SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs761626477 | snp | A/C | | | intron-variant | RBX1 | GRCh38.p7 | 22:40966428 | AGAGGGAGAAGCTGT[A/C]GAATACCCTTCGGTG | 9978 |
rs761626754 | snp | A/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950618 | ACTGAGGAATGCGGA[A/G]TGGGGACTGACACAC | 9978 |
rs761699239 | snp | C/G | 1.65094e-05 | 0.00287305 | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972538 | TTATTCATTTAATGA[C/G]TTTCCCTGCTGTTAC | 9978 |
rs762140529 | snp | A/C | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954164 | ATCCCAGCTACTTGG[A/C]AGGCTGAGGCAGGAG | 9978 |
rs762264026 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967609 | ATGACATTTCTAACA[A/G]ATGCTTTGTTGGAAA | 9978 |
rs762353234 | snp | C/G/T | 6.58994e-05 | 0.00573986 | intron-variant | RBX1 | GRCh38.p7 | 22:40964034 | AGTGATCCTGTTGCT[C/G/T]TTGTTCCCACAGGCA | 9978 |
rs762388863 | in-del | -/AAATAC | | | intron-variant | RBX1 | GRCh38.p7 | 22:40956874 | CCCCGTCTCCACTAA[-/AAATAC]AAAAAATTAGCTGGG | 9978 |
rs762460099 | snp | A/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40968692 | TGAATTTCCCACTGT[A/T]GGCCCCTGCTCCGGC | 9978 |
rs762460140 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954122 | AAAAATACAAAAATT[A/G]GCTGGGCGTACTGGT | 9978 |
rs762582306 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40960724 | TGTATTCCAGTTTCA[A/G]TAAGTTCTTAAATAC | 9978 |
rs762834527 | snp | C/T | | | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973360 | CAGGCAGAGCTCAGG[C/T]GGTAATGCTCGGTCA | 9978 |
rs763045460 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953767 | TCTTCTGTATCTAGT[C/G]TGTTGGTGTGTTTGA | 9978 |
rs763248372 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40968951 | TTTCTTTATGTAAAT[A/G]TACCTTAACTTTTTT | 9978 |
rs763310292 | snp | A/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40970964 | CGTGTAAAATATAAA[A/T]ACATTTGAGACGGTC | 9978 |
rs763386779 | snp | A/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950622 | AGGAATGCGGAGTGG[A/G]GACTGACACACGTTA | 9978 |
rs763570567 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40972218 | AGGCAGCTACTGGCA[C/T]CTGTCAGGTGGGCAT | 9978 |
rs763602027 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40962343 | CTGACTTCAGCCTCT[C/T]ATAGTGCTGGCATTA | 9978 |
rs763819387 | snp | G/T | 1.6492e-05 | 0.00287154 | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972505 | AAAAGACTTCTTCCA[G/T]CAAGCTTAATTGTTT | 9978 |
rs763916851 | snp | A/G | 3.30584e-05 | 0.00406548 | synonymous-codon | RBX1 | GRCh38.p7 | 22:40967855 | ACGACAGGTGTGTCC[A/G]TTGGACAACAGAGAG | 9978 |
rs763928536 | snp | A/C | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950549 | GGTTTCACTACAGCA[A/C]AAGCAGCGGAAAAAG | 9978 |
rs764028863 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40971378 | CAATATTCAAGTAGA[G/T]TTCTTATGAGAAGCT | 9978 |
rs764303766 | snp | A/C | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953803 | AGTAGTTTTTTTATG[A/C]TGTCCTGGAGGCATA | 9978 |
rs764545501 | snp | A/C | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953893 | TTGTGGACGACAGGC[A/C]CTGTTGATTTTTCCT | 9978 |
rs764608379 | snp | C/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950623 | GGAATGCGGAGTGGG[C/G]ACTGACACACGTTAC | 9978 |
rs764642394 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967465 | GGGCCTCCTTTCCCA[A/G]AGAAAGTGGAAGTAT | 9978 |
rs764664350 | snp | A/G | 1.72928e-05 | 0.00294043 | synonymous-codon | RBX1 | GRCh38.p7 | 22:40951455 | CAGCGGCGCGGGCAA[A/G]AAGCGCTTTGAAGTG | 9978 |
rs764732260 | snp | A/C | | | intron-variant | RBX1 | GRCh38.p7 | 22:40966983 | GATTGTCCTTTTCCC[A/C]AATCTAAGCAGACTT | 9978 |
rs765019269 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40968691 | ATGAATTTCCCACTG[C/T]AGGCCCCTGCTCCGG | 9978 |
rs765108337 | in-del | -/CAA | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967030 | ACCAGTGTTCTTGAT[-/CAA]ACTCTTGTCTTTTTA | 9978 |
rs765210794 | snp | C/T | | | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973263 | AGGCAGTAGATGGAC[C/T]GCGCAACCTAGATCC | 9978 |
rs765220300 | snp | G/T | 6.60229e-05 | 0.00574518 | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972539 | TATTCATTTAATGAC[G/T]TTCCCTGCTGTTACC | 9978 |
rs765325929 | in-del | -/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950234 | AGAAAAAAAAAAAAA[-/G]CGGCTCTAGCACTTT | 9978 |
rs765386907 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40963543 | TGGGAGTCTGAGACA[C/T]GAGAATCGCTTGAAC | 9978 |
rs765531309 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40961502 | CACTGCAAGCTCCGC[C/T]TCCCGGGTTCACACC | 9978 |
rs765668013 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954187 | GGCAGGAGAATTGCT[G/T]GAACCTGGGAGGCAG | 9978 |
rs766066687 | snp | C/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40951300 | CTCGCGCGCCAGTAA[C/G]GGGTGGGGTGCGGGA | 9978 |
rs766180086 | snp | A/C | | | intron-variant | RBX1 | GRCh38.p7 | 22:40965598 | GGTGTGTACCACCAC[A/C]CCCAGCTAATTTTTG | 9978 |
rs766244288 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40959459 | TCTTATTTGGTACTC[C/T]AGATTGCAGTAATAT | 9978 |
rs766412818 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40965085 | CGAGGCGGGTGCATC[A/G]TGAGGTCAGCAGATG | 9978 |
rs766796336 | snp | A/T | 6.80353e-05 | 0.00583207 | missense | RBX1 | GRCh38.p7 | 22:40951423 | GCGATGGATGTGGAT[A/T]CCCCGAGCGGCACCA | 9978 |
rs766831340 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40955154 | TAGTCTTTTTTGCCT[A/G]GAATATTCTTCACCT | 9978 |
rs766979564 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40971191 | ATGAAGAATTCCTTA[C/T]CTGGGGCTTTGACTC | 9978 |
rs767135047 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40965259 | AGTGAGCCGAGACCA[C/T]ACCACTGCACTCCAG | 9978 |
rs767224631 | in-del | -/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40962496 | TTTTAATAGTTTTAC[-/T]TTTTTTTTTTTTTTT | 9978 |
rs767315472 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40963454 | CAGCCTGGCCAACAC[A/G]GAGAAACCCCATCTC | 9978 |
rs767502366 | snp | A/G | | | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972910 | TGGGCAGCTGAAAGA[A/G]GGAAGAATGTGGGAT | 9978 |
rs767557412 | snp | A/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950815 | CCCTGAGCAGTTCCC[A/G]AACAGAAATCGGAGA | 9978 |
rs767609895 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40952167 | TGGTGGAACTTGTTA[A/G]GAAAATCCGAGCCCA | 9978 |
rs767778926 | snp | A/G | | | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972666 | GTTGGATTCTGGAAC[A/G]GATGCTCTCTCTTGT | 9978 |
rs767850098 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40965720 | GTGCTGGGATTACAG[A/G]CGTGAGCCACCGTGC | 9978 |
rs767867824 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant | RBX1 | GRCh38.p7 | 22:40953509 | CTAAAGAGTATGTGT[A/G]TGTGTTACAAGCAGA | 9978 |
rs768225599 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953291 | CACTGCACCCGGCCA[G/T]ACTAAATTATTTTAA | 9978 |
rs768419059 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40966392 | CCGTACTGCTGCAAA[C/G]TGCTCAGTGGGTGAG | 9978 |
rs768459265 | snp | C/T | 3.40628e-05 | 0.00412677 | utr-variant-5-prime | RBX1 | GRCh38.p7 | 22:40951385 | GGTCGGACGACAGAC[C/T]GTGTGTTTCCAAAAT | 9978 |
rs768835653 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40970524 | CTTAGCCACTCTGAT[A/G]GGTGACAATCAGTAT | 9978 |
rs768908821 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40960518 | TTAGTAGTGCCATGG[C/T]CACAGTCAAAAGAAA | 9978 |
rs769090852 | in-del | -/CTGTT | | | intron-variant | RBX1 | GRCh38.p7 | 22:40957651 | TCAAAAAGAGAAACA[-/CTGTT]TATTTTTTATTTTTA | 9978 |
rs769124444 | snp | C/G | 1.6477e-05 | 0.00287024 | intron-variant | RBX1 | GRCh38.p7 | 22:40964025 | CCAAGGTCCAGTGAT[C/G]CTGTTGCTCTTGTTC | 9978 |
rs769204474 | snp | A/C | 3.41828e-05 | 0.00413403 | intron-variant | RBX1 | GRCh38.p7 | 22:40964163 | CTTGTAAACATATTT[A/C]CACTTTTCCTGCTTT | 9978 |
rs769323286 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40960662 | AGAGGATCCAGCTTA[A/G]AGGACATCATATTTA | 9978 |
rs769579352 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40951976 | CCTCTCACTTGGAGG[A/G]GTCCTCTCACTTGGA | 9978 |
rs769669141 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40971614 | AGGCTGGAGTGCAGT[G/T]GTTGTGATCTCGGTT | 9978 |
rs769760759 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954624 | GAAATGGAGGAAAGA[A/G]ACTTTAAGTTTCTAG | 9978 |
rs769764421 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40971929 | ACCTCCAAAATCCAC[A/G]CCTAGCTTCTCTTCT | 9978 |
rs769996544 | snp | A/T | 2.14121e-05 | 0.00327194 | intron-variant | RBX1 | GRCh38.p7 | 22:40951523 | GCTAGAGAGGCGCGG[A/T]TCTGGCTGGCAGGCC | 9978 |
rs769998272 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40956186 | TTAGAGTGAAATGCT[G/T]GAGACATCATATTAG | 9978 |
rs770024588 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40968723 | TTGCTGGAGCTAGCC[A/G]TCAGCAACAGGACAG | 9978 |
rs770149004 | in-del | -/AAAAT | | | intron-variant | RBX1 | GRCh38.p7 | 22:40955436 | TCATAAAGTAAAAAG[-/AAAAT]AAAAAGGTGAAATTA | 9978 |
rs770197388 | snp | A/T | 1.69954e-05 | 0.00291503 | utr-variant-5-prime | RBX1 | GRCh38.p7 | 22:40951393 | GACAGACCGTGTGTT[A/T]CCAAAATGGCGGCAG | 9978 |
rs770284946 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40970662 | ATTTTGAATTATTGG[C/T]CATTTTCTTTACTGA | 9978 |
rs770343579 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40970925 | TACTGTTGGGCTCCC[C/T]TCAGCAAAATATATG | 9978 |
rs770376416 | snp | C/T | 1.94414e-05 | 0.00311775 | intron-variant | RBX1 | GRCh38.p7 | 22:40967762 | ATGGCTGAGCCTGCA[C/T]AGAGTTATTTTTAAT | 9978 |
rs770549187 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40964425 | CTTTGGAATATTCTC[A/G]TGGTAGAACTTTGTA | 9978 |
rs770767592 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954784 | AAGCAGCCATGGCCC[C/T]GGCCAGTTTTCCATT | 9978 |
rs771036526 | snp | A/G | 2.1896e-05 | 0.0033087 | intron-variant | RBX1 | GRCh38.p7 | 22:40951528 | AGAGGCGCGGATCTG[A/G]CTGGCAGGCCCGAGG | 9978 |
rs771091520 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40966439 | CTGTCGAATACCCTT[C/T]GGTGAGCCCGACCCC | 9978 |
rs771099967 | snp | A/C | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40949571 | AACTAACAAACAAAT[A/C]TCAGTTCTTTCTCTT | 9978 |
rs771263065 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40972037 | CTATTCTCATTATTA[A/G]CTTTACCCTAAACAT | 9978 |
rs771282028 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40964809 | GGGATAAGAGATTCT[A/G]GAGTCAGACCACCAT | 9978 |
rs771321249 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40961902 | TGATTCTCCTGCCTC[A/G]GCCTCCTGAGTAGCT | 9978 |
rs771425393 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40958075 | ATGATCACCCATCTC[A/G]GCCCCCAAAGTGCTG | 9978 |
rs771615846 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40966248 | AAATTGTACTTTGAC[C/T]GCTAAATATATCCAT | 9978 |
rs771650910 | snp | G/T | 4.95062e-05 | 0.004975 | intron-variant | RBX1 | GRCh38.p7 | 22:40972466 | CAGAGTAATTTACTT[G/T]GTCTTTCAGGTATGG | 9978 |
rs771714461 | snp | A/C | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950099 | CGGGTGGGATGGCTC[A/C]CTCCTGTGATCCCAG | 9978 |
rs771794114 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967524 | GCCACATTCCACGTT[C/G]TCTTAAATAGAAGAG | 9978 |
rs771883869 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40970216 | CAAAAATTAGCCAGG[C/G]ATGGTGGTGCCTATA | 9978 |
rs771908060 | snp | C/G | 1.70528e-05 | 0.00291995 | utr-variant-5-prime | RBX1 | GRCh38.p7 | 22:40951382 | GGTGGTCGGACGACA[C/G]ACCGTGTGTTTCCAA | 9978 |
rs772020034 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967315 | CAGTTCTGGGTGGGC[C/G]GCAGTGACCATGCAC | 9978 |
rs772125538 | in-del | -/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40964454 | ACCTTTGAAACAGGC[-/T]TTTTTTAAAGACCAG | 9978 |
rs772142319 | snp | C/G | 0.000380458 | 0.0137871 | intron-variant | RBX1 | GRCh38.p7 | 22:40953505 | GGTCCTAAAGAGTAT[C/G]TGTGTGTGTTACAAG | 9978 |
rs772292012 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40968332 | CTGATCTCAACTGAT[C/G]TGCCTGCCTCGGTCT | 9978 |
rs772405369 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40959129 | CCCCGTCAGTGTTTT[C/G]AAAGTGTAATCTGTC | 9978 |
rs772492785 | snp | C/T | | | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973056 | GACTAAGTGGCATCA[C/T]GTGGGCACAGAGAGA | 9978 |
rs772494818 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40958377 | TGGATTTATCATTTT[C/T]ATAAAGACAATTTTT | 9978 |
rs772511011 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40956930 | GTCCCAGCTACTTGA[A/G]AGGCTGAGGCAGGAG | 9978 |
rs772841653 | snp | A/G | 3.29527e-05 | 0.00405898 | intron-variant | RBX1 | GRCh38.p7 | 22:40964028 | AGGTCCAGTGATCCT[A/G]TTGCTCTTGTTCCCA | 9978 |
rs773017406 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40962385 | CAACATGCCCGGCCC[A/G]CTTTCCACATTTTCG | 9978 |
rs773037436 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953424 | ATAAGATTAACGTAA[G/T]ATCCAAAAACTTTTG | 9978 |
rs773205549 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953478 | GAGATGATAACTGCA[C/G]CTGCAGCCTGAGGTC | 9978 |
rs773285361 | snp | A/C | | | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973349 | CGCTGATGTGACAGG[A/C]AGAGCTCAGGCGGTA | 9978 |
rs773383770 | snp | C/T | 1.65138e-05 | 0.00287343 | intron-variant | RBX1 | GRCh38.p7 | 22:40951524 | CTAGAGAGGCGCGGA[C/T]CTGGCTGGCAGGCCC | 9978 |
rs773578159 | snp | C/T | 1.69989e-05 | 0.00291533 | utr-variant-5-prime | RBX1 | GRCh38.p7 | 22:40951394 | ACAGACCGTGTGTTT[C/T]CAAAATGGCGGCAGC | 9978 |
rs773588930 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40968776 | ATCTCTTATATGTCC[C/T]GGTATTTACATGGTT | 9978 |
rs773589658 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40957416 | TTTGGGTGGCTGAGG[C/T]GGGCAGATCGCTTGA | 9978 |
rs773604923 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40970923 | GGTACTGTTGGGCTC[C/T]CTTCAGCAAAATATA | 9978 |
rs773685957 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40961151 | GGAGTGCAGTGGTAC[A/G]ATCATGGTGCACTGC | 9978 |
rs773868211 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40955019 | CTCGAACTCCTGACC[G/T]CGGGTGATCCGCGTG | 9978 |
rs774129190 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40965138 | GAAACCCCGTCTCTA[C/G]TAAAAATACAAAAAA | 9978 |
rs774172320 | snp | A/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40949906 | TCTCTTTAGCAATAG[A/G]GTCAGCACGCTCCAT | 9978 |
rs774217130 | snp | A/C | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967250 | CTAGAAATAAAGTTT[A/C]TTTGACCAGAGCTGA | 9978 |
rs774422290 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40962987 | AGGAGTGAGCCATCG[C/T]GCCTGGCCTACTCCT | 9978 |
rs774428670 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967284 | GGGTGTGGGGAGGTT[C/G]GGGAAGTGCCCGTCT | 9978 |
rs774440307 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40960923 | GCCACCCACCACACC[C/G]GGTTAATTGTTTGTA | 9978 |
rs774646069 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40966487 | AAAAATGTCTCTGCT[C/T]TCTGCCTTTTGGAAA | 9978 |
rs774737198 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40972105 | TGATCAGGGCAGCCC[A/G]AAAGTTCAAACTGTC | 9978 |
rs774779049 | in-del | -/AAAG | | | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973505 | TTAGCTTAGAAAAAT[-/AAAG]ATATATATAATCTTG | 9978 |
rs774789482 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40956762 | ACTCTTAGGCCAGGC[A/G]TGGTGGCTTACACCT | 9978 |
rs774815661 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40956904 | GCTGGGTGCGATGGC[A/G]GGCGCCTGTAGTCCC | 9978 |
rs774897118 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954063 | GATCATTTGAGGCCA[A/G]GAGTTGACCAACCTG | 9978 |
rs774914093 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40951654 | GCGTGACGGCGGCCC[A/G]CTGTTGGGGGAAGTG | 9978 |
rs775195770 | snp | C/T | | | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973092 | TGTAAAATGTAAAAC[C/T]GCTATACAAATGTGA | 9978 |
rs775287146 | snp | A/G | 1.64977e-05 | 0.00287203 | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972492 | TATGGGCACTAGGAA[A/G]AGACTTCTTCCATCA | 9978 |
rs775494779 | snp | C/T | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950451 | TGGGCCGAAATCGCG[C/T]CATTACACTCCAGCC | 9978 |
rs775515071 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40964818 | GATTCTAGAGTCAGA[C/T]CACCATTCCCTGTCT | 9978 |
rs775574906 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954785 | AGCAGCCATGGCCCC[A/G]GCCAGTTTTCCATTT | 9978 |
rs775602794 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967327 | GGCGGCAGTGACCAT[G/T]CACTTCTCTACCAAG | 9978 |
rs775738856 | in-del | -/TA | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953502 | TGAGGTCCTAAAGAG[-/TA]TGTGTGTGTGTTACA | 9978 |
rs775799107 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953521 | TGTGTGTGTTACAAG[C/T]AGAATGCACTGTTCC | 9978 |
rs775844671 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40966834 | CACCACAGTGCACCA[A/G]TCACAGACGAAATGA | 9978 |
rs775982646 | snp | G/T | 0.000197765 | 0.00994201 | intron-variant | RBX1 | GRCh38.p7 | 22:40953510 | TAAAGAGTATGTGTG[G/T]GTGTTACAAGCAGAA | 9978 |
rs776014696 | in-del | -/A | | | intron-variant | RBX1 | GRCh38.p7 | 22:40970055 | AATAGACCCAATTTA[-/A]AAAAAAAAAAAAAAA | 9978 |
rs776331514 | snp | C/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950615 | ACAACTGAGGAATGC[C/G]GAGTGGGGACTGACA | 9978 |
rs776343131 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40960555 | GATCAAATTTAAACA[C/T]GATAATGTACCTTGA | 9978 |
rs776466696 | snp | C/T | 3.29886e-05 | 0.00406118 | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972520 | TCAAGCTTAATTGTT[C/T]TGTTATTCATTTAAT | 9978 |
rs776549895 | in-del | -/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40955261 | AAATTTTCTTTTTCC[-/T]TTTTTTTTTTTTTTG | 9978 |
rs776612865 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40972258 | AGAGGGAGAGCCTGT[C/G]CCTAAGAGGGGGCAG | 9978 |
rs776893207 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954895 | GAGTTCAAGTGATTC[G/T]CCTGCCTCAGCCTCC | 9978 |
rs776972865 | snp | C/T | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40949787 | GGGACGGGGTTTCGT[C/T]ATGTTGGCCAGGCTG | 9978 |
rs777013468 | snp | C/G | 0.000118439 | 0.00769451 | intron-variant | RBX1 | GRCh38.p7 | 22:40967751 | GTTGTCGCTCGATGG[C/G]TGAGCCTGCATAGAG | 9978 |
rs777015913 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40956153 | ACAGAAGACAAAGGC[A/G]ATCTATATTGTCTTC | 9978 |
rs777265244 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40968672 | AAAGGGTATACCACA[C/G]AATATGAATTTCCCA | 9978 |
rs777285890 | snp | A/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967519 | AAGGAGCCACATTCC[A/T]CGTTCTCTTAAATAG | 9978 |
rs777386915 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40955029 | TGACCTCGGGTGATC[C/T]GCGTGCCTCTGCCTC | 9978 |
rs777582881 | in-del | -/TAATTGTTTTGTTATTCATTTAATGACTTTCCCTGCTGTTACC | 9.89527e-05 | 0.00703325 | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972512 | TTCTTCCATCAAGCT[lengthTooLong]TAATTACAAATTGGA | 9978 |
rs777597195 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40969614 | ATTAGGCCATGCCTG[A/G]TGGCTCATGCCTGTA | 9978 |
rs777640565 | in-del | -/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967476 | CCAAAGAAAGTGGAA[-/G]GTATCCCCTTACAGG | 9978 |
rs777715387 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40954644 | TAAGTTTCTAGAAAT[G/T]GAATTATAGGAACTT | 9978 |
rs777764791 | snp | C/G | | | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972737 | CCAAGGCTGAAAACT[C/G]AGCTTTTGAAAGTGA | 9978 |
rs777839803 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | RBX1 | GRCh38.p7 | 22:40964076 | GCTAACCAGGCGTCC[A/G]CTACTTCAGAAGAGT | 9978 |
rs777956571 | snp | A/C | | | intron-variant | RBX1 | GRCh38.p7 | 22:40958038 | ACTATGTTGGCCAGG[A/C]TGGTCTCGAGCTCCT | 9978 |
rs777991473 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40959739 | TCACTTGAACCTGGG[A/G]GACAGAGGTTGCAGT | 9978 |
rs778048947 | snp | A/G | 1.64874e-05 | 0.00287113 | intron-variant | RBX1 | GRCh38.p7 | 22:40953678 | TTGAGAAGGTTGCAG[A/G]GATTGTGGCTATCTT | 9978 |
rs778054295 | snp | C/T | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40949610 | TTTTTTGGGGGGGAA[C/T]GGAGTCTCGCTCTGT | 9978 |
rs778165141 | snp | A/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950928 | CCAGCGAGGACTCTT[A/G]GGTTTCGGGGCAGGC | 9978 |
rs778317558 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40964480 | ACCAGGTGTCTAATG[A/G]AACTAAGTTTGATGA | 9978 |
rs778398954 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40951754 | GCGGCGGGAGCCAAG[C/T]GCTTGAGCTGTCACT | 9978 |
rs778525864 | snp | C/T | 1.7149e-05 | 0.00292817 | utr-variant-5-prime | RBX1 | GRCh38.p7 | 22:40951373 | CGCAGGCGCGGTGGT[C/T]GGACGACAGACCGTG | 9978 |
rs778609383 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40964573 | AGATTATTTTTTAAC[A/G]TGGCTTATGCCAGAA | 9978 |
rs778821142 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40955960 | TGCTTGCCAGTTTCT[C/T]GGCCTTGCATTTTCA | 9978 |
rs778901423 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40971648 | TGCAACCTCCAACTC[C/G]CGGGTTGAAGCAGTT | 9978 |
rs778910957 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40959910 | TCACTTGAGGTCAGG[A/G]GTTAAAGACCAGCCT | 9978 |
rs778912574 | snp | A/G | 1.65963e-05 | 0.0028806 | intron-variant | RBX1 | GRCh38.p7 | 22:40967920 | TGACGGGGCTTTTTG[A/G]CTTGCCTCAGGCTGA | 9978 |
rs779417049 | snp | C/T | | | utr-variant-3-prime | RBX1 | GRCh38.p7 | 22:40972979 | CTTGGGTACTGATGG[C/T]AATCTTGGCCAAGTT | 9978 |
rs779479113 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40952442 | TGTCTCATTGTGGCC[A/G]CTGCTGCTCAGTTAC | 9978 |
rs779735648 | in-del | -/CT | | | intron-variant | RBX1 | GRCh38.p7 | 22:40971204 | TATCTGGGGCTTTGA[-/CT]CTGCCACTCTAACTG | 9978 |
rs779743779 | in-del | -/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40969001 | TGCATGTTTTTAACA[-/T]TTTTTTATATTTTTT | 9978 |
rs779788528 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953197 | GATTTTGCCATGTTG[A/G]CCAGGCTGGTCTTGA | 9978 |
rs779852485 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40966354 | CGTGGTATGCTCTGA[C/T]TTAGTTGGGCTCTAC | 9978 |
rs779952010 | snp | C/T | 9.47373e-05 | 0.00688184 | intron-variant | RBX1 | GRCh38.p7 | 22:40951484 | TGAAAAAGGTTGGGT[C/T]TCGCCAGCGCCTTCC | 9978 |
rs780051525 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40958965 | ACTGCAGGTATGCAC[C/T]AGCATGCCCAGCTAA | 9978 |
rs780201903 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40959933 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 9978 |
rs780217794 | in-del | -/AGG | 0.000116373 | 0.00762711 | intron-variant | RBX1 | GRCh38.p7 | 22:40967937 | TTGCCTCAGGCTGAA[-/AGG]AGCGTGGTCTTGGGG | 9978 |
rs780237732 | snp | A/G | 1.66244e-05 | 0.00288304 | intron-variant | RBX1 | GRCh38.p7 | 22:40967931 | TTTGACTTGCCTCAG[A/G]CTGAAAGGAGCGTGG | 9978 |
rs780424080 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40970258 | TTGGGAGGCTGAGGC[A/G]GGAGAATCATCTCTT | 9978 |
rs780440197 | snp | C/T | 3.31329e-05 | 0.00407005 | intron-variant | RBX1 | GRCh38.p7 | 22:40964127 | TGTAACGTAAGGAAG[C/T]ATCTTTACCTGTCAG | 9978 |
rs780474775 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40961904 | ATTCTCCTGCCTCAG[C/G]CTCCTGAGTAGCTGG | 9978 |
rs780562650 | snp | A/C | | | intron-variant | RBX1 | GRCh38.p7 | 22:40960167 | TCTATTTATAGAAAT[A/C]GTTTTTGTTTGCTTG | 9978 |
rs780581721 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40969992 | CTTGAGCCCAGGAGG[C/T]GGAGGTTGCAGTAAG | 9978 |
rs780614090 | in-del | -/AA | | | intron-variant | RBX1 | GRCh38.p7 | 22:40970054 | TAATAGACCCAATTT[-/AA]AAAAAAAAAAAAAAA | 9978 |
rs780669517 | snp | C/T | | | downstream-variant-500B | RBX1 | GRCh38.p7 | 22:40973386 | GGTCACCACCCTGCT[C/T]ACCTCTTGCTGTACA | 9978 |
rs780923476 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40953359 | GTGTTCATATACTCA[C/G]CCTTTTGGAGAATAG | 9978 |
rs781041078 | snp | A/C/T | 1.65809e-05 | 0.00287926 | intron-variant | RBX1 | GRCh38.p7 | 22:40967908 | CTTTGGTTGTTTTGA[A/C/T]GGGGCTTTTTGACTT | 9978 |
rs781064170 | snp | C/T | 3.29495e-05 | 0.00405877 | intron-variant | RBX1 | GRCh38.p7 | 22:40953642 | GATCTTTGTAAGTAA[C/T]TGGAGGAGGATGGGA | 9978 |
rs781129063 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40967205 | GTGAAGTACTGAGCT[C/G]TTGTAATATCAATAT | 9978 |
rs781144005 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40955341 | TGGCTTCAAGTGATC[C/G]TCCCACTTTGGCCTT | 9978 |
rs781232070 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40959067 | GTGATCCACCCGGCT[C/T]GGCCTCCCAAAGTGC | 9978 |
rs781456226 | snp | C/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40962017 | CTCGAACCCTGACAT[C/G]AAGTGATCCGTCACC | 9978 |
rs781577729 | snp | A/T | 1.65258e-05 | 0.00287448 | intron-variant | RBX1 | GRCh38.p7 | 22:40972425 | CAGGTTTTATGTCTC[A/T]AACAGGAAATTATCT | 9978 |
rs781589452 | snp | G/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40971892 | TCTTAGAGCCAAATT[G/T]TGGTTTCTGGGGAAA | 9978 |
rs781620492 | snp | A/G | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40949359 | AGACCTTAATTTACA[A/G]TGGGTTTCTAGTATT | 9978 |
rs781753944 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40969507 | GTGATCCCAACACTT[C/T]AGGAGGCCAAGGTGG | 9978 |
rs796079167 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40964875 | AGGCAAGGCATTTAA[C/T]GTCTCCAATCCTGGG | 9978 |
rs796406450 | in-del | -/A | | | upstream-variant-2KB | RBX1 | GRCh38.p7 | 22:40950233 | AAGAAAAAAAAAAAA[-/A]GCGGCTCTAGCACTT | 9978 |
rs796810679 | snp | A/G | | | intron-variant | RBX1 | GRCh38.p7 | 22:40968409 | TTCCCAACCTTCTAC[A/G]GTCTGTGAAAGTAGA | 9978 |
rs796865530 | in-del | -/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40961104 | TTTTTTTTTTTTTTT[-/T]GATAACAAGGTTTTG | 9978 |
rs796957790 | snp | C/T | | | intron-variant | RBX1 | GRCh38.p7 | 22:40960200 | CAAGTACCAAGAGCC[C/T]AATTTGCACTTGGCA | 9978 |