SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8420 | snp | C/T | 0 | 0 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168223 | CTACCGTATAGTTTT[C/T]TCTATTCTATCATTT | 6613 |
rs13692 | snp | A/C/G | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168048 | GCCACTAATGGAGAA[A/C/G]GGGGGTATTTTCACA | 6613 |
rs752824 | snp | A/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173660 | gcaaaaccctctctt[A/T]acaaaaaaatacaaa | 6613 |
rs899323 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173799 | ATACTTCCAGTTTTG[G/T]CCTAGCAGGGTGGCT | 6613 |
rs899324 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173477 | AAAAAAAAAAAAAAA[C/T]GACTTCCAGTCTTGT | 6613 |
rs1471453 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181349 | CTGCAGGATTTTTCC[G/T]CTTTCACATTGATTT | 6613 |
rs2035252 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171819 | AGTATCTATTGTGCT[A/G]TACTCTCAGTTATTA | 6613 |
rs2035253 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171498 | gagacggagttttgc[C/T]ctgtctcccagactg | 6613 |
rs2127081 | snp | C/T | 0 | 0 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167682 | CTATTTATGTTTTTT[C/T]TAAGCCTCAATTTTC | 6613 |
rs2127082 | snp | A/G | 0.419296 | 0.183954 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176431 | GCGGGGTTTCACCAT[A/G]TTGGCCAGGCTGATC | 6613 |
rs3205678 | snp | A/C | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167983 | AGTTATTTTGCTCTC[A/C]CTGTTTTAACAAAAA | 6613 |
rs3940906 | snp | C/T | 0.0876345 | 0.190099 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183414 | GGAAGCAGGTTGAGA[C/T]TGACTGAGAGGAAGT | 6613 |
rs7213926 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181697 | TTAAAGGAAACACAC[A/G]AACAAAAAAAACAAT | 6613 |
rs7218706 | snp | C/T | 0.499437 | 0.0167637 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175355 | agacagagtcttgct[C/T]tgtcactcaggctgg | 6613 |
rs7225227 | snp | A/G | 0.182296 | 0.240658 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180133 | atcacttgaggtcag[A/G]agttgaggtcaggtc | 6613 |
rs9904412 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177826 | ggtaaaaccccgttt[C/T]tacgaaaaataaatt | 6613 |
rs9912562 | snp | A/G | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172346 | tttttttttttttga[A/G]acaggggctgttacc | 6613 |
rs9913676 | snp | A/G | 0.499995 | 0.00159744 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170617 | CAAAAAACCCACGGC[A/G]ggcgtggtggctcac | 6613 |
rs10401019 | snp | C/T | 0.499987 | 0.00259581 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182216 | TCGGGCCCCTGAGGC[C/T]ATTAAAGTGGGAAAT | 6613 |
rs10401035 | snp | A/T | 0.0926964 | 0.194308 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181601 | ACAAAACAATAAATC[A/T]ACAGCCTGCCATTCA | 6613 |
rs11548468 | snp | A/C/T | 0.00019821 | 0.00995316 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182883 | TCGTTTGGTGCGGAC[A/C/T]TGGTACCTCTTTTGT | 6613 |
rs11657010 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178367 | aaaaatacaaaaatt[A/G]gctgggcacggtggc | 6613 |
rs11870102 | snp | A/T | 0.375 | 0.216506 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180393 | TGAGACTCCCAGCTT[A/T]aaaaaaaaaaaaaaa | 6613 |
rs12940697 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180052 | CCTATTTAGAACAAT[C/T]TGAAGGggccaggca | 6613 |
rs12941564 | snp | C/G | 0.414245 | 0.188477 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180386 | AATAGAGTGAGACTC[C/G]CAGCTTaaaaaaaaa | 6613 |
rs12946898 | snp | C/T | 0.401924 | 0.198543 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184601 | gcacctcagacccag[C/T]aactctcaactaaaa | 6613 |
rs13343264 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179866 | ggattttgccatggt[G/T]gccaggctgatgtca | 6613 |
rs16967636 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171759 | ATAGCAGATAATCCC[A/G]TTTTAGTGGTGGGTA | 6613 |
rs17850328 | snp | C/T | 1.66366e-05 | 0.0028841 | missense | SUMO2 | GRCh38.p7 | 17:75181164 | TCAAATTAATATGAT[C/T]GTTGTTCTCAGTCTT | 6613 |
rs28391127 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177240 | AGGCTAGGTGGCAGG[C/T]GCTGTAATCCCAGTT | 6613 |
rs28437274 | snp | A/C | 0.0926964 | 0.194308 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175200 | GTTGGCCAGGCTGGT[A/C]TCGAACTCCTAACCT | 6613 |
rs28759168 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177080 | CCCAGCTACTCCAGC[C/T]GGAGGTTGAGGGGGG | 6613 |
rs33971007 | in-del | -/C/CTT/CTTT/CTTTT/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172327 | ACTGTACCCAGACTT[-/C/CTT/CTTT/CTTTT/T]TTTTTTTTTTTTTTT | 6613 |
rs34017557 | in-del | -/T/TC/TCTC/TTT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172326 | TACTGTACCCAGACT[-/T/TC/TCTC/TTT]CTTTTTTTTTTTTTT | 6613 |
rs34125225 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170964 | GAAAATATCTTTAAG[-/A]ATACAGTAGATACAG | 6613 |
rs34245817 | in-del | -/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173479 | AAGACTGGAAGTCGT[-/T]TTTTTTTTTTTTTGA | 6613 |
rs34254735 | in-del | -/A | 0.498392 | 0.028309 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169849 | GTGAGACTTGGTCTC[-/A]AAAAAAAAAAAAAAG | 6613 |
rs34641551 | in-del | -/A | 0.374 | 0.217081 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168131 | TAAAAAAAAAAAAAA[-/A]TGCAATATGCTTGTG | 6613 |
rs34969900 | in-del | -/GTT | 0.471673 | 0.115589 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181907 | TCGACCCAACCTAAA[-/GTT]GTCCAAAATCGAGTG | 6613 |
rs35271045 | snp | C/T | 0.441021 | 0.161279 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179199 | CAATTCATAAGTTCA[C/T]GTAGGGTGATTTCAG | 6613 |
rs35302801 | in-del | -/T | 0.107694 | 0.205546 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171067 | CTGTAAGGGGCAGTT[-/T]AAAAAAAAAAAAAAG | 6613 |
rs35348154 | in-del | -/A | 0.488965 | 0.0734569 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179528 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 6613 |
rs35389462 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168835 | TCTCAAACTCCTGAG[-/A]CTCAAGTGATCTGCC | 6613 |
rs35509383 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172121 | CTTTCCCCCGCCCAG[-/A]ATTCTCCTGGCTCAA | 6613 |
rs55817377 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177186 | CAAAAAAAAAAAAAA[-/A]TTAATTAATTAAATA | 6613 |
rs55895120 | snp | A/G | | | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75168345 | GTTCCCTTTTCAGTA[A/G]ACACCTCCCGTCTGC | 6613 |
rs56156468 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172111 | CTGTCTGACACCTTT[C/T]CCCCGCCCAGATTCT | 6613 |
rs56225637 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173745 | GCGTCACAGTGCTGG[C/T]ATTACAAGCACTTTG | 6613 |
rs56335300 | in-del | -/GA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173492 | TTTTTTTTTTTTTTT[-/GA]GAGAGAGGGCCTCAC | 6613 |
rs56705892 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180097 | TGTAATCCCAGCACT[C/T]TGAGAGGCCAAGGTG | 6613 |
rs56739230 | snp | G/T | 0.5 | 0.000399361 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180740 | AAATAATAAAAGACT[G/T]ATAAGTAATTTTACC | 6613 |
rs57535130 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174364 | ACACTGTACTCAAGC[A/C]TGGGCGATGGAGTGA | 6613 |
rs57566541 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179961 | AAAGGAAGTTTTTAT[C/T]TTCACTGATCTTTCA | 6613 |
rs58402695 | in-del | -/A/AAAA | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180421 | AAAAAAAAAAAAAAA[-/A/AAAA]CGACTTCTTGGTTTG | 6613 |
rs58684188 | in-del | -/AAAA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180418 | AAAAAAAAAAAAAAA[-/AAAA]CGACTTCTTGGTTTG | 6613 |
rs59220364 | snp | C/T | 0.109461 | 0.206758 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180895 | TCCTAAGGGTTTTCA[C/T]GAGCTATCAATATAC | 6613 |
rs59613076 | in-del | -/A/AAAAAAA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178011 | AAAAAAAAAAAAAAA[-/A/AAAAAAA]GAATCGCCCAGTGGC | 6613 |
rs60507027 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178528 | AAAAAAAAAAAAAAA[A/G]AAAAGAATACTGTTC | 6613 |
rs60542675 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171164 | GATGGAGTTTCGCTG[C/T]TGTTGCCCAGGGTGG | 6613 |
rs61579555 | in-del | -/AA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179545 | AAAAAAAAAAAAAAA[-/AA]GGTATCTTTATAAGG | 6613 |
rs62085030 | snp | G/T | 0.0134861 | 0.0810011 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167644 | GCTTTATTTCCTTCT[G/T]GAAATGTTACTTCTA | 6613 |
rs62085031 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171816 | TTCTAATAACTGAGA[G/T]TACAGCACAATAGAT | 6613 |
rs62085032 | snp | C/T | 0.309894 | 0.242719 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176259 | TAGCCAGGATGGTCT[C/T]AATTTCCTGACCTCG | 6613 |
rs71159444 | in-del | -/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169863 | CCGCCCCCCCCCACC[-/T]TTTTTTTTTTTTTTG | 6613 |
rs71159445 | in-del | -/TTGT/TTTG | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177837 | CGTGCTCGGCTAATT[-/TTGT/TTTG]TATTTTTCGTAGAAA | 6613 |
rs71361663 | in-del | -/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172343 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGGCTGTT | 6613 |
rs71361664 | in-del | -/TGT | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181909 | GACCCAACCTAAAGT[-/TGT]CCAAAATCGAGTGCA | 6613 |
rs71796908 | in-del | -/CAGT | 0.046775 | 0.145601 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170977 | AAGATACAGTAGATA[-/CAGT]GTTAGGCTAAAAACA | 6613 |
rs73352427 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174323 | TTAAGCATGGCAGGC[A/G]AGGGCTGCCATGACC | 6613 |
rs73995797 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173826 | GTATTTAATGGAACT[C/T]TGAAAGGGTAAAAAG | 6613 |
rs73995798 | snp | G/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184044 | CTTTATTATTTCCTT[G/T]TGTCCCTGAATTTTC | 6613 |
rs74254449 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171070 | CTGTAAGGGGCAGTT[A/T]AAAAAAAAAAAAAGT | 6613 |
rs74326862 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168624 | TTTTTGTTTTTTTTT[G/T]GAGACAGGATTTCTG | 6613 |
rs74976467 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173478 | CAAGACTGGAAGTCA[G/T]TTTTTTTTTTTTTTG | 6613 |
rs75175871 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173491 | CATTTTTTTTTTTTT[G/T]TGAGAGAGGGCCTCA | 6613 |
rs75176740 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176593 | AGCACTCCAGCCTGG[A/G]TGACAGACCAGATTC | 6613 |
rs75264446 | in-del | -/AA | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184094 | TAGAAAAAAAAAAAA[-/AA]GCTCCCAATTCTATG | 6613 |
rs75369313 | snp | C/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176185 | GGGCATGGTGGCACG[C/T]GCCTGTAACCCCAGC | 6613 |
rs75642533 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181714 | ACAAAAAAAACAATC[G/T]AAGAATATCCCGATT | 6613 |
rs75991532 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169068 | TACAAAAAAAAAAAG[A/G]AAAAAAAAAAAAAAT | 6613 |
rs76153429 | snp | G/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173479 | AAGACTGGAAGTCAT[G/T]TTTTTTTTTTTTTGA | 6613 |
rs76340926 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168625 | TTTTGTTTTTTTTTT[G/T]AGACAGGATTTCTGT | 6613 |
rs76359910 | snp | A/C/G | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176150 | CAAGAGGCTGAGGCA[A/C/G]GAGAATCACTTGAAC | 6613 |
rs77301277 | snp | C/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172328 | ACTGTACCCAGACTT[C/T]TTTTTTTTTTTTTTT | 6613 |
rs77515216 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184095 | AGAAAAAAAAAAAAA[A/G]GCTCCCAATTCTATG | 6613 |
rs79205959 | snp | A/C/G/T | 0.00636936 | 0.0560724 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176132 | GAATCACTTGAACCC[A/C/G/T]GGAGGTGGAGGTTGC | 6613 |
rs79249555 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171546 | AAAAAAGCTGGGGAG[A/G]CAGGAGGCCTGCTAA | 6613 |
rs79489412 | snp | A/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169082 | GGAAAAAAAAAAAAA[A/T]TTAGCCAGCCATGGT | 6613 |
rs79661503 | snp | A/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168770 | ACCATGCCCAGCTAA[A/T]TTTTTTGTATTTTTA | 6613 |
rs79694832 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171583 | TTAATTTATCACAAT[C/T]CTGCTATCTAACAAA | 6613 |
rs79815344 | snp | A/G/T | 0.0268644 | 0.113242 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177968 | CACTCCAGTCTGACC[A/G/T]ACAAAGCGAGACTCC | 6613 |
rs80028650 | snp | C/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170403 | GGTGAAACCCTGTTT[C/T]TACCAAAAATACAAA | 6613 |
rs80110636 | snp | A/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168768 | CCACCATGCCCAGCT[A/T]ATTTTTTTGTATTTT | 6613 |
rs80223643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170682 | AGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 6613 |
rs80236856 | snp | A/C | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178511 | AGTGCGAGACTCTCA[A/C]AAAAAAAAAAAAAAA | 6613 |
rs80271291 | snp | A/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169084 | AAAAAAAAAAAAAAT[A/T]AGCCAGCCATGGTGA | 6613 |
rs111392577 | snp | C/T | 0.039522 | 0.134904 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183516 | GCTCAGTCGCCCAGG[C/T]TGGAGTGCAGTGGCA | 6613 |
rs111427495 | snp | C/T | 0.0523666 | 0.153105 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182862 | AGTCTCCTCAGCTGC[C/T]GCTTCACAAAAGAGG | 6613 |
rs111503956 | in-del | -/ACAA | 0.0356815 | 0.128715 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177836 | GTTTCTACGAAAAAT[-/ACAA]TAAATTAGCCGAGCA | 6613 |
rs111658496 | snp | A/C | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174566 | AATTAAAAATAAATG[A/C]ATAAAAACCATTGGC | 6613 |
rs111996518 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181878 | GTTTTATCCTGATTT[A/G]TTTCTTGTAGATTTC | 6613 |
rs112424194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175616 | TAAGACACTGTGCCC[A/G]GCCTGTTTGTTGTTG | 6613 |
rs112453153 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179454 | AATCGCTTGGTCTCG[G/T]GAGGCAGAAGTTGCA | 6613 |
rs112481206 | snp | A/G | 0.0190136 | 0.0958481 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172465 | GCTGGGACTACAGGC[A/G]TGCACCATCATGCCT | 6613 |
rs112539719 | snp | C/G | 0.0926964 | 0.194308 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183696 | CGATCTCCTGACCTC[C/G]TGATCCGCCCGCCTC | 6613 |
rs112640062 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178912 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCTAGC | 6613 |
rs112708142 | snp | A/C | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172186 | CACCACCATGCCCGG[A/C]TAATTTTTGTATTTT | 6613 |
rs112738869 | snp | C/T | 0.109461 | 0.206758 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169462 | GATCTCAGCTCACTG[C/T]AAGCTCCGCCTCCTG | 6613 |
rs113286532 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75182595 | GCGCGCACTCGGAGG[C/G]CGCCGGGGGCGGGAG | 6613 |
rs113671451 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177837 | GTTTCTACGAAAAAT[A/T]AATTAGCCGAGCACG | 6613 |
rs114208328 | snp | C/T | 0.0295035 | 0.117819 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183025 | GAGTAGCCGAAGCCT[C/T]CCATTGGCTGGCGCC | 6613 |
rs115025308 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184715 | CAAGCTGGAAAGGCC[A/G]GCAACATTCCTGACT | 6613 |
rs115187580 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174625 | TCTGTTCCCCTCTGG[C/T]CATACTTCCCAAAGC | 6613 |
rs115318274 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172903 | TAGGATGACAGGTGT[A/G]AACAAGTGCACCTGG | 6613 |
rs115718157 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181555 | TAGAGTCCCTTCTCT[C/T]TTCTAAGCACTTTAA | 6613 |
rs115746148 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176659 | CCTAAAATGCCCCAA[C/T]CTACACCCTTGAACT | 6613 |
rs116177942 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170050 | GGCGCACGCCTGCAC[A/G]CCTGTAATCCCAGCT | 6613 |
rs116297198 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182337 | GAACCCTCGCCCCGC[C/T]GCCGCGGCCCCAGGC | 6613 |
rs116564002 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180196 | GCGCACGCCTGAAAT[C/T]CCAGGTACTCAGGAG | 6613 |
rs116706467 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171356 | TAAACAAATAAAATA[A/G]AAACAAAATTAGCCA | 6613 |
rs116733823 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184809 | TACCAAATCTAATTT[A/C]TTTGGCCTCTGGATG | 6613 |
rs116777884 | snp | G/T | 0.0513262 | 0.151752 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183934 | TTTAATCCTTTCCTC[G/T]TTGCATCCAGTTAAA | 6613 |
rs116864865 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173142 | TCTACTATCACAACA[C/T]TGTAAAATATGTTTC | 6613 |
rs116914410 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170288 | AATAAAAACCCAAAT[A/T]AGGCTGGGCGCCGGG | 6613 |
rs117162506 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176080 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGA | 6613 |
rs117741303 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183768 | CCCGGCCTACAGTGT[C/T]TTCTTCTGTCCTGCT | 6613 |
rs117792069 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174694 | GTTCAAATTCATAAA[C/T]ACAGCTGTTCAAAGA | 6613 |
rs117864065 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178935 | ACTCTAGCCTGGGCA[A/G]TAAGAGCAAAACTCC | 6613 |
rs118066102 | snp | A/G | 0.0126979 | 0.078662 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167713 | TATTTAATATTTCTC[A/G]GAATAAAGAAAACAG | 6613 |
rs137884164 | in-del | -/TTG | 0.0337553 | 0.125452 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175623 | CTGTGCCCGGCCTGT[-/TTG]TTGTTGTTGTTTTTG | 6613 |
rs138120630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173243 | ATCATAACTCACTGC[A/G]GCCTGAAACTCCTGG | 6613 |
rs138122032 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172673 | AGAGACGGGGTTTCT[A/C]CATGTTGGTCGGAGT | 6613 |
rs138443556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177638 | AGTAAGCCTAGATTG[C/T]GCCATTGCATTCAGC | 6613 |
rs138497933 | snp | C/T | 0.0174175 | 0.0916809 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183512 | TCTCGCTCAGTCGCC[C/T]AGGCTGGAGTGCAGT | 6613 |
rs138558745 | snp | A/G | 0.00358779 | 0.0422022 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167581 | GATATTTATAAAACT[A/G]TTATTCTTTGTTTGG | 6613 |
rs138828339 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169157 | GGATCAATTGAGCCC[A/G]TAAGATCAAGGCTGC | 6613 |
rs139205392 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180115 | AGAGGCCAAGGTGGG[C/T]GGATCACTTGAGGTC | 6613 |
rs139448595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175383 | TGGAGGGCAGTGTCG[C/T]GATCTCGGCTCACTG | 6613 |
rs139491904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171006 | AAACACAATTTTAAA[A/G]CTAAGCAGCAGCCAA | 6613 |
rs139843510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170369 | CAGGTCAACAGGTCA[A/C]ACCCATCCTGGCCAA | 6613 |
rs140186027 | snp | C/G/T | 0.0017615 | 0.0296342 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174829 | TTGACAATCCCTGAA[C/G/T]GAGAATTTAAAAGCA | 6613 |
rs140329958 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172516 | TTTTTGAGTTTCGCT[C/T]GTTACCCATGCTCGA | 6613 |
rs140363192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175999 | AATGTTAAATAGAAC[A/T]TACCTTGAGACAAAT | 6613 |
rs140644374 | in-del | -/CTT/TTCT/TTT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172325 | CTACTGTACCCAGAC[-/CTT/TTCT/TTT]TTTTTTTTTTTTTTT | 6613 |
rs140946701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174011 | TCAAACAAAGCTATG[A/G]GACGTGGCAATTAGG | 6613 |
rs140977832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181384 | AGTATTAGATAGCTG[C/T]CAGATACGGAAAAGC | 6613 |
rs141868990 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170237 | ATGTTTAAAGAATCT[C/T]GCTGCACTGCTTAGC | 6613 |
rs141870420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168509 | TTCCACTAAGTTCCA[A/C]GTTTCATTATTTTAG | 6613 |
rs141994247 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173176 | AACTGTAAGTCTTCT[A/G]TTTTTGAGACAGAGT | 6613 |
rs142056162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178880 | GAATCGCTTAAAACT[A/G]GAAGGCGGAGGATGC | 6613 |
rs143061815 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172427 | CGGGTTCAGGTGATT[C/T]TCCTGCCTCAGCCTC | 6613 |
rs143165653 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176274 | CAATTTCCTGACCTC[A/G]TGATCCGCCTGGCTG | 6613 |
rs143190253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174292 | CTACTCTGGGAGGCT[A/G]AGGCAGGAGAATTGC | 6613 |
rs143236337 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182259 | TCCCCCTACCCCCAG[A/G]CCCAGGACGGCGGCC | 6613 |
rs143261404 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177111 | AAAATTGCATGAACC[C/T]GGGAGGTGGAGGTTG | 6613 |
rs144021612 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180175 | CAAAATTAGCCGGGC[A/G/T]TGGTGGCGCACGCCT | 6613 |
rs144096996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176061 | AATTTTTTTTTTTTA[A/G]ATGGAGTCTCGCTCT | 6613 |
rs144270622 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173908 | GACAGAACAAAATGA[A/T]GTGGTACATAAAGAG | 6613 |
rs144378848 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177750 | AGCACTTTGGGAGGC[C/T]GAGGTGGCGAGACGG | 6613 |
rs144406006 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169866 | AAAAAAAAAAAAAGG[G/T]GGGGGGGGGCGGGTG | 6613 |
rs144944859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170440 | CTGGGTGTGGTTGCG[C/T]ACGCCTGTAGTCCCA | 6613 |
rs144972649 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172113 | GTCTGACACCTTTCC[C/T]CCGCCCAGATTCTCC | 6613 |
rs145016494 | snp | C/T | 0.067446 | 0.170804 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171187 | CAGGGTGGAGTGCAA[C/T]GGCGCAATCTTGGCT | 6613 |
rs145504504 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175850 | GTTGGCCAGACTGAT[A/C]TCGAACTCCTGACCT | 6613 |
rs145533317 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168880 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACTG | 6613 |
rs145597449 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172529 | CTCGTTACCCATGCT[C/T]GAGTGCAATGGCGTG | 6613 |
rs145608555 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182114 | GTCTCTCTGCTCGTA[C/T]CTGTGCCTCCAACTT | 6613 |
rs145848784 | in-del | -/CTT/TTTT | 0.49889 | 0.0235361 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172324 | GCTACTGTACCCAGA[-/CTT/TTTT]CTTTTTTTTTTTTTT | 6613 |
rs146186230 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184943 | AACACTCTCAAAAGA[C/G]GCCGGGCATGGTGGC | 6613 |
rs146228129 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179344 | GACCAGTCTGACCAA[C/T]ATGGTGAAACCCCAT | 6613 |
rs146345464 | snp | A/G | 0.119281 | 0.213102 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169917 | CTCAACACTTTGGGA[A/G]GCCGAGGCAGGCAGA | 6613 |
rs146473085 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176163 | TCCTGCCTCAGCCTC[C/T]TCAGTAGCTGGGACT | 6613 |
rs146490994 | snp | G/T | 0.00117537 | 0.0242137 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181036 | TTTTATTCAGTGGAA[G/T]TACACATATGAATTC | 6613 |
rs147001740 | in-del | -/TT | 0.0271762 | 0.113356 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175159 | GGCTAATTTTTGTAG[-/TT]TTTAGTAGAGACTGG | 6613 |
rs147510899 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177318 | TTGCAGTGAGCTGAG[A/C]TCATGCCACTGCACT | 6613 |
rs147546698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174346 | CCATGACCCAAGATC[A/G]TGACACTGTACTCAA | 6613 |
rs147950264 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170531 | GCTGTGATTGCCCCA[C/G]TGCACTCCAGCCTGG | 6613 |
rs148092157 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176424 | AGTTCAAGATCAGCC[C/T]GGCCAATATGGTGAA | 6613 |
rs148533973 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169990 | TGAAACCCAGTCTCT[A/G]CTAAAAATACAAAAA | 6613 |
rs149059706 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172191 | CCATGCCCGGCTAAT[C/T]TTTGTATTTTTAGTA | 6613 |
rs149148407 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182147 | TGAAACCACATGGTG[C/T]TCGCGGATTAGGGGT | 6613 |
rs149419120 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183781 | GTCTTCTTCTGTCCT[A/G]CTGGTAACCCTAGAC | 6613 |
rs149592185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173677 | AGAGAGGGTTTTGCC[A/G]TGTTGCCCAGGCTGG | 6613 |
rs149700459 | snp | A/G/T | 0.141999 | 0.232837 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175696 | GGAGTGCAGTGGTGC[A/G/T]ATCTTGGCTCACTGC | 6613 |
rs149752274 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182012 | AAAGCAGCAAGTCCC[G/T]TGTGCCCCGATGATG | 6613 |
rs150139117 | snp | C/T | 0.0178098 | 0.0926698 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167446 | CTACCCTATACCCTA[C/T]GCTCCGTGCCTCACT | 6613 |
rs150227493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176520 | ATTCGGGAGGCTGAG[A/G]CAGGAGGATCGCTTG | 6613 |
rs150250836 | in-del | -/AAC | 0.439918 | 0.162576 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176618 | AGATTCAATATCAAA[-/AAC]AACAACAACAACAAC | 6613 |
rs150404129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173242 | GATCATAACTCACTG[C/T]GGCCTGAAACTCCTG | 6613 |
rs150703527 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183573 | CTCCCGGGTTCAAGT[C/G]ATTCTCCTGCCTCAG | 6613 |
rs150734961 | in-del | -/T | 9.92625e-05 | 0.00704425 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174742 | TCTAATTAGGAGAGA[-/T]TTTTTTTACCTGTGC | 6613 |
rs180781961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174519 | CCCGGGCAACAGAGA[A/G]GCCCTGTCCCTAAAA | 6613 |
rs180792652 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181398 | GTCAGATACGGAAAA[G/T]CCTACATGCAATACT | 6613 |
rs180903712 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170430 | CAAAAATTAGCTGGG[C/T]GTGGTTGCGCACGCC | 6613 |
rs180904632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178868 | GCTGAGGCAGAAGAA[C/T]CGCTTAAAACTGGAA | 6613 |
rs181115139 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181730 | AAGAATATCCCGATT[C/G]CCCCCGGAACAGCGG | 6613 |
rs181433254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173876 | CAGAAGACAATCCAG[C/T]TGATCCTACAGAAAG | 6613 |
rs181553038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170667 | CAGCCTGGCCAACAT[A/G]GTGAAACCCCGTCTC | 6613 |
rs181669926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182442 | GACTGCAACACCCGA[C/T]GCGGGGTCGACAGAA | 6613 |
rs181788420 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174187 | TTGTGGTCAGCAGTT[C/G]AAGACCAGCCTGGCC | 6613 |
rs182029649 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178564 | CACCAAACTGAAGCA[C/T]GATTCTGTTTGTTTG | 6613 |
rs182124239 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172238 | GCCATGTTGGCCAGG[C/T]TGGTCTTGAACTGCT | 6613 |
rs182212328 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171026 | GCAGCAGCCAACTCG[A/C/G]TGCACTGACTATATA | 6613 |
rs182274650 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171834 | CAGCACAATAGATAC[C/T]TTTTACTATTTCTTT | 6613 |
rs182296155 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177136 | AGGTTGCAATGAGCC[A/G]AGATCGTGCCATTGC | 6613 |
rs182391033 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184493 | TCATTACCATCTCTT[C/T]GCTAATGATCCTCAA | 6613 |
rs182393827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168741 | CCAAGTAGCTGAGAT[C/T]ACAGGCATCCGCCAC | 6613 |
rs182544599 | snp | G/T | 0.00835141 | 0.0640778 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167643 | AGCTTTATTTCCTTC[G/T]TGAAATGTTACTTCT | 6613 |
rs182795532 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183580 | GTTCAAGTGATTCTC[C/T]TGCCTCAGCCTCCCG | 6613 |
rs183064553 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174936 | ATACCTAAATAAACA[A/G]TTGCCAACATGTTAA | 6613 |
rs183249915 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179514 | TCCTGGACAACAGAG[A/C]GAGACTCTGTCTCAA | 6613 |
rs183385070 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172795 | TGGCTAATTTTTGTA[A/T]TTTTTGGCAGACACG | 6613 |
rs183519875 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176126 | TTCAACGCAACCTCC[A/G]CCACCGGAGTTCAAG | 6613 |
rs183635341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179134 | CCCTGTATCCTGAAG[C/G]GGCACTAGTGTTCAA | 6613 |
rs183928507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173653 | GCTAATTTTTGTATT[G/T]TTTTGTAAAGAGAGG | 6613 |
rs184017480 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170578 | TGTCTCAAAAAACAA[A/G]AACAAAAACAAAAAA | 6613 |
rs184320462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181003 | TTGTTCCCATGAAAA[C/T]AAGATTTTTAAAAAT | 6613 |
rs184326963 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170041 | GGGCGTGGTGGCGCA[C/G]GCCTGCACGCCTGTA | 6613 |
rs184427271 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184761 | ACTCCTCATCCAATC[A/G]ATCTTGGCCAAATCT | 6613 |
rs184433754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169262 | AAAAGGCTAGGGCCA[C/T]GCACAATGGCTCACT | 6613 |
rs184521562 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181426 | ACTATCAGTAGCAAC[A/T]ATATGTTTAAAGTTG | 6613 |
rs184563741 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181348 | GAAATCAATGTGAAA[A/G]CGGAAAAATCCTGCA | 6613 |
rs184745256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177417 | GGTGCAGTGGCTCAC[A/G]CCTATAATCCCAACA | 6613 |
rs184785489 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174015 | ACAAAGCTATGGGAC[A/G]TGGCAATTAGGGCTA | 6613 |
rs185224936 | snp | C/T | 0.00052848 | 0.0162469 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174733 | TGGTAATTTTTCTAA[C/T]TAGGAGAGATTTTTT | 6613 |
rs185301441 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178243 | TTCAAGGCCAGGCAC[C/G]AGTGGCTCACACCTG | 6613 |
rs185514293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173150 | CACAACATTGTAAAA[A/T]ATGTTTCAGAAACTG | 6613 |
rs185747733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181787 | CGTTCTCCTCTATTA[G/T]CAGCTTCATTTTTAT | 6613 |
rs185874034 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183575 | CCCGGGTTCAAGTGA[C/T]TCTCCTGCCTCAGCC | 6613 |
rs186265475 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178615 | ATTCTGTCACCCACA[C/G]TGGAGTGCAGCGATG | 6613 |
rs186285484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179161 | TCAAATATAGAAGAT[A/G]CCAGTTTATAAATTA | 6613 |
rs186371701 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182466 | GACAGAAGGTGGAGA[A/C]CCCGCGCGCCCTAAC | 6613 |
rs186390697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178990 | AGATGAGGTCTTACT[A/G]TGTTGTCCAGACTGG | 6613 |
rs186623851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177249 | GGCAGGCGCTGTAAT[A/C]CCAGTTATTCAAGAG | 6613 |
rs186922512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171942 | GCCTTTAAAAAATGA[A/G]GTTCCTGTACCAGCC | 6613 |
rs187065327 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184592 | ATCCCAGAGGCACCT[C/G]AGACCCAGCAACTCT | 6613 |
rs187072880 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169055 | GAGACAACATCTCTA[C/T]AAAAAAAAAAAGGAA | 6613 |
rs187146296 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170866 | CAAAAAAAAAAAAAA[A/C]AAACCCAAATTAATA | 6613 |
rs187219308 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171255 | TGCCTCAGCCTCCCA[A/C]GTAGCTGGGATTACA | 6613 |
rs187263668 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174283 | TAATCCCAGCTACTC[C/T]GGGAGGCTGAGGCAG | 6613 |
rs187766126 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183884 | GAAACAGTATCCATA[A/T]GCGAGAACTACCCAA | 6613 |
rs187842463 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176752 | AATTACTTACTGTCT[C/T]ACTAAAAAACACACT | 6613 |
rs187956403 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179710 | TGTCACCCAGGCTAG[A/G]GTGCAGTGGTGTGAT | 6613 |
rs187977706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178704 | CACTGAAATAGCCTG[A/G]ACTACAGGTATGTGC | 6613 |
rs188056265 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167826 | AGTAATTTATCCCTA[A/C]TTAAAGACAGATTGC | 6613 |
rs188198225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180278 | AAGATTGCACCACTG[A/C]ACTCCAGCCTGGGCA | 6613 |
rs188646683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173719 | TGGACTCAAGTGCTC[C/G]GCCCACCTTGGCGTC | 6613 |
rs188707660 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169573 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 6613 |
rs188752709 | snp | C/G | 0.000992129 | 0.0222504 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75181072 | CTGTCGTTCACAATA[C/G]GCTTTCATTAGTTTA | 6613 |
rs188797112 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170621 | AAACCCACGGCAGGC[A/G]TGGTGGCTCACAAGG | 6613 |
rs188827875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173397 | ACTCCTGGCCTCAAG[A/C]AACCCTCCTGCCAGT | 6613 |
rs188841632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173003 | TCAGGGGCTTTTCCA[A/G]TTTTCAAAGATTATC | 6613 |
rs189026217 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184799 | TCCACCTTCTTACCA[A/G]ATCTAATTTCTTTGG | 6613 |
rs189264719 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170322 | CACGCCTATAATCCC[A/G]ACACTTTGGGAGGCC | 6613 |
rs189281248 | snp | C/T | 0.031825 | 0.122064 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178342 | AATATTGTGAAACCC[C/T]GTCTCTACAAAAAAT | 6613 |
rs189403436 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181386 | TATTAGATAGCTGTC[A/G]GATACGGAAAAGCCT | 6613 |
rs189432066 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174517 | AACCCGGGCAACAGA[C/G]AGGCCCTGTCCCTAA | 6613 |
rs189580263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171278 | GGATTACAGGCATGC[A/G]CCATCATGCCCAGCT | 6613 |
rs189675084 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177912 | GAGAATTGCTTGAAC[C/T]CGGGAGGTGGAGGTT | 6613 |
rs189730668 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168491 | GCTGAAAACATGTAC[A/C]TGTTCCACTAAGTTC | 6613 |
rs189839524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181698 | TAAAGGAAACACACA[A/G]ACAAAAAAAACAATC | 6613 |
rs190086285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174081 | GAATTTCAATTCAGC[A/C]TGTAGAACTAAAATG | 6613 |
rs190089656 | snp | G/T | 0.00123755 | 0.0248444 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174745 | TAATTAGGAGAGATT[G/T]TTTTACCTGTGCAGG | 6613 |
rs190239996 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172558 | TGATCTCCGGCTCAC[C/T]GCAACCTCTGCCTCC | 6613 |
rs190503569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181812 | TTTTATTTTCGGTTA[A/G]GAGCACTTATTCTCC | 6613 |
rs190660346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179428 | ACCTACTCGGGAGAC[G/T]GAGACAGGAGAATCG | 6613 |
rs191041372 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184146 | TCCATTCTTGGCCAA[A/G]CAGCTCGAAAAAATG | 6613 |
rs191329952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179066 | CTATGATTTTCTATT[C/T]TGTATGCAGTTTTGC | 6613 |
rs191349751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173431 | AGTTTCCTAAAGTGA[C/T]AGGACTACAGGTGTG | 6613 |
rs191681488 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175899 | CAGCCTCACAAAACG[C/G]TGGGATTACAGGTGT | 6613 |
rs191958238 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184635 | CTCACTTTACCTTCC[A/G]CATGGGTCCTTCTTC | 6613 |
rs191962512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170962 | AATGAAAATATCTTT[A/C]AGATACAGTAGATAC | 6613 |
rs191967568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169139 | CAGGAAGCCGAGGTG[A/G]GAGGATCAATTGAGC | 6613 |
rs192075861 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182523 | TGGGCCAAGAATCCC[A/C]GTTCGGGGCTGGTGG | 6613 |
rs192124237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181303 | TCTCATACTGTATGC[A/T]AAAACGGCATACTGC | 6613 |
rs192363129 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177389 | AGAAATTAAAAAATT[C/T]GCATGGTGGCCAGGT | 6613 |
rs192452264 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167451 | CTATACCCTATGCTC[C/T]GTGCCTCACTTAATA | 6613 |
rs192623853 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179819 | GTGTAACACCACGCC[C/G]AGCTAATTTTTTTGG | 6613 |
rs192674182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176933 | TCACGCCTGTAATCC[C/T]AGCACCTTGGGAGAC | 6613 |
rs192783064 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180610 | GTAATCCCAGATACT[C/T]AGGAGACTGAGGCAG | 6613 |
rs192905394 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173112 | TTCAAAAGTACATGG[C/G]ATCCAATTTAAATTT | 6613 |
rs193067441 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177922 | TGAACCCGGGAGGTG[C/G]AGGTTGCAGTGAGCC | 6613 |
rs193082311 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75182384 | CCGCGGTTCCTACCC[A/G]AGAGGTGAAGCCCGA | 6613 |
rs193292534 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169630 | CCTCATGATCCACCC[A/T]CCTCGGCCTCCCAAA | 6613 |
rs199509595 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177693 | CTTAAAAAAAAAAAA[-/A]GAAAAGAAAAGCCAG | 6613 |
rs199536449 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176705 | AAAAAAGCACCGCTT[G/T]TTAATTTCCTTTAAT | 6613 |
rs199820776 | in-del | -/AG | 0.0150606 | 0.0854603 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173848 | GGTAAAAAGAAACAA[-/AG]AGCTTCTGCCACAGA | 6613 |
rs199885955 | snp | C/T | 0.000742511 | 0.0192537 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174865 | CAGCATTAAGAGAAA[C/T]AGAATTCTATTTACA | 6613 |
rs200067343 | in-del | -/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180411 | AAAAAAAAAAAAAAA[-/C]AAAAAAAAAACGACT | 6613 |
rs200199376 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181700 | AGGAAACACACAAAC[-/A]AAAAAAAACAATCGA | 6613 |
rs200247743 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178533 | AAAAAAAAAAGAAAA[C/T]AATACTGTTCAAAAC | 6613 |
rs200495495 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169376 | CACCCCATCCCTATT[-/A]AAAAAAAAATTTTTT | 6613 |
rs200988530 | snp | A/G | 4.47788e-05 | 0.00473153 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174861 | TAAACAGCATTAAGA[A/G]AAACAGAATTCTATT | 6613 |
rs201000963 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177534 | CTAAAAATACAAAAT[C/T]AGCCAGGCGTGGTGG | 6613 |
rs201108743 | in-del | -/TG | 0.0142736 | 0.0832652 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171024 | AGCAGCAGCCAACTC[-/TG]GGTGCACTGACTATA | 6613 |
rs201149071 | in-del | -/A | 0.107341 | 0.205301 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180558 | CTCTACTAAAAATAC[-/A]AAAAAAAAAATTGGC | 6613 |
rs201482313 | in-del | -/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173799 | GCCACCCTGCTAGGA[-/C]CAAAACTGGAAGTAT | 6613 |
rs201539626 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176620 | ATTCAATATCAAAAA[A/C]AACAACAACAACAAC | 6613 |
rs201786825 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180802 | TTACATTTCCTTGGT[-/A]AAAAAAAAATTATTG | 6613 |
rs201835747 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177838 | TTTCTACGAAAAATA[A/C]ATTAGCCGAGCACGG | 6613 |
rs201853157 | in-del | -/ACCTC | 0.0146672 | 0.084371 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169614 | AGTCTAGATCTCCTG[-/ACCTC]ATGATCCACCCTCCT | 6613 |
rs201924451 | snp | C/G | 9.41516e-05 | 0.00686054 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168335 | AAAGAAGCAGGTTCC[C/G]TTTTCAGTAGACACC | 6613 |
rs202195617 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180411 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAACGACT | 6613 |
rs367783024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169706 | TTTTTTAAATTAGCC[A/G]GGCATGGTGGCATGT | 6613 |
rs368146840 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171364 | TAAAATAAAAACAAA[A/T]TTAGCCAGGCATCAT | 6613 |
rs368228042 | in-del | -/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168776 | CCAGCTAATTTTTTT[-/T]GTATTTTTAGTAGAG | 6613 |
rs368762032 | snp | C/T | 3.31137e-05 | 0.00406887 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181045 | GTGGAAGTACACATA[C/T]GAATTCCTCACCTGT | 6613 |
rs368853034 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175203 | GGCCAGGCTGGTCTC[A/G]AACTCCTAACCTCAG | 6613 |
rs369106782 | snp | C/T | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167767 | TTAAACAACAAGACG[C/T]TTGACTTGAAGGGAA | 6613 |
rs369197476 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178802 | AACCCAGCACTTTGG[C/G]AGGCTGAGGCGGGTG | 6613 |
rs369234572 | snp | A/T | 1.91206e-05 | 0.00309192 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174828 | ATTGACAATCCCTGA[A/T]CGAGAATTTAAAAGC | 6613 |
rs369337370 | in-del | -/GTT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175634 | CTGTTTGTTGTTGTT[-/GTT]TTTGTTTGTTTGTTA | 6613 |
rs369338045 | snp | C/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183610 | GAGTAGCTGAGACTA[C/G]AGGTACCCGCCACAA | 6613 |
rs369560847 | in-del | -/ACAA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174933 | GAAATACCTAAATAA[-/ACAA]TTGCCAACATGTTAA | 6613 |
rs369707062 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172412 | TTAATCTCCGCCTCT[C/T]GGGTTCAGGTGATTC | 6613 |
rs369736627 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180988 | GTGCTAGTCTAGTTT[G/T]TGTTCCCATGAAAAT | 6613 |
rs370570463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170564 | ACAGAGCAAGACTCT[A/G]TCTCAAAAAACAAAA | 6613 |
rs370892108 | in-del | -/TCT | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183457 | GCCTAAAATGCAGTG[-/TCT]TCTTCTTCTTCTTCT | 6613 |
rs371146078 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174182 | ATTACTTGTGGTCAG[A/C]AGTTCAAGACCAGCC | 6613 |
rs371357028 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180487 | GAAGGCCGAGGCGGG[A/C]GGATCACCTGAGGTC | 6613 |
rs371365057 | in-del | -/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168614 | GATAAAACTTTTTTG[-/T]TTTTTTTTTTGAGAC | 6613 |
rs371482509 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176558 | GAGGCGGAGTTTGCA[-/G]TGAGCCAAGATCGTG | 6613 |
rs371514755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179405 | TGGTGGCGTGCGCCC[A/G]TAGTCCCACCTACTC | 6613 |
rs371813002 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173272 | GGACTCAAGCACCCC[C/T]CCCACTAAACTTCCC | 6613 |
rs371947862 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171447 | TGAACCCAGGAAGCA[G/T]AGGTTGCAGTGAGCT | 6613 |
rs372116798 | snp | C/T | 0.000165986 | 0.00910854 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174711 | CAGCTGTTCAAAGAA[C/T]TACAAATGGTAATTT | 6613 |
rs372175260 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176776 | ACACACTTCAGGAGA[C/T]ATAGGAACCTAGACT | 6613 |
rs372438494 | in-del | -/GAGA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174739 | TTTTTCTAATTAGGA[-/GAGA]TTTTTTTACCTGTGC | 6613 |
rs372539401 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174022 | TATGGGACGTGGCAA[C/T]TAGGGCTATTAGTTC | 6613 |
rs372622781 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172143 | CTGGCTCAATCTCCC[A/G]AGTAGCTGGGATGGG | 6613 |
rs372657036 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172844 | CAGGCTGGTCTCAAA[C/T]TCCTGACCTCAAGCA | 6613 |
rs372851180 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181782 | GTTAACGTTCTCCTC[C/T]ATTAGCAGCTTCATT | 6613 |
rs373069268 | snp | A/G | 7.08207e-05 | 0.00595024 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174867 | GCATTAAGAGAAACA[A/G]AATTCTATTTACATA | 6613 |
rs373109528 | snp | A/G | | | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167547 | AACATGGGACCTAGA[A/G]AAACTTTTGGAACAA | 6613 |
rs373337757 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175918 | GATTACAGGTGTGAG[C/T]CACTGCGCCCAGCCA | 6613 |
rs373564646 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168875 | CTCCCAAAGTGCTGG[C/G]ATTACAGGTGTGAGC | 6613 |
rs373945373 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184267 | TCTCCACAAGGTCAC[C/T]GCAGACTTCTTTGCT | 6613 |
rs373978125 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170919 | AAATACCATATAGCC[A/G/T]TTAAAAAATAAGATT | 6613 |
rs374086048 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183688 | GATGGTCTCGATCTC[C/G]TGACCTCGTGATCCG | 6613 |
rs374308862 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169965 | TTCAAGACCAGCCTG[A/G]CCAAAATGGTGAAAC | 6613 |
rs374586248 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169527 | TAGCTGGGACTACAG[C/G]TGCCCGCCACAACGC | 6613 |
rs374682956 | snp | A/G | 0.000134748 | 0.00820707 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168437 | AATGTAAAAGCACTG[A/G]TTAAGTTCTGAAAAT | 6613 |
rs374699132 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176948 | AGCACCTTGGGAGAC[-/T]TGAGGTGGAAGATCA | 6613 |
rs374758173 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181535 | CCCCCCAAAAAAGTT[A/G]AAAATAGAGTCCCTT | 6613 |
rs374761664 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184045 | TTTATTATTTCCTTT[C/T]GTCCCTGAATTTTCT | 6613 |
rs374771037 | snp | A/G | 2.09672e-05 | 0.00323777 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174851 | TTAAAAGCAATAAAC[A/G]GCATTAAGAGAAACA | 6613 |
rs374831714 | snp | C/G | 3.31318e-05 | 0.00406999 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181033 | TAGTTTTATTCAGTG[C/G]AAGTACACATATGAA | 6613 |
rs374915086 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177161 | CATTGCAAGAGCGAG[A/G]CTCTTGTCTCAAAAA | 6613 |
rs375048393 | in-del | -/GA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169243 | TGTATCAAAAAAAGA[-/GA]AAAAAAGGCTAGGGC | 6613 |
rs375104640 | in-del | -/CA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176804 | ACTGTTTTAGTTACA[-/CA]GTCTATCCCTTGCAC | 6613 |
rs375482259 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178447 | TGAACCCAGGAGGCA[A/C/G]AGGTTGCAGTGAGCC | 6613 |
rs376264973 | snp | A/G | | | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167491 | TACCTGGAAATCCAC[A/G]ATACTATGGCCCAAT | 6613 |
rs376270538 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170494 | AGAATCACTTGAACC[C/T]GTGAAGTGGAGGTTA | 6613 |
rs376324053 | snp | C/T | 0.000249725 | 0.0111714 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174718 | TCAAAGAATTACAAA[C/T]GGTAATTTTTCTAAT | 6613 |
rs376465275 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173401 | CTGGCCTCAAGCAAC[C/T]CTCCTGCCAGTGTCA | 6613 |
rs376671958 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181432 | AGTAGCAACAATATG[C/T]TTAAAGTTGGGTCCT | 6613 |
rs376701238 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180922 | ATACCAAGTGCACGA[C/T]AAAACTGACGTGCCA | 6613 |
rs376795160 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176146 | CGGAGTTCAAGTGAC[C/T]TTCCTGCCTCAGCCT | 6613 |
rs377064141 | snp | A/T | 0.000155988 | 0.00883005 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181019 | AAGATTTTTAAAAAT[A/T]GTTTTATTCAGTGGA | 6613 |
rs377168855 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176531 | TGAGGCAGGAGGATC[A/G]CTTGAACCTGGGAGG | 6613 |
rs377257954 | in-del | -/CAA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176635 | CAACAACAACAACAA[-/CAA]AACCGACCTAAAATG | 6613 |
rs377451906 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183407 | CATGGTTACTTCCTC[C/T]CAGTCAATCTCAACC | 6613 |
rs397772052 | in-del | -/T/TA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171069 | CTGTAAGGGGCAGTT[-/T/TA]AAAAAAAAAAAAAAG | 6613 |
rs527311507 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170883 | AACCCAAATTAATAA[A/T]ACATAGTATGCTCAG | 6613 |
rs527744507 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180373 | TAGCTTAAAAGAAAT[-/A]AGAGTGAGACTCCCA | 6613 |
rs527796361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169663 | GCTGGGATTATAGGC[A/G]TGAACCACTGCACCC | 6613 |
rs527964023 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174468 | CTTTGGGAGGCCAAG[A/G]CTGCAGTGAGCTATA | 6613 |
rs528037951 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181284 | CTTCAAAAATCAACA[A/G]GTTTCTCATACTGTA | 6613 |
rs528045372 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178870 | TGAGGCAGAAGAATC[A/G]CTTAAAACTGGAAGG | 6613 |
rs528462894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176913 | CAAAGGCCAAGTATT[A/G]TGGCTCACGCCTGTA | 6613 |
rs528508996 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175165 | TTTTTGTAGTTTTAG[C/T]AGAGACTGGGTTTCA | 6613 |
rs528575872 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182973 | AGGGTGCGCGCACGT[C/T]GTGCGCTCCCTCCCC | 6613 |
rs528708753 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172483 | CACCATCATGCCTGG[C/G]TAAATTTTTTTTTTT | 6613 |
rs528974942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180250 | ACTCAGGAGGCAGAG[A/G]TTGCAGTGAGCCAAG | 6613 |
rs529167162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169808 | GAGCCAAGATTGTGC[C/T]ACTGGACTCCAACAC | 6613 |
rs529296716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168461 | TGAAAATTAATGATT[G/T]TTGGGTTTAAGTATG | 6613 |
rs529347596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179236 | TCTTCAAATAAGAGT[A/G]TATGGTATCTTGCTG | 6613 |
rs529382472 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167792 | AGGGAAAACTATCTA[A/G]GATTCTTTTTTGTTT | 6613 |
rs529730699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171342 | AAATAAAAACAACAT[A/C]AACAAATAAAATAAA | 6613 |
rs529743704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176699 | AGCTTTAAAAAAGCA[A/C]CGCTTTTTAATTTCC | 6613 |
rs530121450 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170297 | CCAAATTAGGCTGGG[C/T]GCCGGGGCTCACGCC | 6613 |
rs530396417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182198 | GCCGCTGCCCCTCCC[C/T]CTTCGGGCCCCTGAG | 6613 |
rs530883148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178908 | TGCAGTGAGCCGAGA[C/T]TGCGCCACTGCACTC | 6613 |
rs530900241 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172008 | TACATACCATAATTG[C/T]GCCTTTTTTTTTTTT | 6613 |
rs531011543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177634 | TTCCAGTAAGCCTAG[A/G]TTGCGCCATTGCATT | 6613 |
rs531146123 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173254 | CTGCGGCCTGAAACT[C/T]CTGGACTCAAGCACC | 6613 |
rs531310995 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175677 | TTGCTATGTCGCCCA[C/G]GCTGGAGTGCAGTGG | 6613 |
rs531350734 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168685 | TCAGCTCACTGCAAC[A/G]TCCACCCCTCAGGTT | 6613 |
rs531351477 | snp | A/T | 0.000548013 | 0.0165441 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75181156 | CGCCACCTTCAAATT[A/T]ATATGATCGTTGTTC | 6613 |
rs531611960 | in-del | -/TCTTCT | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183456 | GCCTAAAATGCAGTG[-/TCTTCT]TCTTCTTCTTCTTCT | 6613 |
rs531650903 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170320 | CTCACGCCTATAATC[A/C]CAACACTTTGGGAGG | 6613 |
rs531702583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174164 | GGAGGCCAAGGCGGG[C/T]GGATTACTTGTGGTC | 6613 |
rs531908959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182591 | CCCGGCGCGCACTCG[A/G]AGGCCGCCGGGGGCG | 6613 |
rs531945063 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172184 | AGCACCACCATGCCC[A/G]GCTAATTTTTGTATT | 6613 |
rs532056844 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180378 | TTAAAAGAAATAGAG[A/T]GAGACTCCCAGCTTA | 6613 |
rs532114816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171913 | ATGTGAAGTTTTACA[A/G]TGAAACTGTAAATGC | 6613 |
rs532195253 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183756 | TGAGCCACCGCGCCC[A/G]GCCTACAGTGTCTTC | 6613 |
rs532409388 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170834 | CAGCCTGGGTGACAG[G/T]GCGAGACTCCAGGTC | 6613 |
rs532538873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171378 | AATTAGCCAGGCATC[A/G]TGGTGGGCGCCTGTA | 6613 |
rs532739862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176275 | AATTTCCTGACCTCG[A/T]GATCCGCCTGGCTGG | 6613 |
rs532822642 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176771 | AAAAAACACACTTCA[A/G]GAGATATAGGAACCT | 6613 |
rs532873832 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176595 | CACTCCAGCCTGGGT[A/G]ACAGACCAGATTCAA | 6613 |
rs532886533 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182903 | GCACCAAACGAGCAC[A/G]CAAGCAGCACCAGGA | 6613 |
rs532954706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169267 | GCTAGGGCCACGCAC[A/G]ATGGCTCACTCCTGT | 6613 |
rs533144765 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173145 | ACTATCACAACATTG[C/T]AAAATATGTTTCAGA | 6613 |
rs533260052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173892 | TGATCCTACAGAAAG[G/T]GACAGAACAAAATGA | 6613 |
rs533287480 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178164 | GCAAAAGCCTGTCTC[-/A]AAAAAAAAAAGGCAA | 6613 |
rs533449830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172584 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 6613 |
rs533513770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178295 | CCGAAGCAGGCGGAT[C/T]ACGAGGTCAAGAGAT | 6613 |
rs533606193 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178282 | GCACTTTGGGAGGCC[A/G]AAGCAGGCGGATCAC | 6613 |
rs533666393 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168173 | GTGCACATATACCAG[A/T]TACTTTATGTACAAT | 6613 |
rs533678937 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167687 | TATGTTTTTTCTAAG[C/T]CTCAATTTTCTATTT | 6613 |
rs533926735 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181912 | CCAACCTAAAGTTGT[A/C]CAAAATCGAGTGCAG | 6613 |
rs534202377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181266 | CAGCAGCAGCCCTAG[C/T]TGCTTCAAAAATCAA | 6613 |
rs534262897 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180484 | TTGGAAGGCCGAGGC[A/G/T]GGCGGATCACCTGAG | 6613 |
rs534270984 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183824 | CGGGAAAATATTCAT[C/G]TATTCATTCAACGAG | 6613 |
rs534370130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175296 | CCTCTCATTTTCAGT[C/G]AACAGTAAGATGTAG | 6613 |
rs534483222 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172685 | TCTCCATGTTGGTCG[A/G]AGTGGTCTCAAACTC | 6613 |
rs534609549 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174435 | TGGGCACATTGATTC[A/G]TGCCTATAATCCCAT | 6613 |
rs534640727 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177808 | GACCAGCCTGGCCAA[C/T]GTGGTAAAACCCCGT | 6613 |
rs534896130 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168627 | TTGTTTTTTTTTTGA[A/G]ACAGGATTTCTGTCA | 6613 |
rs535013415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171461 | AGAGGTTGCAGTGAG[C/T]TGAGATCACGCCACT | 6613 |
rs535072674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168751 | GAGATTACAGGCATC[C/T]GCCACCATGCCCAGC | 6613 |
rs535161177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175987 | CACAGCTACTATAAT[A/G]TTAAATAGAACATAC | 6613 |
rs535521187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173925 | TGGTACATAAAGAGT[C/T]AAAGGATCAGAGAGC | 6613 |
rs535591968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173551 | ACCATCTTGGGTGAC[A/G]GCAGCCTCCACTTCC | 6613 |
rs535611028 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179926 | CTGGGATTACAGATA[C/T]GAGCCACTGCATCAG | 6613 |
rs535745943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169312 | GGGAGGCTGAAGTGG[A/G]CGGGTCACCTGAGGT | 6613 |
rs535940014 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183511 | GTCTCGCTCAGTCGC[C/T]CAGGCTGGAGTGCAG | 6613 |
rs536018300 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179043 | AGTGCTGGATTACCA[C/T]GCCCAGCCTATGATT | 6613 |
rs536019525 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183084 | CACCCCCACCCCCCG[A/T]CCCACGCCACCGCGT | 6613 |
rs536086460 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184960 | CCGGGCATGGTGGCT[C/T]ATGCCTGTAATCCCA | 6613 |
rs536384228 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169204 | ACCAGCTCACTCCAG[C/T]CTGAGTGACAAAGCA | 6613 |
rs536531679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170037 | AGCTGGGCGTGGTGG[C/T]GCACGCCTGCACGCC | 6613 |
rs536533651 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175833 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGACTGA | 6613 |
rs536601043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178376 | AAAATTGGCTGGGCA[C/T]GGTGGCACGCACCTG | 6613 |
rs536819742 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167874 | CGTACAAAAAAGTTA[C/T]AAAATTGTCCTTGGT | 6613 |
rs536998553 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172782 | GCCCGGCGATGCCTG[C/G]CTAATTTTTGTATTT | 6613 |
rs537123321 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176761 | CTGTCTTACTAAAAA[-/AC]ACACTTCAGGAGATA | 6613 |
rs537480022 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178812 | TTTGGGAGGCTGAGG[C/T]GGGTGGTTCACGAGG | 6613 |
rs537563958 | in-del | -/TCT | 0.0357096 | 0.128762 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183460 | TAAAATGCAGTGTCT[-/TCT]TCTTCTTCTTCTTCT | 6613 |
rs537591011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171092 | AAAAAAAGTACACCC[A/C]AAGGAGCAAAGCAGC | 6613 |
rs537926975 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169406 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCCCTGTGT | 6613 |
rs537989010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174403 | CACAAAAAACAAACA[C/G]AAACCACTGGTGGGG | 6613 |
rs538074752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179616 | GTATTTTCTTATTAC[A/G]TTGTAAATACACTAG | 6613 |
rs538089459 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173086 | TTTTTACTGGGTGAT[-/A]AAAGTTGAAATTCAA | 6613 |
rs538203894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182606 | GAGGCCGCCGGGGGC[G/T]GGAGAGAGCGGCGGG | 6613 |
rs538348507 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175300 | TCATTTTCAGTGAAC[A/G]GTAAGATGTAGTATT | 6613 |
rs538399543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174027 | GACGTGGCAATTAGG[A/G]CTATTAGTTCCTTTT | 6613 |
rs538413666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177718 | AGCCAGGCGTAGTGC[C/T]TCATGCCTGTAATCC | 6613 |
rs538591262 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183155 | GACACGCGCACCCGG[C/G]CCGCCGCGGGGGCGC | 6613 |
rs538678743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175392 | GTGTCGCGATCTCGG[C/T]TCACTGCAACCTCCA | 6613 |
rs538794033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171615 | ATTGGGAGAATAATT[C/G]TAAAACGAATCAATT | 6613 |
rs539030720 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173482 | ACTGGAAGTCATTTT[G/T]TTTTTTTTTTGAGAG | 6613 |
rs539042728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181853 | TTTGTTGTCATGGGT[C/T]AAATACACAGTTTTA | 6613 |
rs539123229 | snp | A/C | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184743 | ACTTCTTCTCCTTCA[A/C]ACACTCCTCATCCAA | 6613 |
rs539214324 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182656 | GGAGGAAGAGAGGGA[A/G]GGAGGAAAATGGCGC | 6613 |
rs539322092 | in-del | -/C | 0.0271762 | 0.113356 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182700 | CTGAGCCGCGGCCGG[-/C]CCCGTGGGGGGCCCG | 6613 |
rs539500000 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172862 | CTGACCTCAAGCAAT[C/T]TGCCTGCCTCAGCCT | 6613 |
rs539539250 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177366 | GCAAGACTCCATCTC[-/A]AAAAAAAAGAAATTA | 6613 |
rs539564225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178412 | CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 6613 |
rs539710419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168663 | GCTGGACTGCAGTGG[C/G]GTGATCTCAGCTCAC | 6613 |
rs539991752 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184894 | ACCTTAGATGTGTGA[C/T]AGGCCAAAGCAGGAA | 6613 |
rs540008293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169667 | GGATTATAGGCGTGA[A/G]CCACTGCACCCGGCC | 6613 |
rs540213222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173713 | AAATCCTGGACTCAA[A/G]TGCTCCGCCCACCTT | 6613 |
rs540361008 | in-del | -/A | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168132 | TTGGCTGTTTAGTTA[-/A]AAAAAAAAAAAAATG | 6613 |
rs540375368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175518 | AGAAACAGGGTTTCG[C/T]CATGTTGGCCAGGCT | 6613 |
rs540560398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180989 | TGCTAGTCTAGTTTT[C/T]GTTCCCATGAAAATA | 6613 |
rs540576948 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177187 | AAAAAAAAAAAAAAA[A/T]TAATTAATTAAATAA | 6613 |
rs540612646 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168246 | TACGGTAGTAGTCAG[C/G]ATGTGGTGGAACCAA | 6613 |
rs540752665 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182756 | GCTCTGGCCGGACCC[C/G]GGCCCGCGCCATGAC | 6613 |
rs540902632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168990 | TACTGGAGGCCAACA[C/T]TGGAGGATTGCTTGA | 6613 |
rs540959259 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184104 | AAAAAAAGCTCCCAA[C/T]TCTATGAAGTTACCA | 6613 |
rs540959884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174082 | AATTTCAATTCAGCA[G/T]GTAGAACTAAAATGG | 6613 |
rs540974408 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171310 | ATTTTGTACTGACTC[C/T]GTCAATACAGAAAAT | 6613 |
rs541007381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171690 | GAAGATTTTAAAATG[A/C]CTCAAGGTCACGGAT | 6613 |
rs541056105 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180439 | ACTTCTTGGTTTGGC[A/G]CGGTGGCTCATGCTT | 6613 |
rs541142274 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170678 | ACATAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 6613 |
rs541225473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182143 | TTCATGAAACCACAT[G/T]GTGTTCGCGGATTAG | 6613 |
rs541283644 | in-del | -/AAAC | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174931 | AAGAAATACCTAAAT[-/AAAC]AATTGCCAACATGTT | 6613 |
rs541371219 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172027 | TTTTTTTTTTTTTTT[G/T]ACAGGGTTTCACTCT | 6613 |
rs541555896 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170151 | CATTGCATGTGACAA[A/G]AAACTGTCTCAAAAA | 6613 |
rs541623182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179250 | TATATGGTATCTTGC[C/T]GGGCACAGTGGCTCA | 6613 |
rs541858527 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184077 | CCTCTCCTCCGTTAG[C/T]ATAGAAAAAAAAAAA | 6613 |
rs542120128 | in-del | -/CTTTT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175323 | GTAGTATTTTTTTTC[-/CTTTT]CTTTTTTTTTTGAGA | 6613 |
rs542230795 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177759 | GGAGGCCGAGGTGGC[A/G]AGACGGGTGGGTCAC | 6613 |
rs542464896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178501 | CCTGGGCAACAGTGC[A/G]AGACTCTCAAAAAAA | 6613 |
rs542544126 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175805 | GCCCAGCTAATTTTT[C/G]TGTTTTTAGTAGAGA | 6613 |
rs542554643 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177846 | AAAAATAAATTAGCC[A/G]AGCACGGTGGTAGGT | 6613 |
rs542573584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174652 | AAGCTCTGAACTCTA[C/T]AAGAACTTATACTCC | 6613 |
rs542574690 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178080 | GGAGGACTGCTTGAG[C/G]CTGGGAGGCAGAGGA | 6613 |
rs542591553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181979 | AAGGCGCGGGAGGCG[A/G]GGGGTGCCACCAAAC | 6613 |
rs542613815 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169121 | TCCATACTCCCAGCT[A/C]CTCAGGAAGCCGAGG | 6613 |
rs542806556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170806 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 6613 |
rs542867835 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176046 | TAGACAAGGAAATGA[A/C]ATTTTTTTTTTTTAA | 6613 |
rs543066728 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169957 | GTCGGGAGTTCAAGA[A/C]CAGCCTGGCCAAAAT | 6613 |
rs543128120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178904 | AGGATGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 6613 |
rs543350860 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169536 | CTACAGGTGCCCGCC[A/T]CAACGCCTGGCTAAT | 6613 |
rs543511982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171039 | CGGTGCACTGACTAT[A/G]TAAGTTAGCCATGCT | 6613 |
rs543604299 | snp | A/G | 6.61529e-05 | 0.00575083 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174859 | AATAAACAGCATTAA[A/G]AGAAACAGAATTCTA | 6613 |
rs543605824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176722 | TAATTTCCTTTAATA[C/T]TTACCCAAATCTGTA | 6613 |
rs544001336 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182885 | AAAAGAGGTACCAGG[G/T]CCGCACCAAACGAGC | 6613 |
rs544722076 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184177 | TCCCCGCCAGCTGTC[C/T]CCAACCCCTCCCCTC | 6613 |
rs544778341 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168149 | AAAAAAAAAAAATGC[A/T]ATATGCTTGTGCACA | 6613 |
rs544873886 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179529 | GAGACTCTGTCTCAA[-/A]AAAAAAAAAAAAAAA | 6613 |
rs544923989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179100 | AGAAGTTCTCCAAAA[C/G]GATTACCTTTTAAAA | 6613 |
rs544961610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170065 | GCCTGTAATCCCAGC[C/T]ACTTGGGAGGCTGAG | 6613 |
rs545015767 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176548 | TTGAACCTGGGAGGC[A/G]GAGTTTGCAGTGAGC | 6613 |
rs545076545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169609 | AGGACAGTCTAGATC[G/T]CCTGACCTCATGATC | 6613 |
rs545357585 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167527 | TGCTAGTATACTTGC[A/G]TATTAACATGGGACC | 6613 |
rs545811435 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172515 | TTTTTTGAGTTTCGC[A/T]CGTTACCCATGCTCG | 6613 |
rs545816366 | in-del | -/A/AAA | 0.0931525 | 0.195027 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178509 | CAGTGCGAGACTCTC[-/A/AAA]AAAAAAAAAAAAAAA | 6613 |
rs545868231 | in-del | -/GAGA | 0.00136032 | 0.0260444 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174737 | AATTTTTCTAATTAG[-/GAGA]GATTTTTTTACCTGT | 6613 |
rs545924267 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174879 | ACAGAATTCTATTTA[C/T]ATAAAAGTACATGCA | 6613 |
rs546334570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171915 | GTGAAGTTTTACAGT[C/G]AAACTGTAAATGCCT | 6613 |
rs546373989 | snp | A/C | | | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182991 | GCGCTCCCTCCCCCC[A/C]CCCTGCGTGCGCGAG | 6613 |
rs546546289 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183560 | CAGCAACCTCTGCCT[C/G]CCGGGTTCAAGTGAT | 6613 |
rs546612074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168729 | TGCCTCAGTCTCCCA[A/G]GTAGCTGAGATTACA | 6613 |
rs546789387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169281 | CAATGGCTCACTCCT[A/G]TAATCTCAACACTTT | 6613 |
rs546806206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172607 | CTGCCTCAGCCTCCC[C/G]AGCAGCTGGGATTAC | 6613 |
rs546928289 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167701 | GCCTCAATTTTCTAT[C/T]TAATATTTCTCAGAA | 6613 |
rs547100419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170889 | AATTAATAAAACATA[C/G]TATGCTCAGATATTA | 6613 |
rs547505626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170435 | ATTAGCTGGGTGTGG[C/T]TGCGCACGCCTGTAG | 6613 |
rs547582002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175817 | TTTGTGTTTTTAGTA[A/G]AGACAGGGTTTCACC | 6613 |
rs547596392 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175313 | ACAGTAAGATGTAGT[A/G]TTTTTTTTCCTTTTC | 6613 |
rs547596492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181728 | CGAAGAATATCCCGA[A/T]TCCCCCCGGAACAGC | 6613 |
rs547823421 | snp | C/G | 1.66032e-05 | 0.0028812 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181020 | AGATTTTTAAAAATA[C/G]TTTTATTCAGTGGAA | 6613 |
rs547861405 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184709 | CTGCCCCAAGCTGGA[A/G]AGGCCAGCAACATTC | 6613 |
rs547988952 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172726 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 6613 |
rs548029059 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182038 | TGATGGGTGTCCCCA[A/G]GTCCTCCCGGGAAGT | 6613 |
rs548181624 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178887 | TTAAAACTGGAAGGC[G/T]GAGGATGCAGTGAGC | 6613 |
rs548601534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177431 | CGCCTATAATCCCAA[A/C]ATTTTGGAAGGCCAA | 6613 |
rs548637163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171965 | TACCAGCCTCATTTA[C/T]CAATAGAATTTAGCT | 6613 |
rs548674912 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182985 | CGTCGTGCGCTCCCT[C/T]CCCCCACCCTGCGTG | 6613 |
rs548708649 | snp | C/T | 0.000148976 | 0.00862935 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181049 | AAGTACACATATGAA[C/T]TCCTCACCTGTCGTT | 6613 |
rs548994820 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174944 | ATAAACAATTGCCAA[C/T]ATGTTAACATACCCT | 6613 |
rs548998737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169313 | GGAGGCTGAAGTGGG[A/C]GGGTCACCTGAGGTC | 6613 |
rs549007310 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174345 | GCCATGACCCAAGAT[C/T]GTGACACTGTACTCA | 6613 |
rs549068765 | in-del | -/CTAGT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180976 | AGTCACTGTAATGTG[-/CTAGT]CTAGTTTTTGTTCCC | 6613 |
rs549103636 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173790 | GCTCTCATGAGCCAC[A/C/G]CTGCTAGGACAAAAC | 6613 |
rs549247370 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167816 | TTTGTTTTAGAGTAA[C/T]TTATCCCTACTTAAA | 6613 |
rs549334258 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169824 | ACTGGACTCCAACAC[C/T]GGTGACAGAGTGAGA | 6613 |
rs549367838 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181736 | ATCCCGATTCCCCCC[C/G]GAACAGCGGTAATAC | 6613 |
rs549378393 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168476 | TTTGGGTTTAAGTAT[C/G]CTGAAAACATGTACA | 6613 |
rs549565647 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173516 | GCCTCACTTTGTCAC[C/T]CAGGCTGGTGTGCAG | 6613 |
rs549921947 | snp | C/T | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167939 | CAATTGAACAAGGTA[C/T]GCAAGGATTTTTATG | 6613 |
rs549954809 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183123 | AGGCGCCCGCCCGGC[A/C]GGCGGGAAGAGGCGC | 6613 |
rs549958219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170945 | AGATTTTCATGTACA[A/G]AAATGAAAATATCTT | 6613 |
rs549970368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176267 | ATGGTCTCAATTTCC[C/T]GACCTCGTGATCCGC | 6613 |
rs550131784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181836 | ATTCTCCCCTCCCCC[C/T]CTTTGTTGTCATGGG | 6613 |
rs550177584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182211 | CCCCTTCGGGCCCCT[A/G]AGGCTATTAAAGTGG | 6613 |
rs550299845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178921 | GATTGCGCCACTGCA[C/T]TCTAGCCTGGGCAAT | 6613 |
rs550313179 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168608 | ACTATTAGATAAAAC[A/T]TTTTTGTTTTTTTTT | 6613 |
rs550373231 | snp | A/G | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183295 | GCCATAGGCCAGGGA[A/G]GGCAGACTTACTAGA | 6613 |
rs550505650 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179084 | TATGCAGTTTTGCTA[-/AAG]AAGTTCTCCAAAAGG | 6613 |
rs550880761 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179389 | AAAAATTAGCTGGGC[A/G/T]TGGTGGCGTGCGCCC | 6613 |
rs550947818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172550 | CAATGGCGTGATCTC[C/T]GGCTCACTGCAACCT | 6613 |
rs551011224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172009 | ACATACCATAATTGC[A/G]CCTTTTTTTTTTTTT | 6613 |
rs551108471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175695 | TGGAGTGCAGTGGTG[C/T]GATCTTGGCTCACTG | 6613 |
rs551408531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169931 | AGGCCGAGGCAGGCA[A/G]ATCACCTGAGGTCGG | 6613 |
rs551484928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175214 | TCTCGAACTCCTAAC[C/T]TCAGGTGCTCCGTCC | 6613 |
rs551500158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169169 | CCCATAAGATCAAGG[A/C]TGCAGTGAACTGAGA | 6613 |
rs551625832 | snp | G/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184297 | TGAATCCAGTATGCT[G/T]CTCAGTTTGTCACTC | 6613 |
rs551679838 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172505 | TTTTTTTTTTTTTTT[G/T]GAGTTTCGCTCGTTA | 6613 |
rs551776657 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183445 | ACCGGACTCTTGCCT[-/A]AAAATGCAGTGTCTT | 6613 |
rs551943036 | snp | C/T | 1.76225e-05 | 0.00296833 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181210 | AAAGAAAAATAAAAG[C/T]ATAATTTGGGAAATG | 6613 |
rs552077069 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178301 | CAGGCGGATCACGAG[C/G]TCAAGAGATCGAGAT | 6613 |
rs552260595 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178384 | CTGGGCACGGTGGCA[C/T]GCACCTGTAGTCCCA | 6613 |
rs552350653 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177741 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 6613 |
rs552497166 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168087 | ATTTTTCCCCATCCC[A/G]TCTCCACTTGATGTC | 6613 |
rs552509173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171387 | GGCATCATGGTGGGC[A/G]CCTGTAATCCCAGCT | 6613 |
rs552594008 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182912 | GAGCACACAAGCAGC[A/T]CCAGGAGCGGCAGAA | 6613 |
rs552620888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176775 | AACACACTTCAGGAG[A/C]TATAGGAACCTAGAC | 6613 |
rs552702586 | snp | G/T | 0.00159617 | 0.0282053 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167554 | GACCTAGAGAAACTT[G/T]TGGAACAAGGTGATA | 6613 |
rs552928767 | snp | C/T | 0.00953873 | 0.0683987 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168009 | TAACTTACTGGAATA[C/T]AAAGATAAGAGCTGA | 6613 |
rs552944718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173540 | TGTGCAGTGGTACCA[C/T]CTTGGGTGACGGCAG | 6613 |
rs553022935 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179538 | GTCTCAAAAAAAAAA[A/T]AAAAAAAGGTATCTT | 6613 |
rs553061874 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177689 | TCCATCTTAAAAAAA[A/C]AAAAGAAAAGAAAAG | 6613 |
rs553077077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179002 | ACTATGTTGTCCAGA[C/T]TGGTCTTCCAGCCTT | 6613 |
rs553307517 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175382 | CTGGAGGGCAGTGTC[A/G]CGATCTCGGCTCACT | 6613 |
rs553401342 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168664 | CTGGACTGCAGTGGC[A/G]TGATCTCAGCTCACT | 6613 |
rs553662506 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184028 | GCTTCTTCCCCCGGG[G/T]CTTTATTATTTCCTT | 6613 |
rs553736917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180493 | CGAGGCGGGCGGATC[A/G]CCTGAGGTCAGGAGT | 6613 |
rs553798224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179777 | GGATTCTCAGCCTCA[C/G]CCTCCGGAGTAGGTG | 6613 |
rs553862967 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176477 | AAAAATTAGCCGAGT[G/T]TGGTGGCATCCGCCT | 6613 |
rs553867299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174095 | CATGTAGAACTAAAA[C/T]GGTGAGGATTTGGCT | 6613 |
rs554054876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181941 | AGAAGCAATTCTGTA[G/T]CCCTAAAACGCTCCA | 6613 |
rs554067210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170023 | AAAACAAAAAAATTA[A/G]CTGGGCGTGGTGGCG | 6613 |
rs554068353 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181400 | CAGATACGGAAAAGC[C/G]TACATGCAATACTAT | 6613 |
rs554126848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171702 | ATGCCTCAAGGTCAC[A/G]GATCCAAACAAATAA | 6613 |
rs554324715 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183427 | CAATCTCAACCTGCT[A/T]CCCACCGGACTCTTG | 6613 |
rs554518683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176445 | ATATGGTGAAACCCC[A/G]CCTCTACTGAAAATA | 6613 |
rs554677883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171062 | GCCATGCTCTGTAAG[A/G]GGCAGTTAAAAAAAA | 6613 |
rs554752598 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178017 | AAAAAAAAAAGAATC[A/G]CCCAGTGGCACAAGC | 6613 |
rs555141821 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168118 | AATCAAAACATACCA[C/T]TGGCTGTTTAGTTAA | 6613 |
rs555194158 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174054 | TTTTTGTTCATGAAG[A/C]CACGTAAAAGAGAAT | 6613 |
rs555352648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168752 | AGATTACAGGCATCC[A/G]CCACCATGCCCAGCT | 6613 |
rs555357432 | in-del | -/ACGCCTGT | 0.00398564 | 0.0444627 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170047 | GTGGCGCACGCCTGC[-/ACGCCTGT]ACGCCTGTAATCCCA | 6613 |
rs555479305 | in-del | -/TCT | 0.0205582 | 0.0992796 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183462 | AATGCAGTGTCTTCT[-/TCT]TCTTCTTCTTCTTCT | 6613 |
rs555547382 | in-del | -/AC | 0.00478085 | 0.0486577 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176801 | TAGACTGTTTTAGTT[-/AC]ACAGTCTATCCCTTG | 6613 |
rs555666231 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179547 | AAAAAAAAAAAAAAG[G/T]TATCTTTATAAGGAA | 6613 |
rs555865962 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169302 | TCAACACTTTGGGAG[A/G]CTGAAGTGGGCGGGT | 6613 |
rs555979948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173615 | AAGTAGCTGGTACTA[A/C]AGGCACGTACCACTG | 6613 |
rs556063440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178560 | AAACCACCAAACTGA[A/G]GCATGATTCTGTTTG | 6613 |
rs556090595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176513 | CCCAGCTATTCGGGA[A/G]GCTGAGGCAGGAGGA | 6613 |
rs556129891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175377 | TCAGGCTGGAGGGCA[C/G]TGTCGCGATCTCGGC | 6613 |
rs556266029 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171406 | GTAATCCCAGCTACT[C/T]GGGAAGCTGAGGCAG | 6613 |
rs556314940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177081 | CCAGCTACTCCAGCC[A/G]GAGGTTGAGGGGGGA | 6613 |
rs556385577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171159 | CTTGCGATGGAGTTT[C/G]GCTGTTGTTGCCCAG | 6613 |
rs556540032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172405 | GCTGACTTTAATCTC[C/T]GCCTCTCGGGTTCAG | 6613 |
rs556656624 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175540 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 6613 |
rs556719062 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177150 | CGAGATCGTGCCATT[C/G]CAAGAGCGAGACTCT | 6613 |
rs556745093 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177959 | ATGTCACTACACTCC[A/G]GTCTGACCGACAAAG | 6613 |
rs556751659 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167927 | ATTAAAATTCTCCAA[C/T]TGAACAAGGTATGCA | 6613 |
rs556921777 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178385 | TGGGCACGGTGGCAC[A/G]CACCTGTAGTCCCAG | 6613 |
rs557249607 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183938 | ATCCTTTCCTCGTTG[C/T]ATCCAGTTAAAACAT | 6613 |
rs557918362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169407 | TTTTTTTTTTGAGAC[A/G]GAGTCTCCCTGTGTC | 6613 |
rs558056908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174473 | GGAGGCCAAGGCTGC[A/C]GTGAGCTATAATGAG | 6613 |
rs558115899 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183201 | GGGCTGTATTGTCCT[C/G]CTTCGTGGTGGAGCA | 6613 |
rs558318007 | in-del | -/TGT | 0.00199481 | 0.0315187 | cds-indel | SUMO2 | GRCh38.p7 | 17:75167953 | ATGCAAGGATTTTTA[-/TGT]TGTTGTTTTTTTTTT | 6613 |
rs558331987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174048 | AGTTCCTTTTTGTTC[A/G]TGAAGACACGTAAAA | 6613 |
rs558393171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179663 | AACATTCTAAAGTTT[G/T]TTTTTTTTTTTCCTT | 6613 |
rs558481769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171621 | AGAATAATTCTAAAA[C/T]GAATCAATTCCAAAT | 6613 |
rs558532313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170093 | GAGGCAGGAGAATCA[C/T]TTGAACCCAGGAGGT | 6613 |
rs558545447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177131 | GGTGGAGGTTGCAAT[A/G]AGCCGAGATCGTGCC | 6613 |
rs558571923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173907 | TGACAGAACAAAATG[A/T]AGTGGTACATAAAGA | 6613 |
rs558668827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170647 | CAAGGTCAGTCATTC[A/G]AGACCAGCCTGGCCA | 6613 |
rs558683027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175934 | CACTGCGCCCAGCCA[A/G]TAAGTCATTCTTTTA | 6613 |
rs558863437 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171864 | TTAAAACCAAACAAG[C/T]CTGTCATCTATCTAC | 6613 |
rs558974902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175440 | ATTTTCCTGCCTCAG[A/C]CTCCTGATTAGCTGG | 6613 |
rs559056064 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181888 | GATTTGTTTCTTGTA[C/G]ATTTCGACCCAACCT | 6613 |
rs559076903 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181253 | ACGTTTTATAAAGCA[A/G]CAGCAGCCCTAGTTG | 6613 |
rs559358070 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172517 | TTTTGAGTTTCGCTC[A/G]TTACCCATGCTCGAG | 6613 |
rs559491513 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178580 | GATTCTGTTTGTTTG[C/T]GGTTTTGAGACAGGG | 6613 |
rs559601536 | snp | A/G | 0.000286779 | 0.0119711 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182803 | GGCGAAGGGGCCGGC[A/G]GCGAGCTCACCTTGG | 6613 |
rs559664818 | in-del | -/A | 0.145642 | 0.227177 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177172 | CGAGACTCTTGTCTC[-/A]AAAAAAAAAAAAAAT | 6613 |
rs559745306 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171920 | GTTTTACAGTGAAAC[C/T]GTAAATGCCTTTAAA | 6613 |
rs559817498 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182970 | GAGAGGGTGCGCGCA[A/C]GTCGTGCGCTCCCTC | 6613 |
rs560038458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178036 | AGTGGCACAAGCCTA[C/T]AGTCCCAACTACCTG | 6613 |
rs560075508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170191 | AATGAAAGCTGAATA[C/T]GTCTGTGTCGAGGGC | 6613 |
rs560170548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179204 | CATAAGTTCATGTAG[A/G]GTGATTTCAGCAAAA | 6613 |
rs560233557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178779 | AGGCGCAGTGGCTCA[C/T]GCCTGTAAACCCAGC | 6613 |
rs560336347 | in-del | -/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179659 | TCAAACATTCTAAAG[-/T]TTTTTTTTTTTTTTT | 6613 |
rs560433410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175521 | AACAGGGTTTCGCCA[G/T]GTTGGCCAGGCTGGT | 6613 |
rs560447640 | snp | C/T | 2.12087e-05 | 0.00325636 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174853 | AAAAGCAATAAACAG[C/T]ATTAAGAGAAACAGA | 6613 |
rs560592931 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169036 | ACCACCTGGGCAACA[C/T]AGGGAGACAACATCT | 6613 |
rs560607806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176681 | CCTTGAACTTCCTGG[A/G]ATAGCTTTAAAAAAG | 6613 |
rs560612995 | in-del | -/AG | 0.00676609 | 0.0577691 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169240 | TCCTGTATCAAAAAA[-/AG]AGAAAAAAAGGCTAG | 6613 |
rs560767946 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171330 | ATACAGAAAATAAAA[A/T]AAAAACAACATAAAC | 6613 |
rs561004353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170907 | TGCTCAGATATTAAA[C/T]ACCATATAGCCGTTA | 6613 |
rs561125048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176211 | TGCTGGGCTAATTTT[C/T]TGTATTTTAGTAGAG | 6613 |
rs561228842 | in-del | -/C | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167821 | TTTAGAGTAATTTAT[-/C]CCTACTTAAAGACAG | 6613 |
rs561542957 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75182500 | CCTCCTCACGCGCGC[A/C]GGCCGGCTGGGCCAA | 6613 |
rs561633074 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184991 | GCACTTTGGGAGGCC[A/G]AGGTGGGAGGATCAC | 6613 |
rs561713808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179927 | TGGGATTACAGATAT[A/G]AGCCACTGCATCAGG | 6613 |
rs561718214 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75182048 | CCCCAAGTCCTCCCG[A/G]GAAGTCTCCGGGTGC | 6613 |
rs561961008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179266 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 6613 |
rs561993908 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183637 | ACAACGCCCGGCTAA[C/T]TTTTCGTAGAGACGG | 6613 |
rs562041506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178157 | CAACAGGGCAAAAGC[C/G]TGTCTCAAAAAAAAA | 6613 |
rs562105606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177611 | CACTGGAACCTGGGA[A/G]GCGGAGGTTCCAGTA | 6613 |
rs562155710 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184082 | CCTCCGTTAGTATAG[A/G]AAAAAAAAAAAAAGC | 6613 |
rs562210469 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177779 | GGGTGGGTCACCTGA[A/G]CTCAGGAGTTCAAGA | 6613 |
rs562299060 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167612 | CATCAGTATCAGTCT[C/G]TCAGAAACACCAAGT | 6613 |
rs562449271 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175646 | GTTGTTTTTGTTTGT[G/T]TGTTAAGACAGAGTT | 6613 |
rs562531945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169538 | ACAGGTGCCCGCCAC[A/G]ACGCCTGGCTAATTT | 6613 |
rs562610913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174117 | GATTTGGCTGGGTGC[A/G]GTGGCTCACACCTGT | 6613 |
rs562677585 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170836 | GCCTGGGTGACAGTG[C/T]GAGACTCCAGGTCTC | 6613 |
rs562740763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170301 | ATTAGGCTGGGCGCC[A/G]GGGCTCACGCCTATA | 6613 |
rs562768992 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176048 | GACAAGGAAATGAAA[A/T]TTTTTTTTTTTAAAT | 6613 |
rs563517823 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171374 | ACAAAATTAGCCAGG[C/T]ATCATGGTGGGCGCC | 6613 |
rs563529059 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170674 | GCCAACATAGTGAAA[C/T]CCCGTCTCTACTAAA | 6613 |
rs563782248 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182888 | AGAGGTACCAGGTCC[C/G]CACCAAACGAGCACA | 6613 |
rs563810966 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172365 | GGGGCTGTTACCCAG[A/G]CTGGAGTGCAGTGGC | 6613 |
rs563881773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177290 | GAGAATTGCTTGAAC[A/C]CAGGAGCAGAGGTTG | 6613 |
rs564165387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180934 | CGACAAAACTGACGT[A/G]CCAAGTGCATATTCA | 6613 |
rs564254265 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184327 | CCTCTTGAACTTTGC[A/G]GGAGGTAGGTTTTCC | 6613 |
rs564353014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174252 | AAAATTAGCCAGGCA[C/T]GGTGGTGCATGCCTG | 6613 |
rs564376962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178281 | AGCACTTTGGGAGGC[C/T]GAAGCAGGCGGATCA | 6613 |
rs564544284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178671 | CCTGCCAAGCTCAAG[C/G]AATCCTCCCACCTCT | 6613 |
rs564547200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171529 | GAAAAATAAAAAAAT[A/T]AAAAAAAGCTGGGGA | 6613 |
rs564589815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173669 | TTTTGTAAAGAGAGG[G/T]TTTTGCCATGTTGCC | 6613 |
rs564599914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182075 | GTGCCTCAAAAGCCG[C/G]GTTCAAAAGTTAAGC | 6613 |
rs564612349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179421 | TAGTCCCACCTACTC[A/G]GGAGACTGAGACAGG | 6613 |
rs564660281 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181700 | AAGGAAACACACAAA[A/C]AAAAAAAACAATCGA | 6613 |
rs564666619 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178271 | CTGTAATCCCAGCAC[A/T]TTGGGAGGCCGAAGC | 6613 |
rs564674890 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168167 | ATGCTTGTGCACATA[C/T]ACCAGTTACTTTATG | 6613 |
rs564712196 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170882 | AAACCCAAATTAATA[A/T]AACATAGTATGCTCA | 6613 |
rs564736241 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167665 | GTTACTTCTAAGCAG[A/G]CCTATTTATGTTTTT | 6613 |
rs564774766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176117 | CAATCTCAGTTCAAC[A/G]CAACCTCCACCACCG | 6613 |
rs565004162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169620 | GATCTCCTGACCTCA[C/T]GATCCACCCTCCTCG | 6613 |
rs565189274 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169944 | CAGATCACCTGAGGT[C/T]GGGAGTTCAAGACCA | 6613 |
rs565572384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178312 | CGAGGTCAAGAGATC[A/G]AGATCATCCTGGCCA | 6613 |
rs565669155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176307 | CACTAACAGGAAATT[C/T]AAAGGAAAAAAATGC | 6613 |
rs565769593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172114 | TCTGACACCTTTCCC[C/T]CGCCCAGATTCTCCT | 6613 |
rs565970974 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176388 | ACTTTAGGAGACCAA[A/G]GCAGATCATCTGAGG | 6613 |
rs566033217 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170874 | AAAAAAAAAAACCCA[A/T]ATTAATAAAACATAG | 6613 |
rs566106618 | in-del | -/T | 0.358728 | 0.225118 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172488 | TCATGCCTGGCTAAA[-/T]TTTTTTTTTTTTTTT | 6613 |
rs566175050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182407 | AAGCCCGAGCCCAGA[A/G]GACTCCTCGCCGCCT | 6613 |
rs566187493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181896 | TCTTGTAGATTTCGA[C/G]CCAACCTAAAGTTGT | 6613 |
rs566381863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176903 | TACTTAAAAACAAAG[A/G]CCAAGTATTGTGGCT | 6613 |
rs566588938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179039 | CCAAAGTGCTGGATT[A/G]CCACGCCCAGCCTAT | 6613 |
rs566610439 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169295 | TGTAATCTCAACACT[C/G/T]TGGGAGGCTGAAGTG | 6613 |
rs566793743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174301 | GAGGCTGAGGCAGGA[A/G]AATTGCTTAAGCATG | 6613 |
rs566970612 | snp | A/C | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184828 | GGCCTCTGGATGGAG[A/C]TGCATTTGCTGGCCT | 6613 |
rs567182415 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173069 | ACATTTATCACTTTC[C/T]AGTTTTTACTGGGTG | 6613 |
rs567293884 | in-del | -/G | 0.0126979 | 0.078662 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181977 | AAAGGCGCGGGAGGC[-/G]GGGGGGTGCCACCAA | 6613 |
rs567562644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175826 | TTAGTAGAGACAGGG[C/T]TTCACCATGTTGGCC | 6613 |
rs567574796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175315 | AGTAAGATGTAGTAT[C/T]TTTTTTCCTTTTCTT | 6613 |
rs567635561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181325 | GCATACTGCTGTTTT[C/G]AGCTGCTGAAATCAA | 6613 |
rs567759060 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175131 | GGGACTACGGTCCCC[C/T]GCCACAACAACCGGC | 6613 |
rs567887760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170029 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGCACGCC | 6613 |
rs567957812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173365 | AGGTCTTGCTATATT[C/G]CCCAGACTGGTCTTA | 6613 |
rs567964410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172767 | GGCATGAGCCACTGC[A/G]CCCGGCGATGCCTGG | 6613 |
rs568027638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178368 | AAAATACAAAAATTG[G/T]CTGGGCACGGTGGCA | 6613 |
rs568052658 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183900 | GCGAGAACTACCCAA[A/C]AATCAAGCTTCCAGC | 6613 |
rs568207393 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167422 | AGAACTTTTTCCTTG[C/T]CACATGTGCTACCCT | 6613 |
rs568444038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171978 | TATCAATAGAATTTA[A/G]CTCCTCCTTGTGGCT | 6613 |
rs568509533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171514 | GCAAAACTCCGTCTC[A/G]AAAAATAAAAAAATA | 6613 |
rs568523623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176986 | TCAGGAGTTCGAGAC[C/T]AGCCTGTCCAACATG | 6613 |
rs568669638 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171166 | TGGAGTTTCGCTGTT[G/T]TTGCCCAGGGTGGAG | 6613 |
rs568806838 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178717 | TGGACTACAGGTATG[C/T]GCCACCACAACCACC | 6613 |
rs568846241 | snp | A/G | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183784 | TTCTTCTGTCCTGCT[A/G]GTAACCCTAGACTTT | 6613 |
rs568851677 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169869 | AAAAAAAAAAGGTGG[G/T]GGGGGGCGGGTGTGG | 6613 |
rs568871872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180303 | TGGGCAACAGAGCAA[A/G]ACTCCATCAAAAACA | 6613 |
rs568914196 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169385 | CCCTATTAAAAAAAA[A/T]TTTTTTTTTTTTTTT | 6613 |
rs569461662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179563 | TATCTTTATAAGGAA[C/G]TACATACAAGAAGGT | 6613 |
rs569784949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177105 | GGGGGGAAAATTGCA[C/T]GAACCCGGGAGGTGG | 6613 |
rs569851695 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183151 | CGCGGACACGCGCAC[A/C]CGGCCCGCCGCGGGG | 6613 |
rs569867910 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183728 | GCCTCCCAAAGTGCT[G/T]GGATTACAGGCGTGA | 6613 |
rs569906623 | in-del | -/TCTTCT | 0.00328204 | 0.0403763 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183457 | GCCTAAAATGCAGTG[-/TCTTCT]TCTTCTTCTTCTTCT | 6613 |
rs569967056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170613 | AAAACAAAAAACCCA[C/T]GGCAGGCGTGGTGGC | 6613 |
rs569976207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181848 | CCCCCTTTGTTGTCA[C/T]GGGTCAAATACACAG | 6613 |
rs570066351 | snp | G/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167963 | TTTTATGTTGTTGTT[G/T]TTTTTTTTTGTTAAA | 6613 |
rs570132558 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181364 | CGGAAAAATCCTGCA[C/G]TAACAGTATTAGATA | 6613 |
rs570267299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175853 | GGCCAGACTGATCTC[A/G]AACTCCTGACCTCAA | 6613 |
rs570359286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168648 | ATTTCTGTCACCCAG[G/T]CTGGACTGCAGTGGC | 6613 |
rs570371449 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167961 | ATTTTTATGTTGTTG[G/T]TTTTTTTTTTTGTTA | 6613 |
rs570435610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182559 | CGGGCGTCCGCTTTC[A/T]GCCCGCCCAACTCGC | 6613 |
rs570616620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173879 | AAGACAATCCAGCTG[A/G]TCCTACAGAAAGTGA | 6613 |
rs570630389 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168948 | ATATTAGCCAGGTGC[A/G]GTGGCTCATGCCTGT | 6613 |
rs570677288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179401 | GGCGTGGTGGCGTGC[A/G]CCCGTAGTCCCACCT | 6613 |
rs570918179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172069 | TAGAGTGAAGTGGCA[C/T]GACCTCCGCGCTCAC | 6613 |
rs570946570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177643 | GCCTAGATTGCGCCA[C/T]TGCATTCAGCCTCAG | 6613 |
rs571211298 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169974 | AGCCTGGCCAAAATG[A/G]TGAAACCCAGTCTCT | 6613 |
rs571279505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175229 | CTCAGGTGCTCCGTC[C/T]GCCTCAGCCTCCCAA | 6613 |
rs571545065 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181239 | TGTGATCAACGAACA[C/T]GTTTTATAAAGCAGC | 6613 |
rs571602689 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180478 | AGCACTTTGGAAGGC[A/C/T]GAGGCGGGCGGATCA | 6613 |
rs571677654 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183234 | ATCAAAATGGCTTCC[A/G]GCTGGTCCTCGGTGG | 6613 |
rs571688400 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175762 | CTCAGCCTCCCGAGT[A/G]GCTGGGATTACAGGC | 6613 |
rs571737530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176653 | AACCGACCTAAAATG[A/C]CCCAACCTACACCCT | 6613 |
rs571800744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182726 | GCCCGGGAAAGCGCT[A/G]GGAGCCAGCGGCGGG | 6613 |
rs571802127 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183964 | AACATACACATGCGT[C/G]CCTCCTGTCTGAAGA | 6613 |
rs571847686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174506 | CACTACACTTCAACC[C/T]GGGCAACAGAGAGGC | 6613 |
rs572224863 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170025 | AACAAAAAAATTAGC[C/T]GGGCGTGGTGGCGCA | 6613 |
rs572266789 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171287 | GCATGCGCCATCATG[C/T]CCAGCTAATTTTGTA | 6613 |
rs572301952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171622 | GAATAATTCTAAAAC[A/G]AATCAATTCCAAATT | 6613 |
rs572342911 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177823 | CGTGGTAAAACCCCG[C/T]TTCTACGAAAAATAA | 6613 |
rs572385494 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171881 | TGTCATCTATCTACT[A/G]AAACAAAATTATCCA | 6613 |
rs572446568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170140 | CAAGATCATGCCATT[A/G]CATGTGACAAGAAAC | 6613 |
rs572456765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175455 | CCTCCTGATTAGCTG[C/G]GACTAGGCAGGCGCC | 6613 |
rs572495990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175976 | TGCTTTTCAGACACA[G/T]CTACTATAATGTTAA | 6613 |
rs572790256 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168014 | TACTGGAATATAAAG[A/G]TAAGAGCTGAATGAG | 6613 |
rs572804797 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173550 | TACCATCTTGGGTGA[C/T]GGCAGCCTCCACTTC | 6613 |
rs572845698 | in-del | -/T | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167960 | ATTTTTATGTTGTTG[-/T]TTTTTTTTTTTTGTT | 6613 |
rs572847438 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167574 | ACAAGGTGATATTTA[C/T]AAAACTGTTATTCTT | 6613 |
rs572911305 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172934 | CCCGTAATTCCTTTT[C/G]AGAGACTGTCACCAG | 6613 |
rs573110247 | in-del | -/AAAAG | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177690 | CCATCTTAAAAAAAA[-/AAAAG]AAAAGAAAAGCCAGG | 6613 |
rs573303726 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179894 | TCAACTGCCACCTGC[C/T]TCAGTCTCCCAAAGT | 6613 |
rs573506792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178463 | AGGTTGCAGTGAGCC[A/G]AGATGGTGCCACTGC | 6613 |
rs573570925 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178069 | AGCCTGAGGTGGGAG[C/G]ACTGCTTGAGCCTGG | 6613 |
rs573705094 | in-del | -/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172011 | TACCATAATTGCGCC[-/T]TTTTTTTTTTTTTTT | 6613 |
rs573728592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180586 | GGCCAGGCCTGGTAG[G/T]GGGCACCTGTAATCC | 6613 |
rs573728698 | snp | C/G/T | 0.00319074 | 0.0398324 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174105 | TAAAATGGTGAGGAT[C/G/T]TGGCTGGGTGCGGTG | 6613 |
rs573857290 | in-del | -/AGTA | 0.00318978 | 0.0398085 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176837 | TAGTAGGTGCTGCTC[-/AGTA]AGTATCAGTGGCATA | 6613 |
rs573868795 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181947 | AATTCTGTAGCCCTA[A/C]AACGCTCCAGAAAGT | 6613 |
rs573907185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176029 | TATGCATTTAAATGA[C/G]TTAGACAAGGAAATG | 6613 |
rs573970929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175565 | CCTCAGATGATCTGA[C/T]CACCTCAGCCTCCCA | 6613 |
rs573985934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181541 | AAAAAAGTTAAAAAT[A/G]GAGTCCCTTCTCTTT | 6613 |
rs574120861 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171745 | TATTTGTAACTACTA[G/T]AGCAGATAATCCCGT | 6613 |
rs574185172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177242 | GCTAGGTGGCAGGCG[C/T]TGTAATCCCAGTTAT | 6613 |
rs574195758 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184360 | TCATCTCTAGCCTGT[C/T]CTTTGTTCTCTCTGC | 6613 |
rs574203899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169533 | GGACTACAGGTGCCC[A/G]CCACAACGCCTGGCT | 6613 |
rs574288441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169095 | AAATTAGCCAGCCAT[A/G]GTGACACATGTCCAT | 6613 |
rs574406227 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172195 | GCCCGGCTAATTTTT[G/T]TATTTTTAGTAGAGA | 6613 |
rs574942737 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171084 | TAAAAAAAAAAAAAA[C/G]TACACCCCAAGGAGC | 6613 |
rs574999502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170707 | TACAAAAAATTAGCT[A/G]GGCATGGTGGCAGGT | 6613 |
rs575365417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168858 | GATCTGCCTGCCTCG[A/G]CCTCCCAAAGTGCTG | 6613 |
rs575368987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179950 | GCATCAGGCCTAAAG[A/G]AAGTTTTTATCTTCA | 6613 |
rs575427454 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168119 | ATCAAAACATACCAT[C/T]GGCTGTTTAGTTAAA | 6613 |
rs575790717 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178045 | AGCCTATAGTCCCAA[C/T]TACCTGGGAGCCTGA | 6613 |
rs575838463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179067 | TATGATTTTCTATTT[C/T]GTATGCAGTTTTGCT | 6613 |
rs575879852 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177937 | GAGGTTGCAGTGAGC[C/T]GAGATTATGTCACTA | 6613 |
rs575921266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182026 | CGTGTGCCCCGATGA[C/T]GGGTGTCCCCAAGTC | 6613 |
rs575937038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173621 | CTGGTACTACAGGCA[C/T]GTACCACTGCTCCCT | 6613 |
rs575999467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173091 | TACTGGGTGATAAAG[C/T]TGAAATTCAAAAGTA | 6613 |
rs576037333 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169679 | TGAACCACTGCACCC[A/G]GCCTAAAAATATTTT | 6613 |
rs576295913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182600 | CACTCGGAGGCCGCC[A/G]GGGGCGGGAGAGAGC | 6613 |
rs576403336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170844 | GACAGTGCGAGACTC[C/T]AGGTCTCAAAAAAAA | 6613 |
rs576470298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180815 | GGTAAAAAAAAATTA[C/T]TGTAAATATAATTTG | 6613 |
rs576677009 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177330 | GAGATCATGCCACTG[C/T]ACTCCAGCCTGGGCA | 6613 |
rs576747244 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167490 | ATACCTGGAAATCCA[C/T]GATACTATGGCCCAA | 6613 |
rs576800747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172821 | ACACGGGGTTTCACC[A/G]TATTGTCCAGGCTGG | 6613 |
rs576865198 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178395 | GGCACGCACCTGTAG[G/T]CCCAGCTACTTGGGA | 6613 |
rs577245255 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175230 | TCAGGTGCTCCGTCC[A/G]CCTCAGCCTCCCAAA | 6613 |
rs577337380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177301 | GAACCCAGGAGCAGA[A/G]GTTGCAGTGAGCTGA | 6613 |
rs577487045 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183959 | GTTAAAACATACACA[A/T]GCGTCCCTCCTGTCT | 6613 |
rs577595705 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183540 | AGTGGCACGATCTCG[C/G]CTCACAGCAACCTCT | 6613 |
rs577831219 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169423 | GAGTCTCCCTGTGTC[A/G]CCCAGGCTGGAGTCC | 6613 |
rs577882037 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181392 | ATAGCTGTCAGATAC[A/G]GAAAAGCCTACATGC | 6613 |
rs578181005 | in-del | -/TACTT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181513 | ATATCACTCCCAAAA[-/TACTT]TACCCCCCAAAAAAG | 6613 |
rs578192625 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179664 | ACATTCTAAAGTTTT[G/T]TTTTTTTTTTCCTTT | 6613 |
rs578234111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168945 | AGAATATTAGCCAGG[C/T]GCGGTGGCTCATGCC | 6613 |
rs578253508 | snp | C/G | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184067 | GAATTTTCTTCCTCT[C/G]CTCCGTTAGTATAGA | 6613 |
rs745526856 | in-del | -/TTA | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184031 | TCTTCCCCCGGGGCT[-/TTA]TTATTTCCTTTTGTC | 6613 |
rs745552901 | in-del | -/AA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179528 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 6613 |
rs745660786 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176778 | ACACTTCAGGAGATA[C/T]AGGAACCTAGACTGT | 6613 |
rs745734014 | in-del | -/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173476 | ACAAGACTGGAAGTC[-/G]ATTTTTTTTTTTTTT | 6613 |
rs745994655 | in-del | -/AC | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172347 | TTTTTTTTTTTTGAG[-/AC]AGGGGCTGTTACCCA | 6613 |
rs746083097 | in-del | -/AA | 1.94365e-05 | 0.00311735 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174832 | CAATCCCTGAACGAG[-/AA]AATTTAAAAGCAATA | 6613 |
rs746155821 | snp | C/T | 1.72507e-05 | 0.00293685 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75182820 | CGAGCTCACCTTGGG[C/T]TTTTCGTCGGCCATG | 6613 |
rs746454605 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173190 | TATTTTTGAGACAGA[A/G]TTTTGCTCTATCGCC | 6613 |
rs746470296 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170438 | AGCTGGGTGTGGTTG[C/T]GCACGCCTGTAGTCC | 6613 |
rs746519441 | in-del | -/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169386 | CCTATTAAAAAAAAA[-/T]TTTTTTTTTTTTTTT | 6613 |
rs747405979 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180884 | TAACCAAATCATCCT[A/C]AGGGTTTTCACGAGC | 6613 |
rs747418519 | snp | C/G | 7.48083e-05 | 0.00611544 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182840 | CGTCGGCCATGGCGA[C/G]CGCCGGAGTCTCCTC | 6613 |
rs747868380 | snp | C/T | 4.09945e-05 | 0.0045272 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168292 | TTGAGAATGTAATCT[C/T]GGTCTTTAAAGAACA | 6613 |
rs748048605 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171982 | AATAGAATTTAGCTC[C/T]TCCTTGTGGCTACAT | 6613 |
rs748123236 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175023 | GTTTTGATCTGTTGT[C/G]AAGGCTGAAGTGCAG | 6613 |
rs748197674 | snp | C/T | 3.97192e-05 | 0.00445623 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174743 | TCTAATTAGGAGAGA[C/T]TTTTTTACCTGTGCA | 6613 |
rs748371173 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180594 | CTGGTAGTGGGCACC[G/T]GTAATCCCAGATACT | 6613 |
rs748518045 | in-del | -/AA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180410 | AAAAAAAAAAAAAAA[-/AA]AAAAAAAAAAACGAC | 6613 |
rs748694031 | snp | A/G | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184244 | CCCCAAAGTTCCACT[A/G]AAACTGCTCTCCACA | 6613 |
rs748736256 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171674 | ATTGCAAATTCAACC[C/T]GAAGATTTTAAAATG | 6613 |
rs748932625 | snp | C/G | 3.33985e-05 | 0.00408633 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168436 | AAATGTAAAAGCACT[C/G]ATTAAGTTCTGAAAA | 6613 |
rs749017403 | snp | C/T | 3.89097e-05 | 0.0044106 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168311 | CTTTAAAGAACAGAG[C/T]TCTGGAGTAAAGAAG | 6613 |
rs749365427 | snp | A/C/G | 0.000216376 | 0.0103993 | missense, synonymous-codon | SUMO2 | GRCh38.p7 | 17:75181165 | CAAATTAATATGATC[A/C/G]TTGTTCTCAGTCTTG | 6613 |
rs749541275 | snp | A/T | 2.42999e-05 | 0.00348559 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174870 | TTAAGAGAAACAGAA[A/T]TCTATTTACATAAAA | 6613 |
rs749702677 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180392 | TGAGACTCCCAGCTT[-/A]AAAAAAAAAAAAAAA | 6613 |
rs749755793 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171070 | CTGTAAGGGGCAGTT[-/A]AAAAAAAAAAAAAGT | 6613 |
rs749766766 | in-del | -/AAC | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176620 | TTCAATATCAAAAAC[-/AAC]AACAACAACAACAAC | 6613 |
rs749777820 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170201 | GAATATGTCTGTGTC[A/G]AGGGCCCACAGAAGG | 6613 |
rs750088010 | snp | C/T | 0.000350079 | 0.0132256 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182765 | GGACCCCGGCCCGCG[C/T]CATGACCCCCACCGC | 6613 |
rs750430043 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181421 | GCAATACTATCAGTA[G/T]CAACAATATGTTTAA | 6613 |
rs750609260 | snp | C/T | 2.76407e-05 | 0.00371747 | missense | SUMO2 | GRCh38.p7 | 17:75168347 | TCCCTTTTCAGTAGA[C/T]ACCTCCCGTCTGCTG | 6613 |
rs750636227 | in-del | -/AAAAT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180714 | AAACTCCATCTCAAA[-/AAAAT]AAAATAAAATAATAA | 6613 |
rs751102338 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171843 | AGATACTTTTTACTA[C/T]TTCTTTTAAAACCAA | 6613 |
rs751339120 | snp | A/C | 0.000533333 | 0.0163212 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182782 | ATGACCCCCACCGCG[A/C]GGCGAGGCGAAGGGG | 6613 |
rs751537967 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168985 | AGTACTACTGGAGGC[A/C]AACATTGGAGGATTG | 6613 |
rs751731535 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181397 | TGTCAGATACGGAAA[A/G]GCCTACATGCAATAC | 6613 |
rs752084407 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175433 | TCAAGCAATTTTCCT[G/T]CCTCAGCCTCCTGAT | 6613 |
rs752127154 | snp | C/T | 5.01857e-05 | 0.00500902 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75168363 | ACCTCCCGTCTGCTG[C/T]TGGAACACATCAATT | 6613 |
rs752221079 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174009 | TGTCAAACAAAGCTA[C/T]GGGACGTGGCAATTA | 6613 |
rs752229100 | snp | C/T | 5.01593e-05 | 0.00500771 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75168390 | AATTGTATCTTCATC[C/T]TCCATTTCCAACTAG | 6613 |
rs752278586 | in-del | -/A | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184081 | CCTCCGTTAGTATAG[-/A]AAAAAAAAAAAAAAG | 6613 |
rs752369851 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179447 | ACAGGAGAATCGCTT[C/G]GTCTCGGGAGGCAGA | 6613 |
rs752422962 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178238 | TAGTGTTCAAGGCCA[C/G]GCACCAGTGGCTCAC | 6613 |
rs752663293 | snp | A/C | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183862 | CTCATCGCCTGTCTT[A/C]CAAGAGGAAACAGTA | 6613 |
rs752697425 | snp | C/T | 6.53488e-05 | 0.00571578 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182867 | CCTCAGCTGCCGCTT[C/T]ACAAAAGAGGTACCA | 6613 |
rs752728769 | snp | A/C | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183532 | TGGAGTGCAGTGGCA[A/C]GATCTCGGCTCACAG | 6613 |
rs753047956 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174161 | TTGGGAGGCCAAGGC[A/G]GGCGGATTACTTGTG | 6613 |
rs753132437 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171087 | AAAAAAAAAAAAGTA[C/T]ACCCCAAGGAGCAAA | 6613 |
rs753204632 | in-del | -/T | 3.98446e-05 | 0.00446326 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168306 | TGGTCTTTAAAGAAC[-/T]AGAGTTCTGGAGTAA | 6613 |
rs753285808 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179400 | GGGCGTGGTGGCGTG[C/T]GCCCGTAGTCCCACC | 6613 |
rs753354464 | snp | C/T | 3.31159e-05 | 0.00406901 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181043 | CAGTGGAAGTACACA[C/T]ATGAATTCCTCACCT | 6613 |
rs753489125 | snp | A/G | 1.92472e-05 | 0.00310214 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174830 | TGACAATCCCTGAAC[A/G]AGAATTTAAAAGCAA | 6613 |
rs753672566 | in-del | -/AACAAC | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176618 | AGATTCAATATCAAA[-/AACAAC]AACAACAACAACAAA | 6613 |
rs753795847 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168867 | GCCTCGGCCTCCCAA[A/G]GTGCTGGGATTACAG | 6613 |
rs753845900 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184950 | TCAAAAGAGGCCGGG[C/T]ATGGTGGCTCATGCC | 6613 |
rs754079810 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172582 | TGCCTCCTGGGTTCA[A/T]GCGATTCTCCTGCCT | 6613 |
rs754734350 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175897 | CTCAGCCTCACAAAA[C/T]GCTGGGATTACAGGT | 6613 |
rs754920378 | snp | C/G | 0.000328515 | 0.0128121 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182799 | GCGAGGCGAAGGGGC[C/G]GGCGGCGAGCTCACC | 6613 |
rs754941027 | snp | A/G | 3.32386e-05 | 0.00407654 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75181159 | CACCTTCAAATTAAT[A/G]TGATCGTTGTTCTCA | 6613 |
rs755122870 | in-del | -/TTTG | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175637 | TTTGTTGTTGTTGTT[-/TTTG]TTTGTTTGTTAAGAC | 6613 |
rs755204763 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181459 | TCCTATTCAGTGTAT[C/T]GCAACGTTCTCTTGA | 6613 |
rs755530217 | snp | A/G | 2.49113e-05 | 0.00352917 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75168366 | TCCCGTCTGCTGTTG[A/G]AACACATCAATTGTA | 6613 |
rs755848380 | snp | A/G | 2.91592e-05 | 0.00381821 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168418 | TAGCATAAAAGAAAA[A/G]ACAAATGTAAAAGCA | 6613 |
rs755858294 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174662 | CTCTACAAGAACTTA[C/T]ACTCCAGTGTCTAAA | 6613 |
rs755871175 | in-del | -/AAAAAAAAAAA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177988 | GCGAGACTCCGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA | 6613 |
rs756189337 | snp | G/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183769 | CCGGCCTACAGTGTC[G/T]TCTTCTGTCCTGCTG | 6613 |
rs756349626 | in-del | -/TA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180740 | AAATAATAAAAGACT[-/TA]TAAGTAATTTTACCA | 6613 |
rs756427540 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169763 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAA | 6613 |
rs756625080 | in-del | -/G | 1.65723e-05 | 0.00287852 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168425 | AAAGAAAAAACAAAT[-/G]TAAAAGCACTGATTA | 6613 |
rs756808379 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174474 | GAGGCCAAGGCTGCA[A/G]TGAGCTATAATGAGG | 6613 |
rs756926588 | snp | A/C | 2.06435e-05 | 0.00321268 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174847 | GAATTTAAAAGCAAT[A/C]AACAGCATTAAGAGA | 6613 |
rs756966274 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174956 | CAACATGTTAACATA[C/T]CCTATAGGTAAAAAG | 6613 |
rs757084410 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181363 | GCGGAAAAATCCTGC[A/T]GTAACAGTATTAGAT | 6613 |
rs757811353 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184000 | CCGATGTGTGTGCAC[C/T]GGATTCCATCTCGCT | 6613 |
rs757909666 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175637 | TTTGTTGTTGTTGTT[A/T]TTGTTTGTTTGTTAA | 6613 |
rs758139947 | snp | A/G | 1.65384e-05 | 0.00287557 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174858 | CAATAAACAGCATTA[A/G]GAGAAACAGAATTCT | 6613 |
rs758192503 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179781 | TCTCAGCCTCAGCCT[C/T]CGGAGTAGGTGGGAT | 6613 |
rs758193075 | snp | A/C | 3.31686e-05 | 0.00407225 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75181138 | CACAGAACCATCCTG[A/C]CCCGCCACCTTCAAA | 6613 |
rs758484889 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181809 | CATTTTTATTTTCGG[C/T]TAAGAGCACTTATTC | 6613 |
rs759002608 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172881 | CTGCCTCAGCCTCCT[A/G]AAGTGCTAGGATGAC | 6613 |
rs759006242 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180948 | TGCCAAGTGCATATT[C/T]ATCCCATCAAAAAGT | 6613 |
rs759299204 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176141 | ACCACCGGAGTTCAA[A/G]TGACTTTCCTGCCTC | 6613 |
rs759391324 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171024 | AAGCAGCAGCCAACT[C/T]GGTGCACTGACTATA | 6613 |
rs759397052 | in-del | -/AAAAAAAAAAAA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180393 | TGAGACTCCCAGCTT[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 6613 |
rs759408795 | snp | C/G | 1.65578e-05 | 0.00287726 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168327 | TCTGGAGTAAAGAAG[C/G]AGGTTCCCTTTTCAG | 6613 |
rs759549197 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175173 | GTTTTAGTAGAGACT[A/G]GGTTTCATCAGGTTG | 6613 |
rs759826780 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171773 | GTTTTAGTGGTGGGT[-/A]AAGGAGGGCTTAAAG | 6613 |
rs760004765 | snp | C/T | 3.31873e-05 | 0.0040734 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181018 | TAAGATTTTTAAAAA[C/T]AGTTTTATTCAGTGG | 6613 |
rs760160309 | snp | C/T | 1.79403e-05 | 0.00299497 | intron-variant, missense | SUMO2 | GRCh38.p7 | 17:75174814 | ATCTGATCTGCCTCA[C/T]TGACAATCCCTGAAC | 6613 |
rs760206802 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176787 | GAGATATAGGAACCT[A/G]GACTGTTTTAGTTAC | 6613 |
rs760443940 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170347 | GAGGCCAAGGTGGGC[A/G]GATCACCAGGTCAAC | 6613 |
rs760495428 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168524 | AGTTTCATTATTTTA[C/G]ATGTCTCATAGCTTA | 6613 |
rs760560779 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184630 | AACTCCTCACTTTAC[C/T]TTCCACATGGGTCCT | 6613 |
rs760567452 | in-del | -/AC | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174864 | ACAGCATTAAGAGAA[-/AC]AGAATTCTATTTACA | 6613 |
rs761211918 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172512 | TTTTTTTTTGAGTTT[C/T]GCTCGTTACCCATGC | 6613 |
rs761342660 | snp | A/G | 5.33927e-05 | 0.00516657 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181218 | ATAAAAGTATAATTT[A/G]GGAAATGTGATCAAC | 6613 |
rs761611027 | in-del | -/AA | 1.71549e-05 | 0.00292868 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182870 | CAGCTGCCGCTTCAC[-/AA]AAGAGGTACCAGGTC | 6613 |
rs761618169 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184555 | GAGTTTCCAGTTGAT[C/T]TCTGAACATCTCCAC | 6613 |
rs761679212 | snp | A/G | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168063 | AGGGGGTATTTTCAC[A/G]GAATCAGTATTTTTC | 6613 |
rs761725594 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180389 | AGAGTGAGACTCCCA[A/G]CTTAAAAAAAAAAAA | 6613 |
rs762216672 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179153 | ACTAGTGTTCAAATA[C/T]AGAAGATGCCAGTTT | 6613 |
rs762248413 | snp | C/T | 0.000434342 | 0.0147303 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182843 | CGGCCATGGCGAGCG[C/T]CGGAGTCTCCTCAGC | 6613 |
rs762268467 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175758 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 6613 |
rs762286303 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176700 | GCTTTAAAAAAGCAC[C/T]GCTTTTTAATTTCCT | 6613 |
rs762569728 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181324 | GGCATACTGCTGTTT[A/T]CAGCTGCTGAAATCA | 6613 |
rs762582733 | snp | C/T | 0.00030689 | 0.0123835 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182775 | CCGCGCCATGACCCC[C/T]ACCGCGCGGCGAGGC | 6613 |
rs762635933 | snp | C/G | 7.07689e-05 | 0.00594806 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182846 | CCATGGCGAGCGCCG[C/G]AGTCTCCTCAGCTGC | 6613 |
rs762665508 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173757 | TGGCATTACAAGCAC[C/T]TTGTAATCTTGAAAA | 6613 |
rs762758484 | snp | A/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183313 | CAGACTTACTAGAGG[A/T]GGAAGGGGATTCCTA | 6613 |
rs762948303 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168887 | TGGGATTACAGGTGT[A/G]AGCCACTGCGCCCAG | 6613 |
rs762992461 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172212 | ATTTTTAGTAGAGAC[A/G]GGGTAGTTTCGCCAT | 6613 |
rs763179877 | snp | C/T | 1.74257e-05 | 0.0029517 | intron-variant, missense | SUMO2 | GRCh38.p7 | 17:75174774 | GGTGTGTCTGTTTCA[C/T]TGATTGGTTGCCCGT | 6613 |
rs763256700 | snp | C/T | 7.86297e-05 | 0.00626966 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75168354 | TCAGTAGACACCTCC[C/T]GTCTGCTGTTGGAAC | 6613 |
rs763309417 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176589 | CCCTAGCACTCCAGC[C/T]TGGGTGACAGACCAG | 6613 |
rs763311931 | in-del | -/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180071 | GGGGCCAGGCACAGT[-/G]GGCCCATGCTTGTAA | 6613 |
rs763393095 | in-del | -/TCT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179243 | TAAGAGTATATGGTA[-/TCT]TCTTGCTGGGCACAG | 6613 |
rs763564386 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180109 | ACTCTGAGAGGCCAA[A/G]GTGGGCGGATCACTT | 6613 |
rs764605588 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175384 | GGAGGGCAGTGTCGC[C/G]ATCTCGGCTCACTGC | 6613 |
rs764658658 | snp | C/G | 0.000354296 | 0.013305 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182764 | CGGACCCCGGCCCGC[C/G]CCATGACCCCCACCG | 6613 |
rs764830067 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179433 | CTCGGGAGACTGAGA[C/T]AGGAGAATCGCTTGG | 6613 |
rs765091383 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75182699 | CCTGAGCCGCGGCCG[A/G]CCCCGTGGGGGGCCC | 6613 |
rs765505334 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174086 | TCAATTCAGCATGTA[C/G]AACTAAAATGGTGAG | 6613 |
rs765844929 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75176812 | AGTTACACAGTCTAT[C/G]CCTTGCACATAGTAG | 6613 |
rs765897797 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179396 | AGCTGGGCGTGGTGG[C/T]GTGCGCCCGTAGTCC | 6613 |
rs766033370 | snp | A/G | 0.000140321 | 0.00837502 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182848 | ATGGCGAGCGCCGGA[A/G]TCTCCTCAGCTGCCG | 6613 |
rs766210088 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183338 | TTCCTAAATCAAAGC[C/T]CCAGCATGAGGTTCT | 6613 |
rs766230639 | snp | C/G | 5.35901e-05 | 0.00517612 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182778 | CGCCATGACCCCCAC[C/G]GCGCGGCGAGGCGAA | 6613 |
rs766325839 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168746 | TAGCTGAGATTACAG[A/G]CATCCGCCACCATGC | 6613 |
rs766370813 | snp | A/G | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184941 | TCAACACTCTCAAAA[A/G]AGGCCGGGCATGGTG | 6613 |
rs766425927 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183836 | CATGTATTCATTCAA[C/T]GAGATCCTTACTCAT | 6613 |
rs766426546 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169053 | GGGAGACAACATCTC[C/T]ACAAAAAAAAAAAGG | 6613 |
rs766702259 | snp | C/T | 3.30945e-05 | 0.0040677 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75168357 | GTAGACACCTCCCGT[C/T]TGCTGTTGGAACACA | 6613 |
rs766710822 | snp | C/G | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183124 | GGCGCCCGCCCGGCC[C/G]GCGGGAAGAGGCGCG | 6613 |
rs766712356 | snp | C/T | 1.73447e-05 | 0.00294483 | intron-variant, synonymous-codon | SUMO2 | GRCh38.p7 | 17:75174782 | TGTTTCATTGATTGG[C/T]TGCCCGTCAAATCGG | 6613 |
rs767154641 | snp | C/T | 0.000131467 | 0.00810654 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182864 | TCTCCTCAGCTGCCG[C/T]TTCACAAAAGAGGTA | 6613 |
rs767182435 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173946 | ATCAGAGAGCATCAC[A/G]TTTTGTAGTAAGGAT | 6613 |
rs767204503 | snp | C/T | 0.000247005 | 0.0111104 | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75168378 | TTGGAACACATCAAT[C/T]GTATCTTCATCCTCC | 6613 |
rs767527416 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75181414 | CCTACATGCAATACT[A/G]TCAGTAGCAACAATA | 6613 |
rs767584241 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172219 | GTAGAGACGGGGTAG[C/T]TTCGCCATGTTGGCC | 6613 |
rs767689529 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171283 | ACAGGCATGCGCCAT[C/T]ATGCCCAGCTAATTT | 6613 |
rs767985449 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169602 | GTTAGCCAGGACAGT[C/T]TAGATCTCCTGACCT | 6613 |
rs768119121 | snp | C/T | 0.00012985 | 0.00805655 | intron-variant, synonymous-codon | SUMO2 | GRCh38.p7 | 17:75174821 | CTGCCTCATTGACAA[C/T]CCCTGAACGAGAATT | 6613 |
rs768208006 | snp | G/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184478 | TGATTTCACCGATTT[G/T]CATTACCATCTCTTT | 6613 |
rs768597746 | in-del | -/TGCCTCTTAATCTTAAACTGC | 1.65449e-05 | 0.00287614 | cds-indel | SUMO2 | GRCh38.p7 | 17:75181099 | TTACTAAGTGGTGTA[-/TGCCTCTTAATCTTAAACTGC]TGCCTCTTAATCTTA | 6613 |
rs768687751 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170443 | GGTGTGGTTGCGCAC[A/G]CCTGTAGTCCCAGCT | 6613 |
rs768778916 | snp | A/G | 0.000103197 | 0.00718248 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168329 | TGGAGTAAAGAAGCA[A/G]GTTCCCTTTTCAGTA | 6613 |
rs768861885 | snp | C/T | 7.45184e-05 | 0.00610358 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182841 | GTCGGCCATGGCGAG[C/T]GCCGGAGTCTCCTCA | 6613 |
rs768892860 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180191 | TGGTGGCGCACGCCT[C/G]AAATCCCAGGTACTC | 6613 |
rs768982534 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170234 | GATATGTTTAAAGAA[A/T]CTCGCTGCACTGCTT | 6613 |
rs769180409 | snp | C/T | 1.77209e-05 | 0.0029766 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181215 | AAAATAAAAGTATAA[C/T]TTGGGAAATGTGATC | 6613 |
rs769245008 | snp | A/G | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184851 | GCTGGCCTTCTGTAG[A/G]TTCTCTTTGGGGAGG | 6613 |
rs769327739 | snp | C/G | 3.3253e-05 | 0.00407742 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168293 | TGAGAATGTAATCTT[C/G]GTCTTTAAAGAACAG | 6613 |
rs769349607 | snp | C/G | 7.21527e-05 | 0.00600592 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182844 | GGCCATGGCGAGCGC[C/G]GGAGTCTCCTCAGCT | 6613 |
rs769448531 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173738 | CACCTTGGCGTCACA[A/G]TGCTGGCATTACAAG | 6613 |
rs769647801 | in-del | -/GCAGGT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170717 | TAGCTGGGCATGGTG[-/GCAGGT]GCCTGTAATCCCAGC | 6613 |
rs769888540 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178613 | TCATTCTGTCACCCA[C/T]ACTGGAGTGCAGCGA | 6613 |
rs770216584 | snp | G/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184191 | CTCCAACCCCTCCCC[G/T]CCCACTCACTCCTCA | 6613 |
rs770643436 | in-del | -/AAGGATC | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173927 | GTACATAAAGAGTTA[-/AAGGATC]AGAGAGCATCACGTT | 6613 |
rs770714092 | snp | C/T | 1.65699e-05 | 0.00287831 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168313 | TTAAAGAACAGAGTT[C/T]TGGAGTAAAGAAGCA | 6613 |
rs770993236 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75175043 | CTGAAGTGCAGTGGC[A/G]TGATCTCAGCTCAAG | 6613 |
rs771067530 | in-del | -/T | 9.92625e-05 | 0.00704425 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174743 | TCTAATTAGGAGAGA[-/T]TTTTTTACCTGTGCA | 6613 |
rs771248076 | snp | C/G | 1.65534e-05 | 0.00287688 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174872 | AAGAGAAACAGAATT[C/G]TATTTACATAAAAGT | 6613 |
rs771377181 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75182030 | TGCCCCGATGATGGG[G/T]GTCCCCAAGTCCTCC | 6613 |
rs771405975 | snp | A/G | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167761 | GTTTATTTAAACAAC[A/G]AGACGCTTGACTTGA | 6613 |
rs771451671 | snp | C/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171696 | TTTAAAATGCCTCAA[C/G]GTCACGGATCCAAAC | 6613 |
rs771632126 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170298 | CAAATTAGGCTGGGC[A/G]CCGGGGCTCACGCCT | 6613 |
rs771990377 | snp | A/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184577 | CATCTCCACTTGGAT[A/T]TCCCAGAGGCACCTC | 6613 |
rs772093107 | in-del | -/AG | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172349 | TTTTTTTTTTGAGAC[-/AG]GGGCTGTTACCCAGG | 6613 |
rs772194967 | in-del | -/A | 1.98817e-05 | 0.00315285 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174838 | CCTGAACGAGAATTT[-/A]AAAGCAATAAACAGC | 6613 |
rs772367595 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179164 | AATATAGAAGATGCC[A/T]GTTTATAAATTATTT | 6613 |
rs772389857 | snp | G/T | 7.75705e-05 | 0.0062273 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182836 | TTTTCGTCGGCCATG[G/T]CGAGCGCCGGAGTCT | 6613 |
rs772473616 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180637 | GCAGGAAAATCGCTT[G/T]AAGTGGAGGTTGCAG | 6613 |
rs772581400 | snp | C/T | 3.53163e-05 | 0.00420201 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181212 | AGAAAAATAAAAGTA[C/T]AATTTGGGAAATGTG | 6613 |
rs772705312 | snp | A/G | 7.1605e-05 | 0.00598309 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182845 | GCCATGGCGAGCGCC[A/G]GAGTCTCCTCAGCTG | 6613 |
rs772919310 | in-del | -/AG | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173920 | TGAAGTGGTACATAA[-/AG]AGTTAAAGGATCAGA | 6613 |
rs772947004 | snp | A/G | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167763 | TTATTTAAACAACAA[A/G]ACGCTTGACTTGAAG | 6613 |
rs772976544 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170343 | TTGGGAGGCCAAGGT[A/G]GGCGGATCACCAGGT | 6613 |
rs773308710 | snp | C/T | 1.74995e-05 | 0.00295795 | intron-variant, missense | SUMO2 | GRCh38.p7 | 17:75174769 | GTGCAGGTGTGTCTG[C/T]TTCATTGATTGGTTG | 6613 |
rs773470925 | in-del | -/TCT | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183459 | TAAAATGCAGTGTCT[-/TCT]TCTTCTTCTTCTTCT | 6613 |
rs773529058 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168625 | TTTGTTTTTTTTTTG[-/A]AGACAGGATTTCTGT | 6613 |
rs773584073 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170739 | CCTGTAATCCCAGCC[A/G]CTCAGGAGGCTGAGG | 6613 |
rs773787121 | snp | C/T | | | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167520 | ATTTTTCTGCTAGTA[C/T]ACTTGCATATTAACA | 6613 |
rs773827646 | snp | C/T | 6.77713e-05 | 0.00582075 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182861 | GAGTCTCCTCAGCTG[C/T]CGCTTCACAAAAGAG | 6613 |
rs773856417 | snp | C/T | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184528 | ATTATTTCTAGTCCA[C/T]GTCTTTCTTCTGAGT | 6613 |
rs774189423 | snp | A/C | 0.000212887 | 0.0103149 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168324 | AGTTCTGGAGTAAAG[A/C]AGCAGGTTCCCTTTT | 6613 |
rs774247346 | snp | G/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174937 | TACCTAAATAAACAA[G/T]TGCCAACATGTTAAC | 6613 |
rs774450157 | in-del | -/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172012 | TACCATAATTGCGCC[-/T]TTTTTTTTTTTTTTG | 6613 |