SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1563 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495905 | TTACAGAATACCTAT[C/T]GAGATATTACACCTA | 115426 |
rs370132 | snp | A/G | 0.49928 | 0.018956 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456221 | gccagttagaatggc[A/G]atcattaaaaagtca | 115426 |
rs370818 | snp | A/C | 0.365232 | 0.22186 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456266 | cattagagaaacgca[A/C]atcaaaaccacactg | 115426 |
rs375835 | snp | A/T | 0.49975 | 0.0111793 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456230 | ccatatcacgccagt[A/T]agaatggcgatcatt | 115426 |
rs380674 | snp | A/T | 0.435837 | 0.167226 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438131 | GACCTGGATTATGAT[A/T]GTTCCCATATTGTAA | 115426 |
rs386632 | snp | C/T | 0.378765 | 0.214288 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456155 | CTCTCTAGAAACATT[C/T]TAAAAAGAAAAAAGC | 115426 |
rs394137 | snp | A/G | 0.435119 | 0.16802 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440619 | ACACACGCAACTTCT[A/G]TTGAGCTAAACCGTA | 115426 |
rs401733 | snp | C/T | 0.497641 | 0.0342639 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455048 | CCTACCTTTGATAGA[C/T]TGAGCTTTTTAAGAG | 115426 |
rs407351 | snp | A/T | 0.348794 | 0.229651 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451638 | GGCGCCCGCCACCAC[A/T]CCCGGCTAATTTTTA | 115426 |
rs414107 | snp | C/T | 0.386123 | 0.209692 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439294 | GGTTCAAACGATTCT[C/T]CTGTCTCAGCCTCCT | 115426 |
rs424119 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439943 | CATTAAGTGGTTAAT[A/G]TAAAAGAAAAAAGGG | 115426 |
rs427077 | snp | A/G | 0.347473 | 0.230215 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451579 | CCCCCCGGGGTTCAC[A/G]CCATTCTCCTGCCTC | 115426 |
rs452135 | snp | A/G | 0.38555 | 0.210062 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441207 | aacatggcaaaaccc[A/G]gtctctacaaaaaaa | 115426 |
rs503315 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439075 | TACAAACACTAAGTT[C/T]ATGAAAAACAGGTTA | 115426 |
rs504698 | snp | A/G | 0.4444 | 0.15719 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463435 | AACGTTAGGAACACA[A/G]TAGCTAAAAAGGAAC | 115426 |
rs513526 | snp | C/T | 0.498964 | 0.02274 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459604 | tcagctcactgccac[C/T]tccacctcctgggtt | 115426 |
rs519674 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450623 | TAATTCCCTAGAATC[C/T]TTCAAAGGTTGACCG | 115426 |
rs524888 | snp | C/T | 0.498059 | 0.0310896 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459274 | GAAAATGGAGACTAT[C/T]GGAATATGCCAGGTT | 115426 |
rs530722 | snp | C/T | 0.442113 | 0.159977 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462813 | TCCCAGCTACATGGG[C/T]GGCTGAGGCAGAGGA | 115426 |
rs531571 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446690 | aaccccgtctctata[C/G]gaaaatttgcttggt | 115426 |
rs535725 | snp | C/T | 0.4973 | 0.0366419 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462346 | AAAAAAAAAATGATG[C/T]GAGGTGTTGAAAACT | 115426 |
rs541378 | snp | A/G | 0.499784 | 0.0103811 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465465 | GTTCTTTTATGGTCA[A/G]TTCGGTTTCTGTAAT | 115426 |
rs553048 | snp | C/G | 0.0547245 | 0.156101 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443567 | ATAACTTAAAAATTT[C/G]TGTTTATCTCTCTAG | 115426 |
rs559438 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455445 | tttccagcttcatcc[A/C]tgtccctacaaagga | 115426 |
rs560059 | snp | A/G | 0.406296 | 0.19512 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447196 | gcccagccAGCACAC[A/G]TACCTTTTAACCTAA | 115426 |
rs563779 | snp | A/C | 0.495291 | 0.0482933 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447591 | TAAGAAGAAATGAAA[A/C]TAAAGGTAAATAAAG | 115426 |
rs568386 | snp | C/T | 0.499234 | 0.0195537 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455777 | AGCTGGTCTCAGACT[C/T]CAGGGCTGAAGCAAT | 115426 |
rs569866 | snp | A/C | 0.44755 | 0.153212 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466285 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 115426 |
rs578124 | snp | C/T | 0.396727 | 0.202413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458054 | aactattccaaacaa[C/T]aggaaaagagggact | 115426 |
rs1044642 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507006 | CTAAATTTTATATTC[A/C]CTATATTCCCTAAAG | 115426 |
rs1156747 | snp | A/G | 0.424814 | 0.178718 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423233 | AAGTACCAGGCTTGG[A/G]TGGCTGAATTGTTTT | 115426 |
rs1156867 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417950 | AAAAATGTTCTTTCA[A/G]TTTCCAGCAGTTTTA | 115426 |
rs1156868 | snp | A/T | 0.084364 | 0.187256 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417972 | GCAGTTTTATCACTT[A/T]AACTGCTATCTTCAT | 115426 |
rs1156869 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418000 | CATTTTTGGAAATAT[C/G]CTACTAGTTAATTTG | 115426 |
rs1156870 | snp | C/T | 0.13446 | 0.221699 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418060 | TATCTTTAAGCACTT[C/T]CATTTAAAAATAGTC | 115426 |
rs1270597 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456954 | catgatgccaccagc[C/T]ttgttctttttgctt | 115426 |
rs1272800 | snp | A/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456975 | ctttttgcttaggat[A/G/T]gtcttggctatacgg | 115426 |
rs1272801 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457078 | atggggacagcattg[A/G]atctataaattactt | 115426 |
rs1381035 | snp | A/T | 0.41408 | 0.188621 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429909 | TAGTAAAACCATCAA[A/T]TATTTGCTGTTGGTA | 115426 |
rs1381036 | snp | A/G | 0.420892 | 0.182472 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429924 | ATATTTGCTGTTGGT[A/G]TTTTCTTTTTTTAAT | 115426 |
rs1381037 | snp | A/G | 0.422 | 0.181428 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430156 | GCTGGGATTACAGGT[A/G]CATGCCACCATGCCC | 115426 |
rs1824537 | snp | A/G | 0.421526 | 0.181876 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430182 | TGCCCGGCTAATTTT[A/G]TACTTTTAGTAGAGA | 115426 |
rs1870696 | snp | G/T | 0.228253 | 0.249052 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452927 | TATTATGCGCTCAAA[G/T]GTTACCTAATATTTT | 115426 |
rs1903419 | snp | A/G | 0.443732 | 0.158012 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433304 | CATTTTGTGTCTTAC[A/G]CCCTGTTCATTTTTA | 115426 |
rs1929929 | snp | A/G | 0.284209 | 0.247648 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499994 | CAAGAGTGAGACCCC[A/G]TCTCAACAACAACAA | 115426 |
rs2065074 | snp | A/G | 0.445855 | 0.155373 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420225 | TACTAGAAATACAAA[A/G]TATTAGCTGGGCGTG | 115426 |
rs2065075 | snp | A/T | 0.441432 | 0.160792 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418041 | TGCTTAAAGATAATT[A/T]AAAAAAACTAACAGT | 115426 |
rs2145991 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451977 | AAAGTGTATTGtgta[C/T]atatgcatttgtata | 115426 |
rs2169283 | snp | A/C | 0.424348 | 0.179172 | intron-variant | UHRF2 | GRCh38.p7 | 9:6413919 | TGTATTTGGTAGGAC[A/C]GCGGCCGTAGGCACT | 115426 |
rs2169286 | snp | A/C | 0.416871 | 0.186156 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425256 | TATGAACTCAtgatc[A/C]aattgttccactttt | 115426 |
rs2295844 | snp | C/G | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460458 | TAAGGACACTTCAAC[C/G]TATTTTACTCTTTCT | 115426 |
rs2297445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496863 | GGGGAAGGGAGAACG[C/T]TGGAAAACTAAAGCA | 115426 |
rs2381444 | snp | C/T | 0.448195 | 0.152377 | intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6413895 | CCGGAGCGCAAATAT[C/T]TCGCCGTTTGTATTT | 115426 |
rs2381445 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446413 | ctcccaaagtgctgg[A/G]tttacaggcgtgagc | 115426 |
rs2381447 | snp | A/G | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460839 | ACTGAATTGATCAAG[A/G]AATGTATTTTTAGGT | 115426 |
rs2777945 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457102 | ttgtgaaaatgccca[C/T]actgcccaaagtaat | 115426 |
rs3070894 | in-del | -/AAG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460836 | TTAACTGAATTGATC[-/AAG]GAATGTATTTTTAGG | 115426 |
rs3739654 | snp | A/G | 0.33514 | 0.235254 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468447 | TGCACCAGAGAATCA[A/G]AGAGAACCAACTGCG | 115426 |
rs4380997 | snp | A/G | 0.429538 | 0.173972 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470639 | TTAAAATATACATAG[A/G]AAAAAAATGCGTGAC | 115426 |
rs4384035 | snp | A/G | 0.318656 | 0.240388 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457938 | aggatttttgcatca[A/G]tgttcatagggatat | 115426 |
rs4463484 | snp | C/T | 0.422315 | 0.181128 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480382 | CATTTATCCCCAGCA[C/T]GAAAATAGTGCCTTG | 115426 |
rs4556138 | snp | C/T | 0.447938 | 0.152711 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469486 | ttgcgccactgcact[C/T]cagcctggcgacaga | 115426 |
rs4740844 | snp | C/T | 0.434253 | 0.168969 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424566 | agatttgtagcaaaa[C/T]tgaagatagtagaga | 115426 |
rs4740845 | snp | A/G | 0.451234 | 0.14834 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424634 | AGATCTTAAGTTAGT[A/G]TGGTGTATTTGTTGA | 115426 |
rs4740846 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469793 | ATATATATGTATATA[C/T]GTGTATATATATATT | 115426 |
rs4742198 | snp | A/C | 0.0547245 | 0.156101 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419653 | CAAGCACTGATTAAA[A/C]ATAAAACTTGAGAAA | 115426 |
rs4742199 | snp | C/T | 0.452103 | 0.147154 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419853 | taaagtgatctccca[C/T]ctcagcctcctgagt | 115426 |
rs4742200 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430254 | acctcaggtgatcca[C/T]ccaccctggccccct | 115426 |
rs4742201 | snp | C/T | 0.421684 | 0.181726 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430502 | ggagagactgccctt[C/T]ttcctagagctagct | 115426 |
rs4742202 | snp | A/G | 0.421526 | 0.181876 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430598 | cgagtccatgcactt[A/G]actacctcccttatc | 115426 |
rs4742203 | snp | A/G | 0.079617 | 0.182947 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435768 | gcttggtaccacacc[A/G]ggctaattcttctat | 115426 |
rs4742204 | snp | C/G | 0.439918 | 0.162576 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435819 | TCACTATGTTGGCCA[C/G]GGTGGTCTCGAACTC | 115426 |
rs4742205 | snp | C/G | 0.32955 | 0.237006 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448912 | TGGATTTTCAATTGC[C/G]TAGCATTTGTGTTTA | 115426 |
rs5896148 | in-del | -/G | 0.0607341 | 0.163335 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412951 | AACGGCAACCGATGT[-/G]GGTAGCCGCGCAATC | 115426 |
rs5896151 | in-del | -/GGA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460838 | AACTGAATTGATCAA[-/GGA]ATGTATTTTTAGGTA | 115426 |
rs5896152 | in-del | -/A | 0.495056 | 0.049474 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462293 | TACTTTCTGGCTCTT[-/A]CGTGGGAAAAGTTTG | 115426 |
rs6477085 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458548 | ctagcttttgaatgt[A/G]tttgctcttgcttct | 115426 |
rs6477086 | snp | A/G | 0.44755 | 0.153212 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470232 | aaaaaatttagccat[A/G]cgtggtagtgcacac | 115426 |
rs6477087 | snp | A/C | 0.43978 | 0.162738 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472714 | atattataactaaaa[A/C]gtagaaggGAAATAT | 115426 |
rs7020390 | snp | A/G | 0.496245 | 0.0431677 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470921 | GCAGAAACAAACACA[A/G]CTGTATCAGCCTTTA | 115426 |
rs7021472 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489735 | gggtttttgtttttt[G/T]TTTTTTTTTTTACCA | 115426 |
rs7027302 | snp | G/T | 0.379746 | 0.213696 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458236 | gtttcgtcttgggag[G/T]gtgtatgtgtccagg | 115426 |
rs7027361 | snp | A/G | 0.488545 | 0.074807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451088 | AAATCACAGTTCCTA[A/G]TGATATCACTGATTT | 115426 |
rs7028825 | snp | C/T | 0.292523 | 0.246357 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428575 | ttttttttttttgaa[C/T]gatctcattctgtca | 115426 |
rs7029498 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446673 | cctggccaacgtggt[A/G]aaaccccgtctctat | 115426 |
rs7029772 | snp | A/T | 0.437683 | 0.165152 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497589 | AAGGTTTTTTTTTTT[A/T]AAATGTAAGTGTATG | 115426 |
rs7030161 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446477 | gtagaagcagggttt[C/T]gccatgttgcccagg | 115426 |
rs7033570 | snp | A/G | 0.191461 | 0.24305 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440123 | TAAATTCACAAAACT[A/G]ACAGCAGTCTTGCAA | 115426 |
rs7033940 | snp | C/G | 0.343701 | 0.231776 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440419 | TCTATTAAACTGTCT[C/G]ACTCAAGAGCCCAAG | 115426 |
rs7034328 | snp | A/C | 0.227369 | 0.248974 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477350 | accaacatggagaaa[A/C]cccatctctactaaa | 115426 |
rs7037825 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444862 | ctgccccggcctccc[A/G]aagtgctgggattac | 115426 |
rs7041671 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415361 | ATAAACCAGTAGGGT[A/T]GAGGAATAGACCTTT | 115426 |
rs7042490 | snp | A/G | 0.0396438 | 0.135094 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412271 | AAGGCGGGGTGGGGG[A/G]TGGGGGAAGCCCTGT | 115426 |
rs7043824 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427721 | GAAGTTATTTATTGC[C/T]CAATATCATTATTTT | 115426 |
rs7044749 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415241 | AGACTTTCAGTAAAC[C/T]AGGAAGCTCATTCCA | 115426 |
rs7467926 | snp | A/G | 0.365646 | 0.221644 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459221 | taaattttaaaaaaa[A/G]aaagaaagaaactgg | 115426 |
rs7847139 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452937 | GTAACATTTGAGCGC[A/G]TAATAGGTTCCCGAC | 115426 |
rs7848831 | snp | C/G | 0.444267 | 0.157354 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504049 | TTTTTTTTTTAAGAC[C/G]GAGTCTCGCTCTGTC | 115426 |
rs7850918 | snp | C/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477573 | TATGAGATTCATAGA[C/T]ATAAAAAATGTTTTA | 115426 |
rs7851003 | snp | C/T | 0.423881 | 0.179625 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469705 | acacgtatatacata[C/T]atatacacacatata | 115426 |