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 |