/G]GCCGGCCGCCGCCAC | 8453 |
rs541125129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055745 | AAGATCATACTCTTT[A/T]TTTTCCCCTTTAAAA | 8453 |
rs541134453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082804 | TCAGGACTACTTGGG[G/T]ATCTTTCTCTTGATG | 8453 |
rs541134454 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063750 | CGGGTGGCATTTCCT[-/T]TTTTTTTTTTTTTTT | 8453 |
rs541176764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35117361 | CCCACCTCAGCTCTC[A/G]AGTATTGGGACTATA | 8453 |
rs541185493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061400 | GAATCACTTGAACCC[A/G]ATCGCACCGAGACCC | 8453 |
rs541198051 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040843 | CCTTGCATGCAGAGT[C/T]CACAATGGAGTTTGC | 8453 |
rs541202446 | snp | A/G | 3.295e-05 | 0.00405881 | missense | CUL2 | GRCh38.p7 | 10:35035270 | CAGTGGACACAGCAC[A/G]GAGTAAGACGTACAT | 8453 |
rs541206462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35028310 | ACCTGACTGGTTACA[A/G]GACTCTCCTCTATTA | 8453 |
rs541235026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020197 | AAATCACAAATAAGT[A/G]ATCCAAAGTACTGGA | 8453 |
rs541262765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069788 | TGTAGTCATCTATAA[A/C]CAACTCCTCTTCCCT | 8453 |
rs541325178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35053509 | ATTGCTGAATGTTGG[A/G]TGCTGAAATTTTACA | 8453 |
rs541333850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35103717 | TGCCCACCTCAGCCT[C/T]CTAAAGTGCTGGGAT | 8453 |
rs541344601 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037351 | ATGCTTGGGTTGTTT[C/G]TAGGATCTCTTATTT | 8453 |
rs541358902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062878 | CAAGCTGACCTTGAT[A/G]AAAGTTCTACACTGG | 8453 |
rs541388643 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35039826 | CACCACTGCACTCCA[G/T]CCTGTGTGACAGAGT | 8453 |
rs541388789 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058430 | ATTCTTTGCTAGCCT[C/T]GAAACCATTAAAATG | 8453 |
rs541490328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079433 | GTCTCTGGGGATCCC[C/T]TGCTGAGTCTTCAAA | 8453 |
rs541542240 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087528 | ACCTACTTCTCACCT[A/C]CACTTGAACAACGAA | 8453 |
rs541578128 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35057737 | TAATATGGACACCAT[A/T]CTTATTTTATAAGTC | 8453 |
rs541605882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121412 | TTGTATTTTTAGTAG[A/C]GATGGGGTTTCGCCA | 8453 |
rs541618047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35108364 | TGGGAGGCTAAGGTG[A/G]GAGGATCACCTGAGC | 8453 |
rs541621836 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35103299 | GGCGCCCGCCACCAG[A/G]CCAAGCTAATTTTTT | 8453 |
rs541629169 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35067745 | TGAGACCCTGCCACA[A/C]AAAAAAAAAAAAATT | 8453 |
rs541636598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011767 | GTTATTTCTGTATCC[C/T]CTTTAAGAAGAAAGA | 8453 |
rs541640284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109442 | CTTACATTCCAGTGA[A/G]CAGAGACAGATAAAA | 8453 |
rs541648702 | in-del | -/A | 0.378174 | 0.214642 | intron-variant | CUL2 | GRCh38.p7 | 10:35045545 | AGCAAGACCCCATAC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs541712031 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35050521 | AAAAGAGTAATAAAA[A/C]ATTCCTGTATTCACT | 8453 |
rs541731949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35092886 | TTGCTAAAGTGTAGG[C/T]ATATTTCTATTAATA | 8453 |
rs541747366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046699 | GAGTTAGAGAGCAGC[C/G]TGGCCAACATGGTGA | 8453 |
rs541785151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043214 | GCCACCACTTGCCAG[G/T]GGCATATTTTTGACA | 8453 |
rs541789858 | in-del | -/T | 0.0705314 | 0.174043 | intron-variant | CUL2 | GRCh38.p7 | 10:35036465 | GCTGGGGGGTGGTTA[-/T]TATGTTTAGGAGAAC | 8453 |
rs541792305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093348 | ACCCATCTGGCCATT[A/T]CAATGGAAGGCCATT | 8453 |
rs541806357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030771 | AGTGGTGCACACCTA[C/T]TGTCCCAGCTGCTCA | 8453 |
rs541815591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119814 | GCTTCAAGCAGTCAT[C/T]CCACTTCGGCCTCCT | 8453 |
rs541855743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086091 | ATACAAAAATTAGCT[C/G]AGAGTGGTGGAGGGC | 8453 |
rs541873227 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35022646 | GAACAAAAATAAAAT[A/G]AAAAATGTTGATCAA | 8453 |
rs541873662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35023314 | GTTTTCAGTACCTTC[A/G]GTGACTCAAAACAAA | 8453 |
rs541929651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128833 | CCCGGCCTTTTTTTC[C/T]TAGTCTTGATTCTTT | 8453 |
rs541936493 | snp | G/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35065041 | ACCTTAATAAAATTT[G/T]AAAGTTTATGTTTTA | 8453 |
rs541996866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016068 | GGAGCGTACAGTAAC[A/G]TAGTGAATACAAGTG | 8453 |
rs542044472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106788 | AAGCAGAGTGGTTAT[A/G]ATCTGAAAAAGGATT | 8453 |
rs542053657 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35117115 | TTGAGTTCCCAGGAC[-/A]AAAAAACTGGTCCAA | 8453 |
rs542056652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35100406 | TAGAAAAGATTGGAG[C/G]CATGGCCCCTATTGC | 8453 |
rs542077197 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35018930 | TGGGAATACCAAGAG[-/A]AAAAATTCATAGCCC | 8453 |
rs542163181 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126974 | GAGGACGGGGCGGGA[A/G]GACGCGGTTCGGTCG | 8453 |
rs542228640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120600 | CTGAAAGGAAATTGC[C/G]TAAAGAATGTGCTGA | 8453 |
rs542240213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019343 | ATCATTTACTTCTTA[C/T]TGAGTTCATTCTTTC | 8453 |
rs542264294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35113224 | TCAGCGGCCAGGTGC[A/G]GTGGCTCACTTCTGT | 8453 |
rs542280179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35117075 | CTTCCTTCAAATTAC[A/G]GAGTATTTTTGAATT | 8453 |
rs542289909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072530 | CCCGCCACCATGCCC[A/G]GCTCATTTTTTGTAT | 8453 |
rs542337709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069632 | TAACAGTGACTGAAG[A/G]GGTCACTTTCCAGGG | 8453 |
rs542392735 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35110653 | TGGTAGGGTTGGTTT[A/C]CTCTGAGGGCCTAAG | 8453 |
rs542395221 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103649 | ATTTTTAATAGAGAC[A/G]AGGTTTAAGTATGTA | 8453 |
rs542411188 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104858 | CCTCAGCCTCCTGAG[C/T]AGCTGGGATTACAGG | 8453 |
rs542453590 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091963 | TTTGTTTTTGTTTTT[G/T]ACACAGGGTCTCCCT | 8453 |
rs542456832 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100185 | CCTAAAAAAAGGTTA[A/G]CAACATCTTGCTTCC | 8453 |
rs542487321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35083924 | AAAAGCAACCTACAA[C/T]AGAGAAAGACTAAGT | 8453 |
rs542499320 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35084431 | GATCCAACACCACAA[C/T]CTTAACCTAACACTA | 8453 |
rs542505018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088211 | GACACTCCAAGAGGA[C/T]AGAAATTTAATGGGT | 8453 |
rs542507715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35077338 | AAACAAACAAAAAAA[A/C]CAAACAAAAATTAGC | 8453 |
rs542542461 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027651 | GCAAATCATCACTAA[A/G]GCAGGATGGATTAAT | 8453 |
rs542555841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119013 | ACACACCACACTTCC[A/G]AATGTCTTGGCTGGT | 8453 |
rs542563267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026232 | TGAACAGGAGATGAC[C/T]AGCACCTGGAATACT | 8453 |
rs542563541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35113788 | CTCAGCTTGCTGCAA[C/T]CTCTCCCTCCCAGGT | 8453 |
rs542595590 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058765 | ATGTTTTAAGGAAAA[C/T]GTATAAACACTAACC | 8453 |
rs542625082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102374 | GCCAGGAGTTCAAGA[C/T]CAGCCTGGCCAACAT | 8453 |
rs542625401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110796 | TAATTACACCAGTCA[C/T]ATGGGATTAAGGTCC | 8453 |
rs542658692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012531 | AAGCAGAGAAGCCAG[A/G]AGAGGGGGCCTATCT | 8453 |
rs542667360 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35094299 | GGAGTGCAATGGTGC[A/G]ATCTTGGCTCACTGC | 8453 |
rs542682959 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35061483 | AAAAAAAAAAATCAC[A/C]CTTATAATGTAACCT | 8453 |
rs542773878 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118814 | ACTTGGGAAAAAGGT[A/G]TATCTCATGTCAAAG | 8453 |
rs542779920 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35103426 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 8453 |
rs542812447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114508 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 8453 |
rs542865504 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35017399 | GAATGTTTTCATAAA[A/T]ATGTTCTATATGTGC | 8453 |
rs542870126 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081159 | AGCAAAGGAGACTTC[A/G]AGGTTACATTAAGCT | 8453 |
rs542960966 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077085 | TTATTCATAAAGGCC[C/T]TTGAAATAGCTCAAG | 8453 |
rs542997857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35010936 | GACCAGCCCAGCTGT[C/G]TATCACATGGTAGGC | 8453 |
rs542998104 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35011520 | CTACTCGGGAGGCTG[A/C]GGCAGGAGACTCACT | 8453 |
rs543026714 | in-del | -/GCCAGGAGTTCAAGACCA | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35096392 | GAAGGGTTACTTGAG[-/GCCAGGAGTTCAAGACCA]GCCTGGGCAACAGAG | 8453 |
rs543033783 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097252 | TAAATACTGAACTTC[C/T]TGCGAACCTCTTTGG | 8453 |
rs543052641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099158 | AGCACTTTGGGAGGC[C/T]GAGGAGGGCAGATCA | 8453 |
rs543079718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094963 | TAATGCTACATTTTA[A/C]AAAACTGTGTTTTGG | 8453 |
rs543102271 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092015 | AGGAGTGCAGTGGCC[C/T]GATCATAGCTCACTG | 8453 |
rs543121315 | in-del | -/CAAAACAAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046922 | CAAAACAAAACAAAA[-/CAAAACAAAA]ACAAAAAACTGGGTT | 8453 |
rs543133421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045126 | AGTTCAAGATACTAT[C/G]TCAGTAATAAGATAA | 8453 |
rs543171511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045946 | TTATCATCATTCCCT[A/T]GTAAGAGCTTGTTGC | 8453 |
rs543227477 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35115248 | GTCTAAAAAATAAAA[C/T]AAAAATAAAATGGAG | 8453 |
rs543228969 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35032932 | CTATCCAGAACATAT[A/C]AGATTAAAAATTCCC | 8453 |
rs543252845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35071435 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 8453 |
rs543255956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35112355 | CAGTGCAGGACTGTG[A/G]TCCCCGAGCAAAGGG | 8453 |
rs543257213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35025018 | TTTAATGGGGAAAGG[C/T]TGATGGAGGAGAAAA | 8453 |
rs543278791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35105539 | TGGAAACCCGTCTCT[A/G]CTAAAAAAATACAAA | 8453 |
rs543312913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014619 | GGGCAGATTACTTGA[A/G]CTCAGGAGTTTGAGA | 8453 |
rs543354815 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022950 | CTCAGAAGGCTGAGG[A/C]AGGAGAATCACTTGA | 8453 |
rs543355661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35056898 | TCAGTCAGTCTTCCT[G/T]TCTTCCTAAAGTATG | 8453 |
rs543359736 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095195 | TGGGCATAGTGCTGC[A/G]TGCCTGAAATCCCAG | 8453 |
rs543370266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055931 | CAGATATTCTGAGGG[C/T]AGTCAGTCCCCTTTC | 8453 |
rs543370621 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070125 | TTCCTTATCCGTTAC[A/C]GTCAAGTAATTATTT | 8453 |
rs543397793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35049193 | AGTGTTAACCACTCT[C/G]AGCCATGGGTAGAGT | 8453 |
rs543428552 | in-del | -/CAAAA | 0.0984455 | 0.198825 | intron-variant | CUL2 | GRCh38.p7 | 10:35046892 | AGTGAGACTCTGTCT[-/CAAAA]CAAAACAAAACAAAA | 8453 |
rs543483693 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037758 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 8453 |
rs543511601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070656 | AACACACTTCCACCC[C/G]AGTCACTGAACTTGC | 8453 |
rs543512068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35077265 | AGCCACTGCACTCCA[C/G]TCTGGGCAACAGAGC | 8453 |
rs543521828 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061185 | ATCCATAATAGAGAA[C/T]AAACTGAGCCGAGCG | 8453 |
rs543527987 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022295 | GAGCTAATAACTCCA[A/G]CCACAGGTCTTCTGA | 8453 |
rs543536420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35049997 | GGTTTTATTATTAGT[C/T]GAAAATCTTAAGAAA | 8453 |
rs543556611 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096475 | AATAGCAGCTGGGTA[C/T]GGTGGTGCATGCCTG | 8453 |
rs543572561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042531 | TCTAATCTTGCCCTA[A/C]CTTTCTGACTGTGGG | 8453 |
rs543595975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111696 | AGTTCCAGACCAGCC[A/T]GGCCAACATGGTGAA | 8453 |
rs543624823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014115 | GCTCATTGCCTAGAG[A/T]TTGACATTTTAATTT | 8453 |
rs543629289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35020922 | CAACACTCTCCTTTA[C/T]GTAGCTTGGTTAAGT | 8453 |
rs543640649 | snp | A/G | 3.32381e-05 | 0.00407651 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35063056 | CACACATAAAGCATA[A/G]ATATCTCTAGTTAAA | 8453 |
rs543764237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034934 | TGTGGAAAGTTAACA[A/G]CTGTTCAATGGACAC | 8453 |
rs543788674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082385 | GATGAGATGTTATCA[A/G]ATGCTGGGGGAAGGG | 8453 |
rs543853202 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125856 | TATTTTTGAGATGGA[A/G]CCTCGCTCTGTCACC | 8453 |
rs543925979 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074581 | AACCTCCACCTCCCA[C/T]GTTCAAGTGATTCAC | 8453 |
rs543964227 | in-del | -/TTC | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35121487 | TTATTAGCTAATGTA[-/TTC]TTCTTCACAAACACT | 8453 |
rs543981616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35028956 | AAAGTAAATATTTAT[C/T]AAATAATCTAAGCAT | 8453 |
rs544028125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103832 | TTTCATACTCTGCCT[C/T]TCATTTATTCTTTCT | 8453 |
rs544042241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096628 | TAAACAAACAAATAA[A/T]CAAAACTGTATAGGT | 8453 |
rs544068087 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35089278 | GTATAGCTCATTTGT[C/T]CATGTGTCTGTCTTG | 8453 |
rs544122539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35040492 | GCTGCTGAGTTGGCC[G/T]GGGCACAAGGAGTGA | 8453 |
rs544131508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35044559 | TTCGATATGTTTTAT[G/T]TCTTACCTTTTCCAT | 8453 |
rs544174542 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053070 | GTGTGCCGTTTTATC[A/G]CAGTTTGAAAAATAA | 8453 |
rs544190115 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079508 | CTTGTCTCTGCTCAT[A/G]TCTTCCACCCACCAG | 8453 |
rs544221315 | snp | C/T | 0.000404948 | 0.0142236 | intron-variant | CUL2 | GRCh38.p7 | 10:35016164 | TAATGCTGATGATGC[C/T]TAAATTCTTTGGAAT | 8453 |
rs544225622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114538 | CAGGCGCCCGCCACC[A/C]CACCTGGCTAATTTT | 8453 |
rs544240401 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35122351 | AAAGTTACAACTTCA[A/G]GGTTATAGTCCTAAT | 8453 |
rs544245115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080289 | TATCAAATGAGCAAG[C/G]CACTGGATGTAACTA | 8453 |
rs544258606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017210 | AATTAATGCTATTAT[G/T]TCTCATAAACAACAT | 8453 |
rs544273177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35113826 | ATTCTCCTGCATCAG[A/G]CCCCTGAGAAGCTGG | 8453 |
rs544320782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065734 | TGTGGTGGCACATGC[C/T]TGTAATGCCAGCTAC | 8453 |
rs544343001 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009394 | CAGGTAGGGGAGGCA[C/T]ATAGAAGGAATATGT | 8453 |
rs544349452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051140 | CTAACAGGGTGAAAC[C/T]CCATCTCTACTAAAA | 8453 |
rs544349706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115294 | AGGCCAGGTGCAGTG[G/T]CTCACACCTGTAATC | 8453 |
rs544349996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123119 | CTCCAGCCAGGGTGA[C/G]AGAGTGAGATCCGAT | 8453 |
rs544352520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35083212 | CTTCTATTTCCCACC[A/G]TCAGAAAATAGCAGT | 8453 |
rs544354367 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35127033 | GGCAGGGAGGCCGCG[G/T]CTACCGCATCACAGC | 8453 |
rs544443584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036890 | AGGTGCACACCACCC[C/T]GCCTGGCTAATGCTT | 8453 |
rs544509162 | snp | A/C | 0.00124275 | 0.0248964 | intron-variant | CUL2 | GRCh38.p7 | 10:35086719 | AGCGAACACCATCTC[A/C]AAATAAATAAATAAA | 8453 |
rs544551410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35022812 | AGCACTTTAGGAGGC[C/T]GAGGTGGGTGGATCA | 8453 |
rs544661649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013900 | TGACCAAGCAAAAAA[A/G]CCTCCACTCTCATAA | 8453 |
rs544707424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058462 | AAATCCTCCCATAAC[A/G]CAAGGACAGGTCCAT | 8453 |
rs544733420 | in-del | -/AAAT | 0.00289495 | 0.0379354 | intron-variant | CUL2 | GRCh38.p7 | 10:35086727 | CATCTCAAAATAAAT[-/AAAT]AAATAAATAAATAAA | 8453 |
rs544747032 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104412 | GATCTCGCCATTGCA[C/T]TGTAGCCTGGGAAGA | 8453 |
rs544809749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055153 | AAATAAAATAAAACA[C/T]GGAGAAAGGACTCGT | 8453 |
rs544816787 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35124935 | ACCTAGTTGTCCCTC[A/C]CCAACAGAGAATTAA | 8453 |
rs544821339 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35123872 | TTAGAATTATCTTTC[-/A]AAAAAATTGGGTATG | 8453 |
rs544844757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078027 | AAGGAATTTAAAAAT[C/T]CTACTCCTCATAAAC | 8453 |
rs544852344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078620 | ATTTTTCATATAAAG[A/G]GATTTGTTCCTGTGA | 8453 |
rs544928525 | snp | A/T | 1.66421e-05 | 0.00288458 | intron-variant | CUL2 | GRCh38.p7 | 10:35031671 | GCTTCTGTATATATC[A/T]CGCCTCAAAGGAGGC | 8453 |
rs544945281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019402 | ACTCTACCAGGGATC[A/G]GGGGTACACTGACCT | 8453 |
rs544978079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095183 | ACAAAAATTAGCTGG[G/T]CATAGTGCTGCATGC | 8453 |
rs544981549 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35110793 | TTATAATTACACCAG[A/T]CATATGGGATTAAGG | 8453 |
rs544995574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104025 | TAGCTTTGTGATAAC[C/T]CATTTCTGTCTCCAA | 8453 |
rs545040675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35087670 | CCAGAATTGACCCAT[C/T]CCAACTGCATGCTCA | 8453 |
rs545083921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054280 | CGTTCCTGAGGATTC[C/T]TAGGAAATCACTATA | 8453 |
rs545108209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35059048 | ATCTCATGATATAAC[C/T]TGAATGGATAAGGAG | 8453 |
rs545121716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35047524 | CTGAGGCAGAAGAAT[C/T]GCTTGAACCCAGCAG | 8453 |
rs545171372 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089166 | GGTGACAAGAGCAAA[A/C]CTCCATCTCAAAACA | 8453 |
rs545194000 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061953 | CTGACCACGTGCAGG[A/G]TTAGACAGTTTAAAT | 8453 |
rs545195247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35027193 | TCTATCACCCAGGCT[A/G]AAGTGCAGTGGCGCA | 8453 |
rs545231436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35059509 | GTGCACATTTTTTTA[A/G]ACAATGCTACTGCAC | 8453 |
rs545255899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025774 | ACAGAACAAAAATAC[A/C]GAGTTCTTTTTTCTT | 8453 |
rs545265853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108113 | ACAAGAGGCCAGAAT[A/G]GATGCAGGCTGATCA | 8453 |
rs545316964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034655 | GTTACAGTCATGTGA[C/T]TGGCAAAGTATTCGA | 8453 |
rs545343884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069650 | TCACTTTCCAGGGAA[A/G]TAATCTATTTCAAAA | 8453 |
rs545365718 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071598 | TTTTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 8453 |
rs545374098 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092071 | GAGTGTACCATCTCA[C/G]TTTCCGAAGCAGCTG | 8453 |
rs545436002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084835 | TAAAAACAACTGATA[A/G]TTGGACAGGCCTGGT | 8453 |
rs545493718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081606 | AACATTGAGAACAAA[C/T]TTTTTGGCTGTGTGC | 8453 |
rs545509406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35046618 | GGTTATTGGCCAGGC[A/G]CAGTGGCTCACACTG | 8453 |
rs545511271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039301 | CAGTCTTATAAGCAA[A/G]AACTAAAGTTAAATA | 8453 |
rs545549970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35039791 | TCCCGGGAGGTGGGG[A/G]TTGTAACGAGCCAAG | 8453 |
rs545555941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064797 | ATCCTTCTGCCTCGG[A/C]CTCCCAAAGTGCTAG | 8453 |
rs545580657 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037000 | TCTTAATGGCCTTTT[A/G]ATAATCCAAAGTTTT | 8453 |
rs545611426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115724 | CATAGTGACACCCCC[A/C]TCACTACAAAAAAAT | 8453 |
rs545629140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128007 | TGCGCCACCACGCCT[A/G]CTAATTTTTGTATTT | 8453 |
rs545631712 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015027 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGAA | 8453 |
rs545640249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018487 | AAAGATTTTAGGCCG[A/G]GCGCAGTGGCTCACG | 8453 |
rs545699927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35052677 | GAGGCAGGCGGATCA[C/T]AAGGTCAGGAGATCG | 8453 |
rs545719588 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35077610 | ATTACCTGAGGTCAC[A/G]AGTTCAAGACCAGCC | 8453 |
rs545755101 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35050408 | AGACCGTAACAGAAA[A/C]AAAGGATTTATGTTA | 8453 |
rs545765220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35100101 | ATGAGCTACTGTGCC[C/T]GGTCTTGTACAGTCA | 8453 |
rs545785199 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042583 | AAGCCCCACCCTGTA[C/G/T]GCTGGGGGAAAGACT | 8453 |
rs545792119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043070 | CTGATGATTGTTGCT[A/G]TGGTGTGAGAGTAGA | 8453 |
rs545810964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050048 | TTAATTTAGGCCAGG[C/T]ACAGTGGGTAACGTC | 8453 |
rs545829439 | snp | A/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126580 | GACCTTAGCTTGGGG[A/T]TGGCGGCGTTAGGAA | 8453 |
rs545879050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071480 | CGTGATCTTGGCTCA[C/T]TGCAAGCTCCGCCTC | 8453 |
rs545917868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063887 | TTTGGGGCCAGACAC[A/G]GTATTAGATTATGAT | 8453 |
rs545960810 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35022502 | AACAGAACTCTGAGA[G/T]ATCTGTCCAGCCTCA | 8453 |
rs545964710 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35037422 | TCTTAATTACTATAG[A/G]TTTTACAATAAGTCT | 8453 |
rs545969281 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35105571 | AAATTTGCCGGGTGT[A/G]GTGGCGGGCGCCTGT | 8453 |
rs545970703 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092317 | GGAATACGGACACTA[C/T]TGATGCCTTAGCAGG | 8453 |
rs546003546 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35014710 | TAGTGGCTTACACCT[A/G]TGGTCCCAGCTACTT | 8453 |
rs546009714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35113025 | GATGAAACCCAGTCT[C/T]TACTAAAAATACAAA | 8453 |
rs546051784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048132 | GATGGATGTAAAATT[G/T]TTAGCACAATGCTTG | 8453 |
rs546159464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35029114 | CCAGGCTTCAATGCA[A/G]TGGCACGATCTCCGC | 8453 |
rs546195522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35083728 | CCATAGGCGGGTCAC[A/G]GTGACTCATGCCTGC | 8453 |
rs546293423 | in-del | -/A | 0.329317 | 0.237084 | intron-variant | CUL2 | GRCh38.p7 | 10:35013345 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs546299091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101587 | CTGAGACCAAGATTA[A/G]TTTTGAACTGAAGAG | 8453 |
rs546347748 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35119610 | TATTTATTTATTTAT[A/T]GAGACAGGGTCTCAC | 8453 |
rs546347756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35112392 | GAGGTGACTCCTACA[A/G]TTGAGCCAGCTTACT | 8453 |
rs546351449 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050180 | ACAAAAATGAGCCTG[A/G]TGTGGTGGCATGCGC | 8453 |
rs546361911 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037981 | AACATGGTGACACCC[A/C/T]GTCTCTACTAAAAAT | 8453 |
rs546362819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051425 | GAGACCATCCTGGCT[A/C]ACATAGTGAAATCCC | 8453 |
rs546399183 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35097518 | AAAAAAAAGAACTTA[C/G]AGTGGTGCAATCTGA | 8453 |
rs546448860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082998 | CCCCATCTCTACTAA[A/C]AATACAAAAATTAGT | 8453 |
rs546465873 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021868 | AGGTGAGGTGGGGTG[A/G]GGTGAGGTGGGGTGA | 8453 |
rs546471159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35079001 | TAAAATGAGAAAATA[C/T]TGAAGACCCAATAAA | 8453 |
rs546472439 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090755 | GCTGTCAATGAGGCA[A/G]TTGCGGTTCGCTGAG | 8453 |
rs546481169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35023858 | TTGACTGGTTGAGAC[A/G]GGGTCTTGCTCTGTT | 8453 |
rs546483972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35076807 | GTAAGCCCAACACTT[C/T]GGGAGGCCAAGGTGG | 8453 |
rs546498490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066632 | AATGAGAAAGAATAC[A/G]GATGCAGTATCTACG | 8453 |
rs546501646 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077466 | CATGCCACTGCACTC[C/T]ACTCTGGACAACAGA | 8453 |
rs546507796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073001 | CAAAGGGAGCGGGTA[A/G]GATGGCGGCCGCACC | 8453 |
rs546520668 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099646 | CTGTGTGTGGTGGTG[A/C]ATGCCTATGATCCTA | 8453 |
rs546524618 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126070 | CAGGTGATCTGCCCA[C/T]GTCTGCCTCCCAAAA | 8453 |
rs546527285 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019258 | GGTTTGAAAGCAGAA[A/T]GAGTCTTCTGCCGTC | 8453 |
rs546539288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35052963 | TATCTCTACAGAATA[A/T]TAAGCTTTCACAAAA | 8453 |
rs546565351 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108868 | TCTCCTCATAAATTG[C/T]TAGCTGTCATACAGA | 8453 |
rs546580382 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009486 | AGAATTAATGGATTA[C/T]GCAACCGAAGAAAGA | 8453 |
rs546623884 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116829 | GGGCGTGGTGGCGCA[C/T]GCCTGTAGTCCCAGC | 8453 |
rs546636221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35010600 | TGTGGAAAATGGATA[C/T]AGCAAAATCTAATAA | 8453 |
rs546640454 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072551 | TTTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 8453 |
rs546640525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042889 | ACTTGTGACTGGTGT[C/T]TGGGGGTGTGCAGGG | 8453 |
rs546725416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037672 | ACATAGTGAAACCTC[A/G]TCTCTACTAAAAATA | 8453 |
rs546770013 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074649 | GTGAGCCATCGCACC[-/CT]AATTTTTGTATTGTT | 8453 |
rs546787645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128358 | CAGTTTCCTTTCTAC[C/T]TAATTTGCCGGGCAG | 8453 |
rs546798968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086193 | GACTCTGTCTCAAAA[A/G]AAAAAAAGAAACAAG | 8453 |
rs546845574 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008800 | AATTTAAATATGAAC[C/T]ACATATTAGATGATA | 8453 |
rs546934334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050718 | CCATGATTTATTTTT[C/T]CACTCTACTGCTGAT | 8453 |
rs546966463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114673 | GGCATGAGCCACCGC[A/G]CCTGGCCCGCAGACA | 8453 |
rs547002355 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050231 | GAGGCTGAGGCAGGA[A/G/T]AATTGCTTGAACCTG | 8453 |
rs547012612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099653 | TGGTGGTGCATGCCT[A/G]TGATCCTAGCTACTT | 8453 |
rs547039150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047745 | AACATGGTGAAAACC[A/G]GTCTCTACTAAAAAT | 8453 |
rs547040935 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069162 | GTGAGACAACGTGCC[C/T]GGCCTGTACTCTTTA | 8453 |
rs547070446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043311 | GCTTCAACAAAAGTC[C/T]AAGGTGCAATAAGGG | 8453 |
rs547086246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35089553 | ATTAATCCATGGGGC[A/T]AAGATGTGGACTTAA | 8453 |
rs547090528 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056802 | GTTTTCTTTTCTGGT[C/G]ACTGGCACCAAGACC | 8453 |
rs547093269 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011372 | CCTGTAACCCCAGCA[C/G]TTTTGGAGGCCGAGG | 8453 |
rs547150302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35022878 | GGTGAAACACCGTCT[C/T]TACTAAAAATACAAA | 8453 |
rs547164729 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041652 | AAGTGATCTTCCCAC[A/C]TCAGCGTCCCAAGAG | 8453 |
rs547174266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35040653 | AGGTCGGGCAAGAAG[A/G]GGTCTAGAGCAGCAG | 8453 |
rs547212630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103536 | CACCGTGTCAGCCAG[G/T]ATGGTCTCGATCTCC | 8453 |
rs547252352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019627 | ATAAAACATTCTGAT[A/C]CATGCATACTTAAAG | 8453 |
rs547297756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057466 | GACCAGTCTGGCCAA[A/C]ATGGTGAAACCCCGT | 8453 |
rs547304101 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35107000 | TTTGTTTTGAGGCAG[A/G]GTTTCACTCTGTCAC | 8453 |
rs547320773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35040037 | AGGTGCCTGTAGCAC[C/G]AGCTACTCGGGAGGC | 8453 |
rs547324017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104114 | AGCATACACATGTGC[A/G]CACACACACGATTTC | 8453 |
rs547337568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35057824 | ATGGGCTGGACGCAG[C/T]GGCTCACGCCTGTAA | 8453 |
rs547379230 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081308 | TGAACTTTAGACTCC[A/C]ATAAGACTGCACAGC | 8453 |
rs547463775 | in-del | -/T | 0.0410537 | 0.137264 | intron-variant | CUL2 | GRCh38.p7 | 10:35087282 | GACTAACATCTTAAA[-/T]TTTTGAGCCATGTGA | 8453 |
rs547469386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082481 | GGTGGTTTTGGAAAT[C/G]GTGGTGAGGGTCACA | 8453 |
rs547477139 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125261 | TGTATCTCACCTCCA[A/G]TATTGATCTTTGTAA | 8453 |
rs547490099 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032942 | CATATCAGATTAAAA[A/G]TTCCCCTTATATAGC | 8453 |
rs547505941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041310 | ATAACTTGGGAGAGA[C/G]AGGCGCATATCAAGA | 8453 |
rs547533601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109235 | TGGGAGACAGAGTGA[C/G]ACCCTGTCTCAAAAA | 8453 |
rs547554577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124439 | AAAATTAAATTAAAA[A/G]AAAAAGAGACGGAAG | 8453 |
rs547565343 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029316 | CCTGCTTTGGCCTCT[A/G]AAAGTGCTGGGATTA | 8453 |
rs547578879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069176 | CCGGCCTGTACTCTT[A/T]AATCATTATTTTTGC | 8453 |
rs547620717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116728 | TCCCAGCATTTTGGG[A/G]GGCCAATGCAGGCAG | 8453 |
rs547652674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061627 | ACCACTTTAACACAC[A/T]TGCTATCAAAAGCAC | 8453 |
rs547682707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095414 | TTTGGGTTGATGTAC[A/G]TAACTCACAATTTAT | 8453 |
rs547704805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096415 | TTCAAGACCAGCCTG[A/G]GCAACAGAGCAAAAC | 8453 |
rs547709922 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122675 | TAGAGTCTTGCTCCA[C/T]GGCCCAGGCTGGAGT | 8453 |
rs547729629 | snp | A/T | 1.66632e-05 | 0.0028864 | intron-variant | CUL2 | GRCh38.p7 | 10:35054404 | ATAAAAACATACTTA[A/T]GTTTGCTAGTCACTT | 8453 |
rs547763317 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | CUL2 | GRCh38.p7 | 10:35016817 | TTGTAATCCTAGCCA[A/C]TTGGGAGGCTGAGGC | 8453 |
rs547771186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026573 | ACCTCTTCAGTAGTA[C/T]TATTTGGTAAAGTTT | 8453 |
rs547810439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078819 | CAAAACTCCTGAATG[A/G]CGATTTATTTCAGTA | 8453 |
rs547834389 | snp | A/G | | | synonymous-codon | CUL2 | GRCh38.p7 | 10:35100867 | GTGGCCATCACCGCA[A/G]TCAGGATACAGAAGA | 8453 |
rs547835419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35068675 | CCATAAATGCATGCT[A/G]AAAGTTCAAATAATA | 8453 |
rs547909743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106533 | GAGATGAGGTTTCAC[C/T]GTGTTAGCCAGGATG | 8453 |
rs547910958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019028 | CAAAAAATTATCATT[C/T]GGAGTATACTATTAA | 8453 |
rs547931244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045372 | GGTGGGAGGATCCCT[C/G]AGTGCTGAATTTGTG | 8453 |
rs547934285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050111 | GCACATCACGAGGTC[A/T]GGAGATCAAGACCAT | 8453 |
rs547942065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065312 | TTGGGAAGCCAAGGC[A/G]GGCAGATCACCAGGT | 8453 |
rs547951653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35027325 | AATTTTTTCTATTTT[C/T]AGTAGAGACGGGGTT | 8453 |
rs547974564 | in-del | -/ACAAACTGTTACAGT | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35034617 | TTGGTGATGGGAAAG[-/ACAAACTGTTACAGT]ACAAACTGTTACAGT | 8453 |
rs548010900 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35051280 | AGATCGCGCCACTGC[A/T]CTCCCGCCCAGGTGA | 8453 |
rs548021678 | in-del | -/CAAAA | 0.0851254 | 0.187927 | intron-variant | CUL2 | GRCh38.p7 | 10:35046896 | GACTCTGTCTCAAAA[-/CAAAA]CAAAACAAAACAAAA | 8453 |
rs548022715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35042706 | TATGTGTCTCCTCAA[A/G]TGGTTGTTTATTTGT | 8453 |
rs548080270 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091343 | GCCCATTTAAAACCC[G/T]GCCTCCAGACCTGAT | 8453 |
rs548105132 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107635 | TGCCTGTAATCCCAG[C/T]ACTTAGGGAGGCCGA | 8453 |
rs548108893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038624 | TATTTCCTTTTTATA[A/G]TCTTTGCCTTTATTC | 8453 |
rs548164969 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CUL2 | GRCh38.p7 | 10:35118903 | CAGATCATTTCACAA[G/T]TCCTCTACTCCAGCC | 8453 |
rs548219799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35022982 | CCCAGAAGGTGGAGG[C/T]TGCAGTGAGCCGAGA | 8453 |
rs548235117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072814 | GGAACATTTTTCTGG[A/C]AAATGTTTTAACAGC | 8453 |
rs548251562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048582 | GAGAAATTATATTAG[A/G]ACTTAGAAGTTTTGT | 8453 |
rs548257280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35056157 | GTACAGTATACAAAG[C/G]AAGAACCTCCTCTTG | 8453 |
rs548266650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014364 | CAAGTGGCCTTTGCT[A/C]AGGGGAAAACTGTTT | 8453 |
rs548312590 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35114057 | GGACTACAGGTGCCC[C/G]CCACCACACCTGGCT | 8453 |
rs548349836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035653 | ATGTATTTTACAGCT[G/T]CACAGTACTCCATTA | 8453 |
rs548366093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099417 | AAAAAAAAATTAACT[G/T]GTACCAAGTGGTTCC | 8453 |
rs548374693 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35029247 | ATTTTTAGTAGAGAC[A/G]GGTTTTCACATGTTG | 8453 |
rs548375595 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092104 | ACTACAGGCGCGTGC[A/G]CCACCACACCCAGCT | 8453 |
rs548385484 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35081915 | CTATAGAAGACACAG[C/G]CATGGAAGAATAATT | 8453 |
rs548431191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098837 | TACTTGGGAGGCTGA[C/T]GCAGGAGAATTGCTT | 8453 |
rs548444232 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068219 | ATGAGCCCAGGGGTT[C/T]GAGACCAGCTTGGCC | 8453 |
rs548464188 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126137 | TCTAATCTAAAAAAA[A/C]AAAAAGAGATGAAGT | 8453 |
rs548484996 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126783 | CCTGACCTTCCTTCT[C/T]CCTATCCCTAGGCCC | 8453 |
rs548493066 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072725 | CAAACTGCATTTAGG[A/T]ATTAGCTGGTTTCTG | 8453 |
rs548546529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127239 | CCCAGCAGCGGGCGA[C/G]GCGGCGCAGGAGGTG | 8453 |
rs548556396 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35018710 | GGAGGTTGCTGTGAG[A/C]CGAGATCGCGCCATT | 8453 |
rs548561026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35112451 | CAGGTAAAGGGAACC[C/T]AGACAGAGCATGGCT | 8453 |
rs548569059 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35070831 | GCTCCAAGCCTCCCC[A/C]ACGTCCTTATCCTGC | 8453 |
rs548576420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014795 | CTGAGATGGCACCAC[C/T]GCACTCCAACCTGGG | 8453 |
rs548603342 | snp | C/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128224 | TTCCTGCATGCTGCT[C/G]AGTGAAGCAGCGGTG | 8453 |
rs548605042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064029 | GGACCTCCTGGTGGT[C/T]ATACTCCAGACTGTT | 8453 |
rs548605954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35063203 | ATACTGTTGTATATA[C/T]GACAAGATAGAATAC | 8453 |
rs548639123 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35021202 | TTTTATTCCATTCTA[A/C]CTGCAGATTAAATTA | 8453 |
rs548641032 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038252 | TCAGAGAGGCCGGGC[A/G]CAGTGGCTCACGCCT | 8453 |
rs548688284 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097851 | GTAGTCCCAGCTACT[G/T]GGGAGGCTGAGACAT | 8453 |
rs548692693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109043 | GATGGCAAAACTCTA[A/T]CTCTACAAAAAATAC | 8453 |
rs548720695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122620 | CAGGTAGTAATAATA[C/T]CCTTATTTTATTTTA | 8453 |
rs548724782 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026910 | ACATATGCATACATG[A/T]GCCATGCTGGTGTGC | 8453 |
rs548740406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024710 | CTGCAAAAAGCTTTA[C/T]TATTGCATTCACTGC | 8453 |
rs548764334 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35020465 | GTCAATAGAATCGTT[A/G]TCTTTTAAGGTATGC | 8453 |
rs548778532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025278 | CAATACTACAAAAGC[A/C]ATGAAAACCATTCAT | 8453 |
rs548779298 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066701 | TTAAATCGAAAATTT[C/T]CAAGTGCACAGCTAG | 8453 |
rs548792802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35076409 | TGAATGGTATGTGAC[A/G]TATATCTCAATAAAG | 8453 |
rs548793661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070272 | GCCCAGAACATAGTT[A/G]GCTTAACAAACTTTT | 8453 |
rs548945760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111817 | ATCACTTGACTCTGG[A/G]AGGCAGAGGTTGCAG | 8453 |
rs548948886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011454 | GAAACCCTGTCTCTA[C/T]GAAAAATACAAAAAT | 8453 |
rs548970409 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35097959 | CCAAGACTCTGACTC[-/A]AAAAAATTAATTAAT | 8453 |
rs549001043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102813 | GCTTGAACCTGGGGG[A/G]CGGAAGTTGCAATGA | 8453 |
rs549035379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116029 | ATCACTACAGATCTG[A/T]TAGACATTAAAGGAT | 8453 |
rs549062461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095482 | AGAACATATAATATA[C/T]ATGCTATTTTGTAGT | 8453 |
rs549074255 | in-del | -/TTG | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35106958 | TTAACCTGTTTTTTT[-/TTG]TTGTTGTTTTTTTGT | 8453 |
rs549124417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074764 | AGTGCTGGGATTATA[A/G]GTGTGAGCCATTGTG | 8453 |
rs549126186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107051 | ATGATCTCAGCTCAC[A/T]GCAAGCTCCACCTCC | 8453 |
rs549127673 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081247 | AGCAGCTACCTGCTT[C/T]CAAAAATAAACCCAC | 8453 |
rs549163980 | in-del | -/AATATATGGATCCAAGTGCAGGAGTAC | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35035352 | TTTCATTTATTAGGT[-/AATATATGGATCCAAGTGCAGGAGTAC]AATATACGGATCCAA | 8453 |
rs549176458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115378 | CAGCCTGGCAAACAT[A/G]ATGAAACCCCGTCTC | 8453 |
rs549181943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086938 | GCTTATATGTCCACA[A/G]ATATTTTTTTCCAAG | 8453 |
rs549186954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073514 | TAGTCTAAGTACCCT[A/G]TACAAACTCGTTTAA | 8453 |
rs549188898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080512 | TTCTGTCACCCAGTG[C/G]AGTGGTGTGATCCTG | 8453 |
rs549189313 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | CUL2 | GRCh38.p7 | 10:35107640 | GTAATCCCAGCACTT[A/T]GGGAGGCCGAGGCGG | 8453 |
rs549223121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35067617 | TTAGCCAGGTCATGC[A/G]CATGTAATCCCAGCT | 8453 |
rs549235176 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35038435 | GGAGTCTGAGGCAGG[A/G]GAATCACTTGAATCT | 8453 |
rs549261939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059866 | CCTCTGTAAAAAACA[A/G]AGATACTAACTAACT | 8453 |
rs549301809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101344 | ATGGAGACAACGGGT[C/T]TACCATTGTAGAAAA | 8453 |
rs549309097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018066 | GAGGTGGAGGCAGGC[A/G]GATCACGAGGTCAGG | 8453 |
rs549309264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35043944 | GTGGTGGTGTGTGCC[C/T]GTAGTCCCAGCTACT | 8453 |
rs549324131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108436 | TACTCTAGCCTGGGC[G/T]ACAGTTAGACCCTGA | 8453 |
rs549360429 | in-del | -/ACAG | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35027828 | TGGAATCAGAATTTT[-/ACAG]ACAGAAACTCACTTC | 8453 |
rs549364045 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35010506 | AAGTAATGACTTTTA[A/G]CCAATCAGTTTAAAG | 8453 |
rs549370377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086283 | GGGAGAATTGTTTGA[G/T]CCCAGGAGTTCGAGA | 8453 |
rs549374366 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042001 | ATCAATGTTTTTAAA[C/T]TGTGGTAAAAACATA | 8453 |
rs549442629 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126182 | TAGGCTGGTCTCCTG[A/G]GCTCAAGCGATCCTC | 8453 |
rs549447949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038046 | CAATCCCAGCTACTT[C/G]GGAGGCTGAGGCAGA | 8453 |
rs549484348 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018495 | TAGGCCGGGCGCAGT[G/T]GCTCACGCCTGTAAT | 8453 |
rs549486146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35090408 | GGAGCGAAGCCCGGG[A/G]AGCCCGCGCGCCGAC | 8453 |
rs549530874 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029834 | CTTTCTTTTTAAAGA[C/T]GTATTTTAAATAAGT | 8453 |
rs549531737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016703 | AGGCCGAGGCAGACA[C/G]ATCACTTTAGGTCAG | 8453 |
rs549545941 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015711 | TGACAGATATTAAAA[A/C]TATATGGTGGTTAAA | 8453 |
rs549549523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35083138 | CTCCAGCCTGCATGA[C/G]AGCAAGACTCCATCT | 8453 |
rs549567309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104918 | ATCTTAAGTAGAAAC[C/G]GAGTTTCTCCATGTT | 8453 |
rs549568727 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009744 | TGTAGGATTTAAATA[G/T]GAGTACAAGTGAATT | 8453 |
rs549568992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35097132 | CCTTTTCTTCAAAGG[A/T]TTACCTTATCTTATG | 8453 |
rs549572779 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | CUL2 | GRCh38.p7 | 10:35103449 | CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGACTA | 8453 |
rs549602541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035669 | CACAGTACTCCATTA[G/T]GTGGATATAATTTCT | 8453 |
rs549630392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35097974 | AAAAAAATTAATTAA[A/T]TAAATAAAATTAAAT | 8453 |
rs549643427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35029338 | CTGGGATTACAGGCA[C/T]AAGCCACCACGCCCA | 8453 |
rs549674336 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35050881 | AATCAAGTGCTCATG[C/G]AGCTTTACTAAATCA | 8453 |
rs549696616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013500 | AAAACCATACCCTTT[A/T]CCTTAGAAAAAACTA | 8453 |
rs549711526 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35051277 | CCGAGATCGCGCCAC[C/T]GCACTCCCGCCCAGG | 8453 |
rs549788403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076133 | CTATCACATGGATGA[A/C]CCTCAAAAACATTCT | 8453 |
rs549790460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069294 | CTGTAATCCTAGCAC[C/T]TTGGGAGGCCAAGGT | 8453 |
rs549829066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069880 | CTCACTAACACACAA[A/G]TAGCAACACTTTTTC | 8453 |
rs549842154 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019492 | CACGACAGGGGAAAG[C/G]AAACTTCAAACTTGG | 8453 |
rs549876066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35076945 | TAGTCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG | 8453 |
rs549912488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071020 | CAACAAATACTTGTT[G/T]AATGAAAGGTTATCA | 8453 |
rs549914625 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35077411 | GCTGAGGAGGAGAAT[C/T]GCTTGAACCTGAGAG | 8453 |
rs549955817 | snp | A/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091051 | CGATAAAGAAACTTC[A/T]CATCTTTTTCACTAA | 8453 |
rs549999080 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081423 | CAATAATCTAGTCAA[A/C/T]GAATTTAAGAAACTG | 8453 |
rs550009456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062418 | CTGTATAAACACTAT[C/T]CAGAGGACGTAGGAG | 8453 |
rs550029576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055327 | ATCTATACATGAATA[G/T]ATACACTTTTCAAAA | 8453 |
rs550032339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35111071 | ATTATTTTAAAAGTA[A/G]CATGCATGGGTTTGC | 8453 |
rs550077909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047790 | GGCGTGGTGGTGCCC[A/G]GCTACTCGGGAGGCT | 8453 |
rs550117890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048421 | TTAGCAAACTAACAA[C/T]CACACTAAAAATTTA | 8453 |
rs550118763 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35088495 | ACAGAGCGAGACTCC[A/G]CCTCAAAAAAAAAAA | 8453 |
rs550152830 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125106 | TTAAAAACCTTATGC[G/T]TCCCCTAAGAGGATA | 8453 |
rs550157537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35081754 | ACAGATCAGCCAGGT[A/G]TGGTGGCATGCACCT | 8453 |
rs550171123 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35027394 | CATGATCCGCCCGCC[C/T]CGGCCTCCCAAGGTG | 8453 |
rs550172511 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35045335 | GGCTCGTGCCTGTAA[C/T]CCCAACACTTTGGGA | 8453 |
rs550176994 | in-del | -/A | 0.0252484 | 0.109484 | intron-variant | CUL2 | GRCh38.p7 | 10:35095323 | CAAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAG | 8453 |
rs550209962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019785 | AAGTTGAAGGCATGA[C/T]AGGATATCACCATTT | 8453 |
rs550210883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065898 | CTAGGTCAGATTTCA[A/T]CTTAAACATTCTTTC | 8453 |
rs550245834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066584 | GATTACAGGCGTGAG[C/T]CACTGCGCCCCGCCA | 8453 |
rs550259473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114177 | TCCGCCTGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 8453 |
rs550288908 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077514 | AAAATAATAATAATA[A/T]AATAAAAAGAAATAA | 8453 |
rs550298431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012716 | GTTTCAAAGTAAATG[A/G]CAGTTAATATTTGTC | 8453 |
rs550304434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35039496 | ATCTAATTATTTTAC[A/G]TTGGTTTCTCTTCTT | 8453 |
rs550322336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107135 | GCCCACCACCGTGCC[C/T]GGCTAATTTTTTGTA | 8453 |
rs550389989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058072 | CACTGCACTCCAGCC[A/G]GGGAAACAGCGAGAC | 8453 |
rs550449231 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009995 | TTAAGATACATTAAA[A/C]AAAAAAAAAAAGACA | 8453 |
rs550471050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072917 | TGAAACATCTTTTCT[C/T]GTCTCCCATCATAGG | 8453 |
rs550479868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084986 | TTAGCTGGGGGTGGT[A/G]GTGGGCGCCTGTAAT | 8453 |
rs550520179 | snp | A/G | 0.000839983 | 0.0204765 | intron-variant | CUL2 | GRCh38.p7 | 10:35049631 | CACTATTTTAAAACC[A/G]TATCAAACAACAAAA | 8453 |
rs550537606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124619 | ATGTGCAACCCGGAA[G/T]TGGCAACTCTGTGGC | 8453 |
rs550545613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121693 | CACATGTCTGTAGTT[C/G]CAGCTACTTAGCCAG | 8453 |
rs550546969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015550 | TTATAAGCACAATAA[C/T]TTGAAGGAGATATAA | 8453 |
rs550594206 | snp | A/C/G | 4.99932e-05 | 0.00499945 | intron-variant | CUL2 | GRCh38.p7 | 10:35031410 | AAAAATATTTTAAAA[A/C/G]ATTACTTCCTTTCTA | 8453 |
rs550594678 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | CUL2 | GRCh38.p7 | 10:35084844 | CTGATAGTTGGACAG[C/G]CCTGGTGGCTCACAC | 8453 |
rs550601086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016936 | TGTCTCAAAAAAAAA[A/C]AAAAAACAAAAAAAA | 8453 |
rs550603116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024404 | AAGGTTATGGCAAAT[A/G]ATTTTCTTGTACCAT | 8453 |
rs550638928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050155 | GCAAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 8453 |
rs550678520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042826 | CCCAAACAGTGTACT[A/G]TAGGACTTCAACTTG | 8453 |
rs550680345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107670 | GGTGAATCACGAGGT[C/T]AGGAGATGGAGACCA | 8453 |
rs550681670 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008099 | TGCAGTGAAGCATAG[A/G]AAATCCTCCTCTCCT | 8453 |
rs550722373 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042631 | TCCACAAAAATCCAA[A/G]AAGACTGGGTTCCAC | 8453 |
rs550729762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35112625 | TGGGCTGTGCATGCA[C/T]GAGAAGAACATGACT | 8453 |
rs550734589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35021295 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 8453 |
rs550741832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017453 | AATCCCAGCACTTTG[A/C]AAGGCCGAGGTGGGC | 8453 |
rs550758457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CREM, CUL2 | GRCh38.p7 | 10:35127413 | CGGCGCCCCCGAGGC[C/G]GCCGGCTCGCCGCCC | 8453 |
rs550790744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35085547 | CAGGAGATCAAGACC[A/C]TCCTGGCTAACACGG | 8453 |
rs550850840 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041447 | GGAAGGCTGTACTGA[C/T]TCATTCCCCAATTAA | 8453 |
rs550906728 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35014914 | TCTGGGCAGCAAAAA[C/T]AGCATGTTTTAGAAA | 8453 |
rs550950076 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067199 | GTTTAAATGGTGGGA[C/G]GATGAACTCATATTC | 8453 |
rs550977504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064049 | TCCAGACTGTTCCAT[G/T]ATAAAGCTATGCCAT | 8453 |
rs550995019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099517 | AAAATAGCATACTTA[G/T]ACTTAGCGAGGCTGA | 8453 |
rs551015492 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098190 | CAGTGGATCCTTTAT[A/G]TTTCTTTGCAGTCAC | 8453 |
rs551047192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053840 | ACATGAACTTACAAG[C/G]TTTTGTGTGCAGGGA | 8453 |
rs551058451 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092193 | CTCCTGAGCTCAAGC[A/G]ATCTGCCCACCTCAG | 8453 |
rs551081618 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35103470 | GCTGGGACTACAGGC[G/T]CGCGCCACCATGCCT | 8453 |
rs551094722 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35039941 | GTGGATCACATGAGG[A/T]CAGGAGTTTGAGACC | 8453 |
rs551122411 | in-del | -/A | 0.0137532 | 0.0817768 | intron-variant | CUL2 | GRCh38.p7 | 10:35077818 | GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAAGAA | 8453 |
rs551126093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030148 | CATGCCACAGCTGCT[A/G]GCTCTTATAAGGTTT | 8453 |
rs551168252 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35018750 | CCTGGGTAACAAGAG[C/T]GAAACTCCGTCTCAA | 8453 |
rs551182542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046965 | AAAAAGGAAAGAAAC[A/G]AACAGTTATTTTGCT | 8453 |
rs551241758 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35010713 | AGCTCTTAGTTCAAA[C/T]ACTTTCTCAAGAAAG | 8453 |
rs551244813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071599 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 8453 |
rs551258175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065142 | CTATTCAAATATCCA[A/G]CCAACCAGGAAACGT | 8453 |
rs551402248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35096318 | AAAGAAGTGGCTGAC[A/G]TGATGGCCGGGTACA | 8453 |
rs551415188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109751 | GCATAATGAAAAGGA[A/G]GACCAAAGCCAAATC | 8453 |
rs551446682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35122701 | GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 8453 |
rs551454282 | in-del | -/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126908 | GAGTTCGAGCCTGGA[-/T]TTTTTTTCCTCGGGG | 8453 |
rs551500133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123555 | CATTTAGCATAGGGC[A/C]TGGAACATAGCAGGC | 8453 |
rs551506654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115452 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 8453 |
rs551519932 | in-del | -/GGAGGT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127247 | GGGCGACGCGGCGCA[-/GGAGGT]GGAGGTGGAGGTGGA | 8453 |
rs551543662 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35028979 | TAAGCATCTAAAACA[-/T]TTTTTTTCTTCCTCA | 8453 |
rs551553880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35101494 | TATTCCTGTTTTACT[A/G]GAAGCTACAATGAAG | 8453 |
rs551556818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081240 | ACAAAAAAGCAGCTA[A/C]CTGCTTCCAAAAATA | 8453 |
rs551570098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109151 | CTGGAGGTTGAGGCT[C/G]CAGTGAGCCATGTTC | 8453 |
rs551613841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034012 | AATAATCCTGAGAAC[A/G]GAGACCCCTTGAACT | 8453 |
rs551640356 | snp | A/C/T | 3.34213e-05 | 0.00408773 | intron-variant | CUL2 | GRCh38.p7 | 10:35060972 | CTCCAAAACTCTCTA[A/C/T]ATAAAGAGGAAAAAT | 8453 |
rs551684021 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35102899 | GAAAAAAAAAAAAAA[A/T]ATTTTAAGAAGAAAC | 8453 |
rs551687024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102014 | CCATTGCCAGGCAGG[C/T]CAATCACCTGAAGTA | 8453 |
rs551702591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023354 | TTATAAGGTTCTCTT[C/T]CCAAAGGAAGTAACT | 8453 |
rs551724473 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061521 | AAAATTGCAAAAAAA[A/T]TATTAATGTCTTACA | 8453 |
rs551731525 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35087201 | GTACTACAGGCGTGC[A/G]CCACCACGCCTGGCT | 8453 |
rs551737151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084142 | ATTAGTCAGGTGTGG[G/T]GGCAGACACCTATAG | 8453 |
rs551751356 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073075 | GAAGAGAGCTCAAGG[A/G]ATCCCAGGAATAGAC | 8453 |
rs551758469 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35033238 | AACAAATTTACCATG[C/T]ACTTCCAAAACTGAC | 8453 |
rs551769599 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35038470 | GGCGGAGGTTGCAGC[A/G]AGCCAAGAGCACGCC | 8453 |
rs551783513 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35051791 | TCTTAATAAAAGCTA[C/G]AGTTTTTTATATATT | 8453 |
rs551786945 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080715 | CAGCCTTGGCCTCCC[A/C]AATTACTAGGATTAC | 8453 |
rs551824143 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116236 | TAATCCCAGCTACTC[C/T]GGAGGCTGAGGCACA | 8453 |
rs551843571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119185 | TTGTTAAATAATTGT[A/G]TAACTGGGAAATTCA | 8453 |
rs551860554 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126672 | GGATTTCTGGCGCAC[A/G]CGCGGCGCGGCACGG | 8453 |
rs551876462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35074033 | GGTGCTCTAGGCTGC[C/T]GTGTGCAACCATGCT | 8453 |
rs551889282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030251 | TTCTATTTAGGCATA[A/T]TTTTAATAGCATCTA | 8453 |
rs551893886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025321 | ATTAAAGCCCATCTG[C/G]TTTACCTCCTTCTTT | 8453 |
rs551902517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120068 | AGAAAACTGATCATC[C/T]ATGGGGACTGCATGT | 8453 |
rs551913022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35067708 | AAGATCACACCACTG[A/C]ACTCCAACCTGGGCA | 8453 |
rs551917683 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35077426 | CGCTTGAACCTGAGA[C/G]GTGGAGGTTGTGGTG | 8453 |
rs551932655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35010567 | GGGCCAAATTAAGTA[C/T]GAAAATAGGAACTAC | 8453 |
rs551943258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048901 | ATACCACGGCTTTGA[C/T]AAAGTATTCCTCATA | 8453 |
rs551955481 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023313 | TGTTTTCAGTACCTT[C/T]GGTGACTCAAAACAA | 8453 |
rs551956365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071614 | GGGGTTTCACTGTGT[A/T]AGCCAGGATGGTCTT | 8453 |
rs551959878 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090500 | ACAGGGGCGGTAGGG[A/G]GGGGGGGAAAGGGGA | 8453 |
rs552022800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35083215 | CTATTTCCCACCGTC[A/G]GAAAATAGCAGTTAT | 8453 |
rs552048500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35048509 | TATAACAGTATTGTC[A/G]TTATACTTTTAAATA | 8453 |
rs552174721 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35036456 | GGGAGGTAAAGCTGG[C/G]GGGTGGTTATATGTT | 8453 |
rs552198238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070703 | AGCACACTCTTCCCC[A/C]CAAAATCACATGGCT | 8453 |
rs552225603 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014521 | AAGACATTCTGCTAA[C/G]GAATGGACAGATTCA | 8453 |
rs552233708 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35127116 | CGCCGCTGCTGAGCG[C/G]CGGTCGGGCTCGCCG | 8453 |
rs552235050 | snp | G/T | 0.000276697 | 0.0117589 | intron-variant | CUL2 | GRCh38.p7 | 10:35063096 | TTTTCATATTTATTG[G/T]AGACAATTTTAAAAC | 8453 |
rs552255955 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35072149 | CAGTATAAGATTAGG[A/G]AAGAAATTTACATTT | 8453 |
rs552287337 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052024 | TCAAGCTTTGCCTTT[C/T]ACATTTAGGCCTTTA | 8453 |
rs552287878 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124647 | GGCCTTCCTTATAGG[G/T]CTAGCAGTGCCAACA | 8453 |
rs552311130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064224 | GAAGATAAAGGACCT[A/C]TGAGCAACCTGAGAC | 8453 |
rs552314601 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063616 | TTAAGTTTCTGAACA[A/C/T]CAACTAAGTACCTTG | 8453 |
rs552424588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104982 | GATCCACCCGCCTGG[G/T]CCTCCCAATGTGCTG | 8453 |
rs552437514 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036114 | TCATGCCTCCTTCCA[A/G]TCACACACTCTTGCT | 8453 |
rs552456036 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097387 | AGACCAGCCTGGGGA[G/T]GCTGAGGTGGAAGGA | 8453 |
rs552457942 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019286 | GTCTTTCAGCACCAC[A/G]AGACCCAAAGAGCAT | 8453 |
rs552458524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069949 | TGTTCCACAGAAAAA[G/T]TAGCTATCTAATTCA | 8453 |
rs552479406 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101411 | TCTAGCCATACACAG[A/G]AATCTGTTTTAATAT | 8453 |
rs552498313 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35041473 | ATTAACTAAATGGAG[A/G]GCAAAGCCCAGGGTT | 8453 |
rs552499305 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033533 | TGAGGTCAGGAGATC[A/G]AGACCATCCTGGCCA | 8453 |
rs552499345 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066441 | TAGCTGGGATTACAG[C/T]TGAGCGCCACCATGC | 8453 |
rs552532958 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35042038 | AAAATTTACATTAGC[C/T]ATTTTTATGTGGGCA | 8453 |
rs552550546 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101715 | TAATCTTTTGTATCA[C/T]TCAATTCTACTCCAG | 8453 |
rs552561587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104299 | AAAAATACAAAAATT[A/G]GCTAGACATGGTGTA | 8453 |
rs552566327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076306 | CCAACAGGGTGAGGA[A/C]AATGCTCTAAAGTTG | 8453 |
rs552619550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013644 | GTAAACACTTGTAAA[C/G]TCCAATGCTTAAATG | 8453 |
rs552627954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054689 | GAATTATGTAGAGAT[G/T]AGAAATATAATAAAA | 8453 |
rs552675188 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127506 | AGTTGGAAAATCCTC[C/T]CTGAGAGAGCCGTGC | 8453 |
rs552682084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073633 | TTTGAGATGGAGTCT[C/T]GCTGTTGTCAGCCTG | 8453 |
rs552685583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35085980 | GGGTAACAAACCTAC[A/G]TGTGTACCTCCTGAA | 8453 |
rs552712209 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35016753 | TCAACATAGTAAAAC[C/T]CCATCTTTACTAAAA | 8453 |
rs552743049 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35027515 | ACAATTAAGATTGAC[G/T]GGCCTAAAGTATAAA | 8453 |
rs552761505 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095684 | ATGCCTCAGACTCCC[A/G]AGTAGCTGGAACTAC | 8453 |
rs552762878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35047483 | GGTGTGGTGGTGCGC[A/G]TCTGTAGTCCCAGCT | 8453 |
rs552769508 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075512 | TCCCATCAAGTTAAC[C/T]GCAAAAATCCAAATC | 8453 |
rs552815990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066053 | TAGCTGCAACCAAAA[C/G]ACAGTCCTAACCAGC | 8453 |
rs552816973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35044387 | AGGGTATTGTAAAGA[A/G]CAATGACTTATCAAT | 8453 |
rs552825402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093979 | ATTATTTTTAAAATT[A/G]ATCAGTAATTTAAAA | 8453 |
rs552852747 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35058118 | AGTAATAAAATTTTT[A/T]AAAAAAGAACATTTA | 8453 |
rs552887519 | snp | G/T | 3.35683e-05 | 0.00409671 | utr-variant-5-prime, missense | CUL2 | GRCh38.p7 | 10:35071331 | ATTGTGCAAGTGTAG[G/T]GTTGAAATCTGTCAA | 8453 |
rs552895644 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35101019 | CAGTCATTTCTGACC[A/G]CTTGAGCCTTGGAAC | 8453 |
rs552910875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036741 | ATCCAGTGGTTTTAA[C/T]GGCTTTTTTTGAGAC | 8453 |
rs552936585 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071609 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 8453 |
rs552952292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35117456 | TCTGGTCTTGAACTC[C/T]TGAGCTCAAGCAATT | 8453 |
rs552955269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093263 | GTGACTGGCCTTGGG[A/T]CAATTAAACACTTTC | 8453 |
rs552981108 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010063 | ACCCAACCGAATTTC[C/T]ACTTTTCAGCAATAC | 8453 |
rs553010099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043596 | TAAACTAACACAAAC[A/C]ATCCCAAAATAAAAT | 8453 |
rs553031745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016984 | TAGAAATGCTAAGAC[C/T]TAGGCAGAAAAAGAA | 8453 |
rs553041924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35100102 | TGAGCTACTGTGCCC[A/G]GTCTTGTACAGTCAT | 8453 |
rs553057543 | snp | G/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075356 | AGTTTACACAAGGAT[G/T]TGAAAGAGACAGGGC | 8453 |
rs553096373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023225 | CAGATACAATTTTTA[C/T]GTGTCAATTGTATCT | 8453 |
rs553168142 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008185 | TGCACAGCAGGGCGG[C/T]CAGGTCAGAGCTCTG | 8453 |
rs553187280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119632 | GGGTCTCACTCTGTT[A/T]TCCAGGTTACAGTCC | 8453 |
rs553285797 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35114264 | AGACAGTGTTTCCCC[A/C]TGTTGGCCAGGATAG | 8453 |
rs553289929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106641 | CGGGCCAAATGTTTG[C/T]TGTTTATAAGCCACC | 8453 |
rs553303158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034305 | GAGTAATAAACCTGA[A/G]TACTATAAACTAATA | 8453 |
rs553338483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048967 | CACAGATATAGGTGG[A/G]GTGGCCATTATTACA | 8453 |
rs553339589 | snp | C/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127977 | CAGCCTCCCGAGTAG[C/T]TGGGATTACAGGCAT | 8453 |
rs553341066 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009117 | AGGGGTGTGGTGGTG[C/G]TGGTGATGGTGTGGA | 8453 |
rs553364912 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039853 | GAGTGAGACACTGTC[A/T]CAAAAAAATAAAAAT | 8453 |
rs553386605 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35078535 | CAAACTCCCAACCTC[A/T]GGTGATCCCCCTGCC | 8453 |
rs553410107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35085023 | TACTTGGGAAGCTGA[A/G]GCAGGAGAGTCTCTT | 8453 |
rs553439498 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | CUL2 | GRCh38.p7 | 10:35120466 | AAAAGGTTACATTTT[A/G]TTTGAAGAAAACAAA | 8453 |
rs553450168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026925 | TGCCATGCTGGTGTG[C/G]TGCACCCACTAACTC | 8453 |
rs553550007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098997 | TAGGAACAAAGAAAG[C/T]GAACAAGTCAAATGT | 8453 |
rs553565763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124769 | GATCTGATATGGGAA[A/C]GAAATGACATCTAAC | 8453 |
rs553593028 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103418 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 8453 |
rs553627952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35116952 | ACAGGGTGAGATTCC[A/G]TCTCAAAAAAAAAAA | 8453 |
rs553648427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102977 | AATCGAAGTTGAACA[A/G]TGCTGCCTGTCTATT | 8453 |
rs553649819 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35056569 | ACTCCCATTCAACAT[C/T]GGCTGAGGGTATATC | 8453 |
rs553651545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042333 | TTGTATCATGTATAA[C/T]TTCAATTCTTTTTAA | 8453 |
rs553707577 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089001 | GCCAACATGGTGAAA[A/C]CCCATCTCCACTAAA | 8453 |
rs553720653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115599 | TAAATTAATTAATCT[A/G]AATGTTGGTTCTGGC | 8453 |
rs553722667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107913 | AAAAAAAAAAAAAGT[A/T]GAAGACCTGGTTCCT | 8453 |
rs553750488 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088379 | TGGGCGTGGTGACGT[A/G]CGCCTGTAGTGCCAG | 8453 |
rs553760944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046415 | AAACATCTACATATG[C/T]GTACAACAGAAACAA | 8453 |
rs553764485 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025505 | TCTGAATAATACTAA[C/G]ATGGACTTTATAAAT | 8453 |
rs553780431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35068973 | CCCAGGGTTTAAGCA[A/G]TTCTCCTGCCTCAGC | 8453 |
rs553795586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039651 | AGGTGGATCATCTGA[A/G]GTCAGGAGTTTGAGA | 8453 |
rs553825935 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022821 | GGAGGCCGAGGTGGG[A/T]GGATCACGAGGTCAG | 8453 |
rs553870104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35019293 | AGCACCACGAGACCC[A/G]AAGAGCATTAGGAGA | 8453 |
rs553871269 | snp | C/T | 0.00222758 | 0.0332991 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074233 | TCTGTACATAAAGTA[C/T]AAAGTTTGTTGTTTC | 8453 |
rs553881309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018248 | GCCGAGATCGCACCA[C/T]TGCACTCCAGCCTGG | 8453 |
rs553945510 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116820 | AGAATAGCTGGGCGT[A/G]GTGGCGCACGCCTGT | 8453 |
rs554012619 | snp | C/T | 0.000399281 | 0.0141238 | missense | CUL2 | GRCh38.p7 | 10:35039019 | CATGAATCACCTTAG[C/T]ATATGAACTTGGATG | 8453 |
rs554048615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053158 | AGTTCAGAAAAGATG[A/C]GAACTAAATTGTTTA | 8453 |
rs554075001 | snp | C/G | | | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079205 | TATGCTATAATAAAA[C/G]TTACATGACCATGGT | 8453 |
rs554098904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017844 | ATAATATGGCAAACA[C/T]GTCTACACTCTGTAA | 8453 |
rs554144190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088073 | GGAAGTTCTTTTCTG[C/G]TTACAGTATCTGAAG | 8453 |
rs554157628 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35106038 | CTATAGAAAAAATGC[A/G]TTCCCCCAAAATTCG | 8453 |
rs554177510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122781 | TAGCTGGGATTACAG[A/G]CATGCGCCACCATGC | 8453 |
rs554238381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059348 | AGACATTGCCACAGC[C/T]TCCCCAACCTTCAGC | 8453 |
rs554275772 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35010868 | TCCCCCATTAAACTG[C/T]GAACTCCAAAAAAGC | 8453 |
rs554288976 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35102330 | CAATCCCAACACTTC[A/G]GGAAGCCAAGGCAGG | 8453 |
rs554292382 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008240 | TGATGACTTCAATCT[A/C]CTGACCTAACTTGAC | 8453 |
rs554356889 | snp | G/T | 0.000148347 | 0.00861113 | intron-variant | CUL2 | GRCh38.p7 | 10:35032431 | CAGCAACCACCAAAC[G/T]TACCAGTTCAGGTGC | 8453 |
rs554368955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038179 | ATTAAATAAAATATA[A/C]ATATTTATTATCTTT | 8453 |
rs554399267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073591 | TTTTCTTTTCTTTTT[C/T]TTTTTCTTTTTCTTT | 8453 |
rs554407643 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094177 | CATTATAACAATACA[A/G]GAATGGCATAATACA | 8453 |
rs554459269 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070117 | AGATCAGTTTCCTTA[A/T]CCGTTACAGTCAAGT | 8453 |
rs554503534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35112929 | CCAGGCGTGGTGGCT[C/T]ACGTCTGTAATCCCA | 8453 |
rs554505768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032902 | CAGTACTAAAAATTG[C/T]AAAATTATGCATGTC | 8453 |
rs554518541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071425 | GTTTGTTTGCTTTGA[A/G]ACGGAGTCTCGCTCT | 8453 |
rs554546381 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023797 | TGGTCCAGCATTTTT[G/T]TCTTAAAATCAATTA | 8453 |
rs554547569 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35118795 | TGCTCCACAAGAGTT[A/T]AGGACTTGGGAAAAA | 8453 |
rs554558861 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35015198 | CTCAGGAGGCTGAGA[C/T]AGGAGAATCATTTGA | 8453 |
rs554574928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064543 | GATGATTTATTAAAT[C/T]CTGCTGAAGGAAAGG | 8453 |
rs554579634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35022284 | TAATAAGTTGTGAGC[C/T]AATAACTCCAGCCAC | 8453 |
rs554676900 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031205 | ATTTAACCAGATGAA[C/T]TGTTTCCTGTTACTG | 8453 |
rs554680945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082816 | GGGGATCTTTCTCTT[A/G]ATGTCACATTATTCA | 8453 |
rs554690108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35089900 | CGCACTCTCACCTTC[C/T]CTCCTTCGAAGGAAA | 8453 |
rs554704382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35047879 | CACCGCACTCCAGCC[C/T]AGTAGACAGAGTGGG | 8453 |
rs554738948 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067937 | ACGGTGAAACCCTGT[C/G]TCTACTAAAAAAATA | 8453 |
rs554752918 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067675 | CTTAAACCCAGGAGG[C/G]GGAGGCTGCAGTGAG | 8453 |
rs554768448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062049 | AAGTGAGTTGCCCGT[C/G]GTTACAACAGCTAAT | 8453 |
rs554811408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054136 | AGTACTTGTCCCCTG[C/T]ACTTTTTAACTACAG | 8453 |
rs554839080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019975 | TCTGGTGGTTACCGC[A/C]TTCATCAAGTGACCA | 8453 |
rs554844037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054938 | AGAAATGCAATTTTT[C/T]ATTTTTAAACAAAAA | 8453 |
rs554859511 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118954 | AAAGGGAAAGAATAG[C/G]GGGACAATGGGGTCC | 8453 |
rs554875807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012920 | AAGTCCCCTCCTCAC[A/G]CTGGCCTGTCAGTAC | 8453 |
rs554901786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35029433 | ATTTATGAATCATTT[G/T]TATCAACGTACTGAA | 8453 |
rs554984456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35044500 | CAAGAAAACTAAGAA[C/T]GATGTTAAATAAAAC | 8453 |
rs555005459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080211 | CACAATGACCAAATA[C/T]GTTGCCATCATTTAA | 8453 |
rs555025567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045647 | TTGAGCCCAGGAGGA[A/G]TCGAGGCTACAGTGA | 8453 |
rs555050035 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125766 | TGATTTCTAAGAACC[C/T]ATCGTTAAGTGAGGA | 8453 |
rs555067414 | in-del | -/TT | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35070124 | TTCCTTATCCGTTAC[-/TT]AGTCAAGTAATTATT | 8453 |
rs555068300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094548 | CTAGAGTAATTTTTA[A/C]GCGTGTAAAGAAACT | 8453 |
rs555077242 | in-del | -/A | 0.367708 | 0.220556 | intron-variant | CUL2 | GRCh38.p7 | 10:35116956 | GTGAGATTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs555082873 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090581 | CCGGCTTTGCCCAAC[A/G]CACACCCTCCGGTCT | 8453 |
rs555116239 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35035358 | TTATTAGGTAATATA[C/T]GGATCCAAGTGCAGG | 8453 |
rs555133547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35087312 | AATACAGTTTTTGTT[C/G]AAAACATTAGTATAC | 8453 |
rs555134851 | in-del | -/GACA | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35017048 | GGAGAAGGAGAAATG[-/GACA]GACAAAGGGCAAAGT | 8453 |
rs555153083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110444 | GTGGTGCACGCCTAT[A/G]GTCCCAGATACTCTG | 8453 |
rs555156342 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094482 | TCAGGTGATTTGCCC[A/G]CCTGGGCCTCCCAAA | 8453 |
rs555161687 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023541 | ATTTTCAAACTAAAT[C/T]CCAATGGCTAAAAAA | 8453 |
rs555186560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038686 | AGGAAATTAGCTCTT[G/T]TAATATATAAAAATG | 8453 |
rs555208784 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35051129 | AACCATCCTGGCTAA[C/G]AGGGTGAAACCCCAT | 8453 |
rs555216253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103741 | CTGGGATTATAGGCA[G/T]GGGCCACCATACCTG | 8453 |
rs555238526 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35048617 | AGTGTTCTTTTAGTT[-/CA]CAGTTTTGTAAAGAA | 8453 |
rs555270763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096591 | GCACTACAGACTGGG[A/T]AACAGAGCCAGACCC | 8453 |
rs555309224 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128404 | TCCCTTGAAACAAAG[A/C]TCTAGATTGAACAGT | 8453 |
rs555344500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086689 | TAAAAATACAAACTC[C/T]AGCCTGGGTGACAGA | 8453 |
rs555350969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104526 | TTTTGATTGCCTAGA[A/T]CCTTGGTGTAGGGAA | 8453 |
rs555402713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093355 | TGGCCATTACAATGG[A/C]AGGCCATTTTTACTT | 8453 |
rs555427253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037711 | AGCCAGGTGTGGGGG[C/T]GGATGCCTGTAGTCC | 8453 |
rs555431763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032292 | CATTCCTTACATAAA[G/T]GCCAAACTATATACA | 8453 |
rs555456421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032954 | AAAATTCCCCTTATA[C/T]AGCATAATCACGGGA | 8453 |
rs555468884 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050902 | TACTAAATCAAGCCA[A/G]ATGATTTTCCAATTT | 8453 |
rs555476500 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35085712 | AAAAAAAAAAAAAAA[A/C]AAAAAACTGATAGTG | 8453 |
rs555502371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122190 | AATCCTAAAGTTTGA[A/G]TAGAAACGGCCTGCA | 8453 |
rs555511525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017087 | CAGCAACAGCCTCAA[C/G]TGCTGTCGATAGCTG | 8453 |
rs555527935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066109 | GTTCTCTATTAAAAG[A/G]TGTTTCCTACGCTTG | 8453 |
rs555530878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099749 | AAGACTCCACCCAAA[A/G]TAAAATAAAAAAATA | 8453 |
rs555531356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065656 | ATTTAAAAAAAGAGA[C/T]TGAGACCATCCTGGC | 8453 |
rs555556807 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020217 | AAAGTACTGGATATT[C/G]TACAAGACAACTGGC | 8453 |
rs555560190 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35113729 | TTTATTTTTTTGAGA[C/T]GGAGTTTCGCTCTGT | 8453 |
rs555564710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058353 | CAGACCCCCGTGGTA[A/C]GGCAAAAAGCCTCAG | 8453 |
rs555614361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107799 | AGGCAGGAGACTGGC[A/G]TGAACCTGGGAGGAG | 8453 |
rs555666660 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008950 | AAATTTTGTGTTGGA[C/T]GGATGCAGTGGCTCA | 8453 |
rs555670309 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091984 | GGGTCTCCCTCTGTC[A/G]CTGAGGCTGGAGTGC | 8453 |
rs555703164 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125492 | GACCTACGAAAATTA[G/T]ATTTGAACAAAGGTT | 8453 |
rs555724383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101679 | TTCTGAATCAACTCT[C/T]GTAACTCTTCAGTTC | 8453 |
rs555764173 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35036803 | CAGTGGCAGGATCTC[A/G]GCTCACTGCAACCAC | 8453 |
rs555797770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078601 | CTACTGCACCCAGCC[C/T]GACATTTTTCATATA | 8453 |
rs555810660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121108 | TAACGCATTCCCCAT[A/C]ATGTCATGTCTTCCT | 8453 |
rs555834221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019993 | CATCAAGTGACCAAA[G/T]TTAGCATCTCTAATA | 8453 |
rs555834481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072537 | CCATGCCCGGCTCAT[C/T]TTTTGTATTTTTAGT | 8453 |
rs555835985 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35028636 | AGCATTTTAGTATCA[A/G]TATTAGTAACTACAA | 8453 |
rs555872533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114375 | CAGCTGCATTCAAGT[A/G]TTTTTGTTGTTGTTT | 8453 |
rs555886627 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070655 | AAACACACTTCCACC[C/T]CAGTCACTGAACTTG | 8453 |
rs555930011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096520 | CTGGAGGCTGAAATG[A/G]GAGGATCACTTGAGT | 8453 |
rs555996368 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35062754 | AGGTGGGAGGATCAC[A/G]TAAGCCAGGGAAGTC | 8453 |
rs556005420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042976 | GTGTTAGAGTTGAAC[G/T]GGAGGACACCTAGCT | 8453 |
rs556039135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050275 | GCAGTGAGCCCAGAT[C/T]GTGCCACTGCACTCC | 8453 |
rs556041927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037279 | TGCGTGTTGAAAAGA[C/T]CATCTTTTACCTGCC | 8453 |
rs556089387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117121 | TTCCCAGGACAAAAA[A/T]CTGGTCCAAAATCTA | 8453 |
rs556134110 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117601 | GTATTGTATGTTTAC[A/G]GCATTTGTAAAAGTG | 8453 |
rs556143902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082195 | GCACTCCAGCCTGGG[A/C]AACAGAGCCAGACCT | 8453 |
rs556156529 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35103146 | CTTGACTCAAAAAAA[A/T]TTTTTTTTGTTTTTG | 8453 |
rs556214692 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012413 | TACAGAATCTTTCAT[G/T]ACGCTTTTAGATGGA | 8453 |
rs556217263 | snp | A/G | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008520 | GATAAGACTTAATTT[A/G]ACATTTATAAATATT | 8453 |
rs556264949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103566 | CTGACCTCGTGATCC[A/G]CCCGTCTCGGCCTCC | 8453 |
rs556265081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35095836 | AAAGAGTTGAGATTA[C/T]AGGCGTGAGCCACCA | 8453 |
rs556269390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070407 | GGCATTCAGAACAAG[C/G]TGAACTACTATCTTA | 8453 |
rs556271048 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082498 | TGGTGAGGGTCACAA[G/T]GACACTGTAAATGCA | 8453 |
rs556303148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093932 | GTTATTTTTCATAAA[A/C]GCATGCAATTTATGT | 8453 |
rs556313123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088290 | TGAGGAGGGCGGATC[A/G]TGAGGTCAAGAGATC | 8453 |
rs556329855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061200 | TAAACTGAGCCGAGC[A/G]CAGTGGCTCACGCCT | 8453 |
rs556338291 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080884 | AGGGTGACACGGTGG[C/G]GAGTAGGGAATGTAT | 8453 |
rs556375938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074482 | CCTAACTCCCACTGA[G/T]AGTCTAACCTTGGTC | 8453 |
rs556414482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074966 | TACCAAAAAGCTAGC[A/G]ATGCTCCCCTCACAT | 8453 |
rs556435111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35033511 | GGAGGCTGAGGCGGG[C/T]GGATCATGAGGTCAG | 8453 |
rs556436997 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022967 | GGAGAATCACTTGAA[C/T]CCAGAAGGTGGAGGT | 8453 |
rs556498624 | snp | C/T | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054743 | CTCTGCAAGCCCTTA[C/T]AATACCCTTCTAGCC | 8453 |
rs556532444 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35096327 | GCTGACGTGATGGCC[A/C/G]GGTACAGTGGCTCAT | 8453 |
rs556554728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35100014 | TCTTGCTATGTTGCC[C/T]AGGCTGGTCTGAAAC | 8453 |
rs556567500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019136 | TTATTTCTGCAATGA[C/T]GACTTAATCATATGC | 8453 |
rs556590214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35068771 | CCTTAAAATTTCCAC[C/T]TAAGATATTAAGGGT | 8453 |
rs556669817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35092670 | GACCTCATTGATTTA[A/G]TCTTGCTTCTGACCT | 8453 |
rs556672004 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35036282 | GCATGGCTTTAATTT[A/G]TTCATTTCCACTCCT | 8453 |
rs556679196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053301 | CTCATTGATCTTTTT[C/G]TCTATATCATCTTTT | 8453 |
rs556758773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123009 | CAGGCATGGTGGTGC[A/G]CACCTGTAGTCCTAG | 8453 |
rs556774150 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35071686 | GTGCTGGGATTACAG[C/G]CATGAACCATCACAC | 8453 |
rs556800172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050934 | TACTTGCATAGCAAA[A/G]CACAAGATTTCCCAT | 8453 |
rs556810908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072508 | CGAGTAGCTGGGACT[A/G]CAGGCGCCCGCCACC | 8453 |
rs556825909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35060399 | TAGGAAACTACAAGT[A/G]ATTCAATATGCCTAG | 8453 |
rs556837111 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042673 | CTCCTGCACTCATGG[C/T]GATTTCAGACCTTCC | 8453 |
rs556848185 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026330 | AAGTATGATCTGACT[A/G]ACTAATAACTCCCAG | 8453 |
rs556859207 | snp | A/G | 0.000118715 | 0.00770348 | intron-variant | CUL2 | GRCh38.p7 | 10:35033132 | ATGATAGAGTTTTAT[A/G]TACATATATAGTATA | 8453 |
rs556870739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35106584 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 8453 |
rs556871554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123910 | AACTAAAGAAAATAC[C/T]GTTTGAGGACAGTAT | 8453 |
rs556894687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041679 | AGAGCTATGACCAGA[C/T]GACTACACCACCATG | 8453 |
rs556926008 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009101 | TGTATGTTGAGGGAG[A/G]AGGGGTGTGGTGGTG | 8453 |
rs556928872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018430 | AAGGATAATTAGTAA[C/T]TCTGATTAAGGTTTT | 8453 |
rs556930635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026666 | ACTACAAAGACTCTC[A/G]TATCTATAGCTAGTC | 8453 |
rs556953698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35112987 | TCACAAGGTCAGGAG[A/G]TGGAGACCATCCTGG | 8453 |
rs556965665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016009 | GGCACATGGCACCAA[C/T]TCACACAGCATGCTC | 8453 |
rs556966825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35057632 | CACTCCAGCCTGGGC[A/G]ACGGAGCAAGACTCC | 8453 |
rs556988177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35056933 | ACTTCCTCTCACTAC[C/T]TCCTTTGACTTCCAA | 8453 |
rs556995019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35077271 | TGCACTCCAGTCTGG[A/G]CAACAGAGCAAGACT | 8453 |
rs556997604 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35055426 | AAGACAACAATTTTG[G/T]GAAACAATTAAACAC | 8453 |
rs557001168 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35122448 | AAGGGGTTTATTTTG[A/G]CTTCTAAGTTCTCAG | 8453 |
rs557002039 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35050336 | TCAAAAAAAAAAAAA[A/C]AACTTAATTTTTTGA | 8453 |
rs557030040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042233 | TGTCTGTTCTAGATA[C/T]TTCCTATAAATTGAA | 8453 |
rs557074483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35030658 | AAAGTGCTACTATTA[C/T]AGGCATGAACCACCA | 8453 |
rs557117108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35077646 | AACATGGAGAAACCC[A/G]GTCTCTACTAAAAAT | 8453 |
rs557157269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119465 | ATGGACTAATTTTAG[C/T]TCTCTGTGAAAATCA | 8453 |
rs557169611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036027 | CTGAATTATCACAAG[C/T]GAACACACAACACAC | 8453 |
rs557201152 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | CUL2 | GRCh38.p7 | 10:35022104 | CCTACTAGACATGAG[-/T]TTTTTTTTGAGGGCC | 8453 |
rs557215781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048055 | ATGTCAAGGATGTCA[C/T]GCATGTAAAATGGTG | 8453 |
rs557269662 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35120228 | AAATTAATTGTCATG[A/C]CAGGCTGGGCACAGT | 8453 |
rs557287859 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35022422 | TGAGCTGGGAATGTA[C/G]AAATAGACTAGGCAA | 8453 |
rs557306635 | in-del | -/TTC | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35021263 | TCTTTCTTTCTTTCT[-/TTC]TTTTTTTTTTTGAGA | 8453 |
rs557317404 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35054984 | GGTAAGAAAATGGAA[C/T]ACAGTGTTACAGATA | 8453 |
rs557324508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023142 | GTGAGAAGCTACTTA[A/T]GTTAATTAGCTTGAG | 8453 |
rs557326463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015370 | AAAATTATGAAAACA[C/T]TGATTTGAATTTCAG | 8453 |
rs557393009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35084232 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTACA | 8453 |
rs557395688 | snp | A/C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091529 | AATCTAGTGATTCTC[A/C/G]AAGTGTGGTCCCCAG | 8453 |
rs557410225 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065105 | TAATTTTAACCAATT[A/G]ACTATGTTCTTTTTC | 8453 |
rs557421259 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020514 | TTTTATTCTGGCAAA[C/T]ACTAGTAACTACCAA | 8453 |
rs557460606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35036657 | CAGTGCCTGTTTTTT[A/G]AGCATTTTATATTTT | 8453 |
rs557480876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111943 | AAACTCATAGCCTAC[C/T]GTCCAGAGATTGGGA | 8453 |
rs557539084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35011490 | AAGTATGGTGGTGCA[C/T]GCCTGTATTCCCAAC | 8453 |
rs557544575 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35104695 | GAATCCAATATATAT[A/T]TTTTTAACATGAACA | 8453 |
rs557545562 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055613 | ACTCCAAAGTGGTAT[A/G]CCCACAACCATTTAC | 8453 |
rs557547068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35105397 | CGCCACTGCACTCCA[G/T]CCTGGGCGACAGGGA | 8453 |
rs557600737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034270 | GTAATAATGTAAACT[A/G]GTAAGTTTGACAAAT | 8453 |
rs557617282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055491 | TAATCCCAGTGCTTT[A/G]GGAGGCTGAGGCGGG | 8453 |
rs557627152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108503 | CAGTTATTTGGACTA[C/G]AATAGTTGTGGGAAA | 8453 |
rs557651067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045695 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACCC | 8453 |
rs557704156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121882 | TAAATAATTCAGGAG[C/T]TTGGGTTTTTATTAT | 8453 |
rs557704242 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35114442 | GGCTGGAGTGCTATG[A/G]CACAATCTTAGCTTA | 8453 |
rs557736838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017212 | TTAATGCTATTATGT[C/T]TCATAAACAACATTT | 8453 |
rs557791775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35088019 | TGTTCCTCCCTAAAA[C/T]AGGAAAACTGTTCCC | 8453 |
rs557808248 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35051374 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGCGGGCG | 8453 |
rs557836319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35032799 | GCAGCTTTCCTTTAA[C/T]GTATGCAAAAGTTCA | 8453 |
rs557862448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025840 | ATGATACTGGATGTG[A/T]AAAAGATAAAAACTC | 8453 |
rs557862815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079939 | GGAGGCATCCACAGC[C/G]TAGAGATGCTGGACA | 8453 |
rs557873780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017726 | CTATATGCTAAATGA[A/C]CCTGGGAGCTCTAAG | 8453 |
rs557892792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101725 | TATCATTCAATTCTA[C/T]TCCAGTATCAAAAGC | 8453 |
rs557898148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35123926 | GTTTGAGGACAGTAT[A/G]GAAGATGATGTCCAA | 8453 |
rs557944803 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020164 | GGAATAGAAAACAAA[-/T]TTAAAAAAAAAAAAA | 8453 |
rs557981479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051523 | GAGGCTGAGGCAGGA[A/G]AATGGCGTGAACCGG | 8453 |
rs558002502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35094098 | TCGTGCTTCTTGTAC[A/G]GCCTGCAGAACCATG | 8453 |
rs558039932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121180 | GAGTGTTAACTGAGA[A/C]AAATGCCATCCATGG | 8453 |
rs558113356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094630 | ATGTTCCTCTTAACT[C/G]TGGTTGGAAATGTGA | 8453 |
rs558197292 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009813 | CTGCTTTGAGTCAAT[A/G]TATTTTGTGGTCAAC | 8453 |
rs558215273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066296 | ATTAACAGTAAAAAA[G/T]AATTTGCTGACTTTT | 8453 |
rs558217810 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35112017 | TGTGTAGAGAAGAAC[C/T]TGAAGGCCTCATTAC | 8453 |
rs558232611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020769 | ATCTGTATGTCTTTA[C/T]CAAACTGTTCCTTAT | 8453 |
rs558239225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059312 | AACTGATGCAGCTAA[C/G]TTCATTGTTGTCTTA | 8453 |
rs558254030 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35066869 | TACACATAATCTCCA[C/T]GGTTACTAAGACCTT | 8453 |
rs558273140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35014436 | AAGCCACTGATATCA[C/T]AGAGTGGAATTTCTC | 8453 |
rs558324312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35089821 | AGATGCCCCCCCCCA[C/T]ACACACACACAAACA | 8453 |
rs558329265 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113269 | GGGAGCCCGAGGTGG[A/G]TGGATCACCTGAAGT | 8453 |
rs558335732 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35085891 | ATAAGGGTTGAAAAA[C/T]GGTTGGGTACTATGT | 8453 |
rs558380484 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076736 | ATTCAGATTGTTATA[C/T]ATCTGCTTTTTTCTC | 8453 |
rs558413417 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35105421 | ACAGGGAGAGACACC[A/G]TTTCAAAAAACAAAA | 8453 |
rs558427772 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128716 | ATTTTTAGTAGAAAC[A/G]GGGTTTCACAGTGTT | 8453 |
rs558435779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117755 | ACCATTCCATGAAAG[C/T]TGTAGGCATGAAAGA | 8453 |
rs558484160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037780 | CCCAGGAGGCAGAGG[A/T]TATAGTGAACAGAGA | 8453 |
rs558518947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35076996 | GGCGGAGCTTGCAAT[C/G]AGCCGAGATAAAACT | 8453 |
rs558524152 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048715 | TCTCTAAAAACAATG[A/G]AATCACTCAAACGGT | 8453 |
rs558532006 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085601 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 8453 |
rs558540256 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35083170 | AAAAAAAAAAAAAAA[C/G]AAAGAAAAAGAAAAA | 8453 |
rs558548331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096547 | GAGTCCAGGAGGTCA[A/T]GTTTGCAGTGAGCTG | 8453 |
rs558548769 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043579 | GACCTTTCTTGGCTA[A/C]ATAAACTAACACAAA | 8453 |
rs558615354 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040141 | CTAGGCAATAAGAGC[A/G]AGGCTCTGTCTCAAA | 8453 |
rs558638117 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35103619 | TGAGCCACCGCGCCC[A/G]GCCTAATTTTTTGTA | 8453 |
rs558656946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063416 | TTAGTATCAATAGTA[C/T]CAATGATATTAGTAT | 8453 |
rs558659160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35089107 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 8453 |
rs558677863 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030113 | CTATCTCACTCTCCC[A/G]GTAGCTGGGACTATT | 8453 |
rs558682997 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126162 | TGAAGTCTCACTGTG[C/T]TCCCTAGGCTGGTCT | 8453 |
rs558698131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082280 | GATATTACGCTAAGT[C/G]AAATACACTAGACAC | 8453 |
rs558740192 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026734 | TGGCACTACAAAGAC[C/T]AAAGTTATAAAACCT | 8453 |
rs558746602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034869 | AAACTACGTTATCAA[C/T]GCCAATTACACAAAA | 8453 |
rs558748511 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060384 | GAGACCATGGGCCAT[C/T]AGGAAACTACAAGTA | 8453 |
rs558760447 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35068857 | CCTTATAACAATTAG[C/T]AGCATAGTCTTTTAT | 8453 |
rs558770089 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35047270 | TCTATGATAGTTCCT[C/T]AATTCTGTGAGTGAA | 8453 |
rs558773479 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35065790 | CTTAAACTCAGGAGG[C/T]GGAGGTTGCAGTGAG | 8453 |
rs558795172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069484 | AGGTTGAGGCTGCAG[C/T]GAGCTATAGTCACAC | 8453 |
rs558795571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061326 | TAAATAAAAAAAAAT[C/T]AGCCAGCCGTGGTGG | 8453 |
rs558851082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026826 | GACTAAACTTATTTT[A/G]TTTTTTTAAATTTTA | 8453 |
rs558912079 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040802 | CTCAGGCATTAGATT[A/C]TTCTAAAGAGCGCAC | 8453 |
rs558920901 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121022 | TCCCTTTCTAAGTTC[A/T]TTTTTCCATGATTTA | 8453 |
rs558929550 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067518 | ACTTTAGGAGGCTGA[A/G]GTGGGGGGAATCACT | 8453 |
rs558946562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35085394 | GAGATCGCGCCACTG[C/T]GCTCCAGCCTGGGCG | 8453 |
rs559047120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35092844 | ATGAAAAGCAGCAAG[A/G]ATAGGATTATGGGAG | 8453 |
rs559058619 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009668 | AATCCATAAAAATAA[A/G]GCATTCTTTATGCTG | 8453 |
rs559085449 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025903 | TTATGCCAGTTCAGA[A/T]TTCTGAATAAACTTT | 8453 |
rs559087589 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062097 | TTCTTACGCAGGCAC[C/T]AAATTATCTCATCCA | 8453 |
rs559089427 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35078208 | AATGTGATGTGTTAA[C/G]ATAGCCTGACAAAAT | 8453 |
rs559103085 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079214 | ATAAAAGTTACATGA[C/T]CATGGTCTCTCAGAA | 8453 |
rs559115200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064961 | TCCCATTTCATTCCA[C/T]ATACAGTACTTCTGC | 8453 |
rs559115947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127209 | GTAAGTGGTGCGTCG[G/T]CTCCGGCCCCGAGAC | 8453 |
rs559125350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043144 | TAATATTCCAATGCA[C/T]ATATGTATCACATTT | 8453 |
rs559176196 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062124 | TCCAGTTCCTGATTA[A/G]ATCAGTAGTCTAAAT | 8453 |
rs559185156 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098838 | ACTTGGGAGGCTGAC[A/G]CAGGAGAATTGCTTG | 8453 |
rs559186572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109394 | TGTTCTAGGTGCTGG[A/G]CACAATATTTGTAGG | 8453 |
rs559213418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053411 | AAGTTTCTATGAACA[A/G]TTTTCTGCTATTAAT | 8453 |
rs559254917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098816 | GCAGGCGCCTGTAAT[A/C]CCAGTTACTTGGGAG | 8453 |
rs559259974 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087802 | GGTCTCCTTGTGTCT[C/T]TCTTCTCCAATCAAC | 8453 |
rs559269675 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092098 | GCTGTGACTACAGGC[A/G]CGTGCGCCACCACAC | 8453 |
rs559335186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019882 | TCCTGGAACAGGGTA[C/T]TCATGCCAAAGTATC | 8453 |
rs559336810 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35012379 | CAATAATTTGCAAGA[C/T]CATTTTCTTATCAGT | 8453 |
rs559358200 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35105695 | CCTGGGCGACAGAGC[G/T]AGACTCTGTCTCAAA | 8453 |
rs559375923 | in-del | -/A | 0.00360937 | 0.042328 | intron-variant | CUL2 | GRCh38.p7 | 10:35048918 | AGTATTCCTCATATA[-/A]AAAAAAACTCCTTAT | 8453 |
rs559376256 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064002 | AATGACACCAGAGCA[A/T]CACAGAGGTCAGGAC | 8453 |
rs559391871 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128025 | AATTTTTGTATTTTT[A/G/T]GTAGAGATGGGGTTT | 8453 |
rs559438612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078738 | ATTTTACTTACCTTC[C/T]AAAAGTATAATTATC | 8453 |
rs559466586 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35037423 | CTTAATTACTATAGG[G/T]TTTACAATAAGTCTT | 8453 |
rs559466909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030971 | CTGCTACCACTTATC[A/G]GTATGTAAGCAAGCT | 8453 |
rs559498245 | snp | A/C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066596 | GAGCCACTGCGCCCC[A/C/G]CCAGATTTGCTGGCA | 8453 |
rs559555301 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35104911 | ATTTTGTATCTTAAG[G/T]AGAAACGGAGTTTCT | 8453 |
rs559559845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041264 | CTGAGAGAGGTGAAG[A/G]AGGATGGAAGAAGGA | 8453 |
rs559562722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050095 | TGGGAGGCCAAGGTG[A/G]GCACATCACGAGGTC | 8453 |
rs559582798 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35099283 | GTAGTCCCAGCTACT[C/T]GGGAGACTGAGGCAG | 8453 |
rs559601262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042634 | ACAAAAATCCAAGAA[A/G]ACTGGGTTCCACAGG | 8453 |
rs559644668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35036182 | ACAGATGAGTTTGAA[C/T]TACGTATAAAAATGG | 8453 |
rs559650997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35029725 | GTGTCGGTATTGCTA[A/G]GTCTTTGATCAAAGG | 8453 |
rs559667176 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100004 | AGAGACAGAGTCTTG[C/T]TATGTTGCCCAGGCT | 8453 |
rs559714361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071487 | TTGGCTCACTGCAAG[C/T]TCCGCCTCCCAGGTT | 8453 |
rs559761630 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068169 | CTCACACCTGTAATC[A/T]CAGCACTTCAGGAGT | 8453 |
rs559808140 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35029128 | AGTGGCACGATCTCC[A/G]CTCACTGCAACCTCC | 8453 |
rs559836702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35076847 | CTGAGGTCAGGAGTT[C/T]GAGATCAGCTGGCTG | 8453 |
rs559913859 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35014756 | GATTATCACTTGAGC[C/T]CAGGAGGTGGGGATT | 8453 |
rs559990693 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35018704 | GGAGGTGGAGGTTGC[G/T]GTGAGCCGAGATCGC | 8453 |
rs559992086 | snp | A/T | 1.92699e-05 | 0.00310396 | intron-variant | CUL2 | GRCh38.p7 | 10:35033139 | AGTTTTATGTACATA[A/T]ATAGTATATATGTAT | 8453 |
rs559994872 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107882 | GCGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 8453 |
rs560015353 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126588 | CTTGGGGTTGGCGGC[A/G]TTAGGAAGAAACCGA | 8453 |
rs560069443 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052981 | AGCTTTCACAAAAAA[A/C]AAACTTATGTAAAAA | 8453 |
rs560071888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35067496 | GGCTCATACCTATAA[C/T]CTCAGAACTTTAGGA | 8453 |
rs560109810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35118017 | CATGTTCTACTTGTT[A/C]GAACTGATGAACCTA | 8453 |
rs560169656 | in-del | -/T | 0.128976 | 0.218754 | intron-variant | CUL2 | GRCh38.p7 | 10:35106304 | TAAATGTGTTTTTTG[-/T]TTTTTTTTTTTGTGG | 8453 |
rs560193853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123383 | GTCACTGTAGATTTT[C/T]TAAGAGAAATCACAT | 8453 |
rs560214941 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35038005 | TAAAAATACAAAAAT[G/T]AGCTGGATGTGATGG | 8453 |
rs560266094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35108996 | AGTGGGTGGACCACC[C/T]GCGCTCAGGAGTTGG | 8453 |
rs560266942 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074417 | ACCCTTACTATTTTC[C/T]CTACCTAAAGTGCTT | 8453 |
rs560273443 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083759 | TGTAATCCCAACACT[C/T]TGGGAAACCAAGGCA | 8453 |
rs560327725 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | CUL2 | GRCh38.p7 | 10:35107605 | TAGAAGACTTGGGCC[G/T]GGCGCGGTGGCTCAT | 8453 |
rs560329279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109483 | TGAATGACAAAGATA[A/G]TTTTGTCTAGTAATT | 8453 |
rs560351582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086921 | AAGTGGGAACAATAT[G/T]TGCTTATATGTCCAC | 8453 |
rs560384828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045041 | TTATATCACAGCTGA[A/G]TTAATATTCATGATA | 8453 |
rs560389584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122534 | TTACATTTATTTAAT[G/T]CTTATTTTGTGCCAG | 8453 |
rs560401661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115347 | CGGGCGGATAGCGAG[G/T]TTAGGAATTCAAGAC | 8453 |
rs560420252 | snp | A/C | 0.000171503 | 0.00925864 | intron-variant | CUL2 | GRCh38.p7 | 10:35025219 | AAAAAAAAAAAAAAA[A/C]ACACATTATTTTTAG | 8453 |
rs560431632 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118080 | CATTAGGCTTCATTC[G/T]CAGTGATGTACATTC | 8453 |
rs560434668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35073834 | TGGTCTCAAACTCCT[A/G]ACCTCAAGTGATCCA | 8453 |
rs560448259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121313 | GCTCACTGCAACCCC[C/T]GCCTCACAGGCTCAA | 8453 |
rs560449269 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009496 | GATTATGCAACCGAA[A/G]AAAGACAACTTTTGA | 8453 |
rs560535585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073241 | ATAACGGATTAGCAG[C/T]GATTTTACTCTGCAA | 8453 |
rs560598371 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35076882 | GGTGAAACCCCATCT[A/C]TACTAAAAATACAAA | 8453 |
rs560618877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086219 | ACAAGAAACAAGGCC[A/G]GGCACAGTGGATCAC | 8453 |
rs560621270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024090 | CCCACCTGTCTCAGC[C/T]TCCCCAAGTGCTGGG | 8453 |
rs560622424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093784 | AATTTTCTTTCAAAG[G/T]CCTGAGTTTCTTCAT | 8453 |
rs560657479 | in-del | -/T | 0.451234 | 0.14834 | intron-variant | CUL2 | GRCh38.p7 | 10:35027144 | CACTACTTTAGATAC[-/T]TTTTTTTTTTTTTTT | 8453 |
rs560665955 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018027 | CAGGCGTGGTGGCTC[A/G]CGCCTGTAATCCCAG | 8453 |
rs560670295 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049456 | TAAGCATATTAGGGT[A/G]TAAGAAAAGACCAGA | 8453 |
rs560698452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023628 | TTACTAAAATTACTT[A/T]AGGAGACACATTGAT | 8453 |
rs560712126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110939 | ACACATAACAGCCCA[C/T]AACAGAAGTCAAGAA | 8453 |
rs560714467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072735 | TTAGGAATTAGCTGG[C/T]TTCTGGAACAAAAGG | 8453 |
rs560736343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35090370 | CCGGCCGCCGCCACC[A/G]GCCCCGGAGACGCGG | 8453 |
rs560738632 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030523 | GAGTAACTGGGACTA[C/G]AGGAACACGCCACCA | 8453 |
rs560802299 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021444 | GTATGTATATATATA[C/T]ACACACACACATACA | 8453 |
rs560825129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104182 | CTGGGCGTAGTGGCT[C/T]ACACCTGTAATCCCA | 8453 |
rs560829237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111654 | ACACTTTGGGATGCC[A/G]AGACGGGTGGATCAC | 8453 |
rs560838781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35016673 | GGCTCACGCCTGTAA[C/T]CCCAGCACTGTGGGA | 8453 |
rs560858813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055289 | TACTGACAATACAAG[C/T]ATTTTAGGCAACAAC | 8453 |
rs560876219 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034531 | AGGGCAAACAGCTCT[A/G]CTTAAGAAGAGACAG | 8453 |
rs560880537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020239 | ACAACTGGCCTGGTC[C/T]GTTCAAAACAGTGTG | 8453 |
rs560895703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048314 | CAAAAATAAGACAAG[C/G]AGACCAGATAATCTA | 8453 |
rs560933545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35081710 | GCCAACCTGGGCAAC[A/G]TGGTGAACCCCGCCT | 8453 |
rs560934405 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032977 | TCACGGGACATTCTA[C/T]AAGCATTCAATTTAA | 8453 |
rs560936084 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068493 | CTCCTAGAGAAACGG[A/G]TGGGATTGTGAACTT | 8453 |
rs560941783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062355 | GCTGAAAATAATAAA[A/G]ACAGAGATTTACCAA | 8453 |
rs560955195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35098750 | AACCTGGCCAACATG[A/G]CGAAACCCCATCTCT | 8453 |
rs561062575 | in-del | -/AAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107907 | AAAAAAAAAAAAAAA[-/AAAA]GTAGAAGACCTGGTT | 8453 |
rs561063755 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090838 | CAATATGTTGGAATG[G/T]TGCTTTCAACAGAAG | 8453 |
rs561084117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076062 | GGTTAAAATGCAATA[C/T]AGCCATACAATAAAT | 8453 |
rs561175531 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35018421 | TTCCCTCTCAAGGAT[A/G]ATTAGTAACTCTGAT | 8453 |
rs561218379 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125052 | TATTTTTTAAAATCT[A/G]CAATAATCCTAACAG | 8453 |
rs561233277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020842 | TTTCAGGATTTTTCT[C/T]ACTCTGTCACATCTG | 8453 |
rs561307258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034499 | ACGTCTATACACAGA[C/T]ACTATCTTATAGATG | 8453 |
rs561320543 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042004 | AATGTTTTTAAATTG[C/T]GGTAAAAACATAGAT | 8453 |
rs561331651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078820 | AAAACTCCTGAATGA[A/C]GATTTATTTCAGTAC | 8453 |
rs561336214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35096141 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 8453 |
rs561346132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034905 | GTTATTTAAAAATGG[C/T]GAGCTTATTTTCCTG | 8453 |
rs561352254 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35027386 | CCTGACCTCATGATC[C/T]GCCCGCCTCGGCCTC | 8453 |
rs561369636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072815 | GAACATTTTTCTGGC[A/C]AATGTTTTAACAGCC | 8453 |
rs561419324 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35103300 | GCGCCCGCCACCAGG[A/C]CAAGCTAATTTTTTT | 8453 |
rs561482722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095458 | ATTAAATATATTTTT[A/G]TACGTATCAGAACAT | 8453 |
rs561505116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012513 | TGGCATTTTATGTGG[C/T]TCAAGCAGAGAAGCC | 8453 |
rs561516927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086120 | GCGCCTGTAGTCCCA[C/G]CTCGGGAAGTGGAGG | 8453 |
rs561528464 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107753 | CAGGCGTGGTGGCAG[A/G]CGCTTGTGGTCCCAG | 8453 |
rs561535518 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095526 | TTCTCTGATTTTGAT[A/C/G]TTTATGAAAATGCAA | 8453 |
rs561536716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057773 | AGTATTTTACAATCA[A/C]ATTTATTAACCACAT | 8453 |
rs561555968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120973 | GATATAATTCCCTTA[C/T]GTTTTATAGAGACTT | 8453 |
rs561572525 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35037829 | GCCTGGGCCACAGAG[C/T]GGGACTCCGTCTCAA | 8453 |
rs561574866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050539 | TCCTGTATTCACTAC[A/C]CAGTTTAAGAAATAC | 8453 |
rs561664462 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35057996 | CCAGCTACTCAGGAG[G/T]CTGAGGAAGGAGAAT | 8453 |
rs561704619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35022652 | AAATAAAATGAAAAA[C/T]GTTGATCAAAGGGGA | 8453 |
rs561730443 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043908 | CCCCATCTCTATAAC[A/G]AATTTTAAAAGTTGC | 8453 |
rs561747637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032571 | ATATAAGCCATAATC[C/T]GTACATCCAAAAATT | 8453 |
rs561748008 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35023681 | ACCAAGAATGTTTAA[A/G]CTCCCCCAGACAGAT | 8453 |
rs561771748 | in-del | -/AAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051612 | AAGACTCCGTCTCAA[-/AAC]AACAACAACAACAAC | 8453 |
rs561786647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35024245 | TGCTCAGTAAAGATC[A/G]ACTTATATAAGTAAT | 8453 |
rs561794873 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022320 | TTCTGATTCTAAATT[C/T]CCCCAAACACCACCT | 8453 |
rs561816853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35100479 | ATTTTTAAATGACCC[A/G]GGCCAGGCGTGGTGG | 8453 |
rs561822669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35114523 | GAGTAGCTGGGATTA[C/T]AGGCGCCCGCCACCA | 8453 |
rs561890551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014902 | ACTTTGTCAATTTCT[G/T]GGCAGCAAAAATAGC | 8453 |
rs561900844 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35104693 | GGAATCCAATATATA[-/T]TTTTTTTAACATGAA | 8453 |
rs561966879 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108838 | CCTGTGGACCTCTCC[A/C]TGGGACTTCCTGGAT | 8453 |
rs561976297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128098 | CCACCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 8453 |
rs561983164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35043233 | ATATTTTTGACAGCC[A/G]GACAGAGCAAAGTGC | 8453 |
rs562014028 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102229 | GACAGAGCGAGACTC[C/T]ATCTCAAAAAACAAT | 8453 |
rs562027088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030030 | TGCCCATGCTGCAAC[A/G]CAGTGGCTATTCATT | 8453 |
rs562034867 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35127010 | AGCGCTACTTTTGGT[C/G]CGGGGTCGGCAGGGA | 8453 |
rs562059834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030799 | TCAGGAGGCTGAGGC[A/G]GGAGGATCGCTTGAG | 8453 |
rs562076700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35113233 | AGGTGCGGTGGCTCA[C/T]TTCTGTAATCCCAGC | 8453 |
rs562100720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019348 | TTACTTCTTATTGAG[C/T]TCATTCTTTCATTGT | 8453 |
rs562193794 | in-del | -/ACACACACAC | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35021461 | CACACACACATACAT[-/ACACACACAC]AAATATGTAGTGATA | 8453 |
rs562201680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106824 | TGATGACTTTGAAAG[C/T]AGGCTGAAGGCTAAG | 8453 |
rs562205945 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35099447 | CTGAATACTGGGTTT[G/T]CTCAACATCAGTGTT | 8453 |
rs562206735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015516 | ATAAAAACAAAACAT[A/T]ATTTATAGGAATTTT | 8453 |
rs562232875 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35119080 | TTCCAATGCTCCTTG[A/C]GTGTTCCTTTTATCT | 8453 |
rs562245406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35112471 | AGAGCATGGCTCTCT[A/G]GCTAAGTTGAGGAGA | 8453 |
rs562276522 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103654 | TAATAGAGACGAGGT[A/T]TAAGTATGTAGCCCA | 8453 |
rs562310611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109630 | CCAGCCCCACAAACA[C/T]TTGCAGAACAAGATT | 8453 |
rs562313213 | in-del | -/TTAAT | 0.000798403 | 0.0199641 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008513 | ATACCAGGATAAGAC[-/TTAAT]TTAACATTTATAAAT | 8453 |
rs562331374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35077960 | AATAAAAGGGACATG[G/T]GGATTTATTACAATA | 8453 |
rs562378522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123487 | GGTAATAGTGGGAAT[A/G]AAAAAAAAAGGGATG | 8453 |
rs562381475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061484 | AAAAAAAAAATCACA[A/C]TTATAATGTAACCTA | 8453 |
rs562407390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35119821 | GCAGTCATCCCACTT[C/T]GGCCTCCTACCTCAA | 8453 |
rs562413975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053754 | TAATGCTGCCTCTTA[A/G]CCTGTTTATTTCCTT | 8453 |
rs562414093 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122024 | ATGGTATTTCCCATG[C/T]TGGAACACAGAACTG | 8453 |
rs562438963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012598 | AGCAGACCATGCCAC[A/G]TTAAGAGGATCTCCT | 8453 |
rs562472471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35018719 | TGTGAGCCGAGATCG[C/T]GCCATTGCACTCCAG | 8453 |
rs562496910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35094309 | GGTGCGATCTTGGCT[C/T]ACTGCAACCTCCGCC | 8453 |
rs562500719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35033981 | AAAGGCTGAGAGAAA[A/G]GAGAGTTAAAAAGCC | 8453 |
rs562526807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081168 | GACTTCAAGGTTACA[A/T]TAAGCTACAATGGCA | 8453 |
rs562536030 | snp | C/G | 0.00638156 | 0.0561253 | intron-variant, nc-transcript-variant | CUL2, MIR3611 | GRCh38.p7 | 10:35079608 | TTGACAGCAAAACTA[C/G]TAAGAATTTCTTTCT | 8453 |
rs562550564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103434 | GGTTCACGCCATTCT[C/G]CTGCCTCAGCCTCCC | 8453 |
rs562551289 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056293 | CAGTAGAACACAAAC[A/C]TGGAAAAGCAGCCTG | 8453 |
rs562552140 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077122 | TCAACTGATAAATGG[C/T]TAAAATGCAATATAT | 8453 |
rs562603656 | in-del | -/ACTA | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35026327 | CAGAAGTATGATCTG[-/ACTA]ACTAATAACTCCCAG | 8453 |
rs562613982 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103881 | AGGTTTACAATAAAA[A/T]GTAACCTCTCCAAGG | 8453 |
rs562636940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35013144 | AGGAGATCGAGACCA[C/T]CCTGGCTAACACAGT | 8453 |
rs562681344 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088925 | TCAGGCCTGTAATCC[A/C]AGCACTTTGGGAGGC | 8453 |
rs562709278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107648 | AGCACTTAGGGAGGC[C/T]GAGGCGGGTGAATCA | 8453 |
rs562725049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081543 | AAGCCCATCGTGTAT[C/G]AATACTAGACAAAGC | 8453 |
rs562782981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034403 | ATTATTGTGGCATAA[C/T]ATAAAAACTAAAAAT | 8453 |
rs562799362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116050 | ATTAAAGGATAAAAA[A/T]AAATATTATGGGCCG | 8453 |
rs562830135 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027918 | TTTAAAGAGTTAAAA[A/G]CTATAAATAGAAAAT | 8453 |
rs562869572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35087590 | CCCATACAACAGCCT[G/T]CTTCCCCCAACCTCT | 8453 |
rs562902505 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091112 | CAGTTTGAAGGGTTT[A/T]CCTCCCTTGGAGTTT | 8453 |
rs562903466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115267 | AATAAAATGGAGCAC[A/G]AAGAGAAAACAAGGC | 8453 |
rs562916556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045138 | TATGTCAGTAATAAG[A/G]TAACACTTCTTTAAT | 8453 |
rs562916596 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35052588 | GTTCACTGCAGTGTT[A/G]TTTGTAATAACAAAA | 8453 |
rs562918059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35087167 | ACCTGGTCATCTGGC[C/T]TCAGCTTCCCAACAG | 8453 |
rs562934393 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35034204 | TCCCAGCCTTGACAC[-/A]AAAATTCGATGCTTC | 8453 |
rs562943388 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35067958 | TAAAAAAATACAAAA[A/C]AATTAGCCGGGCATT | 8453 |
rs562952000 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030137 | GACTATTGGCACATG[C/T]CACAGCTGCTGGCTC | 8453 |
rs562953459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046032 | CATCCAGGCAATTAC[C/T]TTTACATACTAGAGT | 8453 |
rs562954000 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066408 | GGGTTCAAGCAATTA[C/T]CCTGCCTACCTCCTG | 8453 |
rs562962149 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092031 | GATCATAGCTCACTG[C/T]GGCCTCAAACTCCTG | 8453 |
rs562981440 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35038458 | TTGAATCTGGGAGGC[A/G]GAGGTTGCAGCGAGC | 8453 |
rs563014599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059476 | TTTTTTAGCAATAAA[A/G]TAATTTTAAATTAAG | 8453 |
rs563031930 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052274 | TTAATAGCATGAATG[G/T]GGGTTGGGGAGGCAA | 8453 |
rs563073726 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL2 | GRCh38.p7 | 10:35012709 | ATTTTAGGTTTCAAA[A/G]TAAATGGCAGTTAAT | 8453 |
rs563097743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066460 | GCGCCACCATGCCTG[A/G]CTAATTTTTTTGTAT | 8453 |
rs563134478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058742 | TTGCCTCACTGCCAC[C/T]ACCCCTCATGTTTTA | 8453 |
rs563137987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35071473 | GCAATGGCGTGATCT[C/T]GGCTCACTGCAAGCT | 8453 |
rs563172860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017861 | TCTACACTCTGTAAT[A/G]TTCCATACGTGTTTA | 8453 |
rs563183434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051701 | ATTCTTTAATGTTTA[C/T]TGTCCATTTTGGGTT | 8453 |
rs563193801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35010523 | CAATCAGTTTAAAGT[C/G]CCTCAAATGTACTGA | 8453 |
rs563197180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046047 | CTTTACATACTAGAG[C/T]CCTTCCCTGCCTCTG | 8453 |
rs563222182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036331 | TGAATATACTGTACT[A/G]TTCTACAGTAACTGG | 8453 |
rs563272303 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100779 | AAAAAAAAAAAAAAA[-/AA]GACCCTACAGTAAAA | 8453 |
rs563317098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050006 | ATTAGTTGAAAATCT[C/T]AAGAAATAATTGATT | 8453 |
rs563373561 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35055355 | AAATTCACTACACCA[A/T]AATGAAGGGTCCACT | 8453 |
rs563381716 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071829 | TATCCAGACAAGAAA[C/T]TTCACAGACTATTTA | 8453 |
rs563404357 | in-del | -/A | 0.0119304 | 0.0763076 | intron-variant | CUL2 | GRCh38.p7 | 10:35048918 | AAGTATTCCTCATAT[-/A]AAAAAAACTCCTTAT | 8453 |
rs563428849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084804 | ATTCTAGGGCTGATC[C/T]TGTCATCAATTTACT | 8453 |
rs563478130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35102080 | CCCCATCTCTACCAA[A/G]AATACAAAAATTAGC | 8453 |
rs563525487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094392 | AAGCACGTGCCACCA[C/T]GCCCAGCTAATTTTG | 8453 |
rs563549609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35031763 | GTCTTGCTCTGTTGC[C/T]AGGCTGGATTGCAGT | 8453 |
rs563624253 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35040557 | ATAAAAATGAGGCTC[C/T]AGACAGTAGGTTCCC | 8453 |
rs563657543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035439 | GCCCACCTCCCAGCC[A/G]CCCAAGCCCCTCTCC | 8453 |
rs563666416 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075185 | AGCCAACGTGCAAGA[A/G]GCACCAGCCTCGTGA | 8453 |
rs563710913 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125881 | GTCACCCAGACTGGA[C/G]TGCAGTGGAACGATC | 8453 |
rs563792901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35067182 | GACAACAGTATGCCT[C/G]GGTTTAAATGGTGGG | 8453 |
rs563803763 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078774 | TGTAAATGGCTAACC[A/G]CTTACTATTTTGATT | 8453 |
rs563848510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35034960 | GACACCCTCCGTATG[A/G]CTAAGCAGCAGCCTA | 8453 |
rs563885594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35033098 | ATACTAGAATTCTGA[C/T]CTTGAAACTGCCTAA | 8453 |
rs563915887 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077340 | ACAAACAAAAAAAAC[A/C]AACAAAAATTAGCCG | 8453 |
rs563943910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073717 | TGAAGTGATTCTCCA[C/G]CCTCAGCCTCCCAAG | 8453 |
rs563991606 | in-del | -/CTGGGAG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088430 | GAGAATTGCTTGAAC[-/CTGGGAG]TGGGAGGTTGCAGTG | 8453 |
rs563993438 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125183 | ACTGCATGGTTTTTA[A/G]GTCTATTACATCTTA | 8453 |
rs564002642 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080139 | GGGAAGTGGAATACC[A/G]TATTAACTTGGCATT | 8453 |
rs564061916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038297 | TTGGGAGGCTGAGGC[A/G]GGCGGACCACAAGGT | 8453 |
rs564164414 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35115300 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 8453 |
rs564183253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115850 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 8453 |
rs564196547 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35017935 | TGCTTCCTAAAGCAC[C/G]AAGTTGTGGTTTGAC | 8453 |
rs564229486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093567 | GGGAGGCTGAGGTGG[A/G]AGAATCACTTGAACC | 8453 |
rs564250224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043303 | ATCTAGAGGCTTCAA[C/T]AAAAGTCTAAGGTGC | 8453 |
rs564283437 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114749 | AAGTAGAGGAAAACA[C/T]GAGCATGGTGAGGAG | 8453 |
rs564334424 | in-del | -/TTTAATCTGAATGTTTTCATAAAAATGAAAAACA | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35017341 | GTTTTCATAAAAATG[lengthTooLong]TTTAATCTGAATGTT | 8453 |
rs564336397 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35055994 | TGTGCCCTGAACCCC[-/AG]AGGAGTTAGCCTTCA | 8453 |
rs564395262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058469 | CCCATAACACAAGGA[A/C]AGGTCCATTGTAACT | 8453 |
rs564405436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086746 | TAAATAAATAAATGA[A/T]CTTAACAAGGGCAGG | 8453 |
rs564407273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107447 | ACCTCCAAAAAGATA[A/C]ATGCCTAAGTGTTGC | 8453 |
rs564428602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032622 | GCATTGCCGGTAGTT[C/T]GTTAATATTTTCATG | 8453 |
rs564434981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35051143 | ACAGGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 8453 |
rs564439701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120763 | TAGCCTGGCATGGTG[A/T]TGCACACCCGTAGTC | 8453 |
rs564448310 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079526 | TTCCACCCACCAGTG[G/T]AATGCCTTTTCCAAA | 8453 |
rs564461856 | in-del | -/CTTAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070123 | TTTCCTTATCCGTTA[-/CTTAT]CAGTCAAGTAATTAT | 8453 |
rs564469048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065751 | GTAATGCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 8453 |
rs564475558 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35106976 | GTTGTTTTTTTGTTT[G/T]TTTGTTTTTTTGTTT | 8453 |
rs564512159 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009434 | AGATTTCCTAAGACT[C/T]AGGGAAGGCCACAGA | 8453 |
rs564545653 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071734 | TTTAAAGCACTACAT[A/G]ATTAAATAGCATGAT | 8453 |
rs564553764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35100677 | TGAAGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 8453 |
rs564559123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127799 | CTTTTTAGGGCCATC[G/T]GGTAAGGTTTCCAGA | 8453 |
rs564616283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35092968 | CTTCCCCAGTTGCTC[C/T]TATAAATAACATCAG | 8453 |
rs564661118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030881 | AAAAAGAAAAAGGAA[A/G]AAAGGAATGCATATT | 8453 |
rs564668695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045248 | AACTACAAAGTCTTA[A/G]TCATATTAAGACATG | 8453 |
rs564681177 | snp | A/T | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074121 | GAGGATACAGTGGAC[A/T]AAACAAAGTTCTTGA | 8453 |
rs564684139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078032 | ATTTAAAAATCCTAC[C/T]CCTCATAAACATTAA | 8453 |
rs564689247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072076 | TGGGGAATGAGGCAG[C/T]ATGCAAGGGAATATG | 8453 |
rs564701855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104060 | TGGAAAACGTTAAAC[A/G]TAGTCCATTAGCTGT | 8453 |
rs564726101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072597 | ATGGCCTTCATCTCC[C/T]GACCTCGTGATCCGC | 8453 |
rs564727954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065179 | CTTATGAAGAACACC[G/T]ACGAAAATGAGATTT | 8453 |
rs564771881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116718 | AAGCCTGTAATCCCA[G/T]CATTTTGGGAGGCCA | 8453 |
rs564792927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35047593 | CCAACCTGGGCAACA[A/G]AGCAAGACTGTCTCA | 8453 |
rs564813572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35097030 | GGCCAGGCTGGTCTC[A/G]AACTCCTGTCTCCAC | 8453 |
rs564833710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35117242 | TGCGGAATTCACGAA[A/G]GCTGGTGTGGACTGG | 8453 |
rs564835587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109778 | AATCTTGTAGGACTT[C/T]ATCAACTTTGATAGA | 8453 |
rs564872722 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089415 | TTTACTACGAAGGTA[C/G]GCTTGGCCAGGTCTA | 8453 |
rs564936743 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052824 | AGTGTGAACCTGGGA[C/G]GCAGAGCTTGCAGTG | 8453 |
rs564937859 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059214 | AGAGGACTGACTCCA[A/G]TTTCGTAAGAATTTC | 8453 |
rs564958951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055236 | AACAGTCACCACCTA[A/T]AACTATTCATTTGAA | 8453 |
rs564979559 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35104745 | CAAAGACTTTTCTGG[G/T]GGGGGGACAGTCTTG | 8453 |
rs564995550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048198 | ATGCCTTAGTTTCCT[C/T]AACTTTAACATGCAA | 8453 |
rs565019041 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35089340 | ACAGTGTTTTGAATG[G/T]TTTTAAGCGATTATT | 8453 |
rs565021387 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35019484 | TGGGAAGACACGACA[G/T]GGGAAAGGAAACTTC | 8453 |
rs565040251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35097631 | TGTGATCATCCTCCC[A/C]AAACCCCTAAGCCCA | 8453 |
rs565119243 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35026355 | TCCCAGGGATATCAA[-/T]AAAATTCAATCACTA | 8453 |
rs565120454 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35124958 | AGAATTAACTATCAC[C/T]TAGGTGAGGAGCCCC | 8453 |
rs565128228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059576 | TATGCACTGGGAAAC[C/G]AAACAACTTGTGTGA | 8453 |
rs565133089 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050157 | AAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAT | 8453 |
rs565175604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35028141 | AATAACCTTGGATTA[C/T]AGTCTGCCCCATCCA | 8453 |
rs565205081 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082929 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACTTGAG | 8453 |
rs565212575 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35020166 | AATAGAAAACAAATT[A/T]AAAAAAAAAAAAAAT | 8453 |
rs565257327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124406 | GGACAAGAGACTCCA[C/T]GTCTACATATAAAAA | 8453 |
rs565277878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081653 | AATCCCAGCACTTTG[C/T]GAGGCCAAGATGGGC | 8453 |
rs565306396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108826 | TTCCATGCAGTCCCT[G/T]TGGACCTCTCCATGG | 8453 |
rs565327969 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35046643 | ACACTGGTAATCCCA[A/G]CACTTTAGGAGGCTG | 8453 |
rs565334362 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35015060 | TTGGGAAAGACAGGT[A/G]GATCACCTGAGGTCA | 8453 |
rs565365387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039794 | CGGGAGGTGGGGGTT[A/G]TAACGAGCCAAGATC | 8453 |
rs565395001 | snp | C/G | 0.00165426 | 0.0287122 | intron-variant | CUL2 | GRCh38.p7 | 10:35023594 | TTCTTATACACCACT[C/G]GTTGTTAAAATGAGC | 8453 |
rs565402112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034485 | GCTCCTGAACAGTGA[C/T]GTCTATACACAGATA | 8453 |
rs565403252 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023233 | ATTTTTATGTGTCAA[C/T]TGTATCTTATCAAAG | 8453 |
rs565412613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35052691 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 8453 |
rs565422854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102665 | CGAGGCGGGTGGATC[A/C]TGAGGTCAGGAGTTC | 8453 |
rs565430069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35112819 | ATCAAGATTAAAGGC[C/T]GTTCTTTACTTACAC | 8453 |
rs565443185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011185 | ACAAGTGTGCCGCCA[C/T]AACTGGCTAATTTTT | 8453 |
rs565445438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018562 | TGAGGTCTGGAGTTC[A/G]AGACCAGCCTGACCA | 8453 |
rs565482999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011704 | AATTGTGAGTGAGTA[C/T]GATTCTGATTAAGTA | 8453 |
rs565512397 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090502 | AGGGGCGGTAGGGAG[G/T]GGGGGAAAGGGGAGA | 8453 |
rs565522082 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35038248 | AAAATCAGAGAGGCC[A/G]GGCGCAGTGGCTCAC | 8453 |
rs565584552 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35048963 | TGAGCACAGATATAG[C/G]TGGAGTGGCCATTAT | 8453 |
rs565625466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35083227 | GTCAGAAAATAGCAG[C/T]TATAAATAAAGGGGA | 8453 |
rs565629522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120086 | GGGGACTGCATGTAT[C/T]ATCAAGCTATGGTAT | 8453 |
rs565634074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35077434 | CCTGAGAGGTGGAGG[C/T]TGTGGTGAGCCAAGA | 8453 |
rs565670752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071619 | TTCACTGTGTTAGCC[A/G]GGATGGTCTTGATCT | 8453 |
rs565678010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072198 | ATGAATTATGGAGTA[C/G]AATATAAAATTCACA | 8453 |
rs565680799 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022755 | GTAAACTTGAAAATT[A/T]CTGTGACAAGGCTGG | 8453 |
rs565686608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084152 | TGTGGTGGCAGACAC[C/T]TATAGTCCCAGCTAC | 8453 |
rs565713017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062492 | ATTTACTAATTACGA[C/G]ATGCTGAGCAAGTAA | 8453 |
rs565714710 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35055393 | TACAGACAAATTAAA[A/C]ACGAAGACAACCAAA | 8453 |
rs565726762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030353 | TCTCTAATCTTGAAA[C/T]ATAAAAAGCTCATTA | 8453 |
rs565753800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063162 | AAAAAACATTTCTTT[G/T]TGTGGTTTAGCTTAT | 8453 |
rs565792501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015111 | CCAGCCTGGCCAACA[C/T]TGTGAAACCCTATCT | 8453 |
rs565820176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35064259 | CTAACTAAAGATGCA[G/T]ATACAAACTGGAAAT | 8453 |
rs565829822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035102 | ATCTTTCAAAACAAT[A/G]AAGTCAAAGGAAAGG | 8453 |
rs565855940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048543 | GAATTCCAAGTCAAA[A/G]GAAAAGTTAGTATAT | 8453 |
rs565859992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35077075 | CACTGTAGTATTATT[C/T]ATAAAGGCCCTTGAA | 8453 |
rs565913539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35033553 | CATCCTGGCCAACAC[A/G]GTGAAACCCCGTCTC | 8453 |
rs565934432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069494 | TGCAGTGAGCTATAG[C/T]CACACCACTGTACTC | 8453 |
rs565945785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035851 | AACCACAGCTGCCAA[C/T]AGCAGAGAGTTCCTT | 8453 |
rs565971194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035111 | AACAATAAAGTCAAA[A/G]GAAAGGCTCCACGCT | 8453 |
rs565975216 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064255 | CAGCCTAACTAAAGA[A/T]GCAGATACAAACTGG | 8453 |
rs565990134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35029423 | TCAGGCATCCATTTA[C/T]GAATCATTTGTATCA | 8453 |
rs566096845 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124677 | AGTTTTCAAGAGGCA[C/T]GATACTAACACATTT | 8453 |
rs566106233 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075562 | CCTTTTAGTTTCCTT[G/T]TGAGTTCCACTCTTG | 8453 |
rs566147106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051429 | CCATCCTGGCTAACA[C/T]AGTGAAATCCCGTCT | 8453 |
rs566162361 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35105021 | GGCGTGAGCCACCGT[A/G]CCCAGCCCAAAGACT | 8453 |
rs566167209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35014300 | CTGTGACCTGGGGTG[A/G]TGGTGAAAACATTTA | 8453 |
rs566176459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098276 | AGGAAAAGCCCACTA[C/T]TTGAGATAGATAACT | 8453 |
rs566180847 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35092728 | ATAGGCCAACTTAAT[C/T]TGGGGAGGAAGTTAG | 8453 |
rs566186049 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047645 | CATAAAGGCCGGGTG[C/T]GGTGGCTCACTCCTG | 8453 |
rs566192313 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35027560 | ATTACAGCTTTAATT[C/G]CACAGTTTTGAGATA | 8453 |
rs566204591 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35117996 | CCTATCAACATCCTG[C/T]ACCAGCATGTTCTAC | 8453 |
rs566229470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019909 | TATCATCCCTCAGAC[C/T]GTCTGCTAAGCTAAC | 8453 |
rs566251787 | in-del | -/CAAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046927 | CAAAACAAAACAAAA[-/CAAAA]ACAAAAAACTGGGTT | 8453 |
rs566265511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076315 | TGAGGAAAATGCTCT[A/G]AAGTTGATTGTCATG | 8453 |
rs566278341 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35062237 | GTACAGCATACTAAT[-/A]AAAAAAACTGGTCAC | 8453 |
rs566305673 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35116917 | AGTCGAGACTGTGCC[A/C]CTGCACTCCAGCCTG | 8453 |
rs566320871 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083871 | GGCTGAGATATTTTT[A/T]AAAATTTACATATGG | 8453 |
rs566326953 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075391 | AAGAAAAAGGACCAC[A/G]GTCACACTATTTCTA | 8453 |
rs566349173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35028524 | AGCTTTCTTCTGATA[C/T]CAACATTTTTATAAT | 8453 |
rs566362886 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35049830 | AACATTTCCTCAAGG[-/T]TTTTTTTTAACTAAA | 8453 |
rs566368767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35117517 | TTACAGGCGTGAGTC[A/G]CTGCAACTGGCTTTT | 8453 |
rs566369924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032689 | TTACAAAATATCTAT[A/G]TATCCTGTTGCTATT | 8453 |
rs566385649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35088334 | CCAACATGTTGAAAC[C/T]CAGTCTCTACTAAAA | 8453 |
rs566438531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108316 | GAAAAAATTAGTGGG[C/G]TGTTGTGGTGTGTGC | 8453 |
rs566486827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094468 | TTGAACTCCTGACCT[C/T]AGGTGATTTGCCCGC | 8453 |
rs566516852 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35044403 | CAATGACTTATCAAT[A/C/T]GATATTATATAATAA | 8453 |
rs566519860 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108977 | CAGCACTTTGGGAGG[C/T]CGAAGTGGGTGGACC | 8453 |
rs566521677 | in-del | -/T | 0.438526 | 0.164189 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127854 | CATTATTAAACATAC[-/T]TTTTTTTTTTTGAGA | 8453 |
rs566539475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093981 | TATTTTTAAAATTAA[C/T]CAGTAATTTAAAAAT | 8453 |
rs566555384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037209 | GTATATGGTATCTTG[A/G]GGTAGTGATCAAATT | 8453 |
rs566628427 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35032074 | TATAATTTTTGACAT[C/T]GAACAAGTACTTTAA | 8453 |
rs566645708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073008 | AGCGGGTAGGATGGC[A/G]GCCGCACCACCAGCC | 8453 |
rs566689263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106481 | CCGGCCACCACGCCC[A/G]GCTAATTTTTTTTTT | 8453 |
rs566697162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35114316 | TGATTCTCCCTACCT[C/T]GGCCTCCTCAAGTGC | 8453 |
rs566704222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35093073 | GAACTGGTCCTATGG[C/T]CCCACCCAGAGGCAG | 8453 |
rs566704736 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35023898 | GGAGTGCAGTGGCAC[A/G]ATCATGGCTCACTGC | 8453 |
rs566735042 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011645 | AAAAAGGATTACAGG[C/T]ATGAGCCACTGTGCC | 8453 |
rs566746762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050725 | TTATTTTTCCACTCT[A/G]CTGCTGATGACTGCT | 8453 |
rs566782463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043330 | GTGCAATAAGGGCTA[A/G]GAGCTTAGAACCACT | 8453 |
rs566821687 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008886 | GCCTTACTGAAGTAT[C/T]ATAAGTGAAATAATT | 8453 |
rs566851355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042897 | CTGGTGTCTGGGGGT[A/G]TGCAGGGCAGTCTTG | 8453 |
rs566885280 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35085666 | GAATGGTGTGAACCC[A/G]GGAACCAGAGACACA | 8453 |
rs566898746 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072610 | CCTGACCTCGTGATC[A/C]GCCCACCTCGGCCTC | 8453 |
rs566908605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128377 | TTTGCCGGGCAGATG[A/T]GGGTGTACCTTTCCC | 8453 |
rs567028675 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35028621 | TATGACATTCTTCTT[A/G]GCATTTTAGTATCAA | 8453 |
rs567046411 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35065301 | ATCCCAGCACTTTGG[G/T]AAGCCAAGGCGGGCA | 8453 |
rs567083483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057468 | CCAGTCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 8453 |
rs567091355 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35103551 | GATGGTCTCGATCTC[C/G]TGACCTCGTGATCCG | 8453 |
rs567108757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050235 | CTGAGGCAGGAGAAT[G/T]GCTTGAACCTGGGAG | 8453 |
rs567124687 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35027168 | TTTTTTTTTTGAGGC[A/G/T]GAGTCTCGCTCTATC | 8453 |
rs567131262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099692 | GAGGCACGAGAATCG[C/T]TTGAACCTGAGAGGC | 8453 |
rs567158109 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059400 | GCAGCCATCAACACC[A/G]AGGTAAGAAGACTGG | 8453 |
rs567201314 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35103963 | AATGCAAATAAAAAA[A/C/T]GCTAGTGCCTGGCAT | 8453 |
rs567206798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35089706 | ACCCTAAGGGTTGAG[A/G]CAAGAAGTCTAGCAT | 8453 |
rs567263404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047763 | CTCTACTAAAAATAC[A/G]AAAATTAGCAGGGCG | 8453 |
rs567264450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117687 | AAGTCCTTCTGCTAC[A/G]TGTGAGTGGTGTATT | 8453 |
rs567276028 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35025637 | ATTAGACACAAATAC[A/G]AAGTTTTAGGGTATA | 8453 |
rs567284473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35040668 | GGGTCTAGAGCAGCA[A/G]TCCCTAACCTTTTAG | 8453 |
rs567323802 | snp | C/T | 9.89446e-05 | 0.00703296 | missense | CUL2 | GRCh38.p7 | 10:35035192 | CCTGAGTAAGGTTGC[C/T]GGTTGCTCGAAGGCC | 8453 |
rs567379908 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117238 | GAATTGCGGAATTCA[C/T]GAAGGCTGGTGTGGA | 8453 |
rs567414815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109258 | CTCAAAAACAAAACA[A/C]AACACAACAAAAAAC | 8453 |
rs567416617 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35076419 | GTGACGTATATCTCA[A/C]TAAAGCTGCTATACA | 8453 |
rs567419434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047033 | TAGGTGAGAAGAAGC[A/G]TATCTTGATAAAATT | 8453 |
rs567427167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35110067 | GTGGTCTCAGCTACT[C/T]GGGAGGCTGAGTTAG | 8453 |
rs567427189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103128 | AACTCCATCCCAAAT[C/G]TACTTGACTCAAAAA | 8453 |
rs567427818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096467 | TACAACAAAATAGCA[C/G]CTGGGTATGGTGGTG | 8453 |
rs567452598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35061812 | AGTGTCTCACTATAT[C/T]GCCCAGGCTGCTCTT | 8453 |
rs567523289 | snp | A/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128333 | AACACTGTGGCTTAC[A/G]TACGTGACTCAGTTT | 8453 |
rs567540065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074894 | TTAGAGTACTTCATC[A/G]CTCTGAACTGTAATT | 8453 |
rs567566851 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120291 | GCTGAGTTGGAGGAT[C/T]GCTTGAGCCTGGGAG | 8453 |
rs567591020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35097053 | GTCTCCACATGACCC[A/G]TCCACCTCAACCTCC | 8453 |
rs567638172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019093 | AGTTTGGAAAATGTA[A/C]GTAAAACATTACATA | 8453 |
rs567668259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081377 | AGCTTGAAGTTTAAC[A/G]CCATTTTCACTTGCT | 8453 |
rs567673098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012212 | GTATGCACCACAATA[C/T]TGAGCAAATTATATA | 8453 |
rs567701077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072403 | AGACAGAGTCTCACT[C/G]TGTTGCCCAGGCTGG | 8453 |
rs567722873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35061189 | ATAATAGAGAATAAA[C/T]TGAGCCGAGCGCAGT | 8453 |
rs567737584 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35116799 | CATCTCTACTAAAAA[C/T]ACAAAAGAATAGCTG | 8453 |
rs567793996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038645 | GCCTTTATTCCTACT[G/T]TTTATCAGGAATTCT | 8453 |
rs567807170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106535 | GATGAGGTTTCACCG[C/T]GTTAGCCAGGATGGT | 8453 |
rs567819384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107068 | CAAGCTCCACCTCCC[A/G]GGTTCACACCATTCT | 8453 |
rs567832949 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35090265 | GCCCCGGCGAGGAAG[C/G]TGGGCGGAGGCGGCG | 8453 |
rs567876945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35123663 | AGGATGACAAGGAGC[C/T]GAAAAGTGCCATTAA | 8453 |
rs567901836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122799 | TGCGCCACCATGCCC[A/G]GCTTATTTTTGTATT | 8453 |
rs567914257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039423 | TTCAGAACAGGTGAT[C/T]TCTGTTATGAATAAC | 8453 |
rs567928236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35033364 | TATTAGTAAATTTTT[A/C]CTCAAGGAAATTATG | 8453 |
rs567967318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025622 | TAGCTTCCACATTCA[A/G]TTAGACACAAATACG | 8453 |
rs567984668 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075024 | CATATTATACACACT[A/G]CTTGTAAATTAGTTT | 8453 |
rs568014924 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35083079 | GGAGAATCGCTTGAA[A/C]CCAGGAGGCAAAGGT | 8453 |
rs568024984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065876 | AAAGAAAAAAAACAC[A/G]AAATAACTAGGTCAG | 8453 |
rs568052669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35114165 | CTGACCTCGTGATCC[A/G]CCTGCCTCGGCCTCC | 8453 |
rs568059434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078312 | TTTTTTTTTTTTTTT[C/T]GAGATGGAGTTTCTG | 8453 |
rs568067863 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35065369 | CTCACGCCTGTAATC[A/C]CAGCACTTTAGGAGG | 8453 |
rs568082271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35113534 | AAAAAAAAAAAATTC[C/T]GCAAGATCCAGTAAC | 8453 |
rs568083151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016797 | CCAGGCATGGTGGCT[C/T]ATGCTTGTAATCCTA | 8453 |
rs568110083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055471 | GGCGTCGGGGCTCAC[A/G]CCTGTAATCCCAGTG | 8453 |
rs568110717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057552 | CAGCTACTCAGGAGG[C/G]TGAGGCAGGAGAATC | 8453 |
rs568139158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35015993 | AAATCAAACTATAAA[C/T]GGCACATGGCACCAA | 8453 |
rs568148491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048685 | TCAGTATTGCCTTTC[C/T]TCTCCAGCTCTCTAT | 8453 |
rs568161338 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051871 | TGCTCGGTTTCTTTA[C/T]TGTGTTTTGGTAAAA | 8453 |
rs568179074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084933 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCGT | 8453 |
rs568202157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35084219 | GAGGCAGAGGTTGCA[A/G]TGAGCTGAGATCGCG | 8453 |
rs568224542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119292 | GGTTCAGTTATTTTA[A/T]CTTAAAAAGGAGGTA | 8453 |
rs568246778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037114 | CAAGGTTATGAAGAT[A/G]TTCTTCTATATTATC | 8453 |
rs568291148 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35036622 | TATGTTTATTGGCCA[A/T]CTGGGTATCTTCTAT | 8453 |
rs568310769 | snp | C/T | 0.0166325 | 0.0896639 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126855 | CATTTCATTGTTGGA[C/T]TGTGGCGCTTCACTC | 8453 |
rs568322857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127272 | GGTGGAGGCAGGAGG[C/T]GGAGCGGAGCCGGGT | 8453 |
rs568326858 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052679 | GGCAGGCGGATCACA[A/G]GGTCAGGAGATCGAG | 8453 |
rs568342073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35030610 | CTGGTCTTGAACTAC[C/T]GAGCTCAAACAATCT | 8453 |
rs568350465 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059081 | GCTTCTTATGGATGA[A/G]AAAGTGGTTTCTTGA | 8453 |
rs568366060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120163 | CTAAAAACTCAGATA[C/T]AGAAGTCCCTGAGTG | 8453 |
rs568381479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35022304 | ACTCCAGCCACAGGT[C/G]TTCTGATTCTAAATT | 8453 |
rs568381861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35031271 | TGAATGAATTTCTAG[A/G]ACAATACCACATTAA | 8453 |
rs568395698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35021236 | TCCATGTTAATCTGC[A/G]GCATGTTTTCTTTCT | 8453 |
rs568427062 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064832 | ACAGGTATGAGCCAC[C/G]GCTCAATATATCCAC | 8453 |
rs568429229 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100320 | GATAAATCTGCTGGG[C/T]CTTTTATAACCTGCA | 8453 |
rs568429858 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098448 | AAAATACCCCAGGCA[A/C/T]GGTGGCTTACACCTG | 8453 |
rs568430770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041641 | CTCTCAGGCTCAAGT[G/T]ATCTTCCCACCTCAG | 8453 |
rs568431823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35105686 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 8453 |
rs568432925 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066892 | AAGACCTTCTTCTTC[C/T]AACACTTGTGAAAAG | 8453 |
rs568440959 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090593 | AACACACACCCTCCG[C/G]TCTCCTTCTTCCGCT | 8453 |
rs568446118 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097908 | AGGTTGCAGTGAGCC[A/G]CAATCATGCCACTGC | 8453 |
rs568511460 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096155 | CAGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 8453 |
rs568546960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070329 | ATTAAATGGTTTTCT[G/T]TTGGTCTAAAGAACT | 8453 |
rs568547741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042210 | TCTATCTTCTGTCCT[C/T]TTGAATTTGTCTGTT | 8453 |
rs568548096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098844 | GAGGCTGACGCAGGA[A/G]AATTGCTTGAACCTA | 8453 |
rs568568710 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036515 | CATAATATATCCCAC[A/T]TAGCGGTCAGTGCCA | 8453 |
rs568585650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35046240 | CTCATTTCCTTGGCT[C/T]GGGTCACATGCGTGA | 8453 |
rs568643824 | snp | A/C/G | 0.000119519 | 0.00772967 | intron-variant | CUL2 | GRCh38.p7 | 10:35013824 | AAAAATAAAACATTT[A/C/G]TATTTATAAAAACCA | 8453 |
rs568663532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35070852 | CTTATCCTGCTTTCA[C/T]TTATCACGACCTCTT | 8453 |
rs568663795 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35121607 | AGCCCTTTTCCAATA[G/T]GAAATATATTGACAA | 8453 |
rs568665528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35025298 | AAACCATTCATATTA[A/G]AAGAGACATTAAAGC | 8453 |
rs568698230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063212 | TATATATGACAAGAT[A/G]GAATACATAACCATG | 8453 |
rs568726412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35111844 | GCAGTGAGCTGAGAT[C/T]GCATCATTGCACTCC | 8453 |
rs568729527 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35107124 | GGACTACATGCGCCC[-/A]CCACCGTGCCCGGCT | 8453 |
rs568756968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014375 | TGCTCAGGGGAAAAC[C/T]GTTTAGGCAATTTTT | 8453 |
rs568774565 | snp | G/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35105199 | GGGAGGCCGAGGCGG[G/T]CGGATCACGAGGTCA | 8453 |
rs568801813 | snp | C/G/T | 1.86291e-05 | 0.00305192 | missense | CUL2 | GRCh38.p7 | 10:35011916 | CTATAGCAGCTTGGA[C/G/T]ATACATTTTCCGGTC | 8453 |
rs568804739 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35018147 | AAAAAACTAGCAGGG[C/T]GCAGTGGCGGACACC | 8453 |
rs568896583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128416 | AAGATCTAGATTGAA[C/G]AGTGAGAGGTCCGCT | 8453 |
rs568905705 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053558 | CCCTATTAACAATGA[C/T]TGCAAAGAATACTTT | 8453 |
rs568907505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038704 | ATATATAAAAATGTA[C/T]AAACACAATTTCCCA | 8453 |
rs568915774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35087414 | AGAAATTTTTTAACC[A/G]CTATATCCACACATC | 8453 |
rs568922040 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115813 | CAGAAGGATGGGTTG[A/G]ACCTGGGAGGCTGAG | 8453 |
rs568956838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095523 | TACTTCTCTGATTTT[G/T]ATCTTTATGAAAATG | 8453 |
rs568969912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121870 | ATCTTATAGTTTTAA[A/G]TAATTCAGGAGCTTG | 8453 |
rs568993168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35115432 | AGGCATGCTGGCAGG[C/T]GCCTGTAATCCCAGC | 8453 |
rs569013973 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35059951 | ACTAAAAGTTCACAA[A/G]TAGCACCAATTTAAT | 8453 |
rs569031401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35122692 | GCCCAGGCTGGAGTG[C/T]AGTGGCACAATCTTG | 8453 |
rs569053976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059134 | ACGGTATGAACATTG[C/T]TGAAATGACAACAAA | 8453 |
rs569056655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073979 | AAGGTCACAAAGCTA[C/T]GTAATGGTGGCATCA | 8453 |
rs569066497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35107837 | CAGTGAGCCTAGATC[A/G]CGCCACTGCACTCCA | 8453 |
rs569085346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35011455 | AAACCCTGTCTCTAC[A/G]AAAAATACAAAAATT | 8453 |
rs569125473 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35010742 | AGTTTTCCCCAGCAG[C/T]CCCTAGGCCAGGATA | 8453 |
rs569235234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032717 | ATTCCAAGATATTCT[A/G]TAACTCATTATCGAA | 8453 |
rs569244500 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079180 | CAGTAAGATATAACA[A/T]TTATAACAATATGCT | 8453 |
rs569278352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35012617 | AGAGGATCTCCTCAC[A/G]GCGTTTCAAAGACAA | 8453 |
rs569280093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032304 | AAATGCCAAACTATA[C/T]ACAATGTAGATAATT | 8453 |
rs569357005 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35114916 | TAGAAACTATCTAAA[A/C]TGGAGCACAAAGAAG | 8453 |
rs569369898 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126640 | ACAACAGCCGTTACT[A/C]TGGCTGACAAGTCAT | 8453 |
rs569426247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35021318 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 8453 |
rs569432319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119150 | CTACACATAGCAGCC[A/G]AACAAATAACATTCA | 8453 |
rs569503861 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050904 | CTAAATCAAGCCAAA[G/T]GATTTTCCAATTTAT | 8453 |
rs569543602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037716 | GGTGTGGGGGCGGAT[A/G]CCTGTAGTCCCAGCT | 8453 |
rs569576520 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35085724 | AAAAAAAAAACTGAT[A/T]GTGCATATGAAACAT | 8453 |
rs569577555 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35043979 | AGGCTGAGACAGGAG[C/G]ACCACTTGAGCCTGG | 8453 |
rs569631486 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021248 | TGCAGCATGTTTTCT[G/T]TCTTTCTTTCTTTCT | 8453 |
rs569639023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35076968 | GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGGC | 8453 |
rs569658715 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090471 | GTCCAAGGCCGCCGC[C/T]GCTCCCCGGCGGGAC | 8453 |
rs569680222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035672 | AGTACTCCATTATGT[C/G]GATATAATTTCTTAA | 8453 |
rs569699863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069337 | TGAGCCCAGGAGCTC[A/G]AGATCAGCCTGGGCA | 8453 |
rs569736479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35069888 | CACACAAGTAGCAAC[A/G]CTTTTTCAACTTTTA | 8453 |
rs569774902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35087674 | AATTGACCCATCCCA[A/G]CTGCATGCTCATCCA | 8453 |
rs569808125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103569 | ACCTCGTGATCCGCC[C/T]GTCTCGGCCTCCCAA | 8453 |
rs569902691 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026255 | GGAATACTTCAGATT[C/G]CCTGCTTAGTTCTAA | 8453 |
rs569903323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047813 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 8453 |
rs569937768 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35040734 | CACAGACGGAGTGCG[C/G]GCGGCATTGGTGGGG | 8453 |
rs569976879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35041421 | TATAAGAGGAACGCA[A/G]CAAGGAGGCAGGAAG | 8453 |
rs569982236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110165 | ATTCTGTCTCAGAAA[C/T]AAAACAAAACAACAA | 8453 |
rs569986972 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063371 | AATTACCCAGAATCC[C/T]ACAAAATAAGGTTTA | 8453 |
rs570013828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053957 | CTTCTTTCACAATCA[A/G]CATAATTTTCCATAT | 8453 |
rs570091473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062426 | ACACTATCCAGAGGA[C/T]GTAGGAGCACATTTT | 8453 |
rs570093317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065974 | CAAAAACTCCTCTAT[C/T]TATGAACTTTCCAGT | 8453 |
rs570119188 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081446 | AGAAACTGACATTTT[A/T]AAAAAAAACTATTCT | 8453 |
rs570129865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066590 | AGGCGTGAGCCACTG[C/T]GCCCCGCCAGATTTG | 8453 |
rs570130276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111141 | ATCAGTTTTTGGCCT[A/G]AGCAACTTGGTTGCC | 8453 |
rs570188877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35088609 | TTAATAAATATCTGT[C/T]AACTGCCAGACAACG | 8453 |
rs570200018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034216 | ACACAAAATTCGATG[C/T]TTCTATGCCCAATGT | 8453 |
rs570238197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35081771 | GGTGGCATGCACCTG[C/T]AGTCCCAGCTACTAG | 8453 |
rs570291526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116278 | AACCTGGGAGGTGGA[A/G]GTTGTGTAGCAAGCT | 8453 |
rs570293396 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029864 | TGAATAAAAACCACC[C/T]ATCTAGGAACAATAA | 8453 |
rs570310904 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35123923 | ACTGTTTGAGGACAG[C/T]ATAGAAGATGATGTC | 8453 |
rs570316060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072516 | TGGGACTACAGGCGC[C/T]CGCCACCATGCCCGG | 8453 |
rs570326010 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35124634 | TTGGCAACTCTGTGG[A/C]CTTCCTTATAGGGCT | 8453 |
rs570342464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026670 | CAAAGACTCTCGTAT[A/C]TATAGCTAGTCAAGA | 8453 |
rs570351217 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075327 | AAAAATGTTTAATAA[C/T]AACATTCAGGGAAAG | 8453 |
rs570363229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037660 | ACCAGCCGGCCAACA[C/T]AGTGAAACCTCGTCT | 8453 |
rs570375797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050116 | TCACGAGGTCAGGAG[A/T]TCAAGACCATCCTGG | 8453 |
rs570409902 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012226 | ATTGAGCAAATTATA[C/T]AGTTATGTTGTGCCA | 8453 |
rs570414641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016938 | TCTCAAAAAAAAAAA[A/C]AAAACAAAAAAAAAA | 8453 |
rs570444588 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052065 | ATATTTTCCCCACAT[A/G]GAGTATAAATTATTC | 8453 |
rs570456006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072925 | CTTTTCTCGTCTCCC[A/G]TCATAGGGGAAAGGG | 8453 |
rs570480686 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108438 | CTCTAGCCTGGGCGA[C/G]AGTTAGACCCTGACT | 8453 |
rs570493414 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084970 | TAAAAATACAAAAAA[A/G]TTAGCTGGGGGTGGT | 8453 |
rs570547305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042293 | CTTTTTCCACTTAGC[A/G]TAACATTTTCATGGT | 8453 |
rs570550726 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010054 | AAGCATGGTACCCAA[C/T]CGAATTTCCACTTTT | 8453 |
rs570552692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017464 | TTTGAAAGGCCGAGG[C/T]GGGCAGATCACTTAA | 8453 |
rs570560336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35078861 | CACCAATAAAAATTT[A/G]GCATCCAAAAATTAT | 8453 |
rs570581335 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113293 | CTGAAGTCAGGAGTT[C/T]GTGACCAGCCTGGCC | 8453 |
rs570582403 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096119 | CTGGGCTGGTGGTGT[A/G]TGCCTGTAATCCCAG | 8453 |
rs570584531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35042855 | TGAAAGCCAGTCGGT[A/C]AGTAGTCCGGAGGCC | 8453 |
rs570587332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35010575 | TTAAGTATGAAAATA[C/G]GAACTACAATGTGGA | 8453 |
rs570593546 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35078459 | CGCCACCACACCGGT[A/G]TAATTTTGTATTTTT | 8453 |
rs570607986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CREM, CUL2 | GRCh38.p7 | 10:35127431 | CGGCTCGCCGCCCCA[A/C]GCCCGCTTCGTGCGC | 8453 |
rs570665749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35022094 | ATGTCTGTCTTCCTA[C/T]TAGACATGAGTTTTT | 8453 |
rs570671338 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116759 | ATCACAAGGTCAAGA[G/T]ATTGAGACCATCCTG | 8453 |
rs570701629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023190 | TAAACATAACAAAGC[A/G]TCACACTGTACACTG | 8453 |
rs570706153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120384 | CTTTCTCAATAAATA[A/C]ATAACATAAAATATA | 8453 |
rs570714616 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084523 | AAGCCAAATATAAAG[C/T]ACTGATATAGAAATC | 8453 |
rs570716405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121018 | CATATCCCTTTCTAA[A/G]TTCATTTTTCCATGA | 8453 |
rs570779813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35114211 | ACAAGTGTGAGCCAC[C/T]GCACCTGGCCCCGTA | 8453 |
rs570799927 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036926 | TTTTTGCAGAGATGG[A/G]ATACTGTCATGTTGC | 8453 |
rs570801504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35014998 | TTAACCTTAAGAAAT[C/T]CCTATTTTGGCCAGG | 8453 |
rs570939112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039603 | GACATGGTGGCTCAC[A/G]CCTGTAATCCCAGTA | 8453 |
rs570957909 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008159 | CTGTTTTGCCCACTC[A/G]CACTAGTTACTGCAC | 8453 |
rs570970995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084993 | GGGGTGGTGGTGGGC[A/G]CCTGTAATCCCAGTT | 8453 |
rs570972103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35039970 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 8453 |
rs570989508 | in-del | -/T | 0.266273 | 0.24947 | intron-variant | CUL2 | GRCh38.p7 | 10:35061770 | CCTTACTTATGAGGG[-/T]TTTTTTTTTTTTTTT | 8453 |
rs570994761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35105399 | CCACTGCACTCCAGC[C/T]TGGGCGACAGGGAGA | 8453 |
rs571062142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35011491 | AGTATGGTGGTGCAC[A/G]CCTGTATTCCCAACT | 8453 |
rs571063265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35112628 | GCTGTGCATGCACGA[C/G]AAGAACATGACTGGG | 8453 |
rs571076875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35064107 | TGTCTCCAAGGTAAA[A/G]ATAATGAATCTTTCC | 8453 |
rs571144431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046374 | ACTGGCAAAACTCTA[A/C]GTATACACACCCTAT | 8453 |
rs571145433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35109167 | CAGTGAGCCATGTTC[A/G]CACCTAGCAGAAATG | 8453 |
rs571168375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35098933 | AGCAAGACTCTGTCT[C/T]GAAATAAATAAATTA | 8453 |
rs571237500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35088034 | TAGGAAAACTGTTCC[C/T]TCAGAATTTCAAACT | 8453 |
rs571270092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35124732 | AAAAAGGCTGTAGGT[A/G]TGACTCTTGGTAATT | 8453 |
rs571303804 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054078 | TACAATAAATTTGTT[A/G]TATCCATAAATTTGT | 8453 |
rs571447383 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35068532 | ACGTGTTTCGGGTGG[A/C/G]GGTTATAGTGAATGT | 8453 |
rs571448179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35102929 | CAACCTAGGTGACAA[G/T]GTTAGTTCCAGCCAC | 8453 |
rs571449054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35060105 | TCTCTACAAAAAATG[A/C]ACAACATTAGCCAGG | 8453 |
rs571481764 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35093967 | TGTGTTTGGTTTATT[A/G]TTTTTAAAATTAATC | 8453 |
rs571517557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080745 | CAGGCGTGTGCCACC[A/G]CACCCAGCCTAGAAT | 8453 |
rs571593045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086516 | GGTCTCAAGCTGCTG[A/G]GCTCAAGTGATCCAC | 8453 |
rs571622210 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35034366 | GGAATTTGAAGAAAT[-/A]AAAAAAATAGAAAAC | 8453 |
rs571625651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025353 | ACAGAGGAGAAAGCA[C/T]GTTCCTGTGGTCCCT | 8453 |
rs571627879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019165 | GCAGAAATAAGTAGA[A/G]AATTATGCATCAAGC | 8453 |
rs571654928 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35087202 | TACTACAGGCGTGCG[A/C]CACCACGCCTGGCTA | 8453 |
rs571738501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051333 | AAAGAAAAAAAACCG[G/T]CCAGGCGCGGTGGCT | 8453 |
rs571779135 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113358 | AAAAAACTAGCCAGG[C/T]GTAGTGGTATGTGCC | 8453 |
rs571796472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35105474 | CCGGGTGCGGTGGCT[C/G]ACGCCAGTAATCCCG | 8453 |
rs571831441 | snp | C/G | 0.0013878 | 0.0263054 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010281 | GGTGATGGCAATGAT[C/G]TTCTCACACCACGCT | 8453 |
rs571862158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35081912 | CTGCTATAGAAGACA[A/C]AGGCATGGAAGAATA | 8453 |
rs571896076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35044348 | AGGATTTATCAAAAA[C/G]CATCAATTATGATGA | 8453 |
rs571981648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038474 | GAGGTTGCAGCGAGC[A/C]AAGAGCACGCCGCTG | 8453 |
rs571995301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35021442 | ATGTATGTATATATA[C/T]ACACACACACACATA | 8453 |
rs572073586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35063447 | TCATAGTATCAATGA[A/C]GGGCTATGGAATATG | 8453 |
rs572073625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055258 | TCATTTGAAAGGTTC[C/T]GCTAGTGTAAATAGC | 8453 |
rs572107914 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35098702 | TTGGGAAGCCAACAC[A/G]GGTGGATCACCTGAG | 8453 |
rs572121535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075975 | TCACATAAAAACTGG[C/T]ACACAAATGTTCACT | 8453 |
rs572123671 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35124993 | GCTAGACACTGGACT[A/G]ACGTAAACATGAGTA | 8453 |
rs572127183 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093694 | AAAGAAAAGAAAAGA[A/C]GAAGAAATTACCACT | 8453 |
rs572158842 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058171 | ATATCATTATGAACA[-/G]GTGATTAGAAGATGC | 8453 |
rs572165224 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026803 | CTTATTAGTAAAAAA[C/T]ATATGTTGACTAAAC | 8453 |
rs572175752 | snp | A/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128733 | GGTTTCACAGTGTTA[A/G]CCAGGATGGTCTCGA | 8453 |
rs572181029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35028209 | CTAAAATAGTCTGTG[C/G]TACAATCTCTTTTCA | 8453 |
rs572183644 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35089124 | AGGTTGCAGTGAGCC[C/G]AGATCGCACCACTGC | 8453 |
rs572212582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055673 | AGGCTCTAGACTCCA[C/T]GGCTTACAACCTTGA | 8453 |
rs572217280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35076590 | ACGACCTCATTGCCA[C/T]CTCCCATTGAATGAG | 8453 |
rs572243109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082285 | TACGCTAAGTCAAAT[A/G]CACTAGACACAAGGT | 8453 |
rs572243414 | snp | A/C | 0.0599851 | 0.162463 | intron-variant | CUL2 | GRCh38.p7 | 10:35089822 | GATGCCCCCCCCCAC[A/C]CACACACACAAACAC | 8453 |
rs572243608 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35032878 | GTATTATGGCCAAAG[-/A]AAAAAAATCAGTACT | 8453 |
rs572260262 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35034897 | AAAACACAGTTATTT[A/T]AAAATGGCGAGCTTA | 8453 |
rs572262031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35040814 | ATTCTTCTAAAGAGC[A/G]CACATCCTAGACCCC | 8453 |
rs572268629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35118630 | TATAGCTAGTTCTAC[A/G]TATTGTTTTAGCAGT | 8453 |
rs572271674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35068867 | ATTAGTAGCATAGTC[C/T]TTTATTTATTTATTT | 8453 |
rs572275724 | snp | A/G | 5.17531e-05 | 0.00508664 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35028819 | ACTTACCATCTGTAC[A/G]CTTTTTTCTAATTCC | 8453 |
rs572299046 | snp | C/G/T | 9.90482e-05 | 0.00703671 | intron-variant | CUL2 | GRCh38.p7 | 10:35035342 | TCCCAAATATTTTCA[C/G/T]TTATTAGGTAATATA | 8453 |
rs572316170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020786 | AAACTGTTCCTTATC[A/G]TTAATTCTATCCAAA | 8453 |
rs572330351 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35046649 | GTAATCCCAGCACTT[G/T]AGGAGGCTGAGGTGG | 8453 |
rs572385708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054110 | TTTCCTCTCCTCTAG[A/C]CTGTCTTTTAAGTAC | 8453 |
rs572445434 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35062015 | ATAAAGTCAAAACTC[A/C]GTCCATAAGGTAGTT | 8453 |
rs572486659 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35043525 | TTGTGACTTGTGGCC[G/T]AGGGATGTAGGATGA | 8453 |
rs572501038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051046 | CTTGGCCAGGCACAG[C/T]GGCTCACGCCTGTAA | 8453 |
rs572501845 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038491 | AGAGCACGCCGCTGC[A/C]CTCCAGCCTGGGCGA | 8453 |
rs572527394 | in-del | -/CTA | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35053439 | AATTTATCCATTTGC[-/CTA]CTTTTATAACAAAAT | 8453 |
rs572580784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086061 | CAACATAGTGAAACC[C/T]TGTCTCTACTAAAAA | 8453 |
rs572587053 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35065273 | TGGCTGGGCATGATG[C/G]CTGATGCCTGTAATC | 8453 |
rs572642281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086594 | ACGTGGCCGGAAACA[A/G]CTTTTTAAACAACTC | 8453 |
rs572667871 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057005 | TATGACTGGGCTCTA[C/T]TTCAGTTTCTGGCAT | 8453 |
rs572691614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053488 | CATTCTTCTTCCATG[A/C]TTTTTATTGCTGAAT | 8453 |
rs572693830 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35093893 | TTTCCTCTGATCAAA[-/T]TTTTTTTTATTTTGG | 8453 |
rs572702531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103701 | CTGACCTCAAGTGAT[C/T]TGCCCACCTCAGCCT | 8453 |
rs572723630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057729 | TTTCATTTTAATATG[A/G]ACACCATTCTTATTT | 8453 |
rs572746470 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35016858 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGCAAG | 8453 |
rs572760902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35050502 | TAAAAAGAGCAAGTC[A/G]GTTAAAAGAGTAATA | 8453 |
rs572760991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35058183 | ACAGGTGATTAGAAG[A/G]TGCTGATTCTATAAA | 8453 |
rs572764354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012474 | TGCATACTGGATCAG[A/G]CTTCAAAGGGAAGAG | 8453 |
rs572766511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110288 | TAGAAATTTATCCAG[A/G]CACAGTGGCTCATGC | 8453 |
rs572767479 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35043644 | GCAGATTTAAAAACC[C/T]GGCTAGAAGTTCTAA | 8453 |
rs572799274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012856 | GATAGAAACAGTCTA[A/T]CCCAGACCAAAGCAA | 8453 |
rs572893708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35036782 | TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGCAGG | 8453 |
rs572938215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35065606 | CCTGGGCTACAGAGC[A/G]AGACTCCATCTCAAA | 8453 |
rs573000045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016052 | ACGCTCGCAGCTCTA[G/T]GGAGCGTACAGTAAC | 8453 |
rs573006040 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078004 | TGTGTTTACAATTTT[C/T]CATAATAAAGGAATT | 8453 |
rs573053108 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128253 | TGAGTTTGTAATCAC[A/G]TTTTAAGAAATTGGG | 8453 |
rs573097610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35092879 | GTGAACTTTGCTAAA[A/G]TGTAGGCATATTTCT | 8453 |
rs573104956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106644 | GCCAAATGTTTGTTG[C/T]TTATAAGCCACCCAG | 8453 |
rs573107975 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074523 | TTTTTTGTTTGTTCC[C/T]GAGACAGAGTCTCCC | 8453 |
rs573155983 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35036186 | ATGAGTTTGAACTAC[G/T]TATAAAAATGGGATC | 8453 |
rs573167682 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35121234 | GGCTTTATTTATTTA[-/T]TTTTTTTGGGATGGA | 8453 |
rs573168764 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126969 | GAGGGGAGGACGGGG[A/C]GGGAGGACGCGGTTC | 8453 |
rs573192138 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117207 | CAACCAGATACTGGT[A/G]TATGTTTAGCTAGAA | 8453 |
rs573203222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071698 | CAGGCATGAACCATC[A/G]CACCCGGCCAGTTAT | 8453 |
rs573207015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35120585 | TACTACTCTAAAATG[C/T]TGAAAGGAAATTGCC | 8453 |
rs573248850 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35077925 | ACAGCTTGCTCATGA[A/G]TTGATAACTGTTAAG | 8453 |
rs573285671 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35078550 | AGGTGATCCCCCTGC[C/G]TCAACCTCCCAAAGT | 8453 |
rs573293478 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35015466 | CAAAATGAATTAATG[A/C]GAGAAATAAACTGTA | 8453 |
rs573306551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35072526 | GGCGCCCGCCACCAT[A/G]CCCGGCTCATTTTTT | 8453 |
rs573344241 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35026941 | TGCACCCACTAACTC[A/G]TCATTTAGCATTAGG | 8453 |
rs573364708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35049000 | ACAATTCACTGGTCT[A/T]GATAATTCCTATAAC | 8453 |
rs573370678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35027779 | TCCCTCTACTGGTAA[C/T]TGGAGACAATTCAAA | 8453 |
rs573373667 | snp | A/G | 2.01802e-05 | 0.00317643 | intron-variant | CUL2 | GRCh38.p7 | 10:35049774 | ATGCTAGCTGCCGGG[A/G]AAAACGAAAATCATC | 8453 |
rs573403569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041825 | TACAGGTCTGAGCCA[A/C]CGTGCCCAGCCTGAA | 8453 |
rs573436752 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091917 | ACAGGCCTGAGCCAC[C/T]GTGTCAGGCCCCCCC | 8453 |
rs573442505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35106171 | TACAAAAGAGTTCCC[A/G]GAGAGCTCCCTCACT | 8453 |
rs573480045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103612 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTAATT | 8453 |
rs573525534 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35025396 | ACACATATATTCCAG[-/CT]CTTTTAATTGACAAC | 8453 |
rs573541891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124181 | AGCGAGACTCTGCCT[C/T]TAAGTAAATACATTT | 8453 |
rs573554661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35083885 | TAAAAATTTACATAT[A/G]GCAAATCCATGTTTC | 8453 |
rs573563590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069007 | CCAAGTAGCTGAGAT[C/T]CCAGGCACCCACAAC | 8453 |
rs573584147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35098667 | GGGGCACAGTGGCTC[A/G]TGCCTGTAATCCCAG | 8453 |
rs573602154 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35116549 | TTTTTTTGTGATCTC[A/G/T]TTTAACCCTCTTTGA | 8453 |
rs573619239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084345 | AAAGCTTAAAGCAAA[A/C]GGAAATATTCCACCT | 8453 |
rs573620896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124798 | ACTTACAGTTGGATT[C/T]GGAGAGGAAAAAGAG | 8453 |
rs573650027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075311 | GAAAATTAAGTTTCT[C/T]AAAAATGTTTAATAA | 8453 |
rs573657067 | in-del | -/TT | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35038627 | TTCCTTTTTATAGTC[-/TT]TGCCTTTATTCCTAC | 8453 |
rs573668940 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061946 | TCTACTCCTGACCAC[A/G]TGCAGGGTTAGACAG | 8453 |
rs573670984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35012521 | TATGTGGCTCAAGCA[A/G]AGAAGCCAGGAGAGG | 8453 |
rs573688228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019980 | TGGTTACCGCCTTCA[C/T]CAAGTGACCAAATTT | 8453 |
rs573697806 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35061453 | TGACAGAGCAAGACT[C/T]TGTCTCCCAAAAAAA | 8453 |
rs573720307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35087556 | GAAATCCAACTTAAC[A/G]TGTCCAATCCAACCC | 8453 |
rs573726856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35108710 | TCTCATGAGATTTCA[A/G]TCAAAGTATTGGCCT | 8453 |
rs573728956 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110766 | TGTGCATGCATCCCT[C/T]GTATCCCCCTCTTAT | 8453 |
rs573737430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35109542 | AATAAAGTGATGGGG[A/G]ATACTACATTAGCTA | 8453 |
rs573750969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045908 | GCATTAATAATGTCA[C/T]AAAGAGAGCAACAGA | 8453 |
rs573786827 | snp | C/G | 4.76781e-05 | 0.00488229 | intron-variant | CUL2 | GRCh38.p7 | 10:35039118 | AGTCATGAACACAAA[C/G]TTTTACTATGAGGAA | 8453 |
rs573813086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046440 | AAACAAGAGTGGTGT[C/T]AGTGGAAAAACTGGA | 8453 |
rs573839636 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058541 | CTGCTAGCATCCACC[A/T]GATAAGTGTCGATTC | 8453 |
rs573850314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35039721 | AATATAAAAATTAGC[C/T]GGGCATGCCTGTAAT | 8453 |
rs573869291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080078 | CAGACCCCATTGACC[A/G]TGGGTAACTAAAATG | 8453 |
rs573888199 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | CUL2 | GRCh38.p7 | 10:35023551 | TAAATTCCAATGGCT[-/A]AAAAACTATGTGCAT | 8453 |
rs573901019 | in-del | -/CTCA | 0.0115144 | 0.0749975 | intron-variant | CUL2 | GRCh38.p7 | 10:35070761 | TCTAATGTCACCATC[-/CTCA]CTCAGGGAGGCCTTC | 8453 |
rs573979055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081136 | GGCTAAGGTGGGAGC[C/T]TGGCTTGAGCAAAGG | 8453 |
rs574006438 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35088470 | CGTGCCACCGCACTT[A/C]AGCCTGGTGACAGAG | 8453 |
rs574011701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107938 | GTTCCTACTCTTCCT[A/G]AGTTAATTGCTCCTT | 8453 |
rs574018317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081533 | ATGACTAGGCAAGCC[C/T]ATCGTGTATGAATAC | 8453 |
rs574023464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018280 | CAACAGAGCAAGACT[C/T]CATCTCACAAAAAAA | 8453 |
rs574053786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35094909 | CAAACCTCAAATCCT[A/G]GTTCATCTATGATTG | 8453 |
rs574069232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059351 | CATTGCCACAGCCTC[C/T]CCAACCTTCAGCAAC | 8453 |
rs574105944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35060286 | AATAAAAAAAAGGAC[A/C]AAATAAAAGAAAGAA | 8453 |
rs574129580 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097236 | ATTTAAGAAAAATGT[A/G]TAAATACTGAACTTC | 8453 |
rs574140312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35052537 | TAACACAGACGGGTT[C/G]AAAAATACTTAATGA | 8453 |
rs574151334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073242 | TAACGGATTAGCAGC[G/T]ATTTTACTCTGCAAA | 8453 |
rs574169818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35038203 | TATCTTTCCTGCCTA[A/T]AAAAGTAATGCATGT | 8453 |
rs574190664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099125 | GGGCTGGGTGCATTG[C/G]CTCATGCCTTTAATC | 8453 |
rs574204051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35115165 | TTCTCTTGAACCCAG[A/G]AAGCAGAGGTTGCAG | 8453 |
rs574218157 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099231 | ACCTGTTCTTCTAAA[A/G]TACAAAAAAATTAGC | 8453 |
rs574258152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017849 | ATGGCAAACATGTCT[A/G]CACTCTGTAATGTTC | 8453 |
rs574263492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35077256 | CCACAAAATAGCCAC[C/T]GCACTCCAGTCTGGG | 8453 |
rs574265754 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011474 | AATACAAAAATTAGC[C/T]AAGTATGGTGGTGCA | 8453 |
rs574290370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115637 | GGTGGCTCACACCTG[G/T]AAACTCAGCACTTTG | 8453 |
rs574315181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35032908 | TAAAAATTGCAAAAT[C/T]ATGCATGTCTATCCA | 8453 |
rs574358289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024966 | AATTATAAAATACTA[C/T]GAAAAAGTGCTATAC | 8453 |
rs574373910 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CUL2 | GRCh38.p7 | 10:35023925 | CTGCAGCCTCCAGCT[C/T]GTGGGCTCAAGTGAT | 8453 |
rs574409035 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067828 | AGAACCACAAAAGGG[C/T]CGGACGTGGTGGCTC | 8453 |
rs574499817 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35066268 | TTGACAATTAAAAAA[A/T]ATATATAATAAAATT | 8453 |
rs574533244 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35117916 | GAACAATTTTAGGTG[A/C]ACAGCAAAAACGAGC | 8453 |
rs574583912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071428 | TGTTTGCTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 8453 |
rs574592610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35037651 | GAGTTCGAGACCAGC[C/T]GGCCAACATAGTGAA | 8453 |
rs574622594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35118796 | GCTCCACAAGAGTTT[A/G]GGACTTGGGAAAAAG | 8453 |
rs574623664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35076607 | TCCCATTGAATGAGG[C/T]AATAAATGTTATATG | 8453 |
rs574662663 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048646 | GAAAAGAGGAAGAAA[A/G]ACAACGGGTTACACC | 8453 |
rs574672948 | snp | A/C/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126440 | AGTCAGAAGAAGCAC[A/C/G/T]CCTGCAGTCCCAGCT | 8453 |
rs574692422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014586 | GTCTGTAATCCCACC[A/C]CTTTGGGAGGCTGAG | 8453 |
rs574711373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054168 | GCCGTCAACACTTTA[A/T]AATTGTTTCTGAGTT | 8453 |
rs574727621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020920 | CTCAACACTCTCCTT[C/T]ACGTAGCTTGGTTAA | 8453 |
rs574736724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35040425 | TGTGTAATTAGAGTT[C/T]CTGAAATTAAGTGTT | 8453 |
rs574743235 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35089904 | CTCTCACCTTCCCTC[C/T]TTCGAAGGAAAATGG | 8453 |
rs574747971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35047404 | TCACGAGGTCAGGAG[A/T]TAGAGACCATCCTGG | 8453 |
rs574749912 | snp | C/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008693 | CATTATATAAGTCAT[C/T]ATAAGTTCAGTAGAT | 8453 |
rs574750027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35054963 | CAAAAAAGATCACAA[C/T]CAGTAGGTAAGAAAA | 8453 |
rs574754319 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053495 | CTTCCATGCTTTTTA[G/T]TGCTGAATGTTGGAT | 8453 |
rs574785728 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061164 | TCTTCAAAATGAAAG[C/T]GAAGCATCCATAATA | 8453 |
rs574826883 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095413 | GTTTGGGTTGATGTA[C/T]ATAACTCACAATTTA | 8453 |
rs574843445 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35035936 | GATCTCTCAGTGTAG[C/T]AGGTTTAATTTTAAA | 8453 |
rs574872190 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036440 | CCAGGCATTGGCAGT[C/G]GGGAGGTAAAGCTGG | 8453 |
rs574880961 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069572 | AAAAAAAAAAAAGGA[C/T]AACTAAACCATATTA | 8453 |
rs574893024 | snp | A/T | 3.89249e-05 | 0.00441145 | intron-variant | CUL2 | GRCh38.p7 | 10:35044540 | TACAAAATAGATAAA[A/T]GTATTCGATATGTTT | 8453 |
rs574991269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35028948 | CTAAATTCAAAGTAA[A/G]TATTTATTAAATAAT | 8453 |
rs575024724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35096592 | CACTACAGACTGGGT[A/C]ACAGAGCCAGACCCT | 8453 |
rs575037140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35089199 | AAAACTGTGTACTTC[C/T]CTTATCTCACGCGAC | 8453 |
rs575039332 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35093997 | CAGTAATTTAAAAAT[G/T]TTTATCCTTTAAATT | 8453 |
rs575054872 | in-del | -/A | 0.300169 | 0.244914 | intron-variant | CUL2 | GRCh38.p7 | 10:35050322 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs575101246 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35086696 | ACAAACTCCAGCCTG[G/T]GTGACAGAGCGAACA | 8453 |
rs575114621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35103778 | CAAAATGTTTTCACC[A/G]ATGCAGGATTTTCCC | 8453 |
rs575118809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35051132 | CATCCTGGCTAACAG[A/G]GTGAAACCCCATCTC | 8453 |
rs575155474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043758 | ATAACCAATATGTAC[C/T]GGTTTAGTGATCAAT | 8453 |
rs575200577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35104583 | CCAATTTTTAGTTGT[A/G]TTAAGCATAGGGTAA | 8453 |
rs575222047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35033082 | CTACATCAGAAACCT[C/G]ATACTAGAATTCTGA | 8453 |
rs575249997 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048310 | ACAACAAAAATAAGA[C/G]AAGCAGACCAGATAA | 8453 |
rs575285122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35121118 | CCCATAATGTCATGT[C/T]TTCCTATAGGCGATT | 8453 |
rs575302135 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010186 | CACTGGTGATGTTGT[A/C]AACAGCAGAAAACAG | 8453 |
rs575308618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35033512 | GAGGCTGAGGCGGGC[A/G]GATCATGAGGTCAGG | 8453 |
rs575329041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080956 | TGGTGGCTCACACCT[A/G]TAATCCTAGTACTTT | 8453 |
rs575350138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017151 | GGTCCACAGCCACAT[A/G]GAAAATGCTTTTGAG | 8453 |
rs575409347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107766 | AGGCGCTTGTGGTCC[A/C]AGCAACTCGGGAGGC | 8453 |
rs575413003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025076 | AAACCTCTTTCTAAA[C/T]TAATATAATCATCAG | 8453 |
rs575429691 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35063886 | CTTTGGGGCCAGACA[-/C]GGTATTAGATTATGA | 8453 |
rs575441114 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35127018 | TTTTGGTCCGGGGTC[A/G]GCAGGGAGGCCGCGG | 8453 |
rs575502891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35086121 | CGCCTGTAGTCCCAG[C/T]TCGGGAAGTGGAGGC | 8453 |
rs575506820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127675 | AACCTGGGCCGGAGG[C/G]CCTCGCAGCTGAGTC | 8453 |
rs575517718 | snp | C/G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104744 | TCAAAGACTTTTCTG[C/G/T]GGGGGGGACAGTCTT | 8453 |
rs575606265 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35093503 | ATCTCTACAAAAAAT[A/G]CAAAATTTAGCCAGG | 8453 |
rs575615489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117167 | CTGCAGGAAGAGAAG[A/G]GCACTAGCTTACTTG | 8453 |
rs575617712 | in-del | -/TCCG | 0.00716551 | 0.0594257 | intron-variant | CUL2 | GRCh38.p7 | 10:35104813 | CAGCTCACTACAACC[-/TCCG]CCTCCTGGGTTCAAG | 8453 |
rs575650586 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35106912 | CTCCTGTTAGCAATA[A/C/G]GGAAAAAGGATAAAT | 8453 |
rs575669925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35107308 | AAGCAGAGTGATTAT[A/G]ATCTGAAAAAGAATT | 8453 |
rs575670526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020032 | ATCTGACATTAGATG[C/T]CTTTGAAATATGCAA | 8453 |
rs575673162 | snp | G/T | 3.90999e-05 | 0.00442136 | intron-variant | CUL2 | GRCh38.p7 | 10:35016159 | AGCTTTAATGCTGAT[G/T]ATGCTTAAATTCTTT | 8453 |
rs575677069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35117712 | TGTATTACTGAAGGT[A/T]CCTATTATGTGGAAC | 8453 |
rs575679746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35072548 | TCATTTTTTGTATTT[G/T]TAGTAGAGACGGGGT | 8453 |
rs575711208 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009326 | TAAGCACATCTGTGA[C/T]TGATGAGAGTGACTC | 8453 |
rs575717643 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078776 | TAAATGGCTAACCAC[A/T]TACTATTTTGATTCT | 8453 |
rs575830914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35036837 | CTCCCAGATTCAAGT[A/G]ATCCTCCCACCTCAG | 8453 |
rs575902715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35124825 | AGAGGTGCTCCTCCC[A/G]ACCCAGAAAGGGAGG | 8453 |
rs576003173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35110757 | TTGTCTCTGTGTGCA[G/T]GCATCCCTCGTATCC | 8453 |
rs576045134 | snp | C/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126018 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 8453 |
rs576045592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35111436 | TTTTCTATTCATTCT[C/T]TTTATAGAGATGGAG | 8453 |
rs576053046 | snp | A/C | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079869 | TGAACACAAATACTG[A/C]AAAACTGCAACAGTC | 8453 |
rs576060896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35103183 | AGTCTTGCTCTGTTG[C/T]CCAGGCTGCACTGCA | 8453 |
rs576063246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095042 | TAATGTTGGCGGGGC[A/G]CAATGGCTCACACTT | 8453 |
rs576076622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35069649 | GTCACTTTCCAGGGA[A/G]GTAATCTATTTCAAA | 8453 |
rs576079923 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095098 | AGGCTGGTGGATCAC[G/T]TGAGGTAAGGTGGAT | 8453 |
rs576110164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081580 | CAACCAGCCTTTACA[C/G]AAATTATCAAAACAT | 8453 |
rs576111081 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35104738 | GAAGAATCAAAGACT[C/T]TTCTGGGGGGGGGAC | 8453 |
rs576111359 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35070451 | TTTCTAAAGAATGTA[C/T]GCCCCATATAATGAG | 8453 |
rs576124696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35095871 | CGGCCAGTTATGTCA[C/T]GTATTAAACATTTTT | 8453 |
rs576129398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35062780 | AAGTCGGGGCTGCAG[C/T]GAGCCATGATCGCGC | 8453 |
rs576157397 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35088957 | TAAGCAGGCGAATCA[A/C]CTGAGGTCAGGAGTT | 8453 |
rs576190373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35020923 | AACACTCTCCTTTAC[A/G]TAGCTTGGTTAAGTC | 8453 |
rs576194069 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35034406 | ATTGTGGCATAACAT[A/G]AAAACTAAAAATTAT | 8453 |
rs576195536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35067014 | AAATGATAGGTGTGG[C/T]AGCGCATGCCTGTAA | 8453 |
rs576250449 | in-del | -/ATC | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35032145 | GGTTACCCAAACTTT[-/ATC]ATCAGATTTCCTTTA | 8453 |
rs576261150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35034822 | TGCAAGTCGTCTATA[G/T]TACCACTGATTAATA | 8453 |
rs576277788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082246 | TCCGATATATGCTAC[A/G]ACAAGGATTAACCTT | 8453 |
rs576278679 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057759 | TTATAAGTCACTGTA[A/G]TATTTTACAATCAAA | 8453 |
rs576287796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35027923 | AGAGTTAAAAACTAT[A/G]AATAGAAAATAATTA | 8453 |
rs576332465 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093241 | GTGATAACTCCAGTT[C/G]TCCTATGTGACTGGC | 8453 |
rs576336065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35052670 | AGAAGCGGAGGCAGG[C/T]GGATCACAAGGTCAG | 8453 |
rs576354916 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065276 | CTGGGCATGATGGCT[A/G]ATGCCTGTAATCCCA | 8453 |
rs576369480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35061211 | GAGCGCAGTGGCTCA[C/T]GCCTGTAATTCCAGC | 8453 |
rs576397048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075365 | AAGGATGTGAAAGAG[A/T]CAGGGCAAAGAAGAA | 8453 |
rs576405863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35053348 | GTATTCAACATATAC[C/G]TATAATTTTGTGTCC | 8453 |
rs576433883 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055065 | AAAATGAATTATACT[A/G]AAAATGTTTAATATA | 8453 |
rs576457605 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067976 | TTAGCCGGGCATTGT[A/G]GTGGGCGCCTGTAGT | 8453 |
rs576467022 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092055 | ACTCCTGGGCTCAAG[C/T]GAGTGTACCATCTCA | 8453 |
rs576529306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35092763 | TGGTTTAACTTGAAA[A/G]CTAAGTTCCTCCCTA | 8453 |
rs576535347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35026466 | TTCTCAAAACACTTT[C/T]GGAAATGAGAAATTC | 8453 |
rs576540924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35085328 | CCAGCTACTTTGGAG[A/G]CTGAGGCAGGAGAAT | 8453 |
rs576562637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35115271 | AAATGGAGCACAAAG[A/C]GAAAACAAGGCCAGG | 8453 |
rs576566051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35046606 | TCTTAAAAACTGGGT[C/T]ATTGGCCAGGCGCAG | 8453 |
rs576627006 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023084 | TGTGACAGTAATTGC[C/T]GTGACAGTAGATGTT | 8453 |
rs576704175 | in-del | -/TGTT | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35038644 | TGCCTTTATTCCTAC[-/TGTT]TATCAGGAATTCTAA | 8453 |
rs576721461 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35093332 | GCAGTAGCCAAGAAG[-/A]ACCCATCTGGCCATT | 8453 |
rs576741732 | snp | A/T | 2.77882e-05 | 0.00372738 | intron-variant | CUL2 | GRCh38.p7 | 10:35013668 | TTAAATGTTTCCCCC[A/T]CAAAAAAAACTTGAC | 8453 |
rs576748168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35050025 | AAATAATTGATTATT[A/T]TAAAACCTTAATTTA | 8453 |
rs576749989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017869 | CTGTAATGTTCCATA[A/C]GTGTTTAAAAAAAAA | 8453 |
rs576751610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35025673 | GGATTATTCTTTTGC[C/T]GATATTATTGTGAAC | 8453 |
rs576786617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35018486 | TAAAGATTTTAGGCC[A/G]GGCGCAGTGGCTCAC | 8453 |
rs576798757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35100074 | GCCTCCCAAAGTGCT[A/G]GAATTATAGGCATGA | 8453 |
rs576802307 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35058560 | AAGTGTCGATTCTTA[C/G]CTGATAATTCCCAGG | 8453 |
rs576816530 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35041752 | ACGTTGCCCAGGCTT[C/G]TCCTGAACTCCTGGA | 8453 |
rs576828530 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035929 | GAATAATGATCTCTC[A/G]GTGTAGTAGGTTTAA | 8453 |
rs576861481 | snp | C/T | 0.000801282 | 0.02 | intron-variant | CUL2 | GRCh38.p7 | 10:35104812 | TCAGCTCACTACAAC[C/T]TCCGCCTCCTGGGTT | 8453 |
rs576872015 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35090404 | GTGGGGAGCGAAGCC[C/T]GGGGAGCCCGCGCGC | 8453 |
rs576908955 | in-del | -/A | 0.0726307 | 0.176182 | intron-variant | CUL2 | GRCh38.p7 | 10:35052908 | TCAAAAAAAAAAAAG[-/A]AAAAAAAAAATTAAA | 8453 |
rs576946076 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124080 | CCCAACACTTTGGGA[A/G]GCCGAGGTGGGAGGA | 8453 |
rs576951522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35071479 | GCGTGATCTTGGCTC[A/G]CTGCAAGCTCCGCCT | 8453 |
rs576962524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043007 | GGTGTCTGCTGCTTG[G/T]TGTGTGGGAGAAGAG | 8453 |
rs577026336 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35106173 | CAAAAGAGTTCCCAG[A/C]GAGCTCCCTCACTTC | 8453 |
rs577038138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35048118 | GGATTAAATGGGAAG[A/G]TGGATGTAAAATTTT | 8453 |
rs577073007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35041063 | CCTGAGGGTCAGGGA[A/C]CCCTGGTCTAGAGGA | 8453 |
rs577086443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35106592 | CCACCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 8453 |
rs577093821 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35081827 | GAGCCCAAGATGTGA[C/G]CGCACCACTACAATC | 8453 |
rs577095655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35119466 | TGGACTAATTTTAGC[G/T]CTCTGTGAAAATCAA | 8453 |
rs577142020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35083607 | GAAGGTGCTTTCCCC[C/T]CACAAAGAGGGTGGG | 8453 |
rs577155521 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35113016 | GGCCAACATGATGAA[A/C]CCCAGTCTCTACTAA | 8453 |
rs577167745 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35113618 | AAAGAAACAACAAAA[C/T]ATAATTCATAATCAG | 8453 |
rs577193091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35036050 | CAACACACCCATGTA[A/C]TCACACGCAGGATAA | 8453 |
rs577206188 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034580 | CTCTCTTGCTCATCA[A/G]ACATTACCAGTAATA | 8453 |
rs577208462 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35038865 | AGGGTGACTAGAGGA[A/T]GATATAAAAGGTGGA | 8453 |
rs577222207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35016035 | TGCTCTGTGATGCCT[G/T]AACGCTCGCAGCTCT | 8453 |
rs577242615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35029714 | TTAATAATAATGTGT[C/T]GGTATTGCTAGGTCT | 8453 |
rs577267749 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35030676 | GCATGAACCACCACA[C/T]CTGGCCAACACTACT | 8453 |
rs577283368 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35034284 | TAGTAAGTTTGACAA[A/C]TAATAGAGTAATAAA | 8453 |
rs577294670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35077673 | AAATACAAAATTAGC[C/T]GGGCACGGTGGCACA | 8453 |
rs577345957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35055016 | TAAGTATGGGCAAGA[C/T]TGACAGATACAAGAT | 8453 |
rs577353579 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126576 | CGCGGACCTTAGCTT[A/G]GGGTTGGCGGCGTTA | 8453 |
rs577398942 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033756 | AAACAACAACAACAA[-/C]AAAAAAAAAAAAAAA | 8453 |
rs577460945 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099606 | CCCGTCTCTACTAAA[A/G]ATAAAAAAATAAAAT | 8453 |
rs577467677 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35038300 | GGAGGCTGAGGCGGG[C/T]GGACCACAAGGTCAG | 8453 |
rs577483378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35082934 | AGGCCAAGGCGGGCA[C/G]ATCACTTGAGGTCAG | 8453 |
rs577487950 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122039 | TTGGAACACAGAACT[A/G]TTAACTCTCTAATAG | 8453 |
rs577546190 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029949 | AAAATGCCCCGTTAC[C/T]ATACATAAGATACCT | 8453 |
rs577548848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35097445 | CAGTGAACTGTGATC[A/G]CACCATTGCCCTCCA | 8453 |
rs577611177 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35090030 | GTCACTTACAGGATA[A/C]CATCTTCCCGGGCCT | 8453 |
rs577611325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35098652 | TAAAAATAAGCAGGC[A/G]GGGCACAGTGGCTCA | 8453 |
rs577636573 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35025924 | AATAAACTTTTAGCA[C/T]GATGTACCATATATA | 8453 |
rs577638884 | in-del | -/CTC | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35078403 | CAGGTGTGAGCAATT[-/CTC]CTGCCTCAGCCTCCC | 8453 |
rs577655931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081477 | CATATATGTATCCCC[A/G]ATCTCAGGTAAATTA | 8453 |
rs577678344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35026833 | CTTATTTTATTTTTT[A/T]AAATTTTATTATTAT | 8453 |
rs577693909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075196 | AAGAAGCACCAGCCT[C/T]GTGAAACACACCAAA | 8453 |
rs577702587 | snp | C/T | 5.16961e-05 | 0.00508383 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010306 | CACGCTGGAGGAGAG[C/T]GACATCACGCGACGT | 8453 |
rs577702634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35017745 | GGGAGCTCTAAGAGA[C/T]AGAGCAAGTATTATG | 8453 |
rs577737258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35010806 | CCTTCAGTGCATGCT[A/G]ATGTAATTTTACATT | 8453 |
rs577742942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051535 | GGAGAATGGCGTGAA[A/C]CGGCCGGGCGGAGCC | 8453 |
rs577759721 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020594 | TACTGTCTGGTGAAG[-/T]TTTTTTTTATCTTCC | 8453 |
rs577779048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35044724 | ATTAGAACAAGCAGT[G/T]TAAGAAATTAACAGT | 8453 |
rs577820189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35045706 | TGGGTGACAGAGCAA[A/G]ACCCTGTCTCAAAAA | 8453 |
rs577831022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35116455 | TTTTTTAGTAAGAAA[C/T]AGATAAGCTGAAAAG | 8453 |
rs577897062 | in-del | -/TCC | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35070125 | TCCTTATCCGTTACA[-/TCC]GTCAAGTAATTATTT | 8453 |
rs577934175 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | CUL2 | GRCh38.p7 | 10:35073585 | ATTTTCTTTTCTTTT[C/T]TTTTTTTTTTTCTTT | 8453 |
rs578007603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35087446 | GGTTTAAAGCTGGTG[C/T]TTGAGAAGCCCTCGT | 8453 |
rs578035515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35101813 | AGTACAGCTTGTGCT[C/T]GGCTCCCTGCTCTAA | 8453 |
rs578039740 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35037767 | GAATCGCTTGAACCC[-/A]AGGAGGCAGAGGTTA | 8453 |
rs578043541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35066310 | AGAATTTGCTGACTT[C/T]TTTTTTTTTTGAGAC | 8453 |
rs578044445 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110207 | ATACTGCTATAGGAA[C/T]AAGGAGGTATAATTG | 8453 |
rs578087177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35078716 | AAGATGCATTTTGGT[A/G]TTTTGTATTTTACTT | 8453 |
rs578107410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127856 | ATTATTAAACATACT[C/T]TTTTTTTTTGAGACG | 8453 |
rs578141943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128752 | GGATGGTCTCGATCT[C/T]CTGACCTCGTGATCC | 8453 |
rs578144046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35031714 | CAAGGTAAGATCAGC[A/G]GACAGAATTTTTGCT | 8453 |
rs578152813 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017727 | TATATGCTAAATGAC[A/C]CTGGGAGCTCTAAGA | 8453 |
rs578171514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059313 | ACTGATGCAGCTAAC[G/T]TCATTGTTGTCTTAT | 8453 |
rs578179066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079279 | GGTGTGAGACAATAC[A/G]ATGCCTATGTAATGA | 8453 |
rs578200174 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078365 | CAATGGCATGATCTC[A/G]GCTCACCACAACCTT | 8453 |
rs578207901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35073152 | AAGAGGGTATGCCTT[G/T]TTGAACCACATCCTC | 8453 |
rs578210165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043556 | CAGCTCACCCACTTA[A/C]ACTACTCGACCTTTC | 8453 |
rs578238345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35051440 | AACATAGTGAAATCC[C/G]GTCTCTACTAAAAAT | 8453 |
rs745305876 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093682 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAGAA | 8453 |
rs745313778 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116414 | TAGAGAAATTCTCTG[A/G]AAGGCATAAACTACA | 8453 |
rs745319292 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100431 | TATTGCACTGTTTTA[A/T]ACTTTATTTTCTGTT | 8453 |
rs745336041 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034576 | ATTTCTCTCTTGCTC[A/G]TCAAACATTACCAGT | 8453 |
rs745341555 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069430 | CCTGTAGTCCCAGCT[A/G]CTCAGGAGGCTGAGA | 8453 |
rs745365979 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017460 | GCACTTTGAAAGGCC[A/G]AGGTGGGCAGATCAC | 8453 |
rs745373494 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066975 | TCTATGTTTGAAAGA[A/G]ATGCCTGATAGAATA | 8453 |
rs745386748 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115553 | TGACAGAGCAATACT[A/C]CATCTCAAAAGAAAA | 8453 |
rs745453112 | in-del | -/CT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033330 | TCAAGGATATCCAAA[-/CT]ATGAGGTTTATTAGA | 8453 |
rs745503360 | snp | G/T | 1.74958e-05 | 0.00295764 | missense | CUL2 | GRCh38.p7 | 10:35016193 | ATATTACTACATACC[G/T]TTTCTGAATCATGGT | 8453 |
rs745517381 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045170 | TTAACAAAGTAGATA[C/T]GAGCCCATCAATTCA | 8453 |
rs745534715 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078061 | AATATTTTCATAAAT[G/T]TAGGGGAGAAAGCAC | 8453 |
rs745583517 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010097 | ACTCATTCTTTTAAT[A/G]AAGTTTTAAGAAATG | 8453 |
rs745596063 | snp | G/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091121 | GGGTTTTCCTCCCTT[G/T]GAGTTTTAAACGGTA | 8453 |
rs745618869 | snp | C/T | 0.000436534 | 0.0147674 | intron-variant | CUL2 | GRCh38.p7 | 10:35033324 | AGAGGTTCAAGGATA[C/T]CCAAACTATGAGGTT | 8453 |
rs745632943 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059042 | GCTGCAATCTCATGA[C/T]ATAACTTGAATGGAT | 8453 |
rs745638401 | snp | C/G | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008505 | ACAATTAGATACCAG[C/G]ATAAGACTTAATTTA | 8453 |
rs745678471 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085102 | TCCAGCCTGGGTGAC[A/G]GTGTGAGACTCCATC | 8453 |
rs745687629 | snp | C/T | 2.00922e-05 | 0.0031695 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35038981 | AAACTGTAAGTGGTC[C/T]GCTACCATTCGTTGT | 8453 |
rs745697903 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022943 | CCAGCTACTCAGAAG[A/G]CTGAGGCAGGAGAAT | 8453 |
rs745727814 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106574 | CCTGACCTCATGATC[C/T]GCCCACCTCGGCCTC | 8453 |
rs745747856 | snp | A/T | 5.62683e-05 | 0.00530386 | intron-variant | CUL2 | GRCh38.p7 | 10:35049817 | CTTAGTATATGTTTA[A/T]CATTTCCTCAAGGTT | 8453 |
rs745776912 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121696 | ATGTCTGTAGTTCCA[A/G]CTACTTAGCCAGCTG | 8453 |
rs745790485 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045282 | GTGAAATGTTAGCTT[C/T]TCTAATAAAAGGAAT | 8453 |
rs745835919 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071444 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 8453 |
rs745859076 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021445 | TATGTATATATATAC[A/G]CACACACACATACAT | 8453 |
rs745862194 | snp | C/T | 3.97591e-05 | 0.00445847 | intron-variant | CUL2 | GRCh38.p7 | 10:35029445 | TTTGTATCAACGTAC[C/T]GAAATGATTAGTAAA | 8453 |
rs745877863 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083336 | ACACATATACATGCA[A/G]ATAAAAAGATATAAA | 8453 |
rs745901649 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120522 | TACAAAATAAGAGGT[C/T]GTCAATTTATGAAGA | 8453 |
rs745950813 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077045 | TATTCACATAAAAAC[C/T]GGTACACAAATGTTC | 8453 |
rs745985174 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117529 | GTCACTGCAACTGGC[-/T]TTTTTTTTTTTTTTA | 8453 |
rs746025713 | snp | C/T | 1.65002e-05 | 0.00287225 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071264 | GGCTTTTATTGTCGT[C/T]AAAAGTTTGTTCCAT | 8453 |
rs746035003 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050093 | TTTGGGAGGCCAAGG[C/T]GGGCACATCACGAGG | 8453 |
rs746062698 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097007 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC | 8453 |
rs746063878 | in-del | -/CTT | 4.98591e-05 | 0.0049927 | cds-indel | CUL2 | GRCh38.p7 | 10:35044613 | GTAATAAATTTGAAG[-/CTT]CTTGTTTGTAATACT | 8453 |
rs746083042 | snp | A/C | 4.68856e-05 | 0.00484155 | intron-variant | CUL2 | GRCh38.p7 | 10:35038880 | TGATATAAAAGGTGG[A/C]TTTATAATTTAATTT | 8453 |
rs746131251 | in-del | -/GA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064548 | TTATTAAATCCTGCT[-/GA]GAAGGAAAGGAGATG | 8453 |
rs746136553 | snp | C/T | 3.31087e-05 | 0.00406857 | intron-variant | CUL2 | GRCh38.p7 | 10:35071158 | TTTTCAACAAATTTA[C/T]CAATTTTAGAACATT | 8453 |
rs746142109 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011324 | AACAAGACATTCAGA[-/T]TTACAGGTGTCCACT | 8453 |
rs746156781 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014054 | ATAAGCTATTTTCTG[A/G]TCCTACTATTCTATA | 8453 |
rs746169932 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118235 | AGAAATCCCAAAGTT[-/A]AGAGTTGGCCTTTTT | 8453 |
rs746192982 | in-del | -/GA | 3.38089e-05 | 0.00411136 | intron-variant | CUL2 | GRCh38.p7 | 10:35010475 | AGTCAAACTACTGCC[-/GA]AGTTCTTCAGCTATT | 8453 |
rs746229501 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075864 | TTGTCAATAATAATT[A/G]CAAAAGTGAATTATA | 8453 |
rs746243692 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103895 | ATGTAACCTCTCCAA[-/G]GGATAGATCTTGGAA | 8453 |
rs746277337 | snp | G/T | 1.6507e-05 | 0.00287284 | missense | CUL2 | GRCh38.p7 | 10:35044798 | ATTTTTTCTTATACT[G/T]TTCAACATGAACAAA | 8453 |
rs746282793 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074730 | AGGCTCAAGTGATCC[A/G]CCCGCCTTGGCCTCC | 8453 |
rs746293731 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089211 | TTCTCTTATCTCACG[C/T]GACTCTTTTGGAAGG | 8453 |
rs746325247 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029156 | TCCGCCTCTGGGGTT[C/G]AAGCAATTCTCCTGC | 8453 |
rs746331208 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35092788 | CCCTAAAACTACCCC[-/T]TGCTCTTGCTTAGGG | 8453 |
rs746373244 | in-del | -/TATAACAAT | | | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079173 | AAACTAGCAGTAAGA[-/TATAACAAT]TATAACAATATGCTA | 8453 |
rs746375032 | snp | C/T | 4.985e-05 | 0.00499225 | intron-variant | CUL2 | GRCh38.p7 | 10:35031661 | TACAAAGGGTGCTTC[C/T]GTATATATCACGCCT | 8453 |
rs746375723 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040700 | CACCAGGCTCTGCTT[C/T]TGTGGAAGACAATTT | 8453 |
rs746416508 | in-del | -/AG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054862 | TTCCAAAAATTAAAC[-/AG]AGAATGGTTAAAAGA | 8453 |
rs746430187 | snp | A/C | 3.29919e-05 | 0.00406138 | intron-variant | CUL2 | GRCh38.p7 | 10:35031485 | ACTTTTCTGTTCACA[A/C]CATACCTTTTGAAAG | 8453 |
rs746451648 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077735 | GGCAGGAGAATCGCT[C/T]GAACCCAGGAGGCGG | 8453 |
rs746503175 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095217 | AAATCCCAGCTACTC[-/A]GGAGGCTGAGGCAGG | 8453 |
rs746527430 | snp | A/C | 0.000740065 | 0.019222 | intron-variant | CUL2 | GRCh38.p7 | 10:35033298 | AAATATAAGTACAAA[A/C]CCACATTTTAAGAGG | 8453 |
rs746576301 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091037 | CATACATGTATTTTC[A/G]ATAAAGAAACTTCAC | 8453 |
rs746576419 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079796 | CTGGTGTATCCATAT[C/T]GCTAGGATCACTACT | 8453 |
rs746582051 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076577 | ACCACTCCCGTGTAC[A/G]ACCTCATTGCCACCT | 8453 |
rs746633785 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025399 | CATATATTCCAGCTC[C/T]TTTAATTGACAACTT | 8453 |
rs746637100 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106364 | TCACTCTGTAGCCCA[C/G]GCTGGAGTGCAGTGG | 8453 |
rs746661583 | snp | A/C | 1.91845e-05 | 0.00309707 | intron-variant | CUL2 | GRCh38.p7 | 10:35025207 | ATTCAAACTGTAAAA[A/C]AAAAAAAAAAACACA | 8453 |
rs746714817 | snp | A/G | 6.60012e-05 | 0.00574423 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35035172 | TCCCACACAACTCAC[A/G]TTTTCCTGAGTAAGG | 8453 |
rs746756243 | snp | C/G | 1.7327e-05 | 0.00294333 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010298 | TCTCACACCACGCTG[C/G]AGGAGAGCGACATCA | 8453 |
rs746780917 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120147 | TTCCAAATTTTGTAT[A/G]CTAAAAACTCAGATA | 8453 |
rs746797859 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056081 | AGTAATTGCTACTAT[A/G]TGAAATAATCCTATG | 8453 |
rs746825450 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044507 | ACTAAGAACGATGTT[A/C]AATAAAACCAGGCCA | 8453 |
rs746852983 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070196 | AACATAAAAAATATA[A/T]AAGATCTTTTCAAAC | 8453 |
rs746952358 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035712 | GAAATTTAGGTGGTT[C/T]CCAGTCTCTTGATAT | 8453 |
rs746970624 | snp | A/G | | | synonymous-codon, intron-variant | CUL2 | GRCh38.p7 | 10:35049754 | CAATTTCCTCCACAT[A/G]TCCAATGCTAGCTGC | 8453 |
rs746988587 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041912 | TTCCCTTTTAACACC[C/T]TGAGATGTAATTTAC | 8453 |
rs746997931 | snp | C/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127282 | GGAGGCGGAGCGGAG[C/T]CGGGTGCGGTGGAGC | 8453 |
rs747047947 | in-del | -/T | 2.45432e-05 | 0.003503 | intron-variant | CUL2 | GRCh38.p7 | 10:35039125 | AACACAAAGTTTTAC[-/T]ATGAGGAAAAATCTG | 8453 |
rs747076400 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048658 | AAAAACAACGGGTTA[C/T]ACCCTACTGCTTCAG | 8453 |
rs747104750 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036518 | AATATATCCCACTTA[A/G]CGGTCAGTGCCAGTT | 8453 |
rs747115885 | snp | C/T | 1.97595e-05 | 0.00314315 | intron-variant | CUL2 | GRCh38.p7 | 10:35016154 | GAAAAAGCTTTAATG[C/T]TGATGATGCTTAAAT | 8453 |
rs747122300 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095509 | TAGTCAGCTATTTGT[A/G]CTTCTCTGATTTTGA | 8453 |
rs747136747 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030265 | ATTTTTAATAGCATC[C/T]ACTGAGTGCTGAAGA | 8453 |
rs747148285 | snp | C/T | 1.6552e-05 | 0.00287676 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071302 | CAAAATCTACTACTC[C/T]TGGTTTCAAAGACAT | 8453 |
rs747152179 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100577 | GACCAGCCTGGCCAA[A/C]ATGGCGAAACCTCGT | 8453 |
rs747185663 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088598 | AAACCAGGTGCTTAA[G/T]AAATATCTGTCAACT | 8453 |
rs747193853 | snp | C/T | 1.98218e-05 | 0.0031481 | intron-variant | CUL2 | GRCh38.p7 | 10:35044532 | AGGCCAGATACAAAA[C/T]AGATAAATGTATTCG | 8453 |
rs747206993 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109683 | TGAAAAAGCCTGAAG[A/G]ATGGATGAGTTAGGT | 8453 |
rs747209407 | snp | C/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125949 | ATTCTCCTGCCTCAG[C/T]CTCCCAACTAGCTGG | 8453 |
rs747229768 | snp | A/T | 1.95835e-05 | 0.00312911 | intron-variant | CUL2 | GRCh38.p7 | 10:35029460 | TGAAATGATTAGTAA[A/T]TGCTCATAGTAAAAC | 8453 |
rs747253526 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074636 | GGGGATTACAGGCGT[A/G]AGCCATCGCACCCTA | 8453 |
rs747274039 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061721 | GTAGAGCATTTTCCA[A/G]TATTTTCAGGGAAAC | 8453 |
rs747280845 | snp | G/T | 1.85806e-05 | 0.00304794 | missense | CUL2 | GRCh38.p7 | 10:35039033 | GTATATGAACTTGGA[G/T]GTAGGTATTTTCGAC | 8453 |
rs747314999 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087696 | GCTCATCCAAAACAT[A/G]ACAATTTCAATAAGT | 8453 |
rs747316191 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028697 | ACTATAATTTCTGAA[G/T]CTATTTTTATCACAT | 8453 |
rs747333860 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124615 | GTAAATGTGCAACCC[A/G]GAATTGGCAACTCTG | 8453 |
rs747341139 | in-del | -/CT | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008278 | CAACTCTTCCCAGCA[-/CT]CTCTGCAGGGGAAGG | 8453 |
rs747347284 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051662 | TTGTGGTTTTAACTC[C/T]CATTTTACTGAATGA | 8453 |
rs747350694 | in-del | -/ACA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018287 | GCAAGACTCCATCTC[-/ACA]AAAAAAAAAAAAAAA | 8453 |
rs747375161 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040642 | GTCACAGACTCAGGT[C/T]GGGCAAGAAGGGGTC | 8453 |
rs747387096 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078339 | TCTGTCTTGTTGCCC[A/T]GGCTGGAGTGCAATG | 8453 |
rs747399156 | snp | C/T | 6.36409e-05 | 0.0056406 | intron-variant | CUL2 | GRCh38.p7 | 10:35049786 | GGGAAAAACGAAAAT[C/T]ATCAGGGCTGAATTA | 8453 |
rs747418588 | snp | C/T | 4.95536e-05 | 0.00497738 | intron-variant | CUL2 | GRCh38.p7 | 10:35071181 | AGAACATTGATCAAG[C/T]TGCCATTAAAAGGAT | 8453 |
rs747431711 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086446 | GCCTGCACCACCACA[C/T]CTGGCTAATTTCTGT | 8453 |
rs747484676 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101339 | TCAGCATGGAGACAA[C/T]GGGTCTACCATTGTA | 8453 |
rs747485716 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102297 | AAGAAACAGGCTGGG[G/T]GCTGTGACTCACACC | 8453 |
rs747493399 | in-del | -/TA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101282 | CTGGCAATAGTGGCT[-/TA]TATAATTGTGGGACA | 8453 |
rs747510933 | snp | A/G | 0.000165486 | 0.00909482 | intron-variant | CUL2 | GRCh38.p7 | 10:35032497 | CTGACGTAAGGGCCT[A/G]AATAAAAAAACACGC | 8453 |
rs747526826 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053053 | AGGCTGTAGAACTTT[A/G]TGTGTGCCGTTTTAT | 8453 |
rs747539598 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019198 | CAAGATGATTAAGTG[A/G]CACCATCAGCCAGGA | 8453 |
rs747598780 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057474 | TGGCCAACATGGTGA[A/G]ACCCCGTCTCTACTA | 8453 |
rs747599984 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089321 | AGATTCTAAAGGGTA[A/G]GCAACAGTGTTTTGA | 8453 |
rs747621432 | snp | C/T | 1.71182e-05 | 0.00292554 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35028822 | TACCATCTGTACACT[C/T]TTTTCTAATTCCTGG | 8453 |
rs747644498 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025203 | AATAATTCAAACTGT[-/AA]AAAAAAAAAAAAAAC | 8453 |
rs747665531 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089703 | CAGACCCTAAGGGTT[A/G]AGACAAGAAGTCTAG | 8453 |
rs747682593 | snp | A/T | 5.81401e-05 | 0.00539135 | intron-variant | CUL2 | GRCh38.p7 | 10:35025084 | TTCTAAATTAATATA[A/T]TCATCAGGTAAATTT | 8453 |
rs747752441 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088033 | ATAGGAAAACTGTTC[A/C]CTCAGAATTTCAAAC | 8453 |
rs747812808 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021182 | AGCCATGGACATGGT[A/G]ACAATTTTATTCCAT | 8453 |
rs747819683 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075991 | ACACAAATGTTCACT[A/G]TAGTATTATTCATAA | 8453 |
rs747825622 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069969 | TATCTAATTCAAAGG[A/C]AGAATCTATATTGGT | 8453 |
rs747839869 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050788 | GAAACAATGCTGTGA[C/T]TCCTGTATGCATCAT | 8453 |
rs747851747 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118193 | TGCACTCCCCTTGGT[C/T]ATTCTAAATTTTCAT | 8453 |
rs747852318 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044271 | AAATCCAGTATAAAC[-/T]TGATTATTCTGCCAA | 8453 |
rs747874118 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035588 | TATTTGTAGCTTCAG[A/C]ACACATTTTAACTTA | 8453 |
rs747886885 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35081682 | GCAGACTGCTTGAGC[C/T]CAGGAGTTCGCAGCC | 8453 |
rs747886896 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068890 | ATTTATTTTTGAAAC[A/G]GAGCCTTGCTCTTAT | 8453 |
rs747928775 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060921 | GCTGTATTCTTCCCA[A/G]TACCTATGATACATA | 8453 |
rs747951991 | snp | A/G | 1.66468e-05 | 0.00288498 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35010437 | AGCTCTTGACTGGCT[A/G]ATCACCTGTGGAAGA | 8453 |
rs748087959 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095036 | CAAAAGTAATGTTGG[A/C]GGGGCACAATGGCTC | 8453 |
rs748091949 | snp | C/T | 1.64925e-05 | 0.00287158 | missense | CUL2 | GRCh38.p7 | 10:35035200 | AGGTTGCTGGTTGCT[C/T]GAAGGCCCTCATCAT | 8453 |
rs748092557 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046681 | CAGATCATCTGAGGT[C/T]GGGAGTTAGAGAGCA | 8453 |
rs748127834 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093456 | TTGAGTGTAGGAATT[G/T]GAGATCAGCCTGGAC | 8453 |
rs748147033 | snp | C/G | 1.87359e-05 | 0.00306065 | intron-variant | CUL2 | GRCh38.p7 | 10:35033310 | AAAACCACATTTTAA[C/G]AGGTTCAAGGATATC | 8453 |
rs748152668 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35010754 | CAGCCCCTAGGCCAG[G/T]ATATTTAAATACATT | 8453 |
rs748163737 | snp | C/T | 1.67371e-05 | 0.0028928 | intron-variant | CUL2 | GRCh38.p7 | 10:35062952 | ATCACGTATGTATCA[C/T]TGCTTACCTTATGCA | 8453 |
rs748186127 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012131 | CGCTCTCAGCTCACC[A/G]CAACCTCCATCTCCT | 8453 |
rs748195914 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084920 | GTCAGGAGTTCAAGA[C/T]CAGCCTGGCCAACAT | 8453 |
rs748225841 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060775 | AATGCTTTAGTTTTG[C/T]ATATGTGAATGAGAA | 8453 |
rs748227953 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124394 | CCAGACTAGCCTGGA[C/T]AAGAGACTCCATGTC | 8453 |
rs748247223 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058824 | CCACAGATGCATCTG[C/T]GCCTTGCGTTTTTCC | 8453 |
rs748280473 | snp | A/G | 1.91452e-05 | 0.0030939 | intron-variant | CUL2 | GRCh38.p7 | 10:35044543 | AAAATAGATAAATGT[A/G]TTCGATATGTTTTAT | 8453 |
rs748339350 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026619 | CAATATGCCAAAAGA[A/T]GATACTGATTCATCC | 8453 |
rs748366590 | snp | C/T | 1.71226e-05 | 0.00292592 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010309 | GCTGGAGGAGAGCGA[C/T]ATCACGCGACGTAGC | 8453 |
rs748386184 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039628 | CCAGTACTTTGGGAG[C/G]CCAAGGCAGGTGGAT | 8453 |
rs748408138 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100397 | TTCTCTTATTAGAAA[A/T]GATTGGAGGCATGGC | 8453 |
rs748435681 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072918 | GAAACATCTTTTCTC[A/G]TCTCCCATCATAGGG | 8453 |
rs748461914 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101179 | CTGGAAGAGTCTCAT[A/G]GCCAGTTGGGCATTT | 8453 |
rs748463118 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074575 | CACTGCAACCTCCAC[C/T]TCCCACGTTCAAGTG | 8453 |
rs748489809 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012266 | AACCACTGCTAAAAC[A/G]TCTACAATTTCTAGG | 8453 |
rs748495793 | in-del | -/CAGCTACTCGGGACTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051496 | GGGCGCCTGTAGTCC[-/CAGCTACTCGGGACTA]CAGCTACTCGGGAGG | 8453 |
rs748502141 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051542 | GGCGTGAACCGGCCG[A/G]GCGGAGCCTGCAGTG | 8453 |
rs748511014 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037880 | GATTAATGGCCGGGC[A/G]CGGTGACTCACACCT | 8453 |
rs748538876 | snp | A/G | 3.78924e-05 | 0.00435256 | missense | CUL2 | GRCh38.p7 | 10:35039054 | TATTTTCGACATCGA[A/G]TTTCTTCATCTTTTA | 8453 |
rs748548689 | in-del | -/T | 0.000656814 | 0.0181101 | frameshift-variant | CUL2 | GRCh38.p7 | 10:35038922 | TGGTGTCACTTACCA[-/T]TTTTTTTCTCTTGTC | 8453 |
rs748568230 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017071 | AAGGGCAAAGTGATA[-/T]CAGCAACAGCCTCAA | 8453 |
rs748588900 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106305 | TAAATGTGTTTTTTG[-/T]TTTTTTTTTTGTGGG | 8453 |
rs748590354 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099960 | TAAGAATTGTGTAGT[A/G]GGGTTTTTGTTTTCT | 8453 |
rs748620115 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126859 | TCATTGTTGGATTGT[A/G]GCGCTTCACTCCTGC | 8453 |
rs748620515 | in-del | -/CCACATT | 1.8175e-05 | 0.0030145 | intron-variant | CUL2 | GRCh38.p7 | 10:35031278 | ATTTCTAGGACAATA[-/CCACATT]AAAGACTTACATTAC | 8453 |
rs748628850 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065791 | TTAAACTCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 8453 |
rs748654273 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098254 | CACTGAAAAAGAACT[C/T]ATTTTGAGGAAAAGC | 8453 |
rs748661795 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033350 | AGGTTTATTAGACTT[A/G]TTAGTAAATTTTTCC | 8453 |
rs748684850 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033675 | CAGGGAGGTGGAGGT[C/T]GCAGTGAGCAGAGAT | 8453 |
rs748692279 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102585 | TCAAAAAAATAATAA[A/T]AAATAAATAAATTTA | 8453 |
rs748725559 | snp | A/G | 1.66985e-05 | 0.00288946 | utr-variant-5-prime, synonymous-codon | CUL2 | GRCh38.p7 | 10:35071327 | AGACATTGTGCAAGT[A/G]TAGTGTTGAAATCTG | 8453 |
rs748737957 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009047 | CCTGGGAAACATGGC[A/G]AAACCCCGTCTCTTA | 8453 |
rs748782505 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021052 | ATACTCCTGCCTCAG[A/C]CTCCCACAGTGCTAG | 8453 |
rs748863648 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118054 | CACATCATAATCATC[C/G]AAAGTGCATACATTA | 8453 |
rs748871761 | snp | C/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008827 | GATACTAAGTAATTA[C/T]TGTTTTTGTTAGGAG | 8453 |
rs748907278 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019646 | GCATACTTAAAGTAA[A/G]CCAACAATAAATAAT | 8453 |
rs748915051 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067018 | GATAGGTGTGGTAGC[A/G]CATGCCTGTAATCCC | 8453 |
rs748930790 | snp | G/T | 3.29989e-05 | 0.00406182 | missense, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054490 | CATAGCCATACTGAA[G/T]GTCCGCTTCTGTTAA | 8453 |
rs748932897 | snp | A/C | 5.00221e-05 | 0.00500085 | intron-variant | CUL2 | GRCh38.p7 | 10:35032507 | GGCCTGAATAAAAAA[A/C]CACGCCATAATTAAC | 8453 |
rs748936156 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072882 | CACCAACCTAGTCTG[C/T]AGCCAAGGCCAAAAA | 8453 |
rs748963099 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099953 | AATATACTAAGAATT[C/G]TGTAGTGGGGTTTTT | 8453 |
rs748991198 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074391 | TCAGCCTGATTCATA[C/T]ACTTGCCTTTACCCT | 8453 |
rs748991588 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080793 | CAAAAACAAATGAGT[C/T]GGGGAAAAAAGAGTG | 8453 |
rs749025471 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046600 | TCATTATCTTAAAAA[C/G]TGGGTTATTGGCCAG | 8453 |
rs749025711 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094911 | AACCTCAAATCCTAG[A/T]TCATCTATGATTGCT | 8453 |
rs749078155 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060695 | ACACTCCCTGGCTCC[C/T]AAATACCCACCTTAC | 8453 |
rs749129854 | snp | A/G | 1.7419e-05 | 0.00295114 | intron-variant | CUL2 | GRCh38.p7 | 10:35063102 | TATTTATTGGAGACA[A/G]TTTTAAAACATAATG | 8453 |
rs749206504 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107641 | TAATCCCAGCACTTA[C/G]GGAGGCCGAGGCGGG | 8453 |
rs749222379 | snp | A/G | 1.69493e-05 | 0.00291108 | missense | CUL2 | GRCh38.p7 | 10:35028850 | TGGGGAATTGCAAAC[A/G]TAGATGAAGGAGCCT | 8453 |
rs749259890 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059147 | TGTTGAAATGACAAC[A/G]AAGGATTCAAATATT | 8453 |
rs749304728 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026384 | TACTATATAATTCAC[A/T]ATTTATAACACATTT | 8453 |
rs749336858 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106752 | ATAAATTATGTCTGC[A/G]TTGCCCTTACCTGGT | 8453 |
rs749337166 | snp | A/C/T | 3.31649e-05 | 0.00407204 | intron-variant | CUL2 | GRCh38.p7 | 10:35031633 | AGCTCATGTAGAAAT[A/C/T]GATAATAAATCTTAC | 8453 |
rs749342739 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123387 | CTGTAGATTTTCTAA[C/G]AGAAATCACATCACC | 8453 |
rs749342795 | snp | A/C | 1.67806e-05 | 0.00289656 | intron-variant | CUL2 | GRCh38.p7 | 10:35010460 | GTGGAAGAGATGTGG[A/C]AGTCAAACTACTGCC | 8453 |
rs749345180 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055398 | ACAAATTAAAAACGA[A/C]GACAACCAAAACAAG | 8453 |
rs749358263 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039504 | ATTTTACGTTGGTTT[A/C]TCTTCTTGTAAATGG | 8453 |
rs749364650 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072758 | ACAAAAGGGTCCCAA[A/G]TTAAAAGAGAAACTT | 8453 |
rs749388586 | snp | C/T | 3.30387e-05 | 0.00406427 | intron-variant | CUL2 | GRCh38.p7 | 10:35031450 | CATTCAGAAATAAAG[C/T]TGACCAAAATACAAA | 8453 |
rs749400273 | snp | A/G | 1.65592e-05 | 0.00287738 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35062971 | TTACCTTATGCAAAT[A/G]CCGAACATGATTTTC | 8453 |
rs749403904 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082297 | AATACACTAGACACA[A/T]GGTGAAAAATATCTT | 8453 |
rs749407335 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019477 | GAAGGGGTGGGAAGA[-/C]ACGACAGGGGAAAGG | 8453 |
rs749417640 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071590 | TTTGTATTTTTTTTT[A/G]GTAGAGACGGGGTTT | 8453 |
rs749443608 | snp | A/G | 4.95103e-05 | 0.00497521 | missense | CUL2 | GRCh38.p7 | 10:35011871 | TAAGGGCATTGTGCC[A/G]AAGCACTTTTCGTGC | 8453 |
rs749484746 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037814 | CGCCACTGCATTATA[G/T]CCTGGGCCACAGAGC | 8453 |
rs749609534 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115142 | ACTTGAACCCAGGAG[A/G]CAGGAGATTCTCTTG | 8453 |
rs749610528 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098376 | GATTGCAAGGACTTA[C/T]ACATGACATGTGAAA | 8453 |
rs749619133 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029645 | CCACAGGCTTGCTAT[-/AA]AAAAGTTTTAGAAAA | 8453 |
rs749630417 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015716 | GATATTAAAAATATA[C/T]GGTGGTTAAAAACAG | 8453 |
rs749667862 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050148 | TAACATGGCAAAACC[A/C]TGTCTCTACTAAAAA | 8453 |
rs749671105 | snp | A/T | 2.69705e-05 | 0.00367213 | intron-variant | CUL2 | GRCh38.p7 | 10:35016402 | AACTTCACCTACAAT[A/T]AAAACAAAAACTGAC | 8453 |
rs749693327 | snp | C/T | 0.000185787 | 0.00963634 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074239 | CATAAAGTACAAAGT[C/T]TGTTGTTTCCTTCTA | 8453 |
rs749735921 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111506 | TCAAGCCATCCTCTG[C/T]CTTGGTCTCCCAAAA | 8453 |
rs749754983 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014200 | CACATTTTTTTTTAC[A/G]AATGCCGCAGTAACA | 8453 |
rs749766109 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042769 | AAACATTAAGTGAGT[A/G]TTTCCCTAAGTTCTG | 8453 |
rs749780907 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120967 | AATATGGATATAATT[C/T]CCTTATGTTTTATAG | 8453 |
rs749791085 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076222 | GATTATCAAGAATAG[A/G]CAAATCTAGAGACAG | 8453 |
rs749801344 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056566 | TCCACTCCCATTCAA[C/T]ATCGGCTGAGGGTAT | 8453 |
rs749804706 | snp | C/T | 1.66668e-05 | 0.00288672 | intron-variant | CUL2 | GRCh38.p7 | 10:35044745 | AATTAACAGTCTGAT[C/T]ATTTGTTTTTAAAGG | 8453 |
rs749808020 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031232 | ACTGTACACAATGCT[G/T]CAATGAACATCTTTA | 8453 |
rs749833858 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046694 | TCGGGAGTTAGAGAG[-/C]CAGCCTGGCCAACAT | 8453 |
rs749856215 | snp | G/T | 5.50929e-05 | 0.00524818 | intron-variant | CUL2 | GRCh38.p7 | 10:35044549 | GATAAATGTATTCGA[G/T]ATGTTTTATTTCTTA | 8453 |
rs749889449 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059939 | GCTGCAACATTTACT[-/AA]AAGTTCACAAATAGC | 8453 |
rs749894093 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080573 | AGTGATCCTCCCGCC[C/T]CAGCCTCCTGAGCAG | 8453 |
rs749907206 | snp | C/T | 1.65002e-05 | 0.00287225 | missense | CUL2 | GRCh38.p7 | 10:35010385 | CTATCAGAACTTCAA[C/T]ACACTTCTTAATCAT | 8453 |
rs749946219 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095920 | TACCCCTAGATACTG[C/T]ACAACAGTTTTAACG | 8453 |
rs749956128 | in-del | -/ACTTAG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099512 | TTTCTAAAATAGCAT[-/ACTTAG]ACTTAGCGAGGCTGA | 8453 |
rs749965312 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012818 | CAAGGACTGCACACC[A/G]GAGGCAATCAGGAAG | 8453 |
rs749992329 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061462 | AAGACTCTGTCTCCC[A/C]AAAAAAAAAAAAAAA | 8453 |
rs750011394 | in-del | -/AAC | 1.70496e-05 | 0.00291967 | intron-variant | CUL2 | GRCh38.p7 | 10:35071353 | ATCTGTCAATTAAAA[-/AAC]AATAACAATGTTAGC | 8453 |
rs750014294 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058272 | GAGGCTGAGTCATGC[C/T]AAATGGCCATCCTCT | 8453 |
rs750016309 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011555 | CCTGGGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA | 8453 |
rs750018715 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102885 | GAGACTCTGTCTCAG[-/A]AAAAAAAAAAAAAAA | 8453 |
rs750020937 | snp | C/T | 1.67441e-05 | 0.0028934 | intron-variant | CUL2 | GRCh38.p7 | 10:35011833 | AAGAAGCCCTGAGGA[C/T]TGCCCTCCTTTTACC | 8453 |
rs750045607 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046466 | CTGGAAGGAACCTAA[C/T]ATACGCCACTAGGAG | 8453 |
rs750047433 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073996 | TAATGGTGGCATCAG[C/G]ATTCAGACCCGTGCT | 8453 |
rs750051425 | in-del | -/ATTTTTTTTCTCTTGTCGAATTA | 1.64773e-05 | 0.00287026 | splice-acceptor-variant | CUL2 | GRCh38.p7 | 10:35035297 | CATATTTGCCATGTC[-/ATTTTTTTTCTCTTGTCGAATTA]TGAGAGGAAAAAGAC | 8453 |
rs750068331 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123147 | GATCTACAAACAAGC[A/G]AAACATAACAAAAAA | 8453 |
rs750093421 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060442 | GCAGAACTTCAAGGG[A/G]AAAATAACCCAGTAA | 8453 |
rs750135791 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108892 | ATACAGAAATCTGAT[C/G]TTTGCTGAATTAATG | 8453 |
rs750137157 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060469 | GTAATTTATCTAACA[C/T]CGTTTGCATCAAACA | 8453 |
rs750141186 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028230 | TCTCTTTTCAAAGAA[C/G]ATGTAAGAAGTCCTA | 8453 |
rs750142194 | snp | C/G/T | 0.000379854 | 0.0137765 | intron-variant | CUL2 | GRCh38.p7 | 10:35060852 | GCTGCTTAGCTTGTC[C/G/T]AGATTTTAAAGGCAC | 8453 |
rs750192504 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026264 | CAGATTGCCTGCTTA[A/G]TTCTAATCCAGACAA | 8453 |
rs750259942 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085815 | AACACAAAACAAACA[A/G]TGCAAACTTTTGTAA | 8453 |
rs750311435 | snp | A/G | 1.70255e-05 | 0.00291761 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35016306 | ATAACTGACAGTTTC[A/G]CTGTTGTTAAAGGCA | 8453 |
rs750311815 | snp | A/C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123091 | TGCAGTGAGCTGTGA[A/C/T]GGCACCACTGCACTC | 8453 |
rs750318468 | snp | C/T | 1.75776e-05 | 0.00296454 | missense | CUL2 | GRCh38.p7 | 10:35029603 | ATATCTGTATACATC[C/T]GATGTAGCTTGCTGG | 8453 |
rs750326348 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011345 | GGTGTCCACTGGGCA[C/T]GGTGGCTCACACCTG | 8453 |
rs750335004 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052206 | TCTGATCCATTGGTA[A/G]TTAAGCATCTGTCTT | 8453 |
rs750347709 | snp | A/G | 1.66239e-05 | 0.00288299 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35044650 | TGTTTCAGTCAGAAA[A/G]GGAGACTCAAAAATT | 8453 |
rs750365429 | in-del | -/TCAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040221 | TCATAGTCAAGTATG[-/TCAA]TCAAGACTTTTATTA | 8453 |
rs750367729 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017668 | ACTGCACTCAAACCT[C/G]GGCGACAGAATGAGT | 8453 |
rs750380601 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084541 | TGATATAGAAATCTA[C/T]ACATTCTTAAAGGTA | 8453 |
rs750406676 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116019 | GAAAGATGATATCAC[C/T]ACAGATCTGATAGAC | 8453 |
rs750437596 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099234 | TGTTCTTCTAAAATA[C/T]AAAAAAATTAGCTGG | 8453 |
rs750491293 | snp | A/G | 4.97913e-05 | 0.00498931 | intron-variant | CUL2 | GRCh38.p7 | 10:35032537 | CCACCAGCCATAGGG[A/G]AAAAGTACAGCTAGT | 8453 |
rs750502325 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070690 | TCACTCTCCAGCAAG[C/T]ACACTCTTCCCCCCA | 8453 |
rs750519997 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066446 | GGGATTACAGTTGAG[C/T]GCCACCATGCCTGGC | 8453 |
rs750548235 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041531 | ATTATTTCCTGAAAT[A/G]AGCTTTTCTTTTTCT | 8453 |
rs750578771 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115084 | GGATGTGATGATGTG[C/T]GCCTTTAATCCCAAC | 8453 |
rs750666560 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032050 | ACCTAGGTGAGTTTC[A/G]AGTGGTTTTATAATT | 8453 |
rs750679864 | in-del | -/AAATA | 2.03971e-05 | 0.00319345 | intron-variant | CUL2 | GRCh38.p7 | 10:35013848 | AAAACCAAAATCTTT[-/AAATA]AGAGTTTGCTGCAAG | 8453 |
rs750680369 | snp | A/C | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091930 | ACCGTGTCAGGCCCC[A/C]CCTGCTTTTTGTTTT | 8453 |
rs750711158 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068232 | TTCGAGACCAGCTTG[C/G]CCAACATGGCAAAAC | 8453 |
rs750750129 | snp | A/G | 2.11763e-05 | 0.00325388 | intron-variant | CUL2 | GRCh38.p7 | 10:35028904 | TAGAAGGAAAAAAAT[A/G]AAATAAAATAAGCTA | 8453 |
rs750823832 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083822 | AGCCTGGAGCATAGC[C/T]TGTACTTTCTCTCCT | 8453 |
rs750824406 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025672 | TGGATTATTCTTTTG[A/C]TGATATTATTGTGAA | 8453 |
rs750904366 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018029 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 8453 |
rs750918481 | in-del | -/TTTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119569 | AATTAATTTTATTTA[-/TTTA]TTTATTTATTTATTT | 8453 |
rs750935921 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35081851 | TACAATCTACTGTAT[C/T]TGCTGACTGCTATAT | 8453 |
rs750956232 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070882 | TCTTGAAAGCAATGA[C/T]ATTAGATTTTTTTTT | 8453 |
rs750984751 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109654 | CAAGATTTCCAAACA[C/G]TGGGAGCAGCAAGTG | 8453 |
rs750997014 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037093 | TTAAAATATCTTTCC[C/T]TGTCTCAAGGTTATG | 8453 |
rs751000336 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092636 | CTGCCTTTGCAAAAC[A/G]TGATAGTAAGAGGAA | 8453 |
rs751017334 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108621 | GTTTCCAGATTTGGG[A/T]ATGTATTAGCTGTGC | 8453 |
rs751039528 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021004 | GGTCTCACTATGTTG[C/G]CCAGGCTGATCTTGA | 8453 |
rs751065630 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030967 | GAACCTGCTACCACT[C/T]ATCGGTATGTAAGCA | 8453 |
rs751065740 | snp | C/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009866 | AAGGCATTCTATTTC[C/T]TTATTTTTTTTTTAT | 8453 |
rs751086054 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107448 | CCTCCAAAAAGATAA[A/G]TGCCTAAGTGTTGCC | 8453 |
rs751094766 | in-del | -/TGTTTTCCTGAGTAAGGTTGCTGGTTGC | 1.69899e-05 | 0.00291456 | frameshift-variant | CUL2 | GRCh38.p7 | 10:35033272 | CAAATAGTGTTGGCA[-/TGTTTTCCTGAGTAAGGTTGCTGGTTGC]TCTAAAAATGAAATA | 8453 |
rs751105475 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027893 | GAAGACTATACATCA[A/T]CAAATAAAGTTTAAA | 8453 |
rs751114221 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058071 | CCACTGCACTCCAGC[C/T]GGGGAAACAGCGAGA | 8453 |
rs751128379 | snp | A/G | 1.65162e-05 | 0.00287365 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35011860 | TACCTCTTGAATAAG[A/G]GCATTGTGCCGAAGC | 8453 |
rs751129269 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073217 | CTTCAACTCATTCCC[A/G]AACTATCTATAACGG | 8453 |
rs751139305 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122778 | AAGTAGCTGGGATTA[C/T]AGGCATGCGCCACCA | 8453 |
rs751141733 | snp | A/G | 3.40124e-05 | 0.00412372 | intron-variant | CUL2 | GRCh38.p7 | 10:35062942 | ACATATTTATATCAC[A/G]TATGTATCATTGCTT | 8453 |
rs751158897 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025653 | AAGTTTTAGGGTATA[C/T]CTCTGGATTATTCTT | 8453 |
rs751170730 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123937 | GTATAGAAGATGATG[C/T]CCAAGGACAGAAAAT | 8453 |
rs751182647 | in-del | -/ATG | 5.95055e-05 | 0.00545428 | intron-variant | CUL2 | GRCh38.p7 | 10:35029449 | TATCAACGTACTGAA[-/ATG]ATTAGTAAATGCTCA | 8453 |
rs751235123 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072130 | CTTTACCTTCCTGGA[A/G]CATCAGTATAAGATT | 8453 |
rs751246115 | snp | A/G | 3.29527e-05 | 0.00405898 | missense | CUL2 | GRCh38.p7 | 10:35035293 | ACGTACATATTTGCC[A/G]TGTCTGAGAGGAAAA | 8453 |
rs751270337 | snp | A/G | 0.00011623 | 0.00762243 | intron-variant | CUL2 | GRCh38.p7 | 10:35044881 | TCACTAAAACAAGGT[A/G]TAACACAAAATATTC | 8453 |
rs751316244 | snp | A/G | 1.66646e-05 | 0.00288652 | intron-variant | CUL2 | GRCh38.p7 | 10:35031407 | TTTAAAAATATTTTA[A/G]AAGATTACTTCCTTT | 8453 |
rs751335162 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052096 | CAGTACTGAAAACCA[A/T]TTTTTTGTTTGTTTG | 8453 |
rs751400846 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050837 | AGATTCTCTGATATA[C/T]ATCTACAAGTTGAGA | 8453 |
rs751456199 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065395 | GGAGGCCAAGGTGGG[C/G]AGATCATGAGGTCAG | 8453 |
rs751459576 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032925 | TGCATGTCTATCCAG[A/G]ACATATCAGATTAAA | 8453 |
rs751464070 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066393 | CAAACTTCACCCTCC[A/G]GGTTCAAGCAATTAT | 8453 |
rs751467579 | snp | A/G | 1.65831e-05 | 0.00287945 | missense | CUL2 | GRCh38.p7 | 10:35010423 | CTGGGATTAAACCTA[A/G]CTCTTGACTGGCTAA | 8453 |
rs751481438 | snp | C/T | | | missense | CUL2 | GRCh38.p7 | 10:35016353 | GGTATGTTGTAACCA[C/T]GGCTACATATGGTTT | 8453 |
rs751501219 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099122 | CTTGGGCTGGGTGCA[G/T]TGGCTCATGCCTTTA | 8453 |
rs751513619 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032952 | TAAAAATTCCCCTTA[C/T]ATAGCATAATCACGG | 8453 |
rs751540503 | snp | C/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126346 | CAAGCTTCTTTTGGA[C/G]AAGGACTCAACCAGC | 8453 |
rs751543875 | snp | G/T | 1.72695e-05 | 0.00293845 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35016318 | TTCACTGTTGTTAAA[G/T]GCAAGAAGAACTGCC | 8453 |
rs751555798 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071571 | ACCATGCCCAGCTAA[-/T]TTTTTTGTATTTTTT | 8453 |
rs751590305 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015376 | ATGAAAACATTGATT[C/T]GAATTTCAGAATATG | 8453 |
rs751590375 | in-del | -/AATT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038155 | ACTCCATCTCAAAAA[-/AATT]AATTAATTAAATAAA | 8453 |
rs751595627 | snp | C/T | 1.66344e-05 | 0.0028839 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35033253 | CACTTCCAAAACTGA[C/T]TCCACAAATAGTGTT | 8453 |
rs751642127 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063932 | GTTTCATATGCTGCC[C/T]CCAACTACTGTGACA | 8453 |
rs751674135 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076922 | CCAGGTGTGGTTGTG[A/G]GCACCTGTAGTCCCA | 8453 |
rs751731343 | snp | C/G | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35089928 | AAAATGGGGCCGCGG[C/G]AGAGGCGGCCAAGAT | 8453 |
rs751742526 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042452 | AGTTATAATGTTGAG[C/T]GTGTTAGGTCTCAGG | 8453 |
rs751789223 | snp | A/G | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008072 | CTGAGGGTTTTGCTT[A/G]CTTGTGTTTTCTGCA | 8453 |
rs751793726 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041482 | ATGGAGAGCAAAGCC[C/T]AGGGTTTTGCCCTTG | 8453 |
rs751801583 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116532 | GTACCCAGCTGTGGC[-/T]TTTTTTTTGTGATCT | 8453 |
rs751808356 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104668 | AATTAATTAAATGTA[A/T]AAGTAACCATGGAAT | 8453 |
rs751843874 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056703 | ATAAGATTTCGTCAG[A/G]AGCGGTGCTCCCTCA | 8453 |
rs751855457 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089123 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 8453 |
rs751872876 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104993 | CTGGGCCTCCCAATG[C/T]GCTGGGATTACAGGC | 8453 |
rs751890321 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022396 | AAATTAACCTTTTCT[A/T]GGGTATTCCATGAGC | 8453 |
rs751895357 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055591 | AATAATAACTCCTAG[A/G]AAATTGACTCCAAAG | 8453 |
rs751925949 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107027 | TCACCCAGAGTAGAG[C/T]GCAGTGGCATGATCT | 8453 |
rs751927412 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119126 | CTCTCTGGCTCACAT[C/T]TTCTTCACCTACACA | 8453 |
rs751929559 | snp | A/G | | | synonymous-codon, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054491 | ATAGCCATACTGAAG[A/G]TCCGCTTCTGTTAAT | 8453 |
rs751959092 | in-del | -/CCAGTGAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063702 | TTTACCTTTCACTAG[-/CCAGTGAT]CCAGTGATCTTAACC | 8453 |
rs752022195 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069590 | CTAAACCATATTAGA[C/T]GGACCAAACAAATAA | 8453 |
rs752035128 | snp | A/G | 5.19908e-05 | 0.0050983 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35029533 | CAAATCTATTACTGT[A/G]TCTTGGTTTTTGATA | 8453 |
rs752044857 | snp | A/G | 3.30874e-05 | 0.00406726 | intron-variant | CUL2 | GRCh38.p7 | 10:35060828 | TGTCAACTACTGAAT[A/G]CAGGCAACGCTGCTT | 8453 |
rs752053946 | in-del | -/TTTG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071407 | TTTTTGTTGTTGTTT[-/TTTG]TTTGTTTGCTTTGAG | 8453 |
rs752057906 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036152 | AAAGGTAACCACTGC[C/T]GTGACTTCTAAATCA | 8453 |
rs752170798 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023992 | GGTGTGCTCCACCAC[A/G]CCTGGCTAATTTTTG | 8453 |
rs752209436 | in-del | -/AAAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046932 | AAAACAAAACAAAAA[-/AAAAA]CAAAAAACTGGGTTA | 8453 |
rs752213158 | snp | C/T | 2.22576e-05 | 0.00333591 | missense | CUL2 | GRCh38.p7 | 10:35038956 | TTATATTATGACATT[C/T]TGCATGTAAAAACTG | 8453 |
rs752224240 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105829 | AGGCAATGTCCTGAA[-/A]AAAAAAAAAAAAAGT | 8453 |
rs752232160 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037366 | CTAGGATCTCTTATT[C/T]TATTAGGATATCTGT | 8453 |
rs752243870 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072034 | AAGGTTTTGGCCCCA[A/G]ATCCTTGTGGTTTGC | 8453 |
rs752261010 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071248 | ATTCCAACATGACCA[C/T]GGCTTTTATTGTCGT | 8453 |
rs752266272 | snp | A/C | 1.64904e-05 | 0.00287139 | intron-variant | CUL2 | GRCh38.p7 | 10:35035331 | TGAGGGTTAACTCCC[A/C]AATATTTTCATTTAT | 8453 |
rs752298963 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071037 | ATGAAAGGTTATCAA[A/T]TACTGATTGCCATAA | 8453 |
rs752309764 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098807 | GGCACGGTGGCAGGC[A/G]CCTGTAATCCCAGTT | 8453 |
rs752329880 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077989 | TATTCTTTTTTTGTA[C/T]GTGTTTACAATTTTC | 8453 |
rs752332569 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014566 | GGCCAGGCATGGTGG[C/G]TCACGTCTGTAATCC | 8453 |
rs752374286 | snp | C/T | 2.35624e-05 | 0.00343229 | intron-variant | CUL2 | GRCh38.p7 | 10:35028917 | ATAAAATAAAATAAG[C/T]TAAATGGATCAACAT | 8453 |
rs752383212 | snp | A/G | 9.88875e-05 | 0.00703093 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35032437 | CCACCAAACTTACCA[A/G]TTCAGGTGCTTTGCA | 8453 |
rs752410935 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050666 | GCCATAGCTCAATCA[C/T]TGGCACTGCTATACA | 8453 |
rs752451742 | snp | A/G | 1.65089e-05 | 0.00287301 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35011863 | CTCTTGAATAAGGGC[A/G]TTGTGCCGAAGCACT | 8453 |
rs752461340 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036430 | GTATATATGTCCAGG[C/T]ATTGGCAGTGGGGAG | 8453 |
rs752468137 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049592 | AAACCAGCCCCAAGG[C/T]TAGTCACTGGCTCTG | 8453 |
rs752491475 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096278 | AAAACAGCTATTTTG[A/G]GCTTACAAAAGTGCG | 8453 |
rs752537212 | snp | A/G | 4.96438e-05 | 0.00498191 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35031614 | GTTGTCACAGTACTT[A/G]GCAAGCTCATGTAGA | 8453 |
rs752569322 | snp | A/G | 1.71396e-05 | 0.00292737 | intron-variant | CUL2 | GRCh38.p7 | 10:35063088 | TATTAAGGTTTTCAT[A/G]TTTATTGGAGACAAT | 8453 |
rs752574858 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014988 | CCATAATTAATTAAC[C/T]TTAAGAAATCCCTAT | 8453 |
rs752579429 | in-del | -/AAAAT | 3.99018e-05 | 0.00446647 | intron-variant | CUL2 | GRCh38.p7 | 10:35028899 | CAGCCTAGAAGGAAA[-/AAAAT]AAAATAAAATAAGCT | 8453 |
rs752591906 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35112244 | TGCTTTCAGCGAAGA[C/T]GGAAAGACCAGAACT | 8453 |
rs752593659 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075352 | GGAAAGTTTACACAA[A/G]GATGTGAAAGAGACA | 8453 |
rs752594283 | in-del | -/A | 3.47527e-05 | 0.00416835 | intron-variant | CUL2 | GRCh38.p7 | 10:35032500 | CGTAAGGGCCTGAAT[-/A]AAAAAAACACGCCAT | 8453 |
rs752594496 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063244 | TTACTTTATCTAAGA[C/T]TCATTCACTTATTCA | 8453 |
rs752612909 | snp | A/G | 6.66956e-05 | 0.00577437 | intron-variant | CUL2 | GRCh38.p7 | 10:35011991 | AAGAAAAGAAAAAAG[A/G]CCCAACAAGACATTA | 8453 |
rs752710326 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089032 | AATACAAAATTAGCC[A/G]GGCATGGTGGCGCAT | 8453 |
rs752736077 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030613 | GTCTTGAACTACTGA[C/G]CTCAAACAATCTACA | 8453 |
rs752782779 | in-del | -/TC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086814 | ATCCTCTTTCTACAT[-/TC]TCTGTGTTCTCATCC | 8453 |
rs752848187 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047570 | AGCTAAGATCGTGCA[A/G]TTGCACTCCAACCTG | 8453 |
rs752865367 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054104 | TTTGTGTTTCCTCTC[C/T]TCTAGCCTGTCTTTT | 8453 |
rs752868045 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087534 | TTCTCACCTCCACTT[C/G]AACAACGAAATCCAA | 8453 |
rs752902160 | snp | A/G | 3.34644e-05 | 0.00409036 | intron-variant | CUL2 | GRCh38.p7 | 10:35044719 | AAGAAATTAGAACAA[A/G]CAGTTTAAGAAATTA | 8453 |
rs752914995 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055475 | TCGGGGCTCACGCCT[A/G]TAATCCCAGTGCTTT | 8453 |
rs752965349 | in-del | -/GCCATCACACCCGGCCAGTTATTTGTTT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071691 | GGATTACAGGCATGA[-/GCCATCACACCCGGCCAGTTATTTGTTT]ACCATCACACCCGGC | 8453 |
rs752972605 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022782 | CTGGGCACGGTGGCT[C/T]ATGCCTGTAATCCCA | 8453 |
rs753007772 | in-del | -/TTTT | 1.88382e-05 | 0.003069 | intron-variant | CUL2 | GRCh38.p7 | 10:35071390 | ATTCCATGAGCTTAG[-/TTTT]TTTGTTGTTGTTTTT | 8453 |
rs753031315 | snp | A/G | | | synonymous-codon | CUL2 | GRCh38.p7 | 10:35035193 | CTGAGTAAGGTTGCT[A/G]GTTGCTCGAAGGCCC | 8453 |
rs753129544 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019068 | TAAAAAGGACTCTTA[C/T]CAACATTTAAGTTTG | 8453 |
rs753143707 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061462 | AAGACTCTGTCTCCC[-/AA]AAAAAAAAAAAAAAA | 8453 |
rs753167338 | snp | A/C | 1.65296e-05 | 0.00287481 | missense | CUL2 | GRCh38.p7 | 10:35010343 | ATTCATCTGCCGACG[A/C]CTGGCTGCGTTCTAT | 8453 |
rs753175619 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116313 | TCATGCCACTGCACT[A/C]CAGCCTGGGCGACGG | 8453 |
rs753221929 | snp | C/T | 2.32258e-05 | 0.00340769 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35016384 | GCCCAAATAGTTCAT[C/T]TTAACTTCACCTACA | 8453 |
rs753251147 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090780 | GCTGAGCTGATGGAC[A/G]CAGTACCCACCCACT | 8453 |
rs753258062 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036232 | GTCTGGCTTCTTGTG[C/T]TCAACATGTGTATAA | 8453 |
rs753288684 | snp | A/C | 2.00359e-05 | 0.00316505 | intron-variant | CUL2 | GRCh38.p7 | 10:35029437 | ATGAATCATTTGTAT[A/C]AACGTACTGAAATGA | 8453 |
rs753291553 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119364 | TCTCTATTTCTGTGG[A/G]TCTCCATTTGCACTG | 8453 |
rs753314497 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013983 | ACAAACAGGAAAAAA[A/C]CCAATTATTTTCTAC | 8453 |
rs753352576 | snp | C/T | 8.66754e-05 | 0.00658257 | missense | CUL2 | GRCh38.p7 | 10:35029577 | TATTGTTGAGATCAG[C/T]GCTGACACTCATATC | 8453 |
rs753363533 | in-del | -/AAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017218 | CTATTATGTCTCATA[-/AAC]AACATTTTTCTTTCC | 8453 |
rs753391185 | snp | C/G | 2.53875e-05 | 0.00356274 | intron-variant | CUL2 | GRCh38.p7 | 10:35039130 | AAAGTTTTACTATGA[C/G]GAAAAATCTGTAATA | 8453 |
rs753395829 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082571 | TAAATTTTATGTCAT[G/T]TATGTTTTAAGTGCT | 8453 |
rs753403438 | in-del | -/TTTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068868 | TTAGTAGCATAGTCT[-/TTTA]TTTATTTATTTTTGA | 8453 |
rs753415159 | snp | G/T | 1.66043e-05 | 0.00288129 | missense | CUL2 | GRCh38.p7 | 10:35031371 | TTAAACGTTTTGCCA[G/T]CATTCTTGCGTAGAA | 8453 |
rs753424754 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075545 | CTGAAATCACCACAG[C/T]CCCTTTTAGTTTCCT | 8453 |
rs753533886 | snp | C/T | 8.60499e-05 | 0.00655878 | intron-variant | CUL2 | GRCh38.p7 | 10:35013804 | ATCAATATCTTCCTA[C/T]ATTTAAAAATAAAAC | 8453 |
rs753536592 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048029 | GTCAGATCACCACCA[C/T]TGACTTTTGCATGTC | 8453 |
rs753566158 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013191 | TAAAAGTACAAAAAA[C/T]AAAATTAGCCAGGCA | 8453 |
rs753595826 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011705 | ATTGTGAGTGAGTAC[A/G]ATTCTGATTAAGTAT | 8453 |
rs753638778 | in-del | -/A | 4.44454e-05 | 0.00471389 | intron-variant | CUL2 | GRCh38.p7 | 10:35016442 | ACCATTCAAAGAAAC[-/A]TTTCAAATTTACTTT | 8453 |
rs753643801 | in-del | -/C | 2.0947e-05 | 0.00323621 | intron-variant | CUL2 | GRCh38.p7 | 10:35025223 | AAAAAAAAAAACACA[-/C]ATTATTTTTAGCTAC | 8453 |
rs753649246 | snp | C/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091436 | TTATTTCAGTAAAGG[C/G]TTTTTATATACGAAA | 8453 |
rs753690645 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124182 | GCGAGACTCTGCCTC[C/T]AAGTAAATACATTTA | 8453 |
rs753693309 | snp | A/C | 0.000667089 | 0.018251 | intron-variant | CUL2 | GRCh38.p7 | 10:35032521 | AACACGCCATAATTA[A/C]CCACCAGCCATAGGG | 8453 |
rs753703112 | snp | C/T | 2.09932e-05 | 0.00323978 | missense | CUL2 | GRCh38.p7 | 10:35038970 | TCTGCATGTAAAAAC[C/T]GTAAGTGGTCTGCTA | 8453 |
rs753727663 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063750 | TCGGGTGGCATTTCC[-/T]TTTTTTTTTTTTTTT | 8453 |
rs753728450 | snp | C/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125343 | AAGACTACATACATA[C/T]GGGAGTAAAATACTG | 8453 |
rs753739913 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087209 | GGCGTGCGCCACCAC[A/G]CCTGGCTAATGTTTT | 8453 |
rs753761620 | snp | A/C | 1.64779e-05 | 0.00287031 | intron-variant | CUL2 | GRCh38.p7 | 10:35071372 | ATAACAATGTTAGCA[A/C]TAATTCCATGAGCTT | 8453 |
rs753764893 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050236 | TGAGGCAGGAGAATT[A/G]CTTGAACCTGGGAGG | 8453 |
rs753788827 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047607 | GAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs753812741 | snp | C/T | 3.29919e-05 | 0.00406138 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071257 | TGACCACGGCTTTTA[C/T]TGTCGTCAAAAGTTT | 8453 |
rs753818658 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077593 | GAGGCCGAGGCAGGC[A/G]CATTACCTGAGGTCA | 8453 |
rs753978296 | snp | A/G | 1.70188e-05 | 0.00291704 | intron-variant | CUL2 | GRCh38.p7 | 10:35044918 | ATACAAATTATCTAT[A/G]GAAATATACCCAAAA | 8453 |
rs753981353 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021017 | TGCCCAGGCTGATCT[C/T]GAACTCCTGGGCTCA | 8453 |
rs754003879 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018008 | ATTATAAATGAAATT[A/G]GGCCAGGCGTGGTGG | 8453 |
rs754055620 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067673 | CACTTAAACCCAGGA[C/G]GGGGAGGCTGCAGTG | 8453 |
rs754060882 | snp | G/T | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008068 | ACTTCTGAGGGTTTT[G/T]CTTACTTGTGTTTTC | 8453 |
rs754073291 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052464 | GAGATACACATAAAT[A/G]TAACTCCATGAGCAT | 8453 |
rs754079281 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116117 | GGAGGCCGAGGTGGG[C/T]AGATAACCTGAGGTC | 8453 |
rs754088220 | in-del | -/CT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086322 | GGCAACACAATGAAA[-/CT]CTCTTAGTTCTGTCA | 8453 |
rs754103665 | snp | C/T | 1.648e-05 | 0.0028705 | missense | CUL2 | GRCh38.p7 | 10:35032446 | TTACCAGTTCAGGTG[C/T]TTTGCAAACAGACTT | 8453 |
rs754119589 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046164 | TAATTCTGTCAGTCA[C/T]AGAGAATCTTGATAT | 8453 |
rs754126665 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034262 | CTATAAACGTAATAA[C/T]GTAAACTAGTAAGTT | 8453 |
rs754137586 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043961 | TAGTCCCAGCTACTT[C/G]GTAGGCTGAGACAGG | 8453 |
rs754150305 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078865 | AATAAAAATTTGGCA[G/T]CCAAAAATTATCAGT | 8453 |
rs754165409 | snp | A/T | 0.000329301 | 0.0128274 | missense | CUL2 | GRCh38.p7 | 10:35025190 | ATGTTGGCTATAAAA[A/T]AATTCAAACTGTAAA | 8453 |
rs754172444 | snp | C/T | 3.32033e-05 | 0.00407438 | intron-variant | CUL2 | GRCh38.p7 | 10:35035147 | TGATTAGGAGGAAAA[C/T]ATTGCAGTTTCCCAC | 8453 |
rs754237950 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022616 | GAGAAACTTTTTGTT[A/G]AATGAATAAATGGAG | 8453 |
rs754239563 | snp | G/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126698 | CACGGGCAGCTTCCG[G/T]TTTCCAGCCTTGCCC | 8453 |
rs754249159 | snp | A/C | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092255 | GCCACCATGCCTGGC[A/C]TCCTCTGTCTTTTTG | 8453 |
rs754301277 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084308 | ACAGTATCAGTCTGA[A/C]TTTTTAATTCTCCAG | 8453 |
rs754321625 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043929 | TAAAAGTTGCTGGGC[C/G]TGGTGGTGTGTGCCT | 8453 |
rs754369641 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099388 | AGTGAGACTCCGTCT[-/A]AAAAAAAAAAAAAAA | 8453 |
rs754372041 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090802 | CCACCCACTACCCGT[C/T]AGTTCAGGGACTGCT | 8453 |
rs754395910 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35112806 | GAAATCAAAATAGAT[A/C]AAGATTAAAGGCCGT | 8453 |
rs754397525 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070893 | ATGACATTAGATTTT[A/T]TTTTTTACCTGTTTA | 8453 |
rs754411084 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025403 | TATTCCAGCTCTTTT[A/C]ATTGACAACTTGTTC | 8453 |
rs754464605 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055968 | GTCTCAGCACAGACA[C/T]ACCTTTCAGGTGTGC | 8453 |
rs754499892 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077749 | TTGAACCCAGGAGGC[A/G]GGGGTTGCGGTGAGT | 8453 |
rs754509044 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119462 | GTTATGGACTAATTT[C/T]AGCTCTCTGTGAAAA | 8453 |
rs754523246 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069918 | ATTAAGATTCTTGCC[C/G]CAAATCAATCCATAA | 8453 |
rs754541279 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082669 | CTCTAAAAATTTTTA[A/G]ATGGATGCATTCTAA | 8453 |
rs754593505 | in-del | -/GCAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046890 | GAGTGAGACTCTGTC[-/GCAAA]TCAAAACAAAACAAA | 8453 |
rs754601261 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011703 | AAATTGTGAGTGAGT[A/T]CGATTCTGATTAAGT | 8453 |
rs754620314 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035568 | GTGTACTGTATTTTG[C/T]ATATTATTTGTAGCT | 8453 |
rs754641323 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043213 | TGCCACCACTTGCCA[-/G]TGGCATATTTTTGAC | 8453 |
rs754655036 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025215 | TGTAAAAAAAAAAAA[A/C]AAACACACATTATTT | 8453 |
rs754713861 | snp | A/G | 6.61748e-05 | 0.00575178 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35062974 | CCTTATGCAAATGCC[A/G]AACATGATTTTCCAA | 8453 |
rs754717106 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096143 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAGGAG | 8453 |
rs754745671 | snp | A/G | 4.94328e-05 | 0.00497131 | intron-variant | CUL2 | GRCh38.p7 | 10:35035299 | ATATTTGCCATGTCT[A/G]AGAGGAAAAAGACAT | 8453 |
rs754749290 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110635 | AGTCCAAGATCAAGA[A/T]GCTGGTAGGGTTGGT | 8453 |
rs754769882 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027658 | ATCACTAAGGCAGGA[A/T]GGATTAATTTACATG | 8453 |
rs754828470 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094165 | TCTCAGGTATTTCAT[A/T]ATAACAATACAAGAA | 8453 |
rs754835290 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094943 | TCCTTGTTTTACTTT[G/T]TAGCTAATGCTACAT | 8453 |
rs754838575 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061981 | AATAAAACTGTGTTG[C/T]TTTATTCCCATTTTA | 8453 |
rs754850217 | snp | A/G | | | synonymous-codon | CUL2 | GRCh38.p7 | 10:35011872 | AAGGGCATTGTGCCG[A/G]AGCACTTTTCGTGCT | 8453 |
rs754853022 | snp | A/C/G | 3.3028e-05 | 0.00406363 | missense | CUL2 | GRCh38.p7 | 10:35011861 | ACCTCTTGAATAAGG[A/C/G]CATTGTGCCGAAGCA | 8453 |
rs754887780 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060733 | ATAGACCTTTCCCCA[C/T]AGCAGAGAAAAGTCC | 8453 |
rs754889445 | snp | C/G | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074188 | AGACACAAAAATAAC[C/G]TACCTAAGCCAAAAA | 8453 |
rs754930313 | snp | C/T | 1.69542e-05 | 0.0029115 | intron-variant | CUL2 | GRCh38.p7 | 10:35062943 | CATATTTATATCACG[C/T]ATGTATCATTGCTTA | 8453 |
rs754962706 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021025 | CTGATCTTGAACTCC[C/T]GGGCTCAAGTGATAC | 8453 |
rs754974055 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028379 | TTACTACTTACTCTA[C/T]TAGCAGTTACTTCAC | 8453 |
rs755001158 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047210 | TAAAAGAAAGATGTG[A/G]CTCACATCAGAAACC | 8453 |
rs755013132 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073432 | CCCTACAAATGATCC[A/G]GAATCAGGCCCTCAG | 8453 |
rs755025910 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085930 | TGAGTGACGGGATCA[C/T]TGTATCCTAAACCTC | 8453 |
rs755042662 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040216 | TTTAGTCATAGTCAA[A/G]TATGTCAATCAAGAC | 8453 |
rs755043491 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087395 | ACTTAAGTTCCATGA[A/G]GCCAGAAATTTTTTA | 8453 |
rs755074217 | snp | A/T | 0.000371402 | 0.0136222 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074169 | CAGATCTTGCCCTTA[A/T]CAAAGACACAAAAAT | 8453 |
rs755099992 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110219 | GAACAAGGAGGTATA[A/G]TTGTTGGCTAGGGCT | 8453 |
rs755103954 | snp | C/T | 1.67245e-05 | 0.00289171 | intron-variant | CUL2 | GRCh38.p7 | 10:35044710 | TCATATTAGAAGAAA[C/T]TAGAACAAGCAGTTT | 8453 |
rs755114827 | snp | A/G | 1.75422e-05 | 0.00296155 | missense | CUL2 | GRCh38.p7 | 10:35016328 | TTAAAGGCAAGAAGA[A/G]CTGCCATTTGGTATG | 8453 |
rs755148727 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101172 | CTTCTATCTGGAAGA[G/T]TCTCATAGCCAGTTG | 8453 |
rs755160659 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043972 | ACTTCGTAGGCTGAG[A/G]CAGGAGGACCACTTG | 8453 |
rs755167712 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054001 | GTACCTCAAGAACTT[G/T]AATGGACCAAACTGC | 8453 |
rs755220646 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052621 | TTAAAAATTGGGGGG[C/T]GCGGTGGCTCATACC | 8453 |
rs755235469 | snp | C/T | 1.97276e-05 | 0.0031406 | intron-variant | CUL2 | GRCh38.p7 | 10:35044536 | CAGATACAAAATAGA[C/T]AAATGTATTCGATAT | 8453 |
rs755236453 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061171 | AATGAAAGTGAAGCA[A/T]CCATAATAGAGAATA | 8453 |
rs755276256 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099721 | GCAGAGGTTGCAGCC[G/T]GGGCGACAGAGCAAG | 8453 |
rs755279691 | snp | C/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126743 | CGCCCCACCTCCAGG[C/G]TAGTTCCTCCTCTTG | 8453 |
rs755288962 | in-del | -/T/TT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029076 | TGTTTTTTTTTTTTG[-/T/TT]AGATGGAGTCTCACT | 8453 |
rs755309836 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, intron-variant | CUL2 | GRCh38.p7 | 10:35054457 | TTTCCATAAGTGGTT[C/T]ATTCATATCTACACC | 8453 |
rs755317119 | in-del | -/A | 1.64792e-05 | 0.00287042 | intron-variant | CUL2 | GRCh38.p7 | 10:35035304 | GCCATGTCTGAGAGG[-/A]AAAAAGACATCTGAG | 8453 |
rs755325474 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066764 | ATATAATTTAGAATA[C/G]GGTCAGGCAGTTGCT | 8453 |
rs755334797 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100009 | CAGAGTCTTGCTATG[C/T]TGCCCAGGCTGGTCT | 8453 |
rs755376683 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078895 | TAAGATACAATAGAG[C/T]GGTCTAAGTTGACTT | 8453 |
rs755423014 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115171 | TGAACCCAGGAAGCA[C/G]AGGTTGCAGTGAGCC | 8453 |
rs755454304 | snp | C/T | 1.66818e-05 | 0.00288802 | missense | CUL2 | GRCh38.p7 | 10:35033258 | CCAAAACTGACTCCA[C/T]AAATAGTGTTGGCAT | 8453 |
rs755457474 | snp | C/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009528 | TGAAAAGCTCTCTCT[C/G]TGCCAGACTTGAGGT | 8453 |
rs755461053 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092343 | GCAGGGATCAAGACA[A/G]TGCCACCAACCTGTC | 8453 |
rs755517521 | snp | G/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090879 | TTGTTTCAGACCTAT[G/T]TGAATATCCTAAGAC | 8453 |
rs755529441 | snp | A/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081456 | ATTTTTAAAAAAAAC[A/T]ATTCTCATATATGTA | 8453 |
rs755537074 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058613 | AGTAATCATTCCTTC[C/G]CTGAGATGTCTGCAC | 8453 |
rs755543916 | snp | C/T | 2.21222e-05 | 0.00332575 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35038957 | TATATTATGACATTC[C/T]GCATGTAAAAACTGT | 8453 |
rs755583126 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034920 | CGAGCTTATTTTCCT[A/G]TGGAAAGTTAACAAC | 8453 |
rs755653884 | snp | C/T | 1.69149e-05 | 0.00290812 | missense | CUL2 | GRCh38.p7 | 10:35028842 | CTAATTCCTGGGGAA[C/T]TGCAAACGTAGATGA | 8453 |
rs755688137 | in-del | -/A | 5.12229e-05 | 0.00506052 | intron-variant | CUL2 | GRCh38.p7 | 10:35071356 | TGTCAATTAAAAAAC[-/A]ATAACAATGTTAGCA | 8453 |
rs755721861 | snp | A/T | 2.13796e-05 | 0.00326946 | intron-variant | CUL2 | GRCh38.p7 | 10:35049787 | GGAAAAACGAAAATC[A/T]TCAGGGCTGAATTAC | 8453 |
rs755749802 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046470 | AAGGAACCTAATATA[C/T]GCCACTAGGAGAAGA | 8453 |
rs755767099 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011603 | AGCCTGGGCGACAGA[A/G]CAAGACTCTGTCTCA | 8453 |
rs755779782 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094584 | GTTTGAGAACCACTG[C/G]TCTAACTCATGAAAT | 8453 |
rs755842952 | in-del | -/C | 7.03334e-05 | 0.00592973 | intron-variant | CUL2 | GRCh38.p7 | 10:35016427 | CTGACAGTGAATTGA[-/C]CCATTCAAAGAAACA | 8453 |
rs755846385 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028258 | CTAATTTAGCCTCCT[A/G]TTCTGAAAGTCTATC | 8453 |
rs755861188 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097365 | ATTGCTTGAGGCCAG[A/C]AGTGCAAGACCAGCC | 8453 |
rs755885769 | snp | C/T | 2.3491e-05 | 0.00342709 | intron-variant | CUL2 | GRCh38.p7 | 10:35028918 | TAAAATAAAATAAGC[C/T]AAATGGATCAACATC | 8453 |
rs755913866 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040102 | AGGTTGCAGTGAGCC[A/G]ACATCACGCCACTGC | 8453 |
rs755941948 | in-del | -/CA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35024556 | ATCTTCAGGCAACTC[-/CA]CACACAGTCCACAAT | 8453 |
rs755969745 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073377 | TCCTATCATCAACTG[C/T]GCACATGAGTATTTC | 8453 |
rs755999799 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107611 | ACTTGGGCCTGGCGC[A/G]GTGGCTCATGCCTGT | 8453 |
rs755999817 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124151 | TGCACCACTGTACTC[C/T]AACCTGGGTGACAGA | 8453 |
rs756023244 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085833 | CAAACTTTTGTAAAG[A/T]CTCACAAAAAGAAAC | 8453 |
rs756061053 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040772 | CTTCCAGGTGAAGTA[-/T]TTCCACCTCAGATCC | 8453 |
rs756067265 | snp | C/T | 1.64996e-05 | 0.0028722 | intron-variant | CUL2 | GRCh38.p7 | 10:35035337 | TTAACTCCCAAATAT[C/T]TTCATTTATTAGGTA | 8453 |
rs756121965 | snp | C/T | 7.30434e-05 | 0.00604288 | intron-variant | CUL2 | GRCh38.p7 | 10:35012002 | AAAGACCCAACAAGA[C/T]ATTAAGTCACTGAAC | 8453 |
rs756145566 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084593 | CAATATGACAGATAC[A/G]TTACCAGTAAGATTC | 8453 |
rs756230822 | snp | A/G | 1.65529e-05 | 0.00287683 | missense | CUL2 | GRCh38.p7 | 10:35031615 | TTGTCACAGTACTTA[A/G]CAAGCTCATGTAGAA | 8453 |
rs756240121 | snp | C/T | 1.67365e-05 | 0.00289275 | intron-variant | CUL2 | GRCh38.p7 | 10:35044720 | AGAAATTAGAACAAG[C/T]AGTTTAAGAAATTAA | 8453 |
rs756246734 | in-del | -/C | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128769 | TGACCTCGTGATCCG[-/C]CCGCGTCGGCCTCCC | 8453 |
rs756256845 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107512 | ATGTGTCCTTTAATG[C/T]TGTTGTATCTTTAAT | 8453 |
rs756265311 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108468 | TCAAAAAAAAAAAAA[-/G]GAAAAAAAGAAAAAA | 8453 |
rs756268022 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078664 | AGCAAAAAAACAATT[C/T]AGATAATTTCAGCAG | 8453 |
rs756268592 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018055 | CAGCATTTTGGGAGG[C/T]GGAGGCAGGCGGATC | 8453 |
rs756281739 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043956 | GCCTGTAGTCCCAGC[G/T]ACTTCGTAGGCTGAG | 8453 |
rs756332152 | snp | A/G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051091 | GAGGCTGAGACGGGC[A/G/T]GATCACGAGGTCAGG | 8453 |
rs756375755 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111554 | TAAGCCATTGCACCC[A/T]GCCAATAATTCTAAT | 8453 |
rs756378379 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083855 | AACTGAATTAAAACA[A/G]GGCTGAGATATTTTT | 8453 |
rs756386044 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015513 | AAAATAAAAACAAAA[A/C]ATTATTTATAGGAAT | 8453 |
rs756409534 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032153 | AAACTTTATCATCAG[A/C]TTTCCTTTAGATTTC | 8453 |
rs756412362 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35112820 | TCAAGATTAAAGGCC[A/G]TTCTTTACTTACACC | 8453 |
rs756413953 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073794 | TTTTTAGTAGAGACA[-/G]GGTTTTTCACCATGT | 8453 |
rs756456811 | snp | A/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128480 | CGCTGTTTTTTATTT[A/G]TTGTTTTTTTGTTTT | 8453 |
rs756467238 | snp | C/T | 3.35345e-05 | 0.00409465 | intron-variant | CUL2 | GRCh38.p7 | 10:35044906 | ATATTCTTGAGAATA[C/T]AAATTATCTATGGAA | 8453 |
rs756514558 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090493 | CGGCGGGACAGGGGC[A/G]GTAGGGAGGGGGGGA | 8453 |
rs756520379 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028720 | ATCACATGAACCCTT[-/A]AAGACTCTGAAAAAA | 8453 |
rs756531940 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042690 | ATTTCAGACCTTCCC[C/T]TATGTGTCTCCTCAA | 8453 |
rs756542165 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058364 | GGTAAGGCAAAAAGC[C/T]TCAGCCATTTCCTGA | 8453 |
rs756551863 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057290 | TAAAATTTAAACTAA[C/T]TTACATTAACTATGT | 8453 |
rs756560415 | snp | C/T | 1.71914e-05 | 0.0029318 | missense | CUL2 | GRCh38.p7 | 10:35025176 | TTCCTTCCACTGAAA[C/T]GTTGGCTATAAAATA | 8453 |
rs756566341 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089238 | AAGGATCTTCCAGAT[A/G]CTGTATAAGGGCAAA | 8453 |
rs756667141 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021007 | CTCACTATGTTGCCC[A/G]GGCTGATCTTGAACT | 8453 |
rs756693703 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023933 | TCCAGCTCGTGGGCT[C/G]AAGTGATCCTCCCAT | 8453 |
rs756720081 | snp | A/T | | | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079192 | ACAATTATAACAATA[A/T]GCTATAATAAAAGTT | 8453 |
rs756757263 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046297 | GTGAGATACTGATCT[A/G]AACTGTTACCTATTT | 8453 |
rs756758027 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097154 | TATCTTATGTAAACT[A/G]TAGATTTACTGAGCA | 8453 |
rs756801647 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35092726 | GCATAGGCCAACTTA[A/C]TTTGGGGAGGAAGTT | 8453 |
rs756814511 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122970 | TAGAGAACCCATCTA[C/T]ATAAAAAAATTAAAA | 8453 |
rs756851436 | in-del | -/G | 1.93272e-05 | 0.00310857 | intron-variant | CUL2 | GRCh38.p7 | 10:35033319 | TTTTAAGAGGTTCAA[-/G]GATATCCAAACTATG | 8453 |
rs756872966 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056146 | CTCTCTAGAATGTAC[A/G]GTATACAAAGCAAGA | 8453 |
rs756885884 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060297 | GGACAAAATAAAAGA[A/C]AGAAAAATAGAAAAA | 8453 |
rs756887696 | snp | A/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009871 | ATTCTATTTCTTTAT[A/T]TTTTTTTTATTTGAC | 8453 |
rs756901851 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073259 | TTTTACTCTGCAAAA[C/T]TGAGGGGAAGGTGAG | 8453 |
rs756926688 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107470 | AGTGTTGCCTCTGGG[C/G]AGAACTAGAGAAGTA | 8453 |
rs756941202 | in-del | -/ATTC | 1.87089e-05 | 0.00305845 | intron-variant | CUL2 | GRCh38.p7 | 10:35029480 | CATAGTAAAACACAT[-/ATTC]ATACCTGTAGAACAT | 8453 |
rs756949853 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072493 | CCTGCCTGAACCTCC[C/T]GAGTAGCTGGGACTA | 8453 |
rs756976043 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120657 | ATCTCAGCAATTTGA[C/G]AGGCCAAGGCAGGCA | 8453 |
rs756985251 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044966 | CCTTATTCTATTGGT[C/T]TAATCAAAGTGTAAA | 8453 |
rs756987801 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054967 | AAAGATCACAATCAG[-/T]AGGTAAGAAAATGGA | 8453 |
rs757003353 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084394 | AATCAACAGGGTTCA[A/G]GGCACCCCGGAAGTT | 8453 |
rs757018756 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122911 | CCTCCCAATGTGCTA[C/G]AATTATAGGCGTGGG | 8453 |
rs757021969 | snp | C/T | 3.29973e-05 | 0.00406172 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071261 | CACGGCTTTTATTGT[C/T]GTCAAAAGTTTGTTC | 8453 |
rs757038133 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038804 | TAATCTGTAAAAGGT[C/T]ATTTAAAATATTTTA | 8453 |
rs757095324 | snp | A/C | 0.000101066 | 0.00710795 | intron-variant | CUL2 | GRCh38.p7 | 10:35044517 | ATGTTAAATAAAACC[A/C]GGCCAGATACAAAAT | 8453 |
rs757145505 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047684 | ACACTTTTGGAGGCC[A/G]AGAAAGTTGGATCTC | 8453 |
rs757149198 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121471 | TATTAAAACCTTTAT[C/G]TTATTAGCTAATGTA | 8453 |
rs757156045 | snp | A/C | 2.00242e-05 | 0.00316413 | intron-variant | CUL2 | GRCh38.p7 | 10:35029440 | AATCATTTGTATCAA[A/C]GTACTGAAATGATTA | 8453 |
rs757170845 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071681 | CCAAAGTGCTGGGAT[C/T]ACAGGCATGAACCAT | 8453 |
rs757175443 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099098 | AAGGTGGTTGATCAA[C/T]AATATTAACTTGGGC | 8453 |
rs757201046 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083241 | GTTATAAATAAAGGG[G/T]AAAGGCAAGCATTAA | 8453 |
rs757219190 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35016511 | TTTATTAAATTGTTG[C/T]AAAGCCACTGCTGTT | 8453 |
rs757230267 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097712 | ACGCCTGCAATTGAC[A/T]CTTTGGGAGTCCATG | 8453 |
rs757245856 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050846 | GATATACATCTACAA[A/G]TTGAGATCCTGTACT | 8453 |
rs757282699 | snp | G/T | 6.27937e-05 | 0.00560294 | missense | CUL2 | GRCh38.p7 | 10:35038971 | CTGCATGTAAAAACT[G/T]TAAGTGGTCTGCTAC | 8453 |
rs757303119 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065425 | GGAGATCGAGACCAT[C/G]CTGGCTAACATGGTG | 8453 |
rs757343613 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064073 | ATGCCATCTTATCAG[C/T]ACGATGACCACCACC | 8453 |
rs757351667 | snp | A/C | 2.84184e-05 | 0.0037694 | intron-variant | CUL2 | GRCh38.p7 | 10:35013657 | AAGTCCAATGCTTAA[A/C]TGTTTCCCCCTCAAA | 8453 |
rs757352610 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35112533 | TTTTCAGGACAGACT[G/T]CAAGAGAAGACAGAG | 8453 |
rs757393911 | snp | C/T | 3.51927e-05 | 0.00419465 | missense, intron-variant | CUL2 | GRCh38.p7 | 10:35049746 | TCAACCATCAATTTC[C/T]TCCACATATCCAATG | 8453 |
rs757396152 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015391 | TGAATTTCAGAATAT[A/G]CCTTTTACAGTTGTT | 8453 |
rs757406258 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047446 | AACCCCGTCTCCACT[-/A]AAAAAAAAAAAAAAA | 8453 |
rs757430261 | snp | A/T | 1.65625e-05 | 0.00287766 | intron-variant | CUL2 | GRCh38.p7 | 10:35071152 | TCTCAGTTTTCAACA[A/T]ATTTATCAATTTTAG | 8453 |
rs757453589 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091378 | CCCTAGAGCCTTCCT[C/G/T]CTCTTCTAATCTGCT | 8453 |
rs757455791 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042540 | GCCCTACCTTTCTGA[C/G]TGTGGGTCATAAGAC | 8453 |
rs757465568 | in-del | -/AACAAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051613 | AAGACTCCGTCTCAA[-/AACAAC]AACAACAACAACAAA | 8453 |
rs757482120 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038781 | AGTCTTTCAAAATAA[A/G]GTATTAATAATCTGT | 8453 |
rs757497334 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077293 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAACAAA | 8453 |
rs757534501 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030274 | AGCATCTACTGAGTG[A/C]TGAAGAAAACTATTT | 8453 |
rs757549484 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078409 | TGAGCAATTCTCCTG[A/C]CTCAGCCTCCCAAGT | 8453 |
rs757555127 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126035 | GGGTTTCACCATGTT[A/G]GCCAGGCTGCTCCTG | 8453 |
rs757561853 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056885 | TTGCCTGCTTTAATC[A/T]GTCAGTCTTCCTGTC | 8453 |
rs757571213 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041601 | GGAGGGCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 8453 |
rs757621625 | snp | A/G | 1.64822e-05 | 0.00287068 | missense | CUL2 | GRCh38.p7 | 10:35032457 | GGTGCTTTGCAAACA[A/G]ACTTAGGTTCTCTGT | 8453 |
rs757657329 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104692 | ATGGAATCCAATATA[C/T]ATTTTTTTAACATGA | 8453 |
rs757658264 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089174 | GAGCAAAACTCCATC[G/T]CAAAACAAAAAAACT | 8453 |
rs757673967 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055777 | GCCATTTATTCCTTC[C/T]TCTCTATCCTCACTG | 8453 |
rs757703473 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102458 | ATGCCTGTAATTCCA[C/G]CTACTTGGGAGGCTG | 8453 |
rs757729085 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069606 | GGACCAAACAAATAA[C/T]ATCAGAGAAATAACA | 8453 |
rs757738743 | in-del | -/AAAAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110567 | GAGACCTTGTCTAAA[-/AAAAT]AAAATAAAATAAACA | 8453 |
rs757764906 | snp | C/T | 3.73846e-05 | 0.0043233 | intron-variant | CUL2 | GRCh38.p7 | 10:35028795 | AGTCTTCTAATATAT[C/T]TCCTGCAAACTTACC | 8453 |
rs757777927 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119218 | GGACATTTTCAACCA[C/T]ATTCTCAATCTTGGA | 8453 |
rs757801294 | snp | A/C | 1.94362e-05 | 0.00311732 | intron-variant | CUL2 | GRCh38.p7 | 10:35049636 | TTTTAAAACCATATC[A/C]AACAACAAAATAAAA | 8453 |
rs757814437 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105018 | ACAGGCGTGAGCCAC[C/G]GTGCCCAGCCCAAAG | 8453 |
rs757866553 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020610 | TTTTTTTTATCTTCC[G/T]TGAGTTCATCATTTC | 8453 |
rs757867201 | snp | C/T | 1.65015e-05 | 0.00287237 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35010389 | CAGAACTTCAATACA[C/T]TTCTTAATCATGCTG | 8453 |
rs757867618 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042867 | GGTCAGTAGTCCGGA[C/G]GCCCAGACTTGTGAC | 8453 |
rs757891742 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105828 | GAGGCAATGTCCTGA[-/AA]AAAAAAAAAAAAAGT | 8453 |
rs757899808 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119950 | CTGAGGTTACTCTTT[C/T]GGCTCCACACATTAA | 8453 |
rs757922787 | snp | A/C | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008313 | GCGCTGCAATGAATT[A/C]CAAACATTGCTCCCT | 8453 |
rs757923822 | in-del | -/AAAAT | 3.99018e-05 | 0.00446647 | intron-variant | CUL2 | GRCh38.p7 | 10:35028898 | CAGCCTAGAAGGAAA[-/AAAAT]AAAATAAAATAAAAT | 8453 |
rs757925970 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058780 | TGTATAAACACTAAC[C/T]CTCCTAAGAACCTCT | 8453 |
rs757993909 | snp | C/G | 1.77745e-05 | 0.00298109 | intron-variant | CUL2 | GRCh38.p7 | 10:35033291 | AAAAATGAAATATAA[C/G]TACAAAACCACATTT | 8453 |
rs757994523 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057521 | AGCCAGGCATGGTGG[C/T]GGTTGCCTGTAATCC | 8453 |
rs757998610 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121158 | AATTCAGGAGCTATT[A/C]GAGAAAGAGTGTTAA | 8453 |
rs758018494 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022839 | ATCACGAGGTCAGGC[A/G]TTCGAGACCAGCCTG | 8453 |
rs758044779 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028110 | CTTTGGGATGTATCC[G/T]TTCTGCAAAATTTGT | 8453 |
rs758052537 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072036 | GGTTTTGGCCCCAAA[G/T]CCTTGTGGTTTGCAC | 8453 |
rs758098855 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078018 | TCCATAATAAAGGAA[G/T]TTAAAAATCCTACTC | 8453 |
rs758103864 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071038 | TGAAAGGTTATCAAA[C/T]ACTGATTGCCATAAA | 8453 |
rs758119784 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068544 | TGGGGGTTATAGTGA[A/G]TGTGGACAATGTTCT | 8453 |
rs758128541 | snp | A/G | 8.80568e-05 | 0.00663481 | intron-variant | CUL2 | GRCh38.p7 | 10:35062923 | GTAAAGTATACAACT[A/G]TCAACATATTTATAT | 8453 |
rs758139069 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097326 | GTACCCTTAAGCTGG[A/C]TCAGTACACCTCAAG | 8453 |
rs758160456 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067743 | GTGAGACCCTGCCAC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs758168482 | snp | A/C/G | 6.01261e-05 | 0.0054827 | intron-variant | CUL2 | GRCh38.p7 | 10:35044524 | ATAAAACCAGGCCAG[A/C/G]TACAAAATAGATAAA | 8453 |
rs758230553 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083031 | GTGTGGTGGCAGGTG[C/T]CTGTAATCCCAGCTA | 8453 |
rs758275232 | snp | C/T | 1.66441e-05 | 0.00288474 | intron-variant | CUL2 | GRCh38.p7 | 10:35031390 | TCTTGCGTAGAACTA[C/T]ATTTAAAAATATTTT | 8453 |
rs758367308 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015182 | CCTGTAGTCCCAGCT[A/G]CTCAGGAGGCTGAGA | 8453 |
rs758398296 | snp | A/G | 1.79088e-05 | 0.00299234 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35029617 | CCGATGTAGCTTGCT[A/G]GTAAACTCATAACCA | 8453 |
rs758409900 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110767 | GTGCATGCATCCCTC[A/G]TATCCCCCTCTTATA | 8453 |
rs758475326 | snp | C/T | 1.66205e-05 | 0.00288271 | intron-variant | CUL2 | GRCh38.p7 | 10:35032543 | GCCATAGGGAAAAAG[C/T]ACAGCTAGTTCAATA | 8453 |
rs758509610 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071389 | AATTCCATGAGCTTA[A/G]TTTTTTTGTTGTTGT | 8453 |
rs758529247 | snp | A/T | 0.000159105 | 0.0089178 | intron-variant | CUL2 | GRCh38.p7 | 10:35013672 | ATGTTTCCCCCTCAA[A/T]AAAAACTTGACATTA | 8453 |
rs758541531 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029981 | AAAAGGATTTTATGT[C/T]GTGTTTTGTTTTAAA | 8453 |
rs758553647 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124522 | TACAACCCCTGCCTT[G/T]CCTTCTTCTCTTGAG | 8453 |
rs758560263 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089103 | TTGCTTGAACCCGGG[A/G]GGCGGAGGTTGCAGT | 8453 |
rs758583162 | snp | C/G | 1.87735e-05 | 0.00306372 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35039011 | TTGACATTCATGAAT[C/G]ACCTTAGTATATGAA | 8453 |
rs758590754 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054325 | ATCTTTTAAATCTTG[A/C]CCATTTTAAGCTAGC | 8453 |
rs758608177 | snp | A/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091042 | ATGTATTTTCGATAA[A/T]GAAACTTCACATCTT | 8453 |
rs758664158 | in-del | -/TCAG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056883 | TTTTGCCTGCTTTAA[-/TCAG]TCAGTCTTCCTGTCT | 8453 |
rs758676209 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040357 | CTCAAGACAAAACAA[C/T]AACATATACACAGAC | 8453 |
rs758690956 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014661 | AACAAAGCAAAACCC[A/G]GTCTCTACTAAAAAT | 8453 |
rs758700311 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049184 | AGGGTAAAAAGTGTT[-/A]ACCACTCTGAGCCAT | 8453 |
rs758719685 | snp | A/G/T | 2.25197e-05 | 0.0033555 | intron-variant | CUL2 | GRCh38.p7 | 10:35028913 | AAAAATAAAATAAAA[A/G/T]AAGCTAAATGGATCA | 8453 |
rs758737566 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012271 | CTGCTAAAACATCTA[C/T]AATTTCTAGGGTTAA | 8453 |
rs758752521 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102101 | AAAAATTAGCCAAGC[A/G]TGGTGGCACATGCCT | 8453 |
rs758759504 | snp | C/G | 5.97175e-05 | 0.00546399 | intron-variant | CUL2 | GRCh38.p7 | 10:35016146 | CATCTCATGAAAAAG[C/G]TTTAATGCTGATGAT | 8453 |
rs758764566 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116349 | GACTCCATCTCAAAA[A/T]AAAAATTATGAACAA | 8453 |
rs758784812 | snp | A/G | 3.30049e-05 | 0.00406219 | missense | CUL2 | GRCh38.p7 | 10:35032487 | TAATTTACAACTGAC[A/G]TAAGGGCCTGAATAA | 8453 |
rs758790479 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020548 | ATACTATGATGTAGG[C/G]TTCACAAAATTCTAG | 8453 |
rs758791361 | in-del | -/TG | 0.000185718 | 0.00963455 | intron-variant, frameshift-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074220 | TTGACCATGTTACTC[-/TG]TACATAAAGTACAAA | 8453 |
rs758811243 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117732 | TTATGTGGAACCTAT[A/T]TGACTGGACCATTCC | 8453 |
rs758826490 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068214 | AACACATGAGCCCAG[A/G]GGTTCGAGACCAGCT | 8453 |
rs758833604 | snp | C/G | 3.29489e-05 | 0.00405874 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35035271 | AGTGGACACAGCACG[C/G]AGTAAGACGTACATA | 8453 |
rs758851578 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101236 | TAAAGGTGAGAGGTA[G/T]TAAGCCATCAACAGA | 8453 |
rs758877445 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080524 | GTGCAGTGGTGTGAT[C/G]CTGGTTCACTGCAGC | 8453 |
rs758877564 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066919 | AAAGTGTCAAGGATA[C/T]AGGTACTTGCCTCAA | 8453 |
rs758893130 | snp | C/T | 1.65767e-05 | 0.00287891 | intron-variant | CUL2 | GRCh38.p7 | 10:35054417 | TATGTTTGCTAGTCA[C/T]TTAAAGAATGTCCTA | 8453 |
rs758940420 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064556 | ATCCTGCTGAAGGAA[A/G]GGAGATGCAAAATCA | 8453 |
rs759017654 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050529 | AATAAAACATTCCTG[G/T]ATTCACTACCCAGTT | 8453 |
rs759057552 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017108 | CGATAGCTGGGCTCT[-/C]CCCAGGTAAGGTTCA | 8453 |
rs759070970 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083820 | CCAGCCTGGAGCATA[A/G]CCTGTACTTTCTCTC | 8453 |
rs759072446 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35016039 | CTGTGATGCCTTAAC[A/G]CTCGCAGCTCTATGG | 8453 |
rs759079979 | snp | A/G | 5.04732e-05 | 0.00502335 | intron-variant | CUL2 | GRCh38.p7 | 10:35011978 | TCCTGTTTTACAGAA[A/G]AAAAGAAAAAAGACC | 8453 |
rs759148217 | snp | C/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127981 | CTCCCGAGTAGCTGG[C/G]ATTACAGGCATGCGC | 8453 |
rs759202896 | snp | A/C/T | 3.38434e-05 | 0.00411349 | intron-variant | CUL2 | GRCh38.p7 | 10:35071343 | TAGTGTTGAAATCTG[A/C/T]CAATTAAAAAACAAT | 8453 |
rs759204952 | snp | C/G | 1.64893e-05 | 0.0028713 | missense | CUL2 | GRCh38.p7 | 10:35038930 | CTTACCATTTTTTTT[C/G]TCTTGTCGAATTATA | 8453 |
rs759215806 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105826 | AAGAGGCAATGTCCT[-/G]AAAAAAAAAAAAAAA | 8453 |
rs759220759 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064811 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTATGA | 8453 |
rs759239147 | snp | C/T | 2.05857e-05 | 0.00320818 | missense | CUL2 | GRCh38.p7 | 10:35013764 | TACTGCTAAAGTTCA[C/T]ATTTAATGAAAACGA | 8453 |
rs759248766 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097291 | GCCAGATGCATCTGT[A/G]CCTTGGATTTTTCCT | 8453 |
rs759269260 | in-del | -/ATT | 4.28394e-05 | 0.00462794 | intron-variant | CUL2 | GRCh38.p7 | 10:35025224 | AAAAAAAAAACACAC[-/ATT]ATTTTTAGCTACTAT | 8453 |
rs759272841 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111989 | AGTCACTGCTCAACT[A/G]TACAAGGGTCTATGT | 8453 |
rs759274850 | in-del | -/AC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025338 | TTACCTCCTTCTTTT[-/AC]AGAGGAGAAAGCACG | 8453 |
rs759278401 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032823 | AAGTTCATGTAAAAC[A/G]TATCTATTCTCTTTT | 8453 |
rs759305906 | in-del | -/GCTTTGCAAACAGACTTAG | 1.65704e-05 | 0.00287836 | intron-variant | CUL2 | GRCh38.p7 | 10:35031624 | ACTTAGCAAGCTCAT[-/GCTTTGCAAACAGACTTAG]GTAGAAATTGATAAT | 8453 |
rs759325657 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071241 | TCGACGTATTCCAAC[A/G]TGACCACGGCTTTTA | 8453 |
rs759344285 | snp | A/G | 3.32132e-05 | 0.00407499 | intron-variant | CUL2 | GRCh38.p7 | 10:35044883 | ACTAAAACAAGGTAT[A/G]ACACAAAATATTCTT | 8453 |
rs759393549 | snp | C/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126410 | ACTAGTCAAGGTATG[C/T]AGATAGCTTTTAGAA | 8453 |
rs759409241 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030375 | GCTCATTAACACTAC[-/T]TTTTTTTTTGTAATT | 8453 |
rs759433843 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107882 | GCGAGACTCCATCTC[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAGTAG | 8453 |
rs759442192 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042328 | CCATGTTGTATCATG[C/T]ATAACTTCAATTCTT | 8453 |
rs759449302 | snp | C/T | 1.74449e-05 | 0.00295332 | synonymous-codon, intron-variant | CUL2 | GRCh38.p7 | 10:35049694 | TCACTTTTTGATTTC[C/T]CGGAGCAGCATTCGG | 8453 |
rs759465505 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070538 | AGCAGATCACTGTCA[C/T]GGAGGAACACAGGAA | 8453 |
rs759505941 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055362 | CTACACCAAAATGAA[-/G]GGTCCACTCAGCATT | 8453 |
rs759568609 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041035 | CAGGCCACAGGTCAG[C/T]ACTGGTCCTCAGCCT | 8453 |
rs759591916 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055458 | TAATTCCTGGCCAGG[C/T]GTCGGGGCTCACGCC | 8453 |
rs759598753 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107600 | AAAAGTAGAAGACTT[-/G]GGCCTGGCGCGGTGG | 8453 |
rs759607277 | in-del | -/AAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018289 | AAGACTCCATCTCAC[-/AAA]AAAAAAAAAAAAAAA | 8453 |
rs759639903 | snp | A/G | 1.66261e-05 | 0.00288319 | intron-variant | CUL2 | GRCh38.p7 | 10:35035127 | GAAAGGCTCCACGCT[A/G]GATCTGATTAGGAGG | 8453 |
rs759641989 | snp | A/G | 1.654e-05 | 0.00287571 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35062975 | CTTATGCAAATGCCG[A/G]ACATGATTTTCCAAA | 8453 |
rs759722735 | snp | A/C | 1.77445e-05 | 0.00297858 | intron-variant | CUL2 | GRCh38.p7 | 10:35025125 | GATATAATTAAATGC[A/C]TTTTACCTGTACACA | 8453 |
rs759727750 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081143 | GTGGGAGCTTGGCTT[A/G]AGCAAAGGAGACTTC | 8453 |
rs759733563 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35112972 | GCCAAGGCAGGCAGA[C/T]CACAAGGTCAGGAGA | 8453 |
rs759736653 | in-del | -/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091933 | GTGTCAGGCCCCCCC[-/T]GCTTTTTGTTTTGTT | 8453 |
rs759761091 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035888 | CAATGTGTTGCCAAA[C/T]GTTTTGATCTCTAAC | 8453 |
rs759795914 | snp | C/T | 2.10431e-05 | 0.00324363 | intron-variant | CUL2 | GRCh38.p7 | 10:35028767 | ATATGAAGACAATTA[C/T]TAAAATTCCTTTAGT | 8453 |
rs759801116 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35035220 | GCCCTCATCATGGAT[A/G]TGGTTTTGCAGCTCC | 8453 |
rs759814133 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048954 | TCTTCTTGATGAGCA[C/T]AGATATAGGTGGAGT | 8453 |
rs759820906 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109814 | TCGATTTTATTTCAA[C/T]CACATGGAAGTCACT | 8453 |
rs759895201 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094091 | GCCAGGATCGTGCTT[C/T]TTGTACAGCCTGCAG | 8453 |
rs759919051 | snp | C/T | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35090331 | CAGCGCTGCCATTAC[C/T]GTGCGCCGAGGCCGC | 8453 |
rs759992099 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046173 | CAGTCATAGAGAATC[C/T]TGATATCTTGATATC | 8453 |
rs759998362 | snp | C/T | 7.02914e-05 | 0.00592796 | intron-variant | CUL2 | GRCh38.p7 | 10:35031294 | CACATTAAAGACTTA[C/T]ATTACCTTTAATTTG | 8453 |
rs760001219 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035020 | CAAAATGAGTCCAAC[-/A]AATTCTAGGTTTAAA | 8453 |
rs760041775 | snp | C/G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049320 | CTTCCTCAATAGGTG[C/G/T]TCCTCACGAGGATTT | 8453 |
rs760062913 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066488 | TATTTTTAGTAAAGA[C/T]GGGGTTTAACCATGT | 8453 |
rs760071752 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108577 | GATATTGGAATTGAG[A/G]TAGGAGGAAGTTATC | 8453 |
rs760097873 | snp | C/T | 1.65507e-05 | 0.00287664 | intron-variant | CUL2 | GRCh38.p7 | 10:35060833 | ACTACTGAATGCAGG[C/T]AACGCTGCTTAGCTT | 8453 |
rs760128946 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123893 | ATTGGGTATGATTAG[A/G]TAACTAAAGAAAATA | 8453 |
rs760132887 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025650 | ACGAAGTTTTAGGGT[A/G]TATCTCTGGATTATT | 8453 |
rs760162380 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062785 | GGGGCTGCAGTGAGC[C/T]ATGATCGCGCCACTG | 8453 |
rs760176822 | snp | A/C | 1.73966e-05 | 0.00294924 | intron-variant | CUL2 | GRCh38.p7 | 10:35044561 | CGATATGTTTTATTT[A/C]TTACCTTTTCCATAT | 8453 |
rs760209658 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35090175 | CGACCCTCAGCGGGG[A/T]TACCTTCTGCAGAAG | 8453 |
rs760234162 | snp | C/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126313 | ACCCTAAGAAGCAGG[C/T]GAATTGTCTCAGGAG | 8453 |
rs760257740 | snp | C/T | 3.33239e-05 | 0.00408177 | missense | CUL2 | GRCh38.p7 | 10:35016262 | GTCAGTTCCTTTTCA[C/T]TCATCTGAGTGCTGT | 8453 |
rs760291801 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075138 | AGGAAAATACAGTTA[C/T]AATCCATGCTTGGAT | 8453 |
rs760325750 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101343 | CATGGAGACAACGGG[A/T]CTACCATTGTAGAAA | 8453 |
rs760333719 | snp | C/G | 8.66228e-05 | 0.00658057 | missense | CUL2 | GRCh38.p7 | 10:35029545 | TGTGTCTTGGTTTTT[C/G]ATAAAATTGTTGAAC | 8453 |
rs760333768 | in-del | -/AAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113499 | GCAAGACTCTGCCTC[-/AAA]AAAAAAAAAAAAAAA | 8453 |
rs760378291 | snp | A/G | 3.46675e-05 | 0.00416323 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35029578 | ATTGTTGAGATCAGC[A/G]CTGACACTCATATCT | 8453 |
rs760412363 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088169 | ATTTCTTATATACTG[C/T]CTGTCTCTCCATCCC | 8453 |
rs760414443 | snp | C/T | 0.000485437 | 0.0155719 | intron-variant | CUL2 | GRCh38.p7 | 10:35074045 | TGCTGTGTGCAACCA[C/T]GCTACCTCACTAACA | 8453 |
rs760429521 | snp | C/T | 2.41485e-05 | 0.00347472 | intron-variant | CUL2 | GRCh38.p7 | 10:35039122 | ATGAACACAAAGTTT[C/T]ACTATGAGGAAAAAT | 8453 |
rs760467343 | snp | A/G | 2.28089e-05 | 0.00337697 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35013792 | CGAAGATTCTGCATC[A/G]ATATCTTCCTACATT | 8453 |
rs760467598 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087196 | AGCGGGTACTACAGG[C/T]GTGCGCCACCACGCC | 8453 |
rs760496169 | in-del | -/CCTC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025326 | AGCCCATCTGGTTTA[-/CCTC]CTTCTTTTACAGAGG | 8453 |
rs760516034 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101931 | AACATACCTAAGTTA[C/T]TTAGTGTCTGCACTT | 8453 |
rs760517043 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040828 | CGCACATCCTAGACC[C/T]CTTGCATGCAGAGTT | 8453 |
rs760517797 | snp | C/T | 3.33823e-05 | 0.00408534 | intron-variant | CUL2 | GRCh38.p7 | 10:35054400 | GTGTATAAAAACATA[C/T]TTATGTTTGCTAGTC | 8453 |
rs760521364 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103994 | AGGGCCTTGGGAAAT[G/T]AAATTTAAGCTTCTT | 8453 |
rs760545956 | snp | C/T | 3.29625e-05 | 0.00405958 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35032438 | CACCAAACTTACCAG[C/T]TCAGGTGCTTTGCAA | 8453 |
rs760567386 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117162 | GATGCCTGCAGGAAG[A/G]GAAGGGCACTAGCTT | 8453 |
rs760591711 | snp | A/C/T | 4.9747e-05 | 0.00498713 | intron-variant | CUL2 | GRCh38.p7 | 10:35032519 | AAAACACGCCATAAT[A/C/T]AACCACCAGCCATAG | 8453 |
rs760597341 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055036 | AGATACAAGATGACT[C/T]TGTCTACCAGAGGAA | 8453 |
rs760598906 | snp | A/C | 1.69951e-05 | 0.00291501 | intron-variant | CUL2 | GRCh38.p7 | 10:35033160 | ATATATGTATTTAAA[A/C]CTTACCTTATCCAAC | 8453 |
rs760616346 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081071 | AATAAAATTATAGTA[A/G]CTGGGCCCTCTGGTA | 8453 |
rs760695191 | in-del | -/AAAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046928 | AAAACAAAACAAAAC[-/AAAAA]CAAAAAACTGGGTTA | 8453 |
rs760730198 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029063 | TAGGACCTTTTTTTG[-/T]TTTTTTTTTTTTGAG | 8453 |
rs760730269 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053844 | GAACTTACAAGCTTT[C/T]GTGTGCAGGGACCTT | 8453 |
rs760730294 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069015 | CTGAGATTCCAGGCA[A/C]CCACAACCACGCCCA | 8453 |
rs760778559 | snp | C/T | 1.91812e-05 | 0.00309681 | intron-variant | CUL2 | GRCh38.p7 | 10:35028790 | CCTTTAGTCTTCTAA[C/T]ATATTTCCTGCAAAC | 8453 |
rs760790602 | in-del | -/A | 2.49262e-05 | 0.00353022 | intron-variant | CUL2 | GRCh38.p7 | 10:35031456 | GAAATAAAGTTGACC[-/A]AAATACAAATGAAAC | 8453 |
rs760792608 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034157 | TCAGTTGGATTTGAG[A/T]CTACCACAAATGTAT | 8453 |
rs760802495 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017735 | AAATGACCCTGGGAG[C/T]TCTAAGAGATAGAGC | 8453 |
rs760824982 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116041 | CTGATAGACATTAAA[C/G]GATAAAAAAAAATAT | 8453 |
rs760860123 | in-del | -/AAG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096304 | GTGCGAGTCTCTTTA[-/AAG]AAGTGGCTGACGTGA | 8453 |
rs760878655 | in-del | -/C | 0.000327579 | 0.0127938 | intron-variant | CUL2 | GRCh38.p7 | 10:35025219 | AAAAAAAAAAAAAAA[-/C]ACACATTATTTTTAG | 8453 |
rs760885140 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059523 | AGACAATGCTACTGC[A/G]CACTTAACAGACTAC | 8453 |
rs760909291 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046111 | TTATTTGGATATTCT[A/G]AGAACTATTTTTTGG | 8453 |
rs760914033 | snp | A/G | 1.76755e-05 | 0.00297278 | intron-variant | CUL2 | GRCh38.p7 | 10:35061008 | TACTTGAAAAGCAAT[A/G]ATCATTTTCACTGTC | 8453 |
rs760920198 | snp | A/G | 1.72952e-05 | 0.00294063 | missense, intron-variant | CUL2 | GRCh38.p7 | 10:35049710 | CGGAGCAGCATTCGG[A/G]TAAGGATGGCCTGAA | 8453 |
rs760939607 | snp | A/T | 1.81059e-05 | 0.00300876 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35028885 | AAGAGGCCACGCACC[A/T]GCCTAGAAGGAAAAA | 8453 |
rs760981428 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125830 | TATTCCTGATATCCC[A/G]TTACTTTTTTTATTT | 8453 |
rs761004488 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073080 | GAGCTCAAGGAATCC[C/G]AGGAATAGACTCCAT | 8453 |
rs761037764 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123681 | AAAGTGCCATTAACA[C/T]TGCTAAAACAACAAT | 8453 |
rs761040013 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107164 | TATTTTCAGTAGAGA[A/C]GGGGTTTCACTGTGT | 8453 |
rs761056785 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049489 | CCCCCCACCAAAAAG[-/A]AAAAAAAAAGAAAGA | 8453 |
rs761090783 | snp | A/C | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008848 | TTGTTAGGAGTAATA[A/C]TATCACTGTGGATTT | 8453 |
rs761112365 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096249 | TCTGTCTCAGAAAAG[-/A]AAAAAAACAAAACAA | 8453 |
rs761115604 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35035268 | ACCAGTGGACACAGC[A/G]CGGAGTAAGACGTAC | 8453 |
rs761150131 | snp | A/G | 1.68559e-05 | 0.00290304 | intron-variant | CUL2 | GRCh38.p7 | 10:35011823 | CCTCTACCCTAAGAA[A/G]CCCTGAGGACTGCCC | 8453 |
rs761159244 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058525 | TCCTAAAACCTAAGG[A/T]CTGCTAGCATCCACC | 8453 |
rs761164504 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122172 | CTATCTTTGTAAGTC[C/T]CAAATCCTAAAGTTT | 8453 |
rs761173231 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087137 | TGGTGCAATCACAGA[G/T]CACTGCCACTTCCAA | 8453 |
rs761216478 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071856 | TTTACATTCATTACA[A/C]GCTCTAGGAAATGGA | 8453 |
rs761229617 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085387 | GTGAGCTGAGATCGC[A/G]CCACTGCGCTCCAGC | 8453 |
rs761264734 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058096 | GCGAGACTCGGTCCC[A/T]AAAATTAGTAATAAA | 8453 |
rs761272137 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040763 | GGGCAGGTGGCTTCC[A/C]GGTGAAGTATTCCAC | 8453 |
rs761306803 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35031512 | AAAGACGTCCTTGTC[A/G]TCAATGTATTTGAAC | 8453 |
rs761312417 | snp | A/T | 3.30087e-05 | 0.00406242 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35062994 | TGATTTTCCAAAAAA[A/T]TCTTAGTTTCTGTAT | 8453 |
rs761327892 | in-del | -/ACAAACTGTTACAGT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034618 | TTGGTGATGGGAAAG[-/ACAAACTGTTACAGT]ACAAACTGTTACAGT | 8453 |
rs761341659 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086876 | CTAAAAAATACAAAT[A/G]TCAAAGTAAAGTGTA | 8453 |
rs761342178 | in-del | -/ATA | 1.75807e-05 | 0.0029648 | intron-variant | CUL2 | GRCh38.p7 | 10:35063112 | AGACAATTTTAAAAC[-/ATA]ATGAGATTTACCTTG | 8453 |
rs761347793 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35112002 | CTGTACAAGGGTCTA[C/T]GTGTAGAGAAGAACC | 8453 |
rs761350976 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109954 | TGAGGCAGGAGGATT[A/G]CTTCAGGCCAGGAGT | 8453 |
rs761359281 | snp | A/T | 1.66142e-05 | 0.00288216 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35044635 | TTTGTAATACTCTCC[A/T]GTTTCAGTCAGAAAG | 8453 |
rs761422103 | snp | A/C | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125050 | GATATTTTTTAAAAT[A/C]TACAATAATCCTAAC | 8453 |
rs761425703 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083721 | TTATAAACCATAGGC[A/G]GGTCACAGTGACTCA | 8453 |
rs761431246 | snp | A/G | 1.64991e-05 | 0.00287215 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35044811 | CTGTTCAACATGAAC[A/G]AAGGAGTTAATAACC | 8453 |
rs761450743 | snp | G/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126427 | GATAGCTTTTAGAAG[G/T]CAGAAGAAGCACGCC | 8453 |
rs761495517 | snp | C/T | 1.65091e-05 | 0.00287303 | missense | CUL2 | GRCh38.p7 | 10:35010351 | GCCGACGCCTGGCTG[C/T]GTTCTATGTATTGTT | 8453 |
rs761506973 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099389 | AGTGAGACTCCGTCT[-/A]AAAAAAAAAAAAAAA | 8453 |
rs761531596 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015676 | AAAAAAGTAATATAC[-/T]TAATGGCTTGTTATT | 8453 |
rs761547163 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101781 | GAACTAGAGCAGTTG[C/G]TATTGACATTTGTAG | 8453 |
rs761586449 | snp | A/G | 9.97208e-05 | 0.00706048 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35031381 | TGCCAGCATTCTTGC[A/G]TAGAACTACATTTAA | 8453 |
rs761603156 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017606 | GGCTAAGGTATAAGA[A/C]TCCTTGAACCTGGGA | 8453 |
rs761604236 | snp | A/G | | | synonymous-codon | CUL2 | GRCh38.p7 | 10:35100897 | AGTTCCATTCTCCCC[A/G]ATAAGCTGTCCTGTG | 8453 |
rs761604323 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116817 | AAAAGAATAGCTGGG[C/T]GTGGTGGCGCACGCC | 8453 |
rs761604695 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053656 | ATTACTTGGTCAAAA[G/T]GTATTAAGTATTTTA | 8453 |
rs761622933 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085617 | GGCATGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 8453 |
rs761635551 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019848 | AGGATCATCAGTGGA[A/G]GCTAAAACTACATTA | 8453 |
rs761658296 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033982 | AAGGCTGAGAGAAAG[A/G]AGAGTTAAAAAGCCA | 8453 |
rs761729071 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062431 | ATCCAGAGGACGTAG[A/G]AGCACATTTTAAAAC | 8453 |
rs761732333 | snp | C/T | 1.65581e-05 | 0.00287728 | missense | CUL2 | GRCh38.p7 | 10:35033201 | AATGCTGATCACCAT[C/T]CAAAACAGTGTTGAT | 8453 |
rs761745070 | snp | C/T | 1.77972e-05 | 0.002983 | intron-variant | CUL2 | GRCh38.p7 | 10:35071381 | TTAGCAATAATTCCA[C/T]GAGCTTAGTTTTTTT | 8453 |
rs761759160 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067366 | GAAATCTGTCCTAAC[A/G]GCTACTAAAAGAGAG | 8453 |
rs761796915 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034669 | ATTGGCAAAGTATTC[C/G]AGAAAGATGAGTATT | 8453 |
rs761809794 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032067 | GTGGTTTTATAATTT[C/T]TGACATTGAACAAGT | 8453 |
rs761812406 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121649 | CTCTTTTCCTCATGC[C/T]TTTCTTCTCCCTTAA | 8453 |
rs761821892 | snp | A/C | 1.8946e-05 | 0.00307777 | intron-variant | CUL2 | GRCh38.p7 | 10:35029475 | ATGCTCATAGTAAAA[A/C]ACATATTCATACCTG | 8453 |
rs761838707 | snp | A/C | 1.88749e-05 | 0.00307198 | intron-variant | CUL2 | GRCh38.p7 | 10:35025105 | AGGTAAATTTCATTA[A/C]GCCAGATATAATTAA | 8453 |
rs761850648 | in-del | -/TTTCTGAATCATGGTTAATCATTTTC | 2.70984e-05 | 0.00368083 | splice-acceptor-variant | CUL2 | GRCh38.p7 | 10:35013802 | CATCAATATCTTCCT[-/TTTCTGAATCATGGTTAATCATTTTC]ACATTTAAAAATAAA | 8453 |
rs761864855 | in-del | -/CCA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089819 | GAGATGCCCCCCCCC[-/CCA]ACACACACACACAAA | 8453 |
rs761933372 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059417 | GGTAAGAAGACTGGC[A/G]AAAGGATTACAACTT | 8453 |
rs761933439 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043789 | TAAAATTTCTTGGCT[G/T]GGTGCAATGGCTCAC | 8453 |
rs761954640 | snp | A/G | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008078 | GTTTTGCTTACTTGT[A/G]TTTTCTGCAGTGAAG | 8453 |
rs761974723 | snp | C/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128390 | TGAGGGTGTACCTTT[C/T]CCTTGAAACAAAGAT | 8453 |
rs762007938 | snp | C/T | 8.30627e-05 | 0.00644395 | intron-variant | CUL2 | GRCh38.p7 | 10:35054411 | CATACTTATGTTTGC[C/T]AGTCACTTAAAGAAT | 8453 |
rs762044671 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105963 | CATATATTTCCAACA[A/C]TCACTGAAGTAACAG | 8453 |
rs762074772 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106936 | GATAAATTATGTCTG[C/T]ATTGCCCTTAACCTG | 8453 |
rs762084838 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055534 | GGCCAGCAGTTTGAG[A/G]GCAGCCTGGGTAACA | 8453 |
rs762106560 | snp | C/T | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35089934 | GGGCCGCGGGAGAGG[C/T]GGCCAAGATCGGGTT | 8453 |
rs762137468 | snp | A/T | | | missense | CUL2 | GRCh38.p7 | 10:35029606 | TCTGTATACATCCGA[A/T]GTAGCTTGCTGGTAA | 8453 |
rs762151173 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083622 | CCACAAAGAGGGTGG[C/G]GGCATATCGAAAGGA | 8453 |
rs762158930 | in-del | -/TT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027144 | CACTACTTTAGATAC[-/TT]TTTTTTTTTTTTTTT | 8453 |
rs762208237 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070213 | AGATCTTTTCAAACT[C/T]TGAAGCCTTCCAAAA | 8453 |
rs762229151 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043765 | ATATGTACTGGTTTA[C/G]TGATCAATTAAAATT | 8453 |
rs762241331 | snp | A/G | 0.000395504 | 0.0140569 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071228 | CCATGTTGCTCTTTC[A/G]ACGTATTCCAACATG | 8453 |
rs762263615 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023859 | TGACTGGTTGAGACA[C/G]GGTCTTGCTCTGTTG | 8453 |
rs762294979 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070839 | CCTCCCCCACGTCCT[C/T]ATCCTGCTTTCATTT | 8453 |
rs762303278 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109372 | ATATATATTATGTGC[A/C]ATGCAATGTTCTAGG | 8453 |
rs762310355 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081029 | AAACAGCCTTAGCAA[C/T]ATAGACAGACCTGGT | 8453 |
rs762310699 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036934 | GAGATGGGATACTGT[C/T]ATGTTGCCCAGGCTG | 8453 |
rs762315396 | snp | A/G | 3.85669e-05 | 0.00439112 | intron-variant | CUL2 | GRCh38.p7 | 10:35028892 | CACGCACCAGCCTAG[A/G]AGGAAAAAAATAAAA | 8453 |
rs762386636 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098511 | GGATTGCTTGAGGTC[A/C]GGAGTTCAAGACAAG | 8453 |
rs762391933 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122553 | ATTTTGTGCCAGGCA[A/C]AATGTTCTATATACT | 8453 |
rs762405468 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050192 | CTGGTGTGGTGGCAT[A/G]CGCCTGTAATCCCAG | 8453 |
rs762434454 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039790 | ATCCCGGGAGGTGGG[G/T]GTTGTAACGAGCCAA | 8453 |
rs762435562 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036185 | GATGAGTTTGAACTA[C/T]GTATAAAAATGGGAT | 8453 |
rs762442220 | snp | C/T | 3.40512e-05 | 0.00412607 | intron-variant | CUL2 | GRCh38.p7 | 10:35038916 | CATGTTTGGTGTCAC[C/T]TACCATTTTTTTTCT | 8453 |
rs762470754 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086752 | AATAAATGAACTTAA[C/T]AAGGGCAGGGACCAA | 8453 |
rs762479566 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | CUL2 | GRCh38.p7 | 10:35049675 | GTAAGATAAATGTCA[A/G]CACTCACTTTTTGAT | 8453 |
rs762487599 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038128 | GCACTCCAGCCTGGG[C/T]GACGGAGCGAGACTC | 8453 |
rs762490782 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073187 | CTCAACATTCCAAAG[C/T]CTCCACCTCCTGGCC | 8453 |
rs762500449 | snp | A/C | 2.52484e-05 | 0.00355296 | missense | CUL2 | GRCh38.p7 | 10:35011943 | GGTCCTCATCAACTG[A/C]ACTTCTAGTCTGCTC | 8453 |
rs762615425 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059458 | AAATGATCAACAGCA[-/T]TTTTTTTTAGCAATA | 8453 |
rs762632693 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052997 | AAACTTATGTAAAAA[-/G]ACAGACAGTAACAAA | 8453 |
rs762642086 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | CUL2 | GRCh38.p7 | 10:35032402 | TAATACTGACTTTTC[A/G]TAAGATTACTTTTCA | 8453 |
rs762649687 | snp | A/T | 1.65258e-05 | 0.00287448 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35063032 | TTCTCCAAGGGGTTC[A/T]GGATAGGCCACACAT | 8453 |
rs762699037 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115815 | GAAGGATGGGTTGAA[C/T]CTGGGAGGCTGAGGC | 8453 |
rs762704954 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017530 | GAAACCTTGTCTCTA[A/C]TAAAAATACAAAAAT | 8453 |
rs762707681 | snp | A/C | 1.66452e-05 | 0.00288484 | intron-variant | CUL2 | GRCh38.p7 | 10:35011840 | CCTGAGGACTGCCCT[A/C]CTTTTACCTCTTGAA | 8453 |
rs762724884 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098959 | AATTAAATAAGTAAT[A/G]TAGGCCATCTCATTT | 8453 |
rs762748077 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114358 | GTGTGAGGCACCGCC[C/T]CCAGCTGCATTCAAG | 8453 |
rs762821752 | snp | C/T | 1.65762e-05 | 0.00287886 | intron-variant | CUL2 | GRCh38.p7 | 10:35044875 | CCACGATCACTAAAA[C/T]AAGGTATAACACAAA | 8453 |
rs762861590 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078188 | AACACATGGTACTGT[C/T]CCTAAATGTGATGTG | 8453 |
rs762862659 | snp | A/T | 1.82477e-05 | 0.00302051 | intron-variant | CUL2 | GRCh38.p7 | 10:35025116 | ATTAAGCCAGATATA[A/T]TTAAATGCATTTTAC | 8453 |
rs762873355 | snp | C/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128093 | TCCACCCACCTCGGC[C/T]TCCCAAAGTGCTGGG | 8453 |
rs762873801 | snp | A/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128321 | AAGAGCTCCTTTAAC[A/T]CTGTGGCTTACGTAC | 8453 |
rs762891575 | in-del | -/TT | 3.56386e-05 | 0.00422114 | intron-variant | CUL2 | GRCh38.p7 | 10:35061013 | GAAAAGCAATAATCA[-/TT]TTCACTGTCAACAAT | 8453 |
rs762909030 | snp | C/T | 1.91488e-05 | 0.0030942 | intron-variant | CUL2 | GRCh38.p7 | 10:35054580 | GATATTAAGTTAAAG[C/T]CAGTAGGAAAGCAAA | 8453 |
rs762924299 | in-del | -/GTG | | | cds-indel | CUL2 | GRCh38.p7 | 10:35013701 | TAAAAGCACTTACTT[-/GTG]GTGTGTCTTTCTGCA | 8453 |
rs762933978 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058193 | AGAAGATGCTGATTC[C/T]ATAAAGGGAAATAAA | 8453 |
rs762980626 | in-del | -/C | 3.33486e-05 | 0.00408328 | intron-variant | CUL2 | GRCh38.p7 | 10:35032507 | GCCTGAATAAAAAAA[-/C]CACGCCATAATTAAC | 8453 |
rs763008122 | in-del | -/CTTCCTTGCTCTAAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118406 | TCCATTTCTTAGTTC[-/CTTCCTTGCTCTAAT]CTTCCGGTTCATGAG | 8453 |
rs763081167 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089764 | ATCAATCTTTGCAGT[C/G]TGCGGAAACAAAAGT | 8453 |
rs763101710 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022208 | ATCAATGAATTTTAC[A/G]ACAATAAAGAGAAGG | 8453 |
rs763137400 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056559 | GAGGTCTTCCACTCC[C/T]ATTCAACATCGGCTG | 8453 |
rs763140913 | snp | C/T | 1.65803e-05 | 0.00287922 | missense | CUL2 | GRCh38.p7 | 10:35033240 | CAAATTTACCATGCA[C/T]TTCCAAAACTGACTC | 8453 |
rs763201420 | snp | A/G | 1.70962e-05 | 0.00292366 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35016309 | ACTGACAGTTTCACT[A/G]TTGTTAAAGGCAAGA | 8453 |
rs763210129 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036033 | TATCACAAGTGAACA[C/T]ACAACACACCCATGT | 8453 |
rs763217318 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077328 | AAAACAAACAAACAA[-/C]ACAAAAAAAACAAAC | 8453 |
rs763242761 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069226 | TGAGAGAAAATTCAT[C/G]ATCAGGTGAAAAATA | 8453 |
rs763243185 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082412 | AGGGGAAATGGGGAG[A/C]TACTGCCTAATGGTT | 8453 |
rs763251795 | in-del | -/GGGCC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021657 | TTTATTTTCTTTTTG[-/GGGCC]GGCCTGCCTGGTCTT | 8453 |
rs763286379 | in-del | -/TTTC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021246 | CTGCAGCATGTTTTC[-/TTTC]TTTCTTTCTTTCTTT | 8453 |
rs763290894 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060943 | TGATACATAACAAGT[A/G]CTTGTTCTTCTGACT | 8453 |
rs763328893 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096000 | AGCCTGTAATCCCAG[A/C]ACTTTCGGAGTCCGA | 8453 |
rs763330160 | in-del | -/CCCTGCCTCTGAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046052 | CATACTAGAGTCCTT[-/CCCTGCCTCTGAA]CCCCTCTAGTCCTCT | 8453 |
rs763362031 | snp | C/T | 1.79754e-05 | 0.0029979 | intron-variant | CUL2 | GRCh38.p7 | 10:35031283 | TAGGACAATACCACA[C/T]TAAAGACTTACATTA | 8453 |
rs763362417 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067443 | TCTATTTATACAAAG[C/T]CCAAAAATCAAAGAA | 8453 |
rs763373059 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081353 | TTAAGTTTTCACATC[A/G]CTCTTATCAGCTTGA | 8453 |
rs763416370 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069938 | TCAATCCATAATGTT[C/T]CACAGAAAAATTAGC | 8453 |
rs763440855 | snp | A/G | 2.07915e-05 | 0.00322418 | intron-variant | CUL2 | GRCh38.p7 | 10:35039085 | ATCTACCTAGAACCT[A/G]TAAAAATATTTTCTT | 8453 |
rs763449777 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027740 | GAAAACTTGGACTTA[A/C]TAGAAAAAAAATAAA | 8453 |
rs763488523 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123902 | GATTAGATAACTAAA[G/T]AAAATACTGTTTGAG | 8453 |
rs763504408 | in-del | -/A | 0.000147269 | 0.00857979 | intron-variant | CUL2 | GRCh38.p7 | 10:35013669 | AAATGTTTCCCCCTC[-/A]AAAAAAAACTTGACA | 8453 |
rs763560093 | snp | A/G | 1.71968e-05 | 0.00293225 | intron-variant | CUL2 | GRCh38.p7 | 10:35071365 | AAAAACAATAACAAT[A/G]TTAGCAATAATTCCA | 8453 |
rs763561954 | snp | A/C | 1.8531e-05 | 0.00304388 | intron-variant | CUL2 | GRCh38.p7 | 10:35029483 | AGTAAAACACATATT[A/C]ATACCTGTAGAACAT | 8453 |
rs763575370 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047244 | CCTCAACCTCCATAT[G/T]TGCTTAATTCTCTAT | 8453 |
rs763580902 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083420 | ACTGAGAAGGGCCTA[-/G]GAGGAATGACACCAC | 8453 |
rs763596585 | snp | C/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009665 | TCTAATCCATAAAAA[C/T]AAAGCATTCTTTATG | 8453 |
rs763645574 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056031 | CAGCCCTAAGCAAGT[A/C]ACTATTTAACGCACA | 8453 |
rs763708311 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084293 | ACAAGCAAACAAGAC[A/T]CAGTATCAGTCTGAA | 8453 |
rs763717969 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073189 | CAACATTCCAAAGCC[C/T]CCACCTCCTGGCCTT | 8453 |
rs763739505 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085529 | GAAGGCGGACCACAA[C/G]GTCAGGAGATCAAGA | 8453 |
rs763740284 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081197 | CACCACCACACTCCA[A/G]CCTGGGCCAAAAGAC | 8453 |
rs763769398 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072060 | TTTGCACTCCTGAAA[A/G]TGGGGAATGAGGCAG | 8453 |
rs763769679 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098998 | AGGAACAAAGAAAGC[A/G]AACAAGTCAAATGTG | 8453 |
rs763779853 | snp | A/C | 2.87261e-05 | 0.00378976 | intron-variant | CUL2 | GRCh38.p7 | 10:35013648 | ACACTTGTAAAGTCC[A/C]ATGCTTAAATGTTTC | 8453 |
rs763832576 | snp | C/T | 1.66999e-05 | 0.00288958 | missense | CUL2 | GRCh38.p7 | 10:35044589 | TATACTGTGAGCAGT[C/T]TGATTCTTGTAATAA | 8453 |
rs763849370 | snp | C/T | 0.000121346 | 0.00778833 | missense | CUL2 | GRCh38.p7 | 10:35029552 | TGGTTTTTGATAAAA[C/T]TGTTGAACTTATTGT | 8453 |
rs763867422 | snp | A/G | | | missense | CUL2 | GRCh38.p7 | 10:35100872 | CATCACCGCAATCAG[A/G]ATACAGAAGAGTTCC | 8453 |
rs763889281 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050705 | TTGCATAAATATGCC[A/C]TGATTTATTTTTCCA | 8453 |
rs763964304 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032759 | AAAATAACGTTACTT[-/A]AAAAAAAAACTTACA | 8453 |
rs763973087 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114361 | TGAGGCACCGCCCCC[A/T]GCTGCATTCAAGTGT | 8453 |
rs764058485 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091206 | GAGGAACAAAAGCCC[A/G]GCCTTAGTGCTTTTT | 8453 |
rs764083967 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065368 | ACTCACGCCTGTAAT[C/T]CCAGCACTTTAGGAG | 8453 |
rs764094156 | snp | A/G | 2.85988e-05 | 0.00378135 | intron-variant | CUL2 | GRCh38.p7 | 10:35013803 | CATCAATATCTTCCT[A/G]CATTTAAAAATAAAA | 8453 |
rs764095679 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026938 | TGCTGCACCCACTAA[C/T]TCGTCATTTAGCATT | 8453 |
rs764121990 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071254 | ACATGACCACGGCTT[C/T]TATTGTCGTCAAAAG | 8453 |
rs764138176 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076894 | TCTCTACTAAAAATA[C/T]AAAAAAAATTAGCCA | 8453 |
rs764147469 | snp | A/G | 1.90427e-05 | 0.00308561 | intron-variant | CUL2 | GRCh38.p7 | 10:35028890 | GCCACGCACCAGCCT[A/G]GAAGGAAAAAAATAA | 8453 |
rs764168202 | in-del | -/AG | 4.00256e-05 | 0.00447339 | intron-variant | CUL2 | GRCh38.p7 | 10:35033122 | TGCCTAAAGAATGAT[-/AG]AGTTTTATGTACATA | 8453 |
rs764184895 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126252 | GCCAGCGGGCCCAGC[A/G]TGCGGACCATTTCCA | 8453 |
rs764198063 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023255 | TTATCAAAGTTGGGA[A/G]GAAAAACAACTCTAA | 8453 |
rs764203386 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118566 | CTGAAGCTCTATTAA[G/T]CTTATTTTCAATTCT | 8453 |
rs764233533 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031880 | GCATGCACAACCACA[C/T]CAGGCTTCTAAAGCT | 8453 |
rs764249127 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052956 | TATTCTGTATCTCTA[C/G]AGAATATTAAGCTTT | 8453 |
rs764280962 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045419 | AGCGAGACCTCATTC[-/A]AAAAAAAAAATTAGC | 8453 |
rs764284271 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056698 | CAAATATAAGATTTC[A/G]TCAGGAGCGGTGCTC | 8453 |
rs764300033 | snp | C/T | 1.65034e-05 | 0.00287253 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35062998 | TTTCCAAAAAAATCT[C/T]AGTTTCTGTATAAAG | 8453 |
rs764303472 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089792 | AGTGAAAACACTCGG[A/G]GTAAGGATGCATGAG | 8453 |
rs764327074 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35024510 | AGTTTAGCAAAAAAA[-/G]GAGAAAATTCAAGTG | 8453 |
rs764329304 | in-del | -/AG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035855 | ACAGCTGCCAACAGC[-/AG]AGAGTTCCTTTGCCA | 8453 |
rs764358407 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105708 | GCGAGACTCTGTCTC[A/G]AAAAAAAAAAAGAAA | 8453 |
rs764412352 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055575 | CTCTTAAGGAAATAA[C/T]AATAATAACTCCTAG | 8453 |
rs764430672 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023449 | CAAATCAACTTATGT[A/G]TCAGCTTAGAAATTT | 8453 |
rs764431861 | snp | A/C | 1.75145e-05 | 0.00295921 | missense, intron-variant | CUL2 | GRCh38.p7 | 10:35049740 | AGTGGTTCAACCATC[A/C]ATTTCCTCCACATAT | 8453 |
rs764455100 | snp | G/T | 4.94173e-05 | 0.00497053 | intron-variant | CUL2 | GRCh38.p7 | 10:35035139 | GCTGGATCTGATTAG[G/T]AGGAAAACATTGCAG | 8453 |
rs764475413 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022224 | ACAATAAAGAGAAGG[A/G]AACAGGCTCAAAGGA | 8453 |
rs764480883 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104655 | TAAATTAATGGCAAA[C/T]TAATTAAATGTATAA | 8453 |
rs764535357 | snp | C/T | 9.88468e-05 | 0.00702948 | missense | CUL2 | GRCh38.p7 | 10:35035269 | CCAGTGGACACAGCA[C/T]GGAGTAAGACGTACA | 8453 |
rs764570025 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095918 | GATACCCCTAGATAC[C/T]GTACAACAGTTTTAA | 8453 |
rs764578148 | in-del | -/A | 0.000147269 | 0.00857979 | intron-variant | CUL2 | GRCh38.p7 | 10:35013670 | AAATGTTTCCCCCTC[-/A]AAAAAAACTTGACAT | 8453 |
rs764579691 | snp | C/T | 1.77565e-05 | 0.00297958 | intron-variant | CUL2 | GRCh38.p7 | 10:35061010 | CTTGAAAAGCAATAA[C/T]CATTTTCACTGTCAA | 8453 |
rs764605915 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043626 | TGCTTGAAATCCAAC[A/G]CTGCAGATTTAAAAA | 8453 |
rs764614737 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121809 | GTAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs764620202 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102065 | GCCAATAAGGTGAAA[-/C]CCCATCTCTACCAAA | 8453 |
rs764625006 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106339 | TTTTTTGTTTGTTTG[A/T]GAAGGAGTCTCACTC | 8453 |
rs764651797 | snp | A/G/T | 0.000149683 | 0.0086499 | missense, synonymous-codon | CUL2 | GRCh38.p7 | 10:35031384 | CAGCATTCTTGCGTA[A/G/T]AACTACATTTAAAAA | 8453 |
rs764687612 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049186 | GGTAAAAAGTGTTAA[C/G]CACTCTGAGCCATGG | 8453 |
rs764695170 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070203 | AAAATATAAAAGATC[-/T]TTTCAAACTTTGAAG | 8453 |
rs764764876 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023985 | GACTACAGGTGTGCT[C/T]CACCACGCCTGGCTA | 8453 |
rs764798632 | snp | C/T | 1.65002e-05 | 0.00287225 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35010365 | GCGTTCTATGTATTG[C/T]TTGTCTATCAGAACT | 8453 |
rs764863864 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097308 | CTTGGATTTTTCCTA[A/G]CTGTACCCTTAAGCT | 8453 |
rs764875879 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014941 | GAAAAAAATATAAAA[C/T]CTTTAAGAATTTACT | 8453 |
rs764882931 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098796 | AAAATTAGCTGGGCA[C/T]GGTGGCAGGCGCCTG | 8453 |
rs764893153 | snp | G/T | 1.68069e-05 | 0.00289882 | intron-variant | CUL2 | GRCh38.p7 | 10:35011827 | TACCCTAAGAAGCCC[G/T]GAGGACTGCCCTCCT | 8453 |
rs764953983 | in-del | -/A | 1.65004e-05 | 0.00287227 | intron-variant | CUL2 | GRCh38.p7 | 10:35032404 | ATACTGACTTTTCAT[-/A]AGATTACTTTTCAGC | 8453 |
rs764958342 | snp | C/T | 1.64874e-05 | 0.00287113 | missense | CUL2 | GRCh38.p7 | 10:35031517 | CGTCCTTGTCATCAA[C/T]GTATTTGAACACTGT | 8453 |
rs765041819 | snp | A/G | 5.20784e-05 | 0.00510259 | intron-variant | CUL2 | GRCh38.p7 | 10:35063101 | ATATTTATTGGAGAC[A/G]ATTTTAAAACATAAT | 8453 |
rs765063041 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122129 | ACTTACTTGTTTTTA[C/T]CTTTCTCATATATTT | 8453 |
rs765112726 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047585 | ATTGCACTCCAACCT[-/G]GGCAACAGAGCAAGA | 8453 |
rs765142209 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119533 | TATCTAGGTATACTA[C/T]AATTTTTAGGGAGGT | 8453 |
rs765179772 | in-del | -/A | 2.10799e-05 | 0.00324646 | intron-variant | CUL2 | GRCh38.p7 | 10:35028769 | ATGAAGACAATTATT[-/A]AAATTCCTTTAGTCT | 8453 |
rs765192954 | snp | A/G | 2.02075e-05 | 0.00317858 | intron-variant | CUL2 | GRCh38.p7 | 10:35044518 | TGTTAAATAAAACCA[A/G]GCCAGATACAAAATA | 8453 |
rs765197579 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087471 | CCTCGTTGGATGGCT[A/G]AATCACTCCTTAACC | 8453 |
rs765222942 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053639 | TAGGCTTAGGACTTG[C/G]GATTACTTGGTCAAA | 8453 |
rs765230951 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125568 | CACTCTGACACTACA[A/G]TAACTGATATGAAAT | 8453 |
rs765235513 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029816 | TAATCAAAACCTTTC[A/C]AACTTTCTTTTTAAA | 8453 |
rs765243325 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042336 | TATCATGTATAACTT[A/C]AATTCTTTTTAAAGA | 8453 |
rs765244563 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055472 | GCGTCGGGGCTCACG[C/T]CTGTAATCCCAGTGC | 8453 |
rs765273594 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088985 | GTTCAAGACCAGCCT[A/G]GCCAACATGGTGAAA | 8453 |
rs765294922 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022691 | CAGTTAGGACCAGTA[A/C]GTTCTGGAGATCTAT | 8453 |
rs765298264 | snp | A/G | 1.66067e-05 | 0.00288151 | intron-variant | CUL2 | GRCh38.p7 | 10:35054412 | ATACTTATGTTTGCT[A/G]GTCACTTAAAGAATG | 8453 |
rs765304077 | in-del | -/AAAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086720 | GCGAACACCATCTCA[-/AAAT]AAATAAATAAATAAA | 8453 |
rs765368040 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041051 | ACTGGTCCTCAGCCT[C/G]AGGGTCAGGGACCCC | 8453 |
rs765391507 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075054 | AACAGTTGCACAGAC[-/T]TTTTTTTGCTTTATG | 8453 |
rs765487863 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081200 | CACCACACTCCAGCC[C/T]GGGCCAAAAGACCAA | 8453 |
rs765503504 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102070 | TAAGGTGAAACCCCA[C/T]CTCTACCAAAAATAC | 8453 |
rs765505199 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064037 | TGGTGGTTATACTCC[A/T]GACTGTTCCATGATA | 8453 |
rs765505851 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118925 | ACTCCAGCCACTGCT[A/G]CTGATGGAGAGGTAA | 8453 |
rs765535616 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034455 | CTGCAGCTAAGGTAA[C/T]AGCCTCTAAAAAGTG | 8453 |
rs765581050 | snp | C/T | 1.65712e-05 | 0.00287843 | intron-variant | CUL2 | GRCh38.p7 | 10:35032526 | GCCATAATTAACCAC[C/T]AGCCATAGGGAAAAA | 8453 |
rs765624790 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095608 | CCGTTGCCCGGGCTG[A/G]AGTGCAGTGGTGTGA | 8453 |
rs765626519 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080281 | TCTTGCTGTATCAAA[C/T]GAGCAAGCCACTGGA | 8453 |
rs765631766 | snp | C/G/T | 3.67379e-05 | 0.00428577 | intron-variant | CUL2 | GRCh38.p7 | 10:35028799 | TTCTAATATATTTCC[C/G/T]GCAAACTTACCATCT | 8453 |
rs765635858 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047125 | TGACTAAATTACTAA[C/T]TTCTTCATTTCCTTT | 8453 |
rs765648749 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046216 | ATATAATAAGGTCAC[A/T]CATGTGAGCTCATTT | 8453 |
rs765671636 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094183 | AACAATACAAGAATG[A/G]CATAATACAATAGAT | 8453 |
rs765675526 | snp | A/T | 6.36004e-05 | 0.00563881 | intron-variant | CUL2 | GRCh38.p7 | 10:35028903 | CTAGAAGGAAAAAAA[A/T]AAAATAAAATAAGCT | 8453 |
rs765687561 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011288 | AAACTCCTGGACTCA[A/G]GTGATCCTCCTGTCT | 8453 |
rs765728486 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108610 | AGATAATACCTGTTT[C/T]CAGATTTGGGAATGT | 8453 |
rs765802200 | snp | A/G | 1.65315e-05 | 0.00287498 | missense | CUL2 | GRCh38.p7 | 10:35011855 | CCTTTTACCTCTTGA[A/G]TAAGGGCATTGTGCC | 8453 |
rs765841852 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090459 | AAAGACAGCAAAGTC[C/T]AAGGCCGCCGCCGCT | 8453 |
rs765861293 | snp | C/G | 1.64958e-05 | 0.00287187 | intron-variant | CUL2 | GRCh38.p7 | 10:35032411 | CTTTTCATAAGATTA[C/G]TTTTCAGCAACCACC | 8453 |
rs765861415 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068424 | ACGCACTATGTCTAA[-/T]TAAAAAAAAAGAACC | 8453 |
rs765869223 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061769 | CCTTACTTATGAGGG[-/T]TTTTTTTTTTTTTTT | 8453 |
rs765882138 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060013 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGACTGAG | 8453 |
rs765917513 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060358 | GCACCAGGAAAGGCA[-/G]GAAGATGGGAGAGAC | 8453 |
rs765982004 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014506 | TCTCAATAATAATCT[A/G]AGACATTCTGCTAAG | 8453 |
rs766012105 | snp | C/G | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35090205 | GCAGGGCAAGGGGCA[C/G]GGGACAAGGGGAGGG | 8453 |
rs766031957 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035360 | TTAGGTAATATATGG[-/A]ATCCAAGTGCAGGAG | 8453 |
rs766047296 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029700 | ATAAGTCATATTGGT[A/T]AATAATAATGTGTCG | 8453 |
rs766066265 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062918 | AACTAGTAAAGTATA[A/C]AACTATCAACATATT | 8453 |
rs766070174 | snp | C/T | 3.33728e-05 | 0.00408476 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35011962 | TCTAGTCTGCTCCAT[C/T]TCCTGTTTTACAGAA | 8453 |
rs766070704 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075169 | GGATAGCAAATCTGG[A/G]AGCCAACGTGCAAGA | 8453 |
rs766071515 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095934 | GTACAACAGTTTTAA[C/T]GTTTGGAGTGGCTCA | 8453 |
rs766077667 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111756 | AGCTGGGCGTGGTGT[A/G]GCATGTGCCTGCAAT | 8453 |
rs766097319 | snp | A/G | 1.66679e-05 | 0.00288681 | intron-variant | CUL2 | GRCh38.p7 | 10:35044679 | TTTCCTGATAAAACT[A/G]AATAAATCAATTACA | 8453 |
rs766097397 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102884 | GAGACTCTGTCTCAG[-/G]AAAAAAAAAAAAAAA | 8453 |
rs766100810 | in-del | -/AAT | 1.71693e-05 | 0.00292991 | intron-variant | CUL2 | GRCh38.p7 | 10:35071362 | TTAAAAAACAATAAC[-/AAT]GTTAGCAATAATTCC | 8453 |
rs766146214 | in-del | -/CATT | 1.6585e-05 | 0.00287962 | intron-variant | CUL2 | GRCh38.p7 | 10:35016429 | TGACAGTGAATTGAC[-/CATT]CAAAGAAACATTTCA | 8453 |
rs766174228 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103738 | GTGCTGGGATTATAG[C/G]CATGGGCCACCATAC | 8453 |
rs766183838 | in-del | -/AGGAG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045406 | GCCTGGGCAATAGAG[-/AGGAG]CGAGACCTCATTCAA | 8453 |
rs766191663 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088174 | TTATATACTGTCTGT[C/T]TCTCCATCCCAAGCC | 8453 |
rs766219735 | in-del | -/AC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117939 | AAACGAGCAGAAAGT[-/AC]ACAGTTCCTTTCATC | 8453 |
rs766245183 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087197 | GCGGGTACTACAGGC[A/G]TGCGCCACCACGCCT | 8453 |
rs766246661 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027307 | ATGCCACCATGCCCG[G/T]CTAATTTTTTCTATT | 8453 |
rs766274784 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053335 | TATAATTGTATTTGT[A/G]TTCAACATATACCTA | 8453 |
rs766303993 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124158 | CTGTACTCTAACCTG[A/G]GTGACAGAGCGAGAC | 8453 |
rs766322975 | in-del | -/TTTCT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041545 | GAGCTTTTCTTTTTC[-/TTTCT]TTTCTTTTGTCAGAC | 8453 |
rs766324621 | snp | A/G | 1.65853e-05 | 0.00287964 | intron-variant | CUL2 | GRCh38.p7 | 10:35044879 | GATCACTAAAACAAG[A/G]TATAACACAAAATAT | 8453 |
rs766333163 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017081 | TGATATCAGCAACAG[A/C]CTCAAGTGCTGTCGA | 8453 |
rs766354036 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043958 | CTGTAGTCCCAGCTA[C/T]TTCGTAGGCTGAGAC | 8453 |
rs766381102 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075492 | CCACGCGCACTCAGA[C/T]TGTGTCCCATCAAGT | 8453 |
rs766407579 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055046 | TGACTTTGTCTACCA[C/G]AGGAAAATGAATTAT | 8453 |
rs766436208 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077592 | GGAGGCCGAGGCAGG[C/T]GCATTACCTGAGGTC | 8453 |
rs766447793 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079882 | TGCAAAACTGCAACA[C/G]TCTATCTGATAATCA | 8453 |
rs766470371 | snp | A/G | 1.80827e-05 | 0.00300683 | intron-variant | CUL2 | GRCh38.p7 | 10:35025119 | AAGCCAGATATAATT[A/G]AATGCATTTTACCTG | 8453 |
rs766474108 | snp | C/T | 4.97706e-05 | 0.00498827 | missense | CUL2 | GRCh38.p7 | 10:35033243 | ATTTACCATGCACTT[C/T]CAAAACTGACTCCAC | 8453 |
rs766502994 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017805 | ACAGCAGCATGACAT[C/T]AGCACACTGAAAGCT | 8453 |
rs766511450 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035028 | GTCCAACAAATTCTA[A/G]GTTTAAAACATTTGA | 8453 |
rs766532832 | in-del | -/AAAC/AAACA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046928 | AAACAAAACAAAACA[-/AAAC/AAACA]AAAACAAAAAACTGG | 8453 |
rs766538314 | in-del | -/G | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008061 | CTAAAAAACTTCTGA[-/G]GGTTTTGCTTACTTG | 8453 |
rs766566505 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042140 | TTACCCCATCAGAAA[C/T]TTTATAACCATTAAG | 8453 |
rs766581479 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023995 | GTGCTCCACCACGCC[C/T]GGCTAATTTTTGGAT | 8453 |
rs766590778 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070797 | CCACCCATTCTAAAA[A/G]AGCAGCACCCACACA | 8453 |
rs766605113 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098638 | AACTTGTAACTTAAT[A/G]AAAATAAGCAGGCGG | 8453 |
rs766683752 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078690 | AGCAGGTAAAAGTTA[C/T]AGTATCTCAAAAGAT | 8453 |
rs766721243 | snp | C/T | 1.71123e-05 | 0.00292504 | missense | CUL2 | GRCh38.p7 | 10:35016311 | TGACAGTTTCACTGT[C/T]GTTAAAGGCAAGAAG | 8453 |
rs766733024 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092231 | AAAGTTCTGGGATTA[C/T]AGGAGTGAGCCACCA | 8453 |
rs766782272 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059741 | ATGGTAGAATGAAGT[A/G]GTTAAATGGATGGGC | 8453 |
rs766792032 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058529 | AAAACCTAAGGTCTG[C/T]TAGCATCCACCTGAT | 8453 |
rs766829499 | snp | G/T | 1.65674e-05 | 0.00287809 | intron-variant | CUL2 | GRCh38.p7 | 10:35054418 | ATGTTTGCTAGTCAC[G/T]TAAAGAATGTCCTAC | 8453 |
rs766868288 | snp | C/G | 1.64887e-05 | 0.00287125 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071246 | GTATTCCAACATGAC[C/G]ACGGCTTTTATTGTC | 8453 |
rs766931302 | in-del | -/TT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022608 | TAGCGTGTGAGAAAC[-/TT]TTTGTTAAATGAATA | 8453 |
rs766949082 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110118 | AGGTCAAGGCTGCAG[G/T]GAGCCTGATTGTGCC | 8453 |
rs766952651 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055330 | ATACATGAATATATA[-/T]CACTTTTCAAAATTC | 8453 |
rs766954131 | in-del | -/TAACCCTCCACA | 1.68832e-05 | 0.00290539 | splice-acceptor-variant | CUL2 | GRCh38.p7 | 10:35071341 | GTAGTGTTGAAATCT[-/TAACCCTCCACA]GTCAATTAAAAAACA | 8453 |
rs767045521 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072017 | GCAGGACATTCAACC[A/G]AAAGGTTTTGGCCCC | 8453 |
rs767053854 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032966 | ATATAGCATAATCAC[A/G]GGACATTCTACAAGC | 8453 |
rs767066234 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061399 | AGAATCACTTGAACC[C/T]GATCGCACCGAGACC | 8453 |
rs767067504 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011479 | AAAAATTAGCCAAGT[A/G]TGGTGGTGCACGCCT | 8453 |
rs767092472 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047798 | GGTGCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 8453 |
rs767122278 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028153 | TTATAGTCTGCCCCA[C/T]CCAATGAATGTCTGC | 8453 |
rs767152260 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108835 | GTCCCTGTGGACCTC[C/T]CCATGGGACTTCCTG | 8453 |
rs767165082 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111257 | TCTCTTATGAGAAGA[-/T]TTTTTTTTTTTTTGA | 8453 |
rs767171368 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058101 | ACTCGGTCCCAAAAA[C/T]TAGTAATAAAATTTT | 8453 |
rs767185864 | in-del | -/ACTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059871 | GTAAAAAACAGAGAT[-/ACTA]ACTAACTCATATCAT | 8453 |
rs767194774 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073904 | GGCCACTGCGCCTGA[A/C]CTGTTCTCCCCATTT | 8453 |
rs767209995 | snp | A/G | 3.30846e-05 | 0.00406709 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35031608 | CAGTAAGTTGTCACA[A/G]TACTTAGCAAGCTCA | 8453 |
rs767232374 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053692 | TACTGAAAGAAAGAC[A/G]CTGATCAATTTCTTT | 8453 |
rs767264955 | snp | C/T | 1.66156e-05 | 0.00288228 | intron-variant | CUL2 | GRCh38.p7 | 10:35044885 | TAAAACAAGGTATAA[C/T]ACAAAATATTCTTGA | 8453 |
rs767284560 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124036 | GGAGGGAGACTATGT[C/T]AAGAAAGTGGCAGGC | 8453 |
rs767300656 | snp | A/G | 2.40833e-05 | 0.00347003 | missense | CUL2 | GRCh38.p7 | 10:35038943 | TTCTCTTGTCGAATT[A/G]TATTATGACATTCTG | 8453 |
rs767332160 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075326 | TAAAAATGTTTAATA[A/G]TAACATTCAGGGAAA | 8453 |
rs767333021 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085622 | GGTGGCAGGCGCCTG[G/T]AGTCCCAGCTACTCG | 8453 |
rs767335940 | snp | C/G | 1.73525e-05 | 0.0029455 | missense, intron-variant | CUL2 | GRCh38.p7 | 10:35049699 | TTTTGATTTCTCGGA[C/G]CAGCATTCGGATAAG | 8453 |
rs767362559 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038823 | TAAAATATTTTAAAG[A/G]CTATTACTAAAATAG | 8453 |
rs767377523 | in-del | -/GAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105826 | AAGAGGCAATGTCCT[-/GAA]AAAAAAAAAAAAAAG | 8453 |
rs767386928 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049851 | TTTAACTAAAAATAC[C/T]CATCAAAAGAAGTAT | 8453 |
rs767396435 | snp | A/G | 5.60695e-05 | 0.00529449 | intron-variant | CUL2 | GRCh38.p7 | 10:35011983 | TTTTACAGAAGAAAA[A/G]AAAAAAGACCCAACA | 8453 |
rs767452809 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35016693 | GCACTGTGGGAGGCC[A/G]AGGCAGACAGATCAC | 8453 |
rs767504387 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033007 | ACTATTCAGTTAATA[A/G]TTTAAAAATTATATT | 8453 |
rs767560345 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067449 | TATACAAAGTCCAAA[A/G]ATCAAAGAATTCACC | 8453 |
rs767562732 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116003 | TACCAAGATTTGGCT[C/T]GAAAGATGATATCAC | 8453 |
rs767569580 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091850 | CCAGGCTGGTCTTGA[A/G]CTCCTGAGCTCAGGC | 8453 |
rs767590437 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045960 | TAGTAAGAGCTTGTT[A/G]CTCTATATATAGGAT | 8453 |
rs767591713 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034021 | GAGAACAGAGACCCC[G/T]TGAACTCGGCAAGAC | 8453 |
rs767618104 | snp | A/G | 1.72609e-05 | 0.00293771 | missense | CUL2 | GRCh38.p7 | 10:35025147 | CTGTACACAGATAAT[A/G]TAACCATGTAAGTTT | 8453 |
rs767619383 | snp | C/G | 1.66205e-05 | 0.00288271 | intron-variant | CUL2 | GRCh38.p7 | 10:35035128 | AAAGGCTCCACGCTG[C/G]ATCTGATTAGGAGGA | 8453 |
rs767673491 | in-del | -/TA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117429 | GAGACAAGGTCTCAC[-/TA]TGTTTCCCAGTCTGG | 8453 |
rs767680453 | in-del | -/A | 1.98754e-05 | 0.00315235 | intron-variant | CUL2 | GRCh38.p7 | 10:35013839 | ATATTTATAAAAACC[-/A]AAATCTTTAAATAAG | 8453 |
rs767682724 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118936 | TGCTACTGATGGAGA[A/G]GTAAAGGGAAAGAAT | 8453 |
rs767715406 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043790 | AAAATTTCTTGGCTG[C/G]GTGCAATGGCTCACA | 8453 |
rs767727757 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078549 | CAGGTGATCCCCCTG[C/T]CTCAACCTCCCAAAG | 8453 |
rs767741266 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109589 | ATTTTCTGAGGTGAC[A/G]TTTGCGTTTACACGG | 8453 |
rs767781083 | snp | C/G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076962 | GAGGCTGAGGCAGGA[C/G/T]AATGGCGTGAACCCA | 8453 |
rs767846172 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070868 | TTATCACGACCTCTT[C/T]TTGAAAGCAATGACA | 8453 |
rs767893710 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057072 | ACTTTCCTATTCAGA[A/T]TTCTACAGGAGCTTC | 8453 |
rs767967058 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120788 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGTAGTGG | 8453 |
rs768002789 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083636 | GGGGCATATCGAAAG[A/G]ACACAAGTTAAACTA | 8453 |
rs768030628 | snp | C/T | 3.3484e-05 | 0.00409156 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35033262 | AACTGACTCCACAAA[C/T]AGTGTTGGCATCTAA | 8453 |
rs768037297 | snp | C/T | 3.50091e-05 | 0.0041837 | intron-variant | CUL2 | GRCh38.p7 | 10:35031296 | CATTAAAGACTTACA[C/T]TACCTTTAATTTGTT | 8453 |
rs768041454 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022095 | TGTCTGTCTTCCTAC[C/T]AGACATGAGTTTTTT | 8453 |
rs768051221 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023897 | TGGAGTGCAGTGGCA[C/T]GATCATGGCTCACTG | 8453 |
rs768058554 | snp | C/G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054655 | CATGGAATAGCCTAC[C/G/T]AACAAATCCAAAAGA | 8453 |
rs768059806 | in-del | -/TTTT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071581 | AGCTAATTTTTTGTA[-/TTTT]TTTTTAGTAGAGACG | 8453 |
rs768076794 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086826 | CATTCTCTGTGTTCT[C/T]ATCCTATTTCATAAC | 8453 |
rs768092882 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043895 | CAACACAGCAAGACC[A/C]CATCTCTATAACAAA | 8453 |
rs768099073 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028251 | GAAGTCCTAATTTAG[-/C]CCTCCTATTCTGAAA | 8453 |
rs768170800 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068820 | TCTTGGGCAAAATAA[C/T]AGGGAAAATGATGGA | 8453 |
rs768195957 | snp | A/C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085916 | CTATGTTCAGCACCT[A/C/G]AGTGACGGGATCATT | 8453 |
rs768227042 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048596 | GAACTTAGAAGTTTT[A/G]TTGGGAGTGTTCTTT | 8453 |
rs768329803 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053465 | ACAAAATCATATCAT[A/G]TATAATACATTCTTC | 8453 |
rs768389896 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033955 | AAGCAAAGACTGCCT[A/G]CAAAGTCACTAAAGG | 8453 |
rs768397912 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037251 | TGAAATGGATATCCA[A/G]TTGACTGAGCAATGC | 8453 |
rs768410546 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115849 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 8453 |
rs768440846 | snp | A/C | 1.66729e-05 | 0.00288724 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35016270 | CTTTTCATTCATCTG[A/C]GTGCTGTCCTGAAGC | 8453 |
rs768442006 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019750 | CCAGTATCTGTGTCA[A/G]CTCTCTACTCTCTCA | 8453 |
rs768442555 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034791 | CAAATTCAGAGGATA[C/T]GGAAAGGAGGCAAAT | 8453 |
rs768456514 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067256 | AGGCAATATTAAGTC[A/T]CCCCTAACAATCATT | 8453 |
rs768531183 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080823 | GAACAGACATATGGT[A/G]TGTGCCAAAATGTAT | 8453 |
rs768541660 | snp | C/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128336 | ACTGTGGCTTACGTA[C/G]GTGACTCAGTTTCCT | 8453 |
rs768559268 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026467 | TCTCAAAACACTTTC[A/G]GAAATGAGAAATTCC | 8453 |
rs768568007 | snp | A/G | 1.69069e-05 | 0.00290743 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054533 | AATAAACTGGGTGTT[A/G]AGATACCTGGAAAAT | 8453 |
rs768584002 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35024465 | CCTTCTTGTACAAAG[-/A]AAAAGTGATTCAATG | 8453 |
rs768605353 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089584 | CATTAATAACAGTCT[G/T]CAATTCACAGATGTT | 8453 |
rs768606341 | snp | C/T | 1.85765e-05 | 0.00304761 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35039035 | ATATGAACTTGGATG[C/T]AGGTATTTTCGACAT | 8453 |
rs768661168 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059428 | TGGCAAAAGGATTAC[A/T]ACTTGCTGAAGGCTC | 8453 |
rs768661824 | snp | G/T | 1.66305e-05 | 0.00288357 | utr-variant-5-prime, missense | CUL2 | GRCh38.p7 | 10:35071319 | GGTTTCAAAGACATT[G/T]TGCAAGTGTAGTGTT | 8453 |
rs768674595 | snp | A/C/T | 3.6141e-05 | 0.00425082 | intron-variant | CUL2 | GRCh38.p7 | 10:35033299 | AATATAAGTACAAAA[A/C/T]CACATTTTAAGAGGT | 8453 |
rs768722572 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008662 | CTCTTTTGGAAGAAA[A/G]GTAAAATGAGAAATA | 8453 |
rs768724061 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058200 | GCTGATTCTATAAAG[A/G]GAAATAAAATCTCAG | 8453 |
rs768731643 | snp | C/T | 6.66389e-05 | 0.00577192 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35033175 | ACTTACCTTATCCAA[C/T]GCACTCATAAAATGC | 8453 |
rs768731796 | snp | C/T | 9.88582e-05 | 0.00702989 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060907 | TAGTCTGCACCCTTG[C/T]TGTATTCTTCCCAGT | 8453 |
rs768738175 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072828 | GCAAATGTTTTAACA[A/G]CCTCCCTCATGTCTC | 8453 |
rs768772085 | in-del | -/AAAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086723 | ACACCATCTCAAAAT[-/AAAT]AAATAAATAAATAAA | 8453 |
rs768800544 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083568 | TACAAGTTGAACCTA[A/G]AACACCTATGATGTC | 8453 |
rs768812393 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106808 | GAAAAAGGATTACAG[A/G]TGATGACTTTGAAAG | 8453 |
rs768818014 | snp | A/G | 3.00152e-05 | 0.00387385 | intron-variant | CUL2 | GRCh38.p7 | 10:35029685 | TTCAAAAGAAAAATA[A/G]TAAGTCATATTGGTT | 8453 |
rs768889973 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018711 | GAGGTTGCTGTGAGC[C/T]GAGATCGCGCCATTG | 8453 |
rs768925218 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098384 | GGACTTATACATGAC[A/G]TGTGAAAGAAGGGGA | 8453 |
rs768935558 | in-del | -/A | 0.32 | 0.24 | intron-variant | CUL2 | GRCh38.p7 | 10:35029645 | CCACAGGCTTGCTAT[-/A]AAAAAGTTTTAGAAA | 8453 |
rs768947366 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079822 | CTACTCCTGTACTTT[A/G]GGGGCCCTTACTAAG | 8453 |
rs769011965 | in-del | -/AGGAGTTTAAGTCTGTATTACTG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045503 | TGATCCCTTGAGTCC[-/AGGAGTTTAAGTCTGTATTACTG]TGAGTTTGAGACTAG | 8453 |
rs769041408 | snp | A/T | 0.00489358 | 0.0492224 | intron-variant | CUL2 | GRCh38.p7 | 10:35032500 | ACGTAAGGGCCTGAA[A/T]AAAAAAACACGCCAT | 8453 |
rs769150764 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050187 | TGAGCCTGGTGTGGT[A/G]GCATGCGCCTGTAAT | 8453 |
rs769173554 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014292 | TCAATTTGCTGTGAC[C/T]TGGGGTGATGGTGAA | 8453 |
rs769194516 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064408 | CCCCGACACTTCATA[C/T]ACATTCTTCTACAAA | 8453 |
rs769206942 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35124897 | TGTGACTGACAGCCC[A/G]TATTTTCTCAGAAAA | 8453 |
rs769215676 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100596 | GCGAAACCTCGTCTC[C/T]ACTAAAAATAGAAAA | 8453 |
rs769223988 | in-del | -/AAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013344 | GCAAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 8453 |
rs769245871 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076563 | TCAATCTCTCTCCCA[C/T]CACTCCCGTGTACGA | 8453 |
rs769264066 | snp | A/C | 2.6061e-05 | 0.00360968 | intron-variant | CUL2 | GRCh38.p7 | 10:35013677 | TCCCCCTCAAAAAAA[A/C]CTTGACATTAAAAGC | 8453 |
rs769287881 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055942 | AGGGTAGTCAGTCCC[-/C]TTTCATCCGAGTCTC | 8453 |
rs769290138 | snp | A/C | 1.64977e-05 | 0.00287203 | missense | CUL2 | GRCh38.p7 | 10:35044820 | ATGAACAAAGGAGTT[A/C]ATAACCCCATGGATT | 8453 |
rs769291191 | snp | C/G | 1.6507e-05 | 0.00287284 | intron-variant | CUL2 | GRCh38.p7 | 10:35032392 | TCTCATTTTCTAATA[C/G]TGACTTTTCATAAGA | 8453 |
rs769296299 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051860 | AGTAAATCAACTGCT[C/T]GGTTTCTTTATTGTG | 8453 |
rs769363103 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072255 | ATTCCACAGAAATGT[C/T]AGGTTTGCAGTGGAG | 8453 |
rs769374671 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116475 | AAGCTGAAAAGATCT[A/G]TATCTATTGTTTCTC | 8453 |
rs769420737 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066067 | AGACAGTCCTAACCA[C/G]CAGCAAAGTTACTTA | 8453 |
rs769451581 | snp | C/T | 3.61454e-05 | 0.00425105 | intron-variant | CUL2 | GRCh38.p7 | 10:35049670 | ACTCAGTAAGATAAA[C/T]GTCAGCACTCACTTT | 8453 |
rs769460605 | snp | C/G | 5.01107e-05 | 0.00500528 | intron-variant | CUL2 | GRCh38.p7 | 10:35062954 | CACGTATGTATCATT[C/G]CTTACCTTATGCAAA | 8453 |
rs769524123 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058956 | TCAAGACTTCAGGGG[A/G]GGAAGTGACTGGAGG | 8453 |
rs769547777 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089608 | AGATGTTTTATTTGC[A/C]TGCACGTAATGGTAG | 8453 |
rs769596588 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033572 | AAACCCCGTCTCTAC[G/T]AAAAATACAAAAAAA | 8453 |
rs769637257 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35024418 | TGATTTTCTTGTACC[A/G]TCTCTAAGAAATATT | 8453 |
rs769708785 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037799 | AGTGAACAGAGATCG[C/T]GCCACTGCATTATAG | 8453 |
rs769720882 | in-del | -/AAATAAAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086719 | GCGAACACCATCTCA[-/AAATAAAT]AAATAAATAAATAAA | 8453 |
rs769721254 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071465 | GCTGGAGTGCAATGG[C/T]GTGATCTTGGCTCAC | 8453 |
rs769737869 | snp | C/T | 1.84752e-05 | 0.00303929 | intron-variant | CUL2 | GRCh38.p7 | 10:35031254 | ACATCTTTATGTGCT[C/T]GTGAATGAATTTCTA | 8453 |
rs769782135 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083211 | TCTTCTATTTCCCAC[C/T]GTCAGAAAATAGCAG | 8453 |
rs769789936 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106687 | TGTTATGGCAGCCCA[A/G]GTGGAAAGATAGTGT | 8453 |
rs769804277 | snp | C/T | 2.19488e-05 | 0.00331269 | intron-variant | CUL2 | GRCh38.p7 | 10:35025225 | AAAAAAAAACACACA[C/T]TATTTTTAGCTACTA | 8453 |
rs769810020 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023118 | TGCTCTCACCACAAA[C/T]AAAGATAAGTGAGAA | 8453 |
rs769815394 | snp | C/G | | | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079404 | GACTTAGAGTAAATG[C/G]TTTGGTGTCATTCGT | 8453 |
rs769857219 | snp | C/G | 1.64887e-05 | 0.00287125 | missense | CUL2 | GRCh38.p7 | 10:35035201 | GGTTGCTGGTTGCTC[C/G]AAGGCCCTCATCATG | 8453 |
rs769872680 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035916 | AACACTGGGAGGTGA[A/G]TAATGATCTCTCAGT | 8453 |
rs769873351 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083362 | ATAAACATAGATGTT[A/T]GTGTATGCATGGTTG | 8453 |
rs769910709 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121734 | AGGATTGCTTGAGCC[C/T]GGGAGGTCGAGGCTA | 8453 |
rs769970254 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036758 | GCTTTTTTTGAGACA[G/T]GGTCTTACTCTGTCA | 8453 |
rs769994690 | snp | C/T | 1.67531e-05 | 0.00289418 | intron-variant | CUL2 | GRCh38.p7 | 10:35010455 | CACCTGTGGAAGAGA[C/T]GTGGAAGTCAAACTA | 8453 |
rs769999991 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048981 | GAGTGGCCATTATTA[C/T]ACTACAATTCACTGG | 8453 |
rs770041366 | in-del | -/AG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059291 | ATCTTTTGTGAAGAA[-/AG]AGTCAACTGATGCAG | 8453 |
rs770061112 | snp | A/G | 1.68818e-05 | 0.00290527 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35010317 | AGAGCGACATCACGC[A/G]ACGTAGCTGTATTCA | 8453 |
rs770090263 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111343 | TGCAGCCTCAAACTC[A/C]TGGCCTCAAGTACTT | 8453 |
rs770105900 | in-del | -/TTTTTTT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011213 | TTTTAATTTTTTAAT[-/TTTTTTT]TTTTTTTTTTTTTAG | 8453 |
rs770110262 | snp | A/G | 3.81214e-05 | 0.00436569 | intron-variant | CUL2 | GRCh38.p7 | 10:35016168 | GCTGATGATGCTTAA[A/G]TTCTTTGGAATATTA | 8453 |
rs770119667 | in-del | -/TGAT | 1.66969e-05 | 0.00288932 | intron-variant | CUL2 | GRCh38.p7 | 10:35044741 | AAGAAATTAACAGTC[-/TGAT]TATTTGTTTTTAAAG | 8453 |
rs770143614 | snp | C/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126063 | CTGACCTCAGGTGAT[C/T]TGCCCATGTCTGCCT | 8453 |
rs770191114 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120889 | CCATAGAGTAAGAGA[C/T]CCTGTCTCAAAAAAA | 8453 |
rs770196070 | in-del | -/CAAAAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105425 | GGAGAGACACCGTTT[-/CAAAAAA]CAAAAAACAAAAAAC | 8453 |
rs770204922 | in-del | -/GAGC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045404 | GCTGCCTGGGCAATA[-/GAGC]GAGACCTCATTCAAA | 8453 |
rs770206558 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030569 | TGTATTTTTGGTAGA[C/G]ACAGGGTTTTGCCAT | 8453 |
rs770230383 | in-del | -/ACAC | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075642 | GGCCCTAAAACACAC[-/ACAC]ACACACACACACACA | 8453 |
rs770232622 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064177 | ATATATGTTAAAGTA[C/T]TTTATAAACTGTCCA | 8453 |
rs770259522 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029204 | CTGGGATTACAGGCA[C/T]GCACCACCACACCTG | 8453 |
rs770280768 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109901 | ATAGTGGGCCAGGCA[A/T]GGTGGCTCACACCTG | 8453 |
rs770287378 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062465 | ACAAACCCTGAGCTG[A/G]CCCTCTCCTTCATTT | 8453 |
rs770287417 | in-del | -/GGTGTGTCTTTCTGCATTGATGTAGTAA | 3.91229e-05 | 0.00442266 | intron-variant | CUL2 | GRCh38.p7 | 10:35011968 | TGCTCCATTTCCTGT[-/GGTGTGTCTTTCTGCATTGATGTAGTAA]TTTACAGAAGAAAAG | 8453 |
rs770295058 | snp | A/G | 1.86618e-05 | 0.00305459 | intron-variant | CUL2 | GRCh38.p7 | 10:35029480 | CATAGTAAAACACAT[A/G]TTCATACCTGTAGAA | 8453 |
rs770318557 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054959 | TAAACAAAAAAGATC[A/T]CAATCAGTAGGTAAG | 8453 |
rs770322348 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095624 | AGTGCAGTGGTGTGA[C/T]CTCTGCTCACTGCAA | 8453 |
rs770346123 | snp | A/G | 1.97799e-05 | 0.00314476 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35039070 | TTTCTTCATCTTTTA[A/G]TCTACCTAGAACCTA | 8453 |
rs770364268 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064699 | AGCTTTATTTATTTA[C/T]ATTTTTACTTGAAAA | 8453 |
rs770375014 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087899 | CAAAGCCAACATGAT[C/T]CAGCCCCTGGCTAGG | 8453 |
rs770383815 | snp | C/T | 1.88557e-05 | 0.00307042 | intron-variant | CUL2 | GRCh38.p7 | 10:35044546 | ATAGATAAATGTATT[C/T]GATATGTTTTATTTC | 8453 |
rs770392092 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065850 | GCAACAGAGCGAGAC[A/G]CCATCTCAAAAAAGA | 8453 |
rs770399674 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124740 | TGTAGGTATGACTCT[C/T]GGTAATTGAGCAAGA | 8453 |
rs770418017 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033378 | TCCTCAAGGAAATTA[C/T]GTTTCACACATGCAC | 8453 |
rs770434536 | snp | A/G | 0.000185684 | 0.00963366 | intron-variant, missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074207 | CTAAGCCAAAAAGTT[A/G]ACCATGTTACTCTGT | 8453 |
rs770439688 | snp | C/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127782 | TTCTGCCTGAGTCTT[C/G]CCTTTTTAGGGCCAT | 8453 |
rs770456249 | in-del | -/TTACTAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35028364 | CACTATCAATCACTG[-/TTACTAC]TTACTCTACTAGCAG | 8453 |
rs770468882 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095416 | TGGGTTGATGTACAT[A/G]ACTCACAATTTATTT | 8453 |
rs770482546 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091047 | TTTTCGATAAAGAAA[C/T]TTCACATCTTTTTCA | 8453 |
rs770501050 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35092812 | CTTAGGGATGAAAAA[C/T]CACCTTTGGAAGACT | 8453 |
rs770518813 | snp | C/T | 1.86353e-05 | 0.00305243 | intron-variant | CUL2 | GRCh38.p7 | 10:35033144 | TATGTACATATATAG[C/T]ATATATGTATTTAAA | 8453 |
rs770533318 | snp | C/T | 2.05696e-05 | 0.00320692 | missense | CUL2 | GRCh38.p7 | 10:35013754 | TTTGTTCTTTTACTG[C/T]TAAAGTTCATATTTA | 8453 |
rs770569784 | snp | C/G | | | missense | CUL2 | GRCh38.p7 | 10:35033214 | ATTCAAAACAGTGTT[C/G]ATAAGCTGAACAAAT | 8453 |
rs770605634 | snp | C/T | 0.000264389 | 0.0114945 | intron-variant | CUL2 | GRCh38.p7 | 10:35035344 | CCAAATATTTTCATT[C/T]ATTAGGTAATATATG | 8453 |
rs770631885 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108021 | TTCATTGCAATTATT[C/T]AGGCAAGGGAAGAGT | 8453 |
rs770652087 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019181 | AATTATGCATCAAGC[A/G]CCAAGATGATTAAGT | 8453 |
rs770663277 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089489 | GTTAATATTTTGCAT[C/T]TTATCTTCAAAATTT | 8453 |
rs770715832 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104041 | CATTTCTGTCTCCAA[A/C]ATCTGGAAAACGTTA | 8453 |
rs770734874 | snp | C/T | 2.59852e-05 | 0.00360443 | intron-variant | CUL2 | GRCh38.p7 | 10:35025250 | CTACTATAACTTGCC[C/T]AGTTAATTAACACAA | 8453 |
rs770756240 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022899 | AAAATACAAAAATTA[A/G]CTGGGAGTGGTAGTG | 8453 |
rs770764610 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070236 | TTCCAAAATGTCATC[A/G]CCCTTTTACATATCT | 8453 |
rs770774774 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021342 | GCTCACTGCAATCTC[C/T]GCCACCCGGGTTCAT | 8453 |
rs770786163 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123092 | GCAGTGAGCTGTGAC[A/G]GCACCACTGCACTCC | 8453 |
rs770836508 | snp | C/T | 1.69476e-05 | 0.00291093 | missense | CUL2 | GRCh38.p7 | 10:35028851 | GGGGAATTGCAAACG[C/T]AGATGAAGGAGCCTG | 8453 |
rs770883142 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036526 | CCACTTAGCGGTCAG[C/T]GCCAGTTTCCCAAAG | 8453 |
rs770897688 | snp | C/T | 1.68624e-05 | 0.0029036 | intron-variant | CUL2 | GRCh38.p7 | 10:35010471 | GTGGAAGTCAAACTA[C/T]TGCCAGTTCTTCAGC | 8453 |
rs770933722 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120363 | GCCTGGGTGACAGAG[A/G]GAGACCTTTCTCAAT | 8453 |
rs770938221 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035830 | ATCTTGTAGACAGAT[A/C]CTTCTAACCACAGCT | 8453 |
rs770943401 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069025 | AGGCACCCACAACCA[C/T]GCCCAGCTAATTTTT | 8453 |
rs770982031 | in-del | -/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009869 | CATTCTATTTCTTTA[-/T]TTTTTTTTTTATTTG | 8453 |
rs770995531 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100591 | ACATGGCGAAACCTC[A/G]TCTCTACTAAAAATA | 8453 |
rs771001560 | in-del | -/AT | 1.86551e-05 | 0.00305405 | intron-variant | CUL2 | GRCh38.p7 | 10:35044548 | AGATAAATGTATTCG[-/AT]ATGTTTTATTTCTTA | 8453 |
rs771022587 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126065 | GACCTCAGGTGATCT[A/G]CCCATGTCTGCCTCC | 8453 |
rs771034778 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046807 | TGAGGTAGGAAAATT[C/G]GCTTGAACCTGGGAG | 8453 |
rs771050279 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102312 | TGCTGTGACTCACAC[C/T]TGCAATCCCAACACT | 8453 |
rs771067943 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081092 | CCCTCTGGTAACATG[C/T]GCCCGCAGGGAGTCC | 8453 |
rs771071174 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095514 | AGCTATTTGTACTTC[A/T]CTGATTTTGATCTTT | 8453 |
rs771089380 | in-del | -/AGT | 1.65622e-05 | 0.00287764 | splice-acceptor-variant | CUL2 | GRCh38.p7 | 10:35031620 | CAGTACTTAGCAAGC[-/AGT]TCATGTAGAAATTGA | 8453 |
rs771108880 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048701 | TCTCCAGCTCTCTAT[C/G]TCTAAAAACAATGGA | 8453 |
rs771145277 | snp | A/T | 1.80863e-05 | 0.00300713 | intron-variant | CUL2 | GRCh38.p7 | 10:35028803 | AATATATTTCCTGCA[A/T]ACTTACCATCTGTAC | 8453 |
rs771154825 | snp | C/T | 0.000132393 | 0.00813506 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35062973 | ACCTTATGCAAATGC[C/T]GAACATGATTTTCCA | 8453 |
rs771159680 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062323 | ACTTCATATAGCACA[C/T]GAAAGGCAGCTAAAA | 8453 |
rs771187075 | snp | A/G | 9.12201e-05 | 0.0067529 | intron-variant | CUL2 | GRCh38.p7 | 10:35013850 | AACCAAAATCTTTAA[A/G]TAAGAGTTTGCTGCA | 8453 |
rs771209042 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078553 | TGATCCCCCTGCCTC[A/C]ACCTCCCAAAGTGCT | 8453 |
rs771217258 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061962 | TGCAGGGTTAGACAG[A/T]TTAAATAAAACTGTG | 8453 |
rs771239317 | snp | A/G | 1.6517e-05 | 0.00287372 | missense | CUL2 | GRCh38.p7 | 10:35011876 | GCATTGTGCCGAAGC[A/G]CTTTTCGTGCTTTCA | 8453 |
rs771251693 | in-del | -/GTGGGGCGAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021904 | GTGAGGTGGGGTGAG[-/GTGGGGCGAA]GTGGGGCGAAGTGGG | 8453 |
rs771254702 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108492 | GAAAAAAAACACAGT[C/T]ATTTGGACTAGAATA | 8453 |
rs771259916 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051920 | TACTCAAATTTACCA[A/G]TCTTCTTTATCATGG | 8453 |
rs771293266 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058493 | GTAACTCCAGATCTG[-/C]TAGTCTAAAGTCTAG | 8453 |
rs771307540 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033903 | AGGATAACAAGACCT[-/G]AACTACCAGGTCTAT | 8453 |
rs771313758 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012360 | GCAATAAAGGAGGAC[A/T]CAGCAATAATTTGCA | 8453 |
rs771315144 | in-del | -/CACA | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091775 | ACAGAAGCCCGCCAC[-/CACA]CCCGGCTAATTTTTT | 8453 |
rs771347335 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102884 | TGAGACTCTGTCTCA[-/G]AAAAAAAAAAAAAAA | 8453 |
rs771364787 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011082 | GAATTTATTATTATC[A/C]TTTGAGATAGCATCT | 8453 |
rs771382606 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025429 | TGTTCTAGAGTTCTC[C/T]CCACTAAACCACAGC | 8453 |
rs771395498 | in-del | -/AT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115376 | ACCAGCCTGGCAAAC[-/AT]AATGAAACCCCGTCT | 8453 |
rs771405627 | snp | A/T | 1.8231e-05 | 0.00301914 | intron-variant | CUL2 | GRCh38.p7 | 10:35044550 | ATAAATGTATTCGAT[A/T]TGTTTTATTTCTTAC | 8453 |
rs771417229 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123747 | ACAAGACATGTAGTT[C/T]TGAACCTATGAGTTG | 8453 |
rs771431800 | snp | C/T | 4.96931e-05 | 0.00498439 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35010338 | GCTGTATTCATCTGC[C/T]GACGCCTGGCTGCGT | 8453 |
rs771432211 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073662 | TGGGCTGGGGTGCAA[C/T]GGCGCAATCTCGGCT | 8453 |
rs771435956 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039779 | AGAATCACTTCATCC[C/T]GGGAGGTGGGGGTTG | 8453 |
rs771443939 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065120 | AACTATGTTCTTTTT[A/C]TCTAACCTATTCAAA | 8453 |
rs771502254 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031248 | CAATGAACATCTTTA[A/T]GTGCTTGTGAATGAA | 8453 |
rs771506591 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074983 | TGCTCCCCTCACATT[C/T]GCTTTCTCCTCTTAT | 8453 |
rs771512067 | snp | G/T | 1.65059e-05 | 0.00287275 | intron-variant | CUL2 | GRCh38.p7 | 10:35031466 | TGACCAAAATACAAA[G/T]GAAACTTTTCTGTTC | 8453 |
rs771549834 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041916 | CTTTTAACACCTTGA[A/G]ATGTAATTTACATAT | 8453 |
rs771565008 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086523 | AGCTGCTGGGCTCAA[C/G]TGATCCACCCACCTC | 8453 |
rs771592170 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089376 | GTCAGTTGTCAATCA[C/G]ATCAAAGTGATTATT | 8453 |
rs771611879 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085409 | CGCTCCAGCCTGGGC[A/G]ACAAAGCGAGACACC | 8453 |
rs771643405 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104877 | TGGGATTACAGGCAC[C/T]TGCCACCACACCCAG | 8453 |
rs771648401 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092252 | TGAGCCACCATGCCT[A/G]GCCTCCTCTGTCTTT | 8453 |
rs771667640 | snp | C/T | 2.86184e-05 | 0.00378265 | intron-variant | CUL2 | GRCh38.p7 | 10:35016407 | CACCTACAATTAAAA[C/T]AAAAACTGACAGTGA | 8453 |
rs771681575 | snp | C/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126201 | CAAGCGATCCTCCCA[C/G]CTTGGCCTCCCGAAG | 8453 |
rs771721020 | snp | G/T | 5.01542e-05 | 0.00500745 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35016237 | ATCAAGTAATGATTT[G/T]ATTGTTTTTGTCAGT | 8453 |
rs771761967 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103049 | TAATTTAATGTTTTC[A/C]TTGTGTCCAATCTGT | 8453 |
rs771764199 | in-del | -/TA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021433 | TTTTATATATGTATG[-/TA]TATATATATACACAC | 8453 |
rs771829640 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019865 | CTAAAACTACATTAG[C/G]TTCCTGGAACAGGGT | 8453 |
rs771850153 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116905 | GAGGTTGCAGTGAGT[C/T]GAGACTGTGCCACTG | 8453 |
rs771853716 | in-del | -/ACACACACAC | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075636 | CTTATGGGCCCTAAA[-/ACACACACAC]ACACACACACACACA | 8453 |
rs771860394 | snp | A/T | 0.000182091 | 0.00954003 | intron-variant | CUL2 | GRCh38.p7 | 10:35032515 | TAAAAAAACACGCCA[A/T]AATTAACCACCAGCC | 8453 |
rs771879937 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023664 | CTGAAATAATGAGAA[C/T]AACCAAGAATGTTTA | 8453 |
rs771960943 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035604 | ACACATTTTAACTTA[A/G]TGGTCTTTTCCTATC | 8453 |
rs772003964 | snp | C/T | 1.65441e-05 | 0.00287607 | missense, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054510 | GCTTCTGTTAATTTA[C/T]TCTTTTTAATAAACT | 8453 |
rs772006568 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068923 | CCCAGGCTGTAGTGC[A/T]ATGGCCCGATCTTGG | 8453 |
rs772029706 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037622 | AGGCCAAGGCAGGTG[C/G]ATCACGAGCTCAGGA | 8453 |
rs772063222 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35024890 | GGTTGGCTAGAGAAA[-/T]GTAATAAATCAGTAT | 8453 |
rs772090879 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046722 | CATGGTGAAATCCAG[C/T]CTCTACTAAAAATAC | 8453 |
rs772097575 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033715 | GCACTCCAGCTTGGG[C/T]GACAGAGTGAGACTC | 8453 |
rs772103505 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077817 | GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 8453 |
rs772122764 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032072 | TTTATAATTTTTGAC[A/G]TTGAACAAGTACTTT | 8453 |
rs772123391 | snp | C/T | 0.000181259 | 0.00951824 | missense | CUL2 | GRCh38.p7 | 10:35035225 | CATCATGGATGTGGT[C/T]TTGCAGCTCCTGAAT | 8453 |
rs772148074 | in-del | -/AC/C | 0.000608821 | 0.0174367 | intron-variant | CUL2 | GRCh38.p7 | 10:35025217 | AAAAAAAAAAAAAAA[-/AC/C]ACACACATTATTTTT | 8453 |
rs772176900 | snp | A/G | 4.95864e-05 | 0.00497903 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35062978 | ATGCAAATGCCGAAC[A/G]TGATTTTCCAAAAAA | 8453 |
rs772186435 | snp | A/G | | | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079476 | TTTCTGGCACAGTAT[A/G]TTGCCATCAAGTGGA | 8453 |
rs772208734 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058856 | GGGAGCATCCTTAAG[C/G]TAGCTCAATAAACCT | 8453 |
rs772224322 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073007 | GAGCGGGTAGGATGG[A/C]GGCCGCACCACCAGC | 8453 |
rs772224786 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093557 | ACAGCTTCTTGGGAG[A/G]CTGAGGTGGGAGAAT | 8453 |
rs772266081 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012182 | CCTCAGACTCCTGAG[A/C]AGCTGGGATTACAGG | 8453 |
rs772277726 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108239 | GTGGGAGGATTGCTT[A/G]AGCCCAGGAGCTCCA | 8453 |
rs772297563 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038884 | ATAAAAGGTGGATTT[A/G]TAATTTAATTTCTAC | 8453 |
rs772300559 | snp | A/C/T | 0.000226916 | 0.0106494 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35028879 | CTGAGTAAGAGGCCA[A/C/T]GCACCAGCCTAGAAG | 8453 |
rs772327159 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073538 | CGTTTAATCCTCCCA[A/C]CATTCTGACAGGTAG | 8453 |
rs772344340 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123607 | GGCTCCTGAATGACA[A/T]GAGTAGAAGAATGAC | 8453 |
rs772365415 | snp | A/C | 1.65045e-05 | 0.00287263 | missense | CUL2 | GRCh38.p7 | 10:35044803 | TTCTTATACTGTTCA[A/C]CATGAACAAAGGAGT | 8453 |
rs772375682 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086249 | CGCCTGTAATCCTAA[C/T]ACTTAGGGAGGCTGA | 8453 |
rs772384004 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052980 | AAGCTTTCACAAAAA[A/T]CAAACTTATGTAAAA | 8453 |
rs772446986 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026638 | ACTGATTCATCCTTA[C/T]ATTTAAAATCTGACT | 8453 |
rs772475607 | snp | A/C | 1.64738e-05 | 0.00286995 | intron-variant | CUL2 | GRCh38.p7 | 10:35049656 | ACAAAATAAAATTGA[A/C]TCAGTAAGATAAATG | 8453 |
rs772533007 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049069 | TGTGTGACTGACAGA[A/G]TGCTTCTGAGAGTCT | 8453 |
rs772541648 | in-del | -/AAATAA | 2.17621e-05 | 0.00329857 | intron-variant | CUL2 | GRCh38.p7 | 10:35039097 | CTATAAAAATATTTT[-/AAATAA]CTTACAGTCATGAAC | 8453 |
rs772548344 | snp | A/G | 4.9489e-05 | 0.00497414 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35031563 | CCTGTCTTCCACTTC[A/G]TTCTCTGTCATCCCT | 8453 |
rs772554788 | snp | C/T | 3.29832e-05 | 0.00406085 | missense | CUL2 | GRCh38.p7 | 10:35031502 | ATACCTTTTGAAAGA[C/T]GTCCTTGTCATCAAT | 8453 |
rs772576450 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100514 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 8453 |
rs772612501 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051580 | ATCGTGCCACTGCAC[G/T]CCAGCCTGGGCGACA | 8453 |
rs772629706 | in-del | -/A | 1.76558e-05 | 0.00297113 | intron-variant | CUL2 | GRCh38.p7 | 10:35031292 | CCACATTAAAGACTT[-/A]ACATTACCTTTAATT | 8453 |
rs772638934 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100088 | TGGAATTATAGGCAT[A/G]AGCTACTGTGCCCGG | 8453 |
rs772641255 | snp | G/T | 4.986e-05 | 0.00499274 | intron-variant | CUL2 | GRCh38.p7 | 10:35031662 | ACAAAGGGTGCTTCT[G/T]TATATATCACGCCTC | 8453 |
rs772665111 | snp | A/G | 1.68675e-05 | 0.00290405 | missense | CUL2 | GRCh38.p7 | 10:35011898 | GTGCTTTCATGATAC[A/G]AACTATAGCAGCTTG | 8453 |
rs772676889 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086453 | CCACCACACCTGGCT[A/T]ATTTCTGTATTTTTT | 8453 |
rs772680920 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029467 | ATTAGTAAATGCTCA[C/T]AGTAAAACACATATT | 8453 |
rs772715222 | snp | A/T | 1.65141e-05 | 0.00287346 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35044856 | CTGGTTTGGGTCTTC[A/T]CCACCACGATCACTA | 8453 |
rs772716457 | snp | C/T | 1.69361e-05 | 0.00290994 | intron-variant | CUL2 | GRCh38.p7 | 10:35011809 | TACAATGACAATGCC[C/T]TCTACCCTAAGAAGC | 8453 |
rs772759426 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115515 | CAGTGAGCTGAGATC[A/G]CGCCACTACACTCTA | 8453 |
rs772809003 | snp | A/T | 0.000287078 | 0.0119773 | intron-variant | CUL2 | GRCh38.p7 | 10:35031284 | AGGACAATACCACAT[A/T]AAAGACTTACATTAC | 8453 |
rs772811198 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089425 | AGGTAGGCTTGGCCA[C/G]GTCTAGTTCAAAGAC | 8453 |
rs772823607 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068030 | CAGGAGAATGGCATG[-/A]ACCCGGGAGGCGGAG | 8453 |
rs772859933 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115018 | GAAGTTCGAGACCAG[A/C]CTGGCCGATATGGCA | 8453 |
rs772880586 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075106 | CTCTGTTGAGACTGA[C/T]AGATTTCTGGTACCA | 8453 |
rs772901127 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060741 | TTCCCCACAGCAGAG[-/AA]AAGTCCATGTCAGAG | 8453 |
rs772950022 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023736 | AAATCGAACTGCACT[A/G]AGATATATTAGTTTT | 8453 |
rs772978080 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35087069 | TTTTATATTTTGGTT[A/T]TCTGTTTGTTTTAGA | 8453 |
rs773000746 | in-del | -/CTT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025330 | CATCTGGTTTACCTC[-/CTT]CTTTTACAGAGGAGA | 8453 |
rs773016037 | in-del | -/TG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117866 | TATGCTTTAAAAAAC[-/TG]TCTTTGTTTTCTTAA | 8453 |
rs773019447 | in-del | -/CTTGAATAAGGGCATTGTGCCGAAGCACTTTTC | 1.66946e-05 | 0.00288912 | splice-acceptor-variant | CUL2 | GRCh38.p7 | 10:35010444 | ACTGGCTAATCACCT[lengthTooLong]GTGGAAGAGATGTGG | 8453 |
rs773033063 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101814 | GTACAGCTTGTGCTC[A/G]GCTCCCTGCTCTAAT | 8453 |
rs773033821 | snp | A/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125201 | CTATTACATCTTACA[A/G]CAAGGGTATAGCAGA | 8453 |
rs773037005 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35016067 | TGGAGCGTACAGTAA[C/T]GTAGTGAATACAAGT | 8453 |
rs773058108 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056074 | TCTTCACAGTAATTG[C/T]TACTATATGAAATAA | 8453 |
rs773111284 | snp | C/T | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054777 | CAGCTCTTATCCAAG[C/T]TTCAGAATTTCTATA | 8453 |
rs773152969 | snp | C/T | | | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079567 | ACTTATTACACGATA[C/T]AACTATCACTTTTAC | 8453 |
rs773160302 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105755 | TACATACAATAAAGG[A/G]AATATAATTAATGTT | 8453 |
rs773184195 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034906 | TTATTTAAAAATGGC[A/G]AGCTTATTTTCCTGT | 8453 |
rs773208308 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080885 | GGGTGACACGGTGGG[A/G]AGTAGGGAATGTATT | 8453 |
rs773226737 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117095 | ATTTTTGAATTTATC[C/G]AAGAGTTGAGTTCCC | 8453 |
rs773236019 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068941 | GGCCCGATCTTGGCT[C/G]ACTGCAACCTCTGCC | 8453 |
rs773241441 | in-del | -/ATTTAGC | 8.30117e-05 | 0.00644197 | intron-variant | CUL2 | GRCh38.p7 | 10:35031429 | ACTTCCTTTCTAATG[-/ATTTAGC]ATTCAGAAATAAAGT | 8453 |
rs773281928 | snp | A/T | 1.64808e-05 | 0.00287057 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35060942 | ATGATACATAACAAG[A/T]ACTTGTTCTTCTGAC | 8453 |
rs773287602 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067471 | GAATTCACCATTGGC[C/T]GGTCACAGTGGCTCA | 8453 |
rs773312131 | snp | C/T | 7.06889e-05 | 0.0059447 | intron-variant | CUL2 | GRCh38.p7 | 10:35025235 | ACACATTATTTTTAG[C/T]TACTATAACTTGCCT | 8453 |
rs773315784 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098432 | CTGTTACATCATATT[-/A]AAAATACCCCAGGCA | 8453 |
rs773320388 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103471 | CTGGGACTACAGGCG[C/T]GCGCCACCATGCCTG | 8453 |
rs773322765 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037160 | TTTTTTACCTTGTAC[A/C]TTTAGAGAAAAAACT | 8453 |
rs773327348 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095462 | AATATATTTTTATAC[A/G]TATCAGAACATATAA | 8453 |
rs773398808 | snp | A/G | 1.84705e-05 | 0.0030389 | intron-variant | CUL2 | GRCh38.p7 | 10:35031261 | TATGTGCTTGTGAAT[A/G]AATTTCTAGGACAAT | 8453 |
rs773444336 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108311 | AAATAGAAAAAATTA[G/T]TGGGGTGTTGTGGTG | 8453 |
rs773462627 | snp | C/T | 1.65512e-05 | 0.00287669 | missense | CUL2 | GRCh38.p7 | 10:35033212 | CCATTCAAAACAGTG[C/T]TGATAAGCTGAACAA | 8453 |
rs773506279 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057608 | CAGTGAGCCGAGATC[C/G]TGCCACTGCACTCCA | 8453 |
rs773550426 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059507 | TTGTGCACATTTTTT[C/T]AGACAATGCTACTGC | 8453 |
rs773566667 | in-del | -/GAGGT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021831 | GGGGTGAGGTGAGGC[-/GAGGT]GAGGTGAGGTGAGGT | 8453 |
rs773607344 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073025 | CCGCACCACCAGCCA[C/T]GGACTGGGAGAGGCC | 8453 |
rs773618932 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008762 | TTGAATAAACCAATT[A/G]TAAGACCCATCTCAA | 8453 |
rs773647836 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074651 | GAGCCATCGCACCCT[A/G]ATTTTTGTATTGTTA | 8453 |
rs773648259 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039692 | CAATATGGCGAAACC[C/G]TGTCTCTACTAAAAA | 8453 |
rs773654991 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100536 | GGAGGCCGAGGCAGG[C/T]GGATCACTTGAGGTC | 8453 |
rs773661644 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085809 | GGTAGAACACAAAAC[-/A]AAACAGTGCAAACTT | 8453 |
rs773714636 | snp | A/G | 1.68371e-05 | 0.00290143 | utr-variant-5-prime, missense | CUL2 | GRCh38.p7 | 10:35071337 | CAAGTGTAGTGTTGA[A/G]ATCTGTCAATTAAAA | 8453 |
rs773785894 | snp | C/T | 3.59952e-05 | 0.0042422 | splice-acceptor-variant | CUL2 | GRCh38.p7 | 10:35011965 | AGTCTGCTCCATTTC[C/T]TGTTTTACAGAAGAA | 8453 |
rs773789979 | snp | A/C/G | 4.9635e-05 | 0.00498151 | intron-variant | CUL2 | GRCh38.p7 | 10:35032511 | TGAATAAAAAAACAC[A/C/G]CCATAATTAACCACC | 8453 |
rs773795274 | snp | C/T | 2.6541e-05 | 0.00364278 | intron-variant | CUL2 | GRCh38.p7 | 10:35049814 | TTACTTAGTATATGT[C/T]TAACATTTCCTCAAG | 8453 |
rs773812885 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085360 | GCGTAGACCCAGGAG[A/G]CAGAGCTTGCAGTGA | 8453 |
rs773821295 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034453 | TCTGCAGCTAAGGTA[-/T]ACAGCCTCTAAAAAG | 8453 |
rs773823395 | snp | A/G | 1.84602e-05 | 0.00303805 | intron-variant | CUL2 | GRCh38.p7 | 10:35044548 | AGATAAATGTATTCG[A/G]TATGTTTTATTTCTT | 8453 |
rs773824317 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046462 | AAAACTGGAAGGAAC[A/C]TAATATACGCCACTA | 8453 |
rs773865984 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100341 | ATAACCTGCACTACA[C/T]GTAACAAGTTACTCA | 8453 |
rs773886179 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040728 | TTTTTCCACAGACGG[A/G]GTGCGGGCGGCATTG | 8453 |
rs773916513 | snp | G/T | 1.64958e-05 | 0.00287187 | intron-variant | CUL2 | GRCh38.p7 | 10:35032413 | TTTCATAAGATTACT[G/T]TTCAGCAACCACCAA | 8453 |
rs773922837 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039917 | CAGCACTTTGGGAGG[C/T]CGAGGTGGGTGGATC | 8453 |
rs773974824 | in-del | -/AAAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065621 | GAGACTCCATCTCAA[-/AAAT]AAATAAATAAATAAA | 8453 |
rs773986733 | in-del | -/AAGG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023358 | AAGGTTCTCTTTCCA[-/AAGG]AAGTAACTATTTGGT | 8453 |
rs774006319 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101658 | ACACACACAAGCACT[C/T]GTTTCTTCTGAATCA | 8453 |
rs774017334 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086862 | TACTATTTAACACTC[C/T]AAAAAATACAAATGT | 8453 |
rs774038982 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034796 | TCAGAGGATATGGAA[A/G]GGAGGCAAATTGCAA | 8453 |
rs774069037 | snp | C/T | 4.25994e-05 | 0.00461496 | intron-variant | CUL2 | GRCh38.p7 | 10:35028761 | GATATAATATGAAGA[C/T]AATTATTAAAATTCC | 8453 |
rs774099530 | in-del | -/AAGAAGATTGAGAATAG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059668 | AAAGTATGCCTGTAC[-/AAGAAGATTGAGAATAG]AAGAAGATTGAGAAT | 8453 |
rs774100851 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045711 | GACAGAGCAAGACCC[C/T]GTCTCAAAAATTAAA | 8453 |
rs774121537 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068875 | CATAGTCTTTTATTT[A/G]TTTATTTTTGAAACG | 8453 |
rs774124021 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108455 | GTTAGACCCTGACTC[-/A]AAAAAAAAAAAAGGA | 8453 |
rs774125451 | snp | A/G | 1.70429e-05 | 0.0029191 | missense | CUL2 | GRCh38.p7 | 10:35028862 | AACGTAGATGAAGGA[A/G]CCTGAGTAAGAGGCC | 8453 |
rs774131299 | snp | A/T | 1.64833e-05 | 0.00287078 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071233 | TTGCTCTTTCGACGT[A/T]TTCCAACATGACCAC | 8453 |
rs774132649 | snp | A/T | | | synonymous-codon | CUL2 | GRCh38.p7 | 10:35100879 | GCAATCAGGATACAG[A/T]AGAGTTCCATTCTCC | 8453 |
rs774152522 | in-del | -/AAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014393 | TTAGGCAATTTTTAG[-/AAT]AACAACTTCTGTATC | 8453 |
rs774153744 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021767 | AATGTGGGCTGTGAT[C/T]GCGCACCTCCACTCC | 8453 |
rs774194754 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019815 | TTGCAACCAGTAATG[A/T]AACAACTGATTCTGG | 8453 |
rs774233333 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101065 | GTGCCTCTATCCTAG[A/G]AGTGAGAAAAGGGAG | 8453 |
rs774267385 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043750 | AACATATGATAACCA[A/G]TATGTACTGGTTTAG | 8453 |
rs774275322 | snp | A/G | 2.00568e-05 | 0.0031667 | intron-variant | CUL2 | GRCh38.p7 | 10:35029441 | ATCATTTGTATCAAC[A/G]TACTGAAATGATTAG | 8453 |
rs774284479 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033968 | CTGCAAAGTCACTAA[A/C]GGCTGAGAGAAAGGA | 8453 |
rs774298056 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027145 | ACTACTTTAGATACT[-/T]TTTTTTTTTTTTTTT | 8453 |
rs774323243 | snp | C/T | 1.76173e-05 | 0.00296788 | missense, intron-variant | CUL2 | GRCh38.p7 | 10:35049686 | GTCAGCACTCACTTT[C/T]TGATTTCTCGGAGCA | 8453 |
rs774336523 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106893 | TCTGATGTTATCATT[A/G]TAACTCCTGTTAGCA | 8453 |
rs774381411 | snp | A/G | | | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079466 | GGCTCAATGCTTTCT[A/G]GCACAGTATGTTGCC | 8453 |
rs774400336 | snp | A/G | 1.64827e-05 | 0.00287073 | missense | CUL2 | GRCh38.p7 | 10:35035216 | GAAGGCCCTCATCAT[A/G]GATGTGGTTTTGCAG | 8453 |
rs774439854 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035126 | GGAAAGGCTCCACGC[C/T]GGATCTGATTAGGAG | 8453 |
rs774445361 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121581 | GGCCACAGAACAAAA[A/C]TGTGGCATGGAGCCC | 8453 |
rs774460345 | in-del | -/TT | 2.08101e-05 | 0.00322562 | frameshift-variant | CUL2 | GRCh38.p7 | 10:35013738 | TGTAGTAATTTTAAA[-/TT]TTGTTCTTTTACTGC | 8453 |
rs774463945 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121992 | AAAAACCAAAAGCAC[A/G]TAAACACACATACAC | 8453 |
rs774464842 | in-del | -/TGAGAAACGGTCATTCCATGTTGCTCTT | 1.66701e-05 | 0.002887 | frameshift-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35063061 | TAAAGCATAGATATC[-/TGAGAAACGGTCATTCCATGTTGCTCTT]TCTAGTTAAATTATT | 8453 |
rs774477435 | snp | G/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128598 | TGGTCCGCTCTCAGC[G/T]CACTGCAAGCTCCGC | 8453 |
rs774510492 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058311 | GAATAACTCTTACAA[C/G]TTTGTGTCGAAACAT | 8453 |
rs774550462 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073276 | GAGGGGAAGGTGAGA[A/G]TGGAGGAGGTGGGAG | 8453 |
rs774553728 | snp | C/T | 1.68915e-05 | 0.00290611 | intron-variant | CUL2 | GRCh38.p7 | 10:35010474 | GAAGTCAAACTACTG[C/T]CAGTTCTTCAGCTAT | 8453 |
rs774561073 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091607 | CTAGTTTGTTAACAA[C/T]GCAATATGTCTGGTC | 8453 |
rs774670661 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023647 | AGACACATTGATTAT[C/T]GCTGAAATAATGAGA | 8453 |
rs774711251 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120732 | TGGAAACCCCCTCTA[C/T]GAAAAATACAAAAAT | 8453 |
rs774734194 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097176 | TACTGAGCACCAACT[A/G]AAGTGTCACAAGTAG | 8453 |
rs774744754 | in-del | -/AAC | 0.000398804 | 0.0141153 | intron-variant | CUL2 | GRCh38.p7 | 10:35025217 | TAAAAAAAAAAAAAA[-/AAC]ACACATTATTTTTAG | 8453 |
rs774751638 | in-del | -/TCAAAACAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046891 | GAGTGAGACTCTGTC[-/TCAAAACAAA]ACAAAACAAAACAAA | 8453 |
rs774764495 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083616 | TTCCCCCCACAAAGA[G/T]GGTGGGGGCATATCG | 8453 |
rs774783572 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098138 | CTATTTTAAAAGGAA[A/G]TATAAAAAGTATTCT | 8453 |
rs774787446 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064614 | CCTTACTCCAGAAAG[C/T]GCAAGCAGCCCTCTC | 8453 |
rs774809689 | snp | C/T | 1.66774e-05 | 0.00288763 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35016246 | TGATTTGATTGTTTT[C/T]GTCAGTTCCTTTTCA | 8453 |
rs774822085 | snp | A/G/T | 0.000102511 | 0.00715862 | intron-variant | CUL2 | GRCh38.p7 | 10:35071357 | GTCAATTAAAAAACA[A/G/T]TAACAATGTTAGCAA | 8453 |
rs774833519 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015905 | CTAGTTTCAAAATCT[C/T]AATTAATCAAAATCT | 8453 |
rs774852614 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101432 | GTTTTAATATCACCA[C/G]ATTAACTCACATCAA | 8453 |
rs774856533 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096053 | AGGACCTTGAGACCA[A/G]CCTGGCCAATATGGT | 8453 |
rs774870879 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032004 | GACCAATAAAGCAAC[C/T]GATATAAGTAATACA | 8453 |
rs774890083 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036930 | TGCAGAGATGGGATA[C/T]TGTCATGTTGCCCAG | 8453 |
rs774920654 | snp | C/T | 1.78439e-05 | 0.00298691 | intron-variant | CUL2 | GRCh38.p7 | 10:35044554 | ATGTATTCGATATGT[C/T]TTATTTCTTACCTTT | 8453 |
rs774983355 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070184 | GAGGTATCAAACAAC[A/T]TAAAAAATATAAAAG | 8453 |
rs775013175 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109029 | AGCAGCCTGGGCAGG[A/G]TGGCAAAACTCTATC | 8453 |
rs775077663 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114287 | CAGGATAGTCTGGAA[A/C]TCCCGACCTCAAGTG | 8453 |
rs775095338 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038098 | GGGGTTGCAATGAGC[C/T]AAGATCATGCCATTG | 8453 |
rs775103532 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100629 | TAACTGGGCATGGTG[G/T]TGCATACCTGTAATC | 8453 |
rs775116780 | in-del | -/T | 1.65261e-05 | 0.0028745 | frameshift-variant | CUL2 | GRCh38.p7 | 10:35044783 | TACCTTTAAGGGGAA[-/T]TTTTTTCTTATACTG | 8453 |
rs775122827 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078096 | TCTCTAACTGAAAGC[C/T]GTTACTAACCTTCCC | 8453 |
rs775136566 | snp | C/T | 4.41716e-05 | 0.00469934 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35013786 | TGAAAACGAAGATTC[C/T]GCATCAATATCTTCC | 8453 |
rs775253577 | in-del | -/TAAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021509 | TAGATGATATTTCCA[-/TAAT]TAATACATGTTTATA | 8453 |
rs775256275 | snp | C/T | 2.38826e-05 | 0.00345554 | intron-variant | CUL2 | GRCh38.p7 | 10:35039120 | TCATGAACACAAAGT[C/T]TTACTATGAGGAAAA | 8453 |
rs775280921 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017505 | TCGAGACCAGCCTGG[C/T]CAACATGGCGAAACC | 8453 |
rs775282207 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043349 | CTTAGAACCACTGAT[C/T]TAGTGTAACCTGAAC | 8453 |
rs775322339 | snp | G/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128056 | TACCATGTTGGTCAG[G/T]CTGGTCTCGAACTCC | 8453 |
rs775336216 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033615 | GGTGGCGTCCACCTG[C/T]AATCCCAGCTACACG | 8453 |
rs775391564 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032624 | ATTGCCGGTAGTTTG[C/T]TAATATTTTCATGCC | 8453 |
rs775401175 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35056548 | GAAACTCAGGAGAGG[C/T]CTTCCACTCCCATTC | 8453 |
rs775438733 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095322 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs775460224 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023181 | TTTACAATATAAACA[C/T]AACAAAGCATCACAC | 8453 |
rs775460728 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032837 | CATATCTATTCTCTT[C/T]TCAAATATTATTCAA | 8453 |
rs775463844 | snp | A/C | 1.65633e-05 | 0.00287774 | intron-variant | CUL2 | GRCh38.p7 | 10:35032517 | AAAAAACACGCCATA[A/C]TTAACCACCAGCCAT | 8453 |
rs775502573 | snp | C/T | 4.13659e-05 | 0.00454766 | intron-variant | CUL2 | GRCh38.p7 | 10:35038901 | AATTTAATTTCTACT[C/T]ATGTTTGGTGTCACT | 8453 |
rs775504188 | snp | C/T | 3.9582e-05 | 0.00444853 | intron-variant | CUL2 | GRCh38.p7 | 10:35028785 | AAATTCCTTTAGTCT[C/T]CTAATATATTTCCTG | 8453 |
rs775548618 | snp | C/T | 1.65501e-05 | 0.00287659 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054512 | TTCTGTTAATTTATT[C/T]TTTTTAATAAACTGG | 8453 |
rs775551913 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058141 | AACATTTATGATTCA[C/T]GGGAGAAGGTCTAAA | 8453 |
rs775585706 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106707 | AAAGATAGTGTTTCT[A/G]ATGTTATTATAACTC | 8453 |
rs775589058 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015969 | AGCTGTAACAGTATA[A/G]GACAAATAAAATCAA | 8453 |
rs775637319 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070603 | TCTGCATTGTTACAT[A/G]AAACTCTCAATTCAC | 8453 |
rs775639331 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083464 | ACACATAGAACTTAG[A/G]TCTTGGTTTCTAAAT | 8453 |
rs775645873 | snp | C/T | 4.96044e-05 | 0.00497993 | intron-variant | CUL2 | GRCh38.p7 | 10:35071172 | ATCAATTTTAGAACA[C/T]TGATCAAGCTGCCAT | 8453 |
rs775762717 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095723 | GCCAATACACCCAGC[A/G]AATTTTTTTGTATTT | 8453 |
rs775772482 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022059 | TCACATTCAAAACAC[C/T]GTACTGTAACTATGT | 8453 |
rs775777314 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035768 | TACATGAGCAAGAAT[-/A]TATGCAATATAAGTT | 8453 |
rs775827600 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035962 | TTAAACGTTTCATTA[A/C]AGCATCATACATATA | 8453 |
rs775829883 | in-del | -/GAGCCCAGGAGTTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030811 | GCGGGAGGATCGCTT[-/GAGCCCAGGAGTTA]GAGCCCAGGAGTTAG | 8453 |
rs775843495 | in-del | -/CTCCTGAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114147 | CAGGATGGTCTCGAT[-/CTCCTGAC]CTCGTGATCCGCCTG | 8453 |
rs775848961 | snp | A/G | 1.65209e-05 | 0.00287405 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35062981 | CAAATGCCGAACATG[A/G]TTTTCCAAAAAAATC | 8453 |
rs775869742 | in-del | -/AAAAAAAGAAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113198 | AAAAAAAAAAAAAAA[-/AAAAAAAGAAT]TCAGCGGCCAGGTGC | 8453 |
rs775887407 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109937 | TCAGAACTTTGGAAG[G/T]CTGAGGCAGGAGGAT | 8453 |
rs775913563 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097090 | GCTAGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 8453 |
rs775923974 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014091 | ACTTTTTGATAAAAT[A/G]AGAGTCAAGCTCATT | 8453 |
rs775927225 | snp | C/T | 1.69212e-05 | 0.00290866 | intron-variant | CUL2 | GRCh38.p7 | 10:35011814 | TGACAATGCCCTCTA[C/T]CCTAAGAAGCCCTGA | 8453 |
rs775927573 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055242 | CACCACCTAAAACTA[C/T]TCATTTGAAAGGTTC | 8453 |
rs775960117 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030779 | ACACCTATTGTCCCA[C/G]CTGCTCAGGAGGCTG | 8453 |
rs775965368 | in-del | -/AAAGCTGCCAATGGTGCACAATGACCA | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080180 | TCCATAGGTGGGCCC[-/AAAGCTGCCAATGGTGCACAATGACCA]AATATGTTGCCATCA | 8453 |
rs775973367 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069330 | AAGTGATTGAGCCCA[A/G]GAGCTCGAGATCAGC | 8453 |
rs775992545 | in-del | -/AAAAC | 0.000347934 | 0.0131851 | intron-variant | CUL2 | GRCh38.p7 | 10:35025215 | TGTAAAAAAAAAAAA[-/AAAAC]ACACATTATTTTTAG | 8453 |
rs775993310 | snp | A/G | 3.29799e-05 | 0.00406065 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35031503 | TACCTTTTGAAAGAC[A/G]TCCTTGTCATCAATG | 8453 |
rs776013400 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029272 | ATGTTGGCCAGGCTG[A/G]TCTGGAACTCCTGAG | 8453 |
rs776025326 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048986 | GCCATTATTACACTA[C/T]AATTCACTGGTCTAG | 8453 |
rs776027133 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067411 | AAGTAAACTAGAACA[-/G]GGCCAGGTACAGTCT | 8453 |
rs776029183 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095683 | CATGCCTCAGACTCC[C/T]GAGTAGCTGGAACTA | 8453 |
rs776075868 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063709 | TTTCACTAGCCAGTG[A/G]TCTTAACCAAGTTTC | 8453 |
rs776080527 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062602 | CAAGGGAGGCCAAGG[C/T]CGGAGGATCACTGGA | 8453 |
rs776084154 | in-del | -/A | 5.60695e-05 | 0.00529449 | intron-variant | CUL2 | GRCh38.p7 | 10:35011983 | TTTACAGAAGAAAAG[-/A]AAAAAAGACCCAACA | 8453 |
rs776136920 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014615 | AGGTGGGCAGATTAC[C/T]TGAGCTCAGGAGTTT | 8453 |
rs776161868 | snp | A/G/T | 0.000175323 | 0.00936124 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35011905 | CATGATACGAACTAT[A/G/T]GCAGCTTGGAGATAC | 8453 |
rs776187262 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093122 | GTTTTCCACACCCCT[A/G]TGATTCCATCCCCAA | 8453 |
rs776187758 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065115 | CAATTAACTATGTTC[-/T]TTTTCTCTAACCTAT | 8453 |
rs776191393 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35097491 | AAGACCCCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs776205456 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061244 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACCTGA | 8453 |
rs776229284 | snp | C/G | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126357 | TGGAGAAGGACTCAA[C/G]CAGCTGTGACTGGCT | 8453 |
rs776272147 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076699 | GGTATTTTTTTCATC[G/T]GTTTTACATAAATGG | 8453 |
rs776373126 | snp | G/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127976 | TCAGCCTCCCGAGTA[G/T]CTGGGATTACAGGCA | 8453 |
rs776401434 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066672 | TTAGCAAACAAGGAT[-/A]AAAAAATGACTAATT | 8453 |
rs776450784 | snp | A/G | 3.43306e-05 | 0.00414296 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010307 | ACGCTGGAGGAGAGC[A/G]ACATCACGCGACGTA | 8453 |
rs776470201 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35043520 | ATGCTTTGTGACTTG[C/T]GGCCTAGGGATGTAG | 8453 |
rs776499011 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017097 | CTCAAGTGCTGTCGA[C/T]AGCTGGGCTCTCCCA | 8453 |
rs776517378 | in-del | -/TTTATTTATTTA | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080434 | TTTAGAATTCCTATT[-/TTTATTTATTTA]TTTATTTATTTATTT | 8453 |
rs776519335 | snp | C/T | 1.65795e-05 | 0.00287914 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35033190 | CGCACTCATAAAATG[C/T]TGATCACCATTCAAA | 8453 |
rs776548333 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022966 | AGGAGAATCACTTGA[A/T]CCCAGAAGGTGGAGG | 8453 |
rs776550364 | snp | A/G | | | missense | CUL2 | GRCh38.p7 | 10:35044833 | TTAATAACCCCATGG[A/G]TTACTTTCTGGTTTG | 8453 |
rs776550395 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019220 | CAGCCAGGATGTCAC[C/T]GATGCTGTAATATGC | 8453 |
rs776554866 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069066 | TAGAGACGAGGTTTC[A/G]CCATGTTGGTCAGGC | 8453 |
rs776572346 | snp | A/G | 1.69075e-05 | 0.00290748 | missense, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054535 | TAAACTGGGTGTTGA[A/G]ATACCTGGAAAATAA | 8453 |
rs776596651 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082841 | TATTCATTATTTTGG[A/T]AACTATACACTTACA | 8453 |
rs776596711 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055837 | AACCATGCCTTCCAG[C/G]TAAGGAAAGAGGAAT | 8453 |
rs776598796 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042327 | TCCATGTTGTATCAT[A/G]TATAACTTCAATTCT | 8453 |
rs776602488 | snp | A/C | 8.38019e-05 | 0.00647255 | missense | CUL2 | GRCh38.p7 | 10:35016285 | AGTGCTGTCCTGAAG[A/C]TCTTTATAACTGACA | 8453 |
rs776636047 | snp | C/G | 1.92413e-05 | 0.00310166 | intron-variant | CUL2 | GRCh38.p7 | 10:35029469 | TAGTAAATGCTCATA[C/G]TAAAACACATATTCA | 8453 |
rs776649246 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048893 | CATACTAAATACCAC[A/G]GCTTTGACAAAGTAT | 8453 |
rs776649463 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104172 | ACACCAGAGGCTGGG[C/T]GTAGTGGCTCACACC | 8453 |
rs776673989 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108403 | TTGAGGCTGCAGTGA[A/G]CCAAGATCACACCAC | 8453 |
rs776695002 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070267 | TCAGTGCCCAGAACA[C/T]AGTTGGCTTAACAAA | 8453 |
rs776721960 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074783 | TGAGCCATTGTGCCC[A/G]GCCTTCATCTGCTTT | 8453 |
rs776741228 | in-del | -/TTTTTTTT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011212 | TTTTTAATTTTTTAA[-/TTTTTTTT]TTTTTTTTTTTTTAG | 8453 |
rs776745988 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082065 | ATTTTGGGAGGCCAA[C/T]GTGGGAGGATCACTT | 8453 |
rs776748929 | in-del | -/GG | 1.65666e-05 | 0.00287802 | intron-variant | CUL2 | GRCh38.p7 | 10:35031623 | TACTTAGCAAGCTCA[-/GG]TGTAGAAATTGATAA | 8453 |
rs776753957 | in-del | -/C | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080311 | ATGTAACTAAGAATG[-/C]CCTTTCTTATTTGGA | 8453 |
rs776759486 | snp | A/G | | | synonymous-codon | CUL2 | GRCh38.p7 | 10:35100852 | CACTTACAGCCATGC[A/G]TGGCCATCACCGCAA | 8453 |
rs776760683 | snp | C/G | 3.81214e-05 | 0.00436569 | intron-variant | CUL2 | GRCh38.p7 | 10:35028891 | CCACGCACCAGCCTA[C/G]AAGGAAAAAAATAAA | 8453 |
rs776771792 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062427 | CACTATCCAGAGGAC[A/G]TAGGAGCACATTTTA | 8453 |
rs776782155 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118859 | TGATCCAGTTAAAGC[A/G]TTCCCTGTTTTCCCA | 8453 |
rs776804265 | snp | A/G | 4.31835e-05 | 0.00464649 | missense | CUL2 | GRCh38.p7 | 10:35013722 | TGTCTTTCTGCATTG[A/G]TGTAGTAATTTTAAA | 8453 |
rs776824977 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071199 | CCATTAAAAGGATAC[A/G]AGAAACGGTCATTCC | 8453 |
rs776838610 | snp | C/T | 1.87296e-05 | 0.00306014 | missense | CUL2 | GRCh38.p7 | 10:35039045 | GGATGTAGGTATTTT[C/T]GACATCGAATTTCTT | 8453 |
rs776842038 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013074 | GGCCAGGCGCGGTGG[-/T]TCACACCTGTAATCC | 8453 |
rs776852957 | in-del | -/TTTTATTT | 1.80445e-05 | 0.00300365 | intron-variant | CUL2 | GRCh38.p7 | 10:35044552 | AATGTATTCGATATG[-/TTTTATTT]TTTTATTTCTTACCT | 8453 |
rs776901827 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35098811 | CGGTGGCAGGCGCCT[A/G]TAATCCCAGTTACTT | 8453 |
rs776972140 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109801 | TTGATAGAGAAGCTC[A/G]ATTTTATTTCAACCA | 8453 |
rs776982498 | snp | C/T | 7.21891e-05 | 0.00600744 | intron-variant | CUL2 | GRCh38.p7 | 10:35038912 | TACTCATGTTTGGTG[C/T]CACTTACCATTTTTT | 8453 |
rs776994717 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027433 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCAACTTT | 8453 |
rs776999749 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037005 | ATGGCCTTTTAATAA[C/T]CCAAAGTTTTTCATT | 8453 |
rs777008132 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012408 | GTGATTACAGAATCT[C/T]TCATGACGCTTTTAG | 8453 |
rs777020343 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061115 | ACATATTAACTACAC[A/G]TATTAAAAATGAAAC | 8453 |
rs777025103 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108576 | TGATATTGGAATTGA[A/G]GTAGGAGGAAGTTAT | 8453 |
rs777035591 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123858 | TTTGGGTATAAATTT[G/T]AGAATTATCTTTCAA | 8453 |
rs777064038 | snp | A/C/G | 1.79284e-05 | 0.00299397 | intron-variant | CUL2 | GRCh38.p7 | 10:35049674 | AGTAAGATAAATGTC[A/C/G]GCACTCACTTTTTGA | 8453 |
rs777067502 | snp | A/G | 1.65042e-05 | 0.0028726 | synonymous-codon, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35063011 | CTTAGTTTCTGTATA[A/G]AGTCTTTCTCCAAGG | 8453 |
rs777100362 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124662 | GCTAGCAGTGCCAAC[A/T]GTTTTCAAGAGGCAC | 8453 |
rs777120601 | snp | G/T | 7.30078e-05 | 0.0060414 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35011941 | CCGGTCCTCATCAAC[G/T]GCACTTCTAGTCTGC | 8453 |
rs777142826 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35011218 | ATTTTTTAATTTTTT[A/T]TTTTTTTTTTTTTTA | 8453 |
rs777168262 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039782 | ATCACTTCATCCCGG[C/G]AGGTGGGGGTTGTAA | 8453 |
rs777173942 | in-del | -/AC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35034885 | GCCAATTACACAAAA[-/AC]ACAGTTATTTAAAAA | 8453 |
rs777175935 | snp | C/T | 1.6654e-05 | 0.00288561 | utr-variant-5-prime, missense | CUL2 | GRCh38.p7 | 10:35071322 | TTCAAAGACATTGTG[C/T]AAGTGTAGTGTTGAA | 8453 |
rs777209836 | snp | A/C | | | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008352 | GGTGCCTTGGTTGAA[A/C]AGATTTGGCCTCTCT | 8453 |
rs777239820 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090922 | TTGCCACACACTTCC[A/G]TGGGCTTTGCAAATG | 8453 |
rs777279427 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073139 | GCCAAATATCCAAAA[C/G]AGGGTATGCCTTGTT | 8453 |
rs777295179 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054388 | CAAATTACCTCAGTG[C/T]ATAAAAACATACTTA | 8453 |
rs777299724 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121290 | TGGAGTGCTGTGGCG[C/T]GATCTCAGCTCACTG | 8453 |
rs777334325 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117794 | GTTACAGAAATATGT[A/G]ACCTTGAATTCTAAA | 8453 |
rs777387851 | snp | C/T | 4.34622e-05 | 0.00466146 | missense | CUL2 | GRCh38.p7 | 10:35038961 | TTATGACATTCTGCA[C/T]GTAAAAACTGTAAGT | 8453 |
rs777407084 | in-del | -/T | 0.000401 | 0.0141541 | intron-variant | CUL2 | GRCh38.p7 | 10:35028903 | CTAGAAGGAAAAAAA[-/T]AAAATAAAATAAGCT | 8453 |
rs777414932 | snp | C/T | 2.76859e-05 | 0.00372051 | intron-variant | CUL2 | GRCh38.p7 | 10:35028932 | CTAAATGGATCAACA[C/T]CTAAATTCAAAGTAA | 8453 |
rs777421038 | snp | C/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127725 | CAGTCTCCGGAGTGG[C/G]AAGGGCAGAGCCGCG | 8453 |
rs777445356 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058819 | AACAGCCACAGATGC[A/G]TCTGTGCCTTGCGTT | 8453 |
rs777493926 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104908 | CTAATTTTGTATCTT[A/C]AGTAGAAACGGAGTT | 8453 |
rs777500484 | in-del | -/AAA | 0.00486331 | 0.0490714 | intron-variant | CUL2 | GRCh38.p7 | 10:35025203 | AATAATTCAAACTGT[-/AAA]AAAAAAAAAAAAACA | 8453 |
rs777556244 | snp | A/C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036519 | ATATATCCCACTTAG[A/C/T]GGTCAGTGCCAGTTT | 8453 |
rs777573152 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096375 | TTTGGAAGATGGGGA[C/T]AGAAGGGTTACTTGA | 8453 |
rs777616315 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35120131 | TCATTTAAATGATCA[C/T]TTCCAAATTTTGTAT | 8453 |
rs777617885 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063866 | AAGGCAAAGCCCATT[C/T]ATAACTTTGGGGCCA | 8453 |
rs777629207 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071193 | AAGCTGCCATTAAAA[C/G]GATACGAGAAACGGT | 8453 |
rs777644459 | snp | C/T | 1.65809e-05 | 0.00287926 | intron-variant | CUL2 | GRCh38.p7 | 10:35031437 | TCTAATGATTTAGCA[C/T]TCAGAAATAAAGTTG | 8453 |
rs777675857 | snp | C/T | 3.30098e-05 | 0.00406249 | missense | CUL2 | GRCh38.p7 | 10:35011870 | ATAAGGGCATTGTGC[C/T]GAAGCACTTTTCGTG | 8453 |
rs777684354 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070068 | CATCAATTACTACCC[A/G]TATGACCCTGGGCAA | 8453 |
rs777713390 | in-del | -/AAAGT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35086879 | AAAAATACAAATGTC[-/AAAGT]AAAGTGTACTACTGT | 8453 |
rs777735900 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048595 | AGAACTTAGAAGTTT[C/T]GTTGGGAGTGTTCTT | 8453 |
rs777750395 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069075 | GGTTTCGCCATGTTG[A/G]TCAGGCTGGTCTCGA | 8453 |
rs777797865 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084935 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 8453 |
rs777864642 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35127037 | GGGAGGCCGCGGCTA[C/T]CGCATCACAGCTGAC | 8453 |
rs777870654 | snp | C/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125932 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 8453 |
rs777890467 | snp | G/T | 1.67635e-05 | 0.00289507 | intron-variant | CUL2 | GRCh38.p7 | 10:35010457 | CCTGTGGAAGAGATG[G/T]GGAAGTCAAACTACT | 8453 |
rs777929747 | snp | C/T | 1.69352e-05 | 0.00290987 | intron-variant | CUL2 | GRCh38.p7 | 10:35044917 | AATACAAATTATCTA[C/T]GGAAATATACCCAAA | 8453 |
rs777943240 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061665 | AGCAGATAAATGATC[-/A]CATTAGAACACTAAA | 8453 |
rs777976505 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061701 | CATGCCATATACTAT[A/C]AAAAGTAGAGCATTT | 8453 |
rs777989878 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35124614 | TGTAAATGTGCAACC[C/T]GGAATTGGCAACTCT | 8453 |
rs778040291 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041404 | GAAAGAAAGGCCAAA[A/G]CTATAAGAGGAACGC | 8453 |
rs778053193 | snp | A/G | 1.67259e-05 | 0.00289183 | intron-variant | CUL2 | GRCh38.p7 | 10:35044721 | GAAATTAGAACAAGC[A/G]GTTTAAGAAATTAAC | 8453 |
rs778060556 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020577 | AGCCTGATCCATACT[A/G]TGTACTGTCTGGTGA | 8453 |
rs778075130 | snp | A/G | 1.65729e-05 | 0.00287857 | intron-variant | CUL2 | GRCh38.p7 | 10:35031625 | ACTTAGCAAGCTCAT[A/G]TAGAAATTGATAATA | 8453 |
rs778101065 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117882 | GTCTTTGTTTTCTTA[A/G]TAGACTTGATTTTTT | 8453 |
rs778102722 | snp | A/T | 2.66991e-05 | 0.0036536 | intron-variant | CUL2 | GRCh38.p7 | 10:35016401 | TAACTTCACCTACAA[A/T]TAAAACAAAAACTGA | 8453 |
rs778122448 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088102 | AGTAATCTCCCAATC[A/T]CTACCACAACTCCTT | 8453 |
rs778184622 | in-del | -/A | 0.000185718 | 0.00963455 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074227 | TGTTACTCTGTACAT[-/A]AAGTACAAAGTTTGT | 8453 |
rs778272503 | in-del | -/CTT | 2.19286e-05 | 0.00331117 | intron-variant | CUL2 | GRCh38.p7 | 10:35039098 | TATAAAAATATTTTC[-/CTT]TTACAGTCATGAACA | 8453 |
rs778275406 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35053027 | ATAACAAAAAAAAAG[C/G]CAAGAAATATAGGCT | 8453 |
rs778278597 | snp | C/T | 1.71971e-05 | 0.00293227 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35025178 | CCTTCCACTGAAATG[C/T]TGGCTATAAAATAAT | 8453 |
rs778299475 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022758 | AACTTGAAAATTACT[A/G]TGACAAGGCTGGGCA | 8453 |
rs778307189 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080534 | GTGATCCTGGTTCAC[C/T]GCAGCCTTGACCTCC | 8453 |
rs778307415 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066973 | GGTCTATGTTTGAAA[C/G]AGATGCCTGATAGAA | 8453 |
rs778357065 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116355 | ATCTCAAAAAAAAAA[A/T]TATGAACAATTTTAT | 8453 |
rs778373001 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069922 | AGATTCTTGCCCCAA[A/C]TCAATCCATAATGTT | 8453 |
rs778417845 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036428 | TTGTATATATGTCCA[A/G]GCATTGGCAGTGGGG | 8453 |
rs778427034 | snp | A/G | 1.65272e-05 | 0.0028746 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054505 | GGTCCGCTTCTGTTA[A/G]TTTATTCTTTTTAAT | 8453 |
rs778432702 | in-del | -/CAAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046901 | TGTCTCAAAACAAAA[-/CAAAA]CAAAACAAAACAAAA | 8453 |
rs778459196 | snp | C/G | 1.65241e-05 | 0.00287433 | intron-variant | CUL2 | GRCh38.p7 | 10:35060851 | CGCTGCTTAGCTTGT[C/G]TAGATTTTAAAGGCA | 8453 |
rs778469755 | snp | A/G/T | 0.000104625 | 0.00723207 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010292 | TGATCTTCTCACACC[A/G/T]CGCTGGAGGAGAGCG | 8453 |
rs778499466 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119662 | CAGTGGTGCAAACTC[A/C]TAGACCCAAGGGATC | 8453 |
rs778500797 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107023 | TCTGTCACCCAGAGT[-/A]GAGTGCAGTGGCATG | 8453 |
rs778516900 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35070954 | AATTTTTTTTTGTTC[A/T]CCAACTGTATTCCCA | 8453 |
rs778537128 | snp | A/G | 1.73872e-05 | 0.00294844 | missense | CUL2 | GRCh38.p7 | 10:35029588 | TCAGCGCTGACACTC[A/G]TATCTGTATACATCC | 8453 |
rs778562886 | snp | C/T | 1.83417e-05 | 0.00302829 | intron-variant | CUL2 | GRCh38.p7 | 10:35033146 | TGTACATATATAGTA[C/T]ATATGTATTTAAAAC | 8453 |
rs778624215 | snp | A/C | 2.06738e-05 | 0.00321504 | missense | CUL2 | GRCh38.p7 | 10:35038974 | CATGTAAAAACTGTA[A/C]GTGGTCTGCTACCAT | 8453 |
rs778669785 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035572 | ACTGTATTTTGTATA[C/T]TATTTGTAGCTTCAG | 8453 |
rs778685967 | snp | C/T | | | missense | CUL2 | GRCh38.p7 | 10:35011940 | TCCGGTCCTCATCAA[C/T]TGCACTTCTAGTCTG | 8453 |
rs778701371 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021131 | GGTTAGAGCTTCAAC[A/C]GAAGACTTTGTAGGG | 8453 |
rs778715432 | snp | A/C/T | | | | | GRCh38.p7 | 10:35048651 | GAGGAAGAAAAACAA[A/C/T]GGGTTACACCCTACT | 8453 |
rs778761603 | in-del | -/A/AA/AAA | 0.553282 | 0.0975438 | intron-variant | CUL2 | GRCh38.p7 | 10:35025202 | AATAATTCAAACTGT[-/A/AA/AAA]AAAAAAAAAAAAAAA | 8453 |
rs778823465 | snp | A/G | 9.40424e-05 | 0.00685656 | intron-variant | CUL2 | GRCh38.p7 | 10:35038879 | ATGATATAAAAGGTG[A/G]ATTTATAATTTAATT | 8453 |
rs778827563 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013441 | GGGAATTTTCGGAGA[C/G]AATGCATAGTTACAC | 8453 |
rs778829729 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080840 | GTGCCAAAATGTATA[C/T]TGCAGGAAAACATCT | 8453 |
rs778879667 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35060754 | AGAAAAGTCCATGTC[A/G]GAGAGAATGCTTTAG | 8453 |
rs778890615 | in-del | -/AAC | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075467 | TCATTCCTGTGCCTT[-/AAC]GAGATTCCCACGCGC | 8453 |
rs778934652 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073454 | GGCCCTCAGCAGAAA[C/T]AGTAACAGTTAATAT | 8453 |
rs778952806 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094985 | GTGTTTTGGCCTTGT[A/T]TGTTTATTTAATTCC | 8453 |
rs778961718 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018751 | CTGGGTAACAAGAGC[A/G]AAACTCCGTCTCAAA | 8453 |
rs779007706 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35027969 | AAAGAAAAAACTAAA[C/G]GAAAACTTCATTTCT | 8453 |
rs779055618 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052631 | GGGGGCGCGGTGGCT[C/T]ATACCTGTAATCCCA | 8453 |
rs779063351 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044144 | GTGACTCATCCAAAT[C/G]TCTAGAATTACTATA | 8453 |
rs779071382 | snp | A/T | 0.00013185 | 0.00811835 | missense | CUL2 | GRCh38.p7 | 10:35032460 | GCTTTGCAAACAGAC[A/T]TAGGTTCTCTGTAAT | 8453 |
rs779073968 | snp | A/G | 1.65562e-05 | 0.00287712 | intron-variant | CUL2 | GRCh38.p7 | 10:35071153 | CTCAGTTTTCAACAA[A/G]TTTATCAATTTTAGA | 8453 |
rs779075074 | snp | C/T | 1.65343e-05 | 0.00287521 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35011881 | GTGCCGAAGCACTTT[C/T]CGTGCTTTCATGATA | 8453 |
rs779101745 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084731 | CATAACATTCCAAAT[A/C]GCTGCTTGTTTTTCC | 8453 |
rs779131023 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099911 | TGGTTTACTTGACTA[C/G]ATCTCTGTGGGCAAG | 8453 |
rs779136015 | in-del | -/T | 4.62064e-05 | 0.00480636 | intron-variant | CUL2 | GRCh38.p7 | 10:35038885 | TAAAAGGTGGATTTA[-/T]AATTTAATTTCTACT | 8453 |
rs779179057 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066842 | AAAATCTAAGAAAGA[A/G]TGATGGGCTACTACA | 8453 |
rs779180289 | in-del | -/CC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051009 | AATTTTGCCAGTCTG[-/CC]CTGGACATAAAATAG | 8453 |
rs779196067 | snp | C/T | 1.65877e-05 | 0.00287986 | intron-variant | CUL2 | GRCh38.p7 | 10:35031639 | TGTAGAAATTGATAA[C/T]AAATCTTACAAAGGG | 8453 |
rs779197205 | snp | A/G | 0.00814299 | 0.0632865 | intron-variant | CUL2 | GRCh38.p7 | 10:35025204 | ATAATTCAAACTGTA[A/G]AAAAAAAAAAAAAAC | 8453 |
rs779206135 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107774 | GTGGTCCCAGCAACT[C/T]GGGAGGCTGAGGCAG | 8453 |
rs779206505 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021028 | ATCTTGAACTCCTGG[C/G]CTCAAGTGATACTCC | 8453 |
rs779233778 | snp | A/G | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008991 | CCCAGCACTTTGGGA[A/G]ACAGAGATAGGATTG | 8453 |
rs779236298 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058695 | AATGTAGATTTACTG[A/G]GCATTAATTAGTCTC | 8453 |
rs779264469 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017115 | CTGGGCTCTCCCAGG[A/T]AAGGTTCAAGCCTCC | 8453 |
rs779288812 | snp | C/T | | | missense | CUL2 | GRCh38.p7 | 10:35011945 | TCCTCATCAACTGCA[C/T]TTCTAGTCTGCTCCA | 8453 |
rs779291295 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033606 | GCCAGACGTGGTGGC[A/G]TCCACCTGTAATCCC | 8453 |
rs779306285 | snp | C/T | 2.83346e-05 | 0.00376384 | intron-variant | CUL2 | GRCh38.p7 | 10:35013663 | AATGCTTAAATGTTT[C/T]CCCCTCAAAAAAAAC | 8453 |
rs779310723 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35100346 | CTGCACTACATGTAA[C/T]AAGTTACTCACTTGA | 8453 |
rs779329942 | snp | C/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125082 | GGTAGGTACTATTTT[C/T]CTTCCCATTTAAAAA | 8453 |
rs779337862 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35079003 | AAATGAGAAAATACT[A/G]AAGACCCAATAAAGA | 8453 |
rs779414437 | in-del | -/ACA | 1.83321e-05 | 0.0030275 | intron-variant | CUL2 | GRCh38.p7 | 10:35031272 | GAATGAATTTCTAGG[-/ACA]ATACCACATTAAAGA | 8453 |
rs779446884 | snp | A/T | 1.93793e-05 | 0.00311276 | intron-variant | CUL2 | GRCh38.p7 | 10:35049640 | AAAACCATATCAAAC[A/T]ACAAAATAAAATTGA | 8453 |
rs779456695 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115186 | GAGGTTGCAGTGAGC[C/T]GAGGTCATGCTACTG | 8453 |
rs779460175 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | CREM, CUL2 | GRCh38.p7 | 10:35126829 | ACCTTCCCGCCGCCC[C/G]TCCCCGGTTCCATTT | 8453 |
rs779471206 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033336 | ATATCCAAACTATGA[A/G]GTTTATTAGACTTAT | 8453 |
rs779471842 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116512 | GATGTTTAATTTCAC[A/G]GTAATGTACCCAGCT | 8453 |
rs779514134 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044250 | TCTAAACTAACCACT[A/G]AGCATGAAATCCAGT | 8453 |
rs779563158 | snp | A/C | 1.78966e-05 | 0.00299132 | intron-variant | CUL2 | GRCh38.p7 | 10:35033294 | AATGAAATATAAGTA[A/C]AAAACCACATTTTAA | 8453 |
rs779599642 | in-del | -/GGTGA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021818 | GGAGAGGCGAGGTGG[-/GGTGA]GGTGAGGTGAGGCGA | 8453 |
rs779663693 | snp | A/C | 1.65154e-05 | 0.00287358 | missense | CUL2 | GRCh38.p7 | 10:35010407 | CTTAATCATGCTGAT[A/C]CTGGGATTAAACCTA | 8453 |
rs779667272 | in-del | -/TTTTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103329 | TTTTTTTTTTTTTTT[-/TTTTA]TTTTTTTTTGAGACG | 8453 |
rs779712218 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35019295 | CACCACGAGACCCAA[A/C]GAGCATTAGGAGATC | 8453 |
rs779726920 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035420 | CCAGAGAAAAGTCCC[C/G]CATGCCCACCTCCCA | 8453 |
rs779777982 | snp | C/G | 1.64988e-05 | 0.00287213 | intron-variant | CUL2 | GRCh38.p7 | 10:35060864 | GTCTAGATTTTAAAG[C/G]CACACTCACCTATAT | 8453 |
rs779786839 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35059121 | TACTCCTAATAAGAC[A/G]GTATGAACATTGTTG | 8453 |
rs779790620 | snp | A/C | 1.66582e-05 | 0.00288597 | intron-variant | CUL2 | GRCh38.p7 | 10:35016436 | GAATTGACCATTCAA[A/C]GAAACATTTCAAATT | 8453 |
rs779821352 | snp | A/G | | | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079418 | GGTTTGGTGTCATTC[A/G]TCTCTGGGGATCCCT | 8453 |
rs779885391 | snp | A/G | 3.48147e-05 | 0.00417207 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010294 | ATCTTCTCACACCAC[A/G]CTGGAGGAGAGCGAC | 8453 |
rs779899321 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039380 | ACAACATAACATGTA[A/G]CAGGAAAAGTGGGTA | 8453 |
rs779908677 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099921 | GACTAGATCTCTGTG[C/G]GCAAGTGAATAAGAC | 8453 |
rs779928005 | in-del | -/T | | | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074105 | CACCATTCCAAGCTC[-/T]GAGGATACAGTGGAC | 8453 |
rs779950381 | snp | G/T | 1.6516e-05 | 0.00287362 | missense, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35071282 | AAGTTTGTTCCATGT[G/T]TCATCAAAATCTACT | 8453 |
rs779974087 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35109103 | CTATAGTTCCAGCTA[C/G]TTGGGAGGCTGAGGT | 8453 |
rs780005461 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048471 | TATTAAAAAAGATAT[C/T]TCACAAAAGTACATT | 8453 |
rs780022720 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072718 | CCTCAGACAAACTGC[A/G]TTTAGGAATTAGCTG | 8453 |
rs780028780 | in-del | -/CT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110775 | ATCCCTCGTATCCCC[-/CT]CTTATAATTACACCA | 8453 |
rs780032905 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113637 | ATTCATAATCAGGAG[-/A]AAAATAGAAAAATCA | 8453 |
rs780032911 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085873 | CAGCGAGGGAGGAAG[A/G]GCATAAGGGTTGAAA | 8453 |
rs780038266 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021013 | ATGTTGCCCAGGCTG[A/G]TCTTGAACTCCTGGG | 8453 |
rs780054539 | in-del | -/AAGAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023120 | CTCTCACCACAAATA[-/AAGAT]AAGTGAGAAGCTACT | 8453 |
rs780156695 | snp | C/G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050191 | CCTGGTGTGGTGGCA[C/G/T]GCGCCTGTAATCCCA | 8453 |
rs780213556 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068379 | ATGAGCTGAGATCAC[C/T]GCACTATGCCTAACA | 8453 |
rs780221980 | snp | A/G | 1.86364e-05 | 0.00305251 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35039020 | ATGAATCACCTTAGT[A/G]TATGAACTTGGATGT | 8453 |
rs780232438 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015593 | TGCATTTTTAACTAT[G/T]TAAACATCTAGGATA | 8453 |
rs780237474 | in-del | -/GCCTCGGCCTC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064790 | TCAGGCAATCCTTCT[-/GCCTCGGCCTC]CCAAAGTGCTAGGAT | 8453 |
rs780250999 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077003 | CTTGCAATGAGCCGA[A/G]ATAAAACTCCCAAGA | 8453 |
rs780256758 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107576 | TCAATTTAACATTTA[C/T]TAATTTTAAAAAGTA | 8453 |
rs780269355 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113035 | AGTCTCTACTAAAAA[C/T]ACAAAAATTGGCTGG | 8453 |
rs780290311 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017012 | GAAAAGAACAAAAAA[C/T]CCAAACAATAAAAGG | 8453 |
rs780317706 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110492 | ATTGATTGTACCTGG[C/G]AGGTGGAGGTTGCAG | 8453 |
rs780320101 | snp | A/C | 0.000104808 | 0.0072383 | intron-variant | CUL2 | GRCh38.p7 | 10:35013675 | TTTCCCCCTCAAAAA[A/C]AACTTGACATTAAAA | 8453 |
rs780339258 | in-del | -/TTTTG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041550 | TTTTCTTTTTCTTTC[-/TTTTG]TCAGACAGGATCTCG | 8453 |
rs780349401 | snp | C/G/T | 3.73505e-05 | 0.00432136 | intron-variant | CUL2 | GRCh38.p7 | 10:35049660 | AATAAAATTGACTCA[C/G/T]TAAGATAAATGTCAG | 8453 |
rs780375680 | snp | A/C | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090693 | AGCTTCGTGTGATTG[A/C]GAAAGGCCACGGAAA | 8453 |
rs780399442 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032266 | TATTCTTTAAGACAC[A/G]TAGTATATTGCATTC | 8453 |
rs780402529 | in-del | -/CTTTAG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046646 | CTGGTAATCCCAGCA[-/CTTTAG]GAGGCTGAGGTGGGC | 8453 |
rs780409057 | snp | A/C | 2.07786e-05 | 0.00322317 | intron-variant | CUL2 | GRCh38.p7 | 10:35049782 | TGCCGGGAAAAACGA[A/C]AATCATCAGGGCTGA | 8453 |
rs780483408 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065578 | GAGCCAAGATCGCAC[C/T]ACTGCACTCCAGCCT | 8453 |
rs780552017 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076157 | ACATTCTACTAAGTG[A/G]ATGAAGAGGGCCACA | 8453 |
rs780557146 | snp | C/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128791 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 8453 |
rs780574118 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033496 | ATCCCAGCACTTCTG[C/G]GAGGCTGAGGCGGGC | 8453 |
rs780594034 | in-del | -/TTTA | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080437 | GAATTCCTATTTTTA[-/TTTA]TTTATTTATTTATTT | 8453 |
rs780595753 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064265 | AAAGATGCAGATACA[A/T]ACTGGAAATAAGGCT | 8453 |
rs780608497 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127562 | AAAAGGAAAAGGAAT[C/G]CAGAAGTAAGGACCT | 8453 |
rs780686830 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069556 | TAAAAAGTAAAAATT[-/A]AAAAAAAAAAAAGGA | 8453 |
rs780725449 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031433 | CCTTTCTAATGATTT[A/G]GCATTCAGAAATAAA | 8453 |
rs780742797 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35048697 | TCCTCTCCAGCTCTC[-/T]TATCTCTAAAAACAA | 8453 |
rs780758059 | in-del | -/AAA | 8.31635e-05 | 0.00644786 | intron-variant | CUL2 | GRCh38.p7 | 10:35029645 | CCACAGGCTTGCTAT[-/AAA]AAAGTTTTAGAAAAT | 8453 |
rs780781813 | snp | C/G | 1.64814e-05 | 0.00287061 | intron-variant | CUL2 | GRCh38.p7 | 10:35035310 | GTCTGAGAGGAAAAA[C/G]ACATCTGAGGGTTAA | 8453 |
rs780830331 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064735 | TTTTGTAGAAACAGG[G/T]TCTCACCATGTTGTC | 8453 |
rs780859432 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046385 | TCTAAGTATACACAC[C/T]CTATGACCCCAAGCA | 8453 |
rs780860690 | in-del | -/G | 1.66234e-05 | 0.00288296 | intron-variant | CUL2 | GRCh38.p7 | 10:35035127 | GAAAGGCTCCACGCT[-/G]GATCTGATTAGGAGG | 8453 |
rs780904930 | in-del | -/CTGT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35088166 | ATTATTTCTTATATA[-/CTGT]CTGTCTCTCCATCCC | 8453 |
rs780912364 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026047 | CAGCTATATTATGAC[C/T]ACTCCTTAACAGCAA | 8453 |
rs780929636 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071443 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 8453 |
rs780948952 | in-del | -/TGTATGTATATATATA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021428 | ACATTTTTTTATATA[-/TGTATGTATATATATA]CACACACACACATAC | 8453 |
rs780953273 | snp | C/T | 4.9802e-05 | 0.00498984 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35010428 | ATTAAACCTAGCTCT[C/T]GACTGGCTAATCACC | 8453 |
rs780969190 | in-del | -/AAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095323 | GCAAGACTCCATCTC[-/AAAA]AAAAAAAAAAAGAAA | 8453 |
rs781024304 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35106432 | TCACGCCATTCTCCT[C/G]CCTCAGCGTCCCGAG | 8453 |
rs781039768 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058985 | GGTGTGGTGGAAACA[C/T]CAAGAGAACTCAGAA | 8453 |
rs781047257 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35084509 | CCTTTCCCAATGAAA[A/G]GCCAAATATAAAGTA | 8453 |
rs781047749 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095481 | CAGAACATATAATAT[A/G]TATGCTATTTTGTAG | 8453 |
rs781068989 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35072527 | GCGCCCGCCACCATG[C/G]CCGGCTCATTTTTTG | 8453 |
rs781123213 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122982 | CTATATAAAAAAATT[A/T]AAAAAATTAGCCAGG | 8453 |
rs781162829 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058045 | GGATGCTGCAGTGAG[A/C]CAAGATTGTGCCACT | 8453 |
rs781167291 | snp | C/T | 1.76505e-05 | 0.00297068 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35016330 | AAAGGCAAGAAGAAC[C/T]GCCATTTGGTATGTT | 8453 |
rs781246575 | snp | A/G | 1.69012e-05 | 0.00290694 | intron-variant | CUL2 | GRCh38.p7 | 10:35062944 | ATATTTATATCACGT[A/G]TGTATCATTGCTTAC | 8453 |
rs781300498 | snp | C/T | 1.66021e-05 | 0.0028811 | intron-variant | CUL2 | GRCh38.p7 | 10:35029690 | AAGAAAAATAATAAG[C/T]CATATTGGTTAATAA | 8453 |
rs781350644 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35050061 | GGTACAGTGGGTAAC[A/G]TCTGTAATCCCAGCA | 8453 |
rs781355331 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35112739 | TTCTCAAAAGTCACA[A/G]TATTATACAGGGCAT | 8453 |
rs781356330 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35058543 | CTAGCATCCACCTGA[-/T]TAAGTGTCGATTCTT | 8453 |
rs781366207 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030464 | CATGGCTCACAGCAG[A/C]CTTGATGTCCCAGGC | 8453 |
rs781404853 | snp | C/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126048 | TTGGCCAGGCTGCTC[C/T]TGACCTCAGGTGATC | 8453 |
rs781408517 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111223 | TTATGAGATTAAATG[A/C]TTCTTTAAGAATCAC | 8453 |
rs781411787 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038819 | TATTTAAAATATTTT[-/AA]AGACTATTACTAAAA | 8453 |
rs781428364 | snp | C/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091435 | TTTATTTCAGTAAAG[C/G]GTTTTTATATACGAA | 8453 |
rs781442294 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35065436 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 8453 |
rs781462561 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35041199 | TTCAGAGCATACTAT[A/G]GTGACTTTAATCTGC | 8453 |
rs781464834 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015509 | TACAAAAATAAAAAC[-/A]AAACATTATTTATAG | 8453 |
rs781467948 | snp | C/T | 3.81272e-05 | 0.00436602 | intron-variant | CUL2 | GRCh38.p7 | 10:35033141 | TTTTATGTACATATA[C/T]AGTATATATGTATTT | 8453 |
rs781469066 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35032034 | AAATTTTTAAAAGAA[C/T]ACCTAGGTGAGTTTC | 8453 |
rs781484694 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105411 | AGCCTGGGCGACAGG[A/G]AGAGACACCGTTTCA | 8453 |
rs781497542 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35064086 | AGTACGATGACCACC[A/C]CCAAGTGTCTCCAAG | 8453 |
rs781590566 | snp | C/T | 6.59598e-05 | 0.00574243 | missense, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054469 | GTTCATTCATATCTA[C/T]ACCACCATAGCCATA | 8453 |
rs781594491 | snp | A/T | 1.65258e-05 | 0.00287448 | intron-variant | CUL2 | GRCh38.p7 | 10:35032501 | CGTAAGGGCCTGAAT[A/T]AAAAAACACGCCATA | 8453 |
rs781621086 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075552 | CACCACAGTCCCTTT[C/T]AGTTTCCTTGTGAGT | 8453 |
rs781660018 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074713 | CTGGTCTCGAACTCC[C/T]GAGGCTCAAGTGATC | 8453 |
rs781697433 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054579 | GGATATTAAGTTAAA[G/T]TCAGTAGGAAAGCAA | 8453 |
rs781714164 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35079015 | ACTGAAGACCCAATA[A/C]AGAGCCTTACAGCAG | 8453 |
rs781726765 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35102573 | CTAGACTCTGTCTCA[A/C]AAAAATAATAAAAAA | 8453 |
rs781732908 | snp | C/T | 1.94418e-05 | 0.00311778 | intron-variant | CUL2 | GRCh38.p7 | 10:35016161 | CTTTAATGCTGATGA[C/T]GCTTAAATTCTTTGG | 8453 |
rs781770591 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018028 | AGGCGTGGTGGCTCA[A/C]GCCTGTAATCCCAGC | 8453 |
rs781775538 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35061463 | AGACTCTGTCTCCCA[-/A]AAAAAAAAAAAAAAA | 8453 |
rs796105590 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021392 | GAATCTTATTTTCTG[A/C]ACACTGCTGTGTATA | 8453 |
rs796135117 | in-del | -/AAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044064 | CCAAAAAAAAAAAAA[-/AAC]AAAAAAAAAAACACC | 8453 |
rs796161629 | in-del | -/TTTC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021652 | ATTTATTTATTTTCT[-/TTTC]TTTTGGGCCTGCCTG | 8453 |
rs796182707 | in-del | AA/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023758 | TAGTTTTCTTAGGGG[AA/G]AAAAAAAAAAATCTA | 8453 |
rs796224632 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35066479 | ATTTTTTTGTATTTT[-/T]AGTAAAGATGGGGTT | 8453 |
rs796236599 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021559 | TGTATGAATATGTAT[C/T]AAATAAAAACCCATT | 8453 |
rs796251224 | in-del | -/CA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089819 | TGAGATGCCCCCCCC[-/CA]CACACACACACAAAC | 8453 |
rs796344065 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020180 | TTAAAAAAAAAAAAA[-/A]TAAATCACAAATAAG | 8453 |
rs796477220 | in-del | -/AC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025218 | AAAAAAAAAAAAAAA[-/AC]ACACATTATTTTTAG | 8453 |
rs796479312 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033757 | AACAACAACAACAAC[-/AA]AAAAAAAAAAAAAGG | 8453 |
rs796482429 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35040381 | CACAGACAAATGCAC[C/T]GGCTTGGAAACACTC | 8453 |
rs796484644 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103411 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG | 8453 |
rs796504739 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021657 | ATTTATTTTCTTTTT[C/G]GGCCTGCCTGGTCTT | 8453 |
rs796547540 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35085439 | CGTCCCAAAAAAAAA[A/T]AAAAATAAAAATAAC | 8453 |
rs796569020 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055840 | CATGCCTTCCAGCTA[A/C]GGAAAGAGGAATAAG | 8453 |
rs796578851 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090607 | GGTCTCCTTCTTCCG[A/C]TGCTGCCAAATCCCC | 8453 |
rs796613311 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077339 | AACAAACAAAAAAAA[A/C]AAACAAAAATTAGCC | 8453 |
rs796619384 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103472 | TGGGACTACAGGCGC[A/G]CGCCACCATGCCTGG | 8453 |
rs796636539 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021762 | AGGCTAATGTGGGCT[C/G]TGATCGCGCACCTCC | 8453 |
rs796654638 | in-del | -/CA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089818 | TGAGATGCCCCCCCC[-/CA]CACACACACACACAA | 8453 |
rs796656183 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35025218 | AAAAAAAAAAAAAAA[-/A]CACACATTATTTTTA | 8453 |
rs796657043 | in-del | GATCGCTT/TTA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030823 | GCTTGAGCCCAGGAG[GATCGCTT/TTA]GAGTCCAGCCTGGGC | 8453 |
rs796675633 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020980 | TTTTTTTTTTTTTTT[-/T]CAAGACAGGGTCTCA | 8453 |
rs796687101 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021395 | TCTTATTTTCTGCAC[A/G]CTGCTGTGTATAAAC | 8453 |
rs796746702 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033756 | AAACAACAACAACAA[A/C]AAAAAAAAAAAAAAA | 8453 |
rs796791114 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021400 | TTTTCTGCACACTGC[C/T]GTGTATAAACATACA | 8453 |
rs796811790 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089811 | AGGATGCATGAGATG[-/C]CCCCCCCCACACACA | 8453 |
rs796816858 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096810 | TAGCTTCAGGTCCAC[-/T]TTTTTTTTTTTTTTT | 8453 |
rs796847102 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35037642 | CGAGCTCAGGAGTTC[A/G]AGACCAGCCGGCCAA | 8453 |
rs796919253 | in-del | -/TT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094239 | CTAAGTCCTCGATAA[-/TT]TTTTTTTTTTTTGAG | 8453 |
rs796955260 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35022034 | GTGATATGCCCTGGG[C/T]TGGCCTCTATCACAT | 8453 |
rs797009321 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045562 | AAAAAAAAAAAAAAA[A/C]AACTTAGCTGTGCAT | 8453 |