SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4640 | snp | A/G | 0.093777 | 0.195178 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239520 | CAACTGGAGCAGGAC[A/G]GAAGGTTGTCTGTAC | 1643 |
rs11988 | snp | C/T | 0.287867 | 0.247116 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239709 | TAGCTCAGAGGGACA[C/T]GGTCTTGCCTCTCAG | 1643 |
rs326211 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | DDB2 | GRCh38.p7 | 11:47217114 | tgctgggattacagg[C/T]gcgaaccactgcacc | 1643 |
rs326212 | snp | A/G | 0.00251737 | 0.0353894 | synonymous-codon, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216971 | GGAACCCACAGCCAC[A/G]GTGCTGGGGTGAGTT | 1643 |
rs326221 | snp | A/G | 0.0158469 | 0.0875917 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239492 | TACTTGGGAGGGAGT[A/G]GGGAGTGGTGGGAAG | 1643 |
rs326222 | snp | C/T | 0.476322 | 0.1062 | intron-variant | DDB2 | GRCh38.p7 | 11:47238117 | CACCCTCTCCTCATG[C/T]TGACACTCTTGTCTC | 1643 |
rs326223 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DDB2 | GRCh38.p7 | 11:47234352 | AAATCTGTCTGGTTA[C/T]GGCTGGGCCCAGGAT | 1643 |
rs326224 | snp | A/G | 0.4776 | 0.103433 | intron-variant | DDB2 | GRCh38.p7 | 11:47234047 | GGGAGGCTGACTAGG[A/G]GGGTGCTTCAGGGAT | 1643 |
rs830083 | snp | C/G | 0.466927 | 0.124269 | intron-variant | DDB2 | GRCh38.p7 | 11:47232500 | gcccagctaattttt[C/G]tatttttttttttta | 1643 |
rs830084 | snp | A/G | 0.466927 | 0.124269 | intron-variant | DDB2 | GRCh38.p7 | 11:47230101 | tatgtaactcaggcc[A/G]gtctcaaattcctgg | 1643 |
rs830085 | snp | C/T | 0.499839 | 0.00898417 | intron-variant | DDB2 | GRCh38.p7 | 11:47229648 | ACCACAGAGTTGATT[C/T]GAGTTTCTCTCTTTC | 1643 |
rs830086 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DDB2 | GRCh38.p7 | 11:47228337 | TGATCTTAAACCCTC[C/T]GTCTCCACAGACTAG | 1643 |
rs844208 | snp | G/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47231080 | caggctgaagtgcgg[G/T]ggcacaacctcagct | 1643 |
rs901746 | snp | A/G | 0.478204 | 0.102093 | intron-variant | DDB2 | GRCh38.p7 | 11:47238768 | AGATTGGTAACAGAA[A/G]GTGTAAGTCAGACTG | 1643 |
rs1049672 | snp | C/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239374 | CTGGAAAAGAAAGTT[C/T]TAGACTGTGGCCCAG | 1643 |
rs1050244 | snp | C/T | 0.0930568 | 0.194599 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47238926 | TGCAAGCAGAGGTGG[C/T]GATTTGTTAAAGGGC | 1643 |
rs1618238 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | DDB2 | GRCh38.p7 | 11:47231248 | TTCATCATCATTTTC[A/T]TGAATGTTTGGAAGA | 1643 |
rs1667592 | snp | A/C | 0.145642 | 0.227177 | intron-variant | DDB2 | GRCh38.p7 | 11:47231249 | TTCTTCCAAACATTC[A/C]TGAAAATGATGATGA | 1643 |
rs1667593 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231115 | tttttttttttgaga[A/T]gaaggcttgctctgt | 1643 |
rs1685404 | snp | C/G | 0.408359 | 0.193449 | intron-variant | DDB2 | GRCh38.p7 | 11:47222114 | ttgaatatttggaga[C/G]tgatagatagatgag | 1643 |
rs2013867 | snp | C/T | 0.499928 | 0.00598999 | intron-variant | DDB2 | GRCh38.p7 | 11:47238721 | ATTTCTTTACCAAAT[C/T]GTAGGTTTGCGGGCC | 1643 |
rs2029298 | snp | A/G | 0.493881 | 0.054972 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213167 | GTCCACCTAGGAGCA[A/G]CCTGGGACGTGATGG | 1643 |
rs2291120 | snp | C/T | 0.163564 | 0.234582 | intron-variant | DDB2 | GRCh38.p7 | 11:47216129 | TTCAGACTTACTGTT[C/T]GTGGGAGTGTTTTGG | 1643 |
rs2306353 | snp | A/G | 0.461037 | 0.134028 | intron-variant | DDB2 | GRCh38.p7 | 11:47235157 | CCTCTCTAGACAGGA[A/G]CGGAAAGGAAGAGGT | 1643 |
rs2596397 | snp | A/G | 0.491629 | 0.0641526 | | | GRCh38.p7 | 11:47226070 | AATGCTGCAGTGAAT[A/G]TGGATGTGCAAATAT | 1643 |
rs2596398 | snp | C/G | 0.46974 | 0.119223 | | | GRCh38.p7 | 11:47227912 | TTTGGGAGGCCGAGG[C/G]GGTCGGATTATGAGG | 1643 |
rs2596399 | snp | C/G | | | | | GRCh38.p7 | 11:47229979 | atgagcacaggtgtg[C/G]accatcactcccagc | 1643 |
rs2633080 | snp | A/C | 0.469346 | 0.119947 | intron-variant | DDB2 | GRCh38.p7 | 11:47226009 | GTTTATCTGTTTATT[A/C]ATTGACAGACACTTG | 1643 |
rs2633081 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | DDB2 | GRCh38.p7 | 11:47226158 | CATCAAATGGTAATT[G/T]TGTTGTTCATTTTTT | 1643 |
rs2633082 | snp | C/G | 0.488424 | 0.0751925 | intron-variant | DDB2 | GRCh38.p7 | 11:47226499 | gctggtcttgaactc[C/G]cgacctcaggtgatt | 1643 |
rs2633083 | snp | C/T | 0.466927 | 0.124269 | intron-variant | DDB2 | GRCh38.p7 | 11:47227869 | ATTTCTGGCCAGGCG[C/T]GGTGGATCACGCCTG | 1643 |
rs2922976 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | DDB2 | GRCh38.p7 | 11:47221873 | aaaaCCCAggccggg[C/T]gcagtggctcgtgcc | 1643 |
rs2957873 | snp | A/G | 0.488545 | 0.074807 | intron-variant | DDB2 | GRCh38.p7 | 11:47227743 | CATAACATATTTATC[A/G]TTTTTAAATATTACT | 1643 |
rs3740682 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | DDB2 | GRCh38.p7 | 11:47216698 | TTCCAAGATTATTCG[A/T]TCGTGTACATTGCAA | 1643 |
rs3758666 | snp | A/G | 0.469247 | 0.120128 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214743 | CCCACTGCCCTCCAG[A/G]GTGAGCGACAGAGCC | 1643 |
rs3758667 | snp | A/G | 0.469247 | 0.120128 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214747 | CTGCCCTCCAGAGTG[A/G]GCGACAGAGCCAGAC | 1643 |
rs3781619 | snp | A/G | 0.459118 | 0.137002 | intron-variant | DDB2 | GRCh38.p7 | 11:47233766 | TTTCCAGCTAGAGCC[A/G]TGACTCTGACTGCTC | 1643 |
rs3781620 | snp | C/G | 0.461813 | 0.132798 | intron-variant | DDB2 | GRCh38.p7 | 11:47237713 | GTGTTGAGATTACAG[C/G]TGTGAGCCACTGCAC | 1643 |
rs3824866 | snp | C/T | 0.456803 | 0.140473 | intron-variant | DDB2 | GRCh38.p7 | 11:47237302 | AGGCCTGAAGGTGCC[C/T]TAAGGGCCAGGGAGG | 1643 |
rs4237547 | snp | C/G | 0.488545 | 0.074807 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214854 | TGGCACTGGCCCTGG[C/G]GCAGTTCCCGCCCCT | 1643 |
rs4237548 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DDB2 | GRCh38.p7 | 11:47237080 | TCTCTTTTTTAGCCA[C/T]TAGCAATTTTACACT | 1643 |
rs4468307 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213267 | CCTATAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 1643 |
rs4647706 | snp | G/T | 0.0111196 | 0.0737302 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214879 | GCCCCTCCCGGGAGC[G/T]CTGGCACCGCCCCTT | 1643 |
rs4647707 | snp | A/G | 0.181978 | 0.240568 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215017 | CGGGAAGTTGGCTTA[A/G]CTCGGCTACCTGTGG | 1643 |
rs4647708 | snp | C/G/T | 4.94558e-05 | 0.00497251 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215090 | CTCTCAATCCTCCCT[C/G/T]CATGATCTTCGCATA | 1643 |
rs4647709 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | DDB2 | GRCh38.p7 | 11:47215808 | TATAGTGATTGGGTC[C/T]TCAAATACAGTTTGG | 1643 |
rs4647710 | in-del | -/TG | 0.0143877 | 0.0835874 | intron-variant | DDB2 | GRCh38.p7 | 11:47216595 | CGATCACCCAGACTG[-/TG]GTGACTGGCCTACTG | 1643 |
rs4647711 | snp | A/G | 0.0180165 | 0.0931862 | intron-variant | DDB2 | GRCh38.p7 | 11:47217112 | tgggtgcagtggttc[A/G]cgcctgtaatcccag | 1643 |
rs4647712 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | DDB2 | GRCh38.p7 | 11:47217267 | TATAATCCCAGCTAC[G/T]CAGGAGGCTGAGGCA | 1643 |
rs4647713 | snp | A/G | 0.127599 | 0.217986 | intron-variant | DDB2 | GRCh38.p7 | 11:47217719 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAGATA | 1643 |
rs4647714 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | DDB2 | GRCh38.p7 | 11:47217890 | agcgagactccatct[C/T]aaaaaaaaagaaTTG | 1643 |
rs4647715 | snp | A/G | 0.00457664 | 0.0476169 | intron-variant | DDB2 | GRCh38.p7 | 11:47219293 | atgaaatttactttc[A/G]taaccattttaaagt | 1643 |
rs4647716 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | DDB2 | GRCh38.p7 | 11:47219471 | actcaaggaatcctc[C/T]ggcttcagcctccca | 1643 |
rs4647717 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | DDB2 | GRCh38.p7 | 11:47220229 | CCCAGAAAGGCAGTC[A/G]GAGGAGTGCCGCGGA | 1643 |
rs4647718 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | DDB2 | GRCh38.p7 | 11:47223430 | agaggttgcagtgag[C/T]cgagatggtgtcact | 1643 |
rs4647719 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | DDB2 | GRCh38.p7 | 11:47223534 | acctgtaatcccagc[A/G]ctttgggaggccgag | 1643 |
rs4647720 | snp | C/T | 0.133435 | 0.221162 | intron-variant | DDB2 | GRCh38.p7 | 11:47223594 | GACCACCCTGGCTAA[C/T]ACGGTGAAACCCTGT | 1643 |
rs4647721 | snp | C/T | 0.0124219 | 0.0778244 | intron-variant | DDB2 | GRCh38.p7 | 11:47223642 | aaaaaattagccagg[C/T]gtggtggtgggcgcc | 1643 |
rs4647722 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | DDB2 | GRCh38.p7 | 11:47223655 | ggcgtggtggtgggc[A/C/G]cctgtagtcccagct | 1643 |
rs4647723 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | DDB2 | GRCh38.p7 | 11:47223734 | tggcagtgagccgag[A/G]tcggccacttcactc | 1643 |
rs4647724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47223796 | aaataaataaataaa[G/T]aaagaataaaaaTAA | 1643 |
rs4647725 | snp | C/T | 0.462034 | 0.132445 | intron-variant | DDB2 | GRCh38.p7 | 11:47223838 | AGTTGGGCTCAATGG[C/T]TCATGCCTGTAATCT | 1643 |
rs4647726 | snp | A/T | 0.461703 | 0.132974 | intron-variant | DDB2 | GRCh38.p7 | 11:47223943 | gaccccatctctaca[A/T]aaaaatcttaaaaat | 1643 |
rs4647727 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47230409 | CAAAGCTTTCAACAC[A/G]GCTTTTATAGTAGTA | 1643 |
rs4647728 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | DDB2 | GRCh38.p7 | 11:47230556 | CCCTTGGTTTGGTAA[A/G]CATAGAACTCAACTG | 1643 |
rs4647729 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47230599 | GATTGTCATACTACC[A/G]GCAAGCATTTGGCAG | 1643 |
rs4647730 | snp | A/T | 0.0905309 | 0.192535 | intron-variant | DDB2 | GRCh38.p7 | 11:47230686 | TGCCAGTTAGTATGT[A/T]GTGATAGCTAAGTGG | 1643 |
rs4647731 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | DDB2 | GRCh38.p7 | 11:47230703 | TGATAGCTAAGTGGT[C/T]GTTGCATAGAAGAAC | 1643 |
rs4647732 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DDB2 | GRCh38.p7 | 11:47230753 | TGGGATAGCTGCAGC[A/G]TAAAGAAGAAGTGGA | 1643 |
rs4647733 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DDB2 | GRCh38.p7 | 11:47230905 | GCAGGCCAATCACCT[C/G]AGGTCAGGAGTTCGA | 1643 |
rs4647734 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DDB2 | GRCh38.p7 | 11:47231347 | AAAGAGAGCACTGTG[A/G]GAATaacaaattagg | 1643 |
rs4647735 | snp | A/T | 0.154661 | 0.231107 | intron-variant | DDB2 | GRCh38.p7 | 11:47231524 | TTCTATTTTTAATTT[A/T]ATTTTATTTTATTTT | 1643 |
rs4647736 | snp | C/T | 0.128288 | 0.218372 | intron-variant | DDB2 | GRCh38.p7 | 11:47231586 | TAGAGTGCAGTGATT[C/T]GATCGCAACTCACTG | 1643 |
rs4647737 | snp | G/T | 0.459118 | 0.137002 | intron-variant | DDB2 | GRCh38.p7 | 11:47231693 | ATGTCTAAATTTTTT[G/T]TGTGTGTGTAGAGAT | 1643 |
rs4647738 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | DDB2 | GRCh38.p7 | 11:47231759 | TCCTGGCCTCAAGCA[A/G]TCCCCCCGCCTCAGT | 1643 |
rs4647739 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | DDB2 | GRCh38.p7 | 11:47232383 | GGggccagacaaagc[A/G]gctcatgcctgtaat | 1643 |
rs4647740 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | DDB2 | GRCh38.p7 | 11:47232428 | aagccgtggcagggg[G/T]atcgcttgagcttag | 1643 |
rs4647741 | snp | C/T | 0.462691 | 0.131387 | intron-variant | DDB2 | GRCh38.p7 | 11:47232459 | gagttcaagaccagc[C/T]tgggcaacgtgacaa | 1643 |
rs4647742 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | DDB2 | GRCh38.p7 | 11:47232737 | TGCTTCTGTGACGGC[C/G]CAGCATGTGTGCCCA | 1643 |
rs4647743 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47232754 | AGCATGTGTGCCCAG[C/G]CCTGGTTCCTCACGG | 1643 |
rs4647744 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | DDB2 | GRCh38.p7 | 11:47233051 | CCTTAACCCAACCTG[A/G]CCCAGGGAAGAAAGG | 1643 |
rs4647745 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | DDB2 | GRCh38.p7 | 11:47233148 | GGTCCAGGTGGGTTA[C/T]TGCTTTGGGAAGGTG | 1643 |
rs4647746 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DDB2 | GRCh38.p7 | 11:47233619 | gaggctgaagcaaga[A/G]aatcgcttgaaccca | 1643 |
rs4647747 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | DDB2 | GRCh38.p7 | 11:47234018 | GAGCTGAGCTCTTCT[C/G]GCTGAATAGCAGGAT | 1643 |
rs4647748 | in-del | -/G | 0.0880306 | 0.190436 | intron-variant | DDB2 | GRCh38.p7 | 11:47234263 | CAGAACCCGGGGTGT[-/G]GGGGGCAGGCGTGCC | 1643 |
rs4647749 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | DDB2 | GRCh38.p7 | 11:47234438 | CTCACTAGGAATCCA[C/T]GGCAAGACAGTTatt | 1643 |
rs4647750 | snp | C/T | 0.000938511 | 0.021642 | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47234614 | CTGCTAGTAGCCGAA[C/T]GGTGGTCACAGGAGA | 1643 |
rs4647751 | snp | A/G | 0.000183317 | 0.00957208 | missense, intron-variant | DDB2 | GRCh38.p7 | 11:47234931 | AGGCATCCTGTCAAC[A/G]CAGGTGTGATATCCC | 1643 |
rs4647752 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | DDB2 | GRCh38.p7 | 11:47235131 | TTTGTTGTTGTTCAC[A/G]GCCCAGATTCACCTC | 1643 |
rs4647753 | snp | A/G | 0.0110494 | 0.0735024 | intron-variant | DDB2 | GRCh38.p7 | 11:47235178 | TCTAGAGAGGAGTGG[A/G]AGGGAGAGTACCCCT | 1643 |
rs4647754 | snp | C/T | 0.450734 | 0.149016 | intron-variant | DDB2 | GRCh38.p7 | 11:47235789 | TAAGGCAGGGTCTCG[C/T]TCTGTCACCCAGGTG | 1643 |
rs4647755 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DDB2 | GRCh38.p7 | 11:47237308 | GAAGGTGCCCTAAGG[A/G]CCAGGGAGGCCAGCT | 1643 |
rs4647756 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | DDB2 | GRCh38.p7 | 11:47237428 | GCTTGTTACTGGCAA[A/C]TACTACttttttttt | 1643 |
rs4647757 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | DDB2 | GRCh38.p7 | 11:47238442 | TCGCTCTGTCCCCCC[A/G]GGCTGGAGTGCAGTG | 1643 |
rs4647758 | in-del | -/T | 0.0112991 | 0.0743093 | intron-variant | DDB2 | GRCh38.p7 | 11:47238455 | cgggctggagtgcag[-/T]tggcgtgatcttggc | 1643 |
rs4647759 | snp | C/G | 0.133777 | 0.221342 | intron-variant | DDB2 | GRCh38.p7 | 11:47238591 | TTTTAGTAGAGACAG[C/G]GTTTCACCGTGTTAG | 1643 |
rs4647760 | snp | A/C | 0.00835141 | 0.0640778 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239000 | TGGGGCACTGTGGGA[A/C]TGGGACACTTTTATG | 1643 |
rs4647761 | in-del | -/CA | 0.0126979 | 0.078662 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239182 | TATTTGATTTGTGCT[-/CA]CTTTTGATATGGCCA | 1643 |
rs4647762 | snp | A/G | 0.0126979 | 0.078662 | downstream-variant-500B | DDB2, ACP2 | GRCh38.p7 | 11:47239277 | TTGCGTCTCAGAAAT[A/G]AAGAAAAAGCACAGG | 1643 |
rs4647763 | in-del | -/AAC | 0.0392 | 0.1344 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239546 | AGTTGAAGGGGTGAC[-/AAC]GATTCCTGAAGCATT | 1643 |
rs5791754 | in-del | -/A | 0 | 0 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213531 | AAAAAAAAAAAAAAA[-/A]GCAGTGAGGAGGCTG | 1643 |
rs7119952 | snp | C/T | 0.492435 | 0.0610346 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213505 | aacagagtgagactc[C/T]gtctcaaaaaaaaaa | 1643 |
rs7395496 | snp | A/G | 0.469148 | 0.120308 | intron-variant | DDB2 | GRCh38.p7 | 11:47224252 | TTTTCTTTTGAGACA[A/G]AGTCTCACTCTGTCG | 1643 |
rs7395581 | snp | A/G | 0.499971 | 0.00379382 | intron-variant | DDB2 | GRCh38.p7 | 11:47224846 | gcaaagtagcccagc[A/G]tatttttcatttcag | 1643 |
rs7483213 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232648 | tatttcaaaggaaaa[A/G]aaaaagaaGTGAAGG | 1643 |
rs7947269 | snp | C/T | 0.488545 | 0.074807 | intron-variant | DDB2 | GRCh38.p7 | 11:47225434 | cgtctctactaaaaa[C/T]acaaaaaattagctg | 1643 |
rs10544942 | in-del | -/A | 0.214843 | 0.247516 | intron-variant | DDB2 | GRCh38.p7 | 11:47233727 | GCGAAAATCTATCTC[-/A]AAAAAAAAAAAAAAA | 1643 |
rs10577886 | in-del | -/AA | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233726 | GCGAAAATCTATCTC[-/AA]AAAAAAAAAAAAAAA | 1643 |
rs10677833 | in-del | -/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47235949 | TTTTTTTTTTTTTTT[-/T]CTTGAAACGGTCTTG | 1643 |
rs10708891 | in-del | -/A | 0.499971 | 0.00379382 | intron-variant | DDB2 | GRCh38.p7 | 11:47225255 | CGATCCTGTGTCTTT[-/A]AAAAAAAAAAAAAAA | 1643 |
rs10742797 | snp | A/T | 0.469839 | 0.119042 | intron-variant | DDB2 | GRCh38.p7 | 11:47218939 | AAATGTATCACCTTA[A/T]CCATTTAAAAGTGTT | 1643 |
rs10838676 | snp | A/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47224132 | TGAGAAGTCTGCTAC[A/T]ATCCTTATGTTCCTG | 1643 |
rs11039133 | snp | C/T | 0 | 0 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214058 | CTTGGGGATACAGGT[C/T]TGCAAGCCTACTTGG | 1643 |
rs11039134 | snp | A/G | 0.488485 | 0.0749998 | intron-variant | DDB2 | GRCh38.p7 | 11:47220921 | TCCCAGCACTTTGGG[A/G]GGCCGAGGCGGGTGG | 1643 |
rs11039136 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221824 | GACCTCAAGTGATCC[C/G]CCCGCCTCGGCCTCC | 1643 |
rs11039138 | snp | A/G | 0.26818 | 0.249338 | intron-variant | DDB2 | GRCh38.p7 | 11:47227672 | ACGCCCAGCTGGCCC[A/G]ATTGATTTTTAATAG | 1643 |
rs11039139 | snp | C/T | 0.269809 | 0.249214 | intron-variant | DDB2 | GRCh38.p7 | 11:47228768 | tcgagaccagcctgg[C/T]caacatgatgaaact | 1643 |
rs11351835 | in-del | -/A | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213813 | GAGAGGCCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 1643 |
rs11376360 | in-del | -/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47229819 | TTTTTTTTTTTTTTT[-/T]CTTCTTCCTAATAGA | 1643 |
rs11406293 | in-del | -/T/TT/TTT/TTTT | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235926 | TACCCAGGCTGATCC[-/T/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 1643 |
rs11422980 | in-del | -/A | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47232486 | CTTAAAAAAAAAAAA[-/A]TAGAAAAATTAGCTG | 1643 |
rs11444403 | in-del | -/A | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214181 | GACACTGCCTCTAGG[-/A]AAAAAAAAAAAAAAA | 1643 |
rs11445579 | in-del | -/C/T/TT/TTT/TTTT | 0.608682 | 0.181292 | intron-variant | DDB2 | GRCh38.p7 | 11:47229818 | ATTTGATGGCTCTTC[-/C/T/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 1643 |
rs11500475 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47225453 | AAAAATTAGCTGGGC[A/G]TGGTCGTGGGCGCCT | 1643 |
rs11537594 | snp | A/G/T | 1.65059e-05 | 0.00287275 | DDB2 | 11 | allele_origin=G(germline)/A(germline) | 11:47216912 | CGGATATTACAAAAG[A/G/T]CTGCCCCCTTTGACA | 1643 |
rs11600013 | snp | A/G | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47229260 | CAGGGGTGAAGAGTA[A/G]AGGAGGCCGGGCATG | 1643 |
rs11600033 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47229328 | CCACAGGGAGGCCTA[A/G]AGTGGGGTGGCGGAG | 1643 |
rs11603138 | snp | G/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47235828 | gtggggcaagcatgg[G/T]tcattacagccttga | 1643 |
rs11607786 | snp | C/G | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47228497 | aatacacaaaaattc[C/G]ccaagcatggtagca | 1643 |
rs11608203 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228569 | aattgcttgaaccca[A/G]gaggcagaggttgca | 1643 |
rs12221491 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47219960 | acccggctacttttt[A/T]tatattttttagtgg | 1643 |
rs12273133 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227128 | tttttttttttgaga[A/T]ggagttttgctcctg | 1643 |
rs12274713 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | DDB2 | GRCh38.p7 | 11:47236679 | catgcccagcacctg[A/G]taagtactggtaagt | 1643 |
rs12284672 | snp | A/C | 0.101301 | 0.200969 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214367 | CACTCCCCAACTACA[A/C]CCTGTAGGGACCAGC | 1643 |
rs12291341 | snp | A/G | 0.493925 | 0.054776 | intron-variant | DDB2 | GRCh38.p7 | 11:47221210 | AATACAGAGAAAAGT[A/G]TAAAAAATAAATTAA | 1643 |
rs12292830 | snp | C/G | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47221744 | gccaccgtgcccagc[C/G]tgaattttatatttt | 1643 |
rs12418636 | snp | G/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47233971 | GCAAAAGGCAGTGTA[G/T]CATGGATTTGAGAGT | 1643 |
rs12576935 | snp | A/G | 0.133777 | 0.221342 | intron-variant | DDB2 | GRCh38.p7 | 11:47224991 | cttccaggctggagt[A/G]cactggcatgagatc | 1643 |
rs12578030 | snp | A/G | 0.126564 | 0.217402 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213050 | GTCTCTTCTCAGGCT[A/G]GGCAGGACAGCGCGG | 1643 |
rs12790239 | snp | A/C | 0 | 0 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213865 | AAAGAAAAAATAAAA[A/C]CAGCCAACGACCAAA | 1643 |
rs12790377 | snp | C/T | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213810 | agagagaggccctgt[C/T]tcaaaaaaaaaaaaa | 1643 |
rs12792737 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | DDB2 | GRCh38.p7 | 11:47221149 | GCCTGGGCGACACAG[C/T]GAGACTCCATCTCTC | 1643 |
rs17849262 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235406 | CCAGCACCTCACACC[C/T]ATCAAGGTGAGTGGC | 1643 |
rs28365833 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214377 | CTACACCCTGTAGGG[A/T]CCAGCCAATCCCAAA | 1643 |
rs28656827 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221110 | GGAGGTTGCAGTGAG[C/G]TGAGATGGTGCCACT | 1643 |
rs28709669 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221068 | CTCAGGAATCTGAGG[A/C]AGGAGAATCACTTGA | 1643 |
rs34222328 | in-del | -/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47215501 | CGGACTTGTCAGATT[-/C]CCTTGTTCGTATCAG | 1643 |
rs34243882 | in-del | -/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227123 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTTGC | 1643 |
rs34302300 | in-del | -/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47222224 | AGAAATTAATTTACA[-/T]TTTTCTAGAACTATA | 1643 |
rs34447392 | in-del | -/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47222022 | ATAAATTGTACAATT[-/C]CCATGAGTTTTGACA | 1643 |
rs34533481 | in-del | -/A | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218194 | CTTCATGTTTCCCCC[-/A]AGTGTTGATGGGTGT | 1643 |
rs34658569 | in-del | -/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47224649 | GGTTGATGCACTGTT[-/G]CATTTTTGTCTTTTT | 1643 |
rs34897237 | in-del | -/T | 0.375 | 0.216506 | intron-variant | DDB2 | GRCh38.p7 | 11:47222333 | CATTTTTATGTGTAG[-/T]TTTTTTTTTCTTTCT | 1643 |
rs35081905 | in-del | -/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47229238 | TCAGAAGGGCATCCA[-/T]TGTAGGCAGGGGTGA | 1643 |
rs35431351 | in-del | -/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47234714 | CCTCCCTCACCCCCA[-/C]CTCGGTTCTGTGTCC | 1643 |
rs35644155 | in-del | -/C | | | frameshift-variant, intron-variant | DDB2 | GRCh38.p7 | 11:47234805 | CGCATGTGGCCCTGA[-/C]ACCCATGCTGTGATT | 1643 |
rs35772933 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218607 | ATCATCCATTGCTGA[A/G]GGGTGAGTGTGTCGT | 1643 |
rs35908583 | in-del | -/A | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228160 | AAAAAAAAAAAAAAA[-/A]GATTATGCTGATTTC | 1643 |
rs36044881 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239134 | AATGACTTTTCTCCT[-/A]CTCAGTGGGTGGTAG | 1643 |
rs36082302 | in-del | -/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239474 | GTGTGACAAGCAACT[-/C]CCCTTCCCACCACTC | 1643 |
rs41547817 | snp | C/G/T | 0.000153988 | 0.00877328 | intron-variant | DDB2 | GRCh38.p7 | 11:47238207 | GAGGAGAATGTCTCT[C/G/T]ACTTGCCAAGTCCGA | 1643 |
rs55642740 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217202 | CCAACATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 1643 |
rs55749629 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217204 | AACATGGTGAAACCC[C/G]GTCTCTACTAAAAAT | 1643 |
rs55760739 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217166 | GGATCACCTGAGGTA[A/T]GGAGTTTGAGACCAG | 1643 |
rs55811602 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217203 | CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 1643 |
rs55845056 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217155 | CCAAGGTGGGTGGAT[A/C]ACCTGAGGTATGGAG | 1643 |
rs55847708 | snp | A/C/G | 0.000757668 | 0.0194496 | intron-variant | DDB2 | GRCh38.p7 | 11:47234684 | AGAGGTGCGTTCTCC[A/C/G]AGGTCCTGCCTTTCC | 1643 |
rs55884393 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217130 | CCTGTAATCCCAGCA[A/C]TTTGGGAGGCCAAGG | 1643 |
rs56020548 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47234428 | CTGAATGTTCCTCAC[C/T]AGGAATCCACGGCAA | 1643 |
rs56023479 | snp | A/C | 0.0905309 | 0.192535 | intron-variant | DDB2 | GRCh38.p7 | 11:47229256 | TAGGCAGGGGTGAAG[A/C]GTAGAGGAGGCCGGG | 1643 |
rs56042554 | snp | A/G | 0.00162956 | 0.0284978 | intron-variant | DDB2 | GRCh38.p7 | 11:47232979 | GTAGTTTAACTAGCA[A/G]GGGAAAGGGCTTCTA | 1643 |
rs56130625 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217191 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCGT | 1643 |
rs56167102 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217172 | CCTGAGGTATGGAGT[C/T]TGAGACCAGCCTGGC | 1643 |
rs56222682 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217158 | AGGTGGGTGGATCAC[C/T]TGAGGTATGGAGTTT | 1643 |
rs56310830 | snp | G/T | 0.00401557 | 0.044628 | DDB2 | 11 | allele_origin=G(germline)/T(germline) | 11:47216252 | ATTAACCGTGCCGAA[G/T]GAAACAAGGCTTCCT | 1643 |
rs56367299 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217165 | TGGATCACCTGAGGT[A/T]TGGAGTTTGAGACCA | 1643 |
rs56713278 | in-del | -/AAA | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233725 | AAAAAAAAAAAAAAA[-/AAA]TTACAGAATACTCGT | 1643 |
rs58044604 | in-del | -/A | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214206 | AAAAAAAAAAAAAAA[-/A]GGCAAGGAGTTCCAA | 1643 |
rs58216148 | in-del | -/AAA | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47228973 | AAAAAAAAAAAAAAA[-/AAA]GAAATATCTATCTAT | 1643 |
rs58224716 | in-del | -/A/AAA | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47231144 | AAAAAAAAAAAAAAA[-/A/AAA]CACACAAAGAAAATC | 1643 |
rs59098720 | in-del | -/ATCTA/ATCTATCT/ATCTATCTATCTATCT | | | intron-variant | DDB2 | GRCh38.p7 | 11:47229022 | TCTATCTATCTATCT[lengthTooLong]TCCTCTTTCTTCATC | 1643 |
rs60428958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47230996 | GTGATGGTGTGGGCA[C/T]GTAATCCCAGCTACT | 1643 |
rs60712743 | in-del | -/CT | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235962 | TTCTTGAAACGGTCT[-/CT]TGCTCTGTCACCCAG | 1643 |
rs61124822 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | DDB2 | GRCh38.p7 | 11:47229294 | TAGTGAAGTCTGAAG[C/T]GGGGTTGAGGATGCT | 1643 |
rs61273211 | in-del | -/AA | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228660 | AAAAAAAAAAAAAAA[-/AA]GGAAGGAAAGATCAA | 1643 |
rs61741581 | snp | C/T | 0.000642277 | 0.0179088 | synonymous-codon, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47237866 | TCGCTACAACCTCAT[C/T]GTTGTGGGCCGATAC | 1643 |
rs61897858 | snp | A/T | 0.121369 | 0.214369 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213712 | TCCCAGCTACTCGGG[A/T]GGCTGAGGTGGGAGG | 1643 |
rs61897859 | snp | A/G | 0.12932 | 0.218944 | intron-variant | DDB2 | GRCh38.p7 | 11:47225451 | CAAAAAATTAGCTGG[A/G]CATGGTCGTGGGCGC | 1643 |
rs71042661 | in-del | -/GATAGATAGATAGATA | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47228997 | ATAGATAGATAGATA[-/GATAGATAGATAGATA]GATAGATAGATAGAT | 1643 |
rs71457210 | in-del | -/G | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47233430 | CAGAATGCGGCCGGG[-/G]TGCAGTGGCTCATGC | 1643 |
rs71458206 | multinucleotide-polymorphism | AT/TG | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47231248 | TTCATCATCATTTTC[AT/TG]GAATGTTTGGAAGAA | 1643 |
rs71475904 | snp | A/G | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47227291 | TTTGTGCTTTTAGTA[A/G]AGACAGGGTTTCACC | 1643 |
rs73465806 | snp | C/T | 0.103794 | 0.20279 | intron-variant | DDB2 | GRCh38.p7 | 11:47218967 | GTTTTTTTTTTGAGG[C/T]GGACTCTCGCTCTGT | 1643 |
rs73467637 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | DDB2 | GRCh38.p7 | 11:47226713 | ATTTTCTTTGAAGGA[A/G]TGTCTATTCAAGTCC | 1643 |
rs73467642 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DDB2 | GRCh38.p7 | 11:47229106 | CAAGATAGATGTTTA[C/T]GTAGTGGGAAGGCTA | 1643 |
rs74261105 | in-del | -/AA | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218756 | GGAAAAAAAAAAAAA[-/AA]GAATGTATGGTGGTA | 1643 |
rs74457022 | snp | A/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47227521 | TTTTTTTTTTTTTTT[A/T]AATTTTGAGATGGAG | 1643 |
rs74738435 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | DDB2 | GRCh38.p7 | 11:47233866 | ATGAGGAGTGCATGC[A/G]CACGCAAATCAGCAG | 1643 |
rs74781237 | in-del | -/CT | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230131 | AGTGAGACCCTGTCT[-/CT]AAAAAAAAAAAAAAA | 1643 |
rs75282560 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | DDB2 | GRCh38.p7 | 11:47229255 | GTAGGCAGGGGTGAA[C/G]AGTAGAGGAGGCCGG | 1643 |
rs75730438 | snp | A/T | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47225594 | GAGACTCCATCTCTA[A/T]TTTAAAAAAAAAAAA | 1643 |
rs76199809 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230014 | TTTTAATAATTTTTT[A/G]TAGAGGCTGGACCCA | 1643 |
rs76229852 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | DDB2 | GRCh38.p7 | 11:47236818 | TCCATCAGTGTTCCC[A/G]ATAATCCATCTGTCT | 1643 |
rs76383967 | snp | G/T | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47238414 | ATTTCTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 1643 |
rs76406750 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230007 | AGCTAATTTTTAATA[A/T]TTTTTTATAGAGGCT | 1643 |
rs76558898 | snp | G/T | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47227124 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTTTTGCT | 1643 |
rs76692445 | snp | G/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47235887 | TCACTTTTTTTTTTT[G/T]TGTAGAGACAGGGTA | 1643 |
rs76832686 | snp | C/T | 0.465683 | 0.126415 | intron-variant | DDB2 | GRCh38.p7 | 11:47225736 | TTTTTTCTTGTAAAA[C/T]TGAAACTCTATACCC | 1643 |
rs77026843 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235079 | GAACCTTTGTGGCTG[G/T]GGCTGTCCCCATCAG | 1643 |
rs77306647 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232406 | CCTGTAATCTTAGCA[C/T]TTTGGGAAGCCGTGG | 1643 |
rs77417324 | snp | G/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47237453 | TTTTTTTTTTTTTTT[G/T]AGAGTCTTGCTCTGT | 1643 |
rs77418547 | snp | A/C | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47230134 | GAGACCCTGTCTCTA[A/C]AAAAAAAAAAAAAAA | 1643 |
rs77504910 | snp | A/G | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47228161 | AAAAAAAAAAAAAAA[A/G]ATTATGCTGATTTCT | 1643 |
rs77749591 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DDB2 | GRCh38.p7 | 11:47238300 | GCAGTGGCCCACGAA[G/T]AAGATGGCTGGGAGA | 1643 |
rs77822325 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230006 | CAGCTAATTTTTAAT[A/G]ATTTTTTATAGAGGC | 1643 |
rs77897070 | snp | C/G | 0.5 | 0 | missense, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47238846 | AGCCAGGACACGGAA[C/G]TGAGAGACACTAAAG | 1643 |
rs78097793 | snp | G/T | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47238416 | TTCTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 1643 |
rs78253871 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232405 | GCCTGTAATCTTAGC[A/G]CTTTGGGAAGCCGTG | 1643 |
rs78285186 | snp | C/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47235927 | TACCCAGGCTGATCC[C/T]TTTTTTTTTTTTTTT | 1643 |
rs78290488 | snp | A/C | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47233713 | AAAATCTATCTCAAA[A/C]AAAAAAAAAAAAAAT | 1643 |
rs78290566 | in-del | -/G | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47228368 | TATCTGGCTGGGTGC[-/G]GGTGGCTCACTCCTG | 1643 |
rs78443313 | snp | A/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47230135 | AGACCCTGTCTCTAA[A/T]AAAAAAAAAAAAAAA | 1643 |
rs78615445 | snp | A/C | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47228267 | GCACAACTCTGTCTC[A/C]AAAAAAAAAAAAATT | 1643 |
rs78651238 | snp | C/G | 0.5 | 0 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216916 | TATTACAAAAGGCTG[C/G]CCCCTTTGACAGGAG | 1643 |
rs78777104 | snp | A/C | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47228266 | AGCACAACTCTGTCT[A/C]AAAAAAAAAAAAAAT | 1643 |
rs78806813 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DDB2 | GRCh38.p7 | 11:47236995 | TTTAGGAAAATCCCA[C/T]CCAATTCTGCCATTT | 1643 |
rs78811765 | snp | A/C | 0 | 0 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213512 | TGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 1643 |
rs78882057 | snp | G/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47226746 | TGCCTTTTTTTTTTT[G/T]TTTTTTTTTTTTTGA | 1643 |
rs79043473 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232404 | TGCCTGTAATCTTAG[C/G]ACTTTGGGAAGCCGT | 1643 |
rs79073050 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DDB2 | GRCh38.p7 | 11:47225598 | CTCCATCTCTATTTT[A/T]AAAAAAAAAAACAAA | 1643 |
rs79516998 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47220519 | TTTTTTTCTTTGTTG[A/C]ATCACCTTATGACAT | 1643 |
rs79548529 | snp | G/T | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47237452 | TTTTTTTTTTTTTTT[G/T]GAGAGTCTTGCTCTG | 1643 |
rs79684614 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232403 | ATGCCTGTAATCTTA[A/G]CACTTTGGGAAGCCG | 1643 |
rs79712270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47230768 | GTAAAGAAGAAGTGG[A/G]AAAGGTGGAGAAAGG | 1643 |
rs79715620 | snp | A/C | 1.69441e-05 | 0.00291063 | intron-variant | DDB2 | GRCh38.p7 | 11:47234973 | CTCCTGCAGACCCTG[A/C]CTGTCTGACCACTGC | 1643 |
rs79789792 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213510 | AGTGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 1643 |
rs79833271 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230009 | CTAATTTTTAATAAT[G/T]TTTTATAGAGGCTGG | 1643 |
rs79920947 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | DDB2 | GRCh38.p7 | 11:47237232 | GTATCTGGGTCAGGC[G/T]GATGTTAAAACGTTT | 1643 |
rs79988901 | snp | G/T | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47238415 | TTTCTTTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 1643 |
rs111269132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47219826 | GGAGTCTCACTCCGC[C/T]GCCCAGGCTGGAGTG | 1643 |
rs111458546 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DDB2 | GRCh38.p7 | 11:47225297 | TAATACTGCTTTTTT[C/T]AAAAAAAATTGTGGG | 1643 |
rs112403617 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | DDB2 | GRCh38.p7 | 11:47233568 | AAAAAATTAGCTGGG[C/T]GTGGTGGTAGGCCCC | 1643 |
rs112497030 | snp | C/G | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47228246 | CAGTCCAGCCTGAGC[C/G]ACAGAGCACAACTCT | 1643 |
rs112528650 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | DDB2 | GRCh38.p7 | 11:47225389 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCCA | 1643 |
rs112607915 | in-del | -/TATC | 0.5 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47228978 | AAAAAAAAAAAGAAA[-/TATC]TATCTATCTATCTAT | 1643 |
rs112709622 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | DDB2 | GRCh38.p7 | 11:47226136 | ATGCCAATAAGTACG[A/C]TTGCTTCATCAAATG | 1643 |
rs113024016 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231125 | CCTTCATCTCAAAAA[A/G]AAAAAAAAAAAAAAA | 1643 |
rs113508682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47218916 | AATTGTAAAATACAC[A/G]TAACATAAAATGTAT | 1643 |
rs113627237 | snp | G/T | 0.0322114 | 0.122752 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213068 | CAGGACAGCGCGGCC[G/T]CACCTGTGAACCTTC | 1643 |
rs113808506 | snp | C/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47215536 | CTTGCACAGTTAGGA[C/T]GGCTTCAGAGAATCC | 1643 |
rs114456359 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DDB2 | GRCh38.p7 | 11:47223217 | AGGCTGGGCGCTGTG[A/G]CTTACGCCTGTAATC | 1643 |
rs114570667 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | DDB2 | GRCh38.p7 | 11:47237247 | TGATGTTAAAACGTT[A/T]ACCAGTTGGTATGAT | 1643 |
rs114620783 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DDB2 | GRCh38.p7 | 11:47235156 | CACCTCTTCCTTTCC[A/G]CTCCTGTCTAGAGAG | 1643 |
rs114883807 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DDB2 | GRCh38.p7 | 11:47233865 | GATGAGGAGTGCATG[C/T]GCACGCAAATCAGCA | 1643 |
rs115426117 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DDB2 | GRCh38.p7 | 11:47223209 | TGATGTCTAGGCTGG[A/G]CGCTGTGGCTTACGC | 1643 |
rs115443197 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DDB2 | GRCh38.p7 | 11:47221035 | GGGAGTAGTGGTGCA[C/T]GTCTGTAGTTCCAGC | 1643 |
rs115918058 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DDB2 | GRCh38.p7 | 11:47220144 | CACCAGAAAAGGCCA[A/G]GTTAGACAGGTGTGG | 1643 |
rs116081393 | snp | A/G | 0.084728 | 0.187577 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213685 | GCTGAGTGTTGCGGC[A/G]CGCACCTGTAGTCCC | 1643 |
rs116186033 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DDB2 | GRCh38.p7 | 11:47230835 | AGTTCTTAAAACAGT[A/G]CCTGACTGGGCGCAG | 1643 |
rs116818583 | snp | C/T | 0.000197668 | 0.00993955 | intron-variant | DDB2 | GRCh38.p7 | 11:47233011 | GCTTAGGTGTAGTTC[C/T]GGCAAGAGCATCCAG | 1643 |
rs117405518 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239423 | CTCAGGTCCCTGGAG[A/G]CCCCAGCCCAGCTGA | 1643 |
rs117575057 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | DDB2 | GRCh38.p7 | 11:47230240 | AGGAGGTTGGGGCTA[C/T]GCTGAGCCAGGATTG | 1643 |
rs117641284 | snp | A/C/G | 0.0107246 | 0.0724382 | intron-variant | DDB2 | GRCh38.p7 | 11:47226639 | TGTAGTTTCATTTGC[A/C/G]TTTCTCTAATGATTA | 1643 |
rs117733439 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47220560 | TTCTTTACAGTGTAA[A/G]CTTTCTTTACACTGT | 1643 |
rs121434639 | snp | A/G | | | missense, intron-variant | DDB2 | GRCh38.p7 | 11:47234784 | AGAATGCACAAAAAG[A/G]AAGTGACGCATGTGG | 1643 |
rs121434640 | snp | A/G | 3.30437e-05 | 0.00406457 | DDB2 | 11 | allele_origin=G(germline)/A(germline) | 11:47234872 | AAATTTGGGACCTGC[A/G]CCAGGTTAGAGGGAA | 1643 |
rs121434641 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235326 | CAGAAGAGCGAGATC[C/T]GAGTTTACTCTGCTT | 1643 |
rs121434642 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235308 | CGGCTCCTGACCACG[G/T]ACCAGAAGAGCGAGA | 1643 |
rs137929910 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214951 | CGGGGTCTCCGAGAC[C/G]GGTGGGGCCGGAGCT | 1643 |
rs137958929 | snp | C/T | 6.58946e-05 | 0.0057396 | synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235283 | AGCTTGTTTCAGTCC[C/T]GATGGAGCCCGGCTC | 1643 |
rs138255134 | snp | A/G | 0.000330524 | 0.0128512 | synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235373 | CCTGGGCCTGATCCC[A/G]CACCCTCACCGTCAC | 1643 |
rs138346064 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DDB2 | GRCh38.p7 | 11:47228722 | TGACTGTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 1643 |
rs138769111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221196 | TATTCTTATCATAAA[A/G]TACAGAGAAAAGTGT | 1643 |
rs138780245 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214265 | GGATTCGATGGGACT[G/T]TAGTTTCTGGAATCC | 1643 |
rs138812797 | in-del | -/ACA | 0.0256215 | 0.110247 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239544 | CCAGTTGAAGGGGTG[-/ACA]ACGATTCCTGAAGCA | 1643 |
rs138991340 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47234427 | TCTGAATGTTCCTCA[C/G]TAGGAATCCACGGCA | 1643 |
rs139040209 | snp | A/C/G | 0.0364509 | 0.129988 | intron-variant | DDB2 | GRCh38.p7 | 11:47238263 | GCCAGCCTCAGCCCC[A/C/G]CCCTGCCACATTCAC | 1643 |
rs139258155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218124 | TTTCGCTGGTTGTCC[C/T]TACTCATAACGTAGA | 1643 |
rs139290057 | in-del | -/A | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231120 | GCAAGCCTTCATCTC[-/A]AAAAAAAAAAAAAAA | 1643 |
rs139325563 | snp | C/T | 0.000181194 | 0.00951651 | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47234659 | TGATCCTGCTGAACA[C/T]GGACGGCAAAGAGGT | 1643 |
rs139674102 | snp | A/G | 3.30617e-05 | 0.00406568 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216408 | TCCTGCCACCATGCC[A/G]CAGCATCGTCAGGAC | 1643 |
rs139756298 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47235521 | CCTGCCACCCCAGAT[C/T]GCTCCTGGCCCGAGC | 1643 |
rs139895994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47222768 | CAAGTATTTGTGTGG[A/C]TATATGTTTTCATTT | 1643 |
rs139968905 | snp | C/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216991 | CTGTGGGTTCCAAAG[C/G]GGGAGATATCATGCT | 1643 |
rs140307562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224170 | AATTTTTCTTCTGGT[C/T]GCTTTAAAAATGATT | 1643 |
rs140354834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47216693 | TTGCTTTCCAAGATT[A/C]TTCGTTCGTGTACAT | 1643 |
rs140669941 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DDB2 | GRCh38.p7 | 11:47236817 | ATCCATCAGTGTTCC[C/T]GATAATCCATCTGTC | 1643 |
rs140886714 | snp | A/G | 9.88484e-05 | 0.00702954 | synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235307 | CCGGCTCCTGACCAC[A/G]GACCAGAAGAGCGAG | 1643 |
rs140963751 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231438 | CTCAGATGAATCTCA[A/G]AGGCATGATGAGTGA | 1643 |
rs141038935 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236063 | TTAGCCTCGGAAGTA[A/G]ATTGGACTACAGGTA | 1643 |
rs141084415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47225830 | TCTGTGAGTTTGACT[A/G]CTTTAGATATCTCAT | 1643 |
rs141126138 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231968 | GGTTATTTAAGTCTA[C/T]ACATATGTTAAAATT | 1643 |
rs141293157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218786 | TAGGGTCAGGGGTAA[A/G]CTAGAGATGACTGTT | 1643 |
rs141354541 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47237146 | GACAGTGGGGCTCCT[C/G]CAGAACTCAAGTCCT | 1643 |
rs141514762 | in-del | -/TC | 0.0898077 | 0.191933 | intron-variant | DDB2 | GRCh38.p7 | 11:47224762 | CTCCCTTCGTTCCTT[-/TC]TCTCTCTTCTCTTCC | 1643 |
rs141546280 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47227398 | AGGTGTGAGACACTG[A/C/T]GCCCGGCCATGATAT | 1643 |
rs141817382 | snp | A/G | 0.00597247 | 0.0543191 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239648 | GTTCCTTGGGAGCCA[A/G]TGTTTGTACCCCTGG | 1643 |
rs141990819 | snp | C/G | 0.000439271 | 0.0148136 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216338 | TTCTGCTTGGCAGGT[C/G]CTAGCAGAAGATGTG | 1643 |
rs141994037 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DDB2 | GRCh38.p7 | 11:47234484 | TATTTATTGAATGCC[A/C]GCTGTGGGTTAGTCA | 1643 |
rs142203542 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47234666 | GCTGAACATGGACGG[C/T]AAAGAGGTGCGTTCT | 1643 |
rs142424607 | snp | C/T | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214015 | AGCAAGACCTTGTCT[C/T]TACAAAAATAAAAAT | 1643 |
rs142527861 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47235802 | CGCTCTGTCACCCAG[A/G]TGGGAGTACAGTGGG | 1643 |
rs142745076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47222058 | GTACAACTGTGAAGC[C/T]ATCACCACAATTAAA | 1643 |
rs143037895 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DDB2 | GRCh38.p7 | 11:47228732 | GAGGCCGAGGCAGGC[A/G]GATCACTTGAAGTCA | 1643 |
rs143049891 | snp | A/G | 0.00726918 | 0.0598477 | DDB2 | 11 | allele_origin=G(germline)/A(germline) | 11:47238177 | GACACGCTGGCCTCT[A/G]CAATGGGTGAGTAGG | 1643 |
rs143546492 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DDB2 | GRCh38.p7 | 11:47229489 | AAAGAGTCCAAGCAT[C/T]CTAAGGAAGACGTGC | 1643 |
rs143611676 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | DDB2 | GRCh38.p7 | 11:47220010 | TAGCCATGATGGTCT[C/T]GATCTCCTGACCTCG | 1643 |
rs143615033 | in-del | -/GGGG/GGGGGG | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235077 | GGAACCTTTGTGGCT[-/GGGG/GGGGGG]GTGGCTGTCCCCATC | 1643 |
rs143717194 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213107 | GACTTTGGCTGAAGC[G/T]AGGGCGTAGGAGTTC | 1643 |
rs143718979 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DDB2 | GRCh38.p7 | 11:47223908 | CCAGGACTTTAAGAC[C/T]AGCCTAGGAAACACA | 1643 |
rs143877183 | in-del | -/ATAAAA | 0.0162398 | 0.0886349 | intron-variant | DDB2 | GRCh38.p7 | 11:47232328 | CTCCATCTCAAAAAC[-/ATAAAA]ATAAAAATAAAAATA | 1643 |
rs143980626 | in-del | -/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47219238 | TGAGCCACCGCCCCC[-/C]AGCCAACTTTTTAAA | 1643 |
rs144266685 | snp | A/G | 0.00501522 | 0.0498243 | synonymous-codon, intron-variant | DDB2 | GRCh38.p7 | 11:47234792 | CAAAAAGAAAGTGAC[A/G]CATGTGGCCCTGAAC | 1643 |
rs144358907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235040 | ACCTTTACCCCTGAT[A/G]GCGTCTGCCAAGCTG | 1643 |
rs144368453 | snp | A/G | 6.58903e-05 | 0.00573941 | synonymous-codon, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47237926 | TTATGAATTGAGGAC[A/G]ATCGACGTGTTCGAT | 1643 |
rs144530280 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231303 | CCTGCCCTCCTAACT[A/C]AGCCACTGCTCTGAG | 1643 |
rs144729572 | snp | G/T | 9.94876e-05 | 0.00705223 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216874 | GGCTCCAGCAGTCCT[G/T]TTTGCACACTCTGGA | 1643 |
rs144735370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229709 | ATTTAAGGTTTTCAG[C/T]ATACAAAGTAAGACA | 1643 |
rs144744092 | in-del | -/TG | 0.0267878 | 0.112589 | intron-variant | DDB2 | GRCh38.p7 | 11:47216593 | TCCGATCACCCAGAC[-/TG]TGGTGACTGGCCTAC | 1643 |
rs144773443 | snp | A/G | 0.00993419 | 0.0697739 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213874 | ATAAAAACAGCCAAC[A/G]ACCAAACAAATAAAA | 1643 |
rs144989465 | snp | C/T | 3.29451e-05 | 0.00405851 | stop-gained, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47234610 | GTGTCTGCTAGTAGC[C/T]GAATGGTGGTCACAG | 1643 |
rs145167998 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DDB2 | GRCh38.p7 | 11:47234423 | GCAGTCTGAATGTTC[C/T]TCACTAGGAATCCAC | 1643 |
rs145241266 | snp | A/G | 1.66123e-05 | 0.00288199 | missense, intron-variant | DDB2 | GRCh38.p7 | 11:47234916 | TACTCGCTGCCGCAC[A/G]GGCATCCTGTCAACG | 1643 |
rs145264146 | snp | A/C | 4.99147e-05 | 0.00499549 | synonymous-codon, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47217043 | CAAACCCACCTTCAT[A/C]AAAGGGGTGAGCAGT | 1643 |
rs145822896 | snp | C/T | 4.95814e-05 | 0.00497878 | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235372 | CCCTGGGCCTGATCC[C/T]GCACCCTCACCGTCA | 1643 |
rs146590786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218384 | TGGGATGTATACATA[C/T]GAGGTAATTAACAAT | 1643 |
rs146719572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47219356 | AGCAGTCTCCAGAAC[C/T]TCATTATTTTTTTTT | 1643 |
rs146929811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47232382 | AGGGGCCAGACAAAG[C/T]GGCTCATGCCTGTAA | 1643 |
rs146959188 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226273 | TCCCCACCAACATTT[A/C]TTTTCTTTTTTTTTT | 1643 |
rs147169471 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47215999 | ATAAAATTGTGACCC[A/G]GTCCCATCTCGAGTT | 1643 |
rs147297424 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DDB2 | GRCh38.p7 | 11:47217362 | GCCTGGGCAACAAGA[A/G]TGAAACTCCATCTCA | 1643 |
rs147370403 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47222514 | ATACCTGGCTAATTT[A/T]AAAATTTTGTTATAG | 1643 |
rs147994715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226475 | GACGGGTTTTGCCAC[A/G]TTGGCCAGGCTGGTC | 1643 |
rs148013513 | in-del | -/GGGACGTTGAGGTGGAA | 0.130008 | 0.219321 | intron-variant | DDB2 | GRCh38.p7 | 11:47230056 | CTGTAACAGCACTTT[-/GGGACGTTGAGGTGGAA]GGATTGCTTGAGCCC | 1643 |
rs148050067 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47220242 | TCAGAGGAGTGCCGC[A/G]GACAGAGTGGGGTAG | 1643 |
rs148175447 | snp | A/C | 6.59315e-05 | 0.0057412 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215215 | AAGAGGAGCAGGAGT[A/C]CCCTGGAGCTGGAGC | 1643 |
rs148299549 | snp | A/G | 0.000164718 | 0.00907368 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47237933 | TTGAGGACGATCGAC[A/G]TGTTCGATGGAAACT | 1643 |
rs148533855 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DDB2 | GRCh38.p7 | 11:47229911 | TCATAGCTAACTACA[A/G]CCTTGAACTCCTGGG | 1643 |
rs148869406 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DDB2 | GRCh38.p7 | 11:47219612 | GTCTTGTCTTCCCAA[A/G]TTGCTCGGGATTACA | 1643 |
rs149110064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224588 | AAATGAAGAAAAAGA[A/C]CAGTTCTTTTTTTCT | 1643 |
rs149392439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47223155 | TTTATTGCATACAAT[A/G]TATTTGTTCACAGTT | 1643 |
rs149448905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47215488 | TAACAACAGACACAC[A/G]GACTTGTCAGATTCC | 1643 |
rs149583624 | snp | C/G/T | 9.8841e-05 | 0.00702935 | missense, synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47234663 | CCTGCTGAACATGGA[C/G/T]GGCAAAGAGGTGCGT | 1643 |
rs149919159 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | DDB2 | GRCh38.p7 | 11:47224250 | TTTTTTCTTTTGAGA[C/G]AAAGTCTCACTCTGT | 1643 |
rs149970933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218269 | GACCTTTCCTTTCTG[C/G]TTCACCATCCTATTC | 1643 |
rs150119905 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DDB2 | GRCh38.p7 | 11:47237056 | TGATCTGGGGAATGT[A/G]GGTTTCCTTCTCTTT | 1643 |
rs150304708 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214573 | CCCGGACAACAAAGC[A/G]AGACCCCGTCTCTCC | 1643 |
rs150620642 | snp | G/T | 1.65247e-05 | 0.00287438 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216374 | GACTGCCTCTGGGTG[G/T]GGCTGGCTGGCCCAC | 1643 |
rs150822718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47234506 | GGTTAGTCACCGGAG[C/T]GGCAACAGTGAGTAA | 1643 |
rs150875144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228437 | CCTGAGGTCAGGAGT[C/T]CAAGACCAGCCTGGC | 1643 |
rs150925443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47236510 | AATAGTGGTGGGGAG[C/T]GCCAGTTTCCAGCAG | 1643 |
rs150980458 | snp | A/G/T | 0.00319074 | 0.0398324 | intron-variant | DDB2 | GRCh38.p7 | 11:47230847 | AGTGCCTGACTGGGC[A/G/T]CAGTGGCTCACGCCT | 1643 |
rs151064257 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47233910 | CAAGGCTCCAGGCTA[A/C]TCTTCCGCAAGAAAT | 1643 |
rs151146343 | snp | A/C/T | 1.64841e-05 | 0.00287085 | missense, intron-variant | DDB2 | GRCh38.p7 | 11:47234791 | ACAAAAAGAAAGTGA[A/C/T]GCATGTGGCCCTGAA | 1643 |
rs151316703 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DDB2 | GRCh38.p7 | 11:47217939 | TTGACCTCATCTTAC[A/G]CCATTGTCTTTTCTC | 1643 |
rs180861241 | snp | A/G | 0.00018131 | 0.00951957 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215092 | CTCAATCCTCCCTCC[A/G]TGATCTTCGCATAGA | 1643 |
rs180952253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47227402 | GTGAGACACTGCGCC[A/C]GGCCATGATATTAAC | 1643 |
rs181186056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47232189 | TCTCTACTAAAAATA[C/T]ACAATTTAGCCATGC | 1643 |
rs181189502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221777 | GTAGAAACAGGGTTT[C/T]ACCATATTGGCCAGG | 1643 |
rs181404957 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47216580 | CTTGTCAGAGTGGTC[C/T]GATCACCCAGACTGT | 1643 |
rs181435436 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47226869 | GCCTTAGCCACCCGA[C/G]TAACTGGGACTGCAG | 1643 |
rs181604947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47221359 | CCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 1643 |
rs181825071 | snp | A/C | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214343 | GGCACTAGCTCTCTA[A/C]AAAGCCGCCACTCCC | 1643 |
rs182000569 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47233845 | ATCCTGGGCTGTCCC[A/G]CAGGGATGAGGAGTG | 1643 |
rs182004027 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235576 | TCTCTCTCTTCCTTT[A/T]ATCCCACTTCTGCCA | 1643 |
rs182109561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47237516 | ACTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 1643 |
rs182244266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220069 | GCTGGGATTACAGGC[C/G]TGAGCCACTGCACCC | 1643 |
rs182264349 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47215866 | TTCTAATTTCACTTA[A/C]CTCCCCAGAAGTAAC | 1643 |
rs182352408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217144 | ACTTTGGGAGGCCAA[C/G]GTGGGTGGATCACCT | 1643 |
rs182906461 | snp | A/G/T | 0.0135084 | 0.0812711 | intron-variant | DDB2 | GRCh38.p7 | 11:47229391 | AGGGGCGGCCGTGGC[A/G/T]CCTGATGTGGGCAAG | 1643 |
rs182925088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236835 | TAATCCATCTGTCTG[C/T]ATGTCCCAGTTTGTA | 1643 |
rs183159009 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47227655 | AGCTGGCACCCACCA[C/T]CACGCCCAGCTGGCC | 1643 |
rs183195775 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47224940 | CATATTTATTATTTC[C/T]TCTTCTTTCTTTTTT | 1643 |
rs183212099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229269 | AGAGTAGAGGAGGCC[A/G]GGCATGGAATAGTGA | 1643 |
rs183492533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47215502 | CGGACTTGTCAGATT[C/G]CTTGTTCGTATCAGG | 1643 |
rs183716322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47232329 | TCCATCTCAAAAACA[C/T]AAAAATAAAAATAAA | 1643 |
rs183969233 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214256 | AAGCAGCTTGGATTC[G/T]ATGGGACTGTAGTTT | 1643 |
rs183998044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47217892 | CGAGACTCCATCTCA[A/G]AAAAAAAGAATTGAA | 1643 |
rs184093219 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DDB2 | GRCh38.p7 | 11:47223562 | GAGGCAGGCGGATCA[C/T]GAGATCAAGAGATTG | 1643 |
rs184118289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47225604 | CTCTATTTTAAAAAA[A/C]AAAAACAAAAAACTG | 1643 |
rs184185065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218636 | GTCCCCTCTAGGACC[G/T]TTAGCCAGCCCAGCT | 1643 |
rs184648122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47226418 | AGCTGAGATTATAGG[C/T]GCACACCACCATGCC | 1643 |
rs184879437 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DDB2 | GRCh38.p7 | 11:47231013 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 1643 |
rs185023453 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232022 | TGCTATATGTTAATT[A/T]AAAAAAAAAGTAAAA | 1643 |
rs185260634 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213442 | CTTGAACCCGGGAGG[C/T]GGAGATTGCAGTGAG | 1643 |
rs185380045 | snp | C/T | 0.000115305 | 0.00759205 | synonymous-codon, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47237938 | GACGATCGACGTGTT[C/T]GATGGAAACTCAGGG | 1643 |
rs185647092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47220561 | TCTTTACAGTGTAAA[C/T]TTTCTTTACACTGTA | 1643 |
rs185687113 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47216582 | TGTCAGAGTGGTCCG[A/G]TCACCCAGACTGTGG | 1643 |
rs185827759 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227447 | ATGATTTGAAAATAT[C/G]TTCTCCCACTTCATA | 1643 |
rs185930530 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47221513 | GCAGTAGCACGATCT[C/T]GGCCCACTGCAACCT | 1643 |
rs185989773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228233 | GAGTGCACCACTGCA[A/G]TCCAGCCTGAGCGAC | 1643 |
rs186073549 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47229818 | AATTTGATGGCTCTT[C/T]TTTTTTTTTTTTTTT | 1643 |
rs186090142 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DDB2 | GRCh38.p7 | 11:47221832 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAATGC | 1643 |
rs186242614 | snp | C/G/T | 3.29453e-05 | 0.00405854 | intron-variant | DDB2 | GRCh38.p7 | 11:47234563 | CTTACAACACAGTCT[C/G/T]TCCCTCCAGCATCTG | 1643 |
rs186552354 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | DDB2 | GRCh38.p7 | 11:47226971 | CTAAGTTAAAAAAAA[A/T]TTTTTTTTTATAGAG | 1643 |
rs186596100 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236082 | GGACTACAGGTATGC[A/G]CCACCATACCCAGCT | 1643 |
rs186707579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47230281 | TCAAGGTTTTGAACT[C/T]CTGGCCTTAAGCGAT | 1643 |
rs186870004 | snp | A/C/T | 0.00844399 | 0.0644267 | DDB2 | 11 | allele_origin=T(germline)/C(germline) | 11:47216270 | AACAAGGCTTCCTTT[A/C/T]GGGGAATTCAGCAGA | 1643 |
rs186949007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47237265 | CAGTTGGTATGATCT[C/T]AGGAAATGCAAATGA | 1643 |
rs187250799 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218741 | TCCAGAAGCCAGAGT[A/G]GAAAAAAAAAAAAAA | 1643 |
rs187269412 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DDB2 | GRCh38.p7 | 11:47223823 | ATAAAGATGATTTCT[A/C]GTTGGGCTCAATGGT | 1643 |
rs187417387 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47223636 | ATACAAAAAAAATTA[A/G]CCAGGCGTGGTGGTG | 1643 |
rs187941293 | snp | A/C/T | 0.000131985 | 0.0081225 | intron-variant | DDB2 | GRCh38.p7 | 11:47237818 | GTTTACCCTCATGGC[A/C/T]GGCCTCTCCATCTCC | 1643 |
rs188274551 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47229295 | AGTGAAGTCTGAAGC[A/G]GGGTTGAGGATGCTG | 1643 |
rs188348077 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47214977 | GAGCTCCAAGCTGGT[G/T]TGAACAAGCCCTGGG | 1643 |
rs188548355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218304 | TGCCTGGAACAAAGT[C/T]TGGCCTAGAGTAGCT | 1643 |
rs188576126 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213595 | TTGGCAGACCGAGGT[A/G]GATGGATGCCAGGAG | 1643 |
rs188766296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221541 | CCTCTGCCTCCTGAG[C/T]TGAAATGATTCTCCT | 1643 |
rs188781019 | snp | A/G | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213251 | GGCATGGTGGCTCAC[A/G]CCTATAATCCCAGCA | 1643 |
rs188963035 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226278 | ACCAACATTTATTTT[C/T]TTTTTTTTTTTTTTT | 1643 |
rs189010538 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47226674 | TATTGAGCATCTTTA[C/T]GTGTGCTTCTTGGCC | 1643 |
rs189070234 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47237433 | TTACTGGCAAATACT[A/T]CTTTTTTTTTTTTTT | 1643 |
rs189255733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47220930 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACCTGA | 1643 |
rs189260187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47231240 | TGATTATTTTCATCA[C/T]CATTTTCATGAATGT | 1643 |
rs189356916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47219860 | TGGCGCAATCTCGGC[C/T]CACTGCAAGCTCCGC | 1643 |
rs189396398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47227166 | GGCTGGAGTGTAATG[A/G]CTCAATCTCGGCTCA | 1643 |
rs189499095 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47226007 | TTGTTTATCTGTTTA[G/T]TAATTGACAGACACT | 1643 |
rs189807625 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47212977 | GAAAGGCCCAGCAAT[A/G]CCTGAGTAAGCCCAA | 1643 |
rs189836815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47237318 | TAAGGGCCAGGGAGG[A/C]CAGCTAGGGATTAAA | 1643 |
rs189914437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47232089 | TGGCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 1643 |
rs190052956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217092 | CTAAAGAAGTGTTTG[A/T]TGGCTGGGTGCAGTG | 1643 |
rs190327891 | snp | A/C | 0.136166 | 0.22258 | intron-variant | DDB2 | GRCh38.p7 | 11:47231143 | AAAAAAAAAAAAAAA[A/C]ACACACAAAGAAAAT | 1643 |
rs190444068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47215796 | AGACGTCGGACCTAT[A/G]GTGATTGGGTCCTCA | 1643 |
rs190451394 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DDB2 | GRCh38.p7 | 11:47228536 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 1643 |
rs190969000 | snp | C/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47227450 | ATTTGAAAATATCTT[C/T]TCCCACTTCATAGAT | 1643 |
rs190979196 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213091 | GAACCTTCAAGACTT[A/G]GACTTTGGCTGAAGC | 1643 |
rs190994576 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47221876 | ACGAGCCACTGCACC[C/T]GGCCTGGGTTTTTAA | 1643 |
rs191530751 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47219459 | TCCACCTTCCTGACT[C/G]AAGGAATCCTCCGGC | 1643 |
rs191538466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236395 | TTTTTGCCTAAGCCC[A/C]CATGCAGACTGAGCT | 1643 |
rs191773047 | snp | G/T | 1.65318e-05 | 0.002875 | synonymous-codon, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216397 | TGGCCCACAGATCCT[G/T]CCACCATGCCGCAGC | 1643 |
rs191791529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224835 | CTGCTCCATAGGCAA[A/G]GTAGCCCAGCGTATT | 1643 |
rs191828483 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213681 | ATTAGCTGAGTGTTG[A/C]GGCGCGCACCTGTAG | 1643 |
rs192054388 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217532 | TAAATGATGATGATA[C/T]ATATTTTTCTAATGC | 1643 |
rs192093572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47218385 | GGGATGTATACATAC[A/G]AGGTAATTAACAATA | 1643 |
rs192175383 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218758 | AAAAAAAAAAAAAAA[A/G]AATGTATGGTGGTAG | 1643 |
rs192432727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47226407 | CAGCCTCCAGTAGCT[A/G]AGATTATAGGCGCAC | 1643 |
rs192552912 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DDB2 | GRCh38.p7 | 11:47229316 | GAGGATGCTGAACCA[C/T]AGGGAGGCCTAGAGT | 1643 |
rs192627432 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230481 | GCTTAATTAAATTTG[A/G]TGTTAATTGCAATAA | 1643 |
rs192707777 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47225515 | GAGAATCACTTGAAC[C/T]CGGGAGGCAGAAGTT | 1643 |
rs193160239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47231611 | TCACTGCAGCCTCGA[C/T]CTCCAGGCTTCCGTC | 1643 |
rs193220920 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213353 | CTGTCTCTACTAAAA[C/T]ACAAAAAATTAGTCA | 1643 |
rs199502211 | snp | A/G | 0.00112076 | 0.0236458 | intron-variant | DDB2 | GRCh38.p7 | 11:47234718 | CCTCACCCCCACCTC[A/G]GTTCTGTGTCCCCAC | 1643 |
rs199630230 | snp | A/T | 0.000446344 | 0.0149323 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216426 | GCATCGTCAGGACCC[A/T]CCACCAGCATAAGCT | 1643 |
rs199632231 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221289 | CTATTTTTTTTTTTT[C/T]CCAAGTCTGAGTCTT | 1643 |
rs199659792 | in-del | -/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226971 | TAAGTTAAAAAAAAA[-/T]TTTTTTTTTATAGAG | 1643 |
rs199693068 | snp | C/T | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214206 | AAAAAAAAAAAAAAA[C/T]GGCAAGGAGTTCCAA | 1643 |
rs199822504 | snp | C/T | 6.58892e-05 | 0.00573936 | stop-gained, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47232931 | AAAGGCAACATTCTA[C/T]GAGTTTTTGCCAGCT | 1643 |
rs199875336 | snp | C/T | 0.00697544 | 0.0586435 | intron-variant | DDB2 | GRCh38.p7 | 11:47235457 | AGGAGGCTGTGATCA[C/T]GAGGCCGGAGCAGGT | 1643 |
rs199895326 | in-del | -/TC | 0.0926964 | 0.194308 | intron-variant | DDB2 | GRCh38.p7 | 11:47235959 | TTTTTCTTGAAACGG[-/TC]TCTTGCTCTGTCACC | 1643 |
rs199920301 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47237980 | TCAGCTCTATGACCC[A/G]GAATCTTCTGGCATC | 1643 |
rs199945592 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227295 | TGCTTTTAGTAGAGA[C/G]AGGGTTTCACCATGT | 1643 |
rs199965459 | snp | G/T | 0.00365026 | 0.0425653 | intron-variant | DDB2 | GRCh38.p7 | 11:47215268 | GAAGGGCTCCGGTAC[G/T]GCCTGTGCCTGCTGC | 1643 |
rs199967513 | in-del | -/A | | | intron-variant | DDB2 | GRCh38.p7 | 11:47225598 | CTCCATCTCTATTTT[-/A]AAAAAAAAAAACAAA | 1643 |
rs199987013 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47217889 | GAGCGAGACTCCATC[G/T]CAAAAAAAAAGAATT | 1643 |
rs200026126 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232485 | GACAAAACCCCATCT[A/T]AAAAAAAAAAAATAG | 1643 |
rs200094631 | snp | C/T | 0.00199802 | 0.0315439 | synonymous-codon, intron-variant | DDB2 | GRCh38.p7 | 11:47234840 | CCTGGCCACAGCCTC[C/T]GTAGATCAAACAGTG | 1643 |
rs200136414 | snp | A/G | 2.01469e-05 | 0.0031738 | intron-variant | DDB2 | GRCh38.p7 | 11:47235453 | CAGAAGGAGGCTGTG[A/G]TCATGAGGCCGGAGC | 1643 |
rs200136508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229720 | TCAGTATACAAAGTA[A/C]GACAGTTGTGAAGCA | 1643 |
rs200221945 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235527 | ACCCCAGATCGCTCC[C/T]GGCCCGAGCACAGAG | 1643 |
rs200223070 | snp | C/T | 0.0238486 | 0.106562 | intron-variant | DDB2 | GRCh38.p7 | 11:47229836 | TTTTTTTTTTTTTTT[C/T]TTCTTCCTAATAGAG | 1643 |
rs200303229 | in-del | -/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231249 | CATCATCATTTTCAT[-/G]GAATGTTTGGAAGAA | 1643 |
rs200353341 | snp | C/T | 3.34152e-05 | 0.00408736 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47238872 | TAAAGAAGGTGTGGG[C/T]CAGACAAGGCCTTGG | 1643 |
rs200406558 | snp | A/G | 0.00116889 | 0.024147 | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47232934 | GGCAACATTCTACGA[A/G]TTTTTGCCAGCTCAG | 1643 |
rs200856208 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216993 | GTGGGTTCCAAAGGG[A/G]GAGATATCATGCTCT | 1643 |
rs200963195 | snp | C/G/T | 0.000297085 | 0.0121846 | intron-variant | DDB2 | GRCh38.p7 | 11:47237810 | TGTTCTGTGTTTACC[C/G/T]TCATGGCCGGCCTCT | 1643 |
rs201002652 | in-del | -/TC | | | intron-variant | DDB2 | GRCh38.p7 | 11:47223397 | GCTGAGGCATGAGAA[-/TC]TCTTGAACCTGGGAG | 1643 |
rs201088445 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227952 | GGAGACCATCCTGGC[C/T]AACATGGTGAAACCC | 1643 |
rs201229167 | snp | C/T | | | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215188 | TCCGAGATTGTATTA[C/T]GCCCCAGGAACAAGA | 1643 |
rs201259165 | snp | A/C/G | 6.5993e-05 | 0.00574395 | missense, intron-variant | DDB2 | GRCh38.p7 | 11:47234847 | ACAGCCTCCGTAGAT[A/C/G]AAACAGTGAAAATTT | 1643 |
rs201317629 | snp | A/G/T | 0.000346095 | 0.0131503 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215101 | CCCTCCATGATCTTC[A/G/T]CATAGAGCACAGTAC | 1643 |
rs201321118 | in-del | -/A | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235766 | TTTTATTTTTTTATT[-/A]TTTTTTTTAAGGCAG | 1643 |
rs201525567 | snp | A/C/T | 3.29462e-05 | 0.00405857 | missense, synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47234642 | AGACAACGTGGGGAA[A/C/T]GTGATCCTGCTGAAC | 1643 |
rs201531216 | snp | A/G | 1.71455e-05 | 0.00292787 | intron-variant | DDB2 | GRCh38.p7 | 11:47217069 | GCAGTTCCCCATGCC[A/G]GGTCGTGCTAAAGAA | 1643 |
rs201689667 | in-del | -/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47225594 | GAGACTCCATCTCTA[-/T]TTTAAAAAAAAAAAA | 1643 |
rs201703288 | snp | C/G | 0.00141568 | 0.0265676 | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47232868 | CCTCTCAATACCAAC[C/G]AGTTTTACGCCTCCT | 1643 |
rs201842334 | snp | A/G | 4.95896e-05 | 0.00497919 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216898 | CTCTGGATTCTTACC[A/G]GATATTACAAAAGGC | 1643 |
rs202031616 | snp | C/G | 1.64741e-05 | 0.00286998 | intron-variant | DDB2 | GRCh38.p7 | 11:47235236 | CACAGAGGGCTTGTG[C/G]TTCCTTCAGCTCAGG | 1643 |
rs202083037 | snp | C/T | 0.000148249 | 0.00860829 | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47234644 | ACAACGTGGGGAACG[C/T]GATCCTGCTGAACAT | 1643 |
rs202093583 | snp | A/G | 9.8956e-05 | 0.00703336 | intron-variant | DDB2 | GRCh38.p7 | 11:47237819 | TTTACCCTCATGGCC[A/G]GCCTCTCCATCTCCT | 1643 |
rs202117451 | in-del | -/TATCTATC | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228978 | AAAAAAAAAAAGAAA[-/TATCTATC]TATCTATCTATCTAT | 1643 |
rs202120997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47232783 | GGCCAGGCCCATCAT[C/T]ACTCACTGGCTTTTT | 1643 |
rs202149501 | snp | A/G | 0.00199805 | 0.0315442 | intron-variant | DDB2 | GRCh38.p7 | 11:47235415 | CACACCCATCAAGGT[A/G]AGTGGCGGTGGGAAG | 1643 |
rs202165257 | in-del | -/A | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231248 | TTCATCATCATTTTC[-/A]TGAATGTTTGGAAGA | 1643 |
rs367648586 | snp | C/T | 6.59011e-05 | 0.00573988 | intron-variant | DDB2 | GRCh38.p7 | 11:47234676 | GACGGCAAAGAGGTG[C/T]GTTCTCCGAGGTCCT | 1643 |
rs367689636 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | DDB2 | GRCh38.p7 | 11:47228367 | ATATCTGGCTGGGTG[-/T]CGGTGGCTCACTCCT | 1643 |
rs367717420 | snp | C/T | 1.64806e-05 | 0.00287054 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215116 | GCATAGAGCACAGTA[C/T]CCCTTCACACGGAGG | 1643 |
rs367798780 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233781 | GTGACTCTGACTGCT[C/T]CCTGAGGAATTAAGT | 1643 |
rs367829903 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221229 | AAAATAAATTAAATA[C/T]GATCCAAAATCCCCA | 1643 |
rs367856009 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47229506 | TAAGGAAGACGTGCA[A/T]TTGGGGAGTGTGTGG | 1643 |
rs367966832 | snp | C/G | 3.33495e-05 | 0.00408333 | intron-variant | DDB2 | GRCh38.p7 | 11:47216851 | AATTCATTTCTCTCT[C/G]TGGCAGGGGCTCCAG | 1643 |
rs368073045 | snp | C/G/T | 1.65119e-05 | 0.00287327 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215248 | GAGGCCAAGAAGCTC[C/G/T]GTGCGAAGGGCTCCG | 1643 |
rs368317265 | in-del | -/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231862 | ACAGATCAGCCAGGG[-/G]CTGGGGGCGAGGGGA | 1643 |
rs368365566 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213708 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGTGG | 1643 |
rs368460981 | snp | A/G | 3.29478e-05 | 0.00405867 | intron-variant | DDB2 | GRCh38.p7 | 11:47232996 | GGAAAGGGCTTCTAA[A/G]CTTAGGTGTAGTTCC | 1643 |
rs368584907 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230241 | GGAGGTTGGGGCTAC[A/G]CTGAGCCAGGATTGC | 1643 |
rs368605416 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | DDB2 | GRCh38.p7 | 11:47238078 | CAAAAGTGACCAGAA[A/G]TCAGGTGTCTCTGCT | 1643 |
rs368630561 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233654 | GCAGAGGTTGCAGTG[A/G]GCCGAGATGGCGCCA | 1643 |
rs368816614 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231153 | AAAAAAACACACAAA[A/G]AAAATCCCCCCAAAA | 1643 |
rs368849435 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47225593 | CGAGACTCCATCTCT[A/C]TTTTAAAAAAAAAAA | 1643 |
rs368963928 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | DDB2 | GRCh38.p7 | 11:47238195 | ATGGGTGAGTAGGAG[A/G]AGAATGTCTCTGACT | 1643 |
rs369018189 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236408 | CCCCATGCAGACTGA[A/G]CTCTGCTAGTTCTGC | 1643 |
rs369110013 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215156 | CTCCCAAGAAACGCC[C/T]AGAAACCCAGAAGAC | 1643 |
rs369378109 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47238843 | GGAAGCCAGGACACG[G/T]AAGTGAGAGACACTA | 1643 |
rs369552849 | snp | C/T | 9.92162e-05 | 0.0070426 | intron-variant | DDB2 | GRCh38.p7 | 11:47216328 | AATATGTCTGTTCTG[C/T]TTGGCAGGTCCTAGC | 1643 |
rs369612898 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DDB2 | GRCh38.p7 | 11:47227985 | TCTCTACTAAATATG[C/T]AAAAATTAGCTGGGC | 1643 |
rs369707114 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DDB2 | GRCh38.p7 | 11:47223244 | AATCCCAGCATTTTG[A/G]GGGGCCAAGGCAAGT | 1643 |
rs369738157 | snp | C/T | 1.64836e-05 | 0.0028708 | intron-variant | DDB2 | GRCh38.p7 | 11:47238009 | TCAGTTCGGTGAGGC[C/T]TGGGTCCTCAAATAA | 1643 |
rs369978489 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | DDB2 | GRCh38.p7 | 11:47234942 | CAACGCAGGTGTGAT[A/C]TCCCAGACCTCATCT | 1643 |
rs370130760 | snp | A/G | 3.29799e-05 | 0.00406065 | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235345 | TTTACTCTGCTTCCC[A/G]GTGGGACTGCCCCCT | 1643 |
rs370189637 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47225152 | ACCATATTGGCCAGG[C/G]TGGTCTCAGACTCCT | 1643 |
rs370416522 | snp | G/T | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213113 | GGCTGAAGCGAGGGC[G/T]TAGGAGTTCTAAGTA | 1643 |
rs370448159 | snp | C/T | 0.000560058 | 0.0167247 | intron-variant | DDB2 | GRCh38.p7 | 11:47232767 | AGGCCTGGTTCCTCA[C/T]GGCCAGGCCCATCAT | 1643 |
rs370540741 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47232831 | TGGAGCTGGAGGGAG[C/T]ATCACTGGGCTGAAG | 1643 |
rs370554359 | snp | A/T | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213428 | AGGCAGGGGAATCGC[A/T]TGAACCCGGGAGGCG | 1643 |
rs370647279 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47233862 | AGGGATGAGGAGTGC[A/G]TGCGCACGCAAATCA | 1643 |
rs370654581 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47234611 | TGTCTGCTAGTAGCC[A/G]AATGGTGGTCACAGG | 1643 |
rs370952655 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228731 | GGAGGCCGAGGCAGG[C/T]GGATCACTTGAAGTC | 1643 |
rs371257608 | snp | A/G | 7.77046e-05 | 0.00623268 | intron-variant | DDB2 | GRCh38.p7 | 11:47235446 | GAGCTCGCAGAAGGA[A/G]GCTGTGATCATGAGG | 1643 |
rs371281878 | snp | C/G | 4.9436e-05 | 0.00497148 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215127 | AGTACCCCTTCACAC[C/G]GAGGACGCGATGGCT | 1643 |
rs371315799 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47238673 | AAAGTGCTGGGATTA[C/T]AGACTTGAGCCACCG | 1643 |
rs371319666 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221545 | TGCCTCCTGAGTTGA[A/G]ATGATTCTCCTGCCT | 1643 |
rs371454695 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | DDB2 | GRCh38.p7 | 11:47238245 | TCCCAAGGTTCAGTG[C/T]GGGCCAGCCTCAGCC | 1643 |
rs371456569 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235044 | TTACCCCTGATAGCG[C/T]CTGCCAAGCTGATGT | 1643 |
rs371573554 | snp | C/G | 0.000355562 | 0.0133287 | intron-variant | DDB2 | GRCh38.p7 | 11:47234974 | TCCTGCAGACCCTGC[C/G]TGTCTGACCACTGCT | 1643 |
rs371586753 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233740 | AAATTACAGAATACT[C/T]GTCACTTTGATTTCC | 1643 |
rs371594907 | snp | C/T | 0.00017163 | 0.00926204 | intron-variant | DDB2 | GRCh38.p7 | 11:47238220 | CTGACTTGCCAAGTC[C/T]GATCCTACTTCCCAA | 1643 |
rs371699747 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227354 | TCAGGTGATCTACCC[A/G]CCTCGGCCTCCCAAA | 1643 |
rs371704632 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47215447 | AACACCTCTCCCGCT[A/T]GGTAACAGGAAGCAG | 1643 |
rs371732878 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235652 | GAGTTTTTTCAGCCC[A/G]GCTCTGATCTCACTG | 1643 |
rs371781971 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231099 | CACTTCAGCCTGGGC[A/G]ACAGAGCAAGCCTTC | 1643 |
rs371788427 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236532 | TTCCAGCAGCCAGAC[C/T]CCCCGGGTTAGAATC | 1643 |
rs371894900 | in-del | -/C | 0.000652528 | 0.018051 | intron-variant | DDB2 | GRCh38.p7 | 11:47229818 | AATTTGATGGCTCTT[-/C]TTTTTTTTTTTTTTT | 1643 |
rs372407832 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47223270 | CAAGTGGATCATTTG[C/T]GATCATGAGTTTTAG | 1643 |
rs372435540 | snp | C/G | 1.65384e-05 | 0.00287557 | intron-variant | DDB2 | GRCh38.p7 | 11:47238050 | AAGCAGGGATTCAAC[C/G]TACCTTATTGACCAA | 1643 |
rs372523541 | snp | C/T | 3.29478e-05 | 0.00405867 | intron-variant | DDB2 | GRCh38.p7 | 11:47232790 | CCCATCATCACTCAC[C/T]GGCTTTTTCCTTCCT | 1643 |
rs372842821 | snp | C/T | 1.77231e-05 | 0.00297678 | intron-variant | DDB2 | GRCh38.p7 | 11:47235421 | CATCAAGGTGAGTGG[C/T]GGTGGGAAGGAGCTC | 1643 |
rs372993323 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47223546 | AGCGCTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 1643 |
rs373044335 | snp | C/T | 4.97921e-05 | 0.00498935 | missense, intron-variant | DDB2 | GRCh38.p7 | 11:47234911 | TCCTCTACTCGCTGC[C/T]GCACAGGCATCCTGT | 1643 |
rs373164807 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232130 | TGGCGGATTACCTGA[A/G]GGCAGGAGTTCCAGA | 1643 |
rs373220500 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236516 | GGTGGGGAGCGCCAG[G/T]TTCCAGCAGCCAGAC | 1643 |
rs373301292 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | DDB2 | GRCh38.p7 | 11:47234985 | CTGCCTGTCTGACCA[C/T]TGCTGGGGTTTTCCC | 1643 |
rs373309529 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231637 | CCGTCATCTTCCCAC[C/T]TCAGCCTTCTGAGTA | 1643 |
rs373315783 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47238899 | TTGGAGCCCACACAT[A/G]GGATCAAGTCCTGCA | 1643 |
rs373513949 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226932 | TGTTTTGTTTTTTTC[A/G]CTGTCTCTTACAGAA | 1643 |
rs373518343 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228228 | AAGCTGAGTGCACCA[C/T]TGCAGTCCAGCCTGA | 1643 |
rs373622283 | snp | A/G | 0.000428336 | 0.0146282 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215195 | TTGTATTACGCCCCA[A/G]GAACAAGAGGAGCAG | 1643 |
rs373857948 | snp | A/T | 1.64741e-05 | 0.00286998 | intron-variant | DDB2 | GRCh38.p7 | 11:47235242 | GGGCTTGTGGTTCCT[A/T]CAGCTCAGGGGCTTT | 1643 |
rs373863283 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221823 | TGACCTCAAGTGATC[C/T]GCCCGCCTCGGCCTC | 1643 |
rs373937334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218014 | GGGTCTCTGTAATTG[C/T]TGTTCCCTTTGACTG | 1643 |
rs374027588 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221645 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTCG | 1643 |
rs374094218 | snp | A/G | 0.000182671 | 0.00955522 | intron-variant | DDB2 | GRCh38.p7 | 11:47216480 | TCCAGCAGGTAAGGC[A/G]TTTTTTGCCTCAAGT | 1643 |
rs374159574 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220392 | ATGGGAATAGAGGAA[A/C/T]TTAGCTTATGCCTGG | 1643 |
rs374206520 | snp | C/T | 3.30136e-05 | 0.00406273 | intron-variant | DDB2 | GRCh38.p7 | 11:47237808 | CATGTTCTGTGTTTA[C/T]CCTCATGGCCGGCCT | 1643 |
rs374424077 | snp | A/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47222379 | GTTTTTTGTTTTAAG[A/T]CAGGGTCTTGCTGTG | 1643 |
rs374456936 | snp | C/G | 5.00271e-05 | 0.0050011 | intron-variant | DDB2 | GRCh38.p7 | 11:47216290 | AATTCAGCAGAAAAA[C/G]CTTTCGTGAGATTGG | 1643 |
rs374548079 | in-del | -/GAAAGAGAGAAAG | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213833 | AAAAAAAAAAAAAAA[-/GAAAGAGAGAAAG]AAAGAAAGAAAAAAT | 1643 |
rs374929534 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235787 | TTTAAGGCAGGGTCT[C/T]GCTCTGTCACCCAGG | 1643 |
rs375093764 | snp | C/T | 0.000451887 | 0.0150246 | intron-variant | DDB2 | GRCh38.p7 | 11:47216834 | GGGTTTTAATTCAAC[C/T]TAATTCATTTCTCTC | 1643 |
rs375154759 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233947 | GCTTGAAGATATTCA[C/T]AGGGGATGGCAAAAG | 1643 |
rs375166265 | snp | C/T | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213459 | GAGATTGCAGTGAGC[C/T]GAGATTGTGCCACTG | 1643 |
rs375223334 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230293 | ACTCCTGGCCTTAAG[C/T]GATTCTCCTGCCCCA | 1643 |
rs375329024 | in-del | -/CT | | | intron-variant | DDB2 | GRCh38.p7 | 11:47224769 | CGTTCCTTTCTCTCT[-/CT]TCTCTTCCTCTTCCT | 1643 |
rs375446400 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236705 | TAAGTATTCAATAAA[C/T]GATGATTGAATATTG | 1643 |
rs375488493 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant | DDB2 | GRCh38.p7 | 11:47232968 | CCATCAAGTGAGTAG[C/T]TTAACTAGCAGGGGA | 1643 |
rs375532915 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47238032 | TCAAATAATGATGGG[A/G]GGAAGCAGGGATTCA | 1643 |
rs375645261 | snp | A/C/G | 9.88381e-05 | 0.00702929 | intron-variant | DDB2 | GRCh38.p7 | 11:47232807 | GCTTTTTCCTTCCTC[A/C/G]TGTTAGATTGGAGCT | 1643 |
rs375649516 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47237939 | ACGATCGACGTGTTC[A/G]ATGGAAACTCAGGGA | 1643 |
rs375788966 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235336 | AGATCCGAGTTTACT[C/T]TGCTTCCCAGTGGGA | 1643 |
rs375827461 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47225064 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 1643 |
rs375840702 | snp | C/G | 0.00013185 | 0.00811835 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215106 | CATGATCTTCGCATA[C/G]AGCACAGTACCCCTT | 1643 |
rs375859106 | snp | C/T | 5.64701e-05 | 0.00531336 | intron-variant | DDB2 | GRCh38.p7 | 11:47235436 | CGGTGGGAAGGAGCT[C/T]GCAGAAGGAGGCTGT | 1643 |
rs375860199 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226385 | AGTTCAACTGATTCT[C/T]CTGGCTCAGCCTCCA | 1643 |
rs375912946 | in-del | -/ATT | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226692 | TGCTTCTTGGCCATT[-/ATT]TGTATATTTTCTTTG | 1643 |
rs376083611 | snp | C/T | 8.23744e-05 | 0.0064172 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47237852 | GCAGCCTGGCATCCT[C/T]GCTACAACCTCATTG | 1643 |
rs376107098 | in-del | -/TATCTATCTATC | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228977 | AAAAAAAAAAAGAAA[-/TATCTATCTATC]TATCTATCTATCTAT | 1643 |
rs376124278 | in-del | -/TAAAAA | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232347 | AAATAAAAATAAAAA[-/TAAAAA]AAAGAAAGAAATGAA | 1643 |
rs376193077 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215128 | GTACCCCTTCACACG[A/G]AGGACGCGATGGCTC | 1643 |
rs376323752 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47234452 | ACGGCAAGACAGTTA[C/T]TCATTCATTCAACAA | 1643 |
rs376371330 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239424 | TCAGGTCCCTGGAGA[C/G]CCCAGCCCAGCTGAG | 1643 |
rs376431986 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231879 | TGGGGGCGAGGGGAG[A/G]GTGTGATTACAATGG | 1643 |
rs376454200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47225445 | AAAACACAAAAAATT[A/G]GCTGGGCATGGTCGT | 1643 |
rs376471957 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228535 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 1643 |
rs376783024 | snp | C/T | 0.00026621 | 0.011534 | synonymous-codon, intron-variant | DDB2 | GRCh38.p7 | 11:47234924 | GCCGCACAGGCATCC[C/T]GTCAACGCAGGTGTG | 1643 |
rs376834996 | snp | C/T | 4.94499e-05 | 0.00497217 | intron-variant | DDB2 | GRCh38.p7 | 11:47234709 | CTTTCCCTCCCTCAC[C/T]CCCACCTCGGTTCTG | 1643 |
rs376867947 | snp | A/C/G | 3.52108e-05 | 0.00419576 | intron-variant | DDB2 | GRCh38.p7 | 11:47217091 | GCTAAAGAAGTGTTT[A/C/G]TTGGCTGGGTGCAGT | 1643 |
rs377250144 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47229434 | GCATGGTTGAGGGAG[C/T]GGAGAGAGGGAAGAG | 1643 |
rs377410821 | in-del | -/AG | 0.0372196 | 0.131242 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214603 | CAGAAAAAGAAAAAA[-/AG]AGAGAGAGAGAGAGA | 1643 |
rs377549608 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47237660 | CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT | 1643 |
rs377551734 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218154 | ATCCCACTCCTCCAC[C/T]GTCATTCCCTGTATC | 1643 |
rs377568403 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47222411 | CACCCAGGGATGATC[A/G]TGGTTCAGCATAGCC | 1643 |
rs377708556 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218266 | AGGGACCTTTCCTTT[C/G]TGGTTCACCATCCTA | 1643 |
rs386373773 | in-del | -/AAA | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228971 | AAAAAAAAAAAAAAA[-/AAA]AAGAAATATCTATCT | 1643 |
rs386753235 | multinucleotide-polymorphism | ATCA/GGGC | | | intron-variant | DDB2 | GRCh38.p7 | 11:47223246 | TCCCAGCATTTTGGG[ATCA/GGGC]CAAGGCAAGTGGATC | 1643 |
rs398075917 | in-del | -/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228369 | ATCTGGCTGGGTGCG[-/G]GTGGCTCACTCCTGT | 1643 |
rs398097518 | in-del | -/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228370 | TCTGGCTGGGTGCGG[-/G]TGGCTCACTCCTGTA | 1643 |
rs527436250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47226259 | CCAACTTCTCTACTT[C/T]CCCACCAACATTTAT | 1643 |
rs527575291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47234246 | AGTAAAGGAGGCTTG[C/T]TCAGAACCCGGGGTG | 1643 |
rs527810039 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239549 | TGAAGGGGTGACAAC[A/G]ATTCCTGAAGCATTC | 1643 |
rs527857361 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47224304 | ACAATCTCGGCTCAC[C/T]GCAACCTCCACCTCC | 1643 |
rs527924157 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226819 | CAATCATAGCTCACT[A/G]CAGCCTCGAACTTCT | 1643 |
rs527985062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47216022 | CTCGAGTTTTGCAGC[C/T]CAAACTGGGAAGAGT | 1643 |
rs528032033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228850 | TAATCCCAGGTACTT[A/G]GGAAGCTGAGGCTGG | 1643 |
rs528044397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220154 | GGCCAGGTTAGACAG[A/G]TGTGGGAGACTGGAA | 1643 |
rs528072953 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214156 | CACTCCAGCCTGGGT[-/A]ACGGAAGAGAGACAC | 1643 |
rs528136374 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47220091 | ACTGCACCCAGCCAG[C/T]AGGAGGTCTCTTAAG | 1643 |
rs528167829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47228216 | AGAGGTTGTAGTAAG[C/T]TGAGTGCACCACTGC | 1643 |
rs528202410 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47235589 | TTTATCCCACTTCTG[C/T]CATCCCATATGGTTG | 1643 |
rs528355344 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47238572 | CCCAGCTAATTTTTT[A/C/G]TATTTTTAGTAGAGA | 1643 |
rs528468323 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232498 | CTTAAAAAAAAAAAA[C/T]AGAAAAATTAGCTGG | 1643 |
rs528519746 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47234308 | ATGGTATAAGCTTTG[C/T]CTGCTTCAGGGACTT | 1643 |
rs528628601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235063 | CCAAGCTGATGTCTG[A/G]GAACCTTTGTGGCTG | 1643 |
rs528832325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47227358 | GTGATCTACCCGCCT[C/T]GGCCTCCCAAAGTGC | 1643 |
rs529187209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228055 | TGAGGCAAGAGAATC[A/G]TTTGAACTTGGGAAG | 1643 |
rs529200141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47219223 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCCCCC | 1643 |
rs529323758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217113 | GGGTGCAGTGGTTCG[C/T]ACCTGTAATCCCAGC | 1643 |
rs529426130 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47225516 | AGAATCACTTGAACC[C/T]GGGAGGCAGAAGTTG | 1643 |
rs529505328 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47232299 | CAGTGAGCCGAGGTC[A/G]TGACAGAGCAGGACT | 1643 |
rs529671713 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47217877 | GCCTGGGCAACAGAG[C/T]GAGACTCCATCTCAA | 1643 |
rs529681483 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47215467 | ACAGGAAGCAGATGA[C/G]CTCCGTAACAACAGA | 1643 |
rs529699297 | snp | A/G | | | downstream-variant-500B | DDB2, ACP2 | GRCh38.p7 | 11:47239292 | GAAGAAAAAGCACAG[A/G]AAACAGCACTATCAG | 1643 |
rs529808081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47238687 | ACAGACTTGAGCCAC[C/T]GCGCCCGGCCTTCCT | 1643 |
rs529890897 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218670 | GGCTGACATTGGAGG[A/G]CTGTGCTGTGAAAAG | 1643 |
rs530270302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229862 | TAGAGACAGGGTCTT[G/T]CTCTGCCACCCAGGC | 1643 |
rs530406024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47237625 | TATTTTTAGTAGGGA[C/T]GGGGTTTCACCATGT | 1643 |
rs530410881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229287 | CATGGAATAGTGAAG[A/T]CTGAAGCGGGGTTGA | 1643 |
rs530443326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236865 | ATCTAGCCAGGTGTC[A/G]TAAGTCATTACAGCT | 1643 |
rs530518537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220970 | TTCCGAGACCAGCCT[G/T]ACCAACACATAGTGA | 1643 |
rs530717487 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213130 | AGGAGTTCTAAGTAC[C/T]GCTGGCTGCACGCCC | 1643 |
rs530733334 | snp | A/G | 1.64991e-05 | 0.00287215 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215240 | TGGAGCCCGAGGCCA[A/G]GAAGCTCTGTGCGAA | 1643 |
rs530983301 | snp | C/T | 4.94189e-05 | 0.00497062 | synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47234633 | GGTCACAGGAGACAA[C/T]GTGGGGAACGTGATC | 1643 |
rs530986309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236828 | TTCCCGATAATCCAT[C/T]TGTCTGCATGTCCCA | 1643 |
rs531105439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228340 | GTCTGTGGAGACGGA[A/G]GGTTTAAGATCAATA | 1643 |
rs531148027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235691 | TTCTAAGATCCTGAC[C/T]CTCTGTTCTGTCTTC | 1643 |
rs531379329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224683 | TGTTTCATTTTGTGC[A/G]GTTGTTCACTGATCT | 1643 |
rs531508205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47233470 | CAGCACTTTGGGAGG[C/G]CAAGGTGGGTGGATC | 1643 |
rs531581574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47230694 | AGTATGTTGTGATAG[C/T]TAAGTGGTTGTTGCA | 1643 |
rs531989426 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47219507 | CAGGGACTACAGGTA[C/T]GCACCACCATGCCTG | 1643 |
rs532019440 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214616 | AAAGAGAGAGAGAGA[A/G]AGAAATTAGCCGGGC | 1643 |
rs532031039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47223650 | AGCCAGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 1643 |
rs532175283 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47223730 | GAGCTGGCAGTGAGC[C/T]GAGATCGGCCACTTC | 1643 |
rs532180302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47231642 | ATCTTCCCACCTCAG[C/T]CTTCTGAGTAGCTAG | 1643 |
rs532229410 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215029 | TTAGCTCGGCTACCT[A/G]TGGCCCCGCAGTTTT | 1643 |
rs532318596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236081 | TGGACTACAGGTATG[C/T]GCCACCATACCCAGC | 1643 |
rs532684862 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47223048 | TTGCCTTTATTTTGA[-/G]GGAGGATGTTTTTGC | 1643 |
rs532708882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47223211 | ATGTCTAGGCTGGGC[A/G]CTGTGGCTTACGCCT | 1643 |
rs532847739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47230635 | GAGCATTAGAATGAC[C/T]GTGAGGTTAGAATGT | 1643 |
rs532849595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47221872 | AGGCACGAGCCACTG[C/T]ACCCGGCCTGGGTTT | 1643 |
rs532870242 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47238474 | CGTGATCTTGGCTCA[A/G]TGCAAGCTCCGCCTC | 1643 |
rs532889094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229937 | CTGGGCTCAAGTCAC[C/T]ATCCCACCTCAGCCT | 1643 |
rs532911822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47234401 | TCCCCTCTGTCTGGA[C/T]GGTAGAGCAGTCTGA | 1643 |
rs533003333 | snp | C/T | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213988 | GGAGGTCCAGACCAA[C/T]GTGGGAAACATAGCA | 1643 |
rs533109058 | snp | A/T | 1.70023e-05 | 0.00291563 | intron-variant | DDB2 | GRCh38.p7 | 11:47234967 | TCATCTCTCCTGCAG[A/T]CCCTGCCTGTCTGAC | 1643 |
rs533206595 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232762 | TGCCCAGGCCTGGTT[C/T]CTCACGGCCAGGCCC | 1643 |
rs533243217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218144 | CATAACGTAGATCCC[A/G]CTCCTCCACCGTCAT | 1643 |
rs533246784 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DDB2 | GRCh38.p7 | 11:47224530 | GCTGGGATTACAGGC[A/G]TGAGCCACCTTGCCC | 1643 |
rs533299565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226376 | TGCCTCCTGAGTTCA[A/G]CTGATTCTCCTGGCT | 1643 |
rs533417895 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DDB2 | GRCh38.p7 | 11:47227727 | ATAAGTTCATCCTGG[C/T]CATAACATATTTATC | 1643 |
rs533498791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47232591 | CTGCAGTGAGCCGTG[C/T]TTGTGCCACTGCACT | 1643 |
rs533523261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224158 | TCCTGTCTATGTAAT[A/T]TTTCTTCTGGTCGCT | 1643 |
rs533719031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217200 | GGCCAACATGGTGAA[A/G]CCCCGTCTCTACTAA | 1643 |
rs533738977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47225630 | AACTGGTAGAAAACA[C/T]GTAAAACAATTTACA | 1643 |
rs533945496 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217157 | AAGGTGGGTGGATCA[C/T]CTGAGGTATGGAGTT | 1643 |
rs533996278 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228355 | GGGTTTAAGATCAAT[A/G]TCTGGCTGGGTGCGG | 1643 |
rs534061997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47222118 | ATATTTGGAGAGTGA[C/T]AGATAGATGAGTTAT | 1643 |
rs534183217 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221421 | TGGGATTACAGGCAT[A/G]CACCACCACACCAGC | 1643 |
rs534291378 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | DDB2 | GRCh38.p7 | 11:47223248 | CCAGCATTTTGGGGG[C/G]CCAAGGCAAGTGGAT | 1643 |
rs534375494 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239099 | TGTATCTAGCCTGGA[A/G]CCAAGGTTATCTTGG | 1643 |
rs534403007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47219323 | TGCACAGTTCAATGG[C/T]GTTGGGTAAATTGTG | 1643 |
rs534759761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47218491 | GATGAGCGAGGAGGA[A/G]CAGTATTAGATAAAT | 1643 |
rs534858625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226530 | CATTTGCCTTGGCCT[C/T]CCAAATTGCTGGGAT | 1643 |
rs534896311 | snp | A/C | 3.29451e-05 | 0.00405851 | intron-variant | DDB2 | GRCh38.p7 | 11:47234552 | TCCCCAAGAATCTTA[A/C]AACACAGTCTCTCCC | 1643 |
rs535520272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217618 | CCTTCTGGGCTGGGC[G/T]CAGTGGCTCAGGCCT | 1643 |
rs535563772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47225921 | TTTTAAGATTCATCC[A/G]TGTTGTAGCATGTGG | 1643 |
rs535591210 | snp | C/T | 1.65241e-05 | 0.00287433 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216350 | GGTCCTAGCAGAAGA[C/T]GTGACTCAGACTGCC | 1643 |
rs535711980 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233212 | TGTATTAGACTGGAC[C/G]TTGACCCTCACTAGA | 1643 |
rs536446857 | in-del | -/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239369 | TATTCTGGGCCACAG[-/T]TCTAGAACTTTCTTT | 1643 |
rs536535944 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47220360 | TTGTTTTCTTGTTTT[C/G]TCCAGGAGTCTAGGA | 1643 |
rs536561069 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233569 | AAAAATTAGCTGGGC[G/T]TGGTGGTAGGCCCCT | 1643 |
rs536651899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235189 | GTGGGAGGGAGAGTA[A/C]CCCTGCAGGAGAAGG | 1643 |
rs536722953 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236748 | GTACCTCAATCACAT[C/T]CAAGCTCTTAATAAA | 1643 |
rs536838847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47237137 | AGACAGGATGACAGT[A/G]GGGCTCCTCCAGAAC | 1643 |
rs536847229 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47237031 | ACTGCCAGATTTGTT[C/T]TTAGTGGGGTGATCT | 1643 |
rs536980824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47219644 | GGCTGAGCCACTGTG[C/T]TGGGCCTCTAGAACG | 1643 |
rs537258116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47227604 | CAACCTCCACCTCCC[A/G]GGTTCAAGCAATTCT | 1643 |
rs537319701 | in-del | -/TTTGT | 0.00755907 | 0.0610114 | intron-variant | DDB2 | GRCh38.p7 | 11:47226910 | TCATACCTTGCTAAC[-/TTTGT]TTTGTTTTGTTTTTT | 1643 |
rs537390584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235155 | TCACCTCTTCCTTTC[C/T]GCTCCTGTCTAGAGA | 1643 |
rs537623777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47215463 | GGTAACAGGAAGCAG[A/C]TGAGCTCCGTAACAA | 1643 |
rs537987305 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47224297 | CAGTGCCACAATCTC[A/G]GCTCACTGCAACCTC | 1643 |
rs538003695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229423 | AAGTTGTGTCTGCAT[A/G]GTTGAGGGAGTGGAG | 1643 |
rs538249963 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47230060 | AACAGCACTTTGGGA[C/T]GTTGAGGTGGAAGGA | 1643 |
rs538254762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47221337 | GGAGTGCAGTGGTGC[A/G]ATCTCACCTCACTGC | 1643 |
rs538418522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47223346 | AAAAATTAGCTGGGT[A/G]TGGTGGCGCTCACCA | 1643 |
rs538513052 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213425 | CTGAGGCAGGGGAAT[C/T]GCTTGAACCCGGGAG | 1643 |
rs538577535 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213610 | GGATGGATGCCAGGA[C/G]TTCTAGACCAGCCTA | 1643 |
rs538593516 | snp | G/T | 0 | 0 | intron-variant | DDB2 | GRCh38.p7 | 11:47230274 | CACTGCATCAAGGTT[G/T]TGAACTCCTGGCCTT | 1643 |
rs538686021 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47215696 | CTTGAACCTGGGGCT[A/G]TAAGGAGTTTCGAGA | 1643 |
rs538800727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236222 | ACAGGCATGAGCCAC[C/T]GCGCCTGGCAACTTT | 1643 |
rs538835132 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47230846 | CAGTGCCTGACTGGG[C/T]GCAGTGGCTCACGCC | 1643 |
rs538909246 | snp | A/C/G | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213165 | GCCCATCACGTCCCA[A/C/G]GCTGCTCCTAGGTGG | 1643 |
rs539004859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220518 | CTTTTTTTCTTTGTT[A/G]CATCACCTTATGACA | 1643 |
rs539193994 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47232022 | TGCTATATGTTAATT[-/A]AAAAAAAAAGTAAAA | 1643 |
rs539431583 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47222632 | ATTATAGGCGTGAGC[C/G]CCTGCACCCAGCCAC | 1643 |
rs539526230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47215433 | AGTGTTTAGGTTTCA[A/G]CACCTCTCCCGCTAG | 1643 |
rs539784579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47217307 | CTTGAACCCGGGAGG[C/T]AGAGGTTGCAGTGAG | 1643 |
rs539857030 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218852 | TTTTTCTCAAACAAA[A/G]ACACAAATCCTCATT | 1643 |
rs540203075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47215707 | GGCTATAAGGAGTTT[C/T]GAGACACTCAAAAAC | 1643 |
rs540228873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47223577 | CGAGATCAAGAGATT[C/G]AGACCACCCTGGCTA | 1643 |
rs540373978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47231052 | TGGAATCCAGGAGGT[A/G]GAGGCTGCAGTGAGC | 1643 |
rs540505028 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231758 | CTCCTGGCCTCAAGC[A/C]ATCCCCCCGCCTCAG | 1643 |
rs540850799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47238380 | CATGCAATGCCTGGC[A/T]ACTGTCCAGTTTCCT | 1643 |
rs540887945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47237681 | ACCTCGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 1643 |
rs540888883 | snp | A/G | 6.59761e-05 | 0.00574314 | missense, intron-variant | DDB2 | GRCh38.p7 | 11:47234841 | CTGGCCACAGCCTCC[A/G]TAGATCAAACAGTGA | 1643 |
rs541222019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217815 | AGAATCGCTTGAACC[C/T]GGGAGGCGAAGGTTG | 1643 |
rs541233757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226011 | TTATCTGTTTATTAA[C/T]TGACAGACACTTGGG | 1643 |
rs541348323 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213709 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGTGGG | 1643 |
rs541621663 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47229664 | AATCAACTCTGTGGT[A/G]TTGACTTTGAATTGA | 1643 |
rs541629437 | snp | C/G/T | 3.30138e-05 | 0.00406276 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216911 | CCGGATATTACAAAA[C/G/T]GCTGCCCCCTTTGAC | 1643 |
rs541838147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47231373 | TTAGGGCACATCCAT[A/G]TAATGGAATACCTCA | 1643 |
rs541976817 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226462 | TATTTTCAGTAGAGA[C/T]GGGTTTTGCCACGTT | 1643 |
rs542026060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47234099 | AGAAGAGCTCCTGGT[C/T]GTGTTTTTTCCCCCA | 1643 |
rs542195840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236634 | AGGGTTGTTGTGAAG[A/C]TGAGTCAGTATACTT | 1643 |
rs542196154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228057 | AGGCAAGAGAATCGT[C/T]TGAACTTGGGAAGTG | 1643 |
rs542196987 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227456 | AAATATCTTCTCCCA[C/T]TTCATAGATTGCCTT | 1643 |
rs542359887 | in-del | -/AAAT | | | intron-variant | DDB2 | GRCh38.p7 | 11:47223485 | AAGACTGTGTCTCAA[-/AAAT]AAATAAATAAGGCTG | 1643 |
rs542412682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224292 | GTGTGCAGTGCCACA[A/G]TCTCGGCTCACTGCA | 1643 |
rs542462333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220886 | TGTATGGGGCCAGGC[A/G]CAGTGGCCCACGCCT | 1643 |
rs542555298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228818 | ATAACTTAGCTAAGC[A/G]TGGTGGCGTGAGCCT | 1643 |
rs542614119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47218818 | TGCAAAAATGTAGGT[C/T]TTTTGATATCAGATG | 1643 |
rs542774933 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47221362 | CACTGCAACCTCCGC[C/T]TCCTGGGTTCAAGCT | 1643 |
rs542832519 | in-del | -/TTTTTTTTTTTT | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226748 | CCTTTTTTTTTTTTT[-/TTTTTTTTTTTT]GAAACAGGGTCTTAC | 1643 |
rs542981887 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47234192 | CTCTTTGGCTTGTGT[A/C]TCCTTTGGCCTAAAG | 1643 |
rs543028358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217938 | ATTGACCTCATCTTA[C/T]GCCATTGTCTTTTCT | 1643 |
rs543384066 | snp | C/G | 1.68909e-05 | 0.00290606 | intron-variant | DDB2 | GRCh38.p7 | 11:47234969 | ATCTCTCCTGCAGAC[C/G]CTGCCTGTCTGACCA | 1643 |
rs543392705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235456 | AAGGAGGCTGTGATC[A/C]TGAGGCCGGAGCAGG | 1643 |
rs543399358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226134 | TTATGCCAATAAGTA[C/T]GATTGCTTCATCAAA | 1643 |
rs543607706 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47232064 | AGAAATGAAGGGAGG[C/T]GGGGCACGGTGGCTC | 1643 |
rs543621862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218720 | GGAGTCACAAACTTA[C/T]AGGGCTCCAGAAGCC | 1643 |
rs543866656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221561 | ATGATTCTCCTGCCT[C/T]AGCCTCCTGAGTAGC | 1643 |
rs543990740 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218261 | ATGGCAGGGACCTTT[C/T]CTTTCTGGTTCACCA | 1643 |
rs544004062 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236699 | TACTGGTAAGTATTC[A/C]ATAAATGATGATTGA | 1643 |
rs544004346 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47223409 | AGAATCTTGAACCTG[A/G]GAGGCAGAGGTTGCA | 1643 |
rs544148078 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214094 | TGAGGTGGGAGGATC[A/T]GTGAAACTTGAGGTC | 1643 |
rs544158872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47222767 | ACAAGTATTTGTGTG[A/G]ATATATGTTTTCATT | 1643 |
rs544197619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47230532 | AGGTTTGAGAACAAC[A/T]ACAACCAACCCTTGG | 1643 |
rs544360942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47238260 | CGGGCCAGCCTCAGC[C/T]CCGCCCTGCCACATT | 1643 |
rs544742902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47220777 | TCATCTGACCTTGGC[C/T]GTGACCTTTACATTC | 1643 |
rs544812818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47222313 | AATTATTTGAAATTT[A/G]TCTACATTTTTATGT | 1643 |
rs544887330 | snp | A/G | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214864 | CCTGGCGCAGTTCCC[A/G]CCCCTCCCGGGAGCG | 1643 |
rs544891334 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213094 | CCTTCAAGACTTGGA[C/G]TTTGGCTGAAGCGAG | 1643 |
rs544930697 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47223175 | TGTTCACAGTTTTCT[A/C]CTGTCAGTACTTTAA | 1643 |
rs544949331 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47221431 | GGCATGCACCACCAC[A/T]CCAGCTAATTTTTGT | 1643 |
rs545142115 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213838 | AAAAAAAAAAGAAAG[A/C]GAGAAAGAAAGAAAG | 1643 |
rs545876083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47238534 | CTCTCGAGTAGCTAG[G/T]ACTACAGGTGCCCGC | 1643 |
rs545940200 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215031 | AGCTCGGCTACCTGT[A/G]GCCCCGCAGTTTTGT | 1643 |
rs545968688 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47224175 | TTCTTCTGGTCGCTT[A/T]AAAAATGATTATGAT | 1643 |
rs546248614 | in-del | -/A | | | intron-variant | DDB2 | GRCh38.p7 | 11:47217890 | GCGAGACTCCATCTC[-/A]AAAAAAAAAGAATTG | 1643 |
rs546388054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47230785 | AAGGTGGAGAAAGGC[A/G]GACAAGTGGAGAACT | 1643 |
rs546472960 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239570 | TGAAGCATTCTGTCT[A/G]AGTCTAATGGTGGCT | 1643 |
rs546571789 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47215632 | GTCAGTTGTGAGAGC[A/C]CCCAATTCCTTCCTC | 1643 |
rs546898395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221188 | AAACAGTGTATTCTT[A/G]TCATAAAATACAGAG | 1643 |
rs547048936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236003 | AGTGGCACAAACATA[G/T]CTCACTGCAGCCTCA | 1643 |
rs547154283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221801 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 1643 |
rs547234543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229894 | GGAATGCAGTGGCAG[A/G]ATCATAGCTAACTAC | 1643 |
rs547266419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218122 | GCTTTCGCTGGTTGT[C/T]CTTACTCATAACGTA | 1643 |
rs547445968 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | DDB2 | GRCh38.p7 | 11:47223249 | CAGCATTTTGGGGGG[A/C]CAAGGCAAGTGGATC | 1643 |
rs547634751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47226327 | GTCGCCCAGGCTGGA[A/G]TGCAGTGGCACAGCC | 1643 |
rs547761303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47215366 | CCCGAGGCCCGCGCA[A/G]GTCACGGGTGCCTCC | 1643 |
rs548101985 | in-del | -/TT | | | intron-variant | DDB2 | GRCh38.p7 | 11:47224760 | CCCTCCCTTCGTTCC[-/TT]TCTCTCTCTTCTCTT | 1643 |
rs548349114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47230078 | TGAGGTGGAAGGATT[G/T]CTTGAGCCCAGGAAT | 1643 |
rs548422223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47233526 | GCCTGGCCAACATGG[C/T]GAAACCCCCATCTCT | 1643 |
rs548543016 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | DDB2 | GRCh38.p7 | 11:47223246 | TCCCAGCATTTTGGG[A/G]GGCCAAGGCAAGTGG | 1643 |
rs548626444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47235019 | GTGTGGAAGCCACTA[C/T]GTCAAACCTTTACCC | 1643 |
rs548651285 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218164 | TCCACCGTCATTCCC[G/T]GTATCATTACCCTGC | 1643 |
rs548695031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47219274 | ATGATAAAATACATA[C/T]AACATGAAATTTACT | 1643 |
rs548721961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47227359 | TGATCTACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 1643 |
rs548755575 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47220326 | GAAGTCAGAACCCAG[A/C]GCTCAGACAGGAAGA | 1643 |
rs548819460 | in-del | -/A | | | intron-variant | DDB2 | GRCh38.p7 | 11:47224026 | GAATTGCTTAAGCCC[-/A]GGGGGACAAGGCTTC | 1643 |
rs548933392 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214644 | GGCGTGGTGGCGTAC[A/G]CTTGTAGTCCCATCT | 1643 |
rs549041558 | snp | C/T | 3.29554e-05 | 0.00405914 | synonymous-codon, intron-variant, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47235319 | CACGGACCAGAAGAG[C/T]GAGATCCGAGTTTAC | 1643 |
rs549061517 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230542 | ACAACTACAACCAAC[C/T]CTTGGTTTGGTAAGC | 1643 |
rs549583055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228825 | AGCTAAGCGTGGTGG[C/T]GTGAGCCTGTAATCC | 1643 |
rs549726695 | snp | C/G | 0.000841099 | 0.0204901 | intron-variant | DDB2 | GRCh38.p7 | 11:47217057 | TCAAAGGGGTGAGCA[C/G]TTCCCCATGCCAGGT | 1643 |
rs549788260 | snp | C/T | 3.30797e-05 | 0.00406679 | intron-variant | DDB2 | GRCh38.p7 | 11:47216325 | GAAAATATGTCTGTT[C/T]TGCTTGGCAGGTCCT | 1643 |
rs549953445 | in-del | -/A | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233066 | CCCAGGGAAGAAAGG[-/A]AAAGATGTCAGCCAC | 1643 |
rs550024464 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47219093 | GGGACTGCAGGTGCA[C/T]GCTGCCACGCCTGGC | 1643 |
rs550088477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47230102 | CAGGAATTTGAGACT[A/G]GCCTGAGTTACATAG | 1643 |
rs550088892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47227199 | GCAGTCTCCACCTCC[C/T]GGGTTCAAGCAATTC | 1643 |
rs550121214 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213148 | TGGCTGCACGCCCTC[C/T]GGCCCATCACGTCCC | 1643 |
rs550301168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47220980 | AGCCTGACCAACACA[C/T]AGTGAAACCCTGTCT | 1643 |
rs550587671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47233426 | AATTACAGAATGCGG[C/T]CGGGTGCAGTGGCTC | 1643 |
rs550819117 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47219779 | CCAGGAGGAGGTCTC[-/TTTA]TTTATTTATTTGTTT | 1643 |
rs550910285 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | DDB2 | GRCh38.p7 | 11:47228368 | ATATCTGGCTGGGTG[C/G]GGTGGCTCACTCCTG | 1643 |
rs550948806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235788 | TTAAGGCAGGGTCTC[A/G]CTCTGTCACCCAGGT | 1643 |
rs550986100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220182 | GAATTCAAAGTGTGA[A/G]ATGGGTGTTCAAGGA | 1643 |
rs551132159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229257 | AGGCAGGGGTGAAGA[A/G]TAGAGGAGGCCGGGC | 1643 |
rs551722210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47235064 | CAAGCTGATGTCTGG[A/G]AACCTTTGTGGCTGT | 1643 |
rs551948788 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47235590 | TTATCCCACTTCTGC[A/C]ATCCCATATGGTTGA | 1643 |
rs552062744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47232600 | GCCGTGTTTGTGCCA[C/T]TGCACTTCAGCCTAA | 1643 |
rs552140184 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47224975 | TGAGGTCTCACTCTC[C/T]CTTCCAGGCTGGAGT | 1643 |
rs552284946 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47219038 | CAAGCTCCGCCTCCC[A/G]GATTCATGCCATTCT | 1643 |
rs552362641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47231668 | GCTAGAACCACATGC[A/G]CCTACCACCATGTCT | 1643 |
rs552520256 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47229982 | AGCACAGGTGTGCAC[A/C]ATCACTCCCAGCTAA | 1643 |
rs552555611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47237760 | TTTTGATGTTCCTCT[C/T]TGTTCATATTTGTTT | 1643 |
rs552555972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47230676 | GAAGGGAATGTGCCA[A/G]TTAGTATGTTGTGAT | 1643 |
rs552691155 | in-del | -/AAAACAAAAC | 0.0193772 | 0.0965046 | intron-variant | DDB2 | GRCh38.p7 | 11:47224090 | ATCCTGTCTCAATTA[-/AAAACAAAAC]AAAACAAAACATCCT | 1643 |
rs552820428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229593 | TTGAGTAAAATGGGA[A/G]CCACATTTTTCACTG | 1643 |
rs552927622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47221401 | TCCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG | 1643 |
rs553089021 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47219667 | CTAGAACGTCTTAAT[A/T]TTGGCACTGAATGAA | 1643 |
rs553130633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47222140 | ATGAGTTATCTATGC[C/G]CCTTTGTAATCCACC | 1643 |
rs553399430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228578 | AACCCAGGAGGCAGA[G/T]GTTGCAGTGAGCCAA | 1643 |
rs553436685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47227687 | GATTGATTTTTAATA[A/G]TTAAACCAACTTTGC | 1643 |
rs553704743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47215716 | GAGTTTCGAGACACT[C/G]AAAAACGAGCTGGGG | 1643 |
rs553748511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47216514 | CAAGGGTTTACACGT[G/T]CATTTTTACTATTGC | 1643 |
rs553801212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224852 | TAGCCCAGCGTATTT[C/T]TCATTTCAGATACTG | 1643 |
rs554168564 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227603 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCAATTC | 1643 |
rs554393001 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239136 | ATGACTTTTCTCCTC[G/T]CAGTGGGTGGTAGCA | 1643 |
rs554411192 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47214988 | TGGTTTGAACAAGCC[C/T]TGGGCATGTTTGGCG | 1643 |
rs554600010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47231820 | TCTATAGGACATTCT[A/G]TGAGGGCAAAACAAT | 1643 |
rs554676341 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47238975 | GGGTTGGAGCAGGGG[C/T]GCTGGGACCTGGGGC | 1643 |
rs554907760 | in-del | -/ATT | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47226689 | GTGTGCTTCTTGGCC[-/ATT]ATTTGTATATTTTCT | 1643 |
rs555009758 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213060 | AGGCTAGGCAGGACA[G/T]CGCGGCCTCACCTGT | 1643 |
rs555020571 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231339 | GCTCTTCTAAAGAGA[A/G]CACTGTGGGAATAAC | 1643 |
rs555362847 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233284 | GGAGCAACAGCTCAG[A/G]ACTTGAGACTGAATG | 1643 |
rs555611020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47233071 | GGGAAGAAAGGAAAG[A/T]TGTCAGCCACTTTCC | 1643 |
rs555939426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47225097 | AGTGTGCACCACCAC[A/G]CCCAGCTAATTTTTG | 1643 |
rs555960296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47225298 | AATACTGCTTTTTTT[A/T]AAAAAAATTGTGGGC | 1643 |
rs556138833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47225737 | TTTTTCTTGTAAAAC[C/T]GAAACTCTATACCCA | 1643 |
rs556213962 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218194 | CTTCATGTTTCCCCC[A/G]AGTGTTGATGGGTGT | 1643 |
rs556477564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47228773 | ACCAGCCTGGCCAAC[A/G]TGATGAAACTCCATC | 1643 |
rs556536499 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47231082 | CTGAGGTTGTGCCAC[C/T]GCACTTCAGCCTGGG | 1643 |
rs556596767 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | DDB2 | GRCh38.p7 | 11:47224353 | CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGATTA | 1643 |
rs556807253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236511 | ATAGTGGTGGGGAGC[A/G]CCAGTTTCCAGCAGC | 1643 |
rs556908818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228783 | CCAACATGATGAAAC[C/T]CCATCTCTCCTAAAA | 1643 |
rs557099473 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47234002 | TTGAGAGAAAAACTG[G/T]GAGCTGAGCTCTTCT | 1643 |
rs557111187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229433 | TGCATGGTTGAGGGA[A/G]TGGAGAGAGGGAAGA | 1643 |
rs557150203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47219552 | ATGTGGTCTCTCTAT[A/G]TTGCCCAGGCTGGTC | 1643 |
rs557201717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218775 | ATGTATGGTGGTAGG[A/G]TCAGGGGTAAACTAG | 1643 |
rs557586609 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47227652 | AGAAGCTGGCACCCA[C/G]CACCACGCCCAGCTG | 1643 |
rs557614906 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233795 | TCCCTGAGGAATTAA[C/G]TGAGGGTGCTGGGGT | 1643 |
rs557692766 | snp | A/G | 0.000228537 | 0.0106872 | intron-variant | DDB2 | GRCh38.p7 | 11:47235437 | GGTGGGAAGGAGCTC[A/G]CAGAAGGAGGCTGTG | 1643 |
rs557906641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218609 | CATCCATTGCTGAGG[C/G]GTGAGTGTGTCGTCC | 1643 |
rs557941951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217862 | CGCCACTGCACTCCA[A/G]CCTGGGCAACAGAGC | 1643 |
rs557966485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226569 | TGAGCCACCATGCTC[A/G]GCCTTTTCTGTTTTT | 1643 |
rs558383784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47222336 | TTTTATGTGTAGTTT[G/T]TTTTTTCTTTCTGAA | 1643 |
rs558731894 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221598 | TACAGGAGCCTACCA[C/T]CATGCCCAGCTAATT | 1643 |
rs558968369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221306 | CAAGTCTGAGTCTTG[C/T]TCTGTCGCTCAGGCT | 1643 |
rs558971017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236635 | GGGTTGTTGTGAAGA[C/T]GAGTCAGTATACTTA | 1643 |
rs558971355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228193 | TGAATTGCTTGAGCC[C/G]AGGAGGCAGAGGTTG | 1643 |
rs559260647 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213075 | GCGCGGCCTCACCTG[C/T]GAACCTTCAAGACTT | 1643 |
rs559398604 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47238500 | GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 1643 |
rs559400606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220149 | GAAAAGGCCAGGTTA[A/G]ACAGGTGTGGGAGAC | 1643 |
rs559572427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220902 | CAGTGGCCCACGCCT[G/T]TAATCCCAGCACTTT | 1643 |
rs559603599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226187 | TTGAGGAACCGCTAT[A/G]TTGTTTTCCATACTG | 1643 |
rs559738200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47218911 | AAAAAAATTGTAAAA[C/T]ACACGTAACATAAAA | 1643 |
rs559858072 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47226891 | GGACTGCAGGTGCTC[A/C]CCATCATACCTTGCT | 1643 |
rs559929930 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215027 | GCTTAGCTCGGCTAC[C/T]TGTGGCCCCGCAGTT | 1643 |
rs560263916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47223584 | AAGAGATTGAGACCA[C/T]CCTGGCTAACACGGT | 1643 |
rs560527773 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214158 | CTCCAGCCTGGGTAA[C/T]GGAAGAGAGACACTG | 1643 |
rs560656021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47223210 | GATGTCTAGGCTGGG[C/T]GCTGTGGCTTACGCC | 1643 |
rs560692893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47230604 | TCATACTACCAGCAA[A/G]CATTTGGCAGACCAT | 1643 |
rs560713538 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47219852 | GAGTGCAGTGGCGCA[A/G]TCTCGGCTCACTGCA | 1643 |
rs560831081 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47215353 | GTGCTCCGAGGCTCC[C/T]GAGGCCCGCGCAGGT | 1643 |
rs560842794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47237688 | GATCCGCCTGCCTCA[C/G]CCTCCCAAAGTGTTG | 1643 |
rs560894507 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218333 | CTGCTTTATATTTGT[G/T]GAATGAGTGAGGGGC | 1643 |
rs560943922 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226842 | GAACTTCTGGGCTCC[A/G]GTGATCCTGCTGCCT | 1643 |
rs561008710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221756 | AGCCTGAATTTTATA[G/T]TTTTGGTAGAAACAG | 1643 |
rs561047839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229783 | ACCTTAATCTTTTAT[A/C]AGTATCTCACCCTAT | 1643 |
rs561547915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47236848 | TGCATGTCCCAGTTT[A/G]TATCTAGCCAGGTGT | 1643 |
rs561699825 | in-del | -/G | 0.000836995 | 0.0204401 | intron-variant | DDB2 | GRCh38.p7 | 11:47234263 | AGAACCCGGGGTGTG[-/G]GGGGGCAGGCGTGCC | 1643 |
rs561794517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47231443 | ATGAATCTCAGAGGC[A/T]TGATGAGTGAAATGA | 1643 |
rs561846496 | in-del | -/GAAG | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215123 | CACAGTACCCCTTCA[-/GAAG]CACGGAGGACGCGAT | 1643 |
rs561910591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47234165 | GCTCTGAGGAACAGG[A/G]CCAGGCAATCCCTCT | 1643 |
rs561950347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47233566 | ACAAAAAATTAGCTG[A/G]GCGTGGTGGTAGGCC | 1643 |
rs562216283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224296 | GCAGTGCCACAATCT[C/T]GGCTCACTGCAACCT | 1643 |
rs562415686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47223658 | GTGGTGGTGGGCGCC[A/T]GTAGTCCCAGCTACT | 1643 |
rs562435242 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226315 | AAGTCTCCCTCTGTC[A/G]CCCAGGCTGGAATGC | 1643 |
rs562540812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47215822 | CCTCAAATACAGTTT[C/G]GTGATCAGGAGTTGT | 1643 |
rs562600855 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47237626 | ATTTTTAGTAGGGAC[A/G]GGGTTTCACCATGTT | 1643 |
rs562942499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47238556 | GGTGCCCGCTACCAC[A/G]CCCAGCTAATTTTTT | 1643 |
rs563104967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47223643 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGCGCCT | 1643 |
rs563144224 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DDB2 | GRCh38.p7 | 11:47223243 | TAATCCCAGCATTTT[G/T]GGGGGCCAAGGCAAG | 1643 |
rs563180327 | snp | A/G | 3.3845e-05 | 0.00411355 | intron-variant | DDB2 | GRCh38.p7 | 11:47234972 | TCTCCTGCAGACCCT[A/G]CCTGTCTGACCACTG | 1643 |
rs563249959 | snp | A/G | 0.000252221 | 0.0112271 | intron-variant | DDB2 | GRCh38.p7 | 11:47235464 | TGTGATCATGAGGCC[A/G]GAGCAGGTCTGCCCA | 1643 |
rs563332421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220848 | ATGAAGATAGCTTAA[A/T]TTTATTCCTATTATA | 1643 |
rs563442093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47227265 | GCATGCGCCACCATG[A/C]CCGGCTAATTTTTGT | 1643 |
rs563530643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220068 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 1643 |
rs563569443 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DDB2 | GRCh38.p7 | 11:47228023 | CGCACTCCTGTCATC[C/T]CAGCTACCCGGGAGG | 1643 |
rs563598957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47225482 | CTGTAATCCCAGCTA[C/T]TGGGGAGGCTGAGGC | 1643 |
rs563630572 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47230141 | TGTCTCTAAAAAAAA[A/G]AAAAAAAAAAAATTG | 1643 |
rs563635532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47233434 | AATGCGGCCGGGTGC[A/G]GTGGCTCATGCTTGA | 1643 |
rs563771264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47234048 | TCCCTGAAGCACCCT[C/G]CTAGTCAGCCTCCCA | 1643 |
rs564165803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47233192 | GCTCTTCTGTAAGTC[A/C]TACCTGTATTAGACT | 1643 |
rs564166137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224464 | CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCTGA | 1643 |
rs564224763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47234354 | CCTGGGCCCAGCCAT[A/G]ACCAGACAGATTTCT | 1643 |
rs564258082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218963 | AAGTGTTTTTTTTTT[A/G]AGGCGGACTCTCGCT | 1643 |
rs564300982 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47227129 | TTTTTTTTTTGAGAT[C/G]GAGTTTTGCTCCTGT | 1643 |
rs564311013 | in-del | -/T | 0.194902 | 0.243853 | intron-variant | DDB2 | GRCh38.p7 | 11:47237435 | ACTGGCAAATACTAC[-/T]TTTTTTTTTTTTTTT | 1643 |
rs564337726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226358 | TCAGCTTACTGCAAC[C/G]TCTGCCTCCTGAGTT | 1643 |
rs564371184 | snp | C/G | 1.68043e-05 | 0.0028986 | intron-variant | DDB2 | GRCh38.p7 | 11:47234956 | TATCCCAGACCTCAT[C/G]TCTCCTGCAGACCCT | 1643 |
rs564567656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220958 | TGAGGTCAGGAGTTC[C/T]GAGACCAGCCTGACC | 1643 |
rs564757948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47229686 | TTGAATTGAAGACAT[G/T]GATACAAATTTAAGG | 1643 |
rs564861093 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227716 | GCATTCTTGGAATAA[G/T]TTCATCCTGGCCATA | 1643 |
rs565058800 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215014 | TGGCGGGAAGTTGGC[G/T]TAGCTCGGCTACCTG | 1643 |
rs565093153 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47233870 | GGAGTGCATGCGCAC[A/G]CAAATCAGCAGGCAA | 1643 |
rs565244075 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47237577 | CTGGGACTACAGGCA[G/T]GTACCACCACGCCCA | 1643 |
rs565330491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47219888 | CGCCTCCCAGGTTCA[C/T]GCGATTCTCCTGCCT | 1643 |
rs565382192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235648 | TTCTGAGTTTTTTCA[G/T]CCCAGCTCTGATCTC | 1643 |
rs565401298 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47227387 | GCTGGGATTATAGGT[G/T]TGAGACACTGCGCCC | 1643 |
rs565567119 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233424 | GAAATTACAGAATGC[A/G]GCCGGGTGCAGTGGC | 1643 |
rs566038826 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228094 | GCAGTGAGGTGAGAT[C/T]GTACCACTGCACTCC | 1643 |
rs566338163 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47220195 | GAGATGGGTGTTCAA[A/G]GAACAAGTGCCAGAA | 1643 |
rs566446044 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47215637 | TTGTGAGAGCCCCCA[A/G]TTCCTTCCTCCTTAG | 1643 |
rs566631407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47238731 | CAAATTGTAGGTTTG[C/T]GGGCCAGCCCCAGGC | 1643 |
rs566757927 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47233916 | TCCAGGCTACTCTTC[C/T]GCAAGAAATCTTCCT | 1643 |
rs566817503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47219278 | TAAAATACATATAAC[A/G]TGAAATTTACTTTCG | 1643 |
rs566912178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47228714 | GTGGCTCATGACTGT[C/T]GGGAGGCCGAGGCAG | 1643 |
rs566912198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47237054 | GGTGATCTGGGGAAT[A/G]TGGGTTTCCTTCTCT | 1643 |
rs567082210 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47237930 | GAATTGAGGACGATC[A/G]ACGTGTTCGATGGAA | 1643 |
rs567895789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220288 | AAAGAGGCAGGTGAC[C/T]GCTAATAAGGCAGCT | 1643 |
rs568020544 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47231934 | TGTTGCAAATGTTCT[A/G]CATCCTGATTTGGGT | 1643 |
rs568187738 | snp | A/G | 3.30573e-05 | 0.00406541 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47216405 | AGATCCTGCCACCAT[A/G]CCGCAGCATCGTCAG | 1643 |
rs568239617 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47238664 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGACTT | 1643 |
rs568250829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224845 | GGCAAAGTAGCCCAG[C/T]GTATTTTTCATTTCA | 1643 |
rs568295177 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | DDB2 | GRCh38.p7 | 11:47225597 | ACTCCATCTCTATTT[A/T]AAAAAAAAAAAACAA | 1643 |
rs568410197 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | DDB2 | GRCh38.p7 | 11:47223247 | CCCAGCATTTTGGGG[G/T]GCCAAGGCAAGTGGA | 1643 |
rs568674386 | in-del | -/TTTTTTTTTTTT | 0.113334 | 0.209338 | intron-variant | DDB2 | GRCh38.p7 | 11:47226735 | TTCAAGTCCTTTGCC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTGA | 1643 |
rs568689968 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | DDB2 | GRCh38.p7 | 11:47215191 | GAGATTGTATTACGC[C/T]CCAGGAACAAGAGGA | 1643 |
rs568791616 | snp | A/C | 1.68357e-05 | 0.00290131 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47238893 | AAGGCCTTGGAGCCC[A/C]CACATGGGATCAAGT | 1643 |
rs568794187 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214608 | AAAGAAAAAAAGAGA[A/G]AGAGAGAGAGAAATT | 1643 |
rs568965241 | snp | C/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47219329 | GTTCAATGGCGTTGG[C/G]TAAATTGTGTAAGCA | 1643 |
rs569078593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47232733 | GGGGTGCTTCTGTGA[C/T]GGCGCAGCATGTGTG | 1643 |
rs569199115 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47229983 | GCACAGGTGTGCACC[A/C]TCACTCCCAGCTAAT | 1643 |
rs569232837 | snp | A/T | 3.30295e-05 | 0.0040637 | intron-variant | DDB2 | GRCh38.p7 | 11:47237795 | TGTCCCCCTTGATCA[A/T]GTTCTGTGTTTACCC | 1643 |
rs569317393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47221312 | TGAGTCTTGCTCTGT[C/T]GCTCAGGCTGGAGTG | 1643 |
rs569354933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47237094 | ATTAGCAATTTTACA[C/T]TCAGCTCTTAGTTAT | 1643 |
rs569679943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226414 | CAGTAGCTGAGATTA[C/T]AGGCGCACACCACCA | 1643 |
rs569687036 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227826 | ATTGGCCAAATCCTT[A/G]TCACATTTGTGTATC | 1643 |
rs569832530 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47215454 | CTCCCGCTAGGTAAC[A/G]GGAAGCAGATGAGCT | 1643 |
rs569921258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47219132 | GTATTTTTAGTAGAG[A/T]TGGGGTTTCACCGTG | 1643 |
rs569974735 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DDB2 | GRCh38.p7 | 11:47233136 | TGCCCTCACTTTGGT[C/T]CAGGTGGGTTACTGC | 1643 |
rs569983263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47218288 | ACCATCCTATTCCCA[A/G]TGCCTGGAACAAAGT | 1643 |
rs570468778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47233647 | CCAGGAGGCAGAGGT[C/T]GCAGTGAGCCGAGAT | 1643 |
rs570503969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224972 | AGATGAGGTCTCACT[C/G]TCTCTTCCAGGCTGG | 1643 |
rs570576376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47223736 | GCAGTGAGCCGAGAT[C/T]GGCCACTTCACTCCA | 1643 |
rs570615265 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47223333 | CTACTAAAAATACAA[A/G]AATTAGCTGGGTGTG | 1643 |
rs570641641 | in-del | -/CTG | 0.0134861 | 0.0810011 | intron-variant | DDB2 | GRCh38.p7 | 11:47222187 | CTTATTCACTGTAAA[-/CTG]CTGATCTATTTTTTA | 1643 |
rs570674718 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47221905 | AAAATTATATCTTTA[G/T]TGAGGTATAGTGGAC | 1643 |
rs570718428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217286 | GAGGCTGAGGCAGGA[A/G]AATTGCTTGAACCCG | 1643 |
rs570804909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47215374 | CCGCGCAGGTCACGG[A/G]TGCCTCCGGCTGTGC | 1643 |
rs570884853 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214868 | GCGCAGTTCCCGCCC[C/T]TCCCGGGAGCGCTGG | 1643 |
rs570976229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220192 | TGTGAGATGGGTGTT[C/T]AAGGAACAAGTGCCA | 1643 |
rs571027037 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236733 | TTGAGTGGCCCCCAC[A/G]TACCTCAATCACATC | 1643 |
rs571757356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47232525 | CTGGGCATGGTGGCA[C/T]GCACTTGGGAGGCTG | 1643 |
rs572129465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47217750 | CAAAAAATTAGCTGG[A/G]TGTGGTGGTGTGCGC | 1643 |
rs572628631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47225388 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCC | 1643 |
rs572741981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47222258 | AAATAGAATCATAGA[A/G]TATATGGTCTTTTAT | 1643 |
rs572781201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221422 | GGGATTACAGGCATG[C/T]ACCACCACACCAGCT | 1643 |
rs572817980 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47229595 | GAGTAAAATGGGAAC[C/G]ACATTTTTCACTGTC | 1643 |
rs572869712 | snp | A/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47227430 | AACCTCTTATCAGAT[A/C]TATGATTTGAAAATA | 1643 |
rs573177223 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | DDB2 | GRCh38.p7 | 11:47230198 | CCAGCTACTTGGGAG[A/G]CTGAGGCGGGAGGAT | 1643 |
rs573190256 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47235814 | CAGGTGGGAGTACAG[G/T]GGGGCAAGCATGGTT | 1643 |
rs573253499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47235469 | TCATGAGGCCGGAGC[A/G]GGTCTGCCCACAGTG | 1643 |
rs573391037 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226970 | ACTAAGTTAAAAAAA[A/T]ATTTTTTTTTATAGA | 1643 |
rs573459701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47220438 | GTGTAGGGTATTCTA[A/G]GGGAAGAGCTTCCTG | 1643 |
rs573634196 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47236522 | GAGCGCCAGTTTCCA[G/T]CAGCCAGACCCCCCG | 1643 |
rs573716186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47229464 | GGGTGATTGTGCCCT[C/T]GGGAGGGTAAAAGAG | 1643 |
rs573725356 | in-del | -/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47221276 | TGCATGTGTACACTA[-/T]TTTTTTTTTTTTTCC | 1643 |
rs573742184 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47220858 | CTTAATTTTATTCCT[A/G]TTATAAAAACAATGT | 1643 |
rs573878870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47228787 | CATGATGAAACTCCA[A/T]CTCTCCTAAAAATAC | 1643 |
rs573933230 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47236991 | GAAGTTTAGGAAAAT[C/T]CCATCCAATTCTGCC | 1643 |
rs573939618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226725 | GGAATGTCTATTCAA[C/G]TCCTTTGCCTTTTTT | 1643 |
rs574049589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47226146 | GTACGATTGCTTCAT[A/C]AAATGGTAATTTTGT | 1643 |
rs574086699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47234083 | AGTGGTTTGAGGGAC[C/T]AGAAGAGCTCCTGGT | 1643 |
rs574598023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47230580 | TCAACTGGAGGGAGC[C/T]GAAGATTGTCATACT | 1643 |
rs574610228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47225540 | GAAGTTGCAGTGACC[C/T]GAGATTATGCCACTG | 1643 |
rs574659276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47223555 | GGAGGCCGAGGCAGG[C/T]GGATCACGAGATCAA | 1643 |
rs574783690 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DDB2 | GRCh38.p7 | 11:47224673 | TCTTTTTCCCTGTTT[C/T]ATTTTGTGCAGTTGT | 1643 |
rs574859720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47221360 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 1643 |
rs574975145 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213062 | GCTAGGCAGGACAGC[G/T]CGGCCTCACCTGTGA | 1643 |
rs575126747 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47214956 | TCTCCGAGACGGGTG[C/G]GGCCGGAGCTCCAAG | 1643 |
rs575128912 | snp | A/G | | | intron-variant | DDB2 | GRCh38.p7 | 11:47218195 | TTCATGTTTCCCCCA[A/G]GTGTTGATGGGTGTC | 1643 |
rs575176715 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DDB2 | GRCh38.p7 | 11:47223448 | AGATGGTGTCACTGC[A/C]CTCCATTCTGGGTGA | 1643 |
rs575178925 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213909 | AGTGAGAACCAGACA[C/T]GGTGGCTCATGCCTG | 1643 |
rs575244209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47238246 | CCCAAGGTTCAGTGC[C/G]GGCCAGCCTCAGCCC | 1643 |
rs575329462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47237335 | AGCTAGGGATTAAAA[A/G]TGTGCAATGGCAGAG | 1643 |
rs575479150 | in-del | -/TCTG | 0.00199481 | 0.0315187 | intron-variant | DDB2 | GRCh38.p7 | 11:47234391 | CATTATCCCATCCCC[-/TCTG]TCTGGACGGTAGAGC | 1643 |
rs575828033 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DDB2 | GRCh38.p7 | 11:47219925 | CCGAAGTAGCTGGGA[C/T]TACTGGTGCCCGCCA | 1643 |
rs576002349 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DDB2, ACP2 | GRCh38.p7 | 11:47239483 | AGCAACTCCCTTCCC[A/T]CCACTCCCTACTCCC | 1643 |
rs576016254 | snp | C/T | | | upstream-variant-2KB | DDB2 | GRCh38.p7 | 11:47213339 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAATA | 1643 |
rs576108980 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DDB2 | GRCh38.p7 | 11:47225271 | AAAAAAAAAAAAAAA[A/C]CTCTAACAAGTAATA | 1643 |
rs576124732 | snp | G/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47222950 | GTAATATTTTCTTTC[G/T]GCCTGAAGAAATTCC | 1643 |
rs576135909 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DDB2 | GRCh38.p7 | 11:47217580 | GAAGATATAGACTAT[C/T]GATCACCCATAGAAT | 1643 |
rs576196809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47216628 | GCACTCAGCCAGGTA[A/G]AAAATGTCTTATGTT | 1643 |
rs576207321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47215824 | TCAAATACAGTTTGG[C/T]GATCAGGAGTTGTTG | 1643 |
rs576229251 | snp | C/T | | | intron-variant | DDB2 | GRCh38.p7 | 11:47226434 | GCACACCACCATGCC[C/T]GGCTAATTTTTGTAT | 1643 |
rs576538311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47233048 | TTTCCTTAACCCAAC[C/G]TGGCCCAGGGAAGAA | 1643 |
rs576993076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47224171 | ATTTTTCTTCTGGTC[A/G]CTTTAAAAATGATTA | 1643 |
rs577032250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47232194 | ACTAAAAATATACAA[C/T]TTAGCCATGCGTGGT | 1643 |
rs577084182 | in-del | -/C | | | intron-variant | DDB2 | GRCh38.p7 | 11:47228486 | TCTCTACTAAAAATA[-/C]ACAAAAATTCGCCAA | 1643 |
rs577230400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DDB2 | GRCh38.p7 | 11:47216531 | ATTTTTACTATTGCA[C/T]GCTCCCAAATTAGAT | 1643 |