SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14429 | snp | A/T | 0 | 0 | missense | MAP2K5 | GRCh38.p7 | 15:67806716 | GGGTGTGCCGGGCGC[A/T]GGAGGAGAGGCGGAG | 5607 |
rs737226 | snp | A/G | 0.423726 | 0.179776 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548435 | ACACCAATAACTGGA[A/G]TATTACAAAGCTTAC | 5607 |
rs737227 | snp | G/T | 0.239037 | 0.24976 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548571 | TCTCTGTGCCTCACT[G/T]TCCTCATGTGTAATA | 5607 |
rs745212 | snp | A/G | 0.472147 | 0.114677 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767841 | CTGTGTAATGCCTGC[A/G]TGTAATCCTTTGAAC | 5607 |
rs745213 | snp | G/T | 0.450231 | 0.149691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768051 | TTGTAGCCTCTTCGG[G/T]GTTTTTTGTTGTCTG | 5607 |
rs752682 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707427 | AACAAAGTGCATTCT[A/G]TAACATAGTCAACAC | 5607 |
rs868036 | snp | A/T | 0.499203 | 0.0199521 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762675 | TCTTTTTCTCCTAAA[A/T]GTGTTTTGGAAGTTC | 5607 |
rs868037 | snp | C/T | 0.499218 | 0.0197529 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762658 | TGTTTTGGAAGTTCT[C/T]CAGTATTGGGATAAA | 5607 |
rs884202 | snp | A/G | 0.499218 | 0.0197529 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762050 | TTTAGACCAGCCTGA[A/G]CAGGAGACTTCCCAC | 5607 |
rs938874 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660471 | CATAGTCTGATTGTG[A/T]TCCCAGTATCCTTGG | 5607 |
rs938875 | snp | A/G | 0.496416 | 0.0421803 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660584 | GCCATTGCCAAGTCA[A/G]AAGCAACAGAATCAG | 5607 |
rs938876 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707418 | AATCTGAGGAACAAA[A/G]TGCATTCTGTAACAT | 5607 |
rs938877 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707577 | GGAGAGTGGGGCACA[C/G]AGAGCTGAGGAGAGC | 5607 |
rs938878 | snp | A/G | 0.496348 | 0.0425753 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701028 | GGGCAGGATCAAAAA[A/G]GAGGTTAAACACACT | 5607 |
rs938879 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700992 | CATTTGCCCACTGAA[A/C]TATCAAAACAAATGC | 5607 |
rs938880 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700974 | TCAAAACAAATGCAA[A/G]CTGTAAGCTGATAAT | 5607 |
rs951656 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632778 | ATTACATTAGAATTG[C/T]TTATACCTTTTAGTA | 5607 |
rs997295 | snp | G/T | 0.496483 | 0.0417852 | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67724005 | CTCATAAGCAAATGA[G/T]TTTTTTCCTAGTTTT | 5607 |
rs1026731 | snp | A/G | 0.5 | 0.000399361 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802680 | TAACATGCTTTCCGC[A/G]TGAAGGACGGAGGCC | 5607 |
rs1026732 | snp | A/G | 0.5 | 0.000399361 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802747 | TCTTGACAAGCATCT[A/G]TATTGGTGCCTGGGT | 5607 |
rs1026733 | snp | A/G | 0.5 | 0.000399361 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802784 | GAGCTGCACCATGCC[A/G]CGCTTCCATTGTTCC | 5607 |
rs1054650 | snp | C/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762190 | GGCTGCAGAGAAAGA[C/G]GACAATAACGGGTTT | 5607 |
rs1054651 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762195 | CAGAGAAAGAGGACA[A/G]TAACGGGTTTTACTT | 5607 |
rs1054652 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762199 | GAAAGAGGACAATAA[C/G/T]GGGTTTTACTTTTGT | 5607 |
rs1063934 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793558 | ATACTAAGCTTGTTA[G/T]AATCAAGTCTAAAAT | 5607 |
rs1471460 | snp | A/G | 0.499998 | 0.000998401 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796961 | accggcacacattgt[A/G]tctgttcacatggcg | 5607 |
rs1806482 | snp | A/G | 0.296873 | 0.245566 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547759 | ACTGCGCCCATCCCG[A/G]TTTTCTTTTGAAACC | 5607 |
rs1814895 | snp | A/G | 0.323671 | 0.238899 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612048 | GATAAAATTTCCAGG[A/G]AGTCATGTGTTGAAC | 5607 |
rs1878699 | snp | C/T | 0.318896 | 0.240319 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608545 | CCATCAGTTCTTCCT[C/T]AGCCCCCCAGATCTG | 5607 |
rs1878700 | snp | A/G | 0.317692 | 0.240661 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608130 | TACACCCTACAACAC[A/G]GAAGTGCGCTAATGT | 5607 |
rs1878701 | snp | A/C | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660802 | TCTAATTAGTCAGTA[A/C]AAATTTGAACACAGG | 5607 |
rs1878702 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665036 | TTGCTTCACATACTG[C/G]AAAGAAAAACTTTAT | 5607 |
rs1984442 | snp | A/G | 0.496714 | 0.0404017 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713674 | ATCTCGGCTCACTGC[A/G]ACCTCTGCCTCCTGG | 5607 |
rs1984443 | snp | C/T | 0.440471 | 0.161928 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713522 | TCTCAAACTCCCGAC[C/T]TCAGGTGATCAACCC | 5607 |
rs1996482 | snp | C/T | 0.323434 | 0.238972 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603233 | TTAAACAGTAACTCC[C/T]CCATCACTCTGTTAA | 5607 |
rs2045960 | snp | A/G | 0.472052 | 0.11486 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799741 | GCCCACCCACCCAAT[A/G]TTGCCACTCCCTCCC | 5607 |
rs2045961 | snp | A/G | 0.364401 | 0.222289 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799933 | TTGCTGTCACTCCAC[A/G]CAGAGTGGGGGGCAG | 5607 |
rs2045962 | snp | A/G | 0.164873 | 0.23506 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799947 | CACAGAGTGGGGGGC[A/G]GTGGGGGGGATTGTT | 5607 |
rs2127162 | snp | A/C | 0.441977 | 0.16014 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798486 | TGCCCCATCCAACAC[A/C]GTACAACACTGGTCC | 5607 |
rs2127163 | snp | C/T | 0.417521 | 0.185571 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798504 | ACAACACTGGTCCTG[C/T]GGCTGCTCTGTAAGT | 5607 |
rs2241420 | snp | A/G | 0.482083 | 0.0929373 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790478 | TCTGAGGGCACTGCC[A/G]TCTTGTCTGTAGGCT | 5607 |
rs2241421 | snp | A/G | 0.499996 | 0.00139776 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790487 | ACTGCCGTCTTGTCT[A/G]TAGGCTGTGCACAAG | 5607 |
rs2241422 | snp | A/C | 0.473451 | 0.112115 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790734 | AAACAAACAAACAAA[A/C]AAAAAAAAACCTGTG | 5607 |
rs2241423 | snp | A/G | 0.482008 | 0.0931261 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794500 | GTAATTTTCAATCCT[A/G]TAGAAAACTAGACTA | 5607 |
rs2278076 | snp | A/G | 0.433963 | 0.169285 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807262 | TGCTAGCTCCTCGCA[A/G]TTGTGCTGAGGCCCA | 5607 |
rs2288098 | snp | A/C | 0.311123 | 0.242413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693173 | GGGCTTCATTCACAT[A/C]TTGAGCCATCTGACT | 5607 |
rs2414962 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547717 | CCACTTCGGCCCCCC[A/G]AAGTGCTGGGATTAT | 5607 |
rs2414963 | snp | A/G | 0.0513262 | 0.151752 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548914 | ACAGATTTATTTTTG[A/G]AAAAAAAAAAAAGCA | 5607 |
rs2414966 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613000 | TTAGCTGATAGTTAA[A/G]AGAGGAGTTATTTAC | 5607 |
rs2414967 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613001 | TAGCTGATAGTTAAA[A/T]GAGGAGTTATTTACA | 5607 |
rs2414968 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613002 | AGCTGATAGTTAAAA[G/T]AGGAGTTATTTACAG | 5607 |
rs2414969 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621986 | atcaggagttcgaga[C/T]cagcctggacaacat | 5607 |
rs2414970 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622260 | gaagcaatggagcaa[A/G]ccaggtatatattgg | 5607 |
rs2414971 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598963 | TTACTTAGAGAAATG[A/T]TCTAAGGGAATTAGC | 5607 |
rs2414972 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665464 | TTGGGGAATGGAACA[A/G]CATACACATTAGATG | 5607 |
rs2414973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666735 | CAGCCCAATTCCTAC[A/G]GAGAGTAGCCTGCTA | 5607 |
rs2414974 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678359 | TTGCTTTATAGGGGG[A/G]AAAAGTTGAAGAGAA | 5607 |
rs2414975 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679611 | GTTTATCAGGCCTAG[A/T]GCATATCAGTTCTAA | 5607 |
rs2414976 | snp | C/T | 0.0356815 | 0.128715 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680650 | TTCTGCTCACTGATA[C/T]TTTTCTAATAATCTT | 5607 |
rs2414977 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684085 | agtcctagaaaggca[A/G]gaacatgcagagaaa | 5607 |
rs2459919 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577307 | taataaagttaaatg[C/T]cttcctgaaggctac | 5607 |
rs2583571 | snp | C/G | 0.0130921 | 0.0798413 | | | GRCh38.p7 | 15:67564405 | GAGACCCTAATCTTA[C/G]TCAACAGTTAGGTTG | 5607 |
rs2583573 | snp | A/C | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 15:67559590 | CAGCAGATGGTAAAC[A/C]AATATTATGAAGCAA | 5607 |
rs2583575 | snp | G/T | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 15:67573556 | agatttgtgggcggg[G/T]acacaaatccaaacc | 5607 |
rs2583580 | snp | A/G | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 15:67570970 | TTCTTCCATACATCT[A/G]TAACAGGAGAGTTTC | 5607 |
rs2583581 | snp | C/T | 0.0360663 | 0.129354 | | | GRCh38.p7 | 15:67569132 | TGATGCTATTAAATA[C/T]TCAACTTCTAAATGG | 5607 |
rs2583585 | snp | C/T | 0.319856 | 0.240042 | | | GRCh38.p7 | 15:67567381 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 5607 |
rs2583586 | snp | A/G | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 15:67566760 | TCTATTTAAATTACT[A/G]ATAAAAATGTACACT | 5607 |
rs2583587 | snp | A/G | 0.44768 | 0.153045 | | | GRCh38.p7 | 15:67545070 | TGAAAATCAACCTAT[A/G]TAAGTGAGGCACAGA | 5607 |
rs2583588 | snp | C/T | 0.0146672 | 0.084371 | | | GRCh38.p7 | 15:67544798 | CTCAAAATGAAGTTA[C/T]AGAAATCAAATTTTG | 5607 |
rs2583589 | snp | G/T | 0.336879 | 0.245063 | | | GRCh38.p7 | 15:67544302 | TCCCTTACTTTTACC[G/T]TCTCTGAAACTGGAC | 5607 |
rs2583590 | snp | G/T | 0.305934 | 0.243663 | | | GRCh38.p7 | 15:67543915 | TCAAAATAAATTAAT[G/T]AAACAGTGTGCTCAA | 5607 |
rs2583591 | snp | G/T | 0.0107246 | 0.0724382 | | | GRCh38.p7 | 15:67543768 | GGAAAAAACCTCTCT[G/T]CTAGATTCAGCAGTT | 5607 |
rs2583592 | snp | A/G | | | | | GRCh38.p7 | 15:67548168 | GCTATTCCTAAGTAG[A/G]AAGGAACCTAAATTA | 5607 |
rs2583593 | snp | A/G | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 15:67548174 | CCTAAGTAGAAAGGA[A/G]CCTAAATTAATTTGC | 5607 |
rs2589976 | snp | C/T | 0.0333695 | 0.124785 | | | GRCh38.p7 | 15:67577873 | AGCTGGGATTACAGG[C/T]ACCCACCACTGGCCC | 5607 |
rs2589977 | snp | A/G | 0.314301 | 0.241589 | | | GRCh38.p7 | 15:67587332 | CATTACAGGGCCTAC[A/G]AGGCCCCGCATGATA | 5607 |
rs2589978 | snp | C/T | 0.314544 | 0.241524 | | | GRCh38.p7 | 15:67577231 | TATAGGGTTACTGGC[C/T]GGGCACGGTGGCTCA | 5607 |
rs2589979 | snp | C/T | 0.0158469 | 0.0875917 | | | GRCh38.p7 | 15:67577146 | agatcgagaccatcc[C/T]ggctaacaaggtgaa | 5607 |
rs2589980 | snp | C/T | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 15:67587022 | TCTCTTTGGTCAATA[C/T]GTAGCTAGGTTATCT | 5607 |
rs2589981 | snp | A/G | 0.00478085 | 0.0486577 | | | GRCh38.p7 | 15:67573071 | actaaacatacccag[A/G]ttcaggaatgtcctg | 5607 |
rs2589982 | snp | G/T | 0.318656 | 0.240388 | | | GRCh38.p7 | 15:67566259 | TGAACCCAGGAGGCG[G/T]AGGTTGCAGTGAGCC | 5607 |
rs2589983 | snp | G/T | 0.319376 | 0.240181 | | | GRCh38.p7 | 15:67561477 | ATACACTGGTCACTT[G/T]CAGTAATGAAGAAGG | 5607 |
rs2589984 | snp | A/G | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 15:67559414 | CCAATAGAGAGGAGA[A/G]GCAGCCTCAGGTAAG | 5607 |
rs2589985 | snp | C/T | 0.454544 | 0.143743 | | | GRCh38.p7 | 15:67552752 | AAACAGAGCTAATAA[C/T]GTCCTTTTAAGTACT | 5607 |
rs2589986 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 15:67552084 | ATTCATCCACCCCCT[C/T]CCGCCCCCACCAACC | 5607 |
rs2589987 | snp | C/G | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 15:67545381 | ttctGTCCACAGAAC[C/G]ATAATTGCATGCATC | 5607 |
rs2678675 | snp | C/T | 0.314787 | 0.241459 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572791 | tgcaaactcacctct[C/T]gggttcaagtgattc | 5607 |
rs2678676 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574353 | AAGGTGGGTGGATCA[C/T]GTGAGGTCAGGAGTT | 5607 |
rs2678677 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576686 | TAACAGGAGAAAACA[C/T]ATTTTATAATTGCTG | 5607 |
rs2678678 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577092 | AGGCGCCCGCCACCG[C/T]GCCCGGCTAATTTTT | 5607 |
rs2678679 | snp | C/T | 0.321769 | 0.239477 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582687 | ATTAGCCGGGCGTGG[C/T]GCACACTCCTGTTGT | 5607 |
rs2678680 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587492 | ATCCTGCCCTCCTTT[A/G]ATGTTTGACTTCCTA | 5607 |
rs2899726 | snp | A/G | 0.458545 | 0.137872 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614616 | GAGATCAGAATGACT[A/G]TAGTTTCCTTGATCT | 5607 |
rs2899727 | snp | A/G | 0.321769 | 0.239477 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619941 | taggcatggtggttc[A/G]ctcctgtagactcaa | 5607 |
rs2899728 | snp | A/T | 0.32153 | 0.239548 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622414 | ACCAGGGCCCAGATG[A/T]TGAAATCCTTATAAA | 5607 |
rs2899729 | snp | A/G | 0.288906 | 0.246954 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652850 | tgtctctatgtgact[A/G]ctctaggtacctcat | 5607 |
rs3083901 | in-del | -/AA | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664354 | aaaaaaaaaaaaaaa[-/AA]gctaggcatgatggt | 5607 |
rs3223318 | microsatellite | (CA)17/19/20/21/22/23 | 0.744666 | 0.121441 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547079 | caaaaaagangaaaa[(CA)17/19/20/21/22/23]aGATTTCTGTCTAAA | 5607 |
rs3743353 | snp | C/T | 0.299158 | 0.245119 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543032 | ACGGCGGCAGAGACC[C/T]TCACCATAGCGTTCG | 5607 |
rs3743354 | snp | C/T | 0.297636 | 0.24542 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543173 | GTGCCTGCGGGTGCG[C/T]TCCTGATCACCCCTC | 5607 |
rs3784688 | snp | A/G | 0.251296 | 0.249997 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544671 | ATGGAAGACAGAAGC[A/G]GACATTCCGAAAAGC | 5607 |
rs3784689 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548126 | GTTTTCAGTTGGTTG[G/T]TAGAACTCTGCACTT | 5607 |
rs3784691 | snp | G/T | 0.00956916 | 0.0685055 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594266 | ATTGAGGTCCACATC[G/T]GTATCACCTCAGTGC | 5607 |
rs3784692 | snp | C/T | 0.497241 | 0.037038 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695795 | TGAATGTGATGCATC[C/T]ATCTGTTAATTGAAA | 5607 |
rs3784693 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700528 | ACCTGGTAGTTGGTT[G/T]TGTTTTGTTTTGTTT | 5607 |
rs3784694 | snp | A/G | 0.301681 | 0.2446 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710150 | TACAGGTGCACCACC[A/G]CACCCATCTGAAAGC | 5607 |
rs3784695 | snp | C/T | 0.39009 | 0.207062 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710264 | AACCAGTCTCCTGAG[C/T]CTGAGGCATAGAACA | 5607 |
rs3784696 | snp | A/G | 0.288127 | 0.247076 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710701 | TAGAGATGGGGTTTC[A/G]CCATGTTGGCCAGGC | 5607 |
rs3784697 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715238 | TTTTTGGGCGGGGAG[G/T]GGGGGGGTCTAAAAT | 5607 |
rs3784698 | snp | C/G | 0.483995 | 0.0880135 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715244 | GGCGGGGAGGGGGGG[C/G]GTCTAAAATTGTGTG | 5607 |
rs3784699 | snp | C/T | 0.496968 | 0.0388195 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715253 | GGGGGGGGTCTAAAA[C/T]TGTGTGTAACTTAAT | 5607 |
rs3784700 | snp | A/G | 0.451608 | 0.147832 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725414 | TTAAGCCGTCCATTT[A/G]CCATTGCTTAATTCT | 5607 |
rs3784701 | snp | C/T | 0.287085 | 0.247234 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725587 | TACCCAAGTGAATGG[C/T]GCAATGCCTGTGGAA | 5607 |
rs3784702 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736560 | GACTAAAATGAATTA[C/T]TTTTCTGATCCCACA | 5607 |
rs3784703 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736584 | TCCCACAAGAGCCTT[C/G]CTTTACAGACTTTCT | 5607 |
rs3784704 | snp | C/T | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736651 | TAATATATAGAATTA[C/T]ATACAGAATCTCGTC | 5607 |
rs3784705 | snp | G/T | 0.258288 | 0.249863 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736842 | TAGGCCTTCCACTTC[G/T]CTCCCTTTGCTTTTA | 5607 |
rs3784706 | snp | C/T | 0.400325 | 0.199756 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737411 | AGACCTGGCCGAGCT[C/T]TGTTTGAGCATAGAT | 5607 |
rs3784707 | snp | A/C | 0.427119 | 0.176434 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751540 | AGCCTTAGCCATCTG[A/C]TATCTTTGGGGAATA | 5607 |
rs3784708 | snp | A/T | 0.209693 | 0.246729 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763975 | AGATTTACTTTTAAA[A/T]TATAGAGTGTGACTC | 5607 |
rs3784709 | snp | C/T | 0.498182 | 0.0300969 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779937 | CCATGACTCAGCTCA[C/T]TAGAACTTTCTGTTA | 5607 |
rs3784710 | snp | C/T | 0.483418 | 0.0895317 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780120 | CAGCATTTAATTATA[C/T]ATTCATCTTATGGCC | 5607 |
rs3784711 | snp | C/T | 0.498206 | 0.0298983 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780189 | GCAGCTCATCAGAGT[C/T]ACCTCAGAGGTTTAA | 5607 |
rs3784712 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780511 | GATAAAGTAGACACT[A/G]AACAGATAGACAAAC | 5607 |
rs3784713 | snp | C/T | 0.355525 | 0.226637 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780675 | AGGTTTTTGTTTGAC[C/T]TCCTGCTAGGAGAGG | 5607 |
rs3784714 | snp | C/T | 0.155656 | 0.231515 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791644 | GTGCAAATCCCAGCT[C/T]TACCTTGGCCAAATC | 5607 |
rs3784715 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791922 | CACCACCAGGGAGAA[C/T]GTCATGGCTGCAACA | 5607 |
rs3784716 | snp | G/T | 0.360421 | 0.224293 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792112 | GCTTAGAACAGTGGT[G/T]GGAGGTCAGGTTTGC | 5607 |
rs3784717 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805320 | TGAGCATTCTCCTGT[C/G]CCCCACAGTTCTGAC | 5607 |
rs3784718 | snp | C/T | 0.482083 | 0.0929373 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805666 | GGGGCAGGCACATGG[C/T]GCCCTCATCTCCCCC | 5607 |
rs3784719 | snp | C/T | 0.5 | 0.000399361 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805842 | CACCTCTGACTGTGG[C/T]CTGGTAACCCTGGGG | 5607 |
rs3784720 | snp | A/G | 0.208779 | 0.246578 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806053 | AGAGTCCAGCCCCCA[A/G]TGGAACTTCTCACCA | 5607 |
rs3803520 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607904 | GCTATACAAACAACT[G/T]TTCAGTCAATTGAGT | 5607 |
rs3837736 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715237 | TTTTTTGGGCGGGGA[-/G]GGGGGGGGTCTAAAA | 5607 |
rs3837737 | in-del | -/T | 0.464416 | 0.128553 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725236 | TAACATCAGCCATCC[-/T]TTTTTTACCTTGTAC | 5607 |
rs3837738 | in-del | -/A | 0.229136 | 0.249128 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737559 | GAGCTAAGTTCATTG[-/A]AAAAATCAATGAGTT | 5607 |
rs3837739 | in-del | -/T | 0.182933 | 0.240836 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770041 | ACCCATAAAACTGTC[-/T]TGTCACTTAGTGGAA | 5607 |
rs3837740 | in-del | -/AG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805601 | CTGGAGGGAGGAGAG[-/AG]CTGGGGGGAGCGAGG | 5607 |
rs3865018 | snp | C/T | 0.437965 | 0.164831 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600428 | TGAGCTATGTTGTAT[C/T]ATTCCATTTTGACAC | 5607 |
rs3985640 | snp | A/G | 0.0349115 | 0.127424 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680175 | CCTTTTTATTGTTGA[A/G]TAGTATTCCATTGTA | 5607 |
rs3985642 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557929 | GAAAAATGGTCACAA[C/T]AAACCTACACTGAGC | 5607 |
rs4238409 | snp | C/T | 0.208169 | 0.246476 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757638 | TTAAAGAGCAGCTAC[C/T]CTAGTCAGGGAGGCA | 5607 |
rs4238410 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773935 | CTGGATAGCTCAGCT[A/G]TTAAAACAAAGGAAT | 5607 |
rs4238411 | snp | A/T | 0.499295 | 0.0187567 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787086 | GGGGCAGTTGGACGC[A/T]CTTGTTGGTTCTTAA | 5607 |
rs4261476 | snp | C/T | 0.462253 | 0.132093 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628127 | GGGTCTTTGAGAATC[C/T]CCTCTTGAGACAGCT | 5607 |
rs4261477 | snp | G/T | 0.45692 | 0.1403 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781630 | TTTACCGTTTCTCTG[G/T]TCTCTTCATATAAAT | 5607 |
rs4261478 | snp | A/G | 0.499942 | 0.00539106 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781746 | AAATGTAACCCGATT[A/G]ACTCTTAATTGTTAG | 5607 |
rs4268700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778849 | CATTTCCATAGCCCC[C/T]TTAGAGAGTGCTCAT | 5607 |
rs4293328 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620107 | cgggattacaggcgt[G/T]agccgctgcacatgg | 5607 |
rs4296206 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696923 | GGCGGAGGTTGCGGT[A/G]AGCTGAGATCGCACC | 5607 |
rs4300587 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698035 | CTCAAGGAAATACTG[G/T]TTTTTAGGGGCAGAT | 5607 |
rs4304973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602648 | ATTTTAAAACATAGG[C/T]TTGTTTGTTTGTTGG | 5607 |
rs4325504 | snp | A/G | 0.499218 | 0.0197529 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763232 | GTCAGTTCTATCTGC[A/G]TCATGAAATCAAAAA | 5607 |
rs4331293 | snp | A/G | 0.452965 | 0.145963 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695463 | TAAATTAACCTCTGA[A/G]GTCTTCATATCTGTT | 5607 |
rs4334249 | snp | C/T | 0.455621 | 0.142197 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617527 | TAAAATTATTTATGC[C/T]TAGAATTTCAAATTC | 5607 |
rs4343227 | snp | A/G | 0.314544 | 0.241524 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692367 | TTTGAATTTCGGATT[A/G]AGCAGATGATGTCAT | 5607 |
rs4346159 | snp | A/G/T | 0.0154538 | 0.0865337 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600011 | TATATATAAAGTTAC[A/G/T]AAAATGACTTTAATA | 5607 |
rs4356423 | snp | A/C | 0.312348 | 0.242101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678042 | ATAACTTTTATATTG[A/C]AATGTGGTTTTCTCT | 5607 |
rs4363822 | snp | A/G | 0.496348 | 0.0425753 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700245 | TAGTGTGGGTGCCAG[A/G]AGGACTGCCCTTTAA | 5607 |
rs4398061 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713020 | GAAGAAAGAACAGAG[A/G]AAACAAAGGGGAAGA | 5607 |
rs4420481 | snp | G/T | 0.45198 | 0.147323 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557875 | TTGTATATGTAAAAA[G/T]ATAAAGGGTCATTTT | 5607 |
rs4432222 | snp | C/T | 0.081446 | 0.184634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797478 | GTGGATAATTTCTCC[C/T]GAGTACCTTGGAGAT | 5607 |
rs4444286 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700910 | TCTGTGAACATTATC[A/G]CTTTTTCTATTTTTT | 5607 |
rs4451902 | snp | C/T | 0.230603 | 0.249246 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786080 | GTAAACTATGAAGTG[C/T]GAGACATACATGGGG | 5607 |
rs4489954 | snp | G/T | 0.499265 | 0.0191552 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779737 | TATTGGACTGTCATC[G/T]TCCTAGTATCTTGTT | 5607 |
rs4502166 | snp | C/T | 0.261332 | 0.249743 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720065 | AGCTACAAAAGTGGG[C/T]ATTTTTAAATTGAGG | 5607 |
rs4506840 | snp | C/T | 0.290201 | 0.246747 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696337 | ACATGACCACACCCA[C/T]TTGCTTATATATTAT | 5607 |
rs4508384 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618046 | ATTAAAAGATACATC[A/G]TTACAAAGAATAAAC | 5607 |
rs4514626 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605981 | AACAGATACTAAGCA[C/G/T]TGAAGGTTTTAACAT | 5607 |
rs4514627 | snp | A/C | 0.154661 | 0.231107 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790733 | AAAACAAACAAACAA[A/C]AAAAAAAAAACCTGT | 5607 |
rs4533223 | snp | A/C/T | 0.31721 | 0.240796 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605791 | TCATTTTAGCCAAGA[A/C/T]GTACCAAGGGTCTAT | 5607 |
rs4537967 | snp | A/G | 0.312348 | 0.242101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731197 | TGGGGAGGAGGGGCC[A/G]GCTTCAAGACTTGTC | 5607 |
rs4539549 | snp | A/G | 0.361263 | 0.223876 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778281 | TTGGTTGTTCTCTCA[A/G]TTAATCAAGGTATAT | 5607 |
rs4548812 | snp | A/G | 0.483272 | 0.0899109 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768214 | TGTCTTGTAATTACC[A/G]ATCTCATTTTTCTGA | 5607 |
rs4558368 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628193 | CACCCAGCCTTCAGT[A/G]TCTTCTTTAATGCCA | 5607 |
rs4600428 | snp | C/T | 0.323671 | 0.238899 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614772 | ATATACCCCTTTTTA[C/T]TCCCATACCTGCCTC | 5607 |
rs4776366 | snp | A/G | 0.32153 | 0.239548 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589693 | TGTTTGGTTATTTGC[A/G]TCTTTACAATAATTG | 5607 |
rs4776367 | snp | A/G | 0.45866 | 0.137698 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589785 | TGTGTGTGTGTGTAT[A/G]TGTGTGTGTGTGTGT | 5607 |
rs4776368 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610314 | TGTTATTTGGTCTAC[C/G]CTTTGGGTGTCCTTA | 5607 |
rs4776369 | snp | A/T | 0.316243 | 0.241064 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610426 | TTTATAAGACACGTT[A/T]CTTTTTTATAGCTAT | 5607 |
rs4776370 | snp | C/T | 0.437683 | 0.165152 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612173 | GGACTTGCTGGTCTT[C/T]ATAAGGAAGTTAGTT | 5607 |
rs4776371 | snp | A/G | 0.314057 | 0.241654 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652461 | aagagagagaggagg[A/G]aggtcccagacactt | 5607 |
rs4776372 | snp | A/G | 0.314057 | 0.241654 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667990 | CTTGTTAGTCTGGTA[A/G]AAGTTAGTTTATTTG | 5607 |
rs4776373 | snp | A/G | 0.439363 | 0.163222 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668185 | AATGCTAAGAATGTG[A/G]CATGTTTTTATTATA | 5607 |
rs4776374 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773669 | CATCATGAATGCTTT[C/T]CAGGAAGGTACTTTC | 5607 |
rs4776375 | snp | A/G | 0.482384 | 0.0921818 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793217 | TCAAAGGTGTAGTGC[A/G]GAATGATTGTGCTTG | 5607 |
rs4776376 | snp | A/G | 0.5 | 0.000399361 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801097 | GCTCCGCTGGACTGT[A/G]AGATCCCATCTAGTC | 5607 |
rs4776943 | snp | C/T | 0.419936 | 0.183362 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543731 | GCTGGGACACACATA[C/T]AGACACAACCACGCA | 5607 |
rs4776944 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568838 | TGTGAAACCCCATTT[C/T]TACTAAAAATACTAA | 5607 |
rs4776945 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602439 | GCTTCAAATGGAATT[A/T]AAAAATGTTTATTTA | 5607 |
rs4776946 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614952 | ATCTGTGACCTCATA[A/T]CATATTTGACTTGAG | 5607 |
rs4776947 | snp | G/T | 0.318174 | 0.240525 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618350 | TTTACTGTTTTCTTC[G/T]CATCTTTCTGACCTC | 5607 |
rs4776948 | snp | C/T | 0.321769 | 0.239477 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618578 | aaaattatctaaaac[C/T]gagctctttatttct | 5607 |
rs4776950 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622437 | cttataAAGACTTTT[A/G]ATTCAGCAGTTAGAA | 5607 |
rs4776951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623007 | CTCGGGAGGCTGAGG[C/T]GGGAGTATGGCGTGA | 5607 |
rs4776952 | snp | C/T | 0.458315 | 0.13822 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625508 | GAGGTGTATAGTTGT[C/T]TTTTGGTGTAAGCAG | 5607 |
rs4776953 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626247 | ATTTCAggccaagtg[C/T]ggtggctcacacctg | 5607 |
rs4776954 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637287 | tcctattagttctgt[C/T]cctctagagaaccct | 5607 |
rs4776955 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648839 | ccgccttggcctccc[A/G]aggtgctgggattac | 5607 |
rs4776956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658198 | TTACATTTGAGAAAA[A/G]CTGTTACAAAAGACA | 5607 |
rs4776957 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659270 | AGAAGTCATGGGGTG[G/T]TGTGATAGTAAACAA | 5607 |
rs4776958 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659274 | GTCATGGGGTGGTGT[A/G]ATAGTAAACAATTGC | 5607 |
rs4776959 | snp | A/C | 0.0349115 | 0.127424 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661968 | TCCTTCTGTGATAAA[A/C]TTATCATTATTAATA | 5607 |
rs4776961 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701607 | GGAAGGCAGGGAGAT[C/G]TAAAAGGTCATTGTC | 5607 |
rs4776964 | snp | G/T | 0.454182 | 0.144256 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724617 | AAGAAACCATTTTCT[G/T]TTTTACCTCCTCCCA | 5607 |
rs4776965 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729050 | TCACTTTTCAAATTC[A/G]TAGACTTTTTTGTTT | 5607 |
rs4776966 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738079 | CTGGTCTCGAACTCC[C/T]GACCTCAGGTGACCT | 5607 |
rs4776967 | snp | C/T | 0.48955 | 0.071525 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741584 | GCTGACTAATGTAGG[C/T]CTGAACCACCTACCA | 5607 |
rs4776968 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742948 | AAATGAATAATGTTT[C/T]GCTGTACCTCAATGC | 5607 |
rs4776969 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749786 | TCATCAATATCCTCT[A/G]TTATCTTAGATTCCA | 5607 |
rs4776970 | snp | A/T | 0.494484 | 0.0522255 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788548 | GACCAATTTACTGTT[A/T]CTGTTTTTGTAAAAA | 5607 |
rs4776971 | snp | A/C | 0.459004 | 0.137176 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788759 | CAGGAGGATCACTTT[A/C]GCCCAGGAGTTCGAG | 5607 |
rs4776972 | snp | A/C | 0.42803 | 0.175514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791098 | GCTGGGCAGGAGCCA[A/C]GCATCTTCTTTTCAA | 5607 |
rs4776973 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802476 | TTCATTGTGTCTCCA[A/T]CTTCTGTGGCAAAGT | 5607 |
rs4776974 | snp | A/G | 0.5 | 0.000399361 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803589 | CAGCTCCTAACCCCT[A/G]TCTTCCCTCCCTGGG | 5607 |
rs5813450 | in-del | -/AAAAG | 0.32627 | 0.238082 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612998 | ATTTAGCTGATAGTT[-/AAAAG]AGGAGTTATTTACAG | 5607 |
rs5813451 | in-del | -/A | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658891 | TTCCAACTTCTTCTG[-/A]AAAAAAAATGCTGTT | 5607 |
rs5813452 | in-del | -/A/AA/AAA | 0.625 | 0.125 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678980 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GAACTAATCTTACAA | 5607 |
rs5813453 | in-del | -/A/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699988 | AAAAAAAAAAAAAAA[-/A/AA]TCCTCATCACTTGTG | 5607 |
rs5813455 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762582 | AAAAAAAAAAAAAAA[-/A]CAAGCAGACTAAATG | 5607 |
rs5813456 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786031 | TTAGCTGTTAGGTTG[-/T]TTTTTTTTTTTTAAC | 5607 |
rs6494670 | snp | A/G | 0.296873 | 0.245566 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550188 | AAACAGATTATTTAT[A/G]ACCATCATATGGTAC | 5607 |
rs6494671 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565529 | CACTGTGCCCGGCCT[A/G]TCATCATCATTATTA | 5607 |
rs6494672 | snp | A/G | 0.435407 | 0.167703 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576687 | AACAGGAGAAAACAT[A/G]TTTTATAATTGCTGC | 5607 |
rs6494673 | snp | C/G | 0.293037 | 0.246268 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589591 | TTTCTTGGATGAAAG[C/G]CATTCTATAAATGCA | 5607 |
rs6494674 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604009 | TTCACTTGATGGAAT[G/T]TTGGGAATTTCAAGG | 5607 |
rs6494675 | snp | A/G | 0.292008 | 0.246445 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612258 | AGTATATGTGACACC[A/G]TTAAGTTTTAATCTT | 5607 |
rs6494676 | snp | A/G | 0.311614 | 0.242289 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630009 | TTCGTAGACTGAGGT[A/G]GGAGCATCACTTGAG | 5607 |
rs6494677 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643226 | GAGAGATTCCTGGTA[C/T]TTGTCATCATAGTAG | 5607 |
rs6494678 | snp | C/T | 0.457271 | 0.139781 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653909 | gtattttccattttt[C/T]tatgatagaaatctc | 5607 |
rs6494679 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653928 | gatagaaatctcttg[C/T]gatttctttttgacc | 5607 |
rs6494680 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661125 | TGTTATTCAAATTTT[C/T]TCTTGTAAAATGTAT | 5607 |
rs6494681 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662398 | TTCTCATGGGTAATG[A/G]TAGGTTTTCTTGTTC | 5607 |
rs6494684 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666067 | ATCCATTTGACAAAA[G/T]AACTAAAGGAAAAAC | 5607 |
rs6494685 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675306 | cacaacctagatgaa[C/T]ctccagatcattata | 5607 |
rs6494686 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675597 | ggaaactgggtggag[G/T]gtacacaggatgtct | 5607 |
rs6494687 | snp | C/G | 0.0349115 | 0.127424 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680173 | TTCCTTTTTATTGTT[C/G]AATAGTATTCCATTG | 5607 |
rs6494688 | snp | A/G | 0.0349115 | 0.127424 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681571 | AAAATGAGCCACTTT[A/G]CATTGTGCCTTTATC | 5607 |
rs6494689 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690042 | TTTTTTTTAAATCTC[A/T]TCAGCTATTGTTAGT | 5607 |
rs6494690 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693265 | TACTAAAGCGATAAG[C/T]ATCCTGCTTAAGTGA | 5607 |
rs6494691 | snp | G/T | 0.28578 | 0.247426 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717237 | TGTAGCTGGTTTAGT[G/T]TCACCATATTTCAAA | 5607 |
rs6494694 | snp | A/C | 0.499937 | 0.0055907 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764804 | CAAAAATGTAGTCCT[A/C]AGGAATATTTTTTTA | 5607 |
rs6494695 | snp | A/T | 0.274929 | 0.248754 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774202 | GTGTGTGTGTGTGTG[A/T]GAGAGAACATAGGTA | 5607 |
rs7162411 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707784 | AAAAGATAGAGGATC[C/T]CTTCCCCATTTCCCA | 5607 |
rs7162488 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561681 | GTGAGAGCTATGGGT[A/C]ACTGAACAGGACTGG | 5607 |
rs7162980 | snp | A/T | 0.40086 | 0.199352 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758511 | AACTAGACTCTAAGT[A/T]CCTAGACATTTTATT | 5607 |
rs7163007 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710006 | CTGACAGACTTTTCT[A/G]TAGGAGTCAGACTGA | 5607 |
rs7163061 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750110 | CTTACTTGTTTAATT[C/T]GGGCAAAATCATGAG | 5607 |
rs7163462 | snp | A/G | 0.0349115 | 0.127424 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680150 | TTATAGCATGTGTCT[A/G]TAGTTCATTCCTTTT | 5607 |
rs7163787 | snp | C/T | 0.451608 | 0.147832 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620013 | agttcaagtctgcat[C/T]gagctatgattgtca | 5607 |
rs7164011 | snp | A/G | 0.292523 | 0.246357 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616481 | ATGTCTCTGATGGAC[A/G]TCCTATAAATCCCTA | 5607 |
rs7164713 | snp | A/T | 0.296873 | 0.245566 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549596 | TCTATAAGTATTACC[A/T]GACCCATTTTGGAGG | 5607 |
rs7165255 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653428 | gtagctgggattaca[A/G]gcacccagctactct | 5607 |
rs7166237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684066 | gctagaattcacaga[A/G]cagagtcctagaaag | 5607 |
rs7166260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787317 | GGCAGCATGTCACTT[G/T]TCTCTCTTTCTGCAT | 5607 |
rs7166336 | snp | C/T | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757457 | AGAGTATGGGAGATT[C/T]AGATCTCCACCCCCT | 5607 |
rs7166790 | snp | A/C | 0.413582 | 0.189052 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624110 | tttgggaggccaagg[A/C]gggctgatcacaagg | 5607 |
rs7166903 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684133 | taggagttcccttgc[A/G]tctggcctaacatca | 5607 |
rs7166911 | snp | A/C | 0.0349115 | 0.127424 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662687 | GAAGGTAGTACTTGT[A/C]ACCCATATACTTAGG | 5607 |
rs7167080 | snp | A/C | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742122 | gatggtcatgatctg[A/C]cctcgtgatccgccc | 5607 |
rs7167137 | snp | C/G | 0.337386 | 0.23423 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624203 | tattagccaggcgtg[C/G]tggcgggtacctgta | 5607 |
rs7167280 | snp | C/T | 0.296873 | 0.245566 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553342 | TAAACCTCTACTACT[C/T]CAGGTTTACGTTCTG | 5607 |
rs7167339 | snp | C/T | 0.297128 | 0.245518 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558652 | ctctgaacccgtgtg[C/T]ttctccccaaacctc | 5607 |
rs7167477 | snp | C/G | 0.321053 | 0.23969 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624237 | ttagctactcgggag[C/G]ctgaggcaggagaat | 5607 |
rs7168176 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687403 | TTGTTCAGAAAGAAA[A/C]CCCCACTTAGAATAT | 5607 |
rs7168507 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710468 | ACAAGGTCATTGTCA[C/T]TGTCATCCAAGTAAC | 5607 |
rs7168631 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650298 | gctttcttttcaatt[C/T]tgaatgtcttttatt | 5607 |
rs7168821 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710589 | actcattgcaacctc[C/T]gcctcccaggttcaa | 5607 |
rs7168932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642104 | GAATTAGAGTACAGC[A/G]GATTAGCTCCACAAA | 5607 |
rs7169086 | snp | C/T | 0.441977 | 0.16014 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642116 | AGCAGATTAGCTCCA[C/T]AAATACAGTATTCCT | 5607 |
rs7169446 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701807 | ccaaaaactgcacat[G/T]gagaaatactgACCA | 5607 |
rs7169977 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798890 | TCAGAGGCCAAGACa[A/G]ccgggcacggtggct | 5607 |
rs7170143 | snp | C/T | 0.292523 | 0.246357 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621078 | taaaataccaagaca[C/T]agcaaaattgaaagg | 5607 |
rs7170184 | snp | A/G | 0.26818 | 0.249338 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628173 | GTGAAAAAGATATTT[A/G]TTGGTGGCATTAAAG | 5607 |
rs7170299 | snp | A/G | 0.411074 | 0.191194 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580380 | GTAGGTCCAAGCCCA[A/G]TGTGAAGCTTCTTCA | 5607 |
rs7170535 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666355 | AGTTGATGTACCTTT[C/T]GTATTCCTGTATCTA | 5607 |
rs7170841 | snp | A/G | 0.312837 | 0.241974 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660053 | GAGCTACTCTGAAGG[A/G]TTGTTTATATTTGCC | 5607 |
rs7171429 | snp | A/G | 0.209997 | 0.246779 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763606 | TCTATGGAGATCCTT[A/G]GAGGTGAGGGTCCAG | 5607 |
rs7171706 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660284 | CCTCCAAAATGTAGT[G/T]TTTTTTTTGTATGTT | 5607 |
rs7172015 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638890 | tgagaagtgtctgtt[C/T]gtgtcctttgcccac | 5607 |
rs7172055 | snp | C/G | 0.467132 | 0.12391 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645996 | ACTATTGACCTTTGA[C/G]ACCTGGCTTTTTTCT | 5607 |
rs7172298 | snp | C/T | 0.41023 | 0.191902 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580645 | TATTCTCAAGGCTGA[C/T]ATGTATATACCAGCA | 5607 |
rs7172326 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660069 | TTGTTTATATTTGCC[C/T]TTACATTTTTTTTAA | 5607 |
rs7172395 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684756 | ataatgagagaaatg[G/T]aagacaaacaagttg | 5607 |
rs7172511 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660120 | ATATGTGTCCAATTT[C/T]TCCAGCTTTTATGGC | 5607 |
rs7172582 | snp | C/T | 0.464203 | 0.128908 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542218 | TATTTCTTGAATTCT[C/T]GCCTTGCTCTTGCTG | 5607 |
rs7172603 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684823 | aaaaatttcattgat[A/G]gaattaactgaatta | 5607 |
rs7172776 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669227 | agaactcatattcta[G/T]cagtgatagagtggg | 5607 |
rs7174461 | snp | C/G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642602 | AGCACACCCCAAGTA[C/G/T]AGGAAACAGCAGGAG | 5607 |
rs7175009 | snp | A/G | 0.26271 | 0.249677 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702946 | ATAATATCATATAAT[A/G]TTGTGTAATTTGTTA | 5607 |
rs7175517 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785292 | AATTTGTGCCAGGAT[A/G]TAAATCAAGCCTGTC | 5607 |
rs7176845 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739464 | tatatatatatatat[A/T]tTTTttttttttttt | 5607 |
rs7177848 | snp | A/G | 0.182296 | 0.240658 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748961 | CATTCAGTAGGCAAG[A/G]GTCAGAGTTGAAGAG | 5607 |
rs7178987 | snp | G/T | 0.312348 | 0.242101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655779 | tttaggaagtttggg[G/T]tcattgttttctgaa | 5607 |
rs7179975 | snp | A/T | 0.317933 | 0.240593 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606440 | TATATACTGCCTTCA[A/T]GGTGTTTTGAAGGTT | 5607 |
rs7180716 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731570 | AACAGGAAAAACAAT[A/G]GTGTCTTGGCTTCAC | 5607 |
rs7181077 | snp | A/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576930 | ACCCTATATATATAT[A/T]TTTTTTTTTTTTTTT | 5607 |
rs7182031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770540 | CTCCTTCTTAACTAC[A/G]TTGGTCTTCTTTCCC | 5607 |
rs7182417 | snp | A/G | 0.321292 | 0.23962 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565204 | CACCTTCCTCTTTGC[A/G]GGATTTTTTTTATGT | 5607 |
rs7183028 | snp | A/C | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726753 | GATGCTCTCTTAGAT[A/C]CATTAGCGTTAAAGT | 5607 |
rs7183078 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707656 | GAGTCTTCAGTAGAG[A/G]TGTTTACAAAGGACT | 5607 |
rs7183433 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726963 | cagcactttgggagg[A/C]caagccaggcagatc | 5607 |
rs7183639 | snp | A/G | 0.209693 | 0.246729 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758439 | TCTTGGGAGATCACC[A/G]AGCACCTCATTCAAA | 5607 |
rs7495061 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701171 | AAAAAAGGACAGGGG[G/T]TAGGGCAGCATTTAG | 5607 |
rs7495062 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701172 | AAAAAGGACAGGGGT[C/T]AGGGCAGCATTTAGT | 5607 |
rs7496040 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628200 | AAAGAAGATACTGAA[A/G]gctgggtgcagtggc | 5607 |
rs8023643 | snp | A/G | 0.471578 | 0.115772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626555 | aacaaaaaaCATAAT[A/G]TAGGGGATAGGGTTC | 5607 |
rs8024430 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686427 | gcctgggcaacatgg[C/T]gaaacccccgtctca | 5607 |
rs8024530 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547416 | AAAGTATCAAAAAAT[A/G]GTCATCATCAAAATA | 5607 |
rs8025055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723413 | ACTAAGGAACGTCCT[A/G]TTTTTAGAGTGAGAT | 5607 |
rs8025526 | snp | A/T | 0.442113 | 0.159977 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784145 | TCATTTGACCTTCAC[A/T]TGAACACTATAAGGA | 5607 |
rs8025790 | snp | G/T | 0.484138 | 0.0876334 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784061 | TTGATTTATTATATA[G/T]AGAGAAATGGATCTA | 5607 |
rs8025889 | snp | A/G | 0.46865 | 0.121211 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628836 | ATGGACGAAACTTCA[A/G]TGGTCATGGTGGCTT | 5607 |
rs8026496 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732959 | GATAGCTCTGTGGGG[A/G]GGGGGGGCTTAACAG | 5607 |
rs8027125 | snp | A/G | 0.298144 | 0.245321 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565801 | TTTTTGTAGAGATAG[A/G]GTCTTGCTTTGTTGC | 5607 |
rs8027480 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566285 | gttcaagtgattctc[A/C]tgcctcagcctcccg | 5607 |
rs8027606 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566260 | gctcactgcaacctc[C/T]gcctcctgggttcaa | 5607 |
rs8028223 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604949 | cgtaaaaggcttagc[A/G]ctatgactgacactt | 5607 |
rs8028313 | snp | C/G | 0.467642 | 0.123012 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750719 | AGGGCTAAGTCTTCC[C/G]CTTTAGTTCCCACAG | 5607 |
rs8028327 | snp | A/G | 0.317451 | 0.240729 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605255 | ggatggggtttcacc[A/G]tgttggccaggatgg | 5607 |
rs8028813 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566197 | gttttgtttttgaga[C/T]gaagtctcattctgt | 5607 |
rs8028912 | snp | A/G | 0.247053 | 0.249983 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583939 | TTTTTAATAGCGACA[A/G]GGTATCACAGTGTTG | 5607 |
rs8029236 | snp | A/G | 0.0349115 | 0.127424 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671699 | taagttttagggtac[A/G]tgtgcacaatgtgca | 5607 |
rs8029631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671960 | gaatgatgatttcca[A/G]tttcatccatgtccc | 5607 |
rs8030456 | snp | C/T | 0.484209 | 0.0874434 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784518 | CTGCATCTGCAGGGC[C/T]GTGGTCGAGGCAGAG | 5607 |
rs8030476 | snp | A/G | 0.232651 | 0.249397 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754490 | CTCTGCCAGGTGCCG[A/G]GATAAATCCCTGTGC | 5607 |
rs8030996 | snp | C/G | 0.444666 | 0.15686 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739068 | gagactcacgtgagc[C/G]caggagtttgagacc | 5607 |
rs8031524 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690025 | tttttgtgtgtgtgc[A/C]attttttttaaatct | 5607 |
rs8031869 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566291 | gtgattctcatgcct[C/G]agcctcccgggtagc | 5607 |
rs8031870 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566294 | attctcatgcctcag[C/G]ctcccgggtagctgg | 5607 |
rs8032268 | snp | A/G | 0.319616 | 0.240112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550695 | GTAGCATAAGGGCCC[A/G]GATGCTGAGAGGGAT | 5607 |
rs8032516 | snp | A/T | 0.454061 | 0.144427 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605289 | ggatctcctgacgtc[A/T]tgatccacctgcctt | 5607 |
rs8032675 | snp | C/T | 0.496382 | 0.0423778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667126 | GAAATTTACCTTAGA[C/T]TGAGTAGTTGTTAAC | 5607 |
rs8033728 | snp | A/G | 0.323434 | 0.238972 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624987 | ATTCTGTCGCGGCTC[A/G]TCTTGGCTTTGCCAC | 5607 |
rs8034388 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559836 | TCATATCCGGTAACG[C/T]TTTTTTGGTCAGATG | 5607 |
rs8034680 | snp | C/T | 0.000627083 | 0.017696 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693593 | CTTATGCAAAAATAA[C/T]GTTTAAAACCAACAT | 5607 |
rs8035189 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693895 | ATTAACCCTCAAGTA[A/T]CCCCAAATGTCAGTC | 5607 |
rs8035675 | snp | C/T | 0.496245 | 0.0431677 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673243 | CAATGGTAGATCCAC[C/T]GGAAGTTGCAAAAAA | 5607 |
rs8035915 | snp | C/T | 0.033468 | 0.124956 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769681 | GAGCCCGTTTACAAA[C/T]ATGCCATGCCCTCAA | 5607 |
rs8035989 | snp | A/G | 0.453697 | 0.14494 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673282 | GACAGTCCCATCTAA[A/G]GGCATCCTTTTTAAG | 5607 |
rs8036625 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542759 | GCCGCAGCCGCCGCC[A/G]GTCCGCGCGGCCTCG | 5607 |
rs8037011 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748732 | GTATGGCTCTGAGCT[A/G]TGTTACGTGAACTGG | 5607 |
rs8037318 | snp | C/G | 0.312104 | 0.242163 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690899 | AAGATACTGTGCTTG[C/G]AAGGGATACATTTAA | 5607 |
rs8037476 | snp | C/T | 0.453818 | 0.144769 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718813 | catgtgtatggggta[C/T]atgagatattttgat | 5607 |
rs8037887 | snp | G/T | 0.314787 | 0.241459 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676883 | CCAGGTTTAAGTTCT[G/T]GTTCTTCCTCTTAAT | 5607 |
rs8037896 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543246 | ctctgtcctctgccc[C/G]tcactcccctTGTCA | 5607 |
rs8037907 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567528 | cgccaccgcgcccgg[C/G]taattttttgtattt | 5607 |
rs8037986 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611909 | AGGCACATGTATCTT[A/G]TAGATGACCAATATG | 5607 |
rs8038024 | snp | A/C | 0.0539704 | 0.155153 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795038 | ATCACTTCTCCACTT[A/C]TCATCATCTCACACT | 5607 |
rs8038133 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542880 | GTGGTGTGGCGGCCC[C/T]GGGGCTCTTTCTTAA | 5607 |
rs8038578 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543092 | AGTTCCTGCGGGCCT[C/T]TGCCCGCTTCCCGGT | 5607 |
rs8038804 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743835 | TCAAGGAATCTTTGG[A/G]CTTCTCTAGCTCATT | 5607 |
rs8039444 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546849 | gtgggtagatcgctt[A/G]aactcaggagttcga | 5607 |
rs8039738 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615651 | CCTAAAAAGACCAAG[A/C]AATTAGAGGATTAAA | 5607 |
rs8039797 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547055 | gggtcacagagcgag[A/G]ccctatctcaaaaaa | 5607 |
rs8040028 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546925 | caaaaattagtgggg[A/G]cttggtgacactcac | 5607 |
rs8041111 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546990 | agaatctcttgaacc[C/T]agaggtcgaggctat | 5607 |
rs8042042 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779467 | TCCATAGATGTGACC[A/G]CTTAATCTTTTCACA | 5607 |
rs8042233 | snp | C/T | 0.209997 | 0.246779 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756604 | ggcaaattttaaata[C/T]ataatacaggattat | 5607 |
rs8042410 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582350 | caggcgtgagccacc[A/G]cgcccagccAGGAGG | 5607 |
rs8042507 | snp | G/T | 0.400682 | 0.199487 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756636 | aattatactcaccat[G/T]ctatatttatcttat | 5607 |
rs8042567 | snp | A/G | 0.39527 | 0.203462 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683261 | ATATTTTATGCAAGA[A/G]ATAACAAAATTTAAA | 5607 |
rs8043228 | snp | A/T | 0.311369 | 0.242351 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686300 | AACAATAATCAGCAG[A/T]TTGTTTAAAGAAAAA | 5607 |
rs8043459 | snp | C/T | 0.209693 | 0.246729 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756623 | atacaggattattaa[C/T]tatactcaccatgct | 5607 |
rs9302244 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694756 | CAGCCATCCCATTAC[C/T]AGGTATATACCCAAA | 5607 |
rs9302245 | snp | C/T | 0.390277 | 0.206936 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728799 | ACATACTAATTTATG[C/T]ATGGTTAGATTATGC | 5607 |
rs9302246 | snp | A/G | 0.388775 | 0.207946 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728942 | CCTTTACTCAATGAA[A/G]TGTCTCTTTCGTATT | 5607 |
rs9652480 | snp | A/G | 0.253544 | 0.249975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554979 | TGACTGACCCAAGGG[A/G]GTCAAACCTGAGGAG | 5607 |
rs9672402 | snp | A/G | 0.270351 | 0.24917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617135 | AAAAGGGGTATTTCC[A/G]TGCTCATTTTGATAA | 5607 |
rs9783714 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621115 | gtaggggaagatacc[C/T]ggcaaaaactaatca | 5607 |
rs9783715 | snp | A/G | 0.26078 | 0.249767 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677387 | TAAATGAGGTAATGC[A/G]TATGATAATAATGCA | 5607 |
rs9783734 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677238 | ATGCAGTTTGTTAAG[G/T]CTTAAGAGCTTTACT | 5607 |
rs9888652 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736023 | ATTTGGTGTTGTTCC[A/G]GTACTTTAACAGTAC | 5607 |
rs9920956 | snp | A/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655754 | tgtagattcactttt[A/T]aaaatcaaatttagg | 5607 |
rs9972436 | snp | C/G | 0.5 | 0.00019968 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805689 | TCTCCCCCATTCTCT[C/G]TCCTCGCTATGGCTC | 5607 |
rs10152398 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623755 | GGCACCCACCACCAC[A/G]CTGGGCTAATTTTGT | 5607 |
rs10153003 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695134 | GGAGGGGGGAGGGAT[A/G]GCATTGGGAGATATA | 5607 |
rs10153031 | snp | G/T | 0.497271 | 0.0368399 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694955 | tgagttcatgtcctt[G/T]gtagggacatggatg | 5607 |
rs10220844 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663888 | tcagaagaaaaGTTT[C/T]TCCTTGGTCATAAGT | 5607 |
rs10444849 | snp | A/G | 0.402277 | 0.198272 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742096 | agatggggttttacc[A/G]tgttagccaggatgg | 5607 |
rs10518734 | snp | A/G | 0.454182 | 0.144256 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597636 | TCATTTTGAAAAGTC[A/G]AATTAATATCCTTAT | 5607 |
rs10518735 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598880 | TCGTAGAAATTTATG[A/T]CAAGCCATGATGAGA | 5607 |
rs10518738 | snp | C/T | 0.311123 | 0.242413 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721912 | ACAGTTTGATGCTTT[C/T]GTTACATTTATTATC | 5607 |
rs10518739 | snp | C/T | 0.38821 | 0.208322 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722633 | CAGATGATTTAAACT[C/T]TTTCTCTAGGACTGT | 5607 |
rs10518740 | snp | C/T | 0.304438 | 0.244001 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726780 | AAGTCCCTGATGTTG[C/T]GATTCTGCTTTGAAA | 5607 |
rs10518744 | snp | A/G | 0.116838 | 0.211584 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770637 | ACCCTTGGTTCTGTG[A/G]TGTGGCAAAGTAATG | 5607 |
rs10518745 | snp | C/T | 0.207253 | 0.246318 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772302 | CTTTCCTTACTGTCT[C/T]ATCCCAATTACCAAA | 5607 |
rs10529511 | in-del | -/TGTGTGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774194 | GTGTGTGTGTGTGTG[-/TGTGTGTG]TGAGAGAACATAGGT | 5607 |
rs10543669 | in-del | -/CT | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805195 | GCAGCTCTGACAGTG[-/CT]CTGTGTGCCTCTGAG | 5607 |
rs10546581 | in-del | -/TGTGTGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774196 | GTGTGTGTGTGTGTG[-/TGTGTGTG]AGAGAACATAGGTAT | 5607 |
rs10578296 | in-del | -/TT | 0.420096 | 0.183214 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599995 | GAAAAACATGCAAAC[-/TT]ATATATAAAGTTACG | 5607 |
rs10579310 | in-del | -/AC | 0.220544 | 0.248259 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582824 | ATACATTGTCTCAAA[-/AC]ACACACACACACACA | 5607 |
rs10584480 | in-del | -/GTGT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589797 | TGTGTGTGTGTGTGT[-/GTGT]ATAAGAGATAGATGG | 5607 |
rs10593316 | in-del | -/TACG | 0.40157 | 0.198813 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756573 | TGTGTTGATAACACT[-/TACG]ATCTACTCCCTTGGC | 5607 |
rs10609519 | in-del | -/T | 0.375 | 0.216506 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710521 | TTTTTTTTTTTTTTT[-/T]GAGATAGAGTCTCGC | 5607 |
rs10635483 | in-del | -/CCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583976 | TGGTGTCAAACTCCT[-/CCT]GAGCTCAAGCAATCC | 5607 |
rs10665135 | in-del | -/TT/TTT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599698 | GATTTTTTTTTTTTT[-/TT/TTT]CAGGGCTTGCAGTGG | 5607 |
rs10672098 | in-del | -/AC | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582855 | CACACACACACACAC[-/AC]TTCCAATGTTGTGGG | 5607 |
rs10678847 | in-del | -/GT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756562 | TGTGTGTGTGTGTGT[-/GT]TGATAACACTTACGA | 5607 |
rs10679815 | in-del | -/AA | 0.0166325 | 0.0896639 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616186 | AATAAAATGTCACAC[-/AA]AGAGCAAAGAAGCAT | 5607 |
rs10684162 | in-del | -/A/AA | 0.484701 | 0.0861117 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660871 | GAGAAAAAAAAAAAA[-/A/AA]TAGAGGCAGGAGTGG | 5607 |
rs10712444 | in-del | -/C | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661044 | GGTCTAATAATCTGG[-/C]CATGCAAGGCAGGTT | 5607 |
rs10719227 | in-del | -/T | 0.100588 | 0.200439 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556555 | TTTTTCTTTTCTTTC[-/T]TTTTTTTTTTTTTTG | 5607 |
rs10775194 | snp | C/T | 0.420892 | 0.182472 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690742 | TTTTGCCATGTTGGC[C/T]AGGCTGGTCTTGAAC | 5607 |
rs10851775 | snp | A/G | 0.321769 | 0.239477 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594013 | CAGTGCTGTATGGTA[A/G]TGCTTCTGGAGGCCT | 5607 |
rs10851776 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598019 | AGACCAGCCCGGATA[A/T]CATGGTGAAACCCCA | 5607 |
rs11071955 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590319 | TAACCTATTAAAGGT[A/G]CCAAATGGAATATGT | 5607 |
rs11071956 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590446 | CTCTCTCCCTCCCTC[C/T]CTCTCTCTCTCTCTC | 5607 |
rs11071957 | snp | C/T | 0.414576 | 0.188188 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766309 | TGCTTAGAAGTTCAA[C/T]GGAAAAGCATCTGGA | 5607 |
rs11071958 | snp | C/T | 0.414905 | 0.187899 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766524 | GGGAAGTAGCAGCAA[C/T]TGCTTTACTAGAGTC | 5607 |
rs11071959 | snp | A/G | 0.42803 | 0.175514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766565 | TCGGGATGACTAGAT[A/G]CTTTCCCTTCCTGTG | 5607 |
rs11071960 | snp | C/T | 0.381503 | 0.21262 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784784 | TTCTGCCTTTCCACT[C/T]CTGCCATCATGGGTA | 5607 |
rs11071961 | snp | C/T | 0.381503 | 0.21262 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784785 | TCTGCCTTTCCACTT[C/T]TGCCATCATGGGTAT | 5607 |
rs11289969 | in-del | -/A | 0.484209 | 0.0874434 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622145 | GTGAGGCTCCATCTC[-/A]AAAAAAAAAAAAAAA | 5607 |
rs11314980 | in-del | -/A | 0.0898077 | 0.191933 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752898 | CCAAAACAATCATTG[-/A]AAAAAAAAAAAAGAA | 5607 |
rs11334748 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550778 | TCTTTTTCTTTTTTC[-/T]TTTTTTTTTTTGCCG | 5607 |
rs11335365 | in-del | -/T | 0.377977 | 0.21476 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595977 | TAAAGTTATTTTTTC[-/T]TTTTTTTTTTTTGTT | 5607 |
rs11372039 | in-del | -/T | 0.414905 | 0.187899 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765363 | TAATAAAATTTTTTT[-/T]AAAAAGTATAGTACA | 5607 |
rs11374165 | in-del | -/T | 0.499368 | 0.0177603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786025 | TGTTTTTTTTTTTTT[-/T]AACTTACAGAAGATG | 5607 |
rs11374166 | in-del | -/T | 0.484138 | 0.0876334 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785839 | AGCCAAGAAGCAACC[-/T]TGGGAAACTGGAAAG | 5607 |
rs11377061 | in-del | -/T | 0.319136 | 0.24025 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565637 | TCAAATTCAGTGTTT[-/T]AATTATTTTTGTGTT | 5607 |
rs11379051 | in-del | -/TT/TTT/TTTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599685 | TTCCCTGGAAATTGA[-/TT/TTT/TTTT]TTTTTTTTTTTTTCA | 5607 |
rs11395465 | in-del | -/A/AA/AAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664333 | ATCCCTGTTTCTACC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 5607 |
rs11411357 | in-del | -/T | 0.499087 | 0.0213463 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656326 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTAC | 5607 |
rs11418264 | in-del | -/T | 0.316968 | 0.240864 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690538 | ATTTTTTTTTTTTTT[-/T]GAGACAAGTCTCGCT | 5607 |
rs11449677 | in-del | -/C | 0.321769 | 0.239477 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621062 | TATTGGGAGAAAATT[-/C]TAAAATACCAAGACA | 5607 |
rs11449678 | in-del | -/A | 0.429837 | 0.173662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621434 | AAAAAAAAAAAAAAA[-/A]GAACAAAAGTTAATT | 5607 |
rs11504676 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591437 | TGGTGTGCAGTGGTG[C/T]GATCTTGGCTCACTG | 5607 |
rs11504677 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591607 | ATCTCCTGACCTCGT[A/G]ATCCACCTGCACCAG | 5607 |
rs11550176 | snp | A/G | 0.239614 | 0.249784 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542981 | GCTGTATCTCCCCCA[A/G]ACCGAGTCCTTGCCC | 5607 |
rs11629746 | snp | C/T | 0.214843 | 0.247516 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771152 | ACCATGTGTTTTACA[C/T]ATGGTAATGTGTACC | 5607 |
rs11630097 | snp | C/G | 0.239614 | 0.249784 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613227 | TCCAGAAGAGTAAGG[C/G]AAGAACAGTGCAGAA | 5607 |
rs11630417 | snp | C/T | 0.496483 | 0.0417852 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720271 | ATATATACACACACA[C/T]ATGCTTATATATACA | 5607 |
rs11630628 | snp | C/T | 0.314544 | 0.241524 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592113 | ACAAGAGTGAAACTA[C/T]GTCTCAAAAAAAAAA | 5607 |
rs11630730 | snp | A/G | 0.427119 | 0.176434 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565508 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 5607 |
rs11630805 | snp | C/G | 0.238749 | 0.249747 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595697 | TTGTTTTCCTGTTAT[C/G]ACTTTATGTTGGAGT | 5607 |
rs11630854 | snp | A/T | 0.427119 | 0.176434 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565778 | TTGATGAGATAATTT[A/T]AAAAAATTTTTTGTA | 5607 |
rs11630951 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558646 | ttgtttctctgaacc[C/T]gtgtgtttctcccca | 5607 |
rs11631200 | snp | A/G | 0.398354 | 0.201224 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624062 | tgggagagctaggcc[A/G]ggcgcagtggctcac | 5607 |
rs11631249 | snp | C/T | 0.239614 | 0.249784 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613568 | CCCCCTGGAAACCAT[C/T]AGCTTTGAATTTATA | 5607 |
rs11631474 | snp | A/G | 0.392696 | 0.205275 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641829 | GCCATGCTTTTTGCC[A/G]TTGCCTTCAAATAAG | 5607 |
rs11631559 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641962 | ATAGAGAGCATTTGA[A/G]TAGAGTTATTTTAAG | 5607 |
rs11631864 | snp | C/T | 0.328148 | 0.237472 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775424 | TGTGGTTTTCTGGCA[C/T]GTAGCCATGAAGCTA | 5607 |
rs11632574 | snp | A/C | 0.423726 | 0.179776 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560067 | GGCTAGATGGGCTGT[A/C]TATATCCAAGTTTTT | 5607 |
rs11632776 | snp | A/G | 0.40263 | 0.198 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560307 | CCAGTCTTCTCATGG[A/G]TATGGTTACTTTTCT | 5607 |
rs11632827 | snp | G/T | 0.288386 | 0.247035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639305 | TTCTTGTCAGACATG[G/T]ATACCAGCTTTTGAA | 5607 |
rs11632828 | snp | A/G | 0.226484 | 0.248892 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702511 | CTTTGTGAGACCTCC[A/G]TTTCTCTTATTCATT | 5607 |
rs11633668 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590438 | CTCCCTCTCTCTCTC[C/T]CTCCCTCCCTCTCTC | 5607 |
rs11633948 | snp | G/T | 0.265305 | 0.249848 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734683 | ATGTTTACTGATCAC[G/T]CCTGGAATTGCAAAA | 5607 |
rs11634494 | snp | C/G | 0.230896 | 0.249269 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792021 | AGAGCACCAGGCAGA[C/G]GAGGGGCAGGGCCAG | 5607 |
rs11634892 | snp | A/G | 0.264632 | 0.249571 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661771 | TGAGCTATCTTTAAT[A/G]GATAGTTTTTATAAC | 5607 |
rs11635282 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670620 | TTCAAAGGGTCTTGG[A/T]GATTCTGTTATTGTT | 5607 |
rs11635286 | snp | C/T | 0.232943 | 0.249417 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797649 | TTTACTTGGAAATCA[C/T]TGGTTTTTTTTAAAT | 5607 |
rs11635396 | snp | A/G | 0.232651 | 0.249397 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798085 | ACCACACAGCCATCA[A/G]TCACCCCCAGAGACA | 5607 |
rs11635413 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797883 | agacagggtttcacc[A/G]tattggtcaggctgg | 5607 |
rs11635424 | snp | A/G | 0.488846 | 0.0738428 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745240 | TATAAACAGCATTTC[A/G]TATGTTGTGAGGTGC | 5607 |
rs11635944 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645285 | gagttcgagaccagc[C/T]tgagcaacatagtga | 5607 |
rs11636408 | snp | A/G | 0.455144 | 0.142885 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568230 | AGTACAAGAGTCCTT[A/G]TATTTAAGTGAAGTG | 5607 |
rs11636945 | snp | C/T | 0.21725 | 0.247846 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621236 | ATATTTACAACTGAA[C/T]CACAAATACCATGTA | 5607 |
rs11637027 | snp | G/T | 0.495174 | 0.0488838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645417 | tgggaggcagagatt[G/T]cagtgaaccaagatc | 5607 |
rs11637401 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596423 | TGTCTCAAAAAAAAC[C/T]CAACAACAACAGGAA | 5607 |
rs11637445 | snp | G/T | 0.278399 | 0.248382 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699268 | TGCTTATTCCTGAGG[G/T]CATTTGCCTGAATCA | 5607 |
rs11637988 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702529 | TCTCTTATTCATTTG[C/T]TCACGTGTTCATTCC | 5607 |
rs11638507 | snp | C/T | 0.258565 | 0.249853 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581707 | CTAGACTTTCATTAC[C/T]TGTAACTCTCTGAAG | 5607 |
rs11638739 | snp | A/G | 0.261332 | 0.249743 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647274 | CATAAGGTGTACAAC[A/G]TGCTCTAAATTAGTT | 5607 |
rs11638934 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590405 | TTCTTGCTCCTTCct[C/T]cctccctctctccct | 5607 |
rs11638969 | snp | A/T | 0.277778 | 0.248452 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590468 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTTTGTTTC | 5607 |
rs11639267 | snp | C/G | 0.25801 | 0.249872 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722901 | GTTGTCATTCAGCTA[C/G]ATCACTGGCTATATT | 5607 |
rs11854197 | snp | A/G | 0.389527 | 0.207442 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685046 | aaataatttgaagaa[A/G]taatggctgaaaact | 5607 |
rs11854639 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602435 | ATTTGCTTCAAATGG[A/G]ATTAAAAAATGTTTA | 5607 |
rs11855244 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716234 | tagtcccagctactc[A/G]ggaggctgaggcagg | 5607 |
rs11855386 | snp | A/C | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791544 | aagcacctagtgagc[A/C]cctggcacagggtaa | 5607 |
rs11856740 | snp | C/T | 0.316726 | 0.240931 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567585 | TAGCCGGGATGGTCT[C/T]GATCTCCTGACCTCA | 5607 |
rs11856999 | snp | C/T | 0.105924 | 0.204309 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798362 | CCCCTTTAAACAGGC[C/T]AGTGGCACAATTCTG | 5607 |
rs11857017 | snp | A/G | 0.454182 | 0.144256 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680570 | GGCTGATTTTTATTT[A/G]CCTAAAACCACCTAC | 5607 |
rs11858007 | snp | A/G | 0.0364509 | 0.129988 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681385 | TGTATGCTCAGAGAG[A/G]TTTAAATGATTCGTC | 5607 |
rs12050481 | snp | C/T | 0.498084 | 0.0308911 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731471 | TTTCCTTTAGGCCTT[C/T]GGGTTGCATAACTTC | 5607 |
rs12050605 | snp | A/T | 0.199873 | 0.244923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747602 | CTTACTGGACTCTGC[A/T]TTTATTCCCTAAAAA | 5607 |
rs12050676 | snp | A/T | 0.200492 | 0.245049 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747275 | ATAAGGGATTATTAC[A/T]AGTTTCCCTGTATTT | 5607 |
rs12050749 | snp | A/G | 0.200801 | 0.245111 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745033 | CAGCTAATGAAAGAA[A/G]AAAAAAAATCTATGC | 5607 |
rs12050871 | snp | C/T | 0.230603 | 0.249246 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794881 | TTACTTAATTGGCTG[C/T]TTCTTGAAATAAGAT | 5607 |
rs12101607 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672794 | gtttttatggtttta[A/G]gtctaacgtttaagt | 5607 |
rs12102226 | snp | C/G | 0.287085 | 0.247234 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694719 | ttcctcagggatcta[C/G]aactagaaataccat | 5607 |
rs12148363 | snp | C/T | 0.103082 | 0.202275 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585107 | aaaatcaaattaatt[C/T]GTCCCCAAACAATCA | 5607 |
rs12148412 | snp | G/T | 0.227608 | 0.248995 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785841 | GCCAAGAAGCAACCT[G/T]GGAAACTGGAAAGAG | 5607 |
rs12232311 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696183 | AGCTGTTATATTTTA[C/T]AATTTTGAGTTCTAC | 5607 |
rs12232316 | snp | G/T | 0.441841 | 0.160303 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597586 | ATAAGCTTCTAAATA[G/T]CACTTTCTTATATAA | 5607 |
rs12437747 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735670 | TTCAGGAAACCAAGA[A/G]GGTTTCACAGAGTAG | 5607 |
rs12437936 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600626 | CCCAGAGTTGCTTTT[C/T]CTTGACATTTCCATC | 5607 |
rs12438118 | snp | G/T | 0.446547 | 0.154497 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658812 | GTCACACGCTTATGT[G/T]CTCCAACCTGTTCTA | 5607 |
rs12439136 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654599 | ctttcatgttctgtt[A/G]ttgctttcttttata | 5607 |
rs12441512 | snp | C/T | 0.0349115 | 0.127424 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662746 | TCATTCAACTAATTA[C/T]TCTTAACTCAGGCTA | 5607 |
rs12441598 | snp | A/G | 0.360421 | 0.224293 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780867 | GAGCTAGGAGGTGCT[A/G]ACCAGGTGGTGATCA | 5607 |
rs12441715 | snp | A/G | 0.419616 | 0.183658 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568249 | TTAAGTGAAGTGTAA[A/G]TATTCCCTTTGGTGT | 5607 |
rs12441823 | snp | C/T | 0.419616 | 0.183658 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620639 | GACTGTATAAGACAA[C/T]GATAGTAATAATTCA | 5607 |
rs12441975 | snp | A/G | 0.26271 | 0.249677 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705525 | agatcacctgaagtc[A/G]ggagttcgagacaag | 5607 |
rs12443086 | snp | A/C | 0.45692 | 0.1403 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788116 | CTTCCTCTTCATGGA[A/C]CTGCAAGTGTGTTGC | 5607 |
rs12591403 | snp | G/T | 0.191775 | 0.243125 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787117 | GCAGGGAAGTGGCTG[G/T]TCAATGATAGATAGG | 5607 |
rs12592101 | snp | A/G | 0.444533 | 0.157025 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737232 | GCTGACTGGCTATGG[A/G]TCCCTGGGGGGAGAA | 5607 |
rs12592315 | snp | A/G | 0.444267 | 0.157354 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747928 | GTTCACAATCTAGCA[A/G]TATAAAACATTATTT | 5607 |
rs12592373 | snp | C/T | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738901 | TCATCACCATCTCCC[C/T]CCGATTACTTCCTTG | 5607 |
rs12592919 | snp | A/G | 0.179845 | 0.239955 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748526 | CACTGTAAAGATATT[A/G]CATAGAGGCTAATAC | 5607 |
rs12592984 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799973 | TTGTTATTGTGATGC[A/T]TTGGCTTCCTCTTGC | 5607 |
rs12593350 | snp | A/T | 0.157311 | 0.232183 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761602 | TGATGTGGACTTTGG[A/T]TTTACAGTGAGTTCT | 5607 |
rs12593494 | snp | A/G | 0.464629 | 0.128197 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609194 | CCATAAAAACCTTAT[A/G]TCAGGTGTTGCTTGG | 5607 |
rs12593640 | snp | C/G | 0.178785 | 0.239642 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786750 | TCTCCACCTCTAGTT[C/G]CTTATCTACAAAAAT | 5607 |
rs12593664 | snp | A/G | 0.302435 | 0.244439 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691837 | CCAAAAATAATGTAA[A/G]GGAAGAGAAGGATAA | 5607 |
rs12593698 | snp | C/T | 0.15665 | 0.231917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787223 | ATAGGAATGTCCTAA[C/T]CCTTTGGCTGTTTCT | 5607 |
rs12593813 | snp | A/G | 0.489376 | 0.0721049 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744514 | GCTGCAGGGCAAGCC[A/G]TAATTTCAGAGAGTA | 5607 |
rs12595261 | snp | A/G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594231 | TACCTTTAACTTTCA[A/G/T]CAGCCAAAGGTTTGT | 5607 |
rs12708496 | snp | C/T | 0.499203 | 0.0199521 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761760 | ATCAATTTTTTTTCA[C/T]TTAGGCACCTATTAA | 5607 |
rs12900208 | snp | C/G | 0.427119 | 0.176434 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670720 | GCCAGCCAACCCCCC[C/G]ACCCCAAGAAAAAAA | 5607 |
rs12901232 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635357 | tttttttctactttt[A/G]gtagagatggggttt | 5607 |
rs12901703 | snp | C/G | 0.323434 | 0.238972 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626951 | ATTTTCTATATCTTT[C/G]AGACAGAGTCTCGCT | 5607 |
rs12901985 | snp | A/G | 0.200182 | 0.244986 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783886 | AAGGCAGCTTATATC[A/G]TAAGTAAAAGTACCA | 5607 |
rs12902406 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636124 | TGCTTTCTTGAAAGT[A/G]TGAAATgaccgggcg | 5607 |
rs12902505 | snp | C/T | 0.209388 | 0.246679 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759296 | AGGCACGGTGGCTCA[C/T]GCCTGTAATCCTAGC | 5607 |
rs12902780 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636092 | tacaggtgtgagcca[A/G]ggcacctggccTCCT | 5607 |
rs12902804 | snp | A/G | 0.388021 | 0.208447 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696320 | AATAAAGTTTTATTG[A/G]AACATGACCACACCC | 5607 |
rs12902812 | snp | A/G | 0.419456 | 0.183806 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616941 | CCTTCTTTGAAGTAC[A/G]TTATGTGAGAAGTAG | 5607 |
rs12902858 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609675 | CTATTCTATAGGTCT[A/G]TAGATTCTGTAGACC | 5607 |
rs12902904 | snp | A/G | 0.382473 | 0.212016 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784195 | ACTGATGCATAAACT[A/G]GGTCTCAGAGAGGTT | 5607 |
rs12903577 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628786 | CTTtggtggtggttg[G/T]ggaggtgtttttagt | 5607 |
rs12904980 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701392 | AGGTATTAGGTATGT[C/T]TGCCTAGTACTCTCT | 5607 |
rs12904982 | snp | C/T | 0.38934 | 0.207568 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713941 | TGGCACCAACACTTA[C/T]AATCAGTGTGATCTT | 5607 |
rs12905175 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796566 | actccacctcctgtt[C/T]cagtcacctcctacc | 5607 |
rs12905357 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632951 | GGGGGTACAACAGAG[C/T]TTCCTTTGAGATATT | 5607 |
rs12905371 | snp | C/T | 0.42803 | 0.175514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553592 | TTCTGAACCAGAAAT[C/T]CGAACCAATAAATGG | 5607 |
rs12905397 | snp | C/T | 0.398894 | 0.200825 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741812 | aaatatatgaagagc[C/T]gtcattaaacttata | 5607 |
rs12905509 | snp | A/G | 0.392696 | 0.205275 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701770 | AACAGTGAGCACCTC[A/G]GGCAGTTCTGCGATG | 5607 |
rs12905544 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633114 | GGTGCTCACCGAGCG[C/T]GGCCCAGTCGTACCA | 5607 |
rs12905628 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632950 | AGGGGGTACAACAGA[G/T]CTTCCTTTGAGATAT | 5607 |
rs12906959 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641676 | ATTTCAGTTTCTCAC[A/T]TAACCCTTTCTCCAT | 5607 |
rs12907213 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711177 | CATTGCCCTAGTGGG[C/T]ACTCAGTAAATCTTT | 5607 |
rs12907872 | snp | C/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636823 | gtgttaatattcaga[C/G]agattaacatttgag | 5607 |
rs12908383 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637254 | tccttaataaattcc[C/G]cttcatatatacatc | 5607 |
rs12908750 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714414 | TACCCAGCTGCCAGG[A/G]AAAAAAAAAAAAAAA | 5607 |
rs12909310 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639111 | agcgattgcaacaaa[A/G]gcaaaaattgacaaa | 5607 |
rs12910314 | snp | A/C | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614508 | CACATATATTGCCTA[A/C]CAATTCCAGTTCTTT | 5607 |
rs12911125 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642350 | GGGGGATAGAAAAAT[G/T]TACAAGACTCAGCCC | 5607 |
rs12911434 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593499 | CAGTGAGGGACAAAC[A/G]AGCCTTCAGGCCAGT | 5607 |
rs12912155 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584673 | ACCCATATCTTCTCC[C/T]ttttttttttttttt | 5607 |
rs12912176 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651562 | ctctggtaatcatca[C/T]tctactatgtctcca | 5607 |
rs12912382 | snp | A/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547513 | caggctggaatgcag[A/T]ggcgtgatctcggct | 5607 |
rs12912705 | snp | C/G | 0.208779 | 0.246578 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807157 | AGGGGGTCTGTGACC[C/G]CCCCCAGGGCTGGGG | 5607 |
rs12912974 | snp | C/G | 0.392881 | 0.205147 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67682041 | ACTGAATGAAAAGCT[C/G]TATGCCTTCAATTGC | 5607 |
rs12913237 | snp | A/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739350 | CCATGACTTATTTTG[A/T]TTAAATCTATTTTGA | 5607 |
rs12914773 | snp | A/G | 0.496348 | 0.0425753 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727620 | AACTGTCACACACAC[A/G]TAAATGTGAATAATG | 5607 |
rs12915438 | snp | C/T | 0.450734 | 0.149016 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634360 | gtgacagagtaagac[C/T]tcatctcaaaaaaaa | 5607 |
rs12915850 | snp | A/T | 0.463018 | 0.130857 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627484 | TTTGTCCACTCAAGT[A/T]GGAAAAGCAAAATGA | 5607 |
rs12916707 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569977 | TTAAGAGGAATAGCA[C/G]AATTGCTACAGCCTA | 5607 |
rs12916943 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635285 | gttcacaccattctt[A/C]tgcctcagcctcccg | 5607 |
rs12917590 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619326 | ccacctcacatattg[G/T]atatttatttgatta | 5607 |
rs13329413 | snp | C/T | 0.434109 | 0.169127 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804788 | AGGGCACGAGGTCGC[C/T]CCTCCTGAGCCTCCT | 5607 |
rs13380201 | snp | A/G | 0.454182 | 0.144256 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681327 | AATTGTGTGCTCAAC[A/G]CTGAGCATGTGAGTG | 5607 |
rs16950958 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544668 | GGCATGGAAGACAGA[A/C]GCGGACATTCCGAAA | 5607 |
rs16950986 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550667 | AATGAGTCATGCTAC[A/G]ATGAGATAGTCAGTA | 5607 |
rs16951001 | snp | G/T | 0.314301 | 0.241589 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561903 | CTTGTGGTAGGGGAA[G/T]ATCCCTGTGTTGAAC | 5607 |
rs16951002 | snp | A/G | 0.298144 | 0.245321 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567263 | CTGTTTTTATAGCAT[A/G]GTTTCTTGTAAGTTA | 5607 |
rs16951006 | snp | A/G | 0.296619 | 0.245615 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570774 | TGCAAATAGTTGGTT[A/G]GTTTATTGATTATTG | 5607 |
rs16951007 | snp | A/G | 0.295854 | 0.245759 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570897 | GCATGAGTATTCCTT[A/G]TAAGTGAAATACTGT | 5607 |
rs16951010 | snp | A/G | 0.296619 | 0.245615 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571525 | TTTCTGTGTCACCCT[A/G]TTGTTGCGAACATGT | 5607 |
rs16951043 | snp | C/T | 0.314301 | 0.241589 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591780 | CATTATAAAGCTAGA[C/T]GACTTAAGAGCTCCC | 5607 |
rs16951050 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595434 | CTTCGATTTGTGAAG[C/T]AAAGGTCTAGTGATG | 5607 |
rs16951052 | snp | A/G | 0.292523 | 0.246357 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598592 | TTAGGTTGGAGTGCT[A/G]GGAATGTGGATTGGG | 5607 |
rs16951058 | snp | A/C | 0.293037 | 0.246268 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601088 | CTAGTACCCTACGCT[A/C]GTCCCCTGCCTGTTT | 5607 |
rs16951060 | snp | C/T | 0.29278 | 0.246313 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601835 | TTGAAGTAATCTGAT[C/T]CAGTCACCCATTCAG | 5607 |
rs16951061 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603942 | TTTTTCTTTAAAGTG[G/T]AATAAAGCTAATAAG | 5607 |
rs16951062 | snp | A/C | 0.239614 | 0.249784 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606682 | TGACTGTAGAGGCCA[A/C]CTAAAACATTAAATT | 5607 |
rs16951081 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613315 | ATTCCTAAGACAATT[A/C]AAAAATGTATCAGAG | 5607 |
rs16951085 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616602 | TTGAGAGAGTGAACT[A/G]TCTCTGCAATGAGCT | 5607 |
rs16951105 | snp | A/G | 0.420892 | 0.182472 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673356 | CAAAATAGTGTAGGC[A/G]GGTAAATGTTATATA | 5607 |
rs16951125 | snp | A/T | 0.162909 | 0.23434 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688840 | AAAACCCAGGTCATA[A/T]GTCTCCTAGCCCAGA | 5607 |
rs16951127 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689103 | TTAGTATAAAATGTC[A/G]TTAAAGCTGAGTGCA | 5607 |
rs16951147 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699182 | AGCTAAAAAGACAGT[C/G]GGCTACTCCCAGGAC | 5607 |
rs16951157 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713389 | GATCTTCTATACGTA[G/T]AAGTAAACACATAAA | 5607 |
rs16951160 | snp | C/T | 0.0383715 | 0.133092 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719228 | TAGCTACTGATCAGT[C/T]TAAGCAGTGATACGT | 5607 |
rs16951225 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750809 | ATATGCCCAGTTGGG[A/T]TTTGAGCCGTTTTAC | 5607 |
rs16951227 | snp | A/G | 0.206029 | 0.246103 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751095 | AGAGCCAGTCCTGGA[A/G]TGGCCAAAGATGAAT | 5607 |
rs16951230 | snp | C/T | 0.181978 | 0.240568 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751856 | GTTTGGCGCTGACAT[C/T]GATATTCTCGGGCCT | 5607 |
rs16951231 | snp | C/G | 0.181978 | 0.240568 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754677 | CTTTGGAAATACCTT[C/G]ATATTCACAAAATGA | 5607 |
rs16951249 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762990 | ACATGTAATTTGTCA[C/T]GCCTGGCAGCCCAGA | 5607 |
rs16951250 | snp | A/G | 0.157642 | 0.232314 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763794 | TCTGACAGGCAACAC[A/G]CTATCCTGCTGGGCA | 5607 |
rs16951256 | snp | A/G | 0.217551 | 0.247885 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771907 | GACTATCCCATGGAC[A/G]CTCTGAGTTTAGAAC | 5607 |
rs16951258 | snp | A/G | 0.222333 | 0.248464 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773140 | ATGGAGTCCTCTTAG[A/G]TTCATGTAGAATGAA | 5607 |
rs16951259 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776149 | TAAAGGTAAACTAAG[C/T]GTGCAGGCAGCCAAG | 5607 |
rs16951271 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782613 | GCCCCCGTGTTTAAA[C/T]GGGCTTGACAGGAAT | 5607 |
rs16951275 | snp | C/T | 0.484209 | 0.0874434 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784830 | TCCAAGAGATGATGT[C/T]CCTCAAGTTTGGGAG | 5607 |
rs16951297 | snp | C/G | 0.15665 | 0.231917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791038 | TCTACCCAGAGAGAG[C/G]TCCTCACGCCATGAA | 5607 |
rs16951304 | snp | C/T | 0.427575 | 0.175975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797280 | TCAGATTTATCCACA[C/T]GCTTGCCAGTTACTC | 5607 |
rs17240463 | snp | C/T | 0.238749 | 0.249747 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545981 | GCTTAACAGGAAACA[C/T]GAGTGGCCCCACCAC | 5607 |
rs17240546 | snp | A/C | 0.021333 | 0.101051 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549439 | ATGGGTTTATATCGT[A/C]ATGGAAACTTGGGTG | 5607 |
rs17241403 | snp | A/G | 0.253544 | 0.249975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583424 | AAACATAGTCTTTCT[A/G]AGCCAAATTTAAATA | 5607 |
rs17241486 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589222 | AATATTGAGTAAAGT[C/G]AGTCACAGAGAAATT | 5607 |
rs17241808 | snp | A/G | 0.398174 | 0.201356 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600454 | GACACCTTTTATCAA[A/G]CTTTAATGAAATGAC | 5607 |
rs17242046 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611877 | CAGCTGTACTTTGAA[C/T]TTTTATTTTGTGCAC | 5607 |
rs17242186 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613780 | AATTTCTTGAGTTTT[C/T]AATGGAAACGGGTTA | 5607 |
rs17242605 | snp | A/G | 0.393065 | 0.205018 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671098 | TGCCTCTGTTCCCTC[A/G]TGTATACTATGAAAG | 5607 |
rs17243334 | snp | A/G | 0.390277 | 0.206936 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720741 | TCCAGTAATTAGTGT[A/G]TTTTATGGGCCTTTG | 5607 |
rs17244146 | snp | C/G | 0.21303 | 0.247251 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765641 | CCTGCCTGCTCTCAA[C/G]GTCACTAAACGTATT | 5607 |
rs17244601 | snp | A/C | 0.189576 | 0.242588 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780043 | TTTCCCTACTCTTCG[A/C]CTTTACAGTTGCTTG | 5607 |
rs17300356 | snp | A/G | 0.23846 | 0.249734 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560409 | ATCAGACAGTCTCCC[A/G]AAGAGCAGTTTGTAA | 5607 |
rs17300363 | snp | A/C | 0.135825 | 0.222405 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561024 | GTATATTGAAATTCA[A/C]ATATAAGCAGTCTCT | 5607 |
rs17300460 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563058 | TGTTGTGAATGACAT[A/G]AGCAATATTTTAATT | 5607 |
rs17300481 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566912 | GATACATGTGACACG[C/T]GGAATATTGTATTAT | 5607 |
rs17301102 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598259 | ATCAGTTCACAGGCC[A/G]AAGGTTTGCATAACT | 5607 |
rs17301587 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613881 | AGAGGTGCATTTACT[C/G]TTTGACCCACTAGGG | 5607 |
rs17302422 | snp | C/T | 0.258288 | 0.249863 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700828 | AGCTTATTGCAAGAA[C/T]AATTTCCCCAACAAG | 5607 |
rs17303860 | snp | A/G | 0.117886 | 0.21224 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773994 | TAAATGCATGTTTCA[A/G]TGCTGCAATGAGTTG | 5607 |
rs28368738 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548322 | CCTACACTGGCTAGA[A/G]TGAGTGTTCAATAAG | 5607 |
rs28372357 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721396 | TATTGGCACCCGTTA[A/G]GGCGCACTCCTGATG | 5607 |
rs28376010 | snp | G/T | 0.469937 | 0.118861 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771401 | GGGCTGGTCTGAGCA[G/T]CAGGGAGAAAAGTGG | 5607 |
rs28386928 | snp | A/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609500 | CTATAGGTCTATAGA[A/T]TCTGTAGACCTATTC | 5607 |
rs28393658 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609555 | CTATTCTATAGGTCT[A/G]TAGATTCTGTAGACC | 5607 |
rs28393858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635472 | GAGTCACCGTGCCCG[A/G]CCTGGAAATATTTAT | 5607 |
rs28414444 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745054 | AAATCTATGCCCAGA[A/G]AAGGGAAGAGGTTCA | 5607 |
rs28418298 | snp | C/T | 0.453087 | 0.145793 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643407 | TTTGTATTACACTTA[C/T]AGTCTAGTTTACTGA | 5607 |
rs28435327 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570079 | GAGAGGATCCCATAA[A/T]TTTTGGGCCTGTTGC | 5607 |
rs28449612 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718338 | TGCCTGCTGTCAGAG[A/G]ACACAGGTCAGCGTT | 5607 |
rs28450056 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590410 | GCTCCTTCCTTCCTC[C/T]CTCTCTCCCTCCCTC | 5607 |
rs28452558 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604360 | TGTTGCCTCATTTCC[C/T]AAAGTGCTGCAAGTT | 5607 |
rs28453906 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575920 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 5607 |
rs28463100 | snp | C/T | 0.484138 | 0.0876334 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786431 | TTAATCAACAAGTAT[C/T]TGTTGTCCAGGTCTG | 5607 |
rs28478056 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609585 | CTATTCTATAGGTCT[A/G]TAGATTCTGTAGACC | 5607 |
rs28479517 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609645 | CTATTCTATAGGTCT[A/G]TAGATTCTGTAGACC | 5607 |
rs28485607 | snp | C/G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584348 | TCTCTGATTCCTTGG[C/G/T]TAGCCACTTTGTTTA | 5607 |
rs28489575 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610108 | CTGCTTCCCAAGCCA[A/G]GGTTTTTCTGTTTGC | 5607 |
rs28492777 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643812 | GCTTCCCCAAATCAA[C/T]GCCTGGCCAATGTCA | 5607 |
rs28494496 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578918 | CAGTTTTAGACATCT[C/G]TATAATTAACTTGTT | 5607 |
rs28502616 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582240 | CTAATTTTTGTATTT[C/T]TAGCAGAGACAGGGT | 5607 |
rs28504096 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550757 | ATGAGGGCTACTTTT[C/T]TCTTTTCTTTTTCTT | 5607 |
rs28526223 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745233 | AGTTAGTTATAAACA[C/G]CATTTCATATGTTGT | 5607 |
rs28533335 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568103 | TTAACAAAAATAATT[C/T]TCATCATTTTGTCTA | 5607 |
rs28535070 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609650 | CTATAGGTCTGTAGA[A/T]TCTGTAGACCTATTC | 5607 |
rs28558621 | snp | G/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718958 | TACAGTAAATTTTTG[G/T]TGACTGTAATCACCT | 5607 |
rs28562863 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634208 | TACAAAAAATAAAAA[A/T]TAAAAAATAAATTAG | 5607 |
rs28563768 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726755 | TGCTCTCTTAGATCC[A/G]TTAGCGTTAAAGTCC | 5607 |
rs28565266 | snp | C/G | 0.453331 | 0.145452 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645673 | ATCCTCCCACCTCAG[C/G]CTCCCAAGTAGATTG | 5607 |
rs28568344 | snp | A/G | 0.457037 | 0.140127 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804189 | CTGCTCTCGGGTCCT[A/G]CACACTGGCTTTCTC | 5607 |
rs28570354 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766552 | GTCTCTGAACTCCTC[C/G]GGATGACTAGATACT | 5607 |
rs28580436 | snp | A/G | 0.00713661 | 0.0593075 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646223 | TATTAATACCTTTCT[A/G]TATTTAGGTCATACT | 5607 |
rs28587214 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656326 | TGGGGAAACCTTTTA[A/T]TTTTTTTTTTTTTTT | 5607 |
rs28595858 | snp | A/G | 0.311614 | 0.242289 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643729 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 5607 |
rs28608025 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608976 | CTGCAGAGGCAGATT[C/G]TTCACAGCCTAAGGA | 5607 |
rs28612914 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716473 | CTCAACACTAAAATT[C/G]TGAGTCTATGATAAT | 5607 |
rs28620456 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718471 | AATCATTTTTAAAAA[A/T]TTTTTATGGGGGCTG | 5607 |
rs28620621 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597186 | AAAAGAAAAAAAAAA[A/G]AAAAAAAAAAACTAC | 5607 |
rs28625693 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590426 | CTCTCTCCCTCCCTC[C/T]CTCTCTCTCTCCCTC | 5607 |
rs28626095 | snp | C/T | 0.473451 | 0.112115 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774391 | TTGATTTTAAATGAA[C/T]GCATTCCCAGAGGTA | 5607 |
rs28630814 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772355 | ATAAGTTTGAAATAA[A/G]TTGATAATTGAGTCA | 5607 |
rs28637534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592720 | CTTCTTTATTGCTTT[C/T]GATTACTAACAGGGT | 5607 |
rs28651137 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609680 | CTATAGGTCTGTAGA[A/T]TCTGTAGACCTATTC | 5607 |
rs28653027 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711292 | TCTTTAATATAAATG[C/G]CCGTAAGTGTTTGGA | 5607 |
rs28656828 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797867 | TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC | 5607 |
rs28663530 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609530 | CTATAGGTCTGTAGA[A/T]TCTGTAGACCTATTC | 5607 |
rs28668805 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730504 | ACATCATCAAATCAA[A/G]CTTCTCTACAATGTC | 5607 |
rs28671709 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743246 | GTAGATCTTAGAATG[C/T]GAGAATCGTTGGTTC | 5607 |
rs28672247 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590430 | CTCCCTCCCTCCCTC[C/T]CTCTCTCCCTCCCTC | 5607 |
rs28675729 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600444 | ATTCCATTTTGACAC[C/G]TTTTATCAAACTTTA | 5607 |
rs28690569 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609615 | CTATTCTATAGGTCT[A/G]TAGATTCTGTAGACC | 5607 |
rs28693409 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597187 | AAAGAAAAAAAAAAG[A/G]AAAAAAAAAACTACT | 5607 |
rs28694283 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610334 | GGGTGTCCTTATTTA[C/T]CAAAAACTTATAATT | 5607 |
rs28698864 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609077 | ATGTGGCTGTTGTTC[A/G]GAACTGCTGAGAAAA | 5607 |
rs28702447 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561363 | CTTTCTTCTCTCTCT[A/G]CAGCTGGAATGGCAT | 5607 |
rs28709176 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601615 | GATATTAATATGTAT[C/T]TCCAGAGTTGTAAAA | 5607 |
rs28712177 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609525 | CTATTCTATAGGTCT[A/G]TAGATTCTGTAGACC | 5607 |
rs28730805 | snp | A/G | 0.410061 | 0.192043 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587080 | TTAGATTTAGACTGG[A/G]TGCTGAGAAGGCTCT | 5607 |
rs28730806 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587231 | CCAGTTTGGCACAGG[A/G]AGGGGTGCTGGGTTG | 5607 |
rs28730807 | snp | A/T | 1.70525e-05 | 0.00291992 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67592973 | TACTAGCCAATGGCC[A/T]GGTAGGTATTATTAT | 5607 |
rs28730808 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748423 | AGAAATAATAGAACC[C/T]CCTGAGCATCAATGT | 5607 |
rs28730809 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748437 | CTCCTGAGCATCAAT[A/G]TTTTTATAAGAGTTT | 5607 |
rs28730810 | snp | A/G | 0.043519 | 0.140945 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806598 | GAAAGTACAATGAGC[A/G]CGGGAGTCCGAGGAC | 5607 |
rs28730811 | snp | C/T | 0.00618853 | 0.0552808 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806641 | CCTCCTCCTCTTCCC[C/T]GCAGGGCCACCCGTT | 5607 |
rs28735117 | snp | C/T | 0.443464 | 0.15834 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641554 | CTAATTTAAATTGAG[C/T]ACAGAGTAAATTATA | 5607 |
rs28750201 | snp | G/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663391 | TTACTTTGATATTTT[G/T]GAAGAGTACATTGCC | 5607 |
rs34001961 | snp | A/C/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753701 | GAAAAACAGAAAATA[A/C/G]CAATTGGTGACAAGA | 5607 |
rs34004236 | in-del | -/A | 0.430583 | 0.172886 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572708 | ATTATTATTATTATT[-/A]TTTTTTTTTGAGATG | 5607 |
rs34007896 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641282 | CTAGCATTTAAATGG[-/C]ACCATTTGATTAATC | 5607 |
rs34056780 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712366 | CCATGAGCACAGTTT[-/C]CCAGTGAGATTTTCA | 5607 |
rs34106326 | in-del | -/C | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679939 | AGAACATTTTCATCA[-/C]CCCCAAAAAAGTGTC | 5607 |
rs34107836 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714412 | CCTACCCAGCTGCCA[-/G]GGAAAAAAAAAAAAA | 5607 |
rs34145771 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773888 | TTCTAGAGATGGAGA[-/C]CCCATTTACCTTGTG | 5607 |
rs34230819 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604652 | CTGTAATCCCAGCAC[-/T]TTGGGAGGCCGAGGC | 5607 |
rs34240691 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784783 | TTTCTGCCTTTCCAC[-/T]TCTTGCCATCATGGG | 5607 |
rs34264206 | multinucleotide-polymorphism | GC/TT | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632950 | AGGGGGTACAACAGA[GC/TT]TTCCTTTGAGATATT | 5607 |
rs34273323 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605340 | TATAGGCGTGAATCA[-/C]CCACCCCCAGCCAGC | 5607 |
rs34279516 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618672 | GCTAAGGACAAAAAC[-/T]TTTGCAGTCTTTCTT | 5607 |
rs34282083 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653288 | TCTCTGTTTAAAATA[-/T]TTTTTTTTTTTTTTG | 5607 |
rs34286897 | in-del | -/A/AA | 0.472803 | 0.113397 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709478 | AAAAAAAAAAAAAAA[-/A/AA]CTACAGGGCTAAACT | 5607 |
rs34306467 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767877 | AGATTTTATTTCACT[-/C]CCCATTTTTCCTTTG | 5607 |
rs34333817 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773983 | TATTTGTTTGTAAAT[-/G]GCATGTTTCAATGCT | 5607 |
rs34355926 | multinucleotide-polymorphism | CT/GG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768699 | TGGAGTCATTTGCAG[CT/GG]GCCTACTTTATGTGG | 5607 |
rs34365245 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731350 | AGTCAGTGCCCTGGG[-/G]AGCAACATAAAGGTT | 5607 |
rs34367223 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634453 | GTATAATGTCAATTA[A/G]ATCAAGTTGGCTGAT | 5607 |
rs34369642 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590509 | AGGGTCTCATTGCTG[G/T]CACCCCCCCATTCTG | 5607 |
rs34370918 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714697 | TGAGTGAAATCTTAC[C/T]ACATGTTGAATATTC | 5607 |
rs34411457 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675677 | ATCTATAGTTATCTC[-/A]AAAATTAAAAGCTTA | 5607 |
rs34412003 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684728 | TCCAAGGAATTCATA[-/G]GGAAACATGAGCATA | 5607 |
rs34420962 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545184 | CTCTGTGTCATTCTT[-/G]GGTTATGTGCCCCAC | 5607 |
rs34443429 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557664 | CTAAATTGCAATTCT[-/G]GGAAGTTGTAAATTC | 5607 |
rs34459683 | in-del | -/TG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639702 | AGATCCTCCACGACA[-/TG]TCGTCAGTCTGCTTT | 5607 |
rs34462016 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750641 | ATCTACTAGTTTCTC[-/G]GGGTAACTCTCTGCA | 5607 |
rs34471081 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751146 | AGGAGGTGGAATCAT[-/G]GGAACAAAGCCAGAG | 5607 |
rs34473838 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555374 | GAGAGGGCACTGAGT[C/T]ATTCATGGGGGATCC | 5607 |
rs34491417 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666300 | TTATTCTGCCATTAT[-/G]CTTGATTTTTCTTCT | 5607 |
rs34506376 | in-del | -/C | 0.323908 | 0.238825 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619763 | GAGAACCTTGTTCTA[-/C]AAAAAATAAAAATAA | 5607 |
rs34516294 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741028 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 5607 |
rs34583567 | snp | G/T | 0.496314 | 0.0427728 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690943 | ATGCTCCTACCCTGT[G/T]AACTTATTTATTTCT | 5607 |
rs34588322 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712914 | AGAGCAGGCTGTCTC[-/A]AAAAAAAAAAAAGAA | 5607 |
rs34590705 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684862 | AGAAGAAATTGTGAT[A/T]TTGAGGTTAAAGATC | 5607 |
rs34599662 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771429 | GGATAAGGCTTCACC[-/C]TCCCTCCTGTCCAAA | 5607 |
rs34640005 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653595 | CCACCACACCCAGCT[-/A]AAAAAAAATTTTTTC | 5607 |
rs34662750 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647869 | GTGAGACTCTGTCTT[-/A]AAAAAAATAAAAAAA | 5607 |
rs34685592 | in-del | -/G | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720379 | TACACACACACAAGG[-/G]AAAAAAAGAAAATGA | 5607 |
rs34690244 | in-del | -/C | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719346 | GCAAACCAGGCACCT[-/C]CCAGGTTGACCAGTC | 5607 |
rs34726724 | multinucleotide-polymorphism | AG/GC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624654 | GAGTGTGTTTGACGG[AG/GC]TTTCGCTCTTGTTTC | 5607 |
rs34730169 | snp | C/T | 0.021333 | 0.101051 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792199 | AGAAAAAAACTAGGA[C/T]GTTGCTAAGACCCTC | 5607 |
rs34752783 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741342 | GTAAAGCCTAGTCTT[-/C]CCTTGCTGGTTTTAG | 5607 |
rs34765730 | snp | A/G | 0.410737 | 0.191478 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643682 | CGATCTCCTGACCTC[A/G]TGATCTGCCCGCCTC | 5607 |
rs34767566 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688816 | ATTTGTGACAGGATC[-/A]AAAAGACTAAAACCC | 5607 |
rs34792516 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555788 | ATTTGTATTTAATTT[-/C]CCTTTTTTTTTTTTG | 5607 |
rs34805106 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607210 | AAACAAGACATCATC[C/T]TAATGCAAAATTAAA | 5607 |
rs34811815 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555576 | CTGTGTTTGCTCACC[-/A]AAAAGGTAGAACCAA | 5607 |
rs34819968 | snp | C/G | 0.23846 | 0.249734 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558763 | AGCTGCTGCCTCTGC[C/G]TGGAACAGTCTTTCC | 5607 |
rs34858114 | snp | C/T | 0.420733 | 0.18262 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544000 | ACTGCAGCCTCTGCC[C/T]CCTGGGCTCAAGCGA | 5607 |
rs34871225 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762534 | ATGTTTACAACATTT[C/T]TAAGTAAATATAAGT | 5607 |
rs34890838 | in-del | -/ACTT | 0.311614 | 0.242289 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629695 | CATTCCTATCCTAAC[-/ACTT]ACCAGATGAGAGGAA | 5607 |
rs34936528 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741528 | GGCTGCAGTTTCATT[-/G]GGACCAGTTCAACTC | 5607 |
rs34956119 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796005 | AAATTTTATTTTTTG[G/T]TGATATTAATATAGC | 5607 |
rs34960633 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788492 | AGTTACTTCACCCCT[-/G]GGAAACTTTAGTACC | 5607 |
rs34970619 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757283 | GGTTTTTATTTGCAT[-/A]AAAAATAGTATTTCT | 5607 |
rs34973603 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595205 | CTGCCTGGGTTCATT[-/G]GATATAGGTTATGTG | 5607 |
rs34983376 | in-del | -/T | 0.0894459 | 0.191631 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629395 | TAGATTTTTTTTTTT[-/T]GCACCATGCTGTTGA | 5607 |
rs34984883 | in-del | -/T | 0.214843 | 0.247516 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763648 | TTTTTGTTTTTTAGA[-/T]TTTTTTTTTTTAAAC | 5607 |
rs35021732 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742748 | CTAAGCCCCTGCTTT[-/C]CCTTGCAAAATTCAA | 5607 |
rs35029564 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804286 | GACGCTGGGTCCCCT[-/C]CCATGTCTGTCCCCT | 5607 |
rs35041568 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551955 | CATTTTGTAAAATAT[C/T]CAACCACGCTTCCCC | 5607 |
rs35051671 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743346 | CTAATAGACCCACAG[-/C]ACATGATAAGAACTT | 5607 |
rs35058373 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741745 | ATAAGGAAGAAAACA[-/G]GGGATGTTCATTCAA | 5607 |
rs35118494 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606602 | GGCAGTGGGCTGGGG[-/A]ATGGTCCTTGGAGGT | 5607 |
rs35121847 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593881 | CAAGCCTCACTGGCA[-/T]TTTCATGAATCAAGT | 5607 |
rs35123069 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712913 | AGAGCAGGCTGTCTC[-/A]AAAAAAAAAAAAAGA | 5607 |
rs35144669 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727420 | GGTAGAAAATGGATG[-/A]AAAAAACTTTAACAA | 5607 |
rs35160812 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560568 | TCTTTTGGAGTCAGA[-/C]CCCCTAAGGGGAGAG | 5607 |
rs35169066 | in-del | -/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661694 | CTATCAGAATATATT[-/G]GGATTGCCTTCCCCT | 5607 |
rs35193493 | snp | A/C | 0.198324 | 0.244601 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751248 | GACCACAGATCAGGA[A/C]CTGGGAGGGTGGCCA | 5607 |
rs35241595 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654196 | TTTATGTTTCATATA[-/G]TTTTGGCACTCCGTT | 5607 |
rs35258841 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768322 | ATAATGACACGCATA[-/T]TGCAGAGGTGCTTTT | 5607 |
rs35261259 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736726 | AAATAATCAATTTAG[-/C]CCCCCAGAAATAGAA | 5607 |
rs35278102 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771442 | ACCTCCCTCCTGTCC[-/A]AAAAATTAATCAGCT | 5607 |
rs35280849 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761624 | TGAGTTCTCAGAGTC[-/T]TGACTTGATAGTGTT | 5607 |
rs35294921 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664520 | AAAAAAAAAATGTTG[-/A]AATGTATTTAAATAT | 5607 |
rs35303413 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763064 | CTCTGCTCAAGACTT[-/G]ATGTGGAGTAGGATG | 5607 |
rs35307315 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618940 | TGAAATATTAGGTCT[-/C]CCCCTCTGCTCATGA | 5607 |
rs35312559 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791911 | CTGTTCCCCTCACCA[-/C]CCAGGGAGAATGTCA | 5607 |
rs35320674 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543576 | GCAATGGCTACTGCT[-/G]GGCTTCCTGTGGAGG | 5607 |
rs35321070 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666991 | ATATTCATATTTAGC[-/T]TTTTGAGTTTCCCAG | 5607 |
rs35334851 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645351 | GGGTATGGTGGCACA[-/C]CCTGTGGTCCCAGCT | 5607 |
rs35355623 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639705 | TCCTCCACGACATGT[-/C]GTCAGTCTGCTTTTA | 5607 |
rs35373677 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635188 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 5607 |
rs35395156 | snp | A/G | 0.498935 | 0.0230538 | intron-variant, missense | MAP2K5 | GRCh38.p7 | 15:67670425 | TGTTTTTTAGCAAAC[A/G]AAGACCTGTGCACCT | 5607 |
rs35426622 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611389 | AATTCTTAGTGAGTA[-/T]TTTGCAGAGCACAAC | 5607 |
rs35448372 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648821 | CTGACCTCGTGATCT[-/C]CCCCGCCTTGGCCTC | 5607 |
rs35452334 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560808 | CAAAATATTTTGGTT[-/C]TAAGTAGCCTTAAAG | 5607 |
rs35453217 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660294 | GTAGTTTTTTTTTTG[G/T]ATGTTTCCTGAGTAG | 5607 |
rs35476342 | in-del | -/C | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720087 | AATTGAGGGTTTTTT[-/C]CCCCTTTTTTATTTA | 5607 |
rs35484804 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569933 | TTTAAGTGGCAGGTT[-/G]CCCTGAAGCTGCTAT | 5607 |
rs35487718 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627451 | AGTTAAGTTTACCTT[-/C]CCATGACTGGCTTGA | 5607 |
rs35491196 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805596 | GGAAGCTGGAGGGAG[-/G]AGAGAGCTGGGGGGA | 5607 |
rs35507375 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723237 | ACAAAGATTTTTATC[A/G]TGTTATATATTTGGC | 5607 |
rs35509407 | in-del | -/C | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662815 | TTTCTCATTTTATTT[-/C]CCTTGACCTGCCCTT | 5607 |
rs35510441 | in-del | -/T/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650528 | TCTAGTTTGTTGAGT[-/T/TT]TTTTTTTTTTTTTTA | 5607 |
rs35534298 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806262 | CACCAACTGAACCGG[-/A]AAAGCTGGCAACACA | 5607 |
rs35539069 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710433 | TCAACATAGGTAAAG[-/T]AACATAGTCAGAGAA | 5607 |
rs35553590 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806258 | TGGGCACCAACTGAA[-/C]CCGGAAAGCTGGCAA | 5607 |
rs35556314 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775560 | CTTGTTCTAGACTCA[-/C]GCAGAAGATATAAAG | 5607 |
rs35562278 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594325 | AACAAAATCTGACTA[-/C]AAAGCAAAAATATTG | 5607 |
rs35582476 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767456 | CTACTCAGATACTTT[-/C]CAGTACTACACCCTC | 5607 |
rs35602538 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556486 | GTGTCGTATTGTGGG[-/T]TTTTATAAAAAGCAT | 5607 |
rs35622885 | in-del | -/CA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582833 | TCAAAACACACACAC[-/CA]ACACACACACACACA | 5607 |
rs35670580 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752851 | AAACTAATCCTAAAA[-/T]TTCCCATGGAAATAC | 5607 |
rs35683090 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729756 | CAACAGAGCAAGATT[-/T]CCGTCTCAAAAACAA | 5607 |
rs35697256 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678398 | TGCCTCCATTGTCAT[-/C]CCCACAACAGCCACA | 5607 |
rs35723223 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655064 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 5607 |
rs35726621 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743511 | CAGTTTGCTAAAAGT[-/C]CCCATTTGTAGTTAG | 5607 |
rs35733169 | snp | C/G | 0.410568 | 0.191619 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598115 | GAGGCTGAGGCAGGA[C/G]AATCATTTGAACTTG | 5607 |
rs35807809 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795673 | TTCTCTCTTTGCTTG[-/A]AAAAAGTATATATTC | 5607 |
rs35811067 | in-del | -/T/TT | 0.42357 | 0.179927 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632097 | AAGTATTATGCTAGA[-/T/TT]TTTTTTTTTTTTTTT | 5607 |
rs35828534 | in-del | -/A/AA/AAA | 0.499539 | 0.0151687 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678962 | GTGACACTGCATCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 5607 |
rs35832547 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626151 | GTGATGTGGAGGGGG[-/A]AAAATAATATATCAC | 5607 |
rs35839019 | in-del | -/AAAGA | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612999 | TTTAGCTGATAGTTA[-/AAAGA]GGAGTTATTTACAGA | 5607 |
rs35870896 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675972 | GGAAGAGGATAGTTA[-/T]TTTCCCCAGTCCCCA | 5607 |
rs35871652 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695808 | TCTATCTGTTAATTG[-/A]AAATGTGAGGATTAA | 5607 |
rs35903116 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798375 | CCAGTGGCACAATTC[-/T]TGCCATTCACAAGGA | 5607 |
rs35914039 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608128 | TACATTAGCGCACTT[-/C]CCGTGTTGTAGGGTG | 5607 |
rs35918649 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706071 | AGTGCTCTGTGGAGC[A/G]TGACTATAGACAGGC | 5607 |
rs35921672 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569961 | TATTAAAACTTCTAC[-/T]TTAAGAGGAATAGCA | 5607 |
rs35927275 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627406 | AATGAAATATACTTG[-/A]AATTTCTGTATAATT | 5607 |
rs35931346 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792478 | AAAAAGCCTGGTTTG[G/T]CATTGTTTATCTAAT | 5607 |
rs35931405 | in-del | -/A | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669795 | AAAAGAGATAACAAC[-/A]AAAAAACCTGATAAT | 5607 |
rs35932396 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684640 | AAATAGATGCCCCCC[-/T]TCCCACACACACACC | 5607 |
rs35948216 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545310 | AGATAGATATGTTTG[G/T]TTTTGTTTCTTCATA | 5607 |
rs35951451 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608115 | ATCAGGTAAACATTA[-/C]CATTAGCGCACTTCC | 5607 |
rs35960901 | in-del | -/T | 0.493293 | 0.0575177 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555790 | TTCCTTTTTTTTTTT[-/T]GAGACGCAGTCTCAC | 5607 |
rs35968580 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741533 | CAGTTTCATTGGACC[-/A]AGTTCAACTCCCTGT | 5607 |
rs35988425 | in-del | -/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737844 | GGGAATAGAATAGTC[-/T]TTTTTTTTTTTTTTT | 5607 |
rs36004835 | snp | A/C | 0.496314 | 0.0427728 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659204 | TACTATAATGTTCTC[A/C]TAAGTTCCATATTTC | 5607 |
rs36017038 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591878 | GCACTTTGGGAGGCC[C/G]AGGCGGGCAGATCAC | 5607 |
rs36019959 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726533 | TTCTAAAACAATTAC[-/A]AAAGGAGAATTCAGA | 5607 |
rs36038116 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738535 | ACGCACAGAGCTAAC[C/T]TGAGTTCTGGTCTTG | 5607 |
rs36061827 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600625 | CCCAGAGTTGCTTTT[-/C]CCTTGACATTTCCAT | 5607 |
rs36073402 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627390 | TCTTGCTTTTTCTTT[-/A]AAATGAAATATACTT | 5607 |
rs36104348 | in-del | -/CCT | 0.471483 | 0.115954 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627019 | CTCACTGCAGCCTGA[-/CCT]CCTGGACTCAAGCGA | 5607 |
rs36111747 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584672 | ACCCATATCTTCTCC[-/T]TTTTTTTTTTTTTTT | 5607 |
rs36114201 | snp | C/G | 0.200182 | 0.244986 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742910 | GTCCTTTTTTTTCCT[C/G]CTCACTGACTGGCAG | 5607 |
rs36117844 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591834 | AGGACTTTCACGCCA[-/G]GGGGTGGTGGCTCCC | 5607 |
rs36131201 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694967 | TTTGTAGGGACATGG[-/G]ATGAAATTGGAAATC | 5607 |
rs36136516 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694914 | ACATATACACCATGG[-/G]AATACTATGCAGCCA | 5607 |
rs36174707 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694856 | AAGACTTGGAACCAA[-/C]CCCAAATGTCCAACA | 5607 |
rs41305272 | snp | C/T | 0.0221141 | 0.102801 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67807105 | ATAAAAGTATTAATG[C/T]TTTGTGACAGCCTCT | 5607 |
rs41306690 | snp | C/G/T | 3.2954e-05 | 0.00405908 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543440 | CTGGACAGTGCACTC[C/G/T]GGGCCGCAGTTACTC | 5607 |
rs41308580 | snp | A/G | 0.00914312 | 0.0669923 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807369 | GGATCTCAGGCCCCC[A/G]CCATGAGCTCCTTAC | 5607 |
rs55692407 | in-del | -/CTA/CTT/CTTTCTTTCTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575923 | TTTCTTTCTTTTTTT[-/CTA/CTT/CTTTCTTTCTC]TTTTTTTTTTTTTTA | 5607 |
rs55705746 | in-del | -/ATTT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583770 | TTTATTTATTTATTT[-/ATTT]TGGAGACAGAGTCTC | 5607 |
rs55709438 | snp | A/C | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569020 | CAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAACAA | 5607 |
rs55744419 | snp | A/C | 0.00265718 | 0.0363528 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67563347 | GAAGGCAATGCTGTC[A/C]TATGTAAGTATACGA | 5607 |
rs55744816 | in-del | -/AT | 0.0341408 | 0.126114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655531 | TTCTTTCATGTTCAA[-/AT]ATGTCATTCCCCTGC | 5607 |
rs55748942 | in-del | -/C/TTC/TTCTTTC/TTCTTTCTTTC/TTTTTTTTTTTTTTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575921 | TCTTTCTTTCTTTTT[lengthTooLong]TTTTTTTTTTTTTTT | 5607 |
rs55811347 | snp | A/G/T | 9.84204e-05 | 0.00701431 | missense | MAP2K5 | GRCh38.p7 | 15:67806685 | AATGATGGAAATGCC[A/G/T]CCGTGGTGTCCATGT | 5607 |
rs55847901 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754176 | CTGTCACAGGTACAA[C/G]GTTTCTTTTTAGGGT | 5607 |
rs55855141 | snp | C/T | 0.00844213 | 0.0644189 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703412 | TCTTTTATGGAGGTA[C/T]GTTGTTTGCACATAG | 5607 |
rs55873788 | snp | G/T | 0.208474 | 0.246527 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718533 | CTTTGGGAGGCTGAG[G/T]TGGGTGGATCACTTG | 5607 |
rs55877854 | snp | C/T | 9.843e-05 | 0.00701465 | missense | MAP2K5 | GRCh38.p7 | 15:67806713 | TGTGGGTGTGCCGGG[C/T]GCTGGAGGAGAGGCG | 5607 |
rs55908993 | snp | C/T | 0.472241 | 0.114494 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576951 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 5607 |
rs55930868 | snp | A/G | 0.000131889 | 0.00811956 | synonymous-codon, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703393 | TGTCTGGAGCTTAGG[A/G]ATCTCTTTTATGGAG | 5607 |
rs55966838 | snp | C/T | 0.0134655 | 0.080941 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67692480 | TGGTCCCTTTTTAGA[C/T]GTGAAGCCCTCCAAT | 5607 |
rs55986190 | snp | C/T | 0.303187 | 0.244277 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636990 | CTTGCTGAGTCTTCC[C/T]GCCTTCATCTTTCTT | 5607 |
rs55993790 | snp | A/G | 0.394721 | 0.203852 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734184 | AAAGTTTGCTAAATA[A/G]TTGGGTAGTTTTAAT | 5607 |
rs56019646 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725904 | TTGAAAGGAGGTGGG[A/G]TGGGGACAGAGGATG | 5607 |
rs56038097 | snp | A/T | 0.319136 | 0.24025 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612231 | GCTTTCTCCTATCTA[A/T]CATATTTTAAGAGTA | 5607 |
rs56056420 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627843 | AAGTCTCTGTTCTCC[C/T]TGCTGTCATGTCTAA | 5607 |
rs56065367 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628563 | ATATGGAAAAATTGA[A/G]GTGATTGAAATCATG | 5607 |
rs56090924 | snp | A/G | 0.0568808 | 0.158761 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592981 | AATGGCCAGGTAGGT[A/G]TTATTATATATTAAG | 5607 |
rs56151723 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637921 | GTTGATGTGTGTGTG[A/T]GTGTGTGTGTATGTG | 5607 |
rs56161894 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729186 | GGTAACCCATCAAAT[A/T]AAAATTACATTTTCA | 5607 |
rs56176575 | snp | C/T | | | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67806732 | GGAGGAGAGGCGGAG[C/T]CAGCAGGGGCCCCCG | 5607 |
rs56177977 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663802 | ATTGTTTGATCCCAG[A/G]AATTTGAGGTTACAG | 5607 |
rs56188779 | in-del | -/TGCAACCTCCAC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648661 | CACTGCAACCTCCAC[-/TGCAACCTCCAC]CTCCTGGGTTCAAGC | 5607 |
rs56204625 | snp | A/T | 0.316485 | 0.240998 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572085 | AGTGTCTAATCTAGC[A/T]TTGGGGACCAAAAAG | 5607 |
rs56206602 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797979 | TGAGCCACCATGCCC[A/G]GCCTAAAATGTTTTC | 5607 |
rs56211889 | in-del | -/T | 0.375 | 0.216506 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648578 | ATACGTTTTCAGTTC[-/T]TTTTTTTTTTTTGAA | 5607 |
rs56232683 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629113 | GTAGCAGCAGTAGCT[A/G]CGGCAGTGGCAGAAG | 5607 |
rs56241934 | snp | A/G | 3.29549e-05 | 0.00405911 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67585920 | GGGAACGGAACATAC[A/G]TGGCCTGAAGGTACG | 5607 |
rs56254481 | snp | C/T | 0.0233587 | 0.105516 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646390 | ATTTTTGTTACAGTG[C/T]GATTCATCATATATC | 5607 |
rs56264164 | snp | C/T | 0.293551 | 0.246177 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597635 | TTCATTTTGAAAAGT[C/T]GAATTAATATCCTTA | 5607 |
rs56283748 | in-del | -/C/CTGT/CTT/CTTTC/CTTTCT/CTTTCTTTC/CTTTCTTTCTTTC/CTTTCTTTTTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575919 | TTTCTTTCTTTCTTT[lengthTooLong]TTTTTTTTTTTTTTT | 5607 |
rs56304229 | in-del | -/TTAC | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629697 | TTCCTATCCTAACAC[-/TTAC]CAGATGAGAGGAAGA | 5607 |
rs56332896 | snp | C/T | 0.0532157 | 0.154195 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542465 | GTGACCGGGTCGCCG[C/T]GGGCGCTCTGTGGGC | 5607 |
rs56397260 | snp | A/T | 0.49998 | 0.00319482 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576932 | CCTATATATATATTT[A/T]TTTTTTTTTTTTTTG | 5607 |
rs56399438 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708605 | AGTAGCTAGGACTAC[A/G]GGTGTACCACTGCAC | 5607 |
rs56686937 | snp | A/C/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547111 | ACACACACACACAGA[A/C/T]TTCTGTCTAAACTGA | 5607 |
rs56689468 | snp | A/G | 0.305436 | 0.243776 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671703 | TTTTAGGGTACGTGT[A/G]CACAATGTGCAGGTT | 5607 |
rs56700149 | snp | A/G | 0.293294 | 0.246223 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575036 | GCAGAAGACAGGTCT[A/G]GGGTCTGATAGGGGA | 5607 |
rs56735059 | snp | C/T | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739261 | TTCCAGCCTGGGCAA[C/T]AGAGTGAGACCCTGT | 5607 |
rs56804212 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725939 | AACTGAGTCTCTCCC[C/T]TTTCCCTCCCCGTAC | 5607 |
rs56877523 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569033 | AACAAAAAAAAAAAA[A/C]AAAACTCTGTGGGCG | 5607 |
rs56896938 | in-del | -/C/TC/TCTTTCTTTC/TTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575922 | CTTTCTTTCTTTTTT[-/C/TC/TCTTTCTTTC/TTT]TTTTTTTTTTTTTTT | 5607 |
rs56916974 | snp | A/G | 0.43655 | 0.16643 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542213 | AGAACTATTTCTTGA[A/G]TTCTTGCCTTGCTCT | 5607 |
rs56936612 | in-del | -/GTGT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637931 | TGTGAGTGTGTGTGT[-/GTGT]ATGTGTGTTTTAGTA | 5607 |
rs56950303 | snp | G/T | 0.295343 | 0.245854 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582048 | TCCAATGATTAGGAT[G/T]TAGATGATTTCTTTT | 5607 |
rs56951899 | snp | A/G | 0.301177 | 0.244706 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582848 | CACACACACACACAC[A/G]CACACACTTCCAATG | 5607 |
rs57041894 | in-del | -/A | 0.170733 | 0.237101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796699 | TACATTGGTTTGGAA[-/A]TCATATTCTGTTTCT | 5607 |
rs57048756 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693141 | ATTTAGTGTTCATTT[C/G]ATTCTAGTAATGCAT | 5607 |
rs57075395 | snp | A/G | 0.459233 | 0.136827 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568796 | CGGATCATGAGGTCA[A/G]GAGATCGTGACCATC | 5607 |
rs57101762 | snp | A/G | 0.26078 | 0.249767 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681843 | TAAAATCAATGCCCT[A/G]GTATTCATTTGAGCT | 5607 |
rs57116318 | in-del | -/TAATAATAATAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686633 | TAATAATAATAATAA[-/TAATAATAATAA]CATGTTGTAGGGTTT | 5607 |
rs57175545 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774194 | GTGTGTGTGTGTGTG[A/T]GTGTGTGTGAGAGAA | 5607 |
rs57202916 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609414 | CTATAGACCTATTCT[A/G]TAGACCTATTCTATA | 5607 |
rs57236590 | snp | A/C | 0.158632 | 0.232706 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774209 | TGTGTGTGTGAGAGA[A/C]CATAGGTATTTAGAT | 5607 |
rs57488960 | snp | C/T | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740003 | GGGGGGAAGCTGTCT[C/T]AGAAATCTATAGAAC | 5607 |
rs57497468 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752095 | TTTGAGATGGAGTTT[G/T]GCTCTTGTTGCCCAG | 5607 |
rs57569689 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627725 | GTAGAATGTACCCTT[A/T]AAACAAGTGAATGTT | 5607 |
rs57576062 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695375 | TTCATTCAGATACCA[G/T]AATAGCTCATTTTTG | 5607 |
rs57594122 | in-del | -/A/AA | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585095 | AAAAAAAAAAAAAAA[-/A/AA]TCAAATTAATTCGTC | 5607 |
rs57643226 | in-del | -/A | 0.314301 | 0.241589 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759559 | CTCAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 5607 |
rs57650533 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612074 | TTATCTTTGGTTTTC[-/T]TTTTTTTTTTTTTTT | 5607 |
rs57683950 | snp | G/T | 0.311123 | 0.242413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551495 | GCACCACTATGCTTG[G/T]CTAATTTTTAAATTT | 5607 |
rs57701485 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590446 | TCTCTCCCTCCCTCC[-/T]CTCTCTCTCTCTCTC | 5607 |
rs57726475 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774171 | GATGTGTGTGTATGT[A/G]TGTGTGTGTGTGTGT | 5607 |
rs57751829 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787141 | AGATAGGCAGGCAGG[A/G]CGGACAACAGGACTG | 5607 |
rs57758699 | in-del | -/T | 0.413582 | 0.189052 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758519 | CTAAGTTCCTAGACA[-/T]TTTTATTTCTGTCTT | 5607 |
rs57874766 | snp | C/T | 0.212425 | 0.24716 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765251 | GTAGTCCCAGCTACT[C/T]GGGAGGCTAAGGCAG | 5607 |
rs57892823 | snp | C/T | 0.43598 | 0.167067 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542167 | AAGATGATGATCCTC[C/T]GAACCTGTGACTTGG | 5607 |
rs57950818 | in-del | -/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660186 | GGAGTAGAAGAAATG[-/T]TTTTTAATAATTTTG | 5607 |
rs57989358 | snp | A/G | 0.273856 | 0.248859 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635317 | GTAGCTGGGACTACA[A/G]GCGCCTGCCACCACG | 5607 |
rs58049670 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737869 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTGTCAC | 5607 |
rs58112756 | snp | G/T | 0.213333 | 0.247296 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765095 | GCTGGGTGCAGTGGC[G/T]CATGCCTGTAATCCC | 5607 |
rs58243841 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597187 | AAAGAAAAAAAAAAA[-/A]CTACTTGGTATTGTT | 5607 |
rs58351164 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741898 | TTTTTTTTTTTTTTT[-/T]GAGAGGGAGTCTTGC | 5607 |
rs58368149 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725540 | CATGTGAACAGAATT[A/C]TTCCATGGTCCCTGA | 5607 |
rs58386586 | in-del | -/AA/AAA | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541874 | AAAAAAAAAAAAAAA[-/AA/AAA]GATAACCAAGGTTTA | 5607 |
rs58498576 | in-del | -/CATGG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771152 | ACCATGTGTTTTACA[-/CATGG]TAATGTGTACCATGT | 5607 |
rs58511679 | snp | A/G | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735941 | AGCATGGGAAAGGAT[A/G]TGCTAGGTACTCAAG | 5607 |
rs58549750 | snp | C/T | 0.253544 | 0.249975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627800 | TCAGTCCTTTCTGCT[C/T]GTGGACGCCACAGAG | 5607 |
rs58551615 | snp | G/T | 0.164546 | 0.234942 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803683 | TGATGGGAGGAGGGG[G/T]AGTCAGTGACTCTCC | 5607 |
rs58554961 | snp | C/T | 0.0722614 | 0.17581 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663462 | TCCTTTTCTTTTTTT[C/T]ATTCAAGTTAAATCC | 5607 |
rs58568892 | snp | G/T | 0.0032524 | 0.0401948 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658512 | CAGTGCATTGTTCTG[G/T]TAATTTCATTTGTAG | 5607 |
rs58583153 | snp | A/G | 0.212122 | 0.247114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683709 | AGGTGGCAGTGAGCC[A/G]AGATCGCGCCATTGC | 5607 |
rs58648944 | snp | A/G | 0.495708 | 0.0461266 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672764 | TGAATGGTAATGCCT[A/G]GGTTTTCTTCTAGGG | 5607 |
rs58657384 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788989 | AAAAAAAAAAAAAAA[-/A]TTACACAGTACAGAA | 5607 |
rs58737858 | snp | C/G | 0.293551 | 0.246177 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582165 | CTCCCTGGTTCAAGT[C/G]ATTCTCCTGCCTCAG | 5607 |
rs58837886 | snp | A/G | 0.454544 | 0.143743 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558228 | AATGGTACCTGGCAC[A/G]TAATAGGCACTCTAT | 5607 |
rs58880046 | snp | C/G | 0.270351 | 0.24917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643507 | ACTGGTGTGCAGTGG[C/G]GTGATCTCAGCTCAC | 5607 |
rs58943445 | in-del | -/AACTCCTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551426 | AACCTTGAACTCCTG[-/AACTCCTG]GGCTTACACAATCCT | 5607 |
rs58979935 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575889 | CTGTCTCTGTTTTCT[-/C]TTCTTTTTTTCTTTC | 5607 |
rs59012209 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585077 | ATCTGAGAGAGGAGC[-/A]AAAAAAAAAAAAAAA | 5607 |
rs59069542 | snp | C/T | 0.181659 | 0.240478 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754456 | GGGACATTTATTGAG[C/T]TCCTCCTTGGGCTGT | 5607 |
rs59156911 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767812 | CCCATCCACCTCCGT[G/T]TTTCATGTCGTCTCT | 5607 |
rs59158437 | snp | C/T | 0.293037 | 0.246268 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591660 | AGGCATGAGCCACCG[C/T]GCCGGCCCCTTAACA | 5607 |
rs59195439 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630655 | TCATCTATAAAAGGA[C/G]GATAATAATGTATCA | 5607 |
rs59206402 | in-del | -/TCAACATGAGATTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555447 | ATTGGGGATCACTTT[-/TCAACATGAGATTT]GGAGGGGACAAATAT | 5607 |
rs59244439 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575896 | TGTTTTCTCTTCTTT[C/T]TTTCTTTCTTTCTTT | 5607 |
rs59269114 | in-del | -/CACACACACA/CACACACACACACA | 0 | 0 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547108 | ACACACACACACACA[-/CACACACACA/CACACACACACACA]GATTTCTGTCTAAAC | 5607 |
rs59315862 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744398 | TTTCTATTTAAGAGA[A/C]AATAATACAAGCTTG | 5607 |
rs59327254 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562988 | TTGGTTTTTAGTTCC[A/G]CTAACCAAACCTGTT | 5607 |
rs59466769 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561463 | CTCTCAGGACTGTGC[-/C]TTCTTCATTACTGCA | 5607 |
rs59493437 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787945 | TACTGCAGTCTATTA[A/C]CCAAAAATAATAAGG | 5607 |
rs59499364 | in-del | -/T | 0.0228947 | 0.104514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729282 | ATTCAGCTTGGCCAA[-/T]TTGTGAAATCCCCTA | 5607 |
rs59539616 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609811 | GACAGGATGGAATCA[G/T]TATGGGAAAATCTGG | 5607 |
rs59588886 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749908 | TTGCCTACCCAGTTT[C/T]GTGCACAGCCTTCTG | 5607 |
rs59750205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665086 | GGGGTCTTGCTCTGT[C/T]GGCCAGGTTGTTGTT | 5607 |
rs59837680 | in-del | -/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739295 | AAAAAAAAAAAAAAA[-/AA]GATAAAGTAAGTCAA | 5607 |
rs59913200 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734838 | AGGTCTTTAATCAAG[A/G]AAAAAATAGCAATGA | 5607 |
rs59949366 | snp | A/G | 0.237593 | 0.249692 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579150 | GCCTTCCAGAAGCAA[A/G]GGGGTACATGCTGTG | 5607 |
rs59953723 | in-del | -/T/TT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650529 | GTTTTTTTTTTTTTT[-/T/TT]AATTATGAAAGGGTA | 5607 |
rs59960942 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685724 | ATATTACTTGAAGGT[A/G]GACTGTAAGAAATTA | 5607 |
rs59966963 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576006 | CTCACTGCAACCTCT[A/G]CCTCCTGGGTTCAAG | 5607 |
rs59998974 | in-del | -/CACTCTCTCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590476 | TCTCTCTCTCTCTCT[-/CACTCTCTCT]TTGTTTCTTTTTGAG | 5607 |
rs60016009 | snp | A/G | 0.296873 | 0.245566 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548845 | AAAAAATCTCTTTTG[A/G]CTGTAATGAGCAAGG | 5607 |
rs60120818 | in-del | -/TG | 0.296873 | 0.245566 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551895 | GTACGGAAAGATATC[-/TG]TGAAATATTGTTGAA | 5607 |
rs60189100 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627855 | TCCCTGCTGTCATGT[C/T]TAAGTCAGAGTCTCC | 5607 |
rs60338025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651536 | CTTCCTTTCTCACTA[A/C]CCTTCTCAGTCTCTG | 5607 |
rs60344746 | snp | A/G | 0.266273 | 0.24947 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754190 | AGGTTTCTTTTTAGG[A/G]TGGTAGAAATATTTT | 5607 |
rs60375624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749708 | AAAAATGAAGGCATC[A/G]TCCTGAAACAAATGG | 5607 |
rs60404013 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695138 | GGGGGAGGGATGGCA[C/T]TGGGAGATATACCTA | 5607 |
rs60450892 | in-del | -/A | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723764 | TTTTTAAAAAAAAAA[-/A]CTAGACTTAAGCTGC | 5607 |
rs60745485 | snp | A/T | 0.170733 | 0.237101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796541 | GTGAGAACTCACTCC[A/T]TTCTTGAGAACTCCA | 5607 |
rs60924420 | snp | A/G | 0.302184 | 0.244493 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675964 | AATGCAAATGGAAGA[A/G]GATAGTTATTTCCCC | 5607 |
rs60932739 | in-del | -/C | 0.200708 | 0.245092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600654 | ATCCACAGCATGACA[-/C]CCTTTTTGTTTTTCT | 5607 |
rs60967453 | snp | C/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547109 | ACACACACACACACA[C/G]ATTTCTGTCTAAACT | 5607 |
rs60990642 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668833 | GAAGAAAAAAAAAAC[C/T]TATATAGTTGGTGTG | 5607 |
rs61023579 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728577 | AAATGATTCCCCAGT[G/T]TGTGGGGGAAATAAG | 5607 |
rs61067419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803531 | AGCCAGGCCAGCCCC[A/G]AGAATACTCCAGAAT | 5607 |
rs61081821 | snp | A/G | 0.252421 | 0.249988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571862 | AAATGTTTATTGGAT[A/G]GCAGTTCTCTGGCCA | 5607 |
rs61092657 | in-del | -/ACTCTCTC/TCTC | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590475 | CTCTCTCTCTCTCTC[-/ACTCTCTC/TCTC]TTTGTTTCTTTTTGA | 5607 |
rs61101319 | in-del | -/C | 0.462253 | 0.132093 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761244 | TCTATTTTTTCATTT[-/C]CTCTTCTTCCCTCCC | 5607 |
rs61177804 | snp | C/G | 0.0349115 | 0.127424 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718713 | AGGTTGCAGTGAGCC[C/G]AGATCATGCTACTGC | 5607 |
rs61223448 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576931 | CCCTATATATATATT[A/T]TTTTTTTTTTTTTTT | 5607 |
rs61245051 | in-del | -/T/TCTCTCTCTCTCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590445 | CTCTCTCCCTCCCTC[-/T/TCTCTCTCTCTCT]CCTCTCTCTCTCTCT | 5607 |
rs61247537 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668923 | AACTTTTTAAAAATA[C/T]GTTTTTGCAGAAATT | 5607 |
rs61286997 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552168 | TCATTGCCTGTTTTT[A/T]AAAGCTATAATGAGT | 5607 |
rs61414248 | snp | A/T | 0.322007 | 0.239405 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621060 | CTGTATTGGGAGAAA[A/T]TTTAAAATACCAAGA | 5607 |
rs61416098 | snp | C/T | 0.117886 | 0.21224 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734473 | ATAGAGTAGAAAGCA[C/T]ATGTTCTTAAAACTA | 5607 |
rs61439988 | in-del | -/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682235 | CTATTTTTTTTTTTT[-/T]AAGATAGAGTCTTGT | 5607 |
rs61493121 | in-del | -/AA | 0.41408 | 0.188621 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794656 | GGAACATCACAGCTG[-/AA]AAAAAAAAAAAAAAA | 5607 |
rs61495402 | in-del | -/GA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774208 | TGTGTGTGTGAGAGA[-/GA]ACATAGGTATTTAGA | 5607 |
rs61558595 | in-del | -/A | 0.199564 | 0.24486 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769107 | AGTAAAAAAAAAAAA[-/A]TTGATCCAAATTATT | 5607 |
rs61584395 | snp | C/T | 0.223522 | 0.248594 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707113 | GTAGAGACAGGGTTT[C/T]ACCATGTTAGCCAGG | 5607 |
rs61618811 | snp | A/G | 0.305934 | 0.243663 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576635 | AGCTTATTGATTATC[A/G]CTGCAGTTACTGCAT | 5607 |
rs61664255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613245 | GAACAGTGCAGAAAA[C/T]TTAAAAGACTGGCTT | 5607 |
rs61667787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570794 | ATTGATTATTGCTGT[A/C]ATTACTGACTGAGCT | 5607 |
rs62015101 | snp | A/G | 0.327914 | 0.237549 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540951 | GTTGGTTTTCCCCAC[A/G]GTACTTCGAATAAAA | 5607 |
rs62015102 | snp | C/T | 0.0267878 | 0.112589 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541722 | GTAGTCCCAGTTACT[C/T]GGCAGGGGTTGGGGG | 5607 |
rs62015105 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542730 | CTCCTCTCGCCGCTA[C/T]CGCCGTCGCCGCCGC | 5607 |
rs62015106 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542737 | CGCCGCTACCGCCGT[C/T]GCCGCCGCCGCAGCC | 5607 |
rs62015107 | snp | A/G | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548626 | GAGAGCTAGCATCCA[A/G]CTGTAGCTGTTTGGC | 5607 |
rs62015108 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549659 | ATTTTTTTCCCAGAG[A/G]TTCAGACCTACGTCA | 5607 |
rs62015110 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551533 | AGATGGGGTCTTGCT[A/C]TGTTGTCCAGGCTAG | 5607 |
rs62015111 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553628 | ATGTTTAAGAAATAG[C/T]TGAGGCCGGGCGTGG | 5607 |
rs62015112 | snp | C/T | 0.319616 | 0.240112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553641 | AGTTGAGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 5607 |
rs62015113 | snp | A/G | 0.319616 | 0.240112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553685 | TTGGGAGGCCGAGGC[A/G]GGTGGATCATGAGGT | 5607 |
rs62015147 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567592 | GATGGTCTCGATCTC[C/T]TGACCTCATGATCCA | 5607 |
rs62015148 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569078 | AGTTTTGTCCTTACC[C/T]ACAAGGCTGTGTTTT | 5607 |
rs62015152 | snp | A/G | 0.205417 | 0.245993 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576638 | TTATTGATTATCGCT[A/G]CAGTTACTGCATGTA | 5607 |
rs62015155 | snp | C/T | 0.175897 | 0.238765 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587118 | GAGTGACGTTTCTGT[C/T]TTGACCTGAAGAAGC | 5607 |
rs62015157 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592066 | TGGTGAGCCGAGATC[A/G]CACCATTGTACTTTG | 5607 |
rs62015158 | snp | C/T | 0.175897 | 0.238765 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592366 | ATAAAATTGGTATTT[C/T]CCCCATTTTACAGAA | 5607 |
rs62015159 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592748 | GGTTTTAGTCTCTTT[A/G]TTTGATACCTTTTGC | 5607 |
rs62015163 | snp | A/C | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735189 | TCATTATTTTATTTG[A/C]TTAGCCTATGCCAGA | 5607 |
rs62015164 | snp | A/C | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735298 | TAGAAATGTGAAATT[A/C]TTCATTAAAGATAAA | 5607 |
rs62015165 | snp | C/G | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735546 | TGCTCTCAAAAGAGT[C/G]CAGTCCAGTTGGAAG | 5607 |
rs62015167 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736172 | GTCAGGATGGAGATG[A/G]CAAGTGTAGCAGGGA | 5607 |
rs62015168 | snp | A/T | 0.229136 | 0.249128 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738332 | GGTAAAATCCTTTAA[A/T]CAAAAGAAAGTTCCT | 5607 |
rs62015169 | snp | G/T | 0.0693013 | 0.172766 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739751 | CACCCAAAGTGCTAG[G/T]ATTACAGGCATGAGC | 5607 |
rs62015171 | snp | C/T | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740860 | TGGCGAAACCCCGTC[C/T]CTACTAAAAATACAA | 5607 |
rs62015172 | snp | C/T | 0.229136 | 0.249128 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741258 | TTCAGGCAGCTTTCA[C/T]GTCCAGGTAACAGAA | 5607 |
rs62015173 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742574 | AAACTGGATTCTAAA[A/G]TAAGGCCACCCTTCT | 5607 |
rs62015175 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746400 | AAATAACTCCGTTGT[C/T]GAAGCAGATATATCT | 5607 |
rs62015176 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750180 | ATGAAGATTGATGAA[A/G]AACAATAATGTGTAA | 5607 |