SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs744699 | snp | A/C | 0.438246 | 0.16451 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429046 | TTTGGCAACTCTGCA[A/C]CTCTGCCATTATAGC | 5522 |
rs755403 | snp | C/T | 0.493477 | 0.0567349 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6387915 | ACCAATTATCATTCC[C/T]TACTTAGAGACAAGG | 5522 |
rs768636 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6556082 | AGCCTCCTGCGTGAA[A/G]GATGCCTCTGGGGAG | 5522 |
rs872858 | snp | C/T | 0.25801 | 0.249872 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6389318 | GGGGGACTTGCTCCC[C/T]TCGTCCATCACCATA | 5522 |
rs872881 | snp | C/T | 0.243633 | 0.249919 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463074 | TCAAAAAAGTTTTGA[C/T]GCAAACTTTCAAATT | 5522 |
rs872882 | snp | G/T | 0.407158 | 0.194426 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463001 | TTCCCCCCTCCCTCT[G/T]TCCCAGAGAAGGGAG | 5522 |
rs872883 | snp | A/C | 0.473461 | 0.122236 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6462820 | CTCCCCTGCTTTTGG[A/C]TGAAGAATTTTTAGG | 5522 |
rs875579 | snp | A/G | 0.424503 | 0.179021 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6561216 | GGAAATGCCTGACTC[A/G]ACACTCAACTTCCCT | 5522 |
rs875864 | snp | G/T | 0.492287 | 0.0616198 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6384955 | TTTCATTATCTGTAG[G/T]GTGCTTATGGTGGAG | 5522 |
rs878281 | snp | G/T | 0.462034 | 0.132445 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6420749 | GGCTCCATTGTCTCA[G/T]GTTTAACCAGTCCTC | 5522 |
rs878282 | snp | C/T | 0.189261 | 0.242509 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6420730 | TAACCAGTCCTCTTA[C/T]TGGGCATCAGCTTTT | 5522 |
rs878283 | snp | A/T | 0.470521 | 0.117772 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6419942 | TCCAATATGACCTCA[A/T]CTTAACTAGTGACAT | 5522 |
rs1000647 | snp | C/T | 0.265453 | 0.249522 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6444862 | CCATGGATGTGAAGG[C/T]GAACACATGGAAACG | 5522 |
rs1985413 | snp | C/T | 0.410061 | 0.192043 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6448235 | AGGGATCAAACAGTT[C/T]TTAAATCCTGCAGCG | 5522 |
rs2019126 | snp | C/T | 0.151668 | 0.229849 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6428867 | CAGGAAGTGGCAGAG[C/T]GGGTTTCGAACCCAG | 5522 |
rs2240264 | snp | A/G | 0.409721 | 0.192325 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6391152 | CCTGGGTTCCTGGGT[A/G]TCCAGGTTACGTGGG | 5522 |
rs2240265 | snp | C/T | 0.49533 | 0.0480965 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390993 | TGGCCACACTGTCCC[C/T]ACTCTCCCCACCCAA | 5522 |
rs2240266 | snp | G/T | 0.368938 | 0.219895 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390916 | GCTGCAGGAGGAAAC[G/T]TCTCACCAGGCCCGC | 5522 |
rs2240267 | snp | C/T | 0.371987 | 0.218218 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390910 | GGAGGAAACGTCTCA[C/T]CAGGCCCGCTGGAAG | 5522 |
rs2240268 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390615 | CGTCACTCACTCAGT[A/G]CTGATGTCCAGTCCC | 5522 |
rs2269920 | snp | A/C | 0.434109 | 0.169127 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6321727 | CTGAATCAAAATGCC[A/C]AACTACGTGGCTCTG | 5522 |
rs3138737 | microsatellite | (TG)21/22/23/24/25/26/27/28/29/33 | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414071 | AACATAAGTTTTGCC[lengthTooLong]TACAGGTAAATAAAC | 5522 |
rs3220841 | microsatellite | (CA)20/21/22/23/24/25/26/27/28/32 | 0.830862 | 0.0643495 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414073 | TTATTTACCTGTATA[lengthTooLong]AGGCAAAACTTATGT | 5522 |
rs3222647 | microsatellite | (CA)14/18/19/20/21/22 | 0.627222 | 0.137262 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6559391 | agttCTGAAAAAATA[(CA)14/18/19/20/21/22]CAGNACAGAGGCAAA | 5522 |
rs3796398 | snp | C/T | 0.481473 | 0.0944461 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323058 | CCATTTTATGATTTG[C/T]GGCGGTGAACGCTTC | 5522 |
rs3796399 | snp | A/G | 0.00993419 | 0.0697739 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323062 | TTTATGATTTGTGGC[A/G]GTGAACGCTTCCTTT | 5522 |
rs3796400 | snp | C/T | 0.437683 | 0.165152 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323076 | CGGTGAACGCTTCCT[C/T]TCCTTTTTATTTTTT | 5522 |
rs3796401 | snp | A/G | | | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323151 | TGGGGCAGGGAGGGG[A/G]CCCAAACTTCCTGTG | 5522 |
rs3796402 | snp | A/T | 0.460902 | 0.134239 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323291 | TGGCAGGGGCCGGGA[A/T]CTGCACATACCTAGT | 5522 |
rs3796403 | snp | A/G | 0.465209 | 0.127221 | synonymous-codon | PPP2R2C | GRCh38.p7 | 4:6323359 | GTTGTTGGTGGCGGC[A/G]ATGGCAATGATGTTC | 5522 |
rs3924326 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6495353 | GGGTGCTGGTCTGCA[C/T]GGGCCCCAGGCCTGC | 5522 |
rs3934547 | snp | G/T | 0.380529 | 0.213219 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6516319 | GTCATCATCCTCTTT[G/T]CAGGCTGCAATGCCA | 5522 |
rs3934625 | snp | C/T | 0.318656 | 0.240388 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530338 | TTTCCATGCACGCGA[C/T]GTATGTAGAAGCGTG | 5522 |
rs3934626 | snp | A/G | 0.319136 | 0.24025 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530339 | TTCCATGCACGCGAC[A/G]TATGTAGAAGCGTGA | 5522 |
rs4074039 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6477231 | ctccagcctgggcca[C/T]acagcaagattctct | 5522 |
rs4075006 | snp | G/T | 0.34101 | 0.232846 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6521549 | CACCCATTCAGTGTG[G/T]CTTCATCTCCCTGCG | 5522 |
rs4075007 | snp | A/G | 0.499575 | 0.0145705 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6521668 | TCATACGTAGGAGGC[A/G]CTTACACAGGAGCTG | 5522 |
rs4076080 | snp | A/T | 0.463451 | 0.130149 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6522041 | GTTTGGAAACAACAC[A/T]TCTCTGTTCCCAGAG | 5522 |
rs4076293 | snp | C/T | 0.203267 | 0.245593 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6506706 | tcagctaagcccagt[C/T]agtctgcccaaccac | 5522 |
rs4076353 | snp | A/C | 0.280785 | 0.248097 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6473086 | CCCGTTGGGAGCATT[A/C]AGTACATGTGAAGAA | 5522 |
rs4077345 | snp | C/T | 0.210605 | 0.246877 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6471797 | TTTAAACCATTAAAT[C/T]TCCCCGAGATTTCTT | 5522 |
rs4234734 | snp | C/T | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6331403 | ATGAGGCAAAGCATA[C/T]TATGGACTTACCTCA | 5522 |
rs4234735 | snp | C/T | 0.188946 | 0.24243 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6360456 | TTTCACCGAGCACAG[C/T]GAGGCTCATCCAGAT | 5522 |
rs4234736 | snp | A/C | 0.0872718 | 0.189788 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6363122 | CAGCACCATGGACAG[A/C]GCCATGGCACGCAGG | 5522 |
rs4234737 | snp | G/T | 0.160609 | 0.233472 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6363153 | AAGCCCTCAGTCATG[G/T]TGGAGGCTGACTGAC | 5522 |
rs4234738 | snp | C/G | 0.140919 | 0.224948 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375986 | AGCAGCCGGATGGAA[C/G]AGAAGATCCACTTTA | 5522 |
rs4234739 | snp | C/T | 0.114036 | 0.209795 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6386026 | TAAGTGATTACTGTC[C/T]GCCAGGCCCTGCTCT | 5522 |
rs4234740 | snp | G/T | 0.0770498 | 0.180522 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6428100 | GCATCCCTAAGAGCC[G/T]CATGTCACAATCCAT | 5522 |
rs4234742 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6462785 | GATGGAACGGGGAAA[C/T]GACAGGAGTCTTGGA | 5522 |
rs4234743 | snp | A/G | 0.089084 | 0.191327 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6474078 | GTAAATGCAAGGGCC[A/G]GAAGGATGTGCTTGT | 5522 |
rs4234744 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6477895 | AGCCCTTCCCCTCCT[C/T]GAGCCAGCCTCCTCA | 5522 |
rs4234745 | snp | C/T | 0.436265 | 0.166749 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6477966 | CCGTGTTCCCCTTCC[C/T]GGTTCAGATGTTTCC | 5522 |
rs4234748 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6494514 | GAAGCACTGGTCTCC[A/G]AGACGGAGGGCCACC | 5522 |
rs4234749 | snp | A/G | 0.173643 | 0.238054 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6494752 | TGCATGGGAAGGGAG[A/G]AGGCCATACTTGGCC | 5522 |
rs4234750 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6495129 | TGCCAAGGGGCTACG[C/T]GGCCTCCACAGCCAG | 5522 |
rs4234751 | snp | A/G | 0.259397 | 0.249823 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6496929 | CACAGGGAGTGTGAC[A/G]ATGCCATACGTATGG | 5522 |
rs4234752 | snp | C/T | 0.144969 | 0.226867 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6497160 | CAGCACCATGAGCAC[C/T]GGCAGGACACCCAGC | 5522 |
rs4234753 | snp | C/T | 0.483541 | 0.0916089 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6497484 | GAAAAGAAAAAAAAA[C/T]TAAAATCCCTACCTC | 5522 |
rs4234754 | snp | C/T | 0.120674 | 0.21395 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6515559 | CTCATTTAGTCTGCA[C/T]GACAGCTCTTTGAGG | 5522 |
rs4234755 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6515866 | ggaagctgggagagg[C/T]gaggaagaatcctcc | 5522 |
rs4234756 | snp | A/G | 0.159292 | 0.232964 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530610 | CCAGCCCAGCAGTCC[A/G]GCTCAGAGTCACACC | 5522 |
rs4234757 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530795 | TAGTTGGGATGGCCA[C/T]TTACAGTGGTCGCAG | 5522 |
rs4234758 | snp | C/T | 0.488606 | 0.0746142 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6540088 | ATAAGCCATATACCA[C/T]ACACTTTACTTTTAT | 5522 |
rs4234759 | snp | C/T | 0.107694 | 0.205546 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6546963 | AAGAGCAACAGCTAA[C/T]GGCCCCCAAGCACAG | 5522 |
rs4247203 | snp | C/T | 0.434253 | 0.168969 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6349765 | TAGTAGTGGCGTATG[C/T]CTGTAGTCCCAGCTA | 5522 |
rs4247204 | snp | A/C | 0.0984431 | 0.198823 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6349781 | CTGTAGTCCCAGCTA[A/C]TCAGGAGGCTGAGGC | 5522 |
rs4263452 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6468072 | TCTTACTAGGAACCA[C/T]ATGTGTTCTCCTTGG | 5522 |
rs4270639 | snp | A/G | 0.394171 | 0.204242 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390008 | GCCCCACCCACGTCT[A/G]TGAAAGAGACCCTCA | 5522 |
rs4272077 | snp | C/T | 0.040671 | 0.13668 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6449097 | AAACACATAGCCCCA[C/T]GCAGGCATCACACAC | 5522 |
rs4272078 | snp | C/T | 0.164546 | 0.234942 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6367657 | GGCTGCTATCAGTCC[C/T]CATCGCAGCACCTGC | 5522 |
rs4277850 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456946 | GGTGCGGTGGCTTGC[A/G]CCTATAATTCCAGCA | 5522 |
rs4282260 | snp | C/T | 0.406814 | 0.194704 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6409866 | TGCCCAGACTTTCCC[C/T]TCTGCCTGGAACACC | 5522 |
rs4282261 | snp | C/T | 0.141258 | 0.225111 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6358184 | AGAAATAACACCACA[C/T]ATCTACAACCATCTG | 5522 |
rs4293851 | snp | G/T | 0.130008 | 0.219321 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375124 | AAACTTTCTTGGGAC[G/T]GGGGGTGGGGCAGGG | 5522 |
rs4302525 | snp | C/T | 0.25634 | 0.24992 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6550474 | CCTACAACGCCAACC[C/T]GAAACACGTGCTGTT | 5522 |
rs4312829 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6443209 | AGCCTTCCAGGCAGG[A/T]GCCCGGCCGCCGCCT | 5522 |
rs4312830 | snp | A/G | 0.140919 | 0.224948 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6358094 | CAAACTATGCTACAA[A/G]GCTACAGTAACCAAA | 5522 |
rs4321706 | snp | A/C | 0.495368 | 0.0478996 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463793 | TGGACCACGTGTCCA[A/C]TTGTGGCCTCTGCCA | 5522 |
rs4323180 | snp | G/T | 0.404035 | 0.196909 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390092 | AAAAGGGTCTGGAGT[G/T]TGGGGTCTGATTCTG | 5522 |
rs4324617 | snp | A/G | 0.347032 | 0.230401 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6425220 | ACCCTATAATTCCCT[A/G]TCCACCTGTCGGCCC | 5522 |
rs4327561 | snp | A/G | 0.408871 | 0.193029 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6379596 | CGCATCAACCAATCC[A/G]ATCTCTTTCTGCAGC | 5522 |
rs4331842 | snp | C/T | 0.499642 | 0.0133738 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6480054 | GAGACCACAGAGATA[C/T]GGCTGAAGTTCCTTT | 5522 |
rs4334819 | snp | A/G | 0.356169 | 0.226336 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429689 | AAAAGCCAATTTTAT[A/G]ACCGTCTCAGAGTGT | 5522 |
rs4336297 | snp | A/G | 0.473909 | 0.111197 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6458635 | AGGCAGCACAACTAC[A/G]TGCTTTGCTGTCTGT | 5522 |
rs4342255 | snp | G/T | 0.232943 | 0.249417 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6532417 | GGGGTGCCCCAGTCT[G/T]GTCTGGGATGGGCAG | 5522 |
rs4342256 | snp | A/G | 0.387642 | 0.208697 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6532218 | ATGACCAAGGCAGTC[A/G]TGAGGACCATAGATC | 5522 |
rs4345249 | snp | A/G | 0.447809 | 0.152878 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6425343 | TGCACCTCACCTGCT[A/G]TGTGTCCTGGGCACC | 5522 |
rs4346716 | snp | C/T | 0.499703 | 0.0121769 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6561722 | AGATACATACATGGA[C/T]ACATACACACACTGG | 5522 |
rs4352545 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6506730 | tagctgagctgttcc[C/T]tcttggtgttcctca | 5522 |
rs4356980 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6384016 | CAGATGCACATGTCA[C/T]TGAACTTAAAAAGAC | 5522 |
rs4358467 | snp | A/C | 0.320335 | 0.239902 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6549122 | AGCCACTGGTCTAAG[A/C]CACCATCATTGCTCA | 5522 |
rs4370214 | snp | A/C | 0.499609 | 0.0139722 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6524096 | tgtctctactaaaaa[A/C]aaaaaaaatacaaaa | 5522 |
rs4374689 | snp | C/G | 0.499971 | 0.00379382 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6469302 | GGTGGGTATTCCAGG[C/G]AACAGCCATTGCAAA | 5522 |
rs4374690 | snp | C/G | 0.49645 | 0.0419827 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6356862 | TCACAGCTGCAGCCA[C/G]CGGCATGAGACAGGG | 5522 |
rs4379121 | snp | C/G | 0.482905 | 0.0908579 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6418235 | GCTCAACCATTCAGA[C/G]CCACCTACCCACAGG | 5522 |
rs4379122 | snp | A/G | 0.345037 | 0.231231 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6526573 | CCCTCAACATGGAGC[A/G]TTCACGACCACCCCC | 5522 |
rs4380587 | snp | C/T | 0.266 | 0.249487 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6556702 | TTGCCAACCCATGCA[C/T]TAGTGTAGATCCCTA | 5522 |
rs4382106 | snp | A/G | 0.0569829 | 0.158885 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6383725 | GCTTTTATCATCTGT[A/G]GGCTCTCTTCCTGGC | 5522 |
rs4386674 | snp | C/T | 0.484138 | 0.0876334 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463928 | GTTCAAATCCCAAAA[C/T]CTCCTAAGTGTGGTG | 5522 |
rs4386675 | snp | A/G | 0.494315 | 0.0530107 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6350231 | GCTGATTTCTCCAGC[A/G]TCCACCTGGCAGCCC | 5522 |