SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7782 | snp | A/C | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB | MDM4, LOC105371692 | GRCh38.p7 | 1:204557951 | CATCTAGTGAGCTGG[A/C]CACATTCAATAAGTT | 4194 |
rs882935 | snp | A/C | 0 | 0 | nc-transcript-variant, intron-variant | LOC105371692 | GRCh38.p7 | 1:204574171 | TGGCTACATGGACTT[A/C]ATAATTCATCAGAGC | 4194 |
rs885012 | snp | G/T | 0.497091 | 0.0380279 | nc-transcript-variant, intron-variant | LOC105371692 | GRCh38.p7 | 1:204574873 | CCTGCTGCTGCTCCA[G/T]GGCTGCATCCCCTTG | 4194 |
rs898388 | snp | C/T | 0.316 | 0.241131 | intron-variant | MDM4 | GRCh38.p7 | 1:204531129 | TCTTGACCTCTAACA[C/T]TCTAAATCCCACCCA | 4194 |
rs930947 | snp | A/G | 0.33693 | 0.2344 | intron-variant, upstream-variant-2KB | LOC105371692 | GRCh38.p7 | 1:204572069 | CAATGGTGGAAATCC[A/G]GAGGGTGGAGTACAC | 4194 |
rs1046874 | snp | C/T | 0.368324 | 0.220226 | utr-variant-3-prime, upstream-variant-2KB | MDM4, LOC105371692 | GRCh38.p7 | 1:204557932 | TAATAATAATAATAA[C/T]AACAACTTATTGAAT | 4194 |
rs1052644 | snp | C/G | 0 | 0 | missense, utr-variant-3-prime, nc-transcript-variant | MDM4 | GRCh38.p7 | 1:204549618 | GAAGACTAAAGAAGG[C/G]TGGGGCTTCATGCCC | 4194 |
rs1380576 | snp | C/G | 0.497359 | 0.0362457 | intron-variant | MDM4 | GRCh38.p7 | 1:204519150 | CTCAGCACATTTTCA[C/G]TCTTATCTTGCACTG | 4194 |
rs1460036 | snp | C/T | 0.495521 | 0.0471118 | downstream-variant-500B, upstream-variant-2KB | MDM4, LOC105371692 | GRCh38.p7 | 1:204558251 | TTTTAAGTCCATTAA[C/T]TTCCCCAAAGAAGTA | 4194 |
rs1563828 | snp | C/T | 0.498525 | 0.0271165 | intron-variant | MDM4 | GRCh38.p7 | 1:204547449 | AGAAACATGGGGAAA[C/T]AGCAACAAAAAAGCA | 4194 |
rs2045623 | snp | C/T | 0.49533 | 0.0480965 | intron-variant | MDM4 | GRCh38.p7 | 1:204528285 | GCTCAGACAAATCTG[C/T]TCCCTGGGCATCTTT | 4194 |
rs2125855 | snp | C/T | 0.327445 | 0.237702 | intron-variant | LOC105371692 | GRCh38.p7 | 1:204577819 | AGGATGCAGTGGCAC[C/T]GTTACAGCTCACTGC | 4194 |
rs2169135 | snp | G/T | 0.0707826 | 0.174302 | utr-variant-3-prime, nc-transcript-variant | MDM4 | GRCh38.p7 | 1:204550633 | GAGCCCAGGAGGTGG[G/T]CCGTGTTTGCACCAC | 4194 |
rs2169137 | snp | C/G | 0.32768 | 0.237625 | intron-variant | MDM4 | GRCh38.p7 | 1:204528785 | GGCTTCCTAGAGTGA[C/G]AGAAGTACGTGGACC | 4194 |
rs2290853 | snp | A/G | 0.247053 | 0.249983 | intron-variant | MDM4 | GRCh38.p7 | 1:204542576 | AAGTAATGACACTAC[A/G]AACAGATCATCGTTT | 4194 |
rs2290854 | snp | C/T | 0.457869 | 0.13889 | intron-variant, downstream-variant-500B | MDM4 | GRCh38.p7 | 1:204546897 | GCTGGTGCAAAATAG[C/T]TCTTGCTAAAGATTC | 4194 |
rs2290855 | snp | A/G | 0.4973 | 0.0366419 | intron-variant | MDM4 | GRCh38.p7 | 1:204546735 | TGAGGCTAATTAACT[A/G]AAAGCAAAAAAGACA | 4194 |
rs2369244 | snp | C/G | 0.498525 | 0.0271165 | intron-variant | MDM4 | GRCh38.p7 | 1:204546171 | ACGTTTAACAATTTG[C/G]AGCTTTTCTACTCTG | 4194 |
rs2369245 | snp | A/T | | | intron-variant | LOC105371692 | GRCh38.p7 | 1:204581232 | tatatatatatatat[A/T]tatatatatttattt | 4194 |
rs2926531 | snp | A/C | 0 | 0 | intron-variant | MDM4 | GRCh38.p7 | 1:204539421 | CTAAAAGAGCATTAC[A/C]ATCTTTCAAATTGAG | 4194 |
rs2926532 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | MDM4 | GRCh38.p7 | 1:204535124 | ATGGCATCTTCTTGA[C/T]CAAAATGAAAAGTTT | 4194 |
rs3014609 | snp | A/G | | | upstream-variant-2KB | MDM4 | GRCh38.p7 | 1:204515513 | tttgtatttttagta[A/G]aaacgggggtttcgc | 4194 |
rs3014610 | snp | A/T | 0.224116 | 0.248656 | intron-variant | MDM4 | GRCh38.p7 | 1:204527143 | CTAAAAAAAAAAAAA[A/T]AAATACAAAAATTGG | 4194 |
rs3761687 | snp | C/G | 0.00322066 | 0.0399995 | intron-variant | MDM4 | GRCh38.p7 | 1:204538163 | AGTAGAAATAACTGA[C/G]ACCAGGGGATGTAGC | 4194 |
rs3789048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MDM4 | GRCh38.p7 | 1:204548718 | GTCATTCTTTTCTAC[A/G]CTAATAGCAAATGTT | 4194 |
rs3789050 | snp | A/C | 0.262435 | 0.249691 | intron-variant | MDM4 | GRCh38.p7 | 1:204547357 | TAAGAGTGGAATATC[A/C]AGTCTTCTTTAATAG | 4194 |
rs3789051 | snp | A/G | 0.426047 | 0.177503 | intron-variant, utr-variant-5-prime, nc-transcript-variant | MDM4 | GRCh38.p7 | 1:204525308 | TCTGACTACTTTCTA[A/G]TTCTGATTTAATTAA | 4194 |
rs3789052 | snp | A/G | 0.42574 | 0.177808 | intron-variant, upstream-variant-2KB | MDM4 | GRCh38.p7 | 1:204525155 | CCCCAATGGTTATCA[A/G]GTAGAGCACTCTCTA | 4194 |
rs3789053 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | MDM4 | GRCh38.p7 | 1:204516697 | TTTATCTTCCGCGAG[C/T]CCTCATCCCACAACT | 4194 |
rs4245735 | snp | C/T | 0.0132884 | 0.0804216 | intron-variant | MDM4 | GRCh38.p7 | 1:204516761 | CAACAGGTGACAAAC[C/T]TAAAGTCGACGTAGT | 4194 |
rs4245736 | snp | C/G | 0.494936 | 0.050064 | intron-variant | MDM4 | GRCh38.p7 | 1:204517077 | GAAACCCCGTCTCTA[C/G]TAAAAATACAAAAAT | 4194 |
rs4245737 | snp | A/G | 0.497855 | 0.0326773 | intron-variant | MDM4 | GRCh38.p7 | 1:204517114 | TGTGTGTGGTGGCGC[A/G]TGCCTGTAATCCTAG | 4194 |
rs4245738 | snp | C/T | 0.494692 | 0.0512434 | intron-variant | MDM4 | GRCh38.p7 | 1:204536979 | GAAAAATCCAGATTT[C/T]AAGATCCCATAACCC | 4194 |
rs4245739 | snp | A/C | 0.354865 | 0.226944 | utr-variant-3-prime, nc-transcript-variant | MDM4 | GRCh38.p7 | 1:204549714 | AAAATGCATTTATTC[A/C]GTTCACTTACCACAT | 4194 |
rs4252668 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-5-prime, nc-transcript-variant | MDM4 | GRCh38.p7 | 1:204516444 | GCCGAGGCCCTAGGA[C/T]CTGTGACTGCCACCC | 4194 |
rs4252669 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | MDM4 | GRCh38.p7 | 1:204516683 | GGGGGGAGGGGAAGA[C/G]TTGTGGGATGAGGGC | 4194 |
rs4252670 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | MDM4 | GRCh38.p7 | 1:204517364 | ATTTTTGTATACCTT[A/G]AAGCTTGAAAACCAC | 4194 |
rs4252671 | snp | C/T | 0.0222194 | 0.103034 | intron-variant | MDM4 | GRCh38.p7 | 1:204517799 | ATACTTGGAACCTCT[C/T]GGTGTTAAGTATTAC | 4194 |
rs4252672 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MDM4 | GRCh38.p7 | 1:204517840 | TTTAGATTTAGTCTT[C/T]TCTCTCCTCATACAT | 4194 |
rs4252673 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MDM4 | GRCh38.p7 | 1:204518155 | cgcgagagcctgtct[C/T]aaaaaaagagatgag | 4194 |
rs4252674 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MDM4 | GRCh38.p7 | 1:204518375 | AAAGATTTAATCTTC[C/G]CAGTTTAATCTTCCC | 4194 |
rs4252675 | snp | C/T | 0.125182 | 0.216612 | intron-variant | MDM4 | GRCh38.p7 | 1:204525448 | AGGGAATTTTCTGCA[C/T]TAGAATAGATGTTAT | 4194 |
rs4252676 | snp | A/G | 0.00469377 | 0.0482167 | intron-variant | MDM4 | GRCh38.p7 | 1:204525610 | AGGTAAATCATTTTC[A/G]GTATTTCTAGTTTTT | 4194 |
rs4252677 | snp | A/G | 0.497586 | 0.0346604 | intron-variant | MDM4 | GRCh38.p7 | 1:204526125 | CCTGGATATGGTGGC[A/G]TGCACCTGTAGTCCC | 4194 |
rs4252678 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | MDM4 | GRCh38.p7 | 1:204526146 | ctgtagtcccagcta[C/G]tctggaggctgaagt | 4194 |
rs4252679 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MDM4 | GRCh38.p7 | 1:204526506 | tctccctcttttgcc[C/T]aggctggagtgcagt | 4194 |
rs4252680 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | MDM4 | GRCh38.p7 | 1:204526708 | gacctcatgatccat[C/G]cgccttggcctccca | 4194 |
rs4252681 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | MDM4 | GRCh38.p7 | 1:204526718 | tccatccgccttggc[A/C]tcccaaagtgctggg | 4194 |
rs4252682 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MDM4 | GRCh38.p7 | 1:204526752 | acaggcatgagccac[C/T]gcgcctggccAAATT | 4194 |
rs4252683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM4 | GRCh38.p7 | 1:204526904 | CTGTTAGGTTGAACA[C/T]CATATTTCCTTTCTT | 4194 |
rs4252684 | in-del | -/TT | 0.327914 | 0.237549 | intron-variant | MDM4 | GRCh38.p7 | 1:204527701 | AGTTATTTTAAACAC[-/TT]ATGCATTTAAATAAC | 4194 |
rs4252685 | snp | A/C | 0.497586 | 0.0346604 | intron-variant | MDM4 | GRCh38.p7 | 1:204527728 | TAACTTATTTAGCTT[A/C]TGAAGTTTTTTAAAA | 4194 |
rs4252686 | snp | A/G | 0.497586 | 0.0346604 | intron-variant | MDM4 | GRCh38.p7 | 1:204527767 | GTATTCTTTAAGTGG[A/G]AAAGACTCAGTATTA | 4194 |
rs4252687 | snp | C/G | 0.496874 | 0.0394129 | intron-variant | MDM4 | GRCh38.p7 | 1:204528207 | CTGTCCCCTGGAGAT[C/G]GAAGCCGAGCAGAGC | 4194 |
rs4252688 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | MDM4 | GRCh38.p7 | 1:204528228 | CGAGCAGAGCGTGGC[A/G]GGCAAGTGAGGGATC | 4194 |
rs4252689 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MDM4 | GRCh38.p7 | 1:204528754 | TTCTTCTAGAGGGAC[A/G]GGAAAAGAAGAGAGA | 4194 |
rs4252690 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | MDM4 | GRCh38.p7 | 1:204529236 | CATCATGAGGCAGGT[C/T]TCATCATTGAACAAG | 4194 |
rs4252691 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MDM4 | GRCh38.p7 | 1:204529348 | AGGAGTAGGCCTCAT[C/T]CATATTGGGAGGGGA | 4194 |
rs4252692 | snp | C/G | 0.00666659 | 0.0573485 | intron-variant | MDM4 | GRCh38.p7 | 1:204529653 | TTCCTGGCGCTTGCC[C/G]TGCATCTCCAGGGCA | 4194 |
rs4252693 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MDM4 | GRCh38.p7 | 1:204529771 | GGTTATGATGAATTA[C/T]GCCATCTCCTTCATT | 4194 |
rs4252694 | snp | A/G | 0.495521 | 0.0471118 | intron-variant | MDM4 | GRCh38.p7 | 1:204529928 | GTCACCCATGCTGGA[A/G]TGCAGTGGTGGTATC | 4194 |
rs4252695 | snp | G/T | 0.00349039 | 0.0416295 | intron-variant | MDM4 | GRCh38.p7 | 1:204530068 | gttatgtagagacag[G/T]ttttgccatgttgcc | 4194 |
rs4252696 | snp | A/G | 0.0111728 | 0.0739025 | intron-variant | MDM4 | GRCh38.p7 | 1:204531906 | CTGGAAGGAAGGAAT[A/G]GTTTCCAAAAGAGAT | 4194 |
rs4252697 | snp | C/T | 0.307385 | 0.243325 | intron-variant | MDM4 | GRCh38.p7 | 1:204532255 | ACTACAGGTATGTCA[C/T]ATCATATTTCTTCAG | 4194 |
rs4252698 | snp | C/T | 0.00283416 | 0.0375373 | intron-variant | MDM4 | GRCh38.p7 | 1:204532272 | TCATATTTCTTCAGT[C/T]TGTATCACAGCTTTG | 4194 |
rs4252699 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MDM4 | GRCh38.p7 | 1:204532709 | tgatatgtctcataa[A/G]tgtctttaatctata | 4194 |
rs4252700 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MDM4 | GRCh38.p7 | 1:204533078 | ACCTTTTACCTAATG[A/G]CTTTAGCCATCTCTT | 4194 |
rs4252701 | in-del | -/GAAACAGGGTCT | 0.216639 | 0.247764 | intron-variant | MDM4 | GRCh38.p7 | 1:204533389 | ATCTTTTTTTCTTCT[-/GAAACAGGGTCT]CAGGTTGCCCAGGCT | 4194 |
rs4252702 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MDM4 | GRCh38.p7 | 1:204533407 | ggttgcccaggctgg[A/G]gtgcagtggcactat | 4194 |
rs4252703 | snp | C/T | 0.000587084 | 0.017123 | intron-variant | MDM4 | GRCh38.p7 | 1:204536923 | TGACACTTAGAATGT[C/T]GCTTTAGATGAAGAT | 4194 |
rs4252704 | in-del | -/T | 0.316 | 0.241131 | intron-variant | MDM4 | GRCh38.p7 | 1:204537047 | AAAAGCCATACACTC[-/T]TTTCCTTTTGTTTGT | 4194 |
rs4252705 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MDM4 | GRCh38.p7 | 1:204537753 | TTTCTTTGGGTTTGT[A/G]TGTACCTGTGTGTGT | 4194 |
rs4252706 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | MDM4 | GRCh38.p7 | 1:204539011 | agtagctgggattac[A/T]ggcgcacgccaccac | 4194 |
rs4252707 | snp | A/G | 0.342806 | 0.232136 | intron-variant | MDM4 | GRCh38.p7 | 1:204539019 | GGATTACAGGCGCAC[A/G]CCACCACACCCGGCT | 4194 |
rs4252708 | snp | A/G | 0.498459 | 0.0277128 | intron-variant | MDM4 | GRCh38.p7 | 1:204539031 | CACGCCACCACACCC[A/G]GCTAATTTTGTATTT | 4194 |
rs4252709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM4 | GRCh38.p7 | 1:204541039 | AATTTTGGTCTACCT[A/G]GTTACTTTGTAACTA | 4194 |
rs4252710 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | MDM4 | GRCh38.p7 | 1:204541283 | gggtaacatagcgag[A/C]cctcgtctctacaaa | 4194 |
rs4252711 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | MDM4 | GRCh38.p7 | 1:204541338 | TGGGCATGATGGTGC[A/G]CACCAGTCGTCCCAG | 4194 |
rs4252712 | snp | A/G | 0.0110494 | 0.0735024 | intron-variant | MDM4 | GRCh38.p7 | 1:204541356 | ccagtcgtcccagct[A/G]ctcaggaggctgaga | 4194 |
rs4252713 | snp | A/G | 0.425894 | 0.177655 | intron-variant | MDM4 | GRCh38.p7 | 1:204541400 | TGAGCCCAAGAGGTG[A/G]AGATTGCAGTGAGCG | 4194 |
rs4252714 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MDM4 | GRCh38.p7 | 1:204541881 | CACCATATGTACTTC[A/G]GCACACGTTAACCCC | 4194 |
rs4252715 | snp | C/T | 0.00153017 | 0.0276178 | intron-variant | MDM4 | GRCh38.p7 | 1:204542741 | TAGTCTTAGTTATTA[C/T]GTATTGTGCATAGTT | 4194 |
rs4252716 | snp | C/T | 0.0199538 | 0.0978711 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | MDM4 | GRCh38.p7 | 1:204542796 | TAGATGAAGACTTAA[C/T]TGAAAATTTAGCCCA | 4194 |
rs4252717 | snp | C/T | 0.459676 | 0.136146 | intron-variant | MDM4 | GRCh38.p7 | 1:204542972 | TTTGAAGGGAAGTGG[C/T]TTTTTTTCTTTTGAA | 4194 |
rs4252718 | snp | A/T | 0.498009 | 0.0314867 | intron-variant | MDM4 | GRCh38.p7 | 1:204543067 | ATGGCGTTAAATACC[A/T]TCTGTATGCATGTGA | 4194 |
rs4252719 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | MDM4 | GRCh38.p7 | 1:204543413 | GATTCAGCCCcctcc[C/T]tcctcacttcctgtc | 4194 |
rs4252720 | in-del | -/C | 0.0110494 | 0.0735024 | intron-variant | MDM4 | GRCh38.p7 | 1:204543555 | ggaacactgttcccc[-/C]acattctttctttgc | 4194 |
rs4252721 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | MDM4 | GRCh38.p7 | 1:204543670 | CCAGTAGGATCCATT[C/T]GCTTTTTGTTTTGGA | 4194 |
rs4252722 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MDM4 | GRCh38.p7 | 1:204543808 | cactttgtaaaaata[C/T]tgctatattttatgt | 4194 |
rs4252723 | snp | C/T | 0.00332778 | 0.0406548 | intron-variant | MDM4 | GRCh38.p7 | 1:204543834 | tatgtatgtgttgtc[C/T]gtttaccactgaaat | 4194 |
rs4252724 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | MDM4 | GRCh38.p7 | 1:204543893 | tactttttccattac[C/T]tggtacctagaacag | 4194 |
rs4252725 | snp | A/G | 0.494733 | 0.0510469 | intron-variant | MDM4 | GRCh38.p7 | 1:204544128 | ATATTTCTTTAATAA[A/G]CATCCTTGACCATTT | 4194 |
rs4252726 | snp | A/G | 0.424659 | 0.17887 | intron-variant | MDM4 | GRCh38.p7 | 1:204544274 | CTTTTAAACTCTTCA[A/G]TACTGTTTCTTAGGT | 4194 |
rs4252727 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | MDM4 | GRCh38.p7 | 1:204544832 | CCAATTTTAAGATTC[A/G]CATTAAGTAATGTTA | 4194 |
rs4252728 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | MDM4 | GRCh38.p7 | 1:204544877 | AAAAGCCCCTACTTA[-/G]TCAAAAGCAGTAAGC | 4194 |
rs4252729 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | MDM4 | GRCh38.p7 | 1:204545048 | ataaacttttaaaaa[A/C]cattatgagttttct | 4194 |
rs4252730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM4 | GRCh38.p7 | 1:204546288 | gcttactgcaagccg[C/G]aactcttgggctcaa | 4194 |
rs4252731 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | MDM4 | GRCh38.p7 | 1:204546632 | AATGCCAACTAGAAG[C/T]ACAGAATCATGTGTT | 4194 |
rs4252732 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | MDM4 | GRCh38.p7 | 1:204547436 | CAAATGTATACCTTG[C/T]TTTTTTGTTGCTATT | 4194 |
rs4252733 | snp | C/T | 0.316 | 0.241131 | intron-variant | MDM4 | GRCh38.p7 | 1:204547790 | ATGCAATGGCATAAT[C/T]TCGGCTCACTGCAAC | 4194 |