SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs510272 | snp | A/C | 0 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119370943 | CCACTGGGAATCTGC[A/C]TCCTCCCCACACAGG | 9099 |
rs511401 | snp | C/G | 0.207864 | 0.246424 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379350 | TTCAAGAGGAAAGAG[C/G]ATTGAAAAGAGCACA | 9099 |
rs512608 | snp | A/G | 0.206642 | 0.246211 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383087 | tgttATATTTCCTTA[A/G]GGCCCTCATTCCATC | 9099 |
rs513841 | snp | A/T | 0.209084 | 0.246629 | intron-variant | USP2 | GRCh38.p7 | 11:119370539 | CGTGCGGCCTGGACC[A/T]CTTCTTTCTAAAACT | 9099 |
rs514808 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | USP2 | GRCh38.p7 | 11:119370410 | CCTTAGCTTCTGAAC[C/T]TGTGTCCTCCTCTGT | 9099 |
rs565296 | snp | A/G | 0.22576 | 0.248822 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381441 | GGGGATCCGGGAGGG[A/G]GGATTCGGGGATCAG | 9099 |
rs573396 | snp | C/T | 0.449218 | 0.151037 | intron-variant | USP2 | GRCh38.p7 | 11:119368665 | CACACCCTTGCCCTC[C/T]GCTCTAGGACCTGTT | 9099 |
rs576945 | snp | C/T | 0.213635 | 0.247341 | intron-variant | USP2 | GRCh38.p7 | 11:119376186 | CAGGCTGTGCTTTCA[C/T]CTGGAAGGTGCTAGG | 9099 |
rs587726 | snp | C/T | 0.139903 | 0.224452 | intron-variant | USP2 | GRCh38.p7 | 11:119370115 | GGGAGGTGGAGGTTG[C/T]AGTGAGCCGAGATCG | 9099 |
rs587985 | snp | C/T | 0.46772 | 0.122873 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373385 | GGCCCCATAGGAGGA[C/T]GGGGTGTAGGCACCA | 9099 |
rs602492 | snp | G/T | 0.210396 | 0.247097 | intron-variant | USP2 | GRCh38.p7 | 11:119371033 | TAGTTTAGTCTGCGC[G/T]GAGGTTTTCCATCTC | 9099 |
rs614192 | snp | A/G | 0.212425 | 0.24716 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377999 | GAGTTTCAGAAGCAC[A/G]CCTAAACAGGGTTAA | 9099 |
rs615001 | snp | C/T | 0.209388 | 0.246679 | intron-variant | USP2 | GRCh38.p7 | 11:119371567 | TTATCAAAGTTGCTC[C/T]CTCAAGACCTTTAGT | 9099 |
rs619055 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119362701 | GGTCGACAGGGAGAA[A/G]GGGGCCAGAACTGCA | 9099 |
rs656439 | snp | C/T | 0.205723 | 0.246048 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380164 | TTGTGATCCGCCCGC[C/T]TTGGCCTCCCAAAGT | 9099 |
rs658654 | snp | C/T | 0.24134 | 0.24985 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377610 | GCATCTACCCCAGCT[C/T]GGGGCCTTGGGTCCC | 9099 |
rs658921 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | USP2 | GRCh38.p7 | 11:119374475 | CCCAGAGGATCATGA[A/G]TTTTAATCTATCTGT | 9099 |
rs659705 | snp | A/G | 0.212728 | 0.247206 | intron-variant | USP2 | GRCh38.p7 | 11:119374639 | TTAGGGTCAGTTGGG[A/G]ACCCCCAGAGGCCTT | 9099 |
rs670906 | snp | G/T | 0.196844 | 0.244283 | missense, utr-variant-5-prime, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381489 | TGCCTCTTCTTGGAG[G/T]ATGGACGAGTCGAAC | 9099 |
rs674977 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | USP2 | GRCh38.p7 | 11:119375791 | GGAATTGGTATTCTT[C/T]GGGCAGCGCCCCAAG | 9099 |
rs675873 | snp | C/T | 0.459004 | 0.137176 | intron-variant | USP2 | GRCh38.p7 | 11:119375998 | ATTGCCAGACCCCTC[C/T]GCCTCCTCCTAGCAG | 9099 |
rs676465 | snp | C/T | 0.412249 | 0.190198 | intron-variant | USP2 | GRCh38.p7 | 11:119369212 | GCTGAGCTGCGCCCC[C/T]CTGGCCTGGCATTTT | 9099 |
rs677008 | snp | A/G | 0.257176 | 0.249897 | intron-variant | USP2 | GRCh38.p7 | 11:119369361 | AAGTTCGTGTTGCCT[A/G]TTACTGTTAATGAGG | 9099 |
rs679556 | snp | C/G | 0.148326 | 0.228391 | intron-variant | USP2 | GRCh38.p7 | 11:119372005 | AGAGGCGTGTGCGGG[C/G]ATTAGTTGGCGAGCG | 9099 |
rs680268 | snp | A/G | 0.253544 | 0.249975 | intron-variant | USP2 | GRCh38.p7 | 11:119368979 | GGTCTATGGAAGGAC[A/G]AGCTGTTCCCATTGA | 9099 |
rs682006 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383356 | cattctttccccaca[C/T]ttatgtgtagttcac | 9099 |
rs687009 | snp | C/G | 0.213333 | 0.247296 | intron-variant | USP2 | GRCh38.p7 | 11:119375857 | AGTGCTGGGGCCAAA[C/G]GAGGTCCAGAGGACA | 9099 |
rs891290 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | USP2 | GRCh38.p7 | 11:119374300 | CTCTACAAACACAGA[A/T]CTCAAATTGGTCCTG | 9099 |
rs1054953 | snp | A/G | | | synonymous-codon | USP2 | GRCh38.p7 | 11:119357562 | GAGCTTGCTGGTTCG[A/G]ATCCTGGATTCTGAG | 9099 |
rs1133595 | snp | A/T | | | missense | USP2 | GRCh38.p7 | 11:119356872 | GCCAGTTCGTAGAAG[A/T]GCAGGTAGGCGTCGC | 9099 |
rs1652024 | snp | A/C | 0.146623 | 0.228562 | intron-variant | USP2 | GRCh38.p7 | 11:119371846 | TCCATCCATTCATCC[A/C]TGCAATCAGCAGGTC | 9099 |
rs1835210 | snp | G/T | 0 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119362698 | CAGGGTCGACAGGGA[G/T]AAGGGGGCCAGAACT | 9099 |
rs1940804 | snp | C/T | 0.370772 | 0.218893 | intron-variant | USP2 | GRCh38.p7 | 11:119366507 | ATATGTTTATCTTTG[C/T]TTTATAAGTGTTTCA | 9099 |
rs2115645 | snp | A/G | 0.303438 | 0.244222 | intron-variant | USP2 | GRCh38.p7 | 11:119378778 | CAAGCACCTCTGCCC[A/G]GGTACTCTCCTGGTG | 9099 |
rs2195525 | snp | C/T | 0.479095 | 0.100076 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364694 | TCGTGAAGACCCAAA[C/T]TCATGCAGTCTGTGG | 9099 |
rs2195526 | snp | C/T | 0.424193 | 0.179323 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119366041 | CTGGGATTACAGGTG[C/T]GCACCACCACGCCTG | 9099 |
rs2217380 | snp | G/T | 0.126564 | 0.217402 | intron-variant | USP2 | GRCh38.p7 | 11:119369169 | AAGCAGAAGGTGAAG[G/T]CTCAGGGGAGGCCCT | 9099 |
rs2241646 | snp | A/G | 0.408086 | 0.193672 | synonymous-codon | USP2 | GRCh38.p7 | 11:119359254 | AACAAAGCGCGGTGC[A/G]TATCTCTGGATCTGG | 9099 |
rs2288596 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP2 | GRCh38.p7 | 11:119359784 | AGGCTATCCTTTCAT[A/G]GCCTCAAGTTCCTCT | 9099 |
rs2435193 | snp | G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119358512 | gtagagatggggttt[G/T]gccatgttggccagg | 9099 |
rs2509401 | snp | G/T | 0.0360663 | 0.129354 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355222 | CTGCCAACTGATTTC[G/T]CAAAGCTATTATTTA | 9099 |
rs3195469 | snp | A/C | | | missense | USP2 | GRCh38.p7 | 11:119356849 | GAACTGGCCAGCCCG[A/C]CCTCCCGAATGTAGC | 9099 |
rs3195470 | snp | G/T | 0 | 0 | missense | USP2 | GRCh38.p7 | 11:119356838 | CCCGCCCTCCCGAAT[G/T]TAGCGCCAGGAGCCA | 9099 |
rs3751022 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | USP2 | GRCh38.p7 | 11:119366953 | AAAGCTTTAGCGTGG[C/G]AGCACTTTGAGAAGT | 9099 |
rs3833766 | in-del | -/AA | 0.44638 | 0.154709 | intron-variant | USP2 | GRCh38.p7 | 11:119366648 | GTTGATCTTGTCTCT[-/AA]AGAGGGCCAGACCAG | 9099 |
rs4589313 | snp | A/G | 0.399432 | 0.200425 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119366084 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 9099 |
rs4938649 | snp | C/T | 0.0393691 | 0.134665 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119372902 | GTAGTCGACCAGGTA[C/T]TCAGGGCAGCTGGCT | 9099 |
rs5795178 | in-del | -/AG | 0.153997 | 0.230832 | intron-variant | USP2 | GRCh38.p7 | 11:119370608 | CAGGAAATGACGATA[-/AG]AGGGGTGGAGAGATC | 9099 |
rs7115997 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | USP2 | GRCh38.p7 | 11:119375572 | AGACAGACAGAGGCA[A/C]AGGGTCGGGGTGGGG | 9099 |
rs7117852 | snp | C/G/T | 0.100532 | 0.203967 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356534 | CGAGGGTCTTCCCCC[C/G/T]CAAGACACAGTTGTT | 9099 |
rs7126754 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383103 | GGCCCTCATTCCATC[A/G]CTTCATTTTACAGAT | 9099 |
rs7127021 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383276 | taagagctatggggc[A/G]catcaagcaaggagg | 9099 |
rs7927942 | snp | C/T | 0.0345262 | 0.126772 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377906 | TAACCTTCATGGCTT[C/T]TCTCTGCCCAGATCT | 9099 |
rs7929563 | snp | G/T | 0.158962 | 0.232835 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365898 | tattttatttgtttt[G/T]ttttttttttttttg | 9099 |
rs7936181 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119371026 | GGGTCTGTAGTTTAG[C/T]CTGCGCTGAGGTTTT | 9099 |
rs7937208 | snp | C/T | 0.31357 | 0.241783 | intron-variant | USP2 | GRCh38.p7 | 11:119358664 | TGCTTTGTTGAACAC[C/T]AGGCAGAAACAGGCT | 9099 |
rs7937436 | snp | A/G | 0 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119375040 | GCCCTCTGAAGGTCT[A/G]TGATAATATCAGGGC | 9099 |
rs7943722 | snp | C/T | 0.299411 | 0.245069 | upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381738 | CACTGAGTCGCGTCA[C/T]GGCTATTGGCTTGTT | 9099 |
rs7945115 | snp | A/G | 0.123105 | 0.215401 | intron-variant | USP2 | GRCh38.p7 | 11:119369746 | TACAGCCCAGCTGAT[A/G]GGTGTCCAAGGTTAG | 9099 |
rs7949607 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | USP2 | GRCh38.p7 | 11:119371032 | GTAGTTTAGTCTGCG[C/G/T]TGAGGTTTTCCATCT | 9099 |
rs7949694 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119370979 | GATCCCCAGTAAAGG[A/G]GAATACTGCTGTCAT | 9099 |
rs7949724 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119371150 | ATGAATCGTTAAGCC[C/T]TGCAGTGACTCTGAC | 9099 |
rs7949756 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119371261 | CCCGCAGAGGCTTCT[A/G]GGACCCGAGCCCCTC | 9099 |
rs7950073 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119371268 | AGGCTTCTAGGACCC[A/G]AGCCCCTCCGAGGAG | 9099 |
rs10692151 | in-del | -/TTT | 0 | 0 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119379934 | TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTCCG | 9099 |
rs10790291 | snp | A/G | 0.283947 | 0.247685 | intron-variant | USP2 | GRCh38.p7 | 11:119362203 | AGTGCTAATGGGGGT[A/G]GGGAAATGGGAAAAC | 9099 |
rs10892354 | snp | C/T | 0.36955 | 0.219562 | intron-variant | USP2 | GRCh38.p7 | 11:119367671 | AGGCCAAAAGCTCTG[C/T]GCACCTTTGAGCCCA | 9099 |
rs10892355 | snp | C/T | 0.499891 | 0.00738737 | intron-variant | USP2 | GRCh38.p7 | 11:119370099 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 9099 |
rs11217252 | snp | A/G | 0 | 0 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355322 | TTGCCCTTGGGCTCA[A/G]GTTCACAGGTCTTCT | 9099 |
rs11217253 | snp | C/G | 0.406468 | 0.194981 | intron-variant | USP2 | GRCh38.p7 | 11:119357134 | GAGGGTGGAGGAGTG[C/G]GGGGAGAGTGGGTGG | 9099 |
rs11217255 | snp | A/G | 0.422158 | 0.181278 | intron-variant | USP2 | GRCh38.p7 | 11:119360957 | ACTCCTAGAAGTCCA[A/G]TATATAAAGTAACTC | 9099 |
rs11217256 | snp | C/G | 0.23031 | 0.249223 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365880 | TGTAGTAACTATTAC[C/G]TCTATTTTATTTGTT | 9099 |
rs11217257 | snp | A/G | 0.397994 | 0.201489 | intron-variant | USP2 | GRCh38.p7 | 11:119367745 | CTCCTTCTTTTGCAT[A/G]TGTCTCCGTCTGGGG | 9099 |
rs11217258 | snp | C/T | 0.233527 | 0.249457 | intron-variant | USP2 | GRCh38.p7 | 11:119369894 | ATTTAAGAACTTCTT[C/T]TTGGCCAGGCGTGGT | 9099 |
rs11217259 | snp | G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119372642 | GGAGTCGAGCCCTCA[G/T]CCTGGCTGTTCTCCA | 9099 |
rs11217260 | snp | A/G | 0 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119374103 | GGGTGGGCAGGGGAG[A/G]CCGTGAGTGAGCATG | 9099 |
rs11604901 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364653 | TGCACAAACTTTTGT[A/C]TAGAGTTCCGGGGGT | 9099 |
rs11828770 | snp | A/G | 0.0134861 | 0.0810011 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355975 | GGATATTTCAGGAGG[A/G]GCAGTTACCCCCTGG | 9099 |
rs12161775 | snp | C/G | | | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373185 | CCTAAAGGCCGCTCA[C/G]TACCCCGGGTCTGGC | 9099 |
rs12277700 | snp | A/C | 0.229723 | 0.249176 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365982 | TCACTGCAACCTCTG[A/C]CTCCCGGGTTCAAAC | 9099 |
rs12285901 | snp | A/G | 0.232359 | 0.249377 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365250 | TCCCCACATGTACAC[A/G]CACACATGACCACAG | 9099 |
rs12292387 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | USP2 | GRCh38.p7 | 11:119373670 | AGAAGCACACATGCA[C/T]GCAGGTGTGCACAGG | 9099 |
rs12419866 | snp | C/T | 0.319616 | 0.240112 | intron-variant | USP2 | GRCh38.p7 | 11:119369914 | CCAGGCGTGGTGGCT[C/T]ACACCTGTAATCTCA | 9099 |
rs12419879 | snp | C/T | 0.349013 | 0.229557 | intron-variant | USP2 | GRCh38.p7 | 11:119370047 | TGGTGTGGTGGTACA[C/T]GCCTGTAGTCCTAGC | 9099 |
rs12789250 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364394 | CCCAGCCCGCTGACC[C/T]CCGGCCAGGCAGGCC | 9099 |
rs12789449 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364451 | GAGGCCCTGGCCGGC[A/C]TCGGGGTTGAGGCTC | 9099 |
rs33929148 | snp | C/T | 0.0837507 | 0.186711 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372960 | AGCTCCTTGCGCGTC[C/T]GGGCCAGCATGGGGC | 9099 |
rs34432859 | in-del | -/A | | | intron-variant | USP2 | GRCh38.p7 | 11:119360753 | TTTTCAACAACCAAC[-/A]AAAATATTCTTCAGG | 9099 |
rs34691638 | snp | C/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119363433 | GACAGTGAAGGGGAG[C/G]CGGCCCCTTTCTGCC | 9099 |
rs35224356 | snp | A/G | 0.00240695 | 0.0346075 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372792 | GTGTAGCGGCCAATG[A/G]GTCGGTAGGTTGGGC | 9099 |
rs35310980 | snp | A/T | 0.0722614 | 0.17581 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365700 | CTCTAAGGCTGTTTG[A/T]CCACAGGCCCACCAC | 9099 |
rs35560476 | snp | G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119358347 | TTTGAGATGGAGTTT[G/T]GCTCTGTCCCCCAGG | 9099 |
rs35832174 | snp | A/C/G | 3.3872e-05 | 0.00411523 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119372893 | GTTCTCCAGGTAGTC[A/C/G]ACCAGGTATTCAGGG | 9099 |
rs35957161 | snp | A/G | 0.00206093 | 0.0320346 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373021 | AGCTATCTGAGGTCC[A/G]GAGGCTGGAGAAATC | 9099 |
rs36118584 | in-del | -/C | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376420 | CCAATTGGCTGGGAT[-/C]CCCCCATACCCCTCC | 9099 |
rs45521440 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP2 | GRCh38.p7 | 11:119360301 | GTGCTGGGCTCTCTC[A/G]TGCAATTTCTAACCA | 9099 |
rs45533837 | snp | A/G | 0.0245332 | 0.108003 | missense | USP2 | GRCh38.p7 | 11:119359048 | TCGAGGTTCTCAGGG[A/G]TGGACTTAGGTCTCA | 9099 |
rs45539534 | snp | C/T | 0.402454 | 0.198136 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365482 | TGATCTCTACAGTCA[C/T]TGTCCTCACCCAGAC | 9099 |
rs45570535 | snp | A/T | 0.0147044 | 0.0844746 | intron-variant | USP2 | GRCh38.p7 | 11:119358886 | AGCTCAAAACTTAAG[A/T]TTAAGGGTCTGTCAA | 9099 |
rs45575137 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP2 | GRCh38.p7 | 11:119368835 | GAGAGGGTGGCCTGG[A/G]CAGGGTGGGGCAAGG | 9099 |
rs45575236 | snp | A/G | 0.129664 | 0.219133 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356431 | CGGCTCCTCCGCGGC[A/G]CGGGCGTCCAGGCGG | 9099 |
rs45578848 | snp | C/T | 0.016763 | 0.0900027 | intron-variant | USP2 | GRCh38.p7 | 11:119358124 | GGAGAGGGAGTTCAA[C/T]AAGGCGGGCAACTGG | 9099 |
rs45579334 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354719 | ACCTGAAAATGTTTC[A/G]GCAGACAGAATAAAG | 9099 |
rs45580938 | snp | C/T | 0.04875 | 0.148319 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379182 | GACTCGCAGAGATGG[C/T]GAGTGCAACTCACTT | 9099 |
rs45585531 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377807 | GCTCCCTAACCTGCC[C/T]AGCCAGGGGAGGGAC | 9099 |
rs45593833 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365732 | CTCAGTCTTTGACCA[A/C]TGCTGTCAACCAGCC | 9099 |
rs45615134 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP2 | GRCh38.p7 | 11:119361271 | CTGTTGGCCCTATAG[C/T]GGAGGCGGGTGAGGG | 9099 |
rs45619639 | in-del | -/GA | 0.127303 | 0.21782 | intron-variant | USP2 | GRCh38.p7 | 11:119357838 | AGCGACAGCATGTCT[-/GA]GAGACAAGACAAACA | 9099 |
rs45628335 | snp | G/T | 0.097727 | 0.198275 | intron-variant | USP2 | GRCh38.p7 | 11:119368361 | CAGGCCAGTGTGGCT[G/T]CGTGAACGGAGCGAG | 9099 |
rs56047119 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376905 | AGCACCCCAAAAAGT[C/T]TTAGTGCAGGTTTAA | 9099 |
rs57138113 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP2 | GRCh38.p7 | 11:119368234 | ACACAGATTCATGAC[C/G]TCAGGAAGTTCAACC | 9099 |
rs58020786 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356065 | AAAAAAAAAAAAAAA[-/A]CCCAAACCCCCAAAA | 9099 |
rs58651040 | snp | G/T | 0.0248432 | 0.108648 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365893 | ACCTCTATTTTATTT[G/T]TTTTGTTTTTTTTTT | 9099 |
rs58802844 | in-del | -/A/AA | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356065 | AAAAAAAAAAAAAAA[-/A/AA]CCCAAACCCCCAAAA | 9099 |
rs58962753 | in-del | -/AC | | | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354779 | GAACTGTGTGGGTCC[-/AC]TTTCACGTGGATTTT | 9099 |
rs59121503 | snp | C/G/T | 0.0228947 | 0.104514 | intron-variant | USP2 | GRCh38.p7 | 11:119361611 | TGAGGTTGTCAGCTG[C/G/T]GGGGGAGGGGTGTGG | 9099 |
rs59361729 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382910 | TAATTTTTGAATTTT[A/T]AGTAGAGACAGGGTT | 9099 |
rs59501313 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365899 | ATTTTATTTGTTTTG[-/T]TTTTTTTTTTTTTGA | 9099 |
rs59899031 | in-del | -/T | 0.337668 | 0.234125 | intron-variant | USP2 | GRCh38.p7 | 11:119358324 | GCACAGCAGCTTTTA[-/T]TTTTTTTTTTGAGAT | 9099 |
rs59969944 | snp | A/G | 0.368529 | 0.220116 | intron-variant | USP2 | GRCh38.p7 | 11:119362400 | TTAAGGCATCCTTAG[A/G]ACCCTTGGTTGTTAT | 9099 |
rs60019927 | snp | A/T | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365894 | CCTCTATTTTATTTG[A/T]TTTGTTTTTTTTTTT | 9099 |
rs60558211 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | USP2 | GRCh38.p7 | 11:119369962 | GGCGGGTGGATCACC[C/T]GAGGTCAGTTCAAGA | 9099 |
rs60630309 | snp | A/G | | | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355501 | TTATCCAACTATGTA[A/G]GGCAAAATTGAGCCC | 9099 |
rs61753081 | snp | A/C/T | 6.60251e-05 | 0.00574528 | missense | USP2 | GRCh38.p7 | 11:119357819 | CACCGTTTTCTGCCT[A/C/T]GGCAGCGACAGCATG | 9099 |
rs61760208 | snp | C/T | 0.000774395 | 0.0196621 | synonymous-codon | USP2 | GRCh38.p7 | 11:119359080 | TGTCACTCGGTTCAC[C/T]TCGTTATGGAGCCCA | 9099 |
rs61900034 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376894 | TTCATACACAGAGCA[A/C]CCCAAAAAGTCTTAG | 9099 |
rs68152638 | in-del | -/T | 0.277195 | 0.249508 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382739 | ACCACGCCAGGCCGA[-/T]TTTTTTTTTTATAGA | 9099 |
rs71484136 | snp | A/T | 0.5 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119360896 | CCTTACTATAAGAAA[A/T]TTTGAGTCCCAAATC | 9099 |
rs71484137 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP2 | GRCh38.p7 | 11:119372622 | GTCAGTCATCAGTCA[A/G]GTTGGGAGTCGAGCC | 9099 |
rs72423316 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356048 | CCATTCAAAACATTA[-/A]AAAAAAAAAAAAAAA | 9099 |
rs73006920 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119368764 | TTGCAGGTGCCCAGC[C/T]TGCTGACTGTGCTCT | 9099 |
rs73006936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119375515 | GGAAAAGGTAACTGG[A/G]GGATGATGTCACACA | 9099 |
rs73006952 | snp | G/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382606 | TTTTTTGAGACGGAG[G/T]GTCGTCGCTCTTGTT | 9099 |
rs73577381 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP2 | GRCh38.p7 | 11:119363633 | GAGGGAGGGGGCAAG[A/G]GGGACTTCCTCGGAC | 9099 |
rs73579464 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | USP2 | GRCh38.p7 | 11:119376272 | CTATGGGCAGGAGAG[C/T]GGGCTGGGGCCCTGG | 9099 |
rs73579467 | snp | A/G | 0.031825 | 0.122064 | intron-variant | USP2 | GRCh38.p7 | 11:119378837 | CCTTCCTTCTCCTCT[A/G]GGGCGTCATCTTTCC | 9099 |
rs74452020 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119358129 | GGGAGTTCAACAAGG[C/T]GGGCAACTGGGGTGC | 9099 |
rs74540290 | snp | C/G | 0.0237073 | 0.106262 | intron-variant | USP2 | GRCh38.p7 | 11:119362668 | ACCTTTCTTACAGGA[C/G]AAACAATCCTACCTC | 9099 |
rs74695792 | snp | A/C | 0.0209421 | 0.100162 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356248 | GGAGAGCACTCCAGT[A/C]TGAACACTTTAGTTA | 9099 |
rs74789371 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | USP2 | GRCh38.p7 | 11:119367941 | CCCACCCCAGCACCA[C/T]ATTAACTCATGAAGA | 9099 |
rs74815341 | snp | G/T | 0.5 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119369368 | TGTTGCCTATTACTG[G/T]TAATGAGGGAAAGAA | 9099 |
rs75013480 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP2 | GRCh38.p7 | 11:119359928 | TGTGGGAAGTGATGG[A/G]CATCCTTTAGGGGAA | 9099 |
rs75193504 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | USP2 | GRCh38.p7 | 11:119362669 | CCTTTCTTACAGGAC[A/G]AACAATCCTACCTCA | 9099 |
rs75491040 | snp | C/T | 0.0267696 | 0.112553 | intron-variant | USP2 | GRCh38.p7 | 11:119358298 | ATACAGGAAGTAGAG[C/T]ATGGTCTTCTGCACA | 9099 |
rs75953857 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383146 | TGCCAGTCACTCTTC[C/T]AGAAACTGGGGATAT | 9099 |
rs76018648 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | USP2 | GRCh38.p7 | 11:119370742 | CTGCAGGGCATTCCC[A/G]GCTAAAGTGCCTTAT | 9099 |
rs76068261 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | USP2 | GRCh38.p7 | 11:119362021 | TTAAAGCTTGCCCAC[A/C]ACAGAATACCCACCC | 9099 |
rs76141905 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP2 | GRCh38.p7 | 11:119361154 | GAGAATCCTCCCTGC[C/T]TGGCTCAGGTTTCAA | 9099 |
rs76274625 | snp | G/T | 0.5 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119360442 | CTTTTTTTTTTTTTT[G/T]AGACGGAATCTCACG | 9099 |
rs76383543 | snp | C/T | 0.5 | 0 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355126 | GAATTTACAAACTGG[C/T]TGAAACAATGAAATA | 9099 |
rs76560104 | snp | C/T | 0.124491 | 0.216211 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378145 | CTAACAGCATCAGAA[C/T]GTGCTGACCTTGAAG | 9099 |
rs76870367 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | USP2 | GRCh38.p7 | 11:119372481 | CTACTGGACTATCCT[C/T]GAGTGCGCGGGCCCT | 9099 |
rs76917464 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | USP2 | GRCh38.p7 | 11:119367281 | CCTATAGGATAAGTA[A/C]TTTTTGTCACCTTAA | 9099 |
rs77425118 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377289 | GTGCTCTGTCTGCTA[A/T]ATCTGGCCTGAAGCC | 9099 |
rs77833920 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP2 | GRCh38.p7 | 11:119361973 | TGGTGAAACGCTGCA[A/G]AAGTCTCCATGTTGC | 9099 |
rs78312300 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP2 | GRCh38.p7 | 11:119367604 | GAGGGTCAGCCCATC[C/T]TCCCCACTCTCTGTA | 9099 |
rs78339982 | snp | C/T | 0.5 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119368098 | ATGGAGACATCAGTG[C/T]CTTGCTGATTCTAGT | 9099 |
rs78379608 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365786 | CCAAAACTGCCACTC[A/G]TTAAGTACTTATTAG | 9099 |
rs78630472 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | USP2 | GRCh38.p7 | 11:119361988 | AAAGTCTCCATGTTG[C/T]GCACTCGGAACTAAA | 9099 |
rs78794178 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119372154 | TTTCTCCAAAGCCAG[A/G]TGATAAGCATTGCTG | 9099 |
rs78829997 | snp | G/T | 0.5 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119358334 | TTTTATTTTTTTTTT[G/T]GAGATGGAGTTTTGC | 9099 |
rs79033372 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP2 | GRCh38.p7 | 11:119375476 | TTTGCCCACTGTGCC[C/T]AGCACAACTTTCACC | 9099 |
rs79033711 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377773 | CAGCCACTGTCATTT[C/T]CTGTTGCTCACATGA | 9099 |
rs79402968 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | USP2 | GRCh38.p7 | 11:119368294 | GGGAGTAGGTAAGGA[A/C/T]AGACCCCAGGATCTC | 9099 |
rs79464246 | snp | C/T | 0.00418774 | 0.0455668 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373202 | ACCCCGGGTCTGGCT[C/T]TCTGCCCGCTTACCA | 9099 |
rs79637251 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | USP2 | GRCh38.p7 | 11:119360875 | TATATTTGGTACATA[C/T]TGACTCCTTACTATA | 9099 |
rs79691293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119372488 | ACTATCCTCGAGTGC[A/G]CGGGCCCTGAGTGGG | 9099 |
rs80225862 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | USP2 | GRCh38.p7 | 11:119368181 | GGCCAAGGGGCCCCT[C/G]TGGCTTAAGGTCCTT | 9099 |
rs80353234 | snp | A/G | 0.0107246 | 0.0724382 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355973 | AGGGATATTTCAGGA[A/G]GGGCAGTTACCCCCT | 9099 |
rs111251997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363670 | CCGGGGAGGGGACCA[C/T]GAGTAAGCGTGCGAT | 9099 |
rs111476112 | in-del | -/A | 0.0387552 | 0.1337 | intron-variant | USP2 | GRCh38.p7 | 11:119362844 | GTCTTCCTTCCATTC[-/A]GCCATCAGCAAACCT | 9099 |
rs111506730 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356059 | CATTAAAAAAAAAAA[A/C]AAAAAACCCAAACCC | 9099 |
rs111518125 | in-del | -/A | 0.0376037 | 0.131863 | intron-variant | USP2 | GRCh38.p7 | 11:119369503 | GATGTACTTTTTTTT[-/A]ACCTCTGTTTCTCCC | 9099 |
rs111631514 | snp | C/T | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380055 | GAGTAGCTGGGACTA[C/T]AGGCTCCCGCCAGCA | 9099 |
rs111661596 | snp | A/G | 0.0566069 | 0.158427 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382866 | CCCCCGAGTAGCTGG[A/G]ATTACAGGAGCCCAC | 9099 |
rs111737172 | snp | C/T | 0.5 | 0 | missense | USP2 | GRCh38.p7 | 11:119359324 | GAAGTCCATATGGTC[C/T]GAATTAGTTTTGCAA | 9099 |
rs112126688 | in-del | -/C | 0.0119091 | 0.0762411 | intron-variant | USP2 | GRCh38.p7 | 11:119368797 | AGGGCCCTGGGCCAA[-/C]CCCTGGATCTTCTTG | 9099 |
rs112316573 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119366014 | ATTCTCCTGCCTCAG[C/T]TTCCTGAGTAGCTGG | 9099 |
rs112474908 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP2 | GRCh38.p7 | 11:119367473 | CCCAGCATGTGCCTG[C/T]GATTACCACCGCAAA | 9099 |
rs112601044 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | USP2 | GRCh38.p7 | 11:119371807 | TCTACCCGTGTATCC[A/T]CCCACCCACCACCCA | 9099 |
rs112645939 | snp | C/T | 9.26913e-05 | 0.00680713 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119372722 | CATGCCGTCTCTTCC[C/T]GGGGAGCTGGAGCGG | 9099 |
rs112950413 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, nc-transcript-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119381891 | GACTGGAATGTCACA[A/C]GACGGGGCAGCTGGA | 9099 |
rs112952165 | snp | A/T | 0.5 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119369078 | CAGGGCTGAGCCACC[A/T]GAGCTGGCTTGGAGT | 9099 |
rs113259837 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP2 | GRCh38.p7 | 11:119367761 | TGTCTCCGTCTGGGG[C/T]GCTAGTTTTATGTAC | 9099 |
rs113309933 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | USP2 | GRCh38.p7 | 11:119368728 | CAGACTCTGAGCCTC[A/G]GCCCTGGCTCTGCCT | 9099 |
rs113505988 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | USP2 | GRCh38.p7 | 11:119361989 | AAGTCTCCATGTTGC[A/G]CACTCGGAACTAAAT | 9099 |
rs113510614 | in-del | -/A | 0 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119362203 | AGTGCTAATGGGGGT[-/A]GGGAAATGGGAAAAC | 9099 |
rs113727292 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356751 | AGGTTTGTGTGTTGT[C/T]GTTGTTGTTTTGTTT | 9099 |
rs113811075 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP2 | GRCh38.p7 | 11:119359847 | CCCCCACTCCAGGCA[C/T]AGGTGACCTAATTGG | 9099 |
rs113893557 | snp | C/T | 4.96241e-05 | 0.00498092 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373231 | CACCCCCAGTGATGT[C/T]GGGTCTCAGCAGGGG | 9099 |
rs114076992 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356443 | GGCGCGGGCGTCCAG[A/G]CGGTGATGCTCCCAG | 9099 |
rs114095785 | snp | A/G | 0.0337553 | 0.125452 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382613 | AGACGGAGTGTCGTC[A/G]CTCTTGTTGCCAAGG | 9099 |
rs114296723 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377725 | GGGGTTAAAATGAAC[C/T]CTGTCCCCGTGGGGC | 9099 |
rs114331167 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | USP2 | GRCh38.p7 | 11:119374058 | CCCCTGTGAGGCCAA[G/T]GAGGCTCAGGGGAGG | 9099 |
rs115004466 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP2 | GRCh38.p7 | 11:119373566 | GGCCCTGCCAGGTGT[C/T]GGGCTCCCACAGACC | 9099 |
rs115155309 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP2 | GRCh38.p7 | 11:119375369 | CTCCAGCAGTTTTCA[A/G]TCCAGGCTGACATCA | 9099 |
rs115215645 | snp | C/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383273 | TGCTAAGAGCTATGG[C/G]GCACATCAAGCAAGG | 9099 |
rs115308074 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119371062 | TCAGCATGCCTAGAG[A/T]TCACCCAAAGAGCTT | 9099 |
rs115859154 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | USP2 | GRCh38.p7 | 11:119371464 | GCCCTGCCTTGTCAA[A/G]TTCTGAATGTTCTGG | 9099 |
rs116349850 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP2 | GRCh38.p7 | 11:119361589 | GCTGTCAGCAGCTCA[A/G]AGCCCATGAGGTTGT | 9099 |
rs116393325 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP2 | GRCh38.p7 | 11:119363046 | TGTCTTCACACTTGA[A/G]ACCCCAATCAAGGGC | 9099 |
rs116463655 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | USP2 | GRCh38.p7 | 11:119369698 | AGAGGTGGGCAGGGC[A/G]GGCGTGATTGTTCCC | 9099 |
rs116519877 | snp | C/G | 0.00249397 | 0.0352245 | intron-variant | USP2 | GRCh38.p7 | 11:119360327 | AACCAGCTGGAGCCA[C/G]AGGCAGCAGGCCACA | 9099 |
rs116650564 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | USP2 | GRCh38.p7 | 11:119373810 | ACGCAAGCAGGGGCT[A/C]TCTGACCTCCACAGC | 9099 |
rs116701839 | snp | A/C/T | 0.00147342 | 0.0271031 | intron-variant | USP2 | GRCh38.p7 | 11:119358304 | GAAGTAGAGCATGGT[A/C/T]TTCTGCACAGCAGCT | 9099 |
rs116813686 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | USP2 | GRCh38.p7 | 11:119378645 | GGATGGGCCCAGGGC[A/G]GTTTCTATAGGGTGC | 9099 |
rs116860234 | snp | C/T | 0.0287284 | 0.116357 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380868 | TCCAGCTCAGTCCCA[C/T]TCTAAAGGCAGCCAG | 9099 |
rs117187402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119358648 | CTTGCTGTTCCTGCT[C/T]TGCTTTGTTGAACAC | 9099 |
rs117339295 | snp | C/T | 0.000878538 | 0.0209403 | missense | USP2 | GRCh38.p7 | 11:119359560 | AGGGCTGTGTGTGCA[C/T]TGCTGCCGTGGTGCA | 9099 |
rs117436133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119361994 | TCCATGTTGCGCACT[C/T]GGAACTAAATGTTAA | 9099 |
rs117591717 | snp | A/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379728 | TAATAGTGGTCTATC[A/T]CAGTTGTGAGGATTA | 9099 |
rs117719203 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376693 | TCCTCTGCACAGAGG[C/T]ACTGGGCTTCCTGTC | 9099 |
rs138036016 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378327 | GTAGAGTAGGGGATG[C/G]GGGGGCGGGGGCATA | 9099 |
rs138055189 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | USP2 | GRCh38.p7 | 11:119370582 | CTCACCTCAGCAAGA[C/T]GCACTCTGCTCCAGG | 9099 |
rs138072155 | snp | A/G | 0.00124019 | 0.0248708 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373247 | GGGTCTCAGCAGGGG[A/G]CGGCCCCGGTCATAG | 9099 |
rs138094362 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP2 | GRCh38.p7 | 11:119367036 | GACTGCTGCAGGACA[C/T]GGCCACAAAGGACCT | 9099 |
rs138097306 | in-del | -/A | 0.030278 | 0.119257 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355053 | ATTGTTTCAGTTTTT[-/A]AAAAAATTAAACTTA | 9099 |
rs138161083 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP2 | GRCh38.p7 | 11:119375277 | CACACAAGGCTTTGG[A/G]GTAGGTACAGGGGTG | 9099 |
rs138591696 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP2 | GRCh38.p7 | 11:119371299 | AGCCATATTCTAATT[A/G]CCCTGGGGTTGAACA | 9099 |
rs138670632 | snp | A/G | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119366042 | TGGGATTACAGGTGC[A/G]CACCACCACGCCTGG | 9099 |
rs138672113 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383292 | CATCAAGCAAGGAGG[A/C]GGTGCGTTCGGAGAA | 9099 |
rs138963712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119358442 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 9099 |
rs139055772 | snp | C/T | 6.62987e-05 | 0.00575717 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119372956 | GCAGAGCTCCTTGCG[C/T]GTCCGGGCCAGCATG | 9099 |
rs139170156 | snp | A/G | 6.65724e-05 | 0.00576903 | missense | USP2 | GRCh38.p7 | 11:119357230 | CTGTCCCTGGACTGC[A/G]ACAGTAGGCTGTATA | 9099 |
rs139262395 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP2 | GRCh38.p7 | 11:119375532 | GATGATGTCACACAG[C/T]GTTAGAGGGAAACCA | 9099 |
rs139684051 | snp | A/G | 0.000326815 | 0.0127789 | intron-variant | USP2 | GRCh38.p7 | 11:119360156 | TAGGGGGTGGGCCTG[A/G]GGAAGAAGCAGGCCA | 9099 |
rs139719898 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354874 | CTGATTTTCATATAC[A/G]CAGGTTCTGCAGGGG | 9099 |
rs139840069 | snp | C/G | 0.000153816 | 0.00876837 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372881 | CTTGCGACCATAGTT[C/G]TCCAGGTAGTCGACC | 9099 |
rs139873742 | snp | A/C | 1.65026e-05 | 0.00287246 | synonymous-codon | USP2 | GRCh38.p7 | 11:119357580 | CCTGGATTCTGAGAA[A/C]CGCTTCAGATCTGGC | 9099 |
rs139944295 | snp | C/G | 3.30682e-05 | 0.00406608 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373287 | GAGGAGGGGCCATAG[C/G]TACGGGGACGGGTGA | 9099 |
rs140032525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368719 | AGGCTGGGCCAGACT[C/T]TGAGCCTCAGCCCTG | 9099 |
rs140096716 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380567 | GTCTGCTCCCAGGAC[G/T]TTTCTCGATGGCTCT | 9099 |
rs140138747 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377325 | CCCTGCTTCACTCTT[C/G/T]CCTGGCTCTCCATGG | 9099 |
rs140149067 | snp | C/T | 0.000442455 | 0.0148671 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373406 | GTAGGCACCATAGCC[C/T]GACTTGGCATAGTGG | 9099 |
rs140155959 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382006 | CTAAACGTCCCCCAC[A/T]CCCCTTCTCACTGGG | 9099 |
rs140569658 | snp | C/T | 4.94458e-05 | 0.00497197 | missense | USP2 | GRCh38.p7 | 11:119358776 | TCATGCGCTTACCCC[C/T]GATCCTACTGTCTTC | 9099 |
rs140655116 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | USP2 | GRCh38.p7 | 11:119369207 | CAAGTGCTGAGCTGC[C/G]CCCCCCTGGCCTGGC | 9099 |
rs141039753 | snp | A/G | 0.0166325 | 0.0896639 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382760 | TTTTTATAGAGTCTT[A/G]CTCTGTTGTCCAGGC | 9099 |
rs141117796 | snp | C/T | 0.000330191 | 0.0128447 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373156 | GGAATCCGCTGCCCC[C/T]GCTGAGGCCACTGCC | 9099 |
rs141158365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119370348 | ACATACATTATCTTT[G/T]CATTCCTCAAGTAAT | 9099 |
rs141226113 | in-del | -/TT | 0.00795532 | 0.062565 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356731 | AGGTTTGTTTTTCTC[-/TT]GTCAGGTTTGTGTGT | 9099 |
rs141273601 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP2 | GRCh38.p7 | 11:119374525 | ATGCTTATTTGCCCC[C/T]GGCCACACACCAGCA | 9099 |
rs141343760 | snp | A/G | 0.000230608 | 0.0107355 | intron-variant | USP2 | GRCh38.p7 | 11:119357944 | CCCAGTAGGTCCCAC[A/G]GAAATTTGTTCTTGC | 9099 |
rs141614167 | snp | A/C/T | 6.61544e-05 | 0.00575095 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373290 | GAGGGGCCATAGGTA[A/C/T]GGGGACGGGTGAGGA | 9099 |
rs141732562 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP2 | GRCh38.p7 | 11:119370843 | AAAATTCCCTTCACC[A/T]TGGCCCTGGAGCCGG | 9099 |
rs142082562 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-5-prime, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381623 | TCTCTCCCACCTCCG[C/T]CGGGGGCCCAGAAGG | 9099 |
rs142204965 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP2 | GRCh38.p7 | 11:119358651 | GCTGTTCCTGCTTTG[C/T]TTTGTTGAACACTAG | 9099 |
rs142420599 | snp | C/T | 0.000759351 | 0.0194705 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373146 | ACTCCATAAGGGAAT[C/T]CGCTGCCCCCGCTGA | 9099 |
rs142426941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376447 | CTCCCTGCCCAGTGC[A/G]GGGGGCCCCTGCTGC | 9099 |
rs142496697 | snp | A/G | 0.000861926 | 0.0207417 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373323 | CTGCTGGTGGGGACC[A/G]GCTTGAAACCAAGTT | 9099 |
rs142525206 | snp | C/G/T | 7.03227e-05 | 0.00592934 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372811 | GGTAGGTTGGGCTGA[C/G/T]GATTTCAGGGACTCG | 9099 |
rs142665855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373254 | AGCAGGGGGCGGCCC[C/T]GGTCATAGTCCAGGA | 9099 |
rs142754043 | snp | C/T | 5.60522e-05 | 0.00529367 | intron-variant | USP2 | GRCh38.p7 | 11:119359382 | GACAGCTGAGATATT[C/T]TCTATAAGAAACTCT | 9099 |
rs142876394 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119372316 | CCACAGCAAGGAGGC[C/T]CTCCTGCCACAGGGT | 9099 |
rs142971268 | snp | G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119370614 | AATGACGATAAGGGG[G/T]GGAGAGATCAGGGTG | 9099 |
rs143071576 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383379 | AAAGAATGTTCTAGG[C/T]AGAGAGAAGAGTAAA | 9099 |
rs143086154 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119373770 | ACAGGAAGTCAGCGC[A/T]TCCTGGCCATTCAAA | 9099 |
rs143115468 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380380 | CCCCCTTTGCCTAGA[A/T]AAATACGGCAAGTGC | 9099 |
rs143133766 | snp | C/T | 1.65064e-05 | 0.00287279 | splice-acceptor-variant | USP2 | GRCh38.p7 | 11:119357592 | GAACCGCTTCAGATC[C/T]GGCATTGACGTGAGT | 9099 |
rs143214826 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383340 | CTGAGGGAGGCTAGG[C/T]GTGAACTACACATAA | 9099 |
rs143278764 | snp | C/T | 0.000169794 | 0.00921238 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372892 | AGTTCTCCAGGTAGT[C/T]GACCAGGTATTCAGG | 9099 |
rs143418515 | snp | A/C/G | 4.94567e-05 | 0.00497255 | missense | USP2 | GRCh38.p7 | 11:119358199 | CGAAGACCGTAGAAC[A/C/G]GTAACCACAATCTGT | 9099 |
rs143625447 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119371863 | GCAATCAGCAGGTCA[G/T]CCCCCATTGTGGGAG | 9099 |
rs143666340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119367325 | TGAGATGGAGTGATA[C/T]AAATGAAAGTTAGGG | 9099 |
rs143698945 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355983 | CAGGAGGGGCAGTTA[C/T]CCCCTGGTCCCCAAA | 9099 |
rs143805836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364598 | AACCATTTTGAGAAC[A/G]TGATGAAAGCTCTTC | 9099 |
rs143916320 | snp | C/T | 0.00013219 | 0.00812881 | synonymous-codon | USP2 | GRCh38.p7 | 11:119359248 | ATAGCCAACAAAGCG[C/T]GGTGCGTATCTCTGG | 9099 |
rs143947394 | snp | G/T | 0.000282892 | 0.0118898 | missense | USP2 | GRCh38.p7 | 11:119359312 | TCATTGGGGGATGAA[G/T]TCCATATGGTCTGAA | 9099 |
rs144051162 | snp | C/G | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382048 | CCTGTTCCTCAGCCT[C/G]TTCTCTTTTTCTCTG | 9099 |
rs144132190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367406 | CGTGGGCAGCTTAGG[C/T]CAGGGTTTGGTGACA | 9099 |
rs144301997 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119375865 | GGCCAAACGAGGTCC[A/G]GAGGACAGGGACAGA | 9099 |
rs144513344 | snp | G/T | 1.65397e-05 | 0.00287569 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373299 | TAGGTACGGGGACGG[G/T]TGAGGAAGCTGCTGG | 9099 |
rs144633348 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP2 | GRCh38.p7 | 11:119371523 | CACTTCACAGATGGC[A/C]CAACAAAGCCAAGAC | 9099 |
rs144635804 | snp | A/G | 3.64717e-05 | 0.00427019 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372765 | GCCTGACCCTTTCCC[A/G]TCTCCCACAGCGTGT | 9099 |
rs144907324 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379313 | TGGAAGGGGGGCATT[C/T]TGAAGGGGAACAATC | 9099 |
rs145057880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119362146 | CTGGTGACCGTGTCA[A/G]TGTTCACCAAAGCAG | 9099 |
rs145244822 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP2 | GRCh38.p7 | 11:119361671 | TTTCTCAAGAACTGC[C/T]TTACCGATCCCACAA | 9099 |
rs145283051 | snp | A/G | 0.00426348 | 0.0459735 | intron-variant | USP2 | GRCh38.p7 | 11:119360248 | TTCTGTAAGCAAAGA[A/G]CATATGGCAATAAGG | 9099 |
rs145303825 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355287 | TTCTACTCTTGCTTA[C/G]ACAGTAAACAAGTGT | 9099 |
rs145502836 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378157 | GAATGTGCTGACCTT[A/G]AAGGACAAGGTGGGT | 9099 |
rs145530823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377845 | CCAGGAATTCCAGGC[A/G]CTCCTGGCCCTGGGG | 9099 |
rs145543438 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | USP2 | GRCh38.p7 | 11:119374732 | TCAGACGCCTTTCCC[C/G]GAGGGCATCAGGGGC | 9099 |
rs145629117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380772 | GCCCAATCAGCTCTC[C/T]TTTCCTCTGCTTTAC | 9099 |
rs145691521 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355331 | GGCTCAGGTTCACAG[A/G]TCTTCTCTGGAGAAG | 9099 |
rs145848325 | snp | C/T | 1.66192e-05 | 0.00288259 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119372983 | CATGGGGCTGCGGCC[C/T]AGGTTCCTGGGGTCT | 9099 |
rs145903800 | snp | C/T | 0.00161386 | 0.0283606 | intron-variant | USP2 | GRCh38.p7 | 11:119358755 | TGAAAACAGGCATCT[C/T]CCCTTTCATGCGCTT | 9099 |
rs145987190 | snp | A/G/T | 3.30901e-05 | 0.00406743 | intron-variant, synonymous-codon, missense | USP2 | GRCh38.p7 | 11:119373255 | GCAGGGGGCGGCCCC[A/G/T]GTCATAGTCCAGGAG | 9099 |
rs146005919 | snp | C/T | 0.000257796 | 0.0113504 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372870 | GATGCACTGCCCTTG[C/T]GACCATAGTTCTCCA | 9099 |
rs146329875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119371864 | CAATCAGCAGGTCAG[A/C]CCCCATTGTGGGAGG | 9099 |
rs146464241 | snp | C/G/T | 8.24551e-05 | 0.0064204 | missense | USP2 | GRCh38.p7 | 11:119357560 | GTGAGCTTGCTGGTT[C/G/T]GGATCCTGGATTCTG | 9099 |
rs146666365 | snp | A/G | 0.000197742 | 0.00994143 | synonymous-codon | USP2 | GRCh38.p7 | 11:119358152 | TGGGGTGCATACCTT[A/G]GCAATGGGCAGTGAG | 9099 |
rs146824749 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | USP2 | GRCh38.p7 | 11:119368967 | CCCTGGCAGGGCTCA[A/G]TGGGAACAGCTCGTC | 9099 |
rs146836541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119362309 | GCAAGAAGGACACTT[C/T]GTCACCCACGATTAC | 9099 |
rs146943763 | snp | A/G | 8.26153e-05 | 0.00642657 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373210 | TCTGGCTCTCTGCCC[A/G]CTTACCACCCCCAGT | 9099 |
rs146953796 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP2 | GRCh38.p7 | 11:119370449 | TGAGGTCACGCTGCT[A/G]GTAAGCTGAGCACCA | 9099 |
rs147093004 | snp | C/T | 3.29701e-05 | 0.00406005 | synonymous-codon | USP2 | GRCh38.p7 | 11:119358804 | TTCCCGTTCTAGATA[C/T]TTTCTCCACATCTGT | 9099 |
rs147385040 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119366143 | CAAGTGATCCGCCCA[C/T]CTCAGCCTCCCAAAG | 9099 |
rs147455241 | snp | C/T | | | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119372758 | CCCAGGGGCCTGACC[C/T]TTTCCCGTCTCCCAC | 9099 |
rs147488396 | snp | C/T | 0.0271762 | 0.113356 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383420 | CTGAGGTGGGAGCGA[C/T]CTGCCACTTTCGAGG | 9099 |
rs147498305 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380542 | TAGCCTCTCTGGCCT[C/T]GGTGCACTTGTCTGC | 9099 |
rs147539990 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365444 | CTGCTTGTGATCAGT[-/G]AGAGTGGGCATGTGA | 9099 |
rs147552694 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377502 | AAGCCAGGTGCAACT[C/T]GAGCCCCAGAACAAT | 9099 |
rs147562643 | snp | C/T | 1.6949e-05 | 0.00291105 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373399 | ACGGGGTGTAGGCAC[C/T]ATAGCCCGACTTGGC | 9099 |
rs147722450 | snp | C/T | 0.00167798 | 0.0289167 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373038 | AGGCTGGAGAAATCC[C/T]GGGCCAGGTCTGATT | 9099 |
rs147752511 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380798 | TTTACGGGGGTCCAT[C/G]TGGGGGATGTTCTCA | 9099 |
rs147850079 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354835 | ACTGCATTTGTAAGA[C/T]GCAAAACCCACATAT | 9099 |
rs147956525 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376861 | CCCTTGCCATGTGAC[A/G]CATTCTTCTAGATGT | 9099 |
rs148081236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380000 | GCTCACTGCAAGCTC[C/T]GCATCCTGGGTTCAC | 9099 |
rs148175810 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365255 | ACATGTACACGCACA[C/T]ATGACCACAGCTACA | 9099 |
rs148239084 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119374389 | TCCCAGTCCTTCCCT[C/G]CTCCAGTCCTGCAGC | 9099 |
rs148292528 | snp | A/G/T | 6.60671e-05 | 0.00574717 | intron-variant, synonymous-codon, missense | USP2 | GRCh38.p7 | 11:119373192 | GCCGCTCAGTACCCC[A/G/T]GGTCTGGCTCTCTGC | 9099 |
rs148300879 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383341 | TGAGGGAGGCTAGGC[G/T]TGAACTACACATAAG | 9099 |
rs148433430 | snp | A/G | 1.6546e-05 | 0.00287624 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373304 | ACGGGGACGGGTGAG[A/G]AAGCTGCTGGTGGGG | 9099 |
rs148607679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380983 | TCCGGAGCACCGCGT[G/T]CCTGCTTCTGGTTTG | 9099 |
rs148650681 | snp | A/G/T | 3.54807e-05 | 0.00421181 | intron-variant | USP2 | GRCh38.p7 | 11:119359361 | TTGGAAGGAGAGAGT[A/G/T]TACAGGACAGCTGAG | 9099 |
rs148766960 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP2 | GRCh38.p7 | 11:119376093 | CAGTTCCCATGCCTG[C/T]GGAGAGGGTTCCTAC | 9099 |
rs148874001 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378040 | TCCTACTCAGGTGCC[C/T]GGAAAAGGTGAGTGG | 9099 |
rs148934904 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355960 | AGGGAAGAGGCTGAG[G/T]GATATTTCAGGAGGG | 9099 |
rs149013433 | snp | C/T | 4.99197e-05 | 0.00499573 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373020 | TAGCTATCTGAGGTC[C/T]GGAGGCTGGAGAAAT | 9099 |
rs149047828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119373549 | GAGTGTAGTTGTCAG[A/G]GGGCCCTGCCAGGTG | 9099 |
rs149138048 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383298 | GCAAGGAGGAGGTGC[G/T]TTCGGAGAAGGTAAC | 9099 |
rs149216170 | snp | C/G | 1.64819e-05 | 0.00287066 | missense | USP2 | GRCh38.p7 | 11:119358180 | GAGAGGTCCCAGAAG[C/G]GGTCGAAGACCGTAG | 9099 |
rs149314228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119371355 | TGCTCCACTCCAAGC[A/C]CAGCACGCAGCACCC | 9099 |
rs149322772 | snp | C/T | 0.00108986 | 0.0233183 | missense | USP2 | GRCh38.p7 | 11:119359620 | TAATCTCTCAACTCC[C/T]GAGTGTTGCTCAGGC | 9099 |
rs149464743 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | USP2 | GRCh38.p7 | 11:119359070 | TAGGTCTCAGTGTCA[C/T]TCGGTTCACCTCGTT | 9099 |
rs149581274 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119375619 | TTTTGCTTTGGAGAA[C/G/T]TCCATCAATAATGCA | 9099 |
rs149846698 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | USP2 | GRCh38.p7 | 11:119372487 | GACTATCCTCGAGTG[C/T]GCGGGCCCTGAGTGG | 9099 |
rs149898423 | snp | A/T | 0.000714375 | 0.0188859 | missense | USP2 | GRCh38.p7 | 11:119357286 | TGATTGGACACAGCG[A/T]ACAGGTTGTAAACAG | 9099 |
rs149993556 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119361138 | GCTGATTAAAGACTC[C/G]GAGAATCCTCCCTGC | 9099 |
rs150048335 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP2 | GRCh38.p7 | 11:119369900 | GAACTTCTTCTTGGC[C/T]AGGCGTGGTGGCTCA | 9099 |
rs150194851 | in-del | -/CA | 0.0718919 | 0.175435 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354778 | TGAACTGTGTGGGTC[-/CA]CTTTCACGTGGATTT | 9099 |
rs150406697 | snp | C/T | 0.000397108 | 0.0140853 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373241 | GATGTCGGGTCTCAG[C/T]AGGGGGCGGCCCCGG | 9099 |
rs150603723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368521 | CCCCAGGGAAAAATC[A/G]CATGACCTCAGCTTA | 9099 |
rs150639271 | snp | C/T | 0.0337553 | 0.125452 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380142 | GGATGGTCTCGATTT[C/T]CTGACCTTGTGATCC | 9099 |
rs150768738 | snp | A/G | 0.000133551 | 0.00817055 | missense | USP2 | GRCh38.p7 | 11:119357206 | AGTCGTTGAAAGTGT[A/G]CCATTCTCCTGTCCC | 9099 |
rs151018054 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119360832 | ATGTTATTCTCTATT[A/C]TCTGCTACAGTGGAG | 9099 |
rs151028035 | in-del | -/CTCCA | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364722 | GGAGGTCAATGTGCC[-/CTCCA]CAGGTTAAGAAGATG | 9099 |
rs151071928 | snp | A/C/T | 0.0225045 | 0.103662 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356258 | CCAGTCTGAACACTT[A/C/T]AGTTATGGAAATTAA | 9099 |
rs151080852 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | USP2 | GRCh38.p7 | 11:119372439 | GAAGAGTGGTTCATT[C/G]GGCGCAGCAGAGCAT | 9099 |
rs151294772 | snp | C/T | 0.000153988 | 0.00877328 | splice-acceptor-variant | USP2 | GRCh38.p7 | 11:119358254 | CCCAACAAAGAGATC[C/T]GGGGAAGAGAAGGCC | 9099 |
rs180784145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368530 | AAAATCACATGACCT[C/T]AGCTTATATAATCTC | 9099 |
rs180796245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119357916 | CAACTGGATCTGCTG[A/G]TATCAGCCTCTTCCC | 9099 |
rs180830215 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383350 | CTAGGCGTGAACTAC[A/G]CATAAGTGTGGGGAA | 9099 |
rs180922570 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378177 | ACAAGGTGGGTGAGA[A/G]GGGGCCCTGTATCCT | 9099 |
rs180982468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119362310 | CAAGAAGGACACTTC[A/G]TCACCCACGATTACT | 9099 |
rs181039064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363315 | ATAAATGGAGAGGAC[A/G]GAAAGAAGGGGAAGT | 9099 |
rs181464438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364901 | CAATTACCCAGCTCC[A/G]GCTCTCCCATTCTCA | 9099 |
rs181768593 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382724 | ATTACAGGCGTGCGC[C/T]ACCACGCCAGGCCGA | 9099 |
rs181781914 | snp | C/G | | | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356424 | TGGGCGCCGGCTCCT[C/G]CGCGGCGCGGGCGTC | 9099 |
rs181782079 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377627 | GGGCCTTGGGTCCCT[A/G]GCCTGGTTATGAGCA | 9099 |
rs182044654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119369736 | GTCTAGGAAATACAG[C/T]CCAGCTGATAGGTGT | 9099 |
rs182178325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119374009 | AATCCTAGACTGTCT[A/G]TGCTGGAATGACCTG | 9099 |
rs182219147 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379550 | TAGCGAGAAGCAGAA[A/C]GGGGACTAGTACTCA | 9099 |
rs182231950 | snp | A/C | 0.00398564 | 0.0444627 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354757 | GACCTTTGAACAATG[A/C]GGGCTTGAACTGTGT | 9099 |
rs182340997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119371090 | CTTGTGGAAAGAGCA[C/G]CTTCCCAGGCCCCAT | 9099 |
rs182460566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119359912 | GTGATGGACAGAAGT[G/T]TGTGGGAAGTGATGG | 9099 |
rs182786431 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379337 | AACAATCGGGAGATT[C/G]AAGAGGAAAGAGCAT | 9099 |
rs182825989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119367064 | CCTTGGCTCATCTCT[C/T]GGCCAGCCAGGTCTC | 9099 |
rs182933789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119358508 | TTTAGTAGAGATGGG[A/G]TTTTGCCATGTTGGC | 9099 |
rs183211809 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378332 | GTAGGGGATGGGGGG[C/G]CGGGGGCATATTTAT | 9099 |
rs183427737 | snp | A/C | 1.82201e-05 | 0.00301823 | intron-variant | USP2 | GRCh38.p7 | 11:119359372 | GAGTGTACAGGACAG[A/C]TGAGATATTTTCTAT | 9099 |
rs183510472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375854 | AGAAGTGCTGGGGCC[A/G]AACGAGGTCCAGAGG | 9099 |
rs183708505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119374824 | TTGCCCTGTGATGGA[A/C]TAGCTGGGTGATTTT | 9099 |
rs184063510 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP2 | GRCh38.p7 | 11:119375731 | ATGAGCTCATGGCTC[C/T]TCCCCACAGCTCTCC | 9099 |
rs184094209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119369208 | AAGTGCTGAGCTGCG[C/T]CCCCCTGGCCTGGCA | 9099 |
rs184164945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363091 | CACCTGTGTGGTGAG[G/T]GTCGCCCCAAGTCCT | 9099 |
rs184392937 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382242 | TATGTAACCTTCTCC[C/T]GACTCCCCCGATGTT | 9099 |
rs184408272 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355915 | GCAGGATCCCTTTCC[C/T]AGGCGGGTTTGAACA | 9099 |
rs184484372 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119368380 | GAACGGAGCGAGAAC[A/G]TGAGGGACGAGAGGC | 9099 |
rs184557781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119360775 | TTCTTCAGGGCTTTA[C/T]TGAGTGTGTATTGAC | 9099 |
rs184881265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377103 | TTATTAAAGCTTAAA[A/G]CTGCACTAAGGCTTG | 9099 |
rs184925700 | snp | C/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381498 | TTGGAGTATGGACGA[C/G]TCGAACCGGGCACAA | 9099 |
rs185021565 | snp | C/T | 0.00993419 | 0.0697739 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355528 | GCCCACAGGAAAGAA[C/T]CATACAACTGAGGCA | 9099 |
rs185144079 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378202 | TATCCTTCCATCTGC[A/C]CTCTGACCCTGCCTC | 9099 |
rs185457165 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | USP2 | GRCh38.p7 | 11:119363509 | GGTCCAGCGTGCTGC[C/G/T]CTCGCACACCGATCG | 9099 |
rs185705452 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP2 | GRCh38.p7 | 11:119358685 | GAAACAGGCTTCCCC[A/G]GGAGAGTGATTCTTA | 9099 |
rs185777816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119374166 | CCCTTTCCCCAGACA[C/T]CAGCACCTGCTGCAT | 9099 |
rs185811475 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP2 | GRCh38.p7 | 11:119361313 | GAACAGGTGCTGGAT[C/G]GAGGACTCTGAGCTT | 9099 |
rs186420133 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP2 | GRCh38.p7 | 11:119372349 | ACTGGTGGTCTGGGC[A/C]CCCCCGCATCCAGCC | 9099 |
rs186427601 | snp | C/G/T | 0.00319098 | 0.0398384 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382855 | TGCCTCAGCCTCCCC[C/G/T]GAGTAGCTGGGATTA | 9099 |
rs186461000 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383497 | AAAGAGTGGGAGACG[C/T]GATCAGAGAGGTCAG | 9099 |
rs186487170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379253 | CTCACCTTGAGGGGC[C/T]GCCCTTTCGGGCCAG | 9099 |
rs186515873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377832 | AGGGACTTGCTCCCC[A/G]GGAATTCCAGGCGCT | 9099 |
rs186585309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119370658 | GTCTTGTACTATTGA[A/C]CCTGGAGAGGCCTCT | 9099 |
rs186666233 | snp | C/T | 0.000181239 | 0.00951769 | intron-variant | USP2 | GRCh38.p7 | 11:119358107 | GTCAACATGAAAGGA[C/T]AGGAGAGGGAGTTCA | 9099 |
rs186825421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380429 | AGGAGAATGCTTGGC[C/T]CCTCTGGGGTGGTTC | 9099 |
rs187095655 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP2 | GRCh38.p7 | 11:119367332 | GAGTGATATAAATGA[A/C]AGTTAGGGCTAGCTC | 9099 |
rs187180586 | snp | A/C/G | 0.0145336 | 0.0841958 | intron-variant | USP2 | GRCh38.p7 | 11:119356964 | GGAGCGGGCAGGACC[A/C/G]GGAGACCCCCCGCCG | 9099 |
rs187446817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119366186 | AGGCGTGAGCCACCA[C/T]GCCCGGCCTATTACC | 9099 |
rs187568449 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365133 | TTTGGAGCTTGCTGG[C/T]TATTTTTAGCCAGTA | 9099 |
rs187680894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375807 | GGGCAGCGCCCCAAG[C/T]CCGTGACATCCCTTG | 9099 |
rs187681037 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP2 | GRCh38.p7 | 11:119360886 | CATATTGACTCCTTA[C/G]TATAAGAAATTTTGA | 9099 |
rs187689625 | snp | A/C | | | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354851 | GCAAAACCCACATAT[A/C]TAGAAGGCTGATTTT | 9099 |
rs187822085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379345 | GGAGATTCAAGAGGA[A/G]AGAGCATTGAAAAGA | 9099 |
rs188183711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119375228 | GCCAAACCCCAAATG[C/T]GAGGGCTTGGCAGAA | 9099 |
rs188332789 | snp | G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119360281 | GAAGCAAAGATGCTA[G/T]GCCTGTGCTGGGCTC | 9099 |
rs188334472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119368388 | CGAGAACATGAGGGA[C/T]GAGAGGCGAGTTGTA | 9099 |
rs188440727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369460 | GCTGTAGCTCCAGTC[A/G]GCTATCCTGAGAATC | 9099 |
rs188577395 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP2 | GRCh38.p7 | 11:119363175 | CCAGCACGGGAGCTG[G/T]TGCCTGTTACATAAG | 9099 |
rs188587324 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | USP2 | GRCh38.p7 | 11:119376268 | TGCACTATGGGCAGG[A/G]GAGCGGGCTGGGGCC | 9099 |
rs188713986 | snp | A/C/G | 0.000502357 | 0.0158408 | intron-variant | USP2 | GRCh38.p7 | 11:119359500 | AGTGGAGGAGCATCC[A/C/G]GGGGTAGGCAGGGGC | 9099 |
rs189108674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367756 | GCATGTGTCTCCGTC[C/T]GGGGCGCTAGTTTTA | 9099 |
rs189334105 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382998 | AGACCCCCAAAGTGC[A/T]GGGATTACAGGTGTG | 9099 |
rs189344548 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378175 | GGACAAGGTGGGTGA[A/G]AGGGGGCCCTGTATC | 9099 |
rs189487772 | snp | G/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355687 | GAGAAGGGGGCGGGG[G/T]CAGGAAGGCCAGGGG | 9099 |
rs189496946 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382347 | ACCCTTGCAGCTGCC[G/T]TTAACTCCTCCCATC | 9099 |
rs189509916 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356338 | TGTCCCTTCGTCTGT[C/T]CCCTGGAGTTAGCAG | 9099 |
rs189608025 | snp | A/G | 1.65056e-05 | 0.00287272 | synonymous-codon | USP2 | GRCh38.p7 | 11:119357827 | TCTGCCTCGGCAGCG[A/G]CAGCATGTCTGAGAG | 9099 |
rs189748622 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119381922 | AGGTATTGGGAAAGA[A/G]GAGGCGTCATGGGAG | 9099 |
rs189846487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119366947 | ATGCAGAAAGCTTTA[A/G]CGTGGGAGCACTTTG | 9099 |
rs189972810 | snp | C/T | 6.60633e-05 | 0.00574694 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373191 | GGCCGCTCAGTACCC[C/T]GGGTCTGGCTCTCTG | 9099 |
rs190101866 | snp | A/C/T | 0 | 0 | intron-variant | USP2 | GRCh38.p7 | 11:119374662 | GAGGCCTTCCATCAC[A/C/T]GTAAACGTGCAGCCT | 9099 |
rs190160564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377568 | TTTCACCCACTGTGC[C/T]AAGCCCCTGCATGTC | 9099 |
rs190291339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119361847 | AACTTGGCTAGGGCT[C/G]GCAGTATATGGCCCC | 9099 |
rs190636426 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364292 | CCCACCTCGCCTCTA[C/T]CCCGCCCCCGGCGCC | 9099 |
rs191060118 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119358507 | TTTTAGTAGAGATGG[C/G]GTTTTGCCATGTTGG | 9099 |
rs191337751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119369086 | AGCCACCTGAGCTGG[C/T]TTGGAGTCCCCACTT | 9099 |
rs191370123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375810 | CAGCGCCCCAAGCCC[A/G]TGACATCCCTTGACC | 9099 |
rs191427598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378331 | AGTAGGGGATGGGGG[A/G]GCGGGGGCATATTTA | 9099 |
rs191649002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119360529 | CGTGGGTTCAAGCGA[G/T]TTTCCTGCCTCAGCC | 9099 |
rs191702512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379280 | CCAGTGCCAGCCAAG[A/G]AGGTCTGTGAGGACT | 9099 |
rs191849181 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365957 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 9099 |
rs192252456 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355835 | AGAACTTGATGCCCT[A/G]TCGGAAGGAATCTAC | 9099 |
rs192262712 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119367458 | TCTTAAAGCCTGGCT[C/G]CCAGCATGTGCCTGC | 9099 |
rs192281094 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354927 | TGCAGATTTTGGTAT[A/G]TGTGTATCTTGGAAC | 9099 |
rs192313318 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119370928 | GAGGGTTGGGCCATG[C/G]CTGTGTGGGGAGGAG | 9099 |
rs192342386 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379395 | GAACTTGAGACAAAA[A/G]TATGGAGAAAGTGGA | 9099 |
rs192543317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376611 | TGAGGTGTCCTGACC[C/T]TTCCTTCTCTGTCAG | 9099 |
rs192700658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381442 | TGATCCCCGAATCCC[C/G]CCTCCCGGATCCCCG | 9099 |
rs192941938 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382204 | CGAGACAAAACTTGA[A/T]TTTTTGCTGCTCCCA | 9099 |
rs193018811 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119367870 | GTCAGTGGAGCGGCT[C/G]CCCCAGGGGCAAGGA | 9099 |
rs193144349 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP2 | GRCh38.p7 | 11:119375498 | ACTTTCACCCCTTTC[A/T]AGGAAAAGGTAACTG | 9099 |
rs199528569 | snp | A/G | 3.59195e-05 | 0.00423774 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372784 | CCCACAGCGTGTAGC[A/G]GCCAATGGGTCGGTA | 9099 |
rs199646016 | snp | A/C | 8.2558e-05 | 0.00642434 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373165 | TGCCCCCGCTGAGGC[A/C]ACTGCCTAAAGGCCG | 9099 |
rs199765002 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119360427 | ATTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTG | 9099 |
rs199767133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119357855 | GAGACAAGACAAACA[A/G]AAAGAACTTGTGGGG | 9099 |
rs199771100 | snp | C/G/T | 0.000139153 | 0.0083402 | synonymous-codon | USP2 | GRCh38.p7 | 11:119360184 | CCAGGAAAAACTCAC[C/G/T]GTGTTCCCAAGGTTT | 9099 |
rs199887814 | snp | C/T | 1.67002e-05 | 0.00288961 | intron-variant | USP2 | GRCh38.p7 | 11:119357324 | TGAGGAGGAGGCAGC[C/T]GTCAAGCCCCCGAGG | 9099 |
rs199944120 | snp | C/G | 1.83565e-05 | 0.00302951 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372748 | AGCGGCTGGGCCCAG[C/G]GGCCTGACCCTTTCC | 9099 |
rs199985069 | snp | A/T | 0.000136242 | 0.00825242 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372885 | CGACCATAGTTCTCC[A/T]GGTAGTCGACCAGGT | 9099 |
rs200005535 | snp | C/T | 0.000675993 | 0.0183723 | intron-variant | USP2 | GRCh38.p7 | 11:119358863 | GAGAGAGACAACAAT[C/T]GGGTCAAAGCTCAAA | 9099 |
rs200063907 | in-del | -/TTTC | | | intron-variant | USP2 | GRCh38.p7 | 11:119360424 | GTGATTTTCTTTTCT[-/TTTC]TTTTTTTTTTTTTTG | 9099 |
rs200099555 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119379917 | GAAGTGTTCCTTTCT[C/T]TTTTTTTTTTTTTTT | 9099 |
rs200171777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372974 | CCGGGCCAGCATGGG[G/T]CTGCGGCCCAGGTTC | 9099 |
rs200178107 | in-del | -/CGGGGCCT | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377610 | GCATCTACCCCAGCT[-/CGGGGCCT]TGGGTCCCTGGCCTG | 9099 |
rs200223935 | snp | C/T | 3.3305e-05 | 0.00408061 | intron-variant | USP2 | GRCh38.p7 | 11:119359694 | CAATCAGTGGGGAGA[C/T]GAGAGTCCCACCTTC | 9099 |
rs200242839 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | USP2 | GRCh38.p7 | 11:119359290 | GAACTCAGATGGGCT[C/T]ACCACATCATTGGGG | 9099 |
rs200277007 | snp | A/C | 1.6507e-05 | 0.00287284 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373131 | AGGCAGTTGTTGGTC[A/C]CTCCATAAGGGAATC | 9099 |
rs200291387 | snp | A/G | 0.000798297 | 0.0199627 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373003 | TCCTGGGGTCTATCC[A/G]GTAGCTATCTGAGGT | 9099 |
rs200319788 | snp | A/T | 0.00161941 | 0.0284092 | intron-variant | USP2 | GRCh38.p7 | 11:119358998 | ACAAAAGTTTTGCTT[A/T]CCCACAGCATTCTCC | 9099 |
rs200321757 | snp | C/T | 0.001998 | 0.0315438 | synonymous-codon | USP2 | GRCh38.p7 | 11:119358047 | GTCCATTAATGTCAC[C/T]TCAGGATAACCTCGC | 9099 |
rs200432983 | snp | C/G | 8.55074e-05 | 0.00653807 | intron-variant | USP2 | GRCh38.p7 | 11:119357351 | GAGGCCCCCCTGCCC[C/G]GACTTCCCCCCTCCA | 9099 |
rs200511422 | snp | A/G | 0.0004284 | 0.0146293 | intron-variant | USP2 | GRCh38.p7 | 11:119358747 | GGCAACAGTGAAAAC[A/G]GGCATCTTCCCTTTC | 9099 |
rs200564198 | snp | C/T | 5.58821e-05 | 0.00528563 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372712 | GTAAACTCACCATGC[C/T]GTCTCTTCCCGGGGA | 9099 |
rs200595852 | in-del | -/AC | | | intron-variant | USP2 | GRCh38.p7 | 11:119357843 | CAGCATGTCTGAGAG[-/AC]AAGACAAACAGAAAG | 9099 |
rs200712490 | snp | C/T | 1.65119e-05 | 0.00287327 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373168 | CCCCGCTGAGGCCAC[C/T]GCCTAAAGGCCGCTC | 9099 |
rs200755468 | snp | A/G | 0.0242178 | 0.107342 | intron-variant, synonymous-codon, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119363960 | GGGGGCGGCGGGGGG[A/G]TCCTCGGGCAGGGTC | 9099 |
rs200866255 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | USP2 | GRCh38.p7 | 11:119357133 | GGAGGGTGGAGGAGT[C/G]GGGGGAGAGTGGGTG | 9099 |
rs201056943 | in-del | -/TGT | 0.0260105 | 0.111035 | utr-variant-3-prime, cds-indel | USP2 | GRCh38.p7 | 11:119356745 | CTTGTCAGGTTTGTG[-/TGT]TGTTGTTGTTGTTTT | 9099 |
rs201145299 | snp | C/T | 3.4522e-05 | 0.00415449 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119372857 | GGAGGGCACCTGAGA[C/T]GCACTGCCCTTGCGA | 9099 |
rs201189436 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | USP2 | GRCh38.p7 | 11:119357447 | GCCTTGCACACCTGC[A/G]TCTTCATTCTGCCCT | 9099 |
rs201207667 | snp | A/C | 0.000629212 | 0.017726 | intron-variant | USP2 | GRCh38.p7 | 11:119358983 | AAAAATCTCGAGTTC[A/C]CAAAAGTTTTGCTTT | 9099 |
rs201288742 | snp | C/G | 0.0339571 | 0.125933 | intron-variant, synonymous-codon, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119363954 | GGGAAAGGGGGCGGC[C/G]GGGGGGTCCTCGGGC | 9099 |
rs201318408 | in-del | -/TCAC | 0.00199481 | 0.0315187 | intron-variant | USP2 | GRCh38.p7 | 11:119376157 | CCGCAACCCCCAGTT[-/TCAC]TCTCAAAGGTCCTAG | 9099 |
rs201336403 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119362151 | GACCGTGTCAATGTT[C/T]ACCAAAGCAGGCCCT | 9099 |
rs201371336 | in-del | -/G | 0.0123036 | 0.0774623 | intron-variant | USP2 | GRCh38.p7 | 11:119370856 | CTTGGCCCTGGAGCC[-/G]GGGGGGAGGAGCCAG | 9099 |
rs201446799 | snp | C/T | 0.000131785 | 0.00811635 | intron-variant | USP2 | GRCh38.p7 | 11:119357931 | GTATCAGCCTCTTCC[C/T]AGTAGGTCCCACGGA | 9099 |
rs201508297 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP2 | GRCh38.p7 | 11:119358324 | GCACAGCAGCTTTTA[A/T]TTTTTTTTTTGAGAT | 9099 |
rs201511955 | snp | A/G | 3.30267e-05 | 0.00406353 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373148 | TCCATAAGGGAATCC[A/G]CTGCCCCCGCTGAGG | 9099 |
rs201521041 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119366649 | TTGATCTTGTCTCTA[A/G]AGAGGGCCAGACCAG | 9099 |
rs201525721 | snp | A/G | 0.000149131 | 0.00863385 | missense | USP2 | GRCh38.p7 | 11:119359570 | GTGCATTGCTGCCGT[A/G]GTGCAGGTCCCGCAT | 9099 |
rs201575647 | in-del | -/TTTTC | 0.0123065 | 0.0774713 | intron-variant | USP2 | GRCh38.p7 | 11:119360413 | GAGGAATGCCTGTGA[-/TTTTC]TTTTCTTTTCTTTTT | 9099 |
rs201598684 | snp | C/T | 0.00115975 | 0.0240526 | missense | USP2 | GRCh38.p7 | 11:119359567 | TGTGTGCATTGCTGC[C/T]GTGGTGCAGGTCCCG | 9099 |
rs201636268 | snp | A/T | 0.00145054 | 0.0268918 | intron-variant | USP2 | GRCh38.p7 | 11:119358876 | ATTGGGTCAAAGCTC[A/T]AAACTTAAGTTTAAG | 9099 |
rs201752542 | snp | A/G | 1.6686e-05 | 0.00288838 | missense | USP2 | GRCh38.p7 | 11:119357209 | CGTTGAAAGTGTGCC[A/G]TTCTCCTGTCCCTGG | 9099 |
rs201864809 | snp | C/T | 0.000181628 | 0.00952789 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373147 | CTCCATAAGGGAATC[C/T]GCTGCCCCCGCTGAG | 9099 |
rs201872208 | snp | A/C/G | 0.000876283 | 0.0209141 | intron-variant, utr-variant-5-prime | USP2 | GRCh38.p7 | 11:119373513 | AGTGGGGACTGGGAG[A/C/G]CTCATGGGCTGAAAG | 9099 |
rs201877521 | in-del | -/CCACCCA | | | intron-variant | USP2 | GRCh38.p7 | 11:119371809 | TACCCGTGTATCCAC[-/CCACCCA]CCACCCACACATCCA | 9099 |
rs201879324 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119368726 | GCCAGACTCTGAGCC[C/T]CAGCCCTGGCTCTGC | 9099 |
rs201909313 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365912 | TGTTTTTTTTTTTTT[G/T]GAGACGGAGGCTTGC | 9099 |
rs201978255 | snp | A/G | 3.48821e-05 | 0.0041761 | intron-variant, stop-gained | USP2 | GRCh38.p7 | 11:119372826 | TGATTTCAGGGACTC[A/G]TGAGGGAGGGGCCTG | 9099 |
rs202007991 | in-del | -/TA | | | intron-variant | USP2 | GRCh38.p7 | 11:119366647 | TGTTGATCTTGTCTC[-/TA]AAGAGGGCCAGACCA | 9099 |
rs202030286 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364486 | CGGGATAAGTGATCT[C/T]TGGGGCCCGCAGAGG | 9099 |
rs202174709 | snp | A/C | 0.00199792 | 0.0315431 | missense | USP2 | GRCh38.p7 | 11:119358178 | GTGAGAGGTCCCAGA[A/C]GGGGTCGAAGACCGT | 9099 |
rs202223004 | snp | C/T | 0.000181215 | 0.00951706 | missense | USP2 | GRCh38.p7 | 11:119357506 | TCTGAGGCAAATTCT[C/T]TTAAGTCCAGGTCTC | 9099 |
rs367596823 | in-del | -/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119361610 | ATGAGGTTGTCAGCT[-/G]GGGGGGGAGGGGTGT | 9099 |
rs367771245 | snp | A/G | 3.29625e-05 | 0.00405958 | intron-variant | USP2 | GRCh38.p7 | 11:119358733 | CTCAGGCAAGAGCAG[A/G]CAACAGTGAAAACAG | 9099 |
rs367795974 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355986 | GAGGGGCAGTTACCC[C/G]CTGGTCCCCAAATGC | 9099 |
rs367898012 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP2 | GRCh38.p7 | 11:119363325 | AGGACGGAAAGAAGG[A/G]GAAGTTGCCCTCTGT | 9099 |
rs368072999 | in-del | -/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119369503 | GGATGTACTTTTTTT[-/T]ACCTCTGTTTCTCCC | 9099 |
rs368079550 | snp | C/T | 8.31e-05 | 0.00644539 | missense | USP2 | GRCh38.p7 | 11:119359543 | GCCTCTCACCTTCCA[C/T]GAGGGCTGTGTGTGC | 9099 |
rs368095903 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119368007 | ATGGTGCTGGGCACC[A/G]ATTGAGAAATTGAGC | 9099 |
rs368366352 | snp | C/T | | | synonymous-codon | USP2 | GRCh38.p7 | 11:119357987 | GTGACTTACTGGCTT[C/T]TCATCTCCATCAAGC | 9099 |
rs368367349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378096 | GGTTGGGAGCCCCCA[C/T]AGTGGTGACCTCAGA | 9099 |
rs368380796 | snp | C/T | 3.31373e-05 | 0.00407032 | intron-variant | USP2 | GRCh38.p7 | 11:119359224 | GACATGTCTGCAAGG[C/T]CCTTACTTATAGCCA | 9099 |
rs368391551 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119360705 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGTCC | 9099 |
rs368542143 | snp | A/G | 8.37907e-05 | 0.00647212 | intron-variant | USP2 | GRCh38.p7 | 11:119359489 | AGCCCCAGTGGAGTG[A/G]AGGAGCATCCGGGGG | 9099 |
rs368750566 | snp | A/G | 0.000872938 | 0.0208736 | intron-variant | USP2 | GRCh38.p7 | 11:119358130 | GGAGTTCAACAAGGC[A/G]GGCAACTGGGGTGCA | 9099 |
rs368897551 | snp | A/C/T | 8.92827e-05 | 0.00668093 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373439 | ATCTGTGTAGCGGGC[A/C/T]GATTCTGTGTAGCGC | 9099 |
rs368960794 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373226 | CTTACCACCCCCAGT[A/G]ATGTCGGGTCTCAGC | 9099 |
rs369041516 | snp | A/G | 0.00082713 | 0.0203195 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356808 | GGGGCCACCACGGGG[A/G]AGGGAGAAGGGACGT | 9099 |
rs369070032 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378235 | AGCTGCTTGGGTCAC[C/T]TGCTGCACTATCTGG | 9099 |
rs369164717 | snp | A/G | 6.59359e-05 | 0.00574139 | missense | USP2 | GRCh38.p7 | 11:119358794 | TCCTACTGTCTTCCC[A/G]TTCTAGATATTTTCT | 9099 |
rs369207324 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | USP2 | GRCh38.p7 | 11:119357077 | TGCCATCCATTCTCG[A/G]TGTAAGCCGTGCGGG | 9099 |
rs369335154 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP2 | GRCh38.p7 | 11:119369637 | ATTTTATTGATTTCA[C/T]ATTCCTCCACCTTCA | 9099 |
rs369391312 | snp | A/C/G | 0.000115541 | 0.00759993 | intron-variant | USP2 | GRCh38.p7 | 11:119357438 | CTCCCTCCGGCCTTG[A/C/G]ACACCTGCGTCTTCA | 9099 |
rs369501644 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380587 | TCGATGGCTCTCCCC[A/G]AGGACTGGGAGTACC | 9099 |
rs369502700 | snp | C/G | 5.3331e-05 | 0.00516359 | intron-variant | USP2 | GRCh38.p7 | 11:119360168 | CTGGGGAAGAAGCAG[C/G]CCAGGAAAAACTCAC | 9099 |
rs369565638 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119360464 | AATCTCACGCTGTCA[C/T]CCAGGCTGGAGTGCA | 9099 |
rs369644789 | snp | C/T | 1.71097e-05 | 0.00292481 | missense | USP2 | GRCh38.p7 | 11:119360206 | CCAAGGTTTCGAAGA[C/T]CAGCCAGACCCTGGG | 9099 |
rs369667059 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382918 | GAATTTTTAGTAGAG[A/G]CAGGGTTTCACCGTG | 9099 |
rs369730061 | snp | A/G | 9.08142e-05 | 0.00673787 | intron-variant | USP2 | GRCh38.p7 | 11:119356928 | GGGAGTGACGCTGCG[A/G]AGAGAGCGGGGAGTC | 9099 |
rs369739201 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383454 | AACAAAGTCAATGTG[G/T]CTGGAGTGAAGAGAG | 9099 |
rs369792510 | snp | C/T | 1.65086e-05 | 0.00287298 | intron-variant | USP2 | GRCh38.p7 | 11:119357598 | CTTCAGATCTGGCAT[C/T]GACGTGAGTCAAGGA | 9099 |
rs369873806 | in-del | -/AG/GC | | | intron-variant | USP2 | GRCh38.p7 | 11:119370609 | AGGAAATGACGATAA[-/AG/GC]GGGGTGGAGAGATCA | 9099 |
rs369895568 | snp | A/G | 0.000108402 | 0.00736134 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372777 | CCCGTCTCCCACAGC[A/G]TGTAGCGGCCAATGG | 9099 |
rs370011175 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119371929 | TTCCTCCTCTGAGAG[C/T]TTGCCACCTAATGGG | 9099 |
rs370036465 | snp | G/T | 0.000437904 | 0.0147905 | intron-variant | USP2 | GRCh38.p7 | 11:119360292 | GCTAGGCCTGTGCTG[G/T]GCTCTCTCGTGCAAT | 9099 |
rs370046547 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365489 | TACAGTCACTGTCCT[C/T]ACCCAGACTCTGACT | 9099 |
rs370087013 | snp | A/G/T | 0.000247082 | 0.0111124 | intron-variant | USP2 | GRCh38.p7 | 11:119357967 | GTTCTTGCTATTACC[A/G/T]AAGGGTGACTTACTG | 9099 |
rs370128324 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119373536 | GCTGAAAGACAAGGA[A/G]TGTAGTTGTCAGAGG | 9099 |
rs370215437 | snp | A/G | 1.84371e-05 | 0.00303615 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372736 | CCGGGGAGCTGGAGC[A/G]GCTGGGCCCAGGGGC | 9099 |
rs370338722 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119378902 | GCCCCTGACACCCAC[C/T]GGGCCCAATGGGGTG | 9099 |
rs370371826 | snp | A/G | 1.84126e-05 | 0.00303414 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373453 | CCGATTCTGTGTAGC[A/G]CTTCAGGGTGGAGGA | 9099 |
rs370394270 | snp | C/T | 6.62789e-05 | 0.00575631 | intron-variant | USP2 | GRCh38.p7 | 11:119359163 | AAGGAGGGTGAGCAA[C/T]ACCTCTTGTCCTAAG | 9099 |
rs370403138 | snp | A/G | 1.64923e-05 | 0.00287156 | missense | USP2 | GRCh38.p7 | 11:119359027 | CCTCTTACTTACGGA[A/G]GATGATCGAGGTTCT | 9099 |
rs370434087 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119371212 | CACTGCTGACCATGA[A/G]ACAACCCTTCTCTTC | 9099 |
rs370528685 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119369958 | CCGAGGCGGGTGGAT[C/T]ACCTGAGGTCAGTTC | 9099 |
rs370666027 | snp | A/G | 1.65236e-05 | 0.00287429 | missense | USP2 | GRCh38.p7 | 11:119359249 | TAGCCAACAAAGCGC[A/G]GTGCGTATCTCTGGA | 9099 |
rs370688355 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119362390 | AGAAGCTCCTTTAAG[C/G]CATCCTTAGGACCCT | 9099 |
rs370693896 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381163 | CACGTGGGGAGGGGG[G/T]TTGTCAGTGTCGCTC | 9099 |
rs370779529 | snp | C/T | 3.32088e-05 | 0.00407471 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373052 | CCGGGCCAGGTCTGA[C/T]TGGCTGTCCAGCTTC | 9099 |
rs371069251 | snp | G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119367390 | GCTTCTCTCAGATCT[G/T]CGTGGGCAGCTTAGG | 9099 |
rs371224706 | in-del | -/A | | | intron-variant | USP2 | GRCh38.p7 | 11:119366352 | TTCCTGCTCTCTGCC[-/A]ATTACCTACTTGTAA | 9099 |
rs371245887 | snp | A/C | 4.95864e-05 | 0.00497903 | intron-variant | USP2 | GRCh38.p7 | 11:119357749 | GCCCTGATGGATCTT[A/C]AGGATACGGAGCACC | 9099 |
rs371273889 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381675 | CCACCCAGCGGGCAG[C/T]CGCCTCATCGCGCCT | 9099 |
rs371545281 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383431 | GCGACCTGCCACTTT[C/T]GAGGAAGAACAAAGT | 9099 |
rs371696087 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364686 | TCAGGCCTTCGTGAA[A/G]ACCCAAACTCATGCA | 9099 |
rs371707319 | in-del | -/CTT | | | intron-variant | USP2 | GRCh38.p7 | 11:119369894 | ATTTAAGAACTTCTT[-/CTT]GGCCAGGCGTGGTGG | 9099 |
rs371751796 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119358856 | GGAACCAGAGAGAGA[C/T]AACAATTGGGTCAAA | 9099 |
rs371769053 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364432 | GAGGCAGGACCGGAG[C/T]CCTGAGGCCCTGGCC | 9099 |
rs371849956 | snp | C/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119366350 | ACTTCCTGCTCTCTG[C/G]CAATTACCTACTTGT | 9099 |
rs372189891 | snp | A/C/T | 9.89979e-05 | 0.00703497 | synonymous-codon | USP2 | GRCh38.p7 | 11:119358218 | ACCACAATCTGTACA[A/C/T]GTCAGCGAGCTCTTT | 9099 |
rs372464750 | in-del | -/C | | | intron-variant | USP2 | GRCh38.p7 | 11:119369138 | CCACCATCACTGTTC[-/C]TCCTCTCTGCATTTT | 9099 |
rs372649067 | snp | A/T | 0.000143531 | 0.00847024 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373442 | TGTGTAGCGGGCCGA[A/T]TCTGTGTAGCGCTTC | 9099 |
rs372719272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376915 | AAAGTCTTAGTGCAG[G/T]TTTAAGCTGGGATTC | 9099 |
rs372749743 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119368839 | GGGTGGCCTGGGCAG[A/G]GTGGGGCAAGGGCTG | 9099 |
rs372821125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119379803 | AACATTGATGATTAT[A/G]TTGAATACTTCCACT | 9099 |
rs372906234 | snp | A/C | 4.98981e-05 | 0.00499465 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373010 | GTCTATCCGGTAGCT[A/C]TCTGAGGTCCGGAGG | 9099 |
rs372988717 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119360976 | ATAAAGTAACTCTCA[C/T]AAGAGACACTTTGAG | 9099 |
rs373048536 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119367529 | TGATGGATGAAAAGG[C/T]AGGGGCTCTGAGTCC | 9099 |
rs373153803 | snp | A/G | 8.28699e-05 | 0.00643647 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372957 | CAGAGCTCCTTGCGC[A/G]TCCGGGCCAGCATGG | 9099 |
rs373394831 | snp | G/T | 0.000329598 | 0.0128332 | intron-variant | USP2 | GRCh38.p7 | 11:119357469 | TTCTGCCCTGCCTAC[G/T]CAAAGATACTCACTG | 9099 |
rs373544372 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383489 | AGATAGGGAAAGAGT[A/G]GGAGACGCGATCAGA | 9099 |
rs373576579 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383301 | AGGAGGAGGTGCGTT[C/T]GGAGAAGGTAACATT | 9099 |
rs373700996 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119376078 | TCTGACTTCTAGCTA[C/T]AGTTCCCATGCCTGC | 9099 |
rs373775753 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355994 | GTTACCCCCTGGTCC[C/T]CAAATGCTATAAGGC | 9099 |
rs374005377 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP2 | GRCh38.p7 | 11:119357613 | TGACGTGAGTCAAGG[A/G]TAGTCAAACCAATGC | 9099 |
rs374012357 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378328 | TAGAGTAGGGGATGG[C/G]GGGGCGGGGGCATAT | 9099 |
rs374015674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119358358 | GTTTTGCTCTGTCCC[C/T]CAGGCTGAAGTGCAG | 9099 |
rs374141919 | snp | A/G/T | 5.11446e-05 | 0.00505669 | intron-variant | USP2 | GRCh38.p7 | 11:119357355 | CCCCCCTGCCCCGAC[A/G/T]TCCCCCCTCCAACCT | 9099 |
rs374223922 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119360624 | GAGACAGGGTTTCGT[A/C]ATGTTGGCCAGGCTG | 9099 |
rs374264296 | snp | C/G | 0.00136545 | 0.0260933 | intron-variant | USP2 | GRCh38.p7 | 11:119356946 | AGAGCGGGGAGTCAG[C/G]CCGGAGCGGGCAGGA | 9099 |
rs374271839 | snp | A/C | 3.29821e-05 | 0.00406078 | intron-variant | USP2 | GRCh38.p7 | 11:119358844 | TCGTCATCACTGGGA[A/C]CCAGAGAGAGACAAC | 9099 |
rs374392454 | snp | C/T | 1.6601e-05 | 0.00288101 | intron-variant | USP2 | GRCh38.p7 | 11:119359181 | CTCTTGTCCTAAGAA[C/T]CTGCTCCTACTGCCA | 9099 |
rs374467256 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376699 | GCACAGAGGCACTGG[A/C/G]CTTCCTGTCAGGGCA | 9099 |
rs374585819 | snp | C/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119371536 | GCACAACAAAGCCAA[C/G]ACTCCCTAAGTCATA | 9099 |
rs374663984 | snp | A/G | | | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372946 | CCTGCAGGGTGCAGA[A/G]CTCCTTGCGCGTCCG | 9099 |
rs374677499 | snp | G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119370556 | GTCCAGGCCGCACGA[G/T]CAGGGTTGTTCTCAC | 9099 |
rs374702113 | snp | A/G | 6.68204e-05 | 0.00577977 | missense | USP2 | GRCh38.p7 | 11:119357202 | CTGGAGTCGTTGAAA[A/G]TGTGCCATTCTCCTG | 9099 |
rs374783359 | snp | C/T | 0.000135527 | 0.00823073 | missense | USP2 | GRCh38.p7 | 11:119359334 | TGGTCTGAATTAGTT[C/T]TGCAAACTCTATTGG | 9099 |
rs374791073 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119369855 | GACACTCAAGAACAC[C/T]CAGGGCTGCCTCCCA | 9099 |
rs374841616 | snp | A/G | 6.59e-05 | 0.00573983 | intron-variant | USP2 | GRCh38.p7 | 11:119358090 | AAAAGCAAAGGTCAG[A/G]GGTCAACATGAAAGG | 9099 |
rs374865405 | snp | C/G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119361137 | GGCTGATTAAAGACT[C/G/T]GGAGAATCCTCCCTG | 9099 |
rs374909470 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119368430 | GGAGCTCCAGGACAG[C/T]CCCTGCTATCCGCAA | 9099 |
rs374925014 | snp | A/G | 3.34029e-05 | 0.00408661 | intron-variant | USP2 | GRCh38.p7 | 11:119359513 | CCGGGGGTAGGCAGG[A/G]GCACATGACAGAGGG | 9099 |
rs374949575 | snp | A/G | 1.65029e-05 | 0.00287248 | intron-variant | USP2 | GRCh38.p7 | 11:119357879 | TGTGGGGAAGTCAGT[A/G]GGCCCCAATCCAGTC | 9099 |
rs375500650 | snp | A/G | 0.00262596 | 0.0361398 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381449 | CGAATCCCCCCTCCC[A/G]GATCCCCGACAGGTG | 9099 |
rs375539156 | snp | A/G | 9.91195e-05 | 0.00703917 | missense | USP2 | GRCh38.p7 | 11:119359250 | AGCCAACAAAGCGCG[A/G]TGCGTATCTCTGGAT | 9099 |
rs375805729 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119373525 | GAGCCTCATGGGCTG[A/G]AAGACAAGGAGTGTA | 9099 |
rs375833938 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373015 | TCCGGTAGCTATCTG[A/G]GGTCCGGAGGCTGGA | 9099 |
rs375901656 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379364 | GCATTGAAAAGAGCA[C/T]AGAGGGGTGGGGGTG | 9099 |
rs376129505 | snp | A/C/T | 0.000133138 | 0.0081579 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373002 | TTCCTGGGGTCTATC[A/C/T]GGTAGCTATCTGAGG | 9099 |
rs376144411 | snp | G/T | 3.36525e-05 | 0.00410184 | intron-variant | USP2 | GRCh38.p7 | 11:119357183 | GCCCTGCCCTGGCTC[G/T]CACCTGGAGTCGTTG | 9099 |
rs376176064 | snp | A/C | | | intron-variant | USP2 | GRCh38.p7 | 11:119361096 | GAGACAGGTGGAATT[A/C]CTTCCAGCTGAGCTC | 9099 |
rs376411769 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119367043 | GCAGGACACGGCCAC[A/G]AAGGACCTTGGCTCA | 9099 |
rs376412644 | snp | A/T | 4.94393e-05 | 0.00497164 | intron-variant | USP2 | GRCh38.p7 | 11:119357476 | CTGCCTACTCAAAGA[A/T]ACTCACTGGTGTTTT | 9099 |
rs376417199 | snp | C/G | 0.00159744 | 0.0282165 | intron-variant | USP2 | GRCh38.p7 | 11:119372347 | GCACTGGTGGTCTGG[C/G]CCCCCCCGCATCCAG | 9099 |
rs376546761 | snp | C/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119362332 | ACGATTACTATTCTT[C/G]AGGATCTAACCCCTC | 9099 |
rs376586681 | snp | A/T | 0.000155988 | 0.00883005 | missense | USP2 | GRCh38.p7 | 11:119356911 | ACTTGGCTGGAGGAC[A/T]TGGGAGTGACGCTGC | 9099 |
rs376703545 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365918 | TTTTTTTTTTGAGAC[A/G]GAGGCTTGCTCTGTC | 9099 |
rs376744317 | snp | C/G | 0.000568952 | 0.0168568 | intron-variant | USP2 | GRCh38.p7 | 11:119359711 | AGAGTCCCACCTTCA[C/G]CTGTGTTACTTACTA | 9099 |
rs376881781 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377284 | GACTCGTGCTCTGTC[A/T]GCTATATCTGGCCTG | 9099 |
rs376888884 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | USP2 | GRCh38.p7 | 11:119359008 | TGCTTTCCCACAGCA[G/T]TCTCCTCTTACTTAC | 9099 |
rs376890352 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119360123 | GGGACTCTGGTTATA[G/T]GGCTCCAGTCAGCAT | 9099 |
rs376996523 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381153 | GCTGCACGCACACGT[G/T]GGGAGGGGGTTTGTC | 9099 |
rs377000628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363632 | AGAGGGAGGGGGCAA[A/G]GGGGACTTCCTCGGA | 9099 |
rs377255793 | snp | A/G/T | 3.29777e-05 | 0.00406051 | missense | USP2 | GRCh38.p7 | 11:119359109 | CATCCAGAAGAAAGC[A/G/T]AAGGAACTCCTGAGC | 9099 |
rs377301285 | snp | A/G | 3.44542e-05 | 0.00415041 | synonymous-codon | USP2 | GRCh38.p7 | 11:119360193 | ACTCACCGTGTTCCC[A/G]AGGTTTCGAAGACCA | 9099 |
rs377302244 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380001 | CTCACTGCAAGCTCC[A/G]CATCCTGGGTTCACG | 9099 |
rs377531648 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119360781 | AGGGCTTTATTGAGT[A/G]TGTATTGACTATGTA | 9099 |
rs377533523 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380561 | GCACTTGTCTGCTCC[C/G]AGGACGTTTCTCGAT | 9099 |
rs377604526 | snp | C/T | | | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355255 | CTGTACAAGGTTCCA[C/T]TGTACATTAGACATT | 9099 |
rs377616747 | snp | A/C | 0.000437904 | 0.0147905 | intron-variant | USP2 | GRCh38.p7 | 11:119358710 | TTCTTAGGGCTTTTC[A/C]TGCTCCACTCAGGCA | 9099 |
rs377727221 | snp | C/G | 0.000165986 | 0.00910855 | intron-variant | USP2 | GRCh38.p7 | 11:119356962 | CCGGAGCGGGCAGGA[C/G]CGGGAGACCCCCCGC | 9099 |
rs377758729 | snp | A/C | 0.000153988 | 0.00877327 | intron-variant | USP2 | GRCh38.p7 | 11:119357714 | CCTTGTCATCAGTCA[A/C]CCTTGAAAGTCATGT | 9099 |
rs386758032 | multinucleotide-polymorphism | CA/GG | | | intron-variant | USP2 | GRCh38.p7 | 11:119362668 | ACCTTTCTTACAGGA[CA/GG]AACAATCCTACCTCA | 9099 |
rs386758033 | multinucleotide-polymorphism | CATG/TGTA | | | intron-variant | USP2 | GRCh38.p7 | 11:119367742 | CACCTCCTTCTTTTG[CATG/TGTA]TGTCTCCGTCTGGGG | 9099 |
rs397816714 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119379936 | TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTCCG | 9099 |
rs397824545 | in-del | -/AG | | | intron-variant | USP2 | GRCh38.p7 | 11:119370610 | GGAAATGACGATAAG[-/AG]GGGTGGAGAGATCAG | 9099 |
rs397828846 | in-del | -/A | 0 | 0 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382749 | AGAGCAAGACTCTAT[-/A]AAAAAAAAAATCGGC | 9099 |
rs397897488 | in-del | -/GA | 0.0512465 | 0.151648 | intron-variant | USP2 | GRCh38.p7 | 11:119357842 | ACAGCATGTCTGAGA[-/GA]CAAGACAAACAGAAA | 9099 |
rs398076285 | in-del | -/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119358333 | CTTTTATTTTTTTTT[-/T]TGAGATGGAGTTTTG | 9099 |
rs527357769 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380826 | TCATGCCCATTCCAG[A/G]GGAGGTGAGCAGCCC | 9099 |
rs527500008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119358611 | ATGAGCCACCATGCC[C/T]GGCCTGCACAGCATC | 9099 |
rs527626934 | snp | A/G | 1.66021e-05 | 0.0028811 | intron-variant | USP2 | GRCh38.p7 | 11:119359204 | TACTGCCACCCACCT[A/G]AGAGGACATGTCTGC | 9099 |
rs527670550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119378498 | CTCCCCTGGCAGGGG[G/T]TCATCCAAGGGAATT | 9099 |
rs527812798 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365038 | TGCTGGAAGATCAGG[G/T]GTCTTTAGATTTCGT | 9099 |
rs528078898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364002 | GGTGCGCATGCTGGG[A/G]GGCGGGCGGCGGGCT | 9099 |
rs528099484 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356507 | CGGGCGCTGCGGCGG[A/G]AAGCGGCGCAGCGAG | 9099 |
rs528222393 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119366051 | AGGTGCGCACCACCA[C/T]GCCTGGCTAATTTTT | 9099 |
rs528239016 | snp | C/T | 6.65093e-05 | 0.0057663 | missense | USP2 | GRCh38.p7 | 11:119357242 | TGCGACAGTAGGCTG[C/T]ATAGTGGCCACCCAT | 9099 |
rs528255270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119376174 | ACTCTCAAAGGTCCT[A/G]GCACCTTCCAGGTGA | 9099 |
rs528264658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369606 | CCCCTTAAGTTTAAA[A/T]GACCTCTTCTGCAGC | 9099 |
rs528353688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119363579 | TAGGTGCCAGGAATT[A/G]AGAGGCCAAGAGCCA | 9099 |
rs528383080 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119357959 | GGAAATTTGTTCTTG[C/T]TATTACCGAAGGGTG | 9099 |
rs528536331 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383718 | CTCATAATGTTTTAA[C/G]AAAGTTTACGAATTT | 9099 |
rs528536577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375736 | CTCATGGCTCCTCCC[C/T]ACAGCTCTCCCTCTC | 9099 |
rs528666834 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119361620 | CAGCTGGGGGGGAGG[C/G]GTGTGGGTGGGGGAG | 9099 |
rs528736402 | snp | C/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119371193 | CAGACCCCACTTTAA[C/G]GAGCACTGCTGACCA | 9099 |
rs528794824 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356190 | GTACTTGGAAAAGCA[A/G]TAAAAGGACCAGTGC | 9099 |
rs528801258 | snp | C/G | 0.00318978 | 0.0398085 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355164 | CCTAATATACTAGGA[C/G]CCCTTCCTAGATTCA | 9099 |
rs528865616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119374344 | AAAGGGGGCCCCCTA[C/G]AGTCCCAAATCTTGC | 9099 |
rs529009270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368228 | CTGCCAACACAGATT[C/G]ATGACCTCAGGAAGT | 9099 |
rs529029848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119374854 | TGCACTAGTCACGTA[A/G]CCTCTCTGAGCCCCA | 9099 |
rs529174101 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381757 | TATTGGCTTGTTCCT[A/T]CTGTGGCGTCATTAG | 9099 |
rs529212380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381282 | TGGCTCTTCCTGGCA[C/T]CCTGGGCTGTCAGCA | 9099 |
rs529439966 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377940 | TGGCTTTCTGGGGTG[A/G]AAGCCTGCTTTGCTA | 9099 |
rs529455123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119359976 | AGGCTGATGGGTAAA[A/C]GGGCAACTTCCTTTT | 9099 |
rs529528040 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119366928 | CAGGAGCAGGGAGGG[C/T]CAGATGCAGAAAGCT | 9099 |
rs529712063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119378868 | TCTGTTCTCAGCCTC[C/T]GGAGGAGCCTTTGGT | 9099 |
rs529775110 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP2 | GRCh38.p7 | 11:119367278 | TTCCCTATAGGATAA[A/G]TAATTTTTGTCACCT | 9099 |
rs529919834 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP2 | GRCh38.p7 | 11:119358510 | TAGTAGAGATGGGGT[C/T]TTGCCATGTTGGCCA | 9099 |
rs530104679 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364294 | CACCTCGCCTCTACC[C/T]CGCCCCCGGCGCCGG | 9099 |
rs530232258 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119378842 | CTTCTCCTCTAGGGC[A/G]TCATCTTTCCTCTGT | 9099 |
rs530244701 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119371141 | TGGGTTTGGATGAAT[A/C]GTTAAGCCCTGCAGT | 9099 |
rs530324045 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365958 | GGAGTGCAGTGGCAC[C/G]ATCTCGGCTCACTGC | 9099 |
rs530528950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119362659 | CCCAGAGTGACCTTT[C/T]TTACAGGACAAACAA | 9099 |
rs530796094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119369495 | GGGACACAGGATGTA[C/T]TTTTTTTTACCTCTG | 9099 |
rs530960072 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355132 | ACAAACTGGTTGAAA[C/T]AATGAAATAGATGGC | 9099 |
rs531339978 | snp | A/G | 2.28022e-05 | 0.00337647 | intron-variant | USP2 | GRCh38.p7 | 11:119373529 | CTCATGGGCTGAAAG[A/G]CAAGGAGTGTAGTTG | 9099 |
rs531389063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119374249 | GGAGTTAGGGCCCTG[G/T]GGCCTCCTAAGAGTT | 9099 |
rs531421548 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119357674 | AAGGTCCGTTTCTTC[C/T]GACTGTTCCCCTCAC | 9099 |
rs531473842 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381695 | TCATCGCGCCTGGGC[C/G]GGCAGAGCCACACCC | 9099 |
rs531783924 | snp | C/G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119375354 | GACCCTGCCTGAGAA[C/G/T]TCCAGCAGTTTTCAG | 9099 |
rs531936603 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364330 | GGACCCGAACGAGGC[G/T]ACAAGGTCGGTCCTC | 9099 |
rs531971365 | snp | A/G | | | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354823 | AGGATAGAAAATACT[A/G]CATTTGTAAGATGCA | 9099 |
rs532014099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119358099 | GGTCAGAGGTCAACA[C/T]GAAAGGACAGGAGAG | 9099 |
rs532015523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119372601 | TGTCTCCACCAGGAG[C/T]AGCCTGTCAGTCATC | 9099 |
rs532071016 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119367292 | AGTAATTTTTGTCAC[C/T]TTAAATCCTTCCTGG | 9099 |
rs532237264 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364750 | ATGGACCTTCACGGC[A/C]TAGGGGCTGAGCTGC | 9099 |
rs532261045 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119366456 | GCATATCGTCAGTCT[A/G]TGCGCATTCAGTTTG | 9099 |
rs532443595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119370537 | CCAGTTTTAGAAAGA[A/G]GTGGTCCAGGCCGCA | 9099 |
rs532451325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377043 | TACAAGAAATTTAAA[C/T]ATGGAAACTTTCAAA | 9099 |
rs532485657 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364234 | CCGGCGCCTCGGGCC[C/T]CGCGACGTCAGCGCT | 9099 |
rs532508119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, splice-donor-variant | USP2 | GRCh38.p7 | 11:119376223 | TGCCCCTTGGCATTA[A/C]CTGCACAGCTGTCCC | 9099 |
rs532732239 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356362 | TTAGCAGCGTGAAGA[C/G]GGCTCTTGGCTCATG | 9099 |
rs532910817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119361784 | TTTAAACCTGCAGCT[A/G]GAGAGAAAGGCCAAT | 9099 |
rs532943839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375552 | GAGGGAAACCATAGC[A/G]GGAGAGACAGACAGA | 9099 |
rs532958791 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119381883 | CAGAGGTGGACTGGA[A/C]TGTCACACGACGGGG | 9099 |
rs533086030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369448 | TAATGAATGCCAGCT[A/G]TAGCTCCAGTCAGCT | 9099 |
rs533238141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375014 | CAGCTACTGCGAGGC[A/G]GCATGGCTCCGCCCT | 9099 |
rs533283155 | snp | A/G | 3.70357e-05 | 0.00430308 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372723 | ATGCCGTCTCTTCCC[A/G]GGGAGCTGGAGCGGC | 9099 |
rs533454194 | snp | C/T | | | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354974 | ACTGGGGGATGGCTG[C/T]ATATTTAAATGTGTT | 9099 |
rs533483614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367489 | GATTACCACCGCAAA[C/T]GGACAGACCGGTGGC | 9099 |
rs533544008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119378904 | CCCTGACACCCACCG[A/G]GCCCAATGGGGTGGC | 9099 |
rs533641127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368071 | ATACAGCCCACAGCC[A/G]GTCTGCAAGGGATGG | 9099 |
rs533931194 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364412 | GGCCAGGCAGGCCCG[C/G]GGGGGAGGCAGGACC | 9099 |
rs533993709 | snp | A/G | 3.32414e-05 | 0.00407671 | intron-variant | USP2 | GRCh38.p7 | 11:119358256 | CAACAAAGAGATCTG[A/G]GGAAGAGAAGGCCAT | 9099 |
rs534064676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367216 | AACTGAGCTGGGCTC[A/G]TTCCTGCATCCTGAC | 9099 |
rs534179775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119371313 | TGCCCTGGGGTTGAA[C/T]AGCACCAGCCGAGTC | 9099 |
rs534204384 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364916 | GGCTCTCCCATTCTC[A/G]AATTTGACTTGTTTT | 9099 |
rs534390610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP2 | GRCh38.p7 | 11:119376331 | AGGACGGGCACTCAC[A/G]TGGCTGCGAGTCTCC | 9099 |
rs534454476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119363703 | CCTGAGGAGGGGGCA[G/T]TCCTTGCCAGGAGAC | 9099 |
rs534506822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377407 | AGGATCCAGGTGTCC[A/G]TCATCCAGTAACAGC | 9099 |
rs534520909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119370695 | TGGCAGTATCTTCTG[A/G]GGCATGAGCTCAGAA | 9099 |
rs534552744 | snp | C/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119376117 | TTCCTACTGGGGCCG[C/G]GGCCTTCCACATGTC | 9099 |
rs534640551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119362827 | GAGAAAGTTTGGACC[C/T]AGTCTTCCTTCCATT | 9099 |
rs534695589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119374644 | GTCAGTTGGGGACCC[C/T]CAGAGGCCTTCCATC | 9099 |
rs534695600 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382811 | TCGGCTCACTGCAAC[A/C]TCCTCCTCCCGGGTT | 9099 |
rs534731375 | snp | A/C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383495 | GGAAAGAGTGGGAGA[A/C/T]GCGATCAGAGAGGTC | 9099 |
rs534802439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375323 | GCTTCCATATAGGCC[C/T]GGAACAGCATTCCTT | 9099 |
rs534823049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368482 | TCCGCTCACTGCAGG[A/G]CAGCATTCAAGTCCA | 9099 |
rs534883599 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356039 | CAACTAAATTCCATT[A/C]AAAACATTAAAAAAA | 9099 |
rs535070080 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119369112 | CACTTGGGTTAGTGA[A/G]CACTTTTTTTCCACC | 9099 |
rs535136718 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383025 | TGTGAGCCACTGCAC[C/G]CGGCCCCAGCTAATT | 9099 |
rs535421302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367743 | ACCTCCTTCTTTTGC[A/G]TGTGTCTCCGTCTGG | 9099 |
rs535641832 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380212 | TTGAGCCACTGCTCC[C/T]GGCCGGAAGTGTGCC | 9099 |
rs535682228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379251 | TGCTCACCTTGAGGG[A/G]CTGCCCTTTCGGGCC | 9099 |
rs535695084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119373628 | AGAGCTCCCAGTCCA[C/T]TTCCACAAGAGGCAG | 9099 |
rs535871695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375792 | GAATTGGTATTCTTC[A/G]GGCAGCGCCCCAAGC | 9099 |
rs535922039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119372288 | TAAAGCCTGCACAAG[A/G]GGGGAGATGCAACCA | 9099 |
rs535972126 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378158 | AATGTGCTGACCTTG[A/G]AGGACAAGGTGGGTG | 9099 |
rs536049463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365479 | TGGTGATCTCTACAG[C/T]CACTGTCCTCACCCA | 9099 |
rs536183953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119358345 | TTTTTGAGATGGAGT[G/T]TTGCTCTGTCCCCCA | 9099 |
rs536185418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119366131 | AACTCCTGACCTCAA[C/G]TGATCCGCCCACCTC | 9099 |
rs536224379 | in-del | -/ACCCCGGGTCTGGCTCTCTGCCCGCTTACC | 8.25716e-05 | 0.00642487 | intron-variant, cds-indel | USP2 | GRCh38.p7 | 11:119373187 | TAAAGGCCGCTCAGT[lengthTooLong]ACCCCCAGTGATGTC | 9099 |
rs536239142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363053 | ACACTTGAGACCCCA[A/G]TCAAGGGCTTTCCCG | 9099 |
rs536310707 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365534 | GACAAACTGCAGCAG[A/C]CTTTCTCCAAGCCTC | 9099 |
rs536317995 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356634 | GTCCAGGCGATCTTC[C/T]CTGCCGGGCCACAGC | 9099 |
rs536355118 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383359 | AACTACACATAAGTG[C/T]GGGGAAAGAATGTTC | 9099 |
rs536379376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363660 | GGACCTCCACCCGGG[G/T]AGGGGACCACGAGTA | 9099 |
rs536834935 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383409 | AAGTAAAGGTCCTGA[A/G]GTGGGAGCGACCTGC | 9099 |
rs537181159 | snp | C/G | | | synonymous-codon | USP2 | GRCh38.p7 | 11:119359589 | CAGGTCCCGCATGTA[C/G]AGCCTCTGGAGGCAG | 9099 |
rs537255168 | snp | C/T | 1.7309e-05 | 0.0029418 | missense | USP2 | GRCh38.p7 | 11:119360188 | GAAAAACTCACCGTG[C/T]TCCCAAGGTTTCGAA | 9099 |
rs537271260 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119379234 | TTAAAGGGGCAGTGG[C/T]GTGCTCACCTTGAGG | 9099 |
rs537444219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119366444 | CTCTCCATTACTGCA[C/T]ATCGTCAGTCTATGC | 9099 |
rs537520783 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119374487 | TGAATTTTAATCTAT[C/G]TGTTATACAGATGGG | 9099 |
rs537557573 | snp | C/T | 0.000162324 | 0.00900755 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119381942 | CGTCATGGGAGAAGG[C/T]TCGGAACTTGAGCCC | 9099 |
rs537569025 | in-del | -/GCGGGGGC | 0.0190459 | 0.0957089 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364041 | CGCTTAACGTTGGCA[-/GCGGGGGC]GCGGGGGGAGTCCCC | 9099 |
rs537754781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119378993 | GCTCAGATACCAAAG[A/G]GGCAGCTACTGACCT | 9099 |
rs537863257 | snp | A/T | 0.0290055 | 0.116882 | intron-variant | USP2 | GRCh38.p7 | 11:119358323 | TGCACAGCAGCTTTT[A/T]TTTTTTTTTTTGAGA | 9099 |
rs537908972 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119376211 | AGCCTGGGTTGGTGC[C/T]CCTTGGCATTACCTG | 9099 |
rs538110242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380064 | GGACTACAGGCTCCC[C/G]CCAGCACGCCCGGCT | 9099 |
rs538258474 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119369702 | GTGGGCAGGGCGGGC[A/G]TGATTGTTCCCTTTT | 9099 |
rs538292766 | in-del | -/T | 0.0236976 | 0.106241 | intron-variant | USP2 | GRCh38.p7 | 11:119358324 | CACAGCAGCTTTTAT[-/T]TTTTTTTTTTGAGAT | 9099 |
rs538321234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377517 | CGAGCCCCAGAACAA[C/T]ACTGATAGGCCGAGA | 9099 |
rs538438424 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119371399 | TTCCCCACCATGCCA[G/T]CTCTGTTGTGACACA | 9099 |
rs538466854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119363625 | GCCACCGAGAGGGAG[A/G]GGGCAAGGGGGACTT | 9099 |
rs538513131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365277 | ACAGCTACATGGGGA[C/T]TGTGTCCAGGACACA | 9099 |
rs538573591 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP2 | GRCh38.p7 | 11:119372203 | AGTATGCCAGTGTCA[C/T]TCAGAGGAGAGTCCC | 9099 |
rs538573706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364548 | GAGCTTCCCCCAAGG[C/T]ACCATTACACTTCCT | 9099 |
rs538839177 | snp | A/C | 0.0150606 | 0.0854603 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356061 | TTAAAAAAAAAAAAA[A/C]AAAACCCAAACCCCC | 9099 |
rs538910937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375397 | TCAGAAAGGCCTGGT[C/T]CATCTTACTGTCTAG | 9099 |
rs539021217 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377474 | GATTTTCCACTGCAG[A/G]TGAATGAAAGTGAAG | 9099 |
rs539039275 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383603 | AACAGGGTTGTCCAA[A/T]CTTTTGGCTTCCCTG | 9099 |
rs539095573 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119362967 | CGGGGGCTCAGGAGA[G/T]CCCTGCCTGGGTTAA | 9099 |
rs539125122 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355244 | TATTATTTATTCTGT[A/G]CAAGGTTCCACTGTA | 9099 |
rs539326366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119360465 | ATCTCACGCTGTCAC[C/T]CAGGCTGGAGTGCAG | 9099 |
rs539481673 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382276 | GAGGAAAATCGCACA[A/T]CCAGGTAGCTGGGTA | 9099 |
rs539719572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368282 | TGATCCCGGGGTGGG[A/G]GTAGGTAAGGACAGA | 9099 |
rs539782398 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP2 | GRCh38.p7 | 11:119374458 | TGTGGAGCTTTGAGA[A/G]CCCCAGAGGATCATG | 9099 |
rs539819058 | in-del | -/G | 0.0134861 | 0.0810011 | intron-variant | USP2 | GRCh38.p7 | 11:119361609 | ATGAGGTTGTCAGCT[-/G]GGGGGGGAGGGGTGT | 9099 |
rs539948302 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356061 | TAAAAAAAAAAAAAA[-/C]AAAACCCAAACCCCC | 9099 |
rs539989778 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | USP2 | GRCh38.p7 | 11:119358060 | ACCTCAGGATAACCT[C/T]GCTGGGAAGGGGAAA | 9099 |
rs540153221 | snp | A/G/T | 4.98511e-05 | 0.00499234 | synonymous-codon | USP2 | GRCh38.p7 | 11:119359544 | CCTCTCACCTTCCAC[A/G/T]AGGGCTGTGTGTGCA | 9099 |
rs540214640 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365746 | ACTGCTGTCAACCAG[C/G]CTGTGCTTATCCTCT | 9099 |
rs540275098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119358434 | GATTCTCCTGCCTCA[A/G]CCTCCCAAGTAGCTG | 9099 |
rs540334066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368577 | TGGAACCCAAGGCTT[C/G]GGAAGATGAGTCAGC | 9099 |
rs540446373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369944 | AGCGCTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 9099 |
rs540483562 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364122 | CAGGACAGCGTCCGC[A/G]GCGCCCGAACGCGCG | 9099 |
rs540493411 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119362033 | CACAACAGAATACCC[A/G]CCCTTACGTCTATTT | 9099 |
rs540538541 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355838 | ACTTGATGCCCTGTC[A/G]GAAGGAATCTACCTG | 9099 |
rs540583754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363135 | AAGCCTGGTGTGGCC[C/G]TGGCACGGGGCAGGG | 9099 |
rs540798267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119362219 | GGGAAATGGGAAAAC[A/G]GAGTCATCTGTCTAC | 9099 |
rs540859877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369370 | TTGCCTATTACTGTT[A/G]ATGAGGGAAAGAAGT | 9099 |
rs541014805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119374965 | AACAACACGTGAAGG[A/G]CTCCACAATGACAGT | 9099 |
rs541016483 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383029 | AGCCACTGCACCCGG[C/T]CCCAGCTAATTTTTT | 9099 |
rs541053553 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382440 | CAGAGAAATCAGACG[A/C]AATCAAGAGGGGAAT | 9099 |
rs541151717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375524 | AACTGGGGGATGATG[A/T]CACACAGCGTTAGAG | 9099 |
rs541214914 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354866 | ATAGAAGGCTGATTT[G/T]CATATACGCAGGTTC | 9099 |
rs541349405 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381557 | GCGCTGGCGCGGCGC[A/G]GTGAGCACCAGCTGA | 9099 |
rs541375380 | snp | G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119358271 | GGGAAGAGAAGGCCA[G/T]GAGATGCTGAAATAC | 9099 |
rs541392541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367963 | TCATGAAGACATCCT[A/G]GAGTGGGGGTGGAGG | 9099 |
rs541451864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119373949 | TCAGGAGTTAAGACC[A/G]CATCTGTCCCTTCTG | 9099 |
rs541489887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119361421 | AACAGTTTGCAGATG[A/C]GTCTGCCACCCCCTC | 9099 |
rs541532450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377557 | GGAAGCCTCCATTTC[A/G]CCCACTGTGCCAAGC | 9099 |
rs541550939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119360622 | TAGAGACAGGGTTTC[A/G]TCATGTTGGCCAGGC | 9099 |
rs541673705 | snp | C/G/T | 3.29648e-05 | 0.00405974 | missense | USP2 | GRCh38.p7 | 11:119359082 | TCACTCGGTTCACCT[C/G/T]GTTATGGAGCCCATC | 9099 |
rs541697441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119372459 | CAGCAGAGCATTCCT[A/G]AGAACACTACTGGAC | 9099 |
rs541734741 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP2 | GRCh38.p7 | 11:119358536 | GGCCAGGCTGGTCTT[A/G]AACTCCTGACCTCAG | 9099 |
rs541986290 | snp | A/C/G | 9.96321e-05 | 0.00705742 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119372928 | TGGCTGTCTGGTAGA[A/C/G]CCCCTGCAGGGTGCA | 9099 |
rs542121594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119366467 | GTCTATGCGCATTCA[A/G]TTTGCATGGTGTTAA | 9099 |
rs542292372 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376603 | ATCTTCACTGAGGTG[A/T]CCTGACCCTTCCTTC | 9099 |
rs542373553 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383684 | AACACTAAAGATAGC[G/T]GATGAGCTTTAAAAA | 9099 |
rs542436075 | snp | C/G | 4.94205e-05 | 0.0049707 | intron-variant | USP2 | GRCh38.p7 | 11:119357952 | GTCCCACGGAAATTT[C/G]TTCTTGCTATTACCG | 9099 |
rs542492865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119362201 | TCAGTGCTAATGGGG[A/G]TAGGGAAATGGGAAA | 9099 |
rs542648092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119370250 | CAGGGACTGTTGCTC[A/G]CACACATCTCTTGCC | 9099 |
rs542698389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364637 | GGGCGAAATACGTAT[A/G]TGCACAAACTTTTGT | 9099 |
rs542741814 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356196 | GGAAAAGCAATAAAA[A/G]GACCAGTGCAACGTC | 9099 |
rs542761446 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, missense, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119363958 | AAGGGGGCGGCGGGG[A/G]GGTCCTCGGGCAGGG | 9099 |
rs542792608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368631 | AGGTATTCAGTTTCC[A/C]AGACCTTTTGCTCCT | 9099 |
rs542929732 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | USP2 | GRCh38.p7 | 11:119361612 | GAGGTTGTCAGCTGG[C/G/T]GGGGAGGGGTGTGGG | 9099 |
rs542930308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119376136 | CTTCCACATGTCTCT[C/T]CCCTCCCGCAACCCC | 9099 |
rs542969476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369226 | CCCTGGCCTGGCATT[C/T]TGTTGGTGCTTACAC | 9099 |
rs543008616 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381718 | CCACACCCCGCGTCT[C/T]GCGTCACTGAGTCGC | 9099 |
rs543235292 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381099 | CGCCCCTAACCCCCT[G/T]TAGCAAACTGACCGG | 9099 |
rs543637654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119360556 | AGCCTCCTGAGTAGC[G/T]GGGACTACAGGTGTG | 9099 |
rs543830677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380488 | CCAGGGCCACAGAGC[C/T]GGGCTGGGCAGGGTC | 9099 |
rs543838425 | snp | G/T | | | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355249 | TTTATTCTGTACAAG[G/T]TTCCACTGTACATTA | 9099 |
rs543893737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119367866 | GGTGGTCAGTGGAGC[A/G]GCTCCCCCAGGGGCA | 9099 |
rs543950972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367358 | AGCTCTATGAGGGCG[A/G]GGACTGAGAGTATTC | 9099 |
rs544108613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377818 | TGCCCAGCCAGGGGA[A/G]GGACTTGCTCCCCAG | 9099 |
rs544119409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119372424 | AAAAGGAGAAGGTGA[A/G]AAGAGTGGTTCATTG | 9099 |
rs544119587 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364764 | CCTAGGGGCTGAGCT[C/G]CCCTCCTCAAAACAG | 9099 |
rs544670375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119376079 | CTGACTTCTAGCTAC[A/T]GTTCCCATGCCTGCG | 9099 |
rs544707105 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383636 | TTATGGTAGAAGAAG[A/G]ATTATTGTTTTGGGC | 9099 |
rs544785816 | snp | A/C | 0.00557542 | 0.0525036 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356399 | GACCGGCGAGCCGTG[A/C]GGGTGGAGATGGGCG | 9099 |
rs544815845 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119363803 | CCAGGGAGAAGGCGG[C/G]ACCCCAGGCCCTCGG | 9099 |
rs544934286 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365853 | TCCCAGTTAATTTCT[A/G]TAACATCATGCTGTA | 9099 |
rs545147351 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355660 | CAAAGGGCCTATTGT[C/T]TAGGAGGCTCTGAGA | 9099 |
rs545261912 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382199 | AAAGCCGAGACAAAA[C/G]TTGAATTTTTGCTGC | 9099 |
rs545316454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119368122 | TTCTAGTCACAAACC[A/G]CAAACCCACTGCCCT | 9099 |
rs545520215 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354985 | GCTGTATATTTAAAT[A/G]TGTTTGTAAACAATT | 9099 |
rs545564557 | snp | A/G | | | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354995 | TAAATGTGTTTGTAA[A/G]CAATTGGTGAATCCA | 9099 |
rs545612274 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381644 | GCCCAGAAGGGACCT[C/T]CCCGGGAAATCGGCG | 9099 |
rs545782190 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377019 | ATTTTCACAATTAAA[A/C]AATAAATATACAAGA | 9099 |
rs546043047 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380362 | AGCCCATCTGGGCTC[C/T]TTCCCCCTTTGCCTA | 9099 |
rs546247582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119378528 | TTGGGTCCATTTCTC[C/T]TTCTTGTGCTCCCAG | 9099 |
rs546599913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363603 | AGAGCCACCACCTGG[A/T]GCCGGGGCCACCGAG | 9099 |
rs546615860 | snp | C/G | 1.66222e-05 | 0.00288285 | missense | USP2 | GRCh38.p7 | 11:119357253 | GCTGTATAGTGGCCA[C/G]CCATGGTGGTTCCGG | 9099 |
rs546631346 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382849 | TTCTTGTGCCTCAGC[C/T]TCCCCCGAGTAGCTG | 9099 |
rs546758870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119362899 | GTTGCAGGGAGCAGA[C/T]GGCACCTTCACCATC | 9099 |
rs546782302 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356202 | GCAATAAAAGGACCA[C/G]TGCAACGTCCCAGCT | 9099 |
rs546788362 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355210 | AGATTCCAACATCTG[C/G]CAACTGATTTCTCAA | 9099 |
rs546878628 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356512 | GCTGCGGCGGGAAGC[A/G]GCGCAGCGAGGGTCT | 9099 |
rs547021443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367483 | GCCTGCGATTACCAC[C/T]GCAAATGGACAGACC | 9099 |
rs547313211 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119372633 | GTCAGGTTGGGAGTC[C/G]AGCCCTCAGCCTGGC | 9099 |
rs547493673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119361063 | AAACTCAAGTAAGCC[C/T]GCCATTCTGAATTGC | 9099 |
rs547567034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381358 | CAGCCGGCTCTCTCC[C/G]TATATTTCTAGTGTC | 9099 |
rs547661876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119366137 | TGACCTCAAGTGATC[C/T]GCCCACCTCAGCCTC | 9099 |
rs547724826 | snp | C/T | 0.000456838 | 0.0151066 | intron-variant | USP2 | GRCh38.p7 | 11:119372685 | TCCCCAGCCTATCCC[C/T]GGTCCCCAAGGGTAA | 9099 |
rs547725386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119373644 | TTCCACAAGAGGCAG[A/G]CTGGCTGCTGAGAAG | 9099 |
rs547727442 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119381819 | ACCGATATACACAGA[C/G]AACCACGTGGAGGAA | 9099 |
rs547789984 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119360010 | AGTGCTTCCTGCTGG[C/G]GGTGGGTAAAGCACA | 9099 |
rs547852039 | snp | A/G | 5.02887e-05 | 0.00501416 | intron-variant | USP2 | GRCh38.p7 | 11:119359488 | CAGCCCCAGTGGAGT[A/G]GAGGAGCATCCGGGG | 9099 |
rs547872500 | snp | C/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119371196 | ACCCCACTTTAAGGA[C/G]CACTGCTGACCATGA | 9099 |
rs547893754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119378877 | AGCCTCCGGAGGAGC[C/T]TTTGGTCTTGCCCCT | 9099 |
rs548021731 | snp | C/G | 1.65086e-05 | 0.00287298 | intron-variant | USP2 | GRCh38.p7 | 11:119357599 | TTCAGATCTGGCATT[C/G]ACGTGAGTCAAGGAT | 9099 |
rs548079365 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119371031 | TGTAGTTTAGTCTGC[A/G]CTGAGGTTTTCCATC | 9099 |
rs548252462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119371180 | CACAGGCAGTCTGCA[A/G]ACCCCACTTTAAGGA | 9099 |
rs548277335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364327 | CGCGGACCCGAACGA[A/G]GCGACAAGGTCGGTC | 9099 |
rs548342612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377321 | AGACCCCTGCTTCAC[C/T]CTTCCCTGGCTCTCC | 9099 |
rs548405937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364989 | GCTCAGCTGGCATGG[C/G]GCGAGTGTTCTACTC | 9099 |
rs548850719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP2 | GRCh38.p7 | 11:119376297 | CCCTGGCCGGAGTCT[C/T]GCTGCGCAAGACAGG | 9099 |
rs548865420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119375705 | TCAGATACAATCCCC[C/T]CAACAAGGGTATGAG | 9099 |
rs549010492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369502 | AGGATGTACTTTTTT[A/T]TACCTCTGTTTCTCC | 9099 |
rs549064024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363245 | GGCAGCGCCCAGCCT[C/T]GGCCCCGGCATTCCC | 9099 |
rs549117342 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356459 | CGGTGATGCTCCCAG[A/C]GAGCTCCAGAGGGCG | 9099 |
rs549127007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368999 | TTCCATAGACCCCGG[A/G]AACAGGAGAAGTGGG | 9099 |
rs549207842 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP2 | GRCh38.p7 | 11:119368203 | AAGGTCCTTTAGTGA[C/T]CTTCTCATGCTGCCA | 9099 |
rs549208796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375256 | GAAAGCTCTAGAATC[C/G]CAGTCCACACAAGGC | 9099 |
rs549357649 | in-del | -/TGGC | 0.00517822 | 0.0506191 | intron-variant | USP2 | GRCh38.p7 | 11:119361799 | GAGAGAAAGGCCAAT[-/TGGC]TGGCAGCAGGTGGGA | 9099 |
rs549367776 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355140 | GTTGAAACAATGAAA[C/T]AGATGGCCCCTAATA | 9099 |
rs549469215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367680 | GCTCTGTGCACCTTT[A/G]AGCCCAGGCAGTCTG | 9099 |
rs549521675 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119368995 | GTCCTTCCATAGACC[C/T]CGGGAACAGGAGAAG | 9099 |
rs549539301 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119357915 | TCAACTGGATCTGCT[A/G]GTATCAGCCTCTTCC | 9099 |
rs549617817 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355640 | CATCCCTGAGAAACT[C/G]GGTCCAAAGGGCCTA | 9099 |
rs549793730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380990 | CACCGCGTGCCTGCT[C/T]CTGGTTTGGGACTGG | 9099 |
rs549901604 | in-del | -/TAA | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365338 | GCAGCAATTTCATGC[-/TAA]TGAGAGAGGGATGGG | 9099 |
rs550181137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119366878 | GCCAGCTTGCTCTCC[C/T]TCTTCCCTGGGATTT | 9099 |
rs550341664 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364261 | CGCTGGGGCGGGGCC[A/T]GGCCCTAAGCCCCGC | 9099 |
rs550364735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119372243 | GATGTCTTATGTCCA[A/G]ATGTAAAGCCAGGCC | 9099 |
rs550575715 | in-del | -/A | | | intron-variant | USP2 | GRCh38.p7 | 11:119368795 | GGAGGGCCCTGGGCC[-/A]ACCCCTGGATCTTCT | 9099 |
rs550621045 | snp | A/G | 5.13817e-05 | 0.00506836 | intron-variant | USP2 | GRCh38.p7 | 11:119357352 | AGGCCCCCCTGCCCC[A/G]ACTTCCCCCCTCCAA | 9099 |
rs550657786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP2 | GRCh38.p7 | 11:119376248 | TGTCCCTGGAGGCCA[C/T]AGAATGCACTATGGG | 9099 |
rs550694753 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119374382 | GTGGCATTCCCAGTC[-/CTT]CCCTGCTCCAGTCCT | 9099 |
rs551151684 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119369150 | TTCCTCCTCTCTGCA[-/T]TTTAAGCAGAAGGTG | 9099 |
rs551339656 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119361817 | GCAGCAGGTGGGATA[A/T]AAGCATCCTTAGAGA | 9099 |
rs551377804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369450 | ATGAATGCCAGCTGT[A/G]GCTCCAGTCAGCTAT | 9099 |
rs551440761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368916 | GAGGGGTGGAGCTGA[C/G]GGGGATTAGGAAGGA | 9099 |
rs551474929 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355262 | AGGTTCCACTGTACA[C/T]TAGACATTCTTCTAC | 9099 |
rs551604989 | snp | C/T | 3.66885e-05 | 0.00428286 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373452 | GCCGATTCTGTGTAG[C/T]GCTTCAGGGTGGAGG | 9099 |
rs551718305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375023 | CGAGGCAGCATGGCT[C/T]CGCCCTCTGAAGGTC | 9099 |
rs551746389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119360806 | TATGTATCTCCCTGC[C/T]CCCCATCTTTATGTT | 9099 |
rs551798553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119378932 | GGCCTCTCACATGCT[C/T]TCCCAGATTCACTGA | 9099 |
rs551799628 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP2 | GRCh38.p7 | 11:119378455 | TCAGGGGCTAGCACC[C/T]GCTGATCCACCAGCC | 9099 |
rs551823925 | in-del | -/A | 0.00282542 | 0.0374797 | intron-variant | USP2 | GRCh38.p7 | 11:119362668 | CCTTTCTTACAGGAC[-/A]AAACAATCCTACCTC | 9099 |
rs552071331 | snp | A/G | 1.76052e-05 | 0.00296686 | intron-variant | USP2 | GRCh38.p7 | 11:119360174 | AAGAAGCAGGCCAGG[A/G]AAAACTCACCGTGTT | 9099 |
rs552601623 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119372489 | CTATCCTCGAGTGCG[C/T]GGGCCCTGAGTGGGC | 9099 |
rs552650134 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119372067 | AGAGCCTCTTCCCTC[A/G]TTCCAGCTGAGGCAG | 9099 |
rs552662850 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365987 | GCAACCTCTGCCTCC[C/T]GGGTTCAAACAATTC | 9099 |
rs552758503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377426 | TCCAGTAACAGCATG[C/T]GGTGTACAGACTCTG | 9099 |
rs552920014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119378073 | AGTCCCAGCCAGTCC[C/T]GCCAGGTGGTTGGGA | 9099 |
rs553191497 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355576 | CAGGCTCCAGCTCCC[A/G]GGGCAGGACTGGAGA | 9099 |
rs553231473 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382069 | TTTTTCTCTGCTGTC[A/G]AAGACACTCTCCGCT | 9099 |
rs553282367 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376978 | CTTTGGACAGATTAA[-/AT]ATTATTTAAATTAAA | 9099 |
rs553312283 | snp | C/T | 0.000627254 | 0.0176984 | intron-variant | USP2 | GRCh38.p7 | 11:119360417 | AATGCCTGTGATTTT[C/T]TTTTCTTTTCTTTTT | 9099 |
rs553328386 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356058 | ACATTAAAAAAAAAA[A/C]AAAAAAACCCAAACC | 9099 |
rs553334685 | in-del | -/AACTT | 0.00238897 | 0.0344787 | intron-variant | USP2 | GRCh38.p7 | 11:119358878 | TGGGTCAAAGCTCAA[-/AACTT]AAGTTTAAGGGTCTG | 9099 |
rs553386801 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376748 | CACCCCAGCTGGCTG[A/G]TGCTGATCACCTCTG | 9099 |
rs553441354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119361449 | CTCTCTCAGGGAGGG[C/G]ACTGGGAGCAGGCAA | 9099 |
rs553475922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119360374 | CAACTTTACCCATCT[A/G]TGTACTTTGTAGGAA | 9099 |
rs554232006 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119369060 | GGGGCTCCTGGGTCT[C/T]TGCAGGGCTGAGCCA | 9099 |
rs554240989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119371699 | CAAAATGTATTTGTC[C/G]TAGGAGTAGGGAGGG | 9099 |
rs554507207 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356210 | AGGACCAGTGCAACG[C/T]CCCAGCTATGAAGAG | 9099 |
rs554645870 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356764 | GTTGTTGTTGTTTTG[C/T]TTTTGTCTTTTTAAA | 9099 |
rs554660846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119372341 | CAGGGTGCACTGGTG[G/T]TCTGGGCCCCCCCGC | 9099 |
rs554699683 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383410 | AGTAAAGGTCCTGAG[A/G]TGGGAGCGACCTGCC | 9099 |
rs554972228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119370605 | GCTCCAGGAAATGAC[A/G]ATAAGGGGTGGAGAG | 9099 |
rs555298611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368373 | GCTGCGTGAACGGAG[C/T]GAGAACATGAGGGAC | 9099 |
rs555440869 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119355469 | AACAGCTTTACTCTC[C/T]AGGACAGCACAGAGT | 9099 |
rs555563375 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119361323 | TGGATCGAGGACTCT[C/G]AGCTTATTTGTCAAG | 9099 |
rs555701931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119361906 | AGTCAGCAAGAGGGC[C/T]GCAACAGAGATAATT | 9099 |
rs555705180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367226 | GGCTCATTCCTGCAT[C/T]CTGACTGCCGTTCCT | 9099 |
rs555708722 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365205 | CTGTTACTCATCTGT[A/G]GGCTCCTTCTGTTCC | 9099 |
rs555768503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119366445 | TCTCCATTACTGCAT[A/G]TCGTCAGTCTATGCG | 9099 |
rs555842144 | snp | C/T | 9.95041e-05 | 0.00705281 | intron-variant | USP2 | GRCh38.p7 | 11:119359674 | CACTGCAAGAGATGA[C/T]CAGGCAATCAGTGGG | 9099 |
rs556002679 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP2 | GRCh38.p7 | 11:119376338 | GCACTCACGTGGCTG[C/T]GAGTCTCCCTGTTGC | 9099 |
rs556296655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP2 | GRCh38.p7 | 11:119379049 | TGGGGGCTTCTCCTT[C/T]CCCAGCAGGGCAGGG | 9099 |
rs556303000 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119360514 | CTGCAACCTCCACCT[C/T]GTGGGTTCAAGCGAT | 9099 |
rs556655360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376453 | GCCCAGTGCGGGGGG[C/T]CCCTGCTGCCCAGCT | 9099 |
rs556762841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364569 | TACACTTCCTAACTC[C/T]TGAGGGGGCTGCAAA | 9099 |
rs556899856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365407 | TGGGAGGAGGGGGCA[C/G]GGGACAGGAACCACA | 9099 |
rs556903048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119362041 | AATACCCACCCTTAC[G/T]TCTATTTTTGGCAGT | 9099 |
rs556917130 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119356114 | CCCAGGTCTACTGTG[A/G]CTGTGCTTGGGGCCT | 9099 |
rs557002246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377550 | TGGTCCAGGAAGCCT[C/T]CATTTCACCCACTGT | 9099 |
rs557041953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119362992 | GGTTAATGCAGAGGT[A/G]GCATCTGGGCACCCT | 9099 |
rs557083310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119370859 | TGGCCCTGGAGCCGG[A/G]GGGAGGAGCCAGGGT | 9099 |
rs557098761 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | USP2 | GRCh38.p7 | 11:119356561 | TGTTTCTGACACATA[A/G]GAAGACCACAAGTTT | 9099 |
rs557105228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119374750 | GGGCATCAGGGGCTC[C/T]TGGGGGGCTTTCTAG | 9099 |
rs557154114 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119361031 | AAACACCTTGAGTTT[C/T]GATCTTCAGTTGGGA | 9099 |
rs557219256 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383675 | AAATACACTAACACT[A/T]AAGATAGCTGATGAG | 9099 |
rs557245286 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382858 | CTCAGCCTCCCCCGA[C/G]TAGCTGGGATTACAG | 9099 |
rs557354329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375460 | CCTTCATGTACACTC[C/T]TTTGCCCACTGTGCC | 9099 |
rs557420425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380246 | CTAATGCCAGAGAAC[A/G]GTCCCTTGGTTTTCT | 9099 |
rs557513269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119361214 | TGGAGATGGCAGATT[C/G]GGCCCGCAGAGGCAA | 9099 |
rs558014970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119373724 | ACACCTCGGTGAGAG[C/T]GCGAGGGATGAGGTG | 9099 |
rs558015012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119367344 | TGAAAGTTAGGGCTA[A/G]CTCTATGAGGGCGGG | 9099 |
rs558037004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119360515 | TGCAACCTCCACCTC[A/G]TGGGTTCAAGCGATT | 9099 |
rs558102481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380405 | AAGTGCAGCTTCCCC[C/T]AGGCCACCAGGAGAA | 9099 |
rs558276463 | snp | G/T | 1.654e-05 | 0.00287571 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373294 | GGCCATAGGTACGGG[G/T]ACGGGTGAGGAAGCT | 9099 |
rs558331615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119376059 | ATGGAAGCTGCCTCT[C/T]GGCTCTGACTTCTAG | 9099 |
rs558625397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119366187 | GGCGTGAGCCACCAC[A/G]CCCGGCCTATTACCT | 9099 |
rs558995786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119363754 | GGCTGGGAAGAATCC[A/G]TCCCCTCACCTAGGG | 9099 |
rs559166074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119370741 | ACTGCAGGGCATTCC[C/T]GGCTAAAGTGCCTTA | 9099 |
rs559177584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369384 | TAATGAGGGAAAGAA[C/G]TCTGGCTAGAACTGT | 9099 |
rs559237180 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119376407 | CAGTGGGAGGCAAGC[C/T]AATTGGCTGGGATCC | 9099 |
rs559258081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119368745 | CCCTGGCTCTGCCTC[C/T]GAGTTGCAGGTGCCC | 9099 |
rs559378524 | in-del | -/CGGGGGTCC | 0.00161063 | 0.0283323 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119363821 | CCCAGGCCCTCGGCG[-/CGGGGGTCC]CGGAAAAGGGCCCGC | 9099 |
rs559397218 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119374999 | TACCATCTCCTCCCC[C/G]AGCTACTGCGAGGCA | 9099 |
rs559478072 | snp | A/G | 0.000189804 | 0.00973992 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373421 | CGACTTGGCATAGTG[A/G]GCATCTGTGTAGCGG | 9099 |
rs559521383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368048 | CAGTACCAAGGCTAA[C/G]GGCCAGGATACAGCC | 9099 |
rs559620062 | snp | C/T | | | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354740 | CAGAATAAAGTACAG[C/T]TGACCTTTGAACAAT | 9099 |
rs559680512 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119382519 | CAGTGAAAGAGGCAC[C/T]CCTGTTCTTGTCCAA | 9099 |
rs559886183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119358559 | GACCTCAGGTGATCT[A/G]CCCGCCTTGGCCTCC | 9099 |
rs560027726 | snp | A/G | 1.65269e-05 | 0.00287457 | intron-variant | USP2 | GRCh38.p7 | 11:119359146 | CTGACTGAACCCAAA[A/G]GAAGGAGGGTGAGCA | 9099 |
rs560062977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119366473 | GCGCATTCAGTTTGC[A/G]TGGTGTTAATCTATC | 9099 |
rs560247011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119371976 | GAAAAGGCAGATGTC[A/G]TCAGTGCCCCAAGAG | 9099 |
rs560439950 | snp | G/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119361481 | TCTGGAGCAACACTG[G/T]GGCATGCGTGGGGCC | 9099 |
rs560481885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119378485 | CTAATCCTCTTGCCT[A/C]CCCTGGCAGGGGGTC | 9099 |
rs560708816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119368502 | ATTCAAGTCCAAAGT[C/T]CCACCCCAGGGAAAA | 9099 |
rs560715050 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | USP2 | GRCh38.p7 | 11:119357981 | CGAAGGGTGACTTAC[C/T]GGCTTTTCATCTCCA | 9099 |
rs560750521 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119383700 | GATGAGCTTTAAAAA[A/C]AACTCATAATGTTTT | 9099 |
rs560884960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119376150 | TCCCCTCCCGCAACC[A/C]CCAGTTTCACTCTCA | 9099 |
rs560973962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119370997 | ATACTGCTGTCATGA[C/T]TGGGGCTGAGGGTGG | 9099 |
rs560995235 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355815 | GCTAGAGGACGTGGG[C/T]GGGAAGAACTTGATG | 9099 |
rs561256222 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355149 | ATGAAATAGATGGCC[C/T]CTAATATACTAGGAG | 9099 |
rs561507298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119369341 | AGCTGAGTCTGTGAT[A/G]TTCAAAGTTCGTGTT | 9099 |
rs561689698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119374326 | TCCTGGCGATGCTTG[C/T]GCAAAGGGGGCCCCC | 9099 |
rs561891891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119360617 | TTTAGTAGAGACAGG[A/G]TTTCGTCATGTTGGC | 9099 |
rs561902287 | snp | A/C/G | 0.000177132 | 0.00940929 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119381425 | GAGCTCCAAACCGGC[A/C/G]CTGATCCCCGAATCC | 9099 |
rs562152744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119359936 | GTGATGGGCATCCTT[C/T]AGGGGAATGATCCAG | 9099 |
rs562221523 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | USP2 | GRCh38.p7 | 11:119366825 | ATGACTTAGACACAG[C/T]GATGTAAGCACTCCC | 9099 |
rs562293419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364866 | GCTCCTGAAAAGAAC[A/C]TTTTCTGGTCTCTTC | 9099 |
rs562405453 | snp | C/T | 1.65957e-05 | 0.00288055 | intron-variant, synonymous-codon | USP2 | GRCh38.p7 | 11:119373064 | TGATTGGCTGTCCAG[C/T]TTCTGGGTTAGGGTC | 9099 |
rs562419332 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | USP2 | GRCh38.p7 | 11:119369137 | TCCACCATCACTGTT[-/C]CTCCTCTCTGCATTT | 9099 |
rs562494648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119372432 | AAGGTGAGAAGAGTG[A/G]TTCATTGGGCGCAGC | 9099 |
rs562618939 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP2 | GRCh38.p7 | 11:119371098 | AAGAGCAGCTTCCCA[G/T]GCCCCATCCCGAGAG | 9099 |
rs562716794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119371851 | CCATTCATCCCTGCA[A/G]TCAGCAGGTCAGCCC | 9099 |
rs562877885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119377247 | CCAAAGTCACACTGG[A/G]AGCAGTGGCAGAGCT | 9099 |
rs563062231 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | USP2 | GRCh38.p7 | 11:119357124 | GGTTTGGGGGGAGGG[G/T]GGAGGAGTGGGGGGA | 9099 |
rs563102833 | snp | A/G | 0.000725777 | 0.0190358 | intron-variant, missense, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119363895 | GTGGAGAGCAGCAGG[A/G]ACGGGGAGAGAGGGG | 9099 |
rs563136648 | snp | A/C | | | intron-variant | USP2 | GRCh38.p7 | 11:119362973 | CTCAGGAGAGCCCTG[A/C]CTGGGTTAATGCAGA | 9099 |
rs563433669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119375578 | ACAGAGGCACAGGGT[C/T]GGGGTGGGGGCCCAG | 9099 |
rs563494945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368168 | TAGTACAGCTCCTGG[C/T]CAAGGGGCCCCTCTG | 9099 |
rs563501745 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119354999 | TGTGTTTGTAAACAA[C/T]TGGTGAATCCAGATG | 9099 |
rs563630453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119368547 | GCTTATATAATCTCC[A/C]TGTCACTGAACAGCT | 9099 |
rs563651521 | snp | C/G | | | downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355165 | CTAATATACTAGGAG[C/G]CCTTCCTAGATTCAA | 9099 |
rs563752359 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119360614 | ATTTTTAGTAGAGAC[-/AG]GGTTTCGTCATGTTG | 9099 |
rs564092043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119359859 | GCATAGGTGACCTAA[C/T]TGGTTATTTACTATA | 9099 |
rs564167292 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119374851 | TTTTGCACTAGTCAC[A/G]TAACCTCTCTGAGCC | 9099 |
rs564240736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2, USP2-AS1 | GRCh38.p7 | 11:119380951 | GGGCTTCCCTTGACT[A/G]TTGAGAAGTTGCTCT | 9099 |
rs564427911 | snp | C/T | 1.66333e-05 | 0.00288381 | intron-variant, missense | USP2 | GRCh38.p7 | 11:119373009 | GGTCTATCCGGTAGC[C/T]ATCTGAGGTCCGGAG | 9099 |
rs564488735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119372595 | CTTGTTTGTCTCCAC[C/T]AGGAGCAGCCTGTCA | 9099 |
rs564563829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119366511 | GTTTATCTTTGCTTT[A/G]TAAGTGTTTCAAAGA | 9099 |
rs564686765 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119367235 | CTGCATCCTGACTGC[C/T]GTTCCTCAGAACCTG | 9099 |
rs564756231 | snp | A/G/T | 0.000166723 | 0.00912885 | intron-variant | USP2 | GRCh38.p7 | 11:119357316 | GCATGGTCTGAGGAG[A/G/T]AGGCAGCCGTCAAGC | 9099 |
rs564798038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119378622 | ATCCTGACTGGTGGA[A/G]AAGAAGTGGATGGGC | 9099 |
rs564829311 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119368643 | TCCCAGACCTTTTGC[C/T]CCTAGAAACAGGTCC | 9099 |
rs564831838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119371829 | CACCACCCACACATC[C/G]ATCCATCCATTCATC | 9099 |
rs564864576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119358084 | GGGGAAAAAAGCAAA[A/G]GTCAGAGGTCAACAT | 9099 |
rs564925400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364700 | AGACCCAAACTCATG[A/C]AGTCTGTGGAGGTCA | 9099 |
rs564968926 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119365781 | AAAAACCAAAACTGC[A/C]ACTCATTAAGTACTT | 9099 |
rs565015659 | snp | A/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119370126 | GTTGTAGTGAGCCGA[A/G]ATCGCACCACTGCAC | 9099 |
rs565027344 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP2 | GRCh38.p7 | 11:119364204 | CTCTCGCGCTCCGGC[C/T]GACTGGCGGCCCCGC | 9099 |
rs565034518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119376210 | CAGCCTGGGTTGGTG[C/T]CCCTTGGCATTACCT | 9099 |
rs565107171 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, downstream-variant-500B | USP2 | GRCh38.p7 | 11:119355887 | TGCAATGCACAACGA[A/G]CCAGGGCTAAGGGCA | 9099 |
rs565446118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119363151 | TGGCACGGGGCAGGG[C/G]ACGCACTGCCAGCAC | 9099 |
rs565558772 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP2 | GRCh38.p7 | 11:119368254 | GAAGTTCAACCTCCT[C/T]AGGGTGGCTTAGTGA | 9099 |
rs565759810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119361673 | TCTCAAGAACTGCCT[C/T]ACCGATCCCACAAGT | 9099 |
rs565945306 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP2 | GRCh38.p7 | 11:119367752 | TTTTGCATGTGTCTC[C/T]GTCTGGGGCGCTAGT | 9099 |
rs565973913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119374451 | TGCTGAATGTGGAGC[A/T]TTGAGAGCCCCAGAG | 9099 |
rs566010351 | snp | A/T | 0.00113425 | 0.0237873 | upstream-variant-2KB, nc-transcript-variant | USP2, USP2-AS1 | GRCh38.p7 | 11:119381874 | GAGCAGGAACAGAGG[A/T]GGACTGGAATGTCAC | 9099 |
rs566021803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP2 | GRCh38.p7 | 11:119373658 | GGCTGGCTGCTGAGA[A/C]GCACACATGCACGCA | 9099 |
rs566085068 | snp | C/T | | | intron-variant | USP2 | GRCh38.p7 | 11:119371277 | GGACCCGAGCCCCTC[C/T]GAGGAGAGCCATATT | 9099 |
rs566361644 | snp | A/G | 0.000115404 | 0.0075953 | synonymous-codon | USP2 | GRCh38.p7 | 11:119358200 | GAAGACCGTAGAACA[A/G]TAACCACAATCTGTA | 9099 |
rs566543627 | snp | A/G | 9.42338e-05 | 0.00686353 | intron-variant | USP2 | GRCh38.p7 | 11:119372694 | TATCCCCGGTCCCCA[A/G]GGGTAAACTCACCAT | 9099 |
rs566608015 | snp | C/G | | | intron-variant | USP2 | GRCh38.p7 | 11:119367072 | CATCTCTCGGCCAGC[C/G]AGGTCTCTGTGAGAC | 9099 |
rs566621045 | snp | C/T | 1.65094e-05 | 0.00287305 | missense | USP2 | GRCh38.p7 | 11:119357807 | AACTTCTTTATACAC[C/T]GTTTTCTGCCTCGGC | 9099 |