SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15468 | snp | A/C | 0 | 0 | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972594 | AGCAAACTGAAAAAA[A/C]AAAGCAGAAAAAAAC | 9978 |
rs2003733 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | RBX1 | GRCh38.p7 | 22:40957950 | CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGATTAC | 9978 |
rs2413631 | snp | A/G | 0.309894 | 0.242719 | intron-variant | RBX1 | GRCh38.p7 | 22:40963782 | gcccaggaagtcaag[A/G]ctgcagtgagccatg | 9978 |
rs5751014 | snp | A/T | 0.261884 | 0.249717 | intron-variant | RBX1 | GRCh38.p7 | 22:40962088 | tactcccagccTTTT[A/T]TGgtttgtttgtttg | 9978 |
rs5758139 | snp | C/T | 0.089084 | 0.191327 | intron-variant | RBX1 | GRCh38.p7 | 22:40956191 | GTGAAATGCTTGAGA[C/T]ATCATATTAGGCTTT | 9978 |
rs5758144 | snp | C/T | 0 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40964404 | ccttcaaaacctaca[C/T]gcaccctttggaata | 9978 |
rs5758145 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | RBX1 | GRCh38.p7 | 22:40965589 | GGGATTACAGGTGTG[C/T]ACCACCACACCCAGC | 9978 |
rs5995968 | snp | A/G | 0.031825 | 0.122064 | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40949802 | catgttggccaggct[A/G]gtctcaaactcctga | 9978 |
rs5995969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBX1 | GRCh38.p7 | 22:40954145 | gtactggtgcatgtc[G/T]gtaatcccagctact | 9978 |
rs5995970 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RBX1 | GRCh38.p7 | 22:40956220 | TTCAGTGGGATACCT[A/G]TTTTGTTTCATAATA | 9978 |
rs5995971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBX1 | GRCh38.p7 | 22:40958423 | AAGAATCTAGATTTA[A/G]CAACGGTTGTATTTT | 9978 |
rs5995972 | snp | G/T | 0.284471 | 0.247612 | intron-variant | RBX1 | GRCh38.p7 | 22:40962889 | ttttagtagagacgg[G/T]gtttcactatgttgg | 9978 |
rs5995973 | snp | C/G | 0.031825 | 0.122064 | intron-variant | RBX1 | GRCh38.p7 | 22:40966154 | TGCTTGCCTGCCAGG[C/G]TTGATGTGAGGCCTC | 9978 |
rs5995974 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | RBX1 | GRCh38.p7 | 22:40971908 | TGGTTTCTGGGGAAA[A/G]CAGAAACCTCCAAAA | 9978 |
rs6002207 | snp | A/G | 0.151001 | 0.229563 | intron-variant | RBX1 | GRCh38.p7 | 22:40951809 | GACAGGGTAGGGTGG[A/G]GTGGGGTGGGTGGAA | 9978 |
rs6002208 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RBX1 | GRCh38.p7 | 22:40955789 | ACTGGTCATGTATTG[C/T]CCTTGGCTTCTTTGA | 9978 |
rs6002212 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RBX1 | GRCh38.p7 | 22:40969844 | cagtgagcagagatc[A/G]tgccactgcactcca | 9978 |
rs6002213 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972809 | CGCATCACTTAGTGA[A/C]GAGGAATCCAACAGC | 9978 |
rs7284740 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RBX1 | GRCh38.p7 | 22:40970263 | aggctgaggcaggag[A/G]atcatctcttgaacc | 9978 |
rs7290224 | snp | C/T | 0.133093 | 0.220981 | intron-variant | RBX1 | GRCh38.p7 | 22:40954983 | gtagagacacagttt[C/T]accgtgttggccagg | 9978 |
rs7510862 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40965189 | gcgcctgtagtccca[G/T]ctactcgggaggctg | 9978 |
rs8138994 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RBX1 | GRCh38.p7 | 22:40967675 | GAACTTTTGCCTCTC[A/G]TTGTCTTCTTTTCTT | 9978 |
rs9607760 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40969718 | ggtaaaaccccgtct[C/T]tactttaaaaaatac | 9978 |
rs9611443 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | RBX1 | GRCh38.p7 | 22:40963700 | caaaaaatacaaaca[A/G]ttagctggtgtggtg | 9978 |
rs9611444 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40969716 | atggtaaaaccccgt[C/T]tctactttaaaaaat | 9978 |
rs9611445 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RBX1 | GRCh38.p7 | 22:40972170 | CTTTCACAACCACCA[A/G]TGACTTTTCCCTCTC | 9978 |
rs9619925 | snp | C/G | 0.130694 | 0.219696 | intron-variant | RBX1 | GRCh38.p7 | 22:40968173 | ttggctcactgcaac[C/G]tccacctcccagatt | 9978 |
rs9619926 | snp | C/T | 0.133093 | 0.220981 | intron-variant | RBX1 | GRCh38.p7 | 22:40970126 | tttaggaggctgagg[C/T]gggtggatcacctga | 9978 |
rs9623291 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | RBX1 | GRCh38.p7 | 22:40952677 | AAGAGTCTAAACATA[C/T]AAAAGTTGAGAACAT | 9978 |
rs9623292 | snp | A/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953013 | TTTTTTTTTTTGAGA[A/T]GGAGTCTCACTCTGT | 9978 |
rs9623293 | snp | A/C | 0.0854556 | 0.188216 | intron-variant | RBX1 | GRCh38.p7 | 22:40955531 | aaaaaaaaatgagat[A/C]ttttacattctgtct | 9978 |
rs9623294 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40968882 | TTTGTACATTTTGGA[A/G]ATTTTCCATTTCCAC | 9978 |
rs12159069 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RBX1 | GRCh38.p7 | 22:40959499 | ACATTTTTGTTCTTT[G/T]TTAGGAATTTTGTAG | 9978 |
rs12159237 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RBX1 | GRCh38.p7 | 22:40959488 | ATCCCTCCTATACAT[C/T]TTTGTTCTTTGTTAG | 9978 |
rs12166456 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | RBX1 | GRCh38.p7 | 22:40967241 | TGAATAAATCTAGAA[A/G]TAAAGTTTCTTTGAC | 9978 |
rs12170314 | snp | C/T | 0.0159141 | 0.0877712 | intron-variant | RBX1 | GRCh38.p7 | 22:40964212 | TAGGGAAAAAAATGA[C/T]TAGTCCACCTTTCTC | 9978 |
rs12170666 | snp | C/G | | | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973336 | aatctaacgctgccg[C/G]tgatgtgacaggcag | 9978 |
rs12484508 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954229 | agccgagatcacacc[A/G]ctgcactacaacctg | 9978 |
rs12628111 | snp | G/T | 0 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40953345 | TGACATTAATTTCTG[G/T]GTTCATATACTCAGC | 9978 |
rs13055975 | snp | A/G | 0.5 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40965268 | agaccacaccactgc[A/G]ctccagcctgggtga | 9978 |
rs13056347 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40956796 | atcccagcactttgg[C/G]aggccaaggcgggca | 9978 |
rs13058204 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40951837 | gaatggggAGTCGAA[A/G]CGAATGCGGCGGTGG | 9978 |
rs17347451 | snp | C/G | 0.477853 | 0.102875 | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973104 | AACCGCTATACAAAT[C/G]TGACCTTTGGTTGTG | 9978 |
rs28457022 | snp | C/G | 0.133435 | 0.221162 | intron-variant | RBX1 | GRCh38.p7 | 22:40965974 | AAGGAGAGATTCTCT[C/G]AGAGAGCCTGCCGTA | 9978 |
rs28534703 | snp | G/T | | | missense | RBX1 | GRCh38.p7 | 22:40953579 | GTAGCCCTCTGGGCC[G/T]GGGATATTGTGGTTG | 9978 |
rs28564047 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40960883 | CCTGCCTCAGCCTCT[C/T]TAGTAGCTGGGATTA | 9978 |
rs28624654 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40962963 | GGCCTCCCAAAGTGC[G/T]GAGATTACAGGAGTG | 9978 |
rs28657837 | snp | A/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950137 | GGAGGCCGAAGTGGG[A/G]GGATCACTTGGGCCC | 9978 |
rs34126667 | in-del | -/CAAA | | | intron-variant | RBX1 | GRCh38.p7 | 22:40952715 | TTTATGGTAAGAATC[-/CAAA]AAAATTCTAGTGAAT | 9978 |
rs34304315 | in-del | -/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40963827 | TGTAGCCTGGGCAAC[-/G]GGGAGTGAGATGTGC | 9978 |
rs34618218 | in-del | -/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40952984 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 9978 |
rs34633210 | snp | A/G | 0.133777 | 0.221342 | intron-variant | RBX1 | GRCh38.p7 | 22:40968250 | TGTGTGCCACCATGC[A/G]CAGCTAATTTTTGTA | 9978 |
rs34654213 | snp | G/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40951342 | GGAGGTGGGGGGAGC[G/T]AAGTGTGCGCTGCTG | 9978 |
rs34768759 | in-del | -/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953523 | GTGTGTTACAAGCAG[-/T]AATGCACTGTTCCCT | 9978 |
rs34805534 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40965258 | TAGTGAGCCGAGACC[A/G]CACCACTGCACTCCA | 9978 |
rs34892959 | in-del | -/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40952490 | AAAATAATAGAAGTA[-/G]GGGGCTTTTCCTCCA | 9978 |
rs35620343 | in-del | -/A | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967004 | AGCAGACTTCTAGCT[-/A]CCCTGTCAGTTACCA | 9978 |
rs35646973 | in-del | -/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953546 | GTTCCCTCTTTTTGT[-/G]CTTTGCAGTGGAATG | 9978 |
rs35944121 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40955569 | ATCTTTGAAATTCTG[G/T]GTATTTTACACTTAC | 9978 |
rs56080538 | snp | C/G | 0.480064 | 0.0978296 | intron-variant | RBX1 | GRCh38.p7 | 22:40958883 | CAGTGGCATGATCTC[C/G]GTGCACTGCAACCTC | 9978 |
rs56970864 | in-del | -/CAAA | 0.0715661 | 0.175284 | intron-variant | RBX1 | GRCh38.p7 | 22:40952714 | ATGGTAAGAATCAAA[-/CAAA]ATTCTAGTGAATTGT | 9978 |
rs57128854 | in-del | -/GTTTG | | | intron-variant | RBX1 | GRCh38.p7 | 22:40958828 | GTTTGGTTTGGTTTG[-/GTTTG]TTTGAGACAGAGTCT | 9978 |
rs58457576 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950221 | AAAAAATTAAAAAAG[-/A]AAAAAAAAAAAAGCG | 9978 |
rs58909804 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40965990 | AGAGAGCCTGCCGTA[A/G]AAGAGAGCCAGCATG | 9978 |
rs59870929 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | RBX1 | GRCh38.p7 | 22:40962887 | TTTTTTAGTAGAGAC[G/T]GTGTTTCACTATGTT | 9978 |
rs62237046 | snp | A/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40959391 | AAGCTGGAAAACTTT[A/T]GTATTGAGCACATTT | 9978 |
rs67333529 | in-del | -/T | 0.123798 | 0.215808 | intron-variant | RBX1 | GRCh38.p7 | 22:40956065 | TTTATATAACCCTGA[-/T]TTTTTTTTCTCTATA | 9978 |
rs67482133 | in-del | -/T | 0.260504 | 0.249779 | intron-variant | RBX1 | GRCh38.p7 | 22:40954335 | CAAAGGAAAGAAGCG[-/T]TAAGGAGTGAGGATT | 9978 |
rs71325200 | snp | C/T | 0.5 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40969862 | CCACTGCACTCCAGT[C/T]TAAATGACAGAGTGA | 9978 |
rs71325201 | snp | C/T | 0.5 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40969953 | GTAGTCCCAGCTGCT[C/T]TGGAGGCTGAGGTGG | 9978 |
rs71325202 | snp | A/G | 0.5 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40972148 | GGGAGTGAGCAGGCG[A/G]AGCTCCCTTTCACAA | 9978 |
rs71328760 | in-del | -/C | 0.5 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40963748 | CAGCTACTCAGGAGG[-/C]TGAGGGAGAATCACC | 9978 |
rs71328761 | in-del | -/AA | 0.5 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40970053 | TAATAGACCCAATTT[-/AA]AAAAAAAAAAAAAAA | 9978 |
rs71695312 | in-del | -/A | 0.135484 | 0.22223 | intron-variant | RBX1 | GRCh38.p7 | 22:40955515 | ACATGTAATTGATGT[-/A]AAAAAAAAATGAGAT | 9978 |
rs73174614 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBX1 | GRCh38.p7 | 22:40955234 | AGCCAGTACAAACAC[A/G]TATATAATTTTAAAT | 9978 |
rs73174620 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40963948 | ATTCATTAAAAAACA[A/G]TTATGGCTAATTAAC | 9978 |
rs73174621 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RBX1 | GRCh38.p7 | 22:40967230 | CAATATGTCTGTGAA[C/T]AAATCTAGAAATAAA | 9978 |
rs73414647 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | RBX1 | GRCh38.p7 | 22:40966525 | CTTTCTCTTTTTCAC[A/C]GTGAGTTATACAAGA | 9978 |
rs73885712 | snp | A/C | 0.00429586 | 0.0461462 | intron-variant | RBX1 | GRCh38.p7 | 22:40951525 | TAGAGAGGCGCGGAT[A/C]TGGCTGGCAGGCCCG | 9978 |
rs73885713 | snp | C/T | 0.123452 | 0.215605 | intron-variant | RBX1 | GRCh38.p7 | 22:40951895 | GAACCTGAGGTCCTA[C/T]CGCATTAGAGGCCTC | 9978 |
rs75149872 | snp | A/C | 0.00185631 | 0.0304091 | utr-variant-5-prime | RBX1 | GRCh38.p7 | 22:40951383 | GTGGTCGGACGACAG[A/C]CCGTGTGTTTCCAAA | 9978 |
rs75270024 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | RBX1 | GRCh38.p7 | 22:40959330 | GAACAGTTCCTGCCC[A/G]TTTAAACTAACTGGA | 9978 |
rs75322488 | snp | C/T | 0.5 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40955283 | TTTTTTTTGTTTTTT[C/T]CAGAGACGGGATCTC | 9978 |
rs75431775 | snp | G/T | 0 | 0 | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40949607 | ATTTTTTTTGGGGGG[G/T]AACGGAGTCTCGCTC | 9978 |
rs75612763 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | RBX1 | GRCh38.p7 | 22:40954411 | ATCTAAATAAATAAT[C/T]AATTGCACTAAAGAA | 9978 |
rs76329433 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RBX1 | GRCh38.p7 | 22:40952001 | CTTGGAGGGATCCTC[A/G]CTGAACCGAGGCCTC | 9978 |
rs76537927 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950232 | AAAGAAAAAAAAAAA[A/G]AGCGGCTCTAGCACT | 9978 |
rs77585056 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RBX1 | GRCh38.p7 | 22:40955840 | TTCACACTACAGCCA[A/G]GGAAGATCAGCACCT | 9978 |
rs77809930 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40959291 | CCGTTATGTGCCACT[G/T]TCAACCTGTTCTGGG | 9978 |
rs77844793 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RBX1 | GRCh38.p7 | 22:40964523 | TTGAAGTCTCTGTGT[A/G]TGTGTGTTTTAAGTG | 9978 |
rs77951373 | snp | G/T | 0.5 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40957844 | AATTTTTTTTTTTTG[G/T]AGGCGGAGTCTCACA | 9978 |
rs79034706 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40957530 | GTGGTCCCAGCTACT[G/T]GGGAGGCTGAGGTGG | 9978 |
rs79478629 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40972430 | TTTATGTCTCAAACA[A/G]GAAATTATCTTGGAA | 9978 |
rs79505309 | snp | C/T | 0.0861826 | 0.188849 | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973125 | TTTGGTTGTGTATGA[C/T]AGCAGTCCCCAACCT | 9978 |
rs79531119 | snp | A/C | 0.5 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40956110 | TATGTGTCTCTGGAT[A/C]TGAGAGAATGTACTT | 9978 |
rs111290195 | snp | C/T | 0 | 0 | intron-variant | RBX1 | GRCh38.p7 | 22:40960752 | TACACTGCATAGACC[C/T]TAGATCCCTTTTTTG | 9978 |
rs111298861 | snp | G/T | 0.477684 | 0.103247 | intron-variant | RBX1 | GRCh38.p7 | 22:40957451 | AGGAGTTCAAGACCA[G/T]CCTGGGCAACATGGC | 9978 |
rs111379559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBX1 | GRCh38.p7 | 22:40966255 | ACTTTGACCGCTAAA[C/T]ATATCCATTAATACA | 9978 |
rs111469799 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RBX1 | GRCh38.p7 | 22:40967723 | TCACCCATGCCACTA[A/C/T]CCTGTGGGACCTGTT | 9978 |
rs111528055 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972936 | GGGATTCAGTCATCA[A/T]ACCCAGTTCTGAGTC | 9978 |