| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs536206368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68811378 | ATTTGTTGGCTTTTG[A/C]ATTTCATATCATGCT | 4193 |
| rs536331496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68810412 | GCTCACCAAAAGGCT[C/T]TAACAGTTTCACTCC | 4193 |
| rs536429604 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841309 | CCTGTGTTGCCCAGG[A/C]TGGTCTCGAACTCCT | 4193 |
| rs536442303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832031 | GCTGAGATCACGCCA[C/T]TGCACTGCAGCCTGG | 4193 |
| rs536556585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68831599 | GCCAGCCTTTAAGAG[C/T]CAGGGCTTTTATGCT | 4193 |
| rs536580728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828299 | ATAAAAACTTTATTA[G/T]ATAGATTAAATTGTG | 4193 |
| rs536862468 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834066 | AATAATATACTTTGT[G/T]TCTGTTTTTAAAACT | 4193 |
| rs536895321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68817143 | TGTTTGAAACCTAGC[C/G]CAATCATTTACTAGT | 4193 |
| rs536923318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68839150 | TATTTTATATAAAAC[A/G]TGAAACACTGAATAT | 4193 |
| rs537208262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68816264 | GCAGAGTTAAAGTCT[A/C]CAAGGAAAAAAACCT | 4193 |
| rs537455815 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845161 | AAAAGTTTTTAGTTG[C/T]GCTTTATGGGTGGAT | 4193 |
| rs537498131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68814940 | AGCTTCCATTTTTCT[C/T]TTTCCTCTCCAGCTA | 4193 |
| rs537566818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813261 | AGCTTGCAATAAGCT[C/T]GTTGGATCAGTACGG | 4193 |
| rs537611260 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808340 | CGTCCCTCCCCGGAT[A/T]AGTGCGTACGAGCGC | 4193 |
| rs537639197 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | MDM2 | GRCh38.p7 | 12:68834903 | TATTATTGCCCTGAA[-/G]GTCTTACTAGGTTCT | 4193 |
| rs537649961 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835449 | GGAGGGGTGTCTAGT[A/T]GAAGACAGACGAAGA | 4193 |
| rs537682720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828025 | AATCCCAGCTACTTG[A/G]AAGCTGAAGTCACAA | 4193 |
| rs538103355 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68820941 | TTTTACAACCTACTT[A/T]CCATGAGAAAAGCCC | 4193 |
| rs538178819 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68826543 | AATCCCAGCTACTTG[C/G]GAGGCTGAGGCAGGA | 4193 |
| rs538228098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68830398 | GGAGCTGTTACTTAT[A/G]TAGACCGCTAGATGG | 4193 |
| rs538240457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68832815 | GAGCCACCACCTCCA[A/G]CCTGATGCTTTTTAA | 4193 |
| rs538240593 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841711 | CCAGTTTTAGAAACC[C/T]GTGAATTCAGAAAAG | 4193 |
| rs538270585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68825887 | GAGGTGGAACTAGAA[C/T]AAATGGTAGTTACTT | 4193 |
| rs538462144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68820893 | GTTCCAGAAAGATGC[A/G]CATGTATATATACAT | 4193 |
| rs538555797 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821788 | TTCCTAGAATGAATT[A/G]ACCACTCCCTTGTAC | 4193 |
| rs538620827 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68817316 | CAAGTATTAGCTGTA[G/T]CTATTATAACTTTTT | 4193 |
| rs538655246 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830435 | GAGCTCCTGCTCAGT[C/T]TGAGAGCAGGTTCTT | 4193 |
| rs538730784 | snp | A/G | 6.72303e-05 | 0.00579747 | intron-variant | MDM2 | GRCh38.p7 | 12:68824675 | GAATATTTATTTGAC[A/G]CATTCACACAGCTTT | 4193 |
| rs538764544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68816217 | TTTTGCTGCCTTTTC[C/T]CTTCCTAATATGTTA | 4193 |
| rs538791706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68811923 | GGTAATTTTTGTATA[C/T]TTAATAGAGACGGAG | 4193 |
| rs538824634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68839032 | TCTTGAATAGTTAAC[C/T]TTTCTTGTGTGTATG | 4193 |
| rs538884571 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822697 | AGTTTGGTTTAGATA[C/T]CAGTAGAATTAACTT | 4193 |
| rs538953532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68811144 | TGCTGGGATTACAGG[C/T]GTGAATCACTGCACC | 4193 |
| rs539285268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823689 | CTTCTGCTTAAAATT[A/G]CCATTTAGGGGTTCA | 4193 |
| rs539321938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828698 | ACTAAGTTTCTGTAC[A/G]AATAGGTACTCAAAA | 4193 |
| rs539416797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68836213 | TCAATAGACCTCAAT[G/T]AACATGCTTATTATA | 4193 |
| rs539556569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827346 | GACTCAAGATTTTTC[A/G]TATGTTTATTAGTCA | 4193 |
| rs539724891 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68829680 | CTGAGGCAGGAGAAT[C/T]GCTCGAACCCAGGAG | 4193 |
| rs539809452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827988 | ATACAAAAATTATCC[A/T]GGCATGGTGGTGTGC | 4193 |
| rs539860653 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819742 | GTGATCTGCCGGACT[C/T]GGCCTTCCGAAGTGC | 4193 |
| rs539900459 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MDM2 | GRCh38.p7 | 12:68818888 | GGTGCACACTACTAT[A/G]AGCAGCTAATTTTTT | 4193 |
| rs539954474 | snp | A/G | | | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845584 | CATACTTGAATTCGT[A/G]TTGCTTTCCTTTAAA | 4193 |
| rs540196661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832983 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 4193 |
| rs540239420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68831640 | TTTTTCTGGAGCTAC[A/G]AAAAACCTTCCAAGG | 4193 |
| rs540415373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68818072 | GTGCTGGGATTACAG[A/G]TGTGAGCAACCACAC | 4193 |
| rs540473443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832456 | AATTCTAGGTATTTT[G/T]GACTACAAAGATCTA | 4193 |
| rs540530073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68817567 | CCAGCCTGACCAACA[C/T]GGAGAAACCCTGTCT | 4193 |
| rs540733421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68829774 | CCATCTCAAAAAAAA[A/T]AAAAAAAAATGCAGG | 4193 |
| rs540763754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68830995 | TGTGAGCCACCTGCC[C/T]GGACCCCTATTTAAT | 4193 |
| rs540790142 | snp | A/C | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806804 | TTCTCACTGCTTGAG[A/C]TTTTCTTTCATCCAG | 4193 |
| rs540805322 | in-del | -/GGA | 0.00159681 | 0.0282109 | intron-variant | MDM2 | GRCh38.p7 | 12:68810484 | TATTTTTTTTGAGGC[-/GGA]GGAGTCTTGCTCTGT | 4193 |
| rs540929584 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826544 | ATCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 4193 |
| rs541018501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68815768 | ATTTCTAATACAGTG[A/G]TAATAATCTTATGAA | 4193 |
| rs541092135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822730 | GAACTCCTATTCCAT[A/G]TTCTCAACTTTGTCA | 4193 |
| rs541127230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823259 | ATGTTTCCAAGGGGG[A/G]TAGTAAAGGGTATTT | 4193 |
| rs541400551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68826932 | CTGTAATCCCAGCAC[C/G]TTGGGAGGCCGAGGA | 4193 |
| rs541517660 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841995 | TCTGCAGCTGTTGCA[A/G]GGTGTTCAGATTGTA | 4193 |
| rs541601942 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MDM2 | GRCh38.p7 | 12:68834169 | TGATATGGGCTGGGC[A/G]AGGTGGCTCACAGGT | 4193 |
| rs541647114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813478 | CCTTTATTGAACTTG[A/C]TGGATATGTTTGCTG | 4193 |
| rs541684876 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806541 | CGATCTCCGCTCACT[G/T]CAACCTCTGCCTCCC | 4193 |
| rs541685461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827627 | CTCCACCCCAGCATT[A/G]TAAGAATATTTTGTT | 4193 |
| rs541949615 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842960 | CCTGAAATAACTGAC[A/G]CTATATAATTTCTGC | 4193 |
| rs542012136 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828385 | CTCAGCCTAGGCAAC[A/C]TGGTGAAACCCTGTC | 4193 |
| rs542033527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814412 | TGAAATGTTTGCCAT[A/G]AGTACAGTATGATAG | 4193 |
| rs542280034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832917 | GGATCACAAGGTCAG[A/G]AGATCGAGACCATCC | 4193 |
| rs542310591 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MDM2 | GRCh38.p7 | 12:68818399 | CTAAGAAAAGTAAAG[A/G]AAAAAAAAGGACTGT | 4193 |
| rs542380378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68810707 | ACCTGGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 4193 |
| rs542471908 | snp | G/T | | | intron-variant, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68814689 | TCTTTCTGGGATAGA[G/T]GTGAGCTGATTCATG | 4193 |
| rs542500540 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68832158 | TTTTTCTTCTTCGTT[C/T]TAATTTCCCTCATTT | 4193 |
| rs542522399 | in-del | -/GAAAA | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845211 | TGATACTTATAAAAA[-/GAAAA]AGTATTTCTTCAGCT | 4193 |
| rs542746280 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821388 | GAGCTGTCTCTAATA[C/T]ACTACACTGCTCCTA | 4193 |
| rs542860790 | snp | A/C/T | 6.628e-05 | 0.00575635 | missense | MDM2 | GRCh38.p7 | 12:68839425 | AACTGGAAAACTCAA[A/C/T]ACAAGCTGAAGAGGG | 4193 |
| rs542886737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68830879 | CTAATTTTTGTATTT[C/T]TAGTAGAGATGGGGT | 4193 |
| rs542954588 | in-del | -/CT | 0.487 | 0.0795687 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843703 | TTGCTTCAAAACTCT[-/CT]CTCTCTCTCTCTGTC | 4193 |
| rs542963064 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68842010 | AGGTGTTCAGATTGT[A/G]TAAACATAAATGTCA | 4193 |
| rs542985276 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826660 | TCTTAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAA | 4193 |
| rs543065388 | snp | A/T | 0.00279162 | 0.0372561 | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845619 | TCCTTTAAAGACTTT[A/T]AAAAAAATTCGATAG | 4193 |
| rs543172919 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808704 | AGGAGGGCGGGATTT[C/T]GGACGGCTCTCGCGG | 4193 |
| rs543205365 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MDM2 | GRCh38.p7 | 12:68816593 | TTATCTCCTGACCTC[A/G]TGATCCATCCGCTTC | 4193 |
| rs543221794 | in-del | -/TTA | 0.0023933 | 0.0345097 | utr-variant-3-prime, cds-indel | MDM2 | GRCh38.p7 | 12:68840149 | ACATTTAAATGTAAC[-/TTA]TTATTTTTTTTGAGA | 4193 |
| rs543242081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68810087 | GAGGCCAAGGCGGAC[C/T]GATCACCTGAGATGA | 4193 |
| rs543261761 | in-del | -/TATATTA | 0.0170251 | 0.090679 | intron-variant | MDM2 | GRCh38.p7 | 12:68818542 | TTGTATTATAATTTG[-/TATATTA]TATATTATAATATAC | 4193 |
| rs543334129 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68808062 | CCACTCCATCATCCC[A/G]GAGGTGGTGCGGCCG | 4193 |
| rs543352406 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MDM2 | GRCh38.p7 | 12:68829692 | AATCGCTCGAACCCA[A/G]GAGTTGGAGGTTGCA | 4193 |
| rs543372390 | snp | C/T | 0.00205761 | 0.0320089 | intron-variant | MDM2 | GRCh38.p7 | 12:68815688 | GCTCAAGGGATCTGC[C/T]TACCTCGGCCTCCTA | 4193 |
| rs543404564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68822598 | ATGTATTCATTCCTT[C/T]ATTTGTTTAAATAAA | 4193 |
| rs543441185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68815293 | GCTAAACTATGTAAC[A/G]GTAGTGTATGTATTG | 4193 |
| rs543499678 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68837922 | AAATTCAAGAGTTTC[C/G]AAAATTTTTACTGTA | 4193 |
| rs543738664 | snp | A/G | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68807459 | GGTGACCGCCACCAC[A/G]CCCGACTAATTTTTG | 4193 |
| rs543769141 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841630 | AACAACTCTAAGACA[C/T]TTTAAAGTACCTTCT | 4193 |
| rs543787728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68833075 | AGCTTGCAGTGAGCC[C/G]AGATGGTGCCACTGC | 4193 |
| rs543797133 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806488 | TTTTCTTCTGAGATG[A/G]AGTCTTGCTCTGTCA | 4193 |
| rs543850697 | in-del | -/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810874 | TTGTTTTTGTTTTTG[-/T]TTTTTTTTGAGACAG | 4193 |
| rs543869982 | snp | A/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843738 | CTCAATAAATGGCCA[A/T]AGGGATTAGTAGTTT | 4193 |
| rs543917249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813451 | ATCCTCCCCAGCATT[G/T]TTTCCAAATCCCCTT | 4193 |
| rs544071476 | snp | A/T | 4.97863e-05 | 0.00498906 | intron-variant | MDM2 | GRCh38.p7 | 12:68820418 | ATACCATAAAAACGT[A/T]TTAAAGACATTTTTG | 4193 |
| rs544076056 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MDM2 | GRCh38.p7 | 12:68833934 | CTTGACTTGTGATTC[G/T]AATCTGATTGGTAGT | 4193 |
| rs544138988 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843727 | TCTCTGTCTGTCTCA[A/G]TAAATGGCCAAAGGG | 4193 |
| rs544314610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68818198 | CGTTCACCTGAGACA[A/G]TTAACTAGCTTCTGC | 4193 |
| rs544356425 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MDM2 | GRCh38.p7 | 12:68812229 | ATCAGAAAAATTAAT[A/C]ATTCAATTCTATATG | 4193 |
| rs544427556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68821133 | ACTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 4193 |
| rs544524382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68811530 | TTACAAATGCTATTA[C/T]CTTTTATAGCTGTTT | 4193 |
| rs544644568 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810565 | TCCCCGGGTTCACGC[A/C]ATTCCCCTGCCTCAG | 4193 |
| rs544690526 | snp | G/T | | | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808721 | GACGGCTCTCGCGGC[G/T]GTGGGGGTGGGGGTG | 4193 |
| rs544699628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68824933 | TGGGGTGTGGTGGCT[C/T]ACGCCTGGCTCACGC | 4193 |
| rs544728722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832230 | TTGTGAAGGGAGTTA[A/C]AGGAAAGTGCATTCC | 4193 |
| rs544910094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68819139 | ACTTGAAAAGGATAT[G/T]AATTAAAAATATTGT | 4193 |
| rs544978326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68809886 | TAGTATTCCACAGCA[C/T]GAGTATACCATTTTA | 4193 |
| rs545145004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68816508 | CTCCCTAATAGCTGG[G/T]ATTACAGGTGTCTGC | 4193 |
| rs545148355 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844854 | TCACTGCAACCTCTG[C/T]CTCCTGGCTGTGTTC | 4193 |
| rs545204105 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823691 | TCTGCTTAAAATTAC[A/C]ATTTAGGGGTTCATT | 4193 |
| rs545268278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68830745 | TCTCTCTGTCTCCCA[C/G]GCTGGAGTGCAGTGG | 4193 |
| rs545352706 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806653 | ATTTTTAGTAGAGAC[A/G]AGGTTTCACCATCTT | 4193 |
| rs545586380 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807539 | ACTCCTGACCTCAAG[A/T]GATCCACCCGCCTCG | 4193 |
| rs545586642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68815187 | TTATTATCATTGGAT[A/G]ATCAGTTAAGGAAAC | 4193 |
| rs545589949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827803 | TAAAATGAAATGGAA[A/G]CTTTTTACTGGTTTT | 4193 |
| rs545623375 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68808028 | CTCACAGCCCGCCGC[A/G]CCCGCGGGGCGACAC | 4193 |
| rs545696973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814506 | CCTACATTTATAATC[A/G]AAGGAAAAGCTAAAT | 4193 |
| rs545763146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828198 | GAGTAAATTAAACAC[C/T]TTGGCTCTTTTCGGA | 4193 |
| rs545782400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822573 | GAGTTTTCTGAAGTA[C/T]GTAACCCTGATGTAT | 4193 |
| rs546027719 | in-del | -/GCA | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68823836 | TCTGCGGGGAAGAAT[-/GCA]GCAGTGATAAGGGAA | 4193 |
| rs546045095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68821878 | TTTGTTTGTTTTTGA[A/G]ATGGGCTCTCACTCT | 4193 |
| rs546210830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68812907 | ATTGACCCCTAATCT[A/G]GTTGGCAGGCTCCTT | 4193 |
| rs546225760 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68835307 | AAAGGCTTAGTCAAA[G/T]AAGGATGAATAGGAT | 4193 |
| rs546249427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68838983 | TAAATAGTGAAATGA[G/T]CACTACAGTCAAGCA | 4193 |
| rs546286342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68819496 | GTTAATAAGTTTCTT[G/T]TTTTTCTTCCCTGAG | 4193 |
| rs546293440 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68831854 | GGGCGGATCACCTGA[C/G]GTCAGGAGTTCAGGA | 4193 |
| rs546337000 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815514 | TGGCATGATCACTGC[G/T]CGCTGCAGCCTGGAC | 4193 |
| rs546434508 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838363 | ATTGCATGGTGGAAA[C/G]GTTTGTGGGATAAAA | 4193 |
| rs546464680 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844039 | ATTATAAACATAGTA[C/T]ACTTGATATATGGAG | 4193 |
| rs546520713 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838412 | GCATTGAGCAGTTAC[A/G]AAGATGAGAACACAG | 4193 |
| rs546731856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823668 | TTGCTAGAGTGATTT[G/T]TCACTCTTCTGCTTA | 4193 |
| rs546733138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68830188 | TTTTTGGTAATATGG[C/T]AGTGTCTCATGGCCA | 4193 |
| rs546744535 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822420 | TATTTCCTTTTTTTT[A/T]AATTATTATACTTTA | 4193 |
| rs546846385 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840516 | TGTTTTTTTGTTTGT[C/T]TGTTTGTTTGTTTGT | 4193 |
| rs546868454 | in-del | -/CTC | 0.0023933 | 0.0345097 | utr-variant-3-prime, cds-indel | MDM2 | GRCh38.p7 | 12:68840613 | CGGGTTCAAGCCATT[-/CTC]CTGGCTCAGCCTCTG | 4193 |
| rs546915922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68825589 | ACTGGGGAGGCAGAG[C/T]TTACAGTGAGCCGAG | 4193 |
| rs546958394 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68817889 | TGCAACCTCCGTCTC[C/T]TGGGTTCAAGTGATT | 4193 |
| rs547067995 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808189 | AGGGGGCGCGCACCG[A/C]GGCACCGCGGCGAGC | 4193 |
| rs547206405 | in-del | -/A | 0.00199481 | 0.0315187 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806893 | ATCTTTTTAAAAGCC[-/A]CATATTAAATCTCTT | 4193 |
| rs547239439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68809467 | CTGTTAAGAACTGGT[C/T]AGTATTTTTTTAGCC | 4193 |
| rs547288760 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68837786 | ATTATAGGTTTTTTT[A/T]AAACTATTGTGCTTT | 4193 |
| rs547418677 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844082 | ATTTTTACAAAATTT[A/G]AATCTGCAAATGGAT | 4193 |
| rs547510849 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843283 | AAAGTACTAATCCCT[C/T]TGGCCATTTATTGAG | 4193 |
| rs547560670 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842480 | ACTTATTTTTTATAT[A/C]AGGTCACTCCGATGA | 4193 |
| rs547586341 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MDM2 | GRCh38.p7 | 12:68829591 | GCCAACAAGATGAAA[C/T]CATGTCTTTACTGAA | 4193 |
| rs547601727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68834536 | GAGGTCAGGAGTTCA[A/G]GACCAGCCTGGCCAA | 4193 |
| rs547696481 | snp | C/T | 1.65726e-05 | 0.00287855 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68836744 | GATCCTGAAATTTCC[C/T]TAGCTGTAAGTATAC | 4193 |
| rs547747517 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828237 | GATGAGCTCTTATAT[C/T]TTAAAGTTTGGTTTT | 4193 |
| rs547758987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68819719 | TGGTCTTGAGCTCCA[A/G]GCCTCGGGTGATCTG | 4193 |
| rs547819048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828464 | TACCAGCTACTCGGG[A/G]GGCTGAGGTTGAGGT | 4193 |
| rs547866305 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828677 | TTTTGAACTAATTTT[A/G]TTGAAACTAAGTTTC | 4193 |
| rs547991505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68822055 | AGAGACGGTGTTGCT[A/G]TGTTGCCCAGGCTAG | 4193 |
| rs548037175 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830522 | ATACAGTGGTAGTCA[A/G]GGTAGATATGGTTCT | 4193 |
| rs548043833 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68820510 | AATAAAAGTATGATA[A/C]ATTTATTAGAAGTAC | 4193 |
| rs548066631 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827883 | GGCCTGTAATCCCAG[A/C/T]ACTTTGGGAGGCTGA | 4193 |
| rs548359008 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68817803 | ATTATTCTTTTTTTT[G/T]TTTGTTTGTTTTGAG | 4193 |
| rs548394193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68811055 | TTTTTAGTAGAGATG[C/G]GGTTTTTCCATGTTG | 4193 |
| rs548467550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813104 | CCTGGGTTGTTATCT[C/T]TGATCTGTTCTTAAT | 4193 |
| rs548516834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68832626 | AAGCAATCCTTCCTC[C/T]TCAGCCTTGAGAGTT | 4193 |
| rs548551423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68811650 | TGGTCTGTTGCCCAG[A/G]CTGGAGTGCAGTGGC | 4193 |
| rs548627051 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840632 | TGGCTCAGCCTCTGG[A/G]GCAGCTGGGATTACA | 4193 |
| rs548781303 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841546 | CTAGATTACATCAGG[C/T]CCTTTTTCACACACA | 4193 |
| rs549018020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828631 | GTGTTCTGCTGTAAC[A/G]GTTGGACAGATTCAA | 4193 |
| rs549137166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68817199 | TTAAACCTGCTTCCC[C/T]ATTTATAAAATAGGG | 4193 |
| rs549163249 | snp | C/T | 0.000249715 | 0.0111712 | intron-variant | MDM2 | GRCh38.p7 | 12:68836616 | TTATTACTAGGAAGC[C/T]TTCTGATTGAAGGAA | 4193 |
| rs549173803 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824529 | TGTTAAGTTTGTTGT[A/G]TTTTATTTTTTTCCT | 4193 |
| rs549223522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68815951 | TTTATTAATGGTTCA[A/G]AGTCATTATTTTGAT | 4193 |
| rs549238695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823646 | TCTGCCCTCTTTTTC[A/T]TATGTTTTGCTAGAG | 4193 |
| rs549310763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68809354 | GAAGTGATAAACTAA[A/G]TTTCGTATACCTCAA | 4193 |
| rs549358378 | in-del | -/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823256 | AAATGTTTCCAAGGG[-/C]GGGTAGTAAAGGGTA | 4193 |
| rs549365233 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806683 | TGGCCAGGCTGGTCT[C/T]GAACTCCTAACCTCG | 4193 |
| rs549401674 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807642 | GAGTAACCGCTCCCC[G/T]CCCCGCCAACGGTAA | 4193 |
| rs549460311 | snp | A/C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822475 | GTGCAGGTTGGTTAC[A/C/G]TATGTATACCTGTTG | 4193 |
| rs549615967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68815431 | GGGGCCAGTTTCTTC[C/T]TCTTTTTTTTTTTTT | 4193 |
| rs549820222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68821307 | TGCCTCGGCCTTCCA[A/G]AGTCCTGGGATTACA | 4193 |
| rs549965230 | snp | A/C/G | 3.31286e-05 | 0.00406982 | intron-variant, missense | MDM2 | GRCh38.p7 | 12:68835925 | GAAGTTGAATCTCTC[A/C/G]ACTCAGAAGATTATA | 4193 |
| rs550036168 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841761 | AACAGAATTGTTATT[A/T]AAAAACTAACTGGAA | 4193 |
| rs550078504 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844008 | TTTTCTGAGGAGTAT[C/T]GGTAGCATAAATGTG | 4193 |
| rs550168792 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842368 | GTTAACAGGATGCAG[A/G]CATGGCAGAGGTTTC | 4193 |
| rs550218952 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840412 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA | 4193 |
| rs550219273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68831995 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 4193 |
| rs550268037 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840194 | CTGTTACCCAGGCTG[A/G]AGTGCAGTGGCGTGA | 4193 |
| rs550286670 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819023 | AGACGTGAGCCACTG[C/T]GCCTGGTCTGAATAT | 4193 |
| rs550292009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68825659 | TGTCTAAAAAAAAGA[A/G]AGAGAGAGAAAATAG | 4193 |
| rs550306872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832549 | ACAGTCTCTCACTCC[A/G]TTGCCCAGGCGGGAG | 4193 |
| rs550383295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827852 | AGGGTACTGAAGAGC[A/C]GGGCTTAGTGGCTTA | 4193 |
| rs550410140 | snp | G/T | 0.000298142 | 0.0122058 | intron-variant | MDM2 | GRCh38.p7 | 12:68809187 | TTTCCAGTTTTCATC[G/T]TGTCTTTTTTTTCCT | 4193 |
| rs550498816 | in-del | -/CCTG | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68830304 | CTATTCTTGTTACTT[-/CCTG]CCTGTATTATCTTTT | 4193 |
| rs550541822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827204 | TAAAAAAAGTCCTTT[C/T]AGAAATCTGTGATAC | 4193 |
| rs550557179 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68810331 | AAAAAAAAGAAAAGA[A/G]AAAGATTTTAGAGAA | 4193 |
| rs550575881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68818833 | CCTCCTGGGTTCAAG[C/T]GATTCTCTTGCCTCA | 4193 |
| rs550783815 | snp | C/G | 0.000399281 | 0.0141238 | missense | MDM2 | GRCh38.p7 | 12:68839797 | AAAGGAATAAGCCCT[C/G]CCCAGTATGTAGACA | 4193 |
| rs550793066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68812509 | TTACATTCCCCTCCC[C/T]CATGACAATTATTTT | 4193 |
| rs550803998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68817005 | CATTTCAGTTCACCT[C/T]TACCCTCATTCACTT | 4193 |
| rs550903035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68811929 | TTTTGTATATTTAAT[A/G]GAGACGGAGTTTCAC | 4193 |
| rs550946584 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68817763 | CATCTGAAAAAAAAA[A/T]TTTTTTAATATATAT | 4193 |
| rs551508465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835717 | GCAGCAGGCCCATCC[C/T]CCAACTGTTACACCC | 4193 |
| rs551520155 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | MDM2 | GRCh38.p7 | 12:68809078 | GCCACTTTTTCTCTG[C/T]TGATCCAGGTAAGCA | 4193 |
| rs551543680 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824881 | CCCACTGGAGTTTAT[A/G]GTTAGCCAACTCTCT | 4193 |
| rs551583182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68831108 | GCCTTGTTACTGATA[C/T]GGCTTTGAGGAGTAG | 4193 |
| rs551751524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813201 | GAAGATTGATAACAG[G/T]ACCCACTCTAAAGAT | 4193 |
| rs551771022 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | MDM2 | GRCh38.p7 | 12:68828258 | GTTTGGTTTTGACAG[-/A]AAAAAATTCCTAGAT | 4193 |
| rs551866771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68821228 | AATTTTTGTATTTTT[A/G]GTAGAGAGGGGGTTT | 4193 |
| rs551997224 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68815355 | TTCTGGGGCACACAG[G/T]AAGGTAGTGAAAGCT | 4193 |
| rs552020374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822216 | TGTGCATCACACACT[A/G]TAGTGTTTTATTAAT | 4193 |
| rs552035806 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808320 | GCTTTCGCAGCCAGG[A/C]GCACCGTCCCTCCCC | 4193 |
| rs552221341 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68827126 | GAGGTTGCAGTGTGC[C/T]GAGATTGTGCCATTA | 4193 |
| rs552274922 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830465 | TCATTTGTAGATATT[C/T]AAGTTTATACCAAAT | 4193 |
| rs552303956 | in-del | -/A | 0.485495 | 0.0839169 | intron-variant | MDM2 | GRCh38.p7 | 12:68812200 | TGTAAGCACAGTTAA[-/A]AAAAAAAAAAGTGAT | 4193 |
| rs552450983 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806554 | CTGCAACCTCTGCCT[C/T]CCGAGATCAAGCGAT | 4193 |
| rs552478533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68826503 | AAAATACAAAAATTA[A/G]CCAGGTGTGGTGGCA | 4193 |
| rs552498304 | snp | C/T | 0.000804923 | 0.0200453 | intron-variant | MDM2 | GRCh38.p7 | 12:68824468 | TCTAATGTAATATTA[C/T]TTGCAAATTGGAAAG | 4193 |
| rs552528660 | in-del | -/ATT | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68818601 | ACAAATATATGTATA[-/ATT]ATTATTTTTTATTGA | 4193 |
| rs552672525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68811892 | GGCATGAGCCACTGC[A/G]CCTGGCCCACACCTG | 4193 |
| rs552751768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68830669 | TTGATGAGTATCCAA[A/C]CTACAAGTTTGGTTA | 4193 |
| rs552754515 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68820483 | TTAAAAGTTGCTTTA[A/G]TTAAATATTGTAATA | 4193 |
| rs552860902 | snp | C/G | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806772 | CAGCCTATCACTTAT[C/G]TTTTCATGCTTACAT | 4193 |
| rs552864495 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841667 | GGGTTACATGGTTCC[C/T]AGCCTAGGTTTCAGA | 4193 |
| rs552952565 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68842173 | AAGAACTATGGAATA[A/G]AACTACTGATGCAGT | 4193 |
| rs553072649 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808544 | GGCTCTGACGGTGTC[C/T]CCTCTATCGCTGGTT | 4193 |
| rs553094498 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68815460 | TTTTTTTTTTTTTAT[G/T]TGACAGTTTCTCACT | 4193 |
| rs553196031 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68838883 | GTGTACTTACTCTAC[-/T]TTAGGAGAGACTGTT | 4193 |
| rs553289455 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845624 | TAAAGACTTTAAAAA[A/G]AATTCGATAGGCATT | 4193 |
| rs553404997 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819743 | TGATCTGCCGGACTC[A/G]GCCTTCCGAAGTGCT | 4193 |
| rs553476085 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68808015 | ACCCCCACCCCGCCT[C/T]ACAGCCCGCCGCGCC | 4193 |
| rs553477763 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823000 | CCCACCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 4193 |
| rs553553241 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806710 | CTCGTGATCCACCCA[A/C]CTCAGCCTCCCAAAG | 4193 |
| rs553696127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68821857 | TTTGTTTTACTTGTG[G/T]GTTTTTTTGTTTGTT | 4193 |
| rs553753538 | snp | A/C/G | 0.00319106 | 0.0398404 | intron-variant | MDM2 | GRCh38.p7 | 12:68835590 | CTTAATCTAGTTTCA[A/C/G]TATGCAGGATGGATC | 4193 |
| rs553773055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68836126 | ACTAACACATTGGTT[G/T]GTGGACTTGAGGATT | 4193 |
| rs553794444 | snp | A/G | 0.00023198 | 0.0107674 | missense | MDM2 | GRCh38.p7 | 12:68839476 | AAAAAACTATAGTGA[A/G]TGATTCCAGAGAGTC | 4193 |
| rs553809971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828681 | GAACTAATTTTATTG[A/G]AACTAAGTTTCTGTA | 4193 |
| rs553903277 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843059 | GATCTAGAAGCAGAT[A/G]TTATCTCAGTGCCTT | 4193 |
| rs553992635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828183 | TTAAGAATACCATAT[G/T]AGTAAATTAAACACT | 4193 |
| rs554126241 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68812800 | ATGCAACCATGCCCG[C/T]TGGTTTACATAGTAG | 4193 |
| rs554163760 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68826733 | AGTAATCTATCCTAA[-/G]GGATGTAATAAAAAA | 4193 |
| rs554198542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68818051 | CACCTGCCATGGCCT[C/T]CCAAAGTGCTGGGAT | 4193 |
| rs554229551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68833670 | CTACTCAGCCCCGCT[C/T]TTGTAATGCAGGAGC | 4193 |
| rs554239451 | in-del | -/TAT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818554 | TTGtatattatatat[-/TAT]aatatacatataata | 4193 |
| rs554303364 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68833452 | TTTTAAAAATATATA[G/T]AGAGAGAGATAATTT | 4193 |
| rs554321662 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806225 | TTTATTGTATCTCAA[A/T]CAGTCCTCTTATATT | 4193 |
| rs554432677 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841354 | CTCCTGTCTTGGCCT[C/T]GCAAAGTGCTAAGTA | 4193 |
| rs554448048 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825192 | CCAGCCTGGGTAACC[A/G]TGTGAGACTTCGTCT | 4193 |
| rs554667235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68839180 | TTGAGCCCTATGATA[C/T]ACTTTACCTTAGACA | 4193 |
| rs554752703 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841848 | ATGACAGGGTCAGCA[C/T]GTGGAATTCCAAGAT | 4193 |
| rs554953489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68831618 | GGCTTTTATGCTAGA[A/C]AAGAAATTTTTCTGG | 4193 |
| rs555116309 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831130 | GAGGAGTAGAGGAAC[A/G]CCAGGTTTTTTGTTT | 4193 |
| rs555268972 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68832035 | AGATCACGCCATTGC[A/T]CTGCAGCCTGGGCAA | 4193 |
| rs555416364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823224 | TAATGTCCAGGCATG[A/C]GTTCACTGTTAAGAT | 4193 |
| rs555451878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68814945 | CCATTTTTCTTTTTC[C/T]TCTCCAGCTATACTT | 4193 |
| rs555526459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68829718 | TTGCAGTGAGCTGAG[A/G]TTGTGCCACTGCACT | 4193 |
| rs555564659 | in-del | -/AGA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825656 | GACTGTCTAAAAAAA[-/AGA]GAGAGAGAGAAAATA | 4193 |
| rs555619516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822397 | TGAGCTTTAGATTGT[A/G]TCCTTTTTATTTCCT | 4193 |
| rs555651039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823725 | GCTCTCTGGATGTAA[G/T]ATTTTCTGTGAGCTA | 4193 |
| rs555674547 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68820572 | ATGTAAAGTTAAATA[C/T]CCTGTTAGATCAATT | 4193 |
| rs555775132 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68807150 | GTGTTTTTGGGTTTA[A/G]CTAACTCAATTCTTT | 4193 |
| rs555886264 | in-del | -/T | 0.000248682 | 0.0111481 | intron-variant | MDM2 | GRCh38.p7 | 12:68809192 | AGTTTTCATCGTGTC[-/T]TTTTTTTCCTTGTAG | 4193 |
| rs555927718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68836392 | CTATTTCCCTATTAT[C/T]TAATATCTCCATATT | 4193 |
| rs555959732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813262 | GCTTGCAATAAGCTC[A/G]TTGGATCAGTACGGT | 4193 |
| rs556059323 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807921 | ACAAACATAGCGCAA[A/C]GGCTAAAGGAGTGTC | 4193 |
| rs556068485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835460 | TAGTTGAAGACAGAC[A/G]AAGATGTTAATACAG | 4193 |
| rs556130361 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842718 | TAAAATTTTCTTTGC[A/T]GTAAAATATGCCCTT | 4193 |
| rs556178399 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843524 | TTGATTTATATTTAA[A/G]TATGAATCTTAAGCA | 4193 |
| rs556185791 | in-del | -/ATA | 0.00438332 | 0.0466095 | intron-variant | MDM2 | GRCh38.p7 | 12:68815768 | ATTTCTAATACAGTG[-/ATA]ATAATCTTATGAAAT | 4193 |
| rs556226842 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825833 | CCAGAATCTCGTACA[C/T]GCGGGCAGAAGACAG | 4193 |
| rs556531275 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MDM2 | GRCh38.p7 | 12:68819162 | AATATTGTGGGTTTA[A/G]GTTGCTGTATCCTTA | 4193 |
| rs556826845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68817349 | TCCAGAAACAGTATA[A/C]CACCACGTGGTAAAG | 4193 |
| rs556843821 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831011 | GGACCCCTATTTAAT[C/G]TATAGTTTTTGTTAA | 4193 |
| rs556848817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68826572 | GAGAATCGCTTGAAC[C/G]TGGGATGTGGAGGTT | 4193 |
| rs556880336 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840152 | TTTAAATGTAACTTA[G/T]TATTTTTTTTGAGAC | 4193 |
| rs556935394 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | MDM2 | GRCh38.p7 | 12:68832503 | GCCTATCTGATGCTT[-/A]AAAAAAATATATATT | 4193 |
| rs557046053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68809558 | GTTTGTTACGTGACT[G/T]ATTTTTTTTTCCTTT | 4193 |
| rs557066154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68825068 | TACAAAAAGTAGCTG[A/G]GCCTGGTGGCGCACA | 4193 |
| rs557100785 | snp | A/G | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806418 | AGCACAAACCCATTC[A/G]TTCACTTGATATTTA | 4193 |
| rs557114760 | in-del | -/GTT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829258 | TTGGAGTATAGAGTT[-/GTT]TGAGAATTTGAGAGT | 4193 |
| rs557154335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68831339 | TGTGACGGCTGGAGG[A/G]GGTGGTGTCTTATTT | 4193 |
| rs557228097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68838380 | TTTGTGGGATAAAAC[C/G]TTGGGAAAAGGAAGA | 4193 |
| rs557401057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68816220 | TGCTGCCTTTTCCCT[C/T]CCTAATATGTTAGTA | 4193 |
| rs557499913 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841838 | TCCTTCAAGAATGAC[A/G]GGGTCAGCATGTGGA | 4193 |
| rs557514764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68815518 | ATGATCACTGCTCGC[C/T]GCAGCCTGGACCTCG | 4193 |
| rs557585319 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68838210 | CATTTGTGAGGCAAT[C/G/T]TCAAAATGGTTACGG | 4193 |
| rs557729894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68829688 | GGAGAATCGCTCGAA[C/T]CCAGGAGTTGGAGGT | 4193 |
| rs557850283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68821446 | AATGCTCTTAGGCCA[A/G]GTGTGATGGCTCATG | 4193 |
| rs557881873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835612 | GGATGGATCTGAGGA[C/G]GAAATGTGCGTGGCA | 4193 |
| rs558013938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827999 | ATCCAGGCATGGTGG[C/T]GTGCACCTTTAATCC | 4193 |
| rs558166424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813425 | TTCCATGATACTTGC[A/C]TAATGATTAGATCCT | 4193 |
| rs558194253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827399 | CTTTTTCCTGTTTCC[C/T]TAAAAGAAAATACAG | 4193 |
| rs558380236 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807874 | ATTTGTCGCAGTTTC[C/T]ACCGCGGGCGGGAAG | 4193 |
| rs558423268 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841889 | TTCCTCTCAAGCTCC[A/G]TGTTTGGTCAGTGGA | 4193 |
| rs558455219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68833820 | ATTTAATGTTTCTTG[G/T]GATTTACCCCCTTAT | 4193 |
| rs558456326 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842509 | GAAAGGTGATTACAA[A/G]ATCATCTACATTGCT | 4193 |
| rs558459820 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814127 | GCACGATCTCAGCTC[A/G]CTGCAACCTCCGCCT | 4193 |
| rs558497033 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806902 | AAAGCCACATATTAA[A/G]TCTCTTAAGTTAATA | 4193 |
| rs558704965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832091 | ACAACAACAAAATCT[C/T]GTTTTTCAGGTTAAG | 4193 |
| rs558783479 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826412 | CCAGCACTTTGGAAG[G/T]CCGAAGCGGGTGGAT | 4193 |
| rs559130470 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840048 | ATATGTAGCTCATCC[C/T]TTACACCAACTCCTA | 4193 |
| rs559295677 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843820 | AACCAAGCAGAATCT[C/G]TTTTTTTTGGAGGTC | 4193 |
| rs559334299 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844742 | ATAATTAAGATTTTT[A/T]AAATCCTTAATAAGG | 4193 |
| rs559450213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68815321 | TTGTCTGATATAGTT[C/T]TCAGTTATAGGATCT | 4193 |
| rs559556958 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807514 | CCCATGTTGGCCAGG[C/T]TGGTCTTGAACTCCT | 4193 |
| rs559667921 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845763 | ATTCCAAAATTTCAC[A/C]TTTTGTTTGTTTTGT | 4193 |
| rs559708524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835693 | TCCCTCGGGAAGTCC[C/T]GGATCAGAGCAGCAG | 4193 |
| rs559737803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68820569 | CTAATGTAAAGTTAA[A/G]TATCCTGTTAGATCA | 4193 |
| rs559793922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68836503 | TGTGGGTAAGGATTT[C/T]TCTCTCCTCCATTTT | 4193 |
| rs559898453 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814505 | GCCTACATTTATAAT[A/C/T]GAAGGAAAAGCTAAA | 4193 |
| rs559913478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827646 | GAATATTTTGTTATA[G/T]GTACTTGAATGGTTT | 4193 |
| rs559989042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68828527 | TGCAGTGAGCCGAGA[C/T]TGTGCCTCTGTACTC | 4193 |
| rs560006776 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819011 | TGCTGGGATTACAGA[C/T]GTGAGCCACTGTGCC | 4193 |
| rs560024998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835028 | AGTTTATTAAAAAAC[A/G]TAAGTATCTATGACT | 4193 |
| rs560060614 | snp | C/T | 1.66407e-05 | 0.00288446 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813514 | CCTATAGTTCTGGGA[C/T]AATTTTGGAAGTATA | 4193 |
| rs560120495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68821209 | TATGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 4193 |
| rs560224238 | in-del | -/CTCTCT | 0.262883 | 0.249668 | utr-variant-3-prime, cds-indel, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843699 | ATTGTTGCTTCAAAA[-/CTCTCT]CTCTCTCTCTCTGTC | 4193 |
| rs560275937 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806542 | GATCTCCGCTCACTG[C/T]AACCTCTGCCTCCCG | 4193 |
| rs560334954 | snp | A/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844529 | TTTGGGCTAGCCACC[A/G]TACCACTTGTCAGCG | 4193 |
| rs560347295 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | MDM2 | GRCh38.p7 | 12:68836514 | TTTCTCTCTCCTCCA[-/T]TTTTTTCCCCCTTTA | 4193 |
| rs560456842 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841565 | TTTTCACACACAAAA[A/G]AATCCTTTATGGGAT | 4193 |
| rs560552112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68812372 | TAAAGTTAGACAGAG[A/G]ACCGGGGCATATTAA | 4193 |
| rs560630571 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821883 | TTGTTTTTGAGATGG[A/G]CTCTCACTCTGTCAC | 4193 |
| rs560645817 | snp | A/C | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68807417 | TTGTCCTGCCTCAGC[A/C]TCCGGAGTAGAGTAG | 4193 |
| rs560742868 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68817871 | GGCATGATCTTGGCT[-/CA]CTGCAACCTCCGTCT | 4193 |
| rs560912948 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MDM2 | GRCh38.p7 | 12:68830144 | AATTCTTCCAATGTC[A/G]CCCACGGAAACCAAA | 4193 |
| rs560949862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823649 | GCCCTCTTTTTCTTA[C/T]GTTTTGCTAGAGTGA | 4193 |
| rs560992079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68810712 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 4193 |
| rs561233441 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840206 | CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT | 4193 |
| rs561237872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823989 | TGGATACTTTTTCAC[A/G]TGGCGTTTTCTTGGT | 4193 |
| rs561241178 | in-del | -/AAATA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834742 | ATTCCATCTCAAAAT[-/AAATA]AAATAAGTTAAATGA | 4193 |
| rs561302870 | snp | A/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843596 | ATATGTGAATTGTAT[A/G]TACTTAGGTGAAGAC | 4193 |
| rs561339574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68810151 | AACCTGTCTCTACTA[A/C]AAATACAAAAATTAG | 4193 |
| rs561486713 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68832077 | TTCCATCTCAAACAA[C/T]AACAACAAAATCTCG | 4193 |
| rs561547377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68815309 | GTAGTGTATGTATTG[C/T]CTGATATAGTTCTCA | 4193 |
| rs561760184 | snp | C/G | 6.63801e-05 | 0.0057607 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68828862 | TGAAAGCCTGGCTCT[C/G]TGTGTAATAAGGGAG | 4193 |
| rs561787423 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68808102 | CCCAATTGGCGGAAG[C/G]GGGGCCGGTTGTGTG | 4193 |
| rs561796865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822677 | AATTACTTATTTGCA[C/G]TCTGAGTTTGGTTTA | 4193 |
| rs561849151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68814675 | GTACAGTATACTGAT[C/G]TTTCTGGGATAGAGG | 4193 |
| rs562054679 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808740 | GGGGTGGGGGTGGTT[C/T]GGAGGTCTCCGCGGG | 4193 |
| rs562106728 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | MDM2 | GRCh38.p7 | 12:68833084 | TGAGCCGAGATGGTG[C/T]CACTGCACTCCAGCC | 4193 |
| rs562150054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68833945 | ATTCTAATCTGATTG[A/G]TAGTAGAGCCCTTGT | 4193 |
| rs562150111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68826277 | CAGTGCTAATAACTT[G/T]TGTATTAGCACTGAT | 4193 |
| rs562153503 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843267 | AGGACCTCCAAAGGT[A/C]AAAGTACTAATCCCT | 4193 |
| rs562203530 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806525 | CTGGACTGCAGTGGC[A/G]CGATCTCCGCTCACT | 4193 |
| rs562220494 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843763 | TAGTTTACCTGTGGA[C/G]GTCCTCCAAGCATTA | 4193 |
| rs562429730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68826862 | AAGAACTCACGTGCA[G/T]AACTTGTGATCTCGA | 4193 |
| rs562537686 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821480 | ATAATTCCAGCACTT[A/T]AGGAGGCTAAGGCAG | 4193 |
| rs562538244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68829753 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA | 4193 |
| rs562555186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68821147 | CCGCCTCCCAGGTTC[A/C]AGCAATTCTTCTGCC | 4193 |
| rs562580143 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841479 | TGTTATCTGTGAAAA[C/T]AGCCACCATTTACCC | 4193 |
| rs562620775 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823432 | TCTCTTTTAGTGAAT[G/T]GTACCACTCATTTAT | 4193 |
| rs562716967 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813037 | GAAATGTAGACTAAC[A/T]AAGAGGCAGCATGAT | 4193 |
| rs562818818 | snp | A/G | 0.000281688 | 0.0118644 | missense | MDM2 | GRCh38.p7 | 12:68839469 | GATTGTAAAAAAACT[A/G]TAGTGAATGATTCCA | 4193 |
| rs562827930 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68820478 | TCTCTTTAAAAGTTG[A/C]TTTAATTAAATATTG | 4193 |
| rs563025519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68825377 | AAGAGATAAGGGCCG[A/G]GCGCAGTGGCTCACG | 4193 |
| rs563076720 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MDM2 | GRCh38.p7 | 12:68812242 | ATAATTCAATTCTAT[A/G]TGTATTTTAAATTTT | 4193 |
| rs563309568 | snp | C/G | 2.17484e-05 | 0.00329753 | intron-variant | MDM2 | GRCh38.p7 | 12:68836561 | TTGATATTGTCTAAG[C/G]CTTTCTCATATATTG | 4193 |
| rs563323306 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | MDM2 | GRCh38.p7 | 12:68809085 | TTTCTCTGCTGATCC[A/G]GGTAAGCACCGACTT | 4193 |
| rs563344274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68829195 | AATGTCACTGTATGT[A/G]TTAGAGAATATTTGT | 4193 |
| rs563350254 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68833786 | TTGCAGACCCCTACC[A/G]TAGAGTATGTTTTCT | 4193 |
| rs563422638 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MDM2 | GRCh38.p7 | 12:68809972 | TATTACAGATAGTGC[C/T]GCTTTGTACATGCAT | 4193 |
| rs563556868 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810755 | CGTGAGTCACTGCGC[C/T]TGGCCTCTTTTATTA | 4193 |
| rs563736171 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818567 | ATTATAATATACATA[C/T]AATATAATTATATAT | 4193 |
| rs563762756 | snp | C/G | 1.65699e-05 | 0.00287831 | missense, upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68813610 | TGGTGCACAAAAAGA[C/G]ACTTATACTATGAAA | 4193 |
| rs563781093 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810919 | TGCCCAGGCTGGAGT[C/G]CAATGGCGAGATCTT | 4193 |
| rs563854606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823637 | TTTCCTGCCTCTGCC[C/G]TCTTTTTCTTATGTT | 4193 |
| rs563860571 | snp | A/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843941 | CTTTGGAGGTCCTCA[A/G]AGCATTATTGGAGTT | 4193 |
| rs563869852 | snp | A/G | | | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68808109 | GGCGGAAGCGGGGCC[A/G]GTTGTGTGCGCGCGC | 4193 |
| rs563930650 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823855 | GTGATAAGGGAATGA[C/G/T]AGCATGAGTCCTGCT | 4193 |
| rs563998034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822887 | GTGGGATTACAGGTG[C/G]CTGCCACCACGTCCG | 4193 |
| rs564205288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68827809 | GAAATGGAAACTTTT[C/T]ACTGGTTTTGATTTC | 4193 |
| rs564242663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68821252 | GGGGTTTCAGCATGT[G/T]GGCCAGGCTGGTCTC | 4193 |
| rs564386941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68820395 | TTAATTTTGAGCATC[A/G]TGGATAAATACCATA | 4193 |
| rs564511414 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840387 | CTGACCTCGTGATCC[A/G]CCCACCTCGGCCTCC | 4193 |
| rs564545272 | snp | A/C/T | 0.00159649 | 0.0282165 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841396 | GTTAGCCACCACACC[A/C/T]GGCTGTAAAAATGTA | 4193 |
| rs564577782 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68809154 | ATATATGATGTATTT[C/T]CCACAGATGTTTCAT | 4193 |
| rs564618329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68812916 | TAATCTAGTTGGCAG[G/T]CTCCTTGCATACAGG | 4193 |
| rs564636477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68834381 | CCGGAGGCGGAGGTT[G/T]CAGTGAGCTGAGATC | 4193 |
| rs564640759 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843176 | ATTGCACACAAAACC[A/T]CTTTTAATGGGTACA | 4193 |
| rs564678837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835092 | TATTACAAGTGTTGT[A/G]TCTTGTTACGTGTAT | 4193 |
| rs564748601 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MDM2, CPM | GRCh38.p7 | 12:68842260 | AAGAAAAAGGACTAC[A/G]GAAAGTTCAGGACAT | 4193 |
| rs564833664 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MDM2 | GRCh38.p7 | 12:68832994 | AGCCGGGCGTGGTGG[C/T]GGGCACCTATAGTCC | 4193 |
| rs565031548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68825601 | GAGCTTACAGTGAGC[C/T]GAGATCACGCCACTG | 4193 |
| rs565052795 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829894 | AGATGTCACTGAAAG[A/C]AGTTTGGTAAAAAAT | 4193 |
| rs565101533 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68819508 | CTTTTTTTTCTTCCC[G/T]GAGTCGGAGTTTTGC | 4193 |
| rs565113080 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823827 | TTCTGAAGTATCTGC[A/G]GGGAAGAATGCAGTG | 4193 |
| rs565122475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68811439 | CAAATATATTCCTAT[A/G]TTTTCTTCTAGATTT | 4193 |
| rs565171100 | snp | A/G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831473 | ACATTTTACACACGG[A/G/T]GTTATGTGGGGGCGG | 4193 |
| rs565220751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68826175 | TTTTGGTGATTTTTA[A/G]CTTTACAGATAGTAA | 4193 |
| rs565234740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68831042 | AGTTATATCAGAATT[C/T]TAGCTGAATGATATT | 4193 |
| rs565271818 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68824079 | TTGTTTCTCAGACAC[C/T]CCCTGTCCCTACCAA | 4193 |
| rs565282578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68810839 | CTCTAGTTTCTTGGT[C/G]AGGCTGGGCACCTTT | 4193 |
| rs565638469 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844154 | GTTCTTTATAGTACA[C/T]GTGTTGAAAATAAAT | 4193 |
| rs565710743 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68829676 | GGGCCTGAGGCAGGA[G/T]AATCGCTCGAACCCA | 4193 |
| rs565715862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68836211 | AGTCAATAGACCTCA[A/G]TGAACATGCTTATTA | 4193 |
| rs565745776 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830546 | TGGTTCTTGCCTTCA[C/T]TGGGAGATAGATCAT | 4193 |
| rs565746946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823130 | AACCTATTATGTACA[A/C]CTTAAGAAAATTAGT | 4193 |
| rs565817617 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843287 | TACTAATCCCTTTGG[C/T]CATTTATTGAGAGAG | 4193 |
| rs565905084 | in-del | -/TAAAA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826648 | AGTGAGACTCCCTCT[-/TAAAA]AAAAAAAAAAAAGAA | 4193 |
| rs565952485 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MDM2 | GRCh38.p7 | 12:68827950 | AGTGTGGCCAACATG[A/G]TGAAACCCTGTCTCT | 4193 |
| rs565963964 | snp | A/G/T | 0.000382473 | 0.0138237 | intron-variant | MDM2 | GRCh38.p7 | 12:68836764 | TGTAAGTATACATCT[A/G/T]CTTTTTTAAGAAATA | 4193 |
| rs566039595 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | MDM2 | GRCh38.p7 | 12:68827298 | TTTGATCCCTAGGAG[G/T]TAAGAGTTTTTTTTT | 4193 |
| rs566147927 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68834562 | GCCAACATGGTGAAG[C/G]CCTGCCTCTACTAAA | 4193 |
| rs566224821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68826415 | GCACTTTGGAAGGCC[A/G]AAGCGGGTGGATCTC | 4193 |
| rs566297443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68814792 | ATTTTCAGTGACAGA[C/T]TGAGCAACCTTAGGC | 4193 |
| rs566371672 | snp | A/G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68812328 | AAATCTGTTTTTAAG[A/G/T]CATCCCCAATGGGGG | 4193 |
| rs566373856 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842490 | TATATAAGGTCACTC[C/T]GATGAAAGGTGATTA | 4193 |
| rs566407895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822104 | AGATATTCTCACCTC[A/G]GCCTCCCAAAGTTTA | 4193 |
| rs566411803 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814086 | GAGACGAAGTCTCGC[C/T]CTGTCACCCAAGCTG | 4193 |
| rs566483560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68812661 | CTCAGTGTGGCCCAG[A/G]CTGGTCTTGAACACC | 4193 |
| rs566606515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813111 | TGTTATCTCTGATCT[A/G]TTCTTAATTACCCTT | 4193 |
| rs566613854 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815516 | GCATGATCACTGCTC[A/G]CTGCAGCCTGGACCT | 4193 |
| rs566633106 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841044 | AAAGACAGGGTTTCA[C/T]CATGTTAGCCAGGCT | 4193 |
| rs566655723 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822656 | TTATTGAGATGGAAA[C/T]TTACAAATTACTTAT | 4193 |
| rs566796799 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839974 | TAGATTTCTTCTCTT[C/T]AGTATAATTGACCTA | 4193 |
| rs566833165 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819854 | TGAAAGTCAAGATTA[C/T]AATCAAATTCCTATT | 4193 |
| rs566898996 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821968 | TCAAATGATCCTCCC[A/C]CTCAGCCTCCCAAGT | 4193 |
| rs566963658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68833492 | TGGGGCATTCTTTTG[C/T]GAACATTAGCCAAAA | 4193 |
| rs567029541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832658 | GCTGGGACTACAGGT[A/G]TGCACCACCACACCT | 4193 |
| rs567107918 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825547 | AGTCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA | 4193 |
| rs567227090 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MDM2 | GRCh38.p7 | 12:68838932 | ATCTGTTTTGTGTAT[A/G]ATTGAGACATATAAC | 4193 |
| rs567264287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68831210 | GAGCAGAGCGTTTAA[C/T]AGGCAAGAAGGGAGA | 4193 |
| rs567289598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822941 | AGAAAGGGTTTCACC[A/G]TGTTGACCAGGCTGG | 4193 |
| rs567379479 | in-del | -/TTTG | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840507 | TTAGTTTTTTGTTTT[-/TTTG]TTTGTTTGTTTGTTT | 4193 |
| rs567400467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68829504 | TGGGTGCGGTGGCTC[A/C]TGCCTGTAATCAGTA | 4193 |
| rs567417100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822449 | TAAGTTTTAGGGTAC[A/G]TGTGTACAATGTGCA | 4193 |
| rs567490349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68817878 | TCTTGGCTCACTGCA[A/G]CCTCCGTCTCCTGGG | 4193 |
| rs567556601 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MDM2 | GRCh38.p7 | 12:68815436 | CAGTTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 4193 |
| rs567563488 | snp | C/T | 8.49394e-05 | 0.00651632 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824369 | TTCTCTCAGAATCAT[C/T]GGACTCAGGTACATC | 4193 |
| rs567570604 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845957 | ACCTCCCCCGACCCC[A/G]CTGCCACCCGCCCTG | 4193 |
| rs567592541 | snp | A/T | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68812833 | ATGCTTTTTACTTGG[A/T]TAGAACCATTTGTAT | 4193 |
| rs567942092 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MDM2 | GRCh38.p7 | 12:68816142 | ACTAAGTGGCTCCAG[A/C]CCACTGCCATATTTT | 4193 |
| rs567979044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68809361 | TAAACTAAATTTCGT[A/G]TACCTCAATTGTAGC | 4193 |
| rs568063893 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807643 | AGTAACCGCTCCCCT[C/G]CCCGCCAACGGTAAC | 4193 |
| rs568094553 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843527 | ATTTATATTTAAATA[C/T]GAATCTTAAGCAAAA | 4193 |
| rs568134347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | MDM2 | GRCh38.p7 | 12:68835954 | TAGCCTTAGTGAAGA[A/C]GGACAAGAACTCTCA | 4193 |
| rs568204247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68833610 | TCTGTAAAGAGCCAC[A/G]TAGTTAATTATTTGG | 4193 |
| rs568315953 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842402 | AAAATCTCATTATCT[A/C]TAACCATTTCTATAT | 4193 |
| rs568482254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68825668 | AAAAGAGAGAGAGAG[A/G]AAATAGTTGACAGAG | 4193 |
| rs568513324 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841316 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA | 4193 |
| rs568555782 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841835 | TTTTCCTTCAAGAAT[C/G]ACAGGGTCAGCATGT | 4193 |
| rs568587608 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68832608 | CCTCAACCTCCTGGG[A/T]TCAAGCAATCCTTCC | 4193 |
| rs568727776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68817978 | TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACG | 4193 |
| rs568782707 | in-del | -/T | 0.0019964 | 0.0315312 | intron-variant | MDM2 | GRCh38.p7 | 12:68818759 | TATTGAATCTTCTAT[-/T]TTTTTTTCTTTTTTT | 4193 |
| rs569037074 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68810397 | TGCTACTGGTAACTT[C/G]CTCACCAAAAGGCTC | 4193 |
| rs569066290 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819194 | TCCCAAGGATGAAAA[A/C]AGATAGTTGGGATTC | 4193 |
| rs569069451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68822515 | TCTTTAAGAAATTGT[A/G]TGATAGCTAAATATA | 4193 |
| rs569072655 | in-del | -/A | 0.0107246 | 0.0724382 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843211 | TAAATTTGAAGGAAT[-/A]AGTTCTAGCTGAAGT | 4193 |
| rs569078958 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815955 | TTAATGGTTCAAAGT[C/G]ATTATTTTGATTATT | 4193 |
| rs569083510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68812516 | CCCCTCCCCCATGAC[A/T]ATTATTTTTCTCAAG | 4193 |
| rs569147174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68832019 | AGGTTGCAGTGAGCT[A/G]AGATCACGCCATTGC | 4193 |
| rs569324904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68817129 | ATCTTATAAACCAGT[A/G]TTTGAAACCTAGCCC | 4193 |
| rs569466336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68839134 | TGCTGTTTACAGTGA[C/G]TATTTTATATAAAAC | 4193 |
| rs569630411 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830337 | TCTCTTCCAAAGCAG[C/T]GATTGTATGAACGCA | 4193 |
| rs569630923 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835561 | GGAAAATAATGTAGT[A/G]ATAACCTTGAAACCT | 4193 |
| rs569665159 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845285 | ATGTAGCCAGCTTTC[A/G]ATTATATGTAAGAGG | 4193 |
| rs569795510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835730 | CCCCCAACTGTTACA[A/C]CCTGCTGGCAGCAGC | 4193 |
| rs569951421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68822217 | GTGCATCACACACTA[C/T]AGTGTTTTATTAATA | 4193 |
| rs570054755 | in-del | -/AAA | 0.205505 | 0.246009 | intron-variant | MDM2 | GRCh38.p7 | 12:68812198 | TATGTAAGCACAGTT[-/AAA]AAAAAAAAAAGTGAT | 4193 |
| rs570072645 | in-del | -/A | 0.00438332 | 0.0466095 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807811 | CTTAATATATTAAAC[-/A]GCTGTTAATTTTGGT | 4193 |
| rs570239541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813228 | AGATTTATTCATTTC[A/T]CTTTGATTCTCTAAG | 4193 |
| rs570276654 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808329 | GCCAGGAGCACCGTC[C/T]CTCCCCGGATTAGTG | 4193 |
| rs570351913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68814931 | GGCAGGAAGAGCTTC[C/G]ATTTTTCTTTTTCCT | 4193 |
| rs570388582 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807876 | TTGTCGCAGTTTCCA[C/T]CGCGGGCGGGAAGTG | 4193 |
| rs570518030 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834808 | GCAAGTGTAGAATAA[A/G]CCATATCCCGACTTC | 4193 |
| rs570742144 | in-del | -/T/TT | 0.403509 | 0.197319 | intron-variant | MDM2 | GRCh38.p7 | 12:68832689 | GCTAATTTTTTTTAC[-/T/TT]TTTTTTTTTTTCAGA | 4193 |
| rs570820909 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819628 | TCCTGAGTAGCTGGG[A/G]TTACAGGCATGCGCC | 4193 |
| rs570934539 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845351 | GATATCTGAAAGCAC[C/T]AGCACTTGGAAGGTG | 4193 |
| rs570992498 | snp | A/G | 6.62559e-05 | 0.00575531 | missense | MDM2 | GRCh38.p7 | 12:68839574 | CAGCCATCAACTTCT[A/G]GTAGCATTATTTATA | 4193 |
| rs571026325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68819790 | GTGAGCCACTGCGCC[C/T]GGCCTCTGTTAATAC | 4193 |
| rs571231857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68824985 | AGGCCGAGGCTGGCG[G/T]ATCACGAGGTCAGGA | 4193 |
| rs571233042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68831330 | CCAGTTTTATGTGAC[A/G]GCTGGAGGGGGTGGT | 4193 |
| rs571331019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68809525 | TTCCATTACATTGTT[A/G]AGCGTGGTTGAAGTT | 4193 |
| rs571386391 | in-del | -/TAG | 0.00438332 | 0.0466095 | utr-variant-3-prime, cds-indel, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844401 | AATGATGTTGCAAGT[-/TAG]TAGGAGTAAGAAATG | 4193 |
| rs571568316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68810239 | CGCTTGAACCCAGGA[A/G]GCAGAGGTTGCGGTG | 4193 |
| rs571603790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68818684 | TTGGTATATATGGTT[C/T]AATTTTATAAATTTT | 4193 |
| rs571895931 | in-del | -/T/TT | 0.189261 | 0.242509 | intron-variant | MDM2 | GRCh38.p7 | 12:68830060 | CTTAAAATATTATGA[-/T/TT]TTTTTTTTTTTACAA | 4193 |
| rs571993476 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828184 | TAAGAATACCATATG[A/T]GTAAATTAAACACTT | 4193 |
| rs572121311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835035 | TAAAAAACATAAGTA[C/T]CTATGACTCGAGACA | 4193 |
| rs572192142 | snp | A/G | 0.0170251 | 0.090679 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843609 | ATATACTTAGGTGAA[A/G]ACAATAAAATCAACT | 4193 |
| rs572274502 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826528 | GTGGCAGGCGCCTGT[A/T]ATCCCAGCTACTTGG | 4193 |
| rs572354416 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834508 | TTGGGAGGCCAAGGC[G/T]GTTGAATTGCTTGAG | 4193 |
| rs572446251 | snp | A/G | 0.000151926 | 0.00871434 | intron-variant | MDM2 | GRCh38.p7 | 12:68820282 | ACAAATTTTTATTCT[A/G]AAATGTACATCTCTT | 4193 |
| rs572484209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68821091 | CTTGCTCTGTCACTC[A/G]GGCTGGAGTGTAGTG | 4193 |
| rs572660729 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841868 | AATTCCAAGATACCT[C/T]TTGACTTCCTCTCAA | 4193 |
| rs572685622 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806402 | GTCTCTGAACTTTTA[C/T]AGCACAAACCCATTC | 4193 |
| rs572706510 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843090 | TTGCAATTTGTTGTG[A/T]GGGTTTTTTTTTTTT | 4193 |
| rs572822432 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841371 | CAAAGTGCTAAGTAG[C/G]ATTACAGGCGTTAGC | 4193 |
| rs572890302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68811418 | CTCTCCTGTCCCAAG[A/T]TCTTGCAAATATATT | 4193 |
| rs572951563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832944 | ATCCTGGCTAACACG[G/T]CGAAACCCCGTCTCT | 4193 |
| rs573188156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68824844 | TTTTCTGGCTGACTA[C/T]AGCAGGCACAGTTTA | 4193 |
| rs573363279 | snp | C/T | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814544 | AGAAGTTTGTGAAAA[C/T]AAGAATAGAATTTTT | 4193 |
| rs573389701 | snp | C/T | | | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845644 | CGATAGGCATTTTCA[C/T]GTTTCAGTCCTACAA | 4193 |
| rs573439253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832047 | TGCACTGCAGCCTGG[A/G]CAACGAGAACGAAAT | 4193 |
| rs573441053 | snp | A/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843087 | CTTTTGCAATTTGTT[A/G]TGTGGGTTTTTTTTT | 4193 |
| rs573686686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823731 | TGGATGTAATATTTT[A/C]TGTGAGCTAGAAATC | 4193 |
| rs573767450 | in-del | -/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808787 | CACGGGGGCCGGGGG[-/C]TGCGGGGCCGCTTCG | 4193 |
| rs573876805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68816420 | CTCTGTTGCTTAAGC[C/T]GGAGTGCAGTGGCGC | 4193 |
| rs573998914 | snp | A/C | 0 | 0 | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807949 | GTCACAGCGCCAAAC[A/C]TTGCTGGCTCCGCGC | 4193 |
| rs574082516 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68807344 | CCCTGTCGCCCAGGC[G/T]GGAGTGCAATGGCAT | 4193 |
| rs574107103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68836394 | ATTTCCCTATTATTT[A/G]ATATCTCCATATTAG | 4193 |
| rs574139141 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845371 | CTTGGAAGGTGTTCA[C/G]AAGTAACAAATTATA | 4193 |
| rs574224922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68837144 | TTTTTAGTAGAGATG[A/G]GGTTTCACCATGTTG | 4193 |
| rs574272843 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844706 | CCCCTAAGCCAGACG[G/T]GGACTAGCTTTTGGC | 4193 |
| rs574301581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68821644 | AGGAGGATTTTTTGA[C/G]GCTGGGAGGTCAGGA | 4193 |
| rs574327808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68829005 | GTCCTAATAAGGATA[C/T]GGATAGAATGTACAT | 4193 |
| rs574372370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827571 | ATGGTCTAATCTTGA[G/T]AGTCTTTTTATTGAG | 4193 |
| rs574398693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68834968 | AGATGAGCAGCTACA[G/T]AATTTTTTTTAATTG | 4193 |
| rs574489649 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822881 | GAGTAGGTGGGATTA[C/T]AGGTGCCTGCCACCA | 4193 |
| rs574499684 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841987 | GATGTTCATCTGCAG[C/T]TGTTGCAAGGTGTTC | 4193 |
| rs574592221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68830834 | GCCTCCTGAGTAGCT[A/G]GGATTACAGGCTCCC | 4193 |
| rs574659973 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829616 | ACTGAAAATACAAAA[A/C]TTAGCCAGGCGTGGT | 4193 |
| rs574661915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68835528 | TGTTTTTCCTTTATG[C/T]AGTGGGGTTTTGAAC | 4193 |
| rs574787328 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810806 | AAAGGTACTGTACCA[C/T]TGTTTAAATTCATTT | 4193 |
| rs574856994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68825961 | TTTCAAATGAGTTTA[A/G]AAGTTAAATGAAAAA | 4193 |
| rs574926092 | snp | A/G | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841307 | TCCCTGTGTTGCCCA[A/G]GCTGGTCTCGAACTC | 4193 |
| rs574961306 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68832353 | TCTGTCATCTTTGCA[G/T]CCTCAGATTCCATTT | 4193 |
| rs574969023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68825419 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 4193 |
| rs574969087 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838131 | ATGAGCTGTGAAAAA[C/T]CCCCTTCTATAACTT | 4193 |
| rs574970941 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68832897 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACAAGG | 4193 |
| rs575060289 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834869 | ATATATGCTCCTACC[C/T]TTAGCCACTGACAGC | 4193 |
| rs575072191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68812250 | ATTCTATATGTATTT[A/T]AAATTTTTCAATTGT | 4193 |
| rs575195877 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68837276 | CATTTTGATGTTATT[G/T]TGGAAAATTTCAGTG | 4193 |
| rs575263786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68838400 | GAAAAGGAAGAAGCA[C/T]TGAGCAGTTACAAAG | 4193 |
| rs575386269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68831496 | GGGGGCGGCCATGCT[C/G]TTAGGTACCTGATGG | 4193 |
| rs575672176 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845614 | AGCTCTCCTTTAAAG[A/G]CTTTAAAAAAAATTC | 4193 |
| rs575832794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68817922 | CCTGCCTCGGCTTCC[C/G]GAGTAGCTGGGATTA | 4193 |
| rs576062594 | snp | A/G | 3.31807e-05 | 0.00407299 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828801 | AATTATCTGGTGAAC[A/G]ACAAAGAAAACGCCA | 4193 |
| rs576191034 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825884 | GCAGAGGTGGAACTA[C/G]AACAAATGGTAGTTA | 4193 |
| rs576221167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68828295 | GTTAATAAAAACTTT[A/G]TTAGATAGATTAAAT | 4193 |
| rs576267193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68823190 | AATTAATCTATGATA[A/G]TGCATAATTTCAAAA | 4193 |
| rs576278384 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823517 | TATCAAATACCAGGT[C/T]TTGTTGGTTTTTACC | 4193 |
| rs576457443 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841913 | CAGTGGAGGCCCATC[C/T]GAGCTCAGCACTGAG | 4193 |
| rs576507909 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814133 | TCTCAGCTCACTGCA[A/G]CCTCCGCCTCCTAGA | 4193 |
| rs576507921 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806463 | CTATCACTTATCTCT[C/T]TTTTTTTTTTTTTCT | 4193 |
| rs576585841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68834818 | AATAAGCCATATCCC[A/G]ACTTCTAGACTTTTT | 4193 |
| rs576737538 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MDM2 | GRCh38.p7 | 12:68835628 | GAAATGTGCGTGGCA[A/G]CCGGCTCCGGGATGG | 4193 |
| rs576798328 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806967 | ACTATGTTTAAGGAA[A/G]TTTCCTTTCTGGTAG | 4193 |
| rs577001887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68827438 | GATTTGGTAGGACTT[C/T]GTATAATATGTATAC | 4193 |
| rs577010303 | snp | A/G | 3.31895e-05 | 0.00407353 | intron-variant | MDM2 | GRCh38.p7 | 12:68820416 | AAATACCATAAAAAC[A/G]TTTTAAAGACATTTT | 4193 |
| rs577096858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68818135 | GGTTTAGCACAGGCA[A/G]TCCGTGTTGAGCCTT | 4193 |
| rs577183596 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MDM2 | GRCh38.p7 | 12:68821116 | GTAGTGGCATGATTT[C/T]GACTCACTGCAACCT | 4193 |
| rs577207196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68825276 | TTAGTCACCTTAACA[A/G]TTAAATTTTTAAATT | 4193 |
| rs577265341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68832105 | TCGTTTTTCAGGTTA[A/G]GTCCCTAGTTGTGAA | 4193 |
| rs577358858 | snp | C/G/T | 0.00398763 | 0.0445073 | intron-variant | MDM2 | GRCh38.p7 | 12:68833666 | ACAGCTACTCAGCCC[C/G/T]GCTCTTGTAATGCAG | 4193 |
| rs577444865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68825835 | AGAATCTCGTACATG[C/T]GGGCAGAAGACAGGA | 4193 |
| rs577643187 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845454 | AGGCGTGTTCAGTAA[C/G]TTATTCATAATGCAT | 4193 |
| rs577673497 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68837373 | AACTTTTTTTTTTTT[C/G]AATTGAGATAGGGTC | 4193 |
| rs577674957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MDM2 | GRCh38.p7 | 12:68816442 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAGCCTC | 4193 |
| rs577736495 | snp | C/T | | | missense, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809236 | ACCAACATGTCTGTA[C/T]CTACTGATGGTGCTG | 4193 |
| rs577942747 | snp | A/C/T | 6.65174e-05 | 0.00576671 | missense | MDM2 | GRCh38.p7 | 12:68839310 | TGCAATGAAATGAAT[A/C/T]CCCCCCTTCCATCAC | 4193 |
| rs578139052 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MDM2 | GRCh38.p7 | 12:68823336 | GCTCAAAGTCTGTAT[A/T]TCCAACTACAAATGA | 4193 |
| rs578154054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MDM2 | GRCh38.p7 | 12:68830732 | TATTGAGATTGAGTC[C/T]CTCTGTCTCCCAGGC | 4193 |
| rs745346034 | snp | A/G | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806328 | TTCAAGACACAAAAT[A/G]TGTGTGATCTCTGAG | 4193 |
| rs745347613 | snp | C/T | 1.66344e-05 | 0.0028839 | intron-variant | MDM2 | GRCh38.p7 | 12:68836763 | CTGTAAGTATACATC[C/T]ACTTTTTTAAGAAAT | 4193 |
| rs745366647 | snp | A/T | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813101 | GGACCTGGGTTGTTA[A/T]CTCTGATCTGTTCTT | 4193 |
| rs745409858 | in-del | -/AAC | | | intron-variant | MDM2 | GRCh38.p7 | 12:68832074 | AATTCCATCTCAAAC[-/AAC]AACAACAACAAAATC | 4193 |
| rs745463130 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818716 | AAAATAACTATATTG[A/G]TATATTGGTGATTTC | 4193 |
| rs745545777 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68836531 | TTTTTCCCCCTTTAC[A/T]CTCACTTACTCTATT | 4193 |
| rs745584012 | snp | C/T | 1.66181e-05 | 0.00288249 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824649 | GAGCAATTAGTGAGA[C/T]AGGTATATATGAATA | 4193 |
| rs745584795 | snp | A/C | 1.66313e-05 | 0.00288364 | intron-variant | MDM2 | GRCh38.p7 | 12:68816996 | CTGGGCTAACATTTC[A/C]GTTCACCTCTACCCT | 4193 |
| rs745680967 | snp | A/G | 1.66654e-05 | 0.00288659 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828776 | ACATATCCAGAAGAA[A/G]ATTCAGATGAATTAT | 4193 |
| rs745722534 | in-del | -/T | 0.0112104 | 0.0740238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814554 | AAAATAAGAATAGAA[-/T]TTTTTTTTTTCCCAT | 4193 |
| rs745902253 | in-del | -/T | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68812822 | ACATAGTAGCCATGC[-/T]TTTTACTTGGATAGA | 4193 |
| rs745991401 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68832760 | CTGGGCTTATGTGAT[G/T]CTCCTGCTTTGGCTC | 4193 |
| rs746132613 | in-del | -/TTT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821045 | ATGTACACAGTTTGC[-/TTT]TTTTTTTTTTTTTTT | 4193 |
| rs746151513 | snp | A/G | 2.14899e-05 | 0.00327788 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839869 | CCTGTCTATAAGAGA[A/G]TTATATATTTCTAAC | 4193 |
| rs746218072 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810891 | TTTTTTTGAGACAGA[A/G]TTTCACTCCTGTTGC | 4193 |
| rs746284240 | snp | A/G | | | missense, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809243 | TGTCTGTACCTACTG[A/G]TGGTGCTGTAACCAC | 4193 |
| rs746302827 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822427 | TTTTTTTTTAATTAT[C/T]ATACTTTAAGTTTTA | 4193 |
| rs746305992 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823291 | ATGATAATTGTCTGT[A/G]TATCCCAACTCTGAA | 4193 |
| rs746403594 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834337 | ATCTCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 4193 |
| rs746419185 | snp | A/T | 1.76518e-05 | 0.00297079 | intron-variant | MDM2 | GRCh38.p7 | 12:68836593 | AGTACATGATATTTG[A/T]TTAGGACTTATTACT | 4193 |
| rs746439458 | snp | A/G | 1.65644e-05 | 0.00287783 | missense, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809285 | CAGCTTCGGAACAAG[A/G]GACCCTGGTTAGTAT | 4193 |
| rs746461755 | snp | C/T | 1.6855e-05 | 0.00290297 | intron-variant | MDM2 | GRCh38.p7 | 12:68820286 | ATTTTTATTCTAAAA[C/T]GTACATCTCTTGTTA | 4193 |
| rs746505618 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835756 | GCAGCAGAGGCACAG[C/G]GATGAGTTAGGAAAC | 4193 |
| rs746561074 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834290 | CCACTAAAAACATAA[A/G]AATTAGCCGGGTGTG | 4193 |
| rs746564939 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838907 | GACTGTTACATATTG[A/G]CCTTTAAAAATCTGT | 4193 |
| rs746570390 | snp | A/G | | | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807917 | AAATACAAACATAGC[A/G]CAACGGCTAAAGGAG | 4193 |
| rs746619433 | snp | A/T | 4.97706e-05 | 0.00498827 | intron-variant | MDM2 | GRCh38.p7 | 12:68820412 | GGATAAATACCATAA[A/T]AACGTTTTAAAGACA | 4193 |
| rs746641927 | in-del | -/AT | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842655 | ATGGTACTAGACAAC[-/AT]GTAATTAATGACATT | 4193 |
| rs746698549 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819791 | TGAGCCACTGCGCCC[G/T]GCCTCTGTTAATACG | 4193 |
| rs746727108 | in-del | -/AT | 0.000489122 | 0.0156308 | intron-variant | MDM2 | GRCh38.p7 | 12:68836569 | GTCTAAGGCTTTCTC[-/AT]ATATTGTAGTACATG | 4193 |
| rs746732648 | snp | A/G | 1.66261e-05 | 0.00288319 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828917 | AGTGAATCTACAGGG[A/G]CGCCATCGAATCCGG | 4193 |
| rs746741325 | snp | C/T | 1.74163e-05 | 0.00295091 | intron-variant | MDM2 | GRCh38.p7 | 12:68824357 | ATCCTTTTTCTTTTC[C/T]CTCAGAATCATCGGA | 4193 |
| rs746756850 | in-del | -/TAAAA | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844225 | ATTTTTATGAGTTGT[-/TAAAA]TAGAAATTATTTGAA | 4193 |
| rs746815619 | in-del | -/T | 6.68516e-05 | 0.00578112 | intron-variant | MDM2 | GRCh38.p7 | 12:68828963 | AGTAAGGCAAGACTC[-/T]TTACTGTTCAAAGTC | 4193 |
| rs746838444 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828381 | TATTCTCAGCCTAGG[C/T]AACATGGTGAAACCC | 4193 |
| rs746898842 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68827171 | GGACAAGAGTGAGAC[C/T]TTGTCTCAAGAAAAT | 4193 |
| rs746910913 | in-del | -/C | 1.65526e-05 | 0.00287681 | frameshift-variant | MDM2 | GRCh38.p7 | 12:68839309 | TGCAATGAAATGAAT[-/C]CCCCCCCTTCCATCA | 4193 |
| rs746965725 | snp | C/G | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840268 | TCCTGCCTCAGCCTC[C/G]CAATTAGCTTGGCCT | 4193 |
| rs747051496 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823348 | TATATCCAACTACAA[A/G]TGAAACCTATGTGCC | 4193 |
| rs747132793 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834383 | GGAGGCGGAGGTTGC[A/T]GTGAGCTGAGATCAT | 4193 |
| rs747170777 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835317 | TCAAAGAAGGATGAA[C/T]AGGATTTTGAAACTG | 4193 |
| rs747358883 | snp | C/T | 1.69651e-05 | 0.00291243 | intron-variant | MDM2 | GRCh38.p7 | 12:68836604 | TTTGTTTAGGACTTA[C/T]TACTAGGAAGCCTTC | 4193 |
| rs747447453 | snp | A/C | 1.65649e-05 | 0.00287788 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68836713 | AGGGGAGAGTGATAC[A/C]GATTCATTTGAAGAA | 4193 |
| rs747464152 | snp | A/G | 4.00737e-05 | 0.00447608 | intron-variant | MDM2 | GRCh38.p7 | 12:68824316 | GAGTAGCGCCCCGCC[A/G]CCCCCCGCCCACCAC | 4193 |
| rs747476222 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68809822 | GTTGTTCTGTGACTT[A/G]CATCCTTGTCAATAA | 4193 |
| rs747526290 | snp | C/T | 1.6601e-05 | 0.00288101 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813657 | AGAGATAAGTAGTAT[C/T]TCACTAGTTACATGT | 4193 |
| rs747563652 | in-del | -/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815297 | ACTATGTAACAGTAG[-/T]TGTATGTATTGTCTG | 4193 |
| rs747709264 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68827494 | TGCAGATATTATCTT[C/T]GAATTTGACCTTTGC | 4193 |
| rs747786956 | snp | A/C | 4.96816e-05 | 0.00498381 | missense | MDM2 | GRCh38.p7 | 12:68839658 | GAGAGTGTGGAATCT[A/C]GTTTGCCCCTTAATG | 4193 |
| rs747799163 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841103 | TACTCACCTCAGCCT[C/T]CCAAAATGCTGGGAT | 4193 |
| rs747926648 | in-del | -/TGA | 1.65622e-05 | 0.00287764 | cds-indel | MDM2 | GRCh38.p7 | 12:68839604 | GCAGCCAAGAAGATG[-/TGA]TGAAAGAGTTTGAAA | 4193 |
| rs748044533 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829691 | GAATCGCTCGAACCC[A/T]GGAGTTGGAGGTTGC | 4193 |
| rs748061526 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816614 | CATCCGCTTCGGCCT[C/T]CCGAAGTACTGGGAT | 4193 |
| rs748134261 | snp | A/C | 1.6585e-05 | 0.00287962 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828815 | CGACAAAGAAAACGC[A/C]ACAAATCTGATAGTA | 4193 |
| rs748208493 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68812273 | TCAATTGTTAAATAA[A/T]ATTTGTTTTATTGAT | 4193 |
| rs748230740 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824956 | GCTCACGCCTGTAAT[C/T]CCGGCACTTTGGGAG | 4193 |
| rs748254974 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823573 | TCCATGCCTTAGTTT[A/G]GGCTTTAATAGTTTT | 4193 |
| rs748303501 | in-del | -/G | 5.17933e-05 | 0.00508861 | intron-variant | MDM2 | GRCh38.p7 | 12:68835781 | GGAAACAGATACAGA[-/G]GTCAAGAGGTGATGT | 4193 |
| rs748317337 | snp | A/G | | | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824402 | TGAGTGAGAACAGGT[A/G]TCACCTTGAAGGTGG | 4193 |
| rs748340679 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835391 | CAAGATTAGTTGAGG[A/G]AGCAATCTAGATCTG | 4193 |
| rs748376263 | snp | A/G | 4.99214e-05 | 0.00499582 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68828925 | TACAGGGACGCCATC[A/G]AATCCGGTAATGTTC | 4193 |
| rs748388153 | in-del | -/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816363 | AGGCTTAAAAGTAGC[-/T]TTTTTTTTTTTTTTT | 4193 |
| rs748459725 | snp | A/G | 1.71959e-05 | 0.00293217 | missense | MDM2 | GRCh38.p7 | 12:68839275 | TTATTTCATTGAAGG[A/G]CTATTGGAAATGCAC | 4193 |
| rs748461643 | snp | A/G | 1.85201e-05 | 0.00304297 | intron-variant | MDM2 | GRCh38.p7 | 12:68816797 | TAATGCTCAGAAATC[A/G]TATTTGTATTTCAGG | 4193 |
| rs748474309 | snp | A/G | 1.68032e-05 | 0.0028985 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808467 | CCCGACTCCAAGCGC[A/G]AAAACCCCGGATGGT | 4193 |
| rs748549508 | snp | A/T | 1.66106e-05 | 0.00288184 | intron-variant | MDM2 | GRCh38.p7 | 12:68816989 | AAGCCATCTGGGCTA[A/T]CATTTCAGTTCACCT | 4193 |
| rs748597163 | snp | A/G | | | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68846015 | CTGGAGTGCAGTGGT[A/G]CAATCTCGGCTCATT | 4193 |
| rs748598341 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845378 | GGTGTTCAGAAGTAA[C/T]AAATTATAAAATGAG | 4193 |
| rs748776402 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818097 | CCACACCCGGCCTAC[A/G]TTTGGAATTCTTTGT | 4193 |
| rs748820965 | snp | A/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843839 | TTTTTGGAGGTCCTC[A/G]AAGCATTATTTGGAG | 4193 |
| rs748837972 | in-del | -/TAAAC | 4.98873e-05 | 0.00499411 | intron-variant | MDM2 | GRCh38.p7 | 12:68809346 | TATTTTATGAAGTGA[-/TAAAC]TAAATTTCGTATACC | 4193 |
| rs748894728 | snp | A/G | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813254 | CTAAGTTAGCTTGCA[A/G]TAAGCTCGTTGGATC | 4193 |
| rs748989435 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841953 | TTTCTTTGGGACCCA[C/T]CTACCCTGACCACAT | 4193 |
| rs749003450 | snp | A/G | 3.31576e-05 | 0.00407157 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68836746 | TCCTGAAATTTCCTT[A/G]GCTGTAAGTATACAT | 4193 |
| rs749163342 | snp | C/T | 3.34767e-05 | 0.00409112 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68824397 | ATCTGTGAGTGAGAA[C/T]AGGTGTCACCTTGAA | 4193 |
| rs749187947 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819641 | GGATTACAGGCATGC[A/G]CCACCATGCCCAGCT | 4193 |
| rs749231085 | snp | A/T | 1.65732e-05 | 0.00287859 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839804 | TAAGCCCTGCCCAGT[A/T]TGTAGACAACCAATT | 4193 |
| rs749245347 | snp | A/G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68827527 | TTTAACTTTTGTTTG[A/G/T]TATTTTATTTTGTCA | 4193 |
| rs749301960 | snp | C/T | 3.31285e-05 | 0.00406978 | intron-variant, synonymous-codon | MDM2 | GRCh38.p7 | 12:68835927 | AGTTGAATCTCTCGA[C/T]TCAGAAGATTATAGC | 4193 |
| rs749303556 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815135 | GTAGGAAAGGGCCAG[A/G]TTAAATGGTATTTTT | 4193 |
| rs749317078 | snp | A/C | 1.65674e-05 | 0.00287809 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68824596 | GAAACCTTCATCTTC[A/C]CATTTGGTTTCTAGA | 4193 |
| rs749347506 | in-del | -/ATTTATTCAC | 1.69651e-05 | 0.00291243 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839916 | TTTAGACAACCTGAA[-/ATTTATTCAC]ATATATCAAAGTGAG | 4193 |
| rs749406013 | snp | A/G | 1.65605e-05 | 0.0028775 | missense, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809257 | GATGGTGCTGTAACC[A/G]CCTCACAGATTCCAG | 4193 |
| rs749428642 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845458 | GTGTTCAGTAACTTA[C/T]TCATAATGCATCTGA | 4193 |
| rs749452612 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825610 | GTGAGCCGAGATCAC[C/G]CCACTGCACTCCGCC | 4193 |
| rs749518580 | in-del | -/AATTC | | | intron-variant | MDM2 | GRCh38.p7 | 12:68812229 | ATCAGAAAAATTAAT[-/AATTC]AATTCTATATGTATT | 4193 |
| rs749522231 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808197 | CGCACCGAGGCACCG[C/T]GGCGAGCTTGGCTGC | 4193 |
| rs749540448 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838393 | ACGTTGGGAAAAGGA[A/G]GAAGCATTGAGCAGT | 4193 |
| rs749845234 | snp | A/G | 1.68261e-05 | 0.00290048 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808436 | CGTGAAGGAAACTGG[A/G]GAGTCTTGAGGGACC | 4193 |
| rs749855357 | snp | C/T | 1.67211e-05 | 0.00289142 | intron-variant | MDM2 | GRCh38.p7 | 12:68828970 | GCAAGACTCTTACTG[C/T]TCAAAGTCTAGTCCT | 4193 |
| rs749892753 | snp | A/T | 9.97556e-05 | 0.00706172 | splice-acceptor-variant | MDM2 | GRCh38.p7 | 12:68835827 | TTTTTTTCTTGTTTT[A/T]GGATCTTGATGCTGG | 4193 |
| rs749905835 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68833625 | ATAGTTAATTATTTG[A/G]GCTCTGCCGGGCCAT | 4193 |
| rs749943288 | in-del | -/AGG | 1.68176e-05 | 0.00289974 | intron-variant | MDM2 | GRCh38.p7 | 12:68836609 | TTAGGACTTATTACT[-/AGG]AAGCCTTCTGATTGA | 4193 |
| rs749947972 | snp | A/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843458 | TTACAATTATGTATT[A/T]AACATTTAAAATTTC | 4193 |
| rs749981085 | snp | A/C | 1.65674e-05 | 0.00287809 | intron-variant | MDM2 | GRCh38.p7 | 12:68809183 | ATGATTTCCAGTTTT[A/C]ATCGTGTCTTTTTTT | 4193 |
| rs750047925 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68820224 | TGTGTGCAGTAGTTC[A/G]TACTAAGTATGTATG | 4193 |
| rs750098057 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829442 | TAGGTCTAGACATCA[A/G]GTAAGTTCTATTTAC | 4193 |
| rs750156925 | snp | A/G | 1.65704e-05 | 0.00287836 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839414 | TGAGAAAGCCAAACT[A/G]GAAAACTCAACACAA | 4193 |
| rs750222250 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810022 | AAGAAAGATTTTATA[A/G]AATTATAGGCTGGCC | 4193 |
| rs750281940 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821648 | GGATTTTTTGAGGCT[A/G]GGAGGTCAGGACTGT | 4193 |
| rs750304144 | in-del | -/GAAAG | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819818 | ACGTTTTAAGATCAA[-/GAAAG]GAAAGGAAGTTGAAG | 4193 |
| rs750437491 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834752 | AAAATAAATAAAATA[A/G]GTTAAATGATGTTGT | 4193 |
| rs750452466 | snp | A/C | 1.66023e-05 | 0.00288113 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828878 | TGTGTAATAAGGGAG[A/C]TATGTTGTGAAAGAA | 4193 |
| rs750502876 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816468 | GCCTCCACCTCCTGG[A/G]TTCAAGCAATTCTCC | 4193 |
| rs750631361 | in-del | -/CA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824899 | AGCCAACTCTCTGTT[-/CA]AAGATAGTAGGAGGT | 4193 |
| rs750682089 | snp | C/T | 1.65844e-05 | 0.00287957 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68816928 | TGGCGTGCCAAGCTT[C/T]TCTGTGAAAGAGCAC | 4193 |
| rs750728179 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824105 | ACCAAAATAATGACT[C/T]TCCTGTCTCTCTGCT | 4193 |
| rs750827846 | snp | C/G/T | 3.37617e-05 | 0.00410852 | intron-variant | MDM2 | GRCh38.p7 | 12:68824684 | TTTGACGCATTCACA[C/G/T]AGCTTTTTGATATTC | 4193 |
| rs750882198 | in-del | -/G | 1.68196e-05 | 0.00289992 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808446 | ACTGGGGAGTCTTGA[-/G]GGACCCCCGACTCCA | 4193 |
| rs750969650 | in-del | -/TTAAAA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68811236 | TTTCCTTTTAGTTTT[-/TTAAAA]TTTTTCTTAGTAATT | 4193 |
| rs751140188 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834666 | TGCTTGAACTTGGGA[A/G]GTGTAGGTTGCAGTG | 4193 |
| rs751171057 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826545 | TCCCAGCTACTTGGG[A/T]GGCTGAGGCAGGAGA | 4193 |
| rs751275422 | snp | C/T | 1.65605e-05 | 0.0028775 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839720 | ACCTAAAAATGGTTG[C/T]ATTGTCCATGGCAAA | 4193 |
| rs751338961 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829337 | ATATTTTAGCATTTT[A/G]AGGCAAATTTGACTA | 4193 |
| rs751413136 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810400 | TACTGGTAACTTGCT[C/T]ACCAAAAGGCTCTAA | 4193 |
| rs751419968 | snp | G/T | 1.6569e-05 | 0.00287824 | intron-variant, missense | MDM2 | GRCh38.p7 | 12:68835856 | GGTGTAAGTGAACAT[G/T]CAGGTGATTGGTTGG | 4193 |
| rs751458930 | snp | A/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843261 | GCTTTGAGGACCTCC[A/G]AAGGTAAAAGTACTA | 4193 |
| rs751475293 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841670 | TTACATGGTTCCCAG[C/T]CTAGGTTTCAGACTT | 4193 |
| rs751507376 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809015 | CCATGCATTTTCCCA[C/G]CTGTGTTCAGTGGCG | 4193 |
| rs751583857 | snp | C/T | 4.34471e-05 | 0.00466065 | intron-variant | MDM2 | GRCh38.p7 | 12:68836029 | TGGAAAATTATTAAA[C/T]ATTTTCTATGTTCAT | 4193 |
| rs751590195 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68809191 | CAGTTTTCATCGTGT[C/T]TTTTTTTTCCTTGTA | 4193 |
| rs751597055 | snp | C/G | 0.000548141 | 0.016546 | intron-variant | MDM2 | GRCh38.p7 | 12:68816984 | GTAAAAAGCCATCTG[C/G]GCTAACATTTCAGTT | 4193 |
| rs751618188 | snp | A/G | 1.65869e-05 | 0.00287979 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68820345 | TATATACCATGATCT[A/G]CAGGAACTTGGTAGT | 4193 |
| rs751687474 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830404 | GTTACTTATGTAGAC[C/T]GCTAGATGGCATGAT | 4193 |
| rs751908843 | in-del | -/CCGCCCC | 2.00503e-05 | 0.00316619 | intron-variant | MDM2 | GRCh38.p7 | 12:68824313 | CTGAGTAGCGCCCCG[-/CCGCCCC]CCGCCCCCCGCCCAC | 4193 |
| rs751949064 | in-del | -/GTATTTTT | 3.3137e-05 | 0.00407031 | intron-variant | MDM2 | GRCh38.p7 | 12:68809297 | AAGAGACCCTGGTTA[-/GTATTTTT]GTCTCGTGTAACTTT | 4193 |
| rs751953315 | snp | A/G | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813314 | TTTATGGTTGTTTGT[A/G]AGGCAGTAAGCAGGT | 4193 |
| rs752039782 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68836452 | GAATGTTTTGTTTTA[C/T]TCATCCTAAACATCC | 4193 |
| rs752041210 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825166 | GTGAGCCGAAATTGC[A/G]CCACTGCACTCCAGC | 4193 |
| rs752046642 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838077 | GGACTTTTTGATGCA[C/T]TTTTACTCCCATATT | 4193 |
| rs752078756 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839756 | ACATCTTATGGCCTG[C/T]TTTACATGTGCAAAG | 4193 |
| rs752171752 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823930 | TCCAGTAATAATGAA[C/T]TGCTTGTGGTGTCCT | 4193 |
| rs752173209 | snp | A/G | 1.77922e-05 | 0.00298258 | intron-variant | MDM2 | GRCh38.p7 | 12:68839246 | TAAAGGGTTACAGAA[A/G]CTGACTGTGTGTCTT | 4193 |
| rs752188165 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68811720 | AGCAATTCTGCCGCA[A/G]CCTCCCGAGTAGCTG | 4193 |
| rs752208195 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810760 | GTCACTGCGCCTGGC[C/T]TCTTTTATTATTATT | 4193 |
| rs752222682 | snp | C/G | 3.31373e-05 | 0.00407032 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824579 | CAAGAGCTTCAGGAA[C/G]AGAAACCTTCATCTT | 4193 |
| rs752256781 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823994 | ACTTTTTCACATGGC[A/G]TTTTCTTGGTCTGGA | 4193 |
| rs752277202 | snp | A/G | 0.000185649 | 0.00963277 | utr-variant-3-prime, nc-transcript-variant | MDM2, CPM | GRCh38.p7 | 12:68842258 | TCAAGAAAAAGGACT[A/G]CGGAAAGTTCAGGAC | 4193 |
| rs752390412 | snp | C/T | 1.85098e-05 | 0.00304213 | intron-variant | MDM2 | GRCh38.p7 | 12:68828734 | CAATTTTCTAAATCA[C/T]AGTACAGCAATTTAT | 4193 |
| rs752515502 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831306 | GACCTTACATTCTGA[C/T]AATACTAGCCAGTTT | 4193 |
| rs752515895 | snp | A/C | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844691 | GCAGGAGCTTGTGGG[A/C]CCCTAAGCCAGACGG | 4193 |
| rs752517452 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819612 | TTATCCCGCCTCAGT[C/T]TCCTGAGTAGCTGGG | 4193 |
| rs752565420 | snp | A/G | 1.65792e-05 | 0.00287912 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813550 | AGTTCTTTTCTCTTT[A/G]TAGGTTAGACCAAAG | 4193 |
| rs752591665 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831984 | CTGAGACAGGAGAAT[C/T]GCTTGAACCCGGGAG | 4193 |
| rs752618112 | in-del | -/TT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821046 | TGTACACAGTTTGCT[-/TT]TTTTTTTTTTTTTTT | 4193 |
| rs752628448 | snp | A/G | 0.00183823 | 0.0302612 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814601 | CCTGAATTCTATCCA[A/G]GGACTTCTTGGGCAT | 4193 |
| rs752689660 | snp | A/G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825380 | AGATAAGGGCCGGGC[A/G/T]CAGTGGCTCACGCCT | 4193 |
| rs752730895 | snp | C/T | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68807389 | GCAGCCTCTGCCTCC[C/T]GGGTTCACAGGATTG | 4193 |
| rs752761590 | in-del | -/TTT | | | utr-variant-3-prime, cds-indel | MDM2 | GRCh38.p7 | 12:68840503 | AGATTTAGTTTTTTG[-/TTT]TTTTGTTTGTTTGTT | 4193 |
| rs752932923 | snp | C/T | 1.65641e-05 | 0.00287781 | intron-variant, synonymous-codon | MDM2 | GRCh38.p7 | 12:68835924 | TGAAGTTGAATCTCT[C/T]GACTCAGAAGATTAT | 4193 |
| rs753104067 | in-del | -/C | 5.19067e-05 | 0.00509418 | intron-variant | MDM2 | GRCh38.p7 | 12:68835998 | GGTAGTATTTTTTTT[-/C]CCCCTCTAATTATAT | 4193 |
| rs753138941 | snp | A/G | 1.65704e-05 | 0.00287836 | missense | MDM2 | GRCh38.p7 | 12:68839404 | GGGAAATCTCTGAGA[A/G]AGCCAAACTGGAAAA | 4193 |
| rs753201230 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826447 | TGAGGTTAAGAGTTC[A/G]AGACCAACCTGGCCA | 4193 |
| rs753251980 | in-del | -/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818282 | TATTTTATTAAAAAA[-/C]ATAACTTCCTCAGCT | 4193 |
| rs753255764 | snp | A/G | | | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845838 | CTGCAAACATGACTC[A/G]CTACAGCCTCAACCT | 4193 |
| rs753298202 | snp | A/G | 1.65682e-05 | 0.00287817 | missense | MDM2 | GRCh38.p7 | 12:68839554 | AAGAAAGTGAAGACT[A/G]TTCTCAGCCATCAAC | 4193 |
| rs753300168 | snp | A/G | 1.65833e-05 | 0.00287948 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68820370 | GGTAGTAGTCAATCA[A/G]CAGGGTAAGTTAATT | 4193 |
| rs753352746 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830760 | GGCTGGAGTGCAGTG[C/G]TGCAATCTTGGCTCA | 4193 |
| rs753379873 | in-del | -/AC | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824130 | CTGCTAATTTATCTA[-/AC]ACAGTCTTTTAATGT | 4193 |
| rs753442532 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845054 | ATTACAGGCGTGAGC[C/T]GCCACGCCCAGCCTA | 4193 |
| rs753483638 | in-del | -/TAT | 3.35478e-05 | 0.00409546 | intron-variant | MDM2 | GRCh38.p7 | 12:68824463 | CTCATTCTAATGTAA[-/TAT]TATTTGCAAATTGGA | 4193 |
| rs753654969 | snp | A/G | 0.000497884 | 0.01577 | intron-variant | MDM2 | GRCh38.p7 | 12:68815671 | TGGTCTGGAACTCCT[A/G]GGCTCAAGGGATCTG | 4193 |
| rs753663917 | snp | G/T | 1.65831e-05 | 0.00287945 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68816912 | TTCTAGGAGATTTGT[G/T]TGGCGTGCCAAGCTT | 4193 |
| rs753670140 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831444 | CCTTTAATACACAAA[G/T]GCAGGATGCCATGAC | 4193 |
| rs753670742 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821415 | CCTAAAGCCCATCCT[C/T]GAACTACAGTTAAGA | 4193 |
| rs753789378 | snp | C/T | 0.000185649 | 0.00963277 | utr-variant-3-prime, nc-transcript-variant | MDM2, CPM | GRCh38.p7 | 12:68842310 | TCATCTTGACCCCTG[C/T]TGCAGGCAAAGGAAC | 4193 |
| rs753848209 | in-del | -/TC | 0.000158204 | 0.00889253 | intron-variant | MDM2 | GRCh38.p7 | 12:68824355 | TGATCCTTTTTCTTT[-/TC]TCTCAGAATCATCGG | 4193 |
| rs753982883 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841416 | GTAAAAATGTACTTA[C/T]TCTCCAGCCTCTTTT | 4193 |
| rs753985024 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826804 | TTATAATTGCAGCCC[A/G]GCCAAGATCACCTTT | 4193 |
| rs753997820 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840011 | TAGTGGAATAGTGAA[C/T]ACTTACTATAATTTG | 4193 |
| rs754014079 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838230 | AATGGTTACGGAAAT[A/G]CCTCTTACTTAAGAG | 4193 |
| rs754071314 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835306 | CAAAGGCTTAGTCAA[A/G]GAAGGATGAATAGGA | 4193 |
| rs754095005 | snp | C/T | 1.65649e-05 | 0.00287788 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839573 | TCAGCCATCAACTTC[C/T]AGTAGCATTATTTAT | 4193 |
| rs754186779 | snp | A/C | 1.88319e-05 | 0.00306848 | intron-variant | MDM2 | GRCh38.p7 | 12:68824331 | GCCCCCCGCCCACCA[A/C]CAAGTTTCTGATCCT | 4193 |
| rs754384534 | in-del | -/AT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826643 | ACAGAGTGAGACTCC[-/AT]CTCTTAAAAAAAAAA | 4193 |
| rs754409184 | snp | A/G | 1.66482e-05 | 0.0028851 | intron-variant | MDM2 | GRCh38.p7 | 12:68824506 | ACAACAAGTTAGCTT[A/G]CTGGTTATGTTAAGT | 4193 |
| rs754521846 | snp | G/T | 1.6563e-05 | 0.00287771 | missense | MDM2 | GRCh38.p7 | 12:68839590 | GTAGCATTATTTATA[G/T]CAGCCAAGAAGATGT | 4193 |
| rs754522745 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68811145 | GCTGGGATTACAGGC[A/G]TGAATCACTGCACCA | 4193 |
| rs754523661 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808979 | TAAGTCCTGACTTGT[C/T]TCCAGCTGGGGCTAT | 4193 |
| rs754571428 | snp | G/T | 1.73105e-05 | 0.00294193 | intron-variant | MDM2 | GRCh38.p7 | 12:68824359 | CCTTTTTCTTTTCTC[G/T]CAGAATCATCGGACT | 4193 |
| rs754577228 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834698 | GCTGAGATCAGGCCA[C/T]TGCACTCCAGCCTGG | 4193 |
| rs754578340 | in-del | -/ATATA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818564 | TATATTATAATATAC[-/ATATA]ATATAATTATATATA | 4193 |
| rs754592784 | in-del | -/TA | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842736 | AAATATGCCCTTTAT[-/TA]TATAGAAGGGAGGAT | 4193 |
| rs754607777 | snp | C/T | 1.65605e-05 | 0.0028775 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839723 | TAAAAATGGTTGCAT[C/T]GTCCATGGCAAAACA | 4193 |
| rs754627845 | snp | A/G | 6.62756e-05 | 0.00575616 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68824575 | TGTACAAGAGCTTCA[A/G]GAAGAGAAACCTTCA | 4193 |
| rs754668205 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834021 | TCCTAACATTACTCT[A/G]AAAAAGTCTTTTGAT | 4193 |
| rs754763955 | snp | C/G | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806963 | GACCACTATGTTTAA[C/G]GAAGTTTCCTTTCTG | 4193 |
| rs754773002 | in-del | -/GAAGATAAAGGG | 1.65784e-05 | 0.00287905 | cds-indel | MDM2 | GRCh38.p7 | 12:68839367 | GAGAATTGGCTTCCT[-/GAAGATAAAGGG]AAAGATAAAGGGGAA | 4193 |
| rs754784317 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829371 | AGAGTAAAAATATAT[C/T]TTATTACAGCCATCA | 4193 |
| rs754855736 | in-del | -/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844307 | TTTCTGGAATGGCCA[-/T]GCCTGCCCACTTTAG | 4193 |
| rs754920950 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828402 | GGTGAAACCCTGTCT[A/G]TGCAAAAAATACAAA | 4193 |
| rs754946844 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843435 | GTGAAACAGTACATA[C/T]ACCATATTTACAATT | 4193 |
| rs754965312 | snp | C/T | 3.31279e-05 | 0.00406975 | intron-variant | MDM2 | GRCh38.p7 | 12:68809199 | ATCGTGTCTTTTTTT[C/T]CCTTGTAGGCAAATG | 4193 |
| rs754989312 | in-del | -/A | | | intron-variant | MDM2 | GRCh38.p7 | 12:68832130 | GTGAAAGCTTTTGGT[-/A]AGGGCCAGTTTTTTT | 4193 |
| rs755037222 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68836466 | ATTCATCCTAAACAT[A/C]CTTTGTATTGACTTT | 4193 |
| rs755041148 | snp | C/T | 4.97566e-05 | 0.00498757 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68820352 | CATGATCTACAGGAA[C/T]TTGGTAGTAGTCAAT | 4193 |
| rs755174801 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68809578 | TTTTTTCCTTTTTGA[C/T]CTCCCAGTATTTAAT | 4193 |
| rs755225422 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819531 | AGTTTTGCTCTTGTT[A/G]CCCAGGCTGGAGTGC | 4193 |
| rs755256189 | snp | C/T | 1.66269e-05 | 0.00288326 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828918 | GTGAATCTACAGGGA[C/T]GCCATCGAATCCGGT | 4193 |
| rs755327701 | in-del | -/CCCACCA | 5.84368e-05 | 0.00540509 | intron-variant | MDM2 | GRCh38.p7 | 12:68824323 | CCCCGCCGCCCCCCG[-/CCCACCA]CCCACCACCAAGTTT | 4193 |
| rs755429424 | snp | C/T | 1.65707e-05 | 0.00287838 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68836741 | GAAGATCCTGAAATT[C/T]CCTTAGCTGTAAGTA | 4193 |
| rs755437369 | snp | A/C | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813355 | GCTGAAGGAAAAAGT[A/C]ATCTTTGCTCTTTTG | 4193 |
| rs755581488 | in-del | -/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830316 | ACTTCCTGTATTATC[-/T]TTTTTTCTCTTCCAA | 4193 |
| rs755616516 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815764 | CTTCATTTCTAATAC[A/C]GTGATAATAATCTTA | 4193 |
| rs755631246 | snp | C/T | 0.000185684 | 0.00963366 | utr-variant-3-prime, nc-transcript-variant | MDM2, CPM | GRCh38.p7 | 12:68842259 | CAAGAAAAAGGACTA[C/T]GGAAAGTTCAGGACA | 4193 |
| rs755673157 | snp | A/G | 4.9703e-05 | 0.00498488 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68824590 | GGAAGAGAAACCTTC[A/G]TCTTCACATTTGGTT | 4193 |
| rs755712972 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824017 | GGTCTGGAATGGCCT[C/T]TCCTAGCCCTATTTT | 4193 |
| rs755813232 | snp | C/T | 1.65756e-05 | 0.00287881 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813551 | GTTCTTTTCTCTTTA[C/T]AGGTTAGACCAAAGC | 4193 |
| rs756105069 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830624 | CTCTTGAGCGGAAAT[A/G]TATGTGATAAAATTG | 4193 |
| rs756110138 | snp | A/T | 4.96833e-05 | 0.00498389 | missense | MDM2 | GRCh38.p7 | 12:68839760 | CTTATGGCCTGCTTT[A/T]CATGTGCAAAGAAGC | 4193 |
| rs756117122 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815410 | GGATTAAGAGTCAGA[A/G]GAGCTGGGGCCAGTT | 4193 |
| rs756143588 | snp | C/T | 5.41375e-05 | 0.00520248 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839911 | AGGAATTTAGACAAC[C/T]TGAAATTTATTCACA | 4193 |
| rs756183185 | in-del | -/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818853 | CTCTTGCCTCAGCCT[-/C]CTGAGTAGCTGGGAT | 4193 |
| rs756212787 | snp | A/G | | | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68808079 | AGGTGGTGCGGCCGA[A/G]CCCCGGACCCAATTG | 4193 |
| rs756298244 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68836568 | TGTCTAAGGCTTTCT[C/T]ATATATTGTAGTACA | 4193 |
| rs756305304 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68833119 | TGACAGAGCGAGACT[C/T]TGTCTCCAAAAAAAA | 4193 |
| rs756599882 | snp | A/G | 1.65701e-05 | 0.00287833 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839405 | GGAAATCTCTGAGAA[A/G]GCCAAACTGGAAAAC | 4193 |
| rs756673959 | snp | G/T | 1.65982e-05 | 0.00288077 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828867 | GCCTGGCTCTGTGTG[G/T]AATAAGGGAGATATG | 4193 |
| rs756708304 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818087 | ATGTGAGCAACCACA[C/T]CCGGCCTACATTTGG | 4193 |
| rs756828837 | in-del | -/TT | 1.67742e-05 | 0.002896 | intron-variant | MDM2 | GRCh38.p7 | 12:68824464 | CATTCTAATGTAATA[-/TT]TTATTTGCAAATTGG | 4193 |
| rs756911468 | in-del | -/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826647 | AGTGAGACTCCCTCT[-/C]TAAAAAAAAAAAAAA | 4193 |
| rs756933597 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824462 | TCTCATTCTAATGTA[A/G]TATTATTTGCAAATT | 4193 |
| rs756955151 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826811 | TGCAGCCCGGCCAAG[A/G]TCACCTTTTTAAAAA | 4193 |
| rs756995366 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838401 | AAAAGGAAGAAGCAT[C/T]GAGCAGTTACAAAGA | 4193 |
| rs757006444 | snp | C/T | 1.70702e-05 | 0.00292144 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839279 | TTCATTGAAGGACTA[C/T]TGGAAATGCACTTCA | 4193 |
| rs757100640 | in-del | -/TTG | 1.68009e-05 | 0.00289831 | intron-variant | MDM2 | GRCh38.p7 | 12:68820296 | TAAAATGTACATCTC[-/TTG]TTATTTTTTTTTTTT | 4193 |
| rs757161769 | snp | C/T | 1.7013e-05 | 0.00291654 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839846 | GCTAACTTATTTCCC[C/T]TAGTTGACCTGTCTA | 4193 |
| rs757225399 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828748 | ACAGTACAGCAATTT[A/T]TTTTTTTTCCTTACA | 4193 |
| rs757366966 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828114 | CCAGCCTGGGTGGTC[A/G]AGTGTGACTCTGTCT | 4193 |
| rs757379172 | snp | A/G | 1.88724e-05 | 0.00307178 | intron-variant | MDM2 | GRCh38.p7 | 12:68836583 | CATATATTGTAGTAC[A/G]TGATATTTGTTTAGG | 4193 |
| rs757397046 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815209 | TAAGGAAACAAAAAA[G/T]TATGGATTTAGCAGT | 4193 |
| rs757467242 | snp | A/G | 1.65679e-05 | 0.00287814 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68836680 | TTATTAGGTATATCA[A/G]GTTACTGTGTATCAG | 4193 |
| rs757471263 | snp | A/G | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68840044 | TTGAATATGTAGCTC[A/G]TCCTTTACACCAACT | 4193 |
| rs757580574 | snp | A/G | | | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808578 | AGCCTCTGCCCGTTC[A/G]CAGCCTTTGTGCGGT | 4193 |
| rs757679327 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834305 | AAATTAGCCGGGTGT[A/G]GTAGTGGACACCTGT | 4193 |
| rs757683249 | snp | C/T | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813013 | TAAATGTTTGTCAAG[C/T]AGATATTTGAAATGT | 4193 |
| rs757706243 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815008 | TAAATCTAAGTTCTC[C/T]TCCTTTTTCCTTTCC | 4193 |
| rs757715195 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68832892 | AGCACTTTGGGAGGC[A/T]GAGGCGGGCGGATCA | 4193 |
| rs757780201 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816433 | GCCGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 4193 |
| rs757799734 | snp | C/T | 1.65658e-05 | 0.00287795 | intron-variant | MDM2 | GRCh38.p7 | 12:68809186 | ATTTCCAGTTTTCAT[C/T]GTGTCTTTTTTTTCC | 4193 |
| rs757815373 | snp | C/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843003 | TAAGTTCTAACTTGT[C/G]ATTCCTGGTAGAACA | 4193 |
| rs757864152 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68833752 | TATTTATAAAAGTCG[A/G]TGGGTGATGGGCCAC | 4193 |
| rs757888234 | in-del | -/TG | 1.65739e-05 | 0.00287865 | intron-variant | MDM2 | GRCh38.p7 | 12:68836659 | ATTGATGCTAATGAA[-/TG]TGTTTTATTAGGTAT | 4193 |
| rs757970613 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824037 | AGCCCTATTTTCATA[C/T]TGTCCTACAAAATAT | 4193 |
| rs757975502 | snp | G/T | 1.65704e-05 | 0.00287836 | missense | MDM2 | GRCh38.p7 | 12:68839421 | GCCAAACTGGAAAAC[G/T]CAACACAAGCTGAAG | 4193 |
| rs757991854 | snp | C/T | 1.65858e-05 | 0.00287969 | intron-variant | MDM2 | GRCh38.p7 | 12:68820394 | GTTAATTTTGAGCAT[C/T]ATGGATAAATACCAT | 4193 |
| rs758025672 | in-del | -/TG | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821893 | GATGGGCTCTCACTC[-/TG]TCACCCTGCTTGAAG | 4193 |
| rs758087887 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841650 | AAGTACCTTCTTGGC[C/T]TGGGTTACATGGTTC | 4193 |
| rs758148703 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68814894 | AAAACATTTAAGTTT[C/G]TTTCTTACAACGGTA | 4193 |
| rs758204305 | in-del | -/TTT | | | utr-variant-3-prime, cds-indel, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844068 | AGGCAGTGACAGCTA[-/TTT]TTACAAAATTTAAAT | 4193 |
| rs758284427 | snp | C/G | | | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807835 | TTTTGGTTTCTTTTT[C/G]GTAACAGCGACACGG | 4193 |
| rs758319082 | in-del | -/T | 0.000108963 | 0.00738036 | intron-variant | MDM2 | GRCh38.p7 | 12:68828749 | CAGTACAGCAATTTA[-/T]TTTTTTTCCTTACAT | 4193 |
| rs758354449 | snp | G/T | | | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808811 | CGCTTCGGCGCGGGA[G/T]GTCCGGATGATCGCA | 4193 |
| rs758396646 | snp | A/C | 1.66125e-05 | 0.00288201 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828896 | TGTTGTGAAAGAAGC[A/C]GTAGCAGTGAATCTA | 4193 |
| rs758413036 | snp | C/G | 3.31967e-05 | 0.00407397 | missense | MDM2 | GRCh38.p7 | 12:68835832 | TTCTTGTTTTAGGAT[C/G]TTGATGCTGGTGTAA | 4193 |
| rs758517179 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68827719 | TTATGTCTAGTATAA[C/G]GTAGTATTCTCATTT | 4193 |
| rs758550952 | snp | A/G | 1.78886e-05 | 0.00299065 | intron-variant | MDM2 | GRCh38.p7 | 12:68839232 | TGTGACTGAGCAGTT[A/G]AAGGGTTACAGAAAC | 4193 |
| rs758553381 | snp | A/G | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813395 | CTGTCTGTGATCACA[A/G]CTGATACTTGATGAT | 4193 |
| rs758609588 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816509 | TCCCTAATAGCTGGG[A/G]TTACAGGTGTCTGCC | 4193 |
| rs758613549 | snp | C/T | 1.6599e-05 | 0.00288084 | intron-variant | MDM2 | GRCh38.p7 | 12:68816965 | TTCTTCAGTTTAGTC[C/T]ATTGTAAAAAGCCAT | 4193 |
| rs758635058 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829075 | TACTTTAAAATAAAA[C/T]TACTATATTGATCTC | 4193 |
| rs758687398 | in-del | -/TTAAA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826647 | GAGTGAGACTCCCTC[-/TTAAA]AAAAAAAAAAAAAGA | 4193 |
| rs758804649 | in-del | -/T | 0.000248682 | 0.0111481 | intron-variant | MDM2 | GRCh38.p7 | 12:68809191 | AGTTTTCATCGTGTC[-/T]TTTTTTTTCCTTGTA | 4193 |
| rs758856084 | snp | A/C | | | missense | MDM2 | GRCh38.p7 | 12:68839434 | ACTCAACACAAGCTG[A/C]AGAGGGCTTTGATGT | 4193 |
| rs758860429 | snp | A/G | 4.9694e-05 | 0.00498443 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68836696 | GTTACTGTGTATCAG[A/G]CAGGGGAGAGTGATA | 4193 |
| rs758871836 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824244 | AAATACATGTTTAAT[A/G]TTTATTGAAAGGTTA | 4193 |
| rs758958658 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68836340 | TAGTACCCTTAGAGA[C/T]CTGTTTCCCAGAAGT | 4193 |
| rs758979010 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835188 | AGAAACATGCCTGCA[A/G]AATTATGTTTTGCAT | 4193 |
| rs759123173 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835684 | CCGCCGATCTCCCTC[G/T]GGAAGTCCCGGATCA | 4193 |
| rs759141994 | snp | C/T | 1.66175e-05 | 0.00288244 | intron-variant | MDM2 | GRCh38.p7 | 12:68816986 | AAAAAGCCATCTGGG[C/T]TAACATTTCAGTTCA | 4193 |
| rs759244097 | snp | A/T | 3.32602e-05 | 0.00407786 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68816864 | GATTATATGATGAGA[A/T]GCAACAACATATTGT | 4193 |
| rs759294736 | snp | G/T | | | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808730 | CGCGGCGGTGGGGGT[G/T]GGGGTGGTTCGGAGG | 4193 |
| rs759348177 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834380 | CCCGGAGGCGGAGGT[G/T]GCAGTGAGCTGAGAT | 4193 |
| rs759368720 | snp | A/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844544 | GTACCACTTGTCAGC[A/G]TGAAAAGTAAGATTG | 4193 |
| rs759400763 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824909 | TCTGTTAAGATAGTA[C/G]GAGGTGGCTGGGGTG | 4193 |
| rs759410259 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68837186 | CATGAACTCCTGACC[C/T]CAAGTGATCTGCCCA | 4193 |
| rs759423049 | in-del | -/AAGTG | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845001 | CAAACTCCTGACCTC[-/AAGTG]AAGTGATCTGCCCGC | 4193 |
| rs759476008 | snp | G/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844835 | ACAGTGGTGCAATCT[G/T]GGCTCACTGCAACCT | 4193 |
| rs759510005 | snp | C/T | 2.24606e-05 | 0.00335109 | intron-variant | MDM2 | GRCh38.p7 | 12:68836032 | AAAATTATTAAATAT[C/T]TTCTATGTTCATTGA | 4193 |
| rs759556256 | snp | C/T | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813895 | TTGGTAGACTCCTTC[C/T]CAGAATCATGTTTTT | 4193 |
| rs759644422 | snp | G/T | 3.31378e-05 | 0.00407036 | missense | MDM2 | GRCh38.p7 | 12:68839546 | ACAATCACAAGAAAG[G/T]GAAGACTATTCTCAG | 4193 |
| rs759856407 | snp | C/G | 1.71349e-05 | 0.00292697 | intron-variant | MDM2 | GRCh38.p7 | 12:68835795 | AGGTCAAGAGGTGAT[C/G]TTTATTAAGTTATAT | 4193 |
| rs759860190 | in-del | -/AGGA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825847 | ATGCGGGCAGAAGAC[-/AGGA]AGGGCAGAGGTGTCT | 4193 |
| rs759861388 | snp | C/G | 1.67242e-05 | 0.00289168 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824425 | GAAGGTGGGAGTGAT[C/G]AAAAGGTAATCTAAG | 4193 |
| rs760030564 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808213 | GGCGAGCTTGGCTGC[C/T]TCTGGGGCCTGTGTG | 4193 |
| rs760079591 | snp | A/G | 3.31334e-05 | 0.00407009 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839564 | AGACTATTCTCAGCC[A/G]TCAACTTCTAGTAGC | 4193 |
| rs760108963 | in-del | -/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843093 | AATTTGTTGTGTGGG[-/T]TTTTTTTTTTTTTAA | 4193 |
| rs760118560 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821215 | ACCACGCCCGGCTAA[G/T]TTTTGTATTTTTAGT | 4193 |
| rs760127492 | snp | A/C | 1.65767e-05 | 0.00287891 | missense | MDM2 | GRCh38.p7 | 12:68839371 | ATTGGCTTCCTGAAG[A/C]TAAAGGGAAAGATAA | 4193 |
| rs760254648 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68836134 | ATTGGTTTGTGGACT[G/T]GAGGATTTCATAGTT | 4193 |
| rs760269164 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831582 | TTTGCATCTTAAAGG[C/T]TGCCAGCCTTTAAGA | 4193 |
| rs760321000 | snp | A/C | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806545 | CTCCGCTCACTGCAA[A/C]CTCTGCCTCCCGAGA | 4193 |
| rs760399212 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68837375 | CTTTTTTTTTTTTCA[A/G]TTGAGATAGGGTCCT | 4193 |
| rs760454147 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829537 | TTCGGAGGCTGAGGC[A/G]GGTGGATCACCTGAG | 4193 |
| rs760499087 | in-del | -/ATTT | 2.03564e-05 | 0.00319027 | intron-variant | MDM2 | GRCh38.p7 | 12:68816769 | GTATTTACAACTAAC[-/ATTT]AGTTTTCTTTAATGC | 4193 |
| rs760514202 | snp | C/T | | | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845802 | GCGGTCTTGCTCTGT[C/T]GCCCAGGCTGGAATG | 4193 |
| rs760558995 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825788 | TGAAAGAGAATGTCA[G/T]ATCAGTGAAACAGAA | 4193 |
| rs760576245 | snp | A/T | 1.66846e-05 | 0.00288826 | intron-variant | MDM2 | GRCh38.p7 | 12:68836782 | TTTTTAAGAAATAAA[A/T]ATTTCATTAAGGTCA | 4193 |
| rs760583206 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831313 | CATTCTGACAATACT[A/G]GCCAGTTTTATGTGA | 4193 |
| rs760587938 | snp | A/G | 9.95124e-05 | 0.00705311 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68816901 | TTCAAATGATCTTCT[A/G]GGAGATTTGTTTGGC | 4193 |
| rs760631764 | snp | C/G | 0.000366367 | 0.0135296 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814626 | GGGCATCCCTGGATC[C/G]CAGGTTAAGAACTTC | 4193 |
| rs760635168 | snp | G/T | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68812906 | AATTGACCCCTAATC[G/T]AGTTGGCAGGCTCCT | 4193 |
| rs760639175 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68817083 | AATTTTTTAGCTCTG[C/T]GGCATATTATTTGAG | 4193 |
| rs760721754 | snp | C/G | | | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808545 | GCTCTGACGGTGTCC[C/G]CTCTATCGCTGGTTC | 4193 |
| rs760909586 | snp | C/T | 1.65831e-05 | 0.00287945 | intron-variant | MDM2 | GRCh38.p7 | 12:68809309 | TTAGTATTTTTGTCT[C/T]GTGTAACTTTTAAGA | 4193 |
| rs761082043 | snp | A/G | 1.65674e-05 | 0.00287809 | synonymous-codon | MDM2 | GRCh38.p7 | 12:68839561 | TGAAGACTATTCTCA[A/G]CCATCAACTTCTAGT | 4193 |
| rs761138850 | in-del | -/AGAC | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824281 | ATAAGGGTTTGTGTT[-/AGAC]TGATAGCATATCTAC | 4193 |
| rs761179153 | snp | A/G | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841397 | TTAGCCACCACACCC[A/G]GCTGTAAAAATGTAC | 4193 |
| rs761236777 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68827930 | AAGGCCAGGAGTTTG[A/G]GACCAGTGTGGCCAA | 4193 |
| rs761259297 | snp | C/T | 1.65611e-05 | 0.00287755 | missense | MDM2 | GRCh38.p7 | 12:68839664 | GTGGAATCTAGTTTG[C/T]CCCTTAATGCCATTG | 4193 |
| rs761384664 | snp | C/T | 1.73028e-05 | 0.00294128 | intron-variant | MDM2 | GRCh38.p7 | 12:68835998 | AGGTAGTATTTTTTT[C/T]CCCCTCTAATTATAT | 4193 |
| rs761437177 | snp | A/T | | | intron-variant, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68814673 | GAGTACAGTATACTG[A/T]TCTTTCTGGGATAGA | 4193 |
| rs761486425 | in-del | -/TT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824729 | TTAGTGCTTTTAGAC[-/TT]AATTAAATTGTTCCC | 4193 |
| rs761521068 | snp | A/G | 1.69032e-05 | 0.00290711 | intron-variant | MDM2 | GRCh38.p7 | 12:68835807 | GATGTTTATTAAGTT[A/G]TATATTTTTTTCTTG | 4193 |
| rs761541076 | snp | G/T | 1.65707e-05 | 0.00287838 | intron-variant | MDM2 | GRCh38.p7 | 12:68809162 | TGTATTTTCCACAGA[G/T]GTTTCATGATTTCCA | 4193 |
| rs761546875 | snp | C/G | 1.65833e-05 | 0.00287948 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68816914 | CTAGGAGATTTGTTT[C/G]GCGTGCCAAGCTTCT | 4193 |
| rs761558410 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821516 | TCACTTGAGCCGAGG[A/G]GTTCAAGACCAGCCT | 4193 |
| rs761650213 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68833609 | TTCTGTAAAGAGCCA[A/C]ATAGTTAATTATTTG | 4193 |
| rs761713021 | snp | A/G | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813448 | TAGATCCTCCCCAGC[A/G]TTTTTTCCAAATCCC | 4193 |
| rs761906899 | in-del | -/A | 0.000117443 | 0.00766209 | intron-variant | MDM2 | GRCh38.p7 | 12:68820301 | TGTACATCTCTTGTT[-/A]TTTTTTTTTTTTCTG | 4193 |
| rs762025174 | snp | A/G | 3.34835e-05 | 0.00409153 | intron-variant | MDM2 | GRCh38.p7 | 12:68836792 | ATAAAAATTTCATTA[A/G]GGTCAAGATTAGGAG | 4193 |
| rs762030852 | in-del | -/CT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822773 | TGAGATGGAGTCTCA[-/CT]CTGTCACCCAGGCTG | 4193 |
| rs762045078 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68811241 | TTTTAGTTTTTTAAA[A/T]TTTTTCTTAGTAATT | 4193 |
| rs762052814 | in-del | -/A | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831781 | TCCTATCTATAAAAA[-/A]TCTCAGCCGGGCGTG | 4193 |
| rs762080776 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841424 | GTACTTATTCTCCAG[C/T]CTCTTTTGTATAAAC | 4193 |
| rs762132706 | snp | G/T | 3.31214e-05 | 0.00406935 | missense | MDM2 | GRCh38.p7 | 12:68839678 | GCCCCTTAATGCCAT[G/T]GAACCTTGTGTGATT | 4193 |
| rs762220430 | snp | A/G | 1.66493e-05 | 0.0028852 | intron-variant | MDM2 | GRCh38.p7 | 12:68824515 | TAGCTTACTGGTTAT[A/G]TTAAGTTTGTTGTAT | 4193 |
| rs762238313 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68817359 | GTATACCACCACGTG[C/G]TAAAGGCTTACATTT | 4193 |
| rs762294285 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841824 | ATTATGCATCATTTT[C/T]CTTCAAGAATGACAG | 4193 |
| rs762307941 | snp | C/T | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806561 | CTCTGCCTCCCGAGA[C/T]CAAGCGATTCTTCTG | 4193 |
| rs762328343 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829002 | GCAGTCCTAATAAGG[A/G]TACGGATAGAATGTA | 4193 |
| rs762333503 | snp | C/T | | | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845791 | TGTTTTGAGATGCGG[C/T]CTTGCTCTGTCGCCC | 4193 |
| rs762391479 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826346 | TTGATTAAATTTTTC[A/G]GATTATAAAAAAGCT | 4193 |
| rs762393306 | snp | A/T | 1.68156e-05 | 0.00289957 | intron-variant | MDM2 | GRCh38.p7 | 12:68824677 | ATATTTATTTGACGC[A/T]TTCACACAGCTTTTT | 4193 |
| rs762539085 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68827570 | CATGGTCTAATCTTG[A/G]TAGTCTTTTTATTGA | 4193 |
| rs762703355 | in-del | -/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838976 | ACACATGTAAATAGT[-/G]AAATGATCACTACAG | 4193 |
| rs762706473 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810088 | AGGCCAAGGCGGACC[A/G]ATCACCTGAGATGAG | 4193 |
| rs762749628 | snp | C/T | 1.66192e-05 | 0.00288259 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813668 | GTATCTCACTAGTTA[C/T]ATGTAGCCATACTTA | 4193 |
| rs762765084 | snp | C/T | 3.9539e-05 | 0.00444611 | intron-variant | MDM2 | GRCh38.p7 | 12:68824315 | TGAGTAGCGCCCCGC[C/T]GCCCCCCGCCCACCA | 4193 |
| rs762786912 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823768 | ATTTCTTGGACAAAA[A/G]TCCTTTTTAATGGTG | 4193 |
| rs762796150 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822729 | AGAACTCCTATTCCA[C/T]GTTCTCAACTTTGTC | 4193 |
| rs762870651 | snp | A/G | 1.68454e-05 | 0.00290214 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808512 | GGCCCGGCAGCGAGC[A/G]GTCACTTTTGGGTCT | 4193 |
| rs762983354 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830363 | ACGCATACCTGCCCT[C/T]TAGAGTTACTGTACC | 4193 |
| rs763055876 | in-del | -/TGG | 1.65836e-05 | 0.0028795 | cds-indel | MDM2 | GRCh38.p7 | 12:68835840 | TTAGGATCTTGATGC[-/TGG]TGTAAGTGAACATTC | 4193 |
| rs763075161 | snp | G/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844344 | AAATATCACTGGGCA[G/T]CTTGAAGCAGTTGGG | 4193 |
| rs763077109 | in-del | -/TT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816364 | GGCTTAAAAGTAGCT[-/TT]TTTTTTTTTTTTTTT | 4193 |
| rs763077439 | snp | A/G | 0.000165835 | 0.00910439 | missense | MDM2 | GRCh38.p7 | 12:68839350 | GATGTTGGGCCCTTC[A/G]TGAGAATTGGCTTCC | 4193 |
| rs763094430 | snp | A/G | 0.000116166 | 0.00762034 | intron-variant | MDM2 | GRCh38.p7 | 12:68820320 | TTTTTTTTTCTGTCT[A/G]CAAGGAAAATATATA | 4193 |
| rs763134865 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68817593 | TGTCTCTACTAAAAA[A/T]ACAAAATTAGCTGGG | 4193 |
| rs763246240 | snp | C/G | 1.65715e-05 | 0.00287845 | missense | MDM2 | GRCh38.p7 | 12:68839532 | ATTACACAAGCTTCA[C/G]AATCACAAGAAAGTG | 4193 |
| rs763260384 | snp | A/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845302 | TTATATGTAAGAGGG[A/G]CTTTTTGACATTTAC | 4193 |
| rs763423670 | snp | A/G | 1.65897e-05 | 0.00288003 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828848 | TCCCTTTCCTTTGAT[A/G]AAAGCCTGGCTCTGT | 4193 |
| rs763459909 | snp | A/C | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68812914 | CCTAATCTAGTTGGC[A/C]GGCTCCTTGCATACA | 4193 |
| rs763543239 | snp | A/C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831165 | TTGAATTAGATAAAA[A/C/T]GACACGGACACACGT | 4193 |
| rs763587937 | snp | C/G | 8.2969e-05 | 0.00644031 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828860 | GATGAAAGCCTGGCT[C/G]TGTGTGTAATAAGGG | 4193 |
| rs763598977 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826403 | CCTGTAATCCCAGCA[C/G]TTTGGAAGGCCGAAG | 4193 |
| rs763633155 | snp | A/C | 0.000371195 | 0.0136184 | utr-variant-3-prime, nc-transcript-variant | MDM2, CPM | GRCh38.p7 | 12:68842269 | GACTACGGAAAGTTC[A/C]GGACATCAAAGAAGT | 4193 |
| rs763830392 | snp | C/T | 0.000153871 | 0.00876994 | intron-variant | MDM2 | GRCh38.p7 | 12:68835798 | TCAAGAGGTGATGTT[C/T]ATTAAGTTATATATT | 4193 |
| rs763854650 | snp | A/C/G | 3.31451e-05 | 0.00407083 | intron-variant | MDM2 | GRCh38.p7 | 12:68836662 | GATGCTAATGAATGT[A/C/G]TTTTATTAGGTATAT | 4193 |
| rs763864070 | snp | A/G | 0.00168114 | 0.0289438 | intron-variant | MDM2 | GRCh38.p7 | 12:68815635 | TTTTGTAGAGATGGA[A/G]TTTCACTATGTTGCC | 4193 |
| rs763894690 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68837735 | TTAACACTTAAATGT[A/T]TACATCTCATGCATA | 4193 |
| rs763920813 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68820245 | AGTATGTATGTAGAA[A/G]TCTGGTTAGATCCAG | 4193 |
| rs763944701 | snp | G/T | 6.67847e-05 | 0.00577822 | intron-variant | MDM2 | GRCh38.p7 | 12:68836784 | TTTAAGAAATAAAAA[G/T]TTCATTAAGGTCAAG | 4193 |
| rs764034976 | snp | A/G | 1.65855e-05 | 0.00287967 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68816903 | CAAATGATCTTCTAG[A/G]AGATTTGTTTGGCGT | 4193 |
| rs764094226 | in-del | -/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68820094 | TGGTAGTGTGAAATC[-/T]TTCAGCTAGAGAGAC | 4193 |
| rs764138235 | snp | A/G | | | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845831 | TGCAGTGCTGCAAAC[A/G]TGACTCACTACAGCC | 4193 |
| rs764216609 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68817616 | TAGCTGGGTGTGGTG[A/G]TGCATGCCTGTAATT | 4193 |
| rs764246170 | snp | C/T | 1.67713e-05 | 0.00289575 | intron-variant | MDM2 | GRCh38.p7 | 12:68824476 | AATATTATTTGCAAA[C/T]TGGAAAGGTTATTTA | 4193 |
| rs764426270 | snp | G/T | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814147 | AACCTCCGCCTCCTA[G/T]ATTCAAGCCCTTCTT | 4193 |
| rs764465968 | snp | C/T | 1.65608e-05 | 0.00287752 | missense | MDM2 | GRCh38.p7 | 12:68839667 | GAATCTAGTTTGCCC[C/T]TTAATGCCATTGAAC | 4193 |
| rs764473089 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821404 | ACTACACTGCTCCTA[A/T]AGCCCATCCTCGAAC | 4193 |
| rs764486650 | in-del | -/G | 1.65756e-05 | 0.00287881 | intron-variant | MDM2 | GRCh38.p7 | 12:68809305 | CTGGTTAGTATTTTT[-/G]TCTCGTGTAACTTTT | 4193 |
| rs764551277 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842614 | GAAGTGAAATGTGGA[C/T]ATAAAATAGTTACGC | 4193 |
| rs764554024 | snp | C/T | | | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828780 | ATCCAGAAGAAAATT[C/T]AGATGAATTATCTGG | 4193 |
| rs764630209 | snp | A/G | 1.9034e-05 | 0.00308491 | intron-variant | MDM2 | GRCh38.p7 | 12:68824327 | CGCCGCCCCCCGCCC[A/G]CCACCAAGTTTCTGA | 4193 |
| rs764639873 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68827941 | TTTGAGACCAGTGTG[A/G]CCAACATGGTGAAAC | 4193 |
| rs764710762 | snp | A/G | 1.68596e-05 | 0.00290336 | intron-variant | MDM2 | GRCh38.p7 | 12:68835809 | TGTTTATTAAGTTAT[A/G]TATTTTTTTCTTGTT | 4193 |
| rs764730849 | snp | A/C | 1.65704e-05 | 0.00287836 | intron-variant | MDM2 | GRCh38.p7 | 12:68809167 | TTTCCACAGATGTTT[A/C]ATGATTTCCAGTTTT | 4193 |
| rs764783109 | snp | A/G | 1.65987e-05 | 0.00288082 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828869 | CTGGCTCTGTGTGTA[A/G]TAAGGGAGATATGTT | 4193 |
| rs764886405 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822694 | CTGAGTTTGGTTTAG[A/G]TATCAGTAGAATTAA | 4193 |
| rs764918809 | snp | C/T | 1.65888e-05 | 0.00287996 | missense | MDM2 | GRCh38.p7 | 12:68839337 | TCACATTGCAACAGA[C/T]GTTGGGCCCTTCGTG | 4193 |
| rs764959164 | in-del | -/GTA | 4.06711e-05 | 0.00450931 | intron-variant | MDM2 | GRCh38.p7 | 12:68836576 | GCTTTCTCATATATT[-/GTA]GTACATGATATTTGT | 4193 |
| rs764966544 | snp | A/C | 1.66302e-05 | 0.00288355 | intron-variant | MDM2 | GRCh38.p7 | 12:68809347 | ATTTTATGAAGTGAT[A/C]AACTAAATTTCGTAT | 4193 |
| rs764994410 | snp | C/T | 3.31658e-05 | 0.00407208 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68816916 | AGGAGATTTGTTTGG[C/T]GTGCCAAGCTTCTCT | 4193 |
| rs765045035 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826362 | GATTATAAAAAAGCT[G/T]AGATGGCCTGGTGCG | 4193 |
| rs765082422 | snp | G/T | 1.66103e-05 | 0.00288182 | intron-variant | MDM2 | GRCh38.p7 | 12:68820310 | CTTGTTATTTTTTTT[G/T]TTTCTGTCTACAAGG | 4193 |
| rs765129251 | snp | C/G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834396 | GCAGTGAGCTGAGAT[C/G/T]ATGCCACTGCATTTC | 4193 |
| rs765244028 | in-del | -/T | 0.00611517 | 0.0549562 | intron-variant | MDM2 | GRCh38.p7 | 12:68820302 | GTACATCTCTTGTTA[-/T]TTTTTTTTTTTCTGT | 4193 |
| rs765307324 | snp | A/G | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813947 | TAGAATTACAAAGGA[A/G]ACATACTAAAATACG | 4193 |
| rs765330086 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828210 | CACTTTGGCTCTTTT[C/T]GGAAAAAAACAGATG | 4193 |
| rs765367390 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68842149 | GTAACAAGCCTGTCA[A/G]ATATCTGCAAGAACT | 4193 |
| rs765388354 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842627 | GACATAAAATAGTTA[C/T]GCTATTTGGTTAATG | 4193 |
| rs765425166 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841488 | TGAAAATAGCCACCA[C/T]TTACCCGTAAGACAA | 4193 |
| rs765555199 | snp | A/G | 1.65611e-05 | 0.00287755 | missense | MDM2 | GRCh38.p7 | 12:68839686 | ATGCCATTGAACCTT[A/G]TGTGATTTGTCAAGG | 4193 |
| rs765593048 | snp | A/G | 1.68647e-05 | 0.0029038 | intron-variant | MDM2 | GRCh38.p7 | 12:68824683 | ATTTGACGCATTCAC[A/G]CAGCTTTTTGATATT | 4193 |
| rs765625056 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68809990 | TTTGTACATGCATCC[C/T]GTGTGACTATTTCTG | 4193 |
| rs765629495 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68836217 | TAGACCTCAATGAAC[A/C]TGCTTATTATAATGG | 4193 |
| rs765690888 | snp | C/T | 1.66263e-05 | 0.00288321 | intron-variant | MDM2 | GRCh38.p7 | 12:68824531 | TTAAGTTTGTTGTAT[C/T]TTATTTTTTTCCTAA | 4193 |
| rs765704562 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819094 | CTTGAATTCTAAATG[A/T]TGAGAGATAAGAAAT | 4193 |
| rs765714296 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823921 | TGCCTACATTCCAGT[A/C]ATAATGAACTGCTTG | 4193 |
| rs765770696 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825923 | AAAGGTGAAGTTAGA[G/T]CTGTACCTTATGCCA | 4193 |
| rs765812860 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834510 | GGGAGGCCAAGGCGG[C/T]TGAATTGCTTGAGGT | 4193 |
| rs765897838 | in-del | -/TTT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816363 | AGGCTTAAAAGTAGC[-/TTT]TTTTTTTTTTTTTTT | 4193 |
| rs765963793 | snp | A/G | 2.10007e-05 | 0.00324036 | intron-variant | MDM2 | GRCh38.p7 | 12:68836026 | TATTGGAAAATTATT[A/G]AATATTTTCTATGTT | 4193 |
| rs766040958 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68811469 | TAAATTTTTTAAATA[C/T]TTAGATCTTCACCTG | 4193 |
| rs766057047 | snp | C/G | 1.66288e-05 | 0.00288343 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813522 | TCTGGGATAATTTTG[C/G]AAGTATAATAGCAGT | 4193 |
| rs766187015 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831817 | TCATGCCTGTAATCC[C/G]AGCACTTTGGAAGGC | 4193 |
| rs766200891 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816034 | CAGAATTCTCTCAAA[C/G]TGTTTTGTAGCTGTC | 4193 |
| rs766274731 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842879 | GAAGCCTAGTTATGC[C/T]GGACTGTTTTGATCT | 4193 |
| rs766311370 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829737 | TGCCACTGCACTCTA[G/T]CCTGGGTGACAGAGC | 4193 |
| rs766311764 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810112 | AGATGAGGAGTTCAA[C/G]ACTAGCCTGGCCAAC | 4193 |
| rs766335269 | snp | C/T | 1.78407e-05 | 0.00298665 | intron-variant | MDM2 | GRCh38.p7 | 12:68839241 | GCAGTTAAAGGGTTA[C/T]AGAAACTGACTGTGT | 4193 |
| rs766375101 | snp | A/G | 1.65844e-05 | 0.00287957 | missense | MDM2 | GRCh38.p7 | 12:68835838 | TTTTAGGATCTTGAT[A/G]CTGGTGTAAGTGAAC | 4193 |
| rs766424502 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819321 | TCAACGAATACTGGG[A/G]TAAATGAATTATCCT | 4193 |
| rs766428661 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68811834 | CTTGAACTTCTGACC[G/T]CCTGATCTGCCTGTC | 4193 |
| rs766516210 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830366 | CATACCTGCCCTCTA[A/G]AGTTACTGTACCTAA | 4193 |
| rs766541832 | in-del | -/AAC | | | intron-variant | MDM2 | GRCh38.p7 | 12:68832072 | CGAAATTCCATCTCA[-/AAC]AACAACAACAAAATC | 4193 |
| rs766553126 | snp | A/G | 4.97781e-05 | 0.00498864 | synonymous-codon, intron-variant, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68820325 | TTTTCTGTCTACAAG[A/G]AAAATATATACCATG | 4193 |
| rs766558998 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829188 | AATTATCAATGTCAC[C/T]GTATGTATTAGAGAA | 4193 |
| rs766801308 | snp | A/G | 1.65897e-05 | 0.00288003 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828849 | CCCTTTCCTTTGATG[A/G]AAGCCTGGCTCTGTG | 4193 |
| rs766825484 | in-del | -/TAT | 1.68329e-05 | 0.00290106 | intron-variant | MDM2 | GRCh38.p7 | 12:68835989 | AAGATGATGAGGTAG[-/TAT]TTTTTTTCCCCTCTA | 4193 |
| rs766875385 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838025 | TAAATCTATTTTAAG[A/G]CTCAAATTATTTTAG | 4193 |
| rs766898451 | in-del | -/TT | 0.000749285 | 0.0193412 | intron-variant | MDM2 | GRCh38.p7 | 12:68820302 | GTACATCTCTTGTTA[-/TT]TTTTTTTTTTCTGTC | 4193 |
| rs766969276 | snp | G/T | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806668 | AAGGTTTCACCATCT[G/T]GGCCAGGCTGGTCTC | 4193 |
| rs767024509 | snp | C/G | 1.65619e-05 | 0.00287762 | missense | MDM2 | GRCh38.p7 | 12:68839750 | AACAGGACATCTTAT[C/G]GCCTGCTTTACATGT | 4193 |
| rs767042958 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822995 | ATCCTCCCACCTTGG[C/T]CTCCCAAAGTGCTGG | 4193 |
| rs767114198 | snp | C/T | 0.000161616 | 0.00898788 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839949 | AAGTGAGAAAATGCC[C/T]CAATTCACATAGATT | 4193 |
| rs767121919 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826818 | CGGCCAAGATCACCT[G/T]TTTAAAAATAGGGAA | 4193 |
| rs767184413 | in-del | -/TTG | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818418 | AAAAAGGACTGTAGT[-/TTG]TTAACAAAAGGTATT | 4193 |
| rs767192754 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829405 | AAAAAGTCAGCATAG[A/T]CTGAACTTAACATTT | 4193 |
| rs767277336 | snp | C/T | 4.39271e-05 | 0.00468632 | intron-variant | MDM2 | GRCh38.p7 | 12:68836552 | TTACTCTATTTGATA[C/T]TGTCTAAGGCTTTCT | 4193 |
| rs767426126 | snp | A/G/T | 8.29282e-05 | 0.00643879 | intron-variant | MDM2 | GRCh38.p7 | 12:68836639 | TGAAGGAAATAGGGC[A/G/T]ATGAATTGATGCTAA | 4193 |
| rs767475639 | snp | A/G | 3.3168e-05 | 0.00407221 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68820366 | ACTTGGTAGTAGTCA[A/G]TCAGCAGGGTAAGTT | 4193 |
| rs767491109 | snp | G/T | 3.31538e-05 | 0.00407134 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813549 | CAGTTCTTTTCTCTT[G/T]ATAGGTTAGACCAAA | 4193 |
| rs767508610 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68811674 | CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTC | 4193 |
| rs767583596 | snp | C/T | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68807171 | TCAATTCTTTATGTC[C/T]TCAATTTATGAGACC | 4193 |
| rs767588818 | snp | A/C | 1.66421e-05 | 0.00288458 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813679 | GTTACATGTAGCCAT[A/C]CTTAAAGTTTTCAAG | 4193 |
| rs767686947 | snp | C/G | 1.65685e-05 | 0.00287819 | missense | MDM2 | GRCh38.p7 | 12:68839550 | TCACAAGAAAGTGAA[C/G]ACTATTCTCAGCCAT | 4193 |
| rs767692026 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819553 | CTGGAGTGCAATGGC[A/G]TGATCTTGGCTCACC | 4193 |
| rs767746746 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819997 | TCCTGTTTGAAAATA[A/T]GTATGTTCAACCTCT | 4193 |
| rs767922679 | in-del | -/T | 0.00112555 | 0.0236962 | intron-variant | MDM2 | GRCh38.p7 | 12:68835990 | GATGATGAGGTAGTA[-/T]TTTTTTTTCCCCTCT | 4193 |
| rs767959909 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841292 | AATAGAGACAGGGTC[C/T]CCCTGTGTTGCCCAG | 4193 |
| rs768100456 | snp | A/G | 3.31417e-05 | 0.00407059 | missense | MDM2 | GRCh38.p7 | 12:68839394 | AAAGATAAAGGGGAA[A/G]TCTCTGAGAAAGCCA | 4193 |
| rs768252027 | snp | C/T | 1.65899e-05 | 0.00288005 | intron-variant | MDM2 | GRCh38.p7 | 12:68820415 | TAAATACCATAAAAA[C/T]GTTTTAAAGACATTT | 4193 |
| rs768293562 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844539 | CCACCGTACCACTTG[C/T]CAGCGTGAAAAGTAA | 4193 |
| rs768396174 | in-del | -/T | 6.68516e-05 | 0.00578112 | intron-variant | MDM2 | GRCh38.p7 | 12:68828964 | AGTAAGGCAAGACTC[-/T]TACTGTTCAAAGTCT | 4193 |
| rs768454722 | snp | C/G | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813320 | GTTGTTTGTAAGGCA[C/G]TAAGCAGGTAATATA | 4193 |
| rs768460931 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816590 | TCTTTATCTCCTGAC[C/T]TCGTGATCCATCCGC | 4193 |
| rs768500039 | snp | A/G | 1.68576e-05 | 0.00290319 | intron-variant | MDM2 | GRCh38.p7 | 12:68820287 | TTTTTATTCTAAAAT[A/G]TACATCTCTTGTTAT | 4193 |
| rs768623393 | snp | A/G | 1.68046e-05 | 0.00289862 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808463 | GACCCCCGACTCCAA[A/G]CGCGAAAACCCCGGA | 4193 |
| rs768757236 | snp | A/G | 4.04098e-05 | 0.0044948 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839899 | CTATATAACCCTAGG[A/G]ATTTAGACAACCTGA | 4193 |
| rs768793674 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68820996 | ATAGTATAATACTCT[C/G]ATTTGAAGGCTAAAA | 4193 |
| rs768809435 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823501 | TCTTCCTTGCCTTCT[A/G]TATCAAATACCAGGT | 4193 |
| rs768939568 | snp | A/G | 1.66059e-05 | 0.00288144 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813663 | AAGTAGTATCTCACT[A/G]GTTACATGTAGCCAT | 4193 |
| rs768958931 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830178 | TTGGATACATTTTTT[C/G]GTAATATGGCAGTGT | 4193 |
| rs769190317 | snp | A/G | 2.02928e-05 | 0.00318528 | intron-variant | MDM2 | GRCh38.p7 | 12:68816769 | GTATTTACAACTAAC[A/G]TTTAGTTTTCTTTAA | 4193 |
| rs769275340 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68812040 | CCTGAGCCACTGCAC[C/T]TGGCTTCCATTACAG | 4193 |
| rs769299407 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841155 | CTCAGATTTTTGATA[C/T]TCTTAAACCTTCTGA | 4193 |
| rs769381350 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815770 | TTCTAATACAGTGAT[A/G]ATAATCTTATGAAAT | 4193 |
| rs769419446 | snp | A/G | 1.95915e-05 | 0.00312976 | intron-variant | MDM2 | GRCh38.p7 | 12:68836017 | CTCTAATTATATTGG[A/G]AAATTATTAAATATT | 4193 |
| rs769449637 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68809139 | TTGTTTATGTTCTTT[A/G]TATATGATGTATTTT | 4193 |
| rs769588730 | snp | A/G | 1.66776e-05 | 0.00288765 | intron-variant | MDM2 | GRCh38.p7 | 12:68836614 | ACTTATTACTAGGAA[A/G]CCTTCTGATTGAAGG | 4193 |
| rs769663056 | in-del | -/AGTG | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838973 | GACACACATGTAAAT[-/AGTG]AAATGATCACTACAG | 4193 |
| rs769693191 | snp | A/G | 1.65737e-05 | 0.00287864 | missense | MDM2 | GRCh38.p7 | 12:68839508 | TGTGTTGAGGAAAAT[A/G]ATGATAAAATTACAC | 4193 |
| rs769750641 | snp | C/T | 1.67517e-05 | 0.00289406 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68824391 | AGGTACATCTGTGAG[C/T]GAGAACAGGTGTCAC | 4193 |
| rs769801108 | snp | C/T | 1.67103e-05 | 0.00289048 | intron-variant | MDM2 | GRCh38.p7 | 12:68828962 | TAAGTAAGGCAAGAC[C/T]CTTACTGTTCAAAGT | 4193 |
| rs769890846 | snp | A/G | 1.68199e-05 | 0.00289994 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808494 | TGGTGAGGAGCAGGT[A/G]CTGGCCCGGCAGCGA | 4193 |
| rs770001266 | in-del | -/TAAG | 1.70551e-05 | 0.00292015 | intron-variant | MDM2 | GRCh38.p7 | 12:68835801 | AGAGGTGATGTTTAT[-/TAAG]TTATATATTTTTTTC | 4193 |
| rs770052866 | in-del | -/T | 1.65611e-05 | 0.00287755 | frameshift-variant | MDM2 | GRCh38.p7 | 12:68839684 | TAATGCCATTGAACC[-/T]TGTGTGATTTGTCAA | 4193 |
| rs770073233 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68836956 | TGCTGGAATTTGAAC[C/T]TTTTTTTTTTTTTTT | 4193 |
| rs770099930 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819799 | TGCGCCCGGCCTCTG[G/T]TAATACGTTTTAAGA | 4193 |
| rs770102145 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830501 | ACAGTTGAGATGGCA[C/T]TGCAGATACAGTGGT | 4193 |
| rs770125412 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823605 | AGTTTGTATTATTGC[A/G]ATTGTCTAATACTGG | 4193 |
| rs770255535 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831142 | AACACCAGGTTTTTT[A/G]TTTTGAGTTGAATTA | 4193 |
| rs770334560 | snp | C/T | 3.32568e-05 | 0.00407766 | intron-variant | MDM2 | GRCh38.p7 | 12:68816990 | AGCCATCTGGGCTAA[C/T]ATTTCAGTTCACCTC | 4193 |
| rs770391525 | snp | C/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845394 | AAATTATAAAATGAG[C/G]TAACAAACGAAAGGC | 4193 |
| rs770436173 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810002 | TCCCGTGTGACTATT[C/T]CTGTAAGAAAGATTT | 4193 |
| rs770453051 | in-del | -/ATAAAA | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845203 | TTTGATTTGATACTT[-/ATAAAA]ATAAAAAGAAAAAGT | 4193 |
| rs770516319 | in-del | -/T | 4.98202e-05 | 0.00499075 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813531 | ATTTTGGAAGTATAA[-/T]AGCAGTTCTTTTCTC | 4193 |
| rs770591621 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830083 | TTTTACAATTTTTTT[C/T]CTGCTCATCAGCTAT | 4193 |
| rs770629022 | snp | G/T | 1.6591e-05 | 0.00288015 | intron-variant | MDM2 | GRCh38.p7 | 12:68836635 | TGATTGAAGGAAATA[G/T]GGCGATGAATTGATG | 4193 |
| rs770653304 | snp | C/T | 4.9736e-05 | 0.00498653 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68836749 | TGAAATTTCCTTAGC[C/T]GTAAGTATACATCTA | 4193 |
| rs770681512 | snp | G/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843850 | CCTCGAAGCATTATT[G/T]GGAGTTGATAATACT | 4193 |
| rs770704468 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834311 | GCCGGGTGTGGTAGT[A/G]GACACCTGTAATCTC | 4193 |
| rs770743144 | snp | A/G | 1.66344e-05 | 0.0028839 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68816862 | ACGATTATATGATGA[A/G]AAGCAACAACATATT | 4193 |
| rs770763010 | snp | A/T | 1.65729e-05 | 0.00287857 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824618 | GTTTCTAGACCATCT[A/T]CCTCATCTAGAAGGA | 4193 |
| rs770770335 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822355 | TGATGATTTGGCATT[G/T]TATTGTTTTAAAGCT | 4193 |
| rs770802264 | snp | C/T | 3.34403e-05 | 0.00408889 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824407 | GAGAACAGGTGTCAC[C/T]TTGAAGGTGGGAGTG | 4193 |
| rs771046322 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809267 | TAACCACCTCACAGA[C/T]TCCAGCTTCGGAACA | 4193 |
| rs771144765 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825630 | TGCACTCCGCCTGGG[C/T]GACACAGTGAGACTG | 4193 |
| rs771157508 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822038 | TTTTCTGTATGTTTG[C/G]TAGAGACGGTGTTGC | 4193 |
| rs771168652 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845507 | ATATTTAACGTTAGA[A/G]TAATAGTATTTTGAA | 4193 |
| rs771210713 | snp | A/G | 1.65622e-05 | 0.00287764 | missense | MDM2 | GRCh38.p7 | 12:68839617 | ATGTGAAAGAGTTTG[A/G]AAGGGAAGAAACCCA | 4193 |
| rs771246474 | snp | C/T | | | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68808148 | CCGGATGCGCCGCGA[C/T]GACCCGCGCGCTCCC | 4193 |
| rs771373241 | snp | A/G | 1.72704e-05 | 0.00293852 | intron-variant | MDM2 | GRCh38.p7 | 12:68835778 | TTAGGAAACAGATAC[A/G]GAGGTCAAGAGGTGA | 4193 |
| rs771461181 | snp | C/T | 4.96964e-05 | 0.00498455 | intron-variant, synonymous-codon | MDM2 | GRCh38.p7 | 12:68835936 | TCTCGACTCAGAAGA[C/T]TATAGCCTTAGTGAA | 4193 |
| rs771497253 | snp | C/T | 1.6851e-05 | 0.00290263 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808517 | GGCAGCGAGCGGTCA[C/T]TTTTGGGTCTGGGCT | 4193 |
| rs771564622 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834244 | GTCAGGATTTCGAGA[C/G]CAGCCCAGCCAACAT | 4193 |
| rs771625431 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818803 | CTTGCTCTGTTGCCC[A/G]GGCTGCAACCTCTGC | 4193 |
| rs771740174 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819771 | GCTGGGATTACAGGT[G/T]TCTGTGAGCCACTGC | 4193 |
| rs771789870 | in-del | -/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828056 | GAATCACTTGAACCT[-/G]GGAGGCAGAGGTTGC | 4193 |
| rs771870108 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816771 | ATTTACAACTAACAT[C/T]TAGTTTTCTTTAATG | 4193 |
| rs771878671 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825746 | TTGCCTGAGGAAGTC[G/T]CAGTAACTAAGACCG | 4193 |
| rs771968951 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838798 | TTTATAGGTACATGA[A/T]TAATATCACATCACA | 4193 |
| rs771995571 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821321 | AAAGTCCTGGGATTA[C/T]AGGTATGAGCCACTG | 4193 |
| rs771996794 | snp | C/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844789 | ATTTATTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 4193 |
| rs772039014 | in-del | -/T | 0.0112104 | 0.0740238 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68814555 | AAAATAAGAATAGAA[-/T]TTTTTTTTTCCCATC | 4193 |
| rs772049936 | snp | A/G | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841648 | TAAAGTACCTTCTTG[A/G]CCTGGGTTACATGGT | 4193 |
| rs772360712 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808372 | CAGTGCCCTGGCCCG[A/G]AGAGTGGAATGATCC | 4193 |
| rs772361012 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810968 | CCTCACGGGTTCAAG[C/T]GATTCTCTTGCCTCA | 4193 |
| rs772363391 | snp | A/C | 1.66167e-05 | 0.00288237 | intron-variant, synonymous-codon | MDM2 | GRCh38.p7 | 12:68835969 | AGGACAAGAACTCTC[A/C]GATGAAGATGATGAG | 4193 |
| rs772364248 | snp | A/T | 2.55092e-05 | 0.00357127 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839875 | TATAAGAGAATTATA[A/T]ATTTCTAACTATATA | 4193 |
| rs772554005 | snp | A/C | 1.65649e-05 | 0.00287788 | missense, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809288 | CTTCGGAACAAGAGA[A/C]CCTGGTTAGTATTTT | 4193 |
| rs772571641 | snp | A/G | 1.7413e-05 | 0.00295062 | intron-variant | MDM2 | GRCh38.p7 | 12:68836596 | ACATGATATTTGTTT[A/G]GGACTTATTACTAGG | 4193 |
| rs772598655 | snp | A/G | 1.65935e-05 | 0.00288036 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813646 | AAGCTGAATCAAGAG[A/G]TAAGTAGTATCTCAC | 4193 |
| rs772604374 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808386 | GGAGAGTGGAATGAT[C/T]CCCGAGGCCCAGGGC | 4193 |
| rs772616582 | snp | C/T | 1.65707e-05 | 0.00287838 | intron-variant | MDM2 | GRCh38.p7 | 12:68809300 | AGACCCTGGTTAGTA[C/T]TTTTGTCTCGTGTAA | 4193 |
| rs772759928 | snp | A/G | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806678 | CATCTTGGCCAGGCT[A/G]GTCTCGAACTCCTAA | 4193 |
| rs772791413 | snp | C/G | 1.66474e-05 | 0.00288503 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813510 | AGGGCCTATAGTTCT[C/G]GGATAATTTTGGAAG | 4193 |
| rs772845274 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816633 | AAGTACTGGGATTAC[A/G]GGTGTGAGCCACTGC | 4193 |
| rs772865412 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828588 | CAGACAATAAATAAA[A/T]AAACAAATAAATAAA | 4193 |
| rs772867033 | snp | C/G | 1.65723e-05 | 0.00287852 | missense | MDM2 | GRCh38.p7 | 12:68839526 | GATAAAATTACACAA[C/G]CTTCACAATCACAAG | 4193 |
| rs772869332 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823739 | ATATTTTCTGTGAGC[G/T]AGAAATCAGTTTCAT | 4193 |
| rs772975884 | snp | C/T | 1.65957e-05 | 0.00288055 | intron-variant | MDM2 | GRCh38.p7 | 12:68820319 | TTTTTTTTTTCTGTC[C/T]ACAAGGAAAATATAT | 4193 |
| rs772992302 | snp | A/G | 0.00012029 | 0.00775438 | intron-variant | MDM2 | GRCh38.p7 | 12:68824313 | ACTGAGTAGCGCCCC[A/G]CCGCCCCCCGCCCAC | 4193 |
| rs772998686 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835480 | TGTTAATACAGTCAC[A/G]CTGTAGGTACTTTCG | 4193 |
| rs773070021 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68817056 | AAACATATTAAAGAC[A/C]TGCTGAAACTTAATT | 4193 |
| rs773110612 | in-del | -/GCAAAACAGT | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843537 | AAATATGAATCTTAA[-/GCAAAACAGT]GAAAATAACCATCTT | 4193 |
| rs773194659 | snp | C/T | 4.97665e-05 | 0.00498806 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813640 | AGAGGTAAGCTGAAT[C/T]AAGAGATAAGTAGTA | 4193 |
| rs773196530 | snp | C/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844816 | CTGTGGCTCAGGCTG[C/G]AGTACAGTGGTGCAA | 4193 |
| rs773224463 | in-del | -/T | 1.68292e-05 | 0.00290075 | intron-variant | MDM2 | GRCh38.p7 | 12:68835812 | TTATTAAGTTATATA[-/T]TTTTTTCTTGTTTTA | 4193 |
| rs773278707 | snp | A/G | 3.34398e-05 | 0.00408886 | intron-variant | MDM2 | GRCh38.p7 | 12:68828969 | GGCAAGACTCTTACT[A/G]TTCAAAGTCTAGTCC | 4193 |
| rs773349275 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68811421 | TCCTGTCCCAAGATC[G/T]TGCAAATATATTCCT | 4193 |
| rs773351956 | snp | C/T | 1.68281e-05 | 0.00290065 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808499 | AGGAGCAGGTACTGG[C/T]CCGGCAGCGAGCGGT | 4193 |
| rs773408815 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818022 | TGGTCTTGAGCTCCT[A/C]ACCTTCGGTAATCCA | 4193 |
| rs773409112 | snp | A/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68844219 | TCTTAAATTTTTATG[A/T]GTTGTTAAAATAGAA | 4193 |
| rs773441863 | in-del | -/TG | 1.65611e-05 | 0.00287755 | frameshift-variant | MDM2 | GRCh38.p7 | 12:68839685 | AATGCCATTGAACCT[-/TG]TGTGATTTGTCAAGG | 4193 |
| rs773503828 | snp | C/T | 7.55772e-05 | 0.00614678 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839919 | AGACAACCTGAAATT[C/T]ATTCACATATATCAA | 4193 |
| rs773506141 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825065 | AAATACAAAAAGTAG[C/T]TGGGCCTGGTGGCGC | 4193 |
| rs773519801 | snp | C/T | 1.65855e-05 | 0.00287967 | missense | MDM2 | GRCh38.p7 | 12:68839349 | AGATGTTGGGCCCTT[C/T]GTGAGAATTGGCTTC | 4193 |
| rs773525546 | snp | C/T | 5.04197e-05 | 0.00502069 | intron-variant | MDM2 | GRCh38.p7 | 12:68824674 | TGAATATTTATTTGA[C/T]GCATTCACACAGCTT | 4193 |
| rs773552070 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831154 | TTTGTTTTGAGTTGA[A/C]TTAGATAAAACGACA | 4193 |
| rs773583625 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819815 | TAATACGTTTTAAGA[C/T]CAAGAAAGGAAGTTG | 4193 |
| rs773632885 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822886 | GGTGGGATTACAGGT[A/G]CCTGCCACCACGTCC | 4193 |
| rs773662223 | snp | G/T | | | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808496 | GTGAGGAGCAGGTAC[G/T]GGCCCGGCAGCGAGC | 4193 |
| rs773673493 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819098 | AATTCTAAATGTTGA[C/G]AGATAAGAAATAGGA | 4193 |
| rs773714225 | in-del | -/T/TT | 0.194199 | 0.243892 | intron-variant | MDM2 | GRCh38.p7 | 12:68820301 | GTACATCTCTTGTTA[-/T/TT]TTTTTTTTTTTTCTG | 4193 |
| rs773741694 | snp | C/T | 9.96645e-05 | 0.00705849 | intron-variant | MDM2 | GRCh38.p7 | 12:68836757 | CCTTAGCTGTAAGTA[C/T]ACATCTACTTTTTTA | 4193 |
| rs773901901 | snp | A/G | 1.65894e-05 | 0.00288 | intron-variant | MDM2 | GRCh38.p7 | 12:68836637 | ATTGAAGGAAATAGG[A/G]CGATGAATTGATGCT | 4193 |
| rs774006696 | snp | G/T | 0.000166334 | 0.00911808 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813671 | TCTCACTAGTTACAT[G/T]TAGCCATACTTAAAG | 4193 |
| rs774014032 | snp | C/G | 1.6717e-05 | 0.00289106 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824420 | ACCTTGAAGGTGGGA[C/G]TGATCAAAAGGTAAT | 4193 |
| rs774092895 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816982 | TTGTAAAAAGCCATC[C/T]GGGCTAACATTTCAG | 4193 |
| rs774100788 | snp | A/C | 4.98981e-05 | 0.00499465 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68816863 | CGATTATATGATGAG[A/C]AGCAACAACATATTG | 4193 |
| rs774123658 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816624 | GGCCTCCCGAAGTAC[C/T]GGGATTACAGGTGTG | 4193 |
| rs774128626 | snp | A/G | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68812665 | GTGTGGCCCAGGCTG[A/G]TCTTGAACACCTAGC | 4193 |
| rs774204618 | snp | C/G | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841409 | CCCGGCTGTAAAAAT[C/G]TACTTATTCTCCAGC | 4193 |
| rs774279471 | snp | A/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68832670 | GGTGTGCACCACCAC[A/T]CCTGGCTAATTTTTT | 4193 |
| rs774326816 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838123 | TTGGTTTTATGAGCT[A/G]TGAAAAACCCCCTTC | 4193 |
| rs774382161 | snp | A/G | 1.65633e-05 | 0.00287774 | synonymous-codon, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809280 | GATTCCAGCTTCGGA[A/G]CAAGAGACCCTGGTT | 4193 |
| rs774478761 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819881 | TATTTAATGGATTTT[G/T]CGTAACTCAATAGTT | 4193 |
| rs774496699 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831198 | AGTGGTTTTAAGGAG[C/T]AGAGCGTTTAATAGG | 4193 |
| rs774604336 | snp | A/G | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813983 | CAAAATAGTAAACTA[A/G]TTTGTGATATGTGTG | 4193 |
| rs774671243 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845531 | TTTTGAATGAAAACC[A/G]TAGTTGATTGTCTTT | 4193 |
| rs774688124 | snp | A/G | 1.65913e-05 | 0.00288017 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828852 | TTTCCTTTGATGAAA[A/G]CCTGGCTCTGTGTGT | 4193 |
| rs774704532 | snp | C/G | 1.72564e-05 | 0.00293733 | intron-variant | MDM2 | GRCh38.p7 | 12:68835784 | AACAGATACAGAGGT[C/G]AAGAGGTGATGTTTA | 4193 |
| rs774720809 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808180 | TCGGGCGGTAGGGGG[A/C]GCGCACCGAGGCACC | 4193 |
| rs774767562 | snp | A/C/G | 3.3122e-05 | 0.00406941 | missense | MDM2 | GRCh38.p7 | 12:68839636 | GGAAGAAACCCAAGA[A/C/G]AAAGAAGAGAGTGTG | 4193 |
| rs774778416 | snp | A/C | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806220 | ATTTATTTATTGTAT[A/C]TCAAACAGTCCTCTT | 4193 |
| rs774788632 | snp | A/G | 1.68786e-05 | 0.002905 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808528 | GTCACTTTTGGGTCT[A/G]GGCTCTGACGGTGTC | 4193 |
| rs774872609 | in-del | -/A | 1.6851e-05 | 0.00290263 | intron-variant | MDM2 | GRCh38.p7 | 12:68835989 | AGATGATGAGGTAGT[-/A]ATTTTTTTTCCCCTC | 4193 |
| rs775052499 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838832 | AATATATTTTTAGTT[G/T]AGAATTTTTCAGGAT | 4193 |
| rs775062825 | snp | A/G | 8.2991e-05 | 0.00644117 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68816880 | GCAACAACATATTGT[A/G]TATTGTTCAAATGAT | 4193 |
| rs775223325 | snp | A/G | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813183 | ACCTAATCTTTAGAA[A/G]GAGAAGATTGATAAC | 4193 |
| rs775418860 | snp | A/G | | | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68845756 | TTTCCTAATTCCAAA[A/G]TTTCACCTTTTGTTT | 4193 |
| rs775699841 | snp | A/G | 1.65608e-05 | 0.00287752 | missense | MDM2 | GRCh38.p7 | 12:68839659 | AGAGTGTGGAATCTA[A/G]TTTGCCCCTTAATGC | 4193 |
| rs775724620 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834373 | CTTGAACCCCGGAGG[C/T]GGAGGTTGCAGTGAG | 4193 |
| rs775806476 | snp | A/G | 1.66994e-05 | 0.00288953 | intron-variant | MDM2 | GRCh38.p7 | 12:68824664 | CAGGTATATATGAAT[A/G]TTTATTTGACGCATT | 4193 |
| rs775810116 | snp | A/G | 1.65976e-05 | 0.00288072 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813653 | ATCAAGAGATAAGTA[A/G]TATCTCACTAGTTAC | 4193 |
| rs775827390 | snp | C/T | 1.69447e-05 | 0.00291068 | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808543 | GGGCTCTGACGGTGT[C/T]CCCTCTATCGCTGGT | 4193 |
| rs775833695 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68842048 | TTTAAAAGAAGTGCA[A/G]TTCTCAAAAGGTTAG | 4193 |
| rs775909564 | snp | G/T | 0.000119802 | 0.00773866 | intron-variant | MDM2 | GRCh38.p7 | 12:68835992 | ATGATGAGGTAGTAT[G/T]TTTTTTCCCCTCTAA | 4193 |
| rs775949813 | in-del | -/TTGT | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813306 | CTCAGTAATTTATGG[-/TTGT]TTGTAAGGCAGTAAG | 4193 |
| rs775995873 | snp | A/T | | | intron-variant, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68814654 | TTCTGCACTAGAGAT[A/T]CATGAGTACAGTATA | 4193 |
| rs776035870 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826045 | GTATTACATAAAAAG[C/T]CTTCCCAAATCAATA | 4193 |
| rs776196692 | snp | A/G | 5.12466e-05 | 0.00506169 | intron-variant | MDM2 | GRCh38.p7 | 12:68835799 | CAAGAGGTGATGTTT[A/G]TTAAGTTATATATTT | 4193 |
| rs776281610 | snp | C/T | | | upstream-variant-2KB, intron-variant | MDM2 | GRCh38.p7 | 12:68808582 | TCTGCCCGTTCGCAG[C/T]CTTTGTGCGGTTCGT | 4193 |
| rs776287289 | snp | A/G | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841060 | CATGTTAGCCAGGCT[A/G]ATCTTGAACTCCTAA | 4193 |
| rs776289045 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826105 | AAGGGCAGACAGTTC[A/C]CAAAAATTTCTCACA | 4193 |
| rs776303554 | in-del | -/A | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810471 | ATTATTATTATTATT[-/A]TTTTTTTTGAGGCGG | 4193 |
| rs776351918 | snp | C/G | 0.000167283 | 0.00914404 | intron-variant | MDM2 | GRCh38.p7 | 12:68836787 | AAGAAATAAAAATTT[C/G]ATTAAGGTCAAGATT | 4193 |
| rs776440409 | snp | A/G | 1.65899e-05 | 0.00288005 | missense | MDM2 | GRCh38.p7 | 12:68839331 | CTTCCATCACATTGC[A/G]ACAGATGTTGGGCCC | 4193 |
| rs776558865 | snp | C/T | 6.72631e-05 | 0.00579888 | intron-variant | MDM2 | GRCh38.p7 | 12:68824676 | AATATTTATTTGACG[C/T]ATTCACACAGCTTTT | 4193 |
| rs776599202 | snp | C/T | 0.000201959 | 0.0100468 | intron-variant | MDM2 | GRCh38.p7 | 12:68820290 | TTATTCTAAAATGTA[C/T]ATCTCTTGTTATTTT | 4193 |
| rs776664631 | snp | C/T | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841684 | GCCTAGGTTTCAGAC[C/T]TTTGCTTAAGGCCAG | 4193 |
| rs776673832 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815565 | TCCCACCTCAGTGTC[G/T]GCAGTAGCTAGGACT | 4193 |
| rs776774609 | snp | A/G | 1.65866e-05 | 0.00287976 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828807 | CTGGTGAACGACAAA[A/G]AAAACGCCACAAATC | 4193 |
| rs776797879 | in-del | -/TTAT | 1.67888e-05 | 0.00289726 | intron-variant | MDM2 | GRCh38.p7 | 12:68820299 | AATGTACATCTCTTG[-/TTAT]TTTTTTTTTTTCTGT | 4193 |
| rs776853230 | in-del | -/AGTAA | 1.67517e-05 | 0.00289406 | intron-variant | MDM2 | GRCh38.p7 | 12:68828979 | TACTGTTCAAAGTCT[-/AGTAA]AGTCCTGGCAGTCCT | 4193 |
| rs776956465 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822617 | TGTTTAAATAAACTT[C/T]GGCACATTACTAGAA | 4193 |
| rs776992213 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830184 | ACATTTTTTGGTAAT[A/G]TGGCAGTGTCTCATG | 4193 |
| rs777043921 | snp | A/C/T | 0.000129993 | 0.00806117 | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839902 | TATAACCCTAGGAAT[A/C/T]TAGACAACCTGAAAT | 4193 |
| rs777046966 | snp | G/T | 1.66101e-05 | 0.0028818 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813664 | AGTAGTATCTCACTA[G/T]TTACATGTAGCCATA | 4193 |
| rs777046996 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818918 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTTGCCAT | 4193 |
| rs777075587 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | MDM2 | GRCh38.p7 | 12:68839676 | TTGCCCCTTAATGCC[A/G]TTGAACCTTGTGTGA | 4193 |
| rs777082399 | snp | A/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843993 | AAGCAGAATCTGTTT[A/T]TTTCTGAGGAGTATC | 4193 |
| rs777121474 | snp | C/T | 1.65677e-05 | 0.00287812 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68824593 | AGAGAAACCTTCATC[C/T]TCACATTTGGTTTCT | 4193 |
| rs777345763 | snp | A/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843815 | GCTACAACCAAGCAG[A/T]ATCTCTTTTTTTTGG | 4193 |
| rs777346705 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810865 | CCTTTCCTTTTTGTT[G/T]TTGTTTTTGTTTTTT | 4193 |
| rs777448739 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68811891 | AGGCATGAGCCACTG[C/T]GCCTGGCCCACACCT | 4193 |
| rs777489115 | in-del | -/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826648 | AGTGAGACTCCCTCT[-/T]AAAAAAAAAAAAAAA | 4193 |
| rs777525974 | snp | G/T | 1.65715e-05 | 0.00287845 | missense | MDM2 | GRCh38.p7 | 12:68839802 | AATAAGCCCTGCCCA[G/T]TATGTAGACAACCAA | 4193 |
| rs777534936 | in-del | -/TAATT | 4.98012e-05 | 0.0049898 | intron-variant | MDM2 | GRCh38.p7 | 12:68809326 | TGTAACTTTTAAGAA[-/TAATT]TATTTTATGAAGTGA | 4193 |
| rs777568535 | snp | A/C | | | intron-variant | MDM2 | GRCh38.p7 | 12:68819532 | GTTTTGCTCTTGTTG[A/C]CCAGGCTGGAGTGCA | 4193 |
| rs777599995 | snp | C/T | 1.6569e-05 | 0.00287824 | missense, upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68813594 | AGTTATTAAAGTCTG[C/T]TGGTGCACAAAAAGA | 4193 |
| rs777617634 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830699 | AAAAAGAGAATTATT[A/G]TACCCTATTTATTTA | 4193 |
| rs777635548 | snp | A/G | 3.34773e-05 | 0.00409115 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824396 | CATCTGTGAGTGAGA[A/G]CAGGTGTCACCTTGA | 4193 |
| rs777815960 | snp | C/T | 1.65605e-05 | 0.0028775 | synonymous-codon, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809256 | TGATGGTGCTGTAAC[C/T]ACCTCACAGATTCCA | 4193 |
| rs777934813 | snp | A/T | 2.10051e-05 | 0.0032407 | intron-variant | MDM2 | GRCh38.p7 | 12:68836570 | TCTAAGGCTTTCTCA[A/T]ATATTGTAGTACATG | 4193 |
| rs777969898 | snp | C/G | 1.65704e-05 | 0.00287836 | missense | MDM2 | GRCh38.p7 | 12:68839407 | AAATCTCTGAGAAAG[C/G]CAAACTGGAAAACTC | 4193 |
| rs777998477 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834209 | GCATTTTGGGAGGCC[A/G]AGGTGGCGGATCACT | 4193 |
| rs778012866 | snp | G/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838382 | TGTGGGATAAAACGT[G/T]GGGAAAAGGAAGAAG | 4193 |
| rs778024187 | in-del | -/TTTA | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806292 | GGAATATTCTCTGCT[-/TTTA]TTTAAGTCTCACCAT | 4193 |
| rs778031822 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68812612 | TACCTGTTTTTGTTT[C/T]AGTTTTTAAATTTTT | 4193 |
| rs778106898 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821135 | TCACTGCAACCTCCG[C/T]CTCCCAGGTTCAAGC | 4193 |
| rs778253715 | snp | A/G | 1.66147e-05 | 0.0028822 | intron-variant | MDM2 | GRCh38.p7 | 12:68816991 | GCCATCTGGGCTAAC[A/G]TTTCAGTTCACCTCT | 4193 |
| rs778341406 | snp | A/G | 1.65853e-05 | 0.00287964 | intron-variant | MDM2 | GRCh38.p7 | 12:68820390 | GTAAGTTAATTTTGA[A/G]CATCATGGATAAATA | 4193 |
| rs778345390 | in-del | -/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68827952 | TGTGGCCAACATGGT[-/G]AAACCCTGTCTCTAC | 4193 |
| rs778414634 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835722 | AGGCCCATCCCCCAA[C/T]TGTTACACCCTGCTG | 4193 |
| rs778518943 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821619 | TCCTAGCTACTCAGG[A/G]GGCTGAGGCAGGAGG | 4193 |
| rs778582378 | snp | A/C | 1.66535e-05 | 0.00288556 | missense | MDM2 | GRCh38.p7 | 12:68839303 | CACTTCATGCAATGA[A/C]ATGAATCCCCCCCTT | 4193 |
| rs778629802 | in-del | -/TATT | 1.66829e-05 | 0.00288811 | intron-variant | MDM2 | GRCh38.p7 | 12:68824663 | ACAGGTATATATGAA[-/TATT]TATTTGACGCATTCA | 4193 |
| rs778675786 | snp | C/T | 0.000301563 | 0.0122756 | intron-variant | MDM2 | GRCh38.p7 | 12:68828768 | TTTTCCTTACATATC[C/T]AGAAGAAAATTCAGA | 4193 |
| rs778784299 | snp | C/G | 1.66123e-05 | 0.00288199 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68824647 | GAGAGCAATTAGTGA[C/G]ACAGGTATATATGAA | 4193 |
| rs778934678 | snp | G/T | 1.77486e-05 | 0.00297892 | intron-variant | MDM2 | GRCh38.p7 | 12:68836592 | TAGTACATGATATTT[G/T]TTTAGGACTTATTAC | 4193 |
| rs778958802 | snp | A/T | | | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807722 | GCCTGCCTTAAGTGC[A/T]ATTTTTAATCTTTTT | 4193 |
| rs778992117 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68815219 | AAAAAGTATGGATTT[A/G]GCAGTAGATAGAAAT | 4193 |
| rs779003776 | in-del | -/AGC | 3.32143e-05 | 0.00407505 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813532 | TTTTGGAAGTATAAT[-/AGC]AGTTCTTTTCTCTTT | 4193 |
| rs779022475 | snp | A/G | 1.65847e-05 | 0.0028796 | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813636 | TGAAAGAGGTAAGCT[A/G]AATCAAGAGATAAGT | 4193 |
| rs779034414 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830143 | CAATTCTTCCAATGT[C/T]GCCCACGGAAACCAA | 4193 |
| rs779048674 | snp | A/T | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806253 | ATTTTCCTTTCTGTA[A/T]TTTTTGATAATTTTC | 4193 |
| rs779115220 | snp | C/T | 0.000268075 | 0.0115744 | intron-variant | MDM2 | GRCh38.p7 | 12:68824348 | AAGTTTCTGATCCTT[C/T]TTCTTTTCTCTCAGA | 4193 |
| rs779149930 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68809609 | TTTTAAAAATGGTTT[C/T]TAAAAGTCAAAAAAG | 4193 |
| rs779345987 | snp | A/C | 1.65701e-05 | 0.00287833 | intron-variant, missense | MDM2 | GRCh38.p7 | 12:68835951 | TTATAGCCTTAGTGA[A/C]GAAGGACAAGAACTC | 4193 |
| rs779357668 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822300 | TTAAAGCCCAGAAAA[A/G]TATCTCCATTTTATC | 4193 |
| rs779439846 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835090 | AGTATTACAAGTGTT[A/G]TGTCTTGTTACGTGT | 4193 |
| rs779510851 | snp | C/G | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843870 | TTGATAATACTTCAG[C/G]TTCAATTTGGAGTTG | 4193 |
| rs779552981 | snp | C/G | | | upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68807844 | CTTTTTGGTAACAGC[C/G]ACACGGAGATCCGCA | 4193 |
| rs779601429 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68834317 | TGTGGTAGTGGACAC[C/G]TGTAATCTCAGCTAC | 4193 |
| rs779708646 | snp | C/G | 1.65855e-05 | 0.00287967 | intron-variant | MDM2 | GRCh38.p7 | 12:68820397 | AATTTTGAGCATCAT[C/G]GATAAATACCATAAA | 4193 |
| rs779722275 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831865 | CTGAGGTCAGGAGTT[C/G]AGGACCAGCCTCGCC | 4193 |
| rs779733802 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68826895 | AAACGTAAAAATCCC[A/G]GCCAGGTCCAGTGGC | 4193 |
| rs779795138 | in-del | -/AT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68833150 | AAAAAAAAAAAAAAA[-/AT]ATATATATATATATA | 4193 |
| rs779823103 | snp | A/G | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841278 | TTTCTTGATTTAACA[A/G]TAGAGACAGGGTCTC | 4193 |
| rs779881336 | in-del | -/ACTG | 3.55923e-05 | 0.0042184 | intron-variant | MDM2 | GRCh38.p7 | 12:68839246 | TAAAGGGTTACAGAA[-/ACTG]ACTGTGTGTCTTATT | 4193 |
| rs779891495 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824922 | TAGGAGGTGGCTGGG[A/G]TGTGGTGGCTCACGC | 4193 |
| rs779896780 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828317 | AGATTAAATTGTGAT[A/G]TATGGAGATAAAGTT | 4193 |
| rs779913228 | snp | A/G | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68841654 | ACCTTCTTGGCCTGG[A/G]TTACATGGTTCCCAG | 4193 |
| rs779990530 | snp | A/T | 1.66346e-05 | 0.00288393 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68828781 | TCCAGAAGAAAATTC[A/T]GATGAATTATCTGGT | 4193 |
| rs780006768 | snp | A/G | 1.6612e-05 | 0.00288196 | missense, intron-variant | MDM2 | GRCh38.p7 | 12:68828899 | TGTGAAAGAAGCAGT[A/G]GCAGTGAATCTACAG | 4193 |
| rs780013231 | in-del | -/TAAG | 1.66796e-05 | 0.00288782 | intron-variant | MDM2 | GRCh38.p7 | 12:68828947 | GTAATGTTCTCATTT[-/TAAG]TAAGGCAAGACTCTT | 4193 |
| rs780052803 | snp | C/T | 3.31967e-05 | 0.00407397 | intron-variant | MDM2 | GRCh38.p7 | 12:68816967 | CTTCAGTTTAGTCCA[C/T]TGTAAAAAGCCATCT | 4193 |
| rs780101293 | snp | C/T | 3.364e-05 | 0.00410108 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808443 | GAAACTGGGGAGTCT[C/T]GAGGGACCCCCGACT | 4193 |
| rs780123599 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68827479 | TTTTACTATATATGT[C/T]GCAGATATTATCTTC | 4193 |
| rs780149278 | snp | C/T | 2.05046e-05 | 0.00320186 | intron-variant | MDM2 | GRCh38.p7 | 12:68816761 | TATTAAATGTATTTA[C/T]AACTAACATTTAGTT | 4193 |
| rs780285966 | snp | A/T | 1.69986e-05 | 0.0029153 | intron-variant | MDM2 | GRCh38.p7 | 12:68836603 | ATTTGTTTAGGACTT[A/T]TTACTAGGAAGCCTT | 4193 |
| rs780560336 | snp | A/G | 1.65641e-05 | 0.00287781 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68836698 | TACTGTGTATCAGGC[A/G]GGGGAGAGTGATACA | 4193 |
| rs780622085 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810721 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 4193 |
| rs780673045 | snp | A/G | 1.65625e-05 | 0.00287766 | missense | MDM2 | GRCh38.p7 | 12:68839592 | AGCATTATTTATAGC[A/G]GCCAAGAAGATGTGA | 4193 |
| rs780712220 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808982 | GTCCTGACTTGTCTC[C/T]AGCTGGGGCTATTTA | 4193 |
| rs780751561 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823337 | CTCAAAGTCTGTATA[C/T]CCAACTACAAATGAA | 4193 |
| rs780839266 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | MDM2, CPM | GRCh38.p7 | 12:68841714 | GTTTTAGAAACCCGT[G/T]AATTCAGAAAAGTTA | 4193 |
| rs780933636 | in-del | -/TG | | | intron-variant | MDM2 | GRCh38.p7 | 12:68822512 | AGCTCTTTAAGAAAT[-/TG]TGTGATAGCTAAATA | 4193 |
| rs780973303 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68817865 | TGCAGTGGCATGATC[C/T]TGGCTCACTGCAACC | 4193 |
| rs781032929 | in-del | -/G | 1.6571e-05 | 0.0028784 | frameshift-variant | MDM2 | GRCh38.p7 | 12:68839433 | AACTCAACACAAGCT[-/G]AAGAGGGCTTTGATG | 4193 |
| rs781106986 | snp | C/T | 1.68046e-05 | 0.00289862 | upstream-variant-2KB, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68808466 | CCCCGACTCCAAGCG[C/T]GAAAACCCCGGATGG | 4193 |
| rs781159764 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829580 | AGACCAGCATGGCCA[A/G]CAAGATGAAACCATG | 4193 |
| rs781160157 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68832850 | ATAGTATTTAGGTCT[A/G]GTGCAGTGGCTCATG | 4193 |
| rs781195441 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, utr-variant-5-prime | MDM2 | GRCh38.p7 | 12:68809231 | GCAATACCAACATGT[C/T]TGTACCTACTGATGG | 4193 |
| rs781220406 | snp | A/G | 1.66294e-05 | 0.00288347 | synonymous-codon, intron-variant | MDM2 | GRCh38.p7 | 12:68828919 | TGAATCTACAGGGAC[A/G]CCATCGAATCCGGTA | 4193 |
| rs781323600 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828439 | CATTCCTATGGTACC[C/G]TTCCTATGGTACCAG | 4193 |
| rs781398586 | snp | C/G | | | downstream-variant-500B, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68846002 | TCTTTCACCCAGACT[C/G]GAGTGCAGTGGTGCA | 4193 |
| rs781419393 | snp | A/T | 2.01323e-05 | 0.00317265 | intron-variant | MDM2 | GRCh38.p7 | 12:68816776 | CAACTAACATTTAGT[A/T]TTCTTTAATGCTCAG | 4193 |
| rs781438395 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835377 | GGAAGTTGAAATGCC[A/G]AGATTAGTTGAGGAA | 4193 |
| rs781698257 | snp | C/T | 1.66161e-05 | 0.00288232 | intron-variant | MDM2 | GRCh38.p7 | 12:68816987 | AAAAGCCATCTGGGC[C/T]AACATTTCAGTTCAC | 4193 |
| rs781702537 | snp | G/T | 1.7383e-05 | 0.00294808 | intron-variant | MDM2 | GRCh38.p7 | 12:68839269 | TGTGTCTTATTTCAT[G/T]GAAGGACTATTGGAA | 4193 |
| rs796107371 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825389 | CCGGGCGCAGTGGCT[C/G]ACGCCTGTAATCCCA | 4193 |
| rs796122102 | snp | A/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68836403 | TTATTTAATATCTCC[A/G]TATTAGTTATTTATG | 4193 |
| rs796144334 | in-del | AAA/T | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68842532 | CATTGCTGTCTACAA[AAA/T]AGATAATATGGATGT | 4193 |
| rs796162239 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68835077 | AAAAAAACCCATAAG[C/T]ATTACAAGTGTTGTG | 4193 |
| rs796247513 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68817003 | AACATTTCAGTTCAC[C/T]TCTACCCTCATTCAC | 4193 |
| rs796330525 | in-del | -/CTT | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806174 | TCCAAGTTCTTAAAA[-/CTT]CTTCTTGACTTTCAT | 4193 |
| rs796339308 | in-del | -/A | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68807019 | AGGATATAACTTTAT[-/A]AAAAAAAAAAAGCTG | 4193 |
| rs796385055 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68828498 | AGGATCACTTGAGCC[C/T]ATGAGGCAGAGGTTG | 4193 |
| rs796411551 | in-del | -/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68823258 | ATGTTTCCAAGGGGG[-/G]GTAGTAAAGGGTATT | 4193 |
| rs796507690 | snp | C/T | | | intron-variant, upstream-variant-2KB | MDM2 | GRCh38.p7 | 12:68813485 | TGAACTTGATGGATA[C/T]GTTTGCTGCAGGGCC | 4193 |
| rs796519418 | snp | C/G | | | intron-variant | MDM2 | GRCh38.p7 | 12:68816504 | CAGCCTCCCTAATAG[C/G]TGGGATTACAGGTGT | 4193 |
| rs796526206 | in-del | -/CT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68821554 | ATGGCAAAATCCTAA[-/CT]CTGCAAAAACTACAA | 4193 |
| rs796536137 | in-del | -/GA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68825667 | AAAAAGAGAGAGAGA[-/GA]AAATAGTTGACAGAG | 4193 |
| rs796563142 | in-del | -/GA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68830552 | TGCCTTCATTGGGAG[-/GA]ATAGATCATTAATGA | 4193 |
| rs796590099 | in-del | -/GAA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831621 | TTTTATGCTAGACAA[-/GAA]ATTTTTCTGGAGCTA | 4193 |
| rs796613834 | in-del | -/TC | | | utr-variant-3-prime, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843704 | TGCTTCAAAACTCTC[-/TC]TCTCTCTCTCTGTCT | 4193 |
| rs796625013 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68831994 | AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 4193 |
| rs796631937 | in-del | -/TAGTA | | | utr-variant-3-prime | MDM2 | GRCh38.p7 | 12:68839974 | TAGATTTCTTCTCTT[-/TAGTA]TAATTGACCTACTTT | 4193 |
| rs796643799 | in-del | -/GTCTT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68818786 | TTTTTTTGAGATGAA[-/GTCTT]GCTCTGTTGCCCAGG | 4193 |
| rs796674546 | in-del | -/CATATTGACCTTTA | | | intron-variant | MDM2 | GRCh38.p7 | 12:68838912 | TACATATTGACCTTT[-/CATATTGACCTTTA]AAAAATCTGTTTTGT | 4193 |
| rs796675570 | in-del | -/CTT | | | intron-variant | MDM2 | GRCh38.p7 | 12:68824699 | CAGCTTTTTGATATT[-/CTT]TCTCTAATGAAATTA | 4193 |
| rs796790274 | in-del | -/CTT | | | utr-variant-3-prime, cds-indel, intron-variant | MDM2, CPM | GRCh38.p7 | 12:68843505 | CAAACTGTGGATTAA[-/CTT]CTTGATTTATATTTA | 4193 |
| rs796844444 | in-del | -/A | | | intron-variant | MDM2 | GRCh38.p7 | 12:68810468 | TTAATTATTATTATT[-/A]TTATTTTTTTTGAGG | 4193 |
| rs796927345 | snp | C/T | | | intron-variant | MDM2 | GRCh38.p7 | 12:68829732 | GATTGTGCCACTGCA[C/T]TCTAGCCTGGGTGAC | 4193 |
| rs796965240 | snp | A/C | | | upstream-variant-2KB | MDM2, LOC100130075 | GRCh38.p7 | 12:68806837 | TCAAGCACTGAGTCT[A/C]TTAGAAACCCCACTG | 4193 |